[biofuel] Chemistry of washing

2004-08-18 Thread Teoman Naskali

When I wash my test batch, it creates a vaccum in the container it is
washed in. Obviously some kind of chemical reaction takes place. What
could it be? And what does it absorb from the air??? I don't think it is
the Co2 or the O2, could it be the N2??

Please enlighten me, or have I bungled it up yet again.

Teoman




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Re: [biofuel] Chemistry of washing

2004-08-18 Thread Martin Klingensmith



Ken Provost wrote:
 on 8/18/04 5:42 AM, Teoman Naskali at [EMAIL PROTECTED] wrote:
 
 
When I wash my test batch, it creates a vaccum
in the container it is washed in. Obviously
some kind of chemical reaction takes place. What
could it be? And what does it absorb from the
air???
 
 
 Interesting -- I've never noticed that. My guess
 is that methanol is vaporizing out of the unwashed
 fuel before you seal the container, displacing air
 out of the headspace, and then dissolving in the
 wash water after the container is sealed.
 
 Nothing in the air would be taken up by the fuel
 quickly enough to explain it (O2 reacting with
 double bonds in unsaturated fatty acid chains
 would take days, for example). -K
 

Perhaps the air above the biodiesel is warm at first and cools after 
washing, contracting and creating a vacuum.


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Re: [biofuel] Chemistry of washing

2004-08-18 Thread Appal Energy

Teoman,

There is not necessarily any reaction taking place in your wash. Any
sealed vessel creates a slight vacuum when it cools. Ask yourself if what
your experiencing is nothing more than that.

Todd Swearingen

- Original Message - 
From: Teoman Naskali [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Wednesday, August 18, 2004 7:42 AM
Subject: [biofuel] Chemistry of washing


 When I wash my test batch, it creates a vaccum in the container it is
 washed in. Obviously some kind of chemical reaction takes place. What
 could it be? And what does it absorb from the air??? I don't think it is
 the Co2 or the O2, could it be the N2??

 Please enlighten me, or have I bungled it up yet again.

 Teoman





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 http://journeytoforever.org/biofuel.html

 Biofuels list archives:
 http://infoarchive.net/sgroup/biofuel/

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Re: [biofuel] chemistry

2001-12-30 Thread Christian

I re-read the article. No doubt about what it says there. I was really
working out of my memory the other day, so it«s probable I mixed up the
facts. Anyway, if I do find something on the exothermic heating, I«ll let
you know.

Again, thanks.

Chirstian

- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, December 30, 2001 2:33 AM
Subject: Re: [biofuel] chemistry


 Thanks Keith. Though I must clear out something... I was talking of HCl,
 Hydrochloric acid, not Nitric Acid (HNO3), which I do understand is a
main
 chemical in the synthesis of various explosives (a friend of a close
friend
 of mine did pass away in a lab explosion some years ago).

 Yep, sorry, 'twas a bit late in the night - please see correction posted
later.

 The reference to HCl was found in the Morrison  Boyd book on organic
 chemistry (I think it`s Prentice, or Mc Graw)

 If you get any positive results with HCl, please let us know.

 One thing more, somewhere in journeytoforever it said small batches
 were exothermic enough
 to maintain the temperature close enough to 55 ¼C. If so, up to what
volume
 is this true?

 I doubt it - you'll have to find the reference please. The exothermic
 reaction's over by the time the methoxide's properly mixed and you
 add it to the oil, I don't see how it could have any effect on
 maintaining the process temp.

 Mike Pelly says this, in discussing Test batches:

 Start by mixing up the lye and methanol in a blender (one that will
 never be used for food again). First make sure the blender and all
 utensils used are dry. Forming the exothermal sodium methoxide polar
 molecule will heat up the blender container a bit. Keep mixing until
 all the lye has been dissolved.

 He certainly doesn't say it provides enough heat for the
 transesterification process itself. Anyway his test batches are with
 one litre of WVO, the methoxide uses only 150 ml of methanol and 6.25
 g NaOH, not very much heat there. I suggest you read it all again.

 http://journeytoforever.org/biodiesel_mike.html
 Biodiesel recipe from Mike Pelly

 Best wishes

 Keith Addison
 Journey to Forever
 Handmade Projects
 Tokyo
 http://journeytoforever.org/


 Thanks for the advice  concern.
 
 Regards,
 
 Christian



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Re: [biofuel] chemistry

2001-12-29 Thread Keith Addison

Please excuse my chemical terms in english.

I was wondering if you could clear a couple of things I had mixed up:

Greases/oils (are they called fatty acid esters in english?) 
(CH2OCOR-CHOCOR«-CH2OCOR) and methanol (CH3OH) form Glicerol and BD 
(3 RCOOR)... right?

Now this reaction needs either an acid or base catalyst (E.g., dry 
H2SO4 or HCl...

HCl? That's how you'll blow yourself away, like Alfred Nobel's 
brother and many many others. This is what it says among all the info 
in journeytoforever:

CAUTION: If you run out of sulfuric acid NEVER try to make up the 
required volume with nitric acid. It may form small quantities of 
nitroG (nitroglycerine) -- even the smallest amount can cause 
horrible accidents. See High Explosives:
http://journeytoforever.org/biodiesel_glycerin.html#nitrog

By the way, I don't think NaOH is a true catalyst in the process. As 
I understand it (?), a catalyst doesn't take part in a process, 
merely facilitating it, and should be recoverable intact once the 
process is complete. You don't get to recover the NaOH (or KOH, nor 
even H2SO4) from transesterification (or esterification), though 
there may be traces in the wash water.

Anyways, just follow the instructions carefully and you'll be right. 
If you use a single-stage process, it pays to take extra care with 
accurate titration, especially with heavily used cooking oils. If you 
do it right you won't get much soap, if any.

With methoxide, I think it's the other way round: the mixing forms 
the compound and produces an exothermic reaction. Anyway, just mix it 
thoroughly (and carefully!!), be accurate with your measures.

Make mini-batches first, with one or two litres, until you get used 
to the process. Observe all the safety precautions.

Best

Keith Addison
Journey to Forever
Handmade Projects
Tokyo
http://journeytoforever.org/

 

OR NaOH) (here is where I get mixed up).. but NaOH would react with 
the greases/oils to form glicerol  soap (3RCOONa)... So I assume 
the Sodium methoxide is a more efficient catalyst because it 
doesen«t form as much soap?

On the other hand, I traditionally thought sodium methoxide 
CH3O(-)Na(+) was synthesised mainly from dry alcohols and metallic 
sodium (difficult to find + expensive + dangerous).

But from what I gather from all the info in journeytoforever, just 
mixing methanol and NaOH (lye) produces an exothermic reaction which 
forms sodium methoxide. ÀIs this the catalyst or a reactant? If it 
is a catalyst, is it the dissociated (is that how you say it?) 
sodium from the CH3ONa that reacts with the fatty esters 
(greases/oils) to form the bothersome soap which is so important to 
get rid of in the washing stages?

I know all this sounds a bit too chemical, but if anyone feels 
comfortable enough to speak in these terms, please enlighten me a 
bit.

Tank you. (+ Happy new year)

Regards,

Christian


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Re: [biofuel] chemistry

2001-12-29 Thread Keith Addison

 Please excuse my chemical terms in english.
 
 I was wondering if you could clear a couple of things I had mixed up:
 
 Greases/oils (are they called fatty acid esters in english?)
 (CH2OCOR-CHOCOR«-CH2OCOR) and methanol (CH3OH) form Glicerol and BD
 (3 RCOOR)... right?
 
 Now this reaction needs either an acid or base catalyst (E.g., dry
 H2SO4 or HCl...

HCl? That's how you'll blow yourself away, like Alfred Nobel's
brother and many many others. This is what it says among all the info
in journeytoforever:

Whoops! Sorry - that's hydrochloric acid not nitric acid. (Need some 
sleep!) Anyway, use sulphuric acid (H2SO4).

Best

Keith Addison
Journey to Forever
Handmade Projects
Tokyo
http://journeytoforever.org/

 

CAUTION: If you run out of sulfuric acid NEVER try to make up the
required volume with nitric acid. It may form small quantities of
nitroG (nitroglycerine) -- even the smallest amount can cause
horrible accidents. See High Explosives:
http://journeytoforever.org/biodiesel_glycerin.html#nitrog

By the way, I don't think NaOH is a true catalyst in the process. As
I understand it (?), a catalyst doesn't take part in a process,
merely facilitating it, and should be recoverable intact once the
process is complete. You don't get to recover the NaOH (or KOH, nor
even H2SO4) from transesterification (or esterification), though
there may be traces in the wash water.

Anyways, just follow the instructions carefully and you'll be right.
If you use a single-stage process, it pays to take extra care with
accurate titration, especially with heavily used cooking oils. If you
do it right you won't get much soap, if any.

With methoxide, I think it's the other way round: the mixing forms
the compound and produces an exothermic reaction. Anyway, just mix it
thoroughly (and carefully!!), be accurate with your measures.

Make mini-batches first, with one or two litres, until you get used
to the process. Observe all the safety precautions.

Best

Keith Addison
Journey to Forever
Handmade Projects
Tokyo
http://journeytoforever.org/



 OR NaOH) (here is where I get mixed up).. but NaOH would react with
 the greases/oils to form glicerol  soap (3RCOONa)... So I assume
 the Sodium methoxide is a more efficient catalyst because it
 doesen«t form as much soap?
 
 On the other hand, I traditionally thought sodium methoxide
 CH3O(-)Na(+) was synthesised mainly from dry alcohols and metallic
 sodium (difficult to find + expensive + dangerous).
 
 But from what I gather from all the info in journeytoforever, just
 mixing methanol and NaOH (lye) produces an exothermic reaction which
 forms sodium methoxide. ÀIs this the catalyst or a reactant? If it
 is a catalyst, is it the dissociated (is that how you say it?)
 sodium from the CH3ONa that reacts with the fatty esters
 (greases/oils) to form the bothersome soap which is so important to
 get rid of in the washing stages?
 
 I know all this sounds a bit too chemical, but if anyone feels
 comfortable enough to speak in these terms, please enlighten me a
 bit.
 
 Tank you. (+ Happy new year)
 
 Regards,
 
 Christian


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Re: [biofuel] chemistry

2001-12-29 Thread Christian

Thanks Keith. Though I must clear out something... I was talking of HCl,
Hydrochloric acid, not Nitric Acid (HNO3), which I do understand is a main
chemical in the synthesis of various explosives (a friend of a close friend
of mine did pass away in a lab explosion some years ago).

The reference to HCl was found in the Morrison  Boyd book on organic
chemistry (I think it`s Prentice, or Mc Graw)

One thing more, somewhere in journeytoforever it said small batches were 
exothermic enough
to maintain the temperature close enough to 55 ¼C. If so, up to what volume
is this true?



Thanks for the advice  concern.

Regards,

Christian


[Non-text portions of this message have been removed]


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[biofuel] chemistry water

2001-12-29 Thread Christian

Dear Bryan,

I got a bit mixed up with the water... ÀWhich reaction produces it?

If this is an equilibrium reaction, Àcan«t you turn it towards the products 
side by adding more meth?

Best,

Christian


[Non-text portions of this message have been removed]


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Re: [biofuel] chemistry

2001-12-29 Thread Keith Addison

Thanks Keith. Though I must clear out something... I was talking of HCl,
Hydrochloric acid, not Nitric Acid (HNO3), which I do understand is a main
chemical in the synthesis of various explosives (a friend of a close friend
of mine did pass away in a lab explosion some years ago).

Yep, sorry, 'twas a bit late in the night - please see correction posted later.

The reference to HCl was found in the Morrison  Boyd book on organic
chemistry (I think it`s Prentice, or Mc Graw)

If you get any positive results with HCl, please let us know.

One thing more, somewhere in journeytoforever it said small batches 
were exothermic enough
to maintain the temperature close enough to 55 ¼C. If so, up to what volume
is this true?

I doubt it - you'll have to find the reference please. The exothermic 
reaction's over by the time the methoxide's properly mixed and you 
add it to the oil, I don't see how it could have any effect on 
maintaining the process temp.

Mike Pelly says this, in discussing Test batches:

Start by mixing up the lye and methanol in a blender (one that will 
never be used for food again). First make sure the blender and all 
utensils used are dry. Forming the exothermal sodium methoxide polar 
molecule will heat up the blender container a bit. Keep mixing until 
all the lye has been dissolved.

He certainly doesn't say it provides enough heat for the 
transesterification process itself. Anyway his test batches are with 
one litre of WVO, the methoxide uses only 150 ml of methanol and 6.25 
g NaOH, not very much heat there. I suggest you read it all again.

http://journeytoforever.org/biodiesel_mike.html
Biodiesel recipe from Mike Pelly

Best wishes

Keith Addison
Journey to Forever
Handmade Projects
Tokyo
http://journeytoforever.org/

 
Thanks for the advice  concern.

Regards,

Christian


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[biofuel] chemistry

2001-12-28 Thread Christian

Please excuse my chemical terms in english.

I was wondering if you could clear a couple of things I had mixed up:

Greases/oils (are they called fatty acid esters in english?) 
(CH2OCOR-CHOCOR«-CH2OCOR) and methanol (CH3OH) form Glicerol and BD (3 
RCOOR)... right?

Now this reaction needs either an acid or base catalyst (E.g., dry H2SO4 or 
HCl... OR NaOH) (here is where I get mixed up).. but NaOH would react with the 
greases/oils to form glicerol  soap (3RCOONa)... So I assume the Sodium 
methoxide is a more efficient catalyst because it doesen«t form as much soap? 

On the other hand, I traditionally thought sodium methoxide CH3O(-)Na(+) was 
synthesised mainly from dry alcohols and metallic sodium (difficult to find + 
expensive + dangerous).

But from what I gather from all the info in journeytoforever, just mixing 
methanol and NaOH (lye) produces an exothermic reaction which forms sodium 
methoxide. ÀIs this the catalyst or a reactant? If it is a catalyst, is it the 
dissociated (is that how you say it?) sodium from the CH3ONa that reacts with 
the fatty esters (greases/oils) to form the bothersome soap which is so 
important to get rid of in the washing stages?

I know all this sounds a bit too chemical, but if anyone feels comfortable 
enough to speak in these terms, please enlighten me a bit.

Tank you. (+ Happy new year)

Regards,

Christian



[Non-text portions of this message have been removed]


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