Quiklearner
Well-known member
Greetings Forum Members!
First of all, I would like to extend a most sincere thank you to all of you who share your knowledge so freely and to those who ask the questions I don't even know to ask yet.
I am asking for your input to verify my train of thought before I try and perform my first gold drop. I have been recovering the gold from e-waste over the last 2 years and after much labour, I have 2 separate solutions of AR saved up. In the picture attached, I will call the small beaker Solution A and the larger beaker Solution B.
Solution A (~50ml): Denoxed by way of evaporation to syrup and reconstitution with HCl and I believe it to be relatively pure. I am estimating to be a little less than 2g of gold in this solution. A stannous test results in a jet black stain.
Solution B (~250ml): Almost certainly contains an excess of nitric acid and is contaminated with what I suspect to be copper. I estimate that there is around 7g of gold in this solution. A stannous test test results in a jet black stain.
BOTH solutions: Crystal clear with no sediment at the bottom.
This is how I am thinking to proceed:
1) Drop the gold from Solution A using SMB.
2) Wash the precipitant with distilled water until no acid remains.
3) Add this gold to Solution B to consume the excess nitric I suspect is present in it.
4) Add (~1ml) sulphuric acid to remove any lead (which I have not done yet as I JUST obtained some).
5) IF NEEDED, add small doses of nitric to dissolve any remaining gold that is left at the bottom. (I will aim to leave a tiny amount undissolved to prevent overshooting and having an excess)
6) Cool the resulting solution and precipitate the gold with SMB.
To remove the remaining base metal contamination, should I collect and wash the gold mud with distilled water until it is acid free and then treat it in hot dilute nitric before I re-refine it in AR one last time?
I don't have any sulfamic acid at the moment, but I have plenty of Nitric, HCl, Sulphuric acids, and SMB on hand.
Looking forward to your responses!
First of all, I would like to extend a most sincere thank you to all of you who share your knowledge so freely and to those who ask the questions I don't even know to ask yet.
I am asking for your input to verify my train of thought before I try and perform my first gold drop. I have been recovering the gold from e-waste over the last 2 years and after much labour, I have 2 separate solutions of AR saved up. In the picture attached, I will call the small beaker Solution A and the larger beaker Solution B.
Solution A (~50ml): Denoxed by way of evaporation to syrup and reconstitution with HCl and I believe it to be relatively pure. I am estimating to be a little less than 2g of gold in this solution. A stannous test results in a jet black stain.
Solution B (~250ml): Almost certainly contains an excess of nitric acid and is contaminated with what I suspect to be copper. I estimate that there is around 7g of gold in this solution. A stannous test test results in a jet black stain.
BOTH solutions: Crystal clear with no sediment at the bottom.
This is how I am thinking to proceed:
1) Drop the gold from Solution A using SMB.
2) Wash the precipitant with distilled water until no acid remains.
3) Add this gold to Solution B to consume the excess nitric I suspect is present in it.
4) Add (~1ml) sulphuric acid to remove any lead (which I have not done yet as I JUST obtained some).
5) IF NEEDED, add small doses of nitric to dissolve any remaining gold that is left at the bottom. (I will aim to leave a tiny amount undissolved to prevent overshooting and having an excess)
6) Cool the resulting solution and precipitate the gold with SMB.
To remove the remaining base metal contamination, should I collect and wash the gold mud with distilled water until it is acid free and then treat it in hot dilute nitric before I re-refine it in AR one last time?
I don't have any sulfamic acid at the moment, but I have plenty of Nitric, HCl, Sulphuric acids, and SMB on hand.
Looking forward to your responses!