Quote: Originally posted by Organikum  | Surprisingly plain ammonium nitrate will do the job.
As does ozone.
Electrolytic regeneration of the (II)acetate to the (III)acetate is possible but as so often with electrolytic methods so shitty as straightforward in
theory.
If one is able to tackle the real problem of those (III)acetate reactions, whats removing the product from the reaction continously or batchwise
without neutralsing the acetic acid or such but keeping it functional, in use or for further use, whats needed to make the whole thing volumetric less
appalling, then ozone will probably be the winner for not shitting in the bathtub so to say.
Just another girlie reagent/reaction mostly: "to beautiful to be useful"
But there is always hope of course!
Experiment rules.
/ORG |
anybody can confirm,use ammonium nitrate instead of permangenate? |
