Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-19 Thread Pieter Koole



There is a safe way of using nitroglycerin, but I 
would say that nitroglycerine is not a toy. Don't play with it and leave the use 
of it to professionals.

Metvriendelijke groet,Pieter KooleOriginal Message - 


  From: 
  r 
  To: Biofuel@sustainablelists.org 
  
  Sent: Sunday, July 17, 2005 10:45 
PM
  Subject: Re: [Biofuel] Burning glycerol 
  for heat / Acrolein
  How about combining the glycerin with nitrogen to create 
  nitroglycerin? I know, nitrogen is explosive but so is hydrogen. 
  The engines in our vehicles are using what is called "explosion 
  propulsion". Exploding fuel pushes against pistons which are 
  linked to a shaft, which is linked to the transmission. There must be a 
  safe way to use nitroglycerin.[EMAIL PROTECTED] wrote: 
  
The chemical kinetics of fire is not understood very well. 
Smoking a cigarette will produce thousands of intermediate radicals, which 
will lead to thousands of end products, many of which are harmful. 
Altering temperature and other variables will lead to different end 
products. So unless you have empirical evidence on a specific 
substance, it's hard to know what is going to happen. I know people do 
burn it as a fuel, but I wouldn't recommend doing it in your kitchen, for 
instance.
R Del Bueno [EMAIL PROTECTED] 
wrote:
Hello 
  all,I am considering the use of my glycerol coproduct as a burner 
  fuel for process heat generation (indirect via boiler).My glycerol 
  generated while running 20% methanol is of very low viscosity (mostly 
  likely due to the excess methanol), and seems quite usable. This may 
  be more advantageous than recover when heating large batches.I 
  have been searching for emissions information on this, as I have heard 
  that toxic acrolein is produced.when glycerin is burnt at temps below 
  1800degF. (I have heard this about WVO/SVO usage as well).My 
  question is how much?...as acrolein is also produced burning gasoline, 
  diesel, and cigarettes.It seems that if the amount of acrolein 
  produced by burning the gylerol waste is LESS than the amount that 
  would be produced by burning the amount of petro diesel that is offset 
  by the biodiesel..then net amount of acrolein is still a reduction, 
  and hence acceptable.Any data out there?Any chemists out there 
  who may be able to calculate an approximation?Molecular formula C3H4O 
  (..that's little 3, little 
  4)-Rob..Info 
  on Acrolein:Acrolein is principally used as a chemical intermediate in 
  the production of acrylic acid and itsesters. Acrolein is used 
  directly as an aquatic herbicide and algicide in irrigation canals, as 
  amicrobiocide in oil wells, liquid hydrocarbon fuels, cooling-water 
  towers and water treatmentponds, and as a slimicide in the 
  manufacture of paper (IARC, 1985). Combustion of fossil 
  fuels,tobacco smoke, and pyrolyzed animal and vegetable fats 
  contribute to the environmentalprevalence of acrolein (IARC, 
  1985). Acrolein is a byproduct of fires and is one of several 
  acutetoxicants which firefighters must endure. It is also formed from 
  atmospheric reactions of 1,3-butadiene. The annual statewide 
  industrial emissions from facilities reporting under the AirToxics 
  Hot Spots Act in California based on the most recent inventory were 
  estimated to be54,565 pounds of acrolein (CARB, 
  2000).CHRONIC TOXICITY SUMMARYACROLEIN (2-propenal, 
  acraldehyde, allyl aldehyde, acryl aldehyde)CAS Registry Number: 
  107-02-8I. Chronic Toxicity SummaryInhalation reference 
  exposure level 0.06 mg/m3 (0.03 ppb)Critical effect(s) Histological 
  changes in nasal epithelium in ratsHazard index target(s) Respiratory 
  system; eyesII. Physical and Chemical Properties (HSDB, 
  1995)Description Colorless or yellow liquid with 
  piercing,disagreeable odorMolecular formula C3H4O (oops..thats 
  litte 3, little 4)Molecular weight 56.1 g/molDensity 0.843 g/cm3 @ 
  20°CBoiling point 53°CMelting point -88°CVapor pressure 220 
  torr @ 20°COdor threshold 160 ppb (370 mg/m3)(Amoore and Hautala, 
  1983)Solubility Soluble in ethanol, diethyl ether, and up to 20% w/v 
  in waterConversion factor 1 ppm = 2.3 mg/m3 @ 25° C 
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RE: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-19 Thread Chris Lloyd








 How about combining the glycerin with nitrogen to
create nitroglycerin? I know, nitrogen is
explosive but so is hydrogen. 



Nitro-glycerine is a high explosive; the shock wave
expands faster than the speed of sound. Not a good idea inside an enclosed
space. Chris.  



Wessex Ferret Club (http://www.wessexferretclub.co.uk) 

 










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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-19 Thread Mike Weaver

Great.  NOW you tell me.

Chris Lloyd wrote:

How about combining the glycerin with nitrogen to create 

nitroglycerin?  I know, nitrogen is explosive but so is hydrogen. 

 

Nitro-glycerine is a high explosive; the shock wave expands faster 
than the speed of sound. Not a good idea inside an enclosed space. 
Chris.  

 


Wessex Ferret Club  (http://www.wessexferretclub.co.uk)

 

 



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RE: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-19 Thread Joe . Guthrie

Nitrogen is not explosive, infact it
is used as a non flamable protective gas where oxidation is to be prevented.


I'm no expert but I think nitroglycerin
is produced by the action of nitric acid on glycerin. This is a very dangerous
experiment to mess with. Really has nothing to do with internal combustion
engines.






Chris Lloyd [EMAIL PROTECTED]
Sent by: [EMAIL PROTECTED]
07/19/2005 07:58 AM
Please respond to Biofuel

To:
   Biofuel@sustainablelists.org
cc:
   
Subject:
   RE: [Biofuel] Burning glycerol for heat
/ Acrolein

 How about combining the glycerin
with nitrogen to create nitroglycerin? I know, nitrogen is explosive
but so is hydrogen. 

Nitro-glycerine is a high explosive;
the shock wave expands faster than the speed of sound. Not a good idea
inside an enclosed space. Chris. 

Wessex Ferret Club (http://www.wessexferretclub.co.uk)





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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-19 Thread Keith Addison

Hi Rob


ok so this thread has drifted quite far from my original inquiry.


Sorry about that.

I was looking for specific, or even close estimates, of the acrolein 
emissions from glycerol burning in an open flame boiler/burner 
unit..not for its use as a motor fuel, or its combination with 
nitrogen.


Depending on the temperature, the thermal degradation of vegetable 
oils is a polymerisation (200-300 °C), a degradation of vegetable 
oils into acrolein, ketene, fatty acids then formation of alcanes, 
alcenes above 300 °C and finally a formation of a gas-liquid mixture 
from around 500 °C up.

-- ACREVO study:
http://www.biomatnet.org/secure/Fair/F484.htm
BioMatNet Item: FAIR-CT95-0627 - Advanced Combustion Research for 
Energy from Vegetable Oils (ACREVO)


Lower temperature of combustion, more acrolein.

It needs higher temps than 500 deg C to burn the by-product anyway. 
you can burn the glycerin portion, and the excess methanol if you 
haven't removed it, but the burner  soon gunks up with black and 
horribly abused but unburnt soap. I haven't managed to get full clean 
combustion at about 700 deg C and it may have been higher than that. 
Michael Allen reckons it needs 1,000 deg C and five seconds' 
residence time, and maybe pre-heating and atomization too I thought. 
We've been finding good solutions for by-product use, and good 
solutions for burners as well, though we haven't given up yet on 
burning the by-product.


How are you planning to burn it?

Best wishes

Keith



-Rob



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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-19 Thread R Del Bueno

Thanks Keith,

Well I have a few thoughts on the burning...

I WAS hoping I could burn it in a Turk style (perhaps scaled up) burner, to 
heat water for various process uses..but I am concerned with the emissions...


Another idea is to offload it to someone already in the pollution business 
(just kidding) I have a customer who burns around 4000gal/wk of waste motor 
oil in a large open flame jet burner. My thought was for him to use my 
by-product blended with his waste oil. This by-product would end up at a 
blend level no higher than 10%glycerol to 90% motor oil, and hence reduce 
his fuel costs by around 10%


The goal of using it as a BTU additive to other biomass in a biomass 
gasifier seems the best end use, but of course, these units are quite 
expensive. In this case the temp of combustion is up around 1800degF..and 
emissions are not much of an issue.


Thanks,
Rob






Depending on the temperature, the thermal degradation of vegetable oils 
is a polymerisation (200-300 °C), a degradation of vegetable oils into 
acrolein, ketene, fatty acids then formation of alcanes, alcenes above 300 
°C and finally a formation of a gas-liquid mixture from around 500 °C up.

-- ACREVO study:
http://www.biomatnet.org/secure/Fair/F484.htm
BioMatNet Item: FAIR-CT95-0627 - Advanced Combustion Research for Energy 
from Vegetable Oils (ACREVO)


Lower temperature of combustion, more acrolein.

It needs higher temps than 500 deg C to burn the by-product anyway. you 
can burn the glycerin portion, and the excess methanol if you haven't 
removed it, but the burner  soon gunks up with black and horribly abused 
but unburnt soap. I haven't managed to get full clean combustion at about 
700 deg C and it may have been higher than that. Michael Allen reckons it 
needs 1,000 deg C and five seconds' residence time, and maybe pre-heating 
and atomization too I thought. We've been finding good solutions for 
by-product use, and good solutions for burners as well, though we haven't 
given up yet on burning the by-product.


How are you planning to burn it?

Best wishes

Keith



-Rob



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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-18 Thread Keith Addison

LOL

all jokes aside, though, that's actually an interesting idea.  if it were
possible to keep the N and glycerine separate, and inject them into 
the cylinder

where they would combine, then explode. . . .

of course, there's the question of how energy efficient this would be (i'm
assuming it would be pretty efficient since nitroglycerine is so extremely
explosive).  and what emissions would be like.  and whether creating 
nitroglycerine

is as easy and simple as that in the first place.


It's easy to create but it's almost impossible to control. I really, 
really hope this discussion is going to remain entirely 
hypothetical!!!



There must be a safe way to use nitroglycerin.


Only in the form of dynamite it seems. Safe as dynamite, LOL!

High-explosives

The most earth-shattering use of glycerine remains that discovered by 
Italian chemist Ascanio Sobrero 150 years ago when he subjected it to 
nitration to make the world's first real high-explosive, 
nitroglycerin, one of the most dangerous substances ever concocted.


Sobrero's face was badly scarred in an explosion during an early 
experiment. He said nitroglycerin was so dangerous it was useless, 
and it had killed so many people he was ashamed to be its discoverer.


But Swedish chemist Alfred Nobel set about mass-producing the stuff, 
in spite of several explosions -- one of which killed his brother. 
Nobel discovered that nitroglycerin could be mixed with silica 
(diatomaceous earth) to form a stable high-explosive which he called 
dynamite. It made him one of the richest men of the age.


Nitroglycerin is extremely powerful. A mere 10 ml will expand 10,000 
times into 100 litres of gas at an explosive velocity of 7,700 metres 
per second (17,224 miles per hour) -- more powerful than TNT.


It's easy to find recipes for nitroglycerin. You mix deadly compounds 
like sulphuric acid and nitric acid with the glycerine and unless you 
can control the following runaway reaction it explodes in your face. 
Most formulas carry warnings like these:


Caution: Nitroglycerin is extremely sensitive to decomposition, 
heating, dropping, or jarring, and may explode even if left 
undisturbed and cool.


Caution: Nitroglycerin has the capacity to sense when a stupid or 
clumsy person is around and, if given a chance, it will try to kill 
him.


Caution: This formula assumes that the maker has no qualms about 
killing his/her self in the process.


These cautions are VERY well-founded!

Every now and then newspapers rediscover these resources on the 
World Wide Web and set up a hue-and-cry for Internet censorship, 
claiming it promotes terrorism, but any terrorist worth his Semtex 
knows better than these amateurish offerings.


Anyway these things have been around much longer than the Internet. 
We found a nitroglycerin recipe in a general how-to book published 
more than a century ago, along with a dozen other explosives, 
including dynamite. Did Civilization-As-We-Know-It survive? It's hard 
to tell!


-- From: Glycerine
http://journeytoforever.org/biodiesel_glycerin.html

Best wishes for a long, safe, happy and intact future.

Keith




-chris

In a message dated 7/17/05 2:46:35 PM, [EMAIL PROTECTED] writes:

 How about combining the glycerin with nitrogen to create nitroglycerin?

I know, nitrogen is explosive but so is hydrogen.  The engines in our

vehicles are using what is called explosion propulsion.  Exploding

fuel  pushes against pistons which are linked to a shaft, which is

linked to the transmission.  There must be a safe way to use nitroglycerin.



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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-18 Thread r
How about using nitrox, as in used in recreational diving?  I suppose 
that there is a need for energy to combine the nitrogen with the 
glycerin, to make the chemical reaction happen. Maybe carry 2 tanks (one 
of glycerin and one of nitrox)?  There might be a pre-combustion chamber 
where a spark would be set to the glycerin/nitrox mixture, to create the 
nitroglycerin, then the nitroglycerin would be sent to the engine to be 
burned.  Would the design be feasible and realistic?


[EMAIL PROTECTED] wrote:


LOL

all jokes aside, though, that's actually an interesting idea.  if it 
were
possible to keep the N and glycerine separate, and inject them into 
the cylinder

where they would combine, then explode. . . .

of course, there's the question of how energy efficient this would be 
(i'm
assuming it would be pretty efficient since nitroglycerine is so 
extremely
explosive).  and what emissions would be like.  and whether creating 
nitroglycerine

is as easy and simple as that in the first place.



It's easy to create but it's almost impossible to control. I really, 
really hope this discussion is going to remain entirely hypothetical!!!



There must be a safe way to use nitroglycerin.



Only in the form of dynamite it seems. Safe as dynamite, LOL!

High-explosives

The most earth-shattering use of glycerine remains that discovered by 
Italian chemist Ascanio Sobrero 150 years ago when he subjected it to 
nitration to make the world's first real high-explosive, 
nitroglycerin, one of the most dangerous substances ever concocted.


Sobrero's face was badly scarred in an explosion during an early 
experiment. He said nitroglycerin was so dangerous it was useless, and 
it had killed so many people he was ashamed to be its discoverer.


But Swedish chemist Alfred Nobel set about mass-producing the stuff, 
in spite of several explosions -- one of which killed his brother. 
Nobel discovered that nitroglycerin could be mixed with silica 
(diatomaceous earth) to form a stable high-explosive which he called 
dynamite. It made him one of the richest men of the age.


Nitroglycerin is extremely powerful. A mere 10 ml will expand 10,000 
times into 100 litres of gas at an explosive velocity of 7,700 metres 
per second (17,224 miles per hour) -- more powerful than TNT.


It's easy to find recipes for nitroglycerin. You mix deadly compounds 
like sulphuric acid and nitric acid with the glycerine and unless you 
can control the following runaway reaction it explodes in your face. 
Most formulas carry warnings like these:


Caution: Nitroglycerin is extremely sensitive to decomposition, 
heating, dropping, or jarring, and may explode even if left 
undisturbed and cool.


Caution: Nitroglycerin has the capacity to sense when a stupid or 
clumsy person is around and, if given a chance, it will try to kill him.


Caution: This formula assumes that the maker has no qualms about 
killing his/her self in the process.


These cautions are VERY well-founded!

Every now and then newspapers rediscover these resources on the 
World Wide Web and set up a hue-and-cry for Internet censorship, 
claiming it promotes terrorism, but any terrorist worth his Semtex 
knows better than these amateurish offerings.


Anyway these things have been around much longer than the Internet. We 
found a nitroglycerin recipe in a general how-to book published more 
than a century ago, along with a dozen other explosives, including 
dynamite. Did Civilization-As-We-Know-It survive? It's hard to tell!


-- From: Glycerine
http://journeytoforever.org/biodiesel_glycerin.html

Best wishes for a long, safe, happy and intact future.

Keith




-chris

In a message dated 7/17/05 2:46:35 PM, [EMAIL PROTECTED] writes:

 How about combining the glycerin with nitrogen to create 
nitroglycerin?


I know, nitrogen is explosive but so is hydrogen.  The engines in our

vehicles are using what is called explosion propulsion.  Exploding

fuel  pushes against pistons which are linked to a shaft, which is

linked to the transmission.  There must be a safe way to use 
nitroglycerin.




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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-18 Thread r

Who knows, I might be right next to you.  ;-)

[EMAIL PROTECTED] wrote:




r wrote:


How about using nitrox,



nope, it won't work.  Nitrox is just a mixture of oxygen and nitrogen 
with more oxygen than a normal atmosphere.  to make nitroglycerin 
(actually easy) one need only combine fuming nitric, fuming sulfuric, 
and glycerin in the correct proportions, while keeping the whole lot 
cool.  Just let me know when you are going to do it so I can several 
miles away.


In reality it is a very, very dangerous process.  As I recall it was 
Alfred Nobels brother who was killed by a nitroglycerin explosion 
which inspired him to invent dynamite (nitroglycerin + sawdust or a 
similar dispersant)



You could use nitromethane (liquid) or nitrous oxide (gas) but that 
doesn't get to the point of using the glycerin.  I am going to try 
taking the glycerin and esterifying it with short chain fatty acids 
such that I come up with a molecule with about the same mol wt as the 
FAMEs.
For example one could make tributyl glycerate and it should have the 
same viscoity and vapor pressure as FAME.  The only problem is that 
the energy content is lower still than FAME which is slightly lower 
than fossil diesel.




 as in used in recreational diving?  I suppose

that there is a need for energy to combine the nitrogen with the 
glycerin, to make the chemical reaction happen. Maybe carry 2 tanks 
(one of glycerin and one of nitrox)?  There might be a pre-combustion 
chamber where a spark would be set to the glycerin/nitrox mixture, to 
create the nitroglycerin, then the nitroglycerin would be sent to the 
engine to be burned.  Would the design be feasible and realistic?






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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-18 Thread capt3d
hi rich.

i'm not a chemist or engineer.  anything beyond the very general and 
hypothetical comments i made previously are beyond me.  this line of inquiry 
raises so 
many questions which i really don't consider myself competent to comment on 
(and therefore didn't).

keith is right about how volatile and dangerous nitro is.  you can't store 
nitro on board and expect to keep it stable.  surely a spontaneous explosion of 
the nitro while still in the reaction chamber would be inevitable.  i think 
more of a binary fuel-type approach would be called for.  thus my suggestion of 
synthesis and combustion in the same chamber (i.e. the cylinder).

and again, i wouldn't know how to guage the feasibility or practicality of 
this.  after all, depending on the engine, we're talking about maintaining 
anywhere from about 10-20 on up to 50-60 reaction/combustion cycles per 
cylinder 
per second under normal operating conditions.

-chris b.


In a message dated 7/18/05 10:04:06 AM, [EMAIL PROTECTED] writes:

 There might be a pre-combustion chamber 

where a spark would be set to the glycerin/nitrox mixture, to create the 

nitroglycerin, then the nitroglycerin would be sent to the engine to be 

burned.  Would the design be feasible and realistic? 


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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-18 Thread R Del Bueno

ok so this thread has drifted quite far from my original inquiry.
I was looking for specific, or even close estimates, of the acrolein 
emissions from glycerol burning in an open flame boiler/burner unit..not 
for its use as a motor fuel, or its combination with nitrogen.



-Rob



At 01:58 PM 7/18/2005, you wrote:

Who knows, I might be right next to you.  ;-)

[EMAIL PROTECTED] wrote:




r wrote:


How about using nitrox,



nope, it won't work.  Nitrox is just a mixture of oxygen and nitrogen 
with more oxygen than a normal atmosphere.  to make nitroglycerin 
(actually easy) one need only combine fuming nitric, fuming sulfuric, and 
glycerin in the correct proportions, while keeping the whole lot 
cool.  Just let me know when you are going to do it so I can several 
miles away.


In reality it is a very, very dangerous process.  As I recall it was 
Alfred Nobels brother who was killed by a nitroglycerin explosion which 
inspired him to invent dynamite (nitroglycerin + sawdust or a similar 
dispersant)



You could use nitromethane (liquid) or nitrous oxide (gas) but that 
doesn't get to the point of using the glycerin.  I am going to try taking 
the glycerin and esterifying it with short chain fatty acids such that I 
come up with a molecule with about the same mol wt as the FAMEs.
For example one could make tributyl glycerate and it should have the same 
viscoity and vapor pressure as FAME.  The only problem is that the energy 
content is lower still than FAME which is slightly lower than fossil diesel.




 as in used in recreational diving?  I suppose

that there is a need for energy to combine the nitrogen with the 
glycerin, to make the chemical reaction happen. Maybe carry 2 tanks (one 
of glycerin and one of nitrox)?  There might be a pre-combustion chamber 
where a spark would be set to the glycerin/nitrox mixture, to create the 
nitroglycerin, then the nitroglycerin would be sent to the engine to be 
burned.  Would the design be feasible and realistic?


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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-18 Thread bob allen



r wrote:

How about using nitrox,


nope, it won't work.  Nitrox is just a mixture of oxygen and nitrogen 
with more oxygen than a normal atmosphere.  to make nitroglycerin 
(actually easy) one need only combine fuming nitric, fuming sulfuric, 
and glycerin in the correct proportions, while keeping the whole lot 
cool.  Just let me know when you are going to do it so I can several 
miles away.


In reality it is a very, very dangerous process.  As I recall it was 
Alfred Nobels brother who was killed by a nitroglycerin explosion which 
inspired him to invent dynamite (nitroglycerin + sawdust or a similar 
dispersant)



You could use nitromethane (liquid) or nitrous oxide (gas) but that 
doesn't get to the point of using the glycerin.  I am going to try 
taking the glycerin and esterifying it with short chain fatty acids such 
that I come up with a molecule with about the same mol wt as the FAMEs.
For example one could make tributyl glycerate and it should have the 
same viscoity and vapor pressure as FAME.  The only problem is that the 
energy content is lower still than FAME which is slightly lower than 
fossil diesel.




 as in used in recreational diving?  I suppose
that there is a need for energy to combine the nitrogen with the 
glycerin, to make the chemical reaction happen. Maybe carry 2 tanks (one 
of glycerin and one of nitrox)?  There might be a pre-combustion chamber 
where a spark would be set to the glycerin/nitrox mixture, to create the 
nitroglycerin, then the nitroglycerin would be sent to the engine to be 
burned.  Would the design be feasible and realistic?




--
Bob Allen
http://ozarker.org/bob

Science is what we have learned about how to keep
from fooling ourselves — Richard Feynman

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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-17 Thread the skapegoat
The chemical kinetics of fire is not understood very well. Smoking a cigarette will produce thousands of intermediate radicals, which will lead to thousands of end products, many of which are harmful. Altering temperature and other variables will lead to different end products. So unless you have empirical evidence on a specific substance, it's hard to know what is going to happen. I know people do burn it as a fuel, but I wouldn't recommend doing it in your kitchen, for instance.
R Del Bueno [EMAIL PROTECTED] wrote:
Hello all,I am considering the use of my glycerol coproduct as a burner fuel for process heat generation (indirect via boiler).My glycerol generated while running 20% methanol is of very low viscosity (mostly likely due to the excess methanol), and seems quite usable. This may be more advantageous than recover when heating large batches.I have been searching for emissions information on this, as I have heard that toxic acrolein is produced.when glycerin is burnt at temps below 1800degF. (I have heard this about WVO/SVO usage as well).My question is how much?...as acrolein is also produced burning gasoline, diesel, and cigarettes.It seems that if the amount of acrolein produced by burning the gylerol waste is LESS than the amount that would be produced by burning the amount of petro diesel that is offset by the biodiesel..then
 net amount of acrolein is still a reduction, and hence acceptable.Any data out there?Any chemists out there who may be able to calculate an approximation?Molecular formula C3H4O (..that's little 3, little 4)-Rob..Info on Acrolein:Acrolein is principally used as a chemical intermediate in the production of acrylic acid and itsesters. Acrolein is used directly as an aquatic herbicide and algicide in irrigation canals, as amicrobiocide in oil wells, liquid hydrocarbon fuels, cooling-water towers and water treatmentponds, and as a slimicide in the manufacture of paper (IARC, 1985). Combustion of fossil fuels,tobacco smoke, and pyrolyzed animal and vegetable fats contribute to the environmentalprevalence of acrolein (IARC, 1985). Acrolein is a byproduct of fires and is one of several acutetoxicants which firefighters must endure. It is also
 formed from atmospheric reactions of 1,3-butadiene. The annual statewide industrial emissions from facilities reporting under the AirToxics Hot Spots Act in California based on the most recent inventory were estimated to be54,565 pounds of acrolein (CARB, 2000).CHRONIC TOXICITY SUMMARYACROLEIN (2-propenal, acraldehyde, allyl aldehyde, acryl aldehyde)CAS Registry Number: 107-02-8I. Chronic Toxicity SummaryInhalation reference exposure level 0.06 mg/m3 (0.03 ppb)Critical effect(s) Histological changes in nasal epithelium in ratsHazard index target(s) Respiratory system; eyesII. Physical and Chemical Properties (HSDB, 1995)Description Colorless or yellow liquid with piercing,disagreeable odorMolecular formula C3H4O (oops..thats litte 3, little 4)Molecular weight 56.1 g/molDensity 0.843 g/cm3 @ 20°CBoiling point 53°CMelting point -88°CVapor pressure 220 torr @ 20°COdor threshold
 160 ppb (370 mg/m3)(Amoore and Hautala, 1983)Solubility Soluble in ethanol, diethyl ether, and up to 20% w/v in waterConversion factor 1 ppm = 2.3 mg/m3 @ 25° C ___Biofuel mailing listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel at Journey to Forever:http://journeytoforever.org/biofuel.htmlSearch the combined Biofuel and Biofuels-biz list archives (50,000 messages):http://www.mail-archive.com/biofuel@sustainablelists.org/Send instant messages to your online friends http://uk.messenger.yahoo.com ___
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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-17 Thread r




How about combining the glycerin with nitrogen to create
nitroglycerin? I know, nitrogen is explosive but so is hydrogen. The
engines in our vehicles are using what is called "explosion
propulsion". Exploding fuel pushes against pistons which are linked
to a shaft, which is linked to the transmission. There must be a safe
way to use nitroglycerin.

[EMAIL PROTECTED] wrote:

  The chemical kinetics of fire is not understood very well.
Smoking a cigarette will produce thousands of intermediate radicals,
which will lead to thousands of end products, many of which are
harmful. Altering temperature and other variables will lead to
different end products. So unless you have empirical evidence on a
specific substance, it's hard to know what is going to happen. I know
people do burn it as a fuel, but I wouldn't recommend doing it in your
kitchen, for instance.
  
  
  R Del Bueno [EMAIL PROTECTED] wrote:
  Hello
all,

I am considering the use of my glycerol coproduct as a burner fuel for 
process heat generation (indirect via boiler).
My glycerol generated while running 20% methanol is of very low
viscosity 
(mostly likely due to the excess methanol), and seems quite usable.
This 
may be more advantageous than recover when heating large batches.

I have been searching for emissions information on this, as I have
heard 
that toxic acrolein is produced.when glycerin is burnt at temps below 
1800degF. (I have heard this about WVO/SVO usage as well).
My question is how much?...as acrolein is also produced burning
gasoline, 
diesel, and cigarettes.
It seems that if the amount of acrolein produced by burning the gylerol

waste is LESS than the amount that would be produced by burning the
amount 
of petro diesel that is offset by the biodiesel..then net amount of 
acrolein is still a reduction, and hence acceptable.

Any data out there?
Any chemists out there who may be able to calculate an approximation?
Molecular formula C3H4O (..that's little 3, little 4)


-Rob


..
Info on Acrolein:
Acrolein is principally used as a chemical intermediate in the
production 
of acrylic acid and its
esters. Acrolein is used directly as an aquatic herbicide and algicide
in 
irrigation canals, as a
microbiocide in oil wells, liquid hydrocarbon fuels, cooling-water
towers 
and water treatment
ponds, and as a slimicide in the manufacture of paper (IARC, 1985). 
Combustion of fossil fuels,
tobacco smoke, and pyrolyzed animal and vegetable fats contribute to
the 
environmental
prevalence of acrolein (IARC, 1985). Acrolein is a byproduct of fires
and 
is one of several acute
toxicants which firefighters must endure. It is also formed from 
atmospheric reactions of 1,3-
butadiene. The annual statewide industrial emissions from facilities 
reporting under the Air
Toxics Hot Spots Act in California based on the most recent inventory
were 
estimated to be
54,565 pounds of acrolein (CARB, 2000).

CHRONIC TOXICITY SUMMARY
ACROLEIN (2-propenal, acraldehyde, allyl aldehyde, acryl aldehyde)
CAS Registry Number: 107-02-8

I. Chronic Toxicity Summary
Inhalation reference exposure level 0.06 mg/m3 (0.03 ppb)
Critical effect(s) Histological changes in nasal epithelium in rats
Hazard index target(s) Respiratory system; eyes

II. Physical and Chemical Properties (HSDB, 1995)
Description Colorless or yellow liquid with piercing,
disagreeable odor

Molecular formula C3H4O (oops..thats litte 3, little 4)
Molecular weight 56.1 g/mol
Density 0.843 g/cm3 @ 20C
Boiling point 53C
Melting point -88C
Vapor pressure 220 torr @ 20C
Odor threshold 160 ppb (370 mg/m3)
(Amoore and Hautala, 1983)
Solubility Soluble in ethanol, diethyl ether, and up to 20% w/v in water
Conversion factor 1 ppm = 2.3 mg/m3 @ 25 C 


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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-17 Thread Ray J
nitrogen is explosive? .. crap. no one lite a match... lol... the 
earths atmosphere is 78.084% nitrogen



Ray J

r wrote:

How about combining the glycerin with nitrogen to create 
nitroglycerin?  I know, nitrogen is explosive but so is hydrogen.  The 
engines in our vehicles are using




 




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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-17 Thread capt3d
LOL

all jokes aside, though, that's actually an interesting idea.  if it were 
possible to keep the N and glycerine separate, and inject them into the 
cylinder 
where they would combine, then explode. . . .

of course, there's the question of how energy efficient this would be (i'm 
assuming it would be pretty efficient since nitroglycerine is so extremely 
explosive).  and what emissions would be like.  and whether creating 
nitroglycerine 
is as easy and simple as that in the first place.

-chris

In a message dated 7/17/05 2:46:35 PM, [EMAIL PROTECTED] writes:

 How about combining the glycerin with nitrogen to create nitroglycerin?  

I know, nitrogen is explosive but so is hydrogen.  The engines in our 

vehicles are using what is called explosion propulsion.  Exploding 

fuel  pushes against pistons which are linked to a shaft, which is 

linked to the transmission.  There must be a safe way to use nitroglycerin.

 

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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-17 Thread Michael Redler

Have the big black helicopters landed in your back yard yet? How 'bout the guys in the black suits?

All you have to do now is type the word Jihad and.

oops!

Mike[EMAIL PROTECTED] wrote:
LOLall jokes aside, though, that's actually an interesting idea. if it were possible to keep the N and glycerine separate, and inject them into the cylinder where they would combine, then explode. . . .of course, there's the question of how energy efficient this would be (i'm assuming it would be pretty efficient since nitroglycerine is so extremely explosive). and what emissions would be like. and whether creating nitroglycerine is as easy and simple as that in the first place.-chrisIn a message dated 7/17/05 2:46:35 PM, [EMAIL PROTECTED] writes: How about combining the glycerin with nitrogen to create nitroglycerin? I know, nitrogen is explosive but so is hydrogen. The engines in our vehicles are using what is called "explosion propulsion". Exploding fuel pushes against pistons which are
 linked to a shaft, which is linked to the transmission. There must be a safe way to use nitroglycerin.___Biofuel mailing listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel at Journey to Forever:http://journeytoforever.org/biofuel.htmlSearch the combined Biofuel and Biofuels-biz list archives (50,000 messages):http://www.mail-archive.com/biofuel@sustainablelists.org/___
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Re: [Biofuel] Burning glycerol for heat / Acrolein

2005-07-17 Thread the skapegoat
it's not.[EMAIL PROTECTED] wrote:
LOLall jokes aside, though, that's actually an interesting idea. if it were possible to keep the N and glycerine separate, and inject them into the cylinder where they would combine, then explode. . . .of course, there's the question of how energy efficient this would be (i'm assuming it would be pretty efficient since nitroglycerine is so extremely explosive). and what emissions would be like. and whether creating nitroglycerine is as easy and simple as that in the first place.-chrisIn a message dated 7/17/05 2:46:35 PM, [EMAIL PROTECTED] writes: How about combining the glycerin with nitrogen to create nitroglycerin? I know, nitrogen is explosive but so is hydrogen. The engines in our vehicles are using what is called "explosion propulsion". Exploding fuel pushes against pistons which are
 linked to a shaft, which is linked to the transmission. There must be a safe way to use nitroglycerin.___Biofuel mailing listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel at Journey to Forever:http://journeytoforever.org/biofuel.htmlSearch the combined Biofuel and Biofuels-biz list archives (50,000 messages):http://www.mail-archive.com/biofuel@sustainablelists.org/Send instant messages to your online friends http://uk.messenger.yahoo.com ___
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