>I just had this conversation with Girl Mark yesterday at her excellent
>class.
>
>She had some 90% (not 100%) KOH and gave a very general guideline that
>if it were 100%, we'd start with something like 4.9 to 6 g for our
>calculations, and then add whatever we'd calculated from our Titration
>process that we would need.  In our case, we had some good stuff, with
>a Titration of 2.  So, we might use 4.9+2=6.9, or maybe more if we
>took 4.9 as the 'low' figure and wanted a 'middle' figure we could use
>5.5+2=7.5
>
>But, since we had 90% and not 100% KOH, we weren't done calculating.
>After the class, I had to correct my calculation.  I make it to be
>that at 90% KOH, our base-range should be: 5.44 to 6.67 (where 90% of
>5.44 is 4.9 and 90% of 6.67 is 6).  So, if we used 5.44+2=7.44 for
>that 1 liter batch, that might be correct, or maybe a little more if
>we wanted to not use the 'low' figure.  Is this about right?  Hope so.
>
>MM

Hi MM

KOH is never 100%, highest seems to be 92%.

Your calculation is about right. As for "low" and "high" figures for 
the base amount, stick to the low figure (3.5 g NaOH = 4.9 g KOH) for 
low-titration oil like that. Low titration would be anything less 
than about 3 ml. See:

The basic lye quantity -- 3.5 grams?
http://journeytoforever.org/biodiesel_make2.html#lye3.5

Re KOH:

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.

-- From "More about lye"
http://journeytoforever.org/biodiesel_make2.html#lye

Best

Keith


>
>On Fri, 21 May 2004 20:31:33 +0900, you 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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