That's just it. The concentration isn't marked on the container.All 
it says is "technical" which is about as helpful as "guess" to me. 
Sooo, I have re-done the thing using NaOH and will shall see what is 
what soon.
The process is I warm up the oil in a sauce pan with a thermometer 
in it until it reaches 130F or so and then add it to the blender and 
slowly add the methoxide (prepared in my Grolsch bottle- methoxide 
the easy way) :) Blend the lot for 15-18 minutes, pout into a Masson 
jar and let it settle.
I get clear seperation of darker glycerine on the bottom, the 
lighter (but still dark) on top. I take a sample of this top layer 
and add water and shake and I get MAYO freekin' NAISE ! about 1/3 of 
it.My tests are done using 500ml instead of full liters and I just 
divide everything by 2.
I am in the process of revamping my method, going to try some of 
that nice 1% phenolphthalein solution stuff instead of the PH meter 
and see if I get a discrepancy. I now have laboratory grade 
cylendars graded to acuracy for small alcohol stuff (100ml) and a 
larger one (1 liter/1,000ml) for the other stuff, like WVO. A least 
I know the volumes are OK :) My scale is OHAUS electronic 0.1gr-
400gr in 0.1 increments so it's not the scale either. Eliminating 
the variables is important for me 'cause I am not the sharpest tool 
in the shed :)
So, I should be undergoing some adjustments very soon, and hopefully 
will get the testing stuff down before it's time to start loading 
the "real" product into the processor.
I am getting some valuable help though and that is very much 
appreciated.

Luc

--- In biofuel@yahoogroups.com, Keith Addison <[EMAIL PROTECTED]> wrote:
> Hi Luc
> 
> What is the concentration of your potassium hydroxide? I think 
from 
> your figures below that you're presuming 100% concentration, same 
as 
> NaOH (or nearly), but KOH is less concentrated and you have to 
allow 
> for that. I don't have much faith in your figure of "basic 4.9 
> potasium", it should be more, according to the concentration.
> 
> Are you titrating with a KOH solution or a NaOH solution and then 
> converting the results to KOH?
> 
> >More about lye
> >http://journeytoforever.org/biodiesel_make2.html#lye
> >
> >KOH is not as strong as NaOH -- use 1.4 times as much KOH 
(actually
> >1.4025 times). Titration is the same, just use a 0.1% KOH solution
> >instead of NaOH solution, and use 1 gm of KOH for every 
milliliter of
> >0.1% solution used in the titration. But instead of the basic 3.5
> >grams of NaOH lye per liter of oil, use 3.5 x 1.4 = 4.9 grams of 
KOH.
> >So, if your titration was 5 ml, use 5 + 4.9 = 9.9 gm KOH per 
liter of
> >oil.
> >
> >One more complication -- check the purity of your KOH, it's 
generally
> >not as pure as NaOH. Anhydrous grade KOH flake is usually about 
92%,
> >sometimes less -- check the label. We use half-pearls assayed at 
85%.
> >Adjust the basic quantity accordingly: the basic 4.9 grams would 
be
> >5.8 (5.775) grams for 85% KOH, or 5.3 (5.33) grams for 92% KOH.
> >
> >KOH dissolves in methanol much more easily than NaOH does, and
> >doesn't "clump" together as NaOH can do.
> 
> Do a comparison with sodium, and I'd also suggest the "poor man's 
> titration" that Todd outlined for Pierre a few weeks ago.
> http://infoarchive.net/sgroup/BIOFUEL/33676/
> 
> Instead of using jars, do a blender batch for each sample, same as 
> you're doing now. That will mean agitation, temperature etc are 
just 
> the same, with the KOH amount the only variable. You're more 
> interested in tests using more KOH than less.
> 
> Best
> 
> Keith
> 
> 
> >I successfully made one batch using WVO but that required a double
> >processing and came away matching all the numbers I have read 
about,
> >BUT twice now I have doen the folowing and with nearly the same
> >results. Could someone please point out the flaw ?
> >WVO = 500ml heated to 130F.
> >Using the "Better Titration method I titrate it using a PH meter 
to
> >be 1gr extra (4ml%4=1). then I add that to the basic 4.9 potasium
> >Hydroxide for 5.9gr and then divide by two (for the 500ml batch)
> >The methoxide is very well mixed and I add it to the blender oil
> >(still at 130F) slowly and let it blend for 15-18 minutes.
> >After settling I get a distinct seperation of very dark, almost
> >black on the bottom and a redish dark top layer (the BD) but as 
soon
> >as I put it to the shake test (150ml unwashed BD to 150ml water at
> >room temp) I get mayonaise that won't completely break even after
> >two days.
> >I got to be doing something wrong here. I am going to try one more
> >time using sodiuk instead of potassium and see if I get the same
> >results and then I will have to start questioning the PH meter and
> >the source of WVO, not to mention my ability to understand a laid
> >out process.
> >Should I dump the PH meter and go with strips ? Maybe use the 
other
> >liquid penolphalene (or something like that) that makes it go
> >magenta for 10 seconds when it reaches 8.5 PH?
> >My scale is top shelf electronic. The chems are fresh from the 
chem
> >supply house, the oil was still warm when I sampled it :) I am 
using
> >100% isopropyl (I now have LOTS of it,4.5lt)I mix in the oil while
> >the jar is sitting in warm water and it never really does get 100%
> >clear but I keep on stirring it throughout the titration process 
aas
> >I add the .01% lye solution (made according to the Better 
Titration
> >specs)
> >I am now thoughroughly stumped as to what I did wrong.
> >
> >Luc




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