[biofuel] efficiency issue

2002-05-25 Thread Christian

Now that I«ve attained my first objective: effectiveness, I«m moving into the 
efficiency field. At least, I«m trying. My first goal was to make BD, and now 
I«ve become more or less familiarized with the process, so I«m checking out 
ways in which to reduce costs (moneywise and environment wise).

FINDINGS: 
You can use 96¼ Ethanol!

WHY:
Well, methanol is usually cheap, but unattainable at home. Ethanol instead can 
be produced from fermentation and fractional distillation. 96¼ EtOH is hard to 
get to at home (you need a good still), but there are others more experienced 
in that field on the group. 

I used 25% of 96¼ alcohol, and 75% of methanol to make up the ammount I needed 
to transesterify the WVO (i.e., 100 ml WVO, 50 ml EtOH  100 ml MeOH). The lye 
I added freely: I didn«t weigh it (I did this simply because I was testing and 
I sort of trained my eye to the 0,5 g I needed, but this is not recommended). 
The rest of the process was same as always.

The result was one of the clearest batches of BD after the first setting stage. 
I figured that if 96¼ Ethanol was mixed in adecuate proportions with a more 
pure alcohol, as methanol (mine was near 98.8%), the final ammount of water 
would still be low.

In my case: 96% x 0,25 + 98.8% x 0.75 = 98.1%

From what I«ve gathered, less than 2% water usually works OK.

If you can make your ethanol by fermenting free stuff like backyard grapes or 
something, then you could reduce the ammount of methanol required (the first is 
free, the latter you pay for). Anyhow, maybe the effort doesen«t pay off, but 
it«s worth a go.

Regards,

Christian


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[biofuel] water

2002-06-07 Thread Christian

Hi all.

I ran some lab tests on my BD (from M. Pelly«s recipe), including IR 
spectrometry, Flash point, Pour point, Cloud point, Density, Viscosity, 
Residual Carbon and free water  sediment.

My findings showed quite a good BD, except for the water.

ASTM requires 0,05 % vol max of water. I bubble washed my BD, following the 
Univ. of Idaho«s method, and it seems that my level of fre water whent up to a 
value of roughly 0.2% (4 times more than required by ASTM).

I will further treat the BD with anhydrous CaCl2 (calcium chloride), though the 
lab technician also suggested I should use a saturated solution of sodium 
chloride (tablesalt... i.e., brine) to wash the BD. He said that this would 
reduce the presence of water in the washed BD.

The point is: take care with the bubble washes and water washes in general. 
Maybe I was just unlucky, but you should try to check the content of water in 
your BD as the presence of it could be harmful to the motor. I«ve heard some 
people use pure methanol directly to get a BD pure enough to use without 
washing... (I don«t know how good this might be). My BD was very transparent. 
Even more crystaline than diesel fuel bought from my near by gas station.

Comments welcome.

Regards,

Christian


[Non-text portions of this message have been removed]


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Re: [biofuel] water

2002-06-08 Thread Christian

Dear Ken,

I«m not quite sure if I can answer the first question. You should always use
as little lye as necessary to neutralize FFA, plus a little extra to
transesterify the WVO. And the Methanol is calculated by stoichiometry. But
all this falls down in practice, «cause it«s an equilibrium reaction, and
maybe the little extra lye will take ages to transesterify all the WVO,
and maybe the exact ammount of methanol will impede completion of the
reaction.

I can say I«ve heard of people using pure methanol, and then using the BD
straight after settling.

The washing is used to get rid of varius impurities. I somewhere read that
in the fresh BD, half of the methanol is in the BD phase and half of it in
the glycerine. There«s also soaps and sodium ions (and other stuff), which
all usually are carried away by the water. I still think the washing stage
might be imperative. I just don«t quite understand how nobody has come up
with this issue before. I mean, water could cause rusting and other problems
in the motor, and everyone seems to have no trouble with this. Is it simply
than noebody on the list (actually using their BD) has ever measured it«s
water content? The ASTM standard set the limit at 500 ppm fore some reason!

This is just some more thinking. I«m aware this does not quite answer your
question, but I really don«t have a clue. I know as much as you do on this
subject.

Best wishes,

Christian


- Original Message -
From: Ken [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, June 08, 2002 6:04 AM
Subject: Re: [biofuel] water


Christian,

Is there a way to calculate how much catalyst would be needed for how much
a reaction time.  The reason for washing is to get rid of the catalyst in
the newly reacted BD and lower the ph right?  so if we can use lesser
catalyst then washing might not be necessary.  As for the excess
methanol/ethanol, airing it for some time takes care of that.

Regards,
Ken


At 12:05 AM 6/8/02 -0300, you wrote:
Hi all.

I ran some lab tests on my BD (from M. Pelly«s recipe), including IR
spectrometry, Flash point, Pour point, Cloud point, Density, Viscosity,
Residual Carbon and free water  sediment.

My findings showed quite a good BD, except for the water.

ASTM requires 0,05 % vol max of water. I bubble washed my BD, following
the Univ. of Idaho«s method, and it seems that my level of fre water whent
up to a value of roughly 0.2% (4 times more than required by ASTM).

I will further treat the BD with anhydrous CaCl2 (calcium chloride),
though the lab technician also suggested I should use a saturated solution
of sodium chloride (tablesalt... i.e., brine) to wash the BD. He said that
this would reduce the presence of water in the washed BD.

The point is: take care with the bubble washes and water washes in
general. Maybe I was just unlucky, but you should try to check the content
of water in your BD as the presence of it could be harmful to the motor.
I«ve heard some people use pure methanol directly to get a BD pure enough
to use without washing... (I don«t know how good this might be). My BD was
very transparent. Even more crystaline than diesel fuel bought from my near
by gas station.

Comments welcome.

Regards,

Christian


[Non-text portions of this message have been removed]


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Re: [biofuel] water

2002-06-08 Thread Christian

Hi Keith,

I«m answering this letter separate from Ken«s answer.
Regarding I'm really not sure at  this stage whether that's good advice or
not though., my intention is not to freak everyone out. I simply wouldn«t
want anybody to ruin a 2,5lt Grand Cherokee motor by fooling around.

Water, as you«ve mentioned, can bring some benefits in combustion, and often
in chimeneys in industries (for example, when burning hydrocarbons) steam is
injected into the flame area to produce a cleaner combustion. I don«t quite
understand how, but it supposedly does.

In a motor, excess water is said to be a probable cause of rust, and
water-traps do exist in diesel engines for some reason. I«m not quite
familiar wth the related problems, and I«ve found Camillo Holecek«s quote
most interesting. I«ll try to dig into the subject a bit more.

LAB RESULTS were as followed:

Flash Point: Above 118¼C (ASTM PS121 specifies higher than 100¼C, so I
didn«t go much further)
Kinematic Viscosity @ 40¼C: 3.654 cSt
Density: 0.8797 g/cm3
Corrosion: (heating to 100¼C over half an hour with inmersed metal strips)
Aluminum Strip: Slight change in opacity, barely noticeable.
Copper strip: No observed change
Tin strip: No observed change
Iron strip: No observed change
Cloud Point: 9¼C to 10¼C
Pour Point: -4.7¼C
Carbon Residue: 0.0711% (ASTM D189)
Water  Sediment: 1000-2000 ppm

IR Spectrometry: I sent it in attached to [EMAIL PROTECTED]

Best wishes,

Christian

- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, June 08, 2002 7:00 AM
Subject: Re: [biofuel] water


 Hi Christian

 Well, it's interesting. Do those maximums for water content in the
 standards make any sense? Will water in the fuel damage the engine?

 First, this is what Camillo Holecek said about it recently:

 The Austrian Standard ONORM C 1191 said only: No water should
 settle out (i.e. about 1200ppm water would stay in solution in our
 FAME.) All others bother about 500 and even 300 ppm (DIN), which is
 nonsense IMO, as FAME is hygroscopic and will attract humidity from
 air until it is back to 1200ppm. Means, in your car you will have
 anything but 300ppm. (FAME being Fatty Acid Methyl Esters, ie
 biodiesel.)

 Meanwhile quite a lot of people are trying to figure ways of getting
 MORE water into the fuel. See this, for instance:
 http://archive.nnytech.net/index.php?view=835list=BIOFUELS-BIZ

 Also this:
 http://www.epa.gov/otaq/models/analysis/emulsion/emulbibl.pdf

 And this:
 http://www.aquamist.co.uk/dc/reference/refer.html

 There seem to be combustion efficiency gains (with misters into the
 air intake) and emissions reductions (with fuel emulsions), but I
 can't figure which is better and why you wouldn't get both effects
 either way. What's the difference between a water mist injected with
 the air vs water in the fuel that gets misted anyway when it's
 injected with the rest of the fuel?

 Anway, until we settle it one way or the other, if ever, maybe don't
 worry too much about a little excess water. I'm really not sure at
 this stage whether that's good advice or not though. What d you think?

 Christian, what were your lab results, if you don't mind telling us?

 Regards

 Keith




 Hi all.
 
 I ran some lab tests on my BD (from M. Pelly«s recipe), including IR
 spectrometry, Flash point, Pour point, Cloud point, Density,
 Viscosity, Residual Carbon and free water  sediment.
 
 My findings showed quite a good BD, except for the water.
 
 ASTM requires 0,05 % vol max of water. I bubble washed my BD,
 following the Univ. of Idaho«s method, and it seems that my level of
 fre water whent up to a value of roughly 0.2% (4 times more than
 required by ASTM).
 
 I will further treat the BD with anhydrous CaCl2 (calcium chloride),
 though the lab technician also suggested I should use a saturated
 solution of sodium chloride (tablesalt... i.e., brine) to wash the
 BD. He said that this would reduce the presence of water in the
 washed BD.
 
 The point is: take care with the bubble washes and water washes in
 general. Maybe I was just unlucky, but you should try to check the
 content of water in your BD as the presence of it could be harmful
 to the motor. I«ve heard some people use pure methanol directly to
 get a BD pure enough to use without washing... (I don«t know how
 good this might be). My BD was very transparent. Even more
 crystaline than diesel fuel bought from my near by gas station.
 
 Comments welcome.
 
 Regards,
 
 Christian


 Biofuel at Journey to Forever:
 http://journeytoforever.org/biofuel.html

 Biofuels list archives:
 http://archive.nnytech.net/

 Please do NOT send quot;unsubscribequot; messages to the list address.
 To unsubscribe, send an email to:
 [EMAIL PROTECTED]

 Your use of Yahoo! Groups is subject to http://docs.yahoo.com/info/terms/




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mensaje enviado desde http://www.iespana.es

Re: [biofuel] water (Keith)

2002-06-09 Thread Christian

Dear Keith,

I«d find it very interesting (so as to update my thesis), to get the
specifications of ASTM«s new D6751.

Please let me know if you have them, and if so, please pass them on. They«d
really come in handy.

Best wishes,

Christian

- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, June 09, 2002 8:42 AM
Subject: Re: [biofuel] water


 Hi Christian

 Hi Keith,
 
 I«m answering this letter separate from Ken«s answer.
 Regarding I'm really not sure at  this stage whether that's good advice
or
 not though., my intention is not to freak everyone out.

 Oh, I meant my advice might not be good, not yours.

 I simply wouldn«t
 want anybody to ruin a 2,5lt Grand Cherokee motor by fooling around.

 No, nor any motor.

 Water, as you«ve mentioned, can bring some benefits in combustion, and
often
 in chimeneys in industries (for example, when burning hydrocarbons) steam
is
 injected into the flame area to produce a cleaner combustion. I don«t
quite
 understand how, but it supposedly does.
 
 In a motor, excess water is said to be a probable cause of rust, and
 water-traps do exist in diesel engines for some reason.

 Free water in dinodiesel is one thing, an emulsified water-dino blend
 seems to be another, and dissolved water in biod should be more like
 the blend (with its advantages). At least I think so. More in my
 other message on this.

 I«m not quite
 familiar wth the related problems, and I«ve found Camillo Holecek«s quote
 most interesting. I«ll try to dig into the subject a bit more.

 Why not ask Camillo? He's head of Energea in Austria. Here's his address:
 Camillo Holecek [EMAIL PROTECTED]

 LAB RESULTS were as followed:
 
 Flash Point: Above 118¼C (ASTM PS121 specifies higher than 100¼C, so I
 didn«t go much further)

 The new ASTM D-6751 standard specifies 130 deg C, I don't know why.
 Germany and Czech specify 110, all others 100. Maybe it's all just
 politics, the rapeseed vs soy game.

 Kinematic Viscosity @ 40¼C: 3.654 cSt
 Density: 0.8797 g/cm3
 Corrosion: (heating to 100¼C over half an hour with inmersed metal
strips)
 Aluminum Strip: Slight change in opacity, barely noticeable.
 Copper strip: No observed change
 Tin strip: No observed change
 Iron strip: No observed change
 Cloud Point: 9¼C to 10¼C
 Pour Point: -4.7¼C
 Carbon Residue: 0.0711% (ASTM D189)
 Water  Sediment: 1000-2000 ppm

 Cloud point and pour point a bit high, everything else is just fine.
 And the water probably fits in with what Camillo says.

 Well done Christian. It's great we can make good fuel like this eh?
 No need to be Exxon-Mobil!

 IR Spectrometry: I sent it in attached to [EMAIL PROTECTED]

 Thankyou, received.

 All best

 Keith

 Best wishes,
 
 Christian
 
 - Original Message -
 From: Keith Addison [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Saturday, June 08, 2002 7:00 AM
 Subject: Re: [biofuel] water
 
 
   Hi Christian
  
   Well, it's interesting. Do those maximums for water content in the
   standards make any sense? Will water in the fuel damage the engine?
  
   First, this is what Camillo Holecek said about it recently:
  
   The Austrian Standard ONORM C 1191 said only: No water should
   settle out (i.e. about 1200ppm water would stay in solution in our
   FAME.) All others bother about 500 and even 300 ppm (DIN), which is
   nonsense IMO, as FAME is hygroscopic and will attract humidity from
   air until it is back to 1200ppm. Means, in your car you will have
   anything but 300ppm. (FAME being Fatty Acid Methyl Esters, ie
   biodiesel.)
  
   Meanwhile quite a lot of people are trying to figure ways of getting
   MORE water into the fuel. See this, for instance:
   http://archive.nnytech.net/index.php?view=835list=BIOFUELS-BIZ
  
   Also this:
   http://www.epa.gov/otaq/models/analysis/emulsion/emulbibl.pdf
  
   And this:
   http://www.aquamist.co.uk/dc/reference/refer.html
  
   There seem to be combustion efficiency gains (with misters into the
   air intake) and emissions reductions (with fuel emulsions), but I
   can't figure which is better and why you wouldn't get both effects
   either way. What's the difference between a water mist injected with
   the air vs water in the fuel that gets misted anyway when it's
   injected with the rest of the fuel?
  
   Anway, until we settle it one way or the other, if ever, maybe don't
   worry too much about a little excess water. I'm really not sure at
   this stage whether that's good advice or not though. What d you think?
  
   Christian, what were your lab results, if you don't mind telling us?
  
   Regards
  
   Keith
  
  
  
  
   Hi all.
   
   I ran some lab tests on my BD (from M. Pelly«s recipe), including IR
   spectrometry, Flash point, Pour point, Cloud point, Density,
   Viscosity, Residual Carbon and free water  sediment.
   
   My findings showed quite a good BD, except for the water.
   
   ASTM requires 0,05 % vol max of water. I

Re: ASTM Flash point was Re: [biofuel] water (Keith)

2002-06-09 Thread Christian

Todd,

I«ve just asked Keith, but I just as well might ask you.

Could you send me the BD specs as per ASTM D6751?

I«m still working with PS121 (which I have), but it seems some values have
been revised.

Thanks,

Christian

- Original Message -
From: Appal Energy [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, June 09, 2002 1:54 PM
Subject: ASTM Flash point was Re: [biofuel] water (Keith)


  Flash Point: Above 118¼C (ASTM PS121 specifies higher than
 100¼C, so I
  didn«t go much further)
 
  The new ASTM D-6751 standard specifies 130 deg C, I don't know
 why.
  Germany and Czech specify 110, all others 100. Maybe it's all
 just
  politics, the rapeseed vs soy game.

 Christian and Keith,

 As per ASTM D-6751, paragraph X1.21:

 The flash point for biodiesel is used as the mechanism to limit
 the level of unreacted alcohol remaining in the finished fuel.

 As per ASTM D-6751, paragraph X1.22:

 The flash point specification for biodiesel is also of
 importance in connection with legal requirements and safety
 precautions involved in fuel handling and storage, and is
 normally specified to meet insurance and fire regulations.

 Paragraph X1.23 discusses wide variability with the accepted test
 method. This resulted in 130*C being chosen to insure that a low
 end flash point of 100*C is never compromised. Improvements to
 testing are being evaluated, which could result in a revised
 standard at some point in the future.

 Todd Swearingen


 Biofuel at Journey to Forever:
 http://journeytoforever.org/biofuel.html

 Biofuels list archives:
 http://archive.nnytech.net/

 Please do NOT send quot;unsubscribequot; messages to the list address.
 To unsubscribe, send an email to:
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[biofuel] Re: (Todd)

2002-06-09 Thread Christian

Thanks Todd.

I assume all other values the same as PS121?

i.e., Sulfur, copper stri corrosion, cloud point, carbon residue, carbon
residue (Ramsbottom), Acid nœmber  Free glycerin.

One question: I tested my carbon residue (closed cup) and it added up to
0,0711% (as opposed to 0,05 specified by ASTM). How critical is this, and
where does this residue come from?

Thanks again,

Christian

- Original Message -
To: biofuel@yahoogroups.com
Sent: Sunday, June 09, 2002 2:21 PM


 X-MimeOLE: Produced By Microsoft MimeOLE V5.00.2615.200
 From: Appal Energy [EMAIL PROTECTED]
 X-Yahoo-Profile: appalenergy
 MIME-Version: 1.0
 Mailing-List: list biofuel@yahoogroups.com; contact
[EMAIL PROTECTED]
 Delivered-To: mailing list biofuel@yahoogroups.com
 Precedence: bulk
 List-Unsubscribe: mailto:[EMAIL PROTECTED]
 Date: Sun, 9 Jun 2002 13:18:07 -0400
 Subject: Re: ASTM Flash point was Re: [biofuel] water (Keith)
 Reply-To: biofuel@yahoogroups.com
 Content-Type: text/plain; charset=ISO-8859-1
 Content-Transfer-Encoding: 8bit

 Christian,

 Here are the specs.

 Flash point (closed cup):  130*C minimum (150*C average)
 Water and sediment:  0.050 % by volume, maximum
 Kinematic viscosity at 40*C:  1.9 - 6.0 mm2/s
 Sulfated ash:  0.020 % by mass, maximum
 Sulfur:  0.05 % by mass, maximum
 Cetane:  47 minimum
 Carbon residue:  0.050 % by mass, maximum
 Total glycerine (free glycerine and unconverted glycerides
 combined):  0.240 % by mass, maximum
 Phosphorous content:  0.001 % by mass, maximum



 - Original Message -
 From: Christian [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Sunday, June 09, 2002 1:04 PM
 Subject: Re: ASTM Flash point was Re: [biofuel] water (Keith)


 Todd,

 I«ve just asked Keith, but I just as well might ask you.

 Could you send me the BD specs as per ASTM D6751?

 I«m still working with PS121 (which I have), but it seems some
 values have
 been revised.

 Thanks,

 Christian

 - Original Message -
 From: Appal Energy [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Sunday, June 09, 2002 1:54 PM
 Subject: ASTM Flash point was Re: [biofuel] water (Keith)


   Flash Point: Above 118¼C (ASTM PS121 specifies higher than
  100¼C, so I
   didn«t go much further)
  
   The new ASTM D-6751 standard specifies 130 deg C, I don't
 know
  why.
   Germany and Czech specify 110, all others 100. Maybe it's all
  just
   politics, the rapeseed vs soy game.
 
  Christian and Keith,
 
  As per ASTM D-6751, paragraph X1.21:
 
  The flash point for biodiesel is used as the mechanism to
 limit
  the level of unreacted alcohol remaining in the finished fuel.
 
  As per ASTM D-6751, paragraph X1.22:
 
  The flash point specification for biodiesel is also of
  importance in connection with legal requirements and safety
  precautions involved in fuel handling and storage, and is
  normally specified to meet insurance and fire regulations.
 
  Paragraph X1.23 discusses wide variability with the accepted
 test
  method. This resulted in 130*C being chosen to insure that a
 low
  end flash point of 100*C is never compromised. Improvements to
  testing are being evaluated, which could result in a revised
  standard at some point in the future.
 
  Todd Swearingen
 
 
  Biofuel at Journey to Forever:
  http://journeytoforever.org/biofuel.html
 
  Biofuels list archives:
  http://archive.nnytech.net/
 
  Please do NOT send quot;unsubscribequot; messages to the list
 address.
  To unsubscribe, send an email to:
  [EMAIL PROTECTED]
 
  Your use of Yahoo! Groups is subject to
 http://docs.yahoo.com/info/terms/
 
 


 _
 _
 mensaje enviado desde http://www.iespana.es
 emails (pop)-paginas web (espacio ilimitado)-agenda-favoritos
 (bookmarks)-foros -Chat


 Biofuel at Journey to Forever:
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 address.
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 Service.




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Re: ASTM Flash point was Re: [biofuel] water (Keith)

2002-06-10 Thread Christian

Do you know the year in which ASTM D5761 was issued?

Thx

Chistian

- Original Message -
From: Appal Energy [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, June 09, 2002 1:54 PM
Subject: ASTM Flash point was Re: [biofuel] water (Keith)


  Flash Point: Above 118¼C (ASTM PS121 specifies higher than
 100¼C, so I
  didn«t go much further)
 
  The new ASTM D-6751 standard specifies 130 deg C, I don't know
 why.
  Germany and Czech specify 110, all others 100. Maybe it's all
 just
  politics, the rapeseed vs soy game.

 Christian and Keith,

 As per ASTM D-6751, paragraph X1.21:

 The flash point for biodiesel is used as the mechanism to limit
 the level of unreacted alcohol remaining in the finished fuel.

 As per ASTM D-6751, paragraph X1.22:

 The flash point specification for biodiesel is also of
 importance in connection with legal requirements and safety
 precautions involved in fuel handling and storage, and is
 normally specified to meet insurance and fire regulations.

 Paragraph X1.23 discusses wide variability with the accepted test
 method. This resulted in 130*C being chosen to insure that a low
 end flash point of 100*C is never compromised. Improvements to
 testing are being evaluated, which could result in a revised
 standard at some point in the future.

 Todd Swearingen


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Re: [biofuel] How to make calcium chloride?

2002-06-13 Thread Christian

Something in the corner of MY mind, where my little bit of chem-knoledge
resides, tells me that CaO is not the best stuff to dry esters. Yes: CaO and
HCl will produce water and CaCl2, but in a hydrated form. Probably you could
dehydrate the salt (after filtering and evaporating water), by calcination,
but this is an area I don«t know much of, and at high temperatures (I«m
talking of a closed crucible over direct fire) I don«t know if the substance
would decompose in some way.

Someone mentioned to me the other day (I think I recall having mntioned this
on a post some days ago) that CaCl could interfere with traces of methanol
surely present in the BD.

I«m still working on the water issue, as I«ve personally got some problems
here, with water contents of up to 2000 ppm (0,2 % vol) in my BD. A simple
solution seems to be to filter through very dry filter paper. Dry paper
should absorb water quite well (in my case, it worked well with emulsified
water in the final washing stage, removing the water content that impeded
the BD from being totally tranparent). It could work for dissolved water
too.

Regards,

Christian.


- Original Message -
From: Gobert [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Thursday, June 13, 2002 7:50 PM
Subject: Re: [biofuel] How to make calcium chloride?



 - Original Message -
 From: agroefekta [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Thursday, June 13, 2002 7:56 PM
 Subject: [biofuel] How to make calcium chloride?


  I have read some time before that CaCl2 can be used to dry alcohols
  as well as esters.
  I am not good in chemistry, but believe that reaction of CaO and HCl
  can produce CaCl 2.
  Im my country there are many manufacturers of Cao, so I could make it
  quite easy.
 
  One more question. Can this salt be recovered after it has been used
  for dehidration?
 
 agroefekta,  Calcium chloride for chemical drying is usually used in the
 form of fused pellets. Could take quite a bit of energy to get it to that
 state.
 CaO is a very good drying agent, It could be used by itself to dry
 alcohols but the reaction might be a bit vigorous, would suggest try it in
 small ammounts with caution.
 Something in the back of my mind where my limited chemical knowledge
resides
 tells me that it may not be such a good idea from the safety point of
view.
 Regards,  Paul Gobert.




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[biofuel] gas filter (urgent question... I«ve got little time)

2002-06-29 Thread Christian

Hey everyone... 
I«m trying out my BD today, but I«m still one prefilter short.

Does anyone know if an ordinary gasoline in line filter fill be OK (gasoline  
diesel have different viscosities  molecule size, so I don«t know if this 
might represent some trouble). A combined water trap  filter for diesel costs 
way too much, and anyway the car I«m planning to try the BD on has its own 
diesel filter. 

Is there anyone who thinks unsing the gasoline filter as a diesel prefilter 
will bring any problems?

Thanks,

(Please, I need an urgent answer... I«m leaving in 3 hours)

Christian


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Re: [biofuel] gas filter (urgent question... I«ve got little time)

2002-06-29 Thread Christian

Right. Anyhow, I think I«ll be bypassing the tank. I.e., directly plugging
the hose that goes to the filter and pump into a HDPE container.

Regards,

Christian

- Original Message -
From: steve spence [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, June 29, 2002 12:30 PM
Subject: Re: [biofuel] gas filter (urgent question... I«ve got little time)


 If he's never used BD before, it's solvent abilities may very well clean
the
 gook out of his tank and lines. He does not want to clog his diesel filter
 with that, so a clear inline cheapo filter can be the visual sacrificial
 lamb.


 Steve Spence
 Subscribe to the Renewable Energy Newsletter:
 http://www.webconx.com/subscribe.htm

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 http://www.webconx.dns2go.com/2000/humanpower.htm
 [EMAIL PROTECTED]
 - Original Message -
 From: Appal Energy [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Saturday, June 29, 2002 11:19 AM
 Subject: Re: [biofuel] gas filter (urgent question... I«ve got little
time)


  Christian,
 
  Personally, I'd just use the existing filter system.
 
  I am presuming that you're filtering the fuel through at minimum
  a coffee filter before placing it in the tank or resevoir.
 
  Todd Swearingen
 
  - Original Message -
  From: Christian [EMAIL PROTECTED]
  To: biofuel@yahoogroups.com
  Sent: Saturday, June 29, 2002 11:05 AM
  Subject: [biofuel] gas filter (urgent question... I«ve got little
  time)
 
 
  Hey everyone...
  I«m trying out my BD today, but I«m still one prefilter short.
 
  Does anyone know if an ordinary gasoline in line filter fill be
  OK (gasoline  diesel have different viscosities  molecule size,
  so I don«t know if this might represent some trouble). A combined
  water trap  filter for diesel costs way too much, and anyway the
  car I«m planning to try the BD on has its own diesel filter.
 
  Is there anyone who thinks unsing the gasoline filter as a diesel
  prefilter will bring any problems?
 
  Thanks,
 
  (Please, I need an urgent answer... I«m leaving in 3 hours)
 
  Christian
 
 
  [Non-text portions of this message have been removed]
 
 
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Re: [biofuel] gas filter (urgent question... I«ve got little time)

2002-06-29 Thread Christian

Yes... twice. But I«ve noticed 2 (two) specs floating about. Should I
refilter for the third time?

Regards,

Christian

- Original Message -
From: Appal Energy [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, June 29, 2002 12:19 PM
Subject: Re: [biofuel] gas filter (urgent question... I«ve got little time)


 Christian,

 Personally, I'd just use the existing filter system.

 I am presuming that you're filtering the fuel through at minimum
 a coffee filter before placing it in the tank or resevoir.

 Todd Swearingen

 - Original Message -
 From: Christian [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Saturday, June 29, 2002 11:05 AM
 Subject: [biofuel] gas filter (urgent question... I«ve got little
 time)


 Hey everyone...
 I«m trying out my BD today, but I«m still one prefilter short.

 Does anyone know if an ordinary gasoline in line filter fill be
 OK (gasoline  diesel have different viscosities  molecule size,
 so I don«t know if this might represent some trouble). A combined
 water trap  filter for diesel costs way too much, and anyway the
 car I«m planning to try the BD on has its own diesel filter.

 Is there anyone who thinks unsing the gasoline filter as a diesel
 prefilter will bring any problems?

 Thanks,

 (Please, I need an urgent answer... I«m leaving in 3 hours)

 Christian


 [Non-text portions of this message have been removed]


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[biofuel] IT WORKS!!!

2002-06-30 Thread Christian

I tried my BD on a direct injection diesel 504 Peugeot pickup. We bypassed the 
fuel line from the tank into a HDPE container. After two initial chokes (while 
the remaining fuel in the filter was changing, and maybe a bubble or two of 
air)... the engine started running smoothly. We measured gases with an opacity 
measurer (I think it«s scale is congruent with Bacharach scale). 

BTW, thanks to Todd and Steve for their Urgent replies yesterday. In the end, 
I did not use a prefilter (we where one hose  connector short, so we didn«t 
want excessive cuts in the fuel line).

Regards,

Christian


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Re: [biofuel] No more French fry WVO?

2002-06-30 Thread Christian

I received some ordinary post mail from Mr. Hendrik Stein  G. Knothe
concerning various emission tests by  Prof. Krahl in Germany. They reported
traceo of acrolein and aldehides in emissions.

The issue of acrolein was somewhat treated (in part by me) some weeks ago.

Best wishes,

Christian


- Original Message -
From: Appal Energy [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, June 29, 2002 4:21 PM
Subject: Re: [biofuel] No more French fry WVO?


  http://enn.com/news/wire-stories/2002/06/06252002/ap_47645.asp
  - 6/25/2002
  WHO hosts urgent meeting on acrylamide in food

 Permit me to carry the thought process a wee tad further for us
 common laypersons.

 Anyone ever given much thought to the decay product of glycerin
 under conditions of inadequate combustion? Oddly enough it's call
 acrolein - rather toxic to living things, especially breathing
 things,  at least according to every MSDS sheet I've read.

 So take that decay consideration, slap a bunch of potato shreds
 in a high temp tri-glyceride bath, or bake a grain product with a
 high oil content, and what might you think you'll get? Perhaps
 acrilomide?

 Glycerin, in the form of triglycerides, exposed to semi-high
 temps of frying and baking...~350* Fahrenheit.

 But then there is this statement:

 The Swedish researchers said that fried, oven-baked, and
 deep-fried potato and cereal products may contain high levels of
 acrylamide. The same results were not found in boiled products.

 A bit odd that water boils at 212* Fahrenheit, ~140* lower and a
 considerably less destructive temp range than baking or frying.

 Makes one wonder if there won't be a rush in the appliance and
 food processing markets for products that can cook foods in the
 temperature range of boiling, rather than frying and baking.

 Also makes one wonder if there won't be a rush for oils that are
 100% FFAs, rather than a blend of tri-glycerides and FFAs. That
 would sure throw a kink in biodiesel manufacture when using waste
 restaurant oils. It would force every shadetree biodieseler to
 move towards high pressure esterification, rather than STP
 transesterification.

 It would also put some pressure on the animal feed and rendering
 industries to move away from using reprocessed WVOs as
 protein/energy additives to feed. Would be a shame to kill the
 AKC registered family pet simply by feeding it Puppy Chow.

 Todd Swearingen






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Re: [biofuel] Now that you mention Knothe

2002-06-30 Thread Christian

Keith:

Yep... they«re from the ASAE. Yep. The sent me the whole stuff (I think...
it«s rather long and most interesting... still haven«t gone through all of
it. They seem like various reports)

The authors  work:
Krahl J., Baum K., U. Hackbarth H., Jeberien E., Munack A., SchŸtt C.,
Schršder O., Walter N., BŸnger J., MŸller M. M., Weigel A. - Gaseous
Compounds, Ozone Precursors, Particle Number and Particle Size
Distributions, and Mutagenic Effects Due to Biodiesel - 2001 - ASAE, Vol
44(2): 179-191

(The publications sent to me where different works on the same topic:
emissions ant mutagenesis, and each one is written by combinations of the
names listed above)

Your conspiracy theory might be right. Krahl«s RME showed 760 ppm while
their SME showed 1760 ppm (I think those were the values). Evidently RME
holds less water than SME. And we all know Europe favours the first and USA
favours the latter. Who knows. Anyway I see it practically impossible to
vacuum seal (or at least dry seal) our home made BD production... and my
sunflowerME (over 1000 ppm water) worked OK.

A former teacher of mine is currently studying water injection IN DIESEL
ENGINES with very good results (at the Universidad Tecnol—gica Nacional,
which readily favours research... as opposed to my Univ.). I«ve been trying
to contact him but I can never find him. He«s a mechanical engineer (who
tought me thermodynamics and fluid mechanics a couple of years ago). «t
could be interesting to find out what he knows.

Best wishes,

Christian

- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, June 30, 2002 4:59 PM
Subject: Re: [biofuel] Now that you mention Knothe


 Hi Christian

 Dear Keith,
 
 I was also wondering: In the papers the guys from Germany sent me (the
 guys, with all due respect), they showed walues of dissolved water for
SME
 of about 1250 ppm. My own sunflowerME resulted (as previously discussed)
in
 something between 1000 and 2000 ppm.

 Knothe's an American, by the way, he works for ARS. But I guess you
 know that. Did they send you a full copy of the Bunger, Krahl report?

 WHY ON EARTH does DIN specify 300 ppm and why does ASTM specify 500 ppm
max
 if it seems BIODIESEL WILL SUCK UP WATER (either atmospheric or form the
 washing stages) to reach a water saturation content COMFORTABLY ABOVE the
 ammount specified by ASTM  DIN???

 Maybe it's a protection racket.

 As discussed previously, the Euro standards seem to deliberately
 favour rapeseed biodiesel and exclude soy biodiesel, for no good
 reason other than keeping the US out of the market.

 If you recall, it was Camillo Holecek of Energea in Austria who told
 us about these water standards and said they were all nonsense, that
 it would pick up 1200 ppm anyway. Actually he said they were
 producing biodiesel with only 50 ppm. He also said it wouldn't be
 that way anymore by the time it got into a car's tank. But it's
 easily arranged for it to still be 50 ppm on arrival at a quality
 testing lab. On the other hand, that might not be so easily arranged
 for a backyarder or a small-scale operation. I guess you could get it
 down with heat treatment though - cheat, in other words.

 Maybe I just don't trust the big guys. Well, anybody who still does
 hasn't been paying a lot of attention lately. But could be I'm seeing
 plots where there aren't any. Maybe the standards are just stupid.

 Regards

 Keith


 Regards,
 
 Christian
 
 - Original Message -
 From: Keith Addison [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Sunday, June 30, 2002 2:52 PM
 Subject: Re: [biofuel] No more French fry WVO?
 
 
   I received some ordinary post mail from Mr. Hendrik Stein  G. Knothe
   concerning various emission tests by  Prof. Krahl in Germany. They
 reported
   traceo of acrolein and aldehides in emissions.
   
   The issue of acrolein was somewhat treated (in part by me) some weeks
 ago.
   
   Best wishes,
   
   Christian
  
   That's this one, below, Bunger, Krahl et al. I know that Gerhard
   Knothe cites these results, and there's been some controversy about
   that. The other person who cited Bunger, Krahl et al was a certain
   Associate Professor Jim Olsson of the Department of Physical
   Chemistry at Chalmers University of Technology in Gothenburg, Sweden.
   You can find out more about that in the Files section at the list
   website, in a folder marked Swedish_biodiesel_study - Junk science:
   http://groups.yahoo.com/group/biofuel/files/Swedish_biodiesel_study/
  
   A.k.a. the :frying pan study. Rapeseed oil and biodiesel used as a
   green alternative to conventional vehicle fuels can produce 10 times
   more cancer-causing emissions and pollutants than diesel. These
   findings were reported by Reuters. Olsson's flame reactor burned
   the test samples at only 550 deg C (1022 deg F) at normal atmospheric
   pressure, whereas a diesel engine burns the fuel at up to 2000 deg C
   (3632 deg F

[biofuel] In case you«re interested in my opacimeter results

2002-07-01 Thread Christian

The results from my first BD tests (with an opacimeter) were performed on an 
Indenor xd2 engine (a Peugeot 504 pickup) (4 cyl, 2500 cc), Bosch injector pump 
and direct injection over the cylinder. The analyzer was a Maha mdo2-kienzle 
opacimeter (measures how translucent tha smoke is by mesuring light 
transmission through it). It reads the absorption coefficient k (units: 1/m). 
The result was k=5.6/m for dino diesel and k=1.71/m for biodiesel. Some of our 
laws in Argentina state a maximum of around 2,52 (if memory does not fail me). 

The test is performed by accelerating full throttle to clean the carbon 
residue in the exhaust system, and then accelerating to obtain consistent 
peaks, which constitute the value to be read.

BTW, the scale is not linear, so I can«t say there«s an  XX% reduction of 
emissions by dividing the two obtained values. I have to get an L constant 
(which is the length through which the light is forced to pass... through the 
smoke) to convert k into a linear scale, and I still don«t know this L value. 
But the values so far at least tell me that THAT particular pickup would not 
have passed a municipal test running on diesel, but would have comfortably 
passed it if running on my BD.

Steve: regarding the Was there any doubt? question... well, there«s always a 
quota of fear when the engine that might get goofed up is not yours. Of course, 
in that case you«re assuming the motor could get goofed up with biodiesel. Then 
again, it was my home made first batch. I still can«t believe how long t took 
me to find someone who would be willing to lend his car in the name of science.

That«s all for now.

Regards,

Christian 


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Re: [biofuel] salty water (Todd)

2002-07-02 Thread Christian

Todd,

Just as predicted: The mono-, di-  triglycerids made another yucky emulsion
after washing the crystal clear settled biodiesel. Just to confirm once
again the disadvantages of including water in the reaction. I thought water
only caused soaps. Putting pieces together, now it«s clear that water also
prevent the completion of the reaction (forming soaps consumes sodium
necessary for the transesterification)

Christian
- Original Message -
From: Appal Energy [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Friday, June 28, 2002 1:24 PM
Subject: Re: [biofuel] salty water


 Christian,

 Yup. I'm sure. Been that. Done there... in a 350 gallon batch no
 less. Ten gallons of what couldn't be salted out and didn't break
 on its own over time are still sitting in a jug one year later.

 If you get as high a volume of emulsion as you stated, it's an
 incomplete reaction and the presence of mono- and di-glycerides
 that caused the enormity of it, not the soap, as most of the soap
 drops with the glycerin.

 Try this for starters. Take the fluid whose emulsion was broken
 with the salting out and submit it to another wash. It's a safe
 bet that it will emulsify radically all over again. (You might
 also set aside a bit and submit it to a second transeserification
 to see how much glycerin drops out.)

 If you decant the fluid off the top that didn't emulsify and
 submit it to another wash, that might be a fair indicator as to
 how much of your incomplete reaction (mono- and di-glycerides)
 went into the emulsified layer, but would depend greatly upon the
 level of agitation during the initial wash. The decanted layer
 might emulsify every bit as severely as the original washed
 batch.

 I haven't seen any charts that can predict how heavy an emulsion
 will occur in the presence of x mono- or di-glycerides. But I'm
 sure there are some rules of thumb. A quick look at the back of a
 mayonaise jar or many other food products lends one to believe
 that it takes very little to achieve an extensive result.

 A few percent could be all it takes. That same few percent
 wouldn't even be noticeable in a test for viscosity using
 anything but the most advanced and electronically calibrated
 equipment.

 A good number of persons would argue over this, but I'd say pack
 the viscometer up in it's case and rely upon your wash
 characteristics as indicators of a complete reaction, in absence
 of a GC and or in a backyard environment.

 One other thing, relative to the quality of the salted out fluid.
 I used to point out to our chemist that Hell...diesel engines
 will run on straight veg oil! whenever he pointed out that we
 were still none too sure about the quality of our fuel. Then I
 tried running some of the salted out batch mentioned above.

 Sputter...sputtergasp!!hiss..! wheeze... Pure murder
 for the first 3 minutes on a cold start at 50*F. When the fuel
 was exhausted it was replaced with biodiesel from a less
 troublesome batch. The car turned around and slapped a big wet
 one on us in thanks for treating it better.

 Todd Swearingen

 - Original Message -
 From: Christian [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Friday, June 28, 2002 8:52 AM
 Subject: Re: [biofuel] salty water


 Dear Todd,

 Is that so? The mini batch I experimented on seemed to show a
 good
 conversion. Of course I did not run it through a gas
 chromatograph, but the
 BD seemed OK (not emulsified or mixed with oils and mono-  di-
 glycerids).
 The mixture of EtOH and MeOH I used resulted in 98% alcohol, and
 I suppose
 2% water is just in the limit of acceptance for a
 transesterification
 reaction (don«t know... I assume this out of experience). Anyhow,
 the
 ammount of water I had was too much and everything emulsified in
 a thick
 white foam. But the NaCl and a light rewash with the salty water
 reduced
 everything from the former 20% BD, 70% foam, 10% water to a
 50% BD, 5%
 foam, 45% water... or something like that. and the BD is now
 settling its
 turbidity and taking the typical transparent pale golden colour.
 Viscosity
 seems OK (inidcating absence of glycerides?) Are you sure
 it«s such an
 incomplete reaction?

 Thanks again for your help,

 Christian
 - Original Message -
 From: Appal Energy [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Thursday, June 27, 2002 12:15 AM
 Subject: Re: [biofuel] salty water


  Christian,
 
  I believe the emulsion breaking process you are referring to is
  called salting out in chemistry vernacular.
 
  Unfortunately, it's not biodiesel that you are salting out.
  Rather, it's mono- and di-glycerides from an incomplete
 reaction.
 
  Anytime that you have that much of an emulsion problem, you
 can't
  bet your burrow and its saddle that's the problem.
 
  If you take the salted-out, recovered fuel and run it through
  the transesterification process again, you will find that a
 good
  bit more glycerin drops out.
 
  You will also find

[biofuel] what about tap water

2002-07-02 Thread Christian

Hi all.

Can anybody tell me: Can the washing stages use ordinary tap water or do they 
necessarily require distilled water?

I might try to run a recycling program for used oil in the city. Many 
restaurants sell it at around 15 cents/lt (probably reused as second quelity 
oil for cheap chinese restaurants and other places), but distilled water 
increases costs deamatically if I am to make batches of up to 200 liters and 
plan to use the bubble wash method. 

Does free chlorine in the water bring any problems? 

Buying the used oil already makes things expensive, and the pretended volumes 
of WVO aren«t big enough to reach wholesale prices for methanol (Retail 
methanol costs about 2.5 pesos/lt... imagine it were equivalent to 2.5 
dollars/lt, which it is not.. but as salaries  and cost of living have not 
changed since the 1peso = 1 dollar times last year, you can assume no 
devaluation just to picture the price in terms of % of a salary. If I had saved 
dollars, that would roughly be 60 cents of a dollar per liter). To consider 
myself in business, at least for small scale production (the intention is to 
sell the BD... cheaper than dino diesel of course), I need to be very careful 
with costs, and that includes my source of water.

Regards,

Christian


[Non-text portions of this message have been removed]


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[biofuel] tap water?

2002-07-03 Thread Christian

Hi all.

Can anybody tell me: Can the washing stages use ordinary tap water or do
they necessarily require distilled water?

I might try to run a recycling program for used oil in the city. Many
restaurants sell it at around 15 cents/lt (probably reused as second quelity
oil
 for cheap chinese restaurants and other places), but distilled water
increases costs deamatically if I am to make batches of up to 200 liters and
plan to use the bubble wash method.

Does free chlorine in the water bring any problems?

Buying the used oil already makes things expensive, and the pretended
volumes of WVO aren«t big enough to reach wholesale prices for methanol
(Retail methanol costs about 2.5 pesos/lt... imagine it were equivalent to
2.5 dollars/lt, which it is not.. but as salaries  and cost of living have
not changed since the 1peso = 1 dollar times last year, you can assume no
devaluation just to picture the price in terms of % of a salary. If I had
saved dollars, that would roughly be 60 cents of a dollar per liter). To
consider myself in business, at least for small scale production (the
intention is to sell the BD... cheaper than dino diesel of course), I need
to be very careful with costs, and that includes my source of water.

Regards,

Christian


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Re: [biofuel] tap water?

2002-07-04 Thread Christian

Thanks. That«s good news.

Christian

- Original Message -
From: Aleksander Gontarz [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, July 03, 2002 3:41 PM
Subject: RE: [biofuel] tap water?


 Hi Christian!

 I didn't make much biodiesel yet, but I'm a chemist and I can tell you
that
 tap water is perfect (in relation quality - expenses) for washing
biodiesel.
 We are talking here about sub - massive production (not for laboratory
 scale) so distilled water is unnecesary expense.
 Alex



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Re: [biofuel] Re: tap water? methanol use

2002-07-05 Thread Christian

Nope. The scale is so small that the only way to reuse chemicals would be to
pretreat the WVO with the leftover glycrine+meth. But I still can«t separate
methanol at small scale. Furthemore, I can«t distill glycerin to sell it
(that represents a good income) because at the scale I«m talking of (330
lt/week) I can«t afford a vacuum distiller, evaporators or what have you.

regards,

Christian

- Original Message -
From: coachgeo3 [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Thursday, July 04, 2002 11:26 PM
Subject: [biofuel] Re: tap water? methanol use


--- In [EMAIL PROTECTED], Christian [EMAIL PROTECTED] wrote:
 Hi all.
 SNIP
 Buying the used oil already makes things expensive, and the
pretended
 volumes of WVO aren«t big enough to reach wholesale prices for
methanol
 (Retail methanol costs about 2.5 pesos/lt... imagine it were
equivalent to
 2.5 dollars/lt, which it is not.. SNIP
 If I had
 saved dollars, that would roughly be 60 cents of a dollar per
liter). To
 consider myself in business, at least for small scale production
(the
 intention is to sell the BD... cheaper than dino diesel of course),
I need
 to be very careful with costs, and that includes my source of water.

 Regards,

 Christian


Christian does this cost calculation include reuse of the collectable
methanol?



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Re: [biofuel] Re: tap water?

2002-07-05 Thread Christian

Yes. The idea was to leave empty 10 or 20 lt HDPE plastic containers and
pick them up every week or so, or whenever the guys called.

It«s still quite in the air (the project)... but that was the rough idea.
Ideally, we«d pick up the containers in a bio-fueled pick up or something.

Christian

- Original Message -
From: Aleksander Gontarz [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Friday, July 05, 2002 7:27 PM
Subject: RE: [biofuel] Re: tap water?


 Dear Christian,
 Can you tell me how do you want to plan to pick up used oil from the
 restaurants? Will you, for example, leave there your containers and give
 them your phone number or else? Maybe it's a silly question, but I want to
 rus something simmilar in my town (in the future) so I want to know how to
 do it for the best results. Thanks for all the informations!
 Greetings,
 Alex



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Re: [biofuel] (anhydrous) S.M. and glycerol protonisation, titration,

2002-07-09 Thread Christian
 and after
some minutes it turned back to transparent. But after some more additions,
it whent pink and then returned not to transparent, but to a very light
pink. This was past the correct titration ammount, so I had to redo the
experiment and take the readings for the back to transparent volume of
base.

 3. When doing the reaction I thought to add the S.M. and
 methanol already early when the T is still quite low while heating
 the reactor tank, rather than adding it only if the reaction heat is
 reached. That consideration just to save energy and time. However,
 when the ratio of saponification rate to the transesterification at
 lower T is higher than at higher T it should not be done to avoid too
 much soap formation. Could you give a short statement?


Assuming you have used anhydrous methanol and dry oil, saponification will
occur due to the presence of NaOH and the water from the S.M. formation,
making the glycerides exchange their ast H for a Na (I know that«s not what
you asked). Now anhydrous S.M. would reduce soap formation.
Anyhow, I know people who have considered performing the reaction at room
temp for a longer period. I always thought that the equilibrium reaction
would take forever at that temp. However, this guy is a Chemical engineer,
and I he argued the reaction could be performed at room temp with good
yields. I don«t know if he somehow separated unracted oils and centrifuged
the S.M. to add it again in the mixture, thus retrieveing BD as it formed
(and pushing the reaction towards products side).
However I do not know the saponification  transesterification rates at
different temperatures.




One personal question, if I might:

I was looking for a funded PhD in the renewable energies field. I am a
recenly graduated environmental engineer, and an EEC member (French
passport). Do you know if the MSc for Renewable Energy Systems Technology at
Crest (Loughborough, UK.) is funded for EEC members?

Could you help me finding out the entry requirements, maybe a course program
or at least the email of someone in charge of the addmitance for
environmental MSc  PH.D.s?

I«d really appreciate that.

Best wishes,

Christian




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Re: [biofuel] (anhydrous) S.M. and glycerol protonisation, titration,

2002-07-10 Thread Christian

Thanks. I will contact her.

- Original Message -
From: Andreas Jansen [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, July 10, 2002 5:11 AM
Subject: RE: [biofuel] (anhydrous) S.M. and glycerol protonisation,
titration,


Dear Christian,

well first of all thank you very much for all the information, really good.
To the Crest contact: The person in charge for further questions is :Allison
White: [EMAIL PROTECTED]
she is able to  answer your questions about formal matters. Also a look onto
the website might help:
http://www.lboro.ac.uk/crest/MSC/index.htm
As I know is there no possibility to get it funded, otherwise I would have
tried it, but try it your own, it is perhaps worth.

So far. Much lick and the best.
Regards,
Andreas.
  -Original Message-
  From: William Clark [mailto:[EMAIL PROTECTED]
  Sent: 10 July 2002 01:13
  To: biofuel@yahoogroups.com
  Subject: Re: [biofuel] (anhydrous) S.M. and glycerol protonisation,
titration,


  Her is a  link for MSDS on anhydrous S.M..
  http://www.alkalimetals.com/MSDS/SODIUM%20METHOXIDE%20MSDS.htm Does anyone
  know anything about this substance?

  Bill C.
  - Original Message -
  From: Christian [EMAIL PROTECTED]
  To: biofuel@yahoogroups.com
  Sent: Tuesday, July 09, 2002 11:46 AM
  Subject: Re: [biofuel] (anhydrous) S.M. and glycerol protonisation,
  titration,


   Hi Andreas. I doubt I«ll be able t answer all your questions but I«ll
see
  if
   I can help a bit.
  
  
My name is Andreas Jansen, student for Environmental Management in
The Netherlands, however since a year taking part at the MSc for
Renewable Energy Systems Technology at Crest in Loughborough, UK. My
dissertation started 4 weeks ago and is about the topic biodiesel.
Therefore  I have to optimise a small-scale prototype installation
running on used cooking oil for a company, which is just three years
in business, not having much experience yet, which makes the work and
support for me sometimes rather difficult.
For this I read lot of abstracts, however my chemical background is
not so very strong, still for some understanding sufficient. However
there are some topics where I struggle with and cannot find an answer
to:
   
1. When considering Sodium Hydroxide as catalyst for alkaline
based transesterification I wonder about the following things: A
reaction mechanism tells me, that the methanol and sodium hydroxide
form S.M. and water. S.M. catalyses the transesterification and at
the end the H+-ion from the previous formed water is deprotonated by
the diglyceride-ion (or later mono-glyceride- or even later glycerol-
ion) to form a fully alcohol group and finally glycerol. My concern
is whether this combination of H+-ion and (di)glyceride-ion is
necessary to occur or whether in the glycerol-layer after separation
also (di)glyceride-ions may be found if not all (di)glyceride-ions
have had combined with the H+-ions from the water? A catalyst should
be found back at the end (if not saponified), that is what a catalyst
defines, or? Therefore only glycerol but no (di)glyceride-ions should
be found?
Furthermore, if now assumed that anhydrous S.M. powder as catalyst is
used, would that (under the assumption that H+-ions must react with a
(di)glyceride-ions to form the glycerol) mean, that water must be
deprotonated and if water is initially present in the oil this water
would be removed, thus lowering the saponification reaction between
f.f.a., water and Na+-ions?? That would be quite a benefit to
consider buying S.M. powder instead of producing S.M. self by mixing
Me-OH and NaOH!
   
  
   I was unaware of the fact you could buy dehydrated S.M. This would be a
   great improvement, as it would reduce the ammount of water in the
   transesterification. The term catalyst must be carefully used here. From
   what I recover, the catalyst will be somewhat consumed hence disrupting
  its
   own definition. Even more complex solid catalysts used in complex
  industries
   (as pharmaceutical), often patented salts like Titanium tetraalcoxides
and
   so, will probably serve for 20 or so reactions. The end product may
always
   have rmains of mono-  di- glycerides, as 100% efficiency is not
possible.
  
2. When doing previous the reaction a titration to determine the
degree of f.f.a. I take 1 ml oil and dissolve it in 10 ml iso-
propanol. pH meter and litmus-pH-paper give different results during
titration and the indicator (phenolphthalein) is not behaving like
expected. It first tends only very, very light purple but remains
like this, only if ~0,5 ml more NaOH solution is added (than at a pH
of 10) it is turning totally purple. I thought a indicator colours or
does not but the very light purple colour which stays and does not
disappears after stirring more confuses me a lot?
Concerning

[biofuel] Personal matter/opinion

2002-08-06 Thread Christian

Hi all.

I honestly apologize in advance for using this group for a personal question, 
but I consider all members as friends, and am in desperate need of advice. 
(Sorry Keith...hope you understand)

I«ve received a job proposal for a firm in Virginia, USA, which I must answer 
by tomorrow, and would like to know out of American members« experience how 
much the cost of living would roughly be there (per month... rent, food, some 
leisure, savings) to know if the proposal is reasonable or not. I«m 24 years 
old and single.

Thanks to all in advance for your help.

Christian


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Re: [biofuel] Personal matter/opinion

2002-08-06 Thread Christian

Thanks. However, I«m not comparing, as I currently live in Argentina (and
know nothing about the cost of living in other US cities.)
The proposed salary is about 2300 U$S per month. Do you think that will
cover the living costs?

Thanks again,

Christian

- Original Message -
From: [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Tuesday, August 06, 2002 2:31 PM
Subject: Re: [biofuel] Personal matter/opinion


 Christian, it depends on where you live in Virginia.  In the DC area , for
 example, you will encounter one of the highest housing cost places in the
 U.S.   I suggest you try the URL below:

 Http:://www.bestplaces.net/html/citycompare.asp
 Here you can compare any two cities from a wide variety of choices within
the
 50 states.  This will give you the detailed comparisons such as you appear
to
 be wanting between a city that you know and compare it to a city close by
or
 in the city about which you are wanting to know the costs.

 Good luck.

 Glenn Ellis


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Re: [biofuel] Personal matter/opinion

2002-08-07 Thread Christian

Yep.

thanks!

Christian

- Original Message -
From: Curtis Sakima [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, August 07, 2002 12:30 PM
Subject: Re: [biofuel] Personal matter/opinion


 Our U.S. media seems to indicate that the Argentine
 economy is in a real mess.  If that is true, my
 sympathies go out to you on your country's fanancial
 situation.

 Curtis


 --- Christian [EMAIL PROTECTED] wrote:
 ...as I currently live in Argentina...

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[biofuel] back frm the dead

2002-09-03 Thread Christian

Hi all.

I«ve been away for quite some time, mostly preparing the presentation of my 
thesis (on biodiesel production). Now I«ve passed that and I«m oficcialy an 
Environmental Engineer (actually, the paperwork takes about 6 months).

Well, the news is I«ve updated my webpage and uploaded many biodiesel related 
papers. Amongst other stuff, you«ll be able to find an updated 
photo-description of the biodiesel production process (my first batches), as 
well as a spanish and english version of a 10 page summary of my thesis, 
together with the 156 pages long thesis (in spanish). There are also some 
pictures and personal info as my resume.

Please find the mentioned site at: www.clenoir.com

I hope you enjoy it and find it usefult to keep on spreading the word on 
biofuels. 

I would also like to thank the members of the list who were so important for my 
thesis« publication (Specially Keith, Steve, Todd, Manolo, Dana... and so many 
others!) (you were all included in the aknowledgements)

Needless to say, anyone interested is authorised to publish the work or copy it 
to his/her personal sites provided my personal info is attached and mentioned 
as reference and as the source of the work.

Hope you all like it.

Best,

Christian
[EMAIL PROTECTED]



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[biofuel] 55 degs

2001-11-17 Thread Christian

Hi,

My name is Christian and I«m quite new to this group. I«m currently finishing 
Environmental Engineering and to graduate, I must prepare a sort of thesis 
(actually, it«s not a thesis... it«s more of a thorough project). 

Anyway, I was thinking of preparing biodiesel to run it on the lab«s diesel 
engine (a small boat outboard... not much HP) and eventually test NOx and CO 
emissions.

So the question is, in the two stage process, are the 55 ¼C essential, or can 
the temperature be roughly a bit more. Actually, for my batch low-volume 
process, I was thinking of heating the stew with a closed circuit of water in 
copper pipes or something, heated by a fish-tank water heater and pumped by a 
small aquarium water pump. Does anyone think this is feasible? What are the 
ordinary home methods of heating the mixture at 55 degs for over an hour? 
Does the initial heating of the brew (until it reaches the 55 ¼C) count as time?

Thanx.

Christian


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Turbines [biofuel]

2001-11-29 Thread Christian

Just wondering...

Does anybody know of successful experiences concerning BD in turbines? Mainly 
microturbines for small scale power generation.

Any info is welcome.

Thanx

Christian


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Re: [biofuel] washing machine and biodiesel

2001-11-30 Thread Christian

As an Environmental Engineer, I can«t turn my head on some of the previously
discussed issues, but I must agree with Keith. As backyarders, maybe
industrial-level safety should merely be reduced to good ventilation and
other low-budget precautions. You usually can«t get explosion-proof devices
without sky-rocketing your costs.

The again, I«m still in the theory process, and haven«t yet performed a
batch of BD (hopefully this -southern- summer or fall at the latest). So
please don«t laugh at my suggestions if the practice has shown they are not
feasible.

Regarding the thermostat, just to mention one thing, I had thought of using
a small diameter copper piping inside the reactor. A small fish-tank pump
(hopefully would resist 55 deg) could push the water into the piping from a
separate water container. A fish-tank thermostat would heat the water to 55
deg in this separate water tank. So 55 deg water would flow through the
piping into the container. Please someone tell me if this idea is too obtuse
(I don«t know if copper piping can be used in the reactor)... but still, the
idea is that this can be built away from the reactor, and in the worse of
cases, small explosion-proof boxes can be built to house these electric
devices. That is, any hermetic container can have a couple of holes made to
let the tubing through, and these holes can be  hermetically sealed later.
The rest is just proper ventilation. I«m just thinking out loud, because I
still lack the experience, but I think there are home-made solutions
regarding explosion safety.

There«s not much I can say on VOC«s and all the rest of the environmental
concerns, but most RD must leave these issues aside to be able to get
somewhere. It«s like saying developing countries demand to emit an amount of
CO2 to be able to develop.

Christian.

- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Friday, November 30, 2001 9:20 AM
Subject: Re: [biofuel] washing machine and biodiesel


 Hello David

 M Rolan wrote:
  
   Tell me please on wich pieces should I be carefull
 
 If you're using the methoxide process, do not use equipment that is not
 intrinsically safe for use in potentially explosive atmosheres.
 
 washing machine motors have carbon brushes on a commutator which are very
 efficient spark generators

 But many people use electric motors of some ilk to stir their BD. And
 water pumps, and thermostats, and more. Haven't heard of any
 accidents yet. So what would you suggest? Industrial-level safety
 that would pass the official inspectors' tests? For backyarders?

 Solenoid valves - sealed against explosive methanol vapours?
 water pump - ditto plus pressure
 thermostat - and if it fails?
 static protection - you have none
 
 And so it goes on. None of this addresses the toxicity of methanol nor
the
 environmental implications of waste water, VOC emissions or glycerol
 disposal.

 You're talking about a commercial operation here. We've just been
 discussing the toxicity of methanol, we've just established that the
 environmental implications of waste water are essentially a
 non-issue, we've just agreed that glycerine disposal is also a
 non-issue because it's too useful to dispose of.

 Are you saying we should all go full-scale commercial or give up? I'd
 vouch that many or most of the biodiesellers on this list are as
 aware as or more aware of environmental issues than commercial
 operations (which will comply as much as they have to, because they
 have to, not because they care), and we all insist on full safety
 precautions - but this kind of safety overkill will just price us
 right out of the operation. And it is overkill. And seems to be
 rather contrary to your sig, below.

 Best

 Keith Addison
 Journey to Forever
 Handmade Projects
 Tokyo
 http://journeytoforever.org/


 
 Recycling - not a chore more a way of life
 
 Dave Preskett [EMAIL PROTECTED]
 
 The BioComposites Centre
 University of Wales, Bangor
 Deiniol Road
 Bangor
 Gwynedd
 LL57 2UW
 
 
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[biofuel] [biofuels] Short questions

2001-12-09 Thread Christian

I«m planning on building my first reactor this (southern) summer.
I ran into a place just yesterday, which sold stainless steel thermostats for 
$30, electric heaters (big 15A ones) for about $30, digital thermometers for 
about $30 and glass ones for about $10... all in one same shop. So I was quite 
delighted to find so much useful stuff in one place. And the prices are not 
THAT bad for Argentina. I just have one problem, which is I still haven«t 
figured out if I should heat the BD using heated water in pipes, an electric 
submersible heater or an external electrical heater (to heat the metal tank 
from outside). What are your experiences about that?

I have some questions regarding BF:

.- What should the volume of the tank be if I were to produce 1 lt BD? (roughly)

.- Can I distill methyl alcohol like EtOH? Does it form an azeotrope?

.- Should I change to synthetic hoses if using BD50?

.- What metals can be used freely in the construction of the reactor, other tan 
stainless steel, if any?

.- I made a fractional distillation column at home but it«s made out of 
stainless steel (1 in diameter, 30 cm tall) and glass filling, and the top got 
too cold so I got no alcohol distilled. (I used a batch of water + EtOH to test 
it) Do you think a good insulation around the column is the ONLY key to 
success, or can the packing be too tight or the column too tall? If you blow 
through one end, there«s not much resistance, so I doubt the packing is a 
problem «cause the pressure from the boiler should get the steam through.

.- Are attachments (*.jpg) allowed in the newsgroup? (Sorry, I«m new to this)

I«d very much appreciate some short answers.

Thanx,

Christian



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[biofuel] chemistry

2001-12-28 Thread Christian

Please excuse my chemical terms in english.

I was wondering if you could clear a couple of things I had mixed up:

Greases/oils (are they called fatty acid esters in english?) 
(CH2OCOR-CHOCOR«-CH2OCOR) and methanol (CH3OH) form Glicerol and BD (3 
RCOOR)... right?

Now this reaction needs either an acid or base catalyst (E.g., dry H2SO4 or 
HCl... OR NaOH) (here is where I get mixed up).. but NaOH would react with the 
greases/oils to form glicerol  soap (3RCOONa)... So I assume the Sodium 
methoxide is a more efficient catalyst because it doesen«t form as much soap? 

On the other hand, I traditionally thought sodium methoxide CH3O(-)Na(+) was 
synthesised mainly from dry alcohols and metallic sodium (difficult to find + 
expensive + dangerous).

But from what I gather from all the info in journeytoforever, just mixing 
methanol and NaOH (lye) produces an exothermic reaction which forms sodium 
methoxide. ÀIs this the catalyst or a reactant? If it is a catalyst, is it the 
dissociated (is that how you say it?) sodium from the CH3ONa that reacts with 
the fatty esters (greases/oils) to form the bothersome soap which is so 
important to get rid of in the washing stages?

I know all this sounds a bit too chemical, but if anyone feels comfortable 
enough to speak in these terms, please enlighten me a bit.

Tank you. (+ Happy new year)

Regards,

Christian



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[biofuel] Re: chemistry (Bryan)

2001-12-29 Thread Christian

Thanks Bryan

Best wishes,
Christian.


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Re: [biofuel] chemistry

2001-12-29 Thread Christian

Thanks Keith. Though I must clear out something... I was talking of HCl,
Hydrochloric acid, not Nitric Acid (HNO3), which I do understand is a main
chemical in the synthesis of various explosives (a friend of a close friend
of mine did pass away in a lab explosion some years ago).

The reference to HCl was found in the Morrison  Boyd book on organic
chemistry (I think it`s Prentice, or Mc Graw)

One thing more, somewhere in journeytoforever it said small batches were 
exothermic enough
to maintain the temperature close enough to 55 ¼C. If so, up to what volume
is this true?



Thanks for the advice  concern.

Regards,

Christian


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[biofuel] chemistry water

2001-12-29 Thread Christian

Dear Bryan,

I got a bit mixed up with the water... ÀWhich reaction produces it?

If this is an equilibrium reaction, Àcan«t you turn it towards the products 
side by adding more meth?

Best,

Christian


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Re: [biofuel] chemistry

2001-12-30 Thread Christian

I re-read the article. No doubt about what it says there. I was really
working out of my memory the other day, so it«s probable I mixed up the
facts. Anyway, if I do find something on the exothermic heating, I«ll let
you know.

Again, thanks.

Chirstian

- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, December 30, 2001 2:33 AM
Subject: Re: [biofuel] chemistry


 Thanks Keith. Though I must clear out something... I was talking of HCl,
 Hydrochloric acid, not Nitric Acid (HNO3), which I do understand is a
main
 chemical in the synthesis of various explosives (a friend of a close
friend
 of mine did pass away in a lab explosion some years ago).

 Yep, sorry, 'twas a bit late in the night - please see correction posted
later.

 The reference to HCl was found in the Morrison  Boyd book on organic
 chemistry (I think it`s Prentice, or Mc Graw)

 If you get any positive results with HCl, please let us know.

 One thing more, somewhere in journeytoforever it said small batches
 were exothermic enough
 to maintain the temperature close enough to 55 ¼C. If so, up to what
volume
 is this true?

 I doubt it - you'll have to find the reference please. The exothermic
 reaction's over by the time the methoxide's properly mixed and you
 add it to the oil, I don't see how it could have any effect on
 maintaining the process temp.

 Mike Pelly says this, in discussing Test batches:

 Start by mixing up the lye and methanol in a blender (one that will
 never be used for food again). First make sure the blender and all
 utensils used are dry. Forming the exothermal sodium methoxide polar
 molecule will heat up the blender container a bit. Keep mixing until
 all the lye has been dissolved.

 He certainly doesn't say it provides enough heat for the
 transesterification process itself. Anyway his test batches are with
 one litre of WVO, the methoxide uses only 150 ml of methanol and 6.25
 g NaOH, not very much heat there. I suggest you read it all again.

 http://journeytoforever.org/biodiesel_mike.html
 Biodiesel recipe from Mike Pelly

 Best wishes

 Keith Addison
 Journey to Forever
 Handmade Projects
 Tokyo
 http://journeytoforever.org/


 Thanks for the advice  concern.
 
 Regards,
 
 Christian



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[biofuel] Absolute Alcohol

2001-12-30 Thread Christian

Here is something I«d never try, specially in a motor (unless you want to run 
the risk of clogging it to death), but I found an interesting reference as to 
how to dehydrate alcohol and test it:

The abstract is from Henley«s Twentieth Century FORMULAS Processes  Trade 
Secrets, Books Inc, NY, 1957, by Prof. T O«Conor Sloane, A.B., A.M., E.M., 
Ph.D.. 

Yes, it«s as old as hell, and half the formulas it contains would probably 
considered herecy by E.P.A., but it still is interesting:

Absolute Alcohol.- If gelatine be suspended in ordinary alcohol, it will 
absorb the water, but as it is insoluble in alcohol, that substance will remain 
behibd, and thus nearly absolute alcohol will be obtained without distillation.

As to the methods for testing:

Alcohol, Tests for Absolute.- the comittee for the compilation of the German 
Arzneibuch established the following tests for determination of absolute 
alcohol:
Absolute alcohol is clear, colorless, volatile, readily inflammable liquid 
which burns with a faintly luminous flame. Absolute alcohol has a particular 
odour, a burning taste, and does not affect litmus paper. Boiling point, 78.50. 
Specific gravity, 0.795 to 0.797. One hundred parts contain 99.6 to 99.0 parts, 
by weight, of alcohol.
Absolute alcohol should have no foreign smell and should mix with water without 
cloudiness.
After the admixture of 5 drops of silver-nitrate solution, 10 cubic centimeters 
of absolute alcohol should not become turbid or coloured even on heating.
A mixture of 10 cubic centimetres of absolute alcohol and 0.2 cubic centimeter 
of potash lye evaporated down to 1cubic centimeter should not exhibit an odour 
of fusel oil after supersaturation with dilute sulphuric acid.
Five cubic centimeters of sulphuric acid, carefully covered, in a test tube, 
with a stratum of 5 cubic centimeters of absolute alcohol, should not form a 
rose colored zone at the surface of contact, even on standing for some time.
The red color of a mixture of 10 cubic centimeters of absolute alcohol and 1 
cubic centimeter of potassium-permanganate solution should not pass into yellow 
before 20 minutes.
Absolute alcohol should not be dyed by hydrogen sulphide water or by aqueous 
ammonia.
Five cubic centimeters of absolute alcohol should not leave behind a weighable 
residue after evaporation on water bath.

Be warned, most (if not all) of the chemicals mentioned are dangerous and must 
be handled with care. The methods described come back from 1957, and as others 
in the book, are probably outdated by modern, safer methods. Be careful when 
experimenting.

Personally, I tried the potassium-permanganate test after treating 96% EtOH 
with tasteless jello, and I really can«t tell for sure if it worked, as the 
color was a faint orange (not yellow, not pink or red).

I did smell the so called absolute alcohol and my throat is still stinging 
(30 minutes after).

Finally, I wouldn«t recommend this process, as any water mixed in the EtOH CAN 
form jelly, which at room/low temperatures is almost impossible to clean 
(mild/warm/hot water does the job OK). The point is, any jelly left in the 
alcohol (although if well filtered shouldn«t be present) would cause an awful 
lot of sugar to deposit/clog (and ruin) a motor.

On the other hand, maybe doing things slowly and carefully solves the matter. I 
have no way of testing all this, so feel free to send comments. Thinking out 
loud, possibly the hydrated jelly could be dried and reused (?)... dunno.

Please tell me if anyone has a trust-worthy lab method to test Absolute EtOH 
and has found this method works.

Regards,

Christian


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[biofuel] flammability

2001-12-30 Thread Christian

Could anyone please tell me at what water/alcohol ratio the alcohol stops being 
flammable?

Thanks,

Christian


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[biofuel] metals

2001-12-31 Thread Christian

Does anyone know how bronze and niquel-coates (stainless) steel handle BD? 

Somewhere it mentioned NOT to use copper, but I«d appreciate info on the metals 
ALLOWED in the BD processor.

Thanks in advance,

Christian

(BTW, Thanks Brad 4 your answer to flammability... I missed a couple of 
outgoing thank-yous the other day when trying to post on biofuels yahoogroup 
from my other email account.)


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Re: [biofuel] HCL

2001-12-31 Thread Christian

I don«t know if I understand your question, but I«ll give it a go.

HCl may be prepared by direct combination of the elements that form it:  H2
+ X2 -- 2HX
-where X is generic for F, Cl, Br, I (Fluorine, Chlorine, Bromine, Iodine)-

The reaction with F2 to produce HF is explosive and very dangerous. The
reaction with Cl2 does not occur completely in darkness, but performs
quickly in a chain photochemical reaction under light. The luminous energy
is absorbed by the Cl2 molecules which decompose into chlorine radicals
(very reactive atoms with un-paired electrons). These attack the H2
molecules and produce HCl molecules, leaving hydrogen atoms (also radicals)
. The hydrogen radicals also attack Cl2 molecules to form HCl molecules and
chlorine radicals, and so on and so forth. HCl is a colourless gas, melting
point: -114.8 ¡C, Boiling point -84.9 ¡C

A SAFER way of preparing HCl is by the reaction of a metallic chlorine
compound, as NaCl (ordinary table salt) with a non volatile acid
(concentrated H2SO4 or H3PO4)

The formed HCl then bubbles out of the resulting solution.

NaCl (s) + H2SO4 (aq) -- NaHSO4 (s) + HCl (g)

Other reactions, like hydrolysis, that produce HCl:
BCl3 + 3H2O -- H3BO3 + 3HCl
SiCl4 + 2H2O -- SiO2 + 4HCl

CONCLUSION:
So, for small scale production, the best option would be NaCl and sulphuric
acid. How to get sulphuric acid?... well, I do it by making electrolysis out
of a copper sulphate solution (this is a widely available salt). I built my
own electrolysis tub with a couple of the carbon rods inside ordinary 1.5
volt batteries (AA).

The drawback of all this is that HCl is a GAS, so if you want HCl solution,
you«d have to bubble the gas through distilled water, and for wat«s worth
it, you«d be far better off buying ordinary MURIATIC acid (31% HCl in
water).

- Original Message -
From: [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Monday, December 31, 2001 7:23 PM
Subject: [biofuel] HCL


 Can HCL be fomulated on a small scale?


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Re: [biofuel] Solid catalyst,

2002-01-08 Thread Christian

In my humble opinion, the process described seems the counterpart to the
alchemists recipe for turning lead into gold. A process as described would,
as Dana said, revolutionize production.

Count me into the subject, though I don´t know what you´re implying with
this. Sure, when I find some time, I´ll try to look it up. Any hints
regarding a little more detail on the process, or where it came from?...
just so as to get started.

I was currently trying to do some testing with hydrochloric and ethanol..
but my whole first attempt processor project (traditional NaOH  Meth
recipe) is currently quite delayed due to the fact that all imported goods
have gone up by 40% in the past week (due to the currency problems here in
Argentina).

Hope to hear more on the subject

Regards,

Christian


- Original Message -
From: Dana Linscott [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Monday, January 07, 2002 11:30 PM
Subject: Re: [biofuel] Solid catalyst,


 Arne,

 I have not heard any further info on the process you
 describe. Of course this type of continuous process
 biodiesel/glycerin production would REVOLUTIONIZE home
 production of BD if made available. It would also work
 well in conjunction with the inexpensive WVO/SVO
 processing modules I am attempting to design and
 integrate.

 As I stated before even a very expensive catalyst
 module would pay for itself if shared by a group of
 users to maximize its use either by forming a
 cooperative around a shared WVO/SVO/biodiesel
 processor or by shipping the expensive catalyst module
 from one (otherwise inexpensive) home processor to
 another.

 I believe that this deserves more thorough
 investigation. Unfortunately, as you can see from my
 recent posts I already have a rather full plate. If
 there are three or four others that are willing to
 join forces to dig deeper I am more than willing to
 contribute to the effort as best I can.  alarge oart
 of my living hinges on gathering intelligence but I
 can't do it on my own right now.

 Anyone else interested? Ed?,Keith? Others???

 Dana


 --- Arne P. Ryason [EMAIL PROTECTED] wrote:
  Is there any known progress on the INEEL process
  which uses a solid
  catalyst to produce biodiesel and food grade
  glycerin? Two scientists
  have developed a continuous process that eliminates
  the alcohol, base,
  acid,  water wash steps of making biodiesel. Also,
  it is a continuous
  process, versus the batch process that is used now.
  The glycerin
  byproduct is food grade. Selling it would offset the
  refining process,
  making biodiesel competative with petrodiesel.
 
  Anyone with more info on this?
 
 


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[biofuel] Solid catalyst KGPE

2002-01-09 Thread Christian

To all,

Thx all for the posts on solid cat.

I think I recall something from one of my classes (courses?) (...whatever
they«re called), this year.
In some place it mentioned the use of potassium methoxide (KGME, or
CH3-O-CH2-CH2-OK) and KGPE (Potassium Glyme Poly Ethilene). I think it was
used in some dechlorination process for PCBs. The point is that KGPE is
something like this:

KO-[-CH2-CH2-]n-CH2-CH2-O-K  (I think this was what the molecule looked
like)

Being the sodium methoxide the catalyst in the traditional Mike Pelly
recipe (though I«ve never liked the word catalyst here, «cause the methoxide
DOES react with the oil), couldn«t it be possible that the misterious
catalyst mentioned in this whole discussion on solid catalysts, is in fact
something like KGPE, or maybe NaGPE?

Someone mentioned it was a polymer. Plus, the chemical properties of sucha a
polymer shouldn«t differ that much from traditional methoxide. Then again, I
wouldn«t see why this KGME wouldn«t react and dissappear (thus, not being a
catalyst at all)-

Please let me know if this polymer stuff rings a bell somewhere. If so, I«ll
do a bit more research on this KGPE stuff.

Regards,

Christian



- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, January 09, 2002 1:48 AM
Subject: Re: [biofuel] Solid catalyst,


 The Fox-Ginosar process (INEEL) apparently uses a polymer. I posted
 this to the list a long time ago, I don't know if anyone ever picked
 it up:

 A message from Mike Pelly re solid phase catalysts:

 I have been getting ready to pick up some of that type of catalysts
 but have not till now. Not sure just what worked. I understand a
 chemical that is called Dowex works too. (Also need to retrofit my
 processor to make it happen.)

 I'm writing to pass along to you an idea I have on using a solid
 phase catalyst without going through the process of gluing it in
 place. My plans are to contain it in a tube that has screens with
 mesh finer than the catalyst at either end. The grease and alcohol is
 pumped through this in-line (filter-type) device. In simplistic terms
 it would be like placing the catalysts between two sink faucet
 screens and plumbing it in-line on a reactor like the one Dale
 Scroggins built. Also the part with unions at both ends, could be
 easily removed for easy cleaning, back flushing and recharging of
 catalyst.


 David Reid posted this:

 Points to start and research:
 (From the Woollatt book but remember published 1985).

 Bleaching and the treatment of Distillates with ion-exchange resins to
 upgrade quality :
 initial bleaching with 0.2-2.0% activated carbon
 ion-exchange resins from Rohm and Haas instead of or after a.c.
 [Macrorecticular resins (which have large discrete pores capable of
removing
 relatively large molecular mass compounds from the liquid) are normally
best
 for this duty which demands the removal of organic, rather than ionic,
 impurities ]. Sound ideal in this instance to me.
 eg: Amberlite 200 or 200C - strong cation resin  .
   Amberlite IRA-93 - weak base anion resin.
   Amberlite IRA-900 - strong base anion resin
 Deodorization, using heat and open steam, under vacuum, following
treatment
 often necessary.

 Production of refined grades of glycerine without distillation:
 Ion exclusion: process developed by Dow Chemical Co and reviewed in paper
by
 D'Souza (1979) using a bed of granular resin such as Dowex WX8 allowed
 partial purification which could then be completed by ion-exchange.
 Ion-exchange process sounds okay but regeneration using hydrochloric or
 sulphuric acids for the cation resins and caustic soda for the anion resin
 dosnt sound really feasible or realistic for a small plant. Would also not
 be economic I believe.
 Lever Bros installed a plant in L.A. designed by Illinois Water Treatment
Co
 in 1951 but would seriously doubt this was still in operation. Dosnt sound
 too promising. Distillation still seems to be the preferred method.
 Reverse Osmosis also dosnt sound too promising although there could have
 been developments in the last 15 years.
 Refs: Sourirajan and Kimura (1967), review Sourirajan and Matsuura (1982).


 This is also from Mike Pelly:

 From: Goltz, Bob (HR)
 To: '[EMAIL PROTECTED]'
 Subject: Base catalyzed esterification
 Date: Thu, 4 Oct 2001 11:28:27 -0400
 
 Mike Pelly...Thanks for your inquiry. Since you are running this reaction
 as base catalyzed, I think the product you need is DOWEX 1X2 in the OH
form.
 This product comes in several particle sizes... 50-100, 100-200 and
200-400
 mesh. I suggest you try the 50-100 mesh as it will give the lowest
pressure
 drop and still offer short diffusional paths. The resin will catalyze
this
 reaction as long as the resin is in the OH form. If the resin picks up
 chloride or other anions, it will sto working as a catalyst. To restore
the
 DOWEX 1X2 capacity, it can be washed with NaOH as directed in the
 literature.
 More

[biofuel] HCl (again)

2002-01-09 Thread Christian

Yesterday, just for the sake of it, I tried this out:

.- Poured some alcohol through jelly (remember my post on dehydrating 
ethanol?). I have no way to know what the final content of water was after 
drying it with jelly, and for the process I«m about to describe, it probably 
wasn«t even necessary, but still.-

.- Gathered 2 ml EtOH in a test tube.
.- Mixed with 12 ml new sunflower oil
.- Added (0,5ml?... or less... didn«t measure) of Muriatic Acid (35% HCl in 
water)

Then heated at about 57 degrees, mixing for about an hour. I built a mixer 
out of a washing machine little 5W 220V motor, and a flat rod of stainless 
steel (like the type used as oil gauges, in the block of car engines). I also 
have a tea cup warmer (sort of a fancy resistance heater-plate on which to 
leave your cup of coffe). I found out that this plate maintains a 250 ml 
Erlenmeyer full of water at about 57 degrees celsius. So I inmersed my BD test 
tube in a water filled Erlenmeyer, and with the stirrer (clamped to a retort 
stand) in it for about an hour, and left it to settle overnight.

The result:
After a night settling, I can see about 2ml of a very pale yellow not-so-dense 
liquid (Anyone who can tell me if this is BD???)
The rest (about 12 ml) is a murky white-ish stuff... (sort of like glycerin?), 
resting below the supposed-BD.

I guess this could be it:

CH-O-CO---R   CH2OH
CH2-O-CO-R   +   CH3CH2OH  --(HCl, 57¡)--  CHOH +  3 R-OC-O-CH2CH3 
CHO-C-O---R   CH2OH

PLUS:
If anyone«s interested, I also made a batch of H2SO4 (Sulphuric Acid), by 
electrolysis of iron sulphate solution. I still have a lot of colloidal iron, 
but pH is down to about 2 or less.

Best to you all,

Christian


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[biofuel] Pressure

2002-01-11 Thread Christian

I was thinking today (yes.. it«s an ability I sometimes have):

Often chemical processes (specially polimerization) require high pressures. 
High pressure speeds up or even allows many reactions often not attainable at 
normal 1 atm.

If I don«t recall badly, the inventors of Polartec (TM) started out in their 
basement, and made their first Polartec (TM) (or Fleece, or whatever you call 
it) batch in a pressure cooker. Pressure cookers are available in all shapes 
and sizes, and although they are not the cheapest saucepans around, the do a 
very good job in the processes mentioned.

This mail might sound stupid. I don«t need to perform a reaction at high 
pressure for the time being, but I just wanted to remind those who had 
forgotten about this method, of the existance of pressure cookers. (No, I don«t 
sell them).

Regards,

Christian


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[biofuel] for those speaking spanish

2002-01-13 Thread Christian

There«s a very good report on BD, specially focusing on the economics and 
efficiencies in tractor engines in Argentina, published by Monsanto and the 
Agriculture Secretary of Argentina at:

www.sagpya.mecon.gov.ar/0-0/index/institucional/biodiesel/Master.pdf

It«s 80+ pages long, and also covers areas such as energies in the global 
market, oils  prices, taxes, emissions, etc etc. Much of it speaks of these 
variables in Argentina, but if you can read spanish, you might as well give it 
a go. It seems quite extense.

Regards,

Christian



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[biofuel] titration results (Help me Keith)

2002-03-26 Thread Christian

Hi everyone. I«m somewhat confused after my titration results, so anyone (say, 
Keith, Dana, or anyone with experience)... it would be great to hear your 
opinion.

I started my first BD batch today (I«ve gathered 7 lt. of WVO, -corn, 
sunflower-). And I got some queer results for cooked oil. I was following M. 
Pelly«s recipe, where it says I should use Phenolphthalein (which turns pink at 
around pH 8,3-9), but I used Merck (R) universal indicator, so I took two sets 
of values: one to reach pH7 and another to reach pH 8,3+.

My only doubtful step was the weighing. I had a scale and my smalles bronze 
weight was 5g, so I mixed multiple-of-five combinations of nuts, bolts, nails 
and washers, and found out 2 nuts and a washer added up to 1g. That was what I 
used to measure 1g of sodium hydroxide.

QUESTION 1.

ÀShould I titrate to pH 7 or pH 8,3?

RESULTS:

As I took 4 sets of values, I«ve indicated the std. dev. too.

To reach pH7 -- 0,26 ml (+/-0,062) of NaOH (0,025M)

To reach pH 8,3 -- 0,32 ml (+/- 0,052) of NaOH (0,025M)

Note: 0,025 M = concentration of the solution. 1 mole of NaOH weighs 40g, then 
1 g of NaOH is 1/40th of a mole, i.e., 0.025 moles. That, in a liter, is a 
0,025 M solution (0.025 moles/liter).

QUESTION 2.

ÀIsn«t this awfully low for (cooked) WVO?

QUESTION 3.

ÀWhat does thin mean?...ÀIs it very low in FFA?

I suppose the worst that can happen is I«ll get the 3d layer of unreacted oil 
together with the BD (i.e. if my values for NaOH are in fact too short). I«d 
rather get that than the gel formed by an excess of lye.

On the other hand, as I«m still experimenting, I think I«ll go hard on MeOH 
(20% volume of oil).



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[biofuel] PP PET (Todd?)

2002-04-08 Thread Christian

Does anyone know if: 

PC (polycarbonate),
PP (polypropylene), or
PET (polyethylene therfthalate -plastic coke bottles-)

are suitable for the methoxide mix?

I think they are all quite chemical-resistant plastics (at least PET  PC). 
They seem much more available over here.

Thanks,

Christian


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[biofuel] My 2nd titration (to Keith)

2002-04-09 Thread Christian

Dear Keith,

Remember my odd titration results?

Well, now I measured the lye on a precision scale (measures up to hundredths of 
a gram) and made a solution of 1.06 g NaOH/lt (It was the closest I could get, 
given the size of the solid NaOH pips). Close enough. I titrated again, and 
(oops, forgot heating the WVO), titrated to around 1,3 ml.

I figured the first results were low because Phenolphthalein in unheated 
WVO/isoprop takes some time to react with all the prsent FFA, so vigorous 
mixing is needed, as well as -time-.

My results are still low for used oil (ranging from 1,22 ml to 1,5 ml), but now 
they seem closer to reality. I«ll be trying out a liter batch in a couple of 
days, and I«ll try 4g; 4,2g; 4,6g; 4,8g and 5g of NaOH to find the best results 
(these values correspond with titration results varying from 0,5 ml NaOH to 1,5 
ml NaOH). Wish me luck.

I«ve only one doubt, which is the container to use for Methoxide for my 1 lt 
batch. ÀHow hot can the Methoxide get (200ml MeOH + 4,8g NaOH)? ÀIs a 2 lt 
pyrex beaker OK (yes, it«s glass, but I«ll be working in a lab under good 
supervision)? ÀOnce in the WVO, is the mix safer to handle, or should I treat 
it as methoxide for the first minutes?

Regards,

Christian


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[biofuel] SUCCESS!

2002-04-09 Thread Christian

I«ve just completed my FIRST BD BATCH

As small as it may seem, my test batch was as follows:

100 ml WVO
20 ml MeOH
aprox 0,48 g NaOH (measured very unprecisely on a scale)
Initial volume: 120 ml

I mixed the MeOH+NaOH in a 250 ml Erlenmeyer, then poured it into a 150 ml 
beaker which contained the WVO (should have done it in inverse order)... mixed 
(not for long) while I heated it half of the time on the stove and the rest of 
the time on an electric cup warmer (which I know maintains a 250ml Erlenmeyer 
of water at 54 ¡C).

RESULTS:
My BD is settling in a 200 ml probe. Up to now, I can distinguish the 
pale-golden BD atop (aproximately 99 ml) and a brownish denser glycerine (about 
11ml) at the bottom. The BD is translucent but still faintly murky (needs 
settling for at least 12 hs).
Final Volume: 110 ml

INCREDIBLE!

Thanks Keith and all!

Regards,

Christian


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[biofuel] SUCCESS!

2002-04-09 Thread Christian

I«ve just completed my FIRST BD BATCH

As small as it may seem, my test batch was as follows:

100 ml WVO
20 ml MeOH
aprox 0,48 g NaOH (measured very unprecisely on a scale)
Initial volume: 120 ml

I mixed the MeOH+NaOH in a 250 ml Erlenmeyer, then poured it into a 150 ml 
beaker which contained the WVO (should have done it in inverse order)... mixed 
(not for long) while I heated it half of the time on the stove and the rest of 
the time on an electric cup warmer (which I know maintains a 250ml Erlenmeyer 
of water at 54 ¡C).

RESULTS:
My BD is settling in a 200 ml probe. Up to now, I can distinguish the 
pale-golden BD atop (aproximately 99 ml) and a brownish denser glycerine (about 
11ml) at the bottom. The BD is translucent but still faintly murky (needs 
settling for at least 12 hs).
Final Volume: 110 ml

INCREDIBLE!

Thanks Keith and all!

Regards,

Christian


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[biofuel] cloudiness (followup un my 2nd Titration - to Keith)

2002-04-13 Thread Christian

Hi Keith,

My batch of BD settled the glycerine out nicely, though the BD still seemed a 
bit cloudy. It was translucent, but not crystal clear... Is this suspended 
water?

I now bubble-washed it (not for long... the first few minutes produced an 
emulsion of BD+water which seemed murky white-ish/yewllow-ish.

Now I«m settling it. The first wash water is very white (almost like milk). 

QUESTION: If the BD remains non-crystal-clear after some washing  settling, 
should I take it to 105 deg C for some minutes?

Best wishes,

Christian


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[biofuel] Fw: cloudiness (please REPOST answers - email prog problem)

2002-04-14 Thread Christian


- Original Message - 
From: Christian 
To: biofuel@yahoogroups.com 
Sent: Saturday, April 13, 2002 2:55 PM
Subject: cloudiness (followup un my 2nd Titration - to Keith)


Hi Keith,

My batch of BD settled the glycerine out nicely, though the BD still seemed a 
bit cloudy. It was translucent, but not crystal clear... Is this suspended 
water?

I now bubble-washed it (not for long... the first few minutes produced an 
emulsion of BD+water which seemed murky white-ish/yewllow-ish.

Now I«m settling it. The first wash water is very white (almost like milk). 

QUESTION: If the BD remains non-crystal-clear after some washing  settling, 
should I take it to 105 deg C for some minutes?

Best wishes,

Christian


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[biofuel] Is it OK to heat BD to remove water?

2002-04-14 Thread Christian

Is it ok to heat finished  washed Bd to 105 deg C for a couple of minutes to 
boil off remaining dissolved water (and hence remove cloudiness)?

Thanks,

Christian


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[biofuel] Re: Fw: cloudiness (Paul Gobert)

2002-04-17 Thread Christian

Dear Paul,

My third wash left almost crystal clear water, and after settling for 2
daysd, the BD is definitely transparent and non-cloudy.

Today I continued with 4 litres of BD (four 1 liter batches). Im still in
the glys-BD settling stage, and the BD looks much more brownish than my
first batch, and still cloudy. Ill give it a day or so settling to see what
happens.

Anyway, if too much lye forms that sticky gel and too little forms a third
layer of unreacted WVO, then if I only get a layer of glycerine and a layer
of WVO, my proportions should be right, right?.

And very little whit residue (soap?) is left on top of the glycerine layer.
However, the first wash is very dirty (white, milky cloudy almos foamy). So
what should I change to get less soap formation?. Supposedly less water? Can
I wash indefinitely (say, three or four times) to remove all soap?

Best wishes (+ thanks in advance),

Christian

- Original Message -
From: Paul Gobert [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, April 14, 2002 5:18 PM
Subject: Re: [biofuel] Fw: cloudiness



 - Original Message -
 From: Christian [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Monday, April 15, 2002 2:27 AM
  My batch of BD settled the glycerine out nicely, though the BD still
 seemed a bit cloudy. It was translucent, but not crystal clear... Is this
 suspended water?
 
  I now bubble-washed it (not for long... the first few minutes produced
an
 emulsion of BD+water which seemed murky white-ish/yewllow-ish.
 
  Now Im settling it. The first wash water is very white (almost like
 milk).

 Christian, you could have soap problems. Filter a sample of the BD through
a
 filter paper.  It should filter crystal clear and leave a white soapy
 residue on the paper.
 Whatman No. 1 filter papers are rated at 11 micron.
 Processing may have to be adjusted so that not so much soap is formed, or
 use a gentler washing technique such as mist washing.

  QUESTION: If the BD remains non-crystal-clear after some washing 
 settling, should I take it to 105 deg C for some minutes?

 Have done that in past. BD clears up when heated but cloudiness returns
when
 it cools.
 After filtering I trialed heat drying but no water dropped out, I no
longer
 heat dry, filtering is my final step.

 Regards,   Paul Gobert.



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[biofuel] Re: cloudiness again (Paul Gobert)

2002-04-19 Thread Christian

My 100 ml of BD (first batch) are now crystal clear after three washings
(sort of the colour of sunflower oil, maybe clearer). Might need a filtering
just for precaution before using... nothing else.

All my batches come from the same WVO, which hardly titrated to 1.5 ml
(pretty cool for used oil).

My new 4 liters have separated spectacularly well and the glyc is starting
to solidify. BD remains the colour of light tea but amazingly
crystal-transparent.

Looks are good. Ill keep in touch. Hopefully Ill be setting a site up soon
at least to post some pictures (a 36 photo roll)

Best wishes,

Christian

- Original Message -
From: Paul Gobert [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, April 17, 2002 5:39 PM
Subject: Re: [biofuel] Re: Fw: cloudiness (Paul Gobert)



 - Original Message -
 From: Christian [EMAIL PROTECTED]
 [snip]

  Anyway, if too much lye forms that sticky gel and too little forms a
third
  layer of unreacted WVO, then if I only get a layer of glycerine and a
 layer
  of WVO, my proportions should be right, right?.
 [snip]
 Not a definitive guide as to the quality of the BD.
 As an example made two batches of BD from some really well used oil.
 (More about this oil in a few days when I do more tests, get more
 imformation from the distributers.)
 The oil titrated at 9.0ml, pretty well used. Tried neutralising some of
the
 acidity with lime but this oil refused to transesterify after the
treatment.
 Titration was definitely lower but even using levels of NaOH appropriate
for
 the titration on the origional oil, the treated oil/ methoxide mix
remained
 in one phase.
 Going back to the origional oil I made two 1L batches. Both used 250ml of
 methanol.
 Batch A/. 15ml of conc aqueous NaOH added to methanol, Batch B/. 20ml
added
 to methanol.Shaken in 2L bottle, set aside. In half an hour both batches
had
 settled nicely.
 The origional oil is almost black, BD/glycerine interface difficult to see
 in A/., easier to see in B/. (BD in B lighter in colour)

 Yield. A/.  810ml BD, 450ml glycerine.
B/.   710ml BD, 500ml glycerine.

 Glycerine from both batches drained off easily at 25 deg C.
 Batch A/. glycerine was still liquid when last seen 6 hours later.
 Batch B/. glycerine set after four hours, setting seemed to occur from the
 top down even though the beaker was sitting on cold tiles.
 From past experience expect both SG and viscosity of Batch B/. to be lower
 than that from Batch A/.


  And very little whit residue (soap?) is left on top of the glycerine
 layer.
  However, the first wash is very dirty (white, milky cloudy almos foamy).
 So
  what should I change to get less soap formation?

 Use an oil with less FFA.
 Neutralise the FFA in the oil you use.
 Titrate your oil and use the ammount of NaOH indicated by the titration.
 The oil used here titrated to 12.5g NaOH/litre.
 Batch A/. used the equivalent of 12.5g and Batch B/. 16.7g
 Better to err on the high hide than the low side especially if you are
 processing animal fats or the oil you are using has beef tallow residues
in
 it.
 Use 250ml methanol per litre of oil.

  Can I wash indefinitely (say, three or four times) to remove all soap?

 By all means. Make sure that your initial washing is not to vigorous
though
 as it is easy to loose BD through emulsification in the presence of soaps.
 Mist washing combined with prolonged settling works well. Usually only the
 emulsion layer between the BD and the wash water requires prolonged
 settling.

 Would be good to see others have an input to this as these observations
are
 from processing using conc aqueous NaOH to make the methoxide.
 Whilst this method works well for me and the GC results have been
 favourable, its not a method which has acheived universal acceptance.

 Accounts of others experiences in these areas would be appreciated.
 More on that Black Oil later.

 Regards,  Paul Gobert.




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[biofuel] murky

2002-04-25 Thread Christian

Hi everyone.

After my third wash, my 4 lt of BD are still not translucent (after three days 
of settling). Will continue to let it settle for a week more. ÀShould this 
work? ÀOr is my batch ruined?. Does filtering remove the cloudiness? ÀDoes 
heating to over 100¼C to remove water oxidize (spoil) the ester?

Tanks (Keith, Paul, whoever)

Christian Lenoir
@ [EMAIL PROTECTED]
*Juncal 189, Mart’nez (1640)
 Buenos Aires, Argentina
( +54 (11) 4792-1094
Fax:  +54 (11) 4798-8377


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Re: (Todd Paul) [biofuel] murky

2002-04-27 Thread Christian

Thanks to you both for the tips. I still haven«t tried filtering. Heating
to, say, 60¼C, makes the BD clear... even leaving it in full sunshine has
the same effect, but at 20¼C the BD goes back cloudy. (This is regarding
Todd«s 120¼F -49¼C- suggestion)

I«ll try Paul«s suggestion first, just because it«s simpler. Anyway, I don«t
quite understand how filtering removes cloudiness that comes from liquid
particles (either water or glycerides). My reaction times were, I admit it,
perhaps too short. I mixed four independent 1 liter batches, and they were
each left to react for about 30 to 40 minutes. The reaction seemed
complete after 10 minutes or so, and I thought 30-40 min would do.

Washing stage 1 left some emulsion problems, but decanting over night
allowed me to drain the water together with a small emulsified+soap layer in
between. I used a 6lt pyrex with an opening at the bottom, so I always
drained the water from below, rather than syphoning the BD form atop.

Todd: how do I calculate the proportion of lye if I were to follow your
suggestion? Will an excess simply wash out in the washing stage? Or might it
react to form the so feared gel?

My third washing left the water almost clear, and instead of an emulsion, I
sort of got the washing bottle full of bubbles... but not soap bubbles. They
were rather BD bubbles (5mm in diameter) in the water, and water bubbles
(same size) in the BD portion, and they all dissappeared quickly after
turning off the aereator.

Thanks... I«ll keep in touch.

Best to you all,

Christian
- Original Message -
From: Paul Gobert [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Thursday, April 25, 2002 6:13 PM
Subject: Re: [biofuel] murky



 - Original Message -
 From: Christian [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Friday, April 26, 2002 1:28 PM
 Subject: [biofuel] murky


   Does filtering remove the cloudiness?

 Usually works wonders, needs to be fairly fine filter medium though. For
 example a disposable plastic inline fuel filter will pass cloudy BD. A 11
 micron filter paper (Whatman No. 1) produces crystal clear BD from the
same
 murky BD.

 Regards,
 Paul Gobert.


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[biofuel] murky now clear

2002-04-27 Thread Christian

Dear Todd  Paul (and the rest of you),

I used a couple of coffee paper filters in a funnel, filtered the fuel, and the 
BD turned out sparklingly transparent (at room temp).

Thanks again for the help,

Christian.




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Re: [biofuel] murky

2002-04-28 Thread Christian

Right: I found out my filtering also removed a foamy white stuff, leaving
the BD clear.

- Original Message -
From: Paul Gobert [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, April 27, 2002 7:46 PM
Subject: Re: [biofuel] murky



 - Original Message -
 From: Christian [EMAIL PROTECTED]
 [snip]

 Anyway, I don«t
  quite understand how filtering removes cloudiness that comes from liquid
  particles (either water or glycerides).

 Christian, the material that my filtration removes is more of a white
soapy
 mature than water or glycerides. It looks much the same colour as clean
 white tallow but it is more uniform in consistency and does not set at
room
 temp.

 My reaction times were, I admit it,
  perhaps too short. I mixed four independent 1 liter batches, and they
were
  each left to react for about 30 to 40 minutes. The reaction seemed
  complete after 10 minutes or so, and I thought 30-40 min would do.

 In light of what Todd and others have reported I have extended my mixing
 times.
 This may improve the clarity of the BD but I think my use of conc aqueous
 NaOH is a contributing factor.
 Strangely enough results from a test using varying levels of NaOH, with a
 fixed level of methanol on the same feedstock, gave clearer  unwashed BD
for
 higher levels of NaOH than optimum (titration) or low levels. Viscosity
and
 SG were also lower for high levels of NaOH. These tests bear repeating as
 the mixing was of short duration. I suspect that optimum mixing would
level
 out the differences.

 Regards,
 Paul Gobert.


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[biofuel] what could it be?

2002-04-30 Thread Christian

After settling my glycerin, I decided to wash and neutraliza it. I first used 
vinegar, but noticed the pH level whent down very slowly, and I was rather 
diluting the glyc with too much water from the vinegar acetic acid solution. 
So I reached for the HCl 35% (muriatic) acid. 
pH started going upwards, say, 1 pH level per 2 ml (very roughly from what I 
can recall). I was also heating to remove the excess methanol. We know that any 
NaOH will react with vinegar (CH3COOH) to form CH3COONa (a salt) + water. with 
HCl, the reaction forms table salt (NaCl) and water, and table salt wouldn«t 
represent a problem if I were to use the glycerin as a soap... so:
I continued adding HCl, until suddenly the pH whent down drastically, sort of 
as in a buffer effect. 

This is quite possible, as a buffer solution isone which will tend to maintain 
a certain pH for a given ammount of acid or base added. These can be made from 
a) a weak acid and an ionic soluble salt of the weak acid, or b) a weak base 
and a soluble ionic salt of the weak base. For example, CH3COOH (acetic acid) 
and CH3COOH.

So I suddenly forced pH too low, but in the meantime, big flocks of something 
like waxes or thick creamy greasy looking things started forming in the 
mixture. When I finished the heating, and adding some NaOH solution to return 
to pH 7, the remaining liquid was a mixture of glycerin and water below 
(probably + soluble salts), and something atop which looked like very dark 
brown biodiesel.Now, at room temp, there«s a mixture of liquid brown 
something, plus floating and submerged spots and bubbles and skimming 
floating layers of other whiteish solid things (guk). Could these be esterified 
FFA remains with longer chains that remail solid at room temp? How could this 
be if supposedly FFA react FIRST with the catalyst, and then with the WVO, and 
my yield for that batch seemed perfect?

Any ideas?

Regards,

Christian 


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Re: [biofuel] what could it be? (to Ken)

2002-04-30 Thread Christian

Interesting!

Does it always form? And is heating and neutralizaing the usual way of
getting to it?

Thanks

Christian

- Original Message -
From: Ken Provost [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Tuesday, April 30, 2002 1:10 PM
Subject: Re: [biofuel] what could it be?


 Christian writes:

 
 So I suddenly forced pH too low, but in the meantime, big flocks of
 something like
 waxes or thick creamy greasy looking things started forming in the
 mixture. When
 I finished the heating, and adding some NaOH solution to return to
 pH 7, the remaining
 liquid was a mixture of glycerin and water below (probably + soluble
 salts), and
 something atop which looked like very dark brown biodiesel.


 The dark liquid is called acidulated soapstock, and is almost
 entirely free fatty acid.
 (FYI -- Crude oleic acid made this way is also known as red oil.)
 This is the stuff I've been
 playing with for a couple weeks now. You can try to esterify it to
 biodiesel with acid catalyst,
 you can throw it on the nearest dirt road to keep the dust down, you
 can turn it into soap,
 you can react it with Ca(OH)2 to form the calcium salt which you can
 then feed to your
 pigs or dairy cattle as a ruminally inert fat booster, etc,
 etcMany people nowadays are
 frantically looking for wonderful uses for the stuff. Let us know
 what you find.

 Seriously, tho, what you're doing is great -- FFAs are basically the
 final effluent you
 have to deal with after neutralizing everything else. They're fairly
 strong herbicides,
 so you really don't want to just toss 'em in the compost with the
 aqueous phase.


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[biofuel] 2 stages... what if? (new method?)

2002-05-01 Thread Christian
 stirring. A conic floor (for the bucket) would probably 
help (as in a cyclone: apparatus used to settle dust particles from an air 
stream).

Best to you all, and please tell me if anyone is interested in further testing 
this method.

Christian


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Re: [biofuel] 2 stages... what if? (new method?)

2002-05-01 Thread Christian

Sounds logical, (anyway I don«t know if the term phase really applies
here). But it sounds unreasonable to believe the reaction taking place in
the WVO/BD/MeOH layer will have a way of knowing if the layer og glycerin
belw is 1cm, 2cm or a mile deep.

I need to go back to over my books for this one. We need hard references
for the displacement of the reaction how to-s. If what you point is right,
then centrifugating the mixture while processing (just to gather the
glycerine together) should be enough, without havin to tap it out...
assuming you can afford a centrifugue. And if this principle is right,
there«s another implication: In Alek«s 2 stage method, simply stopping the
reaction at 3/4 vol methoxide, and adding the remaining 1/4 the day after in
the same mixture (without separating the glycerin) would be OK... and this
is something important because each time you separate the glyc from the BD
you might be discarding the layer in between (unless you store these
layers for further processings and then separate and gather up all the
leftovers) Am I being clear here? I think not.

The point is that in the traditional 2 stage method, after the first stage
you separate the glycerin and remove it, taking along with it some fine
interphase layer of BD with it. But if the assumtion yuo mentioned is
right, there«d be no need for this and you could simply reheat, proceed with
stage 2 (adding the remaining 1/4 MeOH) and finishing the reaction, and so
you«d avoid removing the glycerin (together with avoiding the drawback of
removing the small interphase layer of BD for every syage) just to remaove
the whole lot of glycerin after the last stage.

Regards,

Christian


- Original Message -
From: Ken Provost [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, May 01, 2002 1:01 PM
Subject: Re: [biofuel] 2 stages... what if? (new method?)


 I don't have any hard references on this, but I believe the precipitation
 of glycerine from the biodiesel reaction as a separate phase is all that
is
 required to shift the equilibrium. Whether a glycerine molecule is in a
 separate droplet a millimeter away, or a separate bucket six feet away,
 it's basically out of the picture.


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Re: [biofuel] 2 stages... what if? (new method?)

2002-05-01 Thread Christian

ANYWAY:

1.- Le Chatelier«s Principle: the position of equilibrium always shifts in
such a direction that eases the tension applied on the system

2.- Chemical reactions DO NOT END in the equilibrium, but rather it is at
this point where the speed of the reacion in one way and the other are
equal. This means that in the equilibrium, there is as much glycerin and BD
combining to produce MeOH and WVO as there is WVO and MeOH combining to
produce glycerin and BD. If you take this into consideration, then I figure
you can say that removing the glycerin to a bucket six feet away is the
only way in which you can favour the equilibrium towards the products side,
«cause if there still is an interfase between glycerin and BD/WVO, you will
still have amounts of glyc/BD in the interfase of the liquids combining to
form more WVO/MeOH. What I still can«t explain is how the amount of (not the
presence of) glycerin may favour the reaction towards one side or the other.


- Original Message -
From: Ken Provost [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, May 01, 2002 1:01 PM
Subject: Re: [biofuel] 2 stages... what if? (new method?)


 I don't have any hard references on this, but I believe the precipitation
 of glycerine from the biodiesel reaction as a separate phase is all that
is
 required to shift the equilibrium. Whether a glycerine molecule is in a
 separate droplet a millimeter away, or a separate bucket six feet away,
 it's basically out of the picture.


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Re: [biofuel] 2 stages... what if? (new method?)

2002-05-01 Thread Christian

Thaks for the compliment. Anyhow, I just made a mini 1 lt batch and
repeating the BD preparation processs I«m seeing the glyc first produced
still needs a couple of minutes to settle gather up at the bottom. More
miportant still, I had also forgotten the methoxide mixed in it and would be
removed if I took away the glyc. -thanks for the reminder-. I think we won«t
be seeing how spiral galaxies influence the BD manufacture process for now.

Well, it takes many failures to get to a good improvement. Anyway it was
worth the chat.

Greetings,

Christian


- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, May 01, 2002 4:03 PM
Subject: Re: [biofuel] 2 stages... what if? (new method?)


 You'll be removing some methanol too, Christian, don't forget. Which
 version of Aleks's method are you using? The updated version has
 quite a few changes, and one of them is that the glyc isn't removed
 after the acid stage, but it is progressively removed during the
 second stage (if your processor permits).

 Thankyou for explaining the spiral galaxy in my coffee, I always
 wondered how it got there without a Big Bang. No, seriously, nice
 explanation, you can watch it forming and see some basic principle at
 work, nice to have it explained. Very interested to know if it leads
 to a process improvement, that would be great, and a nice story to
 tell too.

 Best

 Keith


 Sounds logical, (anyway I don«t know if the term phase really applies
 here). But it sounds unreasonable to believe the reaction taking place in
 the WVO/BD/MeOH layer will have a way of knowing if the layer og
glycerin
 belw is 1cm, 2cm or a mile deep.
 
 I need to go back to over my books for this one. We need hard
references
 for the displacement of the reaction how to-s. If what you point is
right,
 then centrifugating the mixture while processing (just to gather the
 glycerine together) should be enough, without havin to tap it out...
 assuming you can afford a centrifugue. And if this principle is right,
 there«s another implication: In Alek«s 2 stage method, simply stopping
the
 reaction at 3/4 vol methoxide, and adding the remaining 1/4 the day after
in
 the same mixture (without separating the glycerin) would be OK... and
this
 is something important because each time you separate the glyc from the
BD
 you might be discarding the layer in between (unless you store these
 layers for further processings and then separate and gather up all the
 leftovers) Am I being clear here? I think not.
 
 The point is that in the traditional 2 stage method, after the first
stage
 you separate the glycerin and remove it, taking along with it some fine
 interphase layer of BD with it. But if the assumtion yuo mentioned is
 right, there«d be no need for this and you could simply reheat, proceed
with
 stage 2 (adding the remaining 1/4 MeOH) and finishing the reaction, and
so
 you«d avoid removing the glycerin (together with avoiding the drawback of
 removing the small interphase layer of BD for every syage) just to
remaove
 the whole lot of glycerin after the last stage.
 
 Regards,
 
 Christian
 
 
 - Original Message -
 From: Ken Provost [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Wednesday, May 01, 2002 1:01 PM
 Subject: Re: [biofuel] 2 stages... what if? (new method?)
 
 
   I don't have any hard references on this, but I believe the
precipitation
   of glycerine from the biodiesel reaction as a separate phase is all
that
 is
   required to shift the equilibrium. Whether a glycerine molecule is in
a
   separate droplet a millimeter away, or a separate bucket six feet
away,
   it's basically out of the picture.
  



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[biofuel] Important notes

2002-05-07 Thread Christian

I was chatting today with a chemical engineer who happened to write his final 
thesis (the paper you write in order to graduate) on the methyl esters and 
transesterifications. As a chemical engineer, he studied che kinetics of the 
reaction and the reaction speeds, and he designed a production facility for a 
continuous process. He made all sorts of tests using IR spectrography at 
different points of the reaction, and made a very thorough work from the 
chemical point of view. He did not want to show me his thesis (maybe he was 
afraid of me copying methods still not patented), but he did give me some hints 
and opinions, which I try to summarize here, and which you might want to have a 
look at: (This guy used soy oil)

.- Strange enough, he pointed out that some thorough investigations were not 
100% right, but he didn«t say where they were wrong: he just added do the 
experimentation yourself, and you«ll see

.- He said that 50¼C for the reaction was waaay too much. He said he carried 
out his continuous process at room temperature. Besides this, he pointed out 
that the glycerin was very easily decomposed into acrolein and things like 
that, which make it dark brown. I was so curious that just now, when I got 
home, I made a 100ml batch at room temp (now around 18¼C), and mixed for only 
15 minutes. This guy said that they had achieved a 98% conversion after this 
time period. Now I«ve let it settle, and I can see after about an hour settling 
that the glycerin DOES show up much clearer (pure glyc is transparent). He also 
said that in his continuous process he had designed a three stage evaporator to 
remove the water from it, after distilling it to get out the MeOH (I suppose 
he«d do this under vacuum, so as not to heat the glyc and turn it into the 
mentioned brown acrolein). I found this point most interesting.

.- He mentioned they used sulphuric acid (say, 4ml per liter of WVO) to cut 
the reaction and stop the NaOH (this forms sodium sulphate, Na2SO4, which is 
washed with the water). I said I added some drops of vinegar in the washing 
stage and he almost whent crazy: he said tha any ammount of vinegar capable of 
modifying pH would produce great problems with the injectors. He said motors 
are very sensitive to those acid conditions.

.- He also pointed out that I should remove the sulphates (which came from the 
sulphuric acid / lye reaction) from the glycerin, and added that the glycerin 
was full of impurities: sulphates, MeOH, water...

.- He also added that boiling off the MeOH was not a very eco-friendly thing to 
do, and that you«d never be able to boil off 100% of it (eve with a 
distillation column)

.- He said a continuous centrifugue was not har to get, but reaction velocities 
had to be carefully measured when designing a continuous process. He fancied 
this method and said that settling the BD was not a good option, specially 
after vigorous mixing, which always (according to him) brought emulsification 
problems of some kind.

.- Regarding the fact I am an environmental engineer, he pointed out the 
washing stages use a damn great ammount of water (I can«t recall having heard 
of an alternative to this from him). Also, than no reaction is 100% efficient 
and that if I was to measure exhaust gases, then I *should* be checking for 
unburnt traces of methanol, which could produce nasty emissions.

Everything he said sounded most interesting, but presented me with a whole new 
set of questions to be answered. I«m very eager to hear the opinion of those 
with experience in BD making, specially those who use it regularly in their 
cars.

Best to you all,

Christian



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[biofuel] glycerin (Long but interesting)

2002-05-07 Thread Christian

Pasted from: 
http://www.ibiblio.org/herbmed/eclectic/kings/glycerinum.html


Glycerinum (U. S. P.)-Glycerin.
Preparations: Glycerita.-Glycerites - Suppositories of Glycerin - Glycerin 
Lotion - Preparations
Related entry: Sapo (U. S. P.)-Soap
Other tomes: Cook - Felter - Ellingwood - Petersen - BPC - AJP Mar 1871 
(Glycerin quality) - AJP Dec 1871

FORMULA: C3H5(OH)3. MOLECULAR WEIGHT: 91.79.
A liquid obtained by the decomposition of vegetable or animal fats or fixed 
oils, and containing not less than 5 per cent of absolute glycerin (C3H5[OH]3= 
91.79)-(U. S. P.).
SYNONYMS: Glycerina (U. S. P., 1870), Glycerine, Glycerol, Propenyl alcohol.

History and Preparation.-Glycerin was discovered, in 1779, by Scheele in the 
saponification products of olive oil by means of litharge, and later recognized 
by him as a common constituent of other oils and fats, and therefore named the 
sweet principle of fats. Chevreul gave it the name glycerin, and cleared up 
the nature of its combination in the fats. Glycerin, or glycerol, as it is now 
preferably called to indicate its alcohol character, is a trihydric alcohol 
(C3H5[OH]3), containing the trivalent radical glyceryl (C3H5). It exists in 
oils and fats, combined with palmitic, stearic, and oleic acids in the form of 
glycerylesters of these acids (tripalmitin, tristearin, triolein; also see 
under Adeps). In some oils and fats it is combined partially with other 
acids-e. g., in butter-wherein 5 per cent of the total fat is 
glyceryl-tributyrate, or tributyrin; in cod-liver oil it is said to exist in 
part combined with acetic acid, as glyceryl triacetate, or triacetin, etc. 
Glycerin also exists in the yolk of eggs and the human brain in the form of 
phospho-glyceric acid. Pasteur's researches have also established its 
occurrence as a regular constituent among the products of fermentation (see 
Alcohol).

On a small scale glycerin may be obtained in the process which led to its 
discovery, viz., that of making lead plaster (see Emplastrum Plumbi). The late 
Mr. Robert Shoemaker prepared by this method probably the first Commercial 
glycerin in the United States, in 1848, at $4.00 a pound (Amer. Jour. Pharm., 
1879, p. 289). The article became official in the U. S. P., in 1850.

Large quantities of glycerin are now obtained as a by-product in the 
manufacture of soaps and candles. This was formerly thrown away as useless. The 
principle involved is simply that of splitting the fat into its constituents 
(fatty acid and glycerin) by adding the elements of water (see Emplastrum 
Plumbi). The process of saponification is being carried out in several 
different ways: (1) With alkalies; the fatty acids thereby combine with alkali 
and form soap (see Sapo); the glycerin in diluted form is contained in the 
aqueous layer below the soap. (2) With milk of lime (old process of Campbell 
Morfit, see this Dispensatory, previous revision), or with milk of lime and 
water in closed vessels under a pressure of 10 atmospheres and a temperature of 
172¡ C. (242.6¡ F.) (Milly's Autoclave Process, see Prof. S. P. Sadtler, 
Handbook of Indust. Org. Chem., 1895, p. 56). The glycerin water separates from 
the layer of lime soap and fatty acids; glycerin is obtained therefrom best by 
evaporation in vacuo. (3) With superheated steam (aqueous saponification) and 
subsequent redistillation of the raw glycerin. This method was introduced, in 
1855, by Messrs. Wilson and Paine, and marked a great step forward in the 
problem of obtaining a pure article. In saponifying the fats with superheated 
steam, the temperature must not exceed 300¡ C. (572¡ F.), or else decomposition 
products will be formed. Both the fatty acid and the glycerin distill over. In 
redistilling the raw glycerin by superheated steam, the liquid is heated to 
about 180¡ C. (356¡ F.), and the steam has a temperature of about 110¡ C. (230¡ 
F.). For details regarding the manufacture of glycerin, consult the various 
works on chemical technology.

Description.-Glycerin is officially described as follows; A clear, colorless, 
liquid, of a thick, syrupy consistence, oily to the touch, odorless, very sweet 
and slightly warm to the taste. When exposed to the air, it slowly abstracts 
moisture. Specific gravity, not less than 1.260 at 15¡ C. (59¡ F.). Soluble, in 
all proportions, in water or alcohol, also soluble in a mixture of 3 parts of 
alcohol and 1 part of ether, but insoluble in ether, chloroform, carbon 
disulphide, benzin, benzol, and fixed or volatile oils. Glycerin is slowly 
volatilized from an aqueous solution, at or above 100¡ C. (212¡ F.), with the 
vapor of water. Heated by itself to a higher temperature, it yields acrid 
decomposition products, boils at a temperature at or above 165¡ C. (329¡ F.), 
and is finally entirely decomposed and dissipated-(U. S. P.). The exceedingly 
irritating decomposition products are chiefly due to the formation of acrolein 
(allyl aldehyde, C2H3.CHO), which is also formed when 

[biofuel] OILS (Long but interesting)

2002-05-07 Thread Christian

Pasted From:
http://www.ibiblio.org/herbmed/eclectic/kings/olea.html

Olea.-Oils.
Related entries: Olea Infusa (N. F.)-Infused Oils - Index of Oils - Sapo (U. S. 
P.)-Soap
Other tomes: Cook (volatile oils) - Cook (fixed oils) - Potter (volatile oils) 
- Potter (fixed oils)

The term Oil applies to a number of unctuous bodies not miscible with water, 
from both the vegetable and animal kingdoms, which are fluid at ordinary or 
slightly elevated temperature. When placed upon paper they render it 
translucent, or impart to it a greasy stain. Oils may be conveniently divided, 
with reference to their volatility, into two great classes: Fixed or fatty oils 
and fats, to which also belong the waxes (see Cera), and volatile or essential 
oils. Intermediate between the two, although chemically unlike either, stand 
the mineral oils and mineral waxes, or paraffins (see Petrolatum).

Olea Fixa.-FIXED or FATTY OILS (Olea pinguia). Fixed oils derive their name 
from not being volatilized by the vapors of boiling water. The difference 
between fatty oils and fats is merely one of consistency, the former being 
liquid, the latter solid or semisolid at ordinary temperatures. In the 
vegetable kingdom, fixed oils are mostly derived from the seeds of 
dicotyledonous plants, although monocotyledonous plants, such as the palm 
trees, furnish several of the technically important fixed oils. The oil often 
constitutes a large proportion of the seeds, e. g., not less than 25 per cent 
in linseed, 50 per cent in walnuts, about as much in almonds, as against about 
2 per cent in cereals. It is obtained from the crushed oil-bearing material, 
either by cold or warm pressure, in hydraulic presses, or by extracting with 
such solvents as carbon disulphide, or by boiling the crushed material with 
water, whereby the oil floats on top and may be conveniently collected. The 
residual press-cakes, obtained in the first process (oil cakes), are valuable 
feed material for cattle, since they contain much nitrogenous and fatty matter 
(see table in Prof. S. P. Sadtler's Handbook of Indust. Org. Chem., 2d ed., 
1895, p. 70).

The oils and fats derived from the animal kingdom, are obtained from various 
organs of the animal; thus, bone-oil from bones, by boiling with water, or 
extraction with solvents; neat's-foot oil from the feet of oxen by boiling with 
water; cod-liver oil and shark oil, from the respective livers, by spontaneous 
exudation and gentle expression; tallow and lard from the internal abdominal 
fat of sheep and hogs (see Sevum and Adeps), etc. The crude oils and fats as 
obtained in the manner alluded to, are mostly of a yellow, brown or even black 
color, and frequently require more or less purification. This is often effected 
by mechanical treatment, such as filtration with or without charcoal, etc., but 
more frequently, by chemical processes, especially treatment with 1 or 2 per 
cent of strong sulphuric acid (applicable, for example, to linseed oil), or 
with zinc chloride, or alkalies, tanning materials and oxidizers, such as 
potassium bichromate, hydrogen peroxide, etc.

The fatty oils of marine animals, and those from most vegetable sources, are 
fluid at ordinary temperature; palm oil, cacao-butter, nutmeg butter, cocoanut 
oil, and others, are semisolid like butter. When exposed to cold, fixed oils 
solidify at temperatures varying with the oil. Fatty oils are insoluble in 
water, rendering that fluid milky when agitated with it, but the oil finally 
rises upon the surface; if a mucilaginous substance, or alkaline carbonate be 
added, the oil is prevented from rising., and a permanent milky mixture called 
an emulsion is formed. With the exception of castor oil and croton oil, fatty 
oils are nearly insoluble in cold alcohol. They dissolve readily, however, in 
ether, carbon disulphide, chloroform, benzol, petroleum benzin, amyl alcohol, 
acetone, and oil of turpentine, and freely mix with one another, as well as 
with resins and volatile oils. They are all lighter than water, their specific 
gravities ranging from 0.879 to 0.968. Fatty oils are not volatile as such, but 
can be heated to boiling (at about 315¡ C., or 600¡ F.) whereby decomposition 
takes place, acrid fumes of acrolein (see Glycerin) being evolved, together 
with carbonic acid gas, some volatile organic acids and inflammable 
hydrocarbons. Upon condensing the vapors, an empyreumatic oil is obtained. When 
in the state of vapor, fixed oils take fire upon the approach of an ignited 
body; the products of combustion are water and carbonic acid gas.

As to their chemical nature, most fatty oils are mixtures of salts of the 
trivalent alcohol glycerin (C3H5[OH]3), with the saturated palmitic (C16H32O2) 
and stearic acids (C18H36O2), both higher homologues of acetic acid, of the 
general formula CnH2nO2, and the unsaturated oleic acid (C18H34O2), which 
represents the series CnH2n-2O2. The salts are called glycerin esters, or 
glycerides, and are 

[biofuel] Acrolein 2

2002-05-07 Thread Christian

Regarding the message I just sent:

At: http://www.inchem.org/documents/icsc/icsc/eics0624.htm

 (A Chemical safety data sheet) it sais the glycerin decomposes below it«s 
boiling point at 171¼C. (For pure glyc).

Christian


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[biofuel] acrolein

2002-05-08 Thread Christian

I«m a bit concerned with the glycerin/acrolein topic (glycerin thermally 
decomposes into this dangerous substance). I found little on this topic (Keith 
and Todd) in the archives. From a not-so-thorough search in google, acrolein 
forms when heating Glycerol to 290¼C, but that happens when the glycerin is 
pure. The water/glyc mixture boils at a lower temp, near 164 ¼C. A chemical 
engineer told me today that the dark brown colour in the glyc could have to do 
with the formation of acrolein (even at 60¼C). I want to run an IR 
spectrography on my glyc to see if that«s so. Besides, I thought acrolein was a 
gas. But still, it«s a carcinogenic substance you don«t want to mess with. Does 
anyone know more about the subject? I am also concerned with the fact some of 
you are using it as a detergent/grease remover. I«d suppose it will contain at 
least traces of methanol, methoxide, maybe even acrolein, neither of which you 
want on your hands. Please let me know what you think.

Best to you all,

Christian


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[biofuel] Acrolein («twas illegible)

2002-05-07 Thread Christian

I«m a bit concerned with the glycerin/acrolein topic (glycerin thermally 
decomposes into this dangerous substance). I found little on this topic (Keith 
and Todd) in the archives. From a not-so-thorough search in google, acrolein 
forms when heating Glycerol to 290¼C, but that happens when the glycerin is 
pure. The water/glyc mixture boils at a lower temp, near 164 ¼C. A chemical 
engineer told me today that the dark brown colour in the glyc could have to do 
with the formation of acrolein (even at 60¼C). I want to run an IR 
spectrography on my glyc to see if that«s so. Besides, I thought acrolein was a 
gas. But still, it«s a carcinogenic substance you don«t want to mess with. Does 
anyone know more about the subject? I am also concerned with the fact some of 
you are using it as a detergent/grease remover. I«d suppose it will contain at 
least traces of methanol, methoxide, maybe even acrolein, neither of which you 
want on your hands. Please let me know what you think.

Best to you all,

Christian


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[biofuel] Stoichiometric values (to Ken from Phillipines)

2002-05-14 Thread Christian

Hi Ken,

I«ve had my doubts on the stoichiometric values since a beginning (not that
they were wrong or anything, I was just curious), but I never had the tiem
to write it down on paper.

We could briefly try it here, assuming you«ve got the percentages of FA in
coconut oil is as you«ve described:

The corresponding fatty acids are:
46% C12H24O
18% C14H28O
10% C16H32O
4% C18H36O
6% C18H34O

But for each FA chain on the glyceol, there is one H lost in the
esterification, together with the OH group of the glycerin. We«ll assume no
FFA.

So the ester chain in the triglicerid will be as follows:
46% C12H23O = 183 g
18% C14H27O = 211 g
10% C16H31O = 239 g
4% C18H35O = 267 g
6% C18H33O = 261 g

And the glycerol bit will weigh:
CH2-CH-CH2 = 41 g

I suppose we can the say that 1 Mole of WVO (Coconut) will have:
41g + (0.46x183 + 0.18x211 + 0.1x239 + 0.04x267 + 0.06x261) = 213.4 g

Methanol weighs: CH3OH = 32 g/mol

Glyc-R-R«-R«« --(CH3ONa)-- Glyc + ROCH3 + R«OCH3 + R««OCH3 + Na(+)

But we could assume that one mole of WVO will require one mole of Methanol,
as the methyl group in it is exactly what will join the FA in the
transesterification

So every 213.4g of WVO will require 32g of Methanol

Coconut oil«s density at 20¼C is close to 0.919 g/ml (or so I read on the
internet). So 213.4 g (1 mole) will equal 232.201 ml.

On the other side, the density for methanol is 0.79, so 32g of methanol
represent 40.5063 ml.

So, 40.5063 ml in 232.201 ml represent 17.44

The proposed value (M. Pelly«s recipe) is 20% by volume. The value we got to
here is 17.44%
That«s only 2.56% shorter than the proposed value. The 20% value is useful
to push the reaction towards the products side, anyway, you should be able
to use a minimum of 17.4% methanol (in volume) to transesterify your WVO.

I use sunflower oil, and my % is even lower (close to 11% in vol).


Hope to have been of help.

Best wishes,

Christian Lenoir


- Original Message -
From: Christian [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Monday, May 13, 2002 12:39 PM
Subject: Re: Stoichiometric Balance of methanol vs glycerine


 Hello Christian,

 First of all i want to thank you for your posts.  They have been very
 helpful and informative.

 I am Ken and from the Philippines.  I have been making BD for a year now
 thanks to this group.  I use what i make because the price of BD is not
 competitive to regular diesel.

 I was checking the stoichiometric balance of methanol to glycerine when i
 felt something might be wrong and hope maybe you can clear it up for me.

 In our reaction we need 3 moles of methanol to every mole of glycerine to
 be replaced right?  or 1 mole of methanol for every mole of fatty acid(be
 it lauric, myristic, stearic et al).  I use coconut oil and the data for
 coconut oil is as follows

 C12:0 - 46%
 C14:0 - 18%
 C16:0 - 10%
 C18:0 - 4%
 C18:1 - 6%

 in short there is around 1.74 moles of glycerine for every 1000 grams of
 refined coconut oil.  From here i would need 5.22 moles of methanol or 210
 ml of methanol.  The receipe in journey to forever says to use 200 ml of
 methanol for every 1000 ml of oil and they say that has alot of excess
 already.  So this is my dilema, are my calculations wrong.  I wonder how
 Keith and the rest came up with the prescribed volume for methanol.

 Thanks and Best Regards
 Ken





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 mensaje enviado desde http://www.iespana.es
 emails (pop)-paginas web (espacio ilimitado)-agenda-favoritos
(bookmarks)-foros -Chat








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Re: [biofuel] Stoichiometric values (to Ken from Phillipines)

2002-05-14 Thread Christian

I ca«t be too sure on my answer, but wouldn«t it bee too dense?
First of all, it wouldn«t be a transesterification, as the
transesterification implies:
ROH + R«COOR«« -- R««OH + R«COOR
i.e., switching the carbon chains between an ester and an alcohol.

You«d be esterifying the glycerin:
C3H5(OH)3 + RCOOH -- C3H5(OCOR)3 + H2O

Thus forming a triglicerid, the main constituent of vegetable oils, only
that in vegetable oils the fatty acid chains have 14, 16, 18, 20, (etc)
carbons, plus insaturations.

Acetic acid cas only 2 carbons, and would yield:
C3H5(OCOCH3)3 (triacetato de glicerilo, in spanish)

I suppose this substance would have properties similar to oils in some
aspects, but it lacks double bonds, so it would probably be solid. The fatty
acid chains extend in a linear pattern, evidently in zig-zag, due to the
tetrahedic bonds, so these molecules fit weel into one another. The double
bonds in oils make the carbon chains crooked, so molecules have a harder
time regrouping into an ordered consistency (solid state). Therefore, more
insaturations usually make it more difficult for the molecules to pack. So,
the bottom line is: more insaturations reduce the fusion point of greases 
oils.
No saturations:   /\/\/\/\/\/\/\/\/\/\COOH

The structure you propose:

CH2/\/\
CH/\/\
CH2/\/\

Seems to me would solid or of difficult flow. (I«m not an expert in this).

Anyway, don«t let these words bring down your morale. I«m not an expert, as
I«ve said, and it would be good to try this out to see what the results are.

All the best,

Christian

- Original Message -
From: Mccall Tom WP US [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Tuesday, May 14, 2002 2:09 PM
Subject: RE: [biofuel] Stoichiometric values (to Ken from Phillipines)


I there any way to transesterfy the
Glycerin?

It has 3 -OH groups I would think that you
could esterfy with Acetic acid.

If you esterfied all 3 -OH groups you would
have a C9 hydrocarbon with 6 oxygens.

Talk about an oxygenated fuel.

I think that a C-9 is close to the size
of gasoline fuels...?

Could this be a oxygenated additive for
gasoline engines.

Maybe 3-5% Biodiesal would also help to lower
emissions and make up for the BTU loss when
you add the esterfied glycerin to the tank.

Just thinking (typing) out loud.

T

-Original Message-
From: Christian [mailto:[EMAIL PROTECTED]
Sent: Tuesday, May 14, 2002 10:43 AM
To: biofuel@yahoogroups.com
Subject: [biofuel] Stoichiometric values (to Ken from Phillipines)


Hi Ken,

I«ve had my doubts on the stoichiometric values since a beginning (not that
they were wrong or anything, I was just curious), but I never had the tiem
to write it down on paper.

We could briefly try it here, assuming you«ve got the percentages of FA in
coconut oil is as you«ve described:

The corresponding fatty acids are:
46% C12H24O
18% C14H28O
10% C16H32O
4% C18H36O
6% C18H34O

But for each FA chain on the glyceol, there is one H lost in the
esterification, together with the OH group of the glycerin. We«ll assume no
FFA.

So the ester chain in the triglicerid will be as follows:
46% C12H23O = 183 g
18% C14H27O = 211 g
10% C16H31O = 239 g
4% C18H35O = 267 g
6% C18H33O = 261 g

And the glycerol bit will weigh:
CH2-CH-CH2 = 41 g

I suppose we can the say that 1 Mole of WVO (Coconut) will have:
41g + (0.46x183 + 0.18x211 + 0.1x239 + 0.04x267 + 0.06x261) = 213.4 g

Methanol weighs: CH3OH = 32 g/mol

Glyc-R-R«-R«« --(CH3ONa)-- Glyc + ROCH3 + R«OCH3 + R««OCH3 + Na(+)

But we could assume that one mole of WVO will require one mole of Methanol,
as the methyl group in it is exactly what will join the FA in the
transesterification

So every 213.4g of WVO will require 32g of Methanol

Coconut oil«s density at 20¼C is close to 0.919 g/ml (or so I read on the
internet). So 213.4 g (1 mole) will equal 232.201 ml.

On the other side, the density for methanol is 0.79, so 32g of methanol
represent 40.5063 ml.

So, 40.5063 ml in 232.201 ml represent 17.44

The proposed value (M. Pelly«s recipe) is 20% by volume. The value we got to
here is 17.44%
That«s only 2.56% shorter than the proposed value. The 20% value is useful
to push the reaction towards the products side, anyway, you should be able
to use a minimum of 17.4% methanol (in volume) to transesterify your WVO.

I use sunflower oil, and my % is even lower (close to 11% in vol).


Hope to have been of help.

Best wishes,

Christian Lenoir


- Original Message -
From: Christian [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Monday, May 13, 2002 12:39 PM
Subject: Re: Stoichiometric Balance of methanol vs glycerine


 Hello Christian,

 First of all i want to thank you for your posts.  They have been very
 helpful and informative.

 I am Ken and from the Philippines.  I have been making BD for a year now
 thanks to this group.  I use what i make because the price of BD is not
 competitive to regular diesel.

 I was checking the stoichiometric balance of methanol to glycerine when i
 felt something

[biofuel] acetic acid + glycerin (to T)

2002-05-14 Thread Christian

For those who wondered, 

I ran the esterification product from glyc + acetic acid
(triacetato de glicerilo, in spanish.. I suppose in Eng it«s something like 
glycerin triacetate), and the program calculated a melting point of 29.53 ¼C, 
and a boiling point of 263.38 ¼C. That would make it solid at room temp, 
probably making it difficult to use as a fuel additive.

Regards,

Christian


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Re: [biofuel] Stoichiometric values

2002-05-15 Thread Christian

I can«t send HTML on this list, please make a list of those who would want
the mentioned table of FA content of different oils, and I«ll send it to
your personal email (off-list)
please send your request (for this particular table) to
[EMAIL PROTECTED] today.

Regards,

Christian

snip
 Could we figure out a table for the most common oils? Say soy,
 rapeseed/canola, corn, sunflower, cottonseed, peanut, olive, coconut,
 palm, tallow. That would be really useful. We'd need to know the FA
 breakdown of each, SG etc. There are some figures here for the main





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[biofuel] on line.

2002-11-14 Thread Christian Tirabassi

Psicologia del CNR:
Siglato l'accordo per la realizzazione di simulazioni ludico-didattiche basate 
su metodi sviluppati in campi di ricerca d'avanguardia quali l'intelligenza 
artificiale, le scienze cognitive, i sistemi neurali artificiali e gli 
algoritmi genetici. Tali simulazioni saranno utilizzate in previsione dello 
sviluppo di prodotti multimediali per le comunitˆ virtuali, la formazione a 
distanza, l'intrattenimento, l'edutainment.

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[biofuel] Got th job (to Keith... and others too)

2002-09-13 Thread Christian Lenoir

Dear Keith,

I«m just writing to let you know I was given the job in the U.S., at
Environmental Engineering  Technology, so if the US Consulate grants me
the H-1b visa, I«ll be able to go and live over there in Virginia in a
couple of months, after the firm (and it«s law office) has completed all the
paperwork.

I«m a bit off track with the biofuels list, though I«m still receiving it at
home. I«ve had little time to go through it, though, given I«ve been
arranging the job issue (I travelled to the US for the interview last
weekend) and with my graduation and everything.

I plant to keep in touch from time to time, as I have come to consider all
you guys as very good friends. Anyway, I«m not sure if I«ll be able to
continue as an active member, though I«ll check in from time to time.
Special thanks to all of you, but specially to Keith, Todd, Steve, Dana,
Ken, Craig and those who helped me with my first steps in the biodiesel
field.

Thanks for your constant support, and keep up the work the biofuels list
and the journey to forever page are two things you should really be proud
of, and I wish you the best of luck in those projects, as your effort has
enlightened and continues to enlighten the path of those who seek to deepen
their knowledge in this promising field. Your role as a mentor and leader I
value much, and I sincerely wish you all the best.

Sincerely,

Christian Lenoir
Buenos Aires, Argentina
member since mid 2001



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[biofuel] PHOTOS!!!! (BD, of course)

2002-05-04 Thread Christian Lenoir

Too see the photos of my first biodiesel batches, please visit:

http://www.clenoir.com/bd.htm

Best to you all,

Christian



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Re: [Biofuel] Japan Doubles Fukushima Radiation Leak Estimate

2011-06-08 Thread Christian Thalacker
Midori,

This is so sad.

I spent 4 years in Hokkaido as a masters student at Otaru University of 
Commerce.

I spent one month traveling throughout Japan in the Spring of 1999. 

It is hard to believe the damage inflicted.

Christian 

On Jun 08, 2011, at 07:59 AM, Midori Hiraga (JTF) [EMAIL PROTECTED] wrote:

Dear all,

2011/6/8 Keith Addison [EMAIL PROTECTED]:
 http://www.commondreams.org/headline/2011/06/07-1

 According to the latest estimates, 770,000 terabequerels - about 20%
 as much as the official estimate for Chernobyl - of radiation seeped
 from the plant in the week after the tsunami, more than double the
 initial estimate of 370,000.

That's the amount only to the air. 770,000 terabequerels doesn't
include the amount which has been leaking (or poured intentionally)
into the ocean.

Midori

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Re: [Biofuel] Call for Tax on Financial Deals to Fight Global Warming

2011-06-12 Thread Christian Thalacker
Solution:

Tax of 1 basis point on all bond, foreign exchange and commodity transactions 
in the primary (from the issuing entity) and secondary (transacted through a 
broker) markets.

Anything more than 1 basis point would be more altruistic.

Cheers, Christian


On Jun 11, 2011, at 11:13 AM, Keith Addison [EMAIL PROTECTED] wrote:

http://www.commondreams.org/headline/2011/06/08-1

Published on Wednesday, June 8, 2011 by The Irish Times

Call for Tax on Financial Deals to Fight Global Warming

by Frank MacDonald

A tax on international financial transactions could generate real 
funds immediately to help developing countries protect tropical rain 
forests and fight global warming, the latest round of climate talks 
in Bonn heard yesterday.

Bolivian ambassador Pablo Solon, who called on all countries to adopt 
such a tax, complained that most of the $30 billion in fast-start 
finance pledged by developed nations at the Copenhagen climate summit 
in 2009 had not come through.

Instead of countries re-branding aid as climate finance, he said, a 
tax on international financial transactions would be a mechanism 
that can generate real funds . . . to act immediately to address the 
protection of forests and fight climate change.

Mr Solon also called for the Kyoto Protocol to be renewed at the 
Durban climate summit in December, on the basis that there was no 
time to negotiate new legally binding treaty aimed at cutting 
greenhouse gas emissions in developed countries. We cannot come out 
of South Africa with the targets we have now, as the UN Environment 
Programme has shown they will lead us to 4 degrees Celsius of global 
warming. We must have targets that limit temperature rise to between 
1C and 1.5C to preserve life.

More than 3,000 participants from 183 countries are attending the 
two-week session in Bonn, which is meant to lay the groundwork for 
Durban. But few believe that progress will be made on crunch issues 
such as a renewal of Kyoto, which expires next year.

Last week carbon dioxide in the atmosphere reached the highest level 
ever recorded, at nearly 390 parts per million, and the International 
Energy Agency said emissions from energy generation in 2010 were also 
the highest ever - despite the recession.

With carbon emissions at record highs, it's clear that policymakers 
are out of step with the speed of climate change in the real world, 
said Greenpeace's climate policy co-ordinator Tove Maria Ryding. 
[They] need to start delivering proven solutions.

UN climate chief Christiana Figueres said at the opening session that 
governments have an unavoidable responsibility to make clear 
progress towards the 2011 climate objectives which they had agreed 
in at the Cancún climate conference last December.

Governments lit a beacon in Cancún towards a low-emission world 
which is resilient to climate change. They committed themselves to a 
maximum global average temperature rise of 2 degrees Celsius, with 
further consideration of a 1.5 degree maximum.

Now, more than ever, it is critical that all efforts are mobilised 
towards living up to this commitment, Ms Figueres said, adding that 
negotiators were working hard to provide clarity on the architecture 
of the future international climate regime to reduce emissions.

Separately, 18 Greenpeace activists who scaled an Arctic oil rig off 
the coast of Greenland have been arrested. They were demanding that 
operators Cairn Energy reveal its plans to deal with potential oil 
spills.

Cairn Energy had sought an injunction against Greenpeace protesting 
against its operations in the Arctic region. But when the matter came 
before a court in Amsterdam on Monday, the judge also asked the 
company to make its oil spill response plan public.

A final ruling on the injunction application is due tomorrow.

© 2011 The Irish Times


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[Biofuel] Can anyone direct me to the four papers referenced in the NBB article here?

2011-06-30 Thread Christian Thalacker
I am looking for the four full articles/presentations referenced in the 
footnotes:
http://www.biodiesel.org/pdf_files/fuelfactsheets/Lubricity.PDF 

Any additional, relevant articles appreciated.

Christian
Email: [EMAIL PROTECTED]

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[Biofuel] Marc I launched our Biodiesel Co-op in Kentucky and ...

2011-07-16 Thread Christian Thalacker
.. to the question, do community co-ops matter? the answer is: YES!

Do Community Co-Ops Matter?
RFS2 mandates biodiesel production, but local communities need a cooperative 
approach

Eric Williams used to work as a civil engineer in a building owned by a farmer 
co-op that, among many things, made soy biodiesel. Today, Williams works in 
energy efficiency in Omaha and every Friday night he joins up with the members 
of his own co-op, architects, graduate students, financial consultants and 
anyone else interested in making biodiesel. “We realized that it is more 
effective to process the fuels then it would be for any of us to work alone,” 
Williams says. With the help of those architects and financial consultants, he 
formed the Omaha Biofuels Coop, a licensed producer-consumer operation that 
touts the motto: producing, using and promoting biofuels. Back in 2006 as a 
civil engineer, Williams says he also realized that even with large biodiesel 
production facilities scattered across the country, “there were very few 
options for cars in the area to use biodiesel.”


Times have changed since 2006, and today the average driver has greater access 
to biodiesel than ever before (which, unfortunately in some cases, still isn’t 
that great). But, more gallons of available biodiesel haven’t put an end to 
stories like those of Williams and the Omaha Biofuels Coop. In fact, more 
biodiesel co-ops are meeting on Friday nights, sometimes on the loading dock of 
their industrial buildings, than ever before. For a nominal fee, co-op members 
can fill up their Volkswagen diesels, Ford F-250s or even their John Deeres, 
but don’t confuse their stories with a nice back-page feature in the Sunday 
Life section of the local newspaper.


Biodiesel co-ops are doing their part in the continued growth of the industry 
one 5-gallon jug of waste vegetable oil (WVO)  biodiesel at a time. If the 5 
MMgy producers are working to provide an advanced biofuel for mass use, it’s 
the 5-gallon folks who are working to help the end-users understand why such a 
fuel is so special in the first place. Don’t believe it? Think about all the 
times someone you know, or have read about, has made a misinformed statement 
about a biofuel’s negative properties. Eric Williams speaks to people like that 
every day, and every day, he says, his co-op is growing.


Keeping it Rural Matters


Christian Thalacker wasn’t a civil engineer before he started the Louisville 
Biodiesel Cooperative, he was an energy consultant who bought and sold for a 
large wholesale energy company. And, unlike Williams, Thalacker doesn’t cater 
to urban drivers (although he would). Thalacker, along with co-founder Marc 
Verdi, is aiming to supply biodiesel and grow his cooperative by providing 
farmers, particularly family farmers, with biodiesel. His approach is to keep 
his fuel local, and help small cattle operations or horse ranchers in the 
region save a few dollars by purchasing biodiesel from his cooperative that he 
says will be priced lower than the going rate for petro diesel today “You look 
at all the pressures that family farms have, and family ranchers have,” he 
says, “and $4 petrodiesel seems insane.”


Thalacker estimates that the average local farmer in his area uses roughly 
3,000 gallons of fuel per season. Although his co-op is rather new, it started 
in November, he says that farmers in his area (about 70) would love to have 
biodiesel available and “as soon as it is ready,” he adds, “they are ready to 
buy.” The Louisville Biodiesel Cooperative offers up one of the greatest 
benefits of the growing number of co-ops across the country Their model of 
staying local, and being as green and transparent as possible is one that 
nearly every co-op is adopting in its own way, and is a positive medium to 
create a network of public and private relationships of businesses and 
consumers, all holding the same opinion of biodiesel.


“There is a resonance with the restaurants,” he says of the places he collects 
the WVO used to produce his product. “There is a resonance with the big 
commercial-size kitchens,” a mutual feeling he says both parties believe in. 
Thalacker says he isn’t reinventing the wheel though, he’s simply trying to 
mimic the operational standards of arguably the most successful biodiesel co-op 
in the country, Piedmont Biofuels, a co-op he’s talked with several times. He’s 
also trying to take the same approach as people in places like Austin, Texas, 
or Chapel Hill, N.C., who he says are giving back to the restaurants that 
donate their WVO to the co-ops by performing as much marketing as possible for 
those establishments.


While Thalacker does say he has to compete in his area with “the big players” 
who collect WVO for use as animal feed, he might be encouraged to know that 
people like John Campbell, vice president of government relations for Ag 
Processing Inc., an original player in the biodiesel industry, and the model of 
how

[Biofuel] Has anyone seen the 2010 B100 Biodiesel survey from the National Renewable Energy Laboratory?

2011-09-15 Thread Christian Thalacker
Has anyone seen the 2010 B100 Biodiesel survey from the National Renewable 
Energy Laboratory?
If so, please share the link: 

A few National Renewable Energy Lab documents  video on Biodiesel going back 
to 2005

2011: nothing on B100 yet?
B20: http://www.houston-cleancities.org/Clean%20Cities%20Pages/Coalition%20Events/4-27-2011/NREL.pdf
2010: ?
2009: B100 survey?
Biodiesel status 
report: http://www1.eere.energy.gov/cleancities/pdfs/bd_status_issues_final.pdf
http://www.nrel.gov/vehiclesandfuels/npbf/pdfs/44833.pdf
2 NREL video presentations + 1 combined 
MB/Audi/VW/BMW/Bosch http://www.dieselforum.org/index.cfm?objectid=2FB6D266-AF06-11E0-ABD4000C296BA163
my take-away comment: 
NREL sees negligible differences performance-wise between ASTM-spec Biodiesel 
and petro-diesel
versus Walter the Mercedes Benz spokesman 
pushing the urea-exhaust system while admitting quality of hydro-treated 
vegetable oil
versus BP's Rich George talking about the fungible nature of biodiesel versus 
petro diesel
blames the states' individual laws and UL not approving more than 5% use at 
retailers
importance of ASTM spec fuel if big players can distribute biodiesel ... 
Most pipelines don't carry biodiesel = competes with jetfuel
movement to put 100 parts per million of biodiesel with jetfuel ... 
slow movement to B5
expensive to have terminal with heated storage tanks and pipes to carry 
biodiesel 365
business as usual = splash blend
2008: B20 http://www.nrel.gov/vehiclesandfuels/npbf/pdfs/45184.pdf
2007: B100: http://www.nrel.gov/docs/fy08osti/42787.pdf
2006: B100: http://www.nrel.gov/docs/fy07osti/41549.pdf
2005: B100 survey?
Effects of Biodiesel: http://www.nrel.gov/vehiclesandfuels/npbf/pdfs/38296.pdf


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Re: [Biofuel] Capitalism vs. the Climate - Naomi Klein

2011-12-13 Thread Christian Thalacker
The Heartland Institute is a loud  proud  sponsor at various conferences 
(EUEC in Phoenix)  news aggregators (epOverviews) ... 

Wish Stewart @ the Daily Show would make them a weekly feature. 

On Dec 11, 2011, at 1:01 PM, Keith Addison [EMAIL PROTECTED] wrote:

 Heartland Institute - SourceWatch
 http://www.sourcewatch.org/index.php?title=Heartland_Institute
 
 --
 
 http://www.thenation.com/article/164497/capitalism-vs-climate
 
 Capitalism vs. the Climate
 
 Naomi Klein
 
 November 9, 2011
 
 There is a question from a gentleman in the fourth row.
 
 He introduces himself as Richard Rothschild. He tells the crowd that 
 he ran for county commissioner in Maryland's Carroll County because 
 he had come to the conclusion that policies to combat global warming 
 were actually an attack on middle-class American capitalism. His 
 question for the panelists, gathered in a Washington, DC, Marriott 
 Hotel in late June, is this: To what extent is this entire movement 
 simply a green Trojan horse, whose belly is full with red Marxist 
 socioeconomic doctrine?
 
 Here at the Heartland Institute's Sixth International Conference on 
 Climate Change, the premier gathering for those dedicated to denying 
 the overwhelming scientific consensus that human activity is warming 
 the planet, this qualifies as a rhetorical question. Like asking a 
 meeting of German central bankers if Greeks are untrustworthy. Still, 
 the panelists aren't going to pass up an opportunity to tell the 
 questioner just how right he is.
 
 Chris Horner, a senior fellow at the Competitive Enterprise Institute 
 who specializes in harassing climate scientists with nuisance 
 lawsuits and Freedom of Information fishing expeditions, angles the 
 table mic over to his mouth. You can believe this is about the 
 climate, he says darkly, and many people do, but it's not a 
 reasonable belief. Horner, whose prematurely silver hair makes him 
 look like a right-wing Anderson Cooper, likes to invoke Saul Alinsky: 
 The issue isn't the issue. The issue, apparently, is that no free 
 society would do to itself what this agenda requiresŠ. The first step 
 to that is to remove these nagging freedoms that keep getting in the 
 way.
 
 Claiming that climate change is a plot to steal American freedom is 
 rather tame by Heartland standards. Over the course of this two-day 
 conference, I will learn that Obama's campaign promise to support 
 locally owned biofuels refineries was really about green 
 communitarianism, akin to the Maoist scheme to put a pig iron 
 furnace in everybody's backyard (the Cato Institute's Patrick 
 Michaels). That climate change is a stalking horse for National 
 Socialism (former Republican senator and retired astronaut Harrison 
 Schmitt). And that environmentalists are like Aztec priests, 
 sacrificing countless people to appease the gods and change the 
 weather (Marc Morano, editor of the denialists' go-to website, 
 ClimateDepot.com).
 
 Most of all, however, I will hear versions of the opinion expressed 
 by the county commissioner in the fourth row: that climate change is 
 a Trojan horse designed to abolish capitalism and replace it with 
 some kind of eco-socialism. As conference speaker Larry Bell 
 succinctly puts it in his new book Climate of Corruption, climate 
 change has little to do with the state of the environment and much 
 to do with shackling capitalism and transforming the American way of 
 life in the interests of global wealth redistribution.
 
 Yes, sure, there is a pretense that the delegates' rejection of 
 climate science is rooted in serious disagreement about the data. And 
 the organizers go to some lengths to mimic credible scientific 
 conferences, calling the gathering Restoring the Scientific Method 
 and even adopting the organizational acronym ICCC, a mere one letter 
 off from the world's leading authority on climate change, the 
 Intergovernmental Panel on Climate Change (IPCC). But the scientific 
 theories presented here are old and long discredited. And no attempt 
 is made to explain why each speaker seems to contradict the next. (Is 
 there no warming, or is there warming but it's not a problem? And if 
 there is no warming, then what's all this talk about sunspots causing 
 temperatures to rise?)
 
 In truth, several members of the mostly elderly audience seem to doze 
 off while the temperature graphs are projected. They come to life 
 only when the rock stars of the movement take the stage-not the 
 C-team scientists but the A-team ideological warriors like Morano and 
 Horner. This is the true purpose of the gathering: providing a forum 
 for die-hard denialists to collect the rhetorical baseball bats with 
 which they will club environmentalists and climate scientists in the 
 weeks and months to come. The talking points first tested here will 
 jam the comment sections beneath every article and YouTube video that 
 contains the phrase climate change or global warming. They 

Re: [Biofuel] Capitalism vs. the Climate - Naomi Klein

2011-12-14 Thread Christian Thalacker
Keith,

As to why the Heartland Institute is a repeat sponsor at serious energy+ 
conferences and news aggregators, ask the Directors  Owners of the two 
respective firms mentioned:

1. EUEC
    http://www.euec.com/directors.aspx
        

2. epOverviews
    http://www.epoverviews.com/about.php 

Best, 

Christian


On Dec 13, 2011, at 06:56 PM, Keith Addison [EMAIL PROTECTED] wrote:

Hello Christian

The Heartland Institute is a loud  proud  sponsor at various 
conferences (EUEC in Phoenix)  news aggregators (epOverviews) ...

Wish Stewart @ the Daily Show would make them a weekly feature.

Why?

Best

Keith


On Dec 11, 2011, at 1:01 PM, Keith Addison [EMAIL PROTECTED] wrote:

 Heartland Institute - SourceWatch
 http://www.sourcewatch.org/indexphp?title=Heartland_Institute

 --

 http://www.thenation.com/article/164497/capitalism-vs-climate

 Capitalism vs. the Climate

 Naomi Klein

 November 9, 2011

 There is a question from a gentleman in the fourth row.

 He introduces himself as Richard Rothschild. He tells the crowd that
 he ran for county commissioner in Maryland's Carroll County because
 he had come to the conclusion that policies to combat global warming
 were actually an attack on middle-class American capitalism. His
 question for the panelists, gathered in a Washington, DC, Marriott
 Hotel in late June, is this: To what extent is this entire movement
 simply a green Trojan horse, whose belly is full with red Marxist
 socioeconomic doctrine?

 Here at the Heartland Institute's Sixth International Conference on
 Climate Change, the premier gathering for those dedicated to denying
 the overwhelming scientific consensus that human activity is warming
 the planet, this qualifies as a rhetorical question. Like asking a
 meeting of German central bankers if Greeks are untrustworthy. Still,
 the panelists aren't going to pass up an opportunity to tell the
 questioner just how right he is.

 Chris Horner, a senior fellow at the Competitive Enterprise Institute
 who specializes in harassing climate scientists with nuisance
 lawsuits and Freedom of Information fishing expeditions, angles the
 table mic over to his mouth. You can believe this is about the
 climate, he says darkly, and many people do, but it's not a
 reasonable belief. Horner, whose prematurely silver hair makes him
 look like a right-wing Anderson Cooper, likes to invoke Saul Alinsky:
 The issue isn't the issue. The issue, apparently, is that no free
 society would do to itself what this agenda requires·. The first step
 to that is to remove these nagging freedoms that keep getting in the
 way.

 Claiming that climate change is a plot to steal American freedom is
 rather tame by Heartland standards. Over the course of this two-day
 conference, I will learn that Obama's campaign promise to support
 locally owned biofuels refineries was really about green
 communitarianism, akin to the Maoist scheme to put a pig iron
 furnace in everybody's backyard (the Cato Institute's Patrick
 Michaels). That climate change is a stalking horse for National
 Socialism (former Republican senator and retired astronaut Harrison
 Schmitt). And that environmentalists are like Aztec priests,
 sacrificing countless people to appease the gods and change the
 weather (Marc Morano, editor of the denialists' go-to website,
 ClimateDepot.com).

 Most of all, however, I will hear versions of the opinion expressed
 by the county commissioner in the fourth row: that climate change is
 a Trojan horse designed to abolish capitalism and replace it with
 some kind of eco-socialism. As conference speaker Larry Bell
 succinctly puts it in his new book Climate of Corruption, climate
 change has little to do with the state of the environment and much
 to do with shackling capitalism and transforming the American way of
 life in the interests of global wealth redistribution.

 Yes, sure, there is a pretense that the delegates' rejection of
 climate science is rooted in serious disagreement about the data. And
 the organizers go to some lengths to mimic credible scientific
 conferences, calling the gathering Restoring the Scientific Method
 and even adopting the organizational acronym ICCC, a mere one letter
  off from the world's leading authority on climate change, the
 Intergovernmental Panel on Climate Change (IPCC). But the scientific
 theories presented here are old and long discredited. And no attempt
 is made to explain why each speaker seems to contradict the next. (Is
 there no warming, or is there warming but it's not a problem? And if
 there is no warming, then what's all this talk about sunspots causing
 temperatures to rise?)

 In truth, several members of the mostly elderly audience seem to doze
 off while the temperature graphs are projected. They come to life
 only when the rock stars of the movement take the stage-not the
 C-team scientists but the A-team ideological warriors like Morano and
 Horner. This is the true purpose

Re: [Biofuel] Capitalism vs. the Climate - Naomi Klein

2011-12-14 Thread Christian Thalacker
Well Keith, 

Dollars to donuts: 

Stewart @ the Daily Show (and other independent minded citizens like myself) 
find the militant we can piss in the soup, who cares! modus operandi of 
Heartland Institute guests, staff  directors funny at best.

Except, not really funny.

Examples:

7/10 on the Militant-We-Can-Piss-in-the-Soup!-o-meter: 
http://blog.heartland.org/2011/12/coca-cola-playing-a-dangerous-game-by-cuddling-with-environmentalists/

2/10 on the Militant-We-Can-Piss-in-the-Soup!-o-meter: 
http://blog.heartland.org/2011/12/getting-the-enron-story-straight/

10/10 on the Militant-We-Can-Piss-in-the-Soup!-o-meter:
http://news.heartland.org/newspaper-article/2011/12/01/climate-change-weekly-climategate-2-reveals-more-destruction-evidence-s
http://news.heartland.org/newspaper-article/2011/12/09/climategate-conspirator-mann-plays-persecuted-victim

I wish the Daily Show's Stewart would host the Heartland Institute's Managing 
Director James M. Taylor (http://heartland.org/james-m-taylor) and Science 
Director Jay Leher (http://heartland.org/jay-lehr) on the show ...

A little light can go a long way.

Christian

On Dec 14, 2011, at 10:24 AM, Keith Addison [EMAIL PROTECTED] wrote:

No, that's not what I asked.

 Wish Stewart @ the Daily Show would make them a weekly feature.

Why?

Best

Keith


Keith,

As to why the Heartland Institute is a repeat sponsor at serious 
energy+ conferences and news aggregators, ask the Directors  Owners 
of the two respective firms mentioned:

1. EUEC
 http://www.euec.com/directors.aspx
 

2. epOverviews
 http://www.epoverviews.com/about.php 

Best, 

Christian


On Dec 13, 2011, at 06:56 PM, Keith Addison 
[EMAIL PROTECTED] wrote:

Hello Christian

The Heartland Institute is a loud  proud  sponsor at various
conferences (EUEC in Phoenix)  news aggregators (epOverviews) ...

 Wish Stewart @ the Daily Show would make them a weekly feature.

Why?

Best

Keith


On Dec 11, 2011, at 1:01 PM, Keith Addison 
[EMAIL PROTECTED] wrote:

 Heartland Institute - SourceWatch
 http://www.sourcewatch.org/indexphp?title=Heartland_Institute

 --

 http://www.thenation.com/article/164497/capitalism-vs-climate

 Capitalism vs. the Climate

 Naomi Klein

 November 9, 2011

 There is a question from a gentleman in the fourth row.

 He introduces himself as Richard Rothschild He tells the crowd that
 he ran for county commissioner in Maryland's Carroll County because
 he had come to the conclusion that policies to combat global warming
 were actually an attack on middle-class American capitalism. His
 question for the panelists, gathered in a Washington, DC, Marriott
 Hotel in late June, is this: To what extent is this entire movement
 simply a green Trojan horse, whose belly is full with red Marxist
 socioeconomic doctrine?

 Here at the Heartland Institute's Sixth International Conference on
 Climate Change, the premier gathering for those dedicated to denying
 the overwhelming scientific consensus that human activity is warming
 the planet, this qualifies as a rhetorical question. Like asking a
 meeting of German central bankers if Greeks are untrustworthy. Still,
 the panelists aren't going to pass up an opportunity to tell the
 questioner just how right he is.

 Chris Horner, a senior fellow at the Competitive Enterprise Institute
 who specializes in harassing climate scientists with nuisance
 lawsuits and Freedom of Information fishing expeditions, angles the
  table mic over to his mouth. You can believe this is about the
 climate, he says darkly, and many people do, but it's not a
 reasonable belief. Horner, whose prematurely silver hair makes him
 look like a right-wing Anderson Cooper, likes to invoke Saul Alinsky:
 The issue isn't the issue. The issue, apparently, is that no free
 society would do to itself what this agenda requires·. The first step
 to that is to remove these nagging freedoms that keep getting in the
 way.

 Claiming that climate change is a plot to steal American freedom is
 rather tame by Heartland standards. Over the course of this two-day
 conference, I will learn that Obama's campaign promise to support
 locally owned biofuels refineries was really about green
 communitarianism, akin to the Maoist scheme to put a pig iron
 furnace in everybody's backyard (the Cato Institute's Patrick
 Michaels). That climate change is a stalking horse for National
 Socialism (former Republican senator and retired astronaut Harrison
 Schmitt). And that environmentalists are like Aztec priests,
 sacrificing countless people to appease the gods and change the
 weather (Marc Morano, editor of the denialists' go-to website,
 ClimateDepot.com).

 Most of all, however, I will hear versions of the opinion expressed
 by the county commissioner in the fourth row: that climate change is
 a Trojan horse designed to abolish capitalism and replace it with
 some kind of eco-socialism. As conference speaker Larry Bell
 succinctly puts it in his new book Climate of Corruption, climate

Re: [Biofuel] Capitalism vs. the Climate - Naomi Klein

2011-12-14 Thread Christian Thalacker
Well Keith, 

Dollars to donuts: 

Stewart @ the Daily Show (and other independent minded citizens like myself) 
find the militant we can piss in the soup, who cares! modus operandi of 
Heartland Institute guests, staff  directors funny at best.

Except, not really funny.

Examples:
7/10 on the Militant-We-Can-Piss-in-the-Soup!-o-meter: 
http://blog.heartland.org/2011/12/coca-cola-playing-a-dangerous-game-by-cuddling-with-environmentalists/
2/10 on the Militant-We-Can-Piss-in-the-Soup!-o-meter: 
http://blog.heartland.org/2011/12/getting-the-enron-story-straight/
10/10 on the Militant-We-Can-Piss-in-the-Soup!-o-meter:
http://news.heartland.org/newspaper-article/2011/12/01/climate-change-weekly-climategate-2-reveals-more-destruction-evidence-s
http://news.heartland.org/newspaper-article/2011/12/09/climategate-conspirator-mann-plays-persecuted-victim

I wish the Daily Show's Stewart would have the Heartland Institute's Managing 
Director James M. Taylor (http://heartland.org/james-m-taylor) and Science 
Director Jay Leher (http://heartland.org/jay-lehr) on the show ...

A little light can go a long way.

Christian

On Dec 14, 2011, at 10:24 AM, Keith Addison [EMAIL PROTECTED] wrote:

No, that's not what I asked.

Wish Stewart @ the Daily Show would make them a weekly feature.

Why?

Best

Keith
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Re: [Biofuel] Capitalism vs. the Climate - Naomi Klein

2011-12-14 Thread Christian Thalacker
Hi Keith,

You don't sound ratty.

Like Mark Twain? Then you'll love John Stewart @ the Daily Show.

Extended interviews available for free online:

http://www.thedailyshow.com/extended-interviews
Examples

Cheers,

Christian

On Dec 14, 2011, at 12:24 PM, Keith Addison [EMAIL PROTECTED] wrote:

Sorry Christian, I didn't mean to sound ratty. I just don't get it, I 
don't know anything about Stewart @ the Daily Show. How would it help?

By the way:
http://www.mail-archive.com/search?q=Heartland+Institutel=sustainablelorgbiofuel%40sustainablelists.org
55 hits at the List archives for Heartland Institute.

Best

Keith


No, that's not what I asked.

  Wish Stewart @ the Daily Show would make them a weekly feature.

Why?

Best

Keith


Keith,

 As to why the Heartland Institute is a repeat sponsor at serious
energy+ conferences and news aggregators, ask the Directors  Owners
of the two respective firms mentioned:

1. EUEC
 http://www.euec.com/directors.aspx
 

2. epOverviews
 http://www.epoverviews.com/about.php

Best,

Christian


On Dec 13, 2011, at 06:56 PM, Keith Addison
[EMAIL PROTECTED] wrote:

Hello Christian

The Heartland Institute is a loud  proud  sponsor at various
conferences (EUEC in Phoenix)  news aggregators (epOverviews) ...

 Wish Stewart @ the Daily Show would make them a weekly feature.

Why?

Best

Keith


On Dec 11, 2011, at 1:01 PM, Keith Addison
[EMAIL PROTECTED] wrote:

 Heartland Institute - SourceWatch
 http://www.sourcewatch.org/indexphp?title=Heartland_Institute

 --

 http://www.thenation.com/article/164497/capitalism-vs-climate

 Capitalism vs. the Climate

 Naomi Klein

 November 9, 2011

 There is a question from a gentleman in the fourth row.

 He introduces himself as Richard Rothschild He tells the crowd that
 he ran for county commissioner in Maryland's Carroll County because
 he had come to the conclusion that policies to combat global warming
 were actually an attack on middle-class American capitalism. His
 question for the panelists, gathered in a Washington, DC, Marriott
 Hotel in late June, is this: To what extent is this entire movement
 simply a green Trojan horse, whose belly is full with red Marxist
 socioeconomic doctrine?

 Here at the Heartland Institute's Sixth International Conference on
 Climate Change, the premier gathering for those dedicated to denying
 the overwhelming scientific consensus that human activity is warming
 the planet, this qualifies as a rhetorical question. Like asking a
 meeting of German central bankers if Greeks are untrustworthy. Still,
 the panelists aren't going to pass up an opportunity to tell the
  questioner just how right he is.

snip

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Re: [Biofuel] Capitalism vs. the Climate - Naomi Klein

2011-12-15 Thread Christian Thalacker
Keith,

To better understand the companies  people that the Heartland Institute thinks 
their message resonates with, the attached PDF from the upcoming EUEC (Energy, 
Utility  Environment Conference) conference may be helpful. There is also a 
copy of the PDF stored on Google Documents:

https://docs.google.com/open?id=0B83-0weSlvJvYzVlMzYxMWMtYjIzMi00MzIzLWE4ZTctMTQxMmU5YmU4OTRh

The Heartland Institute will be speaking as a conference co-sponsor (see below).

Some of the session titles include:

REDUCING THE CARBON FOOTPRINT IN THE AMERICAS: IS IT WORTH THE COST? James 
Taylor, Senior Fellow, Environment Policy, The Heartland Institute
AIR QUALITY REGULATORY CHALLENGES FOR POWER GENERATORS IN 2012 
UPDATE TO UNITS AT RISK FOR RETIREMENT IN PJM AS A RESULT OF EPA REGULATION
WHAT ABOUT THE NEIGHBORS? ENVIRONMENTAL NUISANCE CLAIMS AND AIR QUALITY 
COMPLIANCE
IMPACT OF SOLID WASTE REGULATION ON ALTERNATIVE FUEL
NO. 6 OIL USE UNDER THE EGU MACT RULE6 OIL USE UNDER THE EGU MACT RULE
FEDERAL GHG REGULATION: IMPLICATIONS FOR BUSINESS
RECENT TRENDS IN EPA AND ACTIVIST GROUP AIR PERMIT CHALLENGE
IMPLICATIONS OF EPA’S PROPOSED CLEAN WATER ACT 316(B) REGULATIONS ON THE POWER 
INDUSTRY
THE FUTURE OF FLYASH AS A CEMENTITIOUS MATERIAL 
ENSURING OPTIMAL COMPLIANCE WITH FUTURE MERCURY REGULATIONS
CARBON TAX OR “CAP-AND-TRADE” SYSTEMS  ITS EFFECT ON U S. REFINING MARKETING
THE CONTINUING SHALE GAS STAMPEDE
SPILLS, SINS  STARBUCKS: HOW WE DESIGNED OUR CITIES AROUND OILS, SINS  
STARBUCKS
BRINGING ENERGY AND SUSTAINABILITY REPORTING INTO THE 21ST CENTURY
NUCLEAR POWER IN A POST-FUKUSHIMA WORLD

Cheers,

Christian

On Dec 13, 2011, at 06:56 PM, Keith Addison [EMAIL PROTECTED] wrote:

Hello Christian

The Heartland Institute is a loud  proud  sponsor at various 
conferences (EUEC in Phoenix)  news aggregators (epOverviews) ...

Wish Stewart @ the Daily Show would make them a weekly feature.

Why?

Best

Keith


On Dec 11, 2011, at 1:01 PM, Keith Addison [EMAIL PROTECTED] wrote:

 Heartland Institute - SourceWatch
 http://www.sourcewatch.org/index.php?title=Heartland_Institute

 --

 http://www.thenation.com/article/164497/capitalism-vs-climate

 Capitalism vs. the Climate

 Naomi Klein

 November 9, 2011

 There is a question from a gentleman in the fourth row.

 He introduces himself as Richard Rothschild. He tells the crowd that
 he ran for county commissioner in Maryland's Carroll County because
 he had come to the conclusion that policies to combat global warming
 were actually an attack on middle-class American capitalism. His
 question for the panelists, gathered in a Washington, DC, Marriott
 Hotel in late June, is this: To what extent is this entire movement
 simply a green Trojan horse, whose belly is full with red Marxist
 socioeconomic doctrine?

 Here at the Heartland Institute's Sixth International Conference on
 Climate Change, the premier gathering for those dedicated to denying
 the overwhelming scientific consensus that human activity is warming
 the planet, this qualifies as a rhetorical question. Like asking a
 meeting of German central bankers if Greeks are untrustworthy. Still,
 the panelists aren't going to pass up an opportunity to tell the
 questioner just how right he is.

 Chris Horner, a senior fellow at the Competitive Enterprise Institute
 who specializes in harassing climate scientists with nuisance
 lawsuits and Freedom of Information fishing expeditions, angles the
 table mic over to his mouth. You can believe this is about the
 climate, he says darkly, and many people do, but it's not a
 reasonable belief. Horner, whose prematurely silver hair makes him
 look like a right-wing Anderson Cooper, likes to invoke Saul Alinsky:
 The issue isn't the issue. The issue, apparently, is that no free
 society would do to itself what this agenda requires· The first step
 to that is to remove these nagging freedoms that keep getting in the
 way.

 Claiming that climate change is a plot to steal American freedom is
 rather tame by Heartland standards. Over the course of this two-day
 conference, I will learn that Obama's campaign promise to support
 locally owned biofuels refineries was really about green
 communitarianism, akin to the Maoist scheme to put a pig iron
 furnace in everybody's backyard (the Cato Institute's Patrick
 Michaels). That climate change is a stalking horse for National
 Socialism (former Republican senator and retired astronaut Harrison
 Schmitt). And that environmentalists are like Aztec priests,
 sacrificing countless people to appease the gods and change the
 weather (Marc Morano, editor of the denialists' go-to website,
 ClimateDepot.com).

 Most of all, however, I will hear versions of the opinion expressed
 by the county commissioner in the fourth row: that climate change is
 a Trojan horse designed to abolish capitalism and replace it with
 some kind of eco-socialism. As conference speaker Larry Bell
 succinctly puts it in his new book Climate of Corruption, climate