I am not sure what you call Ormus, but what others say they make and call Ormus gold, is just a bunch of nonsense, a scam, fiction or magic, manna from heaven, star dust and other fictional magic, just plain old BS. ![]() Where is this place where we can debate, what better place than here where the basis for the discussion is already posted. Make the oxalic additions slowly to avoid possible boil-overs. If you decide to stick with oxalic acid, both the gold solution oxalic acid solution should be near boiling to speed up the reaction. I prefer smb because it reacts faster than oxalic acid. Dilute with water yet again and precipitate with oxalic acid or smb. It is possible that here again you will get oxalic acid precipitating out. Or, you could again evaporate the solution to remove traces of nitric acid. But this will mean the recovered metals will be a mix of all precious metals in solution which will need to be further refined later. The easiest way to recover the precious metals is by cementing out on copper. If the copper is coated with a dark powder, you at least know you have precious metals in solution. ![]() Another way to test is to hold a very bright piece of copper in the solution for a minute or so. The filtered solution should be tested again with stannous chloride for gold presence. If all residue dissolves in hot water, it was oxalic acid. If you are sure you had gold in solution (positive stannous chloride test) and it still has not dropped out, a possible explanation is that you did not evaporate all the nitric acid out.įilter the white powder out and save the filter to later dissolve filtrate in hot water. I think many of us agreed there is no such thing as ormus. I have not used the Oxalic acid to precipitate gold so I cannot help you here, but maybe one of our members who is more knowledgeable with its use can, what temperature, color and concentration was solution while trying to precipitate, also giving details in the steps you took from beginning to end can help the member see where a problem may have occurred or how to resolve the problem. I would like to understand the chemistry here better and know if it could possibly be formed in this manner.Īs far as ormus, this forum and its great members have done a great job of revealing such nonsense, and keeping the real science of gold recovery refining and chemistry, some people seem to want to believe in this type of nonsense, and other people like to spread this nonsense to cheat people, most of the members here on the forum just want to know the truth, true science, and to help other members, although sometimes there can be members here that hide in the shadows and try to prey on other members, but if the light of reality shines on them they will not remain here long, or they will be exposed to our good members and not be able to do their corrupt business here. ![]() But I do not see where the white powder from an attempt to precipitate gold using oxalate acid would form very much if any silver oxalate, or even if it could form a very small amount, (would it not also be mixed in with silver chloride and then not be as dangerous if the dried powder were heated or even if you tried to detonate it?), I do not understand the chemistry of what silver compound could possibly be formed, but at the point of reducing gold from aqua regia, there would not be much silver in solution, silver oxalate normally being made from a silver nitrate solution, not a chloride solution, I wonder if it would even be possible to form silver oxalate in an aqua regia solution when attempting to precipitate gold with oxalic acid.
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