Re: [Biofuel] Modification of cars to use biodiesel and insurance

2006-01-02 Thread Mike Weaver
I have never heard of a biodiesel governing board - who would qualify you?

Here in the states we have the ASE.

Philip Clark wrote:

 Hi TIM
 If you  feel well qualified as a marine engineer, what would it take 
 for you to become a qualified and certified bio diesel installer? Is 
 there anyone on this earth more qualified then you to make that 
 determination? I think not, but that's a matter of philosophy! Where 
 is Leicestershire anyway?

 PHILIP CLARK (USA)




 On 12/31/05, Tim Hadland [EMAIL PROTECTED] wrote:
 
hello from leicestershire!
 
I have just discussed the fact i am going to run my car on bio 
 diesel with
  my insurance company. I have used Norwich union, and the pay as you 
 drive
  option (i am in the merchant navy and dont use my car for 4 month 
 periods
  and i am still a young driver)
 
I wish ships used biodiesel, they use residual or heavy fuel oil 
 - solid
  at room temperature. Nasty stuff, which gets treated through 
 heating and
  settling, heating and purification - centrifuging out water and 
 solids, and
  filtering at various stages before being burnt in the engine. 
 Already and
  ideal set-up for using biodiesel. Would make work feel more healthy 
 with
  reduced nasty fumes and probably much safer.
 
Anyway back to insurance. I was told if i were to have any mod 
 done to my
  fuel system such as a heated fuel filter it would have to be 
 installed by a
  qualified and certified bio diesel installer !? None in 
 Leicestershire, in
  fact i dont know of anyone in the midlands. I feel well qualified as a
  marine engineer.  Has anyone else had insurance probs with 
 modifications?
 
 cheers, and happy new year for tmw.
 
TIM  HADLAND
 
 
 
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Re: [Biofuel] Modification of cars to use biodiesel and insurance

2006-01-02 Thread Sam Critchley

Hi,

I'm quite surprised that running biodiesel is an issue for your insurance 
company, rather than just a warranty issue for the car manufacturer (if it's a 
relatively new car), although I suppose a naysayer legal department might say 
What? Fuel not provided by a big oil company? The car's bound to burst into 
flames and kill everyone within 100 yards/metres! There's no way we'll insure 
it!.

I've got a few thoughts:

1. It might help if the biodiesel you use conforms to the European standard for 
biodiesel EN-14214. If it doesn't you can get it tested by a company like 
Intertek.

2. You probably wouldn't need a heated fuel filter for biodiesel most of the 
time in the UK (unless you live up a mountain or something), but there are a 
couple of places which specialise in car conversions for using SVO (straight 
vegetable oil):

http://www.vegetableoildiesel.co.uk/
http://www.vegburner.co.uk/
http://www.bio-power.co.uk/

3. If you can't get anyone to insure your car if it's running biodiesel, then I 
suggest getting in contact with the AA or the RAC and asking them to help out. 
If this still doesn't work, then try raising it as an issue which is hindering 
national CO2 emission reduction by going to Friends of the Earth, The Carbon 
Trust and the Department of the Environment. I think the Independent and 
Guardian newspapers would also be interested. CO2 reduction is a big story in 
the UK and this is a perfect example of something slowing it down.

Best wishes,


Sam



On Sat, 31 Dec 2005 10:44:04 +0100, Tim Hadland [EMAIL PROTECTED] wrote:


   hello from leicestershire!

   I have just discussed the fact i am going to run my car on bio diesel with
 my insurance company. I have used Norwich union, and the pay as you drive
 option (i am in the merchant navy and dont use my car for 4 month periods
 and i am still a young driver)

   I wish ships used biodiesel, they use residual or heavy fuel oil - solid
 at room temperature. Nasty stuff, which gets treated through heating and
 settling, heating and purification - centrifuging out water and solids, and
 filtering at various stages before being burnt in the engine. Already and
 ideal set-up for using biodiesel. Would make work feel more healthy with
 reduced nasty fumes and probably much safer.

   Anyway back to insurance. I was told if i were to have any mod done to my
 fuel system such as a heated fuel filter it would have to be installed by a
 qualified and certified bio diesel installer !? None in Leicestershire, in
 fact i dont know of anyone in the midlands. I feel well qualified as a
 marine engineer.  Has anyone else had insurance probs with modifications?

cheers, and happy new year for tmw.

   TIM  HADLAND



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[Biofuel] Biodiesel Testing excessive methanol

2006-01-02 Thread JJJN
I just tested a 60 Liter batch and have a few questions; below is what I 
have done with the results and further below are my questions,

The biodiesel used in the tests below was unwashed - glycerin layer 
removed.

1.) Using the test method noted on JtF ( Jan Warnqvist - Methanol test) 
as prescribed 225 ml Methanol combined with 25 ml of the biodiesel.
Results: Biodiesel was fully soluble and formed a clear bright phase no 
contaminants or other phases noted. Results after 24 hours - No change.

2) Using a MODIFIED JtF method,  (combining 4.90875 grams lab grade KOH 
and 100 ml Methanol (Potassium Methoxil) with 1 Liter of the biodiesel) 
- INSTEAD I added 400ml methanol and 4.90875 grams KOH ( Potassium 
Methoxil ) (both lab grade near absolute) to 1 Liter of the Biodiesel. I 
then heated to 120 deg F and mixed for one hour.
Results: after 24 hours  there was a nice amber layer from the bottom of 
the glass jar up to the last say 1/2 inch where a very very slightly 
amber layer resided to the top. there was nothing at the bottom at all.

3) Wash test JtF, In a glass jar I shook 1/2 Bio and 1/2 water at room 
temp till mixed into one phase.
Results: within 1 minute the water and Bio separated and the water was 
quite white. Wash #2 same time of separation water clearer this time. 
Wash # 3 same as #2. Wash # 4 water was not drinking quality but PH is 
close to seven.

O.K why did I increase the Methanol in test #2) above?  I am not sure 
except to see what it would do, but from what I read it would not harm 
so I did.

My Question: Can anyone tell me what the strange clear amber layer on 
top of the other clear amber layer may be?

Could this be the FFA content per L?

Thanks in advance,

Jim

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Re: [Biofuel] Biodiesel Testing excessive methanol

2006-01-02 Thread JJJN
I ran some additional tests on the two layers (see test # 2 below)

Top Layer mixed with water:
Results Soapy and white no separation (yet) (very Soapy- Sudsy)

Bottom Layer mixed with water:
Results Water turns white but a nice clear amber layer of biofuel on top.

Any one?

JJJN wrote:

I just tested a 60 Liter batch and have a few questions; below is what I 
have done with the results and further below are my questions,

The biodiesel used in the tests below was unwashed - glycerin layer 
removed.

1.) Using the test method noted on JtF ( Jan Warnqvist - Methanol test) 
as prescribed 225 ml Methanol combined with 25 ml of the biodiesel.
Results: Biodiesel was fully soluble and formed a clear bright phase no 
contaminants or other phases noted. Results after 24 hours - No change.

2) Using a MODIFIED JtF method,  (combining 4.90875 grams lab grade KOH 
and 100 ml Methanol (Potassium Methoxil) with 1 Liter of the biodiesel) 
- INSTEAD I added 400ml methanol and 4.90875 grams KOH ( Potassium 
Methoxil ) (both lab grade near absolute) to 1 Liter of the Biodiesel. I 
then heated to 120 deg F and mixed for one hour.
Results: after 24 hours  there was a nice amber layer from the bottom of 
the glass jar up to the last say 1/2 inch where a very very slightly 
amber layer resided to the top. there was nothing at the bottom at all.

3) Wash test JtF, In a glass jar I shook 1/2 Bio and 1/2 water at room 
temp till mixed into one phase.
Results: within 1 minute the water and Bio separated and the water was 
quite white. Wash #2 same time of separation water clearer this time. 
Wash # 3 same as #2. Wash # 4 water was not drinking quality but PH is 
close to seven.

O.K why did I increase the Methanol in test #2) above?  I am not sure 
except to see what it would do, but from what I read it would not harm 
so I did.

My Question: Can anyone tell me what the strange clear amber layer on 
top of the other clear amber layer may be?

Could this be the FFA content per L?

Thanks in advance,

Jim

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Re: [Biofuel] HAPPY 2006 AND FRUITFUL NEW YEAR

2006-01-02 Thread damiandolan
Biofuel@sustainablelists.org wrote:


Hi Pannirselvam, to Keith, and list,

many thanks for all great work, and good health, and harmoney to all on list 
and best of luck to make '06 a green and re-newable new year,

dD

  
  --
  Pagandai V Pannirselvam
  Universidade Federal do Rio Grande do Norte - UFRN
  Departamento de Engenharia Qu=EDmica - DEQ
  Centro de Tecnologia - CT
  Programa de P=F3s Gradua=E7=E3o em Engenharia Qu=EDmica - PPGEQ
  Grupo de Pesquisa em Engenharia de Custos - GPEC
  
  Av. Senador Salgado Filho, Campus Universit=E1rio
  CEP 59.072-970 , Natal/RN - Brasil
  
  Residence :
  Av  Odilon gome de lima, 2951,
 Q6/Bl.G/Apt 102
 Capim  Macio
  EP 59.078-400 , Natal/RN - Brasil
  
  Telefone(fone ) ( 84 ) 3215-37690 Ramal210
  32171557
  Telefone(fax) ( 84 ) 3215-3770
  residencia 32171557
  
   Cellular  84  88145083
  
  --=_Part_197_17007032.1136076283115
  Content-Type: text/html; charset=ISO-8859-1
  Content-Transfer-Encoding: quoted-printable
  Content-Disposition: inline
  
  divfont face=3DArial size=3D2Dear Biofuel list=B4s members, my rese=
  arch team members, and my beloved  Biofuel list leader  KEithbr=
  /font/div
  div /div
  divfont face=3DArial size=3D2It is my deepest will and pleasurenbs=
  p; that everyone of you enjoy a=20
  happy and fruitful new year 2006, seeing biomass  based  rural ec=
  o friendly technology taking=20
  off to playing relevant role in today and tomorrow=B4s energy=20
  shares bringing  light and prosperity to the  the  darken ar=
  ea of the rural world.Let us all join for hand to make the colaborative wor=
  k for the same.br/font/div
  div /div
  divfont face=3DArial size=3D2Kindest regards./font/divPannirsel=
  vambr clear=3Dallbr-- br Pagandai V PannirselvambrUniversidade Fe=
  deral do Rio Grande do Norte - UFRNbrDepartamento de Engenharia Qu=EDmica=
   - DEQ
  brCentro de Tecnologia - CTbrPrograma de P=F3s Gradua=E7=E3o em Engenha=
  ria Qu=EDmica - PPGEQbrGrupo de Pesquisa em Engenharia de Custos - GPECb=
  rbrAv. Senador Salgado Filho, Campus Universit=E1riobrCEP 59.072-970 ,=
   Natal/RN - Brasil
  brbrResidence :brAv  Odilon gome de lima, 2951,br n=
  bsp; Q6/Bl.G/Apt 102br   Capim  MaciobrEP 59.078-40=
  0 , Natal/RN - BrasilbrbrTelefone(fone ) ( 84 ) 3215-37690 Ramal210br=
  nb=
  sp;=
     32171557
  brTelefone(fax) ( 84 ) 3215-3770 br  =
    residencia 32171557brbr  =
     Cellular =
   84  88145083
  
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[Biofuel] removing water from WVO

2006-01-02 Thread Lee Eady, D.C.



I am just getting started making BD. I have 
had some trouble getting all the water removed from the WVO. Is it a must 
to heat the oil if so how hot, how long? Will it settle out on its own if 
just sits if so how long do I need to let it settle? Any info will be 
appreciated.
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Re: [Biofuel] acid/base method for conversion of wvo to FAMEs

2006-01-02 Thread Ian Theresa Sims
Some reassurance please.
After months of single stage manufacture and reactor modifications I was 
about to jump into the Foolproof method. But now Bob in a, I assume well 
equiped Lab can't get the process to work completely.
What Gives? How much chance do I have in a back yard with home made and 
jerry rigged equipment.
Alex Kac also states that mixing methanol and sulphuric acid together is can 
cause serious problems. Once again what gives?

Cheers Ian


- Original Message - 
From: bob allen [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Saturday, December 31, 2005 1:42 PM
Subject: Re: [Biofuel] acid/base method for conversion of wvo to FAMEs


 Appal Energy wrote:
 Bob,

 Why not drain the small amount of glycerol that settles out of an
 esterification? The majority of the sulfuric will come out with it. That
 lessens the amount of base catalyst needed for the follow-up
 transesterification.

 again, this is just what I observed:  no glycerin settled out after the 
 acid stage.  Waiting 8 hours
 realistically means another day. Additionally, if I do wait and do get 
 some glycerin to settle out
 with my conditions, wouldn't you think that methanol also would be part of 
 the cocktail, thence
 affecting the equilibrium?


 Fewer chemicals in, fewer problems out.

 Todd Swearingen



 bob allen wrote:


acid/base method for conversion of wvo to FAMEs


In my lab I have had little success with the acid/base method for 
biodiesel production. When my
students and I tried to duplicate the foolproof method

http://journeytoforever.org/biodiesel_aleksnew.html

we  invariably obtained incomplete reactions, plus the longer preparation 
time was less attractive.
 The following is my modification of that procedure which works for us, 
 and takes less time, but
requires more catalyst.


Dissolve 1 ml sulfuric acid in 150 ml methanol and add to 1 liter liter 
dry wvo,  heat to about 60
Celsius for one hour.  Then  dissolve 4.9gm NaOH  in 50 ml methanol and 
add to the reaction
mixture.  Continue heating for an additional hour, stir for one more hour 
and then let set for 8 or
 more hours.  workup as usual.

Now for the why more catalyst. Basically the sulfuric acid used 
neutralizes some of the base
catalyst, hence more must be add to get back to the desired concentration 
of catalyst.  If you don't
know moles and equivalents, the following may be abstruse.

1 ml sulfuric acid is 36 milliequivalents, therefore its presence in the 
reaction mixture
neutralizes 36 milliequivalents of NaOH.  The simple base catalyzed 
method requires 3.5 grams NaOH
which is 90 milliequivalents.  Subtract 36 from 90 and you get 54 
milliequivalents of base left.
This corresponds to to only 2.1 grams NaOH active active catalyst, the 
remainder having been
converted to Na(2)SO(4), sodium sulfate.   In round numbers then you have 
to add an additional 1.4
grams of NaOH on top of the 3.5 grams called for in the simple procedure.

The following instructions are intended for an advanced audience, 
thoroughly familiar with the
simple procedure.  To minimize costs we still do a titration.  If the wvo 
titrates at greater than
1.4 ml, we use this modification, less we use the simple procedure.


All this having be said, I actually use KOH in my procedure but have done 
the calculations with
NaOH, it works either way, one just has to adjust the molar proportions.

Acknowledgment should be given to Kelly Verbel and Josh Lisko, students 
who worked with me on this
part of our biodiesel project.




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[Biofuel] Crude palm oil

2006-01-02 Thread Courtney Blodgett








Hi! Im trying to figure out biodiesel yield from
palm trees. Does anyone know how much crude oil a palm tree can yield
annually? How many palm trees are normally planted per hectare?



Thanks!

Courtney






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Re: [Biofuel] removing water from WVO

2006-01-02 Thread Derick Giorchino








I also had some trouble in the beginning. I
now use a settling drum I found the design on J T F and it works very well. I collect
my wvo in the wee hours on my way to work and have collected 20+ gal of water in
40 gal pickup. I drain the pure water out after a few hours of settling then
heat the balance to 120 f and drain it once more. The separation drum has 2
drain valves one on the bottom and one about 6 inches off the bottom. That where
I get a nice clean product fro processing. It may seem that the energy used is
a waste but I find it is better than 120 liters of failure. 

Good luck Derick











From:
[EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On
Behalf Of Lee Eady, D.C.
Sent: Monday, January 02, 2006
12:05 PM
To: Biofuel@sustainablelists.org
Subject: [Biofuel] removing water
from WVO







I am just getting started making BD. I have had some
trouble getting all the water removed from the WVO. Is it a must to heat
the oil if so how hot, how long? Will it settle out on its own if just
sits if so how long do I need to let it settle? Any info will be appreciated.








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Re: [Biofuel] removing water from WVO

2006-01-02 Thread JJJN
Lee,
I don't know where you are at in the learning process but if you have 
not started with virgin oil and had multiple success in small batches do 
yourself a favor and start there and learn the titration before you 
start with WVO.
As far as heating it there is a whole section on getting the water out 
of WVO:

http://journeytoforever.org/biodiesel_make.html#water

Best
Jim


Lee Eady, D.C. wrote:

 I am just getting started making BD.  I have had some trouble getting 
 all the water removed from the WVO.  Is it a must to heat the oil if 
 so how hot, how long?  Will it settle out on its own if just sits if 
 so how long do I need to let it settle? Any info will be appreciated.



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Re: [Biofuel] acid/base method for conversion of wvo to FAMEs

2006-01-02 Thread Appal Energy
Ian,

I think you'll have to ask Bob what it is that is off the mark for him 
and lends to whatever quandry he may or may not be in.

Acid/base works. It just requires some pretty good understanding of what 
is going on in the reaction, what enhances the reaction and what actions 
are less than beneficial on the operator's part.

There are perhaps only three things that I would suggest to modify in 
the acid/base process.

1) Allow a 24 hour reaction period, of which at least sixteen are under 
agitation.

2) Drain off any glycerol that settles out prior to moving to the base 
stage. As most of the acid will reside there after settling, this will 
reduce the amount of base catalyst consumed in neutralizing the acid.

3) The eighty mililiters of methanol suggested in the acid stage is 
sufficient only for conversion of feedstock up to approximately forty 
percent FFAs. It's almost impossible to imagine any WVO coming from a 
restaurant that would be that degraded. (If it is, they should be shut 
down by the local health department.) But it is theoretically possible. 
Oils that degraded or more will require more methanol in the acid stage 
and less methanol in the base stage.

Todd Swearingen


Ian  Theresa Sims wrote:

Some reassurance please.
After months of single stage manufacture and reactor modifications I was 
about to jump into the Foolproof method. But now Bob in a, I assume well 
equiped Lab can't get the process to work completely.
What Gives? How much chance do I have in a back yard with home made and 
jerry rigged equipment.
Alex Kac also states that mixing methanol and sulphuric acid together is can 
cause serious problems. Once again what gives?

Cheers Ian


- Original Message - 
From: bob allen [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Saturday, December 31, 2005 1:42 PM
Subject: Re: [Biofuel] acid/base method for conversion of wvo to FAMEs


  

Appal Energy wrote:


Bob,

Why not drain the small amount of glycerol that settles out of an
esterification? The majority of the sulfuric will come out with it. That
lessens the amount of base catalyst needed for the follow-up
transesterification.
  

again, this is just what I observed:  no glycerin settled out after the 
acid stage.  Waiting 8 hours
realistically means another day. Additionally, if I do wait and do get 
some glycerin to settle out
with my conditions, wouldn't you think that methanol also would be part of 
the cocktail, thence
affecting the equilibrium?



Fewer chemicals in, fewer problems out.

Todd Swearingen



bob allen wrote:


  

acid/base method for conversion of wvo to FAMEs


In my lab I have had little success with the acid/base method for 
biodiesel production. When my
students and I tried to duplicate the foolproof method

http://journeytoforever.org/biodiesel_aleksnew.html

we  invariably obtained incomplete reactions, plus the longer preparation 
time was less attractive.
The following is my modification of that procedure which works for us, 
and takes less time, but
requires more catalyst.


Dissolve 1 ml sulfuric acid in 150 ml methanol and add to 1 liter liter 
dry wvo,  heat to about 60
Celsius for one hour.  Then  dissolve 4.9gm NaOH  in 50 ml methanol and 
add to the reaction
mixture.  Continue heating for an additional hour, stir for one more hour 
and then let set for 8 or
more hours.  workup as usual.

Now for the why more catalyst. Basically the sulfuric acid used 
neutralizes some of the base
catalyst, hence more must be add to get back to the desired concentration 
of catalyst.  If you don't
know moles and equivalents, the following may be abstruse.

1 ml sulfuric acid is 36 milliequivalents, therefore its presence in the 
reaction mixture
neutralizes 36 milliequivalents of NaOH.  The simple base catalyzed 
method requires 3.5 grams NaOH
which is 90 milliequivalents.  Subtract 36 from 90 and you get 54 
milliequivalents of base left.
This corresponds to to only 2.1 grams NaOH active active catalyst, the 
remainder having been
converted to Na(2)SO(4), sodium sulfate.   In round numbers then you have 
to add an additional 1.4
grams of NaOH on top of the 3.5 grams called for in the simple procedure.

The following instructions are intended for an advanced audience, 
thoroughly familiar with the
simple procedure.  To minimize costs we still do a titration.  If the wvo 
titrates at greater than
1.4 ml, we use this modification, less we use the simple procedure.


All this having be said, I actually use KOH in my procedure but have done 
the calculations with
NaOH, it works either way, one just has to adjust the molar proportions.

Acknowledgment should be given to Kelly Verbel and Josh Lisko, students 
who worked with me on this
part of our biodiesel project.




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Re: [Biofuel] acid/base method for conversion of wvo to FAMEs

2006-01-02 Thread Mike Weaver
FWIW, I tried the foolproof method off and on for a qhile and finally 
went back to the old tried and true.  I never could get it to work reliably.

Ian  Theresa Sims wrote:

Some reassurance please.
After months of single stage manufacture and reactor modifications I was 
about to jump into the Foolproof method. But now Bob in a, I assume well 
equiped Lab can't get the process to work completely.
What Gives? How much chance do I have in a back yard with home made and 
jerry rigged equipment.
Alex Kac also states that mixing methanol and sulphuric acid together is can 
cause serious problems. Once again what gives?

Cheers Ian


- Original Message - 
From: bob allen [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Saturday, December 31, 2005 1:42 PM
Subject: Re: [Biofuel] acid/base method for conversion of wvo to FAMEs


  

Appal Energy wrote:


Bob,

Why not drain the small amount of glycerol that settles out of an
esterification? The majority of the sulfuric will come out with it. That
lessens the amount of base catalyst needed for the follow-up
transesterification.
  

again, this is just what I observed:  no glycerin settled out after the 
acid stage.  Waiting 8 hours
realistically means another day. Additionally, if I do wait and do get 
some glycerin to settle out
with my conditions, wouldn't you think that methanol also would be part of 
the cocktail, thence
affecting the equilibrium?



Fewer chemicals in, fewer problems out.

Todd Swearingen



bob allen wrote:


  

acid/base method for conversion of wvo to FAMEs


In my lab I have had little success with the acid/base method for 
biodiesel production. When my
students and I tried to duplicate the foolproof method

http://journeytoforever.org/biodiesel_aleksnew.html

we  invariably obtained incomplete reactions, plus the longer preparation 
time was less attractive.
The following is my modification of that procedure which works for us, 
and takes less time, but
requires more catalyst.


Dissolve 1 ml sulfuric acid in 150 ml methanol and add to 1 liter liter 
dry wvo,  heat to about 60
Celsius for one hour.  Then  dissolve 4.9gm NaOH  in 50 ml methanol and 
add to the reaction
mixture.  Continue heating for an additional hour, stir for one more hour 
and then let set for 8 or
more hours.  workup as usual.

Now for the why more catalyst. Basically the sulfuric acid used 
neutralizes some of the base
catalyst, hence more must be add to get back to the desired concentration 
of catalyst.  If you don't
know moles and equivalents, the following may be abstruse.

1 ml sulfuric acid is 36 milliequivalents, therefore its presence in the 
reaction mixture
neutralizes 36 milliequivalents of NaOH.  The simple base catalyzed 
method requires 3.5 grams NaOH
which is 90 milliequivalents.  Subtract 36 from 90 and you get 54 
milliequivalents of base left.
This corresponds to to only 2.1 grams NaOH active active catalyst, the 
remainder having been
converted to Na(2)SO(4), sodium sulfate.   In round numbers then you have 
to add an additional 1.4
grams of NaOH on top of the 3.5 grams called for in the simple procedure.

The following instructions are intended for an advanced audience, 
thoroughly familiar with the
simple procedure.  To minimize costs we still do a titration.  If the wvo 
titrates at greater than
1.4 ml, we use this modification, less we use the simple procedure.


All this having be said, I actually use KOH in my procedure but have done 
the calculations with
NaOH, it works either way, one just has to adjust the molar proportions.

Acknowledgment should be given to Kelly Verbel and Josh Lisko, students 
who worked with me on this
part of our biodiesel project.




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-- 
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http://ozarker.org/bob

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

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[Biofuel] quality test questions

2006-01-02 Thread Darryl West
Hi,

I am just after a bit more advice regarding the quality test on a small test
batch.  I followed the Dr Peppers technique using new canola oil and the
process seems to have worked out ok.  When I do the quality test I get
separation in 30 mins, but also get a small (5cm) white layer between the
water and biodiesel, which I believe is soap.  Does this indicate poor fuel?
Would it still be ok to wash and dry and use, or should I not use this batch
and maybe use less methanol and lye?

thanks

Darryl West



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Re: [Biofuel] quality test questions

2006-01-02 Thread Appal Energy
Daryl,

The suggestion is that you understand precisely what it is that you're 
looking at when you see a thick layer of emulsion in a wash. If the fuel 
was manufactured properly, the interface layer between water and fuel in 
a test wash would be only a milimeter or two thick. Five centimeters 
indicates a reasonably incomplete reaction.

As for your suggested resolve? Reducing the methanol and lye? Going that 
direction would only compound the matter.

Todd Swearingen


Darryl West wrote:

Hi,

I am just after a bit more advice regarding the quality test on a small test
batch.  I followed the Dr Peppers technique using new canola oil and the
process seems to have worked out ok.  When I do the quality test I get
separation in 30 mins, but also get a small (5cm) white layer between the
water and biodiesel, which I believe is soap.  Does this indicate poor fuel?
Would it still be ok to wash and dry and use, or should I not use this batch
and maybe use less methanol and lye?

thanks

Darryl West



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Re: [Biofuel] quality test questions

2006-01-02 Thread Derick Giorchino
Not knowing where you are in the process. I would sagest using the stock
methoxide formula listed on J.T.F. after titration I mix the methoxide 1
gram less then the titration # and 1 gram more. I find that the results
often differ with the feed stock used. After figuring out which  1/2 liter
test batch is best I fine tune it 1/2 gram at a time until I start to get
soap. I then go back 1/4 gram and use it for processing. It may seem like a
lot of work but it can be done all at the same time I just mark the tops of
the bottles with the mix used. When I started I found it very hard to see a
change with new oil. After doing 2 qts of new oil just to see the basics I
moved to wvo in 1/2 liter batches. I also found that the group helped me a
lot it seems I thought I was using accurate measurements but only half of
the crap I picked up for measuring was even close.   
Good luck. Derick   
-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Darryl West
Sent: Monday, January 02, 2006 3:37 PM
To: Biofuel@sustainablelists.org
Subject: [Biofuel] quality test questions

Hi,

I am just after a bit more advice regarding the quality test on a small test
batch.  I followed the Dr Peppers technique using new canola oil and the
process seems to have worked out ok.  When I do the quality test I get
separation in 30 mins, but also get a small (5cm) white layer between the
water and biodiesel, which I believe is soap.  Does this indicate poor fuel?
Would it still be ok to wash and dry and use, or should I not use this batch
and maybe use less methanol and lye?

thanks

Darryl West



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Re: [Biofuel] FW: Important, Congress set to gut renewable energy programs

2006-01-02 Thread Greg Ocnos
Title: Re: Important, Congress set to gut renewable energy programs









Has anyone heard anything more about this?
Did NREL get hit hard? 

Just looking for a follow up, who could I
ask?



Thanks





Gregory I. Ocnos





-Original Message-
From:
[EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On
Behalf Of David M. Brockes
Sent: Wednesday,
 November 16, 2005 5:47 PM
To: Awea-Windnet; Biofuel;
Renewable-Energy
Subject: [Biofuel] FW:
Important,Congress set to gut renewable energy programs
Importance: High





Follow-up.





David















-Original
Message-
From: Bob Anderson
[mailto:[EMAIL PROTECTED]
Sent: Wednesday,
 November 16, 2005 3:32 PM
Subject: Re: Important, Congress
set to gut renewable energy programs
Importance: High

Ive
just returned from a meeting at NREL (where I am a small contractor).
The lab expects a 40% cut in the Wind Powering America program.

Bob Anderson



On 11/16/05 1:45 PM, Van Jamison
[EMAIL PROTECTED] wrote:

FYI
- Original Message - 
From: Patrick Judge mailto:[EMAIL PROTECTED] 
To: [EMAIL PROTECTED] ;
[EMAIL PROTECTED] 
Sent: Wednesday,
 November 16, 2005 7:50 AM
Subject: Fwd: Important, Congress
set to gut renewable energy programs

Congress to Terminate National Bioenergy Center
Congress is getting ready this week to terminate the National Bioenergy
Research Center and gut
the Wind Research Program at the National Renewable
Energy Laboratory (NREL). NREL researchers who are CRES members sounded the
alarm over the weekend after finding out on Friday that many of them may be
out of work next month.

Here is what I can piece together about what happened last week. On Tuesday
the House of Representatives passed the House and Senate Conference
Committee markup of the Energy Water and Development Appropriation Bill for
2006. The bill keeps federal funding for renewable energy research
level
with last year's spending.

Unfortunately, it more than doubled the earmarks that take money out of the
Wind Energy and Bioenergy Research Programs and direct it elsewhere.
Earmarks are when individual representatives direct funding to particular
projects in their districts. With passage of the Energy Bill earlier this
year, these earmarks have been in the forefront of the news. In fact, the
American Solar Energy Society said the Energy Bill was so full of pork
barrel spending that ASES did not endorse it.

Congressional leaders usually wait until the conference committee is
meeting
behind closed doors to introduce earmarks. They emerge as part of a much
larger bill that is hundreds of pages long.

It appears that in this case, the House of Representatives voted on this
bill without many of
its members having had time to read it.

It took NREL staff a couple of days of read through the pile of paper and
figure out what it will mean for the research programs. Some of the
earmarks
were listed together to support state initiatives, and others were buried
in
different portions of the massive spending bill. This year these added to
$62 million in total, more than two thirds of the entire research and
development budget for bioenergy. Then the staff had to calculate
DOE's
contractual obligations to its industry partnerships and the 10% cut that
the agency takes from all programs to pay the salaries of its staff.

Staff of the National Bioenergy Center, which
number more than 90 people,
were told Friday afternoon that all that the funding that would be left was
sufficient only to cover their severance checks. The National Wind
Technology Center is
facing similar, severe cutbacks. It seems incredible,
but Congress is getting ready to gut the two research programs in renewable
energy technologies that have enjoyed the most success and commercial
development just at a time when fossil fuel prices are their highest level
in history. In the case of creating transportation fuels from biomass,
these
technologies represent our greatest near-term hope of
reducing imports or fossil fuels.

The Senate is scheduled to take up the appropriations bill today or
tomorrow. Please call Senators Allard and Salazar today and ask them to
vote
no on the appropriations bill from the Energy and Water Committee. Tell
them
that renewable energy RD is one of this country's best investments.

- Wayne Allard: call the Colorado office
at 303-220-7414 or the Washington
office at 202-224-5941, or send an email message at:
http://allard.senate.gov/public/index.cfm?FuseAction=ContactHome

- Ken Salazar: call the Colorado office
at 303-455-7600 or the Washington
office at 202-224-5852, or send an email message at:
http://salazar.senate.gov/contact/email.cfm

Russ Doty, CEO
New World WindPower LLC
PO Box 1734
Billings, MT 59103-1734
406-656-2763
email: [EMAIL PROTECTED]
web site: http://www.newworldwindpower.com









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Re: [Biofuel] Modification of cars to use biodiesel and insurance

2006-01-02 Thread Tim Hadland
Philip

   Leicestershire is in the middle of England, in the Midlands region. 
Where abouts are you in the US, it seems many biofuellers are over there.

  I am not going to make any modifications to start with. I was curious as 
to what the insurance company would say an they will do anything not to pay 
out if i were to make a claim, so i am careful about that.

   Cheers Tim



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Re: [Biofuel] Modification of cars to use biodiesel and insurance *#

2006-01-02 Thread YankeeTrader
Dear Tim,

 I am sure the U.S. Navy produces biodiesel at several locations.
I am afraid the San Diego Naval Base is the only one I can recall without
going to Google.

 Perhaps you should raise this issue with your management team --you 
could
 become a hero and spend the rest of your life as an idea man.

 Good luck !!!

Regards,

Wendell



Tim Hadland wrote:

  hello from leicestershire!

  I have just discussed the fact i am going to run my car on bio diesel with 
my insurance company. I have used Norwich union, and the pay as you drive 
option (i am in the merchant navy and dont use my car for 4 month periods 
and i am still a young driver)

  I wish ships used biodiesel, they use residual or heavy fuel oil - solid 
at room temperature. Nasty stuff, which gets treated through heating and 
settling, heating and purification - centrifuging out water and solids, and 
filtering at various stages before being burnt in the engine. Already and 
ideal set-up for using biodiesel. Would make work feel more healthy with 
reduced nasty fumes and probably much safer.

  Anyway back to insurance. I was told if i were to have any mod done to my 
fuel system such as a heated fuel filter it would have to be installed by a 
qualified and certified bio diesel installer !? None in Leicestershire, in 
fact i dont know of anyone in the midlands. I feel well qualified as a 
marine engineer.  Has anyone else had insurance probs with modifications?

   cheers, and happy new year for tmw.

  TIM  HADLAND



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[Biofuel] Better titration Question

2006-01-02 Thread Logan Vilas
In the better Titration Method I find it's easier to mix my stock solution
with 20grams in 500milliters distilled water. That gives .4% w/v lye
solution when 5ml is added to 45ml distilled water. By doing this I do not
have to divide the titration results. I haven't had any problems yet, but I
was wondering if anyone would know of a reason I shouldn't do it? Or if
there is anyone using this method?

Logan Vilas


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Re: [Biofuel] FW: Important, Congress set to gut renewable energy programs

2006-01-02 Thread Zeke Yewdall
It was all over the news here right before Christmas.  I haven't heard
anything since then -- I think the layoffs were going to start in
January though.

http://www.rockymountainnews.com/drmn/energy/article/0,2777,DRMN_23914_4328252,00.html
http://www.denverpost.com/news/ci_3327991
http://www.9news.com/acm_news.aspx?OSGNAME=KUSAIKOBJECTID=48957dfa-0abe-421a-0002-1de4979db745TEMPLATEID=0c76dce6-ac1f-02d8-0047-c589c01ca7bf
http://home.hamptonroads.com/stories/story.cfm?story=97438ran=116069



On 1/2/06, Greg Ocnos [EMAIL PROTECTED] wrote:



 Has anyone heard anything more about this? Did NREL get hit hard?

 Just looking for a follow up, who could I ask?



 Thanks




 Gregory I. Ocnos



 -Original Message-
  From: [EMAIL PROTECTED]
 [mailto:[EMAIL PROTECTED] On Behalf Of
 David M. Brockes
  Sent: Wednesday, November 16, 2005 5:47 PM
  To: Awea-Windnet; Biofuel; Renewable-Energy
  Subject: [Biofuel] FW: Important,Congress set to gut renewable energy
 programs
  Importance: High




 Follow-up.


 David







 -Original Message-
  From: Bob Anderson [mailto:[EMAIL PROTECTED]
  Sent: Wednesday, November 16, 2005 3:32 PM
  Subject: Re: Important, Congress set to gut renewable energy programs
  Importance: High

 I've just returned from a meeting at NREL (where I am a small contractor).
 The lab expects a 40% cut in the Wind Powering America program.

  Bob Anderson



  On 11/16/05 1:45 PM, Van Jamison [EMAIL PROTECTED] wrote:

 FYI
  - Original Message -
  From: Patrick Judge mailto:[EMAIL PROTECTED]
  To: [EMAIL PROTECTED] ; [EMAIL PROTECTED]
  Sent: Wednesday, November 16, 2005 7:50 AM
  Subject: Fwd: Important, Congress set to gut renewable energy programs

  Congress to Terminate National Bioenergy Center
  Congress is getting ready this week to terminate the National Bioenergy
  Research Center and gut the Wind Research Program at the National
 Renewable
  Energy Laboratory (NREL). NREL researchers who are CRES members sounded
 the
  alarm over the weekend after finding out on Friday that many of them may
 be
  out of work next month.
  
  Here is what I can piece together about what happened last week. On
 Tuesday
  the House of Representatives passed the House and Senate Conference
  Committee markup of the Energy Water and Development Appropriation Bill
 for
  2006.  The bill keeps federal funding for renewable energy research level
  with last year's spending.
  
  Unfortunately, it more than doubled the earmarks that take money out of
 the
  Wind Energy and Bioenergy Research Programs and direct it elsewhere.
  Earmarks are when individual representatives direct funding to particular
  projects in their districts. With passage of the Energy Bill earlier this
  year, these earmarks have been in the forefront of the news. In fact, the
  American Solar Energy Society said the Energy Bill was so full of pork
  barrel spending that ASES did not endorse it.
  
  Congressional leaders usually wait until the conference committee is
 meeting
  behind closed doors to introduce earmarks. They emerge as part of a much
  larger bill that is hundreds of pages long.
  
  It appears that in this case, the House of Representatives voted on this
  bill without many of
  its members having had time to read it.
  
  It took NREL staff a couple of days of read through the pile of paper and
  figure out what it will mean for the research programs. Some of the
 earmarks
  were listed together to support state initiatives, and others were buried
 in
  different portions of the massive spending bill. This year these added to
  $62 million in total, more than two thirds of the entire research and
  development budget for bioenergy. Then the staff had to calculate DOE's
  contractual obligations to its industry partnerships and the 10% cut that
  the agency takes from all programs to pay the salaries of its staff.
  
  Staff of the National Bioenergy Center, which number more than 90 people,
  were told Friday afternoon that all that the funding that would be left
 was
  sufficient only to cover their severance checks. The National Wind
  Technology Center is facing similar, severe cutbacks. It seems incredible,
  but Congress is getting ready to gut the two research programs in
 renewable
  energy technologies that have enjoyed the most success and commercial
  development just at a time when fossil fuel prices are their highest level
  in history. In the case of creating transportation fuels from biomass,
 these
  technologies represent our greatest near-term hope of
  reducing imports or fossil fuels.
  
  The Senate is scheduled to take up the appropriations bill today or
  tomorrow. Please call Senators Allard and Salazar today and ask them to
 vote
  no on the appropriations bill from the Energy and Water Committee. Tell
 them
  that renewable energy RD is one of this country's best investments.
  
  - Wayne Allard: call the Colorado office at 303-220-7414 or the Washington
  office at 

Re: [Biofuel] removing water from WVO

2006-01-02 Thread Mike Weaver
Wow - that's a lot of water - is there any other source of WVO near you?

Derick Giorchino wrote:

 I also had some trouble in the beginning. I now use a settling drum I 
 found the design on J T F and it works very well. I collect my wvo in 
 the wee hours on my way to work and have collected 20+ gal of water in 
 40 gal pickup. I drain the pure water out after a few hours of 
 settling then heat the balance to 120 f and drain it once more. The 
 separation drum has 2 drain valves one on the bottom and one about 6 
 inches off the bottom. That where I get a nice clean product fro 
 processing. It may seem that the energy used is a waste but I find it 
 is better than 120 liters of failure.

 Good luck Derick

  

 

 *From:* [EMAIL PROTECTED] 
 [mailto:[EMAIL PROTECTED] *On Behalf Of *Lee Eady, 
 D.C.
 *Sent:* Monday, January 02, 2006 12:05 PM
 *To:* Biofuel@sustainablelists.org
 *Subject:* [Biofuel] removing water from WVO

  

 I am just getting started making BD.  I have had some trouble getting 
 all the water removed from the WVO.  Is it a must to heat the oil if 
 so how hot, how long?  Will it settle out on its own if just sits if 
 so how long do I need to let it settle? Any info will be appreciated.



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Re: [Biofuel] removing water from WVO

2006-01-02 Thread Mike Weaver
Hi Lee,

I've found it easier to switch to a better WVO source than to fiddle too 
much de-watering.  That said, heat and time will work.

Lee Eady, D.C. wrote:



 I am just getting started making BD.  I have had some trouble getting 
 all the water removed from the WVO.  Is it a must to heat the oil if 
 so how hot, how long?  Will it settle out on its own if just sits if 
 so how long do I need to let it settle? Any info will be appreciated.



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Re: [Biofuel] Better titration Question

2006-01-02 Thread Ken Provost

On Jan 2, 2006, at 3:33 PM, Logan Vilas wrote:

 In the better Titration Method I find it's easier to mix my stock  
 solution
 with 20grams in 500milliters distilled water.


OK -- we now have 4% NaOH soln.


 That gives .4% w/v lye solution when 5ml is added to 45ml distilled  
 water.


Yes, if you add 5ml of your 4% soln. to 45ml of water, you get a
0.4% solution. This is still 4 times the concentration that everyone
else uses.


 By doing this I do not have to divide the titration results.


I don't understand what you mean by this. When using a 0.1% soln.,
the number of milliliters of soln. needed to neutralize 1ml of oil is
equal to the number of grams NaOH which must be added to the
usual 3.5g per liter of oil. With your 4X solution, you will achieve
neutrality at only 1/4 as many milliliters of solution, and thus will
need to multiply by four to calculate the proper excess of NaOH.


 I haven't had any problems yet, but I was wondering if anyone
 would know of a reason I shouldn't do it?


As long as you make the proper multiplication by four, your solution
will work fine.


 Or if there is anyone using this method?


I can't see why anyone would.


-K

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Re: [Biofuel] removing water from WVO

2006-01-02 Thread Derick Giorchino
Yes there is but the titration is off the charts. This has only happened 2
times since I have been doing this about 2 years. And the wvo is normally a
very good quality. Titration at about 2 or 2.25 + the 3.5. As apposed to the
9 to 14 + 3.5 I started with. 
I was advised to not eat at those places. I haven't been back for a FFA
dinner or stock for the process.
I didn't mention before but the settling tank also has the advantage of
settling out the goop you need to filter out for processing. It seems to be
heavier than the oil. This gives me wvo that looks like tan salad oil clear
and clean, I haven't had a failed batch since. Oops I may have just jinxed
myself.  
It seems that the food particles also hold a large amount of water that will
make it harder to process.

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Mike Weaver
Sent: Monday, January 02, 2006 6:56 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] removing water from WVO

Wow - that's a lot of water - is there any other source of WVO near you?

Derick Giorchino wrote:

 I also had some trouble in the beginning. I now use a settling drum I 
 found the design on J T F and it works very well. I collect my wvo in 
 the wee hours on my way to work and have collected 20+ gal of water in 
 40 gal pickup. I drain the pure water out after a few hours of 
 settling then heat the balance to 120 f and drain it once more. The 
 separation drum has 2 drain valves one on the bottom and one about 6 
 inches off the bottom. That where I get a nice clean product fro 
 processing. It may seem that the energy used is a waste but I find it 
 is better than 120 liters of failure.

 Good luck Derick

  

 

 *From:* [EMAIL PROTECTED] 
 [mailto:[EMAIL PROTECTED] *On Behalf Of *Lee Eady, 
 D.C.
 *Sent:* Monday, January 02, 2006 12:05 PM
 *To:* Biofuel@sustainablelists.org
 *Subject:* [Biofuel] removing water from WVO

  

 I am just getting started making BD.  I have had some trouble getting 
 all the water removed from the WVO.  Is it a must to heat the oil if 
 so how hot, how long?  Will it settle out on its own if just sits if 
 so how long do I need to let it settle? Any info will be appreciated.



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Re: [Biofuel] removing water from WVO

2006-01-02 Thread JJJN
Funny you mention this Derick,
I have two sources one gives me 2.5 gallons of water per 5 gallons of 
grease but it is like virgin oil when its cleaned up. My other source 
gives me the oil in clean dry 5 gallon containers with caps but the 
FFA's are really high.  It certainly would be an eye opener for those 
folks that eat the French fries and onion rings if they only knew  
or are they just brave Hm.
Jim

Derick Giorchino wrote:

Yes there is but the titration is off the charts. This has only happened 2
times since I have been doing this about 2 years. And the wvo is normally a
very good quality. Titration at about 2 or 2.25 + the 3.5. As apposed to the
9 to 14 + 3.5 I started with. 
I was advised to not eat at those places. I haven't been back for a FFA
dinner or stock for the process.
I didn't mention before but the settling tank also has the advantage of
settling out the goop you need to filter out for processing. It seems to be
heavier than the oil. This gives me wvo that looks like tan salad oil clear
and clean, I haven't had a failed batch since. Oops I may have just jinxed
myself.  
It seems that the food particles also hold a large amount of water that will
make it harder to process.

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Mike Weaver
Sent: Monday, January 02, 2006 6:56 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] removing water from WVO

Wow - that's a lot of water - is there any other source of WVO near you?

Derick Giorchino wrote:

  

I also had some trouble in the beginning. I now use a settling drum I 
found the design on J T F and it works very well. I collect my wvo in 
the wee hours on my way to work and have collected 20+ gal of water in 
40 gal pickup. I drain the pure water out after a few hours of 
settling then heat the balance to 120 f and drain it once more. The 
separation drum has 2 drain valves one on the bottom and one about 6 
inches off the bottom. That where I get a nice clean product fro 
processing. It may seem that the energy used is a waste but I find it 
is better than 120 liters of failure.

Good luck Derick

 



*From:* [EMAIL PROTECTED] 
[mailto:[EMAIL PROTECTED] *On Behalf Of *Lee Eady, 
D.C.
*Sent:* Monday, January 02, 2006 12:05 PM
*To:* Biofuel@sustainablelists.org
*Subject:* [Biofuel] removing water from WVO

 

I am just getting started making BD.  I have had some trouble getting 
all the water removed from the WVO.  Is it a must to heat the oil if 
so how hot, how long?  Will it settle out on its own if just sits if 
so how long do I need to let it settle? Any info will be appreciated.



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messages):
  

http://www.mail-archive.com/biofuel@sustainablelists.org/

 






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Re: [Biofuel] Better titration Question

2006-01-02 Thread Logan Vilas
Ken

When using the better titration method I'm using 4ml oil and 40ml Isopropyl.


As per the method on JTF you do that then divide by 4. I am just multiplying
the lye solution by 4 before doing the titration to remove the step of
dividing in the end.

I should have said the proportions of my titration ahead of time.

Logan Vilas


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Ken Provost
Sent: Monday, January 02, 2006 9:10 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] Better titration Question


On Jan 2, 2006, at 3:33 PM, Logan Vilas wrote:

 In the better Titration Method I find it's easier to mix my stock  
 solution
 with 20grams in 500milliters distilled water.


OK -- we now have 4% NaOH soln.


 That gives .4% w/v lye solution when 5ml is added to 45ml distilled  
 water.


Yes, if you add 5ml of your 4% soln. to 45ml of water, you get a
0.4% solution. This is still 4 times the concentration that everyone
else uses.


 By doing this I do not have to divide the titration results.


I don't understand what you mean by this. When using a 0.1% soln.,
the number of milliliters of soln. needed to neutralize 1ml of oil is
equal to the number of grams NaOH which must be added to the
usual 3.5g per liter of oil. With your 4X solution, you will achieve
neutrality at only 1/4 as many milliliters of solution, and thus will
need to multiply by four to calculate the proper excess of NaOH.


 I haven't had any problems yet, but I was wondering if anyone
 would know of a reason I shouldn't do it?


As long as you make the proper multiplication by four, your solution
will work fine.


 Or if there is anyone using this method?


I can't see why anyone would.


-K



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Re: [Biofuel] Crude palm oil

2006-01-02 Thread Arttu Aula
http://www.journeytoforever.org/biodiesel_yield.html

The chart there says 5950 l/ha from oil palm.

Googling oil palm cultivation came up with this site (among many others):
http://www.fao.org/documents/show_cdr.asp?url_file=/DOCREP/006/T0309E/T0309E01.htm

leave 7.8 meters between rows and 9 metres between pegs.
In this way you can plant 143 oil palms per hectare; this is the best density.

Are you plannning on growing these things?

-Arttu


On 1/2/06, Courtney Blodgett [EMAIL PROTECTED] wrote:
 Hi!  I'm trying to figure out biodiesel yield from palm trees.  Does anyone
 know how much crude oil a palm tree can yield annually?  How many palm trees
 are normally planted per hectare?



 Thanks!

 Courtney




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[Biofuel] Oooops! to much acid

2006-01-02 Thread mick . ellis
Hi Guys.
I was hoping this day would never come.

I’ve been making Bio from WVO for over 12 months now with great success
using the standard Base catalyst method.

I run it in my 1992 80 series Toyota Land Cruiser with about 340,000 Km on
the clock and she purrs like a Kitten.

I find the web site an excellent wealth of knowledge and a great place to
learn the different theories and ideas from other like minded soles.
Up until now reading and re reading this info has been of great assistance
to me when in doubt/trouble, however this time I’ve ended up with 180
liters of Bio with a PH of  5.8. after stuffing up the calculations with
the acid quench in the wash water.

I now find myself with a self induced problem with this latest batch and I
would like to ask the mailing list for advice so I can go on my annual
camping trip and not have to pay $1.30/Litre at the pump here in Sydney.

I have done a tritation of the washed bio and it gave me a 0.075 tritation
as per the 'Better tritation method. I'm concerned that I have converted
some of the Bio back to FFA's.

My questions are:-
 A. Is this enough catalist to neutralize the acid?
 B. If so how much Methanol should I use for the reaction?
 C. Is this the best method to bring this batch back to PH 7?


Thanks
Mick Ellis



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