Re: [Biofuel] OFM Tube

2005-10-03 Thread Keith Addison
Hello Andrew, John

Quoting john owens [EMAIL PROTECTED]:

  hi
   I just finished designing and building a batch processor based on the
  journey to forever 90 ltr processor I now want to design an ofm flow tube.
  Is there any other sites other than cambridge That would be usefull.
   John

I've thought about this, but think that the OFM technology might not 
be the best
for yields. I know that the Cambridge site mentions biodiesel production but
posts to this list make me think that the agitation may actually harm yield. I
base this on a post I made and the subsequent replies I got when 
Mike Allen was
designing Deep Throat,

Aarghhh! Deep Thort! LOL!

http://www.journeytoforever.org/biodiesel_processor8.html
- I think it was during then, but anyway, someone was designing a reactor...

The designer had mentioned that they where using a motor with a 
gear box so
that the mixing blades rotate at a relatively slow speed hence not churning
everything up.

That's Michael's view, yes. There are 10 big paddles on that mixer 
though, slow speed's all that's needed, 100 rpm. I like that way of 
doing it with a mixer rather than high speeds with a couple of small 
paddles.

I decided to use a pump instead with the JtF 90-litre processor, and 
Michael tut-tutted, all that agitation in the pump chamber, but it 
works very well anyway. Maybe it's different, slow agitation of the 
whole volume inside a tank or fast agitation of just a small part of 
the volume outside the tank with very little agitation inside the 
tank.

I asked the question that wouldn't it be better to flog the crap
out of it so that there was rapid and complete contact between all of the
component chemicals. The reply was that due to the equilibrium (reaction
kinematics???) of the oil/methoxide - biodiesel/glycerine reaction, it was
better to do things slowly and allow the glycerine to drop out of 
the reation,
down to the bottom of the reation, hence a tall slender reator is 
better that a
low squat one. It appears that the presence of the glycerine will hinder the
conversion from oil to BioD.

We hadn't discussed it, but we both ended up with processors that 
drop out a lot of the glycerine during the process, both 
intentionally, but doing it in different ways.

We have the idea that the level of the mixing tank outlet to the 
pump relative to the bottom of the tank is quite important. With our 
processor the mixing outlet is set somewhat higher than the level 
the glycerine by-product will settle at. That level will vary 
according to the oil (and process) you use. Especially with the rose 
at the inlet in the lid, there's not much agitation in the tank, 
mainly just circulation. The necessary agitation takes place inside 
the pump. The pump pulls the oil in from the tank outlet, but that's 
not very violent. As a result, a lot of the glycerine by-product 
settles out during the processing, which is a Good Thing. We think 
almost half of it settles out before the processing's finished. This 
does also remove some of the excess methanol, which is dissolved in 
the by-product.

Aleks Kac's Foolproof two-stage acid-base process has an optional 
step of draining off some of the glycerine during the base stage. 
(The process runs fine without this step, he says. It's just a 
twitch to get higher yield if your processor has a bottom drain.) 
He said this about it:

The process is running on the smallest sensible volume of alcohol. 
While removing a small portion of it with the by-product would seem 
to slow the reaction down, the rather large mass of removed 
by-product will tip the scale toward ester production.

We find that's the case -- the settled out glycerine by-product more 
than offsets any methanol removed, with very satisfactory results.

CAPTION: The sample on the left was taken from the top of the 
processor a couple of minutes before switching the pump off at the 
end of the process. Immediately after processing the whole batch is 
pumped into the holding tank via the processor's bottom drain. What 
comes out first is already-settled glycerine by-product. Pumped into 
the holding tank at the lid, it all gets mixed up again before 
settling. The sample on the right is of the same batch, taken from 
the top of the holding tank immediately after transfer -- twice as 
much glycerine by-product.
-- Journey to Forever 90-litre processor
http://journeytoforever.org/biodiesel_processor10.html

The photograph is interesting.

Best wishes

Keith


How is this relevant to OFM? With the OFM technology, all of the 
components
are in the tube, hence the glycerine does not get a chance to drop 
out, in fact
it is mixed up in the agitating components thus will probably hinder the
reaction. I could see OFM being good for commercial situations where you could
break the reaction down into, say, 3 parts/stages, the first part is run with
the source oil but only a 1/3 of the required methoxide - and some
glycerine is produced, but not enough to 

Re: [Biofuel] OFM Tube

2005-10-03 Thread Andrew Lowe
Quoting Keith Addison [EMAIL PROTECTED]:

 Hello Andrew, John
 
 Quoting john owens [EMAIL PROTECTED]:
 
   hi
I just finished designing and building a batch processor based on the
   journey to forever 90 ltr processor I now want to design an ofm flow
 tube.
   Is there any other sites other than cambridge That would be usefull.
John
 
 I've thought about this, but think that the OFM technology might not
 be the best
 for yields. I know that the Cambridge site mentions biodiesel production but
 posts to this list make me think that the agitation may actually harm yield.
 I
 base this on a post I made and the subsequent replies I got when
 Mike Allen was
 designing Deep Throat,
 
 Aarghhh! Deep Thort! LOL!

I've just gone back to the page and had a look - I'm NOT EVEN GOING TO TRY and
explain that Freudian slip!!!

Andrew

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Re: [Biofuel] OFM Tube

2005-10-03 Thread Keith Addison
Quoting Keith Addison [EMAIL PROTECTED]:

  Hello Andrew, John
 
  Quoting john owens [EMAIL PROTECTED]:
  
hi
 I just finished designing and building a batch processor based on the
journey to forever 90 ltr processor I now want to design an ofm flow
  tube.
Is there any other sites other than cambridge That would be usefull.
 John
  
  I've thought about this, but think that the OFM technology might not
  be the best
  for yields. I know that the Cambridge site mentions biodiesel 
production but
  posts to this list make me think that the agitation may actually 
harm yield.
  I
  base this on a post I made and the subsequent replies I got when
  Mike Allen was
  designing Deep Throat,
 
  Aarghhh! Deep Thort! LOL!

I've just gone back to the page and had a look - I'm NOT EVEN GOING TO TRY and
explain that Freudian slip!!!

Andrew

ROFL!!! It would be superfluous anyway Andrew, I'm sure everyone can 
tell it's just that you spilled coffee on your keyboard and now it 
types all funny sometimes. On a respectable family-values list like 
this too, heavens, whatever next. Clearly it's all Michael's fault.

Keith


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Re: [Biofuel] OFM Tube

2005-10-02 Thread Andrew Lowe
Quoting john owens [EMAIL PROTECTED]:

 hi
  I just finished designing and building a batch processor based on the
 journey to forever 90 ltr processor I now want to design an ofm flow tube.
 Is there any other sites other than cambridge That would be usefull.
  John
 


I've thought about this, but think that the OFM technology might not be the best
for yields. I know that the Cambridge site mentions biodiesel production but
posts to this list make me think that the agitation may actually harm yield. I
base this on a post I made and the subsequent replies I got when Mike Allen was
designing Deep Throat, http://www.journeytoforever.org/biodiesel_processor8.html
- I think it was during then, but anyway, someone was designing a reactor...

The designer had mentioned that they where using a motor with a gear box so
that the mixing blades rotate at a relatively slow speed hence not churning
everything up. I asked the question that wouldn't it be better to flog the crap
out of it so that there was rapid and complete contact between all of the
component chemicals. The reply was that due to the equilibrium (reaction
kinematics???) of the oil/methoxide - biodiesel/glycerine reaction, it was
better to do things slowly and allow the glycerine to drop out of the reation,
down to the bottom of the reation, hence a tall slender reator is better that a
low squat one. It appears that the presence of the glycerine will hinder the
conversion from oil to BioD.

How is this relevant to OFM? With the OFM technology, all of the components
are in the tube, hence the glycerine does not get a chance to drop out, in fact
it is mixed up in the agitating components thus will probably hinder the
reaction. I could see OFM being good for commercial situations where you could
break the reaction down into, say, 3 parts/stages, the first part is run with
the source oil but only a 1/3 of the required methoxide - and some
glycerine is produced, but not enough to hinder the reaction. The results of
this are run through a centrifuge/settling tank with the glycerine being
removed, then the oil with the next 1/3 of the methoxide added is run through
the next section, more glycerine is produced, but once again not enough to
hinder things, the results centrifuged and then the oil plus remaining methoxide
run through the final stage, by now the original oil being fully converted and
the resulting small amount of glycerine centrifuged off. This is probably a
viable process for 100,000l/day plants but with centrifuges costing $10K each,
probably not for the backyarder.

Please bear in mind that this view of things is based on reading posts here,
a bit of other research and being a Civil Engineer, not an organic chemist or
Chemical Engineer. If I've misunderstood anything or got something wrong, please
feel free to correct me.

Regards,
Andrew

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