> >if there is FFA present in the waste oil, and both of them undergo
> >the transesterification, where will the unreacted FFA be present?
> >will the excess methanol and the lye be present all in the glycerine
> >layer? why?

FFAs undergo saponification (soap making). The glycerides undergo
transesterification.

The saponification takes place first and consumes catalyst, leaving no
unreacted FFAs. If the FFA content of the parent oil is not calculated
properly and too little catalyst is used, the transesterification reaction
will not go to completion.

Glycerol and methyl esters (biodiesel) are both solvent in methanol, meaning
that the methanol will reside in both products. Some free catalyst will
remain in the biodiesel layer. The majority of the catalyst will reside in
the glycerol cocktail layer bound up as soap.

> >FFA  reacts with the sodium hydroxide to produce COONa + water? is
> >it correct? if its true, where will these products formed be at? the
> >ester region or the glyerine layer?

The small amount of water that is formed will primarily reside in the
glycerol cocktail layer, as glycerol is far more solvent in water than is
biodiesel.

Todd Swearingen

----- Original Message ----- 
From: "ophelia~" <[EMAIL PROTECTED]>
To: <biofuel@yahoogroups.com>
Sent: Monday, August 30, 2004 8:27 AM
Subject: [biofuel] Transesterfication


> hi ppl...
>
> can anyone answer my questions?? thanks
>
> for the tranesterification,
> >
> >if there is FFA present in the waste oil, and both of them undergo
> >the transesterification, where will the unreacted FFA be present?
> >will the excess methanol and the lye be present all in the glycerine
> >layer? why?
> >
> >FFA  reacts with the sodium hydroxide to produce COONa + water? is
> >it correct? if its true, where will these products formed be at? the
> >ester region or the glyerine layer?
>
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