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) to produce biodiesel in a laboratory, for educational purposes. This is what I've been doing:

 

-         1 liter of virgin oil from supermarket

-         200 mL of methanol

-         3,5 grams of sodium hydroxide

-         Prepared the sodium metoxide by stirring for 24 hours (magnetic stirrer) in an closed Erlenmeyer

-         Preheated the oil to 55ºC

-         Using a flask with an attached Liebig condenser (to prevent methanol vapors to escape), mixed vigorously for 1 hour maintaining agitation and constant temperature (eventually drops to 52ºC when the metoxide is added) and maybe rising to a maximum of 60ºC at some instants.

I do get a clear phase separation after 24 hours, but my biodiesel isn't crystal clear.

When I mix a sample of the unwashed biodiesel with water and shake it, the emulsion won't separate…. It will after some hours, but with a lot of soap formation, widespread in the container.

I'm using good reactants (not p.a. but trustworthy) and anhydrous conditions.

 

There one thing I should say: I never got all the sodium hydroxide to completely dissolve in the methanol. No matter how long I keep stirring, it simply won't dissolve quantitatively. But I do filtrate the remains of solid hydroxide. Do you think this can be the problem? How can I solve it?

 

What can I be doing wrong? Why do I keep getting all this soap? Where do you think the problem might be? In a reactant? Bad quality oil? Do you think I should titrate the virgin oil?

 

Thank you all for your attention

 

 

Duarte Nuno


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