Re: Anhydrification of Xylene
- From: Grecko <grecko@xxxxxxx>
- Date: Wed, 11 Oct 2006 23:52:22 GMT
On Wed, 11 Oct 2006 17:31:01 GMT, <lucasea@xxxxxxxxxxxxx> wrote:
sieves, sieve
"mlundo" <mlundo@xxxxxxx> wrote in message
news:1160560677.104115.78520@xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx
Hallo everybody.
I have to remove water from about 1 liter of o-Xylenes. On the bottle
it's written that there is
0.04%w max of water , but perhaps water is more becouse product is old.
These are my questions:
can i use Na2SO4 or MgSO4 or CaCl2 for anhydrification?
Or is it better to make a distillation? Do Xylenes and water form
azeotropo?
The answer depends on how dry you need it, and thus on what you are going to
do with it. MgSO4 or CaCl2 will get it mostly dry. Better would be
activated 3A molecular seives, but watch out for seive dust. I have had
luck storing it over activated 3A molecular seives, then passing it throughsieves
activated alumina just prior to use, to get rid of residual water and thesieve
seive dust. However, if you need it dry enough to do electropositive
organometallic chemistry, the easiest is to distill it from molten sodium.
Don't bother with ketyl, the low polarity and high distillation temperature
just destroys it. You could also make a ketyl pot (you'll need a *lot* of
tetraglyme to make it purple), and do vacuum transfer instead of
distillation. Polish it up after this (to get rid of benzophenone that
sublimes) by passing it through activated alumina.
Yes, I believe xylenes form azeotropes with water.
Eric Lucas
.
- References:
- Anhydrification of Xylene
- From: mlundo
- Re: Anhydrification of Xylene
- From: lucasea
- Anhydrification of Xylene
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