Ken,

I'm really sorry for not getting to this before I dealt with
other stuff.

Here be the coupe de grace....

An acid/base requires no titration....

Want to here some more good news.....?

Start working acid/base reactions and you can probably reduce
your base catalyst by half or three quarters, thereby reducing
your wash "problems" and increasing your yield.

I just posted a general response to one of Keith's questions,
under the subject line of "Phosphoric." That had some pertinent
thought process throughout.

What I can say unequivocally is that an acid/base reaction,
conducted carefully and "properly," will probably increase your
yield by ~4%.

I certainly wouldn't sneeze at that, as it also reduces your
capital inputs and reduces the cost of your effluent management
programs.

As for taking accumulated recovered FFAs and conducting an acid
esterification that only results in 70% conversion....I'd say
that you are about 10 giant steps in front of most other persons
at the "home biodieseler's" level.

Okay...so you have to reprocess 30% of your original 100% FFAs.
Are you not already 70% ahead of the game?

If you've gone in this direction, I doubt that there is much
holding you back. Your next mission, should you choose to accept
it, (Mission Impossible tele series for those who don't know it)
is to pull off a 100% complete esterification reaction.......

Just one problem there.........esterification reactions happen
best under high temp and pressue.

My best guess under such circumstances is that you would be
better off switching to an acid/base method and not accumulating
recovered FFAs in such high quantities in the first place.

I just don't know exactly what the conversion of FFAs is in an
"STP" acid stage. I have no doubt that it is not entirely
complete. For now, it is considerably better than nothing. In
time, we should have a barnyard and solid answer to this
question. Hopefully in short time.

In the meantime, however, I have to ask........If what you are
trying to convert to esters are 100% FFAs....do you really see
any need to go into a base stage?

Ain't been there...Ain't done that....But fixin' to.....Just
seems like a logical question as the glycerin is already cracked
and non-present.

Todd Swearingen

----- Original Message -----
From: Ken Provost
To: biofuel@yahoogroups.com
Sent: Friday, April 26, 2002 9:25 PM
Subject: Re: [biofuel] Results on Revised 2 Stage Acid/Base
Method


Todd Swearingen wrote:

>We've been doing some testing on acid/base reactions lately....

Great data, I hung on every word!...... The only thing I'd've
liked
woulda been some titrations along the way. My big question is the
obvious one --what does all the acid step really DO for us?
Hopefully, it reduces the FFA level of the original oil from some
gawdawful level, say, 20%, down to 2% before you go into the
base-catalyzed stage, so you can use really dirty oil (or, in my
case, clean oil with lots of FFA intentionally added, having been
recovered as such from the accumulated glycerine phases of weeks
of normal reactions). Unfortunately, my own titrations on that
score seem to indicate I'm only getting about 70% esterification
in the acid step, which still leaves a lot of soap in the base
step.

Did you notice a reduction in the amount of soap from typical to
the 2-stage process? Did you do any pH checks of your wash
water along the way?

I'll be doing some very similar experiments this weekend, using
a combination of clean oil and extracted FFA -- will keep y'all
informed.     -K

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