Lightspeed
Well-known member
I have started a small experiment with what was supposed to be Gold powder. The makeup of which was supposed to be Copper, Zinc, Gold, Silver and Iron as tested by a Gold and Silver dealer friend of mine. I did not witness the test, the result was relayed to me along with the parcel.
My original plan due to the powder makeup was to initially dissolve the unwanted metals in a Nitric/DW 50/50 digestion to put the unwanted metals into solution, before progressing to AR and precip.
The powder was placed into a 5L beaker which was thoroughly rinsed before use, there may have been approximately 10 grams of powder, after rinsing the packaging and washing down the beaker sides I had around 600ml of DW with a lot of the powder floating due to is fineness and surface tension.
I started with 100ml of 68% nitric addition with very little reaction so added another 80ml with a similar result. I stirred the solution then the reaction started as expected with some fuming and the dilution changing to a clear blue colour as I expected. I left the Digestion for less than 5 minutes on very low heat inside the pyroceram safety catchment. When I returned the whole lot had gone into solution.
So no Gold?? I thought gold did not dissolve in nitric, I would have expected the digestion to have gone well due to the lack of concentration of Nitric.
Is it possible the electronic test of the powder was inaccurate and the so called Gold was actually Brass shown by the Copper and Zinc??
Steps forward:
Test solution with stannous, but should be negative according to all I have read regarding Nitric and gold.
If positive and it should not be, where do I go from here to rid the excess of Nitric?
Do I use Sulfamic acid to neutralise, is there another option?
After neutralising solution should i precipitate silver and (gold if existing) with copper?
I am reluctant to go ahead from there and re dissolve in Nitric as if any Gold were present it simply should have stayed as a solid in the initial digestion.
The solution at this stage is clear light blue, with some fine small black bits floating within it. There is no white cloudiness to denote there is a chloride nor settling on the bottom of the beaker.
This is my first experiment in a Gold recovery and refine.
My original plan due to the powder makeup was to initially dissolve the unwanted metals in a Nitric/DW 50/50 digestion to put the unwanted metals into solution, before progressing to AR and precip.
The powder was placed into a 5L beaker which was thoroughly rinsed before use, there may have been approximately 10 grams of powder, after rinsing the packaging and washing down the beaker sides I had around 600ml of DW with a lot of the powder floating due to is fineness and surface tension.
I started with 100ml of 68% nitric addition with very little reaction so added another 80ml with a similar result. I stirred the solution then the reaction started as expected with some fuming and the dilution changing to a clear blue colour as I expected. I left the Digestion for less than 5 minutes on very low heat inside the pyroceram safety catchment. When I returned the whole lot had gone into solution.
So no Gold?? I thought gold did not dissolve in nitric, I would have expected the digestion to have gone well due to the lack of concentration of Nitric.
Is it possible the electronic test of the powder was inaccurate and the so called Gold was actually Brass shown by the Copper and Zinc??
Steps forward:
Test solution with stannous, but should be negative according to all I have read regarding Nitric and gold.
If positive and it should not be, where do I go from here to rid the excess of Nitric?
Do I use Sulfamic acid to neutralise, is there another option?
After neutralising solution should i precipitate silver and (gold if existing) with copper?
I am reluctant to go ahead from there and re dissolve in Nitric as if any Gold were present it simply should have stayed as a solid in the initial digestion.
The solution at this stage is clear light blue, with some fine small black bits floating within it. There is no white cloudiness to denote there is a chloride nor settling on the bottom of the beaker.
This is my first experiment in a Gold recovery and refine.