Hi,

Great information for me working away in the lab. Keep it coming. I'm still
trying to come to terms with methanol ( cheap, easy but oh so toxic) and
ethanol ( expensive, density separation problems, need for excess as a
reactant but great for making products with the glycerine and the
occassional party). Any thoughts here?

Tom Irwin


-----Original Message-----
From: Appal Energy
To: [EMAIL PROTECTED]
Sent: 3/30/05 11:55 AM
Subject: 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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