[Biofuel] Test, please ignore

2013-05-21 Thread Chip Mefford
Changes to the email system behind the list, 
Just checking to see if they are working. 
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[Biofuel] Test drilling for methane to start

2012-02-04 Thread Keith Addison
http://www.japantimes.co.jp/text/nb20120203a4.html

Friday, Feb. 3, 2012

Test drilling for methane to start

Kyodo

NAGOYA - Japan Oil, Gas and Metals National Corp. said Thursday 
preparatory drilling will start around Feb. 14 in Pacific waters off 
central Japan for the world's first seabed methane hydrate production 
tests early next year.

The government-controlled corporation said it and Japan Petroleum 
Exploration Co. plan to launch commercial production in fiscal 2018 
if the tests prove successful.

Methane hydrate, a sherbetlike substance consisting of methane gas 
trapped in ice below the seabed or permanently frozen ground, is 
viewed as a promising next-generation energy source.

We will proceed with research in a bid to contribute to future 
natural gas supply, a JOGMEC official told a press conference.

JOGMEC and Japan Petroleum Exploration will use the deep-sea 
exploration vessel Chikyu of the Japan Agency for Marine-Earth 
Science and Technology to drill four wells up to 300 meters below the 
seabed in 1-km-deep waters 70 to 80 km south of the Atsumi Peninsula, 
Aichi Prefecture, through late March.

Methane hydrate deposits there are estimated at 1 trillion cu. 
meters, enough to supply more than 10 years' worth of natural gas 
consumed in Japan.

If the production tests to be conducted along with an environmental 
effects assessment in the first quarter of 2013 are successful, 
JOGMEC and Japan Petroleum Exploration will conduct additional tests 
in or after fiscal 2016 to ascertain actual production volume.

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Re: [Biofuel] Test drilling for methane to start

2012-02-04 Thread Jason Mier

there's a theory about the bermuda triangle, that when disturbed, these 
hydrates burst (for lack of better terms) and the bubble is large enough to 
sink a ship wholesale, thus the stories of mysterious lost ships.
even if mining hydrates *was* a good idea, i'd be concerned about the crew of 
the survey vessel...
 

 Date: Sat, 4 Feb 2012 21:54:23 +0200
 To: biofuel@sustainablelists.org
 From: [EMAIL PROTECTED]
 Subject: [Biofuel] Test drilling for methane to start
 
 http://www.japantimes.co.jp/text/nb20120203a4.html
 
 Friday, Feb. 3, 2012
 
 Test drilling for methane to start
 
 Kyodo
 
 NAGOYA - Japan Oil, Gas and Metals National Corp. said Thursday 
 preparatory drilling will start around Feb. 14 in Pacific waters off 
 central Japan for the world's first seabed methane hydrate production 
 tests early next year.
 
 The government-controlled corporation said it and Japan Petroleum 
 Exploration Co. plan to launch commercial production in fiscal 2018 
 if the tests prove successful.
 
 Methane hydrate, a sherbetlike substance consisting of methane gas 
 trapped in ice below the seabed or permanently frozen ground, is 
 viewed as a promising next-generation energy source.
 
 We will proceed with research in a bid to contribute to future 
 natural gas supply, a JOGMEC official told a press conference.
 
 JOGMEC and Japan Petroleum Exploration will use the deep-sea 
 exploration vessel Chikyu of the Japan Agency for Marine-Earth 
 Science and Technology to drill four wells up to 300 meters below the 
 seabed in 1-km-deep waters 70 to 80 km south of the Atsumi Peninsula, 
 Aichi Prefecture, through late March.
 
 Methane hydrate deposits there are estimated at 1 trillion cu. 
 meters, enough to supply more than 10 years' worth of natural gas 
 consumed in Japan.
 
 If the production tests to be conducted along with an environmental 
 effects assessment in the first quarter of 2013 are successful, 
 JOGMEC and Japan Petroleum Exploration will conduct additional tests 
 in or after fiscal 2016 to ascertain actual production volume.
 
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[Biofuel] Test Batch on Worst WVO ever

2008-05-29 Thread Thomas Kelly
 I ran a 0.5L test batch using the single stage base method on WVO that 
titrated 19 g KOH/L.
Results:
- No split/no glycerine dropped out.
- Wash test on the mix  bubbly emulsion.

- FFAs dissolve in methanol. This WVO does not dissolve completely. 
- FFAs that I split from the glyc mix titrate about 33.5g KOH/L. The WVO 
titrated 19.
This suggests that there are at least some glycerides in the oil. Why didn't 
they convert to BD  some glycerine drop out?

   Tom

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Re: [Biofuel] Test Batches with Peanut Oil

2008-04-09 Thread Doug Turner
Hi Tom,

  Perhaps Roger is partially or completely colour blind.  As part of the 7
to 10% of the male population that is colour blind, I fully understand
wanting, or rather needing, to use a pH meter.  Most titration indicators
rely upon colour changes I find that are difficult to detect, at least with
any accuracy.  I would be interested in finding out if there are any other
options, other than a pH meter or a titration test, for determining the pH
of a solution.

  Doug Turner,
  Hamilton

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] Behalf Of
Thomas Kelly
Sent: Thursday, April 03, 2008 1:25 PM
To: sustainablelorgbiofuel@sustainablelists.org
Subject: Re: [Biofuel] Test Batches with Peanut Oil


Roger,
  Freshly opened 55 gal drums of methanol usually are good.
By the time you get to the bottom of barrel there is often water present due
to condensation. As the level drops   more air space. Moisture in air
drops out    over time methanol acquires water. Batches have more soap.

 I just picked up some peanut oil. I'll try a test batch to see if I
have any problems.

 You'r insistance on using the pH meter  ???   Because you have one?
   or is it   titration fear?

Phenolphthalein solution (dissolved in alcohol) turns from clear magenta
at the pH range suitable for transesterification, making it suitable for
determining any adjustments that must be made to the WVO we want to convert
to BD.
As Ken has pointed out, pH meters and pH paper are good for determining
the pH of aqueous solutions, but not so for oil.


Tom
- Original Message -
From: Roger [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Thursday, April 03, 2008 10:18 AM
Subject: Re: [Biofuel] Test Batches with Peanut Oil


That is what I was looking for.  I was following the recipe to the 'T'
and was wondering where I was going wrong.  Anything is possible.  The
methanol came from Quaker City Chemical in a 55-Gal Drum, 99.9%.  I
opened the drum, removed 2 liters with a new, unused pump, then sealed
the Nalgene containers and the drum back up.  I assumed it would be
water-less, but I may have missed something.  Suppose there is water in
the drum - does that make it useless?  Any way to fix that?

I used a name brand oil from the grocery store (not sure now what it was
now.)  That shouldn't be the problem.
I'll buy the yellow Heet bottle and try again.

In the meantime, I'll practice titration with my pH meter and find some
phenolphthalein to try as well.  I thought the pH meter would be easy to
use and just as good but I'm not familiar with using one - so training
my be necessary.  I also don't have the calibration solutions yet
either.  Working for a surplus lab equipment company, we get all kinds
of neat stuff - but more often than not it's not all there and that is
even if I know what it is.

The peanut oil I have came from Costco in the big jug. I used half for a
turkey and figured it would be worth trying out. That'll be next.

Thanks for your help,
Roger



Thomas Kelly wrote:
 Roger,
   I'm stumped by the third photo. Why so much soap when you used new
 veg
 oil.
   I'm surprisd it separated at all.
  You are certain the methanol is dry?

  Soap forms when there is water contamination.
  Soap forms when Free Fatty Acids are present.

 Ken P. responded to you on March 31:
 It's ALWAYS a good idea to titrate, even virgin oil. Many oils,
 including palm and olive (don't know about peanut) have high FFA levels as
 typically sold.

  The reason for using new, unused veg oil of our first test batches is
 to decrease the number of variables we are dealing with. It is best to
 avoid
 titration until you get the basic process under your belt. It is assumed
 that new oil doesn't have to be titrated. This may not be the case.

 Suggestions:
  1.  Pick up a container of Heet (brand of gas line antifreeze)  Yellow
 container,  NOT  Red.  (If it is available to you.)   ~ $1.50/300ml.
 (US).
 It is dry methanol.
  2. I did my test batches using a name brand corn oil. The people I have
 helped in my neigborhood have done the same. We had no problems with
 FFAs.
 Maybe you should invest in a bottle of name brand corn oil .   or is
 that what you already did?

 As for pH meters:  (Ken P):
 pH really only makes sense when referring to a water-based solution.
 Sticking pH paper or pH meter into biodiesel gives spurious results
 in most cases. I often measure the pH of my wash water as a check
 of how much lye and soaps may be left in the biodiesel, but never the
 biodiesel (or oil) itself.

  Get Phenolphthalein
  (dissolved in alcohol) for titrations.
  We'll deal with the mysterious peanut oil and with you WVO after you
 succeed w. the test batches.
   I'm now curious about peanut oil. I'll see about getting some and
 doing a test batch myself.
  Tom



 - Original Message -
 From

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-09 Thread Thomas Kelly
Doug,
 Two of my four sons are color-deficient. It should have, but didn't 
occur to me that there might be a problem recognizing color change during 
titration.
 The forms of color deficiency that I am familiar with involves 
distinguishing between colors;   ex:   reds and greens of similar shades.
 Titration, using phenolphthalein, involves color change from clear 
(cloudy white as titration solution is added) to magenta. I would think that 
even those with significant color deficiency would be able to distinguish 
the difference. If nothing other than seeing it change from light to dark. 
I would think that distinguishing the split    biodiesel top, glyc. mix 
bottom, especially from processing unused peanut oil, would have been more 
of a problem.

I'll check with one of my color-deficient sons next time he stops 
by.

  Tom

- Original Message - 
From: Doug Turner [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Wednesday, April 09, 2008 10:10 AM
Subject: Re: [Biofuel] Test Batches with Peanut Oil


Hi Tom,

  Perhaps Roger is partially or completely colour blind.  As part of the 7
to 10% of the male population that is colour blind, I fully understand
wanting, or rather needing, to use a pH meter.  Most titration indicators
rely upon colour changes I find that are difficult to detect, at least with
any accuracy.  I would be interested in finding out if there are any other
options, other than a pH meter or a titration test, for determining the pH
of a solution.

  Doug Turner,
  Hamilton

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] Behalf Of
Thomas Kelly
Sent: Thursday, April 03, 2008 1:25 PM
To: sustainablelorgbiofuel@sustainablelists.org
Subject: Re: [Biofuel] Test Batches with Peanut Oil


Roger,
  Freshly opened 55 gal drums of methanol usually are good.
By the time you get to the bottom of barrel there is often water present due
to condensation. As the level drops   more air space. Moisture in air
drops out    over time methanol acquires water. Batches have more soap.

 I just picked up some peanut oil. I'll try a test batch to see if I
have any problems.

 You'r insistance on using the pH meter  ???   Because you have one?
   or is it   titration fear?

Phenolphthalein solution (dissolved in alcohol) turns from clear magenta
at the pH range suitable for transesterification, making it suitable for
determining any adjustments that must be made to the WVO we want to convert
to BD.
As Ken has pointed out, pH meters and pH paper are good for determining
the pH of aqueous solutions, but not so for oil.


Tom
- Original Message -
From: Roger [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Thursday, April 03, 2008 10:18 AM
Subject: Re: [Biofuel] Test Batches with Peanut Oil


That is what I was looking for.  I was following the recipe to the 'T'
and was wondering where I was going wrong.  Anything is possible.  The
methanol came from Quaker City Chemical in a 55-Gal Drum, 99.9%.  I
opened the drum, removed 2 liters with a new, unused pump, then sealed
the Nalgene containers and the drum back up.  I assumed it would be
water-less, but I may have missed something.  Suppose there is water in
the drum - does that make it useless?  Any way to fix that?

I used a name brand oil from the grocery store (not sure now what it was
now.)  That shouldn't be the problem.
I'll buy the yellow Heet bottle and try again.

In the meantime, I'll practice titration with my pH meter and find some
phenolphthalein to try as well.  I thought the pH meter would be easy to
use and just as good but I'm not familiar with using one - so training
my be necessary.  I also don't have the calibration solutions yet
either.  Working for a surplus lab equipment company, we get all kinds
of neat stuff - but more often than not it's not all there and that is
even if I know what it is.

The peanut oil I have came from Costco in the big jug. I used half for a
turkey and figured it would be worth trying out. That'll be next.

Thanks for your help,
Roger



Thomas Kelly wrote:
 Roger,
   I'm stumped by the third photo. Why so much soap when you used new
 veg
 oil.
   I'm surprisd it separated at all.
  You are certain the methanol is dry?

  Soap forms when there is water contamination.
  Soap forms when Free Fatty Acids are present.

 Ken P. responded to you on March 31:
 It's ALWAYS a good idea to titrate, even virgin oil. Many oils,
 including palm and olive (don't know about peanut) have high FFA levels as
 typically sold.

  The reason for using new, unused veg oil of our first test batches is
 to decrease the number of variables we are dealing with. It is best to
 avoid
 titration until you get the basic process under your belt. It is assumed
 that new oil doesn't have to be titrated. This may not be the case

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-04 Thread Thomas Kelly
Update on peanut oil test batch:
 Because the biodiesel produced from a peanut oil test batch did not 
appear to pass the Jan W. methanol quality test (mix turned white; white 
precipitate settled), I reprocessed the biodiesel layer.
 No glycerin dropped out. The hot, reprocessed mix was clear and light 
yellow in color.

I did a quality test on the reprocessed BD and again, the mix turned 
white.
The methanol I used came from a shed; temp ~ 35F/2C, so I gently heated the 
methanol-BD mix and the white disappeared - clear solution.
The solution stayed clear until it approached room temp (my kitchen: 
65F/18C) at which point it began to cloud up again.
At 70 - 75F (21 - 26C) the BD is completely soluble in methanol = passed 
the test.

   The reprocessed BD remains clear at room temp, but cooling it below 
60F 
wisps of white begin to form.

Ken P. (3/21/08):
 Peanut oil is about 75-80% oleic and linoleic, with the remainder
almost entirely saturated (palmitic, stearic, and longer). I would
expect biodiesel made from it to show precipitates at temperatures
lower than maybe 65 F.

 I think Ken nailed it. The test batch was actually a success. At cool 
temps like my basement, an outdoor shed, or even my kitchen, the BD begins 
to cloud and then gel.

 I put the remaining peanut oil in my refrigerator. At about 40F (5C) 
there is a white layer on the bottom of the container.

 It has been my opinion and experience that the cloud point and pour 
point of biodiesel reflects the cloud and pour point of the veg. oil it was 
made from. Because the peanut oil did not cloud in my basement 55 - 60F (13- 
15C), I didn't think the BD made from it would cloud at that temp. I'm still 
perplexed on that issue, but ... ?

 It might be a good idea to avoid processing peanut oil, especially 
newbies who are doing test batches. What other oils would fall into this 
category?
Again, Ken P:
Many oils, including palm and olive (don't know about peanut) have high FFA 
levels as
typically sold.

 The wash test results on successfully processed peanut oil gives very 
unusual results:
creamy white BD layer on top of a white water layer, with a thin white soap 
layer between. Using hot water gives better definition, but is generally 
viewed as cheating
on the test. The washed/dried BD is very clear and almost colorless.

  Newbies might want to stick to canola, corn, soy oils for test 
batches.

Best to All,
 Tom

- Original Message - 
From: Thomas Kelly [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Thursday, April 03, 2008 8:55 PM
Subject: Re: [Biofuel] Test Batches with Peanut Oil


Roger,
 Peanut oil is interesting stuff.
 I just did a test batch with peanut oil   Planter's  100% pure.

Titration: 0ml0.1% KOH  (90% pure)

Less glycerine dropped out than I expect.  Incomplete reaction?

I let it settle for about an hour and then did a (solubility in
methanol) quality test.
- the mix turned white   a white cloud' is settling in the
methanol.
(I've never seen anything like it w. fresh or waste veg oil.)

I just did a wash test on a small sample  - exactly what you
described:
White, on white, on white:  cloudy white top layer (BD?), cloudy white
bottom layer (water), thin soap layer (white) in between. I had to hold the
container in front of a bright light to see contrast.

 After three shake washes I heated the top layer to get the water to
drop out   clear layer only slightly yellow. I did another quality test
(methanol sol.) and again got white.

 I did a wash test and a quality test on untreated peanut oil --
oil settled out

 Maybe there are unreacted mono- di- glycerides that behave oddly in
the wash and methanol tests. If I get a chance I will reprocess the sample
of biodiesel that remains from the test batch.

 Maybe you just picked the wrong oil to start doing test batches on. I
hope you are having better success with a different oil. I'm on my way to
quality test a batch that is finishing up. Hopefully I'll have better luck
on the mix of waste oil than I did on the peanut oil.
   Tom


 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Monday, March 31, 2008 1:41 PM
 Subject: Re: [Biofuel] Test Batches with Peanut Oil


 Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
 with virgin peanut oil with no luck.

 1L Clean, Virgin, Peanut Oil
 200ml Methanol
 5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
 55°C Temp via Hotplate
 Agitation: Fast Stirring for 30 minutes via Hotplate

 The original separation looks great - waited at least 12 hours but
 separates in about 2 hours.  Obvious layers with a slightly hazy, pale
 yellow

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-04 Thread Roger
Sounds like we ended up at the same place.  Hence why I was very 
perplexed at the wash test results, etc. 
I'll be in touch with my findings this weekend - I'm sure to be busy on 
more test runs.
Thanks,
Roger



Thomas Kelly wrote:
 Update on peanut oil test batch:
  Because the biodiesel produced from a peanut oil test batch did not 
 appear to pass the Jan W. methanol quality test (mix turned white; white 
 precipitate settled), I reprocessed the biodiesel layer.
  No glycerin dropped out. The hot, reprocessed mix was clear and light 
 yellow in color.

 I did a quality test on the reprocessed BD and again, the mix turned 
 white.
 The methanol I used came from a shed; temp ~ 35F/2C, so I gently heated the 
 methanol-BD mix and the white disappeared - clear solution.
 The solution stayed clear until it approached room temp (my kitchen: 
 65F/18C) at which point it began to cloud up again.
 At 70 - 75F (21 - 26C) the BD is completely soluble in methanol = passed 
 the test.

The reprocessed BD remains clear at room temp, but cooling it below 
 60F 
 wisps of white begin to form.

 Ken P. (3/21/08):
  Peanut oil is about 75-80% oleic and linoleic, with the remainder
 almost entirely saturated (palmitic, stearic, and longer). I would
 expect biodiesel made from it to show precipitates at temperatures
 lower than maybe 65 F.

  I think Ken nailed it. The test batch was actually a success. At cool 
 temps like my basement, an outdoor shed, or even my kitchen, the BD begins 
 to cloud and then gel.

  I put the remaining peanut oil in my refrigerator. At about 40F (5C) 
 there is a white layer on the bottom of the container.

  It has been my opinion and experience that the cloud point and pour 
 point of biodiesel reflects the cloud and pour point of the veg. oil it was 
 made from. Because the peanut oil did not cloud in my basement 55 - 60F (13- 
 15C), I didn't think the BD made from it would cloud at that temp. I'm still 
 perplexed on that issue, but ... ?

  It might be a good idea to avoid processing peanut oil, especially 
 newbies who are doing test batches. What other oils would fall into this 
 category?
 Again, Ken P:
 Many oils, including palm and olive (don't know about peanut) have high FFA 
 levels as
 typically sold.

  The wash test results on successfully processed peanut oil gives very 
 unusual results:
 creamy white BD layer on top of a white water layer, with a thin white soap 
 layer between. Using hot water gives better definition, but is generally 
 viewed as cheating
 on the test. The washed/dried BD is very clear and almost colorless.

   Newbies might want to stick to canola, corn, soy oils for test 
 batches.

 Best to All,
  Tom

 - Original Message - 
 From: Thomas Kelly [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Thursday, April 03, 2008 8:55 PM
 Subject: Re: [Biofuel] Test Batches with Peanut Oil


 Roger,
  Peanut oil is interesting stuff.
  I just did a test batch with peanut oil   Planter's  100% pure.

 Titration: 0ml0.1% KOH  (90% pure)

 Less glycerine dropped out than I expect.  Incomplete reaction?

 I let it settle for about an hour and then did a (solubility in
 methanol) quality test.
 - the mix turned white   a white cloud' is settling in the
 methanol.
 (I've never seen anything like it w. fresh or waste veg oil.)

 I just did a wash test on a small sample  - exactly what you
 described:
 White, on white, on white:  cloudy white top layer (BD?), cloudy white
 bottom layer (water), thin soap layer (white) in between. I had to hold the
 container in front of a bright light to see contrast.

  After three shake washes I heated the top layer to get the water to
 drop out   clear layer only slightly yellow. I did another quality test
 (methanol sol.) and again got white.

  I did a wash test and a quality test on untreated peanut oil --
 oil settled out

  Maybe there are unreacted mono- di- glycerides that behave oddly in
 the wash and methanol tests. If I get a chance I will reprocess the sample
 of biodiesel that remains from the test batch.

  Maybe you just picked the wrong oil to start doing test batches on. I
 hope you are having better success with a different oil. I'm on my way to
 quality test a batch that is finishing up. Hopefully I'll have better luck
 on the mix of waste oil than I did on the peanut oil.
Tom


   
 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Monday, March 31, 2008 1:41 PM
 Subject: Re: [Biofuel] Test Batches with Peanut Oil


 Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
 with virgin peanut oil with no luck.

 1L Clean, Virgin, Peanut

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-03 Thread Keith Addison
. The BD will be cloudy because water will be
  suspended in it. The next step is to dry the BD. Heat it gently. You might
  put your tube of BD in a hot water bath. As the mix heats up water will fall
  out and the BD will clear.

   I do my wash tests in the same PET bottles described above. Equal
  volumes of water and BD~150ml of each.   Shake vigorously. With top
  closed, invert, and drain after water settles out. Add clean water  repeat.

   The last batch of 6.0g separated the quickest, less than a minute - the
  others
  
  longer up to 15 minutes or so.


  It might be that your KOH is not 90% pure
  @ 90% purity you would use  5.45g KOH/L of unused oil
  @ 85% purity you would use  5.76g KOH/L of unused oil

  Doing the methanol quality test on the BD before you wash it or after you
  wash and then dry it would tell us more about your success in achieving a
  complete conversion of the veg oil.

  
  And, with the rest of the batch in a jar in the garage, each one has turned
  to mush.  Looks like the inside of a melon or something.


  You're losing me here. Are you referring to the glycerin mix separated from
  the BD?

  Just another word of caution. When you do succeed at 1L test batches and
  feel comfortable w. the process. scale up gardually. We can talk aboput this
  another time.
  Dinner calls.
 Best of Luck to You,
  Tom



  - Original Message -
  From: Roger [EMAIL PROTECTED]
  To: sustainablelorgbiofuel@sustainablelists.org
  Sent: Monday, March 31, 2008 1:41 PM
  Subject: Re: [Biofuel] Test Batches with Peanut Oil


  Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
  with virgin peanut oil with no luck.

  1L Clean, Virgin, Peanut Oil
  200ml Methanol
  5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
  55°C Temp via Hotplate
  Agitation: Fast Stirring for 30 minutes via Hotplate

  The original separation looks great - waited at least 12 hours but
  separates in about 2 hours.  Obvious layers with a slightly hazy, pale
  yellow biodiesel layer and clear, darker by-product layer.
  Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
  of biodiesel for each batch.
  
  It's slightly colder in my garage, but not outside temperate.  I'd say
  roughly 55°F or so.  Each wash test was with 20ml of product and 20ml of
  water in a 50ml plastic tube.  The final wash test I performed inside
  with warmer water.  With each wash test I got cloudy water with a very
  thin white line between.  The biodiesel looks cloudy white.  The last
  batch of 6.0g separated the quickest, less than a minute - the others
  longer up to 15 minutes or so.  However, it doesn't look quite like what
  J2F described as good fuel.  And, with the rest of the batch in a jar in
  the garage, each one has turned to mush.  Looks like the inside of a
  melon or something.

  My first thought was that peanut oil was different enough from vegetable
  oil that I would need to titrate it and change the KOH amount.  However,
  I wasn't having much luck with the pH meter.  One time it would be add
  0.4gm of KOH and the next time 0.01g would be too much.  I thought I
  didn't know how to use the meter.

   The processor I made (assuming I would be using it by now) has 2) 75
  gallon tanks with individual heaters, controls, pumps, and stirrers.  It
  can be used as a 150gal unit or a 2-stage 75gal unit.  (I've attached a
  picture.)  I can't wait to try it but haven't used it yet for fear of
  making a lot of soap.
  
  Your thoughts are greatly appreciated.




  Thomas Kelly wrote:
  
  Roger,
   Back up a bit.


  Has anyone tried this?  It's all I had laying around to start with but I
   keep getting a questionable result.

  
  By tried this do you mean peanut oil?
  If so, I have run batches with peanut oil mixed in.



  Since it was new, I tried the same recipe for virgin vegetable oil and it
  didn't really pass the wash test and as soon as it got cold, it turned
  into sludge.

  
Got cold???The wash test is done at room temp  70-ish F  (20-ish
  C)



  I made a 2x75Gal machine that I
  am dying to use and the used oil is piling up.

  
  (What's a 2x75Gal machine?    a 75 Gal processor? 150 Gal processor?)
  Hold on now cowboy  .  let's not sign up for a marathon run before we
  up
  and walking. You don't want to turn gallons of good oil into gallons of
  goop.

  You might start by telling us  step-by-step what you are doing.
  Ex  1L fresh, unused vegetable oil
200ml methanol
5.45 g of 90% KOH
Method of agitation?
Temp?
30 minutes reaction time
  Do you get a clear split?
  How long do you let it settle?
  How do you separate the settled glycerine mix from the biodiesel
  (separatory funnel?)

  Describe the results of the wash test

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-03 Thread Roger
, even a small amount of
  glycerin/soap contamination will prolong separation time during the wash
  test.

  
   
  With each wash test I got cloudy water with a very
  thin white line between.  The biodiesel looks cloudy white.
  With each wash test I got cloudy water with a very thin white line 
 between.

 
  Do you mean:
  Cloudy water on bottom, with a very thin white line between the cloudy
  water on bottom and something darker on top?
  This would be a good thing.

  When you say:  The biodiesel looks cloudy white.  I'm a bit confused. If
  the biodiesel is white, you wouldn't be able to see the very thin white
  line between. It would just be white on top of white.
   
   Is the biodiesel layer (on top) darker than the thin white line?   
 Again,
 
  a good thing.


   However, it doesn't look quite like what J2F described as good fuel.
   
  
 
  Do you mean after doing a wash test?
  It will not yet be good fuel. It will take more than shaking with water 
 once
  to get the contaminants out of the BD.
   After 3 or 4 washes, the wash water should be clear and the same pH as
  the water that was added. The BD will be cloudy because water will be
  suspended in it. The next step is to dry the BD. Heat it gently. You might
  put your tube of BD in a hot water bath. As the mix heats up water will 
 fall
  out and the BD will clear.

   I do my wash tests in the same PET bottles described above. Equal
  volumes of water and BD~150ml of each.   Shake vigorously. With top
  closed, invert, and drain after water settles out. Add clean water  
 repeat.

   The last batch of 6.0g separated the quickest, less than a minute - the
  others
  
   
  longer up to 15 minutes or so.

 
  It might be that your KOH is not 90% pure
  @ 90% purity you would use  5.45g KOH/L of unused oil
  @ 85% purity you would use  5.76g KOH/L of unused oil

  Doing the methanol quality test on the BD before you wash it or after you
  wash and then dry it would tell us more about your success in achieving a
  complete conversion of the veg oil.

  
   
  And, with the rest of the batch in a jar in the garage, each one has 
 turned
  to mush.  Looks like the inside of a melon or something.

 
  You're losing me here. Are you referring to the glycerin mix separated from
  the BD?

  Just another word of caution. When you do succeed at 1L test batches and
  feel comfortable w. the process. scale up gardually. We can talk aboput 
 this
  another time.
  Dinner calls.
 Best of Luck to You,
  Tom



  - Original Message -
  From: Roger [EMAIL PROTECTED]
  To: sustainablelorgbiofuel@sustainablelists.org
  Sent: Monday, March 31, 2008 1:41 PM
  Subject: Re: [Biofuel] Test Batches with Peanut Oil


  Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
  with virgin peanut oil with no luck.

  1L Clean, Virgin, Peanut Oil
  200ml Methanol
  5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
  55°C Temp via Hotplate
  Agitation: Fast Stirring for 30 minutes via Hotplate

  The original separation looks great - waited at least 12 hours but
  separates in about 2 hours.  Obvious layers with a slightly hazy, pale
  yellow biodiesel layer and clear, darker by-product layer.
  Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
  of biodiesel for each batch.
   
  
 
  It's slightly colder in my garage, but not outside temperate.  I'd say
  roughly 55°F or so.  Each wash test was with 20ml of product and 20ml of
  water in a 50ml plastic tube.  The final wash test I performed inside
  with warmer water.  With each wash test I got cloudy water with a very
  thin white line between.  The biodiesel looks cloudy white.  The last
  batch of 6.0g separated the quickest, less than a minute - the others
  longer up to 15 minutes or so.  However, it doesn't look quite like what
  J2F described as good fuel.  And, with the rest of the batch in a jar in
  the garage, each one has turned to mush.  Looks like the inside of a
  melon or something.

  My first thought was that peanut oil was different enough from vegetable
  oil that I would need to titrate it and change the KOH amount.  However,
  I wasn't having much luck with the pH meter.  One time it would be add
  0.4gm of KOH and the next time 0.01g would be too much.  I thought I
  didn't know how to use the meter.

   
   The processor I made (assuming I would be using it by now) has 2) 75
 
  gallon tanks with individual heaters, controls, pumps, and stirrers.  It
  can be used as a 150gal unit or a 2-stage 75gal unit.  (I've attached a
  picture.)  I can't wait to try it but haven't used it yet for fear of
  making a lot of soap.
   
  
 
  Your thoughts are greatly appreciated.




  Thomas Kelly wrote:
  
   
  Roger,
   Back up

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-03 Thread Roger
That is what I was looking for.  I was following the recipe to the 'T' 
and was wondering where I was going wrong.  Anything is possible.  The 
methanol came from Quaker City Chemical in a 55-Gal Drum, 99.9%.  I 
opened the drum, removed 2 liters with a new, unused pump, then sealed 
the Nalgene containers and the drum back up.  I assumed it would be 
water-less, but I may have missed something.  Suppose there is water in 
the drum - does that make it useless?  Any way to fix that? 

I used a name brand oil from the grocery store (not sure now what it was 
now.)  That shouldn't be the problem. 
I'll buy the yellow Heet bottle and try again. 

In the meantime, I'll practice titration with my pH meter and find some 
phenolphthalein to try as well.  I thought the pH meter would be easy to 
use and just as good but I'm not familiar with using one - so training 
my be necessary.  I also don't have the calibration solutions yet 
either.  Working for a surplus lab equipment company, we get all kinds 
of neat stuff - but more often than not it's not all there and that is 
even if I know what it is. 

The peanut oil I have came from Costco in the big jug. I used half for a 
turkey and figured it would be worth trying out. That'll be next.

Thanks for your help,
Roger



Thomas Kelly wrote:
 Roger,
   I'm stumped by the third photo. Why so much soap when you used new veg 
 oil.
   I'm surprisd it separated at all.
  You are certain the methanol is dry?

  Soap forms when there is water contamination.
  Soap forms when Free Fatty Acids are present.

 Ken P. responded to you on March 31:
 It's ALWAYS a good idea to titrate, even virgin oil. Many oils,
 including palm and olive (don't know about peanut) have high FFA levels as
 typically sold.

  The reason for using new, unused veg oil of our first test batches is 
 to decrease the number of variables we are dealing with. It is best to avoid 
 titration until you get the basic process under your belt. It is assumed 
 that new oil doesn't have to be titrated. This may not be the case.

 Suggestions:
  1.  Pick up a container of Heet (brand of gas line antifreeze)  Yellow 
 container,  NOT  Red.  (If it is available to you.)   ~ $1.50/300ml.  (US). 
 It is dry methanol.
  2. I did my test batches using a name brand corn oil. The people I have 
 helped in my neigborhood have done the same. We had no problems with FFAs. 
 Maybe you should invest in a bottle of name brand corn oil .   or is 
 that what you already did?

 As for pH meters:  (Ken P):
 pH really only makes sense when referring to a water-based solution.
 Sticking pH paper or pH meter into biodiesel gives spurious results
 in most cases. I often measure the pH of my wash water as a check
 of how much lye and soaps may be left in the biodiesel, but never the
 biodiesel (or oil) itself.

  Get Phenolphthalein
  (dissolved in alcohol) for titrations.
  We'll deal with the mysterious peanut oil and with you WVO after you 
 succeed w. the test batches.
   I'm now curious about peanut oil. I'll see about getting some and 
 doing a test batch myself.
  Tom



 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Wednesday, April 02, 2008 2:50 PM
 Subject: Re: [Biofuel] Test Batches with Peanut Oil


 New Results...Better I think.

 I tried another batch last night with vegetable oil with 'better' results.

 1L Clean, Virgin, Vegetable Oil
 200ml Methanol
 5.5g of 90% KOH (All with very similar results)
 55°C Temp via Hotplate
 Agitation: Fast Stirring for 30 minutes via Hotplate

 Here are some pictures of what I have so far...
 http://tesi.servepics.com/roger/BD-4208-01a.JPG
 http://tesi.servepics.com/roger/BD-4208-01b.JPG
 http://tesi.servepics.com/roger/BD-4208-01c.JPG

 I let it settle for 14 hours.  Picture A is of the results.
 Picture B is right after shaking 20ml of BD and 20ml of water (both at
 room temperature)
 Picture C is after an hour of settling.  The is the best wash test I've
 gotten but it looks like a lot of soap in there.

 So my question is...  which way do I need to go to make it better?  More
 KOH?  I'm using very accurate measurements.  (Digital balance accurate
 to 0.001g, Graduated cylinders, etc.)  No water contamination that I'm
 aware of and taking precautions not to have any.  That is the only thing
 missing from J2F, pictures with typical results and adjustments
 necessary to make improvements.  Haven't tried the methanol test yet
 (still at work).

 Now, when I used peanut oil with the same recipe, I got a cloudy, opaque
 water and cloudy whiteish BD after the wash test.  Any thoughts on which
 way I need to go with that?  I presume I'll have to titrate it and make
 adjustments from there.  I need a pH probe to go with my meter before I
 can proceed with the peanut oil or used oil.


 Thomas Kelly wrote:
   
 Roger,
  Now we're getting somewhere

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-03 Thread Keith Addison
.
   

You are getting a clear split. You have made biodiesel. You may well
   have some unreacted mono and di glycerides in with the BD.
- Have you tried a quality test on the unwashed biodiesel?
  i.e. the Jan W. solubility in methanol test describes at JtF?
  
   

   - I would be very careful not to include any glycerin mix when 
you pour the
   biodiesel off the top. In fact I would avoid pouring 
altogether. Draw the BD
   off using a pipette or do the following: Get a few   .5 L - 1L 
clear plastic
   sports drink bottle (PET bottles) that have twist open/close tops. Some
   water bottles have pull-to-open push-to-close tops. Process as 
usual, allow
   to cool a bit and then pour the mix into one of the bottles. Allow the
   biodiesel-glycerin mix to settle in a closed and inverted 
bottle. After 12 -
   24 hours drain out the glycerin from the bottom.

If any unreacted glycerides are present, even a small amount of
   glycerin/soap contamination will prolong separation time during the wash
   test.

 
  
   With each wash test I got cloudy water with a very
   thin white line between.  The biodiesel looks cloudy white.
   With each wash test I got cloudy water with a very thin white 
line between.
   

   Do you mean:
   Cloudy water on bottom, with a very thin white line between the cloudy
   water on bottom and something darker on top?
   This would be a good thing.

   When you say:  The biodiesel looks cloudy white.  I'm a bit 
confused. If
   the biodiesel is white, you wouldn't be able to see the very thin white
   line between. It would just be white on top of white.
  
Is the biodiesel layer (on top) darker than the thin white 
line?   Again,

   a good thing.


However, it doesn't look quite like what J2F described as good fuel.

   

   Do you mean after doing a wash test?
   It will not yet be good fuel. It will take more than shaking 
with water once
   to get the contaminants out of the BD.
After 3 or 4 washes, the wash water should be clear and 
the same pH as
   the water that was added. The BD will be cloudy because water will be
   suspended in it. The next step is to dry the BD. Heat it 
gently. You might
   put your tube of BD in a hot water bath. As the mix heats up 
water will fall
   out and the BD will clear.

I do my wash tests in the same PET bottles described above. Equal
   volumes of water and BD~150ml of each.   Shake vigorously. With top
   closed, invert, and drain after water settles out. Add clean 
water  repeat.

The last batch of 6.0g separated the quickest, less than a minute - the
   others
 
  
   longer up to 15 minutes or so.
   

   It might be that your KOH is not 90% pure
   @ 90% purity you would use  5.45g KOH/L of unused oil
   @ 85% purity you would use  5.76g KOH/L of unused oil

   Doing the methanol quality test on the BD before you wash it or after you
   wash and then dry it would tell us more about your success in achieving a
   complete conversion of the veg oil.

 
  
   And, with the rest of the batch in a jar in the garage, each 
one has turned
   to mush.  Looks like the inside of a melon or something.
   

   You're losing me here. Are you referring to the glycerin mix 
separated from
   the BD?

   Just another word of caution. When you do succeed at 1L test batches and
   feel comfortable w. the process. scale up gardually. We can 
talk aboput this
   another time.
   Dinner calls.
  Best of Luck to You,
   Tom



   - Original Message -
   From: Roger [EMAIL PROTECTED]
   To: sustainablelorgbiofuel@sustainablelists.org
   Sent: Monday, March 31, 2008 1:41 PM
   Subject: Re: [Biofuel] Test Batches with Peanut Oil


   Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
   with virgin peanut oil with no luck.

   1L Clean, Virgin, Peanut Oil
   200ml Methanol
   5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
   55°C Temp via Hotplate
   Agitation: Fast Stirring for 30 minutes via Hotplate

   The original separation looks great - waited at least 12 hours but
   separates in about 2 hours.  Obvious layers with a slightly hazy, pale
   yellow biodiesel layer and clear, darker by-product layer.
   Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
   of biodiesel for each batch.
  
   

   It's slightly colder in my garage, but not outside temperate.  I'd say
   roughly 55°F or so.  Each wash test was with 20ml of product and 20ml of
   water in a 50ml plastic tube.  The final wash test I performed inside
   with warmer water.  With each wash test I got cloudy water with a very
   thin white line between.  The biodiesel looks cloudy white.  The last
   batch of 6.0g separated the quickest, less than a minute - the others
   longer up to 15

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-03 Thread Thomas Kelly
Roger,
  Freshly opened 55 gal drums of methanol usually are good.
By the time you get to the bottom of barrel there is often water present due 
to condensation. As the level drops   more air space. Moisture in air 
drops out    over time methanol acquires water. Batches have more soap.

 I just picked up some peanut oil. I'll try a test batch to see if I 
have any problems.

 You'r insistance on using the pH meter  ???   Because you have one?
   or is it   titration fear?

Phenolphthalein solution (dissolved in alcohol) turns from clear magenta 
at the pH range suitable for transesterification, making it suitable for 
determining any adjustments that must be made to the WVO we want to convert 
to BD.
As Ken has pointed out, pH meters and pH paper are good for determining 
the pH of aqueous solutions, but not so for oil.

 
Tom
- Original Message - 
From: Roger [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Thursday, April 03, 2008 10:18 AM
Subject: Re: [Biofuel] Test Batches with Peanut Oil


That is what I was looking for.  I was following the recipe to the 'T'
and was wondering where I was going wrong.  Anything is possible.  The
methanol came from Quaker City Chemical in a 55-Gal Drum, 99.9%.  I
opened the drum, removed 2 liters with a new, unused pump, then sealed
the Nalgene containers and the drum back up.  I assumed it would be
water-less, but I may have missed something.  Suppose there is water in
the drum - does that make it useless?  Any way to fix that?

I used a name brand oil from the grocery store (not sure now what it was
now.)  That shouldn't be the problem.
I'll buy the yellow Heet bottle and try again.

In the meantime, I'll practice titration with my pH meter and find some
phenolphthalein to try as well.  I thought the pH meter would be easy to
use and just as good but I'm not familiar with using one - so training
my be necessary.  I also don't have the calibration solutions yet
either.  Working for a surplus lab equipment company, we get all kinds
of neat stuff - but more often than not it's not all there and that is
even if I know what it is.

The peanut oil I have came from Costco in the big jug. I used half for a
turkey and figured it would be worth trying out. That'll be next.

Thanks for your help,
Roger



Thomas Kelly wrote:
 Roger,
   I'm stumped by the third photo. Why so much soap when you used new 
 veg
 oil.
   I'm surprisd it separated at all.
  You are certain the methanol is dry?

  Soap forms when there is water contamination.
  Soap forms when Free Fatty Acids are present.

 Ken P. responded to you on March 31:
 It's ALWAYS a good idea to titrate, even virgin oil. Many oils,
 including palm and olive (don't know about peanut) have high FFA levels as
 typically sold.

  The reason for using new, unused veg oil of our first test batches is
 to decrease the number of variables we are dealing with. It is best to 
 avoid
 titration until you get the basic process under your belt. It is assumed
 that new oil doesn't have to be titrated. This may not be the case.

 Suggestions:
  1.  Pick up a container of Heet (brand of gas line antifreeze)  Yellow
 container,  NOT  Red.  (If it is available to you.)   ~ $1.50/300ml. 
 (US).
 It is dry methanol.
  2. I did my test batches using a name brand corn oil. The people I have
 helped in my neigborhood have done the same. We had no problems with 
 FFAs.
 Maybe you should invest in a bottle of name brand corn oil .   or is
 that what you already did?

 As for pH meters:  (Ken P):
 pH really only makes sense when referring to a water-based solution.
 Sticking pH paper or pH meter into biodiesel gives spurious results
 in most cases. I often measure the pH of my wash water as a check
 of how much lye and soaps may be left in the biodiesel, but never the
 biodiesel (or oil) itself.

  Get Phenolphthalein
  (dissolved in alcohol) for titrations.
  We'll deal with the mysterious peanut oil and with you WVO after you
 succeed w. the test batches.
   I'm now curious about peanut oil. I'll see about getting some and
 doing a test batch myself.
  Tom



 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Wednesday, April 02, 2008 2:50 PM
 Subject: Re: [Biofuel] Test Batches with Peanut Oil


 New Results...Better I think.

 I tried another batch last night with vegetable oil with 'better' results.

 1L Clean, Virgin, Vegetable Oil
 200ml Methanol
 5.5g of 90% KOH (All with very similar results)
 55°C Temp via Hotplate
 Agitation: Fast Stirring for 30 minutes via Hotplate

 Here are some pictures of what I have so far...
 http://tesi.servepics.com/roger/BD-4208-01a.JPG
 http://tesi.servepics.com/roger/BD-4208-01b.JPG
 http://tesi.servepics.com/roger/BD-4208-01c.JPG

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-03 Thread Thomas Kelly
Roger,
 Peanut oil is interesting stuff.
 I just did a test batch with peanut oil   Planter's  100% pure.

Titration: 0ml0.1% KOH  (90% pure)

Less glycerine dropped out than I expect.  Incomplete reaction?

I let it settle for about an hour and then did a (solubility in 
methanol) quality test.
- the mix turned white   a white cloud' is settling in the 
methanol.
(I've never seen anything like it w. fresh or waste veg oil.)

I just did a wash test on a small sample  - exactly what you 
described:
White, on white, on white:  cloudy white top layer (BD?), cloudy white 
bottom layer (water), thin soap layer (white) in between. I had to hold the 
container in front of a bright light to see contrast.

 After three shake washes I heated the top layer to get the water to 
drop out   clear layer only slightly yellow. I did another quality test 
(methanol sol.) and again got white.

 I did a wash test and a quality test on untreated peanut oil -- 
oil settled out

 Maybe there are unreacted mono- di- glycerides that behave oddly in 
the wash and methanol tests. If I get a chance I will reprocess the sample 
of biodiesel that remains from the test batch.

 Maybe you just picked the wrong oil to start doing test batches on. I 
hope you are having better success with a different oil. I'm on my way to 
quality test a batch that is finishing up. Hopefully I'll have better luck 
on the mix of waste oil than I did on the peanut oil.
   Tom


 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Monday, March 31, 2008 1:41 PM
 Subject: Re: [Biofuel] Test Batches with Peanut Oil


 Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
 with virgin peanut oil with no luck.

 1L Clean, Virgin, Peanut Oil
 200ml Methanol
 5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
 55°C Temp via Hotplate
 Agitation: Fast Stirring for 30 minutes via Hotplate

 The original separation looks great - waited at least 12 hours but
 separates in about 2 hours.  Obvious layers with a slightly hazy, pale
 yellow biodiesel layer and clear, darker by-product layer.
 Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
 of biodiesel for each batch.

 It's slightly colder in my garage, but not outside temperate.  I'd say
 roughly 55°F or so.  Each wash test was with 20ml of product and 20ml of
 water in a 50ml plastic tube.  The final wash test I performed inside
 with warmer water.  With each wash test I got cloudy water with a very
 thin white line between.  The biodiesel looks cloudy white.  The last
 batch of 6.0g separated the quickest, less than a minute - the others
 longer up to 15 minutes or so.  However, it doesn't look quite like what
 J2F described as good fuel.  And, with the rest of the batch in a jar in
 the garage, each one has turned to mush.  Looks like the inside of a
 melon or something.

 My first thought was that peanut oil was different enough from vegetable
 oil that I would need to titrate it and change the KOH amount.  However,
 I wasn't having much luck with the pH meter.  One time it would be add
 0.4gm of KOH and the next time 0.01g would be too much.  I thought I
 didn't know how to use the meter.

 The processor I made (assuming I would be using it by now) has 2) 75
 gallon tanks with individual heaters, controls, pumps, and stirrers.  It
 can be used as a 150gal unit or a 2-stage 75gal unit.  (I've attached a
 picture.)  I can't wait to try it but haven't used it yet for fear of
 making a lot of soap.

 Your thoughts are greatly appreciated.




 Thomas Kelly wrote:

 Roger,
  Back up a bit.


 Has anyone tried this?  It's all I had laying around to start with but I
 keep getting a questionable result.


 By tried this do you mean peanut oil?
 If so, I have run batches with peanut oil mixed in.



 Since it was new, I tried the same recipe for virgin vegetable oil and 
 it
 didn't really pass the wash test and as soon as it got cold, it turned
 into sludge.


   Got cold???The wash test is done at room temp  70-ish F 
 (20-ish
 C)



 I made a 2x75Gal machine that I
 am dying to use and the used oil is piling up.


 (What's a 2x75Gal machine?    a 75 Gal processor? 150 Gal processor?)
 Hold on now cowboy  .  let's not sign up for a marathon run before we
 up
 and walking. You don't want to turn gallons of good oil into gallons of
 goop.

 You might start by telling us  step-by-step what you are doing.
 Ex  1L fresh, unused vegetable oil
   200ml methanol
   5.45 g of 90% KOH
   Method of agitation?
   Temp?
   30 minutes reaction time
 Do you get a clear split?
 How long do you let it settle?
 How do you separate the settled glycerine mix from the biodiesel
 (separatory funnel?)

 Describe the results of the wash test, done

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-02 Thread Roger
.
 

 You're losing me here. Are you referring to the glycerin mix separated from 
 the BD?

 Just another word of caution. When you do succeed at 1L test batches and 
 feel comfortable w. the process. scale up gardually. We can talk aboput this 
 another time.
 Dinner calls.
Best of Luck to You,
 Tom



 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: sustainablelorgbiofuel@sustainablelists.org
 Sent: Monday, March 31, 2008 1:41 PM
 Subject: Re: [Biofuel] Test Batches with Peanut Oil


 Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
 with virgin peanut oil with no luck.

 1L Clean, Virgin, Peanut Oil
 200ml Methanol
 5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
 55°C Temp via Hotplate
 Agitation: Fast Stirring for 30 minutes via Hotplate

 The original separation looks great - waited at least 12 hours but
 separates in about 2 hours.  Obvious layers with a slightly hazy, pale
 yellow biodiesel layer and clear, darker by-product layer.
 Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
 of biodiesel for each batch.

 It's slightly colder in my garage, but not outside temperate.  I'd say
 roughly 55°F or so.  Each wash test was with 20ml of product and 20ml of
 water in a 50ml plastic tube.  The final wash test I performed inside
 with warmer water.  With each wash test I got cloudy water with a very
 thin white line between.  The biodiesel looks cloudy white.  The last
 batch of 6.0g separated the quickest, less than a minute - the others
 longer up to 15 minutes or so.  However, it doesn't look quite like what
 J2F described as good fuel.  And, with the rest of the batch in a jar in
 the garage, each one has turned to mush.  Looks like the inside of a
 melon or something.

 My first thought was that peanut oil was different enough from vegetable
 oil that I would need to titrate it and change the KOH amount.  However,
 I wasn't having much luck with the pH meter.  One time it would be add
 0.4gm of KOH and the next time 0.01g would be too much.  I thought I
 didn't know how to use the meter.

 The processor I made (assuming I would be using it by now) has 2) 75
 gallon tanks with individual heaters, controls, pumps, and stirrers.  It
 can be used as a 150gal unit or a 2-stage 75gal unit.  (I've attached a
 picture.)  I can't wait to try it but haven't used it yet for fear of
 making a lot of soap.

 Your thoughts are greatly appreciated.




 Thomas Kelly wrote:
   
 Roger,
  Back up a bit.

 
 Has anyone tried this?  It's all I had laying around to start with but I
 keep getting a questionable result.

   
 By tried this do you mean peanut oil?
 If so, I have run batches with peanut oil mixed in.


 
 Since it was new, I tried the same recipe for virgin vegetable oil and it
 didn't really pass the wash test and as soon as it got cold, it turned
 into sludge.

   
   Got cold???The wash test is done at room temp  70-ish F  (20-ish
 C)


 
 I made a 2x75Gal machine that I
 am dying to use and the used oil is piling up.

   
 (What's a 2x75Gal machine?    a 75 Gal processor? 150 Gal processor?)
 Hold on now cowboy  .  let's not sign up for a marathon run before we 
 up
 and walking. You don't want to turn gallons of good oil into gallons of
 goop.

 You might start by telling us  step-by-step what you are doing.
 Ex  1L fresh, unused vegetable oil
   200ml methanol
   5.45 g of 90% KOH
   Method of agitation?
   Temp?
   30 minutes reaction time
 Do you get a clear split?
 How long do you let it settle?
 How do you separate the settled glycerine mix from the biodiesel
 (separatory funnel?)

 Describe the results of the wash test, done at room temp, as to time for
 separation + appearance of layers.

 While it is important to be able to measure accurately, especially for 1L
 test batches, I have gotten along fine w/o a pH meter.
 Best Wishes,

 Tom


 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Monday, March 31, 2008 10:13 AM
 Subject: [Biofuel] Test Batches with Peanut Oil



 
 Has anyone tried this?  It's all I had laying around to start with but I
 keep getting a questionable result.  Since it was new, I tried the same
 recipe for virgin vegetable oil and it didn't really pass the wash test 
 and as soon as it got cold, it turned into sludge.  I wish there was
 more pictures - not sure if I'm adding too much of something or too
 little or what.  I'm using some nice equipment (I work for a laboratory
 surplus equipment company) such as a lab scale, pH meter, quality
 glassware, hotplate stirrer and a 2L reaction vessel.  I'm holding the
 temperature right on, mixing for 30 minutes, etc.  I have 90% KOH and
 99.9% methanol from

Re: [Biofuel] Test Batches with Peanut Oil

2008-04-02 Thread Thomas Kelly
Roger,
  I'm stumped by the third photo. Why so much soap when you used new veg 
oil.
  I'm surprisd it separated at all.
 You are certain the methanol is dry?

 Soap forms when there is water contamination.
 Soap forms when Free Fatty Acids are present.

Ken P. responded to you on March 31:
It's ALWAYS a good idea to titrate, even virgin oil. Many oils,
including palm and olive (don't know about peanut) have high FFA levels as
typically sold.

 The reason for using new, unused veg oil of our first test batches is 
to decrease the number of variables we are dealing with. It is best to avoid 
titration until you get the basic process under your belt. It is assumed 
that new oil doesn't have to be titrated. This may not be the case.

Suggestions:
 1.  Pick up a container of Heet (brand of gas line antifreeze)  Yellow 
container,  NOT  Red.  (If it is available to you.)   ~ $1.50/300ml.  (US). 
It is dry methanol.
 2. I did my test batches using a name brand corn oil. The people I have 
helped in my neigborhood have done the same. We had no problems with FFAs. 
Maybe you should invest in a bottle of name brand corn oil .   or is 
that what you already did?

As for pH meters:  (Ken P):
pH really only makes sense when referring to a water-based solution.
Sticking pH paper or pH meter into biodiesel gives spurious results
in most cases. I often measure the pH of my wash water as a check
of how much lye and soaps may be left in the biodiesel, but never the
biodiesel (or oil) itself.

 Get Phenolphthalein (dissolved in alcohol) for titrations.
 We'll deal with the mysterious peanut oil and with you WVO after you 
succeed w. the test batches.
  I'm now curious about peanut oil. I'll see about getting some and 
doing a test batch myself.
 Tom



- Original Message - 
From: Roger [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Wednesday, April 02, 2008 2:50 PM
Subject: Re: [Biofuel] Test Batches with Peanut Oil


New Results...Better I think.

I tried another batch last night with vegetable oil with 'better' results.

1L Clean, Virgin, Vegetable Oil
200ml Methanol
5.5g of 90% KOH (All with very similar results)
55°C Temp via Hotplate
Agitation: Fast Stirring for 30 minutes via Hotplate

Here are some pictures of what I have so far...
http://tesi.servepics.com/roger/BD-4208-01a.JPG
http://tesi.servepics.com/roger/BD-4208-01b.JPG
http://tesi.servepics.com/roger/BD-4208-01c.JPG

I let it settle for 14 hours.  Picture A is of the results.
Picture B is right after shaking 20ml of BD and 20ml of water (both at
room temperature)
Picture C is after an hour of settling.  The is the best wash test I've
gotten but it looks like a lot of soap in there.

So my question is...  which way do I need to go to make it better?  More
KOH?  I'm using very accurate measurements.  (Digital balance accurate
to 0.001g, Graduated cylinders, etc.)  No water contamination that I'm
aware of and taking precautions not to have any.  That is the only thing
missing from J2F, pictures with typical results and adjustments
necessary to make improvements.  Haven't tried the methanol test yet
(still at work).

Now, when I used peanut oil with the same recipe, I got a cloudy, opaque
water and cloudy whiteish BD after the wash test.  Any thoughts on which
way I need to go with that?  I presume I'll have to titrate it and make
adjustments from there.  I need a pH probe to go with my meter before I
can proceed with the peanut oil or used oil.


Thomas Kelly wrote:
 Roger,
  Now we're getting somewhere.


 The original separation looks great - waited at least 12 hours but
 separates in about 2 hours.  Obvious layers with a slightly hazy, pale
 yellow biodiesel layer and clear, darker by-product layer.
 Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
 of biodiesel for each batch.


  You are getting a clear split. You have made biodiesel. You may well
 have some unreacted mono and di glycerides in with the BD.
  - Have you tried a quality test on the unwashed biodiesel?
i.e. the Jan W. solubility in methanol test describes at JtF?

 - I would be very careful not to include any glycerin mix when you pour 
 the
 biodiesel off the top. In fact I would avoid pouring altogether. Draw the 
 BD
 off using a pipette or do the following: Get a few   .5 L - 1L clear 
 plastic
 sports drink bottle (PET bottles) that have twist open/close tops. Some
 water bottles have pull-to-open push-to-close tops. Process as usual, 
 allow
 to cool a bit and then pour the mix into one of the bottles. Allow the
 biodiesel-glycerin mix to settle in a closed and inverted bottle. After 
 12 -
 24 hours drain out the glycerin from the bottom.

  If any unreacted glycerides are present, even a small amount of
 glycerin/soap contamination will prolong separation time during the wash
 test.


 With each wash test I got cloudy water with a very

[Biofuel] Test Batches with Peanut Oil

2008-03-31 Thread Roger
Has anyone tried this?  It's all I had laying around to start with but I 
keep getting a questionable result.  Since it was new, I tried the same 
recipe for virgin vegetable oil and it didn't really pass the wash test 
and as soon as it got cold, it turned into sludge.  I wish there was 
more pictures - not sure if I'm adding too much of something or too 
little or what.  I'm using some nice equipment (I work for a laboratory 
surplus equipment company) such as a lab scale, pH meter, quality 
glassware, hotplate stirrer and a 2L reaction vessel.  I'm holding the 
temperature right on, mixing for 30 minutes, etc.  I have 90% KOH and 
99.9% methanol from a local chem distributor.  Not sure when I'm doing 
wrong, but any advice would be great.  I made a 2x75Gal machine that I 
am dying to use and the used oil is piling up. 

Also, I don't know if I'm using my pH meter correctly.  Can someone give 
directions on proper use of one of these? 

If anyone needs any special equipment, just ask.  I even have tanks, etc. 

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

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

Search the combined Biofuel and Biofuels-biz list archives (70,000 messages):
http://www.mail-archive.com/biofuel@sustainablelists.org/


Re: [Biofuel] Test Batches with Peanut Oil

2008-03-31 Thread Thomas Kelly
Roger,
 Back up a bit.
Has anyone tried this?  It's all I had laying around to start with but I
 keep getting a questionable result.
By tried this do you mean peanut oil?
If so, I have run batches with peanut oil mixed in.

Since it was new, I tried the same recipe for virgin vegetable oil and it 
didn't really pass the wash test and as soon as it got cold, it turned 
into sludge.

  Got cold???The wash test is done at room temp  70-ish F  (20-ish 
C)

I made a 2x75Gal machine that I
 am dying to use and the used oil is piling up.

(What's a 2x75Gal machine?    a 75 Gal processor? 150 Gal processor?)
Hold on now cowboy  .  let's not sign up for a marathon run before we up 
and walking. You don't want to turn gallons of good oil into gallons of 
goop.

You might start by telling us  step-by-step what you are doing.
Ex  1L fresh, unused vegetable oil
  200ml methanol
  5.45 g of 90% KOH
  Method of agitation?
  Temp?
  30 minutes reaction time
Do you get a clear split?
How long do you let it settle?
How do you separate the settled glycerine mix from the biodiesel 
(separatory funnel?)

Describe the results of the wash test, done at room temp, as to time for 
separation + appearance of layers.

While it is important to be able to measure accurately, especially for 1L 
test batches, I have gotten along fine w/o a pH meter.
Best Wishes,
 Tom


- Original Message - 
From: Roger [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Monday, March 31, 2008 10:13 AM
Subject: [Biofuel] Test Batches with Peanut Oil


 Has anyone tried this?  It's all I had laying around to start with but I
 keep getting a questionable result.  Since it was new, I tried the same
 recipe for virgin vegetable oil and it didn't really pass the wash test  
 and as soon as it got cold, it turned into sludge.  I wish there was
 more pictures - not sure if I'm adding too much of something or too
 little or what.  I'm using some nice equipment (I work for a laboratory
 surplus equipment company) such as a lab scale, pH meter, quality
 glassware, hotplate stirrer and a 2L reaction vessel.  I'm holding the
 temperature right on, mixing for 30 minutes, etc.  I have 90% KOH and
 99.9% methanol from a local chem distributor.  Not sure when I'm doing
 wrong, but any advice would be great.  I made a 2x75Gal machine that I
 am dying to use and the used oil is piling up.

 Also, I don't know if I'm using my pH meter correctly.  Can someone give
 directions on proper use of one of these?

 If anyone needs any special equipment, just ask.  I even have tanks, etc.

 ___
 Biofuel mailing list
 Biofuel@sustainablelists.org
 http://sustainablelists.org/mailman/listinfo/sustainablelorgbiofuel

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

 Search the combined Biofuel and Biofuels-biz list archives (70,000 
 messages):
 http://www.mail-archive.com/biofuel@sustainablelists.org/
 



___
Biofuel mailing list
Biofuel@sustainablelists.org
http://sustainablelists.org/mailman/listinfo/sustainablelorgbiofuel

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

Search the combined Biofuel and Biofuels-biz list archives (70,000 messages):
http://www.mail-archive.com/biofuel@sustainablelists.org/


Re: [Biofuel] Test Batches with Peanut Oil

2008-03-31 Thread Roger
Sorry for the excitement and frustration.  I've made 4 or 5 1L batches 
with virgin peanut oil with no luck.

1L Clean, Virgin, Peanut Oil
200ml Methanol
5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
55°C Temp via Hotplate
Agitation: Fast Stirring for 30 minutes via Hotplate

The original separation looks great - waited at least 12 hours but 
separates in about 2 hours.  Obvious layers with a slightly hazy, pale 
yellow biodiesel layer and clear, darker by-product layer. 
Separated by pouring the biodiesel off the top.  Looks to be about 1.1L 
of biodiesel for each batch. 

It's slightly colder in my garage, but not outside temperate.  I'd say 
roughly 55°F or so.  Each wash test was with 20ml of product and 20ml of 
water in a 50ml plastic tube.  The final wash test I performed inside 
with warmer water.  With each wash test I got cloudy water with a very 
thin white line between.  The biodiesel looks cloudy white.  The last 
batch of 6.0g separated the quickest, less than a minute - the others 
longer up to 15 minutes or so.  However, it doesn't look quite like what 
J2F described as good fuel.  And, with the rest of the batch in a jar in 
the garage, each one has turned to mush.  Looks like the inside of a 
melon or something. 

My first thought was that peanut oil was different enough from vegetable 
oil that I would need to titrate it and change the KOH amount.  However, 
I wasn't having much luck with the pH meter.  One time it would be add 
0.4gm of KOH and the next time 0.01g would be too much.  I thought I 
didn't know how to use the meter. 

The processor I made (assuming I would be using it by now) has 2) 75 
gallon tanks with individual heaters, controls, pumps, and stirrers.  It 
can be used as a 150gal unit or a 2-stage 75gal unit.  (I've attached a 
picture.)  I can't wait to try it but haven't used it yet for fear of 
making a lot of soap. 

Your thoughts are greatly appreciated.




Thomas Kelly wrote:
 Roger,
  Back up a bit.
   
 Has anyone tried this?  It's all I had laying around to start with but I
 keep getting a questionable result.
 
 By tried this do you mean peanut oil?
 If so, I have run batches with peanut oil mixed in.

   
 Since it was new, I tried the same recipe for virgin vegetable oil and it 
 didn't really pass the wash test and as soon as it got cold, it turned 
 into sludge.
 

   Got cold???The wash test is done at room temp  70-ish F  (20-ish 
 C)

   
 I made a 2x75Gal machine that I
 am dying to use and the used oil is piling up.
 

 (What's a 2x75Gal machine?    a 75 Gal processor? 150 Gal processor?)
 Hold on now cowboy  .  let's not sign up for a marathon run before we up 
 and walking. You don't want to turn gallons of good oil into gallons of 
 goop.

 You might start by telling us  step-by-step what you are doing.
 Ex  1L fresh, unused vegetable oil
   200ml methanol
   5.45 g of 90% KOH
   Method of agitation?
   Temp?
   30 minutes reaction time
 Do you get a clear split?
 How long do you let it settle?
 How do you separate the settled glycerine mix from the biodiesel 
 (separatory funnel?)

 Describe the results of the wash test, done at room temp, as to time for 
 separation + appearance of layers.

 While it is important to be able to measure accurately, especially for 1L 
 test batches, I have gotten along fine w/o a pH meter.
 Best Wishes,
  Tom


 - Original Message - 
 From: Roger [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Monday, March 31, 2008 10:13 AM
 Subject: [Biofuel] Test Batches with Peanut Oil


   
 Has anyone tried this?  It's all I had laying around to start with but I
 keep getting a questionable result.  Since it was new, I tried the same
 recipe for virgin vegetable oil and it didn't really pass the wash test  
 and as soon as it got cold, it turned into sludge.  I wish there was
 more pictures - not sure if I'm adding too much of something or too
 little or what.  I'm using some nice equipment (I work for a laboratory
 surplus equipment company) such as a lab scale, pH meter, quality
 glassware, hotplate stirrer and a 2L reaction vessel.  I'm holding the
 temperature right on, mixing for 30 minutes, etc.  I have 90% KOH and
 99.9% methanol from a local chem distributor.  Not sure when I'm doing
 wrong, but any advice would be great.  I made a 2x75Gal machine that I
 am dying to use and the used oil is piling up.

 Also, I don't know if I'm using my pH meter correctly.  Can someone give
 directions on proper use of one of these?

 If anyone needs any special equipment, just ask.  I even have tanks, etc.

 ___
 Biofuel mailing list
 Biofuel@sustainablelists.org
 http://sustainablelists.org/mailman/listinfo/sustainablelorgbiofuel

 Biofuel

Re: [Biofuel] Test Batches with Peanut Oil

2008-03-31 Thread Thomas Kelly
Roger,
 Now we're getting somewhere.

The original separation looks great - waited at least 12 hours but
separates in about 2 hours.  Obvious layers with a slightly hazy, pale
yellow biodiesel layer and clear, darker by-product layer.
Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
of biodiesel for each batch.

 You are getting a clear split. You have made biodiesel. You may well 
have some unreacted mono and di glycerides in with the BD.
 - Have you tried a quality test on the unwashed biodiesel?
   i.e. the Jan W. solubility in methanol test describes at JtF?

- I would be very careful not to include any glycerin mix when you pour the 
biodiesel off the top. In fact I would avoid pouring altogether. Draw the BD 
off using a pipette or do the following: Get a few   .5 L - 1L clear plastic 
sports drink bottle (PET bottles) that have twist open/close tops. Some 
water bottles have pull-to-open push-to-close tops. Process as usual, allow 
to cool a bit and then pour the mix into one of the bottles. Allow the 
biodiesel-glycerin mix to settle in a closed and inverted bottle. After 12 - 
24 hours drain out the glycerin from the bottom.

 If any unreacted glycerides are present, even a small amount of 
glycerin/soap contamination will prolong separation time during the wash 
test.

With each wash test I got cloudy water with a very
thin white line between.  The biodiesel looks cloudy white.
With each wash test I got cloudy water with a very thin white line between.

Do you mean:
Cloudy water on bottom, with a very thin white line between the cloudy 
water on bottom and something darker on top?
This would be a good thing.

When you say:  The biodiesel looks cloudy white.  I'm a bit confused. If 
the biodiesel is white, you wouldn't be able to see the very thin white 
line between. It would just be white on top of white.
Is the biodiesel layer (on top) darker than the thin white line?   Again, 
a good thing.


 However, it doesn't look quite like what J2F described as good fuel.

Do you mean after doing a wash test?
It will not yet be good fuel. It will take more than shaking with water once 
to get the contaminants out of the BD.
 After 3 or 4 washes, the wash water should be clear and the same pH as 
the water that was added. The BD will be cloudy because water will be 
suspended in it. The next step is to dry the BD. Heat it gently. You might 
put your tube of BD in a hot water bath. As the mix heats up water will fall 
out and the BD will clear.

 I do my wash tests in the same PET bottles described above. Equal 
volumes of water and BD~150ml of each.   Shake vigorously. With top 
closed, invert, and drain after water settles out. Add clean water  repeat.

 The last batch of 6.0g separated the quickest, less than a minute - the 
others
longer up to 15 minutes or so.

It might be that your KOH is not 90% pure
@ 90% purity you would use  5.45g KOH/L of unused oil
@ 85% purity you would use  5.76g KOH/L of unused oil

Doing the methanol quality test on the BD before you wash it or after you 
wash and then dry it would tell us more about your success in achieving a 
complete conversion of the veg oil.

And, with the rest of the batch in a jar in the garage, each one has turned 
to mush.  Looks like the inside of a melon or something.

You're losing me here. Are you referring to the glycerin mix separated from 
the BD?

Just another word of caution. When you do succeed at 1L test batches and 
feel comfortable w. the process. scale up gardually. We can talk aboput this 
another time.
Dinner calls.
   Best of Luck to You,
Tom



- Original Message - 
From: Roger [EMAIL PROTECTED]
To: sustainablelorgbiofuel@sustainablelists.org
Sent: Monday, March 31, 2008 1:41 PM
Subject: Re: [Biofuel] Test Batches with Peanut Oil


Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
with virgin peanut oil with no luck.

1L Clean, Virgin, Peanut Oil
200ml Methanol
5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
55°C Temp via Hotplate
Agitation: Fast Stirring for 30 minutes via Hotplate

The original separation looks great - waited at least 12 hours but
separates in about 2 hours.  Obvious layers with a slightly hazy, pale
yellow biodiesel layer and clear, darker by-product layer.
Separated by pouring the biodiesel off the top.  Looks to be about 1.1L
of biodiesel for each batch.

It's slightly colder in my garage, but not outside temperate.  I'd say
roughly 55°F or so.  Each wash test was with 20ml of product and 20ml of
water in a 50ml plastic tube.  The final wash test I performed inside
with warmer water.  With each wash test I got cloudy water with a very
thin white line between.  The biodiesel looks cloudy white.  The last
batch of 6.0g separated the quickest, less than a minute - the others
longer up to 15 minutes or so.  However

Re: [Biofuel] Test Batches with Peanut Oil

2008-03-31 Thread Ken Provost
Roger:

Peanut oil is about 75-80% oleic and linoleic, with the remainder
almost entirely saturated (palmitic, stearic, and longer). I would
expect biodiesel made from it to show precipitates at temperatures
lower than maybe 65 F.

I'm not clear from your wash test whether you are actually washing
your biodiesel before the test -- this might help :-).

pH really only makes sense when referring to a water-based solution.
Sticking pH paper or pH meter into biodiesel gives spurious results
in most cases. I often measure the pH of my wash water as a check
of how much lye and soaps may be left in the biodiesel, but never the
biodiesel (or oil) itself.

It's ALWAYS a good idea to titrate, even virgin oil. Many oils,  
including
palm and olive (don't know about peanut) have high FFA levels as
typically sold.




On Mar 31, 2008, at 9:41 AM, Roger wrote:

 Sorry for the excitement and frustration.  I've made 4 or 5 1L batches
 with virgin peanut oil with no luck.

 1L Clean, Virgin, Peanut Oil
 200ml Methanol
 5.4g, 5.5g, 5.6g, 6.0g of 90% KOH (All with very similar results)
 55°C Temp via Hotplate
 Agitation: Fast Stirring for 30 minutes via Hotplate

 The original separation looks great - waited at least 12 hours but
 separates in about 2 hours.  Obvious layers with a slightly hazy, pale
 yellow biodiesel layer and clear, darker by-product layer.
 Separated by pouring the biodiesel off the top.  Looks to be about  
 1.1L
 of biodiesel for each batch.

 It's slightly colder in my garage, but not outside temperate.  I'd say
 roughly 55°F or so.  Each wash test was with 20ml of product and  
 20ml of
 water in a 50ml plastic tube.  The final wash test I performed inside
 with warmer water.  With each wash test I got cloudy water with a very
 thin white line between.  The biodiesel looks cloudy white.  The last
 batch of 6.0g separated the quickest, less than a minute - the others
 longer up to 15 minutes or so.  However, it doesn't look quite like  
 what
 J2F described as good fuel.  And, with the rest of the batch in a  
 jar in
 the garage, each one has turned to mush.  Looks like the inside of a
 melon or something.

 My first thought was that peanut oil was different enough from  
 vegetable
 oil that I would need to titrate it and change the KOH amount.   
 However,
 I wasn't having much luck with the pH meter.  One time it would be add
 0.4gm of KOH and the next time 0.01g would be too much.  I thought I
 didn't know how to use the meter.

 The processor I made (assuming I would be using it by now) has 2) 75
 gallon tanks with individual heaters, controls, pumps, and  
 stirrers.  It
 can be used as a 150gal unit or a 2-stage 75gal unit.  (I've  
 attached a
 picture.)  I can't wait to try it but haven't used it yet for fear of
 making a lot of soap.

 Your thoughts are greatly appreciated.




 Thomas Kelly wrote:

 Roger,
  Back up a bit.


 Has anyone tried this?  It's all I had laying around to start  
 with but I
 keep getting a questionable result.


 By tried this do you mean peanut oil?
 If so, I have run batches with peanut oil mixed in.



 Since it was new, I tried the same recipe for virgin vegetable  
 oil and it
 didn't really pass the wash test and as soon as it got cold, it  
 turned
 into sludge.



   Got cold???The wash test is done at room temp  70-ish F   
 (20-ish
 C)



 I made a 2x75Gal machine that I
 am dying to use and the used oil is piling up.



 (What's a 2x75Gal machine?    a 75 Gal processor? 150 Gal  
 processor?)
 Hold on now cowboy  .  let's not sign up for a marathon run  
 before we up
 and walking. You don't want to turn gallons of good oil into  
 gallons of
 goop.

 You might start by telling us  step-by-step what you are doing.
 Ex  1L fresh, unused vegetable oil
   200ml methanol
   5.45 g of 90% KOH
   Method of agitation?
   Temp?
   30 minutes reaction time
 Do you get a clear split?
 How long do you let it settle?
 How do you separate the settled glycerine mix from the biodiesel
 (separatory funnel?)

 Describe the results of the wash test, done at room temp, as to  
 time for
 separation + appearance of layers.

 While it is important to be able to measure accurately, especially  
 for 1L
 test batches, I have gotten along fine w/o a pH meter.
 Best  
 Wishes,
   
 Tom


 - Original Message -
 From: Roger [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Monday, March 31, 2008 10:13 AM
 Subject: [Biofuel] Test Batches with Peanut Oil




 Has anyone tried this?  It's all I had laying around to start  
 with but I
 keep getting a questionable result.  Since it was new, I tried  
 the same
 recipe for virgin vegetable oil and it didn't really pass the  
 wash test 
 and as soon as it got cold, it turned into sludge.  I wish there was
 more pictures

Re: [Biofuel] Test Batch Success......Thanks Keith

2006-09-03 Thread Keith Addison
Hello Marc

Good for you! Sometimes it takes perseverance, but it pays off, well done.

Thankyou for your thanks, you are most welcome, I'm sure everyone 
else thinks so too.

All best

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

 


Finally after many months of failed or mediocre wash test results I am
achieving quick and clean separation of unwashed biodiesel(wvo) and
water with a paper thin white layer, and all this as a result of the
useful and encouraging information and instructions provided by JTF!  To
any of you who are about to take on the task of making quality biodiesel
pay attention to Keith's emphasis on taking one's time to learn the process.

I must relay and repeat how important accurate titration, quality
catalyst, proper heat control, and proper agitation are for successful
wvo test batches.  Regarding titration I started out with a good digital
scale and pH meter, but poor volume measurement instruments(2ml
eyedroppers) resulted in too much catalyst = failed wash test.  Free 1ml
graduated syringes work beautifully.  Regarding catalyst, initially I
purchased at a small department store a 3kg tub of lye that turned out
to be poorly sealed resulting in = failed test batches.  Quality KOH
measured out while in clear plastic bags has proved to work much
better.  In the test batch processing department, I went through 2 leaky
blenders before I put together a permanent system much like the one on
JTF that relies on consistent heat and agitation.  Combined, these
variables have inevitably led to complete reactions that are washed free
from emulsions.  Now on to scaling up.

Thanks to Keith and anyone else that has contributed information on the
JTF website.

Peace

Marc


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[Biofuel] Test Batch Success......Thanks Keith

2006-08-31 Thread Marc DeGagne
Finally after many months of failed or mediocre wash test results I am 
achieving quick and clean separation of unwashed biodiesel(wvo) and 
water with a paper thin white layer, and all this as a result of the 
useful and encouraging information and instructions provided by JTF!  To 
any of you who are about to take on the task of making quality biodiesel 
pay attention to Keith's emphasis on taking one's time to learn the process.

I must relay and repeat how important accurate titration, quality 
catalyst, proper heat control, and proper agitation are for successful 
wvo test batches.  Regarding titration I started out with a good digital 
scale and pH meter, but poor volume measurement instruments(2ml 
eyedroppers) resulted in too much catalyst = failed wash test.  Free 1ml 
graduated syringes work beautifully.  Regarding catalyst, initially I 
purchased at a small department store a 3kg tub of lye that turned out 
to be poorly sealed resulting in = failed test batches.  Quality KOH 
measured out while in clear plastic bags has proved to work much 
better.  In the test batch processing department, I went through 2 leaky 
blenders before I put together a permanent system much like the one on 
JTF that relies on consistent heat and agitation.  Combined, these 
variables have inevitably led to complete reactions that are washed free 
from emulsions.  Now on to scaling up.

Thanks to Keith and anyone else that has contributed information on the 
JTF website.

Peace

Marc

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Re: [Biofuel] test please

2006-08-11 Thread D.V Subramanian
Yes, I got yr test msg. 
D.V.S. ManiOn 8/11/06, root [EMAIL PROTECTED] wrote:
please reply if this gets through, i changed email clients, and now ikeep getting rejected emails from [EMAIL PROTECTED]___
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[Biofuel] test please

2006-08-10 Thread root
please reply if this gets through, i changed email clients, and now i
keep getting rejected emails from [EMAIL PROTECTED]


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Re: [Biofuel] test please

2006-08-10 Thread MK DuPree
getting through
- Original Message - 
From: root [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Thursday, August 10, 2006 6:10 PM
Subject: [Biofuel] test please


 please reply if this gets through, i changed email clients, and now i
 keep getting rejected emails from [EMAIL PROTECTED]


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Re: [Biofuel] test please

2006-08-10 Thread Kirk McLoren
I do too and I dont have an account with blogger. Its like our posts are being echoed to them  Kirkroot [EMAIL PROTECTED] wrote:  please reply if this gets through, i changed email clients, and now ikeep getting rejected emails from [EMAIL PROTECTED]___Biofuel mailing listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel at Journey to Forever:http://journeytoforever.org/biofuel.htmlSearch the combined Biofuel and Biofuels-biz list archives (50,000 messages):http://www.mail-archive.com/biofuel@sustainablelists.org/ 
		Talk is cheap. Use Yahoo! Messenger to make PC-to-Phone calls.  Great rates starting at 1¢/min.___
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Re: [Biofuel] test please

2006-08-10 Thread root
well crud, now i have THAT to track down...
oh well, thanks folks.

On Thu, 2006-08-10 at 18:22 -0500, MK DuPree wrote:
 getting through
 - Original Message - 
 From: root [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Thursday, August 10, 2006 6:10 PM
 Subject: [Biofuel] test please
 
 
  please reply if this gets through, i changed email clients, and now i
  keep getting rejected emails from [EMAIL PROTECTED]
 
 
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Re: [Biofuel] test please

2006-08-10 Thread tanuki
got through

ken

- Original Message -
From: root [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, August 11, 2006 7:10 AM
Subject: [Biofuel] test please


 please reply if this gets through, i changed email clients, and now i
 keep getting rejected emails from [EMAIL PROTECTED]


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Re: [Biofuel] test please

2006-08-10 Thread Keith Addison
I do too and I dont have an account with blogger. Its like our posts 
are being echoed to them
Kirk

That seems to be right Kirk, I can't find out who it is and can't 
figure out a way to stop it. Probably everybody is receiving them. A 
bit like the folks who join mailing lists and then leave an 
auto-reply whenever they leave the office for more than 9.3 
nanoseconds. Okay, so it's a bit of a misunderexaggeration but you 
know what I mean.

Anyway, sorry folks, these things are sent to try us, among other 
things that are also sent to try us, please bear with it, of such is 
life, as such, it's all part of the Great Golden Tapestry, etc.

Thankyou.

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

 

root [EMAIL PROTECTED] wrote:

please reply if this gets through, i changed email clients, and now i
keep getting rejected emails from [EMAIL PROTECTED]


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[Biofuel] Test Batches

2005-10-17 Thread bio
I have made a few test batches and they all seem to end up hazy with a dark
layer on top. Is this what happens when the reaction is not complete?

I use Phenolphthalein and am concerned that it is not working correctly. I
checked the PH with PH paper after titrating and the PH was 7. I had to add
2 more ml of lye solution to get the PH to 8. I think this is causing me to
have incomplete reactions.

Should the BD be hazy after the reaction takes place? 




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Re: [Biofuel] Test Batches

2005-10-17 Thread Keith Addison
I have made a few test batches and they all seem to end up hazy with a dark
layer on top. Is this what happens when the reaction is not complete?

No, but what's the dark layer on top? Do you mean you think the 
biodiesel layer is darker than it should be?

I use Phenolphthalein and am concerned that it is not working correctly. I
checked the PH with PH paper after titrating and the PH was 7. I had to add
2 more ml of lye solution to get the PH to 8.

Should be 8.5. You're correcting a phenolphthaleihn solution reading 
with pH test strips? That doesn't sound wise. If your phenolphthalein 
is fresh it should be fine. Store it in a dark place.

I think this is causing me to
have incomplete reactions.

Should the BD be hazy after the reaction takes place?

Usually. Are you using SVO or WVO? I don't know what method you're 
using and you don't describe what you did. Do it this way:

Make your first test batch
http://journeytoforever.org/biodiesel_make.html#biodnew

Check your test batches with the wash-test:
http://journeytoforever.org/biodiesel_vehicle.html#quality

Best wishes

Keith


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Re: [Biofuel] Test Batches

2005-10-17 Thread tanuki
Hi Keith,

I'm not sure but I had that first experience too.  I just posted my results
a few minutes ago.

If you look at the picture at the JTF Make your own biodiesel contd page
(biodiesel_make2.html) you will notice a thin layer seemingly on the top
portion.  I noticed that too when I made my test batch yesterday.  It that a
reflection or something?

best regards,

Ken Uy (tanuki)

- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, October 18, 2005 3:09 AM
Subject: Re: [Biofuel] Test Batches


 I have made a few test batches and they all seem to end up hazy with a
dark
 layer on top. Is this what happens when the reaction is not complete?

 No, but what's the dark layer on top? Do you mean you think the
 biodiesel layer is darker than it should be?



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Re: [Biofuel] Test Batch Help

2005-10-07 Thread Bobby Clark

Looks to me like all you need to do is wash and you'll have good biodiesel

Bobby



From: [EMAIL PROTECTED]
Reply-To: Biofuel@sustainablelists.org
To: Biofuel@sustainablelists.org
Subject: [Biofuel] Test Batch Help
Date: Thu, 06 Oct 2005 21:09:01



Could somebody give me a clue as to what I am doing wrong? All my batches 
except one have turned out pale in color. I am using new oil in 1 liter 
batches. My measurements are accurate. Taking a big breath now...




Here is a picture of my samples.

http://evocm.com/ethanol/pvc_pics/DSC03856.JPG 



Most have turned out looking like the jar on the right.

I thought by looking at them one of you could give me a hint.

In the meantime I'll keep plugging away.



Any help is appreciated.



Ben






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Re: [Biofuel] Test Batch Help

2005-10-07 Thread Keith Addison
Hello Ben

Could somebody give me a clue as to what I am doing wrong? All my 
batches except one have turned out pale in color. I am using new oil 
in 1 liter batches. My measurements are accurate. Taking a big 
breath now...

Here is a picture of my samples.
http://evocm.com/ethanol/pvc_pics/DSC03856.JPGhttp://evocm.com/etha 
nol/pvc_pics/DSC03856.JPG 

Most have turned out looking like the jar on the right.
I thought by looking at them one of you could give me a hint.
In the meantime I'll keep plugging away.

Any help is appreciated.

Ben

Why do you think there's a problem with the colour? The colour's 
fine, but that's a LOT of glycerine by-product for virgin oil. What 
exactly did you do?

Anyway, do a wash-test and if all's well go ahead ahead with washing.

Wash-test:
http://journeytoforever.org/biodiesel_vehicle.html#quality

Washing:
http://journeytoforever.org/biodiesel_bubblewash.html

Best wishes

Keith


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Re: [Biofuel] Test Batch Help

2005-10-07 Thread Jason and Katie



Ben,
 looks like it just needs a wash, 
i had the same questions when i started, but it is usually kind of pale when you 
use new oil. it doesn't tend to be darker until you use WVO.

jason
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[Biofuel] Test Batch Help .....Thanks

2005-10-07 Thread biofuel

http://evocm.com/ethanol/pvc_pics/DSC03856.JPG



Thanks guys, I thought I was doing something wrong. 
Apparently, most of the pictures I see are wvo.


Keith, the sample is a combination of two pour offsso there is a liters worth of glycerin in the jar.
I don’t have any translucent containers big enough to hold an entire batch yet, but I do have a 1000 or so mason jars.

Thanks for the Help

Ben

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[Biofuel] Test Batch Help

2005-10-06 Thread biofuel

Could somebody give me a clue as to what I am doing wrong? All my batches except one have turned out pale in color. I am using new oil in 1 liter batches. My measurements are accurate. Taking a big breath now...

Here is a picture of my samples.
http://evocm.com/ethanol/pvc_pics/DSC03856.JPG

Most have turned out looking like the jar on the right.
I thought by looking at them one of you could give me a hint.
In the meantime I'll keep plugging away.

Any help is appreciated.

Ben

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[Biofuel] test

2005-08-28 Thread keith
Mail  failed.  For further assistance, please contact!



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[Biofuel] test

2005-08-28 Thread keith
Mail  failed.  For further assistance, please contact!



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Re: [Biofuel] Test data on SVO/WVO fuel; better than diesel.

2005-07-20 Thread capt3d
i would definitely like to see test data.

-chris b.

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Re: [Biofuel] Test data on SVO/WVO fuel; better than diesel.

2005-07-20 Thread YardPicker
Hello,
I have a 97 Passat burning SVO, and would be interested in the newer Passat, 
but had heard that the newer model TDI (2004 and up?), which is more powerful, 
might be problematic because of more advanced, higher pressure injectors (or 
something to that effect.  Have you heard such a concern?

Chris

In our every deliberation, we must consider the impact of our decisions on

the next seven generations.


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[Biofuel] Test batch no. 2

2005-02-15 Thread Lars Andersson

This message was sent earlier (2005-01-05) but seems to have been lost 
somewhere... Now i am (almost) ready to make the first bigger batch and do 
not want to be a not so proud owner of 100 l. of  glop.. Could anyone 
encourage me to move on with this oil (of course with titration and so on) or 
tell me not to with some hints about how to proceed..?

Thank You

Lars A


Lars Andersson
VŠstanskogsgatan 7
590 71 Ljungsbro
013-66574/070-5334054



Good evening everybody and thank You for this amount of information 
communicated here. This is my first post here after at least six months of just 
reading and thinking while building a reactor from 200l drums.

I made a quick page (for some reason with very poor picture quality, please 
excuse that) about the test batch mentioned by GoHoff and it all looked quite 
allright to me but after the water test i could not resist to shake it once 
more the next day and after that it separated again but i got some kind of 
fluff between the water and the BD (no pictures of that).. It lies on top of 
the water and looks bad... Is that something that a normal wash would take care 
of or something that is bad ?? I have bubble washed the rest of the batch in 
another PET bottle turned upside down with the bottom cut of and  a outlet in 
the screw plug.. The fourth water (this is better than siphoning (??) the 
used wash water out but some of the milky water still gets caught in there) is 
very clear.

http://user.tninet.se/~qrg733j/Krympta/Snoddastest_1.html 

Any comments on the rsults of my test batch would be very appreciated.

Lars A


Lars Andersson
VŠstanskogsgatan 7
590 71 Ljungsbro
013-66574/070-5334054
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[Biofuel] test message - multiples

2005-01-17 Thread Martin K


to myself (NOT the list)
thank you.
--
Martin K
http://wwia.org/sgroup/biofuel/
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[Biofuel] test

2005-01-03 Thread Martin Klingensmith


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Re: [Biofuel] test

2005-01-03 Thread Phillip Wolfe

Biofuel Readers, 

Are they ways to influence U.S. local cities to
officially adopt biofuels, alternative transporation,
and smart growth? 

Yes, via the General Plan.  In the United States each
city is required to adopt a General Plan. By state
law, the General Plan should contain elements.  The
General Plan requires public participation and is an
avenue for you to influence public policy to include
biofuels and clean fuels via the Circlation Element
and the Conservation Element, - cities may not have
the same elements. 

For a general background on the General Plan, please
refer to see below weblinks:

http://www.lib.berkeley.edu/ENVI/genplans.html#intro

What is a general plan? General plans have many
synonyms, among them comprehensive plan, development
plan, land-use plan, master plan, and urban plan.
Simply stated, a general plan is the official
statement of a municipal legislative body which sets
forth its major policies concerning desirable future
physical development... (Kent, The Urban general
plan, 1964). 

As further elaborated in Planning made easy (Toner, et
al., 1994), a general plan is: 
--A public guide to community decision making 
--An assessment of the community's needs 
--A statement of community values, goals, objectives 
--A blueprint for the community's physical development

--A public document adopted by the government 
--Continuously updated as conditions change 

Note that California state law requires that each city
general plan contain the following seven (7) elements:


1)circulation (transportation)!
2)conservation! 
3)housing 
4)land use 
5)noise 
6)open-space 
7)safety 

Have a Prosperous New Year.

Phillip Wolfe
Certificate in Urban  Regional Planning
BA-BioScience/Environment
MBA-Planning





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[Biofuel] test

2004-12-24 Thread Martin K


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Re: [Biofuel] test batches and the JtF quality test

2004-12-21 Thread John Guttridge


again. I will post the results when done.

John

Keith Addison wrote:

Thankyou John.

I hope this discussion can resume now.

Best wishes

Keith Addison
List owner



to todd and the list in general,

I would like to sincerely apologize for allowing myself to get 
involved in this flame war. It was inappropriate and not at all 
constructive.


Further I apologize for my use of inappropriate language.

I still have unanswered questions that I hope I can get answered here. 
I will continue to post the results of my tests in the hope that they 
will further the goal of making the production of high quality 
biodiesel accessible to all.


Sincerely,
John Guttridge



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Re: [Biofuel] test batches and the JtF quality test

2004-12-20 Thread John P Gochoco



Not that you would be interested to know...

So called linscott...aka dana linscott...aka dana can still be found over 
at the biodiesel yahoogroups performing exactly the same manner to which you 
have just describedunfortunately for most.


Late...

John(yet another John)



- Original Message - 
From: Keith Addison [EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Sunday, December 19, 2004 11:18 AM
Subject: Re: [Biofuel] test batches and the JtF quality test



Hello John

Actually, it takes a brave man to tell a few home truths to John Tillman 
(aka tillyfromparadise, aka about 30 false IDs created to give the 
impression of group support) - you run the risk of precipitating a 
tireless, relentless, truly mindless, vicious and utterly integrity-free 
hate war against you for the next three years or so. I really hope that 
won't happen to you. In fact it doesn't even need home truths - what 
started his hate war against me, Journey to Forever, Aleks Kac (who he's 
never encountered in any way), Todd Swearingen, Steve Spence, and the 
Biofuel list? Nothing. That's right, nothing at all. I asked him some 
questions, that needed asking, without being in any way confrontational or 
rude or anything, and he decided I'd insulted him. Nobody else could see 
it, lots of people asked him to come off it, but no. Hate hate hate! Ever 
since, for the last three years. One sick puppy - a liar, a thief, a 
plagiarist, a multiple imposter, all very well documented. You can read a 
history of it here, if you really want to:

http://groups.yahoo.com/group/Biodiesel/message/4254

Actually there are two of them, they often work in concert. The other 
one's a total creep named Linscott, who used to be a member here until, to 
loud public demand, very belatedly, after he'd wrought a lot of harm, he 
got the boot, also about three years ago or something. He's has lost no 
opportunity to stir it up wherever he can ever since. There's some 
background on him here:

http://infoarchive.net/sgroup/BIOFUEL/37931/

A right couple of psychos, these two. Apart from the above ref 
(necessary), instead of using the list as a platform to wage war from, 
I've been at considerable pains to keep this vomitous stuff away from the 
Biofuel list - unlike Tillscott, who've taken it everywhere they can and 
totalled several previously useful forums in the doing, and done the 
biofuels movement a deal of damage. As if they care. It's easy to be 
destructive.


And yes, both of them lurk around here whispering their noxious BS to 
newcomers offlist. There's not much we can do about it, but we figured 
long ago that if you can't figure that out for yourself you probably won't 
be able to do much else worth half a damn anyway, and so it's proved, you 
being a case in point. There's also someone here right now who proves the 
opposite case in point, but that's his problem. He's going to have to 
choose, he can't have it both ways.


In fact, interestingly, despite all the wreckage elsewhere, these two 
maniacs haven't succeeded in doing us any damage at all, not me, nor 
Journey to Forever, nor the Biofuel list, nor Todd, Aleks and Steve. For 
our part, only damaging *truths* could do that, and there aren't any.


Anyway, John, I'm glad you put it in perspective, but generally we can do 
very well without any acknowledgement of this worthless stuff, thankyou 
very much.


As for this:


I would like to state to the list in general and especially kieth that
no one should take any of this personally.


This is how these creeps can distort things. John, if I got furious and 
took it personally every time somebody here or elsewhere criticised 
something at Journey to Forever, how would we ever have developed the 
resources there the way we have? Criticism and critical thinking are 
positive, or should be, not just a personal attack. It's a major factor at 
this forum and one reason we started it in the first place. There's a lot 
of original work at the Journey to Forever website biofuels section, but 
even there we can acknowledge a big debt to the Biofuel list and what 
we've learnt from the group over the years, and I have often acknowledged 
that. Genuine criticism is of course always welcome, right or wrong. Then 
it gets debated and the whole thing moves forward. Axe-grinding is not 
welcome. They're easily distinguished.


And this:

also I have observed that keith frequently expresses frustration that 
things get gone over again and again


Do I? I've seen other people saying that. I just wish (often!) that more 
people would make better use of the archives, but also I can remember 
saying quite a few times that a question's been asked before but no harm 
in asking again, and pulling previous answers out of the archives for an 
airing rather than just giving the link. It can generate new responses, 
and even if not it makes the stuff easier to find in the archives next 
time.


Best wishes

Keith Addison
Journey to Forever
KYOTO

Re: [Biofuel] test batches and the JtF quality test

2004-12-20 Thread John Guttridge



Appal Energy wrote:

John,

I don't know why you find it necessary to proclaim specific matters to 
be sore spots or as having been tak[en]... personally.


because you are being pissy about this whole thing.



What I do find perplexing is the amazing number of people who don't read 
or follow instructions when available, modify them under the premise of 
experimentation, even when they're trying out their first batches and 
should be adhering to them more rigidly than any other time, and then 
proclaim that they don't work, or aren't reproducable.


you will note that the reason that I posted it was to do a sort of peer 
review process. you pointed out that I made a mistake in my 
experimentation and then I took steps to correct that mistake.




What I find even more amazing (actually, not) is the fact that those 
very same people, once it is discerned or they reveal that the available 
instructions weren't adhered to, continue to find fault with everything 
but their own failure to read and follow.


you will note that in my first reply to this I said that I understood 
that the volume could be a problem, then in my second I said that I 
would make a bigger test batch and repeat the experiment with the 
suggested volume.




My personal belief is that if you want to dally in your laboratory, 
great. But if you wish to lay claims that aren't accurate pursuant to 
dalliances that are at great variance from any instructions (baseline) 
that you might imply as having followed, then you probably deserve any 
frustrations that acrue. Mind you the instructions did say to add 150 ml 
of water, not 150 ml of icecubes, or chilled water, or even heated 
water, much less 4 ml in a culture tube. (Hopefully, you did take note 
of the mention of magnified error when working in such micro-quantities.)


the reason that I did this experiment at all was because I kept making 
1L batches following the instructions to the letter that washed nicely 
but failed the quality test. I figured I could save oil by doing micro 
tests. you pointed out the error in that and I am taking steps to 
eliminate that error.




And if your preference is to declare that your failing to run the middle 
course is a sore spot with others who might point this out, then I'd 
have to say with certainty you're welcome to whatever frustration you 
create for yourself. Yes indeed, you are entitled to them.


what??? I suggested that others with cold water may have problems, luc 
backed me up.




My bet is that if you're sharp enough to conduct all your variances and 
question your results, you might eventually learn from error and begin 
to acknowledge the basic necessity of using (and following) a map  when 
venturing into the unknown, rather than just sticking a wetted finger 
into the air and presuming that all winds blow from the north.


following the map doesn't yield arrival at the destination and I start 
questioning the map. I am doing the best to have peer review of my 
questionings. if you were a good scientist you would say silly john, 
you made an error here and I would say oh, I am sorry, you are right, 
let me fix that and try again and we would have advancement.




Nothing personal. Just taking note of your obstinance.


I post results which are questioned and then agree to make the steps to 
fix the questions. I ask more questions and answer those asked of me, 
you wave you dick around and call me a bad scientist without answering 
the majority of my questions. who is being obstinate?


nothing personal, just making note of your hipocracy.

John


Todd Swearingen

Post script:

We've been washing with well/ground water, averaging ~55*F, for the past 
five years now. Do you think perhaps we should wedge open the shop doors 
and windows during the winter months in hopes that washes and reactions 
will work better? There are reasons why shops and labs are kept at 
reasonable temperatures, the first and foremost is not just to keep the 
human occupants fuzzy and comfortable.


- Original Message - From: John Guttridge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Sunday, December 19, 2004 1:28 AM
Subject: Re: [Biofuel] test batches and the JtF quality test



Todd,

sorry to have stuck a sore spot with you, please stop taking this all 
personally. I never meant any of this as an attack at anyone, I am 
picking at things until I understand them. the purpose of this forum 
seems to be streamlining the process of learning. also I have observed 
that keith frequently expresses frustration that things get gone over 
again and again, lets make the instructions more specific to avoid this.


Appal Energy wrote:


John,


I still think that temperature has a drastic effect on seperation time




And you're correct. But there aren't too many people out there who 
are going to be washing with water direct from a glacier fed stream.



I live in the northeast, my basement is cold and the pipes run through 
there, this has an effect

Re: [Biofuel] test batches and the JtF quality test

2004-12-20 Thread Appal Energy



I certainly hope I didn't hear you right.

And if I did, I suggest you find a new approach, because the antagonistic 
one you're pursuing certainly isn't going to gain you anything.


I'd also suggest that you reread those answers given you. You will find that 
virtually every one of your questions (as few as they were) and a number of 
your statements were addressed. Since you choose to ignore that minor detail 
and opt instead to issue insult, distort what was actually written, pencil 
in what wasn't and instigate arguement, one can only be lead to believe that 
answers are not what you're primary interest is.


Good day.

- Original Message - 
From: John Guttridge [EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Sunday, December 19, 2004 9:38 PM
Subject: Re: [Biofuel] test batches and the JtF quality test



todd,

Appal Energy wrote:

John,

I don't know why you find it necessary to proclaim specific matters to be 
sore spots or as having been tak[en]... personally.


because you are being pissy about this whole thing.



What I do find perplexing is the amazing number of people who don't read 
or follow instructions when available, modify them under the premise of 
experimentation, even when they're trying out their first batches and 
should be adhering to them more rigidly than any other time, and then 
proclaim that they don't work, or aren't reproducable.


you will note that the reason that I posted it was to do a sort of peer 
review process. you pointed out that I made a mistake in my 
experimentation and then I took steps to correct that mistake.




What I find even more amazing (actually, not) is the fact that those very 
same people, once it is discerned or they reveal that the available 
instructions weren't adhered to, continue to find fault with everything 
but their own failure to read and follow.


you will note that in my first reply to this I said that I understood that 
the volume could be a problem, then in my second I said that I would make 
a bigger test batch and repeat the experiment with the suggested volume.




My personal belief is that if you want to dally in your laboratory, 
great. But if you wish to lay claims that aren't accurate pursuant to 
dalliances that are at great variance from any instructions (baseline) 
that you might imply as having followed, then you probably deserve any 
frustrations that acrue. Mind you the instructions did say to add 150 ml 
of water, not 150 ml of icecubes, or chilled water, or even heated water, 
much less 4 ml in a culture tube. (Hopefully, you did take note of the 
mention of magnified error when working in such micro-quantities.)


the reason that I did this experiment at all was because I kept making 1L 
batches following the instructions to the letter that washed nicely but 
failed the quality test. I figured I could save oil by doing micro tests. 
you pointed out the error in that and I am taking steps to eliminate that 
error.




And if your preference is to declare that your failing to run the middle 
course is a sore spot with others who might point this out, then I'd have 
to say with certainty you're welcome to whatever frustration you create 
for yourself. Yes indeed, you are entitled to them.


what??? I suggested that others with cold water may have problems, luc 
backed me up.




My bet is that if you're sharp enough to conduct all your variances and 
question your results, you might eventually learn from error and begin to 
acknowledge the basic necessity of using (and following) a map  when 
venturing into the unknown, rather than just sticking a wetted finger 
into the air and presuming that all winds blow from the north.


following the map doesn't yield arrival at the destination and I start 
questioning the map. I am doing the best to have peer review of my 
questionings. if you were a good scientist you would say silly john, you 
made an error here and I would say oh, I am sorry, you are right, let me 
fix that and try again and we would have advancement.




Nothing personal. Just taking note of your obstinance.


I post results which are questioned and then agree to make the steps to 
fix the questions. I ask more questions and answer those asked of me, you 
wave you dick around and call me a bad scientist without answering the 
majority of my questions. who is being obstinate?


nothing personal, just making note of your hipocracy.

John


Todd Swearingen

Post script:

We've been washing with well/ground water, averaging ~55*F, for the past 
five years now. Do you think perhaps we should wedge open the shop doors 
and windows during the winter months in hopes that washes and reactions 
will work better? There are reasons why shops and labs are kept at 
reasonable temperatures, the first and foremost is not just to keep the 
human occupants fuzzy and comfortable.


- Original Message - From: John Guttridge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Sunday, December 19, 2004 1:28 AM
Subject

Re: [Biofuel] test batches and the JtF quality test

2004-12-20 Thread Keith Addison




Hi Keith,

Not that you would be interested to know...

So called linscott...aka dana linscott...aka dana can still be 
found over at the biodiesel yahoogroups performing exactly the same 
manner to which you have just describedunfortunately for most.


Yup, he's there, and Tillman, and a bunch of others too. That used to 
be a good group. Very few of the longer-term members ever post there 
now. Mostly just this misbegotten bunch leading newcomers astray. 
Sad. People of the lie:

http://www.amasci.com/maglev/levbill1.html
The Pathological Dishonesty Disease


Late...

John(yet another John)


:-) A fine name, to be sure.

Best wishes

Keith


- Original Message - From: Keith Addison 
[EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Sunday, December 19, 2004 11:18 AM
Subject: Re: [Biofuel] test batches and the JtF quality test



Hello John

Actually, it takes a brave man to tell a few home truths to John 
Tillman (aka tillyfromparadise, aka about 30 false IDs created to 
give the impression of group support) - you run the risk of 
precipitating a tireless, relentless, truly mindless, vicious and 
utterly integrity-free hate war against you for the next three 
years or so. I really hope that won't happen to you. In fact it 
doesn't even need home truths - what started his hate war against 
me, Journey to Forever, Aleks Kac (who he's never encountered in 
any way), Todd Swearingen, Steve Spence, and the Biofuel list? 
Nothing. That's right, nothing at all. I asked him some questions, 
that needed asking, without being in any way confrontational or 
rude or anything, and he decided I'd insulted him. Nobody else 
could see it, lots of people asked him to come off it, but no. Hate 
hate hate! Ever since, for the last three years. One sick puppy - a 
liar, a thief, a plagiarist, a multiple imposter, all very well 
documented. You can read a history of it here, if you really want 
to:

http://groups.yahoo.com/group/Biodiesel/message/4254

Actually there are two of them, they often work in concert. The 
other one's a total creep named Linscott, who used to be a member 
here until, to loud public demand, very belatedly, after he'd 
wrought a lot of harm, he got the boot, also about three years ago 
or something. He's has lost no opportunity to stir it up wherever 
he can ever since. There's some background on him here:

http://infoarchive.net/sgroup/BIOFUEL/37931/

A right couple of psychos, these two. Apart from the above ref 
(necessary), instead of using the list as a platform to wage war 
from, I've been at considerable pains to keep this vomitous stuff 
away from the Biofuel list - unlike Tillscott, who've taken it 
everywhere they can and totalled several previously useful forums 
in the doing, and done the biofuels movement a deal of damage. As 
if they care. It's easy to be destructive.


And yes, both of them lurk around here whispering their noxious BS 
to newcomers offlist. There's not much we can do about it, but we 
figured long ago that if you can't figure that out for yourself you 
probably won't be able to do much else worth half a damn anyway, 
and so it's proved, you being a case in point. There's also someone 
here right now who proves the opposite case in point, but that's 
his problem. He's going to have to choose, he can't have it both 
ways.


In fact, interestingly, despite all the wreckage elsewhere, these 
two maniacs haven't succeeded in doing us any damage at all, not 
me, nor Journey to Forever, nor the Biofuel list, nor Todd, Aleks 
and Steve. For our part, only damaging *truths* could do that, and 
there aren't any.


Anyway, John, I'm glad you put it in perspective, but generally we 
can do very well without any acknowledgement of this worthless 
stuff, thankyou very much.


As for this:


I would like to state to the list in general and especially kieth that
no one should take any of this personally.


This is how these creeps can distort things. John, if I got furious 
and took it personally every time somebody here or elsewhere 
criticised something at Journey to Forever, how would we ever have 
developed the resources there the way we have? Criticism and 
critical thinking are positive, or should be, not just a personal 
attack. It's a major factor at this forum and one reason we started 
it in the first place. There's a lot of original work at the 
Journey to Forever website biofuels section, but even there we can 
acknowledge a big debt to the Biofuel list and what we've learnt 
from the group over the years, and I have often acknowledged that. 
Genuine criticism is of course always welcome, right or wrong. Then 
it gets debated and the whole thing moves forward. Axe-grinding is 
not welcome. They're easily distinguished.


And this:

also I have observed that keith frequently expresses frustration 
that things get gone over again and again


Do I? I've seen other people saying that. I just wish (often!) that 
more people would make better use of the archives

Re: [Biofuel] test batches and the JtF quality test

2004-12-20 Thread John Guttridge



I would like to sincerely apologize for allowing myself to get involved 
in this flame war. It was inappropriate and not at all constructive.


Further I apologize for my use of inappropriate language.

I still have unanswered questions that I hope I can get answered here. I 
will continue to post the results of my tests in the hope that they will 
further the goal of making the production of high quality biodiesel 
accessible to all.


Sincerely,
John Guttridge

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Re: [Biofuel] test batches and the JtF quality test

2004-12-20 Thread Keith Addison



I hope this discussion can resume now.

Best wishes

Keith Addison
List owner



to todd and the list in general,

I would like to sincerely apologize for allowing myself to get 
involved in this flame war. It was inappropriate and not at all 
constructive.


Further I apologize for my use of inappropriate language.

I still have unanswered questions that I hope I can get answered 
here. I will continue to post the results of my tests in the hope 
that they will further the goal of making the production of high 
quality biodiesel accessible to all.


Sincerely,
John Guttridge


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http://infoarchive.net/sgroup/biofuel/



Re: [Biofuel] test batches and the JtF quality test

2004-12-19 Thread Appal Energy




I still think that temperature has a drastic effect on seperation time


And you're correct. But there aren't too many people out there who are going 
to be washing with water direct from a glacier fed stream.



I am pointing out a sticking point
that people may have (if I am having this problem other people are
probably having it too).


Some people get stuck. Some eventually recognize it for what it is and 
adapt.



one of the problems that I have with all of this
is that the instructions are really general


Not really. They're pretty specific. They may not have had an exact 
temperature pasted all over them, but they were specific beyond that. You 
could at least note that you opted to go off the beaten path and then lay 
claim as to unreproducable. That in itself is a little bit misleading to 
those who read it or who come to it later.


Making biodiesel is not rocket science. It's not exactly bucket science 
either, as you have to use a little common sense and stick somewhere close 
to the middle of what's known to work.


Todd Swearingen

- Original Message - 
From: John Guttridge [EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Saturday, December 18, 2004 5:17 PM
Subject: Re: [Biofuel] test batches and the JtF quality test


Resending the following because I am unsure if it was caught in the 
outage:



Understood. I will produce a batch large enough to make several runs at
the 150mL test and post the results.

I consumed the remains of my last test batch in a 125mL run (it was all
that was left) and I followed your agitation (10 times up and down
violently). it had seperated in to two clearly stratified sections
within abbout 1 minute with 60*F water however it still had lots of
tiny bubbles in both parts (sort of a milky yellow and a milky white). is 
that what you mean by clear seperation?


I still think that temperature has a drastic effect on seperation time
which I will test and post the results and methods of my experiment.

I would like to state to the list in general and especially kieth that
no one should take any of this personally. I am posting my results so
that people can point out errors. I am pointing out a sticking point
that people may have (if I am having this problem other people are
probably having it too). any good science is a process of peer review.
one posts methods and results others duplicate ones experiments and if
they prove reporducable and consistant then they are seen by the
community to be valid. one of the problems that I have with all of this
is that the instructions are really general and I fear that there are
factors that are important but are not mentioned such that they can be
controlled.

John

Appal Energy wrote:

John Guttridge,

If you're looking for reproducability, you need to follow baseline, not 
modify a test/experiment so as to suit your own preference or conditions.


You've apparently neglected to consider increases in sampling error that 
occur when conducting tests at micro-levels/volumes. You compound any 
flaw in your final evaluations by conducting not only the wash but the 
esterification with miniscule volumes. Unless your preparations are made 
with electronic scales to the thousandth of a gram, your alcohol and 
feedstock volumes determined by weight using the same scale, rather than 
relying upon glassware that forewarns of + or - 5% error factor, not to 
mention the + or - 10% human error factor (whether you know what end of 
the miniscus to take your measurements from or not) you only compound the 
degree of errors that are or can be represented by your conclusions.


There is an enormous world of difference between reproducablity/results 
achieved on 150 ml samples and samples no bigger than single liters, even 
when conducted by professionals with decades of experience.


As to your questioning the time frame that I mentioned for separation of 
well processed fuel, you need to take notice of the difference between 
the agitation period stated in my post and the general guideline you 
opted to modify.


You also need to take notice that the wash test is not represented as 
anything more than a quick and simple manner of determing how an operator 
may care or feel reasonably safe to proceed with what he or she may 
believe to be biodiesel.


The guidelines that are offered on this list and at Journey to Forever 
are intended to assist the general public in getting their fuel near or 
to the level that would pass the scrutiny of spec fuel, despite the fact 
that they may be working on dimestore budgets.


If you can afford the luxury and it's absolute guarantees of finished 
product quality that you seek, I would suggest that you establish a 
procedural regimen, produce what you have reason to believe is a 
well-crafted product and then submit the sample to the testing methods 
established in D-6751. You'll quickly surprise yourself at how easily 
that standard can be neared or met in a meticulous homebrewer's 
environment

Re: [Biofuel] test batches and the JtF quality test

2004-12-19 Thread Legal Eagle



- Original Message - 
From: Appal Energy [EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Saturday, December 18, 2004 8:46 PM
Subject: Re: [Biofuel] test batches and the JtF quality test



John,


I still think that temperature has a drastic effect on seperation time


And you're correct. But there aren't too many people out there who are 
going to be washing with water direct from a glacier fed stream.


Except that I have posted a few times stating that I use well water direct 
and not word one was ever mentioned until I started asking if wash water 
temperature is important.
Point is, not that I went without for awhile, but that now the question IS 
being adressed.
I had a few problems with emulsion, but only in the last two batches when 
the weather changed and it started getting cold. Prior to that, and none of 
the variables had changed, everything was clean and precise and good fuel 
resulted every time.
This question of wash water temperature needs to be added as a requisite in 
the instructional stages of making good fuel. Just assuming that Eskimos 
will not be interested doesn't make it. So it seems that now it has been 
addressed, and I for one am very pleased that it has.
Now it only leaves to have that information readily available to anyone 
wanting to learn the methodology of home brewing biodiesel. I suggest that 
it be added in the washing section at JtF somewhere. That is where I got 
my education from, and I must say that I am very pleased with what I was 
taught, so in the interest of those coming afterward it should be added 
somewhere evident.
I am now in the process of not only adding a second settling tank (insulated 
of course) but also of adding a water pre-heat tank using a 115V immersion 
heater to warm up the well water I will again be using to wash in the Spring 
when I get my production back on line.
Just leaving this information in the archives doesn't cut it either, it 
needs to be accessible in the tutorials.(Sorry Keith, I don't want to tell 
you what to do, but this seems to be an important detail in the end goal of 
proper biodiesel production.) It obviously has been an oversight, and that 
is part of what this forum is all about, the betterment of the end user 
product, so there it is.

Luc


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Re: [Biofuel] test batches and the JtF quality test

2004-12-19 Thread John Guttridge



sorry to have stuck a sore spot with you, please stop taking this all 
personally. I never meant any of this as an attack at anyone, I am 
picking at things until I understand them. the purpose of this forum 
seems to be streamlining the process of learning. also I have observed 
that keith frequently expresses frustration that things get gone over 
again and again, lets make the instructions more specific to avoid this.


Appal Energy wrote:

John,


I still think that temperature has a drastic effect on seperation time



And you're correct. But there aren't too many people out there who are 
going to be washing with water direct from a glacier fed stream.


I live in the northeast, my basement is cold and the pipes run through 
there, this has an effect. that doesn't sound that uncommon.





I am pointing out a sticking point
that people may have (if I am having this problem other people are
probably having it too).



Some people get stuck. Some eventually recognize it for what it is and 
adapt.


right, so lets put it in the instructions so that no one gets stuck in 
the first place. as you may have noticed I am of the second group, now I 
want to make things different for the next batch of newbies.





one of the problems that I have with all of this
is that the instructions are really general



Not really. They're pretty specific. They may not have had an exact 
temperature pasted all over them, but they were specific beyond that. 
You could at least note that you opted to go off the beaten path and 
then lay claim as to unreproducable. That in itself is a little bit 
misleading to those who read it or who come to it later.


there was no mention of temperature. that is a factor that can cause 
problems, I would say that makes the instructions fairly general.


mix 150mL of that with 150mL of this and shake the hell out of it for 
10 seconds, let sit for 30 minutes and see what you get is pretty general.




Making biodiesel is not rocket science. It's not exactly bucket science 
either, as you have to use a little common sense and stick somewhere 
close to the middle of what's known to work.


Todd Swearingen

- Original Message - From: John Guttridge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Saturday, December 18, 2004 5:17 PM
Subject: Re: [Biofuel] test batches and the JtF quality test


Resending the following because I am unsure if it was caught in the 
outage:



Understood. I will produce a batch large enough to make several runs at
the 150mL test and post the results.

I consumed the remains of my last test batch in a 125mL run (it was all
that was left) and I followed your agitation (10 times up and down
violently). it had seperated in to two clearly stratified sections
within abbout 1 minute with 60*F water however it still had lots of
tiny bubbles in both parts (sort of a milky yellow and a milky white). 
is that what you mean by clear seperation?


I still think that temperature has a drastic effect on seperation time
which I will test and post the results and methods of my experiment.

I would like to state to the list in general and especially kieth that
no one should take any of this personally. I am posting my results so
that people can point out errors. I am pointing out a sticking point
that people may have (if I am having this problem other people are
probably having it too). any good science is a process of peer review.
one posts methods and results others duplicate ones experiments and if
they prove reporducable and consistant then they are seen by the
community to be valid. one of the problems that I have with all of this
is that the instructions are really general and I fear that there are
factors that are important but are not mentioned such that they can be
controlled.

John

Appal Energy wrote:


John Guttridge,

If you're looking for reproducability, you need to follow baseline, 
not modify a test/experiment so as to suit your own preference or 
conditions.


You've apparently neglected to consider increases in sampling error 
that occur when conducting tests at micro-levels/volumes. You 
compound any flaw in your final evaluations by conducting not only 
the wash but the esterification with miniscule volumes. Unless your 
preparations are made with electronic scales to the thousandth of a 
gram, your alcohol and feedstock volumes determined by weight using 
the same scale, rather than relying upon glassware that forewarns of 
+ or - 5% error factor, not to mention the + or - 10% human error 
factor (whether you know what end of the miniscus to take your 
measurements from or not) you only compound the degree of errors that 
are or can be represented by your conclusions.


There is an enormous world of difference between 
reproducablity/results achieved on 150 ml samples and samples no 
bigger than single liters, even when conducted by professionals with 
decades of experience.


As to your questioning the time frame that I mentioned for separation

Re: [Biofuel] test batches and the JtF quality test

2004-12-19 Thread Appal Energy



I don't know why you find it necessary to proclaim specific matters to be 
sore spots or as having been tak[en]... personally.


What I do find perplexing is the amazing number of people who don't read or 
follow instructions when available, modify them under the premise of 
experimentation, even when they're trying out their first batches and 
should be adhering to them more rigidly than any other time, and then 
proclaim that they don't work, or aren't reproducable.


What I find even more amazing (actually, not) is the fact that those very 
same people, once it is discerned or they reveal that the available 
instructions weren't adhered to, continue to find fault with everything but 
their own failure to read and follow.


My personal belief is that if you want to dally in your laboratory, great. 
But if you wish to lay claims that aren't accurate pursuant to dalliances 
that are at great variance from any instructions (baseline) that you might 
imply as having followed, then you probably deserve any frustrations that 
acrue. Mind you the instructions did say to add 150 ml of water, not 150 ml 
of icecubes, or chilled water, or even heated water, much less 4 ml in a 
culture tube. (Hopefully, you did take note of the mention of magnified 
error when working in such micro-quantities.)


And if your preference is to declare that your failing to run the middle 
course is a sore spot with others who might point this out, then I'd have to 
say with certainty you're welcome to whatever frustration you create for 
yourself. Yes indeed, you are entitled to them.


My bet is that if you're sharp enough to conduct all your variances and 
question your results, you might eventually learn from error and begin to 
acknowledge the basic necessity of using (and following) a map  when 
venturing into the unknown, rather than just sticking a wetted finger into 
the air and presuming that all winds blow from the north.


Nothing personal. Just taking note of your obstinance.

Todd Swearingen

Post script:

We've been washing with well/ground water, averaging ~55*F, for the past 
five years now. Do you think perhaps we should wedge open the shop doors and 
windows during the winter months in hopes that washes and reactions will 
work better? There are reasons why shops and labs are kept at reasonable 
temperatures, the first and foremost is not just to keep the human occupants 
fuzzy and comfortable.


- Original Message - 
From: John Guttridge [EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Sunday, December 19, 2004 1:28 AM
Subject: Re: [Biofuel] test batches and the JtF quality test



Todd,

sorry to have stuck a sore spot with you, please stop taking this all 
personally. I never meant any of this as an attack at anyone, I am picking 
at things until I understand them. the purpose of this forum seems to be 
streamlining the process of learning. also I have observed that keith 
frequently expresses frustration that things get gone over again and 
again, lets make the instructions more specific to avoid this.


Appal Energy wrote:

John,


I still think that temperature has a drastic effect on seperation time



And you're correct. But there aren't too many people out there who are 
going to be washing with water direct from a glacier fed stream.


I live in the northeast, my basement is cold and the pipes run through 
there, this has an effect. that doesn't sound that uncommon.





I am pointing out a sticking point
that people may have (if I am having this problem other people are
probably having it too).



Some people get stuck. Some eventually recognize it for what it is and 
adapt.


right, so lets put it in the instructions so that no one gets stuck in the 
first place. as you may have noticed I am of the second group, now I want 
to make things different for the next batch of newbies.





one of the problems that I have with all of this
is that the instructions are really general



Not really. They're pretty specific. They may not have had an exact 
temperature pasted all over them, but they were specific beyond that. You 
could at least note that you opted to go off the beaten path and then lay 
claim as to unreproducable. That in itself is a little bit misleading 
to those who read it or who come to it later.


there was no mention of temperature. that is a factor that can cause 
problems, I would say that makes the instructions fairly general.


mix 150mL of that with 150mL of this and shake the hell out of it for 10 
seconds, let sit for 30 minutes and see what you get is pretty general.




Making biodiesel is not rocket science. It's not exactly bucket science 
either, as you have to use a little common sense and stick somewhere 
close to the middle of what's known to work.


Todd Swearingen

- Original Message - From: John Guttridge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Saturday, December 18, 2004 5:17 PM
Subject: Re: [Biofuel] test batches and the JtF quality test

Re: [Biofuel] test batches and the JtF quality test

2004-12-19 Thread Keith Addison



Actually, it takes a brave man to tell a few home truths to John 
Tillman (aka tillyfromparadise, aka about 30 false IDs created to 
give the impression of group support) - you run the risk of 
precipitating a tireless, relentless, truly mindless, vicious and 
utterly integrity-free hate war against you for the next three years 
or so. I really hope that won't happen to you. In fact it doesn't 
even need home truths - what started his hate war against me, Journey 
to Forever, Aleks Kac (who he's never encountered in any way), Todd 
Swearingen, Steve Spence, and the Biofuel list? Nothing. That's 
right, nothing at all. I asked him some questions, that needed 
asking, without being in any way confrontational or rude or anything, 
and he decided I'd insulted him. Nobody else could see it, lots of 
people asked him to come off it, but no. Hate hate hate! Ever since, 
for the last three years. One sick puppy - a liar, a thief, a 
plagiarist, a multiple imposter, all very well documented. You can 
read a history of it here, if you really want to:

http://groups.yahoo.com/group/Biodiesel/message/4254

Actually there are two of them, they often work in concert. The other 
one's a total creep named Linscott, who used to be a member here 
until, to loud public demand, very belatedly, after he'd wrought a 
lot of harm, he got the boot, also about three years ago or 
something. He's has lost no opportunity to stir it up wherever he can 
ever since. There's some background on him here:

http://infoarchive.net/sgroup/BIOFUEL/37931/

A right couple of psychos, these two. Apart from the above ref 
(necessary), instead of using the list as a platform to wage war 
from, I've been at considerable pains to keep this vomitous stuff 
away from the Biofuel list - unlike Tillscott, who've taken it 
everywhere they can and totalled several previously useful forums in 
the doing, and done the biofuels movement a deal of damage. As if 
they care. It's easy to be destructive.


And yes, both of them lurk around here whispering their noxious BS to 
newcomers offlist. There's not much we can do about it, but we 
figured long ago that if you can't figure that out for yourself you 
probably won't be able to do much else worth half a damn anyway, and 
so it's proved, you being a case in point. There's also someone here 
right now who proves the opposite case in point, but that's his 
problem. He's going to have to choose, he can't have it both ways.


In fact, interestingly, despite all the wreckage elsewhere, these two 
maniacs haven't succeeded in doing us any damage at all, not me, nor 
Journey to Forever, nor the Biofuel list, nor Todd, Aleks and Steve. 
For our part, only damaging *truths* could do that, and there aren't 
any.


Anyway, John, I'm glad you put it in perspective, but generally we 
can do very well without any acknowledgement of this worthless stuff, 
thankyou very much.


As for this:


I would like to state to the list in general and especially kieth that
no one should take any of this personally.


This is how these creeps can distort things. John, if I got furious 
and took it personally every time somebody here or elsewhere 
criticised something at Journey to Forever, how would we ever have 
developed the resources there the way we have? Criticism and critical 
thinking are positive, or should be, not just a personal attack. It's 
a major factor at this forum and one reason we started it in the 
first place. There's a lot of original work at the Journey to Forever 
website biofuels section, but even there we can acknowledge a big 
debt to the Biofuel list and what we've learnt from the group over 
the years, and I have often acknowledged that. Genuine criticism is 
of course always welcome, right or wrong. Then it gets debated and 
the whole thing moves forward. Axe-grinding is not welcome. They're 
easily distinguished.


And this:

also I have observed that keith frequently expresses frustration 
that things get gone over again and again


Do I? I've seen other people saying that. I just wish (often!) that 
more people would make better use of the archives, but also I can 
remember saying quite a few times that a question's been asked before 
but no harm in asking again, and pulling previous answers out of the 
archives for an airing rather than just giving the link. It can 
generate new responses, and even if not it makes the stuff easier to 
find in the archives next time.


Best wishes

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




Tilly,

not really trying to say that keith has made a mistake on his site. 
instead I was asking for more information on how to conduct the test 
in a reproducible manner. I have a lot of respect for keith and what 
he does. you seem to lack that and I would be interested to 
understand why.


I think that it is probably a good test to weed out the grossly 
under reacted batches and the way too much catalyst batches. I 

Re: [Biofuel] test batches and the JtF quality test

2004-12-19 Thread Keith Addison




G'day all;

- Original Message - From: Appal Energy [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Saturday, December 18, 2004 8:46 PM
Subject: Re: [Biofuel] test batches and the JtF quality test



John,


I still think that temperature has a drastic effect on seperation time


And you're correct. But there aren't too many people out there who 
are going to be washing with water direct from a glacier fed stream.


Except that I have posted a few times stating that I use well water direct


We have a well, but it's defunct, and we've been using mains water. 
We want to get the well going again, but I take it you'd suggest we 
leave it to the spring? LOL! Ah, I wish we had a glacier-fed stream! 
Full of freshly-ground minerals, the secret of Hunza. But I could 
probably do without the glacier itself...


and not word one was ever mentioned until I started asking if wash 
water temperature is important.
Point is, not that I went without for awhile, but that now the 
question IS being adressed.
I had a few problems with emulsion, but only in the last two batches 
when the weather changed and it started getting cold. Prior to that, 
and none of the variables had changed, everything was clean and 
precise and good fuel resulted every time.
This question of wash water temperature needs to be added as a 
requisite in the instructional stages of making good fuel. Just 
assuming that Eskimos will not be interested doesn't make it. So it 
seems that now it has been addressed, and I for one am very pleased 
that it has.
Now it only leaves to have that information readily available to 
anyone wanting to learn the methodology of home brewing biodiesel. I 
suggest that it be added in the washing section at JtF somewhere. 
That is where I got my education from, and I must say that I am very 
pleased with what I was taught, so in the interest of those coming 
afterward it should be added somewhere evident.
I am now in the process of not only adding a second settling tank 
(insulated of course) but also of adding a water pre-heat tank using 
a 115V immersion heater to warm up the well water I will again be 
using to wash in the Spring when I get my production back on line.
Just leaving this information in the archives doesn't cut it either, 
it needs to be accessible in the tutorials.(Sorry Keith, I don't 
want to tell you what to do, but this seems to be an important 
detail in the end goal of proper biodiesel production.)


No problem, but let's get it all sorted out and settled first.

In fact the whole washing section at JtF is currently being reworked, 
been due for it for awhile. For one thing, it needs to be more 
closely linked to quality control. I'll start uploading it soon, when 
I can.


It obviously has been an oversight, and that is part of what this 
forum is all about, the betterment of the end user product, so there 
it is.


Oversight? Perhaps, or maybe it's just the normal course of 
development. We'll see what comes out of it.


Regards

Keith



Luc


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Re: [Biofuel] test batches and the JtF quality test

2004-12-18 Thread John Guttridge



not really trying to say that keith has made a mistake on his site. 
instead I was asking for more information on how to conduct the test in 
a reproducible manner. I have a lot of respect for keith and what he 
does. you seem to lack that and I would be interested to understand why.


I think that it is probably a good test to weed out the grossly under 
reacted batches and the way too much catalyst batches. I couldn't figure 
out why I kept following the instructions to the letter and getting 
batches that failed the quality test. 'it is cold here' seems to be the 
answer. maybe also 'I have soft water' is the answer.


also your generalized quest against all things JtF gives you very little 
veracity as I have found that JtF is an invaluable resource. you and the 
other one that contacted me off list and tried to direct me at some 
other site seem to both be on another planet than the rest of the 
community and the rest of the community seems to be happily functioning 
and making high quality fuel that works well. I wasted a lot of time 
listening to your advice, when see new people on the list I want to warn 
them not to listen.


I am scientific and skeptical, unless someone can give me good reasons 
and solid instructions their advice is usually out the door (often to my 
own detriment, but at least I really learn things when I do).


John

tillyfromparadise wrote:

Hello John,
It takes a brave man to tell Keith he has a mistake on JTF
 
You are correct.  The water shake test has many problems and at best 
only picks up Grossly under-reacted batches. 
Passing the shake test is certainly NOT an indication that the fuel 
is *well within the standard specifications* as claimed on JTF,  It is 
only an indication that the fuel is probably not grossly under-reacted.

You are also correct that what is in the water makes a difference.
Hard water seperates MUCH quicker than soft water.
It is also important to allow the biodiesel to sit at least over night 
before doing the test.
 
There is NO simple home made test for checking whether your biodiesel 
meets ASTM or not.  I suspect very few people actually achieve ASTM 
standard biodiesel
The best home test is a Viscosity test. 
These have limitations too as the viscosity of biodiesel varies 
slightly depending on what the original oil was.  But it is a darn site 
better than the Shake-em up test on JTF.
But then Keith has officially declaired that viscosity is not an 
indicator of quality so that is never going to be discussed.
 
I wonder what the penality for telling Keith he has a mistake on his web 
site is?
 
Good Luck

Squire Tilly KE
 
the quality test listed here:


http://journeytoforever.org/biodiesel_vehicle.html#quality

doesn't have enough information to be reproducible.

separation time seems to be based on a number of factors including but
probably not limited to:

ambient temperature
initial temperature of the H2O and the FAME
snip

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Re: [Biofuel] test batches and the JtF quality test

2004-12-18 Thread John Guttridge



the 70*F batch was mostly separated within about 5-10 minutes but didn't 
really reach completion until the end of 25 minutes.


thirty seconds to a minute???

http://journeytoforever.org/biodiesel_vehicle.html#quality

says Then let it settle. The biodiesel should separate from the water 
in half an hour or less, with amber biodiesel on top and milky water below.


at 140 it separated right quick.

I understand how volume could have such a big effect, bubbles of the 
fuel seemed to form and get stuck on one another's surface tension while 
the separation was happening. only problem is that 150mL is just about 
all of my test batch so I won't be able to perform the test multiple 
times and vary the parameters.


what I was trying to suggest here is that there are some factors that 
drastically affect the results that aren't even mentioned such that they 
can be controlled.


John

Appal Energy wrote:

John,

It is reproducable if you use larger volumes than the 8 ml total volume 
that you're using. A couple of fluid ounces would be more appropriate. 
The method suggests ~150 ml, or approximately five fluid ounces.


If you're not getting anything resembling a clean separation for 25 
minutes using 70*F water, something is not right. Same for the 50*F wash 
yielding three layers.


The suggestion would be to work on getting more complete reactions.

If the reaction went to completion, you should be able to take a 50/50 
sample of water and fuel, shake radically/vertically ten times, and get 
a clean separation within 30 seconds to one minute, using the first 
water that comes out of a cold tap (ambient temp).


Todd Swearingen

- Original Message - From: John Guttridge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Friday, December 17, 2004 3:25 PM
Subject: [Biofuel] test batches and the JtF quality test



the quality test listed here:

http://journeytoforever.org/biodiesel_vehicle.html#quality

doesn't have enough information to be reproducible.

separation time seems to be based on a number of factors including but
probably not limited to:

ambient temperature
initial temperature of the H2O and the FAME

I made a test batch yesterday and then performed the quality test on it
a number of times varying different factors, I did 2 with the coldest
water that would come out of my tap and 2 with the hottest water that
would come out of my tap, and one with appx 70 degree water (cold was
about 55 degrees F and hot was about 140 degrees F) I also did 2 that
sat in a bath of 140 degree water while they were separating, ambient
temperature in my kitchen is approximately 60 degrees F. the two that
sat in the 140 degree water had separated completely in less than 2
minutes, the 2 that were made with the hot water had completely
separated (less cleanly than the ones in the hot water bath) in 18
minutes, the one that was made with 70 degree water separated fully in
25 minutes, and the ones that were made with the cold water separated
into three layers of approximately the same volume one that was straw
yellow and slightly milky one that was a much lighter yellow and much
more milky and one that was milky white. these were all prepared in
13x100mm culture tubes with 4mL of H2O and 4mL of FAME.

I also presume, although I have not yet tested this that the contents 
of one's tap water and the shape of one's container make a difference 
in the results.


John Guttridge

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Re: [Biofuel] test batches and the JtF quality test

2004-12-18 Thread Appal Energy



If you're looking for reproducability, you need to follow baseline, not 
modify a test/experiment so as to suit your own preference or conditions.


You've apparently neglected to consider increases in sampling error that 
occur when conducting tests at micro-levels/volumes. You compound any flaw 
in your final evaluations by conducting not only the wash but the 
esterification with miniscule volumes. Unless your preparations are made 
with electronic scales to the thousandth of a gram, your alcohol and 
feedstock volumes determined by weight using the same scale, rather than 
relying upon glassware that forewarns of + or - 5% error factor, not to 
mention the + or - 10% human error factor (whether you know what end of the 
miniscus to take your measurements from or not) you only compound the degree 
of errors that are or can be represented by your conclusions.


There is an enormous world of difference between reproducablity/results 
achieved on 150 ml samples and samples no bigger than single liters, even 
when conducted by professionals with decades of experience.


As to your questioning the time frame that I mentioned for separation of 
well processed fuel, you need to take notice of the difference between the 
agitation period stated in my post and the general guideline you opted to 
modify.


You also need to take notice that the wash test is not represented as 
anything more than a quick and simple manner of determing how an operator 
may care or feel reasonably safe to proceed with what he or she may believe 
to be biodiesel.


The guidelines that are offered on this list and at Journey to Forever are 
intended to assist the general public in getting their fuel near or to the 
level that would pass the scrutiny of spec fuel, despite the fact that they 
may be working on dimestore budgets.


If you can afford the luxury and it's absolute guarantees of finished 
product quality that you seek, I would suggest that you establish a 
procedural regimen, produce what you have reason to believe is a 
well-crafted product and then submit the sample to the testing methods 
established in D-6751. You'll quickly surprise yourself at how easily that 
standard can be neared or met in a meticulous homebrewer's environment.


Todd Swearingen

- Original Message - 
From: John Guttridge [EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Friday, December 17, 2004 10:35 PM
Subject: Re: [Biofuel] test batches and the JtF quality test



Todd,

the 70*F batch was mostly separated within about 5-10 minutes but didn't 
really reach completion until the end of 25 minutes.


thirty seconds to a minute???

http://journeytoforever.org/biodiesel_vehicle.html#quality

says Then let it settle. The biodiesel should separate from the water in 
half an hour or less, with amber biodiesel on top and milky water below.


at 140 it separated right quick.

I understand how volume could have such a big effect, bubbles of the fuel 
seemed to form and get stuck on one another's surface tension while the 
separation was happening. only problem is that 150mL is just about all of 
my test batch so I won't be able to perform the test multiple times and 
vary the parameters.


what I was trying to suggest here is that there are some factors that 
drastically affect the results that aren't even mentioned such that they 
can be controlled.


John

Appal Energy wrote:

John,

It is reproducable if you use larger volumes than the 8 ml total volume 
that you're using. A couple of fluid ounces would be more appropriate. 
The method suggests ~150 ml, or approximately five fluid ounces.


If you're not getting anything resembling a clean separation for 25 
minutes using 70*F water, something is not right. Same for the 50*F wash 
yielding three layers.


The suggestion would be to work on getting more complete reactions.

If the reaction went to completion, you should be able to take a 50/50 
sample of water and fuel, shake radically/vertically ten times, and get a 
clean separation within 30 seconds to one minute, using the first water 
that comes out of a cold tap (ambient temp).


Todd Swearingen

- Original Message - From: John Guttridge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Friday, December 17, 2004 3:25 PM
Subject: [Biofuel] test batches and the JtF quality test



the quality test listed here:

http://journeytoforever.org/biodiesel_vehicle.html#quality

doesn't have enough information to be reproducible.

separation time seems to be based on a number of factors including but
probably not limited to:

ambient temperature
initial temperature of the H2O and the FAME

I made a test batch yesterday and then performed the quality test on it
a number of times varying different factors, I did 2 with the coldest
water that would come out of my tap and 2 with the hottest water that
would come out of my tap, and one with appx 70 degree water (cold was
about 55 degrees F and hot was about 140 degrees F) I also did 2 that
sat

[Biofuel] test

2004-12-18 Thread Martin K


The mailing list was down for a few hours today sorry for the trouble.
--
Martin Klingensmith
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Re: [Biofuel] test batches and the JtF quality test

2004-12-18 Thread John Guttridge




Understood. I will produce a batch large enough to make several runs at
the 150mL test and post the results.

I consumed the remains of my last test batch in a 125mL run (it was all
that was left) and I followed your agitation (10 times up and down
violently). it had seperated in to two clearly stratified sections
within abbout 1 minute with 60*F water however it still had lots of
tiny bubbles in both parts (sort of a milky yellow and a milky white). 
is that what you mean by clear seperation?


I still think that temperature has a drastic effect on seperation time
which I will test and post the results and methods of my experiment.

I would like to state to the list in general and especially kieth that
no one should take any of this personally. I am posting my results so
that people can point out errors. I am pointing out a sticking point
that people may have (if I am having this problem other people are
probably having it too). any good science is a process of peer review.
one posts methods and results others duplicate ones experiments and if
they prove reporducable and consistant then they are seen by the
community to be valid. one of the problems that I have with all of this
is that the instructions are really general and I fear that there are
factors that are important but are not mentioned such that they can be
controlled.

John

Appal Energy wrote:

John Guttridge,

If you're looking for reproducability, you need to follow baseline, not 
modify a test/experiment so as to suit your own preference or conditions.


You've apparently neglected to consider increases in sampling error that 
occur when conducting tests at micro-levels/volumes. You compound any 
flaw in your final evaluations by conducting not only the wash but the 
esterification with miniscule volumes. Unless your preparations are made 
with electronic scales to the thousandth of a gram, your alcohol and 
feedstock volumes determined by weight using the same scale, rather than 
relying upon glassware that forewarns of + or - 5% error factor, not to 
mention the + or - 10% human error factor (whether you know what end of 
the miniscus to take your measurements from or not) you only compound 
the degree of errors that are or can be represented by your conclusions.


There is an enormous world of difference between reproducablity/results 
achieved on 150 ml samples and samples no bigger than single liters, 
even when conducted by professionals with decades of experience.


As to your questioning the time frame that I mentioned for separation of 
well processed fuel, you need to take notice of the difference between 
the agitation period stated in my post and the general guideline you 
opted to modify.


You also need to take notice that the wash test is not represented as 
anything more than a quick and simple manner of determing how an 
operator may care or feel reasonably safe to proceed with what he or she 
may believe to be biodiesel.


The guidelines that are offered on this list and at Journey to Forever 
are intended to assist the general public in getting their fuel near or 
to the level that would pass the scrutiny of spec fuel, despite the fact 
that they may be working on dimestore budgets.


If you can afford the luxury and it's absolute guarantees of finished 
product quality that you seek, I would suggest that you establish a 
procedural regimen, produce what you have reason to believe is a 
well-crafted product and then submit the sample to the testing methods 
established in D-6751. You'll quickly surprise yourself at how easily 
that standard can be neared or met in a meticulous homebrewer's 
environment.


Todd Swearingen

- Original Message - From: John Guttridge [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Sent: Friday, December 17, 2004 10:35 PM
Subject: Re: [Biofuel] test batches and the JtF quality test



Todd,

the 70*F batch was mostly separated within about 5-10 minutes but 
didn't really reach completion until the end of 25 minutes.


thirty seconds to a minute???

http://journeytoforever.org/biodiesel_vehicle.html#quality

says Then let it settle. The biodiesel should separate from the water 
in half an hour or less, with amber biodiesel on top and milky water 
below.


at 140 it separated right quick.

I understand how volume could have such a big effect, bubbles of the 
fuel seemed to form and get stuck on one another's surface tension 
while the separation was happening. only problem is that 150mL is just 
about all of my test batch so I won't be able to perform the test 
multiple times and vary the parameters.


what I was trying to suggest here is that there are some factors that 
drastically affect the results that aren't even mentioned such that 
they can be controlled.


John

Appal Energy wrote:


John,

It is reproducable if you use larger volumes than the 8 ml total 
volume that you're using. A couple of fluid ounces would be more 
appropriate. The method suggests ~150 ml, or approximately five

[Biofuel] test batches and the JtF quality test

2004-12-17 Thread John Guttridge



http://journeytoforever.org/biodiesel_vehicle.html#quality

doesn't have enough information to be reproducible.

separation time seems to be based on a number of factors including but
probably not limited to:

ambient temperature
initial temperature of the H2O and the FAME

I made a test batch yesterday and then performed the quality test on it
a number of times varying different factors, I did 2 with the coldest
water that would come out of my tap and 2 with the hottest water that
would come out of my tap, and one with appx 70 degree water (cold was
about 55 degrees F and hot was about 140 degrees F) I also did 2 that
sat in a bath of 140 degree water while they were separating, ambient
temperature in my kitchen is approximately 60 degrees F. the two that
sat in the 140 degree water had separated completely in less than 2
minutes, the 2 that were made with the hot water had completely
separated (less cleanly than the ones in the hot water bath) in 18
minutes, the one that was made with 70 degree water separated fully in
25 minutes, and the ones that were made with the cold water separated
into three layers of approximately the same volume one that was straw
yellow and slightly milky one that was a much lighter yellow and much
more milky and one that was milky white. these were all prepared in
13x100mm culture tubes with 4mL of H2O and 4mL of FAME.

I also presume, although I have not yet tested this that the contents of 
one's tap water and the shape of one's container make a difference in 
the results.


John Guttridge

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Re: [Biofuel] test batches and the JtF quality test

2004-12-17 Thread Appal Energy



It is reproducable if you use larger volumes than the 8 ml total volume that 
you're using. A couple of fluid ounces would be more appropriate. The method 
suggests ~150 ml, or approximately five fluid ounces.


If you're not getting anything resembling a clean separation for 25 minutes 
using 70*F water, something is not right. Same for the 50*F wash yielding 
three layers.


The suggestion would be to work on getting more complete reactions.

If the reaction went to completion, you should be able to take a 50/50 
sample of water and fuel, shake radically/vertically ten times, and get a 
clean separation within 30 seconds to one minute, using the first water that 
comes out of a cold tap (ambient temp).


Todd Swearingen

- Original Message - 
From: John Guttridge [EMAIL PROTECTED]

To: [EMAIL PROTECTED]
Sent: Friday, December 17, 2004 3:25 PM
Subject: [Biofuel] test batches and the JtF quality test



the quality test listed here:

http://journeytoforever.org/biodiesel_vehicle.html#quality

doesn't have enough information to be reproducible.

separation time seems to be based on a number of factors including but
probably not limited to:

ambient temperature
initial temperature of the H2O and the FAME

I made a test batch yesterday and then performed the quality test on it
a number of times varying different factors, I did 2 with the coldest
water that would come out of my tap and 2 with the hottest water that
would come out of my tap, and one with appx 70 degree water (cold was
about 55 degrees F and hot was about 140 degrees F) I also did 2 that
sat in a bath of 140 degree water while they were separating, ambient
temperature in my kitchen is approximately 60 degrees F. the two that
sat in the 140 degree water had separated completely in less than 2
minutes, the 2 that were made with the hot water had completely
separated (less cleanly than the ones in the hot water bath) in 18
minutes, the one that was made with 70 degree water separated fully in
25 minutes, and the ones that were made with the cold water separated
into three layers of approximately the same volume one that was straw
yellow and slightly milky one that was a much lighter yellow and much
more milky and one that was milky white. these were all prepared in
13x100mm culture tubes with 4mL of H2O and 4mL of FAME.

I also presume, although I have not yet tested this that the contents of 
one's tap water and the shape of one's container make a difference in the 
results.


John Guttridge

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Re: [biofuel] Test wash turned completely white

2004-07-10 Thread Appal Energy

 whole thing turned in to a white foam. And it took
 about 5 - 10 mins for the white stuff to separate from
  my biodiesel. Is there anything wrong here?

Yup. You have an incomplete reaction. Take 250 ml of your fuel, reprocess
it with 1/4 of the standard amount of NaOH and MeOH. Sit back and watch some
more glycerin drop. Then try your test wash again after letting it all
settle for 12-24 hours.

Pay no attention to what color your finished fuel is. It will vary dependant
upon the feedstock and the degree of abuse it received prior to your
converting it. It will look slightly cloudy after washing, even if the fuel
is perfectly processed. This cloudiness clears up over time or with the
application of modest heat.

Todd Swearingen

- Original Message - 
From: Teoman Naskali [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Thursday, July 08, 2004 8:16 PM
Subject: [biofuel] Test wash turned completely white


 I just did a test wash on 25 ml of my first batch and
 25 ml of water in a jar. I mixed the 2 together by
 violently shaking the jar for about 30 seconds. The
 whole thing turned in to a white foam. And it took
 about 5 - 10 mins for the white stuff to separate from
  my biodiesel. Is there anything wrong here?

 Even now after half an hour my biodiesel is a very
 light yellowish color, but it looks like diluted urine
 whith a few drops of milk in it, i hope it is not the
 chemical or use wise equivalent.

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[biofuel] Test wash turned completely white

2004-07-09 Thread Teoman Naskali

I just did a test wash on 25 ml of my first batch and
25 ml of water in a jar. I mixed the 2 together by
violently shaking the jar for about 30 seconds. The
whole thing turned in to a white foam. And it took
about 5 - 10 mins for the white stuff to separate from
 my biodiesel. Is there anything wrong here?

Even now after half an hour my biodiesel is a very
light yellowish color, but it looks like diluted urine
whith a few drops of milk in it, i hope it is not the
chemical or use wise equivalent.

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Re: [biofuel] Test wash turned completely white

2004-07-09 Thread Keith Addison

Hello Teoman

I just did a test wash on 25 ml of my first batch and
25 ml of water in a jar. I mixed the 2 together by
violently shaking the jar for about 30 seconds. The
whole thing turned in to a white foam. And it took
about 5 - 10 mins for the white stuff to separate from
 my biodiesel. Is there anything wrong here?

No. It could be better (quicker separation) but the fact that it 
separated at all instead of turning into mayonnaise shows you're on 
the right track, well on your way. Please read this:
http://journeytoforever.org/biodiesel_vehicle.html#quality

Please also read Todd's message today, Re: [biofuel] washing 
biodiesel in large processor (Appal Energy).

Even now after half an hour my biodiesel is a very
light yellowish color, but it looks like diluted urine
whith a few drops of milk in it, i hope it is not the
chemical or use wise equivalent.

It'll clear eventually. Whether it separated or not, how long it 
took, and whether there's an emulsion interface (white) between the 
two layers, how thick it is, these are the indicators.

Not quite sure what your thin red layer on top is, but if you're 
managing to wash it and pass the wash test maybe it doen't matter 
much. Did it vanish in the wash?

Best wishes

Keith



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[biofuel] Test Batches using SVO

2004-06-16 Thread gregg2560

I've only been a member of this group for a short time, but I've 
learned a few tricks to making biodiesel thanks to other more 
experienced members.I am currently working on getting a supply of WVO 
from a fast food place near to where I work. In my test batches, I've 
used 500mls of straight corn  canola oils. I've gone almost by 
the rule of thumb as to the amounts of methanol  NaOH to use, but 
I have found that if I add .5 to 1 ml of H2SO4 to the oil, it breaks 
down the FFA's better than NaOH alone. I hope to have 1 or 2 litres 
made by the weekend. Wish me luck.

Any comments, help, or suggestions are welcomed.

Gregg




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Re: [biofuel] Test batch

2004-06-08 Thread RGMTRUCK

 
In a message dated 06/04/2004 11:27:39 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Rick,

Go to your kitchen and take some of the vegetable oil from  your pantry and
run a sample. Do everything the same as you did with the  WVO.

If the same thing happens you know it's not your oil that's the  problem.

Todd Swearingen






Now why didn't I think  of that.
 
Rick


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




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[biofuel] Test batch

2004-06-05 Thread RGMTRUCK

I just did another test batch and there is something wrong.  I am  doing 
small test batches trying to make sure my measurements are correct.   I have 
done 
5 small batches and have had the same results with all.  I  don't understand 
what is wrong as I have made about 50 gallons of fuel that came  out great.  I 
am useing the same oil that I have been using all  along.
I started out with 1/2 liter of oil and 100 ml of meth and 3-1/2 grams of  
lye.  My oil is the color of like coffee before I add the meth and  lye.  I am 
mixing the meth and lye very good so I am sure that is  okay.  As soon as I add 
the meth and lye to my oil it turns the oil to a  creamy carmel color.  Kinda 
looks like you poured milk into your coffee and  mixed it up.  After it is 
mixed and poured out of the blender it just goes  solid like it is to much lye 
or something.  I have decreased the lye by 1/2  gram of lye all the way down to 
2 grams with the same amount of oil and meth and  get the same results.
I am at a loss as to what is wrong.  Anyone have any  suggestions?
Rick


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




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Re: [biofuel] Test batch

2004-06-05 Thread Keith Addison

I just did another test batch and there is something wrong.  I am  doing
small test batches trying to make sure my measurements are correct. 
I have done
5 small batches and have had the same results with all.  I  don't understand
what is wrong as I have made about 50 gallons of fuel that came  out great.  I
am useing the same oil that I have been using all  along.
I started out with 1/2 liter of oil and 100 ml of meth and 3-1/2 grams of
lye.  My oil is the color of like coffee before I add the meth and  lye.  I am
mixing the meth and lye very good so I am sure that is  okay.  As 
soon as I add
the meth and lye to my oil it turns the oil to a  creamy carmel color.  Kinda
looks like you poured milk into your coffee and  mixed it up.  After it is
mixed and poured out of the blender it just goes  solid like it is to much lye
or something.  I have decreased the lye by 1/2  gram of lye all the 
way down to
2 grams with the same amount of oil and meth and  get the same results.
I am at a loss as to what is wrong.  Anyone have any  suggestions?
Rick

So your titration of this oil gave a result of 3.5 ml? What sort of 
oil is it? This is the same lye amount that you used for the 50 
gallons you've made - 7 g/litre oil? How are you mixing the methoxide 
for the blender batches? What temperature is the oil?

Keith



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Re: [biofuel] Test batch

2004-06-05 Thread Appal Energy

Rick,

Go to your kitchen and take some of the vegetable oil from your pantry and
run a sample. Do everything the same as you did with the WVO.

If the same thing happens you know it's not your oil that's the problem.

Todd Swearingen

- Original Message - 
From: [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Friday, June 04, 2004 11:41 AM
Subject: [biofuel] Test batch


 I just did another test batch and there is something wrong.  I am  doing
 small test batches trying to make sure my measurements are correct.   I
have done
 5 small batches and have had the same results with all.  I  don't
understand
 what is wrong as I have made about 50 gallons of fuel that came  out
great.  I
 am useing the same oil that I have been using all  along.
 I started out with 1/2 liter of oil and 100 ml of meth and 3-1/2 grams of
 lye.  My oil is the color of like coffee before I add the meth and  lye.
I am
 mixing the meth and lye very good so I am sure that is  okay.  As soon as
I add
 the meth and lye to my oil it turns the oil to a  creamy carmel color.
Kinda
 looks like you poured milk into your coffee and  mixed it up.  After it is
 mixed and poured out of the blender it just goes  solid like it is to much
lye
 or something.  I have decreased the lye by 1/2  gram of lye all the way
down to
 2 grams with the same amount of oil and meth and  get the same results.
 I am at a loss as to what is wrong.  Anyone have any  suggestions?
 Rick


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[biofuel] test batches

2004-06-02 Thread RGMTRUCK

Greetings list,
I have a question.  If you do a test batch and you get a glob of what  looks 
like hard grease or bad looking soap,  wouldn't that mean that you  probably 
used to much lye?
Rick M
Brownstown, Mi.


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[biofuel] test batch

2004-02-04 Thread wormmister1

x-charset ISO-8859-1Hi everyone...i was just wondering how long you have to 
let it sit
after  its completed the process and been transfered to a new container



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Re: [biofuel] test batch

2004-02-04 Thread Keith Addison

Hi everyone...i was just wondering how long you have to let it sit
after  its completed the process and been transfered to a new container

Hi, and welcome

You mean after processing and before washing? 24 hours, some people 
say longer is better, which it probably is, others say you should 
have the stuff in your tank within 12 hours of starting the process 
and that washed biodiesel's bad for your car anyway, which is 
ridiculous nonsense but they say it anyway.

Let it settle for 24 hours or more, then separate the glycerine 
by-product (at the bottom) and wash the biodiesel (on top), either in 
the processor or (much better) in a separate wash-tank.

regards

Keith


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Re: [biofuel] Test Batches and Theory vs Practice

2004-01-03 Thread James Slayden

Ken,

I wonder how things would go with titrations between 2-3 ml NaOH?  That
seem to be somewhat average WVO that I am collecting.  I sure do need to
get over to MAX's to get some of that stuff your collecting ..  ;-)

This is a great thread and I am glad your doing the experiments to figure
out what is the limit for Eth processing.  And for everyone out there, I
have been over to Ken's for processing and the setup is EXTREEMELY ludite
and Ken is getting good results with a 5:1 Eth:Meth ratio for titrations
under 2 ml NaOH.  So, it is possible to be as Eco as possible using just a
small amount of Meth.

Good work Ken!!!

James Slayden

BTW, did you ever get another drum of that Parallel Products Eth?  I know
you and Dave Shaw were in contact so I wanted to see if it finally got off
the ground.

On Tue, 30 Dec 2003, Ken Provost wrote:

 on 12/30/03 8:26 AM, Dan Maker at [EMAIL PROTECTED] wrote:
 
  I want to make biodiesel from WVO and Ethanol.  So far
  the only ethyl esters I've heard discussed are from
  virgin oil, or mostly virgin oil with only a small
  percentage of WVO.
 
 
 Well, not exactly. I've been using about half 'n' half
 WVO and flush oil (overall 0.9 ml NaOH titer), but I'm
 doing a sample of straight WVO (1.7 ml NaOH) tonite with
 90:10 eth:meth just to prove you wrong :-)
 
 Now I know that's not very high still, but I'm truly
 shocked to read of fokes trying to use 8- and 9-ml
 stuff. Hey, garbage is garbage -- we can't work miracles
 here. I get my oil from Hammerhead Fish House and Maxx's
 Ribs -- it's 1.7 after 6 mos. in my garage. There's no
 need (for me at least) to get any worse.
 
 If I really needed to use the WORST I've EVER seen in
 my area (4.0 ml Na titr), and I wanted to use mostly
 ethanol, I'd do acid-base with 9:1 eth:meth. I bet it
 would work, tho I can't say fer sure.  -K
 
 
 
 
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Re: [biofuel] Test Batches and Theory vs Practice

2003-12-31 Thread Ken Provost

on 12/30/03 8:26 AM, Dan Maker at [EMAIL PROTECTED] wrote:

 I want to make biodiesel from WVO and Ethanol.  So far
 the only ethyl esters I've heard discussed are from
 virgin oil, or mostly virgin oil with only a small
 percentage of WVO.


Well, not exactly. I've been using about half 'n' half
WVO and flush oil (overall 0.9 ml NaOH titer), but I'm
doing a sample of straight WVO (1.7 ml NaOH) tonite with
90:10 eth:meth just to prove you wrong :-)

Now I know that's not very high still, but I'm truly
shocked to read of fokes trying to use 8- and 9-ml
stuff. Hey, garbage is garbage -- we can't work miracles
here. I get my oil from Hammerhead Fish House and Maxx's
Ribs -- it's 1.7 after 6 mos. in my garage. There's no
need (for me at least) to get any worse.

If I really needed to use the WORST I've EVER seen in
my area (4.0 ml Na titr), and I wanted to use mostly
ethanol, I'd do acid-base with 9:1 eth:meth. I bet it
would work, tho I can't say fer sure.  -K




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Re: [biofuel] Test Batches and Theory vs Practice

2003-12-31 Thread Dan Maker

Ken Provost said:
 
 Well, not exactly. I've been using about half 'n' half
 WVO and flush oil (overall 0.9 ml NaOH titer), but I'm
 doing a sample of straight WVO (1.7 ml NaOH) tonite with
 90:10 eth:meth just to prove you wrong :-)

Great to hear you are having such success with wvo.  Now can you
do that with out any methanol?  Using that 10% methanol to mix with
NaOH will give you the methoxide you'll need as a catylist, allowing
most of the transesterfication to be done by the ethanol.  It should
work just fine.  But with out the methanol, even with KOH, you won't
get enough catylist, at least not from what I've figured, so it's not
something I want to try.

While what you are going to do tonight will be very good, it won't
prove me wrong.  Eleminate the methanol, and use just WVO with what
ever process you like, base only, acid base, something entirely new,
and you will have proved me wrong.

 If I really needed to use the WORST I've EVER seen in
 my area (4.0 ml Na titr), and I wanted to use mostly
 ethanol, I'd do acid-base with 9:1 eth:meth. I bet it
 would work, tho I can't say fer sure.  -K

Yup, and this is where the theory ends and you have to get out the gloves
and go to work.

Happy New Year
Dan
-- 
Jack of all trades, master of none.
Fiber Artist - Genealogist - Kilt Maker - Linux Geek - Piper - Woodworker
http://www.xmission.com/~redbeard

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Re: [biofuel] Test Batches and Theory vs Practice

2003-12-30 Thread Keith Addison

Hi Dan

Keith Addison said:

Sorry it's taken me so long to reply, hollidays and finishing up a
down draft gasifier to burn waste wood have taken a lot of time.  The
gasifier is working nicely, I now need to build the heat exchanger.

  If you accidently measure out an extra .1 gram NaOH in each batch it
  represents it represents 28.5% too much in the 1 liter batch but only 1.4%
  too much in the 20 liter batch.
 
  That's wrong Dan. This is virgin oil, so it should be:

I'll have to check my numbers.

You just dropped a decimal place. Yes, check the quantities you used 
in your test batches, but I'd guess you just got it wrong in the 
calculation for your post, not for making the test batches (or it 
wouldn't have worked at all). You'd said:

1 liter oil requires 0.2 liters of Methanol and .35 grams NaOH

That's only one-tenth the required amount of NaOH, it should be 3.5 
grams. You say the opposite thing about the iffy test batch below: I 
think I had too much NaOH in it...

  It's worth stating. Mark's right though, eh? - it doesn't lend itself
  to armchair theorising. Why we always advise people to start at the
  beginning instead of rushing straight at the two-stage processes or
  designing a full-scale processor before they've made their first
  batch. One erstwhile hopeful complained most bitterly to me because

There are two seperate issues here.  Practical experience using your
tools and familiarity with the process is one.  The other is
understanding the reaction you are attempting.  There is no substitute
for practical, hands on experience, but there is also no substitute
for theory either.

That's quite right. There's also a rational sequence to it though. 
Your theorizing is likely to be much more focused and productive if 
you first gain the basic practical hands-on experience. As with your 
baking example below, you'd want to be competent at the basic recipes 
and techniques before moving on to new recipes and new, untried 
ground, which will need both theory and practical competence. If you 
can't break an egg without breaking the yolk and getting bits of 
shell in it, or if you've never tried breaking an egg, better learn 
how first. Hence our Where do I start? section - start with a small 
test batch of virgin oil, etc, it's a logical progression, easy to 
follow, with the horse at the right end of the cart.

With out understanding the theory you are just following the recipe.
That works, most of the time, as long as the recipe is for the right
thing.  If you are trying to come up with a new recipe you need to
understand the theory.  When you start trying out your new recipe you
need to have good lab skills and practices.

It's much like baking, in that all the experience in the world, at
following somebody elses recipe, will only go so far toward creating
your own recipe.

Conversely, without that experience you're not going to know whether 
the existing recipes are adequate for your purposes or if you need to 
develop a new one of your own.

It may give you a strong intuitive feel for the
product, but it will not be as helpful as understanding the theory and
chemistry. And for any of you that say there's no chemistry in baking,
you need to make Sweedish Lemon Angels,
http://www.recipesource.com/baked-goods/desserts/cookies/01/rec0162.html

:-)

There's a LOT of chemistry in baking! Even short of playing with it.

  Dan, what quite is happening to the test batch you made that isn't
  biodiesel? Why not try rescuing it?

I think I had too much NaOH in it, it was cloudy and not seperating. I
need to go back and double check my figures after you pointed out my
error in the example I gave above for large batches vs. small batches. I
know I wasn't measuring as accurately as I'd like to have.  The scale
I'm using isn't realy up to the task and needs to be replaced before I
make any further efforts.  As for rescuing it, it's only 1.4 liters, and
it's looking realy cool as I've left it to sit and seperate over the last
few weeks.  I have water in there too and so I have a very interesting mix
of glycerin, soap biodiesel and sodium catylist.  My second small batch
worked out nicely, even with the postage scale, but as I said, I'll be
getting a more accurate scale before I try any further test batches.

Worth it, IMO.

Best wishes

Keith


Cheers,
Dan
--
Jack of all trades, master of none.
Fiber Artist - Genealogist - Kilt Maker - Linux Geek - Piper - Woodworker
http://www.xmission.com/~redbeard


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Re: [biofuel] Test Batches and Theory vs Practice

2003-12-30 Thread Dan Maker

Keith Addison said:
 
 That's only one-tenth the required amount of NaOH, it should be 3.5 
 grams. You say the opposite thing about the iffy test batch below: I 
 think I had too much NaOH in it...

Yes, I didn't trust my initial calculations or measurements on my initial
test batch and added in more NaOH, that's why I think I ended up with too
much.

 It's much like baking, in that all the experience in the world, at
 following somebody elses recipe, will only go so far toward creating
 your own recipe.
 
 Conversely, without that experience you're not going to know whether 
 the existing recipes are adequate for your purposes or if you need to 
 develop a new one of your own.

No, not entirely.  It already seems that the recipe I want isn't out
there, at least not in the liturature I've read or seen discussed.  I
want to make biodiesel from WVO and Ethanol.  So far the only ethylesters
I've heard discussed are from virgin oil, or mostly virgin oil with only
a small percentage of WVO.  It could well be that I've misunderstood, and
someone is using fry vat oil with Ethanol, but it wasn't clear to me.

I am not arguing that practical hands on experience, with small batches,
is very helpful before proceeding to large batches.  And that experience
using the equipment and materials is important to become comptetent with
them.

I am saying that it is not necessary to actually make a batch of
biodiesel to understand how the process works, or to contemplate ways of
changing or improving the process.  However it is entirely possible to
make bd without having any understanding of the chemical reactions
involved.  To verify that the new process does work would require using
it to make bd.  And here, starting with a known process, to acheive known
results, before testing the new process, in hopes of acheiving the same
results, is a good idea.

As an example of how thought process is important, consider Albert
Einstein's thought experiments.  He used his thought experiments to
formulate and initially test his theories.

http://www.uh.edu/engines/epi576.htm

 http://www.recipesource.com/baked-goods/desserts/cookies/01/rec0162.html
 
 :-)
 
 There's a LOT of chemistry in baking! Even short of playing with it.

A word of warning to those that may not be aware, the recipe referenced
above will NOT make cookies, just a large mess all over your work surface.

Still thinking (and doing),
Dan
-- 
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Fiber Artist - Genealogist - Kilt Maker - Linux Geek - Piper - Woodworker
http://www.xmission.com/~redbeard

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[biofuel] Test Batches and Theory vs Practice [was - Re: Simple 5-gallon processor]

2003-12-29 Thread Dan Maker

Keith Addison said:

Sorry it's taken me so long to reply, hollidays and finishing up a
down draft gasifier to burn waste wood have taken a lot of time.  The
gasifier is working nicely, I now need to build the heat exchanger.

 If you accidently measure out an extra .1 gram NaOH in each batch it
 represents it represents 28.5% too much in the 1 liter batch but only 1.4%
 too much in the 20 liter batch.
 
 That's wrong Dan. This is virgin oil, so it should be:

I'll have to check my numbers.

 It's worth stating. Mark's right though, eh? - it doesn't lend itself 
 to armchair theorising. Why we always advise people to start at the 
 beginning instead of rushing straight at the two-stage processes or 
 designing a full-scale processor before they've made their first 
 batch. One erstwhile hopeful complained most bitterly to me because 

There are two seperate issues here.  Practical experience using your
tools and familiarity with the process is one.  The other is
understanding the reaction you are attempting.  There is no substitute
for practical, hands on experience, but there is also no substitute
for theory either.

With out understanding the theory you are just following the recipe.
That works, most of the time, as long as the recipe is for the right
thing.  If you are trying to come up with a new recipe you need to
understand the theory.  When you start trying out your new recipe you
need to have good lab skills and practices.

It's much like baking, in that all the experience in the world, at
following somebody elses recipe, will only go so far toward creating
your own recipe.  It may give you a strong intuitive feel for the
product, but it will not be as helpful as understanding the theory and
chemistry. And for any of you that say there's no chemistry in baking,
you need to make Sweedish Lemon Angels,
http://www.recipesource.com/baked-goods/desserts/cookies/01/rec0162.html

 Dan, what quite is happening to the test batch you made that isn't 
 biodiesel? Why not try rescuing it?

I think I had too much NaOH in it, it was cloudy and not seperating. I
need to go back and double check my figures after you pointed out my
error in the example I gave above for large batches vs. small batches. I
know I wasn't measuring as accurately as I'd like to have.  The scale
I'm using isn't realy up to the task and needs to be replaced before I
make any further efforts.  As for rescuing it, it's only 1.4 liters, and
it's looking realy cool as I've left it to sit and seperate over the last
few weeks.  I have water in there too and so I have a very interesting mix
of glycerin, soap biodiesel and sodium catylist.  My second small batch
worked out nicely, even with the postage scale, but as I said, I'll be
getting a more accurate scale before I try any further test batches.

Cheers,
Dan
-- 
Jack of all trades, master of none.
Fiber Artist - Genealogist - Kilt Maker - Linux Geek - Piper - Woodworker
http://www.xmission.com/~redbeard

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[biofuel] test batch questions

2003-12-01 Thread whc281

Hello.  I'm a newbie, so go easy.

We gathered our materials (WVO, Red Devil, methanol, old blender, 
fish tank heater, measuring gear, etc.) and have mixed several test 
batches, but it doesn't look right.

One liter WVO, 200 ml CH3OH, and varied the amount of lye (3.0 g, 4.0 
g, 4.5 g, 5.5 g).  Mixed lye into CH3OH for 5 minutes, while WVO 
preheated to ~110F, then added and ran heater/mixer at ~120F for 1 
hour.  Poured into clear plastic jugs and allowed to settle overnight.

The batches range from 10% to 5% to none, of clear golden oil on top 
of light brown jellied glob (90% to 99%)in the bottom.  Some have 
white crusty island on top of the glob.

Where do we go from here?  I was thinking next test batch I'd try way 
more lye... say 8.0 g.

Thanks,
Bill



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[biofuel] Test Batch

2003-10-11 Thread dave01632002

Hi,

I tried a 500 mL test batch with some used vegetable shortening from 
Long John Silvers.  I used 100 mL of Methanol and 2.8 g of NaOH.  I 
got two distinct layers, but there was some glycerine floating in my 
biodiesel layer.  Then I took about 150 mL of biodiesel/ glycerin 
layer and mixed that with about 150 mL of water.  I got 4 layers!  
The top was clear enough to see through and sort of golden color and 
about 1/4 of the mixture volume.  The second layer was very cloudy, 
fairly golden color and about 1/3 of the mixture volume.  The thrid 
was opaque ad white and of insignificant volume.  The bottom layer 
was cloudy and grey and about 1/2 of the mixture volume.  I only used 
2.8 g of lye.  What went wrong?  And if this happens on a large scale 
batch, what should I do?  Could I possibly filter out the glycerin 
after the reaction?

Dave



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[biofuel] Test-batch mini-processor - one or two litres

2003-08-03 Thread Keith Addison

http://journeytoforever.org/biodiesel_processor7.html

Test-batch mini-processor
For one or two litres
This mini-processor is easy to make from not very much, mostly kichen 
stuff and a couple of tools. It's effective and safe, closed and 
virtually air-tight, with no splashing or leaking of hot fumes. It 
will make one- or two-litre batches for test-batch or demonstration 
purposes, suitable for single-stage or two-stage processes, with full 
agitation and temperature control. And you can take it anywhere.


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[biofuel] TEST

2003-07-29 Thread Raffingora Garage

I WOULD LIKE TO DO A TEST USING 60Lt  WVO AND ETHANOL.CAN ANYONE HELP WITH A 
SIMPLE AND WORKABLE FORMULA.I AM QUITE DESPERATE AS I LIVE IN ZIMBABWE WHERE 
DIESEL IS A VERY SCARES PRODUCT. 
THANKS FOR YOUR HELP
CHRIS.


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



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Re: [biofuel] TEST

2003-07-29 Thread Keith Addison

I WOULD LIKE TO DO A TEST USING 60Lt  WVO AND ETHANOL.CAN ANYONE 
HELP WITH A SIMPLE AND WORKABLE FORMULA.I AM QUITE DESPERATE AS I 
LIVE IN ZIMBABWE WHERE DIESEL IS A VERY SCARES PRODUCT.
THANKS FOR YOUR HELP
CHRIS.

No need to shout! :-)

Test batches should be maybe one litre, not 60.

There's information for you here:

Ethanol biodiesel
http://journeytoforever.org/ethanol_link.html#ethylester

On the other hand, you could perhaps just mix the WVO and the 
ethanol, a la the ACREVO study:

Report of the European Advanced Combustion Research for Energy from 
Vegetable Oils (ACREVO) study of the use of straight vegetable oil as 
diesel fuel. Investigates the burning characteristics of vegetable 
oil droplets from experiments conducted under high pressure and high 
temperature conditions. Very interesting study, worth a thorough read 
(4,400 words).
http://www.nf-2000.org/secure/Fair/F484.htm

WVO should be good quality, ethanol can be 95% (190-proof), mix at a 
ratio of 9% ethanol. But you'll still need to pre-heat it - a 
two-tank system in other words:
http://journeytoforever.org/biodiesel_svo.html
Straight vegetable oil as diesel fuel: Journey to Forever

Best

Keith


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[biofuel] Test B100 without motors

2003-03-14 Thread kmyerkconline

Question and Hi everybody (I'm new to this group),

I am looking into feasability of homemade biodiesel but I don't have 
a car (yet) that I can test the fuel in. Looking for other ways to 
use my experimental batches.

Can I use B100 in a kerosene forced air heater? The one I have is the 
bullet style (sometimes called a salamander) heater that you see at 
football games or in warehouses. Can I use 100% biodiesel or should I 
mix with some proportion of kerosene? 

I use this heater in my garage in the winter when working on my cars. 
Would also be great to get rid of that horrible kerosene smell!

Anyone here experiment with forced air heaters of this type and 
biodiesel?

How does biodiesel compare to kerosene anyway?

Thanks for the help,
Kelly





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Re: [biofuel] Test B100 without motors

2003-03-14 Thread Craig Pech

Kelly,

We did some experimenting this winter. The two problems are the gelling of
the BioD and the air feed needs to be regulated at a different mixture. We
had success with a shut off valve for an ice maker feed - it screws into the
back of the unit. It will operate best when the valve is almost closed.

Do your tests in an open area until you get the right mixture - the initial
ignition will generate a huge amount of very unpleasant smoke. The colder it
gets, the more kero you will have to use. If you can keep your fuel tank
inside until it will be used it will help keep the fuel warmer.

We did not do long term testing - don't know what the BioD will do to the
seals.

Craig
- Original Message -
From: kmyerkconline [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Friday, March 14, 2003 10:27 AM
Subject: [biofuel] Test B100 without motors


 Question and Hi everybody (I'm new to this group),

 I am looking into feasability of homemade biodiesel but I don't have
 a car (yet) that I can test the fuel in. Looking for other ways to
 use my experimental batches.

 Can I use B100 in a kerosene forced air heater? The one I have is the
 bullet style (sometimes called a salamander) heater that you see at
 football games or in warehouses. Can I use 100% biodiesel or should I
 mix with some proportion of kerosene?

 I use this heater in my garage in the winter when working on my cars.
 Would also be great to get rid of that horrible kerosene smell!

 Anyone here experiment with forced air heaters of this type and
 biodiesel?

 How does biodiesel compare to kerosene anyway?

 Thanks for the help,
 Kelly






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 http://journeytoforever.org/biofuel.html

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

 Please do NOT send Unsubscribe 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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[biofuel] test - please ignore

2002-05-25 Thread Keith Addison

Test only, sorry.

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Re: [biofuel] test

2002-03-30 Thread Neoteric Biofuels Inc.

See:


http://www.dieselperformanceproducts.com/home.html


on 3/30/02 8:25 AM, steve spence at [EMAIL PROTECTED] wrote:

 diesels always add air at atmospheric pressure? most diesels are turbo or
 supercharged.
 
 Steve Spence
 Subscribe to the Renewable Energy Newsletter:
 http://www.webconx.com/subscribe.htm
 
 Renewable Energy Pages - http://www.webconx.dns2go.com/
 Human powered devices, equipment, and transport -
 http://www.webconx.dns2go.com/2000/humanpower.htm
 [EMAIL PROTECTED]
 - Original Message -
 From: useravav [EMAIL PROTECTED]
 To: biofuel@yahoogroups.com
 Sent: Sunday, March 24, 2002 6:59 PM
 Subject: [biofuel] test
 
 
 I tested my 1985 VW Jetta diesel for it operation on propane as I
 intend to modify it for multi-fuels use.
 
 While idling on diesel I injected gaseous propane from my hand torch
 and its RPM doubled, there was no pre-ignition, knocking, missing or
 smoke coming out of the tailpipe.
 
 The air in the engine is compressed to a ratio of 23 to 1, getting
 quite hot but that does not ignite gaseous propane as its compresses
 with the air, but it is ignited when the diesel fuel is injected into
 the cylinder, diesel fuel ignites at a far lower temperature then
 propane and supplies the ignition for the propane.
 
 Not only should this allow diesels to operate on propane but probably
 also natural gas, methane and wood-gas.
 When idling the diesel engine uses very little diesel or bio-diesel
 fuel and can be used as a simple way to operate engines on gaseous
 fuels.
 
 With gasoline engines air fuel ratios must be constant throughout its
 range of operation but with a diesel engine air always enters the
 cylinder at atmospheric pressure and its power is controlled only by
 the addition of fuel.
 
 Does anyone know of where there is information on using diesel engines
 for gaseous fuel operation?
 
 George
 
 
 
 
 
 Biofuel at Journey to Forever:
 http://journeytoforever.org/biofuel.html
 Please do NOT send unsubscribe messages to the list address.
 To unsubscribe, send an email to:
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 Your use of Yahoo! Groups is subject to http://docs.yahoo.com/info/terms/
 
 
 
 
 
 
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 http://journeytoforever.org/biofuel.html
 Please do NOT send unsubscribe messages to the list address.
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Re: [biofuel] test

2002-03-30 Thread steve spence

yep, it's a nice kit. I can't make my own propane, so I'm not really
interested, unless I get back into methane digestion.


Steve Spence
Subscribe to the Renewable Energy Newsletter:
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[EMAIL PROTECTED]
- Original Message -
From: Neoteric Biofuels Inc. [EMAIL PROTECTED]
To: Biofuel-JTF biofuel@yahoogroups.com
Sent: Saturday, March 30, 2002 12:35 PM
Subject: Re: [biofuel] test


 See:


 http://www.dieselperformanceproducts.com/home.html


 on 3/30/02 8:25 AM, steve spence at [EMAIL PROTECTED] wrote:

  diesels always add air at atmospheric pressure? most diesels are turbo
or
  supercharged.
 
  Steve Spence
  Subscribe to the Renewable Energy Newsletter:
  http://www.webconx.com/subscribe.htm
 
  Renewable Energy Pages - http://www.webconx.dns2go.com/
  Human powered devices, equipment, and transport -
  http://www.webconx.dns2go.com/2000/humanpower.htm
  [EMAIL PROTECTED]
  - Original Message -
  From: useravav [EMAIL PROTECTED]
  To: biofuel@yahoogroups.com
  Sent: Sunday, March 24, 2002 6:59 PM
  Subject: [biofuel] test
 
 
  I tested my 1985 VW Jetta diesel for it operation on propane as I
  intend to modify it for multi-fuels use.
 
  While idling on diesel I injected gaseous propane from my hand torch
  and its RPM doubled, there was no pre-ignition, knocking, missing or
  smoke coming out of the tailpipe.
 
  The air in the engine is compressed to a ratio of 23 to 1, getting
  quite hot but that does not ignite gaseous propane as its compresses
  with the air, but it is ignited when the diesel fuel is injected into
  the cylinder, diesel fuel ignites at a far lower temperature then
  propane and supplies the ignition for the propane.
 
  Not only should this allow diesels to operate on propane but probably
  also natural gas, methane and wood-gas.
  When idling the diesel engine uses very little diesel or bio-diesel
  fuel and can be used as a simple way to operate engines on gaseous
  fuels.
 
  With gasoline engines air fuel ratios must be constant throughout its
  range of operation but with a diesel engine air always enters the
  cylinder at atmospheric pressure and its power is controlled only by
  the addition of fuel.
 
  Does anyone know of where there is information on using diesel engines
  for gaseous fuel operation?
 
  George
 
 
 
 
 
  Biofuel at Journey to Forever:
  http://journeytoforever.org/biofuel.html
  Please do NOT send unsubscribe 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/
 
 
 
 
 
 
  Biofuel at Journey to Forever:
  http://journeytoforever.org/biofuel.html
  Please do NOT send unsubscribe messages to the list address.
  To unsubscribe, send an email to:
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  Your use of Yahoo! Groups is subject to
http://docs.yahoo.com/info/terms/
 
 



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Re: [biofuel] test

2002-03-29 Thread Paul Gobert


- Original Message -
From: useravav [EMAIL PROTECTED]
[snip]
 Does anyone know of where there is information on using diesel engines
 for gaseous fuel operation?
[snip]
 George,
The technique is called fumigation.
Quite a bit about it on web, a google search will bring up plenty of
information.

Regards,
Paul Gobert.



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Re: Yahoo - was Re: [biofuel] Test

2002-03-07 Thread Martin Klingensmith

I'm up for it
How many people are on this list?
Is there any way to get a list of emails?
I'm just trying to figure out how you would automatically switch people over.
Or if you would just ask them to subscribe to the new list. I still have to set
up listserv software, but that is trivial.
Let me know
-Martin

--- Keith Addison [EMAIL PROTECTED] wrote:
 Time for a move maybe? What think you, Martin, if you're reading this?
 
 Best
 
 Keith Addison
 Journey to Forever
 Handmade Projects
 Osaka, Japan
 http://journeytoforever.org/
 
 List owner
 
 
 
 Biofuel at Journey to Forever:
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 Please do NOT send unsubscribe messages to the list address.
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http://www.nnytech.net/


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[biofuel] Test

2002-03-06 Thread Greg and April

Test

Time sent -- 21:43

Please excuse this post. Something is going on with my e-mail, I've posted a
few times today, but, have only recieved 1 of my post to come back thru the
group e-mail.  So I am seeing how long it is taking to get back to me, in
effort to find out were the problem is.

Greg H.




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Re: [biofuel] Test

2002-03-06 Thread Greg and April

Time recieved -- 17:11 the next day.


- Original Message - 
From: Greg and April 
To: biofuel@yahoogroups.com
Sent: Tuesday, March 05, 2002 21:43
Subject: [biofuel] Test


 Test
 
 Time sent -- 21:43
 



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Re: [biofuel] Test

2002-03-06 Thread StanJhnnyb

Remove me from your e-mail list now!
 Stanjhnnyb

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Re: [biofuel] Test

2002-03-06 Thread studio53

It's Yahoo.
ref http://

Jesse Parris|studio53| graphics / web design|
stamford, ct|[EMAIL PROTECTED]

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- Original Message -
From: Greg and April [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Tuesday, March 05, 2002 8:43 PM
Subject: [biofuel] Test


 Test

 Time sent -- 21:43

 Please excuse this post. Something is going on with my e-mail, I've posted
a
 few times today, but, have only recieved 1 of my post to come back thru
the
 group e-mail.  So I am seeing how long it is taking to get back to me, in
 effort to find out were the problem is.

 Greg H.





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