Beirdo
Well-known member
I have a pile of CPUs (P3, P4) with the pins removed. About half of them, I hand-removed the capacitors with a hot-air rework station setup. The other half, I did not. I removed all of the plated copper caps from the processors so all that is left is the fiber board and the IC itself.
The half with the capacitors, I have dissolved off the solder with hydrochloric acid (32%), and this has removed the capacitors as well, of course. The result is hydrochloric acid with black precipitate (and a fair amount of it) and capacitors in the dregs... and a nice purple hue. That is where my mind went "Oh crud!".
I filtered off the solids, and have a nice bottle with amethyst-hued purple solution in it. I then went to wash the precipitate with water, and it instantly went from black to a nice milk white, and is settling over the day now.
Here is what I think I have:
- purple solution = HCl + stannous chloride + gold stannate (from the wee bit of gold on the surfaces of the processors for pin 1, etc)
- black precipitate in HCl = silver (maybe lead)
which turned into:
- white precipitate in water (likely actually fairly dilute HCl solution) = silver chloride + maybe lead chloride
So, my questions:
1) what are the chances of dropping any gold from the purple solution? I've read that hot sulfuric might precipitate gold from such a solution, but I'm loathe to work with that stuff unless necessary. I'm aware that I may be losing some to colloidal gold here, but there wasn't that much (I thought) in the first place.
2) am I correct on the black precipitate in HCl?
3) I'm assuming that I can separate lead and silver chlorides with the use of hot water to dissolve the lead chlorides. Is there anything else I'm missing here?
4) if there is cupric chloride in the solution (or precipitate) is there a simple way to separate it?
I'll go back to continuing to read Hoke, BTW. It is a great read, and there is still much to learn (which I'm sure is still obvious!)
The half with the capacitors, I have dissolved off the solder with hydrochloric acid (32%), and this has removed the capacitors as well, of course. The result is hydrochloric acid with black precipitate (and a fair amount of it) and capacitors in the dregs... and a nice purple hue. That is where my mind went "Oh crud!".
I filtered off the solids, and have a nice bottle with amethyst-hued purple solution in it. I then went to wash the precipitate with water, and it instantly went from black to a nice milk white, and is settling over the day now.
Here is what I think I have:
- purple solution = HCl + stannous chloride + gold stannate (from the wee bit of gold on the surfaces of the processors for pin 1, etc)
- black precipitate in HCl = silver (maybe lead)
which turned into:
- white precipitate in water (likely actually fairly dilute HCl solution) = silver chloride + maybe lead chloride
So, my questions:
1) what are the chances of dropping any gold from the purple solution? I've read that hot sulfuric might precipitate gold from such a solution, but I'm loathe to work with that stuff unless necessary. I'm aware that I may be losing some to colloidal gold here, but there wasn't that much (I thought) in the first place.
2) am I correct on the black precipitate in HCl?
3) I'm assuming that I can separate lead and silver chlorides with the use of hot water to dissolve the lead chlorides. Is there anything else I'm missing here?
4) if there is cupric chloride in the solution (or precipitate) is there a simple way to separate it?
I'll go back to continuing to read Hoke, BTW. It is a great read, and there is still much to learn (which I'm sure is still obvious!)