Re: [Biofuel] two stage proccess... doubts

2005-12-19 Thread Joe Street




Hi Vakin;



Thanks for your input. When you say 200 ml RO do you mean you wash a 1
liter test batch with 200 ml of reverse osmosis water?
BTW 95 deg. C is pretty warm it may dry the fuel quicker but there are
some notes on J2F that indicate biodiesel can oxidize. It may be
accelerated at that temperature unless you use CO2 or N2 blanket to
keep air away. Also it takes more energy to heat the fuel that much.
Just a thought.

Also I heard one can use an automotive air conditioner compressor as a
vacuum pump. Don't know what level of vacuum it can produce but it is
worth a try if the price is right.

Joe

Vaklin Hristov wrote:

  Hi!

Some time before (I mean early '80) many automotive enthusiast add a 
water injector to their carburetors. Bit better mileage with the same power.

Return line for diesel engines has a enough quantity of fuel to do 
"stir washing" of your BD. Important is to not get fresh water into 
the pump! This can be done with some modernization of your fuel tank.


BTW my test batches (200 ml RO)  with NaOH as catalyst every time 
looks bit "waterized" after third stir wash and this stay at least 
three days. Maybe more but I have gave the batch for physical 
analysis. With KOH water goes out more rapidly. In both processes 
esterification is 92-93%. In monday I'll know how much water has in 
the batch after third wash and after 95 degrees Celsius for one hour. 
Will inform about results, but I think the quantity will be in ppm's.



At 23:13 17.12.05, you wrote:
  
  
 Just an addition:
 In my early batches I was so curious how the BD will
affect the engine I did that test-after the third wash
the fuel was something like Fanta orange,with lot of
water dispersed within,but I pour it in the tank.My
Renault 11 was just fine.Then I heated the BD to
dewater it and what I found?The MPG raised and some
loss of power appeared(5-8%).The same BD with water
was better fuel than without water.The mean problem is
that the water does not stays dispersed!I recall in
the early `80 there was a Russian invention how to mix
gasoline with water by means of
piezo-quartz(ultrasonic frequency)submerged in the
tank,but all I can remember is only the idea!Nowadays
I read somewhere someone was trying to rich the same
effect by azeothrop agents.

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Bulgaria
Phone: +359887000332
FAX: +35997382758 


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Re: [Biofuel] two stage proccess... doubts

2005-12-19 Thread Vaklin Hristov


Hi
At 16:48 19.12.2005 'ã.', you wrote:
Hi Vakin;

Thanks for your input. When you say 200 ml RO do you mean you wash
a 1 liter test batch with 200 ml of reverse osmosis
water?
No. I mean 200 ml methil ester washed with 56 ml pure water. After
heating for couple of minutes up to 55 deg. C it looks just
fine.
BTW 95 deg. C is pretty warm it
may dry the fuel quicker but there are some notes on J2F that indicate
biodiesel can oxidize. 
This is only to test quantity of water inside the BD. Really I noticed
well done drying is possible with 55-60 deg C (the same temperature used
by me for the main process.
It may be accelerated at
that temperature unless you use CO2 or N2 blanket to keep air away.
Also it takes more energy to heat the fuel that much. Just a
thought.

Also I heard one can use an automotive air conditioner compressor as a
vacuum pump. Don't know what level of vacuum it can produce but it
is worth a try if the price is right.

These pumps are not expensive in the US, but here they are about $500.
Oil inside the pump is extremely water sensitive. 15 or 25 micron of
vacuum isn't necessary for this job. Better is to use simple vacuum pump
for old dentist chair for example. Or few years before (now I don't know)
was wide available in eBay vacuum pumps motorized by compressed
air.
Joe
Vaklin Hristov wrote:

Hi!

Some time before (I mean early '80) many automotive enthusiast add a 
water injector to their carburetors. Bit better mileage with the same
power.

Return line for diesel engines has a enough quantity of fuel to do 
stir washing of your BD. Important is to not get fresh water
into 
the pump! This can be done with some modernization of your fuel tank.


BTW my test batches (200 ml RO) with NaOH as catalyst every time 
looks bit waterized after third stir wash and this stay at
least 
three days. Maybe more but I have gave the batch for physical 
analysis. With KOH water goes out more rapidly. In both processes 
esterification is 92-93%. In monday I'll know how much water has in 
the batch after third wash and after 95 degrees Celsius for one hour. 
Will inform about results, but I think the quantity will be in ppm's.



At 23:13 17.12.05, you wrote:



Just an addition:
In my early batches I was so curious how the BD will
affect the engine I did that test-after the third wash
the fuel was something like Fanta orange,with lot of
water dispersed within,but I pour it in the tank.My
Renault 11 was just fine.Then I heated the BD to
dewater it and what I found?The MPG raised and some
loss of power appeared(5-8%).The same BD with water
was better fuel than without water.The mean problem is
that the water does not stays dispersed!I recall in
the early `80 there was a Russian invention how to mix
gasoline with water by means of
piezo-quartz(ultrasonic frequency)submerged in the
tank,but all I can remember is only the idea!Nowadays
I read somewhere someone was trying to rich the same
effect by azeothrop agents.

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CAR DIAGNOSE Ltd.
P.O. Box 79
3320 Kozloduy
Bulgaria
Phone: +359887000332
FAX: +35997382758 


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19.12.2005 ã.

Vaklin Hristov
CAR DIAGNOSE Ltd.
P.O. Box 79
3320 Kozloduy
Bulgaria



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Re: [Biofuel] two stage proccess... doubts

2005-12-19 Thread fresheggs141
a/c compressors or refrigerator compressors will produce enough vacuum but they 
are also designed to allow thier crankase oil to circulate through the system. 
if it is not captured and returned they don't run for very long
 -- Original message --
From: Joe Street [EMAIL PROTECTED]
 Hi Vakin;
 
 
 
 Thanks for your input.  When you say 200 ml RO do you mean you wash a 1 
 liter test batch with 200 ml of reverse osmosis water?
 BTW 95 deg. C is pretty warm it may dry the fuel quicker but there are 
 some notes on J2F that indicate biodiesel can oxidize.  It may be 
 accelerated at that temperature unless you use CO2 or N2 blanket to keep 
 air away.  Also it takes more energy to heat the fuel that much.  Just a 
 thought.
  
 Also I heard one can use an automotive air conditioner compressor as a 
 vacuum pump.  Don't know what level of vacuum it can produce but it is 
 worth a try if the price is right.
 
 Joe
 
 Vaklin Hristov wrote:
 
 Hi!
 
 Some time before (I mean early '80) many automotive enthusiast add a 
 water injector to their carburetors. Bit better mileage with the same power.
 
 Return line for diesel engines has a enough quantity of fuel to do 
 stir washing of your BD. Important is to not get fresh water into 
 the pump! This can be done with some modernization of your fuel tank.
 
 
 BTW my test batches (200 ml RO)  with NaOH as catalyst every time 
 looks bit waterized after third stir wash and this stay at least 
 three days. Maybe more but I have gave the batch for physical 
 analysis. With KOH water goes out more rapidly. In both processes 
 esterification is 92-93%. In monday I'll know how much water has in 
 the batch after third wash and after 95 degrees Celsius for one hour. 
 Will inform about results, but I think the quantity will be in ppm's.
 
 
 
 At 23:13 17.12.05, you wrote:
   
 
  Just an addition:
  In my early batches I was so curious how the BD will
 affect the engine I did that test-after the third wash
 the fuel was something like Fanta orange,with lot of
 water dispersed within,but I pour it in the tank.My
 Renault 11 was just fine.Then I heated the BD to
 dewater it and what I found?The MPG raised and some
 loss of power appeared(5-8%).The same BD with water
 was better fuel than without water.The mean problem is
 that the water does not stays dispersed!I recall in
 the early `80 there was a Russian invention how to mix
 gasoline with water by means of
 piezo-quartz(ultrasonic frequency)submerged in the
 tank,but all I can remember is only the idea!Nowadays
 I read somewhere someone was trying to rich the same
 effect by azeothrop agents.
 
 __
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 Tired of spam?  Yahoo! Mail has the best spam protection around
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 messages):
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 --
 No virus found in this incoming message.
 Checked by AVG Free Edition.
 Version: 7.1.371 / Virus Database: 267.14.1/206 - Release Date: 16.Dec.05
 
 
 
 
 CAR DIAGNOSE Ltd.
 P.O. Box 79
 3320 Kozloduy
 Bulgaria
 Phone: +359887000332
 FAX: +35997382758 
 
 
 ___
 Biofuel mailing list
 Biofuel@sustainablelists.org
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 Search the combined Biofuel and Biofuels-biz list archives (50,000 messages):
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---BeginMessage---




Hi Vakin;



Thanks for your input. When you say 200 ml RO do you mean you wash a 1
liter test batch with 200 ml of reverse osmosis water?
BTW 95 deg. C is pretty warm it may dry the fuel quicker but there are
some notes on J2F that indicate biodiesel can oxidize. It may be
accelerated at that temperature unless you use CO2 or N2 blanket to
keep air away. Also it takes more energy to heat the fuel that much.
Just a thought.

Also I heard one can use an automotive air conditioner compressor as a
vacuum pump. Don't know what level of vacuum it can produce but it is
worth a try if the price is right.

Joe

Vaklin Hristov wrote:

  Hi!

Some time before (I mean early '80) many automotive enthusiast add a 
water injector to their carburetors. Bit better mileage with the same power.

Return line for diesel engines has a enough quantity of fuel to do 
"stir washing" of your BD. Important is to not get fresh water into 
the pump! This can be done with some modernization of your fuel tank.


BTW my test batches (200 ml RO)  with NaOH as catalyst every time 
looks bit "waterized" 

Re: [Biofuel] two stage proccess... doubts

2005-12-19 Thread Vaklin Hristov


Again here main problem is water. Compressors for R134a are lubricated
with ester oil and the ester oil loses lubricant feature very shortly in
high humidity. As Rumen said, the best way is vacuum pump from any diesel
engine.
At 04:13 20.12.05, you wrote:
a/c compressors or refrigerator
compressors will produce enough vacuum but they are also designed to
allow thier crankase oil to circulate through the system. if it is not
captured and returned they don't run for very long
-- Original message --
From: Joe Street [EMAIL PROTECTED]
 Hi Vakin;
 
 
 
 Thanks for your input. When you say 200 ml RO do you mean you
wash a 1 
 liter test batch with 200 ml of reverse osmosis water?
 BTW 95 deg. C is pretty warm it may dry the fuel quicker but there
are 
 some notes on J2F that indicate biodiesel can oxidize. It may
be 
 accelerated at that temperature unless you use CO2 or N2 blanket to
keep 
 air away. Also it takes more energy to heat the fuel that
much. Just a 
 thought.
 
 Also I heard one can use an automotive air conditioner compressor as
a 
 vacuum pump. Don't know what level of vacuum it can produce
but it is 
 worth a try if the price is right.
 
 Joe
 
 Vaklin Hristov wrote:
 
 Hi!
 
 Some time before (I mean early '80) many automotive enthusiast
add a 
 water injector to their carburetors. Bit better mileage with the
same power.
 
 Return line for diesel engines has a enough quantity of fuel to
do 
 stir washing of your BD. Important is to not get
fresh water into 
 the pump! This can be done with some modernization of your fuel
tank.
 
 
 BTW my test batches (200 ml RO) with NaOH as catalyst
every time 
 looks bit waterized after third stir wash and this
stay at least 
 three days. Maybe more but I have gave the batch for physical

 analysis. With KOH water goes out more rapidly. In both
processes 
 esterification is 92-93%. In monday I'll know how much water has
in 
 the batch after third wash and after 95 degrees Celsius for one
hour. 
 Will inform about results, but I think the quantity will be in
ppm's.
 
 
 
 At 23:13 17.12.05, you wrote:
  
 
  Just an addition:
  In my early batches I was so curious how the BD will
 affect the engine I did that test-after the third wash
 the fuel was something like Fanta orange,with lot of
 water dispersed within,but I pour it in the tank.My
 Renault 11 was just fine.Then I heated the BD to
 dewater it and what I found?The MPG raised and some
 loss of power appeared(5-8%).The same BD with water
 was better fuel than without water.The mean problem is
 that the water does not stays dispersed!I recall in
 the early `80 there was a Russian invention how to mix
 gasoline with water by means of
 piezo-quartz(ultrasonic frequency)submerged in the
 tank,but all I can remember is only the idea!Nowadays
 I read somewhere someone was trying to rich the same
 effect by azeothrop agents.
 
 __
 Do You Yahoo!?
 Tired of spam? Yahoo! Mail has the best spam
protection around


http://mail.yahoo.com
 
 ___
 Biofuel mailing list
 Biofuel@sustainablelists.org


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(50,000 messages):


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 --
 No virus found in this incoming message.
 Checked by AVG Free Edition.
 Version: 7.1.371 / Virus Database: 267.14.1/206 - Release
Date: 16.Dec.05
  
 
 
 
 CAR DIAGNOSE Ltd.
 P.O. Box 79
 3320 Kozloduy
 Bulgaria
 Phone: +359887000332
 FAX: +35997382758 
 
 
 ___
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(50,000 messages):


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From: Joe Street [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] two stage proccess... doubts
Date: Mon, 19 Dec 2005 14:49:09 +
Content-Type: Multipart/mixed;
boundary=NextPart_Webmail_9m3u9jl4l_25556_1135044792_1
Hi Vakin;

Thanks for your input. When you say 200 ml RO do you mean you wash
a 1 liter test batch with 200 ml of reverse osmosis water?
BTW 95 deg. C is pretty warm it may dry the fuel quicker but there are
some notes on J2F that indicate biodiesel can oxidize. It may be
accelerated at that temperature unless you use CO2 or N2 blanket to keep
air away. Also it takes more energy to heat the fuel that
much. Just a thought.

Also I heard one can use an automotive air conditioner compressor as a
vacuum pump. Don't know what level of vacuum it can produce but it
is worth a try if the price is right.
Joe
Vaklin

Re: [Biofuel] two stage proccess... doubts

2005-12-17 Thread Keith Addison
Hello Mike, Joe and all

Along the lines of  testing or thinking outside the box I've been up to
5 things which may be on interest:
1.  Titrating - I've taken to using titrating more as a starting point
these days - now I usually make 6 - 8 mini batches
and just look to see which gives the best yield.  I am putting together
a more formal system.  8 small batches of MoX and then into
8 mini Dr Pepper method small bottles.
Since this I haven't had any
strange results.  This is not to say I didn't have a lot of failures -
plenty of glop,
weird seperations and so on.  Most were useful in that I learned what
not to do.
2.  Been tinkering with Silica beads to absorb any left over water.
Work well in practice but haven't scaled it up yet.
3.  (This not new) - been heating the final product - I have an odd
collection of home-built processors - one has a sealed glass lid so I
can watch what goes on.
Interesting thing seems to be that even with settled washed BD sometimes
I see a little residue at the end of the heating process which seems to
be water.  Not a constant phenomenon.  I would have to do more research
before I would say that the heat releases water?  Could well be a fluke.

When you heat it and cool it some of any water content drops out at 
the bottom and some evaporates, so use vented containers for cooling. 
Probably it'll just reabsorb some of what it just lost from the air 
but maybe it doesn't matter, diesel fuel-water emulsions have good 
emissions results, any dissolved water in biodiesel might do the 
same, if it stays dissolved.

4.  Will and have been tinkering with using ISA w/ Methanol.  I don't
think this will prove too useful to anyone except me, as I have 55
gallons of the stuff on hand.
Someone did email me curious about whether it improved the cold weather
behavior of the BD.  He suggested a freezer test.  The only real value I
see here is if there is any improvement of the final product.

It does allegedly have much better cold-weather properties and quite 
a few people have tried it, but without any success. Maybe a mix 
might work, it would be interesting to know. Pure isopropanol 
biodiesel apparently needs an enzyme process, I just posted a patent 
on it in the BioButanol thread. One list member did try enzymes, but 
it was the wrong enzyme and they couldn't get hold of the right one.

5.  As most listers know, I have been struggling off and on with using
BD to power the whole process. I have a 10 gallon stainless reactor
which I want to heat with a PetroMax stove.  My current workshop it
unheated so I have been not at this recently.  It's been very cold for
this part of the country.

The Ballad of the Cold Shed, I know it well... Our workshop's below 
freezing all the time now. There's a kero space heater there but it's 
not the equal of the shed's really good ventilation. (Very old shed.)

I am sure some of the above has been covered.  If anything proves useful
or interesting I will write it up and post it.

Please do!

-Mike

Joe Street wrote:

 Good points there Todd;
 
 I would like to add though that it is really informative to those of us
 on the list with less experience when we read posts such as these and
 though information may be somewhat anecdotal or even if somewhat
 scientific if it is less than rigorous it may still be of use if it is
 taken as such.  If we do have time we should investigate these
 questions.  For instance recently I posted a question similar to this
 asking the membership for a feeling on how much water content can be
 lived with in oil at the starting point.  I know I had at least one cc
 of water in my last batch of 25 liters which equals at least 40 ppm
 water content.  The batch still washed very easily and passes the water
 and methanol tests.

It's a hard question to give a straight answer to, too many variables 
and nobody does exactly the same thing. So everyone (including me) 
says No water, but as you discovered it's not strictly true. It's 
good advice just the same, especially for novices, no need for 
variables you can quite easily get rid of. Once you've got all the 
other factors in your processing stable then it makes sense. The 
higher the FFA level of the oil the more water it's likely to 
contain, the more difficult it will be to remove the water, and the 
less tolerant of water the process will be, and vice versa. So at 
below what FFA level will the process (whichever process) tolerate 
how much water? I think KOH is more water-tolerant than NaOH, but I 
haven't done any tests.

There's often some water in our oil, though it's very little, and I 
take no notice of it, with the same results as you - easy washing and 
it passes all the tests, including lab tests. But we don't use a 
standard process so giving a measure probably wouldn't help much even 
if I had one.

I have not reprocessed it but I will have NMR
 results for it in time.  It would be good to know just where the limits
 are with this.  Also how much glycerine will 

Re: [Biofuel] two stage proccess... doubts

2005-12-17 Thread Joe Street
Kewl!  A form of water injection.  Well I think the water will not be 
good for the injection pump.  If only it was machined from stainless 
steel it would be ok I think.  Keeping the fuel and water emulsified 
would be a bit of a trick, and in cold weather.uh oh.

Joe

Rumen Slavov wrote:

 Just an addition:
 In my early batches I was so curious how the BD will
affect the engine I did that test-after the third wash
the fuel was something like Fanta orange,with lot of
water dispersed within,but I pour it in the tank.My
Renault 11 was just fine.Then I heated the BD to
dewater it and what I found?The MPG raised and some
loss of power appeared(5-8%).The same BD with water
was better fuel than without water.The mean problem is
that the water does not stays dispersed!I recall in
the early `80 there was a Russian invention how to mix
gasoline with water by means of
piezo-quartz(ultrasonic frequency)submerged in the
tank,but all I can remember is only the idea!Nowadays
I read somewhere someone was trying to rich the same
effect by azeothrop agents.


  



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Re: [Biofuel] two stage proccess... doubts

2005-12-17 Thread Vaklin Hristov
Hi!

Some time before (I mean early '80) many automotive enthusiast add a 
water injector to their carburetors. Bit better mileage with the same power.

Return line for diesel engines has a enough quantity of fuel to do 
stir washing of your BD. Important is to not get fresh water into 
the pump! This can be done with some modernization of your fuel tank.


BTW my test batches (200 ml RO)  with NaOH as catalyst every time 
looks bit waterized after third stir wash and this stay at least 
three days. Maybe more but I have gave the batch for physical 
analysis. With KOH water goes out more rapidly. In both processes 
esterification is 92-93%. In monday I'll know how much water has in 
the batch after third wash and after 95 degrees Celsius for one hour. 
Will inform about results, but I think the quantity will be in ppm's.



At 23:13 17.12.05, you wrote:
  Just an addition:
  In my early batches I was so curious how the BD will
affect the engine I did that test-after the third wash
the fuel was something like Fanta orange,with lot of
water dispersed within,but I pour it in the tank.My
Renault 11 was just fine.Then I heated the BD to
dewater it and what I found?The MPG raised and some
loss of power appeared(5-8%).The same BD with water
was better fuel than without water.The mean problem is
that the water does not stays dispersed!I recall in
the early `80 there was a Russian invention how to mix
gasoline with water by means of
piezo-quartz(ultrasonic frequency)submerged in the
tank,but all I can remember is only the idea!Nowadays
I read somewhere someone was trying to rich the same
effect by azeothrop agents.

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3320 Kozloduy
Bulgaria
Phone: +359887000332
FAX: +35997382758 


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Re: [Biofuel] two stage proccess... doubts

2005-12-15 Thread Robert Carr
Teoman,
Sounds like suspended water particles in your BD. I get this all the time,
especially with more aggressive washing techniques.
Leave your BD to stand for a week or so, or warm it up a little, and the
water should settle out leaving you with clear BD again. If you have tried
re-processing without any more glycerin dropping out, but are still doubtful
of the quality, try some of the other JtF recommended quality tests, such as
dissolving a sample in pure methanol. If you get a portion that does not
dissolve, you may still have unprocessed oil in your batch.
Hope this helps.
Reg'ds
Bob
 - Original Message -
From: Teoman Naskali [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, December 15, 2005 2:28 AM
Subject: Re: [Biofuel] two stage proccess... doubts


 I let some of my BD settle for about 2 months (indoors, 22 degrees
 celcius) and by the time I got to the washing stage I noticed that it
 was rather clear with some white sediment at the bottom. And when I
 washed It I did not observe much soap formation. And the separation was
 almost immediate like I was mixing vegetable oil and water.

 Now after two days the water still looks fairly clear. The bd is
 slightly cloudy.

 First I worried that I hadnt completed the process and that what I was
 washing was more vegetable oil rather thatn Bd, but reprocessing it
 didn't give any glycerine.



 Is there any error here?


 Thanks for any advice
 Teoman

 -Original Message-
 From: [EMAIL PROTECTED]
 [mailto:[EMAIL PROTECTED] On Behalf Of Appal Energy
 Sent: Wednesday, December 14, 2005 3:01 PM
 To: Biofuel@sustainablelists.org
 Subject: Re: [Biofuel] two stage proccess... doubts

 ReZn0r,

 Settling time is simply letting gravity do the separation work for
 you, rather than enlisting equipment such as centrifuges. The more
 glycerol/soap that is extracted by settling the less impediment to the
 subsequent step, whether it be stage two or washing.

 Todd Swearingen

 Hi
  We are making BD with a homemade reactor (80 liters). We have
 used de single stage and de two stage (base-base) methods succesfuly,
 but we still having many doubts :)
 
  In the two stages method described in journeytoforever, the mix
 settle around 12 h between first and second stage before extract the
 glycerine. It?s necessary to settle so many time? It?s bad if any
 glycerine is not decanted and is mixed in the second stage? Is there any
 trick to avoid to wait 12 h between first and second stage?
 
 Many thx in advance and sorry for my bad english
 
 
 


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Re: [Biofuel] two stage proccess... doubts

2005-12-15 Thread Joe Street
Good points there Todd;

I would like to add though that it is really informative to those of us 
on the list with less experience when we read posts such as these and 
though information may be somewhat anecdotal or even if somewhat 
scientific if it is less than rigorous it may still be of use if it is 
taken as such.  If we do have time we should investigate these 
questions.  For instance recently I posted a question similar to this 
asking the membership for a feeling on how much water content can be 
lived with in oil at the starting point.  I know I had at least one cc 
of water in my last batch of 25 liters which equals at least 40 ppm 
water content.  The batch still washed very easily and passes the water 
and methanol tests.  I have not reprocessed it but I will have NMR 
results for it in time.  It would be good to know just where the limits 
are with this.  Also how much glycerine will poison the wash.  I'm sure 
some people have a better feel for this than others even if it may not 
be completely scientific.
There have been a few brave souls on here who have talked about their 
failures but not many since I've been here (about a year now I guess).  
Human nature I guess but if anyone does have some experience that sheds 
light on some of these questions please share.
Personally I am trying to find out how much I can shorten settling times 
also.  I think time can be saved especially in the early washes by 
reducing settling times for one example but I only learn a little bit 
with each batch and there are a lot of things I want to investigate.  
Does it make sense for us to organize some type of 'controlled' testing 
amongst a group of us who have a stable reliable process? I can only 
change one variable at a time but if I can get 10 people to do the same, 
with different variables or differing amounts of the same variable it 
will reduce the learning curve considerably. Is anyone else interested 
or willing to put effort into the idea?

Joe

Appal Energy wrote:

Snip

ReZn0r,
All this is done in microscopic amounts and may not amount to any 
discernible difference between samples that have settled twelve hours or 
samples that have settled six. There is really only one way to determine 
whether or not there is any significant difference between the two end 
results. That would be to conduct the testing.

On a firsthand note, as we don't use two-stage base processing, opting 
instead for acid/base processing. As a result, we're not exactly in a 
position to inform you definitively one way or the other. It's also 
rather doubtful that very many people are in such a position, if only 
for the reason that it would take some rather controlled experimentation 
and the majority probably don't have the time or facilities to conduct 
such testing.

On the other hand, it shouldn't be too terribly difficult to conduct 
some basic/crude testing at your own leisure to see if you can discern 
any noticeable difference.

A fair guess is that you wouldn't notice much, if any. Perhaps what 
another question might be is Do you really have need of expediting a 
process? If so, such as in an industrial/commercial environment, 
testing might hold more validity for you than other bears of average brain.

Todd Swearingen
  

  



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Re: [Biofuel] two stage proccess... doubts

2005-12-15 Thread Mike Weaver
Along the lines of  testing or thinking outside the box I've been up to 
5 things which may be on interest:
1.  Titrating - I've taken to using titrating more as a starting point 
these days - now I usually make 6 - 8 mini batches
and just look to see which gives the best yield.  I am putting together 
a more formal system.  8 small batches of MoX and then into
8 mini Dr Pepper method small bottles.  Since this I haven't had any 
strange results.  This is not to say I didn't have a lot of failures - 
plenty of glop,
weird seperations and so on.  Most were useful in that I learned what 
not to do.
2.  Been tinkering with Silica beads to absorb any left over water.  
Work well in practice but haven't scaled it up yet.
3.  (This not new) - been heating the final product - I have an odd 
collection of home-built processors - one has a sealed glass lid so I 
can watch what goes on.
Interesting thing seems to be that even with settled washed BD sometimes 
I see a little residue at the end of the heating process which seems to 
be water.  Not a constant phenomenon.  I would have to do more research 
before I would say that the heat releases water?  Could well be a fluke.
4.  Will and have been tinkering with using ISA w/ Methanol.  I don't 
think this will prove too useful to anyone except me, as I have 55 
gallons of the stuff on hand.
Someone did email me curious about whether it improved the cold weather 
behavior of the BD.  He suggested a freezer test.  The only real value I 
see here is if there is any improvement of the final product.
5.  As most listers know, I have been struggling off and on with using 
BD to power the whole process. I have a 10 gallon stainless reactor 
which I want to heat with a PetroMax stove.  My current workshop it 
unheated so I have been not at this recently.  It's been very cold for 
this part of the country.

I am sure some of the above has been covered.  If anything proves useful 
or interesting I will write it up and post it.

-Mike

Joe Street wrote:

Good points there Todd;

I would like to add though that it is really informative to those of us 
on the list with less experience when we read posts such as these and 
though information may be somewhat anecdotal or even if somewhat 
scientific if it is less than rigorous it may still be of use if it is 
taken as such.  If we do have time we should investigate these 
questions.  For instance recently I posted a question similar to this 
asking the membership for a feeling on how much water content can be 
lived with in oil at the starting point.  I know I had at least one cc 
of water in my last batch of 25 liters which equals at least 40 ppm 
water content.  The batch still washed very easily and passes the water 
and methanol tests.  I have not reprocessed it but I will have NMR 
results for it in time.  It would be good to know just where the limits 
are with this.  Also how much glycerine will poison the wash.  I'm sure 
some people have a better feel for this than others even if it may not 
be completely scientific.
There have been a few brave souls on here who have talked about their 
failures but not many since I've been here (about a year now I guess).  
Human nature I guess but if anyone does have some experience that sheds 
light on some of these questions please share.
Personally I am trying to find out how much I can shorten settling times 
also.  I think time can be saved especially in the early washes by 
reducing settling times for one example but I only learn a little bit 
with each batch and there are a lot of things I want to investigate.  
Does it make sense for us to organize some type of 'controlled' testing 
amongst a group of us who have a stable reliable process? I can only 
change one variable at a time but if I can get 10 people to do the same, 
with different variables or differing amounts of the same variable it 
will reduce the learning curve considerably. Is anyone else interested 
or willing to put effort into the idea?

Joe

Appal Energy wrote:

Snip

  

ReZn0r,
All this is done in microscopic amounts and may not amount to any 
discernible difference between samples that have settled twelve hours or 
samples that have settled six. There is really only one way to determine 
whether or not there is any significant difference between the two end 
results. That would be to conduct the testing.

On a firsthand note, as we don't use two-stage base processing, opting 
instead for acid/base processing. As a result, we're not exactly in a 
position to inform you definitively one way or the other. It's also 
rather doubtful that very many people are in such a position, if only 
for the reason that it would take some rather controlled experimentation 
and the majority probably don't have the time or facilities to conduct 
such testing.

On the other hand, it shouldn't be too terribly difficult to conduct 
some basic/crude testing at your own leisure to see if you can discern 
any noticeable difference.


Re: [Biofuel] two stage proccess... doubts

2005-12-15 Thread Joe Street
I would concur with you on point number three.  Right from my first test 
batch with 1 liter of new oil I noticed that the BD at the end of 
washing is cloudy and I heated it with a stainless immersion (rod) 
heater (in a 2 liter flask) and little drops of water would form at the 
heater and drop out.  Now I do everything in the reactor and after the 
last wash I heat the whole thing again to 50 degrees C and some liquid 
water can be drained out.  Then I evacuate the reactor until I get to 
28 Hg and the BD comes out crystal clear and ready for use. It remains 
clear upon cooling. What I find in the liquid trap, ahead of my vacuum 
pump, appears to be water. I haven't tasted it ;-)

Pics of my stuff are here:

http://www.nonprofitfuel.ca/Reactor.html

Joe

Mike Weaver wrote:

Along the lines of  testing or thinking outside the box I've been up to 
5 things which may be on interest:
1.  Titrating - I've taken to using titrating more as a starting point 
these days - now I usually make 6 - 8 mini batches
and just look to see which gives the best yield.  I am putting together 
a more formal system.  8 small batches of MoX and then into
8 mini Dr Pepper method small bottles.  Since this I haven't had any 
strange results.  This is not to say I didn't have a lot of failures - 
plenty of glop,
weird seperations and so on.  Most were useful in that I learned what 
not to do.
2.  Been tinkering with Silica beads to absorb any left over water.  
Work well in practice but haven't scaled it up yet.
3.  (This not new) - been heating the final product - I have an odd 
collection of home-built processors - one has a sealed glass lid so I 
can watch what goes on.
Interesting thing seems to be that even with settled washed BD sometimes 
I see a little residue at the end of the heating process which seems to 
be water.  Not a constant phenomenon.  I would have to do more research 
before I would say that the heat releases water?  Could well be a fluke.
4.  Will and have been tinkering with using ISA w/ Methanol.  I don't 
think this will prove too useful to anyone except me, as I have 55 
gallons of the stuff on hand.
Someone did email me curious about whether it improved the cold weather 
behavior of the BD.  He suggested a freezer test.  The only real value I 
see here is if there is any improvement of the final product.
5.  As most listers know, I have been struggling off and on with using 
BD to power the whole process. I have a 10 gallon stainless reactor 
which I want to heat with a PetroMax stove.  My current workshop it 
unheated so I have been not at this recently.  It's been very cold for 
this part of the country.

I am sure some of the above has been covered.  If anything proves useful 
or interesting I will write it up and post it.

-Mike
  

  



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Re: [Biofuel] two stage proccess... doubts

2005-12-14 Thread Appal Energy
ReZn0r,

Settling time is simply letting gravity do the separation work for 
you, rather than enlisting equipment such as centrifuges. The more 
glycerol/soap that is extracted by settling the less impediment to the 
subsequent step, whether it be stage two or washing.

Todd Swearingen

Hi
   We are making BD with a homemade reactor (80 liters). We have used de 
 single stage and de two stage (base-base) methods succesfuly, but we still 
 having many doubts :)

   In the two stages method described in journeytoforever, the mix  settle 
 around 12 h between first and second stage before extract the glycerine. It?s 
 necessary to settle so many time? It?s bad if any glycerine is not decanted 
 and is mixed in the second stage? Is there any trick to avoid to wait 12 h 
 between first and second stage?

Many thx in advance and sorry for my bad english 

  



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Re: [Biofuel] two stage proccess... doubts

2005-12-14 Thread ReZn0r
Hi Appal,

Con fecha miércoles, 14 de diciembre de 2005, 14:00:32, escribiste:

Hi
   We are making BD with a homemade reactor (80 liters). We have used de 
 single stage and de two stage (base-base) methods succesfuly, but we still 
 having many doubts :)

   In the two stages method described in journeytoforever, the mix  
 settle around 12 h between first and second stage before extract the 
 glycerine. It?s necessary to settle so many time? It?s bad if any glycerine 
 is not decanted and is mixed in the second stage? Is there any trick to 
 avoid to wait 12 h between first and second stage?

Many thx in advance and sorry for my bad english 

  


AE ReZn0r,

AE Settling time is simply letting gravity do the separation work for 
AE you, rather than enlisting equipment such as centrifuges. The more 
AE glycerol/soap that is extracted by settling the less impediment to the
AE subsequent step, whether it be stage two or washing.

AE Todd Swearingen
Hi Todd

Thx for reply

I Agree with this and for sure is very important to let settle before wash, but 
I want to know if is there any problem in the second stage if we have 5% for 
example of total glycerine from the first stage inside the mix of the second 
one... (I think 95% of glycerine settles in less than 1 hour, correct me if I 
am wrong)

AE ___
AE Biofuel mailing list
AE Biofuel@sustainablelists.org
AE http://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.org

AE Biofuel at Journey to Forever:
AE http://journeytoforever.org/biofuel.html

AE Search the combined Biofuel and Biofuels-biz list archives (50,000 
messages):
AE http://www.mail-archive.com/biofuel@sustainablelists.org/




-- 
Un Saludo,
 ReZn0rmailto:[EMAIL PROTECTED]



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Re: [Biofuel] two stage proccess... doubts

2005-12-14 Thread Kenji James Fuse
I've had a question about the two-stage, base-base method as well. My
second stage resulted in such a little amount of glycerin it didn't seem
worth the extra time or effort. Any comments? I suppose the removal of
this last
tablespoon of glycerin gets my BD to ASTM standards for free glycerin, but
it seems alot of work for a little result, when I'm only using the stuff
myself.

KF

On Wed, 14 Dec 2005, ReZn0r wrote:


 Hi
   We are making BD with a homemade reactor (80 liters). We have used de 
 single stage and de two stage (base-base) methods succesfuly, but we still 
 having many doubts :)

   In the two stages method described in journeytoforever, the mix  settle 
 around 12 h between first and second stage before extract the glycerine. It?s 
 necessary to settle so many time? It?s bad if any glycerine is not decanted 
 and is mixed in the second stage? Is there any trick to avoid to wait 12 h 
 between first and second stage?

 Many thx in advance and sorry for my bad english



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Re: [Biofuel] two stage proccess... doubts

2005-12-14 Thread Teoman Naskali
I let some of my BD settle for about 2 months (indoors, 22 degrees
celcius) and by the time I got to the washing stage I noticed that it
was rather clear with some white sediment at the bottom. And when I
washed It I did not observe much soap formation. And the separation was
almost immediate like I was mixing vegetable oil and water.

Now after two days the water still looks fairly clear. The bd is
slightly cloudy.

First I worried that I hadnt completed the process and that what I was
washing was more vegetable oil rather thatn Bd, but reprocessing it
didn't give any glycerine.



Is there any error here?


Thanks for any advice
Teoman

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Appal Energy
Sent: Wednesday, December 14, 2005 3:01 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] two stage proccess... doubts

ReZn0r,

Settling time is simply letting gravity do the separation work for 
you, rather than enlisting equipment such as centrifuges. The more 
glycerol/soap that is extracted by settling the less impediment to the 
subsequent step, whether it be stage two or washing.

Todd Swearingen

Hi
   We are making BD with a homemade reactor (80 liters). We have
used de single stage and de two stage (base-base) methods succesfuly,
but we still having many doubts :)

   In the two stages method described in journeytoforever, the mix
settle around 12 h between first and second stage before extract the
glycerine. It?s necessary to settle so many time? It?s bad if any
glycerine is not decanted and is mixed in the second stage? Is there any
trick to avoid to wait 12 h between first and second stage?

Many thx in advance and sorry for my bad english 

  



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Re: [Biofuel] two stage proccess... doubts

2005-12-14 Thread Appal Energy
ReZn0r,

All chemical reactions, in one way shape or form, are reactions of 
equilibrium. And the results of many reactions are less than desired if 
the chemical balance is only  one of stoichiometric balance. Hence the 
need on many occasions to use excess amounts of one chemical or another 
in an equation to drive the reaction in the direction desired.

Relative to allowing enough time for the glycerol cocktail (glycerin, 
methanol, excess catalyst and soap) to settle out of the first stage 
before conducting the second?

Without controlled testing to quantify the differences between 
trials/samples, about all that can be said is that the presence of 
glycerol will naturally attract some of the methanol (like seeks like), 
as might whatever fraction of soap is present, possibly preventing an 
unknown fraction of the methanol from randomly interacting with the 
unconverted glycerides as it might have normally had the first stage 
been allowed to settle sufficiently.

The same holds true for the catalyst, as some water is generated in a 
transesterification. This small amount largely settles out with 
everything else in a base reaction. As the catalyst is hydrophyllic, its 
first tendency is to gravitate towards water, which in turn will bind up 
a small portion rather than allowing it to perform its function.

All this is done in microscopic amounts and may not amount to any 
discernible difference between samples that have settled twelve hours or 
samples that have settled six. There is really only one way to determine 
whether or not there is any significant difference between the two end 
results. That would be to conduct the testing.

On a firsthand note, as we don't use two-stage base processing, opting 
instead for acid/base processing. As a result, we're not exactly in a 
position to inform you definitively one way or the other. It's also 
rather doubtful that very many people are in such a position, if only 
for the reason that it would take some rather controlled experimentation 
and the majority probably don't have the time or facilities to conduct 
such testing.

On the other hand, it shouldn't be too terribly difficult to conduct 
some basic/crude testing at your own leisure to see if you can discern 
any noticeable difference.

A fair guess is that you wouldn't notice much, if any. Perhaps what 
another question might be is Do you really have need of expediting a 
process? If so, such as in an industrial/commercial environment, 
testing might hold more validity for you than other bears of average brain.

Todd Swearingen

Hi Appal,

Con fecha miércoles, 14 de diciembre de 2005, 14:00:32, escribiste:

  

Hi
  We are making BD with a homemade reactor (80 liters). We have used de 
 single stage and de two stage (base-base) methods succesfuly, but we still 
 having many doubts :)
  


  

  In the two stages method described in journeytoforever, the mix  
 settle around 12 h between first and second stage before extract the 
 glycerine. It?s necessary to settle so many time? It?s bad if any glycerine 
 is not decanted and is mixed in the second stage? Is there any trick to 
 avoid to wait 12 h between first and second stage?
  


  

Many thx in advance and sorry for my bad english 
  


  

 
  



AE ReZn0r,

AE Settling time is simply letting gravity do the separation work for 
AE you, rather than enlisting equipment such as centrifuges. The more 
AE glycerol/soap that is extracted by settling the less impediment to the
AE subsequent step, whether it be stage two or washing.

AE Todd Swearingen
Hi Todd

Thx for reply

I Agree with this and for sure is very important to let settle before wash, 
but I want to know if is there any problem in the second stage if we have 5% 
for example of total glycerine from the first stage inside the mix of the 
second one... (I think 95% of glycerine settles in less than 1 hour, correct 
me if I am wrong)

AE ___
AE Biofuel mailing list
AE Biofuel@sustainablelists.org
AE http://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.org

AE Biofuel at Journey to Forever:
AE http://journeytoforever.org/biofuel.html

AE Search the combined Biofuel and Biofuels-biz list archives (50,000 
messages):
AE http://www.mail-archive.com/biofuel@sustainablelists.org/




  



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