Re: [Biofuel] Methanol as a motor fuel

2014-11-26 Thread Jan Warnqvist
Darryl, methanol is already used as motor fuel in Indy Car and Speedway. 
Metanol is similar to ethanol, but more. It means that of all properties 
that ethanol has, methanol has more of them. Methanol is slightly more 
corrosive than water and has an oxygene content of 50% by weight. The flash 
point is slightly lower than for ethanol. Incomplete combustion of methanol 
generates formaldehyde and other toxic substances. It is also known that 
methanol can cause wear in excess in connection with the motor oil , unless 
the oil is specially suited for methanol. Your vehicle will consume double 
the amount of fuel compared to gasoline and cold starts will be very 
difficult unless you add some gasoline to the metanol fuel.
However, you can expect a very high fuel effiency if your motor is fully 
adapted to the methanol fuel.
That is the brief version, I also have designed a method for purification of 
sulfate methanol (derived from paper pulping) but that technology is 
currently classfied due to pending patent.

I hope this information did not scar you off, but increased your curiosity.

Best
Jan Warnqvisr

-Ursprungligt meddelande- 
From: Darryl McMahon

Sent: Wednesday, November 26, 2014 4:03 PM
To: Sustainablelorgbiofuel@lists.sustainablelists.org
Subject: [Biofuel] Methanol as a motor fuel

In Canada, it is illegal to produce ethanol for fuel without a federal
permit, and these are effectively never granted to a home brewer.

I have been pondering the idea of using methanol (wood alcohol) as an
alternative to ethanol fuel, but have not taken the time to research it.

Has somebody else already done this, and can save me the effort?

My recollection is it is possible to use methanol as a motor fuel, which
is supported by this document.

https://web.anl.gov/PCS/acsfuel/preprint%20archive/Files/20_2_PHILADELPHIA_04-75_0059.pdf

I know that during the war years (1939 to 1945), a number of people ran
engines on wood gas (the images of large gas bladders on vehicle roof
racks come easily to mind).

I do have access to wood waste and fruit waste material, but working
space is at a premium.  Also, the processes I see seem to be based on
having process heat available (e.g., for pyrolysis).  However, I don't
think I need a lot - our third vehicle travels about 400 km a month, and
I figure the methanol will only displace about 20 litres a month of
gasoline at a maximum, probably less.

I can buy methanol commercially, but in small quantities (retail), it is
more expensive than gasoline.  However, could be an option for
experimentation in the vehicle before committing to home production.

I also have not yet investigated regulatory and safety issues, but
expect the latter to be manageable.

Thoughts, experience, pointers to relevant experience or information?


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Re: [Biofuel] Keith Addison passed away

2014-11-07 Thread Jan Warnqvist
My sincere condolences to you Midori. Keith´s life work has been of immense 
importance to many people and we are all in debt to him for his comittment 
and doings.


Jan Warnqvist

-Ursprungligt meddelande- 
From: David Penfold

Sent: Thursday, November 06, 2014 2:28 PM
To: sustainablelorgbiofuel@lists.sustainablelists.org
Subject: Re: [Biofuel] Keith Addison passed away

Sincere condolences to you, Midori, and anyone who knew Keith.

He has been an inspiration and helped spark my interest in many
alternative technologies.

David Penfold
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Re: [Biofuel] Used mustard oil is the new source of bio-diesel, thanks to AMU students

2014-04-01 Thread Jan Warnqvist
Interesting. Mustard oil have usually high levels of erucic acid (C22:1) 
and is usually disregarded by biodieselers because of that content. It is 
assumed that biodiesel with erucic acid is hard to comply to both EN and 
ASTM standards due to the increased boiling point and decreased ester 
content. The thumb rule is, that longer the fatty acid chain, the more 
difficult the alkylation.  Would be nice to see some data from their 
experiments.


-Ursprungligt meddelande- 
From: Darryl McMahon

Sent: Tuesday, April 01, 2014 7:18 PM
To: Sustainablelorgbiofuel@lists.sustainablelists.org
Subject: [Biofuel] Used mustard oil is the new source of bio-diesel,thanks 
to AMU students


http://ibnlive.in.com/news/used-mustard-oil-is-the-new-source-of-biodiesel-thanks-to-amu-students/461853-3-242.html

Used mustard oil is the new source of bio-diesel, thanks to AMU students

Apr 01, 2014 at 07:21pm IST

A group of engineering students from Aligarh Muslim University have
succeeded in extracting bio-diesel from refined and used mustard oil,
university officials said on Tuesday.

Third-year students of the Diploma in Engineering at the AMU Polytechnic
designed a bio-diesel extraction plant as part of the recently developed
Alternative Fuel and Combustion Engineering Lab, said M. Yunus Khan,
assistant professor of mechanical engineering.

The process can help in directly replacing diesel in conventional
engines, thereby reducing India's dependence on imported oil and
emissions of various pollutants, officials said.

Bio-diesel is a renewable fuel derived from vegetable oil that can be an
additive to or entirely replace diesel in engines.
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Re: [Biofuel] Tar Sands Report

2012-05-16 Thread Jan Warnqvist
Hello Keith. Glad to have you back.

Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Wednesday, May 16, 2012 1:43 AM
Subject: Re: [Biofuel] Tar Sands Report


 Hi Robert

 And then there's this...

 http://truth-out.org/news/item/8403-keystone-xls-dirty-little-secret

 Keystone XL's Dirty Little Secret

 Monday, 09 April 2012 09:18

 By Jim Hightower, OtherWords | News Analysis

 The people and companies pushing the tar-sands pipeline don't want
 you to know that most of this oil won't be made into gasoline for our
 vehicles.

 It's certainly true, declared Energy Secretary Stephen Chu, that
 having Canada as a supplier for our oil is much more comforting than
 to have other countries supply our oil.

 He was referring to the Canadian tar sands oil that TransCanada
 Corporation intends to move through the Keystone XL pipeline it wants
 to build from Alberta to refineries on the Texas Gulf Coast. He and
 lobbyists for the pipeline assert that filling America's gas tanks
 with fuel derived from Canadian crude will cut U.S. dependency on the
 oil we get from unstable and unfriendly nations.

 Good point! If it were true. However, ask yourself this question: why
 go to the expense of piping this stuff 2,000 miles through six
 states, endangering water supplies and residents with inevitable
 toxic spills, when there are oil refineries much closer to Canada in
 the Midwest? What's the advantage of sending Canadian crude to
 refineries way down in Port Arthur, Texas? Aha - because it's a port!

 What the pushers of Keystone want to keep secret from you and me is
 that this oil will not be made into gasoline for our vehicles. Most
 of it will be refined into diesel and jet fuel and exported to
 Europe, China, and Latin America.

 The claim that the pipeline will reduce our reliance on OPEC is an
 outright lie. Such oil giants as Valero, Motiva, and Total have
 already rejiggered their Port Arthur refineries specifically to make
 diesel and jet fuel, nearly all of which will then be piped into
 tanker ships at the port and sent abroad. In presentations to
 investors, Valero openly touts its export strategy, even showing
 world maps with convenient arrows pointing from Port Arthur to its
 foreign customers.

 You'd think our energy secretary would know this dirty little secret
 and come clean with the American people.

 National radio commentator, writer, public speaker, and author of the
 book, Swim Against The Current: Even A Dead Fish Can Go With The
 Flow, Jim Hightower has spent three decades battling the Powers That
 Be on behalf of the Powers That Ought To Be - consumers, working
 families, environmentalists, small businesses, and just-plain-folks.


Interesting reading . . .

http://forestethics.org/downloads/FEA_Tar_Sands_funding_briefing.pdf

Robert Luis Rabello
Adventure for Your Mind
http://www.newadventure.ca

Meet the People video:
http://www.youtube.com/watch?v=txsCdh1hZ6c

Crisis video:
http://www.youtube.com/watch?v=mZedNEXhTn4

The Long Journey video:
http://www.youtube.com/watch?v=vy4muxaksgk


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Re: [Biofuel] Bio Engine Oil

2012-01-22 Thread Jan Warnqvist
Hello Keith and all. I can answer that question. A few years back I visited 
a company recycling engine oil and they managed to remove the inorganic 
content (water, metals, old additives etc) from the oil ending up with a 
clear and bright base oil which was analyzed as such (viscosity etc) and 
then sold back to the lubricant manufacturers as base oil. It seems that the 
base oil is very stable but this recycling should not be possible for 
indefinite time, since nature has its course, eventually cracking the oil 
into different other products. It´s a way of prolonging the life of the 
petro industry.

Best to you all
Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, January 22, 2012 1:54 AM
Subject: Re: [Biofuel] Bio Engine Oil


 Hi Zeke

 Is filtering all that's required? Filtering what, I wonder, little
 bits of engine that get worn off? Isn't that what the oil is supposed
 to prevent? By the time it needs changing, isn't the oil itself
 somewhat worn out, having been subjected to all that heat and high
 pressure?

 Just asking.

 Regards

 Keith


Bio based, no... but I have seen, in the last few months, introduction of 
a
whole line of recycled engine oils in the local auto parts stores here.
I'm not really sure what the recycled content is percentage wise, but
apparently it's using old engine oil, filtering all the bad stuff out, and
adding back in the additives that have been used up.  It's supposed to 
meet
the same standards as new petro-based engine oil.

Z

On Sat, Jan 21, 2012 at 7:29 AM, Jan Warnqvist 
[EMAIL PROTECTED] wrote:

  Hello Keith et al.
  I am not surprised on the market non-introduction of castor oil 
 lubricants.
  Castor oil, although a classic, is not ideal as a raw material for
  lubricant
  formulations. The castor oil has two hydroxyl groups on the fatty acid
  (ricinic acid) chain which will want to polymerize and releasing water 
 into
  the system, giving the lubricant an unnecessary short life. What 
 attracts
  the lubricant inventors is the high viscosity and the expected high
  viscosity index of the oil which both looks promising enough. But I 
 would
  prefer a more stable material to start with and then adjusting the
  viscosity
  values chemically.
  A good lubricant consist from a base oil and then added a number of
  additives in order to adjust the properties of the lubricant. It is 
 then
  preferable to bring as favourable properties already in the base oil in
  order to minimize the addition of additives.

  Best to you all
  Jan W
  - Original Message -
  From: Keith Addison [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Sent: Saturday, January 21, 2012 2:13 PM
  Subject: Re: [Biofuel] Bio Engine Oil


   Hi Chris and Dawie
  
   The answer seems to be No. Sorry to say.
  
   It was first discussed here in 2001. Lots of interesting stuff in the
   list archives:
   http://www.mail-archive.com/biofuel@sustainablelists.org/
  
   Try bio engine oil or biolubricant.
  
   (Don't forget, the whole thread is hotlinked at the end of each 
 find.)
  
   If you do a web search, you'll find lots of talk, lots of products
   that are simply biodegradeable, green lubricants to replace the
   likes of WD-40 or 2-stroke oil, and a few commercial bio engine oils,
   with claims that they're made from renewable resources but they don't
   say what, or they're a marriage of renewables (pig fat) and
   nano-tech, or whatever, but nothing DIYable.
  
   I knew some people in Japan who were making bio engine oil from
   castor oil. They wouldn't tell me how they were doing it, but they
   gave me a bottle of it. Clear, light yellow, sort of oily smell. But
   after a while it started degrading, whisps of cloudiness started
   appearing. Not perfect, and they never brought a product to market.
  
   Still, castor oil is probably the best bet. It's strange stuff - give
   this a read:
   http://www.georgiacombat.com/CASTOR_OIL.htm
  
   IIRC Brazil's Petrobras had plans for producing castor oil-based
   engine oil, but I can't find any details.
  
   HTH, and good luck - best
  
   Keith
  
  
  This is something I've also been wondering about.-D
  
  
From: C Pinelli [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Sent: Saturday, 21 January 2012, 1:56
  Subject: [Biofuel] Bio Engine Oil
  
  
  Hi all.
  I'm still new to biofuels but have been making biodiesel and
  ethanol for my vehicles for a few months now and am thrilled with
  it. However, I can't stand filling up my gas tank with home made,
  environmentally friendly fuel, then changing the oil with expensive
   petroleum. So, I have been doing some research into making
  Bio-Engine Oil, it seems possible which makes me very enthusiastic.
  
  Does anybody know anything about making vegetable based motor oil?
  Or does anybody have any experience with using it?
  
  Thanks very much

Re: [Biofuel] Bio Engine Oil

2012-01-21 Thread Jan Warnqvist
Hello C Pinelli et al. The lubricant industry is not very interested in 
bringing in new raw materials (e.g. vegetable oils and/or derivates) since 
there are standards on the final lubricants that have to be met. Taking in 
new materials may make it necessary to formulate new standards, which is a 
time-consuming and costly process, however not carrying that new standards 
is equal to lack of quality.
In contrast to the petro fuel industry, the lubricant industry was awake 
concerning EU regulation proposals and managed to stop a proposal similar to 
the one on the fuel , demanding a certain amount of renewable material of 
the total sales. Instead came an EU regulation regarding special labelling 
of renewable lubricants in the EU, which they have to apply to get. I have 
seen nothing of this labelling out in the shops so far, and this regulation 
is since 2004 or 2005.
So, similar to the biodesel industry, it takes new actors on the market to 
make it happen. With financial strength and patience, of course.
I have developed a nice vegetable based two-stroke oil (which is among the 
most difficult to formulate, due to the high working temperatures) which is 
still pending for market introduction. So there it is. Any comments ?

With best to everybody
Jan W
- Original Message - 
From: C Pinelli [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, January 21, 2012 12:56 AM
Subject: [Biofuel] Bio Engine Oil



 Hi all.
 I'm still new to biofuels but have been making biodiesel and ethanol for 
 my vehicles for a few months now and am thrilled with it. However, I can't 
 stand filling up my gas tank with home made, environmentally friendly 
 fuel, then changing the oil with expensive petroleum. So, I have been 
 doing some research into making Bio-Engine Oil, it seems possible which 
 makes me very enthusiastic.

 Does anybody know anything about making vegetable based motor oil? Or does 
 anybody have any experience with using it?

 Thanks very much
 Chris

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Re: [Biofuel] Bio Engine Oil

2012-01-21 Thread Jan Warnqvist
Hello Keith et al.
I am not surprised on the market non-introduction of castor oil lubricants. 
Castor oil, although a classic, is not ideal as a raw material for lubricant 
formulations. The castor oil has two hydroxyl groups on the fatty acid 
(ricinic acid) chain which will want to polymerize and releasing water into 
the system, giving the lubricant an unnecessary short life. What attracts 
the lubricant inventors is the high viscosity and the expected high 
viscosity index of the oil which both looks promising enough. But I would 
prefer a more stable material to start with and then adjusting the viscosity 
values chemically.
A good lubricant consist from a base oil and then added a number of 
additives in order to adjust the properties of the lubricant. It is then 
preferable to bring as favourable properties already in the base oil in 
order to minimize the addition of additives.

Best to you all
Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, January 21, 2012 2:13 PM
Subject: Re: [Biofuel] Bio Engine Oil


 Hi Chris and Dawie

 The answer seems to be No. Sorry to say.

 It was first discussed here in 2001. Lots of interesting stuff in the
 list archives:
 http://www.mail-archive.com/biofuel@sustainablelists.org/

 Try bio engine oil or biolubricant.

 (Don't forget, the whole thread is hotlinked at the end of each find.)

 If you do a web search, you'll find lots of talk, lots of products
 that are simply biodegradeable, green lubricants to replace the
 likes of WD-40 or 2-stroke oil, and a few commercial bio engine oils,
 with claims that they're made from renewable resources but they don't
 say what, or they're a marriage of renewables (pig fat) and
 nano-tech, or whatever, but nothing DIYable.

 I knew some people in Japan who were making bio engine oil from
 castor oil. They wouldn't tell me how they were doing it, but they
 gave me a bottle of it. Clear, light yellow, sort of oily smell. But
 after a while it started degrading, whisps of cloudiness started
 appearing. Not perfect, and they never brought a product to market.

 Still, castor oil is probably the best bet. It's strange stuff - give
 this a read:
 http://www.georgiacombat.com/CASTOR_OIL.htm

 IIRC Brazil's Petrobras had plans for producing castor oil-based
 engine oil, but I can't find any details.

 HTH, and good luck - best

 Keith


This is something I've also been wondering about.-D


  From: C Pinelli [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, 21 January 2012, 1:56
Subject: [Biofuel] Bio Engine Oil


Hi all.
I'm still new to biofuels but have been making biodiesel and
ethanol for my vehicles for a few months now and am thrilled with
it. However, I can't stand filling up my gas tank with home made,
environmentally friendly fuel, then changing the oil with expensive
petroleum. So, I have been doing some research into making
Bio-Engine Oil, it seems possible which makes me very enthusiastic.

Does anybody know anything about making vegetable based motor oil?
Or does anybody have any experience with using it?

Thanks very much
  Chris


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Re: [Biofuel] How do I get the paper thin white layer

2011-09-17 Thread Jan Warnqvist
One suggestion is that if you have a lot of methanol in excess, the wash 
test will form an emulsion, since the methanol is soluble both in water and 
in biodiesel. But it will pass my test. And it did ?
- Original Message - 
From: Ian and Jubilee Miller [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Friday, September 16, 2011 8:55 PM
Subject: Re: [Biofuel] How do I get the paper thin white layer


I just reprocessed this last batch using 100ml of methanol and 5.5g KOH. It
 turned darker and there are little cooties floating around in it. Also,
 nothing settled out. Upon doing the wash test, it immediately formed an
 emulsion, although the methanol test yields a nice clear phase with no
 settle material. I am confused. I'm going to move on and make another 
 batch,
 but I'd like to know what went wrong so I can at least learn something. 
 Any
 ideas?

 On Sat, Sep 10, 2011 at 10:10 AM, Ian and Jubilee Miller 
 [EMAIL PROTECTED] wrote:

 I've let the BD separate for over 24 hours, which I thought should be
 enough time. My method for separating could be suspect. I'm decanting out 
 of
 a settling bottle and tried to be careful, but it is possible that some
 glycerine sneaked past. I think getting a better set up going is going to
 make it a lot easier to be consistent.

 I just put my third batch through the methanol and wash tests and this 
 time
 I've got some settling in the methanol so I think I'm going to reprocess 
 it.
 The wash test turned out the same. Here's a link to a picture:
 https://picasaweb.google.com/ianandjubilee/Biodiesel?authuser=0authkey=Gv1sRgCNSD4sbwsfyjYAfeat=directlink

 I also was wondering it our water softener could have an effect. Could
 softened water create more of a problem?

 Thanks for the help,

 Ian


 On Sat, Sep 10, 2011 at 8:44 AM, Jan Warnqvist 
 [EMAIL PROTECTED] wrote:

 Hello C Pinelli. Did you check the FFA and water contents on your raw
 material before processing ? FFA levels above 5 mg KOH/g (2,5%) will
 produce
 a lot of soaps, making the processing bad and the separation even worse.
 The
 water content will promote the soap production and will also compete 
 with
 the methanol. The highest acceptable water content is around 1,5% and 
 the
 lower the better.
 - Original Message -
 From: C Pinelli [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Saturday, September 10, 2011 3:26 PM
 Subject: Re: [Biofuel] How do I get the paper thin white layer


 
  I am having a similar problem, I have experience making ethanol
  successfully, but I'm new to biodiesel.
  I've been trying to get it right for some time with many many test
  batches, without too much success.
  I've followed the instructions as closely as possible, but still can't
  quite get it right. I use 90% KOH Flakes,
  a scale thats accurate to the hundreth of a gram, and am incredibly
  meticulous in my measurements.
  I've had mixed (but mostly good)results with the methanol test, but 
  have
  never consistantly passed the
  wash test. Sometimes I get a very thick separation line between the 
  two,
  sometimes I get clear water on
  the bottom with a yellowy mayo like substance on top. Sometimes it 
  seems
  to have the reverse result,
  where it appears to be clear biodiesel on top, with very murky white
 water
  underneath.
 
  I've tried various amount of KOH and methanol, and varying my 
  processing
  times, but I can't seem to get it
  down. As soon as my schedule permits, I'm going to try to get some new
  chemicals, because im worried
  that my lye might be water contaminated.
 
  Any help deciphering these results would be really appreciated.
 
 
  Date: Wed, 7 Sep 2011 12:51:30 -0500
  From: [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Subject: [Biofuel] How do I get the paper thin white layer
 
  Hello to all. I've made two test batches of biodiesel using new oil
 using
  the instructions on the JTF site, which I've read and re-read, along
 with
  many of the mailing list posts. I'm enjoying everything I'm learning,
 but
  still have a ton to learn. I also have a question. In both my test
  batches
  I've performed the quality tests recommended. The fuel passes the
  methanol
  test fine, with no glycerine settling out. When I come to the wash
 test,
  I
  have perhaps an eighth of an inch of white foam between the water and
 the
  biodiesel. It separates quite well though. I've tried to follow all
  instructions to the letter and I ordered my chemicals from 
  DudaDiesel,
 so
  I
  assume they are a good quality. I assume the foam is soap. It could 
  be
  that
  my measurements aren't precise enough, but if they aren't it's 
  because
 of
  my
  instruments. I have been very meticulous in my measurements.
 
  I've gone ahead and washed the biodiesel from both batches, and they
 also
  have a lot of white foam, although they also separate very quickly.
 With
  both batches I've just kept washing until there's

Re: [Biofuel] How do I get the paper thin white layer

2011-09-10 Thread Jan Warnqvist
Hello C Pinelli. Did you check the FFA and water contents on your raw 
material before processing ? FFA levels above 5 mg KOH/g (2,5%) will produce 
a lot of soaps, making the processing bad and the separation even worse. The 
water content will promote the soap production and will also compete with 
the methanol. The highest acceptable water content is around 1,5% and the 
lower the better.
- Original Message - 
From: C Pinelli [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Saturday, September 10, 2011 3:26 PM
Subject: Re: [Biofuel] How do I get the paper thin white layer



 I am having a similar problem, I have experience making ethanol 
 successfully, but I'm new to biodiesel.
 I've been trying to get it right for some time with many many test 
 batches, without too much success.
 I've followed the instructions as closely as possible, but still can't 
 quite get it right. I use 90% KOH Flakes,
 a scale thats accurate to the hundreth of a gram, and am incredibly 
 meticulous in my measurements.
 I've had mixed (but mostly good)results with the methanol test, but have 
 never consistantly passed the
 wash test. Sometimes I get a very thick separation line between the two, 
 sometimes I get clear water on
 the bottom with a yellowy mayo like substance on top. Sometimes it seems 
 to have the reverse result,
 where it appears to be clear biodiesel on top, with very murky white water 
 underneath.

 I've tried various amount of KOH and methanol, and varying my processing 
 times, but I can't seem to get it
 down. As soon as my schedule permits, I'm going to try to get some new 
 chemicals, because im worried
 that my lye might be water contaminated.

 Any help deciphering these results would be really appreciated.


 Date: Wed, 7 Sep 2011 12:51:30 -0500
 From: [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Subject: [Biofuel] How do I get the paper thin white layer

 Hello to all. I've made two test batches of biodiesel using new oil using
 the instructions on the JTF site, which I've read and re-read, along with
 many of the mailing list posts. I'm enjoying everything I'm learning, but
 still have a ton to learn. I also have a question. In both my test 
 batches
 I've performed the quality tests recommended. The fuel passes the 
 methanol
 test fine, with no glycerine settling out. When I come to the wash test, 
 I
 have perhaps an eighth of an inch of white foam between the water and the
 biodiesel. It separates quite well though. I've tried to follow all
 instructions to the letter and I ordered my chemicals from DudaDiesel, so 
 I
 assume they are a good quality. I assume the foam is soap. It could be 
 that
 my measurements aren't precise enough, but if they aren't it's because of 
 my
 instruments. I have been very meticulous in my measurements.

 I've gone ahead and washed the biodiesel from both batches, and they also
 have a lot of white foam, although they also separate very quickly. With
 both batches I've just kept washing until there's no more white junk and 
 the
 water is clear. Does this take care of the soap (if that's what it is), 
 or
 is there still something to be concerned about? Also, any suggestions on 
 how
 to get that paper thin white layer instead of the thicker one I have 
 now?
 I'm using new oil, what I think are quality chemicals, and I'm being as
 meticulous as I know how to be. As far as I know, I'm following your
 instructions to the letter.

 I thank you for your help,

 Ian
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Re: [Biofuel] Ethanol and gasoline

2011-09-02 Thread Jan Warnqvist
Hello Keith and all. I agree with you to some extent. Gasoline is a 
non-polar mix of 100:s and 100:s of hydrocarbons. In order to be corrosive 
there has to be
a) metal ions (Lewis acids) producing a low pH and
b) water or other polar compounds in the system.
Anhydrous ethanol stays anhydrous reasonably long assuming that it is kept 
in a closed vessel, preferably with dehydration air filters.
No I have not heard if Absolut is into juridical problems. But me, I prefer 
Lithuanian Gold vodka or Wyborowa, so it does not matter.
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, August 29, 2011 10:44 PM
Subject: Re: [Biofuel] Ethanol and gasoline


 Hij Jan

 Thanks for your reply.

 What I was asking about is the 4% (4.37%) water in the azeotrope mix
 that won't separate from the water by distillation. When 190-proof
 ethanol is blended with gasoline, the overall proportion of water is
 even lower. Zeolite will remove the last of the water, but it's
 another processing step and you have to buy it, and how long will the
 ethanol stay absolute?

 I thought that today's engines were built to resist rust and
 corrosion. Gasoline is also corrosive.

 There's also this, in a previous message:

 Biodiesel as an anti-wear and smog additive for gasoline fuel is
 very encouraging. - Franklin Del Rosario, January 2004, Biodiesel
 in gasoline engines - scroll down the page to Biodiesel in 4-stroke
 gasoline engines
 http://journeytoforever.org/biodiesel_make2.html#gas

 It sounds like a good ethanol additive too.

 Has Absolut Vodka been sued yet for making false advertising claims?
 :-) Since it sure isn't absolute. Is it still just as good now that
 it's French? Somebody once gave me a bottle of 100-proof Absolut,
 wonderful stuff.

 All best

 Keith


Hello all. I wish to comment that like this:
Gasoline engines are sensitive to water, too sensitive to accept anything
but a very small portion of water containing alcohol in the gasoline. Any
alcohol blend in gasoline should originate from anhydrous alcohol.The fact
that ethanol in water is corrosive does not make it better. Some of the
ethanol will drop a hydrogen atom to the water and create acid and an
ethoxide ion, both are aggressive.
The diesel engines, as a contrast, can accept up to four per cents of 
water
without even long-term problems. But then the engine in question has to be
prepared for ethanol as fuel, of course.
Best regards
Jan W
- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, August 28, 2011 6:59 PM
Subject: [Biofuel] Ethanol and gasoline


  Hi all

  Would someone who has David Blume's Alcohol Can Be a Gas! please
  look up something for me? I can't get at my copy at the moment.

  What does Mr Blume say about blending 95% ethanol (190-proof) with
  gasoline? Miscible or not?

  Thanks!

   Keith


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Re: [Biofuel] Ethanol and gasoline

2011-08-28 Thread Jan Warnqvist
Hello all. I wish to comment that like this:
Gasoline engines are sensitive to water, too sensitive to accept anything 
but a very small portion of water containing alcohol in the gasoline. Any 
alcohol blend in gasoline should originate from anhydrous alcohol.The fact 
that ethanol in water is corrosive does not make it better. Some of the 
ethanol will drop a hydrogen atom to the water and create acid and an 
ethoxide ion, both are aggressive.
The diesel engines, as a contrast, can accept up to four per cents of water 
without even long-term problems. But then the engine in question has to be 
prepared for ethanol as fuel, of course.
Best regards
Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, August 28, 2011 6:59 PM
Subject: [Biofuel] Ethanol and gasoline


 Hi all

 Would someone who has David Blume's Alcohol Can Be a Gas! please
 look up something for me? I can't get at my copy at the moment.

 What does Mr Blume say about blending 95% ethanol (190-proof) with
 gasoline? Miscible or not?

 Thanks!

 Keith

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Re: [Biofuel] The Green Revolution Backfires: Sweden's Lesson for Real Sustainability

2011-06-12 Thread Jan Warnqvist
Hello all, sincerely Swedish I have never heard of this article. Neither 
have I heard any of the conclusions in the article. The truth is that people 
driving flexible fuel cars fill with gasoline if the gasoline is cheaper 
than the E85 (15% gasoline, 85% ethanol). It is also true that the diesel 
car sector has been growing rapidly during the past years. But that was from 
a very low level, seen from European standards. How that can increase the 
CO2 is a riddle. The big CO2 cut is however in  heat production. The heat 
power plants producing hot water for houses and flats are nowadays almost 
exclusively burring CO2 neutral fuels, such as waste vegetable oils.
I do not think that the article has been published in Sweden, even though 
there are, even here, strong forces aiming to turn the energy consumption 
back to only fossil fuels and - in worst case- nuclear power. I suppose they 
are fighting that battle in other countries too.

Jan W
- Original Message - 
From: Darryl McMahon [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Sunday, June 12, 2011 3:20 PM
Subject: Re: [Biofuel] The Green Revolution Backfires: Sweden's Lesson for 
Real Sustainability


 Something is rotten in the state of Sweden.  Or not.  But I do smell a
 dead rat in here somewhere.

 We have studies from the U.S. that switching from petro-fuel to
 electricity for transportation reduces emissions, including greenhouse
 gases, even when the electricity comes entirely from coal-fired plants.

 However, in Sweden, the primary energy sources are hydro and nuclear
 (over 90% of the generation from those two sources).  Fossil sources
 produce considerably less than 10% of the electricity mix.  (This
 document is a bit dated, but presents the information nicely in a graph
 on page 2.
 http://ec.europa.eu/energy/energy_policy/doc/factsheets/mix/mix_se_en.pdf)

 So, Sweden is switching from conventional gasoline and diesel vehicles
 to electric and plug-in hybrids, charging from a grid that is over 90%
 supplied from essentially zero-GHG sources, but the emissions are going
 up?  And, the actual market penetration is still trivially small - I'm
 guessing well below 1% of the total road-going fleet in the country.
 Doesn't pass the smell test.  Unfortunately, the article doesn't bother
 to cite the evidence used to support it's conclusion.  My suspicion:
 the Swedish 'transportation sector' includes something other than
 private cars that might be driving the numbers up (e.g., ships burning
 bunker C crude).

 Actually, after a very limited Web search, I could not find anything
 credible that looked like the 'evidence' for the article - just lots of
 copy-cat items that also did not provide citations for the desired data.

 I did find this, dated January 2011:
 http://www.eea.europa.eu/data-and-maps/figures/change-in-total-ghg-emissions,
 which shows Sweden's transportation GHG emissions going up 9% from 1990
 to 2008.  The catch is that Sweden did not get serious about EV
 incentives until about 2008-2009, a time period not covered by the data
 for this report.

 Here's someone else's response (found while searching for the 'evidence').

 http://dagblog.com/link/what-if-green-products-make-us-pollute-more-10581 
 (check
 the comments by quinn)

 Darryl

 On 11/06/2011 1:10 PM, Keith Addison wrote:
 http://www.commondreams.org/view/2011/06/10-3

 Published on Friday, June 10, 2011 by CommonDreams.org

 The Green Revolution Backfires: Sweden's Lesson for Real Sustainability

 by Firmin DeBrabander

 What if electric cars made pollution worse, not better? What if they
 increased greenhouse gas emissions instead of decreasing them?
 Preposterous you say? Well, consider what's happened in Sweden.

 Through generous subsidies, Sweden aggressively pushed its citizens
 to trade in their cars for energy efficient replacements (hybrids,
 clean diesel vehicles, cars that run on ethanol). Sweden has been so
 successful in this initiative that it leads the world in per capita
 sales of 'green cars.' To everyone's surprise, however, greenhouse
 gas emissions from Sweden's transportation sector are up.

 Or perhaps we should not be so surprised after all. What do you
 expect when you put people in cars they feel good about driving (or
 at least less guilty), which are also cheap to buy and run?
 Naturally, they drive them more. So much more, in fact, that they
 obliterate energy gains made by increased fuel efficiency.

 We need to pay attention to this as GM and Nissan roll out their new
 green cars to great fanfare. The Chevy Volt, a hybrid with a
 lithium-ion battery, can go 35 miles on electric power alone (after
 charging over night, for example), and GM brags on its website that
 if you limit your daily driving to that distance, you can commute
 gas-free for an average of $1.50 a day. The Volt's price is listed
 at a very reasonable $33K (if you qualify for the maximum $7500 in
 tax credits). The fully electric Nissan 

Re: [Biofuel] Flex Fuel Ford Ranger and methanol

2011-04-01 Thread Jan Warnqvist
Hello all and Tom especially.
There is a saying explaining that methanol is like ethanol but more. This 
is used to point out that the disadvantages of ethanol is more with 
methanol.
I suppose that Ford is too mean to equip the fuel system for methanol.. 
Methanol is corrosive, even more that water. The engine will consume twice 
as much with metanol than with gasoline. And if I remember correctly, 
methanol has a higher vapour generating value than ethanol, meaning that it 
demands more energy to enter the gas phase, which can lead to cold starting 
problems. And during warm-up of the engine the methanol produces more of the 
even so corrosive substances, such as formaldehyde which also is poisonous. 
It is a well-known fact that most motor oils are not able to neutralize 
these corrosion agents, so one can expect an engine wear of twice the value 
than for gasoline. Apart from this is methanol an excellent fuel, especially 
if there was methanol from biological sources available.

Best regards to you all

Jan W
- Original Message - 
From: Tom Kelly [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Friday, April 01, 2011 3:49 PM
Subject: [Biofuel] Flex Fuel Ford Ranger and methanol


 In an earlier post I asked about using a methanol/ethanol blend in my
 flex fuel Ford Ranger. It has been brought to my attention that Ford
 recommends against such a blend:
 Do not use fuel containing methanol. It can damage critical
  fuel systems components.

  Tom


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Re: [Biofuel] Query on breaking emulsions

2011-03-06 Thread Jan Warnqvist
Hello Seth. Using heat exchangers is most of the time a good idea. Just keep 
in mind that they internally have to be acid resistant , at least down to pH 
4, which corresponds to the acid constant of the free fatty acids, which you 
in any case will have.
You are welcome and good luck.

Jan W
- Original Message - 
From: Seth Macdonald [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Monday, March 07, 2011 2:08 AM
Subject: Re: [Biofuel] Query on breaking emulsions


 Thanks Jan.

 I have opted NOT to use it in the hydronic system and decided instead to 
 build a
 heat exchanger into the next phase of the processor instead. Thank you for 
 the
 info.

 Seth





 
 From: Jan Warnqvist [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Sun, February 27, 2011 1:32:19 PM
 Subject: Re: [Biofuel] Query on breaking emulsions

 Hello Seth. Biodiesel is usually processed at as low temperature as
 possible, 60oC is almost ideal. Any temperature above that is threateing.
 The hotter the faster the crack.
 - Original Message - 
 From: Seth Macdonald [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Sunday, February 27, 2011 10:08 PM
 Subject: Re: [Biofuel] Query on breaking emulsions


 At what temp does Bio-Diesel start to crack? Perhaps it is not a great 
 idea
 to
 use it in a hydronic system. If the Bio-diesel is only circulated for 24 
 hrs
 before being replaced by the next batch, am I still in danger of losing
 quality?

 Dredneck




 
 From: Jan Warnqvist [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Tue, February 22, 2011 11:27:24 AM
 Subject: Re: [Biofuel] Query on breaking emulsions

 Biodiesel is not as chemically stable as gas oil, or water for heating
 purposes. High temperatures may cause the biodiesel to crack and form
 solids, so filtering is necessary to keep the circulation running. And the
 biodiesel will in each case loose quality in connection to heating. The
 higher degree of unsaturation, the greater the quality loss.But the 
 process
 can be buffered by the use of anti-oxidants, preferably the BHT based.
 - Original Message - 
 From: Seth Macdonald [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Tuesday, February 22, 2011 8:16 PM
 Subject: Re: [Biofuel] Query on breaking emulsions


 Thanks for the tips Keith.

 the Journey to Forever website has revolutionized my family's life!
 Everything
 I have learned thus far about Bio-Diesel has been learned from going to
 your
 site and hands on experience. I've got a long way to go, but my community
 is now
 addicted to the concept of running on renewable energies!


 Thanks to all who have worked to research and develop the future of 
 energy
 in
 our society. I'll send some photos etc. of my facility when it is
 finished.

 Another concept I am about to explore is using the biodiesel in my
 hydronic
 heating system thereby drying it while heating the floor of my shop.I
 installed
 an infloor pex pipe system in a concrete slab in the fall and I'm about 
 to
 hook
 it up as the final stage in the processor. Once the fuel has circulated
 through
 the floor and had ample time to return to the reservoir and dry, it would
 be
 siphoned off as fuel, making room for the next batch that needs to be
 dried to
 take it's place. Only washed bio-diesel would be used for this. Are there
 any
 problems inherent with heating bio-diesel to 140 degrees?

 Seth Dredneck Macdonald

 Dunster BC
 CANADA





 
 From: Keith Addison [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Thu, February 17, 2011 10:11:09 PM
 Subject: Re: [Biofuel] Query on breaking emulsions

Hi all,

Seth Macdonald here from Northern BC CANADA. I run a very small 
bio-diesel
refinery with plans to sell/trade with local organic farmers this
coming spring.
This winter has been particularly harsh up here and I am having problems
maintaining constant temperatures in my shop. This has led to a variety 
of
problems.

 You might consider this:

 http://journeytoforever.org/RSwoh1.html

Does anyone out there have any ideas on breaking an emulsion with a
large batch
of fuel that will NOT separate from the wash water? I know, it
should never have
happened in the first place.

 That's right - emulsions shouldn't happen.

Cross-contamination due to cooled glycerin in the
processor lines is likely the culprit. Even though the product DID
pass the wash
test.

 And the methanol test?

I have tried heating and cooling, but it is taking a ridiculous amount of
energy to heat 40 gallons of emulsified fuel and I can't seem to get it
hot
enough to make any difference.

Any help on this issue will be greatly appreciated.

 http://journeytoforever.org/biodiesel_bubblewash.html#emulsion

 Best

 Keith


Seth The Dredneck Macdonald
Robson Valley Bio-fuels
Dunster BC

Re: [Biofuel] Query on breaking emulsions

2011-02-27 Thread Jan Warnqvist
Hello Seth. Biodiesel is usually processed at as low temperature as 
possible, 60oC is almost ideal. Any temperature above that is threateing. 
The hotter the faster the crack.
- Original Message - 
From: Seth Macdonald [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Sunday, February 27, 2011 10:08 PM
Subject: Re: [Biofuel] Query on breaking emulsions


At what temp does Bio-Diesel start to crack? Perhaps it is not a great idea 
to
use it in a hydronic system. If the Bio-diesel is only circulated for 24 hrs
before being replaced by the next batch, am I still in danger of losing
quality?

Dredneck





From: Jan Warnqvist [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Tue, February 22, 2011 11:27:24 AM
Subject: Re: [Biofuel] Query on breaking emulsions

Biodiesel is not as chemically stable as gas oil, or water for heating
purposes. High temperatures may cause the biodiesel to crack and form
solids, so filtering is necessary to keep the circulation running. And the
biodiesel will in each case loose quality in connection to heating. The
higher degree of unsaturation, the greater the quality loss.But the process
can be buffered by the use of anti-oxidants, preferably the BHT based.
- Original Message - 
From: Seth Macdonald [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Tuesday, February 22, 2011 8:16 PM
Subject: Re: [Biofuel] Query on breaking emulsions


 Thanks for the tips Keith.

 the Journey to Forever website has revolutionized my family's life!
 Everything
 I have learned thus far about Bio-Diesel has been learned from going to
 your
 site and hands on experience. I've got a long way to go, but my community
 is now
 addicted to the concept of running on renewable energies!


 Thanks to all who have worked to research and develop the future of energy
 in
 our society. I'll send some photos etc. of my facility when it is
 finished.

 Another concept I am about to explore is using the biodiesel in my
 hydronic
 heating system thereby drying it while heating the floor of my shop.I
 installed
 an infloor pex pipe system in a concrete slab in the fall and I'm about to
 hook
 it up as the final stage in the processor. Once the fuel has circulated
 through
 the floor and had ample time to return to the reservoir and dry, it would
 be
 siphoned off as fuel, making room for the next batch that needs to be
 dried to
 take it's place. Only washed bio-diesel would be used for this. Are there
 any
 problems inherent with heating bio-diesel to 140 degrees?

 Seth Dredneck Macdonald

 Dunster BC
 CANADA





 
 From: Keith Addison [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Thu, February 17, 2011 10:11:09 PM
 Subject: Re: [Biofuel] Query on breaking emulsions

Hi all,

Seth Macdonald here from Northern BC CANADA. I run a very small bio-diesel
refinery with plans to sell/trade with local organic farmers this
coming spring.
This winter has been particularly harsh up here and I am having problems
maintaining constant temperatures in my shop. This has led to a variety of
problems.

 You might consider this:

 http://journeytoforever.org/RSwoh1.html

Does anyone out there have any ideas on breaking an emulsion with a
large batch
of fuel that will NOT separate from the wash water? I know, it
should never have
happened in the first place.

 That's right - emulsions shouldn't happen.

Cross-contamination due to cooled glycerin in the
processor lines is likely the culprit. Even though the product DID
pass the wash
test.

 And the methanol test?

I have tried heating and cooling, but it is taking a ridiculous amount of
energy to heat 40 gallons of emulsified fuel and I can't seem to get it
hot
enough to make any difference.

Any help on this issue will be greatly appreciated.

 http://journeytoforever.org/biodiesel_bubblewash.html#emulsion

 Best

 Keith


Seth The Dredneck Macdonald
Robson Valley Bio-fuels
Dunster BC
CANADA
V0J 1J0

PH: 250-968-4411


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Re: [Biofuel] Query on breaking emulsions

2011-02-22 Thread Jan Warnqvist
You are welcome. But have you analyzed the batch with the methanol test as 
initiated by undersigned ? That will give you useful information on the 
state of the batch.

With best regards
Jan W
- Original Message - 
From: Seth Macdonald [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Tuesday, February 22, 2011 7:44 PM
Subject: Re: [Biofuel] Query on breaking emulsions


 Thank you for the info Jan.

 As far as I know the excess methanol has already been evaporated as the 
 batch
 was heated (probably excessively) outside the shop in a barrel over a 
 three
 burner stove! Glycerin layer has also been removed. I'm thinking this 
 batch did
 not completely react.Perhaps incorrect titration. Thanks very much for the 
 tip
 on using weakly acidified water.

 Seth




 
 From: Jan Warnqvist [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Thu, February 17, 2011 10:13:13 AM
 Subject: Re: [Biofuel] Query on breaking emulsions

 Hello Seth. I think that the emulsion problem is caused by another issue
 that just the temperature itself. Any BD emulsion will break with the help
 of weakly acified water, preferably by sulphuric acid. Salty water (NaCl) 
 is
 also an option. This will work assuming that you can have 20oC and that 
 you
 have a reasonably good reaction of the BD. Have you evaporated the excess
 methanol ?

 With best regards
 Jan Warnqvist
 - Original Message - 
 From: Seth Macdonald [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Thursday, February 17, 2011 6:21 PM
 Subject: [Biofuel] Query on breaking emulsions


 Hi all,

 Seth Macdonald here from Northern BC CANADA. I run a very small 
 bio-diesel
 refinery with plans to sell/trade with local organic farmers this coming
 spring.
 This winter has been particularly harsh up here and I am having problems
 maintaining constant temperatures in my shop. This has led to a variety 
 of
 problems.

 Does anyone out there have any ideas on breaking an emulsion with a large
 batch
 of fuel that will NOT separate from the wash water? I know, it should
 never have
 happened in the first place. Cross-contamination due to cooled glycerin 
 in
 the
 processor lines is likely the culprit. Even though the product DID pass
 the wash
 test. I have tried heating and cooling, but it is taking a ridiculous
 amount of
 energy to heat 40 gallons of emulsified fuel and I can't seem to get it
 hot
 enough to make any difference.

 Any help on this issue will be greatly appreciated.

 Seth The Dredneck Macdonald
 Robson Valley Bio-fuels
 Dunster BC
 CANADA
 V0J 1J0

 PH: 250-968-4411


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Re: [Biofuel] Query on breaking emulsions

2011-02-22 Thread Jan Warnqvist
Biodiesel is not as chemically stable as gas oil, or water for heating 
purposes. High temperatures may cause the biodiesel to crack and form 
solids, so filtering is necessary to keep the circulation running. And the 
biodiesel will in each case loose quality in connection to heating. The 
higher degree of unsaturation, the greater the quality loss.But the process 
can be buffered by the use of anti-oxidants, preferably the BHT based.
- Original Message - 
From: Seth Macdonald [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Tuesday, February 22, 2011 8:16 PM
Subject: Re: [Biofuel] Query on breaking emulsions


 Thanks for the tips Keith.

 the Journey to Forever website has revolutionized my family's life! 
 Everything
 I have learned thus far about Bio-Diesel has been learned from going to 
 your
 site and hands on experience. I've got a long way to go, but my community 
 is now
 addicted to the concept of running on renewable energies!


 Thanks to all who have worked to research and develop the future of energy 
 in
 our society. I'll send some photos etc. of my facility when it is 
 finished.

 Another concept I am about to explore is using the  biodiesel in my 
 hydronic
 heating system thereby drying it while heating the floor of my shop.I 
 installed
 an infloor pex pipe system in a concrete slab in the fall and I'm about to 
 hook
 it up as the final stage in the processor. Once the fuel has circulated 
 through
 the floor and had ample time to return to the reservoir and dry, it would 
 be
 siphoned off as fuel, making room for the next batch that needs to be 
 dried to
 take it's place. Only washed bio-diesel would be used for this. Are there 
 any
 problems inherent with heating bio-diesel to 140 degrees?

 Seth Dredneck Macdonald

 Dunster BC
 CANADA





 
 From: Keith Addison [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Thu, February 17, 2011 10:11:09 PM
 Subject: Re: [Biofuel] Query on breaking emulsions

Hi all,

Seth Macdonald here from Northern BC CANADA. I run a very small bio-diesel
refinery with plans to sell/trade with local organic farmers this
coming spring.
This winter has been particularly harsh up here and I am having problems
maintaining constant temperatures in my shop. This has led to a variety of
problems.

 You might consider this:

 http://journeytoforever.org/RSwoh1.html

Does anyone out there have any ideas on breaking an emulsion with a
large batch
of fuel that will NOT separate from the wash water? I know, it
should never have
happened in the first place.

 That's right - emulsions shouldn't happen.

Cross-contamination due to cooled glycerin in the
processor lines is likely the culprit. Even though the product DID
pass the wash
test.

 And the methanol test?

I have tried heating and cooling, but it is taking a ridiculous amount of
energy to heat 40 gallons of emulsified fuel and I can't seem to get it 
hot
enough to make any difference.

Any help on this issue will be greatly appreciated.

 http://journeytoforever.org/biodiesel_bubblewash.html#emulsion

 Best

 Keith


Seth The Dredneck Macdonald
Robson Valley Bio-fuels
Dunster BC
CANADA
V0J 1J0

PH: 250-968-4411


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Re: [Biofuel] Query on breaking emulsions

2011-02-17 Thread Jan Warnqvist
Hello Seth. I think that the emulsion problem is caused by another issue 
that just the temperature itself. Any BD emulsion will break with the help 
of weakly acified water, preferably by sulphuric acid. Salty water (NaCl) is 
also an option. This will work assuming that you can have 20oC and that you 
have a reasonably good reaction of the BD. Have you evaporated the excess 
methanol ?

With best regards
Jan Warnqvist
- Original Message - 
From: Seth Macdonald [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Thursday, February 17, 2011 6:21 PM
Subject: [Biofuel] Query on breaking emulsions


 Hi all,

 Seth Macdonald here from Northern BC CANADA. I run a very small bio-diesel
 refinery with plans to sell/trade with local organic farmers this coming 
 spring.
 This winter has been particularly harsh up here and I am having problems
 maintaining constant temperatures in my shop. This has led to a variety of
 problems.

 Does anyone out there have any ideas on breaking an emulsion with a large 
 batch
 of fuel that will NOT separate from the wash water? I know, it should 
 never have
 happened in the first place. Cross-contamination due to cooled glycerin in 
 the
 processor lines is likely the culprit. Even though the product DID pass 
 the wash
 test. I have tried heating and cooling, but it is taking a ridiculous 
 amount of
 energy to heat 40 gallons of emulsified fuel and I can't seem to get it 
 hot
 enough to make any difference.

 Any help on this issue will be greatly appreciated.

 Seth The Dredneck Macdonald
 Robson Valley Bio-fuels
 Dunster BC
 CANADA
 V0J 1J0

 PH: 250-968-4411


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Re: [Biofuel] Season's greetings

2010-12-23 Thread Jan Warnqvist
In accordance with Keith.
Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Thursday, December 23, 2010 3:31 PM
Subject: [Biofuel] Season's greetings


 Dear All

 Compliments of the season to all the Christians, happy solstice to
 everyone else, and here's wishing a happy, prosperous and wonderful
 New Year to one and all - everything you wish for yourselves. Have a
 great holiday!

 Regards

 Keith

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Re: [Biofuel] A metalworking question

2010-11-03 Thread Jan Warnqvist
Hello all, I just have to point out that castor oil was widely used as a 
lubricant during pre-industrial era and it was working very well. The reason 
for its absence nowadays is that the petroleum-based base oils in use 
nowadays (still) is cheaper.
Anybody who is interested in how to use biological oils as raw materials for 
high-performance lubricants, feel free to adress me.

Jan Warnqvist
- Original Message - 
From: Dawie Coetzee [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Wednesday, November 03, 2010 2:58 PM
Subject: Re: [Biofuel] A metalworking question


Keith

Or use some linseed oil, or this:

Anti-rust Paint from Fish-Scraps - A short guide to the technique
by M. L. Allen, Prince of Songkla University, Thailand
http://journeytoforever.org/farm_library/FishPaintJTF.pdf

Interesting, thanks. Flax is a wonderful thing, isn't it? I've often said 
that
there's nothing wrong with pre-industrial linseed-oil-based paints, and that 
99%
the development of paint technology over the past century has been about 
nothing
but faster drying times. That and getting rid of skilled labour, as is the 
case
in the rest of industry, not to mention agriculture.

That sounds hopeful. But wouldn't hammering along the edge thin the
metal and expand it rather than compacting it? I'd thought of
hammering in the middle to expand it, hopefully making the whole
thing bulge out, but I didn't want to make the middle thinner, and
weaker. Maybe if I started out with slightly thicker metal. And,
indeed, heat it to light yellow.

That was my initial reaction at the time, so I went back and re-read. 
Indeed,
one hammers onto a dolly on anvil where one wants the metal shrunk. I'd
guess that the resulting compaction influences the thermal expansion
characteristics, causing the compacted metal to contract more when cooling. 
But
as I said, I haven't had the opportunity to try it myself.

I've just done a quick search (heat shrinking metal) and, as is often the 
case
with crafts, there are differences both of technique and opinion out there. 
The
technique I've described is found more among those who wish creatively to 
form
compound curves out of flat sheetmetal. Those trying to remove dents in 
fenders
and doorskins tend to favour a higher heat, hammering just off the heated 
area,
and quenching with wet rags.

A circular domed part of a car? I can't think of one, but I'll
certainly have a look.

Try the front and rear corners (unfortunately the areas most likely to be
damaged) or the rear corners of roofs. And don't forget mechanical bits: 
I've
made damper towers out of water pump pulleys!

Simplest of all, see if steel merchants don't have what you want off the 
shelf.
It's surprising what they do have. Round pole caps for palisade fences might
just be perfect for the job.

All the best

-Dawie






From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Wed, 3 November, 2010 11:29:19
Subject: Re: [Biofuel] A metalworking question

Hi Dawie

Keith

It looks to me, unless I've misunderstood the failed attempt, that
you want a worked sheetmetal piece rather than a casting or moulding.

That's right. It's just thin metal, like a tin can. I think anything
much heavier might upset the balance, which is just right - as you
walk the cans more or less empty themselves, you don't have to tip
them much, if at all.

And then the trouble would be to get the domed shape into it: I take
it the shape is necessary for the proper functioning of the rose.

Yes, it widens the spread, and some of the water goes up, which
extends the reach.

The first thing that springs to mind is to scour vehicle breaker's
yards for bits of body panels that have a suitable dome. As you only
need a small piece an otherwise irreparable panel might do.

A circular domed part of a car? I can't think of one, but I'll
certainly have a look.

Otherwise one could start with flat sheetmetal and work in the dome
using traditional bodywork techniques.

That's probably my problem, I don't know much about bodywork techniques.

The problem is that one would be working in ungalvanized metal,
though one could cold galv it afterwards.

Or use some linseed oil, or this:

Anti-rust Paint from Fish-Scraps - A short guide to the technique
by M. L. Allen, Prince of Songkla University, Thailand
http://journeytoforever.org/farm_library/FishPaintJTF.pdf

To form the dome, heat a metal disc until a light yellow oxide bloom
appears. Then hammer along the edge of the disc to compact the
metal. You'll probably have to heat, hammer, and let cool a few
times to achieve the desired domed shape. I haven't done this myself
but have read somewhat on the subject.

That sounds hopeful. But wouldn't hammering along the edge thin the
metal and expand it rather than compacting it? I'd thought of
hammering in the middle to expand it, hopefully making the whole
thing bulge out, but I didn't want to make the middle

Re: [Biofuel] SVO Vehicles in USA

2010-08-30 Thread Jan Warnqvist
Hello Paul, maybe you know me from The Jan Warnqvist Methanol Test?
I belong to that group of people that consider SVO as not suitable for 
diesel engines in general, simply because it is very difficult to have good 
function with SVO as fuel, even if the engines are equipped to handle that 
fuel, you will not be able to get over the obvious disadvantages with SVO:
- High viscosity
- (Too) High boiling point
- (Too) Bad ignition properties
- Unregulated content of metal salts which will generate deposits inside the 
engine.
Biodiesel of good quality is a far better alternative, since all the 
biodiesel turns the above mentioned disadvantages to acceptable properties. 
And - the CO2 neutrality will be almost the same.so why go for SVO ?

With best regards
Jan W
- Original Message - 
From: Paul Landis [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Monday, August 30, 2010 6:29 PM
Subject: [Biofuel] SVO Vehicles in USA


 August 30, 2010

 I am new to this list.

 I learned about SVO as Fuel from Keith and his great web site.

 I am NOT a technician.

 I am an activist who hates Oil Companies.

 I am looking to promote SVO as a capability here in the USA.

 Elsbett has people here in the USA and I have spoken to Taavi McMahon

 If any of you know people in the USA  or are in the USA and
 would like to help let people know about the capabilities of SVO,
 especially if you have a vehicle that is so equipped,
 please let me know.

 Thank you.


 Paul Landis
 50 Columbus Avenue  Apt. F21
 Tuckahoe, NY 10707 USA

 914-771-9114

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Re: [Biofuel] Acid-base chemistry

2010-04-19 Thread Jan Warnqvist
Hello Keith. Moles means molecules. There is one water molecule formed for 
each molecule of fatty acid alkylated.
It is true that some water is produced during saponification of free acidity 
and it is also true that water is formed when mixing NaOH or KOH in an 
alcohol. But neither of these reactions are esterification or 
transesterification reactions..
It is considered that the transesterifiction reaction takes place in two or 
more steps, where the first step is the collapse of the glycerine-formed 
ester (the triglyceride etc) forming free glycerine and free acidity. Water 
is consumed in that step. In another step the new esters are formed where 
the equal amount of  water is released. Conclusion: Some free water is good 
for the first step of the reaction. Does it make sense ?
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, April 18, 2010 7:27 PM
Subject: Re: [Biofuel] Acid-base chemistry


 Hello Jan

 Thankyou!

The acid esterification produces water with 1M /M alkylated fatty acid.

 I have difficulty with moles. I do know how to figure it out, in
 theory, but I'm not confident of the result. Would you mind writing
 it as a formula equation, if that's the right term:

 A + B -- D + E

 Moles gives quantities though, which I'd like to know. Is it possible
 to translate 1M /M alkylated fatty acid into ml of water per litre
 of oil or something similar?

The trans-esterification does not produce any water,

 We've had people saying it does, and others that it doesn't. It's
 been said that some water is produced by the saponification of free
 fatty acids, though it's very little, and someone else said some
 water might be formed during the reaction that produces the methoxide:

 CH3OH + KOH  --- CH3OK + H2O
 or
 CH3OH + NaOH --- CH3ONa + H2O

 Any comments?

but some water present
(0,1%)  is necessary to make the process run well.

 I didn't know that. Can you explain how it works?

 I did know that esterification will also perform some
 transesterification if it has the chance, but it's slow.

 Thanks again Jan - all best to you

 Keith


The acid esterification
produces water with 1M /M alkylated fatty acid. This process will also
perform trans-esterification assuming that there is some material to
trans-esterify and that the operator in question lets the process 
continue.

With best regards
Jan W
- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, April 17, 2010 11:58 AM
Subject: [Biofuel] Acid-base chemistry


  Hello all

  A question...

  Even when everything is dry, including the oil, the
  transesterification process itself produces some water, though not
  very much.

  IIRC acid esterification also produces water, I think more water than
  transesterification does, and via a different process.

  Does anybody know if that's correct, and what the chemical equations
   are? With KOH and H2SO4.

  Thanks!

  All best

   Keith



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Re: [Biofuel] Acid-base chemistry

2010-04-17 Thread Jan Warnqvist
Hello Keith and all.
The trans-esterification does not produce any water, but some water present 
(0,1%)  is necessary to make the process run well. The acid esterification 
produces water with 1M /M alkylated fatty acid. This process will also 
perform trans-esterification assuming that there is some material to 
trans-esterify and that the operator in question lets the process continue.

With best regards
Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, April 17, 2010 11:58 AM
Subject: [Biofuel] Acid-base chemistry


 Hello all

 A question...

 Even when everything is dry, including the oil, the
 transesterification process itself produces some water, though not
 very much.

 IIRC acid esterification also produces water, I think more water than
 transesterification does, and via a different process.

 Does anybody know if that's correct, and what the chemical equations
 are? With KOH and H2SO4.

 Thanks!

 All best

 Keith

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Re: [Biofuel] Cuphea Oil seed

2010-01-24 Thread Jan Warnqvist
Hello Keith. Opposite your opinion, I am quite optimistic concerning the 
relation of cold properties/cetane number of the biodiesel.  Palm oil, lard, 
or coconut oil do not have cloud points of -9 to -10oC. For instance, Palm 
oil biodiesel has a CFPP of +6 - +8oC and a cetane number of around 60. The 
cloud point is always higher than the CFPP, and the cloud point means less 
when it comes to driveability, especially since most additives when treating 
rape seed methyl ester can accomplish an improvement with 10o or more when 
it comes to the CFPP value.
So I still find Cuphea oil biodiesel interesting.

Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, January 24, 2010 7:41 AM
Subject: Re: [Biofuel] Cuphea Oil seed


 Hello Jan

Hello all. The Cuphea oil is similar to coconut oil with an iodine value 
of
approx 17. This confirms its high content of saturated fatty acids, should
as biodiesel create a nice cetane number. The catch could be the biodiesel
final boiling point which should turn out scientifically lower that 350oC.
Good or bad ? It would be nice to judge  that from a report on the
properties of Cuphea oil biodiesel.

 The other catch is the cloud point, I'm not sure I believe the report
 I quoted that it's -9 to -10 deg C, especially not as you confirm the
 low IV of 17. More likely it starts to gel as soon as the weather
 gets cool, same as palm oil, coconut oil, lard, etc. If it does, then
 one wonders why it's being promoted in the US as a substitute for
 palm oil. Hot tip: invest all your bucks and your grandmother's life
 savings in US companies making pour-point depressants.

 Ref. Iodine Values
 http://journeytoforever.org/biodiesel_yield.html#iodine

 Further catch is that it's an awkward crop to process. The seeds are
 tiny, and they tend to shatter. Cuphea isn't really domesticated yet,
 it's more like a wild weed.

 Actually the biodiesel is just a sideshow, the main attraction is the
 caprylic and lauric acid, valuable industrial feedstocks, cloud point
 irrelevant.

 Industry enthusiasm, hm. In the US that means either B20 or B5, maybe
 a low cloud point doesn't matter if you're going to mix it with 80%
 or 95% petrodiesel.

 Best

 Keith


Jan W
- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, January 23, 2010 6:31 PM
Subject: Re: [Biofuel] Cuphea Oil seed


  Hi Tony

  It should be okay for biodiesel, it's been raising quite a lot of
  enthusiasm in the industry in the US, but maybe that just means it's
  better than soy. It's supposed to be similar to palm oil and coconut
  oil (high caprylic and lauric acid content), yet the cloud point is
   low, -9 to -10 deg C. I didn't find an Iodine Value for it though.

  HTH - best

  Keith


Hello List,
Has anyone used cuphea for bio-fuel?  If yes, what were the results?
Any additional information is appreciated.

Thanks

Tony Marzolino

3624 Wilson Creek Rd, Berkshire, NY  13736

  http://www.marzfarm.com/


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Re: [Biofuel] Cuphea Oil seed

2010-01-23 Thread Jan Warnqvist
Hello all. The Cuphea oil is similar to coconut oil with an iodine value of 
approx 17. This confirms its high content of saturated fatty acids, should 
as biodiesel create a nice cetane number. The catch could be the biodiesel 
final boiling point which should turn out scientifically lower that 350oC. 
Good or bad ? It would be nice to judge  that from a report on the 
properties of Cuphea oil biodiesel.

Jan W
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, January 23, 2010 6:31 PM
Subject: Re: [Biofuel] Cuphea Oil seed


 Hi Tony

 It should be okay for biodiesel, it's been raising quite a lot of
 enthusiasm in the industry in the US, but maybe that just means it's
 better than soy. It's supposed to be similar to palm oil and coconut
 oil (high caprylic and lauric acid content), yet the cloud point is
 low, -9 to -10 deg C. I didn't find an Iodine Value for it though.

 HTH - best

 Keith


Hello List,
Has anyone used cuphea for bio-fuel?  If yes, what were the results?
Any additional information is appreciated.

Thanks

Tony Marzolino

3624 Wilson Creek Rd, Berkshire, NY  13736

http://www.marzfarm.com/


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[Biofuel] Merceds-Benz

2009-10-17 Thread Jan Warnqvist
Hi all. Did anybody experience or heard of anybody experiencing severe problems 
with MB CDI engines in connection with biodiesel ?

Jan W
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Re: [Biofuel] Merceds-Benz

2009-10-17 Thread Jan Warnqvist
I had a colleague whose MB 320 CDI suddenly broke down due to suspected 
injection pump scar. When you ask MB owners about this they all say:
Neverthis cannot happen with a Mercedes- Benz! As a MB owner myself I am 
very curious about other´s experiences concerning this..
- Original Message - 
From: Zeke Yewdall [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Cc: biofuel@sustainablelists.org
Sent: Saturday, October 17, 2009 5:13 PM
Subject: Re: [Biofuel] Merceds-Benz


 Haven't really heard either way.  I have heard lots of rumors about quite 
 a
 few of the common rail diesel's having problems with biodiesel, due to
 polymerization of the biodiesel at extremely high pressures that those
 engines have, but I cannot remember any details or specific examples of 
 any
 of them right now.  And I don't recall what sort of biodiesel and what
 iodine numbers they were running.

 Z

 On Sat, Oct 17, 2009 at 4:23 AM, Jan Warnqvist 
 [EMAIL PROTECTED] wrote:

 Hi all. Did anybody experience or heard of anybody experiencing severe
 problems with MB CDI engines in connection with biodiesel ?

 Jan W
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Re: [Biofuel] Merceds-Benz

2009-10-17 Thread Jan Warnqvist
Hello Keith, Zeke and all. If polymerisation is the issue should it be 
related to the oxidation stability of the BD. It should therefore be 
important to use anti-oxidants in order to improve the stability. The 
connection is higher pressure - higher temperatures - quicker 
polymerisation. And the higher the iodine number the lower stability. Sorry 
about that, ASTM.
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, October 17, 2009 9:09 PM
Subject: Re: [Biofuel] Merceds-Benz


 Hi Zeke, Jan and all

Haven't really heard either way.  I have heard lots of rumors about quite 
a
few of the common rail diesel's having problems with biodiesel, due to
polymerization of the biodiesel at extremely high pressures that those
engines have, but I cannot remember any details or specific examples of 
any
of them right now.

 Maybe they're just rumours, but I think DI diesels might indeed have
 problems with polymerised biodiesel in the US. But is it because of
 the high pressures? Can high pressure cause oxidation? I don't know,
 but it's only from US sources that I ever hear that.

 Most biodiesel in the US is soy biodiesel, which doesn't need high
 pressure to oxidise and polymerise, it's a semi-drying oil, it'll
 polymerise anyway. The IV is well above the EU biodiesel standard
 upper limit. (See Iodine Values
 http://journeytoforever.org/biodiesel_yield.html#iodine, National
 standards for biodiesel
 http://journeytoforever.org/biodiesel_yield2.html#biodstds.) The
 biodiesel industry in the US seems to be more are less in denial
 about this, but then the US National Biodiesel Board is a creature of
 US Big Soy.

 Hm, I must check how the US-EU row over the US dumping cheap soy
 biodiesel on the EU market is progressing. IIRC last time I looked
 the US was accusing the EU of protectionism, on the basis of what
 sounded like GMO-style substantial equivalence of America's soy and
 Europe's rapeseed oil, though they're not equivalent when it comes to
 iodine values and polymerisation. Rapeseed oil has a much lower IV
 and is much less likely to polymerise. Nonetheless, a lot of
 Europeans use anti-oxidant with their biodiesel, while very little
 anti-oxidant is used in the US, by contrast. Also, in the US most
 biodiesel is the NBB's commercial B20, a low blend with a lower risk
 of polymerisation, so they have to care about it that much less.

 They're never going to accept that soy could be anything less than
 ideal. I get the impression that, even if there is such a thing,
 high-pressure polymerisation could be just a convenient scapegoat for
 soy's shortcomings.

 Best

 Keith


And I don't recall what sort of biodiesel and what
iodine numbers they were running.

Z

On Sat, Oct 17, 2009 at 4:23 AM, Jan Warnqvist 
[EMAIL PROTECTED] wrote:

  Hi all. Did anybody experience or heard of anybody experiencing severe
  problems with MB CDI engines in connection with biodiesel ?

   Jan W


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Re: [Biofuel] Merceds-Benz

2009-10-17 Thread Jan Warnqvist
hello Denise, I think that US BD is more or synonomous with soy biodiesel 
although it may be a myth. US is the biggest soy producer in the world and 
that is not a myth.
- Original Message - 
From: denise farley [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Saturday, October 17, 2009 11:34 PM
Subject: Re: [Biofuel] Merceds-Benz


 Keith,
 Just out of sheer curiosity, where does the information that Most 
 biodiesel
 in the US is soy biodiesel come from?

 I was wondering too, since I cannot find the information even on the NBB
 (unless I am blind which is never outside the realm of possibility), where
 might be a good source to look for a list of currently operating biodiesel
 plant?  Ours closed and is in bankruptcy and of the other two in the local
 area, only one is operating.  We couldn't compete even switching to animal
 fats - and all those inherent processing problems.  Of course, the one
 operating is big-bucks AGP and, yes, uses soy.

 Hmmm.  D'ya think I might have sort of answered my own question here?
 Although I will say there is a soybean processing coop south of here that
 ceased production of biodiesel in their facility for at least 6 months 
 last
 I heard.  They sold their soybean oil to AGP during that period.  Sigh.

 Thanks so much!
 Denise


 On Sat, Oct 17, 2009 at 2:09 PM, Keith Addison
 [EMAIL PROTECTED]wrote:


 Most biodiesel in the US is soy biodiesel, which doesn't need high
 pressure to oxidise and polymerise, it's a semi-drying oil, it'll
 polymerise anyway. The IV is well above the EU biodiesel standard
 upper limit. (See Iodine Values
 http://journeytoforever.org/biodiesel_yield.html#iodine, National
 standards for biodiesel
 http://journeytoforever.org/biodiesel_yield2.html#biodstds.) The
 biodiesel industry in the US seems to be more are less in denial
 about this, but then the US National Biodiesel Board is a creature of
 US Big Soy.

 Hm, I must check how the US-EU row over the US dumping cheap soy
 biodiesel on the EU market is progressing. IIRC last time I looked
 the US was accusing the EU of protectionism, on the basis of what
 sounded like GMO-style substantial equivalence of America's soy and
 Europe's rapeseed oil, though they're not equivalent when it comes to
 iodine values and polymerisation. Rapeseed oil has a much lower IV
 and is much less likely to polymerise. Nonetheless, a lot of
 Europeans use anti-oxidant with their biodiesel, while very little
 anti-oxidant is used in the US, by contrast. Also, in the US most
 biodiesel is the NBB's commercial B20, a low blend with a lower risk
 of polymerisation, so they have to care about it that much less.

 They're never going to accept that soy could be anything less than
 ideal. I get the impression that, even if there is such a thing,
 high-pressure polymerisation could be just a convenient scapegoat for
 soy's shortcomings.

 Best

 Keith


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Re: [Biofuel] Titration

2008-05-07 Thread Jan Warnqvist
Hello Brian et al.
The standard solutions for titration are for example KOH 0,1M and KOH 0,5M 
which are corresponding to 5,61g and 28,05g of KOH / dm3. But the 
concentration of the titration solution really doesn´t matter as long as the 
analysis is performed correctly and that the acid number is calculated from 
the analysis, and that the compensation need is calculated from the acid 
number. Please note that NaOH has a lower mass than KOH, so the weight will 
be lower for the corresponding concentration.
You did not say how much your sample mass was when having that result. Do 
that, and we will work the values out properly.

With best regards
Jan Warnqvist
- Original Message - 
From: Brian Schneider [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Tuesday, May 06, 2008 5:45 PM
Subject: Re: [Biofuel] Titration


 Jan,
 You say that my concentration is very weak compared to the standard
 solutions.  Do you mean the standard solution to titrate waste oil
 with, or are you just meaning weak in general?  If it is weak
 compared to what should be used for waste oil, what is the standard
 strength?  Did I miss read the information on journey to forever?
 Please let me know because right now I am not going to use the waste
 oil that I have because of the high titration rate and am going to
 have to find a new source.
 Thanks
 Brian Schneider

 On May 6, 2008, at 11:07 AM, Jan Warnqvist wrote:

 You should know that your concentration is very weak compared to the
 standard solutions. Your concentration is 0,025M / dm3, and due to its
 weakness, it will almost always produce high titration values. 1 ml
 of the
 solution assuming that your sample mass is 10,0 g corresponds to an
 acid
 number of 0,1, which is normal for refined oils. Consequently is 5 ml
 corresponding to 0,5 for acid number assuming that your sample mass
 is 10,0
 g. 0,5 is a very good value for virgin oils. But, if your sample
 mass is
 1,0g, then the values will become 10 times higher, of course.

 With best regards
 Jan Warnqvist
 - Original Message -
 From: Brian Schneider [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Tuesday, May 06, 2008 1:37 PM
 Subject: Re: [Biofuel] Titration


 I am using the 1 gram per 1000 mL or .1% of NaOH.
 I have tried mixing it several ways, 1 gram in 1 liter and also tried
 Keith's suggestion of 5 grams in .5 L as stock then using 5 mL of
 that in 45 mL of distilled water for the working solution.
 Both give the same result.
 What should New virgin oil titrate out as? or does it?
 Thanks for the help
 Brian Schneider

 On May 6, 2008, at 2:52 AM, Jan Warnqvist wrote:

 Hello Brian et al.
 Which concentration of the titration solution are you using ? The
 figures
 that you stated could be correct, but only assuming that your
 titration
 solution is aimed for the purpose.

 Best regards
 Jan Warnqvist
 - Original Message -
 From: Brian Schneider [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Monday, May 05, 2008 4:35 PM
 Subject: [Biofuel] Titration


 Hi All,
 Have a quick question about titration.
 I have obtained some waste oil that seems to be titrating at 12 -
 15mL.  I have done this numerous times and come up with about the
 same results.
 That seems unusably high.  So I tried to titrate new virgin oil.
 When I did that it only took about .2 - .4 mL is that normal or
 am I
 doing something terribly wrong.
 I am a little confused at this point and any help I could get would
 be really appreciated.
 Thanks

 Brian Schneider
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Re: [Biofuel] Titration

2008-05-06 Thread Jan Warnqvist
Hello Brian et al.
Which concentration of the titration solution are you using ? The figures 
that you stated could be correct, but only assuming that your titration 
solution is aimed for the purpose.

Best regards
Jan Warnqvist
- Original Message - 
From: Brian Schneider [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Monday, May 05, 2008 4:35 PM
Subject: [Biofuel] Titration


 Hi All,
 Have a quick question about titration.
 I have obtained some waste oil that seems to be titrating at 12 -
 15mL.  I have done this numerous times and come up with about the
 same results.
 That seems unusably high.  So I tried to titrate new virgin oil.
 When I did that it only took about .2 - .4 mL is that normal or am I
 doing something terribly wrong.
 I am a little confused at this point and any help I could get would
 be really appreciated.
 Thanks

 Brian Schneider
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Re: [Biofuel] Titration

2008-05-06 Thread Jan Warnqvist
You should know that your concentration is very weak compared to the 
standard solutions. Your concentration is 0,025M / dm3, and due to its 
weakness, it will almost always produce high titration values. 1 ml of the 
solution assuming that your sample mass is 10,0 g corresponds to an acid 
number of 0,1, which is normal for refined oils. Consequently is 5 ml 
corresponding to 0,5 for acid number assuming that your sample mass is 10,0 
g. 0,5 is a very good value for virgin oils. But, if your sample mass is 
1,0g, then the values will become 10 times higher, of course.

With best regards
Jan Warnqvist
- Original Message - 
From: Brian Schneider [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Tuesday, May 06, 2008 1:37 PM
Subject: Re: [Biofuel] Titration


I am using the 1 gram per 1000 mL or .1% of NaOH.
 I have tried mixing it several ways, 1 gram in 1 liter and also tried
 Keith's suggestion of 5 grams in .5 L as stock then using 5 mL of
 that in 45 mL of distilled water for the working solution.
 Both give the same result.
 What should New virgin oil titrate out as? or does it?
 Thanks for the help
 Brian Schneider

 On May 6, 2008, at 2:52 AM, Jan Warnqvist wrote:

 Hello Brian et al.
 Which concentration of the titration solution are you using ? The
 figures
 that you stated could be correct, but only assuming that your
 titration
 solution is aimed for the purpose.

 Best regards
 Jan Warnqvist
 - Original Message -
 From: Brian Schneider [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Monday, May 05, 2008 4:35 PM
 Subject: [Biofuel] Titration


 Hi All,
 Have a quick question about titration.
 I have obtained some waste oil that seems to be titrating at 12 -
 15mL.  I have done this numerous times and come up with about the
 same results.
 That seems unusably high.  So I tried to titrate new virgin oil.
 When I did that it only took about .2 - .4 mL is that normal or am I
 doing something terribly wrong.
 I am a little confused at this point and any help I could get would
 be really appreciated.
 Thanks

 Brian Schneider
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Re: [Biofuel] Fuel from Algae??

2008-04-27 Thread Jan Warnqvist
Hello Doug et al. There are two major concern signs about biodiesel from 
algae oil:
1) The algae have to be fed with CO2 during growth. If this CO2 comes from 
fossile sources, you have achieved almost nothing.
2) The oil from algae is highly unsaturated. This makes it difficult to have 
the biodiesel meet the EN norm and other standards.

Jan Warnqvist
- Original Message - 
From: doug [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, April 27, 2008 5:38 AM
Subject: [Biofuel] Fuel from Algae??


 Hi,
 I ran into a chap travelling around Australia extolling the virtues of
 running on SVO.
 He is to email me more details, but apparently there is a project in
 Australia involved with oil from Algae, aparently using CO2 feedstock from
 generation equipment.
 I googled to try to find more info, but only found foreign references from
 ~2005. Has anyone heard anything about this project?

 regards Doug

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Re: [Biofuel] What's Wrong With This Picture

2007-12-13 Thread Jan Warnqvist
Hello Jonathan et al
The main problem with SVO is the high boiling point. This includes both the 
FFA and the SVO molecule itself. The points of turning the SVO into 
biodiesel are the following:
1) The final boiling point of the fuel will not exceed 370oC, which is 
proper for modern small and middle-size diesel engines.
2) The viscosity will drop til approx. max 5cSt, which is acceptable to 
modern small and middle-size diesel engines.
3) Using the proper recipe when performing the process, the FFA will be 
reduced or saponified. This will make the fuel less corrosive, assuming that 
the alkaline metal content of the biodiesel is taken care of .
4) The chemically bounded glycerine in SVO will partially be released from 
the SVO in hot environment. The glycerine is hard to combust, since it 
rather forms deposits than CO2 and water.

Best regards
AGERATEC AB
Jan Warnqvist
- Original Message - 
From: Jonathan Schearer [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Friday, December 14, 2007 5:01 AM
Subject: Re: [Biofuel] What's Wrong With This Picture


Hello.  Lately, I have been doing a lot of reading on the different systems 
for using SVO.  Elsbett seems to have one of the best single tank systems 
for this.  I have made good biodiesel, but with rising costs of methanol, I 
was looking at alternatives.  I have read about fuel mixing and admit have 
tried the DSE just to see what all the hype was about.  I agree that there 
is nothing really special about their ingredient and most of the thinning 
and diluting is done with the kerosene and gasoline.  It seemed to work fine 
in my 300SD, but the more I read, the more I learned of the negative 
aspects(incomplete combustion, coking, ring sticking, etc.).  I understand 
that I should only try things like this for short term experiments, which I 
have.  Is it the FFA in the vegetable oil that causes all of these problems? 
Is that why biodiesel will not cause these problems, because part of the 
process removes FFA?  I also read about the experiment that concluded that 
in order to
 achieve the same atomization as petrol diesel, the rapeseed oil was heated 
to 150 C.  This is twice as hot as most of the 2 tank SVO systems that are 
on the market now.  Would this mean that you would still have incomplete 
combustion if 150 C cannot be reached?  If Rudolf Diesel invented his engine 
to run on a variety of fuels, including vegetable oil, how come the engines 
of today require more modification or fuel modification to run veg oil?  My 
last question is concerning the Elsbett single tank SVO system.  If you can 
just pour the veg oil in and go, is there a heater on the main tank for cold 
weather?  I am not even sure that SVO will work for me since I drive 12 
miles one way to work.  My car gets up to operation temp. half way there. 
Thanks all.  Jonathan Schearer.

[EMAIL PROTECTED] wrote:  Hallo,

Check out this website if you want to see how well some folks talk out
both sides of their mouths.

http://www.dieselsecret.com

No, it isn't Bio-diesel! Yes, it is the only true Bio-diesel! The
Germans at Mercedes have been doing this since the post World War II years
but we have the only proprietary ingredients! On, and on, and on. Same
old same old.

Happy Happy,

Gustl
-- 
Je mehr wir haben, desto mehr fordert Gott von uns.

We can't change the winds but we can adjust our sails.

The safest road to Hell is the gradual one - the gentle slope,
soft underfoot, without sudden turnings, without milestones,
without signposts.
C. S. Lewis, The Screwtape Letters

Es gibt Wahrheiten, die so sehr auf der Straße liegen,
daß sie gerade deshalb von der gewöhnlichen Welt nicht
gesehen oder wenigstens nicht erkannt werden.

And those who were seen dancing were thought to be
insane by those who could not hear the music.
Friedrich Nietzsche

The best portion of a good man's life -
His little, nameless, unremembered acts of kindness and of love.
William Wordsworth


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Re: [Biofuel] BD disinfo from SVO kit vendors

2007-11-21 Thread Jan Warnqvist
Hello Bruno et al.
The viscosity and the high boiling point of SVO are just a consequence of 
the main molecule of SVO and its composition. The SVO consists from 
triglycerides together with some content of free acidity. Since we are 
mainly dealing with plant oils (or similar) we can expect the dominating 
fatty acid content to consist from oleic or linoic acid. These are C18:s 
which means that the triglyceride will have an approximate sum formula of 
C57H115O6 . This is a large molecule, which in itself is a reason for its 
combustion properties. Furthermore, the fatty acids are tied to a backbone 
of glycerine. This component can be extremely difficult to burn, since its 
urge to create polymeric compounds rather than vaporize is well known to 
anybody who have tried burning it. This property increases with the 
unsaturation of the oil. There are reports suggesting that highly saturated 
oils and fats are more easy to combust in diesel engines.
So the sum is that biodiesel is more suitable than SVO.
The additive we successfully tried was manufactured by Sybron Chemicals (SA) 
and consisted from phenolic compounds, which created soot which diluted 
the deposits.

Jan Warnqvist
- Original Message - 
From: Bruno M. [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Tuesday, November 20, 2007 9:01 PM
Subject: Re: [Biofuel] BD disinfo from SVO kit vendors


Jan,

SVO having a high boiling point doesn't mean it
can't be used instead of dinodiesel
in a diesel car, because, ...
normal Diesel fuel is also completely evaporated before combustion.
What you need is a fine mist, not evaporated fuel in a diesel motor.

Dino diesel has a boiling point, rather a boiling-range, between 340 and 
400°C,
so even dino juice will not be much vaporized at the time of ignition.

But it's possible that the higher the viscosity,
boiling point, and vapor pressure is,
the more difficult it is for your dieselcar's
hardware to make the ultimate mist
who gives the ideal burning of all fuel components.
Thats why SVO conversion kits alway's have a fuel heather device in it to 
lower
the viscosity so the pump - injector combo can
produce a optimal ( or as close as possible ) mist.

At 95°C sunflower oil has around the same viscosity then DD at 15°C.

DOE and other governmental organizations still claim that SVO will shorten
the live span of your motor and more cooking and
reduced motoroil live span will appear.

Mixing with dinojuice or an additive can also help but is not the
best or preferred option if you want to go fossil free.

What additive did you use or tested?

Grts
Bruno M.
~~
At 18:30 20/11/2007, Jan wrote:

Hi all,
I find it difficult to embrace any SVO technology. That is for many 
reasons,
but the most outstanding is the high boiling point of SVO:s. Canola
vaporizes completely at no less than 650-700oC, which is far too high for
modern diesel engines which have a limit of acceptance at approx 350oC. 
This
means that the SVO cannot combust completely in a diesel engine. This leads
to deposits in the engine, some of them lethal to the engine, and
lubricating oil contamination. This is a fact that no SVO kit can cure. I
was into a SVO project during the 90:s and we found one additive that could
keep the deposits at a certain level. But the composition of the additive
was such, that the handling of the fuel became environmentally undesirable,
also from the human health point of view.
If somebody has an attractive technical/chemical solution for this I would
be very interested to hear about it.

Jan Warnqvist
- Original Message -
From: [EMAIL PROTECTED]
Sent: Tuesday, November 20, 2007 5:42 PM
Subject: [Biofuel] BD disinfo from SVO kit vendors

See:
The SVO vs biodiesel argument:
http://journeytoforever.org/biodiesel_svovsbd.html
=


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Re: [Biofuel] BD disinfo from SVO kit vendors

2007-11-20 Thread Jan Warnqvist
Hi all,
I find it difficult to embrace any SVO technology. That is for many reasons, 
but the most outstanding is the high boiling point of SVO:s. Canola 
vaporizes completely at no less than 650-700oC, which is far too high for 
modern diesel engines which have a limit of acceptance at approx 350oC. This 
means that the SVO cannot combust completely in a diesel engine. This leads 
to deposits in the engine, some of them lethal to the engine, and 
lubricating oil contamination. This is a fact that no SVO kit can cure. I 
was into a SVO project during the 90:s and we found one additive that could 
keep the deposits at a certain level. But the composition of the additive 
was such, that the handling of the fuel became environmentally undesirable, 
also from the human health point of view.
If somebody has an attractive technical/chemical solution for this I would 
be very interested to hear about it.

Jan Warnqvist
- Original Message - 
From: [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, November 20, 2007 5:42 PM
Subject: [Biofuel] BD disinfo from SVO kit vendors


See:
The SVO vs biodiesel argument:
http://journeytoforever.org/biodiesel_svovsbd.html

SVO versus biodiesel is a pseudo argument that should not exist. It
creates a false competitive situation between two good things and
distracts from the real issues on how we can minimize the use of fossil
fuels. - Hakan Falk

So many SVO vendors take this approach. There's a growing market for SVO
systems and for all ready-to-use biofuels solutions, why try to chisel off
bits of the biodiesel market by spreading disinfo? I haven't seen Elsbett
slagging biodiesel, for instance.

But then (somehow it's no surprise) this is just yet another two-tank
system, no optimised injector nozzles or anything a real system would
have.

We are market leader in converting diesel engines for straight vegetable
oil in Germany, they said.

:-)

Now what was it Greasecar told me... Throughout the world we are
recognized as the leading manufacturer, seller and producer of SVO
conversion equipment.

LOL!

---

http://www.3egmbh.com/eng/technology.php

Theoretically there are three ways of using vegetable oil as fuel:

1. Manufacturing an engine especially designed to run with vegetable oil:
At this moment in time, this version is inefficient, as the attitude of
the automobile and mineral oil companies only allows a small quantity of
these engines at high prices. Our aim is to change this attitude,
distribute the vegetable oil technology and to establish the vegetable oil
engine.

2. Adaptation of the vegetable oil to the existing engine technology:
It is inefficient to change the vegetable oil into biodiesel using a lot
of energy and chemical processes, which then destroy gaskets and tubes,
decrease the engine's power and increases consumption when the natural
fuel has already better features to offer.

3. Adaptation of existing engines to the natural vegetable oil:
Our company has developed this from of technology. We install additional
components in vehicles so a mode is selectable to use pure vegetable oil
or diesel fuel without having to change the engine. Form and extent of the
alteration depends on the technology of the diesel engine.

3E GmbH Pflanzenöltechnik

From: Frank Wohlberg [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Subject: Your link list
Date: Sat, 17 Nov 2007 14:34:23 +0100

Hi Keith,

is it possible to put a link of our company to your link list?

We are market leader in converting diesel engines for straight vegetable
oil in Germany but I couldn`t find a link to us.

Thank you very much!

Regards

Frank Wohlberg

http://www.3egmbh.com/eng/index.php


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Re: [Biofuel] Off Topic - More on the Holocaust if you can stand it.

2007-10-17 Thread Jan Warnqvist
Hello Guag et al.
The reason for the Germans during ww2 to spend time and resources on 
collecting racial, religious and political non-approved people was simple: 
Idelogical.
Germany was during this time built up on a lie and the money for this lie 
was borrowed from domestic and foreign lone providers so as for building up 
the war industry itself.
It was necessary for the German government to keep this lie, since their 
complete build-up was based upon that. But, when it came to the final 
solution it grew forward little by little, goverened by directives from the 
government and performed practically by the lower parts of the 
administration with the concentration camps adminstrations in the bottom. 
There were meetings held where administrates discussed how to kill as many 
as effiectively as possible within a certain time frama = executing the 
directives from the government.
So, the reason for spending resources on these collection activities was 
that they did not know how the final solution would look like.
A completely mad system from the very beginning until the end, if you ask 
me.

Jan Warnqvist
- Original Message - 
From: Guag Meister [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Wednesday, October 17, 2007 4:57 AM
Subject: [Biofuel] Off Topic - More on the Holocaust if you can stand it.


 Hi Keith and all List Members

 I like the part about Fred Dr. Death Leuchter, the
 designer of the US Prison system's execution
 apparatus, as an expert defense witness who tested
 purported execution gas chambers ON-SITE in
 Auschwitz, Poland  tesitified in a court of law under
 oath and determined they had never been used to kill
 anyone.

 The other question I have is this. The war machine
 runs on fuel. During a time of war for Germany, fuel
 would be incredibly important.  So why would the
 Germans waste precious fuel to transport all the
 prisioners to the camps if they intended to kill them?
 Wouldn't a sharp bayonette be much cheaper?

 Best Regards,

 Peter G.
 Thailand


 20th Anniversary of the Great Holocaust Trial

 by Michael A. Hoffman II

 Copyright 2005 by revisionisthistory.org

 January 7, 2005 marks the 20th anniversary of what
 came to be known throughout the world as The Great
 Holocaust Trial thanks chiefly to the drive,
 determination, courage and vision of one man, Ernst
 Zundel, supported by those he inspired.

 In 1985 Zundel was a German immigrant residing in
 Toronto, Canada where he had built a highly successful
 advertising and graphic arts business based in a
 rambling Victorian mansion in the bohemian
 Cabbagetown section of metropolitan Toronto.

 Zundel viewed the Six million story as a form of
 mental genocide against the German people; ostensibly
 a noble tale of the epoch struggle for human rights
 that in actuality was a form of devious hate
 propaganda, leveling every conceivable blood libel at
 the Germans and branding them with the Mark of Cain.
 Having survived the Allied firebombing of his native
 city of Pforzheim as a child, Zundel was well familiar
 with the war crimes of the hypocritical Allies and he
 made it his life's work to clear the name of his own
 people.

 For this commendable enterprise, Zundel had his
 mailing privileges revoked by the Canadian government
 in 1983, forcing him to open a post office box in
 Buffalo, New York and send a messenger to commute
 hundreds of miles just to receive mail. In 1985 he was
 charged under an archaic False News provision of an
 old Edwardian municipal code, for having published the
 pamphlet Did Six Million Really Die? He faced two
 years in prison if convicted.

 In reponse Zundel put the so-called Holocaust itself
 on trial, hiring a little-known maverick lawyer from
 British Columbia, Douglas Christie, to argue his case
 before Judge Hugh Locke. Seated next to Christie was
 the learned revisionist historian Prof. Robert
 Faurisson of France, who guided Christie's withering
 cross-examination of a long train of saintly
 'Holocaust' survivors offered by the Crown.

 Zundel's defense was initially regarded by the press
 and public as preposterous. How can anyone deny the
 'Holocaust? was the incredulous response to the news
 that Zundel would vigorously defend himself and the
 free speech rights of all Canadians. The trial was
 expected to be a quick and ignominious rout of Zundel
 and his motley crew.

 How wrong the odds-makers were! For the first time in
 history the holy survivors finally had to submit
 their testimony to scrutiny, to the rules of
 evidence and cross-examination, something that has
 never happened before or since. Seated in the press
 gallery, I watched as my colleagues of the fourth
 estate grew ever more surprised and shocked at the
 amazing admissions Christie and Faurisson elicited
 from the eyewitnesses to the gas chambers. TV
 reporters like Claud Adams and journalists from the
 Toronto Star and Globe and Mail produced footage and
 headlines

Re: [Biofuel] Rapeseed Biofuel Produces More Greenhouse Gas Than Oil OrPetrol

2007-10-03 Thread Jan Warnqvist
Dear all, I would really like to read this study this report in 
original,since the article is producing several question marks.
It is well known that the exhaust emissions from fatty acid methyl esters 
are producing higher amounts of nitrious gases than petro diesel does , but 
as far as I can remember, the nitrious oxide corresponds only to a tiny part 
of these. It is also well known that that the higher the cetane number of 
the biodiesel, the lower the emissions of nitrious gases. From that point it 
is a little bit strange to conclude that the the emissions of nitrious gases 
from rape seed oil biodiesel and maize biodiesel are the same, since the 
iodine number of maize oil in general is higher than the corresponding value 
of rape seed oil. This is suggesting in its prolongment that the emissions 
of nitrious gases from BD out of rape seed oil should be lower than from BD 
of maize oil. If the article is displaying the facts from the study 
correctly, then there are two ways to approach this problem:
1) Further product development of the fatty acid methyl esters in order to 
raise the cetane number to a level where the emissions of nitrious gases 
become acceptably lower.
2) New diesel veichles will be equipped with an Exhaust Gas Recirculation 
(EGR) system or an exhaust gas aftertreatment system which will lower the 
production of nitrious gases as required in Euro regulations.
Information on the properties of nitrious oxide can be found at 
http://en.wikipedia.org/wiki/Nitrous_oxide  No doubt has the information on 
the green house effects from nitrious oxide come from this sight,
No matter if the conclusions from the study are right or not, it still makes 
sense to produce biodiesel, not in the least for forcing the development to 
take another path than previous. You know what I mean.

Jan Warnqvist
- Original Message - 
From: Olivier Morf [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Friday, September 28, 2007 6:40 AM
Subject: [Biofuel] Rapeseed Biofuel Produces More Greenhouse Gas Than Oil 
OrPetrol


Source: http://www.timesonline.co.uk/tol/news/uk/science/article2507851.ece
September 22, 2007

Rapeseed Biofuel Produces More Greenhouse Gas Than Oil Or Petrol

By Lewis Smith

A renewable energy source designed to reduce greenhouse gas emissions is
contributing more to global warming than fossil fuels, a study suggests.

Measurements of emissions from the burning of biofuels derived from rapeseed
and maize have been found to produce more greenhouse gas emissions than they
save.

Other biofuels, especially those likely to see greater use over the next
decade, performed better than fossil fuels but the study raises serious
questions about some of the most commonly produced varieties.

Rapeseed and maize biodiesels were calculated to produce up to 70 per cent
and 50 per cent more greenhouse gases respectively than fossil fuels. The
concerns were raised over the levels of emissions of nitrous oxide, which is
296 times more powerful as a greenhouse gas than carbon dioxide. Scientists
found that the use of biofuels released twice as much as nitrous oxide as
previously realised. The research team found that 3 to 5 per cent of the
nitrogen in fertiliser was converted and emitted. In contrast, the figure
used by the International Panel on Climate Change, which assesses the extent
and impact of man-made global warming, was 2 per cent. The findings
illustrated the importance, the researchers said, of ensuring that measures
designed to reduce greenhouse-gas emissions are assessed thoroughly before
being hailed as a solution.

³One wants rational decisions rather than simply jumping on the bandwagon
because superficially something appears to reduce emissions,² said Keith
Smith, a professor at the University of Edinburgh and one of the
researchers.

Maize for ethanol is the prime crop for biofuel in the US where production
for the industry has recently overtaken the use of the plant as a food. In
Europe the main crop is rapeseed, which accounts for 80 per cent of biofuel
production.

Professor Smith told Chemistry World: ³The significance of it is that the
supposed benefits of biofuels are even more disputable than had been thought
hitherto.²

It was accepted by the scientists that other factors, such as the use of
fossil fuels to produce fertiliser, have yet to be fully analysed for their
impact on overall figures. But they concluded that the biofuels ³can
contribute as much or more to global warming by N2 O emissions than cooling
by fossil-fuel savings².

The research is published in the journal Atmospheric Chemistry and Physics,
where it has been placed for open review. The research team was formed of
scientists from Britain, the US and Germany, and included Professor Paul
Crutzen, who won a Nobel Prize for his work on ozone.

Dr Franz Conen, of the University of Basel in Switzerland, described the
study as an ³astounding insight².

³It is to be hoped that those

Re: [Biofuel] Rapeseed Biofuel Produces More Greenhouse Gas ThanOil OrPetrol

2007-10-03 Thread Jan Warnqvist
Ok, my mistake. When reading the article this is not shown very clear. But 
nitrous oxide is N2O and nothing else.
- Original Message - 
From: Chris Burck [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Wednesday, October 03, 2007 2:30 PM
Subject: Re: [Biofuel] Rapeseed Biofuel Produces More Greenhouse Gas ThanOil 
OrPetrol


jan, the study was focused on NO2 released by soil microbes as the
rapeseed crops grow, not on the emissions from burning the fuel.  you
make an excellent point, though.  imo, we should *always* be searching
for ways to reduce the impact of the fuels we burn.

On 10/3/07, Jan Warnqvist [EMAIL PROTECTED] wrote:
 Dear all, I would really like to read this study this report in
 original,since the article is producing several question marks.
 It is well known that the exhaust emissions from fatty acid methyl esters
 are producing higher amounts of nitrious gases than petro diesel does , 
 but
 as far as I can remember, the nitrious oxide corresponds only to a tiny 
 part
 of these. It is also well known that that the higher the cetane number of
 the biodiesel, the lower the emissions of nitrious gases. From that point 
 it
 is a little bit strange to conclude that the the emissions of nitrious 
 gases
 from rape seed oil biodiesel and maize biodiesel are the same, since the
 iodine number of maize oil in general is higher than the corresponding 
 value
 of rape seed oil. This is suggesting in its prolongment that the emissions
 of nitrious gases from BD out of rape seed oil should be lower than from 
 BD
 of maize oil. If the article is displaying the facts from the study
 correctly, then there are two ways to approach this problem:
 1) Further product development of the fatty acid methyl esters in order to
 raise the cetane number to a level where the emissions of nitrious gases
 become acceptably lower.
 2) New diesel veichles will be equipped with an Exhaust Gas Recirculation
 (EGR) system or an exhaust gas aftertreatment system which will lower the
 production of nitrious gases as required in Euro regulations.
 Information on the properties of nitrious oxide can be found at
 http://en.wikipedia.org/wiki/Nitrous_oxide  No doubt has the information 
 on
 the green house effects from nitrious oxide come from this sight,
 No matter if the conclusions from the study are right or not, it still 
 makes
 sense to produce biodiesel, not in the least for forcing the development 
 to
 take another path than previous. You know what I mean.

 Jan Warnqvist
 - Original Message -
 From: Olivier Morf [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Friday, September 28, 2007 6:40 AM
 Subject: [Biofuel] Rapeseed Biofuel Produces More Greenhouse Gas Than Oil
 OrPetrol


 Source: 
 http://www.timesonline.co.uk/tol/news/uk/science/article2507851.ece
 September 22, 2007

 Rapeseed Biofuel Produces More Greenhouse Gas Than Oil Or Petrol

 By Lewis Smith

 A renewable energy source designed to reduce greenhouse gas emissions is
 contributing more to global warming than fossil fuels, a study suggests.

 Measurements of emissions from the burning of biofuels derived from 
 rapeseed
 and maize have been found to produce more greenhouse gas emissions than 
 they
 save.

 Other biofuels, especially those likely to see greater use over the next
 decade, performed better than fossil fuels but the study raises serious
 questions about some of the most commonly produced varieties.

 Rapeseed and maize biodiesels were calculated to produce up to 70 per cent
 and 50 per cent more greenhouse gases respectively than fossil fuels. The
 concerns were raised over the levels of emissions of nitrous oxide, which 
 is
 296 times more powerful as a greenhouse gas than carbon dioxide. 
 Scientists
 found that the use of biofuels released twice as much as nitrous oxide as
 previously realised. The research team found that 3 to 5 per cent of the
 nitrogen in fertiliser was converted and emitted. In contrast, the figure
 used by the International Panel on Climate Change, which assesses the 
 extent
 and impact of man-made global warming, was 2 per cent. The findings
 illustrated the importance, the researchers said, of ensuring that 
 measures
 designed to reduce greenhouse-gas emissions are assessed thoroughly before
 being hailed as a solution.

 ³One wants rational decisions rather than simply jumping on the bandwagon
 because superficially something appears to reduce emissions,² said Keith
 Smith, a professor at the University of Edinburgh and one of the
 researchers.

 Maize for ethanol is the prime crop for biofuel in the US where production
 for the industry has recently overtaken the use of the plant as a food. In
 Europe the main crop is rapeseed, which accounts for 80 per cent of 
 biofuel
 production.

 Professor Smith told Chemistry World: ³The significance of it is that the
 supposed benefits of biofuels are even more disputable than had been 
 thought

Re: [Biofuel] new topic

2007-09-20 Thread Jan Warnqvist
Prifitability to the new energy business is a matter for the government to 
ensure, assuming that the government wants such a development, of course.
In Sweden. Italy and UK (I think) there is a system of green certificates 
for power generation. These systems oblige the power distributors to buy a 
min quote of green certificates, allowing of certain amount of the power 
will be green.
As for the biodiesel or even ethanol, the authorities will have to enforce 
the production and consumption of these, with grants or by quotas.
But there is another factor to take into consideration as well: Big systems 
are sensitive to terrorst attacks, technical malfunctions etc. That in 
itself is a reason to encourage small scale energy production.
- Original Message - 
From: Michael Miller [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Thursday, September 20, 2007 6:14 AM
Subject: Re: [Biofuel] new topic


 On 9/19/07, Jan Warnqvist [EMAIL PROTECTED] wrote:

 Hello all,
 my time here in Ageratec has provided me with some observations which I
 would like the list members to share with me:
 We are in the business of producing energy from sources which originally
 are meant for food purposes or food waste. It is obvious that this new
 energy sector has very few of the traditional energy suppliers, rather 
 new
 actors in this field of green energy.


 I don't think the renewable energy industry is nearly as profitable as the
 existing oil industry. The investments in renewables by big oil is only to
 comply with mandatory state and federal requirements. If renewables ever
 take off and actually threaten their profits the oil giants will have tens
 of billions of dollars available to buyout everyone, and in the end they 
 own
 it all again.

 It is happening with ethanol production. What started as cooperatively 
 owned
 ethanol plants financed by groups of local farmers has grown into highly
 capitalized publicly owned corporations not owned by farmers at all.
 Non-farm investors are buy up ethanol production plants and farmers are 
 back
 to growing a commodity crop and suffering the whims of the market and
 speculators.


 Here in Sweden the farmers are buying wind mills, selling the power to the
 power distributors, the paper and pulp industry is burning the black 
 liqueur
 residue and producing power from it, both for own consumption and for 
 sales.
 Some farmers are growing canola, producing biodiesel from it for own
 consumption and for sales. The ethanol industry has begun to shift from
 approaching ethanol as a solvent to treating it as fuel. There is a new
 combinative proposing that wood should be used for producing methanol for
 energy purposes.
 None of these areas have mineral oil companies,  nuclear, coal  or hydro
 power companies or any other traditional suppliers of energy involved in
 their business. This teaches us that the new energy will be dominated by 
 new
 actors, which means that there is a great need for knowledge and know-how
 both for the energy products as such, and also for the energy business
 itself. This demand exsists not only within the actors, but also within 
 the
 authorities, the traditional actors and the industry used to produce food
 etc.
 The same development will no doubt strike the lubricant industry. The new
 green lubricants will no doubt be forced out into the market by new 
 actors.
 So we are actually into a process which will change the power balance,
 intensely stalled by the traditional actors and anybody who gains from 
 their
 power. This may be a long hard struggle, be the outcome is given on
 forehand:
 If we want to consume energy it has to be renewable. We may have to
 decrease our consumption, but that does not mean that our welfare or
 independence will suffer. On the contrary, this is a major stimulation 
 for
 new technology, new solutions and - for new actors. So - hang in there, 
 even
 to your nails.

 Jan Warnqvist
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Re: [Biofuel] new topic

2007-09-20 Thread Jan Warnqvist
And further:
The developing countries may be able to benefit very well from a more 
de-centralized energy production by taking advantage from the green 
techniques. An example:
A farmer in Africa decides to grow Jatropha plants, because a near-by 
plantation has decided to produce biodiesel for their own consumption, since 
the availability of petrodiesel changes with the wheather and with rebel and 
government activities. The production cost for Jatropha oil biodiesel is far 
less than the cost of petrodiesel. The biodiesel and its by-products can 
also be used to generate electricity and give a surplus back on to the power 
network. A surplus that can be consumed by the farmer and his family. This 
will enable them to increase their standard and even increase the production 
of Jatropha oil.
This is only one example of events that we in the company have seen taking 
place, although mostly concerning palm oil.
- Original Message - 
From: Lugano Wilson [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Thursday, September 20, 2007 10:53 AM
Subject: Re: [Biofuel] new topic


 TRUE,

  governments have key role to play - the development of these new and 
 clean energy systems need be regulated not just left to the multinationals 
 to control everything at their PROFIT.

  serious cases will be to developing countries that have corrupt systems 
 only to throw such precious lands at a token advantage.

  it is clear that these developments are going to spread decentralized 
 energy sevices to remote areas that one could not think of. it should 
 therefore be promoted with much regulation.

  Lugano

 Jan Warnqvist [EMAIL PROTECTED] wrote:
  Prifitability to the new energy business is a matter for the government 
 to
 ensure, assuming that the government wants such a development, of course.
 In Sweden. Italy and UK (I think) there is a system of green certificates
 for power generation. These systems oblige the power distributors to buy a
 min quote of green certificates, allowing of certain amount of the power
 will be green.
 As for the biodiesel or even ethanol, the authorities will have to enforce
 the production and consumption of these, with grants or by quotas.
 But there is another factor to take into consideration as well: Big 
 systems
 are sensitive to terrorst attacks, technical malfunctions etc. That in
 itself is a reason to encourage small scale energy production.
 - Original Message - 
 From: Michael Miller
 To:
 Sent: Thursday, September 20, 2007 6:14 AM
 Subject: Re: [Biofuel] new topic


 On 9/19/07, Jan Warnqvist wrote:

 Hello all,
 my time here in Ageratec has provided me with some observations which I
 would like the list members to share with me:
 We are in the business of producing energy from sources which originally
 are meant for food purposes or food waste. It is obvious that this new
 energy sector has very few of the traditional energy suppliers, rather
 new
 actors in this field of green energy.


 I don't think the renewable energy industry is nearly as profitable as 
 the
 existing oil industry. The investments in renewables by big oil is only 
 to
 comply with mandatory state and federal requirements. If renewables ever
 take off and actually threaten their profits the oil giants will have 
 tens
 of billions of dollars available to buyout everyone, and in the end they
 own
 it all again.

 It is happening with ethanol production. What started as cooperatively
 owned
 ethanol plants financed by groups of local farmers has grown into highly
 capitalized publicly owned corporations not owned by farmers at all.
 Non-farm investors are buy up ethanol production plants and farmers are
 back
 to growing a commodity crop and suffering the whims of the market and
 speculators.


 Here in Sweden the farmers are buying wind mills, selling the power to 
 the
 power distributors, the paper and pulp industry is burning the black
 liqueur
 residue and producing power from it, both for own consumption and for
 sales.
 Some farmers are growing canola, producing biodiesel from it for own
 consumption and for sales. The ethanol industry has begun to shift from
 approaching ethanol as a solvent to treating it as fuel. There is a new
 combinative proposing that wood should be used for producing methanol 
 for
 energy purposes.
 None of these areas have mineral oil companies, nuclear, coal or hydro
 power companies or any other traditional suppliers of energy involved in
 their business. This teaches us that the new energy will be dominated by
 new
 actors, which means that there is a great need for knowledge and 
 know-how
 both for the energy products as such, and also for the energy business
 itself. This demand exsists not only within the actors, but also within
 the
 authorities, the traditional actors and the industry used to produce 
 food
 etc.
 The same development will no doubt strike the lubricant industry. The 
 new
 green lubricants will no doubt

[Biofuel] new topic

2007-09-19 Thread Jan Warnqvist
Hello all,
my time here in Ageratec has provided me with some observations which I would 
like the list members to share with me:
We are in the business of producing energy from sources which originally are 
meant for food purposes or food waste. It is obvious that this new energy 
sector has very few of the traditional energy suppliers, rather new actors in 
this field of green energy. Here in Sweden the farmers are buying wind mills, 
selling the power to the power distributors, the paper and pulp industry is 
burning the black liqueur residue and producing power from it, both for own 
consumption and for sales. Some farmers are growing canola, producing biodiesel 
from it for own consumption and for sales. The ethanol industry has begun to 
shift from approaching ethanol as a solvent to treating it as fuel. There is a 
new combinative proposing that wood should be used for producing methanol for 
energy purposes. 
None of these areas have mineral oil companies,  nuclear, coal  or hydro power 
companies or any other traditional suppliers of energy involved in their 
business. This teaches us that the new energy will be dominated by new actors, 
which means that there is a great need for knowledge and know-how both for the 
energy products as such, and also for the energy business itself. This demand 
exsists not only within the actors, but also within the authorities, the 
traditional actors and the industry used to produce food etc.
The same development will no doubt strike the lubricant industry. The new green 
lubricants will no doubt be forced out into the market by new actors. 
So we are actually into a process which will change the power balance, 
intensely stalled by the traditional actors and anybody who gains from their 
power. This may be a long hard struggle, be the outcome is given on forehand:
If we want to consume energy it has to be renewable. We may have to decrease 
our consumption, but that does not mean that our welfare or independence will 
suffer. On the contrary, this is a major stimulation for new technology, new 
solutions and - for new actors. So - hang in there, even to your nails.

Jan Warnqvist
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Re: [Biofuel] (was Glycerine Settling Time) removing salt/dirt fromwvo

2007-08-13 Thread Jan Warnqvist
Hello Roderick. A definiyion is on its place:
A salt is basically a compound built up from the reaction of a metal and an 
acid.There are other salts too, but we can leave them for now.  This means that 
soaps are salts, since they are built up from metal ions (Na+ or K+ in 
connection with biodiesel) and fatty acids. These are formed as a by-reaction 
in the trans-esterification process, often encouraged by the water content. 
Salt in every-day talk is NaCl sodium chloride , where in this case the 
chlorine is fetched from HCl, hydrochloric acid. Does this spread any light to 
you ?
You are using acetic acid to break the emulsion. This will create the salts 
potassium or sodium acetate and water. 
Best regards
Jan
  - Original Message - 
  From: Roderick Roth 
  To: biofuel@sustainablelists.org 
  Sent: Sunday, August 12, 2007 6:03 PM
  Subject: Re: [Biofuel] (was Glycerine Settling Time) removing salt/dirt 
fromwvo


   Hello Jan
  May I jump into the discussion? Jan you have just mentioned the word salts 
isn't that one of the ingrediants for making very good quality soap? Hence 
possibly helping make a great emultion during the first wash on the quality 
esters. I am assuming that salts will remain in the whole process, not being 
disolved in any manner from the methoxide right? Some salt should be drained 
with the glycern right? Possibly leaving some salt in the unwashed ester.
My last two reactions have had the same feedstock, ( a very popular 
restaurant which salts their fry's heavily, lol) both reactions were two stage 
acid/base reactions becos the titration is consistantly over 14 eww . 
Here are the wash results from both batches of Quality Tested BD:  
   Reaction #21  using 1500L unwashed oil as a feedstock:the resulting 1380 
Litre batch of quality BD required 3.5 litres of pure 99% vinagar to break the 
first wash emultion. 
   Reaction #22 using  1500L PREWASHED oil of the same feedstock : the 
resulting 1450L batch only required 1 Litre of 99% pure vinagar, to break the 
first wash emultion.  
  Jan  does this observation make any sense? Think it could be salt?
   -Rod.

  Jan Warnqvist [EMAIL PROTECTED] wrote:
Hello Joe.
There were probably small amounts of mono- and diglycerides left in the 
biodiesel, and/or possibly soaps which together are excellent emulsifiers. A 
strong acid will divide the glycerides into fatty acids and glycerine ,and the 
soaps into salts and fatty acids, which then goes into a fat phanse and an 
aquaeus phase, possibly with the salts in the bottom.'
Best regards
Jan
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Friday, August 10, 2007 3:45 PM
  Subject: Re: [Biofuel] Glycerine Settling Time


  Hi Jan;

  Ok your post agrees with what Andres said.  So how do we explain Tom's 
experiment then?  To recap (Tom correct me if I miss something here) he took 
washed esters that passed the methanol test and added water and (of course) no 
emulsion when agitated. Whatever mono and diglycerides were in the esters were 
small but present I assume, but yet no emusion. Then added some small quantity 
of glycerol ( which had been separated from the soaps, FFA and salts) and 
agitated again and did get an emulsion.  I have had the feeling glycerin has 
usually been the cause of emulsion problems when I have had them.  No doubt a 
poorly reacted batch is much more likely to have the problem but is that really 
due to the glycerides or is it glycerin which hasn't settled.  Remember we 
started this discussion that the glycerin settles much slower in a poorly 
completed run.

  BTW as an addition to this discussion look what someone just posted on my 
yahoo group!  Using glycerin cocktail to BREAK an emulsion.  Now that's 
radical!!?? 

  http://www.biodieselcommunity.org/breakingemulsions/

  Joe

  Jan Warnqvist wrote:

Hi evereybody. I feel obliged to enter this discussion. Pure glycerine is   not 
a good emulsifier due to the fact that there are three OH-groups and   that the 
carbon s in the first  and third positions are surronded by two   hydrogene 
atoms. This makes the glycerine hydrophilic in five places   alltogether. 
However, the mono- and diglycerides are excellent emulsifiers.   Only small 
amounts of these are sufficient to create stable emulsions. Would   somebody 
agree with me on that ?Jan Warnqvist 
 - Original Message -   From: Keith Addison [EMAIL PROTECTED]  To: 
biofuel@sustainablelists.org  Sent: Friday, August 10, 2007 9:53 AM  Subject: 
Re: [Biofuel] Glycerine Settling TimeHi TomHi Keith,  
Then if you do one-litre test batches first, especially with iffy  batches of 
oil,  Ops.I took Joe's point to be: If you have to 
re-process it is possible to  use info from the QT to determine how much (how 
little) methanol you'll   need  to use.I also took

Re: [Biofuel] Glycerine Settling Time

2007-08-10 Thread Jan Warnqvist
Hi evereybody. I feel obliged to enter this discussion. Pure glycerine is 
not a good emulsifier due to the fact that there are three OH-groups and 
that the carbon s in the first  and third positions are surronded by two 
hydrogene atoms. This makes the glycerine hydrophilic in five places 
alltogether. However, the mono- and diglycerides are excellent emulsifiers. 
Only small amounts of these are sufficient to create stable emulsions. Would 
somebody agree with me on that ?

Jan Warnqvist
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, August 10, 2007 9:53 AM
Subject: Re: [Biofuel] Glycerine Settling Time


 Hi Tom

Hi Keith,

  Then if you do one-litre test batches first, especially with iffy
  batches of oil,

Ops.

 I took Joe's point to be: If you have to re-process it is possible to
use info from the QT to determine how much (how little) methanol you'll 
need
to use.

 I also took that point, there were others though. It's a useful
 method, cheaper reprocessing, but I think we all agree that
 reprocessing itself is to be avoided if at all possible. Or I thought
 we did anyway.

 I think that both Joe and myself have standardize(d) the process
so that passing the QT is the rule, not the exception.

 That's not what Joe said:

 It makes sense. Glycerin is an emulsifier.  Have you ever tried
 dosing the batch again with a little methoxide?  After you remove
 the glycerin it doesn't take much to get the last bit of the
 reaction to go and settle out the remaining glycerin.  Of course
 this is well known already.  Kenji and many others do straight base
 catalysis as a two stage deal. You can do a methanol test of sorts
 and the unreacted oil will settle out.  Then you can use the
 measured amount of unreacted oil in the methanol test vial to
 estimate the percentage unreacted oil in your batch and dose
 accordingly with the stoichiometric amount of methoxide.  Assume
 neutral oil for this calculation.  Rod and I do this regularly if
 the batch fails the QT and it works like a charm.  Will save you
 settling time in the long run.

 Rod and I do this regularly if the batch fails the QT and it works
 like a charm. That if makes it a little ambiguous, but the
 regularly bit puts a question-mark on what's the rule and what's
 the exception.

 Kenji and many others do straight base catalysis as a two stage deal.

 Less methanol notwithstanding, my question remains - why reprocess,
 as a standard procedure, instead of avoiding the problem in the first
 place?

 Could be wrong, but it sounds like Kenji and others might be doing
 this rather than doing a titration - you know the old line: There's
 no need for titration, just use 6.25 g. And then using the methanol
 test to try to fix the regularly ensuing disaster. A different
 version of that here in Japan is to put the stuff through a
 centrifuge, though the product still doesn't pass any quality test or
 standards test.

 What you describe is much the same as what I described, doing
 (whatever) tests during the processing, adjusting accordingly and
 conducting the whole thing as a single stage.

 From Joe's replies so far I can't tell if he (and Rod, and Kenji and
 many others) are doing it that way or not, but it seems not:

 Your question (and mine): Don't you have to heat up the whole batch
 again? (Time and energy)

 Joe's reply: This is all done right after draining the glycerin.  I
 leave the heater on during this period.  Do the rough QT right away
 before wash test.

 Rough QT? Anyway, how long is it settling before he drains the glyc?

 I run a QT towards the end of the reaction because I do not want to
re-process.

 Indeed not.

It takes me a few minutes and I like the certainty of knowing
the BD is good before I pump it into my settling tank.
 If the test should fail when I'm making a batch for my car, I could 
 use
Joe's suggestion to help me better approximate the amount of methanol to
add.

 If the process has been standardized, why bother?

 I think this is a misunderstanding. I didn't say what you say below,
 standardized; can't fail, and I didn't mean that standardising the
 process means there's no need for tests, whether in-process tests or
 1-litre test batches or whatever. Anything can fail. I'm all in
 favour of any tests that are helpful at any stage. So I agree with
 all you say here.

 Indeed, whatever rough might mean, using the methanol test to
 fine-tune the amount of extra methanol needed for reprocessing is a
 useful technique.

 But I'm not in favour of using reprocessing as a standard method,
 which, pending a better explanation, seems to be what's being
 proposed here.

As you say:

 there shouldn't be any batches failing the QT.

 I've had a few failed batches in the past year. It seems to happen 
 when
I think I have it all figured out; standardized; can't fail. On one 
occasion
the pump was making a bit of a funny noise when I

Re: [Biofuel] Glycerine Settling Time

2007-08-10 Thread Jan Warnqvist
Hello Joe.
There were probably small amounts of mono- and diglycerides left in the 
biodiesel, and/or possibly soaps which together are excellent emulsifiers. A 
strong acid will divide the glycerides into fatty acids and glycerine ,and the 
soaps into salts and fatty acids, which then goes into a fat phanse and an 
aquaeus phase, possibly with the salts in the bottom.'
Best regards
Jan
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Friday, August 10, 2007 3:45 PM
  Subject: Re: [Biofuel] Glycerine Settling Time


  Hi Jan;

  Ok your post agrees with what Andres said.  So how do we explain Tom's 
experiment then?  To recap (Tom correct me if I miss something here) he took 
washed esters that passed the methanol test and added water and (of course) no 
emulsion when agitated. Whatever mono and diglycerides were in the esters were 
small but present I assume, but yet no emusion. Then added some small quantity 
of glycerol ( which had been separated from the soaps, FFA and salts) and 
agitated again and did get an emulsion.  I have had the feeling glycerin has 
usually been the cause of emulsion problems when I have had them.  No doubt a 
poorly reacted batch is much more likely to have the problem but is that really 
due to the glycerides or is it glycerin which hasn't settled.  Remember we 
started this discussion that the glycerin settles much slower in a poorly 
completed run.

  BTW as an addition to this discussion look what someone just posted on my 
yahoo group!  Using glycerin cocktail to BREAK an emulsion.  Now that's 
radical!!?? 

  http://www.biodieselcommunity.org/breakingemulsions/

  Joe

  Jan Warnqvist wrote:

Hi evereybody. I feel obliged to enter this discussion. Pure glycerine is 
not a good emulsifier due to the fact that there are three OH-groups and 
that the carbon s in the first  and third positions are surronded by two 
hydrogene atoms. This makes the glycerine hydrophilic in five places 
alltogether. However, the mono- and diglycerides are excellent emulsifiers. 
Only small amounts of these are sufficient to create stable emulsions. Would 
somebody agree with me on that ?

Jan Warnqvist
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, August 10, 2007 9:53 AM
Subject: Re: [Biofuel] Glycerine Settling Time


  Hi Tom

Hi Keith,

  Then if you do one-litre test batches first, especially with iffy
batches of oil,
Ops.

I took Joe's point to be: If you have to re-process it is possible to
use info from the QT to determine how much (how little) methanol you'll 
need
to use.
  I also took that point, there were others though. It's a useful
method, cheaper reprocessing, but I think we all agree that
reprocessing itself is to be avoided if at all possible. Or I thought
we did anyway.

I think that both Joe and myself have standardize(d) the process
so that passing the QT is the rule, not the exception.
  That's not what Joe said:

It makes sense. Glycerin is an emulsifier.  Have you ever tried
dosing the batch again with a little methoxide?  After you remove
the glycerin it doesn't take much to get the last bit of the
reaction to go and settle out the remaining glycerin.  Of course
this is well known already.  Kenji and many others do straight base
catalysis as a two stage deal. You can do a methanol test of sorts
and the unreacted oil will settle out.  Then you can use the
measured amount of unreacted oil in the methanol test vial to
estimate the percentage unreacted oil in your batch and dose
accordingly with the stoichiometric amount of methoxide.  Assume
neutral oil for this calculation.  Rod and I do this regularly if
the batch fails the QT and it works like a charm.  Will save you
settling time in the long run.
  Rod and I do this regularly if the batch fails the QT and it works
like a charm. That if makes it a little ambiguous, but the
regularly bit puts a question-mark on what's the rule and what's
the exception.

Kenji and many others do straight base catalysis as a two stage deal.

Less methanol notwithstanding, my question remains - why reprocess,
as a standard procedure, instead of avoiding the problem in the first
place?

Could be wrong, but it sounds like Kenji and others might be doing
this rather than doing a titration - you know the old line: There's
no need for titration, just use 6.25 g. And then using the methanol
test to try to fix the regularly ensuing disaster. A different
version of that here in Japan is to put the stuff through a
centrifuge, though the product still doesn't pass any quality test or
standards test.

What you describe is much the same as what I described, doing
(whatever) tests during the processing, adjusting accordingly and
conducting the whole thing as a single stage.

From Joe's replies so far I can't tell if he (and Rod, and Kenji and
many others) are doing it that way

Re: [Biofuel] Biofuel Quality Test

2007-08-07 Thread Jan Warnqvist
Hello Shawn. You were looking at all methanol soluble components including 
the glycerine which is rather soluble in methanol. Separate the glycerine 
next time.
Best regards
Jan Warnqvist
- Original Message - 
From: shawn patrick [EMAIL PROTECTED]
To: Biofuel Mailing List biofuel@sustainablelists.org
Sent: Friday, September 07, 2007 3:03 PM
Subject: [Biofuel] Biofuel Quality Test


 Good Day All,

 My question is in regards to the Quality test develop by Jan Warnqvist. Is
 this test to be performed on the product before or after the glycerin has
 been removed, or does it matter. I performed the test with out removing
 glycerin and found that I got a clear bright phase except you could tell
 that there was a more dense substance at the bottom of the flask. I 
 assumed
 that was the glycerin since just extracted a sample from the process 
 without
 separating BD from glycerin. Does the glycerin dissolve in the methanol??
 Was I looking at the unprocessed materials in my BD??

 Regards

 Shawn Patrick



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Re: [Biofuel] biodiesel pH

2007-06-11 Thread Jan Warnqvist
If mixed thourghly the ions from the biodiesel will be more attracted to the 
water phase than the biodiesel phase. The pH value of the biodiesel will 
reflect in the water phase. So the water phase is the place to do the 
measurement in.
With best regards
Jan
- Original Message - 
From: [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, June 09, 2007 4:54 PM
Subject: [Biofuel] biodiesel pH



 hello,
 Yes, you are right Andres and Keith.
 I realise there is no need to measure pH of fresh oil, and to do a
 titration on the used oils instead, I was not specific enough.
 So when the wash water has a pH of 7, the biodiesel should also, as the 
 ions
 should be equal in both solutions. is that right? By the way, whats
 virgin oil then?

 When doing the titration, as the 2 solutions of oil and methanol don't
 mix, do i just need to keep them vigorously shaken? Also would you
 suggest a pH meter for this step.

 Jan, When you say to use 10% biodiesel in 90% distiled water, mix, then
 let separate. Do you mean to test the biodiesel's or the water's pH?

 thankyou to all who replied.

 Josh.

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Re: [Biofuel] Jatropha vs Castor

2007-06-11 Thread Jan Warnqvist
Hello REXIS.
The castor oil is highly questionable as a raw material for biodiesel 
production due to two important issues::
1) The biodiesel from castor oil will have a too high viscosity well outside 
the specs.
2) The fatty acids of castor oil are very special and polymerize easily forming 
heavier compounds while releasing water.
Unsuitable ?  Yes.

With best regards
Jan Warnqvist
  - Original Message - 
  From: Rexis Tree 
  To: biofuel@sustainablelists.org 
  Sent: Monday, June 11, 2007 11:54 AM
  Subject: [Biofuel] Jatropha vs Castor


  I had did some web study on Castor and Jatropha.

  Jatropha, being promoted as the perfect biodiesel crop by India, is receiving 
international highlights and many investors are interested or even start 
investing in planting this crop. This may spoil the original intension of 
promoting Jatropha, when large forest was cleared again to make way for 
Jatropha plantation rather then planting them on the wasteland or marginal land 
where india planned to do. 

  Castor, the beautiful yet deadly seeds of castor, has been long used as an 
non edible oil source by mankind, as well as in other industrial application 
like paint, nylon, food addictive, lubricant, etc. And castor oil is a unuqie 
oil that it can completely dissolve in alcohol(not too sure what that means, no 
catalyst needed?). 

  Our focus here is obviously biofuel. About which is the better choice for 
biodiesel.

  Similarity:
   - drought resistance
   - oily seeds sitable for fuel purpose
   - seed cake made an excellence manure
   - poisonious and therefore producing non eatable oil
   - a kind of weed

  Jatropha advantage
   - it is said that Jatropha would trive on all kind of soil even rocky soil
   - Higher oil yield
   - it can improve the soil quality

  Jatropha disadvantage
   - since it is relatively new crop therefore it was not well understood, and 
inaccurate yield figure estimation may harm profit, more research and real data 
required
   - Jatropha is suitable for India where large area of their land consist of 
arid wasteland, but may not be suitable to other country like those with lots 
of rain forest.

  Castor advantage
   - Castor oil is one of the oldest traded goods, mankind has been trading 
castor oil since a few thousand years ago
   - Castor oil has a lot of industrial usage, therefore a market is already 
exsistance, thou limited
   - Since it was cultivated before in commercial plantation, its biology is 
well understood, and high yield hybrid is available
   - Castor can be found in medium climate area as an annual crop or in 
tropical area as a small tree
   - faster oil yield and long term yield is possible for tropical/warm area

  Castor disadvantage
   - It is said that castor will exhaust the soil quickly, fertilizer required 
to maintain a large castor plantation for a reasonable yield, but castor can 
often been seen as weed growing without attension, therefore it is possible to 
plant it as marginal plant in unattended idle area. 
   - it notorious poison is feared by the public, perhaps a research on castor 
poison(ricin) remedy is necessary.

  I do not have a conclusion currently, but as you can see, I am trying to open 
up Castor as an extra option here.

  Discussion:
   - Cultivation requirement: Jatropha maybe able to trive on most kind of 
soil, but I believe that to yield reasonable harvest, irrigation and fertilizer 
still required. Castor, while the cultivation requirement is better understood 
then Jatropha, it is still unknown about which one gets better yield if left 
unattended in a poor condition area, it is possible that each of them will 
exceed another under specific senarior, intercropping of castor and jatropha 
also an interesting subject. 

   - Harvesting: it seems like it is more labourious to harvest Jatropha, which 
its yield grow as scattered fruit, yes, olive harvester can be modified to 
harvest Jatropha but it will involved high capital. Castor seem to be easier to 
harvest as its yeild made of a branch of fruit, worker can just cut the whole 
branch at once. 

   - Toxicity: It seems that castor seeds are much more deadly then Jatropha, 
its toxic, which was being used in assasination, implies that it is extremely 
deadly and no remedy avaibale; however castor oil is perfectly harmless due to 
the fact that the toxic is only water soluble not oil soluble. Jatropha, even 
though toxic, in some case, was roasted and being eaten dangerously, but note 
that Jatropha toxic is deadly as well can kill a person by a 5-6 seeds, I am 
unable to find more articles about its toxicity and remedy about Jatropha here. 
Both plant is said can be detoxify by simply heating it and thurs destroying 
the toxic protein, confirmation needed here thou. 

   - Cost: this is also a main factor, the lower input with higher outcome is 
desired.

  Any other topics are welcome.

  Just my 1/2 cents, top up or add on are most welcome.




  Regards

Re: [Biofuel] [Norton AntiSpam] Re: Off topic

2007-06-06 Thread Jan Warnqvist
There are a number of factors that in fluence the result of the 
trans-esterification. The general rule is that even if you  have an extremly 
low content of tri-glycerides, you may still have di-glycerides or even, but 
seldom mono-glycerides out of spec. And this may be a sign of too low 
processing temperature. This subject demands more development than suited here, 
I´m afraid.

Best regards
Jan Warnqvist
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Tuesday, June 05, 2007 8:23 PM
  Subject: [Norton AntiSpam] Re: [Biofuel] Off topic


  Hey Jan;

  Since the reaction proceeds in stages from TRi- to Di- to Mono-glycerides and 
then finally to esters, I'm wondering if there is a statistical relationship to 
the fractions??  In other words if we do a reaction and find 8% triglycerides 
remaining can we estimate the fractions of diglycerides and monoglycerides as 
well since they are unmeasureable with this test?  Or would the ratios depend 
on what type of oil was being used and other factors such as FFA content?

  Joe

  Jan Warnqvist wrote:

Dear all. I am very flattered that my methanol method had so much 
attention. Here is a development of the method:
Equipment needed for the analysis

  1.. One 250 ml separatory funnel 
  2.. One 400 ml beaker (Figure 2) 
  3.. One magnetic stirrer 
  4.. Balancer with 0,05g acc. 
  5.. One 50 ml  narrowed neck E-flask 

Chemicals for the analysis

1. Water free methanol, min 225 g
2. FAME with water content less than  500 ppm, clear, bright and without 
visible impurities, min 25 g

Take the clean beaker and put exactly 225 g of methanol in it. Then add 
exactly 25g of the biodiesel. Stir the fluids on the stirrer for 2 minutes. 
Take the beaker off the stirrer ans pour the content into the separation 
funnel.Take the clean e-flask to the balancer and tarate with the flask. Let 
any oil phase separate out from the biodiesel/methanol phase and put it in the  
e-flask. Weigh the content and calculate the result:

1 -  m1/m2 = m3
where m1 is the mass of the biodiesel
m2 is the amount of methanol
m3 is how much of the biodiesel put in that is consisting from methyl 
esters.
The method will show huch much of the material by mass that is soluble in 
methanol. This includes mostl mono- and diglycerides. The residue consists 
therefore mostly from unreacted oil.

With best
Jan Warnqvist
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Tuesday, May 29, 2007 6:22 PM
  Subject: Re: [Biofuel] Newbie Seeking Diesel Van Recommendations


  Hi Ray;

  Sorry for the delay.  Try this forum for more information on Delicas.

  http://delica.ca/forum/index.php

  Joe

  raymond greeley wrote:

I would like to see this van, what did you send it in. I have not been 
able to open
ray




--
  Date: Wed, 23 May 2007 15:48:02 -0400
  From: [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Subject: Re: [Biofuel] Newbie Seeking Diesel Van Recommendations

  Look for a mitsubishi delica.  A buddy of mine just imported one with 
low miles from Japan.  He loves it.

  Joe

  Luke Kareklas wrote:

Hello All, 

I am a Kid's Birthday Party Entertainer, as well as a Juggler, 
Magician, and Balloon Guy.

I live in the Midwest, and have all 4 seasons during the year, if 
this is a helpful bit of information. 

Lately my entertainment business has gotten really busy and it's 
come time for me to buy a larger vehicle. I have been a fan of alternative 
fuels for years, but never pursued a diesel vehicle. 

I would like recommendations on what type of deisel van would you 
recommend that would most easily transfer over to a SVO, WVO, or biodiesel 
system for me to drive? I am looking for a 1/2 or 3/4 ton van, not really a 
minivan type of vehicle. 

Again, I am naive and new to all this and hope your thoughts will 
help ground me and get me pointed in the right direction. I guess I have to go 
buy a diesel vehicle before I can get moving on SVO, WVO, or Biodiesel fueling, 
right? 
Thank you very much. 

Luke

Luke Kareklas
Luke the Juggler
614-764-8010
www.LuketheJuggler.com


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Re: [Biofuel] Meth test (was Off topic)

2007-06-05 Thread Jan Warnqvist
Yes of course. It is very flattering.

With best regards
AGERATEC AB
Jan Warnqvist
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, June 04, 2007 6:44 PM
Subject: Re: [Biofuel] Meth test (was Off topic)


 Greetings Jan

 Sorry for the late reply.

 Just to add my vote of thanks - the methanol test is simple and
 useful, it's helped a lot of people.

 I'd like to add this development to the quality testing section at
 Journey to Forever, would you agree?

 All best

 Keith


Dear all. I am very flattered that my methanol method had so much
attention. Here is a development of the method:

Equipment needed for the analysis

1. One 250 ml separatory funnel
2. One 400 ml beaker (Figure 2)
3. One magnetic stirrer
4. Balancer with 0,05g acc.
5. One 50 ml  narrowed neck E-flask

Chemicals for the analysis

1. Water free methanol, min 225 g
2. FAME with water content less than  500 ppm, clear, bright and
without visible impurities, min 25 g

Take the clean beaker and put exactly 225 g of methanol in it. Then
add exactly 25g of the biodiesel. Stir the fluids on the stirrer for
2 minutes. Take the beaker off the stirrer ans pour the content into
the separation funnel.Take the clean e-flask to the balancer and
tarate with the flask. Let any oil phase separate out from the
biodiesel/methanol phase and put it in the  e-flask. Weigh the
content and calculate the result:

1 -  m1/m2 = m3
where m1 is the mass of the biodiesel
m2 is the amount of methanol
m3 is how much of the biodiesel put in that is consisting from methyl 
esters.
The method will show huch much of the material by mass that is
soluble in methanol. This includes mostl mono- and diglycerides. The
residue consists therefore mostly from unreacted oil.

With best
Jan Warnqvist


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Re: [Biofuel] Meth test (was Off topic)

2007-06-05 Thread Jan Warnqvist
Sorry, there is a confusing definition error in the formula:
m1 = is the amount of undissolved material as a result of the test.
m2 = the amount of biodiesel put into the reaction

m3 = is the amount of biodiesel soluble in methanol in %

All the best
Jan
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, June 04, 2007 6:44 PM
Subject: Re: [Biofuel] Meth test (was Off topic)


 Greetings Jan

 Sorry for the late reply.

 Just to add my vote of thanks - the methanol test is simple and
 useful, it's helped a lot of people.

 I'd like to add this development to the quality testing section at
 Journey to Forever, would you agree?

 All best

 Keith


Dear all. I am very flattered that my methanol method had so much
attention. Here is a development of the method:

Equipment needed for the analysis

1. One 250 ml separatory funnel
2. One 400 ml beaker (Figure 2)
3. One magnetic stirrer
4. Balancer with 0,05g acc.
5. One 50 ml  narrowed neck E-flask

Chemicals for the analysis

1. Water free methanol, min 225 g
2. FAME with water content less than  500 ppm, clear, bright and
without visible impurities, min 25 g

Take the clean beaker and put exactly 225 g of methanol in it. Then
add exactly 25g of the biodiesel. Stir the fluids on the stirrer for
2 minutes. Take the beaker off the stirrer ans pour the content into
the separation funnel.Take the clean e-flask to the balancer and
tarate with the flask. Let any oil phase separate out from the
biodiesel/methanol phase and put it in the  e-flask. Weigh the
content and calculate the result:

1 -  m1/m2 = m3
where m1 is the mass of the biodiesel
m2 is the amount of methanol
m3 is how much of the biodiesel put in that is consisting from methyl 
esters.
The method will show huch much of the material by mass that is
soluble in methanol. This includes mostl mono- and diglycerides. The
residue consists therefore mostly from unreacted oil.

With best
Jan Warnqvist


 ___
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 Biofuel@sustainablelists.org
 http://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.org

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Re: [Biofuel] Meth test (was Off topic)

2007-06-05 Thread Jan Warnqvist
Hello Peter. You forgot the first signs of the formula. It should be: 1 - 
m1/m2 = m3
In your case: 1 - 25/225 = 0,.
There is also a definition error in the formula.
m1 = the amount of undissolved material
m2 = the amount of biodiesel put into the reaction
m3= The amount of biodiesel that is dissolved in methanol in mass%
Sorry about that.

The proportions between methanol and biodiesel is carefully balanced in 
order to make the test reproducable.

Best regards
Jan
- Original Message - 
From: Guag Meister [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, June 05, 2007 3:33 AM
Subject: Re: [Biofuel] Meth test (was Off topic)


 Hi Keith and Jan ;

 I read this with interest but I am quite confused.
 Please can we start by exlaining the underlying basis
 for this test??  Is it that unreacted oil will not
 dissolve in methanol?  Are we trying to dissolve the
 FAME in methanol and measure the remaining?? If we
 are, then why is it so important to measure exactly
 225g methanol.  Why wouldn't 250g be OK for example??
 I can understand exactly 25g of biodiesel is
 necessary, but why exactly 225g methanol?  Perhaps I
 missed this in a previous post.

 Then when I try an example with your formula I again
 get confused.  Let's say we have perfect biodiesel. So
 this means all of if will dissolve in the methanol,
 right?

 By your formula :

 m3=m1/m2
 m3=25g/225g
 m3= 0.1

 So 0.111 is how much of the FAME is methyl esters for
 perfect FAME?  What does this mean??

 Best Regards,

 Peter G.
 Thailand

 --- Keith Addison [EMAIL PROTECTED] wrote:

 Greetings Jan

 Sorry for the late reply.

 Just to add my vote of thanks - the methanol test is
 simple and
 useful, it's helped a lot of people.

 I'd like to add this development to the quality
 testing section at
 Journey to Forever, would you agree?

 All best

 Keith


 Dear all. I am very flattered that my methanol
 method had so much
 attention. Here is a development of the method:
 
 Equipment needed for the analysis
 
 1. One 250 ml separatory funnel
 2. One 400 ml beaker (Figure 2)
 3. One magnetic stirrer
 4. Balancer with 0,05g acc.
 5. One 50 ml  narrowed neck E-flask
 
 Chemicals for the analysis
 
 1. Water free methanol, min 225 g
 2. FAME with water content less than  500 ppm,
 clear, bright and
 without visible impurities, min 25 g
 
 Take the clean beaker and put exactly 225 g of
 methanol in it. Then
 add exactly 25g of the biodiesel. Stir the fluids
 on the stirrer for
 2 minutes. Take the beaker off the stirrer ans pour
 the content into
 the separation funnel.Take the clean e-flask to the
 balancer and
 tarate with the flask. Let any oil phase separate
 out from the
 biodiesel/methanol phase and put it in the
 e-flask. Weigh the
 content and calculate the result:
 
 1 -  m1/m2 = m3
 where m1 is the mass of the biodiesel
 m2 is the amount of methanol
 m3 is how much of the biodiesel put in that is
 consisting from methyl esters.
 The method will show huch much of the material by
 mass that is
 soluble in methanol. This includes mostl mono- and
 diglycerides. The
 residue consists therefore mostly from unreacted
 oil.
 
 With best
 Jan Warnqvist


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 Be a better Heartthrob. Get better relationship answers from someone who 
 knows. Yahoo! Answers - Check it out.
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Re: [Biofuel] pH meters

2007-06-04 Thread Jan Warnqvist
Yes, Andres Secco is right. If you want to determine the free acidity of the 
virgin oil, you should use titration. But if you want to determine the pH 
value of the finished biodiesel (which should be close to 7) a pH meter is 
handy. But the pH has to be measured in a water phase, e.g. 10% biodiesel in 
distilled water, Just make sure that you first let the biodiesel and water 
to mix properly and then separate compleatly after that.

With best regards
AGERATEC AB
Jan Warnqvist
- Original Message - 
From: Andres Secco [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, June 04, 2007 5:47 PM
Subject: Re: [Biofuel] pH meters


Why a pH meter Joshua?.
Acidity does not makes sense in an oil phase. The right thing is to make a
titration
pH has no sense nor numeric sense in a non aqueous systems

- Original Message - 
From: [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, June 04, 2007 6:35 AM
Subject: [Biofuel] pH meters


 Hello,
 Im making some biodiesel and I'm having some difficulty finding a
 reasonably priced electronic pH meter to purchase so I can test the virgin
 oil and the resulting biodiesel. it would be appreciated if anyone with an
 answer or some knowledge in this area could steer me in the right
 direction.

 Joshua

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Re: [Biofuel] [Norton AntiSpam] Re: Meth test (was Off topic)

2007-05-30 Thread Jan Warnqvist
Thank you Joe.
The determination by mass will give you a more precise idea of the methyl ester 
content.
With best
Jan Warnqvist
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Tuesday, May 29, 2007 7:59 PM
  Subject: [Norton AntiSpam] Re: [Biofuel] Meth test (was Off topic)


  Hey Jan;

  Let me take the chance to thank you again for your contributions.  Also I'd 
like to let you know how WE have evolved your idea.  Me and this other dude in 
town ( who might be lurking herelol  - it was his idea actually) have taken 
to doing some kind of variation on your idea which helps us in the middle of 
the process.  I know you are talking about testing clean, washed and dried 
fuel, but check this out;  We take a sample ( I have a small test tube so I use 
3 ml of fuel and 27 ml meoh) after the reaction but before washing.  I know 
this contains catalyst, soap, water and whatever BUT when I stir it up, any 
unreacted oil settles out very quickly and gives me a gauge of how close I came 
to a complete reaction.  I can even measure the percentage of unreacted oil and 
use this to determine how much catalyst and methanol to hit the reactor with in 
order to complete the reaction. The unreacted stuff is treated as neutral oil 
when determining catalyst and methanol amounts ( ie 12% meoh v/v and 4.9 g/l 
koh)  If I am good and the reaction was very complete the first time, then only 
a little white powder (soap/catalyst?) settles in the bottom and the rest is 
clear and bright.  This is more useful than a pop bottle wash test IMHO.

  best regards
  Joe

  Jan Warnqvist wrote:

Dear all. I am very flattered that my methanol method had so much 
attention. Here is a development of the method:
Equipment needed for the analysis

  1.. One 250 ml separatory funnel 
  2.. One 400 ml beaker (Figure 2) 
  3.. One magnetic stirrer 
  4.. Balancer with 0,05g acc. 
  5.. One 50 ml  narrowed neck E-flask 

Chemicals for the analysis

1. Water free methanol, min 225 g
2. FAME with water content less than  500 ppm, clear, bright and without 
visible impurities, min 25 g

Take the clean beaker and put exactly 225 g of methanol in it. Then add 
exactly 25g of the biodiesel. Stir the fluids on the stirrer for 2 minutes. 
Take the beaker off the stirrer ans pour the content into the separation 
funnel.Take the clean e-flask to the balancer and tarate with the flask. Let 
any oil phase separate out from the biodiesel/methanol phase and put it in the  
e-flask. Weigh the content and calculate the result:

1 -  m1/m2 = m3
where m1 is the mass of the biodiesel
m2 is the amount of methanol
m3 is how much of the biodiesel put in that is consisting from methyl 
esters.
The method will show huch much of the material by mass that is soluble in 
methanol. This includes mostl mono- and diglycerides. The residue consists 
therefore mostly from unreacted oil.

With best
Jan Warnqvist
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Tuesday, May 29, 2007 6:22 PM
  Subject: Re: [Biofuel] Newbie Seeking Diesel Van Recommendations


  Hi Ray;

  Sorry for the delay.  Try this forum for more information on Delicas.

  http://delica.ca/forum/index.php

  Joe

  raymond greeley wrote:

I would like to see this van, what did you send it in. I have not been 
able to open
ray




--
  Date: Wed, 23 May 2007 15:48:02 -0400
  From: [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Subject: Re: [Biofuel] Newbie Seeking Diesel Van Recommendations

  Look for a mitsubishi delica.  A buddy of mine just imported one with 
low miles from Japan.  He loves it.

  Joe

  Luke Kareklas wrote:

Hello All, 

I am a Kid's Birthday Party Entertainer, as well as a Juggler, 
Magician, and Balloon Guy.

I live in the Midwest, and have all 4 seasons during the year, if 
this is a helpful bit of information. 

Lately my entertainment business has gotten really busy and it's 
come time for me to buy a larger vehicle. I have been a fan of alternative 
fuels for years, but never pursued a diesel vehicle. 

I would like recommendations on what type of deisel van would you 
recommend that would most easily transfer over to a SVO, WVO, or biodiesel 
system for me to drive? I am looking for a 1/2 or 3/4 ton van, not really a 
minivan type of vehicle. 

Again, I am naive and new to all this and hope your thoughts will 
help ground me and get me pointed in the right direction. I guess I have to go 
buy a diesel vehicle before I can get moving on SVO, WVO, or Biodiesel fueling, 
right? 
Thank you very much. 

Luke

Luke Kareklas

Re: [Biofuel] Off topic

2007-05-29 Thread Jan Warnqvist
Dear all. I am very flattered that my methanol method had so much attention. 
Here is a development of the method:
Equipment needed for the analysis

  1.. One 250 ml separatory funnel 
  2.. One 400 ml beaker (Figure 2)
  3.. One magnetic stirrer 
  4.. Balancer with 0,05g acc.
  5.. One 50 ml  narrowed neck E-flask 

Chemicals for the analysis

1. Water free methanol, min 225 g
2. FAME with water content less than  500 ppm, clear, bright and without 
visible impurities, min 25 g

Take the clean beaker and put exactly 225 g of methanol in it. Then add exactly 
25g of the biodiesel. Stir the fluids on the stirrer for 2 minutes. Take the 
beaker off the stirrer ans pour the content into the separation funnel.Take the 
clean e-flask to the balancer and tarate with the flask. Let any oil phase 
separate out from the biodiesel/methanol phase and put it in the  e-flask. 
Weigh the content and calculate the result:

1 -  m1/m2 = m3
where m1 is the mass of the biodiesel
m2 is the amount of methanol
m3 is how much of the biodiesel put in that is consisting from methyl esters.
The method will show huch much of the material by mass that is soluble in 
methanol. This includes mostl mono- and diglycerides. The residue consists 
therefore mostly from unreacted oil.

With best
Jan Warnqvist
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Tuesday, May 29, 2007 6:22 PM
  Subject: Re: [Biofuel] Newbie Seeking Diesel Van Recommendations


  Hi Ray;

  Sorry for the delay.  Try this forum for more information on Delicas.

  http://delica.ca/forum/index.php

  Joe

  raymond greeley wrote:

I would like to see this van, what did you send it in. I have not been able 
to open
ray




--
  Date: Wed, 23 May 2007 15:48:02 -0400
  From: [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Subject: Re: [Biofuel] Newbie Seeking Diesel Van Recommendations

  Look for a mitsubishi delica.  A buddy of mine just imported one with low 
miles from Japan.  He loves it.

  Joe

  Luke Kareklas wrote:

Hello All, 

I am a Kid's Birthday Party Entertainer, as well as a Juggler, 
Magician, and Balloon Guy.

I live in the Midwest, and have all 4 seasons during the year, if this 
is a helpful bit of information. 

Lately my entertainment business has gotten really busy and it's come 
time for me to buy a larger vehicle. I have been a fan of alternative fuels for 
years, but never pursued a diesel vehicle. 

I would like recommendations on what type of deisel van would you 
recommend that would most easily transfer over to a SVO, WVO, or biodiesel 
system for me to drive? I am looking for a 1/2 or 3/4 ton van, not really a 
minivan type of vehicle. 

Again, I am naive and new to all this and hope your thoughts will help 
ground me and get me pointed in the right direction. I guess I have to go buy a 
diesel vehicle before I can get moving on SVO, WVO, or Biodiesel fueling, 
right? 
Thank you very much. 

Luke

Luke Kareklas
Luke the Juggler
614-764-8010
www.LuketheJuggler.com


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Biofuel

[Biofuel] Chevy diesels

2007-04-23 Thread Jan Warnqvist
Hello everybody in the New World and others.
I have an aquintance who is running his Chevy 6,2 litre truck on biodiesel, and 
he experiences mysterious engine stops etc. The car will start immedeatly again 
after a few seconds. He suspects it to be a computer bug in the injection 
system.Anybody with similar problems ?

AGERATEC AB
Jan Warnqvist___
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Re: [Biofuel] Chevy diesels

2007-04-23 Thread Jan Warnqvist
He is running on 100% BD and the problems began immedeately on the first tank 
of BD.
  - Original Message - 
  From: John Beale 
  To: biofuel@sustainablelists.org 
  Sent: Monday, April 23, 2007 1:55 PM
  Subject: Re: [Biofuel] Chevy diesels


  How long ago did he switch to biodiesel and is he running on 100% BD or a mix?
  John


  On Apr 23, 2007, at 7:09 AM, Jan Warnqvist wrote:


Hello everybody in the New World and others.
I have an aquintance who is running his Chevy 6,2 litre truck on biodiesel, 
and he experiences mysterious engine stops etc. The car will start immedeatly 
again after a few seconds. He suspects it to be a computer bug in the injection 
system.Anybody with similar problems ?
 
AGERATEC AB
Jan Warnqvist___
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Re: [Biofuel] Chevy diesels

2007-04-23 Thread Jan Warnqvist
He has consumed approx. 600 ltrs and encountered problems from the very 
beginning.
  - Original Message - 
  From: John Beale 
  To: biofuel@sustainablelists.org 
  Sent: Monday, April 23, 2007 2:36 PM
  Subject: Re: [Biofuel] Chevy diesels


  But did he make the switch recently or has he been running biodiesel for 
years and he's just now experiencing problems?
  John



  On Apr 23, 2007, at 8:21 AM, Jan Warnqvist wrote:


He is running on 100% BD and the problems began immedeately on the first 
tank of BD.

  - Original Message -
  From: John Beale 
  To: biofuel@sustainablelists.org 
  Sent: Monday, April 23, 2007 1:55 PM
  Subject: Re: [Biofuel] Chevy diesels

  How long ago did he switch to biodiesel and is he running on 100% BD or a 
mix?
  John


  On Apr 23, 2007, at 7:09 AM, Jan Warnqvist wrote:


Hello everybody in the New World and others.
I have an aquintance who is running his Chevy 6,2 litre truck on 
biodiesel, and he experiences mysterious engine stops etc. The car will start 
immedeatly again after a few seconds. He suspects it to be a computer bug in 
the injection system.Anybody with similar problems ?
 
AGERATEC AB
Jan Warnqvist___
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Re: [Biofuel] Chevy diesels

2007-04-23 Thread Jan Warnqvist
Yes, he has. Once was enough.
  - Original Message - 
  From: John Beale 
  To: biofuel@sustainablelists.org 
  Sent: Monday, April 23, 2007 3:15 PM
  Subject: Re: [Biofuel] Chevy diesels


  Ask him if he's replaced his fuel filter since switching to Biodiesel.




  On Apr 23, 2007, at 8:58 AM, Jan Warnqvist wrote:


He has consumed approx. 600 ltrs and encountered problems from the very 
beginning.

  - Original Message -
  From: John Beale 
  To: biofuel@sustainablelists.org 
  Sent: Monday, April 23, 2007 2:36 PM
  Subject: Re: [Biofuel] Chevy diesels

  But did he make the switch recently or has he been running biodiesel for 
years and he's just now experiencing problems?
  John



  On Apr 23, 2007, at 8:21 AM, Jan Warnqvist wrote:


He is running on 100% BD and the problems began immedeately on the 
first tank of BD.

  - Original Message -
  From: John Beale
  To: biofuel@sustainablelists.org 
  Sent: Monday, April 23, 2007 1:55 PM
  Subject: Re: [Biofuel] Chevy diesels

  How long ago did he switch to biodiesel and is he running on 100% BD 
or a mix?
  John


  On Apr 23, 2007, at 7:09 AM, Jan Warnqvist wrote:


Hello everybody in the New World and others.
I have an aquintance who is running his Chevy 6,2 litre truck on 
biodiesel, and he experiences mysterious engine stops etc. The car will start 
immedeatly again after a few seconds. He suspects it to be a computer bug in 
the injection system.Anybody with similar problems ?
 
AGERATEC AB
Jan Warnqvist___
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Re: [Biofuel] Chevy diesels

2007-04-23 Thread Jan Warnqvist
Hello Keith.
He is in Sweden on rapeseed BD. But, as far as I remember, somebody in the 
US wrote about some similar problems with his Chevy.
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, April 23, 2007 4:43 PM
Subject: Re: [Biofuel] Chevy diesels


 Hello everybody in the New World and others.
I have an aquintance who is running his Chevy 6,2 litre truck on
biodiesel, and he experiences mysterious engine stops etc. The car
will start immedeatly again after a few seconds. He suspects it to
be a computer bug in the injection system.Anybody with similar
problems ?

AGERATEC AB
Jan Warnqvist

 Where is he, Jan? In Sweden or in the US? In other words is he using
 rapeseed biodiesel or soy biodiesel?

 Best

 Keith


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Re: [Biofuel] Acids

2007-03-13 Thread Jan Warnqvist
Hello Robin et al.
The acidic step is necessary for neutralisation of the biodiesel. But, 
basically any mineral acid can be used. The most common (and efficient ?) is 
concentrated sulphuric acid. Even hydrochloric acid can be used, however 
usually available as 35-36% solution. For neutralisation similar amounts of 
phosphoric and sulphuric acid are required, all according to the need for 
neutralisation.
With best regards
AGERATEC AB
Jan Warnqvist

- Original Message - 
From: Robin Pentney [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, March 12, 2007 9:49 PM
Subject: [Biofuel] Acids


 Hi!
 Can anyone tell me what the purpose of the Phosphoric acid in the
 'Foolproof method? I would like to try it (the method) but phosphoric
 is only made in Alberta by a fertilizer mfr just down the road from
 me, but they will only make enough for themselves. Rats! The oilfield
 creates a huge demand for it here, so the suppliers who ship it up
 from the states or from Winnipeg mark it up mercilessly. $158.00 for
 a 20 L pail! It is 75% so there's lots of diluting to do , but still
 Can I use another acid for the wash? Can you describe the reaction
 for me ( a neophyte ) In the wash process so I can fully understand
 it? I am striving to achieve the best quality fuel possible so that
 others will not be discouraged when if they see me sitting at the
 side of the road beside my car , with the hood up and my thumb out
 What would I dilute the 75% phosporic with? Distilled water?
 Tnx
 Robin


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Re: [Biofuel] Crude fatty acid distillate

2007-01-24 Thread Jan Warnqvist
Ken, the important thing is that you do the measurements necessary in order 
to decide how to proceed.

With best regards
AGERATEC AB
Jan Warnqvist
- Original Message - 
From: JAMES PHELPS [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Wednesday, January 24, 2007 7:53 PM
Subject: Re: [Biofuel] Crude fatty acid distillate


 Jan, Ken,
 I have pushed the procedure to double the acid amount in the first phase,
 dewatered and went to the second phase (base base) in small batches 
 without
 problem.  I suggest testing in small amounts and working up a procedure 
 that
 fits the product. This will take some time to do but when you get it you
 can get repeatbility thereafter.  I did use Venturi acid introduction so
 that perhaps makes a big difference as well.

 Jim


From: Jan Warnqvist [EMAIL PROTECTED]
Reply-To: biofuel@sustainablelists.org
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Crude fatty acid distillate
Date: Wed, 24 Jan 2007 12:48:10 +0100

If you have that much tri-glycerides you may most likely do one acid
esterification followed by one base trans-esterification. Just check the
FFA
value after the first step after removal of the (acidic) water phase. If
the
FFA value is  5%, go as described above, in any other case as described
before.
With best regards
AGERATEC AB
Jan Warnqvist
- Original Message -
From: [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Wednesday, January 24, 2007 10:02 AM
Subject: Re: [Biofuel] Crude fatty acid distillate


  Thanks again Jan.
 
  Its 71.8% FFA.  But doing acid esterification twice? Do you finish with
a
  base transesterification after the two acid esterification?
  Please pardon my ignorance.  Can you expound a bit.  First time to hear
  about acid esterification twice.  Appreciate very much your help on the
  matter.
 
  Thanks.
 
  Ken
 
  - Original Message -
  From: Jan Warnqvist [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Sent: Tuesday, January 23, 2007 4:46 PM
  Subject: Re: [Biofuel] Crude fatty acid distillate
 
 
  No, if you are working with 100% free fatty acids, you will have to do
  the
  ACID esterification twice with water content evapoation inbetween
 
  With best regards
  AGERATEC AB
  Jan Warnqvist.
  - Original Message -
  From: [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Sent: Tuesday, January 23, 2007 9:22 AM
  Subject: Re: [Biofuel] Crude fatty acid distillate
 
 
   Thanks Jan,
  
   So you are saying that Aleks Kac's two stage process is the way to 
   go
   on
   this one?  Start with the acid-based stage and finish with the
  base-based
   stage.  That's doing it twice right?
  
   Am doing small batches on the single stage base process (about 100
  liters
   veg. oil).  Will blending this with new veg. oil make a difference?
  
   Been reading the Foolproof Method over and over again to familiarize
   myself.
   Looks like it.
  
   Much thanks again.
  
   Ken
  
   - Original Message -
   From: Jan Warnqvist [EMAIL PROTECTED]
   To: biofuel@sustainablelists.org
   Sent: Tuesday, January 23, 2007 3:35 PM
   Subject: Re: [Biofuel] Crude fatty acid distillate
  
  
   Hello Ken,
   fatty acids are possible to esterify with an acid catalyst. The
formed
   water
   has to be drawn off, so it is always nice to start with a low water
   content.
   Performed correctly, the esterification will produce 90-95% esters.
   Usually
   these kinds of reactions are performed twice for a good conversion
  grade.
  
   With best regards
   AGERATEC AB
   Jan Warnqvist
   - Original Message -
   From: [EMAIL PROTECTED]
   To: biofuel@sustainablelists.org
   Sent: Tuesday, January 23, 2007 8:18 AM
   Subject: Re: [Biofuel] Crude fatty acid distillate
  
  
Hi everyone,
   
I sent this out a few days ago.  I was told by someone in the oil
  mill
that
crude fatty acid distillate is just a fancy name for their 
seconds
or
reject
oils, which soap factories take from them and make into soap.
Anyone
   has
any experience with this kind of stock being made into biodiesel?
  Will
such
a high FFA content give problems?
   
Thanks.
   
Ken
   
   
- Original Message -
From: [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, January 18, 2007 10:15 AM
Subject: [Biofuel] Crude fatty acid distillate
   
   
Hi everyone,
   
An oil mill has just told me that they have excess of crude 
fatty
  acid
distillate which they can give me with the following
specifications
  :
   
Free Fatty Acid (As Lauric)  -  71.8%
Iodine Value mg I/g  - 10
Total Fatty Matter- 96%
Moisture  Impurities   - 0.5%
Saponifiable Value mg KOH/g   -  260
Unsaponifiable Matter-  0.32%
   
I am now doing some small production for my own use with a blend
of
WVO
and
new oil on the single stage process

Re: [Biofuel] Crude fatty acid distillate

2007-01-23 Thread Jan Warnqvist
No, if you are working with 100% free fatty acids, you will have to do the 
ACID esterification twice with water content evapoation inbetween

With best regards
AGERATEC AB
Jan Warnqvist.
- Original Message - 
From: [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, January 23, 2007 9:22 AM
Subject: Re: [Biofuel] Crude fatty acid distillate


 Thanks Jan,

 So you are saying that Aleks Kac's two stage process is the way to go on
 this one?  Start with the acid-based stage and finish with the base-based
 stage.  That's doing it twice right?

 Am doing small batches on the single stage base process (about 100 liters
 veg. oil).  Will blending this with new veg. oil make a difference?

 Been reading the Foolproof Method over and over again to familiarize 
 myself.
 Looks like it.

 Much thanks again.

 Ken

 - Original Message -
 From: Jan Warnqvist [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Tuesday, January 23, 2007 3:35 PM
 Subject: Re: [Biofuel] Crude fatty acid distillate


 Hello Ken,
 fatty acids are possible to esterify with an acid catalyst. The formed
 water
 has to be drawn off, so it is always nice to start with a low water
 content.
 Performed correctly, the esterification will produce 90-95% esters.
 Usually
 these kinds of reactions are performed twice for a good conversion grade.

 With best regards
 AGERATEC AB
 Jan Warnqvist
 - Original Message -
 From: [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Tuesday, January 23, 2007 8:18 AM
 Subject: Re: [Biofuel] Crude fatty acid distillate


  Hi everyone,
 
  I sent this out a few days ago.  I was told by someone in the oil mill
  that
  crude fatty acid distillate is just a fancy name for their seconds or
  reject
  oils, which soap factories take from them and make into soap.  Anyone
 has
  any experience with this kind of stock being made into biodiesel?  Will
  such
  a high FFA content give problems?
 
  Thanks.
 
  Ken
 
 
  - Original Message -
  From: [EMAIL PROTECTED]
  To: Biofuel@sustainablelists.org
  Sent: Thursday, January 18, 2007 10:15 AM
  Subject: [Biofuel] Crude fatty acid distillate
 
 
  Hi everyone,
 
  An oil mill has just told me that they have excess of crude fatty acid
  distillate which they can give me with the following specifications :
 
  Free Fatty Acid (As Lauric)  -  71.8%
  Iodine Value mg I/g  - 10
  Total Fatty Matter- 96%
  Moisture  Impurities   - 0.5%
  Saponifiable Value mg KOH/g   -  260
  Unsaponifiable Matter-  0.32%
 
  I am now doing some small production for my own use with a blend of 
  WVO
  and
  new oil on the single stage process.  I've read up on the two stage
  process
  and it looks like the above will take a two stage process with 71.8%
 FFA.
  Am I right?  Anyone out there with some thoughts on the matter?  Its
 free
  stuff for me although its only about 200liters monthly.  Would it be
  better
  to blend it or process it separately?
 
  Thanks
 
  Ken
 
 
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Re: [Biofuel] Crude fatty acid distillate

2007-01-22 Thread Jan Warnqvist
Hello Ken,
fatty acids are possible to esterify with an acid catalyst. The formed water 
has to be drawn off, so it is always nice to start with a low water content. 
Performed correctly, the esterification will produce 90-95% esters. Usually 
these kinds of reactions are performed twice for a good conversion grade.

With best regards
AGERATEC AB
Jan Warnqvist
- Original Message - 
From: [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, January 23, 2007 8:18 AM
Subject: Re: [Biofuel] Crude fatty acid distillate


 Hi everyone,

 I sent this out a few days ago.  I was told by someone in the oil mill 
 that
 crude fatty acid distillate is just a fancy name for their seconds or 
 reject
 oils, which soap factories take from them and make into soap.  Anyone has
 any experience with this kind of stock being made into biodiesel?  Will 
 such
 a high FFA content give problems?

 Thanks.

 Ken


 - Original Message -
 From: [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Thursday, January 18, 2007 10:15 AM
 Subject: [Biofuel] Crude fatty acid distillate


 Hi everyone,

 An oil mill has just told me that they have excess of crude fatty acid
 distillate which they can give me with the following specifications :

 Free Fatty Acid (As Lauric)  -  71.8%
 Iodine Value mg I/g  - 10
 Total Fatty Matter- 96%
 Moisture  Impurities   - 0.5%
 Saponifiable Value mg KOH/g   -  260
 Unsaponifiable Matter-  0.32%

 I am now doing some small production for my own use with a blend of WVO
 and
 new oil on the single stage process.  I've read up on the two stage
 process
 and it looks like the above will take a two stage process with 71.8% FFA.
 Am I right?  Anyone out there with some thoughts on the matter?  Its free
 stuff for me although its only about 200liters monthly.  Would it be
 better
 to blend it or process it separately?

 Thanks

 Ken


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[Biofuel] Question

2007-01-17 Thread Jan Warnqvist
Hi all,
came across some info on Jatropha oil recently. The oil from some spieces is 
considered non-edible, but I have found no reason for it. Can somebody spread a 
little light on this ?

Jan Warnqvist
aGERATEC AB___
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Re: [Biofuel] Water Powered Engine / Electrolysis

2006-12-29 Thread Jan Warnqvist
Hello Doug, Andrew et al.
Hydrogen gas has a fine heat value, which makes it very interesting as an
energy source. However, as Doug pointed out, it will be necessary to obtain
the energy for the electrolysis from an outer source, why not from solar
cells, to make the energy balance favourable. Good Luck !
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, December 29, 2006 5:49 AM
Subject: Re: [Biofuel] Water Powered Engine / Electrolysis


 What this amounts to is a really lousy, incompetent attempt at a perpetual
 motion machine.

 You have to put in the energy to separate the hydrogen from the oxygen,
 then you get back the same energy when they recombine. There would be no
 surplus to run the vehicle even if every stage was perfectly efficient,
 which they are very far from being.

 Doug Woodard
 St, Catharines, Ontario, Canada


  Just trying to pick the brains of the rest of the world
 
  This is pertaining to gasoline engines being run off of hydrogen from an
  electrolysis reaction onboard the vehicle.
  http://www.spiritofmaat.com/archive/feb2/carplans_doc.htm
 
  What is the probability of this working correctly? Anyone done it?
 
  Thanks,
  Andrew



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Re: [Biofuel] Ethanol use

2006-08-22 Thread Jan Warnqvist
Hello Ken, Charles et al.
Ethanol can be somewhat tricky to deal with when it comes to producing
biodiesel.
The glycerine drop is related to the amount of ethyl esters that you have
created during the process. This is suggesting that you will need a certain
qty of ethyl esters produced in order to have a spontaneous glycerol drop.
To make sure that you have a sufficient amount, the ethanol stochiometric
surplus should be at least 75% or rather 100%. The stochiometric
relationships are much more important than increasing of the reaction
temperature, say 5 or 10 degrees. But also note that the ethanol inserted
has to be anhydrous.
Best of luck to you !
Jan Warnqvist
AGERATEC AB


+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Ken Provost [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, August 22, 2006 4:40 AM
Subject: Re: [Biofuel] Ethanol use



 On Aug 21, 2006, at 1:57 PM, Charles List wrote:


  I would like to know, however, if I can increase the temperature
  of the  reaction mixture to cut down the time taken for the reaction
  as  ethanol boils at 78C rather than 65C.


 You probably could, but the separation of glycerol takes such a
 long time with ethanol (hours maybe), and the reactants are all
 in solution that whole time (completely clear, single phase), that
 you probably don't need more than the usual heating to get the
 reaction to go as far as it will.

 -K




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Re: [Biofuel] Water content - was tirating a virgin oil

2006-08-22 Thread Jan Warnqvist



Hello Joe.
If you are trying to recycle the surplus 
methanol you should be aware of this:
MeOH 
+ KOH  MeO  + K+ + H2O
Methanol 
and potassium hydroxide will form water. That is your first water source. The 
second is the water content of the fresh methanol which should be below 0,5%. 
The third water source is the oil, max water content 0,5%. And if you add 1kg of 
KOH you can expect it form 0,322 kgs of water as it dissolves in the methanol. 
So for a batch of 1000 kgs, these are the actual water contents:
Oil: 
5 kgs
Methanol 
: 1kg
KOH 
(20kg): 6,45 kgs
12,45 
kgs of water = 1,25%
So 
now you can understand why itcan benecessary to dry the oil. To 
decrease the water content further I suggest that you purchase ready-made 
anhydrous catalyst, such as Potassium or Sodium Methoxide. In this case the 
surplus methanol will have a low water content and will be recyclable. For the 
water in methanol tests I can only say that this gravimetric method of yours is 
difficult. So far there is no simple quick and reliable method to do 
this.
Best 
of luck to you !

Jan WarnqvistAGERATEC AB


+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Joe Street 
  To: biofuel@sustainablelists.org 
  
  Sent: Tuesday, August 22, 2006 4:15 
  PM
  Subject: Re: [Biofuel] Water content - 
  was tirating a virgin oil
  Jan;Further to my post from yesterday regarding the 
  0.5% water in oil as a limit; I am assuming that this percentage relies 
  on fairly anhydrous methoxide, and therefore is the maximum water that the 
  process can tolerate. Is this a safe assumption? And if so would it be 
  safe then to assume that if the oil is very dry the same absolute amount of 
  water could be present in another source? I am asking because I am 
  working on methanol recovery now. I can dry my oil quite well with 
  vacuum and heat but recovered methanol always has significant water. If 
  I assume methanol is added at 20% of oil volume then the same absolute volume 
  of water present in the methanol can be 5 times higher i.e. 2.5% instread of 
  0.5% of oil volume? Is this correct? If so then I need only dry my 
  methanol to 97.5% to get good results with very dry oil. I would 
  appreciate your thoughts on this.I have purchased a hydrometer in the 
  0.790 to 0.900 range so that I can test the water content of recovered 
  methanol. The hydrometer is calibrated for 15 degrees C which is cooler 
  than room temperature. Also there is the problem that if I add 50 ml 
  methanol and 50 ml water I don't get 100 ml of liquid! Rather than try 
  to compensate the readings what I have decided to do is start with pure 
  methanol and add small amounts of water and record the readings at room 
  temperature to produce my own table based on percentages by volume. I 
  will post these results so that others can benefit from it. My first 
  test which was a mixture of methanol recovered from fuel mixed with methanol 
  recovered from glycerin cocktail measured 0.813 at RT. That's a lot of 
  water. Sigh.Stay tuned for more.JoeJan Warnqvist 
  wrote:
  Hello Emre, Rafal et al.
I have to say that I partially disagree with some of your statements. The
limit of FFA for a flawless trans-esterification is drawn at 5mg KOH/g of
oil. Any value above will demand pre-treatment of the oil. It is always
important to check the water content, which should be below 0,5%. Try to get
hold of a water-in-oil test kit for quick determination.
If we are talking about the EN standard, it is always necessary to process
the oil/catalyst/methanol mix for 90 minutes to obtain the right values for
tri- di- and monoglycerides. And - this assumes that you have correct
stochiometric conditions and no methanol losses during processing.
As for the phophatides and the chlorophyll compounds, my experience is that
these are not very important for the processing result, unless the values of
these are extremely high (thousands of ppms). If so, the oil is usually very
dark. Totally refined oil, on the other hand, may have preservatives added,
and some of these will eat catalyst. So, good oil quality is a tricky thing.
Best of luck to you !
Jan Warnqvist
AGERATEC AB


+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: "EMRE ELMAS" [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, August 20, 2006 10:15 PM
Subject: Re: [Biofuel] tirating a virgin oil


  
Dear Rafal,

First of all, as long as you use cheap oil you should always be prepared
to
  
deal with much more FFA and water than it should normally contain. I think
your emulsion problem occurs as a result of highly contained water. If
that
  
is the problem you should first dry the oil then process the reaction.

Also if you use crude oil you should be very careful about the chemicals,
such as lesitine, in the oil. So always try to use degummed oil, if you
have
  
to process crude oil.

Another thing is, as you pro

Re: [Biofuel] tirating a virgin oil

2006-08-22 Thread Jan Warnqvist
Hello Tom.
Yes, it is likely that the high FFA content of the oil caused you problems
with the methanol test. But, the water content is also important. You should
get yourself a water test kit.
One way of pre-treatment is to do a two-step process. After the first
alkaline step, take off the glycerol and process the oil/ester with methanol
and sulphuric acid as catalyst. This will give you a very high ester
content. The amount of acid added has to be calculated upon the original FFA
value, of course.
With best regards
Jan Warnqvist
AGERATEC AB



+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Thomas Kelly [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, August 22, 2006 7:35 PM
Subject: Re: [Biofuel] tirating a virgin oil


 Jan,
 You wrote:
 The limit of FFA for a flawless trans-esterification is drawn at 5mg
 KOH/g of oil. Any value above will demand pre-treatment of the oil.

  I have been blending the WVO I collect - titration of  2 - 3 g
of
 90%KOH/L. I recently ran a 76L batch of poor quality WVO . It titrated at
 5.5g of 90%KOH/L. For the first time in months, the BD I produced failed
the
 methanol  quality test   not bad, but there were tiny buggers that did
 not dissolve.
  I have been troubled by the failed test. I have never used WVO that
 titrated above 4g  90% KOH/L.
 1. Is it reasonable assume that the failure to make quality BD was due to
 the poor quality of the WVO I used?
 2. What pre-treatment would be appropriate?

  Tom
 - Original Message - 
 From: Jan Warnqvist [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Monday, August 21, 2006 10:39 AM
 Subject: Re: [Biofuel] tirating a virgin oil


  Hello Emre, Rafal et al.
  I have to say that I partially disagree with some of your statements.
The
  limit of FFA for a flawless trans-esterification is drawn at 5mg KOH/g
of
  oil. Any value above will demand pre-treatment of the oil. It is always
  important to check the water content, which should be below 0,5%. Try to
  get
  hold of a water-in-oil test kit for quick determination.
  If we are talking about the EN standard, it is always necessary to
process
  the oil/catalyst/methanol mix for 90 minutes to obtain the right values
  for
  tri- di- and monoglycerides. And - this assumes that you have correct
  stochiometric conditions and no methanol losses during processing.
  As for the phophatides and the chlorophyll compounds, my experience is
  that
  these are not very important for the processing result, unless the
values
  of
  these are extremely high (thousands of ppms). If so, the oil is usually
  very
  dark. Totally refined oil, on the other hand, may have preservatives
  added,
  and some of these will eat catalyst. So, good oil quality is a tricky
  thing.
  Best of luck to you !
  Jan Warnqvist
  AGERATEC AB
 



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Re: [Biofuel] tirating a virgin oil

2006-08-21 Thread Jan Warnqvist
Hello Emre, Rafal et al.
I have to say that I partially disagree with some of your statements. The
limit of FFA for a flawless trans-esterification is drawn at 5mg KOH/g of
oil. Any value above will demand pre-treatment of the oil. It is always
important to check the water content, which should be below 0,5%. Try to get
hold of a water-in-oil test kit for quick determination.
If we are talking about the EN standard, it is always necessary to process
the oil/catalyst/methanol mix for 90 minutes to obtain the right values for
tri- di- and monoglycerides. And - this assumes that you have correct
stochiometric conditions and no methanol losses during processing.
As for the phophatides and the chlorophyll compounds, my experience is that
these are not very important for the processing result, unless the values of
these are extremely high (thousands of ppms). If so, the oil is usually very
dark. Totally refined oil, on the other hand, may have preservatives added,
and some of these will eat catalyst. So, good oil quality is a tricky thing.
Best of luck to you !
Jan Warnqvist
AGERATEC AB


+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: EMRE ELMAS [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, August 20, 2006 10:15 PM
Subject: Re: [Biofuel] tirating a virgin oil


 Dear Rafal,

 First of all, as long as you use cheap oil you should always be prepared
to
 deal with much more FFA and water than it should normally contain. I think
 your emulsion problem occurs as a result of highly contained water. If
that
 is the problem you should first dry the oil then process the reaction.

 Also if you use crude oil you should be very careful about the chemicals,
 such as lesitine, in the oil. So always try to use degummed oil, if you
have
 to process crude oil.

 Another thing is, as you probably know, approximately 95 - 97 % of the
 reaction is completed in the first 35 minutes, so you do not have to wait
 for 2 hours. Also the alcohol boils at 65 C and the closer you get to that
 point, the more alcohol you will lose at the time you need it the most for
 the reaction. This prevents you to complete the reaction 100 %.

 As I mentioned above if you just watch the content of water and the other
 impurities in the oil you will be fine.

 Hopefully the information works for you. I am looking forward to hear from
 you soon.

 Best wishes,

 Emre ELMAS
 Mobile: +90 533 517 72 45





 From: Rafal Szczesniak [EMAIL PROTECTED]
 Reply-To: biofuel@sustainablelists.org
 To: biofuel@sustainablelists.org
 Subject: [Biofuel] tirating a virgin oil
 Date: Sun, 20 Aug 2006 19:31:26 +0200
 
 Hi,
 
 Recently I've came through problems with testing a cheap virgin oil
 in my test processor which every time ended up with incomplete reactions
 (emulsion problems). I did make the process longer (2 hours) and at
 higher temperature (60-63 degC) - still nothing, though by product
 separation is very nice.
 
 Today, I tried to titrate the oil and - to my surprise - it took 0.925ml
 of KOH solution. This was my first experience with titration, so I can
 also tell that the phenolophtalein solution turned pale (but noticable)
 magenta for about 15 secs (as described at JtF) after 0.925ml. After
 adding 1.05ml the colour got more intensive for longer time.
 
 My main question is - is it normal in case of cheap oils ?
 I suppose they contain (as other oils) some amount of FFAs, but so much ?
 
 Additional matter is whether I got titration right. I mean, interpreting
 the colours.
 
 I'm running out of ideas what could be wrong in the process, so any
 help is appreciated.
 
 
 --
 cheers,
 
   Rafal Szczesniak  **mir[at]diament.iit.pwr.wroc.pl
   Samba Team member mi***[at]samba.org
 +-+
   *BSD, GNU/Linux and Samba  http://www.samba.org
 +-+
 
 
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Re: [Biofuel] Sweden how they do it

2006-08-13 Thread Jan Warnqvist



Hello Lugano et al.
As a Swedish native I can provide a more 
detailed and personal picture of the possibilities of oil independence of this 
country. There are a number of buts:
- The power companies are not allowed to 
increase the share of electricity coming from hydropower sources, because 
thereis environmental, nature-protecting legislation. So, in order to 
become more independent of oil, we just have to trust that the 11 nuclear power 
plants running, will keep on to do so without serious accidents or other side 
effects.
- Biodiesel has never been a popular 
product within any administration in this country. This is probably because 
biodiesel production can be performed in small scale. The administrative 
favourite product, ethanol, is a typical large scale product, which complies 
more with the industrial traditions of this country. One can even suspect that 
there is an attitude proclaiming that it is bad enough letting the farmers be in 
control of the food production. Things would get even worse if the farmers were 
in control of the energy production as well.
- The petroleum supplies to this country 
have mainly been coming from the North Sea for a number of decades now, provided 
nominally by Norwegian and British companies. But the northernAtlantic 
production has already passed its peak, making changes necessary in order not to 
be totally depending upon oil from Russia and the middle east, which can be 
considered asa tooadventurous project.
- The result of next election can very 
well over-throw the ambition of oil independence, since the right-liberal-centre 
coalition aiming for office, doesn´t have this target on the agenda. 

- The automotive industry, not only the 
Swedish, has to acknowledge and accept the goal. So far nothing along this line 
has been proclaimed from the industry. In such a small export-depending country 
as Sweden, the automotive industry is very power-ful, and used to 
havingits way.
Jan Warnqvist
+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Lugano 
  Wilson 
  To: biofuel@sustainablelists.org 
  
  Sent: Saturday, August 12, 2006 1:52 
  PM
  Subject: Re: [Biofuel] Sweden how they do 
  it
  
  Yes, 
  
  Sweden is well commited to renewabel energy as part of energy security 
  and environmental considerations. it is projected that in 2010 about 51% of of 
  its electricity will be produced from renewable sources. this is supported by 
  existing huge hydropower sources and strong commitment to bioenergy. renewable 
  electricity like bioenergy, wind, solar, etc. are currently growing in sharing 
  the supply scheme due to existing legislation on certification scheme.
  
  further to this, the transport sector has been targetted for increased 
  efficiency and utilization of renewable energy like ethanol and biodiesel 
  through taxation that based on annual vehicle pollution (emitted CO2) and not 
  the conventional taxation that based on either weight, size, utilization, 
  etc.
  
  the whole of this development is guided by strong policies that are 
  spearheading research, development and utilization. 
  
  follow the following links for: 
  
  1: electricity for renewable sources http://ec.europa.eu/energy/res/publications/index_en.htm
  
  2: 
  green vehicles 
  http://www.gronabilister.se/public/dokument.php?art=272 
  
  have a nice week end. 
  
  Lugano
  Mark` Cookson [EMAIL PROTECTED] 
  wrote:
  Hellow 
every one I was listening to the radio this afternoon here int the UK 
and a programme come on called Costing the Earth. Its subject was how 
Sweden are changing away from fossil fuels.I found it very 
interesting as you may.Follow the link here then go down the left of 
the page to [Listen to the latest programme link] hey 
presto!!!http://www.bbc.co.uk/radio4/science/costingtheearth.shtmlGood 
luckMark___Biofuel 
mailing 
listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel 
at Journey to 
Forever:http://journeytoforever.org/biofuel.htmlSearch the 
combined Biofuel and Biofuels-biz list archives (50,000 
messages):http://www.mail-archive.com/biofuel@sustainablelists.org/..Division 
  of Energy and Furnace Technology,Department of Materials Science and 
  Engineering,Royal Institute of Technology (KTH),Brinellvägen 23,SE 
  100 44 Stockholm,Sweden.[EMAIL PROTECTED]Tel. 0046 8 205 
  204Fax: 0046 8 207 681..
  
  
  Talk is cheap. Use Yahoo! Messenger to make PC-to-Phone calls. MailScanner has detected a possible fraud attempt from "us.rd.yahoo.com" claiming to be Great 
  rates starting at 1¢/min.
  
  

  ___Biofuel mailing 
  listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel 
  at Journey to 
  Forever:http://journeytof

Re: [Biofuel] Sweden how they do it

2006-08-13 Thread Jan Warnqvist



Hello Lugano et al.
As a Swedish native I can provide a more 
detailed and personal picture of the possibilities of oil independence of this 
country. There are a number of buts:
- The power companies are not allowed to 
increase the share of electricity coming from hydropower sources, because 
thereis environmental, nature-protecting legislation. So, in order to 
become more independent of oil, we just have to trust that the 11 nuclear power 
plants running, will keep on to do so without serious accidents or other side 
effects.
- Biodiesel has never been a popular 
product within any administration in this country. This is probably because 
biodiesel production can be performed in small scale. The administrative 
favourite product, ethanol, is a typical large scale product, which complies 
more with the industrial traditions of this country. One can even suspect that 
there is an attitude proclaiming that it is bad enough letting the farmers be in 
control of the food production. Things would get even worse if the farmers were 
in control of the energy production as well.
- The petroleum supplies to this country 
have mainly been coming from the North Sea for a number of decades now, provided 
nominally by Norwegian and British companies. But the northernAtlantic 
production has already passed its peak, making changes necessary in order not to 
be totally depending upon oil from Russia and the middle east, which can be 
considered asa tooadventurous project.
- The result of next election can very 
well over-throw the ambition of oil independence, since the right-liberal-centre 
coalition aiming for office, doesn´t have this target on the agenda. 

- The automotive industry, not only the 
Swedish, has to acknowledge and accept the goal. So far nothing along this line 
has been proclaimed from the industry. In such a small export-depending country 
as Sweden, the automotive industry is very power-ful, and used to 
havingits way.
Jan Warnqvist
+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Lugano 
  Wilson 
  To: biofuel@sustainablelists.org 
  
  Sent: Saturday, August 12, 2006 1:52 
  PM
  Subject: Re: [Biofuel] Sweden how they do 
  it
  
  Yes, 
  
  Sweden is well commited to renewabel energy as part of energy security 
  and environmental considerations. it is projected that in 2010 about 51% of of 
  its electricity will be produced from renewable sources. this is supported by 
  existing huge hydropower sources and strong commitment to bioenergy. renewable 
  electricity like bioenergy, wind, solar, etc. are currently growing in sharing 
  the supply scheme due to existing legislation on certification scheme.
  
  further to this, the transport sector has been targetted for increased 
  efficiency and utilization of renewable energy like ethanol and biodiesel 
  through taxation that based on annual vehicle pollution (emitted CO2) and not 
  the conventional taxation that based on either weight, size, utilization, 
  etc.
  
  the whole of this development is guided by strong policies that are 
  spearheading research, development and utilization. 
  
  follow the following links for: 
  
  1: electricity for renewable sources http://ec.europa.eu/energy/res/publications/index_en.htm
  
  2: 
  green vehicles 
  http://www.gronabilister.se/public/dokument.php?art=272 
  
  have a nice week end. 
  
  Lugano
  Mark` Cookson [EMAIL PROTECTED] 
  wrote:
  Hellow 
every one I was listening to the radio this afternoon here int the UK 
and a programme come on called Costing the Earth. Its subject was how 
Sweden are changing away from fossil fuels.I found it very 
interesting as you may.Follow the link here then go down the left of 
the page to [Listen to the latest programme link] hey 
presto!!!http://www.bbc.co.uk/radio4/science/costingtheearth.shtmlGood 
luckMark___Biofuel 
mailing 
listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel 
at Journey to 
Forever:http://journeytoforever.org/biofuel.htmlSearch the 
combined Biofuel and Biofuels-biz list archives (50,000 
messages):http://www.mail-archive.com/biofuel@sustainablelists.org/..Division 
  of Energy and Furnace Technology,Department of Materials Science and 
  Engineering,Royal Institute of Technology (KTH),Brinellvägen 23,SE 
  100 44 Stockholm,Sweden.[EMAIL PROTECTED]Tel. 0046 8 205 
  204Fax: 0046 8 207 681..
  
  
  Talk is cheap. Use Yahoo! Messenger to make PC-to-Phone calls. MailScanner has detected a possible fraud attempt from "us.rd.yahoo.com" claiming to be Great 
  rates starting at 1¢/min.
  
  

  ___Biofuel mailing 
  listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel 
  at Journey to 
  Forever:http://journeytof

Re: [Biofuel] The amazing properties of Vegtible oil

2006-06-17 Thread Jan Warnqvist
Yes,both Keith and David are right. Unless you are referring to palm oil,
which have an unusual fatty acid composition, the amount of glycerine in
most vegetable oils is roughly 10% by mass.
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Saturday, June 17, 2006 6:48 PM
Subject: Re: [Biofuel] The amazing properties of Vegtible oil


 Is there a chemist amongst our ranks that can that can quantify % and
 molar, how much glycerin is in 1 liter of soybean oil? tallow? canola?
 Fish? (all virgin)Seems like spend time pondering questions like this of
 late.  Any one know?
 
 Jim

 Hello Jim

 The rule of thumb is 79 millilitres of glycerine for every litre of
 oil used (7.9%).
 -- How much glycerine? Why isn't it solid?
 Make your own biodiesel - page 2: Journey to Forever
 http://journeytoforever.org/biodiesel_make2.html#howmuchglyc

 More information here:

 How much methanol?
 http://journeytoforever.org/biodiesel_meth.html

 HTH.

 Best

 Keith


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Re: [Biofuel] Back to the future

2006-06-09 Thread Jan Warnqvist
Håkan, it is obvious that no patent or manufacturing lisence will last for 
one houndrad years, espcecially considering the development of the diesel 
engine. But Scania is the inheritar of the original diesel engine. However, 
it is not flattering for us Swedes to be so historically involved and 
possibly even having promoted the petroleum substitute for the diesel 
engine. Particulary not, since there is a common imagnination that the 
discovery of petroleum made it possible for the combustion engine to arise, 
because of the unique properties of petroleum.
Jan
- Original Message - 
From: Hakan Falk [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, June 09, 2006 9:37 AM
Subject: Re: [Biofuel] Back to the future



Jan,

Manufacturing rights as a whole to the diesel engine cannot be
owned by Scania, only certain modifications that are done the
last 25 years. It is no legal way, that I know of, to protect the
original diesel engine for 100 years. The only legal way to protect
manufacturing rights, is through patents and even they are not
protected in certain countries. Patents are only valid for 25 years
and the normal way is to patent modifications/enhancements to
the original patent to prolong the patent protection of the most
competitive product.

Diesel might have had the idea as student, but he had financing
for his development from the German coal industry. The contract
was to develop his engine to run on coal dust. That is why there
are always mentioning of coal dust, in conjunction with diesel.

Kerrosene was at the time and today, used for lamps and heating.
It is also a quality of kerrosene used for dry cleaning.

The quality of crude that are economical for gasoline, will end
before the crude suitable for fuel for diesel engine. If normal demand
principles are governing the situation, the price gap between
diesel and gasoline should widen in the future. It depends also
on the space heating demands, where heating oil (diesel) is
used for small buildings. Large buildings and Area centrals, use
heavy oil and it will last longer than diesel.

When we are talking of oil depletion, it is a very rough estimation.
Certain oil products like gasoline are depleting faster than the
generally used numbers. Oil products and their depletion is
a much more complex situation.

Hakan


At 08:34 09/06/2006, you wrote:
Yes, I am able to amswer some questions concerning Rudolf Diesel.
He had his idea to his engine when he was a student of the technical
academy. Once he had a ready prototype ( which was tested with several 
fuels
; gasoline, kerrosene and vegetable oils) he realized that he had to supply
the fuel with the machine. So as a result of an agreement with Atlas Copco
Diesel (member of the Wallenberg group) he had oil exploration rights in
Baku, near the Caspian Sea through an oil company with head office in St
Petersbrg Russia. This company was run by two relatives to Alfred Nobel, 
the
founder of the Nobel prize. The aim with this deal was to obtain large qtis
of kerrosene, which was the main petroleum product by that time. But then
the Russian revelution came in 1917 and his rights were expropiated. But 
the
time that he had at his disposal was enough to establish kerrosene as the
main diesel fuel. The manufacturing rights of the diesel engine is now 
owned
by Scania, which also is a member of the Wallenberg group.
The question for Rudolf Diesel was not the fuel itself, it was to have
access to diesel engine fuel, period.
We are now running out of oil, but some really good alternatives are coming
up in practice, don´t you think ?
Jan Warnqvist
- Original Message -
From: lres1 [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, June 09, 2006 4:49 AM
Subject: Re: [Biofuel] Back to the future


  Mike
  The oil engine was in use long before Rudolf Diesel. Bit of chicken or
  egg.
 
  Did Rudolf  invent the fuel?
  He certainly reduced the size of the oil engine principal to enable it 
  to
  fit into land transport use from Sea and machine shop energy sources. I
  have
  been unable to locate any part where he actually invented the mineral 
  oil
  known as Diesel oil. I can only find references to Peanut/vegetable oils
  in
  his early engines.
 
  Can anyone point me in the direction where he invented the Diesel oil?
 
  Prohibition was to stop home making of fuel or to stop alcoholic drinks 
  or
  one was to cover the other? In history wood alcohol was included why?
 
  Henry Ford was a ruthless marketing and business man. (Read some of 
  Edzels
  conflicts with his father before his early death). Fuel was sold in 
  cans.
  How do you sell cars to people well away from fuel sources? Make them 
  able
  to run on multi fuels, until Prohibition. The dates are about correct,
  late
  model T and early model A, AA and AAA. Note the model AAA
  (Triple
  A) was still run on ethanol as was not outlawed as far as my trips and
  research shows.
 
  The globe

Re: [Biofuel] Back to the future

2006-06-09 Thread Jan Warnqvist
No I do not have a connection to Atlas Copco, but I know a little something 
about Rudolf Diesel.
Jan
- Original Message - 
From: Hakan Falk [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, June 09, 2006 12:41 PM
Subject: Re: [Biofuel] Back to the future



Jan,

I did work with Atlas Copco as consultant in acoustics, when they developed
the silent compressors. At the time I was employed by Stellan Dahlstedt,
Akustik Konsult AB. It was very interesting insights in both diesel and
compressor technology.  The person in charge of their acoustic lab. was an
ex. employee in Akustik Konsult. I tell you this, because you obviously have
a connection to them. It was around 40 years ago and I moved out of Sweden
almost 30 years ago, to work full time with CAD/CAM and network products.

The final line of compressors became trend setters in the market and a large
success.

Håkan


At 11:06 09/06/2006, you wrote:
Håkan, it is obvious that no patent or manufacturing lisence will last for
one houndrad years, espcecially considering the development of the diesel
engine. But Scania is the inheritar of the original diesel engine. However,
it is not flattering for us Swedes to be so historically involved and
possibly even having promoted the petroleum substitute for the diesel
engine. Particulary not, since there is a common imagnination that the
discovery of petroleum made it possible for the combustion engine to arise,
because of the unique properties of petroleum.
Jan
- Original Message -
From: Hakan Falk [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, June 09, 2006 9:37 AM
Subject: Re: [Biofuel] Back to the future



Jan,

Manufacturing rights as a whole to the diesel engine cannot be
owned by Scania, only certain modifications that are done the
last 25 years. It is no legal way, that I know of, to protect the
original diesel engine for 100 years. The only legal way to protect
manufacturing rights, is through patents and even they are not
protected in certain countries. Patents are only valid for 25 years
and the normal way is to patent modifications/enhancements to
the original patent to prolong the patent protection of the most
competitive product.

Diesel might have had the idea as student, but he had financing
for his development from the German coal industry. The contract
was to develop his engine to run on coal dust. That is why there
are always mentioning of coal dust, in conjunction with diesel.

Kerrosene was at the time and today, used for lamps and heating.
It is also a quality of kerrosene used for dry cleaning.

The quality of crude that are economical for gasoline, will end
before the crude suitable for fuel for diesel engine. If normal demand
principles are governing the situation, the price gap between
diesel and gasoline should widen in the future. It depends also
on the space heating demands, where heating oil (diesel) is
used for small buildings. Large buildings and Area centrals, use
heavy oil and it will last longer than diesel.

When we are talking of oil depletion, it is a very rough estimation.
Certain oil products like gasoline are depleting faster than the
generally used numbers. Oil products and their depletion is
a much more complex situation.

Hakan


At 08:34 09/06/2006, you wrote:
 Yes, I am able to amswer some questions concerning Rudolf Diesel.
 He had his idea to his engine when he was a student of the technical
 academy. Once he had a ready prototype ( which was tested with several
 fuels
 ; gasoline, kerrosene and vegetable oils) he realized that he had to 
 supply
 the fuel with the machine. So as a result of an agreement with Atlas 
 Copco
 Diesel (member of the Wallenberg group) he had oil exploration rights in
 Baku, near the Caspian Sea through an oil company with head office in St
 Petersbrg Russia. This company was run by two relatives to Alfred Nobel,
 the
 founder of the Nobel prize. The aim with this deal was to obtain large 
 qtis
 of kerrosene, which was the main petroleum product by that time. But then
 the Russian revelution came in 1917 and his rights were expropiated. But
 the
 time that he had at his disposal was enough to establish kerrosene as the
 main diesel fuel. The manufacturing rights of the diesel engine is now
 owned
 by Scania, which also is a member of the Wallenberg group.
 The question for Rudolf Diesel was not the fuel itself, it was to have
 access to diesel engine fuel, period.
 We are now running out of oil, but some really good alternatives are 
 coming
 up in practice, don´t you think ?
 Jan Warnqvist
 - Original Message -
 From: lres1 [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Friday, June 09, 2006 4:49 AM
 Subject: Re: [Biofuel] Back to the future
 
 
   Mike
   The oil engine was in use long before Rudolf Diesel. Bit of chicken or
   egg.
  
   Did Rudolf  invent the fuel?
   He certainly reduced the size of the oil engine principal to enable it
   to
   fit into land

Re: [Biofuel] Back to the future

2006-06-09 Thread Jan Warnqvist
 Nobel,
 the
 founder of the Nobel prize. The aim with this deal was to obtain large
qtis
 of kerrosene, which was the main petroleum product by that time. But then
 the Russian revelution came in 1917 and his rights were expropiated. But
 the
 time that he had at his disposal was enough to establish kerrosene as the
 main diesel fuel. The manufacturing rights of the diesel engine is now
 owned
 by Scania, which also is a member of the Wallenberg group.
 The question for Rudolf Diesel was not the fuel itself, it was to have
 access to diesel engine fuel, period.
 We are now running out of oil, but some really good alternatives are
coming
 up in practice, don´t you think ?
 Jan Warnqvist
 - Original Message -
 From: lres1 [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Friday, June 09, 2006 4:49 AM
 Subject: Re: [Biofuel] Back to the future
 
 
   Mike
   The oil engine was in use long before Rudolf Diesel. Bit of chicken or
   egg.
  
   Did Rudolf  invent the fuel?
   He certainly reduced the size of the oil engine principal to enable it
   to
   fit into land transport use from Sea and machine shop energy sources.
I
   have
   been unable to locate any part where he actually invented the mineral
   oil
   known as Diesel oil. I can only find references to Peanut/vegetable
oils
   in
   his early engines.
  
   Can anyone point me in the direction where he invented the Diesel oil?
  
   Prohibition was to stop home making of fuel or to stop alcoholic
drinks
   or
   one was to cover the other? In history wood alcohol was included why?
  
   Henry Ford was a ruthless marketing and business man. (Read some of
   Edzels
   conflicts with his father before his early death). Fuel was sold in
   cans.
   How do you sell cars to people well away from fuel sources? Make them
   able
   to run on multi fuels, until Prohibition. The dates are about correct,
   late
   model T and early model A, AA and AAA. Note the model AAA
   (Triple
   A) was still run on ethanol as was not outlawed as far as my trips and
   research shows.
  
   The globe was already controlled by the oil industry. Sloan, the most
   powerfull man at the time, could not perhaps change this or was in
   agreement
   with the oil industry.
  
   *   Rudolf Diesel, the inventor of the diesel engine, designed it
   to
 run on vegetable and seed oils like hemp. In fact, when the
   diesel
 engine was first introduced at the World's Fair in 1900, it ran
   on
 peanut oil.
   * Two decades later, Henry Ford was designing his Model Ts to run
   on
 ethanol made from hemp. He envisioned the entire mass-produced
 Model T automobile line would run on ethanol derived from crops
 grown in the U.S.
   * Even in the 1920s, the oil industry had massive lobbying power
in
 Washington. Lobbyists convinced policymakers to create laws
 favoring petroleum based fuels while disgarding the ethanol
   option.
   * Nearly a century later, amidst oil wars in the Middle East,
   Global
 Warming, and a nearly depleted oil supply, the U.S. government
is
 finally shifting attention to fuels that are more along the
lines
 of Diesel and Ford's original ideas.
   * In an interview with the New York Times in 1925, Henry Ford
said:
 The fuel of the future is going to come from fruit like that
 sumac out by the road, or from apples, weeds, sawdust -- almost
 anything. There is fuel in every bit of vegetable matter that
can
 be fermented. There's enough alcohol in one year's yield of an
 acre of potatoes to drive the machinery necessary to cultivate
   the
 fields for a hundred years.
  
   Whose water is it? *Learn more:*
   http://www.organicconsumers.org/2006/article_658.cfm
  
  
 
http://alerts.organicconsumers.org/trk/click?ref=zqtbkk3um_0-ax332x3239551;




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Search the combined Biofuel

Re: [Biofuel] Back to the future

2006-06-09 Thread Jan Warnqvist
  before the crude suitable for fuel for diesel engine. If normal demand
  principles are governing the situation, the price gap between
  diesel and gasoline should widen in the future. It depends also
  on the space heating demands, where heating oil (diesel) is
  used for small buildings. Large buildings and Area centrals, use
  heavy oil and it will last longer than diesel.
 
  When we are talking of oil depletion, it is a very rough estimation.
  Certain oil products like gasoline are depleting faster than the
  generally used numbers. Oil products and their depletion is
  a much more complex situation.
 
  Hakan
 
 
  At 08:34 09/06/2006, you wrote:
  Yes, I am able to amswer some questions concerning Rudolf Diesel.
  He had his idea to his engine when he was a student of the technical
  academy. Once he had a ready prototype ( which was tested with several
  fuels
  ; gasoline, kerrosene and vegetable oils) he realized that he had to
supply
  the fuel with the machine. So as a result of an agreement with Atlas
Copco
  Diesel (member of the Wallenberg group) he had oil exploration rights 
  in
  Baku, near the Caspian Sea through an oil company with head office in 
  St
  Petersbrg Russia. This company was run by two relatives to Alfred 
  Nobel,
  the
  founder of the Nobel prize. The aim with this deal was to obtain large
qtis
  of kerrosene, which was the main petroleum product by that time. But 
  then
  the Russian revelution came in 1917 and his rights were expropiated. 
  But
  the
  time that he had at his disposal was enough to establish kerrosene as 
  the
  main diesel fuel. The manufacturing rights of the diesel engine is now
  owned
  by Scania, which also is a member of the Wallenberg group.
  The question for Rudolf Diesel was not the fuel itself, it was to have
  access to diesel engine fuel, period.
  We are now running out of oil, but some really good alternatives are
coming
  up in practice, don´t you think ?
  Jan Warnqvist
  - Original Message -
  From: lres1 [EMAIL PROTECTED]
  To: biofuel@sustainablelists.org
  Sent: Friday, June 09, 2006 4:49 AM
  Subject: Re: [Biofuel] Back to the future
  
  
Mike
The oil engine was in use long before Rudolf Diesel. Bit of chicken 
or
egg.
   
Did Rudolf  invent the fuel?
He certainly reduced the size of the oil engine principal to enable 
it
to
fit into land transport use from Sea and machine shop energy 
sources.
I
have
been unable to locate any part where he actually invented the 
mineral
oil
known as Diesel oil. I can only find references to Peanut/vegetable
oils
in
his early engines.
   
Can anyone point me in the direction where he invented the Diesel 
oil?
   
Prohibition was to stop home making of fuel or to stop alcoholic
drinks
or
one was to cover the other? In history wood alcohol was included 
why?
   
Henry Ford was a ruthless marketing and business man. (Read some of
Edzels
conflicts with his father before his early death). Fuel was sold in
cans.
How do you sell cars to people well away from fuel sources? Make 
them
able
to run on multi fuels, until Prohibition. The dates are about 
correct,
late
model T and early model A, AA and AAA. Note the model AAA
(Triple
A) was still run on ethanol as was not outlawed as far as my trips 
and
research shows.
   
The globe was already controlled by the oil industry. Sloan, the 
most
powerfull man at the time, could not perhaps change this or was in
agreement
with the oil industry.
   
*   Rudolf Diesel, the inventor of the diesel engine, designed 
it
to
  run on vegetable and seed oils like hemp. In fact, when the
diesel
  engine was first introduced at the World's Fair in 1900, it 
ran
on
  peanut oil.
* Two decades later, Henry Ford was designing his Model Ts to 
run
on
  ethanol made from hemp. He envisioned the entire 
mass-produced
  Model T automobile line would run on ethanol derived from 
crops
  grown in the U.S.
* Even in the 1920s, the oil industry had massive lobbying 
power
in
  Washington. Lobbyists convinced policymakers to create laws
  favoring petroleum based fuels while disgarding the ethanol
option.
* Nearly a century later, amidst oil wars in the Middle East,
Global
  Warming, and a nearly depleted oil supply, the U.S. 
government
is
  finally shifting attention to fuels that are more along the
lines
  of Diesel and Ford's original ideas.
* In an interview with the New York Times in 1925, Henry Ford
said:
  The fuel of the future is going to come from fruit like that
  sumac out by the road, or from apples, weeds, sawdust --  
almost
  anything. There is fuel in every bit of vegetable matter

Re: [Biofuel] Ethanol for diesel engines

2006-06-08 Thread Jan Warnqvist



Just wanting to make some remarks 
.
The Scania ethanol buses are running 
on a special ethanol quality blend consisting from ethanol (95%), a cetane 
improver called Bereid, which I am told is a polyglycol, and a lubricant. The 
injection timing is normal (approx 20 degrees before TDC) and all engines are 
equipped with intercooler which functions as an air heater when the engine runs 
on idle. Ethanol is not self-evident as a diesel fuel, but progress has been 
done.
Jan Warnqvist

  - Original Message - 
  From: 
  FRANCISCO 
  To: biofuel@sustainablelists.org 
  
  Sent: Thursday, June 08, 2006 4:25 
  PM
  Subject: Re: [Biofuel] Ethanol for diesel 
  engines
  HiEthanol is close to gasoline when referring to fueling 
  energy to an engine. Therefore cetane number is low even though ethanol 
  prefers higher pressure than regular gasoline. So ethanol diesel blend to be 
  viable as fuel and easy the blending has to have two supports: cetane improver 
  additive to easy combustion and a electronic/software combination which can 
  adjust ignition timing and pumpin all the time. ( Please remember atomiztion 
  is diferent also!) In order to reduce the amount of additive ( very 
  expensive and it is like TNT - worsening stability) I assume they use some 
  diesel so it helps ignition (Please note) This reminds me the natural 
  gas/diesel dual fuel engine where the diesel is used as the spark plug and the 
  electronics do the rest. Please remember when we have two types of fuel two 
  explosions will always happen and in the case of the diesel/cetane 
  improver/alcohol we might have three explosions and this is not good for the 
  engine so in the long run efficiency is jeopardize severely.Hakan you are 
  right: The cetane improver experiences with alcohol have been done a long time 
  by Scania and in fact they tried to introduce this technology in Brasil. It is 
  not used because it was considered too expensive. The consumption should 
  be much higher than the 100% diesel ( energy content per mass and volume 
  admission in the combustion chamber ) and considering the new refining 
  technologies the emissions of the new blend should not be better. We 
  still do not know the effect of aldehyde on the environment a please pay 
  attention nitrates generates NOx thru exhaust pipe and aldehyde and NOx are 
  always there when using alcohol. Also diesel engines do operate at higher 
  temperatures and this can affect exhaust gases worsening emissions 
  environmentally speaking.In my opinion we have to scrutinize this approach 
  thouruglly and this approach it is not novel. I love ppo svo and 
  biodiesel.very best fo rall of usChicHakan Falk wrote: 
  Keith,

If I remembered right, the Swedish diesel buses are running on a wood 
alcohol mix, with some sort of additive. In Sweden it is now more and 
more common that the buses use biofuel.

Hakan


At 18:47 07/06/2006, you wrote:
  
Hi Tomas


  Hi,

this one fuel combination is interesting.
I've never heard about such possibility before:

http://www.greencarcongress.com/2006/06/xcelplus_acquir.html

--
Tomas Juknevicius
  Fuel-Cycle Energy and Emission Impacts of Ethanol-Diesel Blends in
Urban Buses and Farming Tractors, (July 2003, 992kb pdf)
http://www.transportation.anl.gov/pdfs/TA/280.pdf

The Manual for the Home and Farm Production of Alcohol Fuel
by S.W. Mathewson
Chapter 3 UTILIZATION OF ALCOHOL FUELS
Diesel Engines
http://journeytoforever.org/biofuel_library/ethanol_manual/manual3.html

Best

Keith


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Re: [Biofuel] Biodiesel from wood

2006-06-02 Thread Jan Warnqvist
Hello Steve et al,
if  my memory isn¨t fooling me, is there a fatty acid fraction in tall oil. 
The composition of this reminds very much of that of soy bean oil. But it 
takes a lot of distilling and fractionizing to get this fatty acid fraction 
clean enough. Wood is more suitable for ethanol production I think.
Jan Warnqvist
- Original Message - 
From: Steve Knox [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, June 02, 2006 12:17 PM
Subject: Re: [Biofuel] Biodiesel from wood


I believe that there is a company in Germany (CHOREN) who makes biodiesel
from wood. If my memory is correct, they're getting about 60 or so gallons
per ton. A major oil company has bought an interest in the company.

Steve
- Original Message - 
From: Zeke Yewdall [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Thursday, June 01, 2006 10:30 PM
Subject: Re: [Biofuel] Biodiesel from wood


Using wood as feedstock means using either lignin or cellulose, right?
 If so, alot of stuff could be made into biodiesel -- grass, weeds,
cardboard, etc...  Thermo catalytic cracking is the only thing I can
think of that could do this.  Unless they have some fancy microbes
that can digest lignin and give oil?

I also remember that in WWII germany was trying to distill gasoline
substitutes from pine trees -- I thought this was more like turpentine
though, derived more from the sap than the wood?   I'm not an expert
on this by any means, but perhaps someone else remembers exactly what
they were doing.

Zeke

On 6/1/06, [EMAIL PROTECTED] [EMAIL PROTECTED] wrote:
 Has anyone heard of such a thing? It says Wood-based biodiesel
 production requires the development of new technology. Are they on to
 something or are they still working out if this is even possible?

 Steve

 http://snipurl.com/r8b3

 (2006-05-26) Hydro and Norske Skog have agreed to carry out a joint
 feasibility study relating to the production of biodiesel from wood.
 The intention is to identify the feasibility of establishing a
 biodiesel production facility in south-east Norway. Such a plant could
 come on stream by 2012 at the earliest.

 We consider ourselves to be natural partners as far as wood-based
 biodiesel is concerned. Hydro has wide experience derived from the
 construction and operation of major processing plants and from the
 quest to find new forms of energy. Norske Skog has considerable
 expertise when it comes to wood purchasing and treating wood pulp, say
 senior vice president Alexandra Bech Gjørv of Hydro and vice president
 Terje Engevik of Norske Skog.

 A technically superior product

 The production of biodiesel is currently based on rapeseed or other
 oil-based raw materials. Wood-based biodiesel production requires the
 development of new technology. Once this technology is in place, it
 will be possible to offer an even better product than today?s biodiesel.

 Today only a five-percent biodiesel tank mixture is available.
 Wood-based biodiesel will give us a technically superior product
 without such limitations. By using timber we can also utilize a much
 greater proportion of the raw material and considerably reduce
 greenhouse gas emissions compared with biodiesel produced from rapeseed
 or other plant oils. This means that wood-based biodiesel will be a an
 even more environmentally friendly fuel than today?s biodiesel, the
 two companies say in a press release.

 NEW ENERGY: Alexandra Bech Gjørv is responsible for Hydro's efforts to
 develop renewable energy. (Photo: Kåre Foss)


 Long road to completion

 The road to completion of a possible production plant is, however, a
 long one. To begin with, collaboration between the two companies
 involves a feasibility study that will primarily provide an overview of
 the technologies available in the market, identify the availability of
 raw materials, and create a realistic picture of the external governing
 conditions that must be in place in order to reach an investment
 decision.

 CO2 emissions represent a climate threat that affects all of us, and
 we can see that the political will exists to promote biodiesel as an
 environmentally friendly alternative to regular fuels. There is great
 potential for biodiesel in the market of the future, but if this market
 is going to materialize we are in need of a sound, long-term operating
 framework from the authorities, state Bech Gjørv and Engevik.


 Author: Lars Nermoen
 Published: 2006-05-26


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[Biofuel] American diesels

2006-05-18 Thread Jan Warnqvist



Hello everybody in the Americas! I 
have one question for you concerning BD and the cars consuming it. It seems as 
if you all are prefering European cars for fueling BD instead of American 
diesels. Is that true, and in this case why? Arn´t GM:s diesels good for BD 
?

Jan 
Warnqvist
BEGIN:VCARD
VERSION:2.1
N:Warnqvist;Jan
FN:Jan Warnqvist
ORG:AGERATEC AB
TEL;WORK;VOICE:+46 11 33 53 70
TEL;CELL;VOICE:+46 70 4993845
URL;WORK:http://www.ageratec.com
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Re: [Biofuel] distilling fuel/reactant ethanol

2006-04-23 Thread Jan Warnqvist
Hello Jason and Kate,
the reason for this is simple. The castor oil (unlike most other vegetable
oils) is ethanol soluble. This means that most other oils will not do the
trick.
With best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

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- Original Message - 
From: Jason  Katie [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Sunday, April 23, 2006 6:31 AM
Subject: [Biofuel] distilling fuel/reactant ethanol


 i pulled a paper from the library describing separating ethanol from water
 using castor oil. can this be done using any kind of oil, or are their
 certain characteristics of the oil not described in the paper?

 http://journeytoforever.org/biofuel_library/eth_separate.html


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Re: [Biofuel] best source for WVO

2006-03-22 Thread Jan Warnqvist
Hello Zeke et al.
A very unscientific trial feeding sugar into the air intake(without air
filter) suggested that sugar does not harm the engine at all, just
combusting together with tha gasoline. According to this experiment, the
melting points and boiling points of the sugar (sackarose) are rather close.
Jan
AGERATEC AB
Jan Warnqvist
- Original Message -
From: Zeke Yewdall [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, March 22, 2006 6:21 PM
Subject: Re: [Biofuel] best source for WVO


 What exactly would sugar do to an engine?  The worst I can think of is
 clogging some filters or increasing carbon deposits.

 Zeke

 On 3/22/06, Bob Carr [EMAIL PROTECTED] wrote:
 
  Nor sure about lard, but watch out for sugar in your feedstock. This is
an
  old favourite additive for sabotaging an engine.
  Reg'ds
 
  Bob
 
 
  - Original Message -
  From: ROY Washbish
  To: Biofuel@sustainablelists.org
  Sent: Wednesday, March 22, 2006 12:09 PM
  Subject: Re: [Biofuel] best source for WVO
 
 
  Hi All
  Don't donut shops use LARD that is SOLID at room temp?
  Isn't that lard full of sugar?
  Roy
 
 
  [EMAIL PROTECTED] wrote:
  as i am just starting myself, i am thinking towards donut shops. they
  usually fry no meats in their veg oil and would have less fats.
 
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Re: [Biofuel] Vinegar in WVO

2006-02-18 Thread Jan Warnqvist



Hello Tom, 
if your titration value is 1,9 , there is 
no need for additional treatment, since the acidic ions from the vinegar will be 
included in the titration value. However, you shoulddetermine the water 
content of the oil before processing it. A good value here is max 0,5%. 

Yes, you are right, the oxonium ions from 
the vinegar will produce water when neutralized and the complete reaction will 
be the following :
H3O+ 
+ Ac- + Na+ + OH-  2 H2O + 
Na+ Ac-
but 
NaOH in methanol and in oil with some vinegar the following reaction takes 
place:

Na+ + MeO - + H3O 
+ Ac- + H2O  
MeOH + Na+ Ac- + 2 H2O
This means that instead of one extra water 
molecule you will produce one molecule of methanol, since sodium hydroxide will 
form sodium methoxide and water in methanol.
It is of some comfort, isn´t it ?
Best of luck to you !
Jan
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Thomas 
  Kelly 
  To: Biofuel@sustainablelists.org 
  
  Sent: Friday, February 17, 2006 7:21 
  PM
  Subject: Re: [Biofuel] Vinegar in 
  WVO
  
  Zeke, Mark and Doug,
   Thanks for 
  your thoughts. The oil comes from a nice restaurant.Some of their 
  appetizersare deep fried and could contribute acid to the oil. I just 
  spoke to one of the kitchen staff. He said theyscrub the fryers w. 
  vinegarand it goes, along w. the oil, into the grease dumpster. I 
  suspect most of the vinegar settles out w. the water.
  I am interested in 
  the role these water-soluble acids might play in the reaction and the 
  byproductsmade. 
   Since they are not fatty 
  acids, they should not produce soap themselves, but won't lye + vinegar 
  (acetic acid) produce sodium acetate and water?
   Should I try to 
  neutralize the vinegarbefore dryingthe oil? Should I go to the 
  trouble of washing the oil and allowing it to settle for a few weeks before 
  drying it?
   It is good oil and there 
  is a lot of it. Washed w. water, settled overnight, then dried, it 
  titrates at 1.9g/L .
   Thanks 
  again,
   
  Tom
  - Original Message - 
  
From: 
Doug 
Turner 
To: Biofuel@sustainablelists.org 

Sent: Friday, February 17, 2006 11:58 
AM
Subject: Re: [Biofuel] Vinegar in 
WVO

Hi Tom,

 Some restaurants will use a 
vinegar rinse after cleaning their fryer equipment. The intent is to 
extend the useful oil lifespan by neutralizing any bases (from the soaps) 
that may remain after cleaning. They should do a final water rise but 
many do not. This could be the source of your acid.

 Doug Turner


  - Original Message - 
  From: 
  Thomas 
  Kelly 
  To: biofuel 
  Sent: Friday, February 17, 2006 8:56 
  AM
  Subject: [Biofuel] Vinegar in 
  WVO
  
  Good day to all,
  I have 
  anew source of WVO. It is very clear and light in color. I did a 
  titration w/o drying it. I was surprised to find that it required 3.2ml of 
  .1% lyeto neutralize each ml of oil. 
  We heateda sampleof the oil and 
  some water fell out.The dry oil titrated at 2.6ml of the lye 
  solution. I shake-washed some of the oil in water and then dried the oil 
   titration required only2.3ml of the lye 
  solution.The wash water was ever so 
  slightly acid. There seems to be water soluble 
  acid(s) in this oil.
   While heating the 
  oil, a friend commented on the smell. My wife came home and asked if we 
  wereusing vinegar. 
  Here's the questions:
   1. Do restaurants either 
  fry foods with vinegar in/on them?
  Do acids from frying cheeses (mozarella 
  sticks) leach into the oil?Do restaurants clean their grills/friers 
  w. vinegar?
   2. Am I correct in 
  assuming that these mysterious water-soluble acidswill be 
  neutralized by the lye and will not contribute to soap 
  formation?
  
   
  Thanks for listening,
   
  Tom
  
  

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Re: [Biofuel] KOH carbonated

2006-02-12 Thread Jan Warnqvist
Hello Jim,
if you knew the level of carbonation, it would be much simpler. If you treat
this KOH as ordinary KOH, you will have a buffer solution in water or
methanol. this buffer will not be as effective as you are used to. I suggest
that you try a mini-batch and adjust the input of your new KOH according to
that. Good luck !

Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

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- Original Message - 
From: JJJN [EMAIL PROTECTED]
To: BIO Biofuel@sustainablelists.org
Sent: Sunday, February 12, 2006 6:07 AM
Subject: [Biofuel] KOH carbonated


 Hello everyone,

 I just got 50 #s of KOH for next to nothing. It is in flake form but it
 is carbonated to some extent (unkown).  I have some lab grade KOH that
 is near absolute also.

 Can anyone give me a complete procedure to make a comparison (Strength
 %) of one to the other?  I want to know because if the one is 10% weaker
 than the other then I should be able to increase the weaker by 10% to
 achieve similar results.  I understand that from this point I must still
 tweek some one way or the other.

 Perhaps my thinking is flawed in assuming the relationship is
 proportional and  I should just  use better  KOH?

 Any help would be greatly appreciated.

 Jim

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Re: [Biofuel] pH question

2006-01-30 Thread Jan Warnqvist



I have already been critizised for 
leaving out the sub-understood meaning that the determinations should be carried 
out in a water phase, since the H30 and OH ions are not detectable any where 
else.
Jan

  - Original Message - 
  From: 
  A. Secco 
  
  To: Biofuel@sustainablelists.org 
  
  Sent: Monday, January 30, 2006 4:15 
  PM
  Subject: Re: [Biofuel] pH question
  
  Dear Jan,
  If I understand correctly somethingcan be 
  wrong with the pH measurementswhich Andrew made and 
  reported.
  The pH can only be measured in an aqueous system 
  and not in an oil/fatty phase. It has no sense to put the probe in the oil 
  phase to measure pH. Remember that pH only applies were the water equilibrium 
  constant works.
  Instead of measuring through an pH electrode it 
  is more convenient and accurate to measure the total acidity of the oil 
  phasewhich is made throug a titration with NaOH and reported as "acid 
  value"
  
  Andres Secco
  
- Original Message - 
From: 
Jan Warnqvist 
To: Biofuel@sustainablelists.org 

Sent: Monday, January 30, 2006 3:30 
AM
Subject: Re: [Biofuel] pH 
question

Hello Andrew,
not to worry, that pH value is 
quite in order. When you judge the result of a correctly performed pH 
determination, you should be aware of that the pH scale is logaritmic. 
Example:
pH 7 means that the amounts of 
H3O( acidic)and OH (hydroxide)ions are the same amounts, that is 10 
powered by - 7 moles per dm3 = 0,001 moles/dm3.
If you have pH 6, this means that 
the H3O ions are ten times more than the OH ions, H3O= 10 powered by -6 
moles/dm3 = 0,01, and the OH ions are 10 powered by -8 moles/dm3 = 
0,0001 moles/dm3.For pH 2 you have a concentration for the H3O ions of 
10 powered by -2 = 0.01 moles/dm3 and the corresponding value for OH is 10 
powered by -12 = 0,0001 moles/dm3. This means thatif apH 
determination drops from pH 1 to pH 2, much more has actually happend than a 
drop from pH 6 to pH 7.
The reason for pH 6 on biodiesel 
could be that there is a content of free fatty acids or other acidic remains 
in the biodiesel. Is this right, Bob ?
    
Jan Warnqvist

  - Original Message - 
  From: 
  Andrew 
  Leven 
  To: Biofuel@sustainablelists.org 
  
  Sent: Monday, January 30, 2006 2:09 
  AM
  Subject: [Biofuel] pH question
  
  Hello,
  I'vemade and washed 4 test 
  batches from different wvo oil sources andhave comeup 
  with some quite clear, light amber colored BD but it all seems to test out 
  at pH 6 + or -. This seems a bit low. Any ideas about what would cause a 
  consistent low reading like this?
  Andrew Leven
  
  

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  Internet. Tutopia es Internet para todos.  
  
  

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Re: [Biofuel] pH question

2006-01-29 Thread Jan Warnqvist



Hello Andrew,
not to worry, that pH value is quite 
in order. When you judge the result of a correctly performed pH determination, 
you should be aware of that the pH scale is logaritmic. Example:
pH 7 means that the amounts of H3O( 
acidic)and OH (hydroxide)ions are the same amounts, that is 10 powered by 
- 7 moles per dm3 = 0,001 moles/dm3.
If you have pH 6, this means that the 
H3O ions are ten times more than the OH ions, H3O= 10 powered by -6 moles/dm3 = 
0,01, and the OH ions are 10 powered by -8 moles/dm3 = 0,0001 
moles/dm3.For pH 2 you have a concentration for the H3O ions of 10 powered by -2 
= 0.01 moles/dm3 and the corresponding value for OH is 10 powered by -12 = 
0,0001 moles/dm3. This means thatif apH determination drops 
from pH 1 to pH 2, much more has actually happend than a drop from pH 6 to pH 
7.
The reason for pH 6 on biodiesel 
could be that there is a content of free fatty acids or other acidic remains in 
the biodiesel. Is this right, Bob ?

Jan Warnqvist

  - Original Message - 
  From: 
  Andrew Leven 
  
  To: Biofuel@sustainablelists.org 
  
  Sent: Monday, January 30, 2006 2:09 
  AM
  Subject: [Biofuel] pH question
  
  Hello,
  I'vemade and washed 4 test batches 
  from different wvo oil sources andhave comeup with some quite 
  clear, light amber colored BD but it all seems to test out at pH 6 + or -. 
  This seems a bit low. Any ideas about what would cause a consistent low 
  reading like this?
  Andrew Leven
  
  

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Re: [Biofuel] ethanol method

2006-01-26 Thread Jan Warnqvist
Hello Bias Antonio,
Ken is right, the NaOH dissolves a lot quicker in ethanol if heated. In
order to make ethyl esters the quality of the reactants has to be high:
ethanol min 99,5% pure and
oil with a water content  500 ppm and
a stochiometric surplus of ethanol of at least 75% and why not 100% ?
The economy of this is depending upon your possibilities of recover the
excess ethanol.
Good luck to you
AGERATEC AB
Jan Warnqvist
- Original Message -
From: Ken Provost [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, January 26, 2006 4:55 AM
Subject: Re: [Biofuel] ethanol method



 On Jan 25, 2006, at 11:00 AM, Blas Antonio Guanes wrote:


   the problem is that, methanol costs 4 $ and pure ethanol
  for car costs 0.52 $, NaOH is gotten in any part.. KOH is
  sold in bags of 25  kilos for soap industry.. Here in Paragua
  it is difficult to get chemical products. for that reason I want
  know how I can make with oil, ethanol and NaOH


 Have you tried dissolving NaOH in pure anhydrous ethanol? It is
 difficult. If you can dissolve the required amount (perhaps by
 boiling the ethanol/NaOH mixture under reflux), you could possibly
 make biodiesel out of very clean dry oil. If you only use 3.5g NaOH
 per liter of oil, or if your ethanol or oil contain any water, you will
 probably never achieve separation of a glycerine phase. All your
 ingredients go into a clear solution, and just stay that way forever.
 Until glycerine separates, you don't have biodiesel.

 -K

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Re: [Biofuel] ethanol method

2006-01-26 Thread Jan Warnqvist
Hello Bob,
yes, you are right, recovered ethanol will likely contain  500 ppm of
water. This ethanol can then possibly only be used in small portions for
forward production of ethyl esters. It is however important to find out the
purity of the recovered ethanol before any conclusions can be drawn. It is
also likely that a big part of the water content of the biodiesel will enter
the most polar phase (glycerol phase), which may make it possible to re-use
the ethanol.
It does not sound too thrilling to use E85 as an ethanol source. There are a
number of research projects that have used gasoline-contaning ethanol, and
this with production difficulties from time to time. Assuming that biodiesel
from E85 is produced, the actual gasoline content would be max 15% of the
esterified ethanol ,about 15% of 13-14% which makes max 2,1% in total
gasoline content in the biodiesel. This amount will not influence the
viscosity, nor the density severly. It is doubtful that it will effect the
cetane number or the material compability properties more than marginally.
However, if the ethanol is recovered, it is highly likeky to assume that
some of the gasoline will enter this phase instead of staying in the
biodiesel. The BD may still have an odour of gasoline though.

AGERATEC AB
Jan Warnqvist
- Original Message -
From: bob allen [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, January 26, 2006 5:40 PM
Subject: Re: [Biofuel] ethanol method


Jan, Wouldn't you expect that  500 ppm water would be picked up in any
recovered ethanol, due to even a small amount of soap production?  also
if the ethanol used is for automobile use, is it an  E-85 blend, ie, 15%
gasoline?  If so I would think that the gasoline would partition into
any biodiesel made from this alcohol source.  How would the gasoline
impact the biodiesel?

Jan Warnqvist wrote:
 Hello Bias Antonio,
 Ken is right, the NaOH dissolves a lot quicker in ethanol if heated. In
 order to make ethyl esters the quality of the reactants has to be high:
 ethanol min 99,5% pure and
 oil with a water content  500 ppm and
 a stochiometric surplus of ethanol of at least 75% and why not 100% ?
 The economy of this is depending upon your possibilities of recover the
 excess ethanol.
 Good luck to you
 AGERATEC AB
 Jan Warnqvist
 - Original Message -
 From: Ken Provost [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Thursday, January 26, 2006 4:55 AM
 Subject: Re: [Biofuel] ethanol method


 On Jan 25, 2006, at 11:00 AM, Blas Antonio Guanes wrote:


  the problem is that, methanol costs 4 $ and pure ethanol
 for car costs 0.52 $, NaOH is gotten in any part.. KOH is
 sold in bags of 25  kilos for soap industry.. Here in Paragua
 it is difficult to get chemical products. for that reason I want
 know how I can make with oil, ethanol and NaOH

 Have you tried dissolving NaOH in pure anhydrous ethanol? It is
 difficult. If you can dissolve the required amount (perhaps by
 boiling the ethanol/NaOH mixture under reflux), you could possibly
 make biodiesel out of very clean dry oil. If you only use 3.5g NaOH
 per liter of oil, or if your ethanol or oil contain any water, you will
 probably never achieve separation of a glycerine phase. All your
 ingredients go into a clear solution, and just stay that way forever.
 Until glycerine separates, you don't have biodiesel.

 -K

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Re: [Biofuel] unheated oil for biodiesel?

2006-01-23 Thread Jan Warnqvist
Hello Kenji,
heating the oil means that you are adding energy to the coming reaction. The
reaction will go faster and become more complete than if you didn´t heat the
oil. Trans-esterifucation processes can often take place in temperatures
around 20oC and above.
The glycerol settling will also go smoother and faster with a little
temperature on it, say around 40 - 50ioC.
Good luck to you
AGERATEC AB
Jan Warnqvist
- Original Message -
From: Kenji James Fuse [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, January 24, 2006 5:14 AM
Subject: [Biofuel] unheated oil for biodiesel?


 I've never tried making biodiesel without heating the oil, except in
 little demo batches (2 litre pop bottle). How necessary is it, and can
 anyone describe the chemistry or physics of it to me in dumb-dumb terms?

 Or maybe its in the archives, and someone could point me in the right
 direction.

 Thanks,

 Kenji Fuse


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Re: [Biofuel] Jan's Methanol test

2006-01-15 Thread Jan Warnqvist
 
from this test?And finally should I be concerned by a 
couple of percent contamination in my fuel? I did 
search the mail archive twice using 'methanol test' and also  'Jan 
    Warnqvist' as keywords, but the returns were not so informative. 
List members I need your wisdom! Jan perhaps you are most 
qualified to answer but I would really like to get a sense of the 
percentage of the list members who are running  this test. So chime 
in! Joe 
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Re: [Biofuel] Acid - Base questions

2006-01-08 Thread Jan Warnqvist
Hello Todd,
yes, to my knowledge it is favourable producing methyl esters by turning the
FFA:s into soaps as a first step. There will be amounts of water created
with this method as well, but it seems to be of less importance.
There is no need for scaring people off , but there is a need for
explaining the mechanisms necessary for success. There will also always be a
need for us that are trained to disperse our knowledge with the
responsibility required.
I was referring to acid esterification of FFA:s / oil without passing
through the soap step. These reactions are often incomplete, and moreover,
quite slow.
With best regards
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Appal Energy [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Sunday, January 08, 2006 4:29 AM
Subject: Re: [Biofuel] Acid - Base questions


 Jan,

 Since when are esterifications often incomplete?

 And since when is a good conversion achieved necessarily through base
 catalysis?

 It's relatively simple to take 100% FFAs and achieve a 100% yield of
 esters. Industry does it daily from soap stock.

 Let people satisfy their own curiosities rather than scaring them off
 paths that many have already taken..., and succeeded at one might add.

 Todd Swearingen


 Jan Warnqvist wrote:

 Hello Jim,
 the sensible thing is to spending time and money producing BD from a
cheap
 feedstock, not the other way around.
 Acid esterifications are often incomplete, and I assume that oils and
fats
 with max 20% FFA are worth while bothering about, unless you are willing
to
 do several acid esterification steps and draining off the produced water
 after each step.But in order to have a good conversion into BD, you
finally
 have to run the alkaline transesterification step , also for
neutralization.
 Good luck to you !
 Jan Warnqvist
 AGERATEC AB
 
 [EMAIL PROTECTED]
 
 + 46 554 201 89
 +46 70 499 38 45
 - Original Message - 
 From: JJJN [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Saturday, January 07, 2006 3:26 AM
 Subject: Re: [Biofuel] Acid - Base questions
 
 
 
 
 Thanks Jan,
 If I had developed a method to separate FFA's from base stock without
 using chemicals or water say in the range of 95% separation in WVO
 (still a work in progress but hopeful results) so that I could React the
 Low FFA's in a Base method then would it be feasible to react the High
 FFA's In a separate Acid reaction? Or what problems would I encounter
 like the water problem you noted below?  Would the FFA's be worth the
 trouble?
 
 Thanks Jim
 
 Jan Warnqvist wrote:
 
 
 
 Hello Jim,
 when using the acid esterification, you will have methyl esters,
 
 
 unreacted
 
 
 oil, sulphate ions, oxonium ions and - water.
 Proceeding to the base step you will create more methyl esters,
potassium
 
 
 or
 
 
 sodium soaps, maybe a little unreacted oil or partially reacted oil,
 potassium or sodium sulphates and - even more water.
 This method works fine if the water content can be kept on a reasonable
 level. Please note that the higher the initial FFA level, the more
water
 will be produced.
 With best regards
 Jan
 Jan Warnqvist
 AGERATEC AB
 
 [EMAIL PROTECTED]
 
 + 46 554 201 89
 +46 70 499 38 45
 - Original Message - 
 From: JJJN [EMAIL PROTECTED]
 To: BIO Biofuel@sustainablelists.org
 Sent: Thursday, January 05, 2006 3:01 AM
 Subject: [Biofuel] Acid - Base questions
 
 
 
 
 
 
 I have decided to try the acid/base method in small test batches as I
 have some High FFA (4ml) oil I would like to process.  Since September
I
 have gone to great lengths to get repeatability and accuracy in all my
 work with Biodiesel. I have read and re-read JtF and I know that I
will
 no doubt read it several more times if I get stumped.  I would like to
 start with fully understanding the process first.
 Before I start:
 Can you use KOH with the Acid Base method?  It might be obvious, but I
 did not see it in the recipe as a substitution.
 
 When the acid gets done with Estrification properly then the mix that
is
 left is basically an oil (triglycerides) , Methanol,  and Sulfur ions
?
 Or did I miss something?
 
 When the Methoxil is added the Sulfur gets combined with the Sodium
 ions, (right?) how does this affect the reaction?
 
 Any good experienced information would be helpful,
 
 Jim
 
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 Biofuel@sustainablelists.org
 
 

http://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.org
 
 
 Biofuel at Journey to Forever:
 http://journeytoforever.org/biofuel.html
 
 Search the combined Biofuel and Biofuels-biz list archives (50,000
 
 
 
 
 messages):
 
 
 
 
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Re: [Biofuel] Acid - Base questions

2006-01-07 Thread Jan Warnqvist
Hello Jim,
the sensible thing is to spending time and money producing BD from a cheap
feedstock, not the other way around.
Acid esterifications are often incomplete, and I assume that oils and fats
with max 20% FFA are worth while bothering about, unless you are willing to
do several acid esterification steps and draining off the produced water
after each step.But in order to have a good conversion into BD, you finally
have to run the alkaline transesterification step , also for neutralization.
Good luck to you !
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: JJJN [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Saturday, January 07, 2006 3:26 AM
Subject: Re: [Biofuel] Acid - Base questions


 Thanks Jan,
 If I had developed a method to separate FFA's from base stock without
 using chemicals or water say in the range of 95% separation in WVO
 (still a work in progress but hopeful results) so that I could React the
 Low FFA's in a Base method then would it be feasible to react the High
 FFA's In a separate Acid reaction? Or what problems would I encounter
 like the water problem you noted below?  Would the FFA's be worth the
 trouble?

 Thanks Jim

 Jan Warnqvist wrote:

 Hello Jim,
 when using the acid esterification, you will have methyl esters,
unreacted
 oil, sulphate ions, oxonium ions and - water.
 Proceeding to the base step you will create more methyl esters, potassium
or
 sodium soaps, maybe a little unreacted oil or partially reacted oil,
 potassium or sodium sulphates and - even more water.
 This method works fine if the water content can be kept on a reasonable
 level. Please note that the higher the initial FFA level, the more water
 will be produced.
 With best regards
 Jan
 Jan Warnqvist
 AGERATEC AB
 
 [EMAIL PROTECTED]
 
 + 46 554 201 89
 +46 70 499 38 45
 - Original Message - 
 From: JJJN [EMAIL PROTECTED]
 To: BIO Biofuel@sustainablelists.org
 Sent: Thursday, January 05, 2006 3:01 AM
 Subject: [Biofuel] Acid - Base questions
 
 
 
 
 I have decided to try the acid/base method in small test batches as I
 have some High FFA (4ml) oil I would like to process.  Since September I
 have gone to great lengths to get repeatability and accuracy in all my
 work with Biodiesel. I have read and re-read JtF and I know that I will
 no doubt read it several more times if I get stumped.  I would like to
 start with fully understanding the process first.
 Before I start:
 Can you use KOH with the Acid Base method?  It might be obvious, but I
 did not see it in the recipe as a substitution.
 
 When the acid gets done with Estrification properly then the mix that is
 left is basically an oil (triglycerides) , Methanol,  and Sulfur ions ?
 Or did I miss something?
 
 When the Methoxil is added the Sulfur gets combined with the Sodium
 ions, (right?) how does this affect the reaction?
 
 Any good experienced information would be helpful,
 
 Jim
 
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 Biofuel@sustainablelists.org

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 Biofuel at Journey to Forever:
 http://journeytoforever.org/biofuel.html
 
 Search the combined Biofuel and Biofuels-biz list archives (50,000
 
 
 messages):
 
 
 http://www.mail-archive.com/biofuel@sustainablelists.org/
 
 
 
 
 
 
 
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 Search the combined Biofuel and Biofuels-biz list archives (50,000
messages):
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Re: [Biofuel] In French ?

2006-01-06 Thread Jan Warnqvist
Hello Oliver.
I have some interesting ideas concerning biofuel in Switzerland. Contact me
on
[EMAIL PROTECTED] ASAP for further discussions.
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Mike Weaver [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Saturday, December 10, 2005 5:26 PM
Subject: Re: [Biofuel] In French ?


Bonjour,

in researching the possibility of making BD with Isopropyl Alcohol, I
have noticed than in Europe many countries refer to biodiesel as FAME;
this may be a useful term to search for when looking for French language
information.

-Mike

Keith Addison wrote:

I would highly recommend also using:

http://world.altavista.com/

I would highly recommend also using an online translator such as
AltaVista's
Babelfish (http://world.altavista.com/).  I have used it frequently for
Russian to English, and it seems to have no problem with English to French
when you use the Translate a web page option.

--Randall
Charlotte, NC



Hello Randall

The machine translators are useful, we've discussed using them here
before, but that was for when people wanted to post messages in
Spanish or French or whatever, not for technical instructions on a
website.

How would American biodieselers for instance like it if they had to
get their information from Journey to Forever via Babelfish?

Here's how the Spanish version of Mike Pelly's titration instructions
come out in English via world.altavista.com:

Disolución of a gram of lejía in a distilled liter of water prepares
one. Asegúrate of which it is dissolved totally. This sample serves
like value of reference in valoración. It is important that this
disolución is not contaminated because serˆ used in many valuations.
Mixture in a container pequeño 10 mililiter of isopropílico alcohol
with 1 mililiter of the oil (asegurate of which it is exactly 1
mililiter). It takes to the oil sample después of it to have warmed
up and to have shaken (5 Figure # 1). Añade two drops of
fenolftaleína, that is an indicator ˆ cido-bases colorless in the
presence of ˆ cidos and red in the presence of bases.

English version:

Make up a solution of one gram of lye to one liter of distilled
water. Make sure it dissolves completely. This sample is then used as
a reference tester for the titration process. It's important not to
let the sample get contaminated, it can be used for many titrations.
Mix 10 milliliters of isopropyl alcohol in a small container with a 1
milliliter sample of WVO -- make sure it's exactly 1 milliliter. Take
the WVO titration sample from the reaction vessel (Figure 5 #1) after
it's been warmed up and stirred. Add to this solution 2 drops of
phenolphthalein, an acid-base indicator that's colorless in acid and
red in base.

Not so good eh?

Lots of people in lots of countries speak French. If there aren't any
good biofuels how-to sites in French there should be. Invitation
stands:



If some of the French-speaking list members wanted to translate the
Journey to Forever Biofuels section into French we'd be happy to host
it, like the Spanish-language site.



Best

Keith





- Original Message -
From: Sam Critchley [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Friday, December 09, 2005 11:51 AM
Subject: Re: [Biofuel] In French ?




Hi,

Biodiesel is often called diester in French. Here's a French-language
Wikipedia entry with some links to biodiesel in Switzerland at the
bottom:

http://fr.wikipedia.org/wiki/Diester

I also suggest doing an advanced search on Google for French-language
pages containing the words biodiesel or diester.

Thanks,

Sam

On Fri, 09 Dec 2005 17:01:00 +0100, Keith Addison
[EMAIL PROTECTED] wrote:



Hello Olivier



I have some friends in the French side of Switzerland, Geneva, who are
interested to try to make Biodiesel. They already have a car (a
LandRover I beleive) running on SVO.

But they do not speak (nor read) english.

Do you know by any chance a good web site where they can find
information on how to produce in French ?


I don't. Maybe there isn't one.

If some of the French-speaking list members wanted to translate the
Journey to Forever Biofuels section into French we'd be happy to host
it, like the Spanish-language site.

Regards

Keith Addison
Journey to Forever
KYOTO Pref., Japan
http://journeytoforever.org/






Thanks,
Olivier




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Re: [Biofuel] Biodiesel Testing excessive methanol

2006-01-06 Thread Jan Warnqvist
Hello Jim,
since the methanol solubility test worked out well, you probably have
created some soap from the methyl esters.
With best regards
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: JJJN [EMAIL PROTECTED]
To: BIO Biofuel@sustainablelists.org
Sent: Monday, January 02, 2006 7:32 PM
Subject: [Biofuel] Biodiesel Testing excessive methanol


 I just tested a 60 Liter batch and have a few questions; below is what I
 have done with the results and further below are my questions,

 The biodiesel used in the tests below was unwashed - glycerin layer
 removed.

 1.) Using the test method noted on JtF ( Jan Warnqvist - Methanol test)
 as prescribed 225 ml Methanol combined with 25 ml of the biodiesel.
 Results: Biodiesel was fully soluble and formed a clear bright phase no
 contaminants or other phases noted. Results after 24 hours - No change.

 2) Using a MODIFIED JtF method,  (combining 4.90875 grams lab grade KOH
 and 100 ml Methanol (Potassium Methoxil) with 1 Liter of the biodiesel)
 - INSTEAD I added 400ml methanol and 4.90875 grams KOH ( Potassium
 Methoxil ) (both lab grade near absolute) to 1 Liter of the Biodiesel. I
 then heated to 120 deg F and mixed for one hour.
 Results: after 24 hours  there was a nice amber layer from the bottom of
 the glass jar up to the last say 1/2 inch where a very very slightly
 amber layer resided to the top. there was nothing at the bottom at all.

 3) Wash test JtF, In a glass jar I shook 1/2 Bio and 1/2 water at room
 temp till mixed into one phase.
 Results: within 1 minute the water and Bio separated and the water was
 quite white. Wash #2 same time of separation water clearer this time.
 Wash # 3 same as #2. Wash # 4 water was not drinking quality but PH is
 close to seven.

 O.K why did I increase the Methanol in test #2) above?  I am not sure
 except to see what it would do, but from what I read it would not harm
 so I did.

 My Question: Can anyone tell me what the strange clear amber layer on
 top of the other clear amber layer may be?

 Could this be the FFA content per L?

 Thanks in advance,

 Jim

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Re: [Biofuel] Acid - Base questions

2006-01-06 Thread Jan Warnqvist
Hello Jim,
when using the acid esterification, you will have methyl esters, unreacted
oil, sulphate ions, oxonium ions and - water.
Proceeding to the base step you will create more methyl esters, potassium or
sodium soaps, maybe a little unreacted oil or partially reacted oil,
potassium or sodium sulphates and - even more water.
This method works fine if the water content can be kept on a reasonable
level. Please note that the higher the initial FFA level, the more water
will be produced.
With best regards
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: JJJN [EMAIL PROTECTED]
To: BIO Biofuel@sustainablelists.org
Sent: Thursday, January 05, 2006 3:01 AM
Subject: [Biofuel] Acid - Base questions


 I have decided to try the acid/base method in small test batches as I
 have some High FFA (4ml) oil I would like to process.  Since September I
 have gone to great lengths to get repeatability and accuracy in all my
 work with Biodiesel. I have read and re-read JtF and I know that I will
 no doubt read it several more times if I get stumped.  I would like to
 start with fully understanding the process first.
 Before I start:
 Can you use KOH with the Acid Base method?  It might be obvious, but I
 did not see it in the recipe as a substitution.

 When the acid gets done with Estrification properly then the mix that is
 left is basically an oil (triglycerides) , Methanol,  and Sulfur ions ?
 Or did I miss something?

 When the Methoxil is added the Sulfur gets combined with the Sodium
 ions, (right?) how does this affect the reaction?

 Any good experienced information would be helpful,

 Jim

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Re: [Biofuel] BD and Oil Burner

2006-01-06 Thread Jan Warnqvist



Hello Tom,
the leakage you have spotted is no doubt a 
result of material incompability, something that you will have to live with 
unless you find sealings of a compatible material.
The biodiesel from WVO will in case of 
crystallisation, plug the fuel filter of your burner, not causing 
leakages.
Is the jelly thing clear or emulsified 
?
Best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Thomas 
  Kelly 
  To: biofuel 
  Sent: Friday, January 06, 2006 4:43 
  PM
  Subject: [Biofuel] BD and Oil 
Burner
  
  Hello All,
   I've been using a 30% 
  BD/70% heating oil mix in my heating oil tank since August. My oil burner 
  heats my water as well as my house.All went well (each time I checked 
  the nozzle on the burner it was clean as new) until late in Dec.
   I was away. My 
  wife noticed an odor of diesel fuel in the basement. She found a small puddle 
  of oil under the furnace. Following is the 
  report from the person who serviced the burner:
   Oil leak under the 
  burner
   Nozzle jelled up 
  outside
   Found some sort of jelly 
  built up on end of nozzle
   Oil was dripping down 
  blast tube
  
  I suspect that the 
  difference in the performance of the mix in Dec vs Aug through Nov, is the 
  cold. Although my oil tank is inside, it is in my basement where temps 
  drop below 50F on cold days. The fuel line to the burner is 12 ft long and 
  runs along an exterior wall. 
  During the colder 
  months I use the bestWVO, with the lowest cloud point to made BD for my 
  car and the rest to make BD for my heating fuel. (My caris outdoors, 
  starts on the coldest days and runs well on a 70% BD/30% petro diesel 
  mix. It has a small pre-coolant heater that I plug in for an hour before 
  starting.)
   Questions:
  1. Am I right in assuming 
  that the "jelly" on the nozzle is the thicking of the BD due to the 
  cold?
   2. Can the problem be 
  addressed by heating the fuel line to the burner?
   3. Any other 
  thoughts?
   
  Thanks,
   
  Tom
   
  
  

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Re: [Biofuel] grease trap waste

2005-12-15 Thread Jan Warnqvist
Hello Manuel,
the FFA value does not alter the net heat value, but high FFA oils are
usually quite corrosive. And - oil from grease traps may also contain
mineral oils and other fatty substances.
Good luck to you
AGERATEC AB
Jan Warnqvist
- Original Message -
From: manuel cilia [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, December 14, 2005 1:45 PM
Subject: [Biofuel] grease trap waste


 Has anyone has any experience with grease trap waste. I am looking into an
 idea of collecting grease trap waste and seperating the water from the
 grease, then heating the grease to a level where it can be filtered and
used
 in gas turbines while the water is cleaned up and use for irrigation I
know
 grease trap waste is very high in FFA but does this atler it total energy
 value or just its gelling point.
 - Original Message -
 From: Joey Hundert [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Wednesday, December 14, 2005 8:33 PM
 Subject: Re: [Biofuel] Widescale Biodiesel Production from Algae
 byMichaelBriggs


  Todd,
Please forgive the fact that I'm about to post a previous thread into
  this one, however, the archives don't seem to be working tonight.
 
The following is Keith's last post on this issue.  Subj: RE: Algae -
was
  Re: [Biofuel] Gasoline Prices
 
Todd, if you keep a good personal archive, please also note the thread
  the bad news about biodiesel
 
http://www.mail-archive.com/biofuel@sustainablelists.org/msg58130.html
 
as it also has some kernels.
 
  -Joey
 
 
  Hello Craig
 
 Hello Keith,
 
 I've been doing a bit of research on microalgae production for
 energy and found there is some research going on around the world in
 various places. The NREL's 'Aquatic Species Program' research closed
 in the mid 1990's due, among other things, to pressure for DOE
 funding and the decision to focus their research budgets on ethanol
 production.
 
  Were those the only reasons? I thought there were some negative
  reasons about algae too, could always be wrong though.
 
 Also in the 1990's the Japanese took the idea on in a big way,
 spending more than $250 million on research into hi-tec bioreactors
 with optical fiber devices etc but found they were too expensive to
 be economical. I believe research is continuing there but on a
 smaller scale;
 
  I haven't heard of any such research here, and I'm a bit sceptical.
  As with biodiesel itself - it's quite easy to get the impression that
  there's lots of fancy stuff going on here, especially if you listen
  to several quite noisy people, and there are indeed some fancy
  Japanese patents, but in fact biodiesel hardly exists here, some (or
  most) of the few projects that do exist are very bad, to the extent
  that emissions tests for exemption from the restrictions of the
  anti-diesel campaign here (Tokyo and some other places) will no
  longer allow biodiesel because they've found it's so badly made it
  wrecks the machinery. Tests of our biodiesel have shown it would pass
  and wouldn't mess up any machinery, but they made a blanket rule: NO
  biodiesel, great, thanks guys. More and more people are making their
  own now, since we got involved (not boasting, that's what's
  happened), high-quality fuel, but it doesn't count, too bad. Same
  with ethanol, lots of good research, lots of schemes, but nothing
  happens. Yet.
 
 China and Israel are also leaders in applied phycology and have done
 work on biofuels from algae.
 
 Michael Briggs, of UNH, and his team are currently focusing on
 enclosed systems where the algae will process wastewater too.
 
  Have they made any biodiesel from it yet?
 
 John Benemann, who was involved in the NREL research, is now an
 independent consultant and heading up an international network who
 are researching into it: their website gives a good overview
 
  Thanks, I'll take a look.
 
 http://www.co2captureandstorage.info/networks/Biofixation.htm .
 http://www.co2captureandstorage.info/networks/documents/01roadmp.pdf
 
 Other links...
 NREL research
 http://www.nrel.gov/docs/fy04osti/34796.pdf
 http://govdocs.aquake.org/cgi/reprint/2004/915/9150010.pdf
 
 Further studies
 http://www.unh.edu/p2/biodiesel/pdf/algae_salton_sea.pdf
 http://europa.eu.int/comm/research/energy/pdf/36_qingyu_wu_en.pdf
 
 Discussion forum exchanges
 http://biodiesel.infopop.cc/eve/ubb.x?a=tpcs=447609751f=719605551m
 =932606061r=932606061#932606061
 
  Um... (burp), no thanks.
 
 http://forums.biodieselnow.com/topic.asp?TOPIC_ID=3153.
 http://forums.biodieselnow.com/topic.asp?TOPIC_ID=3414whichpage=1
 http://groups.yahoo.com/group/oil_from_algae/
 
 Algal biodiesel plant planned for California?? (I don't know
 anything more about it)
 http://www.bfi.org/Trimtab/spring02/biodiesel.htm
 
 US Company making algal biodiesel from power station gases
 http://www.greenfuelonline.com/index.htm
 
 
 I find the last link particularly interesting. My only problem with
 it - and with John

Re: [Biofuel] Vehicles suitable for biodiesel operation

2005-12-11 Thread Jan Warnqvist



Hello Win.
assumable nothing else than keeping an 
extra fuel filter with you in the car. And also assuming that the biodiesel is 
of good quality.
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Vin Lava 
  To: Biofuel@sustainablelists.org 
  
  Sent: Sunday, December 11, 2005 8:06 
  AM
  Subject: [Biofuel] Vehicles suitable for 
  biodiesel operation
  
  Hi,
  
  I'm setting up to homebrew biodiesel in a month or so.
  
  I'm being offered a 1985 Mercedes Benz 190D in reasonably decent 
  condition.What do I need to do touse biodiesel in it? What should 
  I look out for?We also have an early 90'sNissan Largo with the 
  small (2.0L?) diesel and a mid-90'sIsuzu Bighorn with the 3.1L 
  intercooler turbodiesel. What do I need to do to run them on biodiesel? Any 
  info would be much appreciated. :-)
  
  Thanks and regards.
  
  Vin Lava
  Manila, Philippines
  
  

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Re: [Biofuel] Adding SVO to petro diesel (lubricity issue)

2005-12-04 Thread Jan Warnqvist
Hello Dana,
you will have full lubricity properties if adding 5% of SVO or BD to the
diesel oil. But, BD is preferrable due to the coking properties of the SVO.
I would suggest a BD with a high content of olelic acid e.g. from canola
,soybean or sunflower oil.
With best regards
AGERATEC AB
Jan Warnqvist
- Original Message -
From: Dana Adams [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Monday, December 05, 2005 2:25 AM
Subject: [Biofuel] Adding SVO to petro diesel (lubricity issue)



 I wonder if someone on this forum could help me?

 I have no biodiesel options around my home, and I'm concerned that running
 the lower sulphur petroleum diesel fuel will damage my injection pump.

 I'd like to add some SVO into the petro diesel to add lubricity to the
fuel,
 and I'm wondering if someone on here could tell me the optimal
percentages?
 I'd like to add enough to give substantial protection to the pump and
 injectors.

 Also, is any particular kind of SVO better for this purpose than another
 type?

 thanks



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Re: [Biofuel] (off topic) looking for Jan Warnqvist

2005-10-25 Thread Jan Warnqvist

Sorry, Chip,
the response failed to reach your e-mail adress twice, and I stored it in my
other computer. I will re-send it again during the weekend
Jan
- Original Message -
From: Chip Mefford [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, October 25, 2005 6:00 PM
Subject: [Biofuel] (off topic) looking for Jan Warnqvist


 -BEGIN PGP SIGNED MESSAGE-
 Hash: SHA1

 After my appeal for ethanol as fuel information a couple of
 weeks back, I was contacted by Jan Warnqvist who asked me
 to reply for more information.

 I did reply, and never heard from you again.

 Perhaps my off-list reply didn't make it for some
 reason.

 But here is the body of my response to you;

 - --

  Jan Warnqvist wrote:
 
 
  Hello Chip.
 
 
  Hy Jan;
 
 
  I read your input on the JTF mailing list.
  I have experience in ethanol as a fuel for
  both 2-stroke and 4-stroke engines. Converting a 4-stroke
  engine to ethanol is not a big thing, however making a 2-stroke
  engine to run safe and properly on ethanol is a different matter
  not in the least due to its way of lubrication.
 
 
  yes, it is interesting.
 
  Were I trying to get a generic old 2 stoke to work, it would be one
  thing, as the older 2stoke engines used fuel/oil as a coolant
  as well as a lubricant/fuel.
 
  However, these newer husqvarna saw engines do a very wonderful
  job of completing the combustion in the combustion chamber, with
  very little un-spent fuel exhausting.
 
  Husqvarna has done an admirable job engineering these engines.
 
  However, here in the US, the alkyate fuels like Aspen are not
  available, or if they are, it's a real mystery as to where.
  Futher, even Aspen is non-renewable. Seems we in the US not
  only use the most petrol, we also use the lower quality petrols.
  Nothing to be proud of.
 
  The small things, like adapting the fuel system, guestimating
  the carb modifications and such are things I could probably do.
  However, trying to determine a good fuel/lubricant ratio
  for ethanol and perhaps using a bio-oil like biodiesel
  as a lubrication additive is quite simply beyond my quite limited
skills.
 
  Any help is greatly appreciated.
 
  Thanks very much for the reply.
 
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