Re: [Biofuel] Acid-base chemistry

2010-04-21 Thread Chris Burck
lol, yeah, moles for sure are kind of tricky.  precisely because of
the things you mention.  (i dropped chem in college.  there was no way
i was going to pass if i stuck it out.)  thanks for sharing your
impression of the youtube guy.  sorry if it was waste of your time.

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Re: [Biofuel] Acid-base chemistry

2010-04-20 Thread Keith Addison
Hi Chris

Thanks!

But...

keith,

don't know if this will help, but. . .:

http://www.youtube.com/user/khanacademy#p/c/166048DD75B05C0D/10/gfBcM3uvWfs

Emperical? H amu is 1.008 but he reads it out as 
one-point-oh-oh-oh-eight. And so on, much sloppiness! I thought it 
was rather poor, I'm sure you can find better resources for brushing 
up your math skills.

Strange to tell, but my high-school chemistry lessons never once 
mentioned moles. :-(

(Don't ask me what kind of school I went to or I'll tell you.)

I can see that moles are useful, and I can figure it out, but moles 
only concern mass, and what I often need is volume. How many people 
would be able to follow titration instructions eg if the quantities 
were given in moles? Not a lot, I think. And for weight, a simple 
measure in grams is clearer.

Going from moles to volumes isn't so easy, the SG ratios make it 
complicated (and it turns out SG is itself controversial, 1cc H2O @ 
4degC weighs 1g isn't the gold standard it used to be). I did get a 
result, I think it's right, but I'm not sure, and not quite sure that 
it works like that anyway.

1 ml H2SO4 + 80 ml CH3OH -- (I think) ? CH4SO4 + ? H2O

(Not sure that's right either.) Can you do it? Give your math some 
practice. :-)

Periodic table of elements:
http://www.chemicalelements.com/

Avocado's cucumber:
http://www.chemistry.co.nz/avogadro.htm

Density, mass, SG of Liquids (useful table):
http://www.simetric.co.uk/si_liquids.htm

Mole (FWIW):
http://en.wikipedia.org/wiki/Mole_(unit)

All best

Keith


and:

http://www.youtube.com/user/khanacademy#p/c/166048DD75B05C0D/11/AsqEkF7hcII
maybe it'll give you what you need to feel more confident doing it
yourself?  i've been meaning to check some of this guy's stuff out myself
(really need to revisit a lot of high school math), but haven't gotten
around to it yet.

-chris
On Sun, Apr 18, 2010 at 1:27 PM, Keith Addison
[EMAIL PROTECTED]wrote:


  I have difficulty with moles. I do know how to figure it out, in
   theory, but I'm not confident of the result.


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Re: [Biofuel] Acid-base chemistry

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


 Hello Jan

 Thankyou!

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

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

 A + B -- D + E

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

The trans-esterification does not produce any water,

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

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

 Any comments?

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

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

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

 Thanks again Jan - all best to you

 Keith


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

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


  Hello all

  A question...

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

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

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

  Thanks!

  All best

   Keith



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Re: [Biofuel] Acid-base chemistry

2010-04-19 Thread Chris Burck
keith,

don't know if this will help, but. . .:

http://www.youtube.com/user/khanacademy#p/c/166048DD75B05C0D/10/gfBcM3uvWfs

and:

http://www.youtube.com/user/khanacademy#p/c/166048DD75B05C0D/11/AsqEkF7hcII
maybe it'll give you what you need to feel more confident doing it
yourself?  i've been meaning to check some of this guy's stuff out myself
(really need to revisit a lot of high school math), but haven't gotten
around to it yet.

-chris
On Sun, Apr 18, 2010 at 1:27 PM, Keith Addison
[EMAIL PROTECTED]wrote:


 I have difficulty with moles. I do know how to figure it out, in
 theory, but I'm not confident of the result.
-- next part --
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Re: [Biofuel] Acid-base chemistry

2010-04-19 Thread Keith Addison
Hello again Jan

Thanks for the explanation.

Hello Keith. Moles means molecules.

Yes, or molecular weights. My problem is with translating moles to 
quantities, such as ml and litres. Which brings in specific gravity / 
relative density... :-( I can manage though.

I arrived at a figure of the acid esterification step producing 17.3 
ml of water per litre of oil processed (rapeseed), 1.73%. I doubt 
it's that precise, but it should be something like that.

There is one water molecule formed for
each molecule of fatty acid alkylated.
It is true that some water is produced during saponification of free acidity
and it is also true that water is formed when mixing NaOH or KOH in an
alcohol. But neither of these reactions are esterification or
transesterification reactions..

No, but the water is there nonetheless.

It is considered that the transesterifiction reaction takes place in two or
more steps, where the first step is the collapse of the glycerine-formed
ester (the triglyceride etc) forming free glycerine and free acidity. Water
is consumed in that step. In another step the new esters are formed where
the equal amount of  water is released. Conclusion: Some free water is good
for the first step of the reaction. Does it make sense ?

Yes it does.

So in acid-base processing, the acid esterification stage should 
provide the water needed for the first step of the base 
transesterification stage, very convenient. The water released in the 
final stage of transesterification should end up in the glycerine 
byproduct layer, or most of it anyway, and washing and settling 
should remove the rest.

Without the preceding acid esterification stage, could some of the 
water required in the first step of transesterification be provided 
by the water formed in mixing the methoxide? I'd imagine that water 
formed during saponification would be in the by-product layer rather 
than available to help initiate transesterification.

Interesting, Jan - thanks very much.

All best to you

Keith


- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Sunday, April 18, 2010 7:27 PM
Subject: Re: [Biofuel] Acid-base chemistry


  Hello Jan

  Thankyou!

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

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

  A + B -- D + E

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

The trans-esterification does not produce any water,

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

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

  Any comments?

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

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

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

  Thanks again Jan - all best to you

  Keith


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

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


   Hello all

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

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

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

   Thanks!

   All best

 Keith
  


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Re: [Biofuel] Acid-base chemistry

2010-04-18 Thread Keith Addison
Hello Jan

Thankyou!

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

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

A + B -- D + E

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

The trans-esterification does not produce any water,

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

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

Any comments?

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

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

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

Thanks again Jan - all best to you

Keith


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

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


  Hello all

  A question...

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

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

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

  Thanks!

  All best

   Keith



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[Biofuel] Acid-base chemistry

2010-04-17 Thread Keith Addison
Hello all

A question...

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

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

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

Thanks!

All best

Keith

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Re: [Biofuel] Acid-base chemistry

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

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


 Hello all

 A question...

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

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

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

 Thanks!

 All best

 Keith

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