Re: [Biofuel] soap or mono- and diglycerides

2006-09-11 Thread Rafal Szczesniak
On Mon, Sep 11, 2006 at 07:14:40AM +0200, Tonom?r Andr?s wrote:
 Hi Rafal,
 
 Do not overcomplicate yourself.
 
 1. Make sure that your oil is dry.
 2. Make sure that your methanol dry, and lye fresh
 3. Reaction parameters - time, temperature, agitation are OK.
 4. Settlig time 24 Hours +
 5 Wash test from the upper layer of reaction wessel. - If failed try +1gr
 lye.
 For example 5.5gr / liter wash test faild, try 6.5 then 7.5 ... (if more
 then 10gr, then something else is really bad)
 
 DO more test batches at a time with 5, 6, 7, 8, 9, 10 gr lye and see wash
 test.

I guess I need to do that ie. process small samples with increasing
amount of lye. Or do the poor man's titration. Or both...

 A washtest is only passed when separating within minutes no matter how long
 and hard you shake it.

It did - much quicker than my previous tests - but there's still about
1 centimeter (in 0.5 litre PET bottle) of white foam layer between water
and biodiesel.

 and the best advice, read JTF website :)))

I have, and I'm still reading it back again after each test I make :)

 If you are unconfy with titration try base - base 2 stage. (not for
 testbatch)
 But You HAVE TO LEARN TITRATION.

Titration is not a problem. My last two batches had increased lye amount
after I titrated the oil. I surely still need a bit of practice and feel
of it, but I've titrated about ten samples so far, and I'm not scared of
it.

 Let me know how it goes,

I can assure you I will let everybody know once I succeed :)

I'm just surprised that it looks I need much more lye. I didn't expect,
when titrating with phenolophtalein, the colour should be so intensive.
For me it was clear enough last time (1.35g KOH more / 1l).

Thanks for word of advice.

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Re: [Biofuel] soap or mono- and diglicerides

2006-09-11 Thread Rafal Szczesniak
On Mon, Sep 11, 2006 at 10:11:35AM -0400, Joe Street wrote:
 Try vacuum dewatering the feedstock before processing and be good and 
 sure about having anhydrous chemicals and you won't have soap.  If you 
 are then still getting emulsions, your process is not going far enough.

Yes, it looks like. Processing time is 2h, temperature in range of
60-64 degC, agitation using medium-size aquarium water pump - I think it's
enough for 5l test container. Maybe I should redesign the container's
inlet and outlet (both in the same lid - two plastic pipes of different
length).


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Re: [Biofuel] soap or mono- and diglycerides

2006-09-10 Thread Rafal Szczesniak
On Sat, Sep 09, 2006 at 05:05:59PM -0700, Ken Provost wrote:
 
 On Sep 9, 2006, at 4:31 PM, Rafal Szczesniak wrote:
 
 
  I'm talking about the result I get from the washing test. I know the
  soap formation is only possible in presence of water dissolving
  the lye. That's probably why aggresive mixing in the test
  could produce the soap in my case.
 
 
 Except by the time you're washing, the NaOH will be so dilute it
 shouldn't produce any additional soap. I think all your glycerides
 and all your soap will be present already -- if you want to know
 the relative proportions, an FFA assay or gas chromatogram
 are possible ways.

One of the reasons I raised this question is that I'd like to know for
sure, after my product fails the wash test, whether I should increase
the amount of lye or decrease it.


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[Biofuel] soap or mono- and diglicerides

2006-09-09 Thread Rafal Szczesniak
Hi all,

Could you tell me how can I tell the difference between emulsion
caused by unfinished process (glicerides left in the product) and
caused by soap formation (too much lye) ?

I have a feeling I misinterpret the result I get from the wash
test...


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Re: [Biofuel] soap or mono- and diglycerides

2006-09-09 Thread Rafal Szczesniak
On Sat, Sep 09, 2006 at 02:18:17PM -0700, Ken Provost wrote:
 
 On Sep 9, 2006, at 11:12 AM, Rafal Szczesniak wrote:
 
  Hi all,
 
  Could you tell me how can I tell the difference between emulsion
  caused by unfinished process (glycerides left in the product) and
  caused by soap formation (too much lye) ?
 
 
 I suppose you could use gentle acidification followed by assaying
 the resulting FFA (soap will produce FFA, mono- and diglycerides
 won't). Sounds complicated. In general, soap formation is a result
 of too much water in the reaction, not too much lye. The concentra-
 tions of NaOH you're working with (even when somewhat excess-
 ive) are not high enough to saponify the oil itself -- in the absence
 of water, only the FFA originally present will form soap.

Yes, I know that. I'm talking about the result I get from the washing
test. I know the soap formation is only possible in presence of water
dissolving the lye. That's probably why aggresive mixing in the test
could produce the soap in my case. I'm trying to find out whether
emulsion I get comes from soap or unfinshed reaction. The product seems
to have pH  7 (tested with the litmus paper).


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[Biofuel] titrating a virgin oil (cont.)

2006-09-03 Thread Rafal Szczesniak
Hi all,

For those who are interested.

Just to let you know - I did another test with lye amount
increased by the titration result, but it failed - emulsion
(a bit less, but still).

There're two possible reasons for that. One is that I had
an accidental spill of methoxide when adding it to the oil
Not much, but who knows what's enough...
Another is that I should probably try to titrate with more
intensive colour of phenolophtalein solution to say that's
it.

I'm going to do one more try with more lye.


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Re: [Biofuel] tirating a virgin oil

2006-08-21 Thread Rafal Szczesniak
On Mon, Aug 21, 2006 at 10:08:58AM -0400, Thomas Kelly wrote:
 Rafal,
  1 - 2L test batches w. virgin oil . Good
 
  99% pure KOH V. Good
  (If you are concerned about the purity and have
   NaOH of known purity you can test the KOH)

I know that. However, KOH that I've bought doesn't look perfectly fresh
ie. it is not completely translucent, as my NaOH was a couple of months
ago. Now, I have both of them slightly calcinated which shows up as a trace
of dust (really, just a little bit) on the bottom of a bottle I use to mix
the methoxide solution.

  Temp and agitation also sound good.
 
  If there is water in the methanol you will make more soap (emulsion) 
 and there will be less methanol --- incomplete reaction (emulsion).

No, the methanol is also very pure - the same supplier. I started with pure
and a bit expensive chemicals, to gain more experience and avoid troubles
that might be caused by urity.

   As I understand it, you have done test batches w virgin oil and 
 have gotten unsatisfactory results    emulsions upon washing. You are 
 concerned about incomplete reactions.

That's right.

 Question #1: Are you careful to exclude the glycerine byproduct from the 
 wash?

Last time I settled the mixture of ester and glycerine byproduct for 24
hours and got nice separation. I carefully removed glycerine from the
bottom (similar construction to the test processor on JtF pages) _and_
I settled the ester with just a bit of byproduct on the bottom (difficult
to remove completely) for the next 12 hours. Then I syphoned off a 200 ml
sample for test using elastic pipe, from the middle of the container. Nice,
clean and pale yellow product. My only concern is that it's not transparent,
but rather cloudy - likely due to incomplete reaction.

 Question #2: The oil titrated at  0.925 ml of .99KOH.. This is significant.
 Have you run a batch with an additional .9 - 1.0 g KOH/L you got from 
 titration?

Not yet - that's why I'm asking for your opinion. After the mails I've
received I'm going to try it. I tried it once, with NaOH, but I didn't add
such a small amount (divided by 1.4), but rather 20% more. I was afraid of
the lye calcination, so I tried to add more, according to what I read. That
was probably too much - no luck and washing problems.

 3.5g 100%NaOH/L of oil = 4.9 g 100%KOH/L of oil

Of course, I realise that.

 Add 0.9 - 1.0 g of the KOH (from titration) you would be using 5.8 - 5.9 g 
 of KOH/L of oil.
 
 This additional .9 -1.0 g represents an increase of  18 - 20% over the 
 amount used for virgin oil w/o FFAs. When you consider that your KOH may be 
 less than 99% pure,
 the amount needed would be even higher. This could very well be the cause of 
 the incomplete reaction.
 
 Treat the virgin oil as if it was WVO. Include your titration results in 
 the amount of KOH to be added and run a batch exactly as you have before. 
 Let us know how it worked out and we'll proceed from there.

Surely I will.

 Of course you could go out and buy some high quality veg oil that 
 titrates zero, but then we would not get the answer to the puzzle.

Exactly. Besides, led by curiousity, I tried to titrate a better oil I had.
It was also pure rapeseed oil, just the quality was better. Titration result
was .750ml or so. I wonder, what would be the result when a really fine
quality oil was tested (sunflower perhaps)...


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Re: [Biofuel] tirating a virgin oil

2006-08-21 Thread Rafal Szczesniak
On Mon, Aug 21, 2006 at 09:57:30AM +0200, Tonom?r Andr?s wrote:
 Hi Rafal,
 
 If it is virgin oil from the supermarket, you should not worry about water.

Yes, that's exactly what it is. Cheap brand made for a supermarket by
a known oil producer (n-th pressing of residues after they make their own
good oil, probably...).

 I had the same problem in my early batches, and I think it is the lye.
 do some additional test batches with more and more lye.
 This eay you have an idea and a feel for the process.

ok, I will. According to titration results.

 What you should look for is a perfect wash test.
 Increase the lye in the batch until you can shake the hell out of it in the
 wash test and still get perfect separation within minutes.
 
 This is what I would be doing.

Thanks for your suggestion.


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[Biofuel] tirating a virgin oil

2006-08-20 Thread Rafal Szczesniak
Hi,

Recently I've came through problems with testing a cheap virgin oil
in my test processor which every time ended up with incomplete reactions
(emulsion problems). I did make the process longer (2 hours) and at
higher temperature (60-63 degC) - still nothing, though by product
separation is very nice.

Today, I tried to titrate the oil and - to my surprise - it took 0.925ml
of KOH solution. This was my first experience with titration, so I can
also tell that the phenolophtalein solution turned pale (but noticable)
magenta for about 15 secs (as described at JtF) after 0.925ml. After
adding 1.05ml the colour got more intensive for longer time.

My main question is - is it normal in case of cheap oils ?
I suppose they contain (as other oils) some amount of FFAs, but so much ?

Additional matter is whether I got titration right. I mean, interpreting
the colours.

I'm running out of ideas what could be wrong in the process, so any
help is appreciated.


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Re: [Biofuel] tirating a virgin oil

2006-08-20 Thread Rafal Szczesniak
On Sun, Aug 20, 2006 at 06:29:51PM -0400, Thomas Kelly wrote:
 Rafal,
  I assume you are doing 1L test batches? Correct me if I'm wrong.

Yes. Actually these are 1 or 2l test batches. For agitation I use a small
water pump originally designed for larger aquaria and also recently used
in water cooling systems for PCs. Manufacturer says it's capacity is 700
liters per hour. Even considering higher viscosity of oil it should be
enough for 5l testing container. Do you think it is ? I can provide some
pictures if it helps (I've done a bit of documentation).

  Do you know the purity of the KOH you are using?

Yes, it's 99% pure from chemical supplier, though I've noticed it's
a little bit calcinated (some flakes are too white, in my opinion).
I have also tried NaOH (same purity) before with the same result.

  I have heard of virgin oil containing some FFA. I have no experience 
 with such oil.

It's probably normal, as it sounds impossible to make fresh oil with
absolutely no FFAs. The question is - what amount is 'normal' and what
is definately not ?


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Re: [Biofuel] safe temperature

2006-08-02 Thread Rafal Szczesniak
On Wed, Aug 02, 2006 at 01:17:02PM +0900, Keith Addison wrote:
 Hi Rafal
 
 What is max temperature you would consider safe for the process ?
 
 I know methanol boils at 64.7 degC, but it starts evaporating before
 reaching this point. Does that mean the temperature higher than
 55 degC kept for, say half a minute, causes that a big part of methanol
 goes away ?
 
 Goes where? If it's a closed processor (as it should be) the methanol 
 vapours won't go very far, most or all of it will condense on the 
 underside of the lid and drop back in again.

Well, I've seen some traces of condensation on the walls (it's a test
reactor), but it didn't seem to drop back.

 Have a look at what it says about it here:
 The 'Deepthort 100B' Batch Reactor
 http://journeytoforever.org/biodiesel_processor8.html

Thanks, Keith. I've missed this description, though I've read nearly
everything at JtF at least a couple of times.

I think I'm going to try out adding methoxide in 2-3 phases. I have
a feeling that in the end - the hardest part - there's not enough exess
methanol. Last time I was careful about the temperature, about measuring
the lye and methanol, but still the process doesn't reach completion.
Biodiesel phase isn't clear (though the colour is quite right) nor does
it separate quickly in the wash test. There's still something wrong... 


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[Biofuel] safe temperature

2006-08-01 Thread Rafal Szczesniak
What is max temperature you would consider safe for the process ?

I know methanol boils at 64.7 degC, but it starts evaporating before
reaching this point. Does that mean the temperature higher than
55 degC kept for, say half a minute, causes that a big part of methanol
goes away ?


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[Biofuel] lye-contaminated batch

2006-07-25 Thread Rafal Szczesniak
Hi all,

I have a small batch that appars to contain too much lye as
wash test shows quite a bit of soap under murky biodiesel
(which after all doesn't wash and remain a chicken soup).
Is there a good way to reprocess it ? I know I can process
unfinished batch (too little lye) as it still contains mono-
and diglicerides to be reacted.

Theoretically, I could just add low concentrated methoxide
or downright pure methanol, reprocess it once again, and lye
still present in the batch should take part of a catalyst.

Am I correct ?


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[Biofuel] degradation of methoxide solution in time

2006-07-16 Thread Rafal Szczesniak
Hi,

Is it possible for methoxide solution to degrade ? I've had
400ml of it in 5l container waiting in a cool and dark place
(basement) for a couple of months. It seemed to have a bit
of some sediment on the bottom, but recently when I tried
to use it, I could clearly see it was quite a bit of white
dust (a bit like a light sand). Also, the solution wasn't
absolutely clear and translucent, and it lost about 50ml in
volume. I thought the container was really hermetic...

The solution I'm talking about took 400ml of methanol and 7g
of NaOH.


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Re: [Biofuel] degradation of methoxide solution in time

2006-07-16 Thread Rafal Szczesniak
On Sun, Jul 16, 2006 at 08:43:29AM -0500, bob allen wrote:
 the methoxide is reacting with CO2 in the the 4.6 L of air in container, 
 making sodium bicarbonate 
 and or sodium carbonate.

That's what I thought. Although my original idea was that lye itself
could have reacted with CO2 from air making it less pure NaOH. When
dissolving in methanol, NaOH gets into the solution and residue is
Na2CO3. The only question is whether or not, sodium bicarbonate
affects the biodiesel reaction ?


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Re: [Biofuel] A new website

2005-10-29 Thread Rafal Szczesniak

On Wed, Oct 26, 2005 at 06:37:47PM -0700, Jeromie Reeves wrote:
 snip
 
 Indeed. You can already switch to safer and open replacements of web browser
 and mail reader as well as office suite (especially with just-released
 OpenOffice 2.0). Isn't it great ? There's a choice finally for average
 user.
 
 This choice exists on Windows to.

That's exactly what I meant :) You can either use Windows or FreeBSD,
or something else and still benefit from the same software. 

 The core windows OS can be very stable 
 (just needs configured correctly, not hard
 just takes more then a average Joe). I personally use OO 2.0, Firefox, 
 and Thunderbird (as does my wife) over IE
 except in those very rare cases where a site is IE only. Avast is hands 
 down the best Windows based AV there is and
 it is free (for home use) too.
 
 No need to. Just wait for unix desktop environments to become mature
 enough to be widely usable.
   
 
 Define mature enough?

It can be said it's mature when you have consistent desktop environment
that handles all subsystems for various components of operating system
and hardware running it. So far each desktop (mainly KDE and Gnome)
differ too much in basic areas to write a single piece of code that
fits in both of them. Also, they have different approach to hardware
interaction (scanners poorly supported, for instance), and they're
way too slow on older boxes (not all machines are modern Intel P4).

 I think its more the add on software that needs to 
 mature more then the OS and GUI environment.

Agreed. 

 One of the issues I find with OSS is there are to many options.

Yes, it's great advance and obstacle at once.

 Since 
 there is not this one app for all monolithic force in
 OSS, how do you get people to try something new, even if it would work 
 very well for them? The Linux Live CD's
 help alot.


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Re: [Biofuel] A new website

2005-10-29 Thread Rafal Szczesniak

On Thu, Oct 27, 2005 at 04:42:43PM +1000, Doug Foskey wrote:
 Rafal,
  congratulations on being part of the Samba team!

Thank you very much :)

 I am constantly amazed how 
 many Biodiesel list members are involved with Open Source software.

I think it is mostly because biodiesel homebrewing and open source have
(among many others) one thing in common - it attracts people with wide
horizons, curious of something new and interesting.

  A comment to others on Linux: there is now a move by the major Linux 
 developers to standardise the way that Linux is seen by programs, so the old 
 issues of differing packages for different flavours of Linux will then be a 
 thing of the past. The common Linux desktop is ever closer.

Yes, many initiatives has been founded in the last 1-2 years focused
on forging standards and base recommendations.


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Re: [Biofuel] A new website

2005-10-27 Thread Rafal Szczesniak

On Wed, Oct 26, 2005 at 03:08:26PM -0600, Zeke Yewdall wrote:
 Unfortunately, there are too many specialized engineering software
 packages that I use every day that can only operate under windows
 (often they are even picky about the version of windows) for me to
 consider Linux.

Yes, I'm in fortunate position of being a programmer and network
engineer. As for now it is a great environment for people of this
profession. I must agree though, engineers using CAD software (of various
fields) still have a hard time when trying to switch to free unix-like
systems. It just needs a bit more time, like many new things.

 If it was just web browsing, spreadsheets, word
 processing, and the like, I'd get rid of windows in a heartbeat.  I've
 already dumped IE and outlook.

Indeed. You can already switch to safer and open replacements of web browser
and mail reader as well as office suite (especially with just-released
OpenOffice 2.0). Isn't it great ? There's a choice finally for average
user.

 I want Google or Mozilla to come out with an operating system.

No need to. Just wait for unix desktop environments to become mature
enough to be widely usable.


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Re: [Biofuel] A new website

2005-10-26 Thread Rafal Szczesniak

On Mon, Oct 24, 2005 at 08:49:14AM -0600, Zeke Yewdall wrote:
 Huh?
 
 On 10/23/05, midori [EMAIL PROTECTED] wrote:
  Content-Type: application/octet-stream;
  name=post[1].htm
  Content-Transfer-Encoding: base64
  Content-ID: L87Md53d
 

Looks like Midori's address has been forged over the net and used to
send out some virus/bug/spyware/whatever. It happens all the time
all over the network. Oh, those spammers... :(


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Re: [Biofuel] A new website

2005-10-26 Thread Rafal Szczesniak

On Wed, Oct 26, 2005 at 04:54:01PM +1000, Doug Foskey wrote:
 Good reason to go Linux.

It doesn't really matter. If one of your addresses is publicly available
(either on a website or mailing list archives) it will be abused this
way sooner or later. I use Linux and FreeBSD all the time and it
happened to me too (several times). Naturally, using Windows mail
readers exposes you more due to impact the mail worms and viruses have
on internet these days, but just using Linux is not an ultimate solution.


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Re: [Biofuel] methoxide solution

2005-10-15 Thread Rafal Szczesniak
On Sat, Oct 15, 2005 at 07:00:21AM -0600, Brian Rodgers wrote:

Brian,

 I will Google Magnetic mixer but an explanation from you would be
 great too. What is? Where to find? Standard lab equipment? Etc. It
 sounds pretty damn cool.

It sounds like a great new toy, but believe me - you don't really need
magnetic mixer to prepare methoxide solution :) If you want to play
with it, that's a different matter, but it's quite enough to use
ordinary thick plastic HDPE bottle carefully swirling it. It takes
a bit of time, but hydroxide must be completely dissolved.


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Re: [Biofuel] methoxide solution

2005-10-13 Thread Rafal Szczesniak
On Wed, Oct 12, 2005 at 03:57:15PM -0500, Juan B wrote:
 Hello, It happen to me too,
 
 I was wonderigh whether that was ok or not ?
 any tips !!

I suspect the amount of methanol was the reason. I wanted to try out
a newly purchased and so I took just 200ml with 3.5g of natrium
hydroxide. As much as is needed to do the test on 1 litre of virgin oil.


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[Biofuel] methoxide solution

2005-10-12 Thread Rafal Szczesniak
Hi,

I've recently bought new fresh methyl alcohol and lye. I have measured
out exact amounts, mixed lye with methanol and - a bit of a surprise,
the solution haven't actually got warm. No temperature, fumes,
whatsoever. Is this normal, or could I have done something wrong ?

The chemicals are most probably pure and good quality. Also, lye has
been completely dissolved.


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Re: [Biofuel] Warning to List Members

2005-09-02 Thread Rafal Szczesniak
On Sun, Aug 28, 2005 at 11:15:44AM -0700, Rumen Slavov wrote:
  Hi, Friends,
   It seems to me all of you are intelligent persons,
 so I wonder why you are using Microsoft bullsh...?

One has really nothing to the other. At the moment, MS software
is just easier to use on desktop PCs. It's going to change fairly
soon (within next few years, likely), but not yet.

 As far as it is well known, there is not such animal -
 virus or worm or Trojan - for Linux! For some time now
 there are several distribution of Live CD`s, which
 work even in an empty hard like Knoppix and many
 others! My OS is Slackware Linux 10.1 and I never had
 any problems in the net. And it is free of charge.

It's Free Software - you can do whatever you want with it.
It doesn't mean it has to be free of charge. Just to be 
clear with exact meaning of term Free Software...

 The OppenOffice 1.1.4 office is well ahead of MS office -

That's absolutely too optimistic statement. I also use Linux and BSD
system, as I'm a software developer, but I wouldn't dare to claim that
current OpenOffice is better than MS Office. True - it can open .doc
files not matter what version of MS Word created them, yet still when
it comes to _details_ ie. to read and render file _exactly_ how it
was saved, OpenOffice reveals its lacks. Version 2 of this office suite
brings significant progress, but it's still unstable.
I use OpenOffice to read various MS Office files that come via email,
but I prefer to work on native OpenOffice file formats instead of using
it as a free replacement for MS Office. It just doesn't work well this
way.

 it opens files no matter which application is involved
 in the creation ( for example MS office XP can not
 open document written with MS office 97). Everything
 can be downloaded free from the net and the
 distributions are equipped with more than 2000
 applications!

... which are often difficult to setup and/or use. Remember, not every
user really feels like to explore what to do, to make it actually work
like I want it to. It's educative and very interesting - just like
biofuel brewing :) - but sometimes people just want to use it... nothing
more.

 All you need is to compile idconfig (the
 network connection) and you are free of problems. Me,
 personally, I do not have antivirus - I don`t need it.

So do I. But I'm more careful when advocating such a system :-)


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Re: [Biofuel] methanol and airmodel engine fuel

2005-07-22 Thread Rafal Szczesniak
On Thu, Jul 21, 2005 at 05:23:11PM -0500, James G. Branaum wrote:
 I buy my methanol in bulk at the local representative of the refinery.  I
 strongly suspect is probably not available in your area.  I also don't think
 you want to use it unless you make it yourself.

What do you mean by making it myself ? Making what ? Sorry, I'm not sure
I understood clearly.


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[Biofuel] methanol and airmodel engine fuel

2005-07-21 Thread Rafal Szczesniak
Hi,

As I've found it nearly impossible buy small (1-2 litres) amounts of
pure methanol here, in Poland, I've taken closer look at model fuels.
They mostly contain methanol (40-85%), castor oil, EDL synthetic oil
and additions.
Now, castor oil might be even good. EDL definately not - luckily not
all fuels do have it. Does anyone know what's in those additions ?
I'm not talking about nitromethan here - that one I know about.

This leads to a more specific question - how those fuels (after a bit
of processing, naturally) can be useful as a source of methanol ?


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Re: [Biofuel] methanol and airmodel engine fuel

2005-07-21 Thread Rafal Szczesniak
On Thu, Jul 21, 2005 at 11:39:30AM -0500, James G. Branaum wrote:
 I have been mixing my own model airplane engine fuel for the last 12 years
 or so.  I normally use 70% methanol, 10% nitro methane (as an igniter) and
 20% oil of various make ups.  I eschew castor because it gums things up
 unless it is hot and can render an expensive 4-stroke engine useless due to
 sticky carbon build up.

Where do you dig up your methanol from ? :)
I don't have such an experience with model engines but I know that
mixture of 80% methanol and 20% castor (no nitromethane) is still the
official FAI fuel for contests.

 Typically the additions to the synthetic oils are things to retard corrosion
 and improve the burn of the oil itself during combustion as in model engines
 it is the source of lubrication and adds nothing to the energy developed.
 Most of the makers of that specific product protect their intellectual
 property rights viciously as there are different compounds that have
 different properties under different conditions.

That's probably why you can't really find any information about kind of
additions at least (not proportions which are significant).


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Re: [Biofuel] methanol and airmodel engine fuel

2005-07-21 Thread Rafal Szczesniak
On Thu, Jul 21, 2005 at 06:30:57PM +0200, Bruno M. wrote:
 Hi  Rafal,
 
 Maybe this model-fuel is meant for 2takt engines,
 and thats whats the mixed-in oil is for?

Yes, it is typical 2-stroke engine fuel.

 If it's only oil, you mite be able ( if you've got equipment)
 to distill the methanol out of it;

That's what I also thought, but it would probably require double
distillation to obtain methanol of enough purity.

 but is this stuff water free?

as far as I know, it is

 And I'm afraid that modelairplain-fuel is way to expensive
 compared to technical  water-free methanol. No?

Surprise. Seems like technical methanol is triple as much as the fuel.

 Maybe search a little further for a supplier of chemicals?

I have. _Only_ one found supplies a non-company with chemicals (methanol
among other stuff). It is however rather an expensive source, though I
was happy to find tonight at all. Others say they don't sell methanol in
small amounts to a private person due to its poisonness (apparently it's
been forbidden to sell it like this... hard to believe).

 Or ask a producer of automotive fluids ( oils and carwindow antifreez / 
 cleaner )
 those winshield antifreez and cleaners (still) contains mostly methanol.
[...]
 [  in most countries of the EU this must now be IPA or Ethanol instead of 
 Methanol,

That's the problem. I haven't seen any of those specifics based on
methanol.


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[Biofuel] adding carbon vs. carbon dioxide to the atmosphere

2005-07-15 Thread Rafal Szczesniak
Hi all,

One thing that's not entirely clear to me is argument of biofuel not
increasing amount of carbon in environment whereas fossil fuels do so.
So far I thought the whole problem of global warming was mostly due to
rasing amount of carbon dioxide and substances of similar properties,
not the carbon itself.

Combustion of biofuel certainly leaves amount of circulating carbon at
constant level. Doing same with fossil fuel like oil derivatives does
not, but (theoretically) in the same time we have to assume that carbon
fuel deposits do not take share in carbon in the environment. That's
likely to be a common assumption and fairly sensible.

The question remains whether preventing the warming is more about
limiting amount of carbon introduced from under the ground (which in
turn often ends up as carbon dioxide) or rather limiting emission of
carbon dioxide itself ? The former is more general approach, and the
latter is more concentrating at one problem at a time.

It's a bit tricky issue, but it's interesting for clarity in this
matter.


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Re: [Biofuel] adding carbon vs. carbon dioxide to the atmosphere

2005-07-15 Thread Rafal Szczesniak
On Fri, Jul 15, 2005 at 10:06:05AM -0400, Appal Energy wrote:
 One thing that's not entirely clear to me is
 argument of biofuel not increasing amount of
 carbon in environment whereas fossil fuels do so.
 
 Nothing tricky about the issue at all Rafal.
 
 Carbon dioxide of plant origin returns to the plants with each growing 
 cycle. This is called carbon neutral.
 
 Carbon dioxide of fossil fuel origin is not recycled annually, as it 
 takes millions of years for coal, natural gas and petroleum to 
 regenerate. Therefore it's considered to be carbon  positive .

That's why I mentioned about assumption of fossil carbon included or not
in circulating carbon share.

 There are arguments that plant-based fuels aren't entirely carbon 
 neutral due to the fossil fuels that go into their production at 
 different steps in the process. However, they remain considerably more 
 carbon negative than fossil fuels.

True, agreed.

 Your trickiness as you call it is really more of a blind rather than 
 anything perplexing, revolving around gross carbon dioxide outputs. Yes, 
 essentially the same amount of carbon dioxide is produced annually, no 
 matter if the sources are plant-based or of fossil origin. However, 
 global CO2 levels essentially plateau after one year's use of 
 plant-based fuels, while they continue to rise under a regimen of fossil 
 fuel use.

I meant trickiness rather as the kind of question raised in some
talks and debates I've heard. It was the argument as to why plant-based
fuels are not so good for warming environment because of emission they
introduce anyway. It was a bit like playing with facts to avoid those
less comfortable for the speaker.

Thank you!


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