I would like to get a copy of those article.  Can you explain what you
mean by the K-O bond being more polar?  I didn't think that there were
any K-O bonds left once the KOH is dissolved (reacted) with the
methanol creating methoxide since that acid-bace reaction is quite
complete.

Andy


On Fri, 14 Jan 2005 09:27:13 +0200, Stelios Terzakis
<[EMAIL PROTECTED]> wrote:
> My experience about KOH+MeOH is that the path of saponification is weaker
> than NaOH+MeOH. I will try to write a chemical explanation for this in my
> thesis. From an first look is seems that the K-O bond is more polar and
> dissociates esterified glycerides more easily...
> 
> Some other authors have made the same conclusion (for those interesting i
> can send them the whole article):
> Kinetic Parameters Affecting the Alkali-Catalyzed Transesterification
> Process of Used Olive Oil
> 
> M. Pilar Dorado,*,? Evaristo Ballesteros,? Martin Mittelbach,€ and Francisco
> J. Lo«pez|
> 
> Departments of Mechanics and Mining and of Physical and Analytical
> Chemistry,
> 
> EUP de Linares, University of Jae«n, C/. Alfonso X el Sabio 28, 23700
> Linares, Jae«n, Spain,
> 
> Institute of Chemistry, Karl-Franzens-UniversitaŹ t Graz, Heinrichstrasse
> 28, A-8010 Graz,
> 
> Austria, and Department of Agricultural Engineering, ETSIAM, University of
> Co«rdoba,
> 
> Avenida Mene«ndez Pidal s/n, 14080 Co«rdoba, Spain
> 
> Received November 21, 2003. Revised Manuscript Received June 9, 2004
> 
> In this study, chemical parameters involved in waste olive oil
> transesterification were investigated and optimized. Better results were
> obtained using KOH and methanol instead of
> 
> NaOH and ethanol, which decreases transesterification rates. The presence of
> KOH and methanol above or below the optimum quantity decreases the ester
> yield because of the presence of soaps
> 
> or unreacted glycerides, respectively. Settling at ambient temperature under
> 25 ĄC increases the difficulty of ester and glycerol separation because of a
> conflict between glycerol solubility
> 
> and low temperatures. This could be solved by increasing the settling
> temperature or the time for settling. In summary, the reaction was optimized
> at ambient temperature using 1.26% KOH,
> 
> 12% methanol, 1 min of stirring, with 90 min of pour-off time, 11.38%
> distilled water by volume at 25 ĄC to purify the ester, and drying over 0.5%
> Na2SO4. Losses of esters during the washing
> 
> process were less than 4%. The ester yield of the reaction was 94%. The
> small presence of unreacted glycerides did not drop the engine performance.
> Fuel specifications were close to those
> 
> of diesel fuel, thus indicating that methyl esters from used olive oil can
> be considered as a fuel candidate.
> 
> ----- Original Message -----
> From: "Andrew Cunningham" <[EMAIL PROTECTED]>
> To: <[EMAIL PROTECTED]>
> Sent: Thursday, January 13, 2005 10:29 PM
> Subject: Re: [Biofuel] Kaliumhydroxide.
> 
> > How does KOH avoid saponifcation?  As far as I knew both NaOH and KOH
> > are equally capable of the saponification reaction.
> >
> > Andy
> > Chemical Engineer
> >
> > "If you want the opinion of a chemist, i think that KOH wich i use gives
> > better product yields (you avoid saponification and problems in the
> > cleaning)
> >
> > This means that in a production cycle it may be less expensive.
> >
> > Stelios"
> > _______________________________________________
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