See below

Thomas Kelly wrote:

Joe,
You wrote: "Have you ever tried dosing the batch again with a little methoxide? After you remove the glycerin it doesn't take much to get the last bit of the reaction to go and settle out the remaining glycerin." I've been concerned about the excess methanol and the catalytic caustic that will leave with the glycerin I remove.

It is in the glycerin anyways, but the glycerin is stopping the reaction so removing it shifts the equilibrium point in favour of completion.

You seem to be suggesting re-processing the BD using info from the QT.

Yep. There will be 1-2% v/v methanol in the esters anyways and the remaining excess is disolved in the glycerin.

Instead of adding 10% (vol/vol) methanol, use an amount that correlates to the volume of unreacted oil (from QT). Ex QT suggests 8% unreacted oil in a 100L batch = 8 L of unreacted oil in the batch. Add 1.6L of methanol (20% vol/vol of the unreacted oil) and re-process. (Much better than the 10L normally required for re-processing).
     Have I got it right?

Yes

Do you still have to add 3.5g of lye (or KOH equivalent)/L ? If so, is it 3.5g lye per liter of unreacted oil (calculated from QT) or per L of batch?

Yes 28 g or 40 etc.

Don't you have to heat up the whole batch again? (Time and energy)

This is all done right after draining the glycerin. I leave the heater on during this period. Do the rough QT right away before wash test.
BTW I still do the 'real' QT after all washing and drying are done.

If so, I suggest my way. Towards the end of the reaction, interrupt the process and test the BD*. If it fails the QT add more methanol** and let the reaction continue for a while.

Well basically yes that's what I'm doing but have drained the glycerin and doing the test with methanol shows you exactly what percentage unreacted stuff you've got so add methanol and 'X'OH for that amount of oil. You can add the remains to the reaction or next batch of course.

* When I drain the sample to be tested, I allow some to flow before taking the sample. In case there was oil in my drain plug I won't get a false negative on the QT. ** I have simply added a liter or two based loosely on the QT. I will now quantify based on the QT and be more accurate (Thanks). >Kenji and many others do straight base catalysis as a two stage deal. Two Stage Base/Base Method?
I know of someone who uses it; no titration  ---> consistently good BD.

I wouldn't skip the titration but rather do the base step in two stages and remove glycerin in between.

It seems to be a bit more time-consuming and uses more energy and caustic than my simple (some would say "primitive") single stage base method.

Yes a little more time since two settling periods but it's hard to get it just perfect with one stage anyways so then some repro is called for and....time.

Big Lunch,
      Tom


LOL U funny!
Cheers
Joe

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