I was chatting today with a chemical engineer who happened to write his final 
thesis (the paper you write in order to graduate) on the methyl esters and 
transesterifications. As a chemical engineer, he studied che kinetics of the 
reaction and the reaction speeds, and he designed a production facility for a 
continuous process. He made all sorts of tests using IR spectrography at 
different points of the reaction, and made a very thorough work from the 
"chemical point of view". He did not want to show me his thesis (maybe he was 
afraid of me copying methods still not patented), but he did give me some hints 
and opinions, which I try to summarize here, and which you might want to have a 
look at: (This guy used soy oil)

.- Strange enough, he pointed out that some "thorough investigations" were not 
100% right, but he didn«t say where they were wrong: he just added "do the 
experimentation yourself, and you«ll see"

.- He said that 50¼C for the reaction was waaay too much. He said he carried 
out his continuous process at room temperature. Besides this, he pointed out 
that the glycerin was very easily decomposed into acrolein and things like 
that, which make it dark brown. I was so curious that just now, when I got 
home, I made a 100ml batch at room temp (now around 18¼C), and mixed for only 
15 minutes. This guy said that they had achieved a 98% conversion after this 
time period. Now I«ve let it settle, and I can see after about an hour settling 
that the glycerin DOES show up much clearer (pure glyc is transparent). He also 
said that in his continuous process he had designed a three stage evaporator to 
remove the water from it, after distilling it to get out the MeOH (I suppose 
he«d do this under vacuum, so as not to heat the glyc and turn it into the 
mentioned brown acrolein). I found this point most interesting.

.- He mentioned they used sulphuric acid (say, 4ml per liter of WVO) to "cut" 
the reaction and stop the NaOH (this forms sodium sulphate, Na2SO4, which is 
washed with the water). I said I added some drops of vinegar in the washing 
stage and he almost whent crazy: he said tha any ammount of vinegar capable of 
modifying pH would produce great problems with the injectors. He said motors 
are very sensitive to those acid conditions.

.- He also pointed out that I should remove the sulphates (which came from the 
sulphuric acid / lye reaction) from the glycerin, and added that the glycerin 
was full of impurities: sulphates, MeOH, water...

.- He also added that boiling off the MeOH was not a very eco-friendly thing to 
do, and that you«d never be able to boil off 100% of it (eve with a 
distillation column)

.- He said a continuous centrifugue was not har to get, but reaction velocities 
had to be carefully measured when designing a continuous process. He fancied 
this method and said that settling the BD was not a good option, specially 
after vigorous mixing, which always (according to him) brought emulsification 
problems of some kind.

.- Regarding the fact I am an environmental engineer, he pointed out the 
washing stages use a damn great ammount of water (I can«t recall having heard 
of an alternative to this from him). Also, than no reaction is 100% efficient 
and that if I was to measure exhaust gases, then I *should* be checking for 
unburnt traces of methanol, which could produce nasty emissions.

Everything he said sounded most interesting, but presented me with a whole new 
set of questions to be answered. I«m very eager to hear the opinion of those 
with experience in BD making, specially those who use it regularly in their 
cars.

Best to you all,

Christian



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