I agree with you Todd. All chemical reactions of this kind carries a number
of side reactions, but the amount or appetence of the glycerol cocktail
cannot be used for judging the success of the transesterification(unless it
is < 10% by mass), but a determination of the content of the glycerol
cocktail might give a clue.
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
----- Original Message ----- 
From: "Appal Energy" <[EMAIL PROTECTED]>
To: <[EMAIL PROTECTED]>
Sent: Wednesday, March 30, 2005 4:55 PM
Subject: @SPAM+++++++++ Re: [Biofuel] liquid glycerine


> Jan & Paul,
>
> > It seems to me that you produced some soap that time.
>
> All base processing creates soap.
>
> What everyone keeps referring to as "glycerine" settling out of a
> transesterification (base) reaction is for the most part soap, diluted
with
> methanol and glycerol.
>
> The volume of glycerol per liter of oil processed is ~7.9% (~79
mililiters).
> The excess alcohol present in this layer (glycerin cocktail) is ~65ml when
> initially using 200 ml per liter. The balance is soap.
>
> Different oil and fat feedstocks produce different types of soap. If your
> feestock was primarily soybean oil on Monday but coconut oil on Tuesday,
the
> latter would in general yield a more solid glyc cocktail. If the
feedstocks
> were soybean oil on both days but Tuesday's was extremely degraded (high
> FFA) then the latter would yield a harder glyc cocktail. If the feedstock
on
> Monday had less animal fat in it than that on Tuesday the latter would
> generally yield a harder or more viscous glyc cocktail.
>
> The same happens when using different catalysts. In soap making sodium
> hydroxide (lye) is used to produce bar soaps (hard) and potassium
hydroxide
> is used to produce liquid soaps (solid like thick bread dough but more
> soluble). When using potassium hydroxide the glyc cocktail generally never
> thickens beyond that of maple syrup.
>
> Hardened or thinned glyc cocktails don't necessarily indicate "mistakes"
or
> "correctness" in processing.
>
> Todd Swearingen
>
> ----- Original Message ----- 
> From: "Jan Warnqvist" <[EMAIL PROTECTED]>
> To: <[EMAIL PROTECTED]>
> Sent: Wednesday, March 30, 2005 3:01 AM
> Subject: Re: [Biofuel] liquid glycerine
>
>
> > Hello Paul.
> > It seems to me that you produced some soap that time. Did you measure
the
> > FFA content before starting ?
> > Best regards
> > Jan Warnqvist
> > AGERATEC AB
> >
> > [EMAIL PROTECTED]
> >
> > + 46 554 201 89
> > +46 70 499 38 45
> > ----- Original Message ----- 
> > From: "Paul Tanner" <[EMAIL PROTECTED]>
> > To: <[EMAIL PROTECTED]>
> > Sent: Wednesday, March 30, 2005 1:00 AM
> > Subject: [Biofuel] liquid glycerine
> >
> >
> >>
> >>
> >>
> >>
> >> Hi,
> >>
> >> I've been making Biodiesel (BD) for a few months, now.. using the Mike
> >> Pelly method.. and a curious thing happened with the last batch (my
> > batches
> >> are in approx. 160 - 180 litres).. the glycerine was liquid after the
> >> reaction. This is the first time this has occurred for me, all other
> >> times
> >> the glycerine formed and settle in my tank, and was solid at low
> >> temperatures.
> >>
> >> I had measured accurately, the quantities of methanol, caustic soda and
> >> volume of oil...( I had an interested observer, who can testify if
> >> required!! :-)  ) I watched the colour of the mixture change, as I was
> >> agitating, from a light caramel colour to a dark molasses colour...
then
> >> observed the glycerine start to settle, as expected. At this time the
> >> glycerine was quite warm, so was still liquid, however, I let the
mixture
> >> settle for a 2 week period and the glycerine has not set firm. maybe I
> >> should not complain.. 'cos it was easy to drain out of the tank! :-)
> >>
> >> Did the reaction not go far enough?  Any further ideas on what has
> >> happened??
> >>
> >> regards,
> >>
> >> Paul.
> >> -------------------------------------------
> >> Paul Tanner
> >> Software IT Architect
> >> Melbourne, Australia
> >>
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> >>
> >
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> >
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>
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