Hi Kirk

>H and Cl combine redily. Have water present and the HCl will go into the
>water. A catalyst on the H line can start the reaction.

What sort of catalyst?

>Don't let a lot of
>gas build up first as it is energetic. Even a bright light can initiate H
>and Cl combining.

Thanks!

Keith


>Kirk
>
>-----Original Message-----
>From: Keith Addison [mailto:[EMAIL PROTECTED]
>Sent: Saturday, November 02, 2002 10:56 PM
>To: biofuel@yahoogroups.com
>Subject: [biofuel] Salt and NaOH
>
>
>Dunno if you remember this, on making NaOH from table salt.
>http://cator.hsc.edu/~kmd/caveman/projects/chloralkali/slideshow/index.html
>
>You end up with hydrogen and chlorine, which I guess you could turn
>into hydrochloric acid, not sure quite how though (nor how to
>concentrate it after that). Anyone have any ideas on that?
>
>I was thinking you could use HCl instead of phosphoric to neutralize
>the glycerin layer, as here:
>http://journeytoforever.org/biodiesel_glycsep.html
>Separating glycerine/FFAs
>
>You'd end up with more table salt - sodium chloride instead of sodium
>phosphate - which you could turn into more NaOH. Does that make any
>sense? This might help close the loop, and phosphoric is expensive.
>Traditionally soapstock is acidulated with strong sulphuric acid, but
>since phosphoric works just as well HCl should be okay, though I'm
>not sure about safety considerations.
>
>I don't know if any of this works - this NaOH from salt would be wet,
>I don't know if drying it would leave you with a pure enough product
>(not carbonated?), but it's interesting.
>
>There's also this:
>
>"Thus an equimolar amount of calcium chloride may be directly added
>to the soapstock and prompt separation of the calcium soap by
>precipitation from a relatively pure saline (NaCl) solution will
>ensue. Calcium soaps are useful industrial ingredients, for instance
>as demoulding agents."
>
>More table salt. And Dubbin, quite nice. Seems to work equally well
>with the glyc layer, glycerine and all.
>
>Keith


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