----- Original Message -----
From: Keith Addison <[EMAIL PROTECTED]>
To: <biofuels-biz@yahoogroups.com>
Sent: Sunday, September 15, 2002 2:03 PM
Subject: Re: [biofuels-biz] High FFA oils - another way


> Hello Paul
<snip>
> >----- Original Message -----
Paul wrote> >Mix the lime into the WVO/BD and heat with occasional stirring
to 100 deg C.
> >The lime appears to dissolve in WVO as heated but is probably just held
in
> >suspension.
> >Cool decant and filter. No problems with ammount of lime just use excess.

Forgot to mention that it is best to make a slurry of the lime and a small
volume of WVO, then add this to WVO.

> Thanks Paul, I'll try that. But this caustic refining step is so easy
> I'm quite satisfied with it, and there's no need for heat, for
> filtering, or for anything you haven't already got.
>
> "... just use excess" - about how much per litre?

Be guided by the titration.
1g NaOH is equivalent in reaction to 1.08g Ca(OH)2


> >Would much rather go acid/base with feedstock with FFA content this high,
>
> Sure, as I said, but a lot of people don't do acid-base. Also,
> acid-base doesn't like this particular oil, it has a lot of salt in
> it (tempura oil). Hot pre-washing solves that problem, but that then
> makes the acid-base process a lot more trouble than this, and a lot
> more energy use, so you're left to choose between much more time and
> hassle for the acid-base advantages, or a quick and easy way like
> this, and there's not much in it. Especially since I think recovered
> FFAs are useful, not wastage. You're not using more methanol, the
> extra lye isn't expensive, so it's really just some extra phosphoric,
> no big deal, as against no sulphuric.

Interesting I didn't think of the salt content.
> >less wastage/recovery
>
> "It's an alternative - better than straight single-stage base for oil
> like this, and while it won't get as a high a production rate as
> acid-base, and it uses more catalyst and gives you more co-products,
> it's very quick and simple, and the product is good."
>
> >and acid stage allows alcohols other than methanol or
> >ethanol to be used. Isopropanol for instance has the potential to reduce
> >cloudpoint.
>
> Have you tried the acid-base process with isopropynol? That'll make
> branched alkyl esters, low cloud-point yes, but I don't know of
> anyone that's had any success with isopropynol or butyl other than
> with enzymes, though I do know people who've tried. Reference
> previously posted in "Cracking" thread, Foglia et al, for instance.
> Pressure maybe.

Have to dig through my records, intended to try acid/base with isoprop in
acid stage but can't remember whether I got around to it.
isopropanol definitely doesn't seem to want to work for transesterification.
I think Aleks was working on BD using either isopropanol or butanol.
>
> Best wishes
>
> Keith
>
>
Regards,   Paul Gobert



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