Separating bromine from BCDMH has been claimed using metabisulfite which supposedly takes Br+ to Br2 and Cl+ to Cl-. len1 wrote a
book about it, and some trials are in this thread somewhere:
https://www.sciencemadness.org/whisper/viewthread.php?tid=69...
Kind of annoying, though, since often you just want HBr, which is much less of a handling issue than Br2. For this, the BCDMH separation by redox is a
lot of extra work!
US 4254092A suggests another method: https://patents.google.com/patent/US4254092A/en
NH4Cl decomposes at 337 C at one atmosphere while NH4Br is stable up to 450 C. So, by precipitating a mixture of ammonium chloride and bromide, it may
be possible to destroy all of the NH4Cl by heating to around 350 C and retain NH4Br.
The patent suggests using organic amines for this, with an eye to recovering everything, but we can afford to lose HCl (usually). Should be tried at
small scale first to determine if aerobic oxidation of bromide will be an issue. |