Re: [biofuel] Methanol and Sodium Hydroxide efficiant mixing method

2004-04-13 Thread gobie

Kevin,
have to agree with you that the preparation of the methoxide can be a
dangerous step.
There are some good methods mentioned on JTF, but most of them take time.
To get around the NaOH dissolving in methanol problem I have developed a
method of using NaOH in the form of a concentrated aqueous solution. The
NaOH dissolves readily into the water and is available as a stock solution
when needed. To make methoxide the Conc Aqueous NaOH is measured out and
poured slowly with stirring into the methanol. Result a crystal clear
methoxide prepared in a minute or two.
Dissolve 100g of NaOH (flakes, pellets or pearls) in 90ml of distilled
water. Some stirring will be needed and the solution will get very hot. Mix
in a heatproof non metalic container and avoid breathing the fumes. This
will give you 1200ml of solution. Store in an airtight plastic bottle at
ground level away from children.
When making up the methoxide multiply the grams of NaOH/litre required by
1.2.
If the ambient temperature is below 20 deg C the conc NaOH solution will
tend to solidify and may need to be shaken or warmed.

One of the golden rules of biodiesel making is to avoid water at all
costs. In this case however the small ammount of water in the Conc NaOH
solution does not seem to have a detrimental effect.

The above advise is offered as asistance, not to prove a point or promote a
particular way of making methoxide. Try it and if you like it great I have
been of help.

There are sure to be a few comments from the detractors of this method.
I'm flying out this evening, not back till Monday, so will not be available
for comment till then.


Regards   Paul Gobert

   - Original Message -
   From: Kevin Shea
   To: biofuel@yahoogroups.com
   Does anyone have suggestions on the best way to agitate the Lye powder
into the methanol?  I use a type 20 Lightning mixer (with small propeller
agitator), but have problems with the dissolving of Sodium Hydroxide

   I mix 3.75 liters of methanol to the appropriate amount of sodium
hydroxide in a 5 gallon carboy (with small hole drilled in cap) and let mix
for 15 minutes.  My problem is that the sodium hydroxide fails to dissolve
completely with the methanol.  I can see lots of clumped Lye!

   I hate this part of the process!!! and it is the most dangerous!!  I
take as much precaution as possible not to expose myself and wear proper
safety protection.  I'm not crazy about mixing for longer period with an
electric mixer or have something happen to cause a catastrophic event, so
I'm trying to minimize this danger window of this process

   Most likely I'll mix the next batch of Sodium Methoxide in a smaller
carboy (HDPE), and that should hopefully help.  Maybe the propeller shaft
should be a larger design??  Anyway, I'm interested in the most efficient
(Safe) methods and how long agitation should be?

   I use the Red Devil powder Lye.


   Thank you,
   Kevin Shea


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Re: [biofuel] Combining small batches into a common settling tank

2004-04-12 Thread gobie

Mark,
I've done much the same thing mixing up 15L batches by hand shaking in 20L
sealable container and bulking them into a larger container. Shouldn't be a
problem on a larger scale.

Regards  Paul Gobert.

- Original Message -
From: Mark McElvy

 I am wondering if there are any ill effects from combining several small
 batches of bio into a large settling tank? For example, Making several 50
 liter batches in one day and put them all into a larger tank to
 separate/wash.



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Re: [biofuel] Hydrated Lye

2004-04-12 Thread gobie

Biobenz,,
Hydrated Lye is not a term I am familiar with. A google search provided
only one link where the words were mentioned i9n a list of ingredients but
no mention of how the material was used.

Hydrated Lime is a common term for Ca(OH)2 or slaked lime. So called because
it can be make by slaking or adding water to Quick lime CaO.

Generally water is to be avoided in BD making. However my std process
involves the use of the NaOH in the form of a concentrated solution. Its a
controversial method but suits my processing.

Regards,
Paul Gobert.





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Re: [biofuel] Re: pre-mixed Phenolphthalein solution ???

2004-04-10 Thread gobie


- Original Message -
From: biobenz
snip
 I figure that if I can eliminate the number of screw-up factors
 then if/when something goes awry that way I will already have most
 of the posible sources discounted :) So I guess I need to give them
 a caall and get the pre-mxed stuff huh? It's not all that dear
 (expensive) and it just eliminates one more item that can go wrong.
 I ain't the sharpest tool in the shed, so I need the averages on my
 side :)Chemistry classes, I think, were for someone else :) and then
 I lost interest. Little did I know

Try to keep detailed records of everything you do this will help to show
what you are doing right and what doesn't work too well.

Regards,
Paul Gobert.





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Re: [biofuel] pre-mixed Phenolphthalein solution ???

2004-04-09 Thread gobie


- Original Message -
From: biobenz
 The chem supply house I am dealing with offers the Phenolphthalein
 in a pre-mixed alcohol solution at 1%. Would this work as well or
 better than the do-it-yourself method ?

Biobenz,
If you are unable to get 95% ethanol or don't want to go to the trouble of
making up the phenolphthalein solution yourself, the premixed solution would
be a great idea. It would also be neutralalised in manufacture. Would indeed
work just as well as or better.

Regards  Paul Gobert.





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Re: [biofuel] Phenolphthalein

2004-04-07 Thread gobie


- Original Message -
From: Dermot

 Thanks for the help Paul,

 Now I can't get ethanol except in 45 gallon drums!
 Is vodka close enough to ethanol and could I mix the phenolphthalein with
 it?

 Regards
 Dermot

Dermot, not being a consumer of things alcoholic I'm not sure of the proof
of vodka. 98% pure alcohol would be almost 200 proof. Don't imaging any
drink for human consumption would be that strong. Whilst working for a
pharmaceutical company once I was analysing one of their raw materials. The
analysis consisted in serial dilutions in pure ethanol with 2% hydrochloric
acid. Sucked a bit too hard on the pipette and got half a mouthful of the
brew. That night whilst eating dinner the 1st layer of skin came away from
the inside of my mouth.

You could give the vodka a try.  Soime brands of methylated Spirits sold out
here in Oz are mostly ethanol could be worth investigating.
Perhaps methanol could be substituted, the phenolphthalein definately
prefers to be disolved in alcohol. Have to be even more careful not to get
this mix on your skin though.

Regards   Paul Gobert.






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Re: [biofuel] 5 micron filtering

2004-04-07 Thread gobie


- Original Message -
From: biobenz

The final filtering of my biodiesel just before it goes into the tank is via
an automotive Diesel filter.
C.A.V. with water trap, 1 micron cartidge, BD gravity fed through the filter
into a storage container.
Admittedly this is a small scale setup and time is not a problem. Good
processing and washing sees the BD crystal clear before it enters the
filter. At one stage I was filtering the finished BD through 1 micron
filterpapers but the setup, with four funnels and the BD metered to them was
very messy.

Regards   Paul Gobert

 Would a standard truck fuel fieter work for the final filtering of
 the biofuel or should I be looking at something else?
 The idea was to get the long filter as well as it's mounting
 hardware and then use a drill pump to push it through. They are
 screw on type filters and are only changed in big trucks every
 35,000Km or so, so one set up shopuld be good for quite some time
 unless you are a big time biodiesel producer, and then you would
 already have a more elaborate and automated system.

 Thanks for any feedback. I am trying to get my ducks in a row and
 these questions keep poping up so I figure the best time to ask is
 when the iron is hot.

 PS: My alter ego LoveMyDiesel2003's password wasn't responding so I
 had to make a new one and this is it. I will be using this one from
 now on.




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Re: [biofuel] Phenolphthalein

2004-04-06 Thread gobie


- Original Message -
From: Dermot Subject: [biofuel] Phenolphthalein


 I've managed at last to get some phenolphthalein to perform titrations but
 unfortunately it's in powder form.
 I think it needs to be mixed with ethanol in a 1% w/v solution.
 Can anyone confirm this?

Dissolve the phenolphthalein in 2/3 of the final volume of ethanol. When it
has all dissolved add with stirring half as much distilled water. Add dilute
sodium hydroxide solution ( the solution you use to titrate will do) until
the phenolphthalein solution just shows a slight pinkish tinge. Store in an
airtight bottle out of light.and away from sources of ignition.


 Can I mix it with isopropyl alcohol instead?

I'm not sure what the solubility of phenolphthalein is in isopropyl alcohol.
Could be worth a try.

Regards   Paul Gobert.






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Re: [biofuel] methanol recovery before separation

2004-03-31 Thread gobie


- Original Message -
From: Kenneth Kron


Catching up on ancient email.

If one continues mixing until the reaction is complete and I have not
heard of any evidence that indicates separation is required for the
reaction to complete and then introduces into the reactor enough acid to
quench the sodium catalyst then I see no reason why you should not be
able to recover the methanol before separation.

Kenneth, I can see a problem here if the process was single base and the
feedstock was high in FFA.
The addition of acid could convert the soap formed from the initial
neutralisation back into FFA. Careful monitoring of the ammount of acid
added might prevent this. Whilst FFA is a good fuel in itself its
compatability with the components of a diesel engine is highly suspect.

In fact if you follow the Fool proof method then you do almost exactly
this.  You separate the glycerin, mix it with phosphoric acid and mix it
back into your biodiesel.  You've quenched the reaction right there and
have everything mixed up.  If it's critical to add the acid to the
glycerin for some reason (which I don't quite see) you should have
plenty on hand from previous reactions.

Another way to strip some of the methanol from the raw biodiesel would be to
use glycerine from which the methanol had already been distilled..  Mix the
raw biodiesel and the glycerine. The methanol will disperse 50/50 in the
biodiesel and the glycerine. The methanol can be distilled from the
glycerine. But would it be cost effective?

Regards,   Paul Gobert.





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Re: [biofuel] Methanol Hazards - provocative mail

2004-03-06 Thread gobie

x-charset ISO-8859-1Whilst I in no way advocate carelessness when handling 
chemicals the dangers
should be put into perspective. A comparison of the Material Safety Data
Sheets for methanol and petrol (gas in US) show some similarities in
dangers. Chemicals can be handled safely. Be forewarned of the dangers and
design your processing around them.

Regards,

Paul Gobert.
- Original Message -
From: Go Hoff [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, March 06, 2004 1:09 AM
Subject: [biofuel] Methanol Hazards - provocative mail


 There are warnings all over alt fuel sites about dealing with methanol
 because of course it is nasty poisonous stuff. I have not been
experimenting
 with the process cuss the info on 'journey' and elsewhere scared me.

 However I just started re-talking to an old friend who has been driving
 methanol race cars for 34 years.

 He is a non drooling family man with 5 children and a multitude of
 grandchildren with a vitality many 30 year olds lack. Apart from messing
 with methanol 6 months of the year he does a lot of head slamming, violent
 body 'G' forced exercises, explosions, engulfing fires and heavy
 disagreements between crew and promoters - between rounds, routinely.

 I get the impression that he and his crew sort of slop methanol around
from
 the barrel to the container to the race car - he assures me they do not
wear
 special clothing or breathing apparatus, he doesn't remember if they wear
 gloves but supposes they do if they have them on at the time.

 I remember buying an USA made hammer in the 70*s it was hung with labels
and
 stuff saying to wear protective glasses, gloves, overalls etc and to keep
 children and pets away, not to leave it unattended and to hide it or lock
it
 up from potential thieves - failure to do any of that stuff would void
it's
 warranty - it was a hammer for goodness sakes - are you Americans nuts?

 Anyway, I would really like to know if anyone has died by handling - not
 drinking because that is deathly - methanol, and if so if the poison
 intrudes through the skin or the airways.

 Hmm... I Guess this is a bit beyond our competence maybe but even my
doctor
 agrees, stay curiouse - try and work it out.










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/x-charset


Re: [biofuel] First Batch

2004-01-19 Thread gobie

x-charset ISO-8859-1
- Original Message -
From: Keith Addison [EMAIL PROTECTED]
 As I recall your conc. aq. lye soln. method was found wanting by
 someone with extensive knowledge and experience who submitted your results
to a GC test.

Keith I'm not aware of any such GC test. A non-GC test on a very early test
batch indicated that the glycerides were slightly high.

GC Analysis was performed on samples from a test to compare BD made from the
same feedstock using methoxides prepared by
a). dissolving sodium metal in methanol
b). dissolving solid sodium hydroxide in methanol and
c).conc aqueous sodium hydroxide mixed into methanol
the resultant BD was warmed to evaporate any excess methanol but was not
washed.

I have revisited the results
The only significant difference in the figures is at the highest peak which
is for 9-Octadecenoic acid (Z)-, methyl ester, 10-Octadecenoic acid, methyl
ester and 6-Octadecenoic acid, methyl ester.
a).  60.79   b). 64.37   c).64.34.
The lower peaks were all methyl esters with a difference of less than 0.05
of a % total between them.

These results are open to interpretation to those more knowledgable about
interpreting GC results than myself.
Factors to consider are:
1/. The GC only detects the chemicals for which the column is designed and
calibrated.
2/. Only organic chemicals are detected.

Taking the above into consideration the results indicated that there was
very little difference between these analysis results for the Biodiesels
made using  methoxides b).and c).

Regards Paul Gobert.





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/x-charset


Re: [biofuel] First Batch

2004-01-18 Thread gobie


- Original Message -
From: Keith Addison [EMAIL PROTECTED]
 Increasing the basic lye amount from 3.5 to 4.5 grams per litre of
 oil is not good advice.
snip
And  then? Spend a whole lot of time developing super-gentle washing
 methods to hide the fact that you're not processing the stuff
 properly in the first place, etc etc etc. Sheesh.

Keith tests that I have run varying the ammount of lye in steps 0.5g either
side of the ammount indicated by titration have shown that the batches using
higher than titration levels of lye wash much easier than those using the
titration ammount or less.


 There are times when it's advisable to increase the basic amount, but
 NOT as a general rule, and certainly not for virgin oil. It might not
 make too much difference with virgin oil, because virgin oil is very
 forgiving of bad technique, but I've had several cases of good WVO
 with low titration - less than 2ml - which nonetheless would not
 process well with anything more than the basic lye quantity of 3.5
 gm/litre plus the exact titration amount: anything even slightly
 above that brought lower production, more soap, and difficult
 washing. These were just tests, using single-stage, there weren't any
 problems processing the oil with acid-base, but it's single-stage
 we're talking about here. I did a lot of tests with various oils and
 found that the usual base figure of 3.5 grams per litre of oil is
 correct, 4.5 grams is generally bad advice. Other people's tests have
 confirmed that. Since then we've encountered many cases where using
 4.5 grams as the basic quantity would give poor results. There are
 times when the basic quantity should be increased, but these
 exceptions are quite specific, not at all some sweeping,
 across-the-board measure:

 As the ammount of lye is increased above the titration ammount both the
density and the viscosity of the washed BD decrease indicating more complete
conversion of tri, di and mono glycerides to BD. At the same time the volume
of yield drops, so a compromise has to be reached where the fuel is regarded
as suitable for use. Conversly using less than the titration ammount of lye
gives a yield above 100%.
A conversion of near 100% may be required to meet standards but less than
that may be quite ok as fuel. Some BD makers are using low levels of
Methanol ( below 20%) without extending the reaction time. Whilst the
conversion might not be 100% it may still be suitable fuel, Would be
interesting to know what degree of conversion is required to produce a fuel
suitable for troublefre longterm use, especially in situations where the
fuel is heated before being injected.

Adding methanol/lye mix to Oil.
My reason for mentioning this is that tests I have done retreating BD have
shown that if a the BD is treated with a methanol/lye mix which has a higher
than normal ratio of lye to methanol, the result will be jelly.
Slow addition of methanol/lye to stirred oil prevents the oil/methoxide
interface which can result from a sudden addition of one component to the
other. This interface between the two phases, I feel favours, the production
of soap.

Regards,
Paul Gobert.






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Re: [biofuel] First Batch

2004-01-18 Thread gobie


- Original Message -
From: Keith Addison [EMAIL PROTECTED]
snip
 Paul, I'm afraid I'm inclined to take all your test results with a
 grain of salt (not to break the emulsion, LOL!) because of the
 methods you use. You use your concentrated aqueous lye solution as
 standard, yes?
snip

For my production batches yes but not for test batches, like to eliminate as
many variables as possible.

Many or most of us here do not use this method, we've
 examined it at length and in depth and find the practice of
 deliberately adding water to the process as your method does adds
 unneeded variables which would discount the reliability of your
 results, and it's superfluous anyway.

Superflous for you practical for me. To each their own with tollerance for
the other persons preference.


 Please let's not have this argument again here now, and again please
 let's not have any of the extremely dubious endorsements so to speak
 that the method has had from elsewhere.

Keith arguments are something I don't enter into unless I have something to
gain.
I presented the method, others have tried it and it suited their production
methods..If others want to use it I am happy to help . At no time do I
insist that it is the only way to go. Wether or not anyone uses the method
is of no concern to me. What does concern me however is when my results are
denigrated. My work has been conducted in a scientific manner, is fully
documented and can be duplicated by anybody given the same materials and
conditions.
Can the same be said for the detractors of the method?
Very few of us in this group have access to facilities and equipment to
provide definitive test results.
At best we can only offer guidelines which are often subjective. My
objective is to follow the old principle, First know the rules then bend
them
I'm a stubborn old bugger who likes to learn by his mistakes, and on the way
have come to some interesting conclusions on BD making based on scientificly
conducted investigations.

Of course I'm not disagreeing
 with your use of your conc. aq. lye soln., it works for you so
 fine, no problem, but when you start giving test results using the
 conc. aq. lye soln. you should say so, because it is not a standard
 method and gives different results, or at the least adds variables.
 I'm saying this now because you've done that before without
 specifying it, I had to ask you, as I'm having to ask you again now.

In the future if the test results I quote involve the use of conc aqueous
NaOH or any other variation from the standard methodI will state such.

Regards   Paul Gobert.




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Re: [biofuel] First Batch

2004-01-17 Thread gobie

Rick,
Would suggest adding the methanol/lye mix to the oil, the slower the better.
Adding oil to methanol/lye might require less equipment but its a great way
to make soap. You could also increase the ammount of lye slighlty to say
4.5g per litre which will push the process al;ong nicely.

Regards,
Paul Gobert.
- Original Message -
From: [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, January 17, 2004 2:39 AM
Subject: [biofuel] First Batch


 Well I made my first blender batch of Biodiesel last night.  I am proud to
 say that I made a great batch of GLOP

 I am not sure what I did wrong.  I think maybe the Lye and Methanol did
not
 get mixed good enough.  I used 1 liter of new oil, 200 ml of Methanol, and
3.5
 grams of lye.  What do you suppose went wrong?  I blended the lye for
almost a
 min then added the new veggie oil and blended for another 15 min.  It made
a
 real nice batch of goo.

 Any suggestion?

 Rick M
 Brownstown. Mi





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Re: [biofuel] effects of using BD without retarding the pump

2004-01-14 Thread gobie


- Original Message -
From: [EMAIL PROTECTED]


 What would happen if you wanted to retain the pump setting used for
 petrodiesel so you could use it if you ahd to and not have the timing too
 far retarded.  Will this cause the diesel engine to produce massive
 amounts of pollution and/or unmanageable EGTs?  If not, are there any
 other downsides to leaving the pump in its dynamic timing for #2?  Thanks,
 J.D.

J.D.  from what I have observed very few people change the timing on their
diesels when using BD.
My Hilux is a smokey runner on petroleum diesel but with biodiesel or strong
BD/petro mixes the exhaust cleans up nicely.
There is reportedly a slight drop in power when using BD, but my vehicle
seems to run better. This might be because there is a lot of fat in the oil
I use to make BD which results in a high cetane number fuel. It certainly
quietens the diesel knock
regards,
Paul Gobert





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Re: [biofuel] Re: Was deodorant..

2004-01-01 Thread gobie


- Original Message - 
From: Grahams [EMAIL PROTECTED]
 The Anti-Smoking Manifesto Bra
 
 It seems to be over someone's top.
 
 Caroline 
 
LOL, good on you Caroline you are a good sort.

Regards,
Paul Gobert 





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O.T. Deodorants ( was Re: [biofuel] Digest Number 1902)

2003-12-31 Thread gobie

Caroline here is something that looks to me to be completely over the top. I
might add that I'm a millitant antismoker.

Courier Mail  6th Nov 2003 (Australia)
snip
The Anti-Smoking Manifesto Bra comes with capsules containing lavender and
jasmine fragrances mounted in the cleavage. These capsules have two
purposes, said Triumph spokeswoman Megumi Ishii.
They were supposed to calm the nerves of people trying to quit.
And they were designed as aversion therapy for hardcore smokers as the
fragrances made cigarettes taste unpleasant.
But it doesn't end there. The surface of the bra and shorts are coated with
liquified titanium oxide, a substance which could break down unpleasant
smoke smells. And if that fails, a pad attached to the Triumph bra could be
used as a face mask in smokey bars.

Regards,
Paul Gobert.




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Re: [biofuel] Re: test batch questions

2003-12-30 Thread gobie

Bill I think the problem is the high acidity of your oil.
It requires so much lye to neutralise the freefatty acids that a lot of soap
is being formed which prevents the separation of the BD and glycerine.

To rescue it you could add some acetic acid and mix it all up to a slurry.
You will get separation this way but the soap formed before will revert to
free fatty acids, leaving a mixture of BD and FFA.

oil with such a high free fatty acid content is better processed using a two
stage acid/base method.

One way to process it using single stage base, is to  neutralise the free
fatty acids before adding the methoxide.
Heat the oil up to about 100 deg C and stir in some lime. The ammount to use
coresponds roughly to the titration in grams.
Stir for about an hour (less could work). The lime neutralises the FFA and
forms calcium soaps which are insoluble in the oil.
Allow to settle,cool, pour off the oil and process. Titration should be now
much lower and less lye requyired, thereby giving much less soap in the
final product and a good separation should result.

Be sure to use lime in the form of Calcium hydroxide (slaked lime), some
lime sold over here in hardware stores is calcium carbonate (powdered
limestone) and that won't work.

Regards,
Paul Gobert.

- Original Message -
From: whc281 [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Tuesday, December 30, 2003 1:13 PM
Subject: [biofuel] Re: test batch questions


 Still making goo.

 I heated a liter of the oil really hot (~300 F) on the stove to see
 if any water would boil off.  I decided the oil doesn't have any
 entrained water.

 I did a titration and determined the needed amount of lye to
 neutralize the free fatty acids to be 8 to 9 grams/liter, + 3.5 grams
 for the esterification, = 11.5 to 12.5 grams/liter!

 I made test batch #9.  A one liter batch.  Preheated oil (~140 F).
 Premixed the lye into 200 ml of methanol until dissolved (5
 minutes).  Then poured them together in a sealed jar (no methanol
 evaporation).  Shook for 10-12 minutes.  Allowed to settle at room
 temp.  Result: about 10% oil, 90% goo.

 What now?!  Help!

 Should I keep it warm during settling?  Should I mix the sodium
 methoxide longer?

 Bill





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Re: [biofuels-biz] Ist Biodiesel Limo and taxi company

2003-11-06 Thread gobie


 Bill Althouse wrote:

 Hi,

 America's first biodiesel Limousine rolled out onto the Interstate today!

 The Limo is a factory built 300D always stored inside with 50,000 original
 miles, mint condition.  I ran the tank nearly empty and filled up with
 World
 Energy Biodiesel with the engine running. About 60 seconds after I began
 pouring the biodiesel, the engine suddenly got much more quiet. Anyone
know
 why biodiesel made the engine more quiet?
snip

Bill the engine would be quieter on biodiesel if the cetane number of the
biodiesel is higher than the deisel it displaced.
The higher the cetane the less time it takes for the flame propogation of
the burning fuel and hence less knock. I find that in summer I can use
biodiesel made from tallow  Tallow Biodiesel has a high cetane number and
the engine runs very quietly on it..

regards,   Paul Goibert




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Re: [biofuel] Phenolphthalein solution for titration

2003-10-06 Thread gobie


- Original Message -
From: simonswb6 [EMAIL PROTECTED]

 i found this online 'Phenolphthalein Indicating Solution, 1% in
 Alcohol, 125ml'

 is this ok for doing titration?  it has 1% Alcohol?


Yes that solution will be quite suitable.
It is more likely 1% phenolphthalein in alcohol which is a standard mix for
phenolphthalein indicator.

Regards,   Paul Gobert





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Re: [biofuel] Diesel redline

2003-09-21 Thread gobie


- Original Message -
From: Alan Petrillo [EMAIL PROTECTED]


 Here's a question for you engineers out there.

 What limits the rev redline on diesel engines?

 I've noticed that a lot of diesels are limited to revs down in the 3000
 rpm range, and IMHO this is one of the things that limits their power to
 weight ratio.


 AP

Alan, whilst I am certainly no engineer, as an owner of a diesel vehicle I
can report some observations and pose a few more questions.

Perhaps the solider construction and hence weight of the pistons, rods and
crank limit the revs. Some large truck engines are lucky to rev to 2000 and
large marine diesels don't even see 1000 rpm.

The tacho on my Hilux 2.2l diesel goes yellow at 4300  rpm and red at 4800
rpm.
In practise it just runs out of go at 4000 rpm, downhill runs have seen in
excess of 4000 rpm come up but I rarely do that out of respect for the
vehicle, its dynamics just aren't suited to that use. My usual practise is
to keep the revs between 2500 and 4000. Steep hills with a full load test
the limitations of the four speed box especially the gap between second and
third. Often second gear has to held because the revs would be too low in
third, the engine will happily run up the revs in second so I back off on
the throttle and maintain a reasonable rpm. There is a healthy ammount of
torque available at the 3000+ level and if you can get the revs up there in
top gear the vehicle will run happily at 100 to 110 kph all day, empty or
fully loaded.

Having been a petrol head in my younger days I often wonder whether
camshaft profile ( valve timing) influences diesel engines as much as it
does petrol engines.
Would individual inlet pipes be better than the branched manifolds that are
usually standard?  Certainly headers are available aftermarket and big bore
exhaust systems. Would porting and pollishing or even chamber shape
modification have an effect?

Regards,   Paul Gobert.



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Re: [biofuel] mixing pumps

2003-09-01 Thread gobie


- Original Message -
From: Appal Energy [EMAIL PROTECTED]
snip
 At minimum you would also want the drive motor enclosure to be TEFC, fan
 cooled, continuous duty and preferable thermal overload protected.
snip

Pardon my ignorance but wouldn't, totally enclosed, fan cooled be an
oxymoron? Surely the cooling air has to enter and exit?

Regards Paul Gobert.



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Re: [biofuel] mixing pumps

2003-09-01 Thread gobie

I stand corrected there Todd, got to thinking after I made that post.
As you say a motor in a finned encapsulated case wth a fan on the dead end
of the output shaft flowing air through the fins would qualify.
- Original Message -
From: Appal Energy [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Tuesday, September 02, 2003 2:20 AM
Subject: Re: [biofuel] mixing pumps


  wouldn't, totally enclosed, fan cooled be an
  oxymoron?

 Paul,




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Re: [biofuel] Ooops! - Re: milk fat

2003-08-31 Thread gobie


- Original Message -
From: Keith Addison [EMAIL PROTECTED]

snip
 dewatering the butter is easy enough. Take 400 g of butter, heat
 (indirect) to 60 deg C, maintain for 15 minutes. It sort of clarifies
 and a bunch of thick whitish gunk falls out at the bottom
 (buttermilk?). You're left with 315 g butter and 100 g buttermilk.

 That should have been: You're left with 315 ml butter and 100 ml
buttermilk.
snip

Not too sure that the dairy industry would call the residue buttermilk
Keith.
Buttermilk is the liquid which is drained from the butter after churning.
Usually about 1% fat which when compared with the 45% fat in the cream used
for buttermaking, makes for a pretty efficient conversion to butter.

Regards,Paul Gobert.




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Re: [biofuel] milk fat

2003-08-30 Thread gobie

Can I use cow's milk fat to make biodiesel?

Keith, Brent,

Butter contains water, its an emulsion of water in  milk fat which is
accomplished during the churning, can't remember offhand the % of water
present. Ghee or dehydrated butter would be a better feedstock
One of the tests on butter in dairy labs is water content. The water is
boiled out of a known weight of butter. End result is a golden liquid with a
crumb-like deposit in the bottom of the flask (could be proteins, milk
solids and salt). Filtering would be required or a more gentle heat
treatment. The residue from the moisture test is then used for the salt
test.
The salt may be a factor to be taken into account, better to use unsalted
butter.

 From: Keith Addison [EMAIL PROTECTED]
 Hi Brent
 
 When you say cow's milk fat you mean butter?
snip

Ghee would be the purest form of milk fat available.
Whilst cheese contains up to 30% fat in some varieties the fat would have to
be extracted by solvent extraction/digestion.
Milk from currently used Freezian cows runs at about 4% butterfat.
the traditional method of testing milk for butterfat involved the use of
near concentrated sulphuric acid and centrifuging to release the fat from
the proteins and allow it to accumulate in the neck of a graduated test
flask, this was the Babcock test.
Today Lab instruments, made mainly by Foss are used to analyse milk.
Other mammals besides cows yield much higher fat contents in their milk.
Sheep milk is higher in fat content and Wallrus milk is about 50% fat I seem
to remember. Can't imaging farming/milking the latter.

regards   Paul Gobert.



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Re: [biofuel] Porsche diesel coming for 2005...

2003-08-25 Thread gobie

- Original Message -
From: Neoteric Biofuels Inc [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, August 24, 2003 7:03 PM
Subject: [biofuel] Porsche diesel coming for 2005...


snip
Wow, Ed that will be some diesel A true tribute to old Ferdinand.
Not much room there for a two tank SVO system.
As they say at the end of the article it will be interesting to hear it in
action, will expect a nice purr under engine braking.

Regards,Paul Gobert.





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Re: [biofuel] Ammoniac ( NH3 )

2003-08-22 Thread gobie


- Original Message -
From: Pieter Koole [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Friday, August 22, 2003 6:02 AM
Subject: [biofuel] Ammoniac ( NH3 )


 Hi all,
 I think I have asked this question before, but I can't remember about
 getting an answer to it.
 In Holland we are having big problems with NH3 polution from chicken
houses
 and pig houses, where the farmers keep hundreds of thouthands of
chickens
 or thouthands of pigs.
 The air coming out of these houses, contain very much NH3.
 Is there a way to clean this air, and use the NH3 as a fuel ?

 Met vriendelijke groeten,
 Pieter Koole
 Netherlands.

Pieter, the air can be easily stripped of ammonia by spraying a fine mist of
water into it. Ammonia is very soluble in water.
The resultant solution of ammonium hydroxide can be used as a fertiliser.
Not sure how it could be captured and used directly as a fuel. ammonia forms
explosive mixtures with air over quite a range of concentraion.

Regards,  Paul Gobert.



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Re: [biofuel] Fitting a turbo (was SVO in turbodiesels)

2003-08-19 Thread gobie


- Original Message -
From: Juan Boveda [EMAIL PROTECTED]
 Hello Paul.
 I would consider a good maintenance for that engine, first of all.

Engine reconditioned about 10,000k ago after picking up a bigend. Running
like a swiss watch after some annoying oil leaks caused by installation of
poor quality seals by reconditioner. I should have stuck with the local
Toyota dealership who did a good job on the engine's first recondition.

 I used to drive a Toyota Hi-Lux pick up with the 2.2 L engine, a 1981
 model, from brand new up to about 600,000 Km on it :-) without cargo its
 acceleration was good but with more than 800 kg on it, I suffer from its
 slugish acceleration.

Mine is the dual cab 4wd, even more sluggish than the standard pickup. It
will run all day at 110kph and beyond if you let it but don't mention hills.
With patience and the adaption of the planning required when driving low
powered vehicles it doesn't embarass itself.

 It is a good engine if its copression is Ok and the fuel injectors are in
 good shape. Besides its fuel consuption is really low for a 1 ton pick up
 without cargo, I used to get about 8 litres/100 Km at 90 Km/h on road with
 it (the model did not have air conditioner from factory).

With all the extra hardware the 4wd has to carry(including the add-ons of
Bullbar, winch and longrange fuel tank) my mileage is more like 9.5
litres/100km, the freewheel hubs help .

Its a fairly crude vehicle for this day and age, rough ride and all but the
log book figures have shown me it has been the most reliable, economical
vehicle I have ever owned and that tray in the back gets plenty of use
including transporting drums of WVO and WAF.

If I need comfort, speed and agility along with a rewarding driving
experience, well there a a couple of Pug 504's in the back yard almost ready
for registration, and one is a diesel.
 Regards,
 Paul Gobert.




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Re: [biofuel] Fitting a turbo (was SVO in turbodiesels)

2003-08-19 Thread gobie


- Original Message -
From: Alan Petrillo [EMAIL PROTECTED]
 Many aircraft are turbocharged this way.  Instead of being rigidly
 mounted to the engine core the turbo is mounted behind it on the
 firewall, and connected with flexible exhaust pipes.  I don't know what
 the pitfalls of such an installation would be for cars.  I suspect the
 added plumbing would make for a lot of turbo lag, which isn't a problem
 for airplanes but could be for cars.

Greetings Alan,
Yes turbo lag could be a problem, but heck if I can live with low power and
planning every passing move five minutes in advance the addition of turbo
lag could be interesting. At least there could be power there when I want
it. Guess i could hold the lower gear longer to get the turbo spinning and
then take advantage of its inertia to get power on the upchange, would be
quite a different driving technique than present.
Just out of interest, I have heard  very little about modifying camshafts in
diesels as is done in petrol engines to shift power and torque bands or
optimise for modifications.
Perhaps fumigation could be incorporated to alleviate the lag, plenty of
room in the back for a LPG tank. Plenty available secondhand in this area as
the price of a litre of LPG has rissen above 2/3 that of a litre of petrol .

.

  Do turbos rely on  the sudden pulses of the exhaust gas as it exits the
  exhaust ports and expands or  the total flow of the exhaust gas?.  .

 Um... well, the answer to that question is yes.  Depending on the
 design of the turbine.

Something I would have to investigate before embarking on this modification.

Regards,
Paul Gobert



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Re: [biofuel] Fitting a turbo (was SVO in turbodiesels)

2003-08-18 Thread gobie


- Original Message -
From: craig reece [EMAIL PROTECTED]


 Alan,

 An intercooler will cool the incoming air charge, allowing more fueling
 and power without adding any more heat - unless you turn the fueling up
 a whole lot. Adding a pyrometer (aka EGT gauge - exhaust gas temperature
 ) and a turbo boost gauge at the same time will help you make sure you
 don't add so much power by turning up the fueling than you melt
 something.

 How to add a turbo is another question - if there's anyone who makes a
 kit for it, that'd be easiest, if not, you'll have to get an intercooler
 from a junkyard - I know a guy who's added a Saab or Mustang gas engine
 intercooler to a Mercedes 300D - I could give you his number if you
 contacted me off-list.

 Craig

I have a rather smokey Hilux 2.2 deisel (1982 model). Even smokes a bit on
`100% BD.
Have been thinking of turboing it to reduce smoke and give it a much needed
power boost.
Kits are probably no longer available for this engine and would be expensive
to get a turbo adapted.
Have decided to investigate fitting a secondhand turbo in the exhaust pipe
and mounted on the chassis behind the cab under the tray.
Exhaust will exit through vertical stack/muffer. Air intake will be mounted
on other side feeding through filter to turbo inlet.
Engine/exhaust pipe up to turbo will probably need insulation to maintain
volume of flow. Piping of air from turbo ( along chassis) to engine can be
finned to act as an intercooler.
I'm not after high pressure boost but i'm curious to know if locating a
turbo remote from the engine like this would be effective. Certainly would
make fitting one to an older vehicle much easier.
Do turbos rely on  the sudden pulses of the exhaust gas as it exits the
exhaust ports and expands or  the total flow of the exhaust gas?.  .

Regards,
Paul Gobert.



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Re: [biofuel] Using pH to determine optimum methoxide level.

2003-08-04 Thread gobie


- Original Message -
From: Keith Addison [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Monday, August 04, 2003 1:24 PM
Subject: Re: [biofuel] Using pH to determine optimum methoxide level.


 Hi Paul

 Covered most of this already - see:
 http://archive.nnytech.net/index.php?view=26692list=BIOFUEL

 Best

 Keith

Thanks Keith, must have missed that one. My computer/connection is not
bringing up the page at the moment so will check it later.

Regards Paul.



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Re: [biofuel] ASTM Fuel

2003-08-04 Thread gobie


- Original Message -
From: Jack Kenworthy [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Tuesday, August 05, 2003 5:30 AM
Subject: [biofuel] ASTM Fuel


 Hey All - just thought I would let you all know that I just received my
results from the ASTM tests and we passed all categories.  Just another good
example of a homebrewer in a remote setting (Bahamas) making spec-grade
biofuel!
snip
Congratulations Jack, any particular areas you had to concentrate on to get
the BD to ASTM spec? Large excess of methanol, prolonged agitation, extended
settling time, thorough washing?

Regards,
Paul Gobert.



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Re: [biofuel] NATRIUM METHOXIDE

2003-07-23 Thread gobie


- Original Message -
From: Johnsson Tomas [EMAIL PROTECTED]


 Hello All,

 I was just talking with a soap maker about glycerin when he asked about
the
 the process for manufactutring BD. He suggested the using of natrium
 methoxide have some one experince or information (pros and cons) of using
 natrium methoxide as katalyst.

 /Tomas

Greetings Tomas,

Natrium is another name for Sodium as in Sodium methoxide.
The symbol  Na for sodiu7m is derived from natrium.

Regards,  Paul Gobert.






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Re: [biofuels-biz] Separation of water from WVO

2003-07-22 Thread gobie


- Original Message -
From: David Teal [EMAIL PROTECTED]


 Terry Lohnes' original post reported that :

  Right now, I'm experimenting with separation of 80%
  soybean oil, 20% water (emulsified in a blender) using a CaCl salt
  solution at varying concentrations and temperatures.

 My concern is that this is not representative of typical water
contamination
 percentages

Yes David, I too think that the lower percentages would be of more
relevance.

My main concern however is someone who claimed to be a Chemical Engineer (
could be wrong there Terry, my appologies if I am) using the formulae CaCl
for Calcium chloride.

Regards,   Paul Gobert.




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Re: [biofuel] Monsanto Sues Small Dairy In Maine Over Growth Hormone Comment

2003-07-12 Thread gobie


- Original Message -
From: Appal Energy [EMAIL PROTECTED]



 Has anyone ever noticed the vast discrepancy between the expiration dates
on
 organic milk vs government issue milk?

 Government issue pasteurized usually has at best a week before it's use
date
 is reached, with freshly stocked shelves sometimes having but a day or
two's
 time window.

 Yet organic milk, more frequently than not, has as much as a 30 day +
 expiration window.

Quite a difference on many counts there Todd.

Haven't had much to do with organic milk, but have spent most of my working
life in Dairy Companies in their Labs and on the factory floor.

Often people would bring in samples from their house cows for
microbiological testing. The results would invariably be a much  lower level
of bacterial contamination for this raw milk than the processed milk leaving
the factory. Sometimes we would have to drop the dilution rate by a factor
of ten to get a decent count on an agar plate. With a healthy cow the milk
in the udder is practically sterile, but milk a good media for the growth of
any bacteria that may later contaminate it during milking and handling..

With a disease free cow and clean milking techniques, cow to consumer is the
way to go not only for freshness but also for taste.

With the advent of refrigerated on farm bulk milk tanks decades ago some
following. After packaging there is the delivery/sales delay.
Factories draw their milk from many farms and the milk from one farm is not
necessarily as good as from another.  Quality of supply is maintained by
regular testing, penalties for not meeting standard and exclusion of
substandard milk from processing.

Being a living food milk is succeptable to degredation by bacteria
introduced to it. Regardless of how careful a dairy factory handles, treats
its milk there is always area for bacterial contamination. Pasteurising was
origionally enforced to prevent the spread of TB and other diseases. Today
better farming practises and legislation on cow health have eliminated the
TB threat. Pasteurising kills the harmful bacteria but the thermoduric
bacteria, those which can survive heat treatment remain and are responsible
for the bacterial degredation of the milk. Post factory storage temperature
plays a big part in the shelf life of milk. Maintainance of a low
temperature from factory to glass will see a shelf life in excess of that on
the carton/jug. As consumers we can play our part by transporting our
refrigerated/frozen foodstuffs from supermarket to refrigerator/freezer via
insulated boxes, eskys etc. Allowing temperature sensitive foods to warm up
after purchase accellerates their spoilage.

Pasteurisation and homogenisation take away the natural wholesome taste of
milk. The more processing a dairy product is subjected to the shorter will
be its shelf life.
Selection of cow breed for volume yield has seen the widespread adoption of
the Fresian breed. Although breeding has improved their milk it cannot rival
the taste of milk from a Jersy or Gurnsey cow ( even though their milk is
high in fat content).
Friend and ex workmate has been running an organic dairy not far from here
for for some years, he produces some great dairy foods which are in such
demand that he can only supply the local market.

Regards,
Paul Gobert.



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Re: [biofuel] Monsanto Sues Small Dairy In Maine Over Growth Hormone Comment

2003-07-12 Thread gobie


- Original Message -
From: doug foskey [EMAIL PROTECTED]
 Where in Aus are you? It sounds like it could be NR of NSW?

Greetings Doug, I'm on the Atherton Tablelands inland from Cairns
Queensland. Its the location for Australia's only Tropical Dairying Area and
home of the worlds longest milk run.
Have also worked in Dairy factories across N.S.W. and in Canberra.

First job was in the lab of a large dairy company in Hunter Valley,
Newcastle N.S.W.. In those times milk was delivered to the factory in milk
cans. Each farmers milk would be tipped into one side of a double sided
weighing vat. Part of my job was to sample the milk for methylene blue
quality testing (this was in the days before widespread microbiological
testing and indeed anyone who was capable of such tests was held in godlike
status).
Each farmers milk would have a different fragrance depending upon its
freshness, the mix of cows in the herd and what they were eating. Many times
I succomed to temptation and sucked a little harder on the sampling pipette
to get the taste of a good smelling batch.

(for the internationals, we have an organic dairy near Kyogle who also
sells milk from
 selected cows (A2 milk), supposed to be low in undesirable fats?.)
   This milk (the normal one, anyway) is Jersey milk,  my children will
not
 drink it as it tastes 'different'. To me it tastes like I remember
milk

Some years ago when I worked at an agricultural college a company was
trialing a product that coated feed components and moved them unaltered
through the initial phase of a cows digestive system. The aim was to produce
milk with less saturated fats, not sure of the mechanism or outcome of the
trials.

Guess its what you are used to and expect of a product.
Butter for instance always has a yellower colour in summer because of the
better pasture, winter butter is harder to sell because the comsumer expects
a nice yellow colour, (can remember my grandmother's homemade butter being
very pale and a bit too salty but good), so the buttermakers send a lot of
the butter they make off to cold store. Summer butter gets blended with
winter butter to improve the colour and excess butter from summer gets
shipped to cold store for use in winter.

Another example is any product with a strawberry flavour.The colour the
consumer expects is way in excess of what the proportion of natural fruit
could provide.
This is just an example of the hurdles organic produce face. Marketing has
transfered our selection criteria from our noses and taste buds to our eyes.
Fruit with skin blemishes does not necessarily taste inferior. Indeed it can
have a better taste and nutritional content than a perfect example of a
variety grown specifically for its presentation value, ability to be force
ripened at the required time and its durability to travel. Tomatoes are a
good example of this.

Was given the task of making up a ten gallon batch of custard for a TV ad
crew once. The normal custard was considered too pale and not thick enough
for the filming. Both thickness and colour had to be dramatically increased
for the desired effect until the end result was more like a batch of orange
dyed cement mix.


   As yet in Aus, we do not have a lot of processing on raw veges (that I
lnow
 of anyway..) We still get eyes sprouting on potatoes, etc.

Atherton Tablelands is a potatoe growing area and we can buy bags of spuds
straight from the farm, still covered with the rich red volcanic soil they
grow in.
Ironic part is that even though this soil is reputed to be some of the best
farm soil in the country and will grow almost anything, every time we are
cut off from southern distribution markets by flooding our local
supermarkets run out of vegetables.

BUT unfortunately  we seem to have a govt going down the GM road - even tho
the populace do not
 trust it. I wonder if the US powerbrokers are using pressure to make us go
 this way (So no competitor can be GM free,  have a powerful market
position)
 Ah well, conspiracy theory mode off

 regards Doug

The ultimate insult from GM products would seem to me to be the reports of
fines for farmers whose properties adjoin those with GM crops and find that
some of those crops are sprouting in their fields.  Do GM crops set true to
seed or do they throw back like hybrids?

Enouth of my waffling, its probably information everyone is familiar with
anyway.

Regards,
Paul Gobert.






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To 

Re: [biofuel] Monsanto Sues Small Dairy In Maine Over Growth Hormone Comment

2003-07-12 Thread gobie


- Original Message -
From: Appal Energy [EMAIL PROTECTED]


 Paul,

 What I'm referring to is pasteurized 2% organic (Oregon Tilth) vs
 pasteurized 2% non-organic, both from auto milking environments,
 transportation to packaging houses, storage, transportation to vendors and
 final shelving in the exact same cooling units.

Yes, big difference in quality, natural justice would see the organic dairy
sueing Monstanto for claiming that the chemical; milk was as good as the
organic milk. Unfortunately natural justice is a poor cousin compared with
industrial muscle.

A change of subject heading would have been appropriate for my comments
which were about the dairy industry in general.

Regards,
Paul Gobert.




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Re: [biofuel] Problems sep. glycerine

2003-06-25 Thread gobie


- Original Message -
From: Pieter Koole [EMAIL PROTECTED]


 I am still trying to separate glycerin and FFA's, but it does not work.
 Now I used ยธ liter of the bottom layer ( from the very bottom of the
 vessel ) and ยธ liter ( not ยธ ml. but ยธ liter ! ) sulphuric acid ( 98% )
and
 all that happens : no separation.
snip

Pieter, I think you mentioned earlier that the oil you are using is only
used for one day. The acidity should be very low. Perhaps the FFA's aren't
separating because there isn't much there.
( excuse me if I am thinking of the wrong feedstock).
Regards,   Paul Gobert.




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Re: [biofuel] WW2,peroxide power

2003-06-21 Thread gobie


- Original Message -
From: greg [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, June 22, 2003 6:03 PM
Subject: Re: [biofuel] WW2,peroxide power


 i think it was the me 162
 The ME-163 looks like what we are after.

from  http://www.oldgloryprints.com/Herman's%20Comet.htm

(good picture)
The Me-163 Komet.  A rocket powered plane used to intercept raiding
American B-17's and '24's.
As the Komet was about 250 MPH faster than the target, and only flew for
about 3 minutes,
they proved to be very exciting (to the pilot), but relative ineffective in
combat.

The original aircraft used a highly volatile 2 part liquid propulsion
rocket engine for power and had a little propeller on the front as a wind
powered generator. The plane was basically a fuel bomb with wings.

The Komet was the first rocket-powered fighter to be placed in active duty.
It was a very beautiful, well-designed and airworthy craft with a small
drawback; It was deadly! If that simply had referred to the enemy facing the
Komet, it wouldn't be much of a drawback, but unfortunately the pilot and
the ground crew were the ones who were in the greatest danger.

http://homepage.ntlworld.com/andrew.walker6/komet/flight/flight3.htm
A Hellmuth Walter Kiel Kommandogesellschaft HWK 109-509 bi-fueled rocket
powered the first B-model Komets. Throttle positions of off, Idle, 1st, 2nd
and 3rd stages thrust were controllable from 220 lb. to 3,307 lb. The engine
dimensions: length-8 ft. 3.5 in.; height-2 ft. 11 in. Total weight was 813
lb. (fuels system 441 lb.; motor 366 lb., control system 7 lb.). The 163B
was propelled by fuels coded T-Stoff and C-Stoff. C-Stoff was a mixture of
57% methyl alcohol, 30% hydrazine hydrate and 13% water. T-Stoff was 80%
concentrated hydrogen peroxide, to which some additional stabilizers were
added. The T-Stoff fuel tank system consisted of a main fuselage tank and
two smaller tanks on each side of the pilot's seat in the cockpit (see
cockpit photo). Total fuel capacity was 3,717 lb. of T-Stoff and 1,032 lb.
of C-Stoff.

 Interesting reading at
http://homepage.ntlworld.com/andrew.walker6/komet/flight/flight1.htm

Regards,   Paul Gobert.





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Re: [biofuel] Ammonia as Fuel

2003-06-21 Thread gobie


- Original Message -
From: Pieter Koole [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Saturday, June 21, 2003 10:07 PM
Subject: Re: [biofuel] Ammonia as Fuel


 How does one use NH3 as energy source ?
 I ask this, because in Holland we have big problems with NH3 polution
coming
 out of huge animal houses with hundreds of thousends of pigs or chickens.
 If we could filter the NH3 out of the air and use it as a fuel, it would
be
 great.

 Pieter Koole

 - Original Message -
 From: murdoch [EMAIL PROTECTED]
 To: [EMAIL PROTECTED]
 Cc: [EMAIL PROTECTED];
 [EMAIL PROTECTED]; biofuel@yahoogroups.com;
 [EMAIL PROTECTED]
 Sent: Friday, June 20, 2003 9:35 PM
 Subject: [biofuel] Ammonia as Fuel


  It isn't clear to me at what temperature it can become liquid.  It
  seems to me that a big part of why I was advocating other fuels is
  that, in liquid form, they can be transported and used with greater
  energy density.  I do think it's close to being easily made into a
  liquid, but that at room temperature it's gaseous?
 
  http://www.c-f-c.com/specgas_products/ammonia.htm
  http://www.slider.com/enc/2000/ammonia_Properties.htm
 
  There does seem some indication that it is toxic in some extent.
  This is not to preclude your suggestion, just to examine the pros and
  cons a little.
 
  Wasn't ammonia used as a refrigerant and then replaced with CFC's?
 
  Note that several people appear to be cc'ing to other groups in
  response to my own cc's.  When I initiate this, I do it because my
  experience has been that I get a wider range of more-enlightening
  response, even if there are some significant downsides to this, such
  as disjointed conversations.  If you wish for your posts to appear in
  the other groups, I think the way yahoo works, you'd just have to join
  them, otherwise the cc: is wasted.  If it is not that important, then
  fine.  I moderate the evworld.com group and the energyproduction one
  that I just maintain for myself it seems.
 
  But I am not stumping for membership, just going over something that
  seems to now pertain to several people.  I did send out invites for
  the evworld.com group because it seemed a way to alert some that their
  posts were not being seen on that group, in case they weren't fully
  aware.
 
  MM
 
 
  On Thu, 19 Jun 2003 17:11:24 EDT, you wrote:
 
  You're welcome!!
  
  Now, about liquifiable fuels--  You didn't mention one of my favorites,
  ammonia, NH3.  Its energy density is a little lower than methanol, but
 notice that
  it contains no carbon and can be catalytically reduced to hydrogen and
  nitrogen.  I am not aware of environmental problems with this
substance.
 It is
  currently used at very high tonnages for fertilizer without any
reported
 problems.
  
  Ernie Rogers
  
   Thanks for the feedback Ernie.
  
  
  
  
  [Non-text portions of this message have been removed]
  
  
  
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Re: [biofuel] Ammonia as Fuel

2003-06-21 Thread gobie

Ooops sorry about the repeat.

- Original Message -
From: Pieter Koole [EMAIL PROTECTED]


 How does one use NH3 as energy source ?
 I ask this, because in Holland we have big problems with NH3 polution
coming
 out of huge animal houses with hundreds of thousends of pigs or chickens.
 If we could filter the NH3 out of the air and use it as a fuel, it would
be
 great.

 Pieter Koole

Getting the ammonia out of air is no problem, bubble the air through water.
Ammonia is very soluble in water (fountain experiment used in schools).
Don't know how you would derive inergy from it, probably best converted to
fertiliser and used or exported.

Regards Paul Gobert



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Re: [biofuel] McDonald's Tries To Phase Out Use of Antibiotics In Meat

2003-06-21 Thread gobie

Something to consider regarding medication of animals.
If you intend to add some horse manuar to a worm farm make sure that the
manuar is aged. Have been advised that if the horses have recently been
wormed you can kill off some or all of your worms in the farm.
Regards,   Paul Gobert.



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Re: [biofuel] Freezing (was Ammonia)

2003-06-21 Thread gobie

An interesting high school chemistry demonstration is the dry mixing of
Ammonium thyocyanate and Barium hydroxide powders in a flat bottomed flash.
They are stirred together and form a slurry. The flask is placed on a
dampened block of wood. The reaction between the two chemicals is
endothermic. The mixture absorbs heat from the moisture on the wooden block.
Flask and block are bonded together by the ice formed and can be lifted as
one unit.

Regards   Paul Gobert.



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Re: [biofuel] WW2,peroxide power

2003-06-21 Thread gobie


- Original Message -
From: [EMAIL PROTECTED]

 Pilot's seat?  in a German rocket?
 On Saturday, Jun 21, 2003, at 07:02 US/Eastern, gobie wrote:

Yes we could call it plenty of other things. Must have been one hell of a
ride especially under maximum thrust with near empty tanks. All this with
fabric covered wings.
In view of the unusual performance and the potential to self destruct good
pilots were hard to find especially when they were needed for conventional
aircraft.
Some interesting reading on the performance of the aircraft, the training
of the pilots and the techniques the pilots used to get around its
vulnarabilities, especially when it glided back to base.
 http://homepage.ntlworld.com/andrew.walker6/komet/flight/flight1.htm

Wonder has anyone tried deriving oxygen from H2O2 to supercharge an  ICE?

 Regards,   Paul Gobert.




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Re: [biofuels-biz] Peugeot takes it's diesel racing on biofuel

2003-06-20 Thread gobie

Thankyou David and Kirsten

Paul,
I recently visited a very large diester plant in Northern France.  Their
feedstock is 100% French grown rapeseed oil, processing flowchart is bog
standard.  Plant is alongside an oil extraction industry, whose output is
40% to food trade and 60% to diester.  Fuel is shipped (by water transport)
to 3 oil refineries for blending with mineral diesel prior to distribution.

Watch this space for news of a UK biodiesel competition sports car.

David T.


From a commercial manufacturing perspective, SAIPOL, near Rouen, has one of
the largest diester manufacturing sites in the world.  They are a large
producer of BD in France along with ROBBE and COGNIS.  France produced
365,000 tonnes of BD in 2002 and expect to increase by 70,000 tonnes in
2003.

KPS

-

David, I like the name Diester. Aside from purchasing the diester for its
diester blend I wonder what connection/investment Total have in the plants?
Would be interesting to see what industry model has developed.

The competition sports car sounds interesting but the present pug is a
beauty, (what me biased?)
See that Peugeot and Jaguar have signed an agreement to design and build a
V6 diesel about 2.7 L but to appear in many forms.
Hopefully it should be better than the Peugeot/Renault/Volvo V6 petrol of
the seventies.

Kirsten,
Interesting, are these companies independent of Total?
We hear a bit about the production and use in Germany but not too much about
France.
Will search around to see if I can find production figures for Germany.


Regards,   Paul Gobert.




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Re: [biofuels-biz] Peugeot/Citroen/Jaguar/Ford V6 diesel.

2003-06-20 Thread gobie


Re: [biofuel] Sparkling bio-diesel

2003-06-20 Thread gobie


- Original Message - 
From: mark schofield [EMAIL PROTECTED]
 As far as I understand, and I will have it out
 with them shortly, I have to test it for
 certification and then they also test
 periodically when ever they want. Further, they
 can also turn up on site at the drop of a hat and
 demand and take up to 6 years of production data,
 figures etc.
 
 Regards
 
 Mark
 

Pleasant little blighters, hope it doesn't come to that over here.

regards,   Paul Gobert.



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Re: [biofuel] WW2,peroxide power

2003-06-20 Thread gobie

from  http://www.pbs.org/wgbh/nova/lostsub/hist1939.html
1940
German scientist Helmuth Walter demonstrated a prototype for the first true
submarine, a boat that in theory could operate submerged for an indefinite
period, unlimited by battery capacity or the need for atmospheric oxygen.
V.80 gained its power from the decomposition of highly concentrated (95
percent) hydrogen peroxide, H2O2, known as Perhydrol. In essence, when the
chemical breaks down, it releases superheated steam to drive a turbine along
with oxygen to support conventional combustion for additional power or for
crew respiration.

V.80's designer optimized its hull shape for submerged operations, and the
boat indeed demonstrated exceptional speed -- 28 knots submerged. It also
demonstrated exceptionally high fuel consumption, 25 times that of a diesel
engine, at exceptional cost. According to one source, one
six-and-a-half-hour trial run consumed $200,000 worth of Perhydrol.
The design showed great promise, but Hitler thought his war was won, so
plans for production of a series of Walter boats were put on hold. Research
continued, however, and perhaps eight, in several variations between 250 and
300 tons, were put into service in 1943-44.

Not a nice chemical to be trapped in a big pipe with, but then notice that
an early design of American nuclear sub  used an alloy of sodium and
potassium metals to transfere the heat from the reactor to the boilers. I
wonder if anyone who designed these things was game enough to travel in
them.
Conventional deisel generator and battery subs had their problems too.
Saltwater in contact with high current producing chlorine gas. Bad enough to
be in a damaged leaking sub but chlorine as well.

Regards, Paul Gobert.



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Re: [biofuel] Re: how much do you know

2003-06-20 Thread gobie


- Original Message -
From: Forbes Bagatelle-Black [EMAIL PROTECTED]


 At the speeds we are discussing, wind resistance accounts for most of
 the energy consumed.  Other sources of energy consumption are rolling
 resistance of the tires, which remains constant relative to velocity
 (but not vehicle mass), and inefficiencies in the drivetrain and
 engine.  Drivetrain inefficiencies remain relatively constant.  Engine
 efficiencies, on the other hand, vary greatly largely as a function of
 actual torque at a given RPM and peak torque at that RPM.  Efficiency
 tends to increase as actual torque approach peak torque.

Now here is one from the weird ideas department.
What if we could reduce the wind resistance by mechanical means.
Wind resistance increasing vastly as speed increases, mechanical energy
requirements increasing less.
Would need something like a moving skin on the vehicle same speed as the
air.
Its alright folks, very early in the morning here, gpoing to get some sleep
, will be back to normal in a few hours.

Yawns,   Paul Gobert.




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Re: [biofuel] Ammonia as Fuel

2003-06-20 Thread gobie

Ammonia (gaseous) mixed with air in the right ratio forms an explosive
mixture. But then that can be said for a lot of fuels with low vapour
points.

Regards  Paul Gobert.



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Re: [biofuel] WW2,peroxide power

2003-06-20 Thread gobie

Brant, apparently they did use the oxygen from the peroxide to power the
diesel generators.
The V.80 was built in a figure eight cross-section configuration with the
base section intended to hold the peroxide. When the idea didn't work out to
be practical; they filled the bottom section up with additional batteries.
Whilst not a fan of warefare, I admire the technological advances conflict
brings even if they are in a less than social direction.
The site makes for very interesting reading I especially liked the 1935 to
1945 section.
Interesting little snippets like the British training seagulls to sit on
periscopes to make the submerged sub easier to spot.
The  Japanese I Boat that fired a cluster of six torpedos at a ship in a
convoy. Three hit the target sinking it, the other three ran for a further
12 Km, encountered another convoy, damaging two more ships and the sixth
torpedo kept going. Contrast this to the early war scenario where torpedos
were unreliable. On sub fired off its its 24 torpedos during its tour of
duty, plenty of hits but only one exploded. However it did sink one ship
when the unexploded torpedo punctured the rusty hull..
Regards   Paul Gobert.





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Re: [biofuel] WW2,peroxide power

2003-06-20 Thread gobie


- Original Message -
From: jgnat1488 [EMAIL PROTECTED]


 What was used as the reactant in the nazi rocket
 plane? I know that one of the fuels were h2o2 and
 when the other liquid was in contact with it, it
 combusted for more thrust. As i recall the plane was a
 shoort range (12 min. fly time) interceptor placed
 near factories and used drop dollies for take off
 gear. It even had a small prop. on the front that was
 used for power generation to run the radio and such.
 Jason Gnatowsky

Jason couldn't find any mention of the rocket planebut
http://www.constable.ca/v2.htm
details the use of H2O2 in the V2.
Technical Details
The V2 was an unmanned, guided, ballistic missile. It was guided by an
advanced gyroscopic system that sent signals to aerodynamic steering tabs on
the fins. It was generally inaccurate due to errors in aligning the rocket
with it's target, premature shut-off of the motor and inconsistencies in
electric current in the guidance system. It was propelled by an alcohol (a
mixture of 75% ethyl alcohol and water), and liquid oxygen fuel. The two
liquids were delivered to the thrust chamber by two rotary pumps, driven by
a steam turbine. The steam turbine operated at 5,000 rpm on two auxiliary
fuels, namely hydroperoxide (100 %) and calcium permanganate. This system
generated about 55,000 lbs (27,000 to 30,000 Newton) of thrust. The motor
typically burned for 60 seconds, pushing the rocket to around 4,400
ft/second. It rose to an altitude of 52 miles and had a range of 200 - 225
miles.

regards Paul Gobert.



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[biofuels-biz] Peugeot takes it's diesel racing on biofuel

2003-06-19 Thread gobie



 From: Marc Bonanni [EMAIL PROTECTED]
 Date: Fri, 28 Mar 2003 21:23:40 -0500 (EST)
 
 Did you know that Peugeot will use one of the two RC prototypes(born
 in 2002 Geneva Motorshow)in REAL race on circuit 
 
 It will use the same HDI engine than the red one(2.2l, particles
 filter, 175bhp)but using diester oil(more ecological than diesel),
 and 25 examples will be built to race in diffrent circuits in France
 and Belgium...
 
 See the official photographes, it's a really nice sport car
 
 http://ffsa.turbo.m6.fr/images/030321_nogaro//p031492.jpg
 
 http://ffsa.turbo.m6.fr/images/030321_nogaro//p031493.jpg
 
 Thanks!
 Marc Bonanni

Certainly a nice looking car.
Total advertising on car and in pits. Wonder if Total are producing the
diester .
Not sure where the 2% BD used in French diesel comes from. Any ideas
anybody?

Regards   Paul Gobert.



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Re: [biofuel] Some questions and perhaps an idea about BD

2003-06-19 Thread gobie


- Original Message -
From: Pieter Koole [EMAIL PROTECTED]
To: biofuel@yahoogroups.com
Sent: Sunday, June 15, 2003 2:31 AM
Pieter, looks like you didn't get much response to your questions.
A lot of what you are asking about can be found at Journeytoforever.org,
through the archives of this list, at the Mauri discussion list and many
other sites around the net.

 Can anyone explain me, why the excess methanol at the end of the BD
process not just floats on top of the BD , regarding the specific gravity ?

Methanol is miscible with both biodiesel and glycerine, so it stays in
solution. Separation is usually by distillation.

 Another question or may be even a solution :
 When we make methyl esters we can distill the excess (m)ethanol out of
this ? Am I right ?
 When we make our own ethanol, the problem is to get it 99% pure.
 How, if we would mix the ethanol / water mixture with ethyl ester, so that
the ethanol will solve in the ester and the water falls down to the bottom.
 After that, we could distill the water out of the ester.
 Is this a very stupid thought ? As you maybe allready understood, I am not
a chemist.

Not sure on this one, (m)ethanol are very soluble in water and perhaps less
soluble in ester. This is born out by the (m)ethanol being removed from the
ester by water washing, the volume of water involved here is much greater
though.

 Is n't it possible to separate the water and ethanol with some kind of
electrolyse ?

Electrolysis works on ionic solutions, not aware of any such technique that
would separate water and ethanol.

 How come that the pH of the ethanol I use now ( 98% pure, rest is
methanol ) is just below 7 ?
 I thought alcohol is a basic fluid because of the OH  ( r COOH ) ?

Electronic pH measurements of non ionic liquids are unreliable, pH meters
are only accurate for ionised liquids, ethanol is an organic liquid with
very little ionisation.
pH can be measured chemically using indicators, Universal indicator (a
mixture of various indicators) is a handy indicator to guage the progress of
washing etc. Results rely on the interpretation of the colour it produces
and are only accurate to about one half of a pH unit.

 If I would make a still in which I could reach 290ยก C to destilate the
glycerin out of the bottom layer from the BD process, would that be
dangerous ?
 Would it deliver pure glycerine as one of the fractions ?

Danger would be relative to construction,siteing etc, can be done but not
economical unless you have a cheap source of heat for that 290 deg C and a
market for the glycerine.

 Sorry for the mistakes in the language. My parents never tought me to
speak or write in English. I had to learn that later, like learning to make
BD and somehow it works.
 I' have driven just over 100.000 km now without ever having any problems.

Thats a good mileage on BD.
Washed or unwashed BD?
What type of vehicle?

Regards Paul Gobert.



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Re: [biofuel] Sparkling bio-diesel

2003-06-19 Thread gobie


- Original Message -
From: mark schofield [EMAIL PROTECTED]

 In England, dispite the Government crying out for
 cleaner fuels etc, we still have to pay road duty
 at the rate of 25.8p per L (43.3c USD per L) and
 before we are allowed to pay the duty ie use the
 fuel the Customs  Excise have to make sure its
 manufactured to the correct standard etc. Minimum
 requirements include 96.5% Methyl Ester content,
 0.005% sulphur, SG around 0.835 maximum etc.
 These are rough figures off the top of my head.

 And the beat goes on.

 Regards

 Mark

Mark  is the user required to have the fuel analysed or do Customs  Excise
do the analysis?

Regards   Paul Gobert.



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Re: [biofuel] Re: Reusing washing water

2003-06-19 Thread gobie


- Original Message -
From: appalenergy [EMAIL PROTECTED]


 Magnesium sulfate (epsom salt) works. Even plain sodium chloride
 (table salt) will work to some degree.

 Warning! Overkill on salt will produce an even worse problem, as
 saline effluent can yield a dead zone just as readily as soap
 accumulation.

Worse still when reusing the wash water after treatment and filtering,
residual MgSO4, NaCl or CaCl2 in the wash water will deposite the soap
scum within the BD

Regards   Paul Gobert.



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Re: [biofuel] Self-drive cars ahead

2003-06-15 Thread gobie


- Original Message -
From: Keith Addison [EMAIL PROTECTED]

 - Original Message -
 From: Keith Addison [EMAIL PROTECTED]
 
   BBC NEWS | Technology | Self-drive cars ahead
   7 June, 2003, 07:46 GMT 08:46 UK
  
   Self-drive cars ahead
 snip
   I don't mean that we shouldn't have and use cars, just that they
   should be driven by computers and not humans, electronically tethered
   to cars in front and behind, he said.
 
 And they call that driving?, might as well take the bus.
 
 RegardsPaul Gobert.

 Hi Paul

 Might as well, yes. Or the train. If there is a bus or a train, but
 most likely there isn't, and there should be...

 My sympathies, I feel much the same, but on the other hand, how many
 drivers - people with a licence to propel a car - know what
 driving is? Not too many, eh? It's a minority skill, and a real
 charge for those few who have it, but if it has to be sacrificed in
 order to stop the slaughter caused by all those who don't have it,
 nor road sense either, well, so be it, I wouldn't argue. Just as long
 as it really did stop it, and that without the all-too-usual
 unexpected side-effects that turn out to be worse than the original
 problem.

 Best

 Keith

Yet another reason  why I deserted the cities 30 years ago, choice of
lifestyle over material wealth.
. Old habits die hard, double declutching and heel and toeing etc. People
often ask me how come my engine was being reved up whilst I have my brake
lights on, or tell me that my brake lights weren't working when I was using
gears and engine braking to come to a leasurly stop.Replaced the Toyota's
clutch at 550,000 km and 600,000 km sees it still on its second set of brake
linings.The engine braking of a manual diesel makes for smooth driving.
Not so many drivers as road users over here. Tourists from heavily
populated areas seem to be the worst. If they haven't seen another car for a
minute or two they think it is ok to stop their hire car in the middle of
the road around a blind corner to sightsee.
By the way my fleet of Pugs has grown, was confined to one with last wife,
now have 4 504s (including a diesel) and a 505 in the yard, plus a new lady
who doesn't mind them, now that is happiness.If only I could find somewhere
to park the Toyota and for my lady to park her car.

By the way anyone who enjoys movies where the little guy triumphs over the
big banks would enjoy the movie The Bank

Regards Paul Gobert.





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Re: [biofuel] Self-drive cars ahead

2003-06-13 Thread gobie


- Original Message - 
From: Keith Addison [EMAIL PROTECTED]

 BBC NEWS | Technology | Self-drive cars ahead
 7 June, 2003, 07:46 GMT 08:46 UK
 
 Self-drive cars ahead
snip 
 I don't mean that we shouldn't have and use cars, just that they 
 should be driven by computers and not humans, electronically tethered 
 to cars in front and behind, he said.

And they call that driving?, might as well take the bus.

RegardsPaul Gobert.



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Re: [biofuel] Veg-oil lubricant/Complex mixing of fuels

2003-06-12 Thread gobie


- Original Message -
From: kirk [EMAIL PROTECTED]


 Many years ago race cars ran on castor bean oil. I think they promptly
 drained them after the race however. I was told the high heat caused the
oil
 to gel once it cooled. Was the best lubricant around at the time though.

 Kirk

Castrol R or Mobil P, both castor based oils are still the prefered
lubricants in the worm/wheel diffs as fitted to Peugeot 203,403,404.

Regards, Paul Gobert.



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Re: [biofuels-biz] Drying methods

2003-06-09 Thread gobie

How about quick lime, cheaper than Lithium salts, and will neutralise the
FFA at the same time as it grabs the water.

regards,   Paul Gobert.



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Re: [biofuel] Re: Two-stage Process - jelly?

2003-05-28 Thread gobie


- Original Message -
From: girl_mark_fire [EMAIL PROTECTED]

 Check that you are not accidentally evaporating off too much of your
 methanol. What kind of container are you using on that hot plate? If
 it is an Ehrlenmeyer flask you've got a better chance of retaining all
 the methanol than if you are using a beaker, for instance. If you put
 a lid over the container you're better off still.

 mark

A glass funnel placed in the neck of the Ehrlenmeyer flask acts as a nice
condensor. If you want to get fance the neck of the funnel can be blocked at
its tip and the funnel filled with crushed ice, but that should not be
necessary..

Regards,   Paul Gobert.



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Re: [biofuel] Two-stage Process - jelly?

2003-05-28 Thread gobie


- Original Message -
From: mark schofield [EMAIL PROTECTED]

 Hi

 So after playing with the single stage for a
 while, I have produced a good clear final
 product. I have bought a hot plate magnetic
 stirrer for $360 USD that has helped for
 titrations etc.

 I have played with the two stage process and the
 final product has turned to jelly. I have
 followed the 2-stage instructions exactly -
 timer, burettes, +/- 1mg weighing scale, 97%
 H2SO4, hot plate stirrer with closed loop
 temperature control and digit speed and temp
 output. The chemicals are all analytical grade
 and the oil requires only 0.1cc of 0.1M NaOH
 solution to pH 8.5.

 I heat 1000cc of oil up to 35'C. I add 80cc of
 99.5% Methanol and stir for 5 minutes. I then add
 1cc of 97% H2SO4 and stir for 1 hour. I then cut
 the heat and stir for a further hour. The mixture
 does not separate but is left for minimum 8hrs
 usually 12. I re-heat the still liquid mixture to
 55'C and add 3.5g NaOH and 120cc Methanol. I stir
 for 1 hr and leave to settle. The final product
 doesn't settle and congeals over time.

 Keith - I am lost. Some where along the line soap
 is formed. I will re-run the experiment and
 comment tomorrow.

 On a larger scale - could a 1um filter /
 coalescer unit be used to pre-process heated oil?

 Regards

 Mark

Hello Mark,
With oil of 0.1ml 0.1M (0.4%) NaOH titration use of the two stage acid base
method is not waranted. The aim of the acid stage is to esterify any FFA
present. From your titration we can see that the oil has very little FFA in
it to start with. It would be a better candidate for single base method.
Very little would be happening in the acid stage, there is almost no FFA to
esterify and acid catalysed transesterification is very slow. In this case
all that is happening is that you are acidifying (with sulphuric acid) the
oil/methanol mix prior to performing a base catalysed transesterification
and not taking that acidity into account when choosing the ammount of NaOH
to use.
When you rerun the experiment try using a larger quatity of NaOH in the
second stage. If you don't drain off the small ammount of acid/aqueous layer
after the first stage some of  the NaOH will be consumed neutralising it.
Also current thinking is that more than 3.5g/l gives a better conversion.
Both good reasons for using more than 3.5g/l in the second stage.

Would suggest using this oil for single base method and finding some oil
higher in FFA to trial the acid/base method.

Regards   Paul Gobert.





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Re: [biofuel] Need clearification and advice

2003-05-19 Thread gobie


- Original Message -
From: Appal Energy [EMAIL PROTECTED]


(  i see biodiesel in the same light as photography,  learn by the rules
and
  then break them.)

 Problem is, in photography an entire spectrum of end results can be
desired
 and achieved by bending or breaking rules.

 In manufacturing biodiesel there is only one shade of gray that is
 desired. Bending or breaking the rules moves the perpetrator further and
 further away from the desired result.

 Agreeing to disagree doesn't change the end result of bending or
breaking
 the rules either.

 Todd Swearingen


Valid points Todd.

Have found that I have learned a lot from the mistakes I have made by
bending the rules and the investigation of the results.
Bit of a stubborn old bugger here learn by experience.

regards Paul Gobert.


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Re: [biofuel] Need clearification and advice

2003-05-18 Thread gobie


- Original Message -
From: Keith Addison [EMAIL PROTECTED]
 Well, that's one way. As I said, various people adapt it to their
 requirements and preferences, and it seems to adapt well. The best
 way though, according to much feedback, our own findings and Aleks's
 continuing work, is as-is, just the way it's presented:
 http://journeytoforever.org/biodiesel_aleksnew.html
 Foolproof biodiesel process

 Proceed just as instructed, start adapting only if you have problems.
Greetings Keith
 The ammount of NaOH Alex suggests to add in the second stage is the ammount
required for transesterification of a neutral feedstock.
If the first stage product has any residual acidity at all it will
neutralise some of the NaOH, not enough NaOH will be left for all the
oil/fat to be transesterified.

 Paul, I am a bit dubious of your advice here because I think you use
 your concentrated aqueous solution of methoxide, and IMO that adds an
 unnecessary variable, especially with the acid-base process, where
 you'll be adding water to a process that's already water-sensitive.

Once the first stage has been completed we are left with a mixturte of ester
and oil.(plus residual acid).
I have had no problems using Conc Aqueous methoxide to process either this
mix or WVO/F

 This has to be superior:
 Methoxide the easy way
 http://journeytoforever.org/biodiesel_aleksnew.html#easymeth

 And it could hardly be easier, or safer.

I revisited the site Keith.
Whilst Methoxide the easy way is all it claims to be, in comparison with the
Conc Aqueous NaOH method it falls short in speed, convenience and
adaptability.
Using Conc Aqueous NaOH I can prepare any quantity of methoxide of the
desired composition in a minute or two, handy if your batches of oil/fat
turn out to be a bit higher in acid than anticipated or you decide to
process more or less feedstock.
Its one of those proceedures that isn't supposed to work in theory but
works well in practise. Probably waiting for theory to catch up with it.
Once over the doubt hurdle and trying the method most people like it.

I can't see much difference on the safety issue either.
The Conc Aqueous NaOH method involves less handling of either methanol or
NaOH, and certainly no shaking of a potentially leaky containor.
Weighing of the NaOH is required only once to make the stock solution of
conc NaOH, so carbonate and moisture contamination of the NaOH is reduced
(both these contaminations could reduce the ammount of pure NaOH in
subsequent weighings.)

Regards Paul Gobert.




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Re: [biofuel] Need clearification and advice

2003-05-18 Thread gobie


- Original Message -
From: Andreas W Ohnsorge [EMAIL PROTECTED]

 Tomas,

 I had a similar problem with WVO from a restaurant when I tried the
 foolproof recipe allthough it worked fine with virgin oil. I had some
 sort of success using the two stage acid based version with a recipe found
 in the following website (but it requires titrating AND determination of
 peroxide number): http://mars.wiz.uni-kassel.de/agt/biodiesel/rezept.html

Greetings Andreas,
The site you mentioned gives details for the calculation of methoxide
compositions for the base/base two stage method, not the acid/base two stage
method.
Their calculator is interesting. I'm curious as to why they place so much
emphasis on peroxide number instead of say the saturation of the oil/fat
molecules.
Definition of Peroxide Number: The extent of oxidation that has taken place
in a sample pf lipid or lipid fat can be expressed in terms of peroxide
value.

Haven't been able to find much about the expected levels of stored WVO/F.
For fresh oils such as Hemp and Emu  figures of 5meq/kg were quoted.

Ran a few figures through the calculator, the methanol levels stay the same
for all FFA and peroxide levels, its the KOH levels in the two stages that
change
A peroxide number of 10 made very little difference to the result Would be
interesting to find out what figures could be expected for WVO/F stored for
some time.

One of the links that turned up dealt with preventing oxideation of oils,
looks like rosemary comes up tops here.

http://www.geocities.com/RainForest/4124/NSOres.html

Regards   Paul Gobert.


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Re: [biofuel] Need clearification and advice

2003-05-17 Thread gobie


- Original Message -
From: Johnsson Tomas [EMAIL PROTECTED]

 Hello all

 We have been testing Alecs Fool Proof process and find it to work after
 several long and time consuming testings (adding lye/methanol several
times
 and removing the glyrein).

Greetings Johnsson,
I have found with the acid/base method that it is very important to drain
off the acid/aqueous phase from the bottom of the mix after the acid stage.
Any remaining sulphuric acid neutralises part of the NaOH added in the base
stage.
The oil/ester mix should then be titrated to determine the ammount of NaOH
required to neutralise any acidity resulting from residual Sulphuric acid
and any unreacted FFA.
As Keith has already suggested the use of phenolphthalein to determine
neutrality is much more accurate than either ph paper or universal indicator
paper.
When determining the acidity after the first stage a stronger solution of
NaOH may be required. A 10% solution of NaOH may be required to get a
reasonable titration, multiply the result by ten to get the grams per litre
required.
For the second stage use the ammount of NaOH indicated by the titration plus
the ammount for catalysation  (usually 3.5 to 4.5g/l).

Regards,
Paul Gobert.


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