That is a mistake.. There is no good reason to concentrate that solution, and, in fact, it's the wrong thing to do. Assuming there was any silver present, it could have been extracted without concentration, and that, alone, would have minimized the amount of garbage you are dealing with. You should have simply introduced salt to the solution, while it was dilute. That would have precipitated silver as silver chloride. I fully expect there would not have been anything else of value in the solution, and maybe not even silver. Alternately, assuming there was silver in solution, you could have used copper to extract the silver. After the recovery of silver, the solution would most likely be barren of values. It would be, for sure, if copper was used. It would then be eliminated from the process. Under no circumstance should it be kept in the circuit.We took roughly 30 lbs of the concentrates and roasted of the sulfides and dissolved the material in half a gallon of nitric (70%) and 2 gallon of water, filtered and have been putting this solution in 4 crockpots to concentrate.
No one can tell you from the information you have provided if you used enough acid, or not. That would be determined by the nature of the material. You would have been far better served to have worked with a small amount of this material, and kept impeccable records of what you did, and how much acid was consumed. You should have carried the first digest to the point where the further addition of nitric made no difference. If you did not, your work was not complete. It is for that reason you should have run a small test batch. From it you would have learned what it would take to arrive at the point where you could attempt to recover greater values.We know our acid amounts were off now because I have since found this forum.
This leaves me with questions. Did you add the HCl to the original solution, the one that contained nitric? If so, that was a mistake. The objective in using nitric for the initial digest is to eliminate unwanted substances before you attempt to dissolve values. Because silver dissolves in nitric, you would have expected a silver return, assuming you used enough acid. If you did not, it may well still be in the gangue. It also may be in a form that won't dissolve in nitric, so none would have been recovered. Bottom line is, had you not messed with the original solution, you would have been much better off.We also thought 2 gallons of 70% HCI wouldn't hurt. I wish I would have found this forum before that!! I had access to very strong acids but that access is no longer. So I am concentrating the solutions since the metals are quite diluted .
I'm not convinced anyone can tell you what you have. Not without a credible assay, and even then it may not indicate what you're recovering.Now I have a white substance growing everywhere, I assume this is the silver and my acids are getting very brownish green, it has been filtered and I am getting a shiny black mud out of the filters. I read read read and am not understanding.
Silver chloride does not represent itself as crystals. It is best likened to fine cottage cheese. The crystals are almost assuredly not silver.I want so bad to achieve success at this. I have harvested the crystals and they are like fibers and white as snow. Silver I am sure since silver screamed from the assay.
Want my opinion? Most likely nothing of value. The material you described most likely contains iron, along with copper. Combined they will yield a green solution. You may also be getting a false positive from stannous chloride. To test for gold, using stannous chloride, the most reliable test is to place a drop of the unknown solution in a spot plate (or a white plastic spoon ---thanks Palladium for that idea). Leave it for several minutes after applying a drop of stannous chloride. Disregard any color reactions you see when the drop is introduced. After ten or more minutes, rinse off the spoon or spot plate with a rinse bottle. If there is gold present, the test will show a purple stain. No stain--no gold.With my very dark green solutions I am stumped.
crazyman said:It is done. I have learned a lot and am accepting the project as an *** whoopin from nature. I need :roll: a break anyhow. False positive stannous tests took me on one hell of a roller coaster ride. Thank you for all those that gave 110% helping me out. As I said I have learned A LOT. :roll:
renatomerino said:Hello to the forum:
I have long been interested in the roasted ore particularly to gold and silver leaching.
This is a circular oven can be used for small and large quantities.
Basically camera has a fire in the bottom, a separate grill pallet, a combustion chamber on the grill and of course out the coolers and a bag filter to collect the roasted material not seen but I will provide photos later on.
The ore roasting contains 70 kg of silver per ton and the other is the calcined sample obtained.
The calcine is readily leached with solutions of 93% in initial tests.
The kiln feed is performed tires on the grill and the grain size is 100% minus 200 mesh.
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