[biofuel] Re: Residual oil in BD.

2001-06-10 Thread gjkimlin

Re: Paper Chromatography. Are there specific disclosure solutions for 
the glycerol, Esters and oil? I remember(many years ago) spraying an 
essentially invisible separation of esters/oil with some compound 
that disclosed the bands. Can't find a basic text book when you want 
one!!
Regards Harry

--- In [EMAIL PROTECTED], Aleksander lt;kac [EMAIL PROTECTED] wrote:
  
  I don't really think this is true. Using 200ml methanol per liter 
 of WVO is
  about a 60% molar excess (that is, 60% more methanol than is 
 actually
  consumed in the transesterification). The excess helps to shift 
 equilibrium
  in the desired direction, and I think we can expect something 
like 
 95%
  completion. 
 Right. Combined processes need a little less meth, but still a 50% 
 excess.
 
 When you start cheating on the methanol is when you start
  seeing more unconverted oil in the BD -- viscosity will be 
 measurably
  higher as a result.   -K
 You can observe your volumetric yield. With the right quantities of 
 alcohol and catalyst the 95+ % conversion will give 100 to 103% 
volum.
 yield (measured at the same temp). The mass of the ester is 
actually 
 somewhat lower and the volume is 3% higher, which should give at 
 least 10% lower specific gravity (oil/fat vs. ester).
 Oh, and you can determine unreacted triglycs by chromatography. 
 Titration isn't reliable.
 
 Cheers, Aleks


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[biofuel] Re: Residual oil in BD.

2001-06-09 Thread gjkimlin

Titration is working now, (batch 1) alkali only 10% oil (batch 2)acid 
then alkali 20% oil. Got the centrifuge working--no separation from 
batch 1---looks like good whisky. Batch 2 gave a solid deposit ~1/5th 
by volume liquid clear but dark. Tried the titration from the BD on 
the very top after 15min at 3500rpm--still came back 8%. Is this a 
zero error or is the oil/BD so well dissolved that the centrifuge 
does not separate them? Currently distilling 100mls from batch 1. 
Intend to titrate what should be pure BD. let you know!! Harry
--- In [EMAIL PROTECTED], [EMAIL PROTECTED] wrote:
 OK What I intend is to attempt to :
 1) Use bicarb soda to neutralise the acidic BD prior to titration. 
 Hopefully this will give me a constant starting point PH wise.
 2) Seperate about 5gms of both BD and Source oil (palm) by paper 
 chromatography, ether extract fractions and weigh. Should give a 
 standard oil residue to calibrate my titration. Where will the 
 glycerol end up? I'll let you know!!
 3) Boil off esters and weigh remainder. ( oil glycerol?)
 Bit of running around to do first, its 9.47 here I may get to it 
 about 15.00. Thanks for the comments.
 Regards Harry.
 
 --- In [EMAIL PROTECTED], Ken Provost [EMAIL PROTECTED] wrote:
  At best the reaction conditions we are using convert only a 
 fraction of the
  WVO to ester.
  ( Configure the ammount of methanol into the equation for the 
 reaction and
  you will see what I mean).
  The reaction involves equilibrium and as with a lot of organic 
 chemistry
  reactions is not as straightforward as an inorganic reaction. So 
 we can't
  just add more methanol and expect more ester.
  
  I don't really think this is true. Using 200ml methanol per liter 
 of WVO is
  about a 60% molar excess (that is, 60% more methanol than is 
 actually
  consumed in the transesterification). The excess helps to shift 
 equilibrium
  in the desired direction, and I think we can expect something 
like 
 95%
  completion. When you start cheating on the methanol is when you 
 start
  seeing more unconverted oil in the BD -- viscosity will be 
 measurably
  higher as a result.   -K


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[biofuel] Re: Residual oil in BD.

2001-06-08 Thread gjkimlin

OK What I intend is to attempt to :
1) Use bicarb soda to neutralise the acidic BD prior to titration. 
Hopefully this will give me a constant starting point PH wise.
2) Seperate about 5gms of both BD and Source oil (palm) by paper 
chromatography, ether extract fractions and weigh. Should give a 
standard oil residue to calibrate my titration. Where will the 
glycerol end up? I'll let you know!!
3) Boil off esters and weigh remainder. ( oil glycerol?)
Bit of running around to do first, its 9.47 here I may get to it 
about 15.00. Thanks for the comments.
Regards Harry.

--- In [EMAIL PROTECTED], Ken Provost [EMAIL PROTECTED] wrote:
 At best the reaction conditions we are using convert only a 
fraction of the
 WVO to ester.
 ( Configure the ammount of methanol into the equation for the 
reaction and
 you will see what I mean).
 The reaction involves equilibrium and as with a lot of organic 
chemistry
 reactions is not as straightforward as an inorganic reaction. So 
we can't
 just add more methanol and expect more ester.
 
 I don't really think this is true. Using 200ml methanol per liter 
of WVO is
 about a 60% molar excess (that is, 60% more methanol than is 
actually
 consumed in the transesterification). The excess helps to shift 
equilibrium
 in the desired direction, and I think we can expect something like 
95%
 completion. When you start cheating on the methanol is when you 
start
 seeing more unconverted oil in the BD -- viscosity will be 
measurably
 higher as a result.   -K


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http://journeytoforever.org/biofuel.html
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To unsubscribe, send an email to:
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[biofuel] Re: Residual oil in BD.

2001-06-08 Thread Aleksander lt;kac

 
 I don't really think this is true. Using 200ml methanol per liter 
of WVO is
 about a 60% molar excess (that is, 60% more methanol than is 
actually
 consumed in the transesterification). The excess helps to shift 
equilibrium
 in the desired direction, and I think we can expect something like 
95%
 completion. 
Right. Combined processes need a little less meth, but still a 50% 
excess.

When you start cheating on the methanol is when you start
 seeing more unconverted oil in the BD -- viscosity will be 
measurably
 higher as a result.   -K
You can observe your volumetric yield. With the right quantities of 
alcohol and catalyst the 95+ % conversion will give 100 to 103% volum.
yield (measured at the same temp). The mass of the ester is actually 
somewhat lower and the volume is 3% higher, which should give at 
least 10% lower specific gravity (oil/fat vs. ester).
Oh, and you can determine unreacted triglycs by chromatography. 
Titration isn't reliable.

Cheers, Aleks


Biofuel at Journey to Forever:
http://journeytoforever.org/biofuel.html
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To unsubscribe, send an email to:
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