biomechem
Unregistered
Posts: N/A
Registered: N/A
Member Is Offline
|
|
Modification of Castner–Kellner process - bromine
Is it possible, and relatively easy to obtain bromine in the following process.
In a vertical tube, on the bottom is mercury electrode, above it NaBr solution, and carbon electrode. The mixture is heated above 58.8 °C (boiling
point of bromine).
1. Will Br3- formation will be the same as in lower temperature or it will degradate to Br2 and Br-?
2. Does Br3- react (violently) with sodium amalgam?
3. Is it better to use saturated (or conc.) NaBr solutions, or diluted like 0.1M will be better?
[Edited on 13-1-2017 by biomechem]
|
|
Melgar
Anti-Spam Agent
Posts: 2004
Registered: 23-2-2010
Location: Connecticut
Member Is Offline
Mood: Estrified
|
|
Br3- would mostly stay away from the cathode, what with them both having like charges. The trouble happens when Br2 comes into play, and falls to the
bottom due to its density. Then you have mercury bromide in solution. Sure, most of it will be reduced again, but not all of it, and you can't
depend on the solution temperature to remove bromine immediately as it's formed. Maybe a divided cell with sodium carbonate on the mercury side, and
sodium bromide on the other side?
|
|
biomechem
Unregistered
Posts: N/A
Registered: N/A
Member Is Offline
|
|
Quote: Originally posted by Melgar | Br3- would mostly stay away from the cathode, what with them both having like charges. The trouble happens when Br2 comes into play, and falls to the
bottom due to its density. Then you have mercury bromide in solution. Sure, most of it will be reduced again, but not all of it, and you can't
depend on the solution temperature to remove bromine immediately as it's formed. Maybe a divided cell with sodium carbonate on the mercury side, and
sodium bromide on the other side? |
Your solution is definitely better and much more simple, thank you, and please forgive me this poor attempt to reinvent the wheel.
|
|