Andres,
Doesn´t the water poison the catalyst and give you saponification reactions?
From: Andres Secco [mailto:[EMAIL PROTECTED]To: Biofuel@sustainablelists.orgSent: Thu, 16 Feb 2006 00:37:16 -0300Subject: Re: [Biofuel] Trying to produce biodiesel in laboratory scale
Dear Duarte,
The basic
: Re: [Biofuel] Trying to produce
biodiesel in laboratory scale
Andres,
Doesn´t the water poison the catalyst and give you saponification
reactions?
From: Andres Secco [mailto:[EMAIL PROTECTED]To: Biofuel@sustainablelists.orgSent:
Thu, 16 Feb 2006 00:37:16 -0300Subject
Mahoney
To: Biofuel@sustainablelists.org
Sent: Wednesday, February 15, 2006 10:38
PM
Subject: Re: [Biofuel] Trying to produce
biodiesel in laboratory scale
One thing I've never seen mentioned is using
sodium methoxide from a company such as BASF. I am using it in lab
: Thursday, February 16, 2006 4:54
AM
Subject: Re: [Biofuel] Trying to produce
biodiesel in laboratory scale
Andres,
Doesn´t the water poison the catalyst and give you saponification
reactions?
From: Andres Secco [mailto:[EMAIL PROTECTED]To: Biofuel
]
*To:* Biofuel@sustainablelists.org
mailto:Biofuel@sustainablelists.org
*Sent:* Thu, 16 Feb 2006 00:37:16 -0300
*Subject:* Re: [Biofuel] Trying to produce biodiesel in
laboratory scale
Dear Duarte,
The basic reaction you are doing
:[EMAIL PROTECTED]
*To:* Biofuel@sustainablelists.org
mailto:Biofuel@sustainablelists.org
*Sent:* Thursday, February 16, 2006 4:54 AM
*Subject:* Re: [Biofuel] Trying to produce biodiesel in laboratory scale
Andres,
Doesn´t the water poison the catalyst and give
to produce biodiesel in laboratory scale
One thing I've never seen mentioned is using sodium methoxide from a
company such as BASF. I am using it in lab work and find it very
convenient. It is water-free and about 25% in methanol. Take a
look at this web page
http://www.basf.com
@sustainablelists.org
*Sent:* Thursday, February 16, 2006 4:54 AM
*Subject:* Re: [Biofuel] Trying to produce biodiesel in laboratory
scale
Andres,
Doesn´t the water poison the catalyst and give you saponification
reactions
1) Start by compensating with an equal amount of dissolved NaOH for the
undissolved solids you're removing. You can't call them part of the 3.5
requisite grams, take them out of the equation and then expect
everything to work perfectly as if no subtraction was done.
2) Titrate the oil.
How did you utilize the liebig condensor? Wouldnt that condense the gas given off by the reaction into a liquid? Is that the jist of it? Turning it into a less volitile liquid instead of a gas?
On 2/15/06, Duarte Nuno Januário [EMAIL PROTECTED] wrote:
Hi all!
I've been trying (made 5 batches)
YupHe's basically refluxing it, I assume, with the liebig condenser vertically attached to the reaction vessel. A closed container would do the same thing!A good use for the liebig condenser would be to reclaim the excess methanol from the glycerine, but they are usually pretty small, so would
A while back I tried to shake up the methoxide and oil in a closed
container (due to lack of glass blender or lab stirrer), and much like
a shaken soda bottle it expanded a bit and fizzed out a bit. I am
looking for a better test setup that can prevent this type of thing.
Would stirring the
A while back I tried to shake up the methoxide and oil in a closed
container (due to lack of glass blender or lab stirrer), and much
like a shaken soda bottle it expanded a bit and fizzed out a bit.
I am looking for a better test setup that can prevent this type of
thing. Would stirring the
Hello Dennis
Don't you mean sodium methylate?
Best
Keith
One thing I've never seen mentioned is using sodium methoxide from a
company such as BASF. I am using it in lab work and find it very
convenient. It is water-free and about 25% in methanol. Take a
look at this web page
Hi Duarte
I do get a clear phase separation after 24 hours, but my biodiesel
isnt crystal clear.
It really doesn't matter much, or it doesn't matter at all. See, eg.:
Allow to settle for 12-24 hours. Darker-coloured glycerine
by-product will collect in a distinct layer at the bottom of the
One thing I've never seen mentioned is using sodium
methoxide from a company such as BASF. I am using it in lab work and find
it very convenient. It is water-free and about 25% in methanol. Take
a look at this web page
http://www.basf.com/businesses/chemicals/alcoholates/biodiesel/index.html
Dear Duarte,
The basic reaction you are doing is a nucleophilic
reaction were the methoxide replaces the glycerine in the fatty acid. So you get
free methylstearates (if the oil have stearic acid). This substances called
methyl-Stearates or Linoleates arethe Biodiesel.
Now, I have some
Hi, I am trying to construct a similar setup. How do you actually use
the Liebig condensor to pickup the methanol gas? I have never used that
piece of equipment before. Do you have a picture of the setup or
diagram you can send me?
Thanks!
- JaredOn 2/15/06, Duarte Nuno Januário [EMAIL
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