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] 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] 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] 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] phosphatide content in crude oil

2005-06-04 Thread Jan Warnqvist
Hello Subbu.
Since used cooking oil from the beginning probably consists from refined
oil, the phosphatetide content should be  1%.
With best regards
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: Thursday, June 02, 2005 12:03 PM
Subject: [Biofuel] phosphatide content in crude oil



 Hi friends,

 Could someone please tell me how much phosphatide is normally present in
 used cooking oil.

 Many thanks

 regards

 Subbu








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Re: [Biofuel] How would any of you answer this one?

2005-06-06 Thread Jan Warnqvist



More answers:
Even as we speak the green house effect 
will cause seriuos climate changes. It does not matter whether the carbon 
dioxide is generated from fossile oil, fossile gas or coal. As long as we 
maintain our dependence on fossile energy this development will 
proceed.
Concerning the nuclear power, it is a 
fairytale to believe that somebody can guarantee safe keeping of nuclear waste 
for at least 1.000 years ahead. The more we adapt to atomic power, the more 
waste, the bigger the fairytale. And even if technology in the future will 
allow recycling of nuclear waste, splitting atoms to generate electricity 
brings dangerous radiation and another serious nuclear power plant accident will 
take place sooner or later.
Did anybody know that the nuclear power 
plants in Sweden are un-insured ? There is no insurance company willing to take 
the risk of a nuclear accident !
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  bmolloy 

  To: Biofuel 
  Sent: Thursday, June 02, 2005 4:24 
  AM
  Subject: [Biofuel] How would any of you 
  answer this one?
  
  
  Hi Michael,
  
   
  Re your quote from Herron as follows:snip 
  
   Our only real sources of useful and practical energy are oil, 
  gas, coal and nuclear. It's true that our oil supply will eventually decrease, 
  but coal is nearly inexhaustible and newer methods of processing it eliminate 
  the smoke and by-products. 
  
   Nuclear is the energy of the future and must be 
  de-politicized. It will be totally clean, very economical and inexhaustible. 
  In the meantime let's stop hindering our search for oil, including Alaska, 
  off-shore and on federal lands.
  
   Firstly, our uses of, and search for sources of energy are limited 
  only by our imagination. Our current love affair with oil and other fossil 
  fuels is but a temporary aberration. Necessity will force us to use of 
  renewables. Wind energy is but one, solar another, tidal energy is at present 
  almost unharnessed, geothermal (just drill a hole in your backyard and keep 
  going down until you reach useable heat - the New Zealanders currently lead 
  the world in geothermal power) equally so. There are many other completely 
  renewable and environmentally supportive means of energy production, but that 
  is not the nub of this post. I wish only to address the statement that nuclear 
  is the energy of the future. Not only is this not the case. Use of 
  this form of power would eventually remove the possibility of any future at 
  all for the human race.As evidence, I offer the following blast from a medical 
  doctor when the Australian government recently toyed with the idea of nuclear 
  power
  
   Nuclear Power Isn't Clean; It's Dangerous - and Uneconomic
  
   By Dr. Helen Caldicott
  
   Among the many departures from 
  the truth by opponents of the Kyoto protocol, one of the most invidious is 
  that nuclear power is "clean" and, therefore, the answer to global 
  warming. However, the cleanliness of nuclear power is 
  nonsense. Not only does it contaminate the planet with long-lived radioactive 
  waste, it significantly contributes to global warming.While it is claimed that 
  there is little or no fossil fuel used in producing nuclear power, the reality 
  is that enormous quantities of fossil fuel are used to mine, mill and enrich 
  the uranium needed to fuel a  nuclear power plant, as well as to 
  construct the enormous concrete reactor itself. Indeed, a nuclear power plant 
  must operate for 18 years before producing one net calorie of energy. (During 
  the 1970s the United States deployed seven 1,000-megawatt coal-fired plants to 
  enrich its uranium, and it is still using coal to enrich much of the world's 
  uranium.) So, to recoup the equivalent of the amount of fossil fuel used 
  in preparation and construction before the first switch is thrown to initiate 
  nuclear fission, the plant must operate for almost two decades. But 
  that is not the end of fossil fuel use because disassembling nuclear plants at 
  the end of their 30- to 40-year operating life will require yet more vast 
  quantities of energy. Taking apart, piece by radioactive piece, a nuclear 
  reactor and its surrounding infrastructure is a massive operation: Imagine, 
  for example, the amount of petrol, diesel, and electricity that would be used 
  if the Sydney Opera House were to be dismantled. That's the scale we're 
  talking about. And that is not the end of fossil use because much will also be 
  required for the final transport and longterm storage of nuclear waste 
  generated by every reactor. From a medical perspective, nuclear 
  waste threatens global health. The toxicity of many elements in this 
  radioactive mess is long-lived. Strontium 90, for example, is tasteless, 
  odorless, and invisible and remains radioactive for 600 years. Concentrating 
  in the food chain, it emulates the 

Re: [Biofuel] Rapeseed Biodiesel

2005-06-07 Thread Jan Warnqvist



Hello Purbo.
It all depends on the car or the effort 
and interest put in by the car manufacturer. What kind of car do you have ? Nine 
times out of ten it´s a question of hosing.
With best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Purbo J. Wignjosajono 
  
  To: Biofuel@sustainablelists.org 
  
  Sent: Tuesday, June 07, 2005 2:44 
AM
  Subject: [Biofuel] Rapeseed 
  Biodiesel
  
  Dear All,
  
  I read the owner's manual 
  of my car whose engine is a Direct Injection Intercooled Turbo Diesel and 
  found out that biodiesel fuel made of rapeseed is not allowed to be used. Does 
  anybody knows the reason?
  
  Regards,
  Purbo J. W.
  
  

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Re: [Biofuel] Rapeseed Biodiesel

2005-06-07 Thread Jan Warnqvist



Hello Purbo.
I suggest that you ask your dealer what 
will happen if you fill biodiesel. Is it a question of rubber qualities 
orare there electric obstacles ? Some cars have a valve which closes if it 
does not recognize the incoming fuel as fuel.
Best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Purbo J. Wignjosajono 
  
  To: Biofuel@sustainablelists.org 
  
  Sent: Tuesday, June 07, 2005 12:24 
  PM
  Subject: Re: [Biofuel] Rapeseed 
  Biodiesel
  
  Hi Jan,
  
  Thank you for responding. 
  My car is a 2001 Renault Scenic 1.9 dTi with a Direct Injection Intercooled 
  Turbo Diesel engine. The manual mention that "rapeseed oil must not be used in 
  any cirscumtance". I am not whether it is rapeseed oil or biodiesel made of 
  rapeseed oil.
  
  PJW
  
- Original Message - 
From: 
Jan Warnqvist 

To: Biofuel@sustainablelists.org 

Sent: Tuesday, June 07, 2005 1:56 
PM
Subject: Re: [Biofuel] Rapeseed 
Biodiesel

Hello Purbo.
It all depends on the car or the 
effort and interest put in by the car manufacturer. What kind of car do you 
have ? Nine times out of ten it´s a question of hosing.
With best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Purbo J. 
  Wignjosajono 
  To: Biofuel@sustainablelists.org 
  
  Sent: Tuesday, June 07, 2005 2:44 
  AM
  Subject: [Biofuel] Rapeseed 
  Biodiesel
  
  Dear All,
  
  I read the owner's 
  manual of my car whose engine is a Direct Injection Intercooled Turbo 
  Diesel and found out that biodiesel fuel made of rapeseed is not allowed 
  to be used. Does anybody knows the reason?
  
  Regards,
  Purbo J. 
  W.
  
  

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Re: [Biofuel] NaOH

2005-06-13 Thread Jan Warnqvist



Hello Marc.
If your NaOH is not anhydrous, you should 
not use it at all. The best way of finding out the water content is to ask your 
dealer (or his supplier) for a certificate of analysis, where the actual NaOH 
content along with the impurities should be stated properly.
With best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Marc 
  Arends 
  To: Biofuel@sustainablelists.org 
  
  Sent: Monday, June 13, 2005 9:52 AM
  Subject: [Biofuel] NaOH
  
  
  
  
  Hello all, 
  
  I have a questions before i want to start with making my first test batch 
  with the single stage method. 
  
  
  I bought NaOH from a hardware store, but it looks white so it is not 
  pure. Does somebody know how i can mesure the moisture content of this NaOH so 
  i can compensate for all this water? 
  (I can use an oven at my work that canreach1000 degrees 
  Celsius).
  
  Greetings,
  
  Marc
  
  

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Re: [Biofuel] VW Diesel

2005-06-26 Thread Jan Warnqvist
Hello Lyn.
Yes, you are missing something. The main problem with SVO as diesel engine
fuel is not the high viscosity, but the final boiling point and the low
cetane number. Elsbett system have taken action before these disadvantages
and have designed a dual air system in the combustion chamber of the piston.
This makes it possible to combust SVO completely, since the outer air layer
isolates from the inner air layer, where the combustion temperature is high
enough. And although the engine is directly injected, it is equipped with
pre-chamber injectors, on which coke will form, but works self-cleansing due
to the typical design of pre-chamber injectors.
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Lyn Gerry [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Saturday, June 25, 2005 9:53 PM
Subject: Re: [Biofuel] VW Diesel


 I went to the site that Keith recommended and it looks fantastic. What
this
 maker Elsbett sells is a one tank system you can put anything from WVO to
 Dino into. If such a system exists, why are people bothing to make
biodiesel?
 It would be easier, more ecological, economical etc to just use vegetable
oil.

 I think about this problem both in the ecolological sense and the Peak oil
 sense. Particularly with the latter, the fewer things you have to buy, the
less
 exposure you have to being gouged by corporations exploiting scarcity.
 Anyone with access to a few acres of land and a home made oil press can
 create fuel out of a variety of easy to grow crops.

 Am I missing something?

 Lyn

  
  Elsbett. See:
  http://journeytoforever.org/biodiesel_svo.html
  Straight vegetable oil as diesel fuel
  
  Don't get some two-tank system that probably has copper parts in it
  and all it does is pre-heat the oil to lower the viscosity, there's
  a lot more to it than that, even with a Merc.

  forgetting to) - switch on and go, stop and switch off, SVO,
  biodiesel or petro-diesel, in any combination.
 
  We've had a two-tank system for a couple of years but we never used
  it. I just didn't think it addressed the problem fully, and the more
  I learnt the more I thought so. A few months ago we installed a
  single-tank Elsbett system in our Toyota TownAce and we're most
  pleased with it. It does exactly what it claims to do, as we fully
  expected.
 
  http://www.elsbett.com
 
  Best wishes
 
  Keith
 
 
  On 25 Jun 2005 at 8:46, John Hayes wrote:
  
You have the 'SVO destroyed my TDI' folks.
   
And the 'SVO is just fine' pollyannas.
   
  
  I went to the TDIclub site as well. I probably only saw a fraction
  of the posts,
  and what I saw made me realize that I didn't really do Mike's question
justice
  with my previous answer, so this will be long in an attempt to provide
more
  substantive info.
  
  I researched WVO for a while and decided upon the Jetta TDI, which I
bought
  specifically with the intent of doing a WVO conversion. I chose the
Jetta even
  though the golf or beetle would have been more to my personal taste,
because
  the consensus seemed to be that it was desirable to isolate the WVO
tank
  from the passenger area because the tank is heated  - a hot metal tank
of oil
  being not the most desirable presence in a passenger compartment
  
  There are a variety of systems and kits and ways that people have done
these
  conversions and I have no doubt people have ruined their TDI's with
WVO. The
  TDI has very close tolerances, also why it its such a high performance
engine.
   From what I have gathered, gumming up the injectors with WVO is one
of the
  serious risks. Critical issues in the system then are well filtered WVO
and
  that it be HOT.
  
  Just to clarify matters for any readers, a WVO system is a 2 tank
system. Do
  not ever consider just pouring WVO into your regular fuel tank - that
will
  destroy your TDI.
  
  The system I have has :
  
  a heated WVO  tank and fuel lines (the lines are heated by being
bundled
  beside a line filled with  engine coolant) ,
  
  a filter for the WVO (which has already been prefiltered the remove
  the obvious
  particulate  fryer gunk before being put in the tank) This filter
should be
  replaced approximately every 2000 miles,
  
  and a PURGE switch.
  
  The purge switch is a very important part of the system. It is used
when
  switching *back* to diesel from WVO. It pushes the WVO out of the lines
and
  injectors. If you purge for too long, you begin to suck diesel fuel
into your
  WVO tank, but ithat's not really not a problem.
  
  The *problem* in a WVO system *without* a purge function  arises
because,
  if the WVO is not completely cleared from the engine components ,  you
will
  begin to dump some WVO into the diesel tank when you shut off the car.
  After a while, your diesel will be contaminated with WVO. The reason
why this
  is a problem is because your diesel tank is not heated and the WVO is
too
  viscous at room

Re: [Biofuel] VW Diesel

2005-06-27 Thread Jan Warnqvist
Hello Keith.
The system that I am referring to is described at:
http://www.elsbett.com/engl/index.htm
Technology/ 4. The ELSBETT duothermic combustion system.
Quoting:
Only by combining the above mentioned elements it is possible to achieve
the optimum thermal and mechanical conditions required for the combustion of
fuels, such as natural vegetable oils, which are slow to vaporise.
These guys have a lot of know-how which is highly relevant for the
combustion of SVO:s.
With best regards
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: Sunday, June 26, 2005 6:36 PM
Subject: Re: [Biofuel] VW Diesel


 Hello Jan

 Hello Lyn.
 Yes, you are missing something. The main problem with SVO as diesel
engine
 fuel is not the high viscosity, but the final boiling point and the low
 cetane number. Elsbett system have taken action before these
disadvantages
 and have designed a dual air system in the combustion chamber of the
piston.
 This makes it possible to combust SVO completely, since the outer air
layer
 isolates from the inner air layer, where the combustion temperature is
high
 enough. And although the engine is directly injected, it is equipped with
 pre-chamber injectors, on which coke will form, but works self-cleansing
due
 to the typical design of pre-chamber injectors.

 Are you talking about the original Elsbett 3-cylinder multifuel diesel
engine?

 Best wishes

 Keith


 Best regards
 Jan Warnqvist
 AGERATEC AB
 
 jan at carryon.se
 
 + 46 554 201 89
 +46 70 499 38 45
 - Original Message -
 
 I went to the site that Keith recommended and it looks fantastic. What
this
 maker Elsbett sells is a one tank system you can put anything from WVO
to
 Dino into. If such a system exists, why are people bothing to make
 biodiesel?
 It would be easier, more ecological, economical etc to just use
 vegetable oil.
 
 I think about this problem both in the ecolological sense and the Peak
oil
 sense. Particularly with the latter, the fewer things you have to
 buy, the less
 exposure you have to being gouged by corporations exploiting scarcity.
 Anyone with access to a few acres of land and a home made oil press can
 create fuel out of a variety of easy to grow crops.
 
 Am I missing something?
 
 Lyn
 
   
   Elsbett. See:
   http://journeytoforever.org/biodiesel_svo.html
   Straight vegetable oil as diesel fuel
   
   Don't get some two-tank system that probably has copper parts in it
   and all it does is pre-heat the oil to lower the viscosity, there's
   a lot more to it than that, even with a Merc.
 
   forgetting to) - switch on and go, stop and switch off, SVO,
   biodiesel or petro-diesel, in any combination.
  
   We've had a two-tank system for a couple of years but we never used
   it. I just didn't think it addressed the problem fully, and the more
   I learnt the more I thought so. A few months ago we installed a
   single-tank Elsbett system in our Toyota TownAce and we're most
   pleased with it. It does exactly what it claims to do, as we fully
   expected.
  
   http://www.elsbett.com
  
   Best wishes
  
   Keith
  
  
   On 25 Jun 2005 at 8:46, John Hayes wrote:
   
 You have the 'SVO destroyed my TDI' folks.

 And the 'SVO is just fine' pollyannas.

   
   I went to the TDIclub site as well. I probably only saw a fraction
   of the posts,
   and what I saw made me realize that I didn't really do Mike's
 question justice
   with my previous answer, so this will be long in an attempt to
 provide more
   substantive info.
   
   I researched WVO for a while and decided upon the Jetta TDI,
 which I bought
   specifically with the intent of doing a WVO conversion. I
 chose the Jetta even
   though the golf or beetle would have been more to my personal
 taste, because
   the consensus seemed to be that it was desirable to isolate the WVO
tank
   from the passenger area because the tank is heated  - a hot
 metal tank of oil
   being not the most desirable presence in a passenger compartment
   
   There are a variety of systems and kits and ways that people
 have done these
   conversions and I have no doubt people have ruined their TDI's
 with WVO. The
   TDI has very close tolerances, also why it its such a high
 performance engine.
From what I have gathered, gumming up the injectors with WVO
 is one of the
   serious risks. Critical issues in the system then are well
 filtered WVO and
   that it be HOT.
   
   Just to clarify matters for any readers, a WVO system is a 2
 tank system. Do
   not ever consider just pouring WVO into your regular fuel tank
 - that will
   destroy your TDI.
   
   The system I have has :
   
   a heated WVO  tank and fuel lines (the lines are heated by being
bundled
   beside a line filled with  engine coolant) ,
   
   a filter for the WVO (which has already been prefiltered the remove
   the obvious
   particulate

Re: [Biofuel] BD process question

2005-06-28 Thread Jan Warnqvist
Hello Joe.
The cloudiness is most likely caused by water or water soluble substances.
A simple way of approaching your problem is to put your mini batch into
water about 60-65oC, and let it stay there for a few hours. If it becomes
clear, let it stay there for some additional time. If it does not become
clear, try washing it again several times with water only and repeat the hot
water procedure.
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Joe Street [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, June 28, 2005 3:26 PM
Subject: [Biofuel] BD process question


 Hello, I have a question about biodiesel processing I hope someone can
 help me with;
 I read the excellent info on the journey to forever site and checked the
 archives about washing etc.  I am interested in using mechanical
 agitation to speed up the process of washing but I wonder if I am being
 too impatient or something.  Some background on what I am doing
 I have been using the single stage process so far.  I started to learn
 with virgin canola oil and then went to waste canola oil from a local
 pub.  In every case I have done my titrations carefully using a good
 quality burette and stock KOH solution carefully mixed using a
 laboratory grade electronic scale and DI water.  When I did the 1 liter
 test batches I got a clean split with only 2 layers and after 4 washes
 with acetic acid on the first one I have ended up with BD that is
 cloudy.  After heating the BD for drying it became spectrally clear and
 remained that way after cooling.  I had given an extended waiting time
 of more than a week to see if it would clarify on it's own but this did
 not happen.  After the clarification by heating I  took it down to the
 freezing point and it remained clear after thawing.  Then I did my first
 5 gallon batch in a water heater.  My reractor is a vacuum type and I
 use a circulation pump for mixing and washing etc.  Again I obtained a
 good clear split but this time the BD clarified after heating (began to
 clear at about 50 deg. C. and I heated it to 135 deg C.) and I was
 shocked to see it cloudy the following day after it cooled.  I reheated
 again this time to 170 deg. C. and it was better after cooling but not
 near as clear as the other 1 liter test batches. So questions:
 What is it exactly that causes the cloudiness?  Is it water content?  I
 notice the BD from the test batches after all is done has a smell
 similar to oil based paint or linseed oil but had a much sweeter
 aromatic smell while it was being heated.  The large batch more so.  Is
 this due to residual methanol (which I thought I completely removed
 after the reaction using vacuum distillation at 55 deg C and 25 in Hg)?
 Does the cloudiness indicate that the reaction was not correct (excess
 caustic?) I didn't have a problem with soaps.
 Any recommendations?


 Thanks in advance for any help you can offer

 Joe


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Re: [Biofuel] biodiesel and WVO in all liquid cooled Diesel

2005-07-11 Thread Jan Warnqvist
Hello Richard.
Good of you to bring up these thoughts.
Diesel oil is a mixture of a number of hundreds different hydrocarbons,
which together have the properties as stated in the standards. This means
that the properties and the composition of diesel oil will differ depending
upon which diesel standard is current. Diesel engine oil is not homogenous.
The engine manufacturers have solved this problem by using a special
reference diesel fuel for their calibrations and conformity regulations.
Biodiesel is usually methyl esters of fatty acids. There are different
standards for this, for instance the ASTM norm as well as the EN 14214 norm.
There are test methods stated in these standards which the biodiesel should
fulfil.
That´s it.
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Richard Rovinsky [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Monday, July 11, 2005 2:58 AM
Subject: [Biofuel] biodiesel and WVO in all liquid cooled Diesel


 I believe you need to ask someone who knows more about biodiesel
 and the equipment you are powering with it.  Of course, the
 safe answer given by anyone who doesn't know will be no.
 Investigate their knowledge of biodiesel before asking that
 question.  I think the real answer is...it depends.  What is
 biodiesel specifically?  What tests has it passed?
 Chemically speaking, diesel is diesel is diesel once it is
 processed.  The quality of the processes used to generate a
 quality product is what you should be investigating, I believe.
 Any additional byproducts included in the biodiesel may be cause
 for precautions (due diligence in investigation followed by
 appropriate courses of action).
   Since there are so many sources and levels of care taken to
 make it, they may be right in some cases.  Are you planning use
 it in cold weather, where it might become too thick?  So, you
 may need to blend it with dinodiesel.
   Has the biodiesel you plan to use been tested to meet any
 automovitive quality tests for purity, contaminants,
 particle/size?  You may need to test your Biodiesel to be sure,
 otherwise, you may just take a chance.
   From what I understand, biodiesel will generally act as a
 solvent and release any accumulations of dinodiesel residue that
 may have built up in the tanks of older equipment, and so you
 may need to inspect and change filters more often, initially.
 Hope this provides some food for thought.
Richard

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Re: [Biofuel] glycerine ?

2005-07-15 Thread Jan Warnqvist



Yes ,it most certainly will. Glycerine 
residues will have an impact on the equivalence balance for next reaction, that 
most probably will produce less biodiesel.
Contaminations in general are not good for 
biodiesel production either.
With best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  alex 
  burton 
  To: Biofuel@sustainablelists.org 
  
  Sent: Friday, July 15, 2005 10:07 
AM
  Subject: [Biofuel] glycerine ?
  
  
  Hello All
  I have a question about glycerine.
  what is the effect if after i have made biodiesel and let it settel in the 
  prossesor but there is still a small amout of glycerine left in the 
  prossesor after i have drained it and then make another batch will the 
  glycerine that is left in the prossesor have a negative result on the next 
  batch?Thanks for the advice
  Alex
  
  
  

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Re: [Biofuel] theoretical and practical questions

2005-07-18 Thread Jan Warnqvist
Hello Marc.
The method that you are referring to, mixing BD with water in equal
proportions seems to me a dubious method of determining the state of the BD.
If the BD contains small amounts of detergents (common in used cooking oil)
the phases will separate very slowly or not at all. Furthermore, the BD is
slightly polar, which means that it will attract some water during all
conditions. And - small amounts of di- and monoglycerides will also slow the
separation process. This goes concerning any remaining soaps as well.
A good visual hint to ready biodiesel is when the last washing water is
clear and bright. This does not mean that the BD is, for the reasons
mentioned above.
The question about GC catalyst I cannot answer, sorry.
With best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
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- Original Message - 
From: Marc Arends [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Monday, July 18, 2005 12:32 AM
Subject: [Biofuel] theoretical and practical questions


 Hello All,

 I am a beginner with biodiesel and i did a lot of reading the last few
 months and i did quite some test batches with unused sunflower oil with
the
 single stage method (as is advised).
 Now i have some practical questions and theoretical questions.

 Practical questions:
 When you are finished with making the BD (ready to put in the car) and you
 take a small sample of this and shake it with an equal amount of water in
a
 glass jar the water and BD separate,  should the BD layer be completey
clean
 and clear after few minutes? How can you test if your final product is
good
 enough to put in you car?
 I also have some questions about washing my test batches.
 As i am a chemist and work in a laboratory all my test batches were made
in
 laboratory conditions.
 After separating the glycerol layer from the BD layer, i washed the BD 3
 times with water. Then i filtered the BD over a coffee filter and the BD
 looked really nice (clean, clear). But when i shake this BD with water
 again, the BD layer looks not clear again, and it looks like there is
still
 soap in it. How do you know when you are finished washing the BD and
should
 i filter it after every wash?


 Theoretical problems
 As i live in Holland and it can get very could in winter, i am also
 interested in the 2 stage method because BD made with the 2 stage method
 works better in colder conditions. But what is the chemical difference
 between BD made with the single stage and BD with the second stage?
 In my laboratory we also analyze fatty acids and we also make FAME to
 analyze with GC. The difference with making BD and FAME to analyze with GC
 is that we also add Borotrifluoride-methanol complex as a catalyst for...?
 Nobody at my jobs does know why and i asked 2 PhD in organic chemistry but
 they also don't know. So does anyone know why this catalyst is added and
 what it does exactly. Would it help us to when processing our BD?

 Hopefully someone can help me.

 Greetings,

 Marc
 I



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Re: [Biofuel] Re: CUMMINS B5.9TD

2005-07-19 Thread Jan Warnqvist
The thermal stability problems with biodiesel mainly occurs when the
biodiesel consists from highly unsaturated fatty acids. When mixing it with
DINO, the problem should disappear, because a good diesel stock should be
treated with anti-oxidating agents.
These agents can be added to the biodiesel directly, of course.
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Arden B. Norder [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, July 19, 2005 7:38 AM
Subject: RE: [Biofuel] Re: CUMMINS B5.9TD


 Reading this is beginning to make me nervous. I have been researching
biodiesel
 production and considering building around biodiesel and glycerin.

 I have only one question (mainly because I was planning to run B100): When
 can/should I run B100 without blowing up my engine or meltin my fuel lines
or
 gumming up the fuel pump and injectors.

 I am totally in love with my Peugeot HDi diesel - I don't want to end its'
life
 prematurely. HELP!!!

 Greetings,
 Arden

 On Jul 19, 2005 01:49 AM, James G. Branaum [EMAIL PROTECTED] wrote:

  In one of my many conversations with a fuels specialist, he strongly
  suggested that BD has some thermal stability problems when used in over
a
  10% mix with Petro.  He has the degree and over 20 years experience in
the
  field since I first met him.
 
 
 
  -Original Message-
  From: [EMAIL PROTECTED]
  [mailto:[EMAIL PROTECTED] On Behalf Of
  [EMAIL PROTECTED]
  Sent: Monday, July 18, 2005 4:47 PM
  To: Biofuel@sustainablelists.org
  Subject: Re: [Biofuel] Re: CUMMINS B5.9TD
 
 
 
  - Original Message -
  From: Doug Memering [EMAIL PROTECTED]
  Date: Saturday, July 16, 2005 9:40 pm
  Subject: [Biofuel] Re: CUMMINS B5.9TD
 
  
 Any of which can be replaced on an as needed basis. Terry's
   mechanic  should be a little more specific with him, rather than
   issuing a
 sweeping and perhaps unsupported statement.
  
   Perhaps I can shed some light on this topic, as I am an engineer
   at Cummins
   Inc, and work in Fuel System Development.
   Officially, Cummins supports Biodiesel blends up to B5 or 5%
   Biodiesel.There are several concerns the company has with higher
   ratio blends.  There
   are three major areas of concerns that the company has.  These are
   mostlycommercial concerns which will be evident as I explain them
   any of which an
   individual could deal with by being aware and careful about what
   they put
   into their tank.
  
   First, while biodiesel is touted as being cleaner, there are some
   caveats.While the particulate emissions (the ones you can see) are
   considerablyimproved with biodiesel,  the NOx emmission will
   increase and the higher the
   biodiesel ratio the higher the NOx increases.  Up to B5 the
   increase will
   not likely move the engine's NOx emissions beyond the federal
   limit, but B20
   and higher will likely move the NOx emissions outside of the
   box.  Since
   the US tends to hold the manufacturers repsonsible for the
   emissions of the
   engines instead of the users the company must maintain a strict policy
   against recommending or accepting fuels that will violate the
   regulations.
   Second, biodiesel has a lower heating value than Petro diesel,
   therefore the
   higher the biodiesel blend the lower the available power from the
   engine.Most vehicles with B5.9 diesel are substantially
   overpowered so the driver
   may not notice the 2% loss of power with a B5 blend, but it will
   become more
   noticeable as the ratio is increased.  As I said many of the vehicles,
   especially pickups are overpowered for the job they do, so you it
   wouldlikely not be bothered unless you are street racing or
   pulling a large
   (heavy) trailer through the mountains.  But once again as a
   company Cummins
   is in the position that if the sell a 305 Hp engine and the
   customers tend
   to expect to get 305 Hp regardless of what fuel they chose to put
   in the
   tank.
  
   The third and more serious concern for us homegrown biodieselers,
   in my
   opinion, is water.  Most tanks collect water, many vehicles are
   equippedwith water separation filters to protect the fuel system
   components.  The
   problem is the biodiesel has a higher affinity for water than
   petrol diesel,
   so the biodiesel is going to carry the water out of the tank.
   Furthermore,the water separators that are normally used will NOT
   extract the water from
   biodiesel so the water gets carried into the fuel system.  Most
   modern fuel
   systems are very sensitive to water.  The engine will run
   initially but the
   internal fuel system components will quickly corrode which will
   lead to a
   fuel system failure, and usually an expensive one.
  
   The company is also concerned about the quality of the biodiesel
   coming on
   the market.  They have a wide variety from some very high quality
   to some
   very poor quality

[Biofuel] Fw: Lipase

2005-07-26 Thread Jan Warnqvist




Jan Warnqvist

+46 554 201 89+ 46 70 499 38 45
- Original Message - 
From: Jan 
Warnqvist 
To: Biofuel@sustainablelists.org 

Sent: Tuesday, July 26, 2005 4:31 PM
Subject: Lipase

Hello all,
does anybody have a good link to a 
supplier of industrial lipase enzyme ?

Jan Warnqvist

+46 554 201 89+ 46 70 499 38 
45
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Re: [Biofuel] methanol

2005-08-09 Thread Jan Warnqvist



Hello Ian.
Answer #1: Methanol attracts water. So, 
old methanol is not anhydrous, which it has to when producing 
biodiesel.
Answer#2: Yes, but it takes a little 
longer.
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Ian  
  Theresa Sims 
  To: Biofuel@sustainablelists.org 
  
  Sent: Tuesday, August 09, 2005 10:49 
  AM
  Subject: [Biofuel] methanol
  
  I was talking toa friend that races cars 
  and he said that methanol kept for a long??time degraded and didn't work as 
  well. Is this a problem for us?
  As a matter of interest does biodiesel make the 
  sump oil in your car go as black as dinodiesel?
  
  Cheers Ian
  
  

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Re: [Biofuel] methanol

2005-08-10 Thread Jan Warnqvist



Yes, old methanol is always a problem. 
Both for speedway racers and for biodiesel producers.
With best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Ian  
  Theresa Sims 
  To: Biofuel@sustainablelists.org 
  
  Sent: Wednesday, August 10, 2005 3:16 
  AM
  Subject: Re: [Biofuel] methanol
  
  Thanks Jan
  But is that a yes or a no on question 
  1
  
- Original Message - 
From: 
Jan Warnqvist 

To: Biofuel@sustainablelists.org 

Sent: Wednesday, August 10, 2005 12:20 
AM
Subject: Re: [Biofuel] methanol

Hello Ian.
Answer #1: Methanol attracts water. 
So, old methanol is not anhydrous, which it has to when producing 
biodiesel.
Answer#2: Yes, but it takes a little 
longer.
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Ian 
   Theresa Sims 
  To: Biofuel@sustainablelists.org 
  
  Sent: Tuesday, August 09, 2005 10:49 
  AM
  Subject: [Biofuel] methanol
  
  I was talking toa friend that races 
  cars and he said that methanol kept for a long??time degraded and didn't 
  work as well. Is this a problem for us?
  As a matter of interest does biodiesel make 
  the sump oil in your car go as black as dinodiesel?
  
  Cheers Ian
  
  

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Re: [Biofuel] Biodiesel

2005-08-10 Thread Jan Warnqvist



Hello Ian,
if treated with anti-oxidizing agents, and 
produced from oil with a moderate peroxide number, the biodiesel should be 
consumed within three months.
10 microns is a normal filter size for 
diesel engines, unless equipped with a common-rail system. So, filtering at 10 
microns is good, 5 microns even better assuming that the biodiesel has an 
abnormal content of solids which will lead to filter clogging very rapidly. Pay 
attention to the markings "absolute" and "nominal" on the filter spec. There is 
a huge difference between those two. 
The biodiesel should be ready for instant 
consumption if it´s clear and bright and without sediments.
With best regards
Jan WarnqvistAGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89+46 70 499 38 45

  - Original Message - 
  From: 
  Ian  
  Theresa Sims 
  To: Biofuel@sustainablelists.org 
  
  Sent: Wednesday, August 10, 2005 10:59 
  AM
  Subject: [Biofuel] Biodiesel
  
  Does anyone tell me how long Biodiesel will keep 
  after production.
  Can someone clarify the final filter process 
  after production. Some say 5 microns some say 10. Mike pelly's recipe dosn't 
  seem to say anything about it? And how long should it stand or can you pour it 
  straight in?
  Cheers Ian
  
  

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Re: [Biofuel] Re: A beginners titration question

2005-08-11 Thread Jan Warnqvist
Hello Doug.
Keith has made an excellent input to you questions but I felt it necessary
to add some aspects of your problem:
The rule no1 when taking samples is to make sure - as possible- that the
sample is representative for the batch. This sounds simple, but if you are
dealing with high water content together with high FFA levels you will have
different titration values if sampled from the top or from the bottom. If
there are detergents in the oil, this actually may help. It is a
disadvantage when washing the biodiesel though.
By using IPA for titration, the general idea is to have one clear phase
consisting from IPA, water, KOH (or NaOH) and oil. The EN standard for
determination of acid number which is likewise determined by titration
strongly recommends that the amount of IPA should be increased if the
solution becomes cloudy or turbid.
By using methanol for titration, you are out of standard procedure.
And - possibly annoying Keith - the EN requirement for a good titration is
that the solution stays magenta for at least 15 seconds.
Good luck to you further on !
With best regards
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: Thursday, August 11, 2005 9:38 AM
Subject: [Biofuel] Re: A beginners titration question


 Hello Doug

 Hello group,
 I am a beginner in the conversion of WVO to BD and I have been
 having trouble with my titration process.  On JTF there are 2
 reference documents on titration which I have been using as my guide.

 There's more than that there about titration.

 However, I don't seem to get consistent results.  For example, One
 time I will get 1.55ml and the second time I get 3.22 ml  using WVO
 from the same batch and drawing from the same solution of NaOH and
 water.
 
 First is that kind of variability to be expected?

 No.

 Second I noticed in reviewing the tritration documents again, that
 isopropyl alcohol is specifed.

 But how could you not have noticed that the first time round?
 Everywhere is says so.

  I have been using the same methanol that I use in the conversion
 process.  Prefacing this with I ain't no chemist, Is that the
 source of my problem?  If that is the case can someone explain why
 the titration is done with one type of alcohol when the process is
 run with a different one?

 I also ain't no chemist, very few of us are chemists, but we can
 learn, and do. I can't give you a technical comparison of the effects
 of different alcohols, but why depart from established practice when
 you're just starting? It doesn't make a lot of sense anyway,
 titration and processing have different purposes, with titration
 you're only finding out how much acid will have to be neutralised,
 not processing the WVO. The result of the titration is applied to the
 subsequent processing in the form of the amount of lye required, not
 the kind of alcohol to use. If you assume that the two different
 processes should use the same alcohol then why don't you also assume
 that they should use it in the same proportions? - ie 10 litres of
 99%+ isopropyl alcohol per one litre of WVO to be processed?

 Anyway, it is possible to use isopropyl alcohol to make biodiesel,
 called branched-alkyl esters, which have the advantage of much
 improved cold-weather properties. There's discussion of this in the
 list archives, using either isopropyl alcohol or butanol. But it's
 not for homebrewers, though many have tried - it's laboratory-level
 stuff, patented but not used, nobody is using these techniques yet
 AFAIK.

 Also I seem to be having difficulty keeping the WVO and alcohol
 mixed during the titration process, which would be what I would
 attribute to the variation in the results.

 I don't think so.

 I have been carrying out the  titration in a test tube and shaking
 it after each drop, but the oil still seems to settle out.

 Stirring is better. Did you warm the mixture first (and the 0.1% NaOH
 solution)? Use something wider than a test tube that you can stir.

 And even when they are mixed it is a cloudy white solution, not
 clear as the  JTF documents indicate.

 They do not indicate that. What they say is that it should be clear
 (thoroughly mixed) BEFORE you start adding the 0.1% NaOH solution.

 Warm the beaker gently by standing it in some hot water, stir until
 all the oil dissolves in the alcohol and turns clear. Add 2 drops of
 phenolphthalein solution. Using a graduated syringe, add 0.1% lye
 solution drop by drop to the oil-alcohol-phenolphthalein solution,
 stirring all the time, until the solution starts to turn pink and
 stays that way for 10 seconds. ...
 Biodiesel from waste oil
 http://journeytoforever.org/biodiesel_make.html#biodwvo

 Dissolve 1 gram of lye in 1 liter of distilled or de-ionized water
 (0.1% w/v lye solution). In a smaller beaker, dissolve 1 ml of
 dewatered WVO oil in 10 ml of pure isopropyl alcohol. Warm

Re: [Biofuel] Quality Test

2005-08-11 Thread Jan Warnqvist
Hello Jeffery.
The test method that you are using seems to me highly dubious, since there
are a number of pre-assumptions that has to be met.
For a further check I´d suggest this:
Take exactly 25 ml of biodiesel and dissolve it in exactly 225 ml of
methanol in a measuring glass. Now:
The biodiesel should be fully soluble in the methanol forming a clear bright
phase. If not, there is pollution in the biodiesel causing you trouble with
the water test. Each ml of undissolved material is corresponding to 4% by
volume. Are there any undissolved material at the bottom of the measuring
glass ?
If there is, your reaction is not complete and this is causing you trouble
with the water test.
This method does not cover every aspect of quality, but it gives a hint
though
Good luck to you
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Jeffrey Tan [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, August 11, 2005 2:19 PM
Subject: [Biofuel] Quality Test


 Hello all.  Need some explanation and advise here on my experiments
please.

 I have been using virgin cooking palm oil for the experiments.  When
 following the steps for checking on quality, I put in 150ml of de ionised
 battery water and 150ml of the biodiesel obtained but the end result was
 clear yellowish liquid on top and white emulsion like on the bottom.  I
have
 done 3 different batches with the same result.  My further reading and
guess
 is either the NaOH is too much/little or the methanol is too much/little.
 My next step will probably to increase the methanol from 200ml to 400ml
(my
 batches are in 1 liter of new oil).  Any comments or suggestions from the
 gurus out there?

 Can I continue with the bubble washing process with the above 3 test
 batches?

 Jeff

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Re: [Biofuel] Re: Re: A beginners titration question

2005-08-12 Thread Jan Warnqvist
Hello again Doug.
The forming of FFA in the presence of water is an auto-catalyst process,
meaning that the more FFA:s there are, the more rapidly the further
production of FFA:s. This is due to the fact that this is an acid-catalyst
reaction which will continue for as long as there is water present in
adequate amounts. The FFA and water values are in general higher at the
bottom of the vessel, the other way around at the top.
WVO often contains detergents because the cleansing of the frying oil
vessels at the restaurants or factories is done with detergents and water.
Some people pour this stuff into the used oil. The best way of avoiding
this, is of course to let the WVO supplier know that the detergent -
containing WVO is of scientifically less value, since the detergents are
contaminations and cause a great deal of troubles.
The other way of dealing with this is to vacuum -evaporate the WVO at 90oC,
where the emulsions should break up.
The third way is to reduce the water content and react the WVO in the normal
way, adding further washing sequences and expecting a lower yield of
biodiesel than usual.Any soap formation can be scattered with acid
treatment.
IPA is a good solvent for titration, unlike methanol or ethanol, which are
hardly soluble in oil.
I think you have a good base recipe. Do not change it, before you have
examined the quality of your raw material. The solution to your problems is
most likely to be found there.
With best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

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- Original Message - 
From: Doug Memering [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Friday, August 12, 2005 3:50 AM
Subject: [Biofuel] Re: Re: A beginners titration question


 Jan,

 Thanks for the help.
  Hello Doug.
  Keith has made an excellent input to you questions but I felt it
necessary
  to add some aspects of your problem:
  The rule no1 when taking samples is to make sure - as possible- that the
  sample is representative for the batch. This sounds simple, but if you
are

 I am still working with fairly small batches so I have been drawing the
 complete batch
 out of my holding tank and then taking the test sample from that.  I have
 been titrating that batch
 multiple times and getting the variation even from that.

  dealing with high water content together with high FFA levels you will
 have

 Does water content itself cause variation or is it changes in the amount
of
 water content
 that would cause the variation in the titration?

  different titration values if sampled from the top or from the bottom.
If
  there are detergents in the oil, this actually may help. It is a

 Detergents? What's the likelihood of picking up detergents in the WVO from
 a restaurant? Is this something I should watch for or is it simply a
matter
 of more washing?

  disadvantage when washing the biodiesel though.
  By using IPA for titration, the general idea is to have one clear phase
  consisting from IPA, water, KOH (or NaOH) and oil. The EN standard for
  determination of acid number which is likewise determined by titration
  strongly recommends that the amount of IPA should be increased if the
  solution becomes cloudy or turbid.

 The solution was definitely turbid, but Keith's recommendation (unlike
James
 Bond)
  was to do the test in a beaker or jar rather than a test tube so that it
 could be
 stirred and not shaken

  By using methanol for titration, you are out of standard procedure.

 When I started out I got a titration procedure from another site, before I
 found JTF.  The procedures
 were nearly identical except in the list of what you needed it said to use
 either
 Isopropyl, Ethyl, or Methyl.  Since I had already invested in a bunch of
 Methyl alcohol
 for this adventure and didn't have any isopropyl on hand I started using
it.
 My limited college
 chemistry had me in the frame of mind that a solvent is a solvent.  That's
 why I asked for an
 explanation.  I can see where the my results could be shifted by what
 alcohol I am using but it didn't
 make sense to me that the type of alcohol would cause the huge variation
in
 the test.

  And - possibly annoying Keith - the EN requirement for a good titration
is
  that the solution stays magenta for at least 15 seconds.

 This was happening, there was a distinctive cross-over point where the
 solution would
 turn magenta for like 10 seconds and then fade to pink.  It is just that
 event happened at
 substantially different amounts of NaOH.

 Heating was mentioned as well, and that could be a part of my problem too.
 I was heating the WVO then mixing it with the alcohol which was at about
 95F.
 I didn't hear the reagent either.  I gather they should all be near the
 process temperature.

 Thanks again
  Good luck to you further on !
  With best regards
  Jan Warnqvist
  AGERATEC AB



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Re: [Biofuel] Quality Test

2005-08-12 Thread Jan Warnqvist
Hello Jeffery,
the clear phase at the bottom is likely unreacted oil. It seems likely that
your oil has contaminations which inhibit the trans-esterification reaction.
Do not change your recipe at first hand, get yourself a little oil that you
know is OK, maybe from the supermarket and try your recipe on that one by
following the instructions on YTF including the titration. When settled and
washed go through the methanol extraction method again and compare the
results.
Get back to me and report. Add the recipe that you are working with too.
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
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- Original Message - 
From: Jeffrey Tan [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Friday, August 12, 2005 11:52 AM
Subject: Re: [Biofuel] Quality Test


 Jan,
Thanks for the tip.  We tried it and without stirring, there were clear
 yellow deposit on the bottom.  The biodiesel did not disolve fully in the
 methanol like you said.  So does this mean the next time I do another
batch,
 I have to increase the methanol to the sodium?  Any suggestion?

 Jeff

 From: Jan Warnqvist [EMAIL PROTECTED]
 Reply-To: Biofuel@sustainablelists.org
 To: Biofuel@sustainablelists.org
 Subject: Re: [Biofuel] Quality Test
 Date: Thu, 11 Aug 2005 18:51:02 +0200
 
 Hello Jeffery.
 The test method that you are using seems to me highly dubious, since
there
 are a number of pre-assumptions that has to be met.
 For a further check I´d suggest this:
 Take exactly 25 ml of biodiesel and dissolve it in exactly 225 ml of
 methanol in a measuring glass. Now:
 The biodiesel should be fully soluble in the methanol forming a clear
 bright
 phase. If not, there is pollution in the biodiesel causing you trouble
with
 the water test. Each ml of undissolved material is corresponding to 4% by
 volume. Are there any undissolved material at the bottom of the measuring
 glass ?
 If there is, your reaction is not complete and this is causing you
trouble
 with the water test.
 This method does not cover every aspect of quality, but it gives a hint
 though
 Good luck to you
 Jan Warnqvist
 AGERATEC AB
 
 [EMAIL PROTECTED]
 
 + 46 554 201 89
 +46 70 499 38 45
 - Original Message -
 From: Jeffrey Tan [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Thursday, August 11, 2005 2:19 PM
 Subject: [Biofuel] Quality Test
 
 
   Hello all.  Need some explanation and advise here on my experiments
 please.
  
   I have been using virgin cooking palm oil for the experiments.  When
   following the steps for checking on quality, I put in 150ml of de
 ionised
   battery water and 150ml of the biodiesel obtained but the end result
was
   clear yellowish liquid on top and white emulsion like on the bottom.
I
 have
   done 3 different batches with the same result.  My further reading and
 guess
   is either the NaOH is too much/little or the methanol is too
 much/little.
   My next step will probably to increase the methanol from 200ml to
400ml
 (my
   batches are in 1 liter of new oil).  Any comments or suggestions from
 the
   gurus out there?
  
   Can I continue with the bubble washing process with the above 3 test
   batches?
  
   Jeff
  
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Re: [Biofuel] Biofuel College Courses

2005-08-15 Thread Jan Warnqvist
Hi all,
interfering with basic physics:
The mass of the object moving, is of outmost importance, since it takes more
energy to move a heavy object than a less heavy one. This is mathematically
most significant when moving the object up-hill. Compared to these
circumstances, the rolling and wind resistances are of less importance to
the energy consumption.
Are you sure that you calculated your fuel consumption properly ?
With best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

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- Original Message - 
From: Bede [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Monday, August 15, 2005 11:48 AM
Subject: RE: [Biofuel] Biofuel College Courses


 depending on the speed your going a higher torque engine can
 cruise more effcently at a lower rpm than a smaller engine
 trying to do the same work at a higher rpm
 if the road is mainly flat,
 Then the only real diffrence between the 2 cars once up to highway
 speed is the the amount of effort to overcome the rolling and wind
 resistance.
 For such a long trip, things such as if you had a tailwind and
 your avg travling speed also make a big difrence.

 and then theres maunal, automatic trans mission and cruise control.

 What about MIT ?
 Bede

 -Original Message-
 From: [EMAIL PROTECTED]
 [mailto:[EMAIL PROTECTED] Behalf Of Pablo
 Sent: Monday, August 15, 2005 5:51 AM
 To: Biofuel@sustainablelists.org
 Subject: [Biofuel] Biofuel College Courses


 I am 18 and not sure where I want to go to college. I might take the
 year off, as it is so late to be signing up. My question for everyone
 is, does anyone here know of some good colleges, preferably in the New
 England area, that have specialty biofuel(or related) courses? That
 would be a great help to me.  Also, I wanted to add an amazing
 discovery/question that I found this past week. I drive a 1992 honda
 civic. I just did a full tune up, including O2 sensor, plugs, wires,
 cap  rotor, etc. I drove from FL to MA, and i got about 23 MPG. This
 is in a 1.5L engine in a  car weighing maybe 1600 lbs fully loaded
 with 106 base HP. I then drove my father's car south( a 2000 Cadillac
 Deville), from Ma to FL, and got an amazing surprise : his 4.6L
 American engine with about 300 base HP pulling a car weighing maybe
 3000Lbs empty got  28MPG. I also found that in the city, his car's
 gas mileage was 18 MPG, where mine is about 13. Now I admit to owning
 a foot of lead, but does anyone know how this is possible as i drove
 both vehicles, and with regular gas? The calculations were correct for
 MPG. Any input would be appreciated. ~ Paul

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Re: [Biofuel] mercedes/dodge sprinter vans?

2005-08-16 Thread Jan Warnqvist
Hello all,
according to the position of Daimler-Chrysler concerning the use of
biodiesel in MB cars, the most recent information I have is similar to the
one Lars Andersson has. But, it is merely a question of material
compability. From the experiences from previous MB models I can vouch for
that the problems are very small, if any at all ,with B100.
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

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- Original Message - 
From: S. Chapin [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, August 16, 2005 6:37 AM
Subject: Re: [Biofuel] mercedes/dodge sprinter vans?


 Lars Andersson wrote:

 We have a Mercedes Sprinter 316 CDI as a job van. I checked with the
Swedish distributor about using biodiesel as fuel and they answered
something undecided and then that maximum 5% was okey but they did not
want any biodiesel at all in the fuel tank because it was possible to get 4%
once and maybe 6% the next time !! I got an bit annoyed and checked with the
German manufacturers who answered that because of materials used in the fuel
system they did not allow any biodiesel at all with warranties
unbroken.. Boring answer !! It is from late 2003 and company owned so i
will not make any experiments with it..
 
 It pulls a 1800 kg trailer like a dream at about 20-21 mpg.
 
 Lars A
 
 From: S. Chapin [EMAIL PROTECTED]
 
 
 
 
 Does anyone out there have have a (diesel) biofueled Sprinter aka 316
 I think? We are considering one, a CDI 5cyl turbo mercedes, for general
 hauling. My feeling is that there will be no problems with even b100
 (mild climate) but just to see thought of casting about on the list.
 Other than the ford and dodge diesel trucks (maybe 22hwy max) it's all I
 can find (in the US) that gets even close (pathetic really) to
 reasonable mileage (18-30) for the capacity.
 Also, a hemp bill before the congress, I've forgotten the #, needs
 support. A viable source of oil I understand, amoung other uses
 (recreational not amoung them).
 Also, dust off that old copy of Farenheit/9-11 and watch it again. I
 find dragging oneself back through the timeline tends to clear the
 cobwebs of CNN breaking news stories.
 Then a little from Iran-Contra and some Watergate hearing footage
 and if the blood hasnt risen to your rosey cheeks try some footage of
 Wallace, or Jesse Helms.
 Fool me once 
 I looked into the Santa Cruz GM food ban and it looks like a
 response to GM efforts to circumvent state by state restrictions on GM
 experimental plantings. Stealth Monsanto.
 Cheers,
 S. Chapin
 Corralitos Creek Gardens
 
 
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 Many Thanks Lars.
  I have a feeling  that manufacturers, dealers and insurers are finding
 it possible to write off warranties because of BD use. I can imagine
 that in cold climates, with a thickened fuel it would put some strain on
 difertent elements, starters, glow plugs, CDI system... but okay maybe
 b50 or even b10. And perhaps there is  some reluctance because of the
 inconsistent  quality of home brewed BD. The manual transmission trucks
 in the US have a lower tow capacity than the auto trans simply because
 they dont want to cover clutch work on warranty because the driver may
 not know how to drive a manual trans without burning it up. So  in the
 end it's a paperwork rule and, I would think, rarely an issue. What gets
 me is that BD is a better lubricant, hence lower wear, and cleaner hence
 less warranty claims, happier clients etc. but maybe, as with so many
 issues... the reality doesnt make much of an impression.
 I am glad to hear 20-21 with 1800 kg load. I think the lowest mpg
 advertised by Dodge is
 about 16 max load city driving  for the 3500 van (dual rear wheels ).
 Thanks
 S.Chapin

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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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[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
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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
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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
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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] 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

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] 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] 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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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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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] 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] 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] 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] (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

[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] 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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 http://journeytoforever.org/biofuel.html

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 messages):
 http://www.mail-archive.com

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

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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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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 messages):
 
 
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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
 
 

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 Search the combined Biofuel and Biofuels-biz list archives (50,000
 
 
 
 
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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] 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] 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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from fooling ourselves — Richard Feynman

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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] 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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  Visita www.tutopia.com y comienza a navegar más rápido en 
  Internet. Tutopia es Internet para todos.  
  
  

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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]

+ 46 554 201 89
+46 70 499 38 45
- 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] 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]

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  - 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] 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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[Biofuel] Method

2005-02-27 Thread Jan Warnqvist

Hi everyone!
Normally it takes some quite complicated laboratory equipment to establish the 
ester content of a batch biodiesel. Does anybody know of a reliable garage 
method (experimental or algebraic) to do the same job with an accuracy on 
percent level ?
Jan Warnqvist

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[Biofuel] Fw: Method

2005-02-28 Thread Jan Warnqvist


Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

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- Original Message - 
From: Jan Warnqvist 
To: [EMAIL PROTECTED] 
Sent: Sunday, February 27, 2005 3:03 PM
Subject: Method


Hi everyone!
Normally it takes some quite complicated laboratory equipment to establish the 
ester content of a batch biodiesel. Does anybody know of a reliable garage 
method (experimental or algebraic) to do the same job with an accuracy on 
percent level ?
Jan Warnqvist

+46 554 201 89
+ 46 70 499 38 45
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Re: [Biofuel] A problem with WVO

2005-03-06 Thread Jan Warnqvist

Hello.
I think that both the FFA content and water content are too high in that
oil. The water content is the worst enemy for a good trans-etherification.
Try this :
Put the oil in a vessel at 70oC for 24 hrs. The water may form a separate
phase at the bottom of the vessel.
Check the water content. ExxonMobile sells a nice kit called Mobil water
test. The active chemical compound in this is calciumdihydride. It is a
reliable method. Do not try to transesterify again until the water content
is around 0,5%.
And- watch out for any remaining detergents in the oil !
Jan Warnqvist
AGERATEC AB

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- Original Message - 
From: Appal Energy [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Sunday, March 06, 2005 1:25 AM
Subject: Re: [Biofuel] A problem with WVO


 Kitch,

  Any suggestions ?

 Conduct a series of bracket titrations and/or move towards the acid/base
 process.

 Todd Swearingen

 - Original Message - 
 From: [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]
 Sent: Saturday, March 05, 2005 9:54 AM
 Subject: [Biofuel] A problem with WVO


  Hello brothers and sisters.
 
  I have been making my own bio for about three years and have been very
  successful with it. I HAVE had some great failures such as filter
clogging
  raw
  fat in the fuel, gertting it in the tank while some Glycerine was still
  separating - MORE clogged filters, but have learned so much that i now
  give
  free seminars and have about 50 people now brewing their own.
 
  So my problem is this: I have a restaurant that gives me about 20
gallons
  a
  week of Canola oil that they have cooked french fries and hot dogs in.
  Never
  too dirty, but quite dark.
 
  I have had BAD results with this stuff. I titrate and it always needs to
  have
  an excessive amount of lye added and when I do, I get a solid MESS. I
have
  even tried to make various half litre batches with the same results - an
  almost solid block of GLOP. Now, i have added perhaps uip to 20% of this
  oil
  in with my more common crappy soy oil and THEN it works OK.
 
  Any suggestions ?
 
  Kitch in Az
 
  99 Golf diesel
  82 Vanny camper diesel
  82 Vanny diesel grease getter
 
  Small diesels driving truck alternators backing up solar power

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Re: [Biofuel] A problem with WVO

2005-03-07 Thread Jan Warnqvist

Hello.
You are doing the right thing. But, remember that a high FFA content
usually is managed with NaOH or KOH in excess or by a pre-staged acid
transesterification. Water is not.
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

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- Original Message - 
From: [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Sunday, March 06, 2005 4:20 PM
Subject: Re: [Biofuel] A problem with WVO


 Quoting Jan Warnqvist [EMAIL PROTECTED]:

  Hello.
  I think that both the FFA content and water content are too high in that
  oil. The water content is the worst enemy for a good
trans-etherification.
  Try this :
  Put the oil in a vessel at 70oC for 24 hrs. The water may form a
separate
  phase at the bottom of the vessel.
  Check the water content. ExxonMobile sells a nice kit called Mobil water
  test. The active chemical compound in this is calciumdihydride. It is a
  reliable method. Do not try to transesterify again until the water
content
  is around 0,5%.
  And- watch out for any remaining detergents in the oil !
  Jan Warnqvist
  AGERATEC AB
 
  [EMAIL PROTECTED]

 Hi Jan,

 I think my main problem is too much free fat in the oil. If I add 20-25%
of it
 to my other soy oil that is little used for only two days at a street
fair,
 then it converts really well, as the overall free fat content of the
blended
 batch is low enough to work with just a one step lye/meth conversion. SO,
I am
 going to move to a two step acid/meth-lye program with it. Watr saeems not
to
 be a big issur here in the desert, but since you guys warned me, I'll sure
 check for it!!

 Thanks again SO MUCH and let's keep working to save our country from those
 that run it!!

 kitch in Az.

 -
 FastQ Communications
 Providing Innovative Internet Solutions Since 1993

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Re: [Biofuel] (Biofuel)[Fwd: Re: soybeanoil a bad choice for BD making?]

2005-03-07 Thread Jan Warnqvist

Hello Stephan.
The reason for Elsbett«s people (and several others) for rejecting soy bean
oil is its high iodine number. As the case with fish oil, corn oil and
several kinds of sunflower oil. A high iodine number is indicating that the
oil may be chemically unstable due to its unsaturation level and therefore
unsuitable as engine fuel both as SVO and BD.
There are some companies producing me from oil with a high iodine number,
and there is no practical difference between those products and the BD:s
with a iodine number around or under 120 for the consumer.And may I add that
the American B100 standard allows soy bean oil as raw material.
Best regards
Jan Warnqvist
AGERATEC AB

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- Original Message - 
From: stephan torak [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Monday, March 07, 2005 3:19 AM
Subject: [Biofuel] (Biofuel)[Fwd: Re: soybeanoil a bad choice for BD
making?]







 Hi Everyone!
 I am a recent addition to the biodiesel world, due to a malfunction
 in my brain (age related no doubt) that caused me to go and buy a
 190D.(I Love it just as I knew I would) . After I decided that
 buying the conversion kit from Elsbett wasn't necessarily the best
 option (due to local WVO quality concerns)by the way, if you come to
 Hawaii, where I live, and decide to eat in a restaurant, make sure
 you have healthinsurance, the glop they are using here to fry stuff
 in ..
 
 Seriously, though, the WVO I am getting here is is a mix of mostly
 Soybean oil used 100 times over and other unidentified saturated and
unsaturated things.
 So I deciided to make BD.
 Now, Everything is running,  I've done small batches, large batches,
 learned a lot,  I am using itand now I just read that an
 Elsbett engineer said to stay away from Soybean oil, regardless if
 used straight or as feedstock for BD.
 
 Now, in my (brief) dealings with the Elsbett company I had the
 distinctive feeling that they have a little bit of an anti- BD leaning
(maybe I got that because German is my native language)
 
 But in studying the resources further, and considering the high IV
 of soybean oil more questions as to its suitability  seem to emerge
 
 Here are some questions:  As far as suitability as a long term
 source for B100, how serious are the concerns  in using BD made from
 this sort of an oil?
 
 What criteria in evaluating  the finished product (beyond Mike Perry's
criteria of pH and aspect)
 should serve as a go no go test?
 
 does a two step process improve the situation with the high number of
double bonds
 (which leads to the high IV value, as I understand)

 Thanks for your consideration, Aloha




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Re: [Biofuel] (Biofuel)[Fwd: Re: soybeanoil a bad choice for BD making?]

2005-03-07 Thread Jan Warnqvist

Hello Keith !
Of course there is a possibility that unsaturated compounds interact in the
lubricating oil, but if the engine«s combustion is proper, you do not have
to expect big problems. But, there are other ways for the fuel to get in
contact with the engine oil: It the engine is equipped with a row pump, with
one pump element per injector, there is a possibility (due to construction
error) that some of the fuel slips by the pump piston entering the engine
oil. Some engine manufacturers refuse to acknowledge biodiesel, because once
in the oil, it will not vaporise the way ordinary diesel engine fuel does.
But the to be on the safe side, cut the oil change intervals by half, which
is recommended by many engine manufacturers. Maybe you even can get Castrol
to analyse samples of your oil and look for signs of polymerisation.
You can safely assume that the EN 14214 is technically founded, although it
has its shortcomings. For info on me with a high iodine number, I advice you
to enter:
www.scanbio.org
for further information about the products of ESTRA AS.

Best wishes

Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Monday, March 07, 2005 7:56 PM
Subject: Re: [Biofuel] (Biofuel)[Fwd: Re: soybeanoil a bad choice for BD
making?]


 Hello Jan

 Hello Stephan.
 The reason for Elsbett«s people (and several others) for rejecting soy
bean
 oil is its high iodine number. As the case with fish oil, corn oil and
 several kinds of sunflower oil. A high iodine number is indicating that
the
 oil may be chemically unstable due to its unsaturation level and
therefore
 unsuitable as engine fuel both as SVO and BD.

 In other words, it polymerises - to quote Phillip Calais: Drying
 results from the double bonds (and sometimes triple bonds) in the
 unsaturated oil molecules being broken by atmospheric oxygen and
 being converted to peroxides. Cross-linking at this site can then
 occur and the oil irreversibly polymerises into a plastic-like solid.
 -- From Waste Vegetable Oil as a Diesel Replacement Fuel by Phillip
 Calais, Environmental Science, Murdoch University, Perth, Australia,
 and A.R. (Tony) Clark, Western Australian Renewable Fuels Association
 Inc.
 http://www.shortcircuit.com.au/warfa/paper/paper.htm

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

 But that's not quite what Elsbett's Alexander Noack is quoted as
 saying at the East Coast Region-United States Elsbett Workshop:

 Soybean oil is bad. Whether it is straight vegetable oil or soybean
 based biodiesel. It is a no-go in diesel engines. Why? In diesel
 engines you have slight mixing between fuel and lubricating oil.
 There is a fuel property in soybean oil that makes it reactive when
 in contact with engine lubricating oil. It supposedly has a
 polymerizing action with the engine oil, which is detrimental to the
 life of your lubricating system.

 What they do in Europe is use a vegetable-based lubricating oil for
 the engine to prevent any problems with fuel-lubricating oil
 intimacy. What else? They do not use soybean oil; They use rape seed
 also known as canola.

 So it would seem that Elsbett's reservations are not so much with
 polymerisation per se because of the high iodine number as with
 fuel-lubricating oil interactions.

 Can you shed any light on this?

 There are some companies producing me from oil with a high iodine number,
 and there is no practical difference between those products and the BD:s
 with a iodine number around or under 120 for the consumer.

 Can you quote any research that supports the conclusion that there is
 no practical difference? I've heard of drying problems with sunflower
 oil biodiesel, and even with rapeseed oil biodiesel (I don't have the
 reports, I was told they're in German) and I would not want to use
 linseed oil or tung oil.

 And may I add that
 the American B100 standard allows soy bean oil as raw material.

 Of course they do - how much do you think the soy councils and Big
 Soy had to do with that? They were involved at every level. Whatever
 the science may say, do you think it would have been possible for
 them to develop standards that excluded soy?

 Similarly, it's often said that the EU standard's stipulating a
 maximum iodine # of 120 (115 in France and Germany, while the US
 standard doesn't stipulate anything) is politically based, intended
 to exclude soy and protect European rapeseed oil production, but is
 that really all there is to it?

 If you really wanted to exclude drying problems you'd probably have
 to exclude rapeseed oil as well and stop at castor oil (85), but no
 doubt that would be as politically impossible in Europe as excluding
 soy would be in the US. In both, though less so in Europe perhaps,
 biodiesel and biofuels are still seen more as agricultural
 commodities issues than as energy issues.

 There is a whole

Re: [Biofuel] Neophyte seeks advice on runing 1983 Mercedes 300SD on BD

2005-03-10 Thread Jan Warnqvist

Hello Thomas.
Congratulations to a good car choice.
You may have filter clogging problems in the beginning of BD use.
Therefore I recommend you to move the feed pump strainer (it is a strainer,
not a filter) upwards so it can be easily reached from above for swift and
simple exchange. this is done by longer rubber tubes.
This will simplify the filter/strainer replacements.
Good luck to you !
Jan Warnqvist
AGERATEC AB

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- Original Message - 
From: Thomas Giguiere [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Wednesday, March 09, 2005 10:13 PM
Subject: [Biofuel] Neophyte seeks advice on runing 1983 Mercedes 300SD on BD


 Hello. I am an aspiring biodieseler with an elementary background in
 chemistry. I would like to run my 1983 Mercedes 300SD on biodiesel. Can
 anyone recomend a good formulation to use? Should I make any
 modifications to the vehicle before I attempt to change over to BD? Any
 advice would be appreciated.

 Regards,

 Thomas Gigiuiere
 Folsom, CA
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Re: [Biofuel] Re: Drying WVO - Is there a simple way

2005-03-10 Thread Jan Warnqvist

Hi John.
In order to separate water from WVO by using a centrifuge, the most
efficient way is to heat the water/WVO mix to 75-90oC and run it as a round
circuit until the water content drops to a sufficiently low level.
Best rgrds
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
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- Original Message - 
From: John Wilson [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Wednesday, March 09, 2005 3:01 PM
Subject: [Biofuel] Re: Drying WVO - Is there a simple way


 Hi,
 I haven't tried this yet so it is only theory. I bought an old cream
 seperator(Centrifuge) and I am going to filter the wvo first then run it
 through the seperator and hopefully seperate any water  from the WVO. Also
 going to try and recover Methy that way. Did you see the news on CNN that
 there is a country that makes a national drink from methanol called raki.
 WOW! ethanol is bad enough , but drink methanol that is absolutely
 redicilous.
 Yours truly
 John Wilson
 Goldens
 ***
 Wilsonia Farm Kennel Preserve

 Email: [EMAIL PROTECTED]
 Ph-Fax (902)665-2386)

 Web: http://www3.ns.sympatico.ca/goldens/new.htm
 Pups: http://www3.ns.sympatico.ca/goldens/pup.htm
 Politics: http://www3.ns.sympatico.ca/goldens/elect.htm
   http://www3.ns.sympatico.ca/goldens/c68.htm


 In Nova Scotia smoking permitted in designated areas only until 9:00 PM .
 After 9:00 it is okey to kill everyone.



 ^^^


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Re: [Biofuel] Re: Drying WVO - Is there a simple way?

2005-03-10 Thread Jan Warnqvist

It is not recommendable with water together with SVO, WVO or BD for that
matter.
The oils consist from esters which are sensible to hydrolysis. This means
that parts of the oil will crack by the influence of water. A water content
too high will cause:
1) Severe filter clogging problems since many of the compounds formed by the
hydrolysis are in solid shape, not liquid.
2) Corrosion in the fuel system, since many of the hydrolysis products are
bound to be sour.
Jan Warnqvist
AGERATEC AB

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- Original Message - 
From: R Del Bueno [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Wednesday, March 09, 2005 3:16 PM
Subject: Re: [Biofuel] Re: Drying WVO - Is there a simple way?


 This is a good question.

 I have found that gravity will take most of the free water out in time.
 Warming the oil to about 140degF speeds up the process. The use of a
 centrifuge speeds it up even further (but can be costly unless you stumble
 into a good deal on one).

 I know some folks are using some vacuum setups to lower the boiling point,
 and using flash evaporators and or thin film evaporators, but I wonder if
 it is needed.

 (As a side question...how much more efficient is a vacuum assisted
 evaporator from a total energy usage standpoint, than just heat, after all
 one must use energy to create the vacuum?)

 There still seems to be some debate over how dry the oil needs to be.

 For WVO/SVO fuel systems, I am not positive that small quantities of water
 are all that problematic...after all there are water injection systems out
 there, and a few companies that sell diesel /water emulsifiers in order to
 suspend water into diesel fuel as a method of altering combustion
 temperature to reduce NOX emissions. So from a combustion
standpoint..seems
 that small amounts of water will simply turn to steam.

 Free water over time can collect in the fuel system and cause freeze
 issues, and corrode internal components of injection systems...but if you
 are running a dual tank WVO system, switching back to diesel prior to
 shutdown, there should not be water sitting in the injection system.

 Does a small amount of water affect the lubricity value of the
 WVO?..perhaps..but with the initial lubricity of WVO being so high, I
 suspect there is a bit of room to play.

 So far I have been running 10 micron filtered gravity settled oil (about a
 week at around 70degF) with a heated waterblock type filter in vehicle.
 Very little, if any water collects in the clear bowl. I have yet to run
 into any problems that indicate water problems...but only topping out at
 around 10k miles..so nothing definitive.

 I understand the need to dry WVO for biodiesel production, but wonder how
 needed it is for straight WVO as fuel.

 -Rob

 At 08:30 PM 3/8/2005, you wrote:





 Hello to all:
 I'm wondering if anyone is using WVO and drying it before use.  I filter
 it and it looks brite and clear but I worry that there may be water
disolved
 in the oil. Is there a simple test for water content?  Is there a simple
 method of removing moisture?  I don't want to heat 50 gallons to 150C.
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Re: [Biofuel] (Biofuel)[Fwd: Re: soybeanoil a bad choice for BD making?]

2005-03-10 Thread Jan Warnqvist

Hello Keith.
The site is in Norwegian and English.
Anti-oxidants are used as a reinsurance, since the temperatures of the car
fuel tanks can rise to high levels. Anti-oxidants.
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Tuesday, March 08, 2005 1:54 AM
Subject: Re: [Biofuel] (Biofuel)[Fwd: Re: soybeanoil a bad choice for BD
making?]


 Hello Jan

 Hello Keith !
 Of course there is a possibility that unsaturated compounds interact in
the
 lubricating oil, but if the engine«s combustion is proper, you do not
have
 to expect big problems. But, there are other ways for the fuel to get in
 contact with the engine oil: It the engine is equipped with a row pump,
with
 one pump element per injector, there is a possibility (due to
construction
 error) that some of the fuel slips by the pump piston entering the engine
 oil. Some engine manufacturers refuse to acknowledge biodiesel, because
once
 in the oil, it will not vaporise the way ordinary diesel engine fuel
does.
 But the to be on the safe side, cut the oil change intervals by half,
which
 is recommended by many engine manufacturers. Maybe you even can get
Castrol
 to analyse samples of your oil and look for signs of polymerisation.
 You can safely assume that the EN 14214 is technically founded, although
it
 has its shortcomings.

 I'm sure it's technically founded, but I wouldn't assume that it was
 not also subjected to political pressures.

 For info on me with a high iodine number, I advice you
 to enter:
 www.scanbio.org
 for further information about the products of ESTRA AS.

 Fish-oil biodiesel... but I can't read Swedish, apologies. Do you
 quote any research studies there on polymerisation that might support
 your statement that there is no practical difference for the consumer
 between biodiesel made with drying oils (high iodine numbers) and
 biodiesel made with oils with an iodine number around or under 120?

 Oils with an iodine number of around or under 120 are classified as
 semi-drying oils, and both soy and sunflower fall into this
 category, with rapeseed oil (canola) at the lower end of the range.
 Polymerise they do, if not quite as fast as linseed oil will (why
 it's used in paint), as well as fish oils - see, eg:

 Anti-rust Paint from Fish-Scraps
 http://journeytoforever.org/farm_library/FishPaintJTF.pdf

 This is what Ken Provost said here recently about linseed oil biodiesel:

 Being a drying oil, it will crosslink eventually in the presence of
 oxygen, which will cause it to thicken. I have used linseed biodiesel
 in my car, but only as a minor constituent (plenty of soy esters, olive
 esters, etc. in addition to the linseed) and only when I was prepared
 to empty my tank quickly (eg, a long trip where I'd have to refill with
 petrodiesel halfway anyway).

 Fish oils can have a higher iodine # than linseed oil. How do you
 prevent fish-oil biodiesel from drying? Making biodiesel with it
 doesn't affect the degree of unsaturation. Do you hydrogenate the
 oil? That would help, but what does it do for the melting point? The
 semi-drying oils will also dry, but not as quickly.

 Oxidation and thermal stability are one of the concerns about
 biodiesel of the Fuel Injection Equipment (FIE) Manufacturers
 (Delphi, Stanadyne, Denso, Bosch). In their field trials with
 biodiesel they found increased dilution and polymerisation of engine
 sump oil. See:

 FIEM report
 http://journeytoforever.org/biodiesel_FIEM.html

 Results from fleet tests in in Europe (Bosch) have shown that after
 60,000 km even DIN compliant fuel can damage the fuel injection
 system through polymerisation. I know of one such case of injector
 pump damage through polymerised fuel after only 40,000 km on B100.

 I think that if the EU's EN 14214 standard was entirely tchnically
 founded it might have excluded rapeseed oil; instead it has an IV
 cut-off of 120 and stipulates quite strict Oxidation stability
 levels, the only biodiesel standard specification to do so (though
 Australia has now followed suit). That looks like a compromise that
 allows for rapeseed oil as a feedstock and tries to limit the damage.
 There seems to have been a lot of trade in biodiesel anti-oxidants in
 Europe since EN 14214 was announced. Some American companies are also
 starting to offer biodiesel anti-oxidants - what do they know about
 soy biodiesel that we don't know (but are trying to find out)?

 Best wishes

 Keith


 Best wishes
 
 Jan Warnqvist
 AGERATEC AB
 
 [EMAIL PROTECTED]
 
 + 46 554 201 89
 +46 70 499 38 45
 - Original Message -
 From: Keith Addison [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]
 Sent: Monday, March 07, 2005 7:56 PM
 Subject: Re: [Biofuel] (Biofuel)[Fwd: Re: soybeanoil a bad choice for BD
 making?]
 
 
   Hello Jan
  
   Hello Stephan.
   The reason for Elsbett«s people (and several others) for rejecting
soy
 bean
   oil is its

Re: [Biofuel] Re: Drying WVO - Is there a simple way?

2005-03-11 Thread Jan Warnqvist

Hello, Keith and Rob.
The water content in FAME according to EN 14214 is set to 500 ppm.
In the long run you will have problems if the water content exceeds 0,5% and
if the water content exceeds the percentage level, the problems will occur
quickly and rising. BD is basically not storable for more than three months
keeping an acceptable quality.
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Keith Addison [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Thursday, March 10, 2005 5:22 PM
Subject: Re: [Biofuel] Re: Drying WVO - Is there a simple way?


 Hello Jan, Rob

 It is not recommendable with water together with SVO, WVO or BD for that
 matter.
 The oils consist from esters which are sensible to hydrolysis. This means
 that parts of the oil will crack by the influence of water. A water
content
 too high will cause:
 1) Severe filter clogging problems since many of the compounds formed by
the
 hydrolysis are in solid shape, not liquid.
 2) Corrosion in the fuel system, since many of the hydrolysis products
are
 bound to be sour.

 Once hydrolosis has taken its course perhaps. But there is always
 water in biodiesel. The various standards set upper limits of
 500-600ppm, but Camillo Holecek of Energea in Austria told us that no
 matter how dry you get it, it will quickly reabsorb water from the
 atmosphere to an average of about 1,500ppm, and that's what you'll
 have in the tank. That seems to be correct, and it doesn't seem to
 hasten hydrolosis. Frankly, I'm beginning to think all the cautions
 about degraded biodiesel are a myth, because I can't persuade any to
 degrade, and I'm not the only one. Maybe it has more to do with the
 commercial industry's use of the petro-diesel storage and delivery
 infastructure, which isn't all that great.

 We've had this discussion here about water content, water emulsions
 and water injection before a few times, there is quite a lot of
 information in the archives. For instance:

 http://www.dieselnet.com/
 Water in Diesel Combustion [subscriber access]
 DieselNet Technology Guide È Engine Design for Low Emissions
 
 Water in Diesel Combustion
 
 Abstract: Addition of water to the diesel process decreases
 combustion temperatures and lowers NOx emissions. The most common
 methods of introducing water are direct injection into the cylinder,
 a process commercialized in certain marine and stationary diesel
 engines, and water-in-fuel emulsions. Emulsified fuels, due to
 increased mixing in the diesel diffusion flame, can be also
 effective in simultaneous reduction of PM and NOx emissions.
 
 Addition of Water to Diesel Process
 Fumigation of Water into Intake Air
 Direct Injection of Water
 Fuel Emulsions
 Practical Embodiments
 [more...]
 http://wwia.org/pipermail/biofuel/Week-of-Mon-20041115/002962.html

 Water Emulsions - Water-fuel emulsions are one of the few methods
 that can simultaneously control PM and NOx emissions. Depending on
 the engine, emulsions containing 20% water can reduce PM emissions by
 as much as 50%. It should be noted that other methods of water
 addition, such as direct injection, are not effective in controlling
 PM.
 http://infoarchive.net/sgroup/BIOFUEL/37764/
 [Scroll down.]

 Here's a roundup below of some stuff we've had previously and some
 other stuff, on both water injection and water-fuel emulsions...
 http://infoarchive.net/sgroup/BIOFUEL/30409/

 The US EPA lists 23 studies of water emulsions with dino-diesel:

 Following is a list of studies that are being considered for
 inclusion in work being done by EPA to assess the effects of
 water-fuel emulsions on emissions of oxides of nitrogen (NOx),
 hydrocarbons (HC), and particulate matter (PM).
 http://www.epa.gov/otaq/models/analysis/emulsion/emulbibl.pdf

 We've also had reports of successful use of biodiesel-alcohol-water
 mixes in Australia, on quite a large scale. As for hydrolosis, you're
 probably quite safe if you use it in a month or two, probably longer.

 Joe, re WVO:

   Hello to all:
   I'm wondering if anyone is using WVO and drying it before use.  I
filter
   it and it looks brite and clear but I worry that there may be water
 disolved
   in the oil. Is there a simple test for water content?  Is there a
simple
   method of removing moisture?  I don't want to heat 50 gallons to
150C.
   Searching..___

 Heat it to 60 deg C for 15 minutes then let it settle, at least
 overnight; draw from the top. Heating to high temps like 150 deg C
 can lock that water in there rather than boiling it off. If 60 deg C
 doesn't work you probably shouldn't be using that oil in an SVO
 system - find better oil. 60 deg C is safer too, no steam explosions.

 A quick test is to heat a little of the oil in a saucepan; if there's
 water it will start to crackle at 50 deg C or less; if it reaches
 60-65 deg C and still no crackling then you don't have a water
 problem

Re: [Biofuel] Re: Drying WVO - Is there a simple way

2005-03-11 Thread Jan Warnqvist

Hello Norm.
The centrifuge itself is calibrated for water, so its capacity with oil is a
trial and error project. But unless the centrifuge is equipped with a feed
pump, one has to go for a pump with adjustable capacity for starters. And be
precise when choosing the gravity disc and the seal ring size at the outlet.
Everything is working properly when you have sludge and water coming out of
one outlet and pure oil from the other outlet.
Never use a centrifuge or separator working with a water seal.
The water content can be determined with a kit from ExxonMobil, Mobil water
test kit.
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Gmail - GaitedRidge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Thursday, March 10, 2005 1:24 PM
Subject: Re: [Biofuel] Re: Drying WVO - Is there a simple way


 Hi Jan,

 When you say :

 /heat the water/WVO mix to 75-90oC and run it as a round
 circuit until the water content drops to a sufficiently low level./

 From the above statement I envision a closed system like a hot water tank
type heater with an attached pump slowly circulating the WVO.  What flow
rate would you consider appropriate when shopping for a pump to do this and
how are measuring the water content?

 Regards
 Norm Fillion
 [EMAIL PROTECTED]
 Manitoba
 -


  Hi John.
 In order to separate water from WVO by using a centrifuge, the most
 efficient way is to heat the water/WVO mix to 75-90oC and run it as a
round
 circuit until the water content drops to a sufficiently low level.
 Best rgrds
 Jan Warnqvist
 AGERATEC AB

 [EMAIL PROTECTED]

 + 46 554 201 89
 +46 70 499 38 45
 - Original Message - 
 From: John Wilson [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]
 Sent: Wednesday, March 09, 2005 3:01 PM
 Subject: [Biofuel] Re: Drying WVO - Is there a simple way



 Hi,
 I haven't tried this yet so it is only theory. I bought an old cream
 seperator(Centrifuge) and I am going to filter the wvo first then run it
 through the seperator and hopefully seperate any water  from the WVO.
Also
 going to try and recover Methy that way. Did you see the news on CNN
that
 there is a country that makes a national drink from methanol called
raki.
 WOW! ethanol is bad enough , but drink methanol that is absolutely
 redicilous.
 Yours truly
 John Wilson
 Goldens
 ***
 
 
 snip...
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Re: [Biofuel] diesel, is it cleaner?

2005-03-22 Thread Jan Warnqvist

Hi Andrew  Tracy.
There is a Swedish survey performed by Motor Test Center, in which FAME is
compared with Swedish diesel oil Mk 1 and other similar fuels. The survey is
focusing on the cancerogenity of the particulants of the fuel respectively.
The results suggest that the semi-violate phase from biodiesel is more
carcinogenic than the correspondent from diesel fuel. But, on the other hand
that phase is much smaller from biodiesel than from diesel fuel, so it makes
diesel fuel more dangerous anyway.
http://www.mtc.se/eng/freport.htm
Emissions from Use of RME Compared to Environmental Class 1 Diesel Fuel in
a HD Vehicle
It should be pointed out that this report has not brought much attention to
itself.
Best regards
Jan

Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
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- Original Message - 
From: Andrew  Tracey [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Monday, March 21, 2005 11:09 PM
Subject: [Biofuel] diesel, is it cleaner?


Back in the 80's there was a report published about the findings of number
of independant scientists investigating the effects of burning diesel fuel
and the connection to the big increase of asthma in children. Not only did
they find the two very much connected, they also claimed diesel was
responsible for causing cancer. Do you know anybody who has died from lung
cancer that didn't smoke? It also went on to state it was one of the most
dangerous substances known to man because of the increasing volume of usage.
Does anybody remember this report?. I know several people who do- they all
own diesel powered cars. It's funny how we all think that nothing is going
to happen to us, just to the other bloke. Does anyone know of any research
done on the effects of biodiesel on the human body? Is it less harmfull? I
hope it is as i intend to make some.  regards  AT.
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Re: [Biofuel] Salt in WVO problem or not ??

2005-03-29 Thread Jan Warnqvist

Hello Denis.
Addressing your question, the least you can expect is that most of the salt
will dissolve in the rinsing water, if done properly and several times. And
ordinary salt (NaCl) will not affect the pH value of the fuel.
Best regards
Jan Warnqvist
AGERATEC AB

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- Original Message - 
From: Jelatancev Denis [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Tuesday, March 29, 2005 11:45 AM
Subject: [Biofuel] Salt in WVO problem or not ??


 hi to all,

 This is my first mail to the list.

 I am planing to make my first bach of BD, and one question bothering me
for
 some time.

 How salt inside WVO can influence BD production process?
 Is it (salt) somehow taken out during BD production process or it stayes
 inside final product (BD)?

 I am asking that because I do not think that our TDI car engines would
like
 salt in it fuel.

 I have done lot of reading but have never come across this kind of info.

 any visions about it ?

 thanks,

 Denis
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Re: [Biofuel] Cladisporium resinae

2005-03-30 Thread Jan Warnqvist

Hi Phil,
are you referring to the plant producing castor oil ?
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
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- Original Message - 
From: Phil  Elaine [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Wednesday, March 30, 2005 2:12 AM
Subject: [Biofuel] Cladisporium resinae


Hi there good people,
does anyone out there have any experience of the growth of this organism in
Bio? I've had a lot to do with it in my capacity as an aircraft Engineer and
it's got rid of ( or kept under control at least ) by the addition of some
pretty toxic chemicals to the fuel which effectively act as a weedkiller
for want of a better expression.
Look forward to any response.

Phil Lloyd
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Re: [Biofuel] liquid glycerine

2005-03-30 Thread Jan Warnqvist

Hello Paul.
It seems to me that you produced some soap that time. Did you measure the
FFA content before starting ?
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Paul Tanner [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Wednesday, March 30, 2005 1:00 AM
Subject: [Biofuel] liquid glycerine






 Hi,

 I've been making Biodiesel (BD) for a few months, now.. using the Mike
 Pelly method.. and a curious thing happened with the last batch (my
batches
 are in approx. 160 - 180 litres).. the glycerine was liquid after the
 reaction. This is the first time this has occurred for me, all other times
 the glycerine formed and settle in my tank, and was solid at low
 temperatures.

 I had measured accurately, the quantities of methanol, caustic soda and
 volume of oil...( I had an interested observer, who can testify if
 required!! :-)  ) I watched the colour of the mixture change, as I was
 agitating, from a light caramel colour to a dark molasses colour... then
 observed the glycerine start to settle, as expected. At this time the
 glycerine was quite warm, so was still liquid, however, I let the mixture
 settle for a 2 week period and the glycerine has not set firm. maybe I
 should not complain.. 'cos it was easy to drain out of the tank! :-)

 Did the reaction not go far enough?  Any further ideas on what has
 happened??

 regards,

 Paul.
 ---
 Paul Tanner
 Software IT Architect
 Melbourne, Australia

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Re: @SPAM+++++++++ Re: [Biofuel] Set up help

2005-03-30 Thread Jan Warnqvist

Hello Luke.
I agree with you fully, but do not forget that SVO have a lower cetane
number, and they tend to form deposits in the combustion surroundings. These
deposits have a high cracking point (550-600oC) and the diesel engine is
built for fuel with a max boiling point of 350oC, so the deposits will
continue to form and grow until they cause trouble.
Best regards
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
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- Original Message - 
From: WM LUKE MATHISEN [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Wednesday, March 30, 2005 4:13 PM
Subject: @SPAM+ Re: [Biofuel] Set up help


Thanks for you input, I like the idea of capturing the heat and using it.

I did just run into this from Biomass 2004 Biodiesel handling and use
guidelines by the DOE enerty Efficiency and Renewable Energy.

Raw or refined vegetable oil, or recycled greases that have not been
processed into biodiesel, are not biodiesel and should be avoided.  Research
shows that vegetable oil or greases used in CI engines at levels as low as
10% to 20% can cause long-term engine deposits, ring sticking, lube oil
gelling, and other maintenance problems and can reduce engine life.  These
problems are caused mostly by the greater viscosity, or thickness, of the
raw oils (around 40mm 2/s) compared to that of of the diesel fuel for which
the engines and injectors were designed (between 1.3 an d4.1 mm @/s).  To
avoid viscosity-related problems, vegetable oils and other feedstocks are
converted into biodiesel.  Through the process of converting vegetable oil
or greases to biodiesel, we reduce viscosity of the fuel to values similar
to conventional diesel fuel (biodiesel values are typically between 4 and 5
mm 2.s).

I just paid $4000 for a genset and would like it to last the 20,000 to
50,000 hours it was designed for.  Are there any studies out there that
contradict the DOEs studies?
  - Original Message - 
  From: Gene Chaffinmailto:[EMAIL PROTECTED]
  To: [EMAIL PROTECTED]mailto:[EMAIL PROTECTED]
  Sent: 03/29/2005 10:45 PM
  Subject: RE: [Biofuel] Set up help


  Jeremy:  I started with an 8KW china diesel which runs at 2000rpm and
  consumed .8 gallons per hour.  I now do not consider these china diesels
  capable of 24/7 operation, eventhough I did get 6,200 hours out of one.  I
  am now using a Detroit 2-71 12 KW genset which consumes 1.1 gallons per
hour
  of wvo.  I have only been using the Detroit genset for two weeks now but I
  do like the fact that it revolves at a slow 1200 rpm and does not have a
  fuel injection pump like most diesel engines.  I don't just produce
  electricity I also use the waste heat from the cooling system as well as
the
  waste heat from the exhaust.  The waste heat is used to heat up the vege
oil
  and warm the water on my fish farm so the little rascals don't go into
  hybernation.  If you make use of all of the parasitic heat available from
  your genset you will have no problem running straight veg oil, I don't
care
  if you live in Alaska.  It freezes where I am and I still had to install a
  swamp cooler to keep the generator room comfortable.  Make use of the
water
  jacket heat and exhaust heat to provide your domestic hot water and heat
  your house.  I have not had any fuel system maladies.  Most of the
problems
  I was experiencing with the China diesels was with the valve train...they
  needed valve jobs every 2000 hours.  My learning curve is rather long at
  this point so don't hesitate to pick my brain as you progress.  I am now
in
  the process of installing a 20 KW Northern Lights genset which has a
similar
  engine to your Isuzu.  It has the Bosh/Kiki fuel injection pump.  I do not
  expect to have any problems with that conversion to wvo.  Good luck. Gene
  Chaffin  [EMAIL PROTECTED]mailto:[EMAIL PROTECTED]

  -Original Message-
  From: [EMAIL PROTECTED]mailto:[EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED]
  Behalf Of Jeremy
  Sent: Tuesday, March 29, 2005 7:52 AM
  To: [EMAIL PROTECTED]mailto:[EMAIL PROTECTED]
  Subject: Re: [Biofuel] Set up help


  Luke and Gene,

  Running straight WVO through your genset is great if you life in sunny
  california,  but I would not rely on that in Missoula.  WVO in Missoula
  would require a hefty investment in time and materials to create an
  environment equal to that of california in a shed.  Also, it is very
  difficult to collect WVO oil in freezing temps, or do anything with WVO in
  freezing temps.  I have a 12k isuzu generator that I am hoping to run with
a
  diesel/biofuel mix.  I think the best we could do is Biofuel in the summer
  and a mix in the winter, something greater than 50/50.  I think it would
be
  best to process your fuel in the summer, and store it with diesel for the
  winter.  That would require knowing how much fuel you would need over the
  winter, probably close to a half gallon an hour for you lister petter.

  Gene: could you describe your generator, what load you run

Re: @SPAM+++++++++ RE: [Biofuel] Study predicts growth of HCCI engines

2005-03-31 Thread Jan Warnqvist

Hello Tom.
No, quoting:HCCI is a low temperature combustion technology utilizing
compression
ignition of well-mixed air-fuel mixture.Unlike the conventional diesel
engine,
HCCI emits ultra low emissions of NOx and PM. On the negative side,
it can produce increased HC and CO emissions.
This is a diesel engine, no doubt. The Sterling engine works with external
combustion and takes advantage of the expansion (not combustion) of the
working gas (hydrogen, helium, or air).
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Tom Irwin [EMAIL PROTECTED]
To: 'Keith Addison ' [EMAIL PROTECTED]; [EMAIL PROTECTED]
Sent: Wednesday, March 30, 2005 8:37 PM
Subject: @SPAM+ RE: [Biofuel] Study predicts growth of HCCI engines


 Hi all,

 Are these HCCI engines related to the Sterling engine I've just starting
to
 learn about?

 Tom Irwin


 -Original Message-
 From: Keith Addison
 To: [EMAIL PROTECTED]
 Sent: 3/30/05 1:33 PM
 Subject: [Biofuel] Study predicts growth of HCCI engines

 DieselNet UPDATE
 March 2005
 http://www.dieselnet.com/

 Study predicts growth of HCCI engines

 A new study analyzing trends in heavy-duty vehicle powertrain
 technologies by 2020 has been released by TIAX, a collaborative
 product and technology development firm, and Global Insight, an
 industry forecasting firm. One of the findings of the study is a
 predicted growth in homogeneous charge compression ignition (HCCI)
 engine technology which will be displacing conventional heavy-duty
 diesel engines. The study also predicts greater use of heavy-duty
 hybrid vehicles.

 The study, titled The Future of Heavy-Duty Powertrains, was
 commissioned by a group of oil companies, engine and vehicle
 manufacturers, and component suppliers to investigate the impact of
 more stringent emissions regulations, increased traffic congestion,
 and a shortage of skilled drivers for large vehicles on the
 heavy-duty vehicle industry in North America, Europe, and Japan.

 Key findings of the report include:

   - HCCI engines will power nearly 40% of heavy-duty vehicles by 2020.
 Initially HCCI will only be able to power light loads at low speeds
 so early versions of the engine will also incorporate conventional
 diesel combustion to supply more power when greater demand is placed
 on the engine. A full mode HCCI engine will eventually supersede the
 mixed mode HCCI/diesel technology.

 - By 2020, 15-25% of heavy-duty vehicles globally will incorporate
 either hybrid electric or hydraulic hybrid technology. The rapid
 deployment of hybrid technology in the heavy-duty vehicle industry
 will be driven by savings on fuel and brake maintenance by vehicle
 operators.

 - The demand for self-shifting transmission technology in heavy- duty
 vehicles will increase dramatically over the next 15 years. The
 self-shifting transmissions can maximize fuel efficiency and to
 broaden the labor pool from which drivers can be recruited because
 trucks with automated or automatic transmissions are easier to drive.

 HCCI is a low temperature combustion technology utilizing compression
 ignition of well-mixed air-fuel mixture. The major technical
 challenge in HCCI is the control of combustion, with most of today's
 engine prototypes being able to sustain the HCCI combustion mode only
 at low to medium engine loads. Unlike the conventional diesel engine,
 HCCI emits ultra low emissions of NOx and PM. On the negative side,
 it can produce increased HC and CO emissions.

 The predicted growth in HCCI engines is particularly significant in
 that the exhaust gas aftertreatment systems currently being
 developed- -targeting mostly NOx and PM emissions--and expected to
 reach the market in the next few years will start to become obsolete
 by 2020. Instead, HCCI emission aftertreatment would need to target
 HC and CO emissions at very low exhaust temperatures.

 Summary:

 http://www.globalinsight.com/publicDownload/genericContent/03-03-05_P
 T_overview.pdf
 Purchase the report:

 http://www.globalinsight.com/MultiClientStudy/MultiClientStudyDetail1
 629.htm
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Re: @SPAM+++++++++ Re: [Biofuel] liquid glycerine

2005-03-31 Thread Jan Warnqvist

I agree with you Todd. All chemical reactions of this kind carries a number
of side reactions, but the amount or appetence of the glycerol cocktail
cannot be used for judging the success of the transesterification(unless it
is  10% by mass), but a determination of the content of the glycerol
cocktail might give a clue.
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: Appal Energy [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Wednesday, March 30, 2005 4:55 PM
Subject: @SPAM+ Re: [Biofuel] liquid glycerine


 Jan  Paul,

  It seems to me that you produced some soap that time.

 All base processing creates soap.

 What everyone keeps referring to as glycerine settling out of a
 transesterification (base) reaction is for the most part soap, diluted
with
 methanol and glycerol.

 The volume of glycerol per liter of oil processed is ~7.9% (~79
mililiters).
 The excess alcohol present in this layer (glycerin cocktail) is ~65ml when
 initially using 200 ml per liter. The balance is soap.

 Different oil and fat feedstocks produce different types of soap. If your
 feestock was primarily soybean oil on Monday but coconut oil on Tuesday,
the
 latter would in general yield a more solid glyc cocktail. If the
feedstocks
 were soybean oil on both days but Tuesday's was extremely degraded (high
 FFA) then the latter would yield a harder glyc cocktail. If the feedstock
on
 Monday had less animal fat in it than that on Tuesday the latter would
 generally yield a harder or more viscous glyc cocktail.

 The same happens when using different catalysts. In soap making sodium
 hydroxide (lye) is used to produce bar soaps (hard) and potassium
hydroxide
 is used to produce liquid soaps (solid like thick bread dough but more
 soluble). When using potassium hydroxide the glyc cocktail generally never
 thickens beyond that of maple syrup.

 Hardened or thinned glyc cocktails don't necessarily indicate mistakes
or
 correctness in processing.

 Todd Swearingen

 - Original Message - 
 From: Jan Warnqvist [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]
 Sent: Wednesday, March 30, 2005 3:01 AM
 Subject: Re: [Biofuel] liquid glycerine


  Hello Paul.
  It seems to me that you produced some soap that time. Did you measure
the
  FFA content before starting ?
  Best regards
  Jan Warnqvist
  AGERATEC AB
 
  [EMAIL PROTECTED]
 
  + 46 554 201 89
  +46 70 499 38 45
  - Original Message - 
  From: Paul Tanner [EMAIL PROTECTED]
  To: [EMAIL PROTECTED]
  Sent: Wednesday, March 30, 2005 1:00 AM
  Subject: [Biofuel] liquid glycerine
 
 
 
 
 
 
  Hi,
 
  I've been making Biodiesel (BD) for a few months, now.. using the Mike
  Pelly method.. and a curious thing happened with the last batch (my
  batches
  are in approx. 160 - 180 litres).. the glycerine was liquid after the
  reaction. This is the first time this has occurred for me, all other
  times
  the glycerine formed and settle in my tank, and was solid at low
  temperatures.
 
  I had measured accurately, the quantities of methanol, caustic soda and
  volume of oil...( I had an interested observer, who can testify if
  required!! :-)  ) I watched the colour of the mixture change, as I was
  agitating, from a light caramel colour to a dark molasses colour...
then
  observed the glycerine start to settle, as expected. At this time the
  glycerine was quite warm, so was still liquid, however, I let the
mixture
  settle for a 2 week period and the glycerine has not set firm. maybe I
  should not complain.. 'cos it was easy to drain out of the tank! :-)
 
  Did the reaction not go far enough?  Any further ideas on what has
  happened??
 
  regards,
 
  Paul.
  ---
  Paul Tanner
  Software IT Architect
  Melbourne, Australia
 
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  http://infoarchive.net/sgroup/biofuel/
 
 
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  http://infoarchive.net/sgroup/biofuel/
 
 
 
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Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]

2005-03-31 Thread Jan Warnqvist

Hello DB.
Quoting :Trans esterifying triglyceride oils and fats with
monohydric alcohols to form biodiesel largely eliminates the tendency of the
oils and fats to polymerization and auto-oxidation.. I can add that this is
the exact scenario with methyl ester from fish oil and linseed oil.
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: DB [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Thursday, March 31, 2005 9:16 AM
Subject: Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]


 Anyone making bio-diesel should be concerned with the IV of the oil and
the
 polymerzation of the engine. After a careful reading of the australian
 report WVO as a Diesel replacement fuel it is obvious that they are
 concerned with it's use as straight veggy oil and Not  so much
 Bio-diesel.( I would be concerned too) Here is a direct quote from that
 report.  Trans esterifying triglyceride oils and fats with
 monohydric alcohols to form biodiesel largly eliminates the tendency of
the
 oils and fats to polymerization and auto-oxidation.. The base crop for
 european biodiesel being rapeseed with a IV of 98 is a reasonable goal to
 acheve. Most of my stock is soy oil and much of it is hydrogenated. I also
 get cottonseed and peanut oil along with canola (rapeseed) I no longer use
 straight soy oil and try to make a blend. In the past when I only had soy
 oil based biodiesel I would only run BD50. I an no longer worried about
the
 IV of the oil and if you are then just run BD50.Drive down the
road
 Happy...DB ..PS. I have been making biodiesel
 since '02 and have made 1000's of gallons with zero problems.
 - Original Message - 
 From: TLC Orchids and Such [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]
 Sent: Wednesday, March 30, 2005 4:37 PM
 Subject: Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]


  Where can we get the veg-based motor oil?
  Can better oil filtering help with this problem?
  Racor has a motor oil filter used in race cars.
 
  - Original Message - 
  From: stephan torak [EMAIL PROTECTED]
  To: [EMAIL PROTECTED]; stephan torak [EMAIL PROTECTED]
  Sent: Wednesday, March 30, 2005 5:45 PM
  Subject: Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]
 
 
  Thanks for the follow up, Keith.
  I have since spent many hours researching the issue and have found some
  relevant facts here:
 
 
www.blt.bmlf.gv.at/vero/veroeff/0100_Technical_performance_of_methyl_esthers
  _e.pdf
  #www.blt.bmlf.gv.atveroveroeff0100_Tec
  Keith Addison wrote:
 
   Hello Stephan, Jan and all
  
   I asked Elsbett's Alexander Noack for some comment on what he was
   quoted as saying about soy oil, and got a very brief response from
him:
  
   Hi Keith,
  
   this all is nearly correct, but only for direct injection engines.
  
   Mit freundlichen Gr٤en / Best regards
  
   Alexander Noack
   ELSBETT Technologie GmbH
   Weissenburger Stra§e 15
   D-91177 Thalmaessing
   Internet: www.elsbett.com
   e-mail:  [EMAIL PROTECTED]
   phone:  +49 (0)9173 77940
   Fax:  +49 (0)9173 77942
  
  
   This was the quote in question:
  
   Soybean oil is bad. Whether it is straight vegetable oil or soybean
   based biodiesel. It is a no-go in diesel engines. Why? In diesel
   engines you have slight mixing between fuel and lubricating oil.
   There is a fuel property in soybean oil that makes it reactive when
   in contact with engine lubricating oil. It supposedly has a
   polymerizing action with the engine oil, which is detrimental to the
   life of your lubricating system.
  
   What they do in Europe is use a vegetable-based lubricating oil for
   the engine to prevent any problems with fuel-lubricating oil
   intimacy. What else? They do not use soybean oil; They use rape seed
   also known as canola.
  
  
   Best wishes
  
   Keith
  
  
  
   Hello Jan
  
   Hello Stephan.
   The reason for Elsbett«s people (and several others) for rejecting
   soy bean
   oil is its high iodine number. As the case with fish oil, corn oil
   and
   several kinds of sunflower oil. A high iodine number is indicating
   that the
   oil may be chemically unstable due to its unsaturation level and
   therefore
   unsuitable as engine fuel both as SVO and BD.
  
  
   In other words, it polymerises - to quote Phillip Calais: Drying
   results from the double bonds (and sometimes triple bonds) in the
   unsaturated oil molecules being broken by atmospheric oxygen and
   being converted to peroxides. Cross-linking at this site can then
   occur and the oil irreversibly polymerises into a plastic-like
solid.
   -- From Waste Vegetable Oil as a Diesel Replacement Fuel by
Phillip
   Calais, Environmental Science, Murdoch University, Perth, Australia,
   and A.R. (Tony) Clark, Western Australian Renewable Fuels
Association
   Inc.
   http://www.shortcircuit.com.au/warfa/paper/paper.htm
  
   See:
   Iodine Values
   http

Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]

2005-03-31 Thread Jan Warnqvist

Hello DB.
Quoting :Trans esterifying triglyceride oils and fats with
monohydric alcohols to form biodiesel largely eliminates the tendency of the
oils and fats to polymerization and auto-oxidation.. I can add that this is
the exact scenario with methyl ester from fish oil and linseed oil.
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: DB [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Thursday, March 31, 2005 9:16 AM
Subject: Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]


 Anyone making bio-diesel should be concerned with the IV of the oil and
the
 polymerzation of the engine. After a careful reading of the australian
 report WVO as a Diesel replacement fuel it is obvious that they are
 concerned with it's use as straight veggy oil and Not  so much
 Bio-diesel.( I would be concerned too) Here is a direct quote from that
 report.  Trans esterifying triglyceride oils and fats with
 monohydric alcohols to form biodiesel largly eliminates the tendency of
the
 oils and fats to polymerization and auto-oxidation.. The base crop for
 european biodiesel being rapeseed with a IV of 98 is a reasonable goal to
 acheve. Most of my stock is soy oil and much of it is hydrogenated. I also
 get cottonseed and peanut oil along with canola (rapeseed) I no longer use
 straight soy oil and try to make a blend. In the past when I only had soy
 oil based biodiesel I would only run BD50. I an no longer worried about
the
 IV of the oil and if you are then just run BD50.Drive down the
road
 Happy...DB ..PS. I have been making biodiesel
 since '02 and have made 1000's of gallons with zero problems.
 - Original Message - 
 From: TLC Orchids and Such [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]
 Sent: Wednesday, March 30, 2005 4:37 PM
 Subject: Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]


  Where can we get the veg-based motor oil?
  Can better oil filtering help with this problem?
  Racor has a motor oil filter used in race cars.
 
  - Original Message - 
  From: stephan torak [EMAIL PROTECTED]
  To: [EMAIL PROTECTED]; stephan torak [EMAIL PROTECTED]
  Sent: Wednesday, March 30, 2005 5:45 PM
  Subject: Re: [Biofuel] Re: soybeanoil a bad choice for BD making?]
 
 
  Thanks for the follow up, Keith.
  I have since spent many hours researching the issue and have found some
  relevant facts here:
 
 
www.blt.bmlf.gv.at/vero/veroeff/0100_Technical_performance_of_methyl_esthers
  _e.pdf
  #www.blt.bmlf.gv.atveroveroeff0100_Tec
  Keith Addison wrote:
 
   Hello Stephan, Jan and all
  
   I asked Elsbett's Alexander Noack for some comment on what he was
   quoted as saying about soy oil, and got a very brief response from
him:
  
   Hi Keith,
  
   this all is nearly correct, but only for direct injection engines.
  
   Mit freundlichen Gr٤en / Best regards
  
   Alexander Noack
   ELSBETT Technologie GmbH
   Weissenburger Stra§e 15
   D-91177 Thalmaessing
   Internet: www.elsbett.com
   e-mail:  [EMAIL PROTECTED]
   phone:  +49 (0)9173 77940
   Fax:  +49 (0)9173 77942
  
  
   This was the quote in question:
  
   Soybean oil is bad. Whether it is straight vegetable oil or soybean
   based biodiesel. It is a no-go in diesel engines. Why? In diesel
   engines you have slight mixing between fuel and lubricating oil.
   There is a fuel property in soybean oil that makes it reactive when
   in contact with engine lubricating oil. It supposedly has a
   polymerizing action with the engine oil, which is detrimental to the
   life of your lubricating system.
  
   What they do in Europe is use a vegetable-based lubricating oil for
   the engine to prevent any problems with fuel-lubricating oil
   intimacy. What else? They do not use soybean oil; They use rape seed
   also known as canola.
  
  
   Best wishes
  
   Keith
  
  
  
   Hello Jan
  
   Hello Stephan.
   The reason for Elsbett«s people (and several others) for rejecting
   soy bean
   oil is its high iodine number. As the case with fish oil, corn oil
   and
   several kinds of sunflower oil. A high iodine number is indicating
   that the
   oil may be chemically unstable due to its unsaturation level and
   therefore
   unsuitable as engine fuel both as SVO and BD.
  
  
   In other words, it polymerises - to quote Phillip Calais: Drying
   results from the double bonds (and sometimes triple bonds) in the
   unsaturated oil molecules being broken by atmospheric oxygen and
   being converted to peroxides. Cross-linking at this site can then
   occur and the oil irreversibly polymerises into a plastic-like
solid.
   -- From Waste Vegetable Oil as a Diesel Replacement Fuel by
Phillip
   Calais, Environmental Science, Murdoch University, Perth, Australia,
   and A.R. (Tony) Clark, Western Australian Renewable Fuels
Association
   Inc.
   http://www.shortcircuit.com.au/warfa/paper/paper.htm
  
   See:
   Iodine Values
   http

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