Re: [Biofuel] Convert your Microwave oven to make Colloidal Silver

2007-02-06 Thread Logan vilas
Joe

Maybe it helps to know the voltage (capacitors come in many sizes), but if
they make a 3500 volt meter I could definitely get one to use. I know
several offshore electricians who deal with that level of volts and even
higher. That would involve having the microwave pulled apart to see what it
says. I am very familiar working with 440 3 phase, I used to work for a navy
contractor and that's what they gave us for supply power to our equipment.
As for the leads, if the meter is rated for the voltage then I'd be pretty
sure the leads would sustain it. I could easily be wrong I have no formal
training in electronics. I was not aware of dirt allowing the charge to
pass. And I know they COULD have enough electricity to provide another
discharge, but if you are doing something stupid like pulling a microwave
apart in the first place that would be a good first step toward safety.
Notice I said most if not all it would depend on a lot of factors. 

To be honest I have a 5kv megger that has a meter display on it. I know it
will jump if it is plugged into a hot electrical source. I'd be willing to
try that to see if it displays. I'd be cautious of the handle possible
spinning; otherwise leaving it on the capacitor would possible draw the
remaining power out of it.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Joe Street
Sent: Monday, February 05, 2007 3:18 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Convert your Microwave oven to make Colloidal Silver

See! See!  A quick test will a meter might leave you lying on the floor 
witrh your heart all a twitter.  What meter will you use to check 3500 V 
DC?  What voltage are the leads good for?  Did you know that even dirt 
on the outside of the lead wires can be enough of a conductive path to 
let the discharge flow right down the surface to your hands?  No 
probably not.  And it would not be something intuitively obvious to 
anyone who has not been trained how to work with HV. Because it is not 
obvious and everyone has to be taught these things.  Did you know that 
the dielectric in a HV capacitor will usually recharge itself quite 
significantly after a single discharge?  It is also a naive assumption 
that pulling the plug will leave the cap discharged.
No offence to you Logan, but your post just serves to illustrate my point.

Joe

Logan vilas wrote:

If turn on the microwave and pull the plug while it's running that would
discharge most if not all of the power in the capacitor I would think. A
quick test from a meter would verify if it still had power or not.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Kirk McLoren
Sent: Monday, February 05, 2007 2:19 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Convert your Microwave oven to make Colloidal Silver

I think the commercial process was the Katadyne process. You pull an arc
between two silver electrodes under distilled water and filter the result
since you will have a mix of sizes. I think they use something around 30 to
60 volts. High amperage as you want a plasma. When it goes out you
restrike.
 
Kirk

D. Mindock [EMAIL PROTECTED] wrote:

   Hi Joe,
  I would bring the oven to a shop that routinely repairs them to
have that capacitor discharged safely. The thing with
   using the oven's electronics (no magnetron needed) was the very high
rate of production of CS. Also, it is a higher use of the oven as they do
change the characteristics of protein into something dangerous, i.e.,
carcinogenic. My wife thinks they're a godsend. I can't convince her of
their intrinsic danger. I've told her that when the damn thing goes bad
that
I am not replacing it. Myself, I don't use it, even for heating water,
since
it changes the structure of the water. The microwave
   oven is another modern marvel that has lessened life.
   If CS is made with distilled water in a constant current device
using four nines (99.99%) or better pure silver, it will be safe to
consume.
I use it to stop the progression of periodontal disease. I have a bad case
of it. Also am using ozonated
   water. I have no problem with killing of friendly gut flora, but I
do take a good probiotic to hedge my bets. 
   Peace, D. Mindock

   - Original Message - 
   From: Joe Street mailto:[EMAIL PROTECTED]  
   To: biofuel@sustainablelists.org 
   Sent: Thursday, February 01, 2007 12:55 PM
   Subject: Re: [Biofuel] Convert your Microwave oven to make
Colloidal Silver

   OMG please don't do this!
   The capacitor in a microwave oven contains several joules of
energy!  This is sufficient to kill you and has done to more than one
unsuspecting soul who has decided to tinker around inside the microwave
oven.  The article below even goes to the extent of warning you to
discharge
the cap before doing any

Re: [Biofuel] Convert your Microwave oven to make Colloidal Silver

2007-02-05 Thread Logan vilas
If turn on the microwave and pull the plug while it's running that would
discharge most if not all of the power in the capacitor I would think. A
quick test from a meter would verify if it still had power or not.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Kirk McLoren
Sent: Monday, February 05, 2007 2:19 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Convert your Microwave oven to make Colloidal Silver

I think the commercial process was the Katadyne process. You pull an arc
between two silver electrodes under distilled water and filter the result
since you will have a mix of sizes. I think they use something around 30 to
60 volts. High amperage as you want a plasma. When it goes out you restrike.
 
Kirk

D. Mindock [EMAIL PROTECTED] wrote:

Hi Joe,
   I would bring the oven to a shop that routinely repairs them to
have that capacitor discharged safely. The thing with
using the oven's electronics (no magnetron needed) was the very high
rate of production of CS. Also, it is a higher use of the oven as they do
change the characteristics of protein into something dangerous, i.e.,
carcinogenic. My wife thinks they're a godsend. I can't convince her of
their intrinsic danger. I've told her that when the damn thing goes bad that
I am not replacing it. Myself, I don't use it, even for heating water, since
it changes the structure of the water. The microwave
oven is another modern marvel that has lessened life.
If CS is made with distilled water in a constant current device
using four nines (99.99%) or better pure silver, it will be safe to consume.
I use it to stop the progression of periodontal disease. I have a bad case
of it. Also am using ozonated
water. I have no problem with killing of friendly gut flora, but I
do take a good probiotic to hedge my bets. 
Peace, D. Mindock

- Original Message - 
From: Joe Street mailto:[EMAIL PROTECTED]  
To: biofuel@sustainablelists.org 
Sent: Thursday, February 01, 2007 12:55 PM
Subject: Re: [Biofuel] Convert your Microwave oven to make
Colloidal Silver

OMG please don't do this!
The capacitor in a microwave oven contains several joules of
energy!  This is sufficient to kill you and has done to more than one
unsuspecting soul who has decided to tinker around inside the microwave
oven.  The article below even goes to the extent of warning you to discharge
the cap before doing any assembly work but then it goes on at the end in
bold red saying the danger is not in operating the beast but in its
construction.  It doesn't say anythingabout how you are supposed to
discharge the cap before you try to remove the electrode from the jar!  

Trust me colloidal siver can be easily made using voltage as
low as 20 volts and with current limiting.  It will take a little longer (15
minutes) to make a batch ( I do half a litre at a time)  but current
limiting is important because it keeps particle size down in the low
nanometer range where it needs to be in order to make a good colloid.  I use
a little wall wart type transformer for this.  Half a litre IS high volume.
Considering that the most effective way to use the stuff is to put it in a
nasal sprayer and use it directly on ther mucous linings at THE FIRST SIGN
of a sore throat ( not effective at later stages) and you are using perhaps
1ml at a time, half a litre will last your entire family a year or more.
DON'T drink the stuff unless you want to kill off beneficial bacteria in
your GI tract.  Pink eye is easily and quickly cured with repeated misting
of the open eye, but again it is working on contact.  There are many other
uses for the stuff which I won't get into but it is basically a powerful
anit-bacterial which works on contact against single celled organisms.  

The internals of microwave ovens are extremely unforgiving
and even for the initiated there is no room for error or absent mindedness.

Joe

D. Mindock wrote:


Build Your Own High-Volume Colloidal Silver Maker


You want a plague-ready machine that'll make about
40 quarts of strong Colloidal Silver an hour, that you can easily build in
an hour for about $38?? I've built many now for people and I'll tell you how
to make yours. 

This is about the simplest colloidal silver maker
you could build. The unit makes 1 liter of roughly 40 PPM CS in 1.5 minutes
or less using reverse osmosis water; with this kind of power, continuous
production is possible with a spaghetti tube adding and removing water at a
trickle. The primarily ionic silver

Re: [Biofuel] Splenda Explodes Internally, Says Chemist

2007-01-14 Thread Logan Vilas
Yeah, I guess my mind was not working I see that now.
Thanks
Loagn

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of D. Mindock
Sent: Sunday, January 14, 2007 7:05 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Splenda Explodes Internally, Says Chemist


Let's see. If it cost each American one dollar per year that'd be 
300,000,000
dollars annually. I think your math is a little off.
Peace, D. Mindock


 Not trying to be too much of a smartass, but
 300 million Americans, 187 million annually
 =623 thousand per an American annually

 That's a little off somewhere.
 Logan Vilas
 -Original Message-
 From: [EMAIL PROTECTED]
 [mailto:[EMAIL PROTECTED] On Behalf Of D. Mindock
 Sent: Friday, January 12, 2007 11:34 PM
 To: Undisclosed-Recipient:;
 Subject: [Biofuel] Splenda Explodes Internally, Says Chemist

 Splenda Explodes Internally, Says Chemist

 By Shane Ellison, M.Sc.

 Copyright 2006C _www.healthmyths.net http://www.healthmyths.net/
 http://www.healthmyths.net/ _

 NewsWithViews.com

 1-11-7

 If there were a contest for the best example of total disregard for
 human life, the victor would be McNeil Nutritionals---makers of
 Splenda^(TM). Manufacturers of Vioxx^(TM) and Lipitor^(TM) would tie for
 a very distant second.

 McNeil Nutritionals is the undisputed drug-pushing champion for
 disguising their drug Splenda as a sweetener.

 Regardless of its drug qualities and potential for side effects, McNeil
 is dead set on putting it on every kitchen table in America. Apparently,
 Vioxx and Lipitor makers can't stoop so low as to deceptively masquerade
 their drug as a candy of sort. There is no question that their products
 are drugs and by definition come with negative side effects. Rather than
 sell directly to the consumer, these losers have to go through the
 painful process of using doctors to prescribe their dangerous goods.

 A keen student in corporate drug dealing, McNeil learned from aspartame
 and saccharine pushers that if a drug tastes sweet, then let the masses
 eat it in their cake. First though, you have to create a facade of
 natural health. They did this using a cute trade name that kind of
 sounds like splendid and packaged it in pretty colors. Hypnotized, the
 masses were duped instantly. As unquestionably as a dog humps your leg,
 millions of diabetics (and non-diabetics) blindly eat sucralose under
 the trade name Splenda in place of real sugar (sucrose).

 Splenda was strategically released on April fool's day in 1998. This day
 is reserved worldwide for hoaxes and practical jokes on friends and
 family, the aim of which is to embarrass the gullible. McNeil certainly
 succeeded.

 The splendid Splenda hoax is costing gullible Americans $187 million
 annually*^1 *. While many people wonder about the safety of Splenda,
 they rarely question it. Despite its many unknowns and inherent
 dangers, Splenda demand has grown faster than its supply. No longer do I
 have to question my faith in fellow Man. He is not a total idiot, just a
 gullible one. McNeil jokesters are laughing all the way to the bank.

 Splenda is not as harmless as McNeil wants you to believe. A mixture of
 sucralose, maltodextrine, and dextrose (a detrimental simple sugar),
 each of the not-so-splendid Splenda ingredients has downfalls. Aside
 from the fact that it really isn't sugar and calorie free, here is one
 big reason to avoid the deceitful mix . . . think April fool's day:

 Splenda contains a potential poison---the drug sucralose. This chemical
 is 600 times sweeter than sugar. To make sucralose, chlorine is used.
 Chlorine has a split personality. It can be harmless or it can be life
 threatening.

 In combo with sodium, chlorine forms a harmless ionic bond to yield
 table salt. Sucralose makers often highlight this worthless fact to
 defend its safety. Apparently, they missed the second day of Chemistry
 101---the day they teach covalent bonds.

 When used with carbon, the chlorine atom in sucralose forms a covalent
 bond. The end result is the historically deadly organochlorine or
 simply: a Really-Nasty Form of Chlorine (RNFOC).

 Unlike ionic bonds, covalently bound chlorines are a big no-no for the
 human body. They yield insecticides, pesticides, and herbicides---not
 something you want in the lunch box of your precious child. It's
 therefore no surprise that the originators of sucralose, chemists Hough
 and Phadnis, were attempting to design new insecticides when they
 discovered it! It wasn't until the young Phadnis accidentally tasted his
 new insecticide that he learned it was sweet. And because sugars are
 more profitable than insecticides, the whole insecticide idea got canned
 and a new sweetener called Splenda got packaged.

 To hide its origin, Splenda pushers assert that sucralose is made from
 sugar so it tastes like sugar. Sucralose is as close to sugar as
 Windex^(TM) is to ocean water.

 The RNFOC poses a real and present danger

Re: [Biofuel] Splenda Explodes Internally, Says Chemist

2007-01-13 Thread Logan Vilas
Not trying to be too much of a smartass, but
300 million Americans, 187 million annually
=623 thousand per an American annually

That's a little off somewhere. 
Logan Vilas
-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of D. Mindock
Sent: Friday, January 12, 2007 11:34 PM
To: Undisclosed-Recipient:;
Subject: [Biofuel] Splenda Explodes Internally, Says Chemist

Splenda Explodes Internally, Says Chemist

By Shane Ellison, M.Sc.

Copyright 2006C _www.healthmyths.net http://www.healthmyths.net/
http://www.healthmyths.net/ _

NewsWithViews.com

1-11-7

If there were a contest for the best example of total disregard for 
human life, the victor would be McNeil Nutritionals---makers of 
Splenda^(TM). Manufacturers of Vioxx^(TM) and Lipitor^(TM) would tie for 
a very distant second.

McNeil Nutritionals is the undisputed drug-pushing champion for 
disguising their drug Splenda as a sweetener.

Regardless of its drug qualities and potential for side effects, McNeil 
is dead set on putting it on every kitchen table in America. Apparently, 
Vioxx and Lipitor makers can't stoop so low as to deceptively masquerade 
their drug as a candy of sort. There is no question that their products 
are drugs and by definition come with negative side effects. Rather than 
sell directly to the consumer, these losers have to go through the 
painful process of using doctors to prescribe their dangerous goods.

A keen student in corporate drug dealing, McNeil learned from aspartame 
and saccharine pushers that if a drug tastes sweet, then let the masses 
eat it in their cake. First though, you have to create a facade of 
natural health. They did this using a cute trade name that kind of 
sounds like splendid and packaged it in pretty colors. Hypnotized, the 
masses were duped instantly. As unquestionably as a dog humps your leg, 
millions of diabetics (and non-diabetics) blindly eat sucralose under 
the trade name Splenda in place of real sugar (sucrose).

Splenda was strategically released on April fool's day in 1998. This day 
is reserved worldwide for hoaxes and practical jokes on friends and 
family, the aim of which is to embarrass the gullible. McNeil certainly 
succeeded.

The splendid Splenda hoax is costing gullible Americans $187 million 
annually*^1 *. While many people wonder about the safety of Splenda, 
they rarely question it. Despite its many unknowns and inherent 
dangers, Splenda demand has grown faster than its supply. No longer do I 
have to question my faith in fellow Man. He is not a total idiot, just a 
gullible one. McNeil jokesters are laughing all the way to the bank.

Splenda is not as harmless as McNeil wants you to believe. A mixture of 
sucralose, maltodextrine, and dextrose (a detrimental simple sugar), 
each of the not-so-splendid Splenda ingredients has downfalls. Aside 
from the fact that it really isn't sugar and calorie free, here is one 
big reason to avoid the deceitful mix . . . think April fool's day:

Splenda contains a potential poison---the drug sucralose. This chemical 
is 600 times sweeter than sugar. To make sucralose, chlorine is used. 
Chlorine has a split personality. It can be harmless or it can be life 
threatening.

In combo with sodium, chlorine forms a harmless ionic bond to yield 
table salt. Sucralose makers often highlight this worthless fact to 
defend its safety. Apparently, they missed the second day of Chemistry 
101---the day they teach covalent bonds.

When used with carbon, the chlorine atom in sucralose forms a covalent 
bond. The end result is the historically deadly organochlorine or 
simply: a Really-Nasty Form of Chlorine (RNFOC).

Unlike ionic bonds, covalently bound chlorines are a big no-no for the 
human body. They yield insecticides, pesticides, and herbicides---not 
something you want in the lunch box of your precious child. It's 
therefore no surprise that the originators of sucralose, chemists Hough 
and Phadnis, were attempting to design new insecticides when they 
discovered it! It wasn't until the young Phadnis accidentally tasted his 
new insecticide that he learned it was sweet. And because sugars are 
more profitable than insecticides, the whole insecticide idea got canned 
and a new sweetener called Splenda got packaged.

To hide its origin, Splenda pushers assert that sucralose is made from 
sugar so it tastes like sugar. Sucralose is as close to sugar as 
Windex^(TM) is to ocean water.

The RNFOC poses a real and present danger to all Splenda users. It is 
risky because the RNFOC confers a molecule with a set of super powers 
that wreak havoc on the human body. For example, Agent Orange, used in 
the U.S. Army's herbicidal warfare program, is a RNFOC. Exposure can 
lead to Hodgkin's lymphoma and non-Hodgkin's lymphoma, as well as 
diabetes and various forms of cancer! Other shocking examples are the 
war gas phosgene, chlordane, and lindane*^2 *. The RNFOC is lethal 
because it allows poisons to be fat soluble

[Biofuel] ffa in biodiesel

2006-12-31 Thread Logan Vilas
After methanol recovery if acid was added it would split the soaps into ffa
and salts. Then washing should remove the salts and lower the acidity with
very little if any soap in the wash water. It might reduce washing to 1
cycle per a batch. And would be safer to dispose of because no soap just
salt and a slightly acidic ph.

 Would the ffa mixed with biodiesel be a problem?

I would imagine that since we burn ffa attached to methanol then ffa by
themselves should burn, and when mixed with biodiesel they should burn even
better.

Has anyone tried this or have any thoughts on it? I do acid/base method on
anything that titrates 3.0 or higher so my ffa level should be very low. 

Logan Vilas


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[Biofuel] Soap formation

2006-12-28 Thread Logan Vilas
If you have a complete reaction to biodiesel will soap form from the
biodiesel? I mean if you put lye and water into it would it form soap or
would it be incapable of forming soap?

Logan vilas


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Re: [Biofuel] Ethyl Esters (was Making Methanol)

2006-12-01 Thread Logan vilas
Doesn't castor oil absorb alcohol? If so the heat would cause the alcohol to
evaporate out of the water, but it would combine with the Castor oil. That
should raise the alcohol boiling point. Maybe once the Castor oil becomes
saturated with alcohol then any remaining alcohol would appear on the
surface. Also maybe raising the temp more but keeping it under water's
boiling point would cause it to boil out of the castor oil, but keep the
water below the castor.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Joe Street
Sent: Friday, December 01, 2006 8:23 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Ethyl Esters (was Making Methanol)

Hi Tom

Well I put a couple of bottles of my hooch in a flask and dumped enough
castor oil on top to form a layer about 2cm thick. Heated to 60 degrees C
and started to nod off while waiting for something to happen.  So I went to
bed and left the hot plate on overnight..well in the morning..I
crept downstairsfull of anticipation, like a child on Chritmas morning
and..there was this collosal.huge...disappointment.  There was
nothing interesting. Even though I had crossed my heart and hoped to die. So
I  reduced the oil layer to about 2mm to try again.  It is stormy here today
and the temperature controller I am using is digital and uses pulse control
for power modulation with a solid state relay.  I didn't feel comfortable
leaving the experiment running while I went to work in case of a surge on
the electrical which could result in the loss of the relay and the hot plate
then running full blast so I shut it down.  I'll try again over the weekend
if I can.  It looks like the diffusion rate of alcohol through the castor
oil is depressingly slow.  It may still work though but may require a lot of
time.  If so it might be a candidate for some type of solar heated affair
that you just let sit for days.  Dunno. It's no majik bullet at least.
Maybe seives is still the best bet. Haven't tried corn grits yet either

Joe

Thomas Kelly wrote:


Joe,
 What's the word?
 I've had my fingers, eyes,and heart (?) crossed for days now
.  on the edge of my seat, waiting a shivers for the results of the
castor oil screen/ pinot noir experiment. My fingers and eyes are holding up
but my heart is starting to cramp up.
 Encouraging? Discouraging? Inconclusive?
 
 If I recall correctly, any response with the term bat guano in
it means 
Sorry, I don't want to talk about it.
 Tom

- Original Message - 
From: Joe Street mailto:[EMAIL PROTECTED]  
To: biofuel@sustainablelists.org 
Sent: Monday, November 27, 2006 10:09 AM
Subject: Re: [Biofuel] Ethyl Esters (was Making Methanol)

Hi Tom;

Yes you got the idea I am thinking about.  I worked a bit on
the setup last night.  I've got some old pinot noir I made a few years back
( which is a difficult grape at the best of times) which is a bout a  on
the dryness scale.  I'll take a bottle or two and put it in a flask and pour
in some castor oil  which will float on the surface.  Since the flask
narrows at the top it won't take too much castor oil to form the barrier
layer.  I'll heat to just below the boiling point and see what happens.
Perhaps the alcohol molecules will drag some water with them as you said.
The only way to know is to find out.  In the very least I'll have some high
potency ethanol for making herbal tinctures. If I'm lucky I'll have dry
ethanol!!  Fingers crossed, eyes crossed, heart crossed, hoping to find
out.

Tirah
Joe

Thomas Kelly wrote:


Hi Joe,
 I didn't follow you when you wrote:
I am really curious about the castor oil trick.  I
wonder how to do it?  I think the methanol I have recovered is already over
90% pure and I think the castor oil would sink to the bottom.  If there was
a high percentage of water the oil would float on top and you could do
something like normal distillation through the oil layer evaporating pure
alcohol off the top of the oil layer and gradually removing it from the
water below.  I haven't done any experiments yet. Of course the goal is to
move to ethyl eventually as well.
 
 I thought the idea was to dissolve the
distilled alcohol in castor oil, then remove the water that does not
dissolve and then proceed to distill the alcohol from the castor oil.
 
This would require alcohol to be highly soluble
in castor oil (or a lot of castor oil). The more soluble, I think

Re: [Biofuel] Methanol Price Increase?

2006-11-22 Thread Logan vilas
My price went from 2.02 a gallon last month to 3.08 a gallon this month

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Andres Secco
Sent: Wednesday, November 22, 2006 7:51 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Methanol Price Increase?

Think methanol price is strongly dependant of natural gas price which is
linked to fuel prices.

- Original Message - 
From: Thomas Kelly mailto:[EMAIL PROTECTED]  
To: biofuel mailto:Biofuel@sustainablelists.org  
Sent: Wednesday, November 22, 2006 10:14 AM
Subject: [Biofuel] Methanol Price Increase?

Hello All,
 Did I miss the news?
 Has there been a significant increase in the price of methanol
recently?

 I just got the bill for a delivery (two  55gal barrels).
Previous price ( July): $2.60 USD/gallon; current bill: $3.54 USD/ gallon
  35% increase in a few months?
 I'll call my supplier in a little while ...  maybe it's just a
billing mistake. I am just hoping someone has some info.  
 
   Thanks,
 Tom







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[Biofuel] A.O.C.S. glycerol method

2006-11-04 Thread Logan Vilas
Does anyone here, know or have acess to the AOCS method for determing total
glycerine? If you do could you tell me how to perform it?

Logan Vilas


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[Biofuel] NREL Bio-Diesel Analytical Methods August 2002-Jan 2004.

2006-10-31 Thread Logan vilas
This Is a Huge Information Resource. Anyone interested in doing some better
home testing with minimal investment should look at this. Or just if you're
interested in what is happening when ASTM testing occurs. 

Logan Vilas


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[Biofuel] Bio-Diesel Slogan any thoughts

2006-10-27 Thread Logan vilas
Bio-Diesel, Runs more like petro-Diesel.
Just Without belching out black smoke and without the chemical smell.

Logan Vilas


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Re: [Biofuel] new alcohol ideas

2006-10-12 Thread Logan vilas
Would glycerin dissolve in the castor oil or not? If not then castor oil
added to glycerin cocktail should cause the methanol to dissolve in it and
then the methanol can be recovered water free from the castor oil instead of
separating it from the glycerin. It would take much less energy to recover
it in that method. Verses cooking it out of the glycerin.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of bob allen
Sent: Saturday, September 30, 2006 2:16 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] new alcohol ideas

Howdy Jason, there would be no advantage.  In the ethanol/water/castor oil
scheme, one mixes E/W/C. 
only ethanol dissolves in the castor oil.  then heating the C/E mix to about
80 degrees C separates 
the ethanol from the castor oil.

what this does is get around the problem of the azeotrope of ethanol/water
which is the lowest 
boiling component of a mix of water/ethanol.  You can't separate the last 5%
of water from ethanol 
via distillation.

for glycerin this isn't an issue, just heat the stuff to close to 300
degrees C. anything that boils 
off at a lower temp is impurity, after is glycerin. (short form of
discussion)


Jason Katie wrote:
 i just had a bizarre idea. someone please argue with me on this, but if 
 glycerine is categorized as an alcohol, would it work to use castor oil to

 purify it, the same as ethanol? ideas?comments?
 Jason
 ICQ#:  154998177
 MSN:  [EMAIL PROTECTED] 
 
 
 


-- 
Bob Allen, http://ozarker.org/bob
=
The modern conservative is engaged in one of Man's oldest exercises in moral
philosophy; that is, 
the search for a superior moral justification for selfishness  JKG

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Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

2006-09-21 Thread Logan vilas
I know nothing about buildings like that, most of my work involved things
going down into the water, not up. But thanks for the heads up.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of [EMAIL PROTECTED]
Sent: Wednesday, September 20, 2006 7:06 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

Quoting Logan vilas [EMAIL PROTECTED]:

 It's amazing that the Weight of the airplane alone was enough to not cause
 the building to collapse in my opinion.

Without going into the nity grity of structural design, dead load,  
live load, second order effect, dynamics, load factoring, material  
capacity reduction etc etc, take my word for it, if the fire hadn't  
happened, the building would have hardly noticed the impact. Repairs  
would have taken 6 months and then you would probably not even know  
the impact had happened.

 Andrew


 Logan Vilas

 -Original Message-
 From: [EMAIL PROTECTED]
 [mailto:[EMAIL PROTECTED] On Behalf Of robert and
benita
 rabello
 Sent: Wednesday, September 20, 2006 3:35 PM
 To: biofuel@sustainablelists.org
 Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

 Kirk McLoren wrote:

[snip]


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Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

2006-09-21 Thread Logan vilas
Hey Terry, 

The first thing I said is there is a ton of very suspicious
unanswered questions, but I was just saying I can understand how the
building would have gotten hot enough to have molten steel. A lot of shit
happened that day that no one wants to be let out. Right down to the people
who were in the tower steeling money from their businesses and disappearing
forever. The money was thought to be incinerated or lost in the rubble, and
the same for the people. 


Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Terry Dyck
Sent: Wednesday, September 20, 2006 1:08 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

Hi Logan,

What about the building that was not hit by a jet, the building that housed 
all of the investigative people who were close to exposing a stock market 
cover up, it fell to the ground just like the twin towers?

Terry Dyck


From: Logan vilas [EMAIL PROTECTED]
Reply-To: biofuel@sustainablelists.org
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11
Date: Wed, 20 Sep 2006 08:27:47 -0500


D. Mindock,

   I agree with you for the most part there are a ton of very
suspicious unanswered questions. There are 2 things you say that I can
understand and contradict. I don't know how hot the temps were recorded in
the rubble. So you might prove me wrong, but with decent airflow and enough
fuel anything can create very hot temps. I do metal casting I've been doing
it for about 3 years now in my backyard. Look up the Dave gingery book
series or even Lindsey books. When I started I used 1 thick fence boards
cut into 4-6 x6 sections. 3 at a time in my firepot, with a blow drier
feeding it air and that was enough heat to melt steel reliably. It took
about 1/2 hour and 9-12 pieces of wood to melt 12LB's of steel to a
reasonable casting tempeture. 2700F or better.

   The towers would have had huge ventilation shafts running up and
down, it also had 8 elevator shafts if I remember right. A plane holds
thousands of gallons of fuel, then the building it crashed into was at 
least
half burnable material between desks, paper, and all the other stuff 
inside.
That stuff is spread out with a large room for airflow around it causing it
to burn fast and extremely hot. Heat rises up those shafts and it sucks air
into the bottom of the fire and in the side that the plane entered. The 
best
places to give the fire fuel. Those temps could have easily been 3000F or
higher. Then even if the temps were not that high. Look at house fires. The
temp of wood on fire is about 300f. But once it has that heat input for 
long
enough the room will reach temps of 1200f making the room flash over and
everything in it burns. The World Trade Center towers would have kept that
temp in as the fires sucked in air. The floors above the fire would have
gradually taken in BTU's with out anything to cool them off until the metal
melted.

   In the end with a big pile of rubble you can speculate what
happened, but you just won't know unless you were there and saw it happen
yourself. You also have to ask. If you don't believe what they're telling
you about how it fell, or secondary explosions, then why do you even 
believe
them when they say there's molten metal in the rubble or when they tell you
how high the rubble temps were. For that matter Why do you believe that
planes hit them at all.

Logan Vilas


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of D. Mindock
Sent: Wednesday, September 20, 2006 3:27 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

Robert,
The towers and bldg 7 are just part of a larger puzzle. You want to
believe the
buildings all fell down the same exact way, go ahead. But what of the
numerous
explosions throughout the buildings after they were hit by the airliners 
and

before
they fell? What about the molten steel found in the basement? What about 
the
puffs of smoke on the floor levels below the falling floors above? What
about the
very high temperatures recorded in the rubble, much higher than jet fuel is
capable?
Why did bldg 7 fall in the same manner as the towers even though its
construction
was not the same as the towers? Your Occam's Razor is being severely
overused.
And the towers were a minor part of 9/11's strange occurances. What about
Able
Danger? Why was this info ignored by the 9/11 Commission? Etc., etc. You
need
to look at the whole series of bizarre dots to get the whole picture.
Peace, D. Mindock

- Original Message -
From: robert and benita rabello [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, September 19, 2006 7:43 PM
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11


  Kirk McLoren wrote:
 
  To fall straight down means the failures supposedly caused by heat all
  happened at the same time. In the real world they lean

Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

2006-09-20 Thread Logan vilas

D. Mindock,

I agree with you for the most part there are a ton of very
suspicious unanswered questions. There are 2 things you say that I can
understand and contradict. I don't know how hot the temps were recorded in
the rubble. So you might prove me wrong, but with decent airflow and enough
fuel anything can create very hot temps. I do metal casting I've been doing
it for about 3 years now in my backyard. Look up the Dave gingery book
series or even Lindsey books. When I started I used 1 thick fence boards
cut into 4-6 x6 sections. 3 at a time in my firepot, with a blow drier
feeding it air and that was enough heat to melt steel reliably. It took
about 1/2 hour and 9-12 pieces of wood to melt 12LB's of steel to a
reasonable casting tempeture. 2700F or better.

The towers would have had huge ventilation shafts running up and
down, it also had 8 elevator shafts if I remember right. A plane holds
thousands of gallons of fuel, then the building it crashed into was at least
half burnable material between desks, paper, and all the other stuff inside.
That stuff is spread out with a large room for airflow around it causing it
to burn fast and extremely hot. Heat rises up those shafts and it sucks air
into the bottom of the fire and in the side that the plane entered. The best
places to give the fire fuel. Those temps could have easily been 3000F or
higher. Then even if the temps were not that high. Look at house fires. The
temp of wood on fire is about 300f. But once it has that heat input for long
enough the room will reach temps of 1200f making the room flash over and
everything in it burns. The World Trade Center towers would have kept that
temp in as the fires sucked in air. The floors above the fire would have
gradually taken in BTU's with out anything to cool them off until the metal
melted.

In the end with a big pile of rubble you can speculate what
happened, but you just won't know unless you were there and saw it happen
yourself. You also have to ask. If you don't believe what they're telling
you about how it fell, or secondary explosions, then why do you even believe
them when they say there's molten metal in the rubble or when they tell you
how high the rubble temps were. For that matter Why do you believe that
planes hit them at all.

Logan Vilas


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of D. Mindock
Sent: Wednesday, September 20, 2006 3:27 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

Robert,
   The towers and bldg 7 are just part of a larger puzzle. You want to 
believe the
buildings all fell down the same exact way, go ahead. But what of the 
numerous
explosions throughout the buildings after they were hit by the airliners and

before
they fell? What about the molten steel found in the basement? What about the
puffs of smoke on the floor levels below the falling floors above? What 
about the
very high temperatures recorded in the rubble, much higher than jet fuel is 
capable?
Why did bldg 7 fall in the same manner as the towers even though its 
construction
was not the same as the towers? Your Occam's Razor is being severely 
overused.
And the towers were a minor part of 9/11's strange occurances. What about 
Able
Danger? Why was this info ignored by the 9/11 Commission? Etc., etc. You 
need
to look at the whole series of bizarre dots to get the whole picture.
Peace, D. Mindock

- Original Message - 
From: robert and benita rabello [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Tuesday, September 19, 2006 7:43 PM
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11


 Kirk McLoren wrote:

 To fall straight down means the failures supposedly caused by heat all
 happened at the same time. In the real world they lean  to the failed
 side and then forces cause more failures. It is a very tricky business
 making them fall straight down.


But the dust prevented observers from actually witnessing the manner
 in which the lower floors fell.  Additionally, ALL of the force that
 destroyed the towers came from the mass of upper floor falling directly
 on top of lower floors--kind of like crushing a soda can underfoot.
 It's not difficult to understand how this happened, unless one is
 UNWILLING to accept the simplest, most straightforward explanation.

 robert luis rabello
 The Edge of Justice
 Adventure for Your Mind
 http://www.newadventure.ca

 Ranger Supercharger Project Page
 http://www.members.shaw.ca/rabello/



 

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Re: [Biofuel] biodiesel for heating

2006-09-20 Thread Logan vilas
You can not make biodiesel using only 10% Methanol. A chemical reaction
requires things to be just right, which requires a little more then is
actually needed no get the mixtures where they need to be. Also the amount
of Glycerin in your triglyceride is often more then 10% of the entire thing.
The only result you will get with 10% methanol is partial Biodiesel, partial
monoglycerides, partial diglycerides, and partial base oil. Then you are
reprocessing everything except the biodiesel and spending more time and
money to get the same result. Your best bet is to set up a methanol recovery
system if you are worried about the extra money involved in using the extra
methanol.

Either way it just will not be complete the reaction if you don't use 20%
methanol. I find that if you do your 20% calculations by weight instead of
volume there are more consistent and better results. That normally is 22-23%
methanol per a batch.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of [EMAIL PROTECTED]
Sent: Wednesday, September 20, 2006 12:00 PM
To: Biofuel@sustainablelists.org
Subject: [Biofuel] biodiesel for heating

is there anybody out there who makes biodiesel for home heating using only
10% methanol instead of the prescribed 20%? if so can you give any tips on
differences in processing as i am about to begin making test and then 90
liter batches soon?


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Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

2006-09-20 Thread Logan vilas
It's amazing that the Weight of the airplane alone was enough to not cause
the building to collapse in my opinion.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of robert and benita
rabello
Sent: Wednesday, September 20, 2006 3:35 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] WHAT REALLY HAPPENED ON SEPT 11

Kirk McLoren wrote: 


 
Unfortunately since you arent qualified to judge what you read you
accept information based on authority.


What nonsense!!!

Wrap your mind around something written by an engineering firm:

DID THE WORLD TRADE CENTER TOWERS ACTUALLY IMPLODE?
No. They collapsed in an uncontrolled fashion, causing extensive damage to
surrounding structures, roadways and utilities. Although when viewed from a
distance the towers appeared to have telescoped almost straight down, a
closer look at video replays reveal sizeable portions of each building
breaking free during the collapse, with the largest sections--some as tall
as 30 or 40 stories--actually laying out in several directions. The
outward failure of these sections is believed to have caused much of the
significant damage to adjacent structures, and smaller debris caused
structural and cosmetic damage to hundreds of additional buildings around
the perimeter of the site. 

WHY DID THEY COLLAPSE?
Each 110-story tower contained a central steel core surrounded by open
office space, with 18-inch steel tubes running vertically along the outside
of the building. These structural elements provided the support for the
building, and most experts agree that the planes impacting the buildings
alone would not have caused them to collapse. The intense heat from the
burning jet fuel, however, gradually softened the steel core and
redistributed the weight to the outer tubes, which were slowly deformed by
the added weight and the heat of the fire. Eventually, the integrity of
these tubes was compromised to the point where they buckled under the weight
of the higher floors, causing a gravitational chain reaction that continued
until all of the floors were at ground level. 

DID THE TERRORISTS PLANT ANY BOMBS IN THE BUILDINGS IN ADVANCE TO GUARANTEE
THEIR DEMISE?
To our knowledge there is no evidence whatsoever to support this assertion.
Analysis of video and photographs of both towers clearly shows that the
initial structural failure occurred at or near the points where the planes
impacted the buildings. Furthermore, there is no visible or audible
indication that explosives or any other supplemental catalyst was used in
the attack.

HOW DOES THIS EVENT COMPARE WITH A NORMAL BUILDING IMPLOSION?
The only correlation is that in a very broad sense, explosive devices
(airplanes loaded with fuel) were used to intentionally bring down
buildings. However it can be argued that even this vague similarity relates
more to military explosive demolition than to building implosions, which
specifically involve the placement of charges at key points within a
structure to precipitate the failure of steel or concrete supports within
their own footprint. The other primary difference between these two types of
operations is that implosions are universally conducted with the utmost
concern for adjacent properties and human safety---elements that were
horrifically absent from this event. Therefore we can conclude that what
happened in New York was not a building implosion.


You won't likely be happy with this, but that's because you're looking
for a conspiracy that is far better explained by ineptitude.



That is a close second to voting on the truth. It seems odd you see
organised control in the hydrocarbon industry yet the possibility of a Pearl
Harbor type episode in the 9-11 disaster is incomprehensible.


No, it's not incomprehensible at all.  We were attacked by the Japanese
at Pearl Harbor.  Airplanes filled the sky over Pearl Harbor and dropped
torpedos and bombs on our ships.  Many of those ships were sunk in the
attack.  There's a lot of evidence suggesting a degree of threat awareness
at the upper echelons of government, but it wasn't staged by covert American
intelligence operatives, the Mossad, or even a bunch of anti-government
loonies.  There was no conspiracy.  There was a cause / effect
relationship between Japanese torpedos, bombs and sunken ships.

  Likewise, we all witnessed airplanes being flown into buildings on
September 11, 2001.  Not long afterward, the buildings came down.  The
buildings did NOT come down until after the airplanes had flown into them.
What's so hard for you to understand about this?

Now, the question of who financed the operation and is ultimately
responsible for the attack is one that has not been answered to my
satisfaction.  A lot of the facts don't add up, but in my mind, that's more
of an indication of governmental blundering and butt-covering than a
conspiracy.  Did the current administration white wash facts

Re: [Biofuel] sticker on diesel pumps

2006-08-21 Thread Logan Vilas








All new on road vehicles manufactured, for
use in the US,
in model year 2007 and up must have catalytic converts on them to help reduce
exhaust emissions. That includes 18 wheelers. The high sulfur content will plug
them; the ULSD will allow the use. 



Logan Vilas

Bio-Fuel Enterprises, Inc.











From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On
Behalf Of vin
Sent: Sunday, August 20, 2006 8:37
AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] sticker on
diesel pumps







Looks like what happened with leaded vs. unleaded gasoline
fuel is happening with diesel...











http://www.kentuckycleanfuels.org/biodiesel/ulsdupdate.pdf








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Re: [Biofuel] sticker on diesel pumps

2006-08-21 Thread Logan vilas
I have no clue what the effects are or any other little secrets used to make
it more efficient. I would guess that bio-diesel does not cause a problem,
or that the converters for diesel are different.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Kirk McLoren
Sent: Monday, August 21, 2006 3:34 PM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] sticker on diesel pumps

I assume air injection is incorporated. In that case they finish oxidising.

Zeke Yewdall [EMAIL PROTECTED] wrote: 

What does biodiesel do to the catalytic converters?   No sulfur, but
how about all the polyaromatic hydrocarbons?

Z


On 8/21/06, Logan Vilas  [EMAIL PROTECTED]
mailto:[EMAIL PROTECTED]  wrote: 

All new on road vehicles manufactured, for use in the US, in
model year 2007 and up must have catalytic converts on them to help reduce
exhaust emissions. That includes 18 wheelers. The high sulfur content will
plug them; the ULSD will allow the use. 
 
Logan Vilas
Bio-Fuel Enterprises, Inc.
 



From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of vin
Sent: Sunday, August 20, 2006 8:37 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] sticker on diesel pumps

 
Looks like what happened with leaded vs. unleaded gasoline
fuel is happening with diesel...
 
http://www.kentuckycleanfuels.org/biodiesel/ulsdupdate.pdf

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Talk is cheap. Use Yahoo! Messenger to make PC-to-Phone calls. Great rates
starting at 1¢/min.
http://us.rd.yahoo.com/mail_us/taglines/postman7/*http://us.rd.yahoo.com/ev
t=39666/*http://messenger.yahoo.com 


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Re: [Biofuel] Astroturf

2006-08-07 Thread Logan vilas








I dont think Astroturf will work
for biofuell production



Logan Vilas











From:
[EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On
Behalf Of Kirk McLoren
Sent: Monday, August 07, 2006
12:43 PM
To: biofuel
Subject: [Biofuel] Astroturf





Not new though see Kuwait comment.The gvt isnt concerned about what you think. They have created what you think.Kirk++| PR Firm Behind Al Gore YouTube Spoof? || from the new-intarweb-trolls dept. || posted by ScuttleMonkey on Sunday August 06, @18:11 (Republicans)|| http://politics.slashdot.org/article.pl?sid=06/08/06/209244 |++mytrip writes to tell us ABC News is reporting that a supposed amateurvideo posted to YouTube.com may have actually been designed and posted bya Republican [0]public relations firm called DCI. From the article:Public relations firms have long used computer technology to createbogus grassroots campaigns, which are called 'Astroturf.' Now these firmsare being hired to push illusions on the Internet to create the falseimpression of real people blogging, e-mailing and making films.Discuss this story at: http://politics.slashdot.org/comments.pl?sid=06/08/06/209244Links: 0. http://abcnews.go.com/GMA/story?id=2273111page=1









In fact, the most emotionally moving testimony on
October 10 came from a 15-year-old Kuwaiti girl, known only by her first name
of Nayirah. According to the Caucus, Nayirah's full name was being kept
confidential to prevent Iraqi reprisals against her family in occupied Kuwait.
Sobbing, she described what she had seen with her own eyes in a hospital in Kuwait City.
Her written testimony was passed out in a media kit prepared by Citizens for a
Free Kuwait.
I volunteered at the al-Addan hospital, Nayirah said. While I
was there, I saw the Iraqi soldiers come into the hospital with guns, and go
into the room where . . . babies were in incubators. They took the babies out
of the incubators, took the incubators, and left the babies on the cold floor
to die.83

Three months passed between Nayirah's
testimony and the start of the war. During those months, the story of babies
torn from their incubators was repeated over and over again. President Bush
told the story. It was recited as fact in Congressional testimony, on TV and
radio talk shows, and at the UN Security Council. Of all the accusations
made against the dictator, MacArthur observed, none had more impact
on American public opinion than the one about Iraqi soldiers removing 312
babies from their incubators and leaving them to die on the cold hospital
floors of Kuwait City.84

At the Human Rights Caucus, however,
Hill  Knowlton and Congressman Lantos had failed to reveal that Nayirah
was a member of the Kuwaiti Royal Family. Her father, in fact, was Saud Nasir
al-Sabah, Kuwait's
Ambassador to the US,
who sat listening in the hearing room during her testimony. The Caucus also
failed to reveal that HK vice-president Lauri Fitz-Pegado had coached
Nayirah in what even the Kuwaitis' own investigators later confirmed was false
testimony.



 







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Re: [Biofuel] Fluorescent fuel?

2006-07-27 Thread Logan vilas
I was not trying to say anyone is right or wrong. I was just asking if that
was logical, because it makes sense to me. 

I also think that the roots and shoots probably don't use nearly the co2
as would go into the seed production, but it is still potentially co2
negative. I don't think the few plants we grow or that small portion of
roots and shoots is going to make a difference. It took millions of years
without the use of plants in any way to build up deep in the ground. And in
the last 50-100 years we've managed to release most of it back into the
atmosphere. On top of that we've greatly reduced the area to grow the plants
that are needed to remove co2. 

An interesting study would be to track the ppm co2 from year to year in a
sample of air.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Joe Street
Sent: Thursday, July 27, 2006 10:35 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Fluorescent fuel?

Yes that's true.  Depending on what happens to the remains of the plant 
it may stay sequestered. My point was that with the current carbon 
economy and what we currently have with climate change, carbon neutral 
ideologies do not do anything to reverse the problem but have the 
potential to stabilize and maintain things the way they are. But you are 
right this may be slightly carbon negative which is what we really need.

Joe


Logan Vilas wrote:

 The plants require co2 for all of their growth, stem, seeds, leaves, roots
 and we only use a portion of the plant for making fuels. Wouldn't that
left
 over part of the plant be using more co2 then is put out by the burning of
 the oil?
 
 Logan Vilas
 
 -Original Message-
 From: [EMAIL PROTECTED]
 [mailto:[EMAIL PROTECTED] On Behalf Of bob allen
 Sent: Wednesday, July 26, 2006 9:23 AM
 To: biofuel@sustainablelists.org
 Subject: Re: [Biofuel] Fluorescent fuel?
 
 only in that the process in theory is carbon neutral, and replaces 
 fossil fuel which is carbon positive.
 
 first we stop increasing the CO2...
 
 
 
 Joe Street wrote:
 
So if we use a plant to remove CO2 from the atmosphere and that plant 
makes oil that we then burn and release CO2 to the atmosphere how is 
that supposed to reduce atmospheric CO2?

Joe

Bob Molloy wrote:

snip


Phytoplankton, like other plants, absorb carbon dioxide as they grow. 
Scientists have examined the possibility of stimulating growth of the 
single cell plants as a means of reducing the amount of CO2 in the 
atmosphere.
CO2, liberated by burning fossil fuels like coal, oil and gas, is widely 
held responsible for global warming.
 
Bio Fuel Systems said its new fuel would reduce CO2, was free of other 
contaminants like sulphur dioxide and would be cheaper than fossil oil 
is now.


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Re: [Biofuel] Fluorescent fuel?

2006-07-26 Thread Logan Vilas
The plants require co2 for all of their growth, stem, seeds, leaves, roots
and we only use a portion of the plant for making fuels. Wouldn't that left
over part of the plant be using more co2 then is put out by the burning of
the oil?

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of bob allen
Sent: Wednesday, July 26, 2006 9:23 AM
To: biofuel@sustainablelists.org
Subject: Re: [Biofuel] Fluorescent fuel?

only in that the process in theory is carbon neutral, and replaces 
fossil fuel which is carbon positive.

first we stop increasing the CO2...



Joe Street wrote:
 So if we use a plant to remove CO2 from the atmosphere and that plant 
 makes oil that we then burn and release CO2 to the atmosphere how is 
 that supposed to reduce atmospheric CO2?
 
 Joe
 
 Bob Molloy wrote:
 
 snip
 
 Phytoplankton, like other plants, absorb carbon dioxide as they grow. 
 Scientists have examined the possibility of stimulating growth of the 
 single cell plants as a means of reducing the amount of CO2 in the 
 atmosphere.
 CO2, liberated by burning fossil fuels like coal, oil and gas, is widely 
 held responsible for global warming.
  
 Bio Fuel Systems said its new fuel would reduce CO2, was free of other 
 contaminants like sulphur dioxide and would be cheaper than fossil oil 
 is now.
 
 
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--
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--
-
The modern conservative is engaged in one of Man's oldest exercises
in moral philosophy; that is, the search for a superior moral
justification for selfishness  JKG
 


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Re: [Biofuel] Home energy system ...was Re: {Disarmed} Telegraph - US could be going bankrupt

2006-07-17 Thread Logan vilas
Hey Doug,

I have some small machine equipment and some reasonable priced
machine shops in my area, If I can't make it I'm sure I can have it made. I
am interested in stirling engines for the exact same use. If the plans look
good to me I might be willing to build a prototype at my expense and will
gladly let you know how it works or possibly ship it for your testing.

Everyone Else,
http://www.lindsaybks.com/
This Site Has some great books at really good prices, I highly
recommend the Dave Gingery Series. It includes Sand Casting, Making a Metal
Shaper, Lathe, Milling machine, Drill Press, Accessories, and Sheet Metal
Brake from scrap. The plans can be size up easily and everything can be done
really low budget. There is also many other books, all the ones I've gotten
have been on metal working. Right now I'm working on a furnace that will
hold 75lbs of molten aluminum, and turn around the spot. From one of the
local machine shops I have a supply of about 400lbs of alum turnings a month
all I have to do is go pick them up. They use only 6061 and have one machine
that turns out the same part 8 hours a day 7 days a week. So it's a good
clean source for strong castings.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of doug swanson
Sent: Sunday, July 16, 2006 7:14 PM
To: biofuel@sustainablelists.org
Subject: [Biofuel] Home energy system ...was Re: {Disarmed} Telegraph - US
could be going bankrupt

I agree that in tight times, basic or even primitive skills are more 
valuable than gold.  Basics in Agriculture, animal husbandry, health 
maintenance, knowing how to preserve food without supplies you'd have to 
get at a grocer's store, blacksmithing, wood working, etc. are all 
skills that should be present in what I see as being a new birth of 
communities which will establish themselves once TEOTWAWKI happens.

Energy systems can be a large part of this, since my wood heater 
currently relies on a chainsaw to supply fuel, and my biodiesel relies 
on restaurant wastes and petro-derived methanol, and industry produced 
hydroxides, I still don't feel that my current situation is 
sustainable.  Solar makes a lot of sense in my location, and I've been 
working in that direction, but with a twist.  The 10' parabolic 
collector can collect a lot of heat, and rather than convert it 
immediately to electricity, which I'd then have to store in some sort of 
battery (with all the problems that batteries come with, ie. disposal 
when they don't work anymore, and then having to acquire new ones..., ) 
it makes better sense to store the heat from the collector in 55 gallon 
drums of water, which can actually make up the rear greenhouse wall... 

I've been studying Stirling engines for some time now, guess I've read 
everything that Google can show me about them, crammed all the ideas 
into my head, noted the major disadvantages of most of them, (They've 
got to be airtight, precision power piston, most aren't self-starting, 
etc...) and have come up with a design that addresses these problems, 
and eliminates them by integrating much of the engine into 3 moving 
parts.  Heat goes in, electricity comes out.  I really would like to 
build the prototype, but can't afford a machine shop to make a couple of 
its parts.  Maybe someone on this list has the right tools to make the 
parts, and would like to see more detailed plans on this.  Eventually, 
when a working prototype is producing electricity, the plans with step 
by step guidance will be under the open information license  The point 
of the whole system is that wherever possible, the parts should be stuff 
that can be found at the junkyard, and that when completed, a home power 
generation system is running for under 3-400 bucks.  Adding another 
collector just for home heat would be even simpler, under floor heat 
circulation would increase the cost due to plumbing, thermostat control, 
etc., but if the hot water was just circulated through a radiator 
(junkyard again) with a fan behind it, the home could be comfortable 
without huge expense.

The efficiency of a Stirling engine makes it a potential candidate for a 
hybrid vehicle, and I've been working on something along that line also, 
but first things first...

Any ideas are welcome, anything I can do to help pull us out of the mess 
this planet is in, I will do.

doug swanson



Jason Katie wrote:

you dont need money if you can supply a need. i know more than just fuel, i

can build just about anything a person would have as a daily need. house, 
furniture, small macines, engine repair, anyone with a skill is pretty well

safe. it is the people who have never had to work a day in their life
(CEO's 
and politicians) that are screwed.
Jason
ICQ#:  154998177
MSN:  [EMAIL PROTECTED]
- Original Message - 
From: Mike Weaver [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, July 14, 2006 9:01 PM
Subject: Re: [Biofuel

Re: [Biofuel] Manesol pretreatment and washing

2006-05-24 Thread logan vilas
Chris,

I'm guessing you did not titrate the used oil sample after adding 
Mangesol. If you could do that it would be intresting to see the results. 
And that should tell you definately if the FFA's have been neutralized.

Logan Vilas
- Original Message - 
From: Chris Bennett [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Wednesday, May 24, 2006 4:14 AM
Subject: [Biofuel] Manesol pretreatment and washing


 Been having a play with a bag of Magnesol this week with impressive
 resuts. I made a sample batch of diesel, went over the top with the lye
 by about 2 grams per litre. I added the magnesol powder to the finished,
 seperated diesel and mixed for about 5 minuites. I removed the magnesol
 by filtering thru coffee filters several times (it was quite difficult
 to get it all out without a fine enough filter). The result is crystal
 clear biodiesel. I mean CRYSTAL clear, much better than I have EVER been
 able to get with water washing. Adding water to the diesel yields quick
 seperation, clarity is still 100% and the wash water is perfectly clear.
 10grams per litre of magnesol has removed EVERY trace of soap and
 contaminants. Lets just say I will no longer be water washing.
 The next experiment was based on the claims that magnesol neutralises
 FFA. I got 2 samples of WVO and filtered them. One 250ml sample was
 treated with about 1.5g of magnesol and mixed for abut 10 minuites. The
 magnesol was filtered out of the sample. BOTH samples were processed as
 new oil with 3.5g lye per litre and 250ml meth per litre. After
 seperation and cooling the pretreated sample is clear, and the byproduct
 is a redish colour. The untreated sample shows an uncomplete reaction
 and a very dark nearly black byproduct. I have yet to try water washing
 these samples. It appears that the magnesol pretreatment has removed the
 ffa content and then the oil has been able to be processed as new oil.
 It should be quite easy to integrate into a process by adding an
 arbitrary amount of magnesol to the feedstock and mixing, PH
 measurements will tell you if more needs to be added.

 The waste magnesol, according to manufactutrers literature, can be
 composted, put into landfill, and even used as animal feed. The magnesol
 washing could be integrated into a semi continuous process easily, which
 is why I am looking at it. Another comment is that when using it for
 washing biodiesel it also seems to remove colour and odour from the
 biodesel. The magnesol washed samples are always paler than the water
 washed samples.

 If the used magnesol is put into water it instantly goes cramy white, as
 it gives up the soaps etc that it has absorbed.

 Kieth, if you are interested I have some photos of the different samples
 tested and washed. Maybe you could incorporate something aout it into
 the JTF page? If anyone wants these photos emailed let me know! I was
 impressed.

 Chris Bennett


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Re: [Biofuel] Manesol pretreatment and washing

2006-05-24 Thread logan vilas
Synthetic Magnesium Silicate Adsorbent is white fine powder, amorphous, with 
vesicular structure and huge specific area, it is an amphoteric compound 
capable of adsorbing either acid or alkali metal catalyst. It is an 
efficient refining and purifying agent in the production of polyols for its 
excellent depicking, deodorizing, potassium ion adsorbing effects and 
function as filter medium.

- Original Message - 
From: bob allen [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Wednesday, May 24, 2006 9:25 AM
Subject: Re: [Biofuel] Manesol pretreatment and washing


Joe Street wrote:
 I am interested in the pics.  What is magnesol exactly?

good question:

MAGNESOL - (DP - 45)

  MAGNESIUM SILICATE, not much different than talc.

but

MAGNESOL® is based on a linear polyester imide resin.



I suspect you want the former, not the latter.







  Also I just
 wanted to say FYI when you talk about crystal clarity it is anecdotal of
 course and DOES only give some info about particulate or emulsified
 contamination.  A great way to detect very small levels of this type of
 contamination is to put a sample into a glass jar and in a darkened room
 shine a laser (pointer) through the BD. The beam should not be visible
 in the liquid.  Note that this tells you nothing about trigliceride
 levels or methanol contamination but water content will give an
 indication above a certain level.
 Can magnesol be used to pretreat feedstock and be left in to settle out
 with the byproduct?

 Joe

 Chris Bennett wrote:

 Been having a play with a bag of Magnesol this week with impressive
 resuts. I made a sample batch of diesel, went over the top with the lye
 by about 2 grams per litre. I added the magnesol powder to the finished,
 seperated diesel and mixed for about 5 minuites. I removed the magnesol
 by filtering thru coffee filters several times (it was quite difficult
 to get it all out without a fine enough filter). The result is crystal
 clear biodiesel. I mean CRYSTAL clear, much better than I have EVER been
 able to get with water washing. Adding water to the diesel yields quick
 seperation, clarity is still 100% and the wash water is perfectly clear.
 10grams per litre of magnesol has removed EVERY trace of soap and
 contaminants. Lets just say I will no longer be water washing.
 The next experiment was based on the claims that magnesol neutralises
 FFA. I got 2 samples of WVO and filtered them. One 250ml sample was
 treated with about 1.5g of magnesol and mixed for abut 10 minuites. The
 magnesol was filtered out of the sample. BOTH samples were processed as
 new oil with 3.5g lye per litre and 250ml meth per litre. After
 seperation and cooling the pretreated sample is clear, and the byproduct
 is a redish colour. The untreated sample shows an uncomplete reaction
 and a very dark nearly black byproduct. I have yet to try water washing
 these samples. It appears that the magnesol pretreatment has removed the
 ffa content and then the oil has been able to be processed as new oil.
 It should be quite easy to integrate into a process by adding an
 arbitrary amount of magnesol to the feedstock and mixing, PH
 measurements will tell you if more needs to be added.

 The waste magnesol, according to manufactutrers literature, can be
 composted, put into landfill, and even used as animal feed. The magnesol
 washing could be integrated into a semi continuous process easily, which
 is why I am looking at it. Another comment is that when using it for
 washing biodiesel it also seems to remove colour and odour from the
 biodesel. The magnesol washed samples are always paler than the water
 washed samples.

 If the used magnesol is put into water it instantly goes cramy white, as
 it gives up the soaps etc that it has absorbed.

 Kieth, if you are interested I have some photos of the different samples
 tested and washed. Maybe you could incorporate something aout it into
 the JTF page? If anyone wants these photos emailed let me know! I was
 impressed.

 Chris Bennett


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http://ozarker.org/bob

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


Re: [Biofuel] Solar Concentrator PV Modules

2006-05-16 Thread logan vilas
The best heat transfer pastes for processors has silver in it and I belive 
silver is conductive.

Logan Vilas
- Original Message - 
From: Jason  Katie [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Monday, May 15, 2006 7:02 PM
Subject: Re: [Biofuel] Solar Concentrator  PV Modules


 aha, this is where i find a new idea.

 the dielectric heat grease used between processors and heat sinks /should/
 work to electrically insulate the cell from the water pack (not jackets, a
 flat sleeve covering the back with circulated coolant completely filling 
 it)
 while conducting heat into the cooling vanes in the water pack, 
 eliminating
 the risk of breakage, just as you say. the goop isnt exactly cheap, but it
 works rather effectively on high temp applications.

 - Original Message - 
 From: Joe Street [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Monday, May 15, 2006 9:26 AM
 Subject: Re: [Biofuel] Solar Concentrator  PV Modules


 Silicon is quite fragile especially the thin polysilicon material used
 in cells.  You are right but any water pressure would break the cells.
 You need to bond them onto a heat conducting back plate like copper or
 aluminum with a heat conducting cement.  Aso the back is an electrical
 contact so you need isolation there.

 Joe

 Jason  Katie wrote:

 in theory, if one could find a way to waterproof the back of a PV cell 
 it
 could be used as the heat-side plate in this concentrator/boiler found 
 at
 (or after) http://www.ida.net/users/tetonsl/solar/page_46.htm you could
 safely increase the power range of a smaller PV cell without too 
 horrible
 of
 a heat loss. the problem is finding a sealing substance that wont melt 
 or
 burn under these 1200*F temperatures.


 - Original Message - 
 From: logan vilas [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Friday, May 12, 2006 4:54 PM
 Subject: Re: [Biofuel] Solar Concentrator  PV Modules



I am working with the idea of building my own Concentrator with about 50
times the mirror space then collector space. That Is why the question 
was
asked in the first place I was wondering if placeing a 50watt solar 
panel
at
the focal point would increase the power output. I've read that it is
more
then 100% liner increase in power output when increasing the amount of
light
on it. a normal panel at 50 watts would be 2500 watts at 50 suns. I know
it
would need to be kept cool. due to the fact that they are only 20-30%
efficent, but I could use the coolant to heat my biodiesel processor,
then
the hot water going into my home before a tankless heater. If I were to
get
a grid tied inverter It would suppliment my normal power useage and maby
with netmetering it might come close to canceling out my power
requirements
alltogther. a simple temp sensor could be used so if the temp is over
150f
in the coolant it will shut down and not collect the sun anymore. As for
a
solar tracker that is relative easy with very simple electronics. The
setup
to hold everything would be a simple build for most people who can make
their own biodiesel processor. And If I base it off a 7 meter dish I can
get
those free. I just have to use the labor to remove it.

Logan Vilas
- Original Message - 
From: Zeke Yewdall [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Friday, May 12, 2006 3:59 PM
Subject: Re: [Biofuel] Solar Concentrator  PV Modules



I am speaking mostly from experience, from what I have seen work and
fail in the field, and what I can buy to install for my clients. The
reason I talk about trackers on large poles is because that is what is
commercially sold right now (at least in the US, europe is ahead of us
in many areas).  And the biggest reason I see for failed systems is
lack of maintenance (mostly batteries, but also anything that moves).
Also, the number of new innovative PV systems that I have seen come on
the market over the years, only to dissapear within another year...
We're still basically doing the same thing as PV was in the 70's, with
incremental improvements in efficiency and incremental cost decreases.
I called the concrentrating PV exotic merely because I can't call up
one of 200 some suppliers and buy one that meets all current
electrical code, whereas I can with silicon PV modules.  Maybe another
breakthrough is coming, but in the mean time, alot of people will keep
using coal generated power because they are waiting for those
breakthroughs.  I would rather see working PV systems going in today,
even if they aren't all that high tech, rather than people thinking
they have to wait before solar energy can work for them -- and in the
mean time continuing to support coal and oil.   It's not that I want
to limit the new technology, but what I have seen is that the
layperson holds out the possibility of a paradigm shift in the
technology in the future as a reason to do absolutely nothing now.
And if I recall, the original question was about concentrating
sunlight on a normal

[Biofuel] Thermal conductivity Please help

2006-05-16 Thread logan vilas
Thermal conductivity of silicone (300 K) 149 W/(m·K)


Can anyone help me understand this. I've been trying to figure out how to 
read this equasion for 2 days and all I got was a headache.

Logan Vilas 


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Re: [Biofuel] Thermal conductivity Please help

2006-05-16 Thread Logan Vilas


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Zeke Yewdall
Sent: Tuesday, May 16, 2006 8:54 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] Thermal conductivity Please help

This means basically that at 300K average temperature, the thermal
conductivity is 149 W/(m*K).  What the proper units are is actually
W*m/(sq meter *K).  Two of the meters cancel out to leave just one on
the bottom, but it's easier to think of it with them still in there.
If you think about trying to calculate heat transfer in watts per
square meter, you need to cancel out the m on top of the thermal
conductivity, and the K on the bottom.  So, you multiply the
conductivity by the delta T in Kelvins, which cancels the K.  And you
divide it by the thickness of the silicon you are transferring heat
through (because a thicker piece will transfer less heat), which
cancels out the m on top.  This leaves units of W/m^2 for the units of
the answer, which is what we were looking for.  If we want total
watts, we can multiply by the area of the heat transfer area, and
cancel out the m^2, and are left with just watts.

On 5/16/06, logan vilas [EMAIL PROTECTED] wrote:
 Thermal conductivity of silicone (300 K) 149 W/(m.K)


 Can anyone help me understand this. I've been trying to figure out how to
 read this equasion for 2 days and all I got was a headache.

 Logan Vilas


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Re: [Biofuel] Thermal conductivity Please help

2006-05-16 Thread Logan Vilas


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Zeke Yewdall
Sent: Tuesday, May 16, 2006 8:54 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] Thermal conductivity Please help

This means basically that at 300K average temperature, the thermal
conductivity is 149 W/(m*K).  What the proper units are is actually
W*m/(sq meter *K).  Two of the meters cancel out to leave just one on
the bottom, but it's easier to think of it with them still in there.
If you think about trying to calculate heat transfer in watts per
square meter, you need to cancel out the m on top of the thermal
conductivity, and the K on the bottom.  So, you multiply the
conductivity by the delta T in Kelvins, which cancels the K.  And you
divide it by the thickness of the silicon you are transferring heat
through (because a thicker piece will transfer less heat), which
cancels out the m on top.  This leaves units of W/m^2 for the units of
the answer, which is what we were looking for.  If we want total
watts, we can multiply by the area of the heat transfer area, and
cancel out the m^2, and are left with just watts.

On 5/16/06, logan vilas [EMAIL PROTECTED] wrote:
 Thermal conductivity of silicone (300 K) 149 W/(m.K)


 Can anyone help me understand this. I've been trying to figure out how to
 read this equasion for 2 days and all I got was a headache.

 Logan Vilas


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Re: [Biofuel] Solar Concentrator PV Modules

2006-05-13 Thread Logan Vilas
The main concern would be thermal transfer rates of the materials that the
cell is made out of and max temp the cell can handle. I know PV are made
from silicone, but is there any more depective terms for the material? For
example all Iron is not steel and every version of it has different thermal
transfer rates. What is the maximum working temp of PV modules? From Those
two things I can calculate the maximum amount of concentration that should
work. Also approximately how large is a 50watt panel?

I can pick a PV module then based on size and material thermal transfer I
can calculate the thermal transfer it would have in BTUs. I would then
divide by 3.4 and that's the number of watts it can have aimed at it.
There's approximately 1000watts per square meter energy from the sun. The
mirrors are about 92% reflective and I would figure there it going to be
about 10% loss to heating the air between the PV and the mirrors. 82.8
percent of the energy will be transferred to the PV. That's 828watts per
square meter of mirrors. Divide the thermal transfer by 828 and that's the
max concentration that can be focused at that cell to keep it at the same
temp as the input temp of the coolant you are using. 

The overall design should be engineered to keep the cell within working temp
limits without loosing much of the power gain, so under 200F (I'm guessing),
while being able to dissipate 100% of the heat that is concentrated. It
would need to dissipate all the heat because of the chance that no
electricity will be used and all the energy will become heat. When 20-30% of
the energy is being turned into electricity then the cell temp will remain
an equal percentage lower. At these temps it could be done with water and no
additives, but a closed system with relief valve would be best otherwise the
water would evaporate. 

I am thinking a closed loop system of filtered and dewatered UVO. I have
firefighting material called fire blockade that can be added at 1% mixture
and that will ensure the oil is nonflamiable. That would cause the fluid to
not boil off or spontaneously combust.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Zeke Yewdall
Sent: Saturday, May 13, 2006 5:30 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] Solar Concentrator  PV Modules

This is exactly what I did my master's thesis on.  The concept works
pretty well from a theoretical perspective.  I was just investigating
using water cooling for non-concrentrating PV, but it would work even
better for concentrating PV.  You shouldn't really have to deal with
1200F, at least if you are talking about water, because the maximum
working temp for a water based fluid is probably about 400F or so??
(assuming antifreeze additives and increased pressure).  Depends on
how much pressure you are talking about I guess.

On 5/13/06, Jason  Katie [EMAIL PROTECTED] wrote:
 in theory, if one could find a way to waterproof the back of a PV cell it
 could be used as the heat-side plate in this concentrator/boiler found at
 (or after) http://www.ida.net/users/tetonsl/solar/page_46.htm you could
 safely increase the power range of a smaller PV cell without too horrible
of
 a heat loss. the problem is finding a sealing substance that wont melt or
 burn under these 1200*F temperatures.


 - Original Message -
 From: logan vilas [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Friday, May 12, 2006 4:54 PM
 Subject: Re: [Biofuel] Solar Concentrator  PV Modules


 I am working with the idea of building my own Concentrator with about 50
  times the mirror space then collector space. That Is why the question
was
  asked in the first place I was wondering if placeing a 50watt solar
panel
  at
  the focal point would increase the power output. I've read that it is
more
  then 100% liner increase in power output when increasing the amount of
  light
  on it. a normal panel at 50 watts would be 2500 watts at 50 suns. I know
  it
  would need to be kept cool. due to the fact that they are only 20-30%
  efficent, but I could use the coolant to heat my biodiesel processor,
then
  the hot water going into my home before a tankless heater. If I were to
  get
  a grid tied inverter It would suppliment my normal power useage and maby
  with netmetering it might come close to canceling out my power
  requirements
  alltogther. a simple temp sensor could be used so if the temp is over
150f
  in the coolant it will shut down and not collect the sun anymore. As for
a
  solar tracker that is relative easy with very simple electronics. The
  setup
  to hold everything would be a simple build for most people who can make
  their own biodiesel processor. And If I base it off a 7 meter dish I can
  get
  those free. I just have to use the labor to remove it.
 
  Logan Vilas


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Re: [Biofuel] Solar Concentrator PV Modules

2006-05-12 Thread logan vilas
I am working with the idea of building my own Concentrator with about 50 
times the mirror space then collector space. That Is why the question was 
asked in the first place I was wondering if placeing a 50watt solar panel at 
the focal point would increase the power output. I've read that it is more 
then 100% liner increase in power output when increasing the amount of light 
on it. a normal panel at 50 watts would be 2500 watts at 50 suns. I know it 
would need to be kept cool. due to the fact that they are only 20-30% 
efficent, but I could use the coolant to heat my biodiesel processor, then 
the hot water going into my home before a tankless heater. If I were to get 
a grid tied inverter It would suppliment my normal power useage and maby 
with netmetering it might come close to canceling out my power requirements 
alltogther. a simple temp sensor could be used so if the temp is over 150f 
in the coolant it will shut down and not collect the sun anymore. As for a 
solar tracker that is relative easy with very simple electronics. The setup 
to hold everything would be a simple build for most people who can make 
their own biodiesel processor. And If I base it off a 7 meter dish I can get 
those free. I just have to use the labor to remove it.

Logan Vilas
- Original Message - 
From: Zeke Yewdall [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Friday, May 12, 2006 3:59 PM
Subject: Re: [Biofuel] Solar Concentrator  PV Modules


I am speaking mostly from experience, from what I have seen work and
 fail in the field, and what I can buy to install for my clients. The
 reason I talk about trackers on large poles is because that is what is
 commercially sold right now (at least in the US, europe is ahead of us
 in many areas).  And the biggest reason I see for failed systems is
 lack of maintenance (mostly batteries, but also anything that moves).
 Also, the number of new innovative PV systems that I have seen come on
 the market over the years, only to dissapear within another year...
 We're still basically doing the same thing as PV was in the 70's, with
 incremental improvements in efficiency and incremental cost decreases.
 I called the concrentrating PV exotic merely because I can't call up
 one of 200 some suppliers and buy one that meets all current
 electrical code, whereas I can with silicon PV modules.  Maybe another
 breakthrough is coming, but in the mean time, alot of people will keep
 using coal generated power because they are waiting for those
 breakthroughs.  I would rather see working PV systems going in today,
 even if they aren't all that high tech, rather than people thinking
 they have to wait before solar energy can work for them -- and in the
 mean time continuing to support coal and oil.   It's not that I want
 to limit the new technology, but what I have seen is that the
 layperson holds out the possibility of a paradigm shift in the
 technology in the future as a reason to do absolutely nothing now.
 And if I recall, the original question was about concentrating
 sunlight on a normal old PV module -- which isn't the best idea --
 they tried that at the carrizo solar plant in the early 80's, and a
 few years later, a whole lot of used Mud-lams (because the encapsulant
 turned varying shades of brown) flooded the market for off-grid use.

 I do admit that this list's members are not your average layperson,
 and most of us won't just use the news of new inventions as an excuse
 for procrastinating, so I apologize for that.

 Zeke


 On 5/12/06, Michael Redler [EMAIL PROTECTED] wrote:

 By now, you may have noticed my resistance to conventional wisdom 
 whenever
 someone gives negative feedback about a particular energy scheme. Here is 
 an
 example.

 The idea of concentrating light onto PV cells is a relatively new idea in
 some circles. What to do about waste heat is a natural progression in the
 discussion of such technology. But, why is it seen as such an obstacle -
 especially when schemes for harvesting waste heat are so abundant in 
 energy
 related discussions?

 You wrote: ...regular PV is cheap enough that the simplicity of not 
 having

 moving parts will probably outweigh any advantage of trying to get more 
 from
 the same amount of silicon.


 The sweeping statements are getting old Zeke. Adding trackers become
 advantageous when you run out of roof. By the way PV that works on
 concentrated sunlight isn't so exotic and will probably become the PV of
 choice in a large percentage of applications. The large cost of
 concentrating PV is likely to be offset by an increase in power 
 conversion
 requiring the use of heliostats, tracking technology and those pesky 
 moving
 parts.


 Mike

 Zeke Yewdall [EMAIL PROTECTED] wrote:

 Most of the highest efficiency PV cells do use concentrators. These
 are the 35% efficient super exotic ones that NREL and others are
 working on. Compared to 20% which is about the highest commercial
 single sun efficiency right

[Biofuel] Solar Concentrator PV Modules

2006-05-11 Thread Logan Vilas
Would a standard PV module produce more when used with a Solar Concentrator
or does it require a special PV module?

Logan Vilas


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Re: [Biofuel] Water in recovered methanol?

2006-05-05 Thread logan vilas



You probably don't get all of the water out of the 
oil because when it mixes with the oil the boiling point is raised. It would 
probably take 230-240F with a vacuum to pull the water 100% out. Without the 
vacuum the water vapor will still condense slightely on the walls of your 
heating pot. During the reaction you also create water. The combination of these 
is still very small. It might be 1% water to recovered methanol for every batch, 
but the water is not being used in processingso the second batch will have 
2% and it will add up. 

Logan Vilas



From: Jonathan Schearer 

  To: biofuel@sustainablelists.org 
  
  Sent: Friday, May 05, 2006 1:58 PM
  Subject: Re: [Biofuel] Water in recovered 
  methanol?
  I am probably missing something, but where would the water be 
  coming from in the first place? Isn't the waste oil you start with not 
  supposed to contain any water, and if it does, you need to boil it off? 
  Then there's the methanol. It should not contain any water either. 
  I don't believe the catalyst would contain any water either. It is the 
  waste glycerin layer that contains most of the methanol, correct? I have 
  been told that the only stupid question is the one that isn't asked. So 
  I'm asking...where is the water coming from?Michael Gian 
  [EMAIL PROTECTED] wrote: 
  In 
additon, a fractionating column requires a reflux, the partial return 
andrecycling of distillate product from the condenser back down 
thefractionatingcolumn which increases the energy tax (energy costs) 
of purifying themethanol.This is true for tray towers. A more 
elegant setup is a packedfractionating column, aka reflux column. Years 
ago we made one packed withsmall glass beads for jewelry, picked up 
cheap at a garage sale. Ethanolproduction, in this case not intended to 
fuel machinery. What works forethanol will work for methanol, probably 
better, given no water azeotrope.Alcohol Fuel Manual Ch11 has the 
poop.Michael GianMike McGinnessbob allen 
wrote: without getting into excessive detail, the boiling point 
of a mixture is the weighted average of the stuff present. At first 
you have pure methanol coming off. as the temperature rose, 
increasing amounts of water contaminated the 
alcohol. You need a fractionating column to obtain pure 
methanol. Joe Street wrote:  3A sieves will work 
but are normally used for getting tiny amounts of  water out of 
solvents to bring them into the low ppm range. They will  work 
of course but you might saturate them and have to do a second  
stage. There is a significant energy input into regenerating the 
seives  as well. You have to bake them at well over 100 degrees 
C more like  200, but you can get by with lower temps if you 
bake them out with  vacuum. Try putting a thermometer in your 
condenser and monitor vapour  temperature to get a better 
endpoint and you will have an easier time.  You have answered 
some of my own questions. I have recovered some  methanol but 
not tried to use it yet. Sounds like if straight  distillation 
is carefully done the methanol is dry enough to use without  
further drying. Great news and thanks for the post! :)  
 I have some excellent references on solvent drying I can mail you if 
you  want. No soft copy sorry but I might be able to scan 
them.   Joe   Thomas Kelly 
wrote:  Good day to all,  After splitting 
the glycerine coproduct from roughly 1200L of  processed 
WVO, I distilled approximately 100L of the  
glycerine/methanol component.  The first drops of methanol 
began to fall from the condenser at  145F. As the temp rose 
to 150F there was a steady flow of clear liquid  from the 
condenser. Throughout the day I turned the heat off when the 
 flow was steady and back on when it slowed.  I 
filled a 4.5 gal (17.7L) cubie with clear liquid and started a 
 second one. At this point the temp was over 160F. I let the still 
run  up to 200F. At this point the second cubie had 4 
gallons of clear  liquid (and it was now 1AM) giving a total 
of 8.5 gal. I was thrilled  with the result (and tired). I 
used the first 4.5 gal (17.7L) to run  one batch, and while 
that was settling ran a second batch using the  second 4 gal 
of recovered methanol.  The first batch washed OK, but was a 
little slow to separate. It  failed the methanol quality 
test.  The second batch did not even pass the wash 
test.  I have been making consistenly high quality BD for 
several months ...  thank you JtF and list members. I don't 
think I made mistakes in  measurement or titration. 
 My question:  As my distillation temps rose towards 
200F (93C) could I have been  including water in my 
distillate? (The methanol recovered at lower  temps 
performed better than the methanol recovered at higher temps.) 
 If so, can

Re: [Biofuel] Filtering - was Re: Vegtable oil sources...

2006-04-28 Thread logan vilas
Sock filters are relatively cheap and a head can be bought for them from 
http://www.mcmaster.com/ ,search for filter head ,allowing you to pump 
through the filter makeing it last much longer and go faster. I would think 
setteling would be good enough before processing, but once processed I would 
pump it through a sock filter bringing it down to at least 30 microns. The 
filters should be under 5 dollars each and do several hundred gallons of 
processed fuel per a filter. The head is under 20 dollars from them. Then 
use a clearwater pump for about 30 dollars and you will pump fast and have 
clean fuel for your vehicle. Oh remember polypropylene filters not 
polyester. They hold up much better with biodiesel.

Logan Vilas

- Original Message - 
From: Thomas Kelly [EMAIL PROTECTED]
To: biofuel@sustainablelists.org
Sent: Friday, April 28, 2006 11:05 AM
Subject: Re: [Biofuel] Filtering - was Re: Vegtable oil sources...


 Keith,
You wrote:
 So I'm also interested in what folks might have to say about filtering, 
 and
 not filtering.

 I filtered my WVO when I was doing small - 1L, 5L, 15L batches - but
 found it to be too time and energy-consuming when I began to run larger
 (91L) batches.
 Before upscaling my process, I had already set up sources for WVO, and
 was getting far more WVO than I was processing. Cubies of WVO were filling
 up my shed.
 I got a few 55 gal drums to store the oil in and found that after settling
 in the cubies for a few weeks, the oil was very clear.  I now rely on
 gravity/settling and do not filter my WVO.
 I allow the WVO to settle in cubies for a week. I then pour the top 
 80%
 of each cubie into a barrel and consolidate the bottoms of 5 cubies into 
 1.
 Most of this will be ready for the barrel the next week. I have 4 WVO
 barrels. One is settled and is used for processing, two are settling, and
 one is being filled. I pump WVO out of the settled barrel from the top 
 3/4.
 This oil is very clear and requires very little drying.
 Tom
 - Original Message - 
 From: Keith Addison [EMAIL PROTECTED]
 To: biofuel@sustainablelists.org
 Sent: Friday, April 28, 2006 6:00 AM
 Subject: [Biofuel] Filtering - was Re: Vegtable oil sources...


 Hi Jesse and all

Mike
Yup, I too want to know this, please?  We are still fumbling toward our
co-op.  Naturally, I should just look at Keith's archives and SEE IT
ALL!!!
Jesse

 I'm not sure what all is in the archives, maybe not any definitive
 answers. There's nothing about filtering at JtF. I've been sort of
 sporadically working on a section covering filtering, as well as
 collection and so on, for SVO as well as biodiesel, and I'd like to
 finish it and get it uploaded.

 So I'm also interested in what folks might have to say about
 filtering, and not filtering.

 Best

 Keith





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Re: [Biofuel] best source for WVO

2006-03-22 Thread logan vilas
Wouldn't the sugar be washed out of the biodiesel? It will disolve in water 
and most if not all of it would be removed.

Logan Vilas
- Original Message - 
From: Bob Carr [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, March 22, 2006 11:59 AM
Subject: Re: [Biofuel] best source for WVO


 It leaves a horrid toffee like deposit on your valves , pistons, rings and
 every other part that comes into contact with the fuel.
 When your piston rings are glued into their grooves, the sugar deposits 
 will
 find their way into your engine oil where they act as an abrasive on all
 your bearing surfaces.
 I have actually witnessed 2lbs of sugar poured into a guys tank, his 
 engine
 was irreparably damaged within 50 miles

 - Original Message - 
 From: Zeke Yewdall [EMAIL PROTECTED]
 To: Biofuel@sustainablelists.org
 Sent: Wednesday, March 22, 2006 5:21 PM
 Subject: Re: [Biofuel] best source for WVO


 What exactly would sugar do to an engine?  The worst I can think of is
 clogging some filters or increasing carbon deposits.

 Zeke

 On 3/22/06, Bob Carr [EMAIL PROTECTED] wrote:

 Nor sure about lard, but watch out for sugar in your feedstock. This is
 an
 old favourite additive for sabotaging an engine.
 Reg'ds

 Bob


 - Original Message -
 From: ROY Washbish
 To: Biofuel@sustainablelists.org
 Sent: Wednesday, March 22, 2006 12:09 PM
 Subject: Re: [Biofuel] best source for WVO


 Hi All
 Don't donut shops use LARD that is SOLID at room temp?
 Isn't that lard full of sugar?
 Roy


 [EMAIL PROTECTED] wrote:
 as i am just starting myself, i am thinking towards donut shops. they
 usually fry no meats in their veg oil and would have less fats.

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[Biofuel] HELPFUL CREDIT INFO

2006-03-21 Thread logan vilas





  ATTORNEY'S ADVICE -- NO CHARGE

 Read this and make a copy for your files in case you need to refer to 
it someday. Maybe we should all take some of his advice! A corporate 
attorney sent the following out to the employees in his company.

1. Do not sign the back of your credit cards. Instead, put PHOTO ID 
REQUIRED.

 2. When you are writing checks to pay on your credit card accounts, DO 
NOT put the complete account number on the For line. Instead, just put the 
last four numbers. The credit card company knows the rest of the number, and 
anyone who might be handling your check as it passes through all the check 
processing channels won't have access to it.

 3. Put your work phone # on your checks instead of your home phone. If 
you have a PO Box use that instead of your home address. If you do not have 
a PO Box, use your work address. Never have your SS# printed on your checks. 
(DUH!) You can add it if it is necessary. But if you have it printed, anyone 
can get it.

 4. Place the contents of your wallet on a photocopy machine. Do both 
sides of each license, credit card, etc. You will know what you had in your 
wallet and all of the account numbers and phone numbers to call and cancel. 
Keep the photocopy in a safe place. I also carry a photocopy of my passport 
when I travel either here or abroad. We've all heard horror stories about 
fraud that's committed on us in stealing a name, address, Social Security 
number, credit cards.

 Unfortunately, I, an attorney, have firsthand knowledge because my 
wallet was stolen last month. Within a week, the thieve(s) ordered an 
expensive monthly cell phone package, applied for a VISA credit card, had a 
credit line approved to buy a Gateway computer, received a PIN number from 
DMV to change my driving record information online, and more. But here's 
some critical information to limit the damage in case this happens to you or 
someone you know:

 5. We have been told we should cancel our credit cards immediately. But 
the key is having the toll free numbers and your card numbers handy so you 
know whom to call. Keep those where you can find them.

 6. File a police report immediately in the jurisdiction where your 
credit cards, etc., were stolen. This proves to credit providers you were 
diligent, and this is a first step toward an investigation (if there ever is 
one).

 But here's what is perhaps most important of all: (I never even thought 
to do this.)

 7. Call the 3 national credit reporting organizations immediately to 
place a fraud alert on your name and also call the Social Security fraud 
line number. I had never heard of doing that until advised by a bank that 
called to tell me an application for credit was made over the Internet in my 
name. The alert means any company that checks your credit knows your 
information was stolen, and they have to contact you by phone to authorize 
new credit.

 By the time I was advised to do this, almost two weeks after the theft, 
all the damage had been done. There are records of all the credit checks 
initiated by the thieves' purchases, none of which I knew about before 
placing the alert. Since then, no additional damage has been done, and the 
thieves threw my wallet away this weekend (someone turned it in). It seems 
to have stopped them dead in their tracks.

 Now, here are the numbers you always need to contact about your wallet, 
etc., has been stolen:

1.) Equifax: 1-800-525-6285

2.) Experian (formerly TRW): 1-888-397-3742

3.) Trans Union: 1-800-680-7289

4.) Social Security Administration (fraud line): 1-800-269-0271

 We pass along jokes on the Internet; we pass along just about 
everything.

 If you are willing to pass this information along, it could really help 
someone that you care about. 


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Re: [Biofuel] HELPFUL CREDIT INFO

2006-03-21 Thread logan vilas
I personaly put ask for ID on my cards I've never run into a problem with 
it, but I also live in louisiana. Here I've been asked for my ID once ever 
when makeing a c/c purchase and the reason was it was 1200 dollars and the 
machine told the clerk to call. When he called they asked him to check my 
ID. As for the c/c number I can see troubles happening, The payment slip 
that you are souposed to return normally has the full number on it.

Logan Vilas
- Original Message - 
From: Garth  Kim Travis [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, March 21, 2006 11:03 AM
Subject: Re: [Biofuel] HELPFUL CREDIT INFO


 Greetings,
 Unfortunately, this attorney did not do his homework.  Many places
 including the USPS will not accept a credit card that is not
 signed.  Worse, you will be paying late fees on your credit card payment 
 if
 you don't put the full number on your check, many companies just chuck 
 them
 aside until they have time to track down your account number and make your
 payment late.  They can do this as the instruction they send tell you to
 put your full account number on the check.  Ask your company before
 following this attorneys advice.

 The rest of his advice is good, only if you have a safe secure place to
 keep all your photo copies.

 If your credit card will let you put your picture on it, do so.  If they
 allow pin numbers, use one.

 Bright Blessings,
 Kim

 At 09:47 AM 3/21/2006, you wrote:





   ATTORNEY'S ADVICE -- NO CHARGE

  Read this and make a copy for your files in case you need to refer 
 to
it someday. Maybe we should all take some of his advice! A corporate
attorney sent the following out to the employees in his company.

 1. Do not sign the back of your credit cards. Instead, put PHOTO ID
REQUIRED.

  2. When you are writing checks to pay on your credit card accounts, 
 DO
NOT put the complete account number on the For line. Instead, just put 
the
last four numbers. The credit card company knows the rest of the number, 
and
anyone who might be handling your check as it passes through all the check
processing channels won't have access to it.

  3. Put your work phone # on your checks instead of your home phone. 
 If
you have a PO Box use that instead of your home address. If you do not 
have
a PO Box, use your work address. Never have your SS# printed on your 
checks.
(DUH!) You can add it if it is necessary. But if you have it printed, 
anyone
can get it.

  4. Place the contents of your wallet on a photocopy machine. Do both
sides of each license, credit card, etc. You will know what you had in 
your
wallet and all of the account numbers and phone numbers to call and 
cancel.
Keep the photocopy in a safe place. I also carry a photocopy of my 
passport
when I travel either here or abroad. We've all heard horror stories about
fraud that's committed on us in stealing a name, address, Social Security
number, credit cards.

  Unfortunately, I, an attorney, have firsthand knowledge because my
wallet was stolen last month. Within a week, the thieve(s) ordered an
expensive monthly cell phone package, applied for a VISA credit card, had 
a
credit line approved to buy a Gateway computer, received a PIN number from
DMV to change my driving record information online, and more. But here's
some critical information to limit the damage in case this happens to you 
or
someone you know:

  5. We have been told we should cancel our credit cards immediately. 
 But
the key is having the toll free numbers and your card numbers handy so you
know whom to call. Keep those where you can find them.

  6. File a police report immediately in the jurisdiction where your
credit cards, etc., were stolen. This proves to credit providers you were
diligent, and this is a first step toward an investigation (if there ever 
is
one).

  But here's what is perhaps most important of all: (I never even 
 thought
to do this.)

  7. Call the 3 national credit reporting organizations immediately to
place a fraud alert on your name and also call the Social Security fraud
line number. I had never heard of doing that until advised by a bank that
called to tell me an application for credit was made over the Internet in 
my
name. The alert means any company that checks your credit knows your
information was stolen, and they have to contact you by phone to authorize
new credit.

  By the time I was advised to do this, almost two weeks after the 
 theft,
all the damage had been done. There are records of all the credit checks
initiated by the thieves' purchases, none of which I knew about before
placing the alert. Since then, no additional damage has been done, and the
thieves threw my wallet away this weekend (someone turned it in). It seems
to have stopped them dead in their tracks.

  Now, here are the numbers you always need to contact about your 
 wallet,
etc., has been stolen:

 1.) Equifax: 1-800-525-6285

 2.) Experian

Re: [Biofuel] automating titration

2006-03-16 Thread logan vilas
The same could be done with a ph meter with external alarm. Put a relay 
inline to a solenoid valve when it hits the right ph the solenoid valve 
shuts off flow. Just use a measureing device like a burett. when you come 
back to it read the burett and see how many ml was used.

Logan Vilas
- Original Message - 
From: Joe Street [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, March 16, 2006 8:29 AM
Subject: Re: [Biofuel] automating titration


 Hey Jason;

 If you are bent on doing this, why not approach it from a different
 angle?  Make a system that imitates what you do yourself, instead of
 trying to do it numerically just make a system that does what you do.
 It could all be done by way of gravity feed and counting drops by use of
 optical sensors.  You add a few drops of indicator and then keep adding
 titration solution until the indicator goes off and stays for 10
 seconds.  That's 8.4 ph.  Again a photosensor is used to detect the
 colour change condition.
 This will for sure work and eliminates much of the problem with trying
 to meter flows.

 Joe

 Jason  Katie wrote:

Mr. McGinness
i thank you for the advice on the pumps/ flow controls, i hadnt considered
ready-made equipment (i usually build my own rig) ill have to look into
that, but my problem does not lie within the realm of mechanics. i need a
mathematical equation that i can manipulate to find the volume of  base
needed to bring the acid to a pH of 8.4.

the knowns will be:

pH of the base (by reference measurement)
pH of the Oil (by measurement)
volume of the oil (by external input)

the variable will be:

volume of base needed to reach a pH of 8.4

i have the outline of what i need, i just dont know how to put it together
and make it work and pH isnt some simple (A+B)/C= your number here
equation, which is confusing me beyond anything ive ever tried before (im
horrible at math).


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Re: [Biofuel] Methoxide Questions

2006-03-15 Thread logan vilas
Mike,

Thanks mike you answered my question on this and another question I had 
about titration. I'm not one for the facts of chemestry but I can understand 
that 2 different substances with the same ph will take different amounts of 
lye to raise the ph to the same level.

Logan Vilas
- Original Message - 
From: Mike McGinness [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Tuesday, March 14, 2006 11:02 PM
Subject: Re: [Biofuel] Methoxide Questions


 Logan,

 The reaction forms water (H2O) and Sodium Methoxide (CH3ONa) from the 
 methanol
 (CH3OH) and sodium hydroxide (NaOH).

 I think part of the answer to your second question is it will make more 
 soaps
 (not good) if you adjust the pH first.

 Mike McGinness

 Logan Vilas wrote:

 I've searched the archives so please forgive me if I didn't find this
 question.

 What is the chemical reaction when making methoxide? Why do we not 
 correct
 the ph of the oil then add methoxide, made with a standard grams per a
 liter?

 Logan Vilas


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Re: [Biofuel] automating titration

2006-03-14 Thread Logan Vilas
Jason

I personally think that there will be a set amount of grams KOH per liter
depending on the ph of your oil. It might vary slightly based on your Lye
supply but you could test your lye and have a set multiplier to adjust.
People on here have told me I'm wrong. I just can't see it not being that
easy. As I perform titrations I keep a log of the ph before I titrate and
the number of grams per a liter it took to reach ph 8.4. It will just take
time and many batches of data to compare and see if I'm right. 

Bob Allen

Can you verify if there would be a standard for example

IF USED OIL PH=6.2 THEN ADD 2.3 GRAMS PER A LITER OF 100% KOH TO
REACH PH 8.5

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Jason  Katie
Sent: Tuesday, March 14, 2006 7:13 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] automating titration

Mr. McGinness
i thank you for the advice on the pumps/ flow controls, i hadnt considered 
ready-made equipment (i usually build my own rig) ill have to look into 
that, but my problem does not lie within the realm of mechanics. i need a 
mathematical equation that i can manipulate to find the volume of  base 
needed to bring the acid to a pH of 8.4.

the knowns will be:

pH of the base (by reference measurement)
pH of the Oil (by measurement)
volume of the oil (by external input)

the variable will be:

volume of base needed to reach a pH of 8.4

i have the outline of what i need, i just dont know how to put it together 
and make it work and pH isnt some simple (A+B)/C= your number here 
equation, which is confusing me beyond anything ive ever tried before (im 
horrible at math). 


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[Biofuel] Methoxide Questions

2006-03-14 Thread Logan Vilas
I've searched the archives so please forgive me if I didn't find this
question.

What is the chemical reaction when making methoxide? Why do we not correct
the ph of the oil then add methoxide, made with a standard grams per a
liter? 

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Jason  Katie
Sent: Tuesday, March 14, 2006 7:13 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] automating titration

Mr. McGinness
i thank you for the advice on the pumps/ flow controls, i hadnt considered 
ready-made equipment (i usually build my own rig) ill have to look into 
that, but my problem does not lie within the realm of mechanics. i need a 
mathematical equation that i can manipulate to find the volume of  base 
needed to bring the acid to a pH of 8.4.

the knowns will be:

pH of the base (by reference measurement)
pH of the Oil (by measurement)
volume of the oil (by external input)

the variable will be:

volume of base needed to reach a pH of 8.4

i have the outline of what i need, i just dont know how to put it together 
and make it work and pH isnt some simple (A+B)/C= your number here 
equation, which is confusing me beyond anything ive ever tried before (im 
horrible at math). 


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Re: [Biofuel] hybrid efficiency

2006-03-10 Thread logan vilas
Hakan,

The price depends on volume purchased and it doesn't make much sense. 
Distilled water costs 60 cents to 1.50 for a gallon depending on brand. 1/2 
liter bottled water costs 1 dollar, but at the same store I can buy 1 gallon 
of the same brand for .80 cents. I just have to walk down the isle instead 
of grabing it at the checkout counter. Then you can buy filtered water for 
as cheap as 30 cents a gallon. At least that's the local grocery store here 
in Louisiana, USA

So if you buy water by the 1/2 liter it is more expensive then gas, but 
gallon by gallon it's 1/3rd the price or cheaper.

Logan Vilas
Bio-Fuel Enterprises, Inc.

- Original Message - 
From: Hakan Falk [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, March 09, 2006 5:09 PM
Subject: Re: [Biofuel] hybrid efficiency



 David,

 I do not understand why it is silly to want to know the facts about
 the following,

 Jeromie Reeves wrote:

Are you serious? N. America has cheap fuel? Please show me this cheap
fuel as I pay WAY
more for a gallon of gas then I do a gallon of bottled water.

Jeromie

Andrew Netherton wrote:



I'll bet that research would show a mighty quick return on investment
if they had done the study based on European fuel costs, and not our
cheaper-than-bottled-water fuel here in North America.

Andrew Netherton

 I live in Europe and we pay WAY more for the fuel than bottled water.

 Hakan


 At 22:44 09/03/2006, you wrote:
Hakan Falk wrote:
  That means that bottled water is more expensive than gasoline, as I
  understand,
 
 http://www.bairdpetro.com/gasoline_prices/index.htmhttp://www.bairdpetro.com/gasoline_prices/index.htm
  @ $1.453 per gallon.
 
  So, what was wrong with the original statement?
  Nothing as I understand it.
 

This is just silly.

People want to make a point that gasoline is cheap in the US so they
come up with something that makes it sound cheaper than water.

It's not enough that we're going to compare gasoline, an industrial
fuel, to food quality water that's packaged for individual consumption.

Now we're going to compare the industrial, bought in large dollar
quantities, price of gasoline without any kind of road or sales tax to
water packaged for individual consumption with any and all applicable
taxes applied.

If you really want to compare the price of gasoline to water, how about
using the price of water from the water company?  Oh, right, it's
because they charge cents per cubic foot and all of a sudden our
comparison looks silly.


Gasoline IS cheap in the US.  It's not highly taxed compared to the rest
of the world, and it doesn't include any of the external costs which
might double or triple the price.  It doesn't include the costs of its
use (global warming, pollution, health side-effects), the costs of it's
production (pollution, economic and social policies), or its procurement
(military intervention, social and economic policies).

Rather than dredging up platitudes about it being cheaper than water
which just IMHO make people look silly , could we please talk about its
real costs?

Thanks,

--- David

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Re: [Biofuel] A wealth of manuals

2006-03-03 Thread logan vilas
I downloaded it thins morning thanks. I'll also seed it on Torrentspy.com

Logan Vilas
- Original Message - 
From: David Miller [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, March 02, 2006 5:02 PM
Subject: Re: [Biofuel] A wealth of manuals




 I have a mostly idle server with a 100 Mbit connection to the AOL/TW
 backbone.  Obviously,
 using it all would be frowned upon, but I'm willing to put it up and see
 what happens.

 Has anybody already downloaded it?  It sounds like it's not going to
 happen very fast.
 Please let me know asap if you have it.

 Thanks,

 --- David


 OK!  Kirk ([EMAIL PROTECTED]) got a full copy of it and we got it
 onto my server today.

 If you have winzip, pkzip, or gzip and can uncompress a file, save a bit
 of bandwidth on the full ISO with:

 http://renegade.sparks.net/cd3wd.iso.gz  (471 MB)

 If you just need the raw ISO file, click on:

 http://renegade.sparks.net/cd3wd.iso (694 MB)

 Note:  The CD image contains a pile of self extracting .exe files.  You
 have to run them before being able to view any files at all.

 I haven't done this, and I don't and can't vouch for any of the
 programs.  If they're full of virii it's not my fault, and I'm not
 available for help in recovering your system:)

 Also, I'm limiting the server to 75 simultaneous connections until I see
 what bandwidth utilization is like.  If there are lots of people who
 can't connect and the utilization isn't too high I can increase that.
 We'll see how it goes.

 Hope it helps people.

 --- David

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Re: [Biofuel] A wealth of manuals

2006-02-28 Thread Logan Vilas
I'm having the same problems downloading the link, but I'm downloading the
entire web site. I'll see how that goes. So far it's about 30-50kb/s

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of David Miller
Sent: Tuesday, February 28, 2006 7:13 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] A wealth of manuals

Evergreen Solutions wrote:
 If there is somebody who has succeeded in getting these, make a
 .torrent and host it somewhere and put up the link...better sharing
 for everyone.
   

I have a mostly idle server with a 100 Mbit connection to the AOL/TW 
backbone.  Obviously,
using it all would be frowned upon, but I'm willing to put it up and see 
what happens.

Has anybody already downloaded it?  It sounds like it's not going to 
happen very fast. 
Please let me know asap if you have it.

Thanks,

--- David



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Re: [Biofuel] A wealth of manuals

2006-02-28 Thread Logan Vilas
I found the slowdown. It's not a server and with paralleal computing it's
slowed down.

What is Sleekfreak?

Sleekfreak is enjoying its new home in a 1.1 ghz athlon, with a gig of ram
and scsi raid 1 storage. It is running the Woody release of Debian/GNU
linux. It functions as secondary secure wireless access point, router,
authoritative nameserver, web server, smtp/pop3 server, ftp server, cvs
server, ssh server, and irc server for the Sleekfreak Pirate Broadcast. It
also serves as a fully configured multimedia X-Window workstation, complete
with graphics, audio, programming, web design, virtual reality programming,
office, accounting, and network software, in addition to being part of a
heterogenous parallel computing cluster... the ghetto ring

http://sleekfreak.ath.cx:81/technology.html

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of doug
Sent: Tuesday, February 28, 2006 8:30 PM
To: Biofuel@sustainablelists.org
Subject: Re: [Biofuel] A wealth of manuals

Logan Vilas wrote:

I'm having the same problems downloading the link, but I'm downloading the
entire web site. I'll see how that goes. So far it's about 30-50kb/s

Logan Vilas
  

After several attempts at the cd.iso file, I just started going through 
the links and DL the pages that are of primary interest to me at this 
time...  some ag, some fuels, food preservation, energy systems, etc.  
Just using the download link target (Right click in Mozilla) doesn't 
include graphics on each page, and several of the link targets would 
have opened to another index, listing more links.  An FTP would be nice, 
or Torrent,  But this seems to be working.

I'd bet that the biofuels list members flocking to this site and viewing 
and downloading pages may be part of the reason that their server 
appears so slow.  Sure, it could handle the load if it was a high speed 
connection, but I get the impression that it isn't, or it may be restricted.

Loads of great info there though!

doug swanson
-- 

Contentment comes not from having more, but from wanting less.

* * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * *

This email is constructed entirely with OpenSource Software.
No Microsoft databits have been incorporated herein.
All existing databits have been constructed from recycled databits. 


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Re: [Biofuel] Let's accredit ourselves

2006-02-22 Thread logan vilas
 Original Message - 
Kenji James Fuse Wrote

I wasn't talking aboout the ASTM test, although one of these days I'm
 going to talk to politicians and bureaucrats about getting the 'distillate
 curve' off the Canadian specs.

 All I meant is that we write up a 'biodiesel safe' thingy, like those
 silly foodsafe courses waiters and grocery store clerks have to take
 (after wiping your bum, wash your hands). Why let ignorant and
 liability-conscious politicos do it in a year or so, when we could do it
 easily, better and beat them to it?

 KF


Kenji,

I'm willing to put in time and effort.

The polititions will eventually form a board and write rules and
regulations on produceing biofuels for personal and businesses. They will
either say you can't do it personally or they'll make the requirements so
strict that you won't be able to do it LEAGLY. To acredit ourselves and do
it in a weak manner won't do any good in a few years. It would take detailed
process documents, safety regulations, requirements, restrictions of
materials to be used and various other things. Then the documents would have
to be transulated into the major languages of the world. Without this type
of work it would be pointless because the EPA, or various other
orginizations would not reconize any authority you have created.

There would not be a requirement to actually inspect and police the
people doing it. They would be takeing legal responsability and negating
their membership if they did not follow the rules and regulations. If we
work and do it right we could form an associatoin that would be respected
and reconized worldwide while makeing it possiable for people to produce
biodiesel on a personal scale.

Keith, How many members are there for the biofuel list?

Logan Vilas
Bio-Fuel Enterpriese, Inc.



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[Biofuel] Filter bags adaptor heads

2006-02-21 Thread Logan Vilas










I just found the filter bag adaptor heads
in McMaster-Carr. For bags 4 3/32 made from polypro 13.13 or for 7
bags 17.5 instead of 30-35 that Ive found them elsewhere.



Logan Vilas

Bio-fuel Enterprises, Inc.








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Re: [Biofuel] Ethynol vs Biodiesel

2006-02-04 Thread Logan Vilas

Andrew wrote:

Ethanol and Biodiesel are totally different substances and have completely 
different applications. Biodiesel works in engines with a compression ratio

over 50, like most of diesel engines. Explossion in the engine occurs 
because a temperature/pressure ratio (the diesel cicle). Ethanol/Gas blends

and ethanol alone are used in the lower compression ratio engines tipically

10. The explosion occurs because a spark plug initiates the cicle.
There are not engines which can use either ethanol and Biodiesel. Ethanol 
may explode way before the right moment in the high compression diesel 
cicles and Biodiesel do not have the flash point enough for a low 
compression engine.

There might be diesel engines with compression ratio that high, but they
usually don't go over 25:1. Pure ethanol can run in engines as high as 13:1
compression ratio. And there are some very unique engines that can run both.


The US Army duce and a half can run on almost anything you put into it and
it will run a very long time with no problem. They normally run diesel, but
I've been told that they will run on any flammable liquid. There is a set of
controls that can be adjusted based on what type of fuel you put in.

Logan Vilas


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Re: [Biofuel] Cooking oil isn't just for diesels anymore.

2006-01-19 Thread Logan Vilas
Is Cooking oil nonconductive? If so it would work. I've seen pictures of
computers immersed in other nonconductive liquids.

Logan Vilas

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Alan Petrillo
Sent: Thursday, January 19, 2006 4:25 PM
To: Biofuel list
Subject: [Biofuel] Cooking oil isn't just for diesels anymore.

I wouldn't have believed it if I hadn't seen it.  I'm still not sure I 
believe it, frankly.  But if it's a web stunt, then at least it's a 
_good_ web stunt!

http://www.tomshardware.com/2006/01/09/strip_out_the_fans/


AP


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Re: [Biofuel] Dewatering with vacuum.

2006-01-18 Thread logan vilas

- Original Message - 
From: David Miller [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, January 18, 2006 8:49 AM
Subject: Re: [Biofuel] Dewatering with vacuum.


 Those sound about right.  An atmosphere is ~30 mercury and  ~30 feet of
 water.

Just in case anyone is useing it for measurements. One atsmophere of water 
is 33 feet.

Logan Vilas 


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Re: [Biofuel] Dewatering with vacuum.

2006-01-18 Thread logan vilas



Well said, but a higher vacuum can be pulled when 
below sea level and it will read lower when above sea level. So it would be best 
to know your baramic pressure before determining what your vacuum needs to be. 
Forpeople above sea levelthey don't have to get as high ofa 
vacuume because they are already at a lower pressure. If you're up on a 
mountainit will be even easier.

Logan Vilas

  - Original Message - 
  From: 
  Arttu 
  Aula 
  To: Biofuel@sustainablelists.org 
  
  Sent: Wednesday, January 18, 2006 7:08 
  AM
  Subject: Re: [Biofuel] Dewatering with 
  vacuum.
  You're talking about 2 different things.Talking about 
  so-and-so-much vacuum is sort of misleading. Your 30"Hg of vacuum means 
  0"Hg (0 mmHg, 0 mbar, 0 psi) absolute pressure; the vapor pressure points were 
  absolute pressure. Absolute pressure is measured according to how high 
  of a column of mercury it can push upwards with a complete vacuum at the top, 
  gauged pressure with atmospheric at the top. 29.92"Hg (760 mmHg, 1013.25 
  mbar, 14.7 psi) is standard atmospheric pressure at sea level, so that's the 
  maximum height you can pull up mercury with a vacuum if the other end is 
  exposed to air pressure at standard conditions, which means the vacuum reading 
  will vary slightly according to the weather, even if the actual measured 
  pressure stays constant. Absolute pressure is atmospheric pressure 
  minus vacuum.
  
  

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Re: [Biofuel] Dewatering with vacuum.

2006-01-18 Thread logan vilas



To remove water at 55C your pump has to remove 
11(at sea level)times the atsmopheric volume of your container before you 
get to a low enough vacuum to boil off water. If your atsmophericpressure 
is 0.13 PSI lowerat your level.Then yourmultiplier is only 10 
times, and if it's .29 PSI lower it is 9 times.

At sea level 1 cubic foot of free air in your 
vessel will result in 11cfm that your pump has to move and if just a small 
amount of uncondensed water goes through your pump that can add up very 
quickely. Then If your pump is not 100% efficent that adds another 
multiplier.

Logan Vilas


  - Original Message - 
  From: 
  Joe Street 
  To: Biofuel@sustainablelists.org 
  
  Sent: Wednesday, January 18, 2006 11:21 
  AM
  Subject: Re: [Biofuel] Dewatering with 
  vacuum.
  Atmospheric pressure varies by a fraction of an inch (except 
  for at the eye of a hurricane and then dewatering your oil is less 
  important!)logan vilas wrote:
  



Well said, but a higher vacuum can be pulled 
when below sea level and it will read lower when above sea level. So it 
would be best to know your baramic pressure before determining what your 
vacuum needs to be. Forpeople above sea levelthey don't have to 
get as high ofa vacuume because they are already at a lower pressure. 
If you're up on a mountainit will be even easier.

Logan Vilas

  - 
  Original Message - 
  From: 
  Arttu 
  Aula 
  To: 
  Biofuel@sustainablelists.org 
  
  Sent: 
  Wednesday, January 18, 2006 7:08 AM
  Subject: 
  Re: [Biofuel] Dewatering with vacuum.
  You're talking about 2 different things.Talking 
  about so-and-so-much vacuum is sort of misleading. Your 30"Hg of 
  vacuum means 0"Hg (0 mmHg, 0 mbar, 0 psi) absolute pressure; the vapor 
  pressure points were absolute pressure. Absolute pressure is 
  measured according to how high of a column of mercury it can push upwards 
  with a complete vacuum at the top, gauged pressure with atmospheric at the 
  top. 29.92"Hg (760 mmHg, 1013.25 mbar, 14.7 psi) is standard 
  atmospheric pressure at sea level, so that's the maximum height you can 
  pull up mercury with a vacuum if the other end is exposed to air pressure 
  at standard conditions, which means the vacuum reading will vary slightly 
  according to the weather, even if the actual measured pressure stays 
  constant. Absolute pressure is atmospheric pressure minus 
  vacuum.
  
  
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Re: [Biofuel] Dewatering with vacuum.

2006-01-07 Thread logan vilas
David

Sorry if that number's wrong it's what I've been told from the only person I 
know who does AC work.

But that number makes it sound a lot better. You will not have 1 cubic foot 
of water in your oil after you settle and drain it. If you do then you need 
to get a better method. There is likely less then 1 cubic inch after 
setteling and draining. That would only take 6 miniutes to remove.

Logan Vilas

- Original Message - 
From: David Miller [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Friday, January 06, 2006 1:13 PM
Subject: Re: [Biofuel] Dewatering with vacuum.


 logan vilas wrote:

 Water boils off at 43F at 20-50mmhg of vacuum at sea level. At 140F it
 takes about 150-200mmhg. When fluids are mixed togther the Pressure of
 Vaporization changes especially when thouroughly mixed. You do not
 need a condensor if you are useing a AC type vacuum pump(that's what
 they are designed for).

 I know iowa's BECON program flash heats their oil to 230F then runs it
 through a vacuum chamber to achieve dewatering. Unless you have a very
 large vacuum pump or very little water in your oil it will take a long
 time. Water multiplies in volume by 10-18 thousand times when boiled.


 Say WHAT?  I'm not sure what number you mean by 10-18 thousand.  The
 number I remember is about 1700 times.


 1 Cubic foot =  1728 cubic inches
 1 Cubic Inch of water when boiled off = 5.79 cubic feet minimum
 1 gallon = 231 cubic inches

 Vacuum Distilation alone would take a huge amount of time. I would
 still heat then let it settle and remove the water off the bottom.
 Then use vacuum distilation. Remember if you buy a 5CFM vacuum pump
 that is displacement of the piston at no load and full rpm. When you
 start pulling a vacuum that number falls off quickely and at 30 that
 is probably less then 1CFM.


 You have to multiply the CFM by the pressure. 1/30 atmosphere * 5 CFM =
 1/6 CFM.  It you're trying to pump off a cubic foot of water it would
 take something like 1700 * 6 minutes.  That's a long time to wait:)

 --- David


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Re: [Biofuel] Dewatering with vacuum.

2006-01-06 Thread logan vilas



Water boils off at 43F at 20-50mmhg of vacuum at sea 
level.At 140F it takes about 150-200mmhg.When fluids are mixed 
togther the Pressure of Vaporization changes especially when thouroughly mixed. 
You do not need a condensor if you are useing a AC type vacuum pump(that's what 
they are designed for).

I know iowa's BECON program flash heats their oil to 230F 
then runs it through a vacuum chamber to achieve dewatering. Unless you have a 
very large vacuum pump or very littlewater in youroil it will take a 
long time. Water multiplies in volume by 10-18 thousand times when 
boiled.

1 Cubic foot = 1728 cubic inches
1 Cubic Inch of water when boiled off = 5.79 cubic feet 
minimum
1 gallon = 231 cubic inches

Vacuum Distilation alone would take a huge amount of time. 
I would still heat then let it settle and remove the water off the bottom. Then 
use vacuum distilation. Remember if you buy a 5CFM vacuum pump that is 
displacement of the piston at no load and full rpm. When you start pulling a 
vacuum that numberfalls off quickely and at 30" that is probably less then 
1CFM.

A Racor Fuel filter/dewaterar MIGHT work also. They are 
built for Diesel engines, but the ones you can afford havelow flow 
rates.

Logan Vilas

  - Original Message - 
  From: 
  [EMAIL PROTECTED] 
  To: Biofuel@sustainablelists.org 
  
  Sent: Thursday, January 05, 2006 3:35 
  PM
  Subject: [Biofuel] Dewatering with 
  vacuum.
  
  Can vacuum be used alone to dewater oil at room temp?Or even at 
  slightly elevated temp? 55 deg. C would be a good temp so
  when it finished drying it could be sent directly to the processor. I 
  would alsoneed a condenser to keep the evacuated water out of the vacuum 
  pump.A friend of mine (in ACR) uses vacuum @30" water column to 
  take the watercontent to 300 micron. What micron is acceptable other than 
  the obvious 0micron?I am just looking at options vs costs. I seen 
  a post the other day and itmade me sit back and think.As always 
  appreciate your input.John Frey
  
  

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Re: [Biofuel] It was bound to happen - is this the beginning of the endfor BD?

2006-01-03 Thread Logan Vilas
I am not sure about California, but in Louisiana the DEQ considers Waste
Vegetable Oil a solid waste. Their definition of solid waste is trash and
other discarded materials that is not hazardous. The key word is discarded.
If I am purchasing the oil then it is not discarded it is sold. It is an
asset to the restaurant and becomes yours at purchase. I purchase it for
.005 dollars a gallon and meter all the oil I get. I know Louisiana is much
more relaxed then California but there may be some merit. I also refer to it
as USED Vegetable Oil (UVO). If you call it waste then it is waste. But used
Items are not waste. If Used grease was a waste then you would need a permit
to purchase Yellow Grease which is Filtered UVO.

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Mike Weaver
Sent: Tuesday, January 03, 2006 7:42 PM
To: Biofuel@sustainablelists.org
Subject: [Biofuel] It was bound to happen - is this the beginning of the
endfor BD?

Gov Arnold signed into law in Sept 05 a waste collection law AB1065, 
that had no minimum use exemption and classified all restaurant waste as 
waste grease.
There are several of us in California that have developed a letter that 
we have sent to our legislators and the author asking for an amendment. 
This law was sponsored by the refiners as a response to broken 
contracts. Another thing that they have been doing is making new 
contracts that have a all or nothing clause. They will not take the trap 
waste without the fryer oil. This new law requires anyone who collects 
waste grease in any amount to have a liscense and 1million dollar bond 
insurance. This is wrong and we are trying to fight it.  If any of you 
on this list live in CA please contact me so I can get you the copy of 
the letter.


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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] 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] Household electricity consumption questions, remarks, and theorizing.

2005-11-20 Thread logan vilas
I do not know about battary's for your house, but if useing automotive 
battarys I would recomend BAT-CAPS http://www.batcap.net/Model800.html. It 
is a battary with the discharge capability of a capaciter so there will be 
no unexpected brownouts because your battary can't keep up. They can be 
completely drained and recharged many times without a problem. Most auto 
battarys can not do that. They are also half the size of the equilivant 
battary. They can be mounted in any posistion or angle you want.

Logan Vilas


- Original Message - 
From: Michael Nehring [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Saturday, November 19, 2005 12:28 PM
Subject: [Biofuel] Household electricity consumption questions, remarks,and 
theorizing.


 Hi all,
 In about 8 months or so, I and my (future) wife will buy our first
 house. One of my goals is to have a relatively high level of energy
 self-sufficiency (without going bankrupt since we currently don't have a
 ton of cash lying around).

 First question: does anyone know of any charts/statistics of household
 energy consumption. I'm not so much interested in kilowatthours per day,
 but rather how the usage is divided up. This will make it easier to plan
 what areas typically need to be improved.

 On another note, have any of you guys already looked at this:
 http://mtbest.net/chest_fridge.html. It's a fridge that uses only .1
 kw-hours/day (that's around 37 per year, and at $.1/kWh, that's less
 than $4 year if you're on the grid). The idea is surprisingly simple.

 Another question: does anyone know how many kilowatt hours are stored in
 a normal car battery (a battery for a standard sedan, I suppose)? I've
 been thinking about hooking an inverter up to a car battery (or probably
 an array) to power various devices in the house. However, I don't know
 how much power is actually in a fully charged battery.
 Here would be one idea to charge the batteries: I just install a few
 extra alternators in my car, and have those charge the batteries which
 would be stored in the trunk. Assuming the car is running biodiesel,
 then the electricity would be produced by biodiesel. Does the idea sound
 reasonable? Or does it have too many drawbacks and pitfalls? Are there
 other 12V batties that are better designed for household-type uses? (12V
 so that I can charge it with an alternator, since I have a few
 alternators lying around, and can get them for near to free if I go for
 used). How long does it take to charge an empty car battery? If it
 doesn't take long, maybe I could build a simple treadmill-like device
 for the car, so the car spins a wheel, which in turn spins a dozen or so
 alternators to charge a dozen batteries at once. While it isn't the most
 efficient method, it would be cheap, since the motor would stay in the
 car, and the car would serve other purposes (that is, getting places).

 I guess that's it for now. If any of you guys have any tips for common
 sources of waste in a house, I'd be happy to hear them (I'm already
 planning a rainwater harvesting system and a greenhouse for winter food
 production).

 Thanks,
 -Michael

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Re: [Biofuel] bd in furnace and engines

2005-11-18 Thread logan vilas



I use one for casting alumium and have burned 
a20-30 gallonsof Bio-diesel through it. Ifit isn't really 
clean then the flame eye gets sooted overin less then 5 min and you have 
to shut down and clean it, but if the fuel is good it will run a long 
time.Also I've been selling BD to a Diving company who uses it in their 
hot water heaters. They haveused about200-300 gallonsin one of 
their machines and no problems. 

Logan Vilas

  - Original Message - 
  From: 
  Andrew Leven 
  
  To: Biofuel@sustainablelists.org 
  
  Sent: Thursday, November 17, 2005 8:46 
  PM
  Subject: [Biofuel] bd in furnace and 
  engines
  
  Hi All,
  What is the word on using straight bd in a 
  Beckett oil burner? This is a new unit only having burned a few gallons of 
  petro diesel to test it so it is basically a "virgin'. BTW this is a backup 
  unit on my Tarm wood fired boiler. 
  Also has anyone had any issues with the solvent 
  action in a petro diesel engine cleaningthe gunk off the inside of the 
  motor and having it plug up vital item ie: injectors etc.? Once the bd gets 
  past your fuel filter itany degunked stuff is free to pass through the 
  motor unfilterd
  Thanks in advance
  Andrew Leven
  
  

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Re: [Biofuel] Drying KOH

2005-11-15 Thread logan vilas

Why Butyl? I was thinking Buna-N but butyl is not a problem. It's out of 
1/8 steel. A small CO2 scrubber is easy to make and I have plenty of 
sodasorb/sofnolime available. It won't take much because I am not opening it 
often and it is a very small volume. I can even put in some desicant to know 
if the moisture level is low enough before opening the bag. I'll just hope 
for the best from the CO2 scrubber I don't feel like buying a CO2 meter, but 
I could potentially use a Argon or dry nitrogen purge also. Any thoughts?

Logan Vilas


 The cabinet should be metal and aim for a temperature of -60 Deg. C with
 the peltier stack to get the ppm levels of water down.  Oh also make
 sure the seals are of Butyl rubber not neoprene or buna and the gloves
 too.  If this seems like a lot of work then consider getting a vacuum
 pump.  Put the KOH in a bell jar and pump out all the air.  Gentle
 warming while pumping may even remove adsorbed water and the vacuum will
 keep out the nasty CO2's as well.

 Cheers.


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[Biofuel] Drying KOH

2005-11-14 Thread logan vilas

If KOH is exposed to water can it be dryed? If so do ya'll think 
dehumidifaction would dry it?

I am building a cabinet sort of like a sand blast cabinent for measuring 
KOH. I am going to build a small dehumidifyer from peltier junctoins. It 
opens on the right side to put in a bag of KOH. Then I'll let the 
dehumidifier run until it has very little or no liquid removal before 
opening the bag. I will have a box on the left side of the unit. The box's 
top will open, but close when you let it go. That box will have a door on 
the outside of the case. There will be a tray along the back and left side 
of it. Sandblasting gloves in the front and a plexiglas window. My scales 
will be on the tray. Just measure out the amount needed put it in a plastic 
bag. Then drop the bag in the box. Pull your hands out and remove the bag 
from the little door on the left. 


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Re: [Biofuel] acceptable loss

2005-11-04 Thread logan vilas

I call it a micro seperation tank. I am useing a piece of 8 pipe 8' long. I 
have a ball valve on one the bottom and a sight glass connected to a hose. I 
take that boundry layer and just pour it straight into that pipe. When the 
pipe gets close to full I drain off the bottom. I use the sightglass to 
watch for the boundry layer in this micro tank and put it in a 5 gallon 
bucket to go back into the pipe after I am done seperating the majority of 
it.

You want something tall and skiny to minimize that boundry layer and make 
thicker layers of the material which is easier to be seperated.. My 
processor is 4' square which has a large bottom surface area 2300 Square 
inches and that layer is about 1 thinck, but when put into the 8 pipe with 
50 square inch bottom surface area then it fills 3-5 feet of the pipe making 
each layer 18 thick or more

Logan Vilas
Bio-Fuel Enterprises, Inc.

- Original Message - 
From: David Thornton [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, November 03, 2005 12:24 PM
Subject: Re: [Biofuel] acceptable loss


 Hey Ed, something we've added in our co-op to recover that lost fuel is 
 what
 we've dubbed a boundary separator. It is a small 5 gallon conical steel
 tank we rescued from a metal scrap yard. When draining the wash water, we
 take that boundary layer, meaning the layer where it's not quite pure 
 wash
 water or fuel and we put it first in a 5 gallon bucket. Once it's full 
 from
 all 3-4 washes, we empty it into our boundary separator and let it 
 settle.
 Then drain off water, and take the recovered fuel, set it in a 5 gallon
 carboy and add it to the next new wash.
 Hope this helps.


 Ed Normandy writes:


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Re: [Biofuel] Separating Glycerine/FFA

2005-10-31 Thread logan vilas



SODIUM CHLORIDE IS VERY TOXIC STAY AWAY. IT WILL 
TURN INTO A YELLOW CLOUD. IF YOU SMELL IT IT'S TOO LATE FOR YOU. ABOUT 3 SECONDS 
LATER YOU'LL STOP SMELLING IT AND SHOTLY AFTER YOU'LL DROP DEAD.

THAT'S WHY YOU SHOULD NEVER MIX CHEMICALS TRYING TO 
GET A CLOGED SINK OPEN. I ONCE SAW SOMEONE DUMP RED DEVIL(LYE) THEN POUR CHLOROX 
ON TOP OF IT. i BARELY DRAGED HER OUT BEFORE THE CLOUD HIT HER IN THE 
FACE.

Logan Vilas
Bio-Fuel Enterprises, Inc.

  - Original Message - 
  From: 
  Thomas 
  Kelly 
  To: biofuel 
  Sent: Sunday, October 30, 2005 4:19 
  PM
  Subject: [Biofuel] Separating 
  Glycerine/FFA
  
  Hello All,
   I'm having difficulty 
  getting Phosphoric Acid. Can I use Hydrochloric Acid to separate the 
  Glycerine/FFA ? It will produce Sodium Chloride rather than Sodium Phosphate 
  (I use lye), but other than that, any objections?
  
   
  Tom
  

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Re: [Biofuel] Separating Glycerine/FFA

2005-10-31 Thread logan vilas

My mistake, I said sodium chloride without thinking, but I know mixing lye 
with things that contain chlorine can and will for chlorine gas, I don't 
know exactly what because I've never tried experimenting with it. Sorry for 
the confusion.

Logan Vilas
Bio-Fuel Enterprises, Inc.

- Original Message - 
From: Zeke Yewdall [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Sunday, October 30, 2005 9:07 PM
Subject: Re: [Biofuel] Separating Glycerine/FFA


 Sodium chloride is table salt.  Chlorine is the yellow gas you're
 talking about I think.  You can get it from sodium chloride by
 electrolyzing saltwater, or mixing sodium hypochlorite with lye
 aparrently, but it's not all that dangerous by itself.


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Re: [Biofuel] Anyone find a source for used centrifuges?

2005-10-17 Thread logan vilas
http://www.rousselet-robatel.com/products/lls.php

I was quoted about 2 weeks ago. under 16,000 for a rebuilt BXP 130P. The 
same unit new is just under 28,000. That should do about 3 gallons per min. 
but they have some sizes that are not much larger. I don't know about useing 
it to remove large particles, but water seperation would be no problem.  You 
can also get interchangeable Weirs. They take about 15 min to replace. With 
those you can use the centrifuge for preseperating and to skip the washing 
phase. You would still need the setteling phase. The centrifuge does not 
remove 100%, it works at about 90% seperation, To get better results you 
need 2 or 3 running in line.

My Ideal setup is a centrifuge from my WVO storage into a day tank then to 
the processr(capable of 200 gallons of Bio-diesel per hour). Then into a 
2500 gallon seperating tank. Then a battary of 3 centrifuges seperating 
Glycerine/cataylist and Bio-Diesel/Methanol. (This must be done first as 
there is a lot of methanol traped in the glycerine. If you take the methanol 
off the top first then as you seperate the glycerine you will free more 
methanol and have to repeat that stage). Then into another battery of 3 
seperating Bio-Diesel and Methanol. That should leave no more then .01-.02% 
Glycerine/Cataylist/Methanol in my finished product. This will take a lot of 
time and 50-100k gallons sold to make a reality, but that will definately 
meet ASTM unless there is a mojor problem with your WVO to begin with.

Logan Vilas
Bio-Fuel Enterprises, Inc.


- Original Message - 
From: Matt Yarrison [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Sunday, October 16, 2005 8:21 PM
Subject: [Biofuel] Anyone find a source for used centrifuges?


 Dear All-
 I'm helping to set up a small scale (about 5-8 thousand gallons per year)
 processing unit at Rice University. This is a completely student run
 project, and we've got most of the kinks worked out. One problem we have 
 is
 that one of the colleges on campus somehow manages to produce WVO that has 
 a
 large quantity of water and fries, batter, etc in it. So we don't have to
 waste energy to de-water by heating, or spend a few weeks settling (we are
 somewhat limited on space) the gunk out, I'd like to use a small scale
 centrifuge to remove water and junk from the oil. Problem is, the only 
 ones
 I can seem to find are either for use in cars or are much more than we 
 need.
 Does anyone out there have a source for a centrifuge that can process 
 about
 5-10 gpm?
 Cheers!
 - Matt Yarrison


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Re: [Biofuel] Why aren't there more manufacturers?

2005-10-14 Thread logan vilas



Mike,

 I'll do my best to write up some 
plans and explain the harder points. The best thing I can tell you is to start 
looking up homemade turbine. Or Turbocharger engine. I am more of a tinker then 
a planer. I bought a turbo from a local junkyard $25 bucks. I was told it 
worked, but the car wastotaled. Then from several sources I 
hadalready found on the internet I started tinkering. After a few months 
of playing around with it, and a lot of time watching tv, I had a running 
engine. Now I could use it to power something, but what am I going to do 
with5 lbs of thrust that sucks 10lbs of propane in 5 min. Now that I've 
gotten into bio-diesel I was trying to figure out what I can do with my 
byproduct. 

If I plan on selling a lot of this I have to find 
someone to take the glycerine or a way to dispose of it. Well I started thinking 
about it and for any number of reasons it would be nice to have a high volume 
burner then I decided to try glycerine. I had already run diesel, kerosine, 
propane, and a near miss with gasoline. Once it is up to heat on propane then 
put in the glycerine and it works great. it will also take twice the glycerine 
to make as much power as any of the other fuels so you can burn off a lot if you 
need to.

After thinking about it there's a lot of heat lost, 
and I have been dreading the electric bill of heating my batches, but here's a 
good source of excess heat, just beine blown into the atsmophere. now I reclaim 
that and did the math. I get a huge amount of heating power without any 
electricity at all.

Now I think if I add a exhaust turbine in line then 
gear reduce it to turn my genhead I will still reclaim some more of that energy 
and be able to power my processor pumps, and I decided to look at electric bills 
and net metering. Well it technically is a biomass generator, and in louisiana a 
person can produce 25kwh, or commercial can produce 100kwh and send it back out 
the public lines. So now all I have to do is get approved and have a 
electriction wire it into place.

Logan Vilas
Bio-Fuel Enterprises, Inc.

  - Original Message - 
  From: 
  Michael 
  Luich 
  To: Biofuel@sustainablelists.org 
  
  Sent: Thursday, October 13, 2005 3:33 
  PM
  Subject: Re: [Biofuel] Why aren't there 
  more manufacturers?
  Care to share the plans?Mike Luich
  On 10/13/05, logan 
  vilas [EMAIL PROTECTED] 
  wrote:
  I 
have built a turbine engine/burner for my waste glycerine. I know it 
canbe dumped, but mysetup preheats and can produce electricity at the 
same timeof destroying my waste. The burner is just about the same for 
any useage from a half gallon an hour to 10 gallons a hour. It can burn 
a lot. I haveit set up for 1 gallon a hour right now. It is slightely 
loud(like a reallysmall jet engine), so no running it at night if your 
nebighors are going to complain. I figure 1 gallon of glycerine has 
53,000 btu's. That's enoughenergy to produce about 20 HP. You loose 
about 25% in most cases to heat. SoIf my numbers are correct that's 5hp. 
That will turn a 2.5-3kw GeneratorHead. My average electric consumption 
for the last 6 months is 2.2 Kw perhour. Right now the burner just 
exhausts onto a 50 gallon water vat that Iam going to plumb into my 
processor for heating(just waiting on the money for heat exchanger). I 
figure after the energy produced the left over energyin the heat is 
about 37,500 btu's. Then I should get about 3,750 btu's ofheating per 
hour on my water vat.The only reason I have not set up the genhead 
is because durning the normal day there are spikes above 3kw for some 
time, then at night it slows down. Iam trying to get NET METERING. That 
means any electricity I don't use goesout to the general public and I 
get paid for it, but when my demand is more then my output I draw what 
else I need from the utilitys. By the end of themonth they end up oweing 
you for the excess you produced. and you made itinstead of going to the 
dump with your glycerine. Plus that makes the size of your glycerine 
storage much smaller.To produce enough glycerine to burn 24 gallons 
a day you will need to make a75 gallon batch per day. I size my batch by 
wvo put into the processor. Thatmeans you are preheating 562.5 pounds of 
WVO. that's a 6.67 degree rise perhour. and you should have about 22 
hours of heating time at a min per day. Ifigure no more then one hour to 
pump 75 gallons into the processor then 1hour to refill the preheat 
tank. before heat loss that gives you a 146.74degree heat rise from 
ambiant. I figure in a decently insulated containershould have no more 
then 50% heat loss(this could be easily wrong). Thatwould give you a Min 
of 73.37 degree rise above ambiant. It seldom gets below 40F In south 
Louisiana.This could be turned up to 1000 gallons per day and 10 
gallons a hour ofconsumption

Re: [Biofuel] Why aren't there more manufacturers?

2005-10-14 Thread logan vilas
Hey Jason

It is actually a 2' square box that has a 6 tube with baffles in it. 
The exhaust goes into the bottom left, then hits a flat wall where the 
exhaust is directed up through some small plates tacked to either side to 
help catch heat and slow down the air speed. The pipe runs right through the 
middle of the tank There's about 1 8 hole so the water doesn't build 
pressure. In the diving industry they build hot water heaters on almost the 
same basis except they use a becket fuel oil burner for the heat source, and 
most of the time they are much bigger. I am not useing a water heater 
because I am setting up a facility and hopeing to sell at least 1500-2000 
gallons of biodiesel a month. More is alway's better. For that I would have 
to do a batch a day for now I am planning on 4-5 batches a day on the 
weekends they are 200 gallons so it should only take 2-3 days work a week to 
keep up with my hopeful min of 1000 gallons. But I am going to enclose my 
Preheat tank in my facility that way it does help heat durning the winter, 
but during the summer in Louisiana that's gonna add extra heat also.

My burner is in a box made out of 1/4 steel plate, that sits 3' square and 
4' tall with a open top for saftey. If it decides to blow apart that should 
hold it in. I thought last night that If I make a inlet, throught the side 
of the box, and seal my intake to the side of the box, my exhaust is already 
run like this, then I can fill that box with water. That should give me 
aditional water heat, and help keep my turbo even cooler while adding a 
little more safety. If it decides to blow apart then it will have the water 
to slow it down and probably not burst into flames. At the most you'll head 
a thud and the turbine stop. I Think that's the safest way to make this.

Logan Vilas
Bio-Fuel Enterprises, Inc.


- Original Message - 
From: Jason and Katie [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Thursday, October 13, 2005 11:45 PM
Subject: Re: [Biofuel] Why aren't there more manufacturers?


 Damn Logan, this is a tremendous idea!
 i had known about boneyard turbine engines for a while, but i hadnt ever
 put the idea of glyceine to it yet.
 this is fantastic. i have a recommendation though.
why dont you use a gas water heater tank instead of a drum? it already
 has the baffles for heating built into it, and it already has the more
 difficult plumbing pre-assembled for you, if you so choose, you could also
 add to the factory insulation and use it for more than just heating your
 bio. heat the garage, or the shower, or if you're feeling ambitious, heat
 the whole bloody house (you'd probably need two turbines for that though.)
 the tinker gives a damn,
 jason



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Re: [Biofuel] liquid liqid centrifuge

2005-10-13 Thread logan vilas
You're only turning 1400-3000 RPM. How many people do you know cutting on 
engines that are running 6,000 rpm or more. I know I've seen a lot of them 
go wrong, but they're normally not sending things flying in every direction. 
And belive it or not most of the time they work. Also the fact that liquid 
is spinning should help adjust any off balance and smooth out the rotation. 
http://www.rousselet-robatel.com/products/extraction3.php I am planing on 
useing one of their BXP 130p for my setup. I was quoted 15,500US. for 
rebuilt, 27,800us for new. I know that's a lot for the average person 
makeing it in their backyard, but I am setting up for production in south 
Louisiana.

Logan Vilas

- Original Message - 
From: Jason and Katie [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, October 12, 2005 10:14 PM
Subject: Re: [Biofuel] liquid liqid centrifuge




 
  http://www.cheresources.com/centcontactor.shtml
 
  I think it would be possible to build something along these lines
 cheaply,
  take that old blender and put it inline with your reactor?


 i wouldnt be inclined to try building/using it without a damn good 
 machinist
 working for me...

 ---
 [This E-mail scanned for viruses by Declude Virus]


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Re: [Biofuel] Why aren't there more manufacturers?

2005-10-13 Thread logan vilas
I have built a turbine engine/burner for my waste glycerine. I know it can 
be dumped, but mysetup preheats and can produce electricity at the same time 
of destroying my waste. The burner is just about the same for any useage 
from a half gallon an hour to 10 gallons a hour. It can burn a lot. I have 
it set up for 1 gallon a hour right now. It is slightely loud(like a really 
small jet engine), so no running it at night if your nebighors are going to 
complain. I figure 1 gallon of glycerine has 53,000 btu's. That's enough 
energy to produce about 20 HP. You loose about 25% in most cases to heat. So 
If my numbers are correct that's 5hp. That will turn a 2.5-3kw Generator 
Head. My average electric consumption for the last 6 months is 2.2 Kw per 
hour. Right now the burner just exhausts onto a 50 gallon water vat that I 
am going to plumb into my processor for heating(just waiting on the money 
for heat exchanger). I figure after the energy produced the left over energy 
in the heat is about 37,500 btu's. Then I should get about 3,750 btu's of 
heating per hour on my water vat.

The only reason I have not set up the genhead is because durning the normal 
day there are spikes above 3kw for some time, then at night it slows down. I 
am trying to get NET METERING. That means any electricity I don't use goes 
out to the general public and I get paid for it, but when my demand is more 
then my output I draw what else I need from the utilitys. By the end of the 
month they end up oweing you for the excess you produced. and you made it 
instead of going to the dump with your glycerine. Plus that makes the size 
of your glycerine storage much smaller.

To produce enough glycerine to burn 24 gallons a day you will need to make a 
75 gallon batch per day. I size my batch by wvo put into the processor. That 
means you are preheating 562.5 pounds of WVO. that's a 6.67 degree rise per 
hour. and you should have about 22 hours of heating time at a min per day. I 
figure no more then one hour to pump 75 gallons into the processor then 1 
hour to refill the preheat tank. before heat loss that gives you a 146.74 
degree heat rise from ambiant. I figure in a decently insulated container 
should have no more then 50% heat loss(this could be easily wrong). That 
would give you a Min of 73.37 degree rise above ambiant. It seldom gets 
below 40F In south Louisiana.

This could be turned up to 1000 gallons per day and 10 gallons a hour of 
consumption. It will produce the same temp rise because of the added batch 
size, but at 10gph glycerine it would produce 50hp and beable to turn a 
20-25kw gen head. You could also get a larger genhead and burn 10 gallons 
per hour over 2.4 hours that will give the same overall energy consumption 
the same electricity production and heating without the continious running, 
but that genhead gets very expensive and it will be real loud running that 
high speed. Then you would have to start it wait 2 hours for your preheat 
then start processing. I perfer the idea of a running continious, Quiter, 
and less trouble of haveing to restart it and shut it down.

Logan Vilas
Bio-Fuel Enterprises, Inc.

- Original Message - 
From: David Miller [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, October 12, 2005 4:05 PM
Subject: Re: [Biofuel] Why aren't there more manufacturers?


 Bobby Clark wrote:

 I'm slowly starting to think of it, but I'm not convinced yet.

 I think most people who do it do it mostly as a way of not using
 petro-diesel much more than to save money.

 I doubt I'd save much on fuel for my TDI.  I'd have to buy the pieces
 for the processor, buy the chemicals, and go through the process of
 getting WVO, and practice until I get it right.  If I don't get it right
 I run the risk of damaging my engine; rebuilding it or the injection
 pump or replacing the injectors will cost more than I'll save making
 biodiesel in a long, long time, even if the WVO is free.  I have three
 things I want to do with every free hour I have now, so making a
 processor and learning to use it has some serious competition.

 As far as reducing my personal impact on the planet regarding fossil
 fuels I'm more inclined to use the WVO I can get as a replacement for
 some of the home heating oil I use.  I have an extremely well insulated
 house and use ~650 gallons of heating oil last year.  I think next
 summer I'll cut at least 150 off with solar hot water heaters.  If I can
 get 250 gallons of  WVO and mix it with K1 I can save 400 of the 650
 gallons without risking the engine in my TDI:)  That's a significant
 savings, bring me down to 10-20% of what most houses use in these parts.

 I also wonder what people are really doing with the leftover glycerine
 and wash water with excess methanol.  I suspect a lot of both get
 dumped, as do batches that just go bad.  I don't know that, but would
 be interested to hear from those actually making BD what they do with
 their wash water.  I

Re: [Biofuel] cost of B100 versus Petro in the Midwest USA

2005-10-13 Thread logan vilas

Bouchereau Oil CO Inc
   1272 Lafourche Street
   Donaldsonville, LA  70346
   http://www.chevrontexaco.com
 225-473-7662


 They are a bulk seller. They don't like selling it by the drum, but 
they will if you ask nicely. They perfer to sell it by tote tank or bulk 
truck. That number actually forwards you to Gobert oil company. They may be 
able to help you find cheaper in your area.


 Logan Vilas
 Bio-Fuel Enterprises, Inc.


- Original Message - 
From: John Short [EMAIL PROTECTED]

To: Biofuel@sustainablelists.org
Sent: Wednesday, October 12, 2005 5:07 PM
Subject: Re: [Biofuel] cost of B100 versus Petro in the Midwest USA



I would like to know the company that is selling for that price I just
thought I had found a good deal @ $2.36 a gal. here in Dallas, Tx.  And to
get that price it has to be by the drum.


- Original Message - 
From: Brian Rodgers [EMAIL PROTECTED]

To: Biofuel@sustainablelists.org
Sent: Wednesday, October 12, 2005 3:43 PM
Subject: Re: [Biofuel] cost of B100 versus Petro in the Midwest USA



I want some. Even at twice that price
Brian Rodgers


On 10/12/05, logan vilas [EMAIL PROTECTED] wrote:

I don't know if it's just a really good source or what, but I was Quoted
$1.10 per gallon for methanol. If I bring my own container. If I have to
buy
in 55 gallon drums then it is 1.57 per gallon. That was quoted 9/14/05 
in

Thibideaux, Louisiana.

Logan Vilas

- Original Message -
From: Zeke Yewdall [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, October 12, 2005 10:40 AM
Subject: Re: [Biofuel] cost of B100 versus Petro in the Midwest USA


 You forgot to add the road tax and a markup for profit to the
 biodiesel...  Anyone who is selling biodiesel has those costs too.

 On 10/9/05, Jason and Katie [EMAIL PROTECTED] wrote:
 I sat here and figured up the ballpark cost of parts for BD in a 
 390

 gallon batch-( i started my numbers with a full 55 gal. drum of
 methanol)

 for 2 barrels of methanol (have to have
 excess) ~550$
 for 390 gal.
 oil.
 .Haul-off
 for 40 lbs lye(VERY rough
 estimate)~140$
 for one cannister of bottle gas (heat
 source)..~25$

 Total
 C.O.P...
 .~715$

 Results (Approximate)
 ~340 Gallons of ester
 ~47 Gallons reclaimed methanol
 ~43 gallons glycerine

 Market Value of 340 Gal. of diesel @
 2.60$/Gal...~884$
 Your
 Savings.
 ...~169$

 not to mention if you use the glycerine as a heat source through any
 of
 the
 available ways (digester gas, directly burning it, etc.) the heating
 costs
 will fall off entirely, and methanol will become cheaper the more you
 reclaim the excess, and we could always go to ethanol and add that to
 the
 equation, which has it's own COP. there are always options.
  Now, having read this, can you still tell me BD is more expensive
 than
 Petro?

 ---
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Re: [Biofuel] cost of B100 versus Petro in the Midwest USA

2005-10-12 Thread logan vilas
I don't know if it's just a really good source or what, but I was Quoted 
$1.10 per gallon for methanol. If I bring my own container. If I have to buy 
in 55 gallon drums then it is 1.57 per gallon. That was quoted 9/14/05 in 
Thibideaux, Louisiana.

Logan Vilas

- Original Message - 
From: Zeke Yewdall [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Wednesday, October 12, 2005 10:40 AM
Subject: Re: [Biofuel] cost of B100 versus Petro in the Midwest USA


 You forgot to add the road tax and a markup for profit to the
 biodiesel...  Anyone who is selling biodiesel has those costs too.

 On 10/9/05, Jason and Katie [EMAIL PROTECTED] wrote:
 I sat here and figured up the ballpark cost of parts for BD in a 390
 gallon batch-( i started my numbers with a full 55 gal. drum of methanol)

 for 2 barrels of methanol (have to have
 excess) ~550$
 for 390 gal.
 oil.
 .Haul-off
 for 40 lbs lye(VERY rough
 estimate)~140$
 for one cannister of bottle gas (heat
 source)..~25$

 Total
 C.O.P...
 .~715$

 Results (Approximate)
 ~340 Gallons of ester
 ~47 Gallons reclaimed methanol
 ~43 gallons glycerine

 Market Value of 340 Gal. of diesel @
 2.60$/Gal...~884$
 Your
 Savings.
 ...~169$

 not to mention if you use the glycerine as a heat source through any of 
 the
 available ways (digester gas, directly burning it, etc.) the heating 
 costs
 will fall off entirely, and methanol will become cheaper the more you
 reclaim the excess, and we could always go to ethanol and add that to the
 equation, which has it's own COP. there are always options.
  Now, having read this, can you still tell me BD is more expensive than
 Petro?

 ---
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