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Distilled Spirits Council Urges Ban of Alcohol Vapor Devices ("alcohol without liquid" - AWOL)
Yahoo News ^ | 3/21/05

Posted on 03/22/2005 6:02:10 PM PST by Libloather

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To: redgolum
A molecular sieve is what most places use now. Cyclohexane is to nasty to use. Very flammable. I used to work at a plant that made ethanol, and we had a few contractors that would sneak the stuff straight out of the sieves. Gave them one heck of a hangover.

My lab skills are a bit dated. A molecular sieve wasn't common in labs in the mid-70's. The closest approximation was Sephadex gels used to separate salt solutions from larger proteins. The Sephadex gels cause a larger included volume to be experienced by smaller salt particles. Proteins zip on past the outside of the gels due to larger physical size. I usually finished the desalting process with reverse osmosis via semi-permeable membranes.

81 posted on 03/23/2005 9:00:08 AM PST by Myrddin
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To: Myrddin
This is on a large scale with zeolyte (sp?) beads with porous structures. Superheated vapor is passed through the bed of beads, and the water gets "stuck" in the pores. The water is then forced out by recircing some of the finished product back through the beds. It works ok, but makes for a control headache.
82 posted on 03/23/2005 9:05:31 AM PST by redgolum ("God is dead" -- Nietzsche. "Nietzsche is dead" -- God.)
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To: redgolum
Sounds like a similar process to the average water softener albeit at higher temps. Thanks for the description.
83 posted on 03/23/2005 9:07:29 AM PST by Myrddin
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To: Myrddin

LOL! Actually that is a pretty good way to think of it. Only in a water softener, it is done by ion exchange and a mole sieve by size.


84 posted on 03/23/2005 9:22:28 AM PST by redgolum ("God is dead" -- Nietzsche. "Nietzsche is dead" -- God.)
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To: Libloather

What is their beef? That they won't sell as much alcohol? Pathetic.


85 posted on 03/23/2005 10:51:48 AM PST by ClintonBeGone (In politics, sometimes it's OK for even a Wolverine to root for a Buckeye win.)
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To: Myrddin
"Methyl sulphate would be the expected product in this instance."
And where will you get the methyls? You must mean monoethylsulfate, and at higher temperatures ether and ethylene. Diethylsulfate is slightly more difficult to make.
86 posted on 03/23/2005 11:43:23 AM PST by GSlob
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To: GSlob
I did correct my "oops" a couple posts after the "methyl" gaffe.
87 posted on 03/23/2005 1:14:44 PM PST by Myrddin
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