| Pages:
1
2 |
Dr.Bob
International Hazard
Posts: 2659
Registered: 26-1-2011
Location: USA - NC
Member Is Offline
Mood: No Mood
|
|
Not likely. People need to remember that mps are defined for PURE compounds, once a compound is mixed, the mp is depressed, often completely
eliminated. It is one thing to crystallize tBuOH from the liquid to purify it, but trying to freeze out one solvent from another only works in a few
cases, almost impossible in many cases. The more similar two solvents are, the harder it would be to freeze one out. Also, in general
crystallizations work best with nearly pure material to get it really pure, not so well with 50:50 mixtures.
If the NMP bp was much different than GBL's, so you might be able to distill away the GBL away from the NMP, then once the NMP is mostly pure, you
could try to vacuum distill it a second time to purify it. But they are much closer in bp than I would have guessed, only 4 degree F apart.
Distillations are affected by mixtures as well, but they work pretty well when the bps are more than 10-20 C apart. But with only 2 C between them,
they will be very hard to separate that way.
|
|
|
Metacelsus
International Hazard
Posts: 2531
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
If you don't have a good enough column, you might be able to selectively hydrolyze the GBL, distill off the NMP, and then do an esterification to
recover the lactone. However, this probably wouldn't be very economical.
(Of course, if you're just after the lactone hydrolysis product, then this method would be more attractive. But be careful to not do anything you'll
regret.)
|
|
|
| Pages:
1
2 |
|
![[*]](images/xpblue/default_icon.gif){kind=icon}
