So, how would nitric be better at disassociating/oxidize, or just being corrosive?Vinegar and H2O2 may attack metals, sure lots of things will do that, but it is pretty much useless in recovery and refining in general, Period.
Trying to prove something you do not understand is useless as counting on peracetic acid to be some kind of miracle breakthrough or to be a safer alternative.
II is not better or safer and there are no real benefits.
Using it is just as useless as trying to prove it useful, or a safe alternative.
The time spent trying to argue a moot point could be better spent actually learning.
Hydrochloric acid (HCl): pKa = -6.3.
Nitric acid in water has a pKa of -1.3
Acids under 0 get stronger.
I see it Acid prevalence, and Oxidation agent-
Nitric acid is a strong acid, completely ionized into hydronium (H3O+) and nitrate (NO3-) ions in an aqueous solution, and a powerful oxidizing agent.
Same reasoning why AP, or any chlorine + oxidizer work. People still do use Acetic, and H2O2 for home refining.... If you made a stronger solution of the 22 I'd assume the speed would improve. I don't have such luxuries to get HNO3 for $0.50 a FREKAING LITER. That's awesome for Europe though. Good on em me chap.
Shows why Nitric always need a base of water-
Does nitric acid completely ionize in water?
Nitric acid decomposes into water, nitrogen dioxide, and oxygen, forming a brownish yellow solution. It is a strong acid, completely ionized into hydronium (H3O+) and nitrate (NO3−) ions in aqueous solution, and a powerful oxidizing agent (one that acts as electron acceptor in oxidation-reduction reactions).
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