What a helpful site and I am sure the answer to my question is here somewhere. I have read and read to the point that I am confused beyond comprehension. Help from anyone is greatly appreciated and please excuse my ignorance. To that end.... I have made a sulfuric cell for stripping gold plating off of e-waste-mostly pins and contacts. I have used a Pyrex loaf dish and a small battery charger utilizing a clump of lead and copper pipe that I cut and flattened to make a basket for the anode and cathode. The sulfuric acid is new for a auto battery. The cell seems to work fine as it removes the gold from the pis in a matter of seconds when only doing a few. The solution turns black with what I suspect is the gold.
Here are my questions. What is the next step in my final goal of getting the gold. I am confused as I believe I am to let it settle then maybe rinse? I think I am trying to avoid using the auqa-regina method but I am mixed up as what the next step is due to reading about the ar methods. I keep referring back to Hooke and the handbook but my thinking is contaminated by trying to absorb the different methods at one time. I thought it better to ask then cause a castropy. Thank you in advance.-Aptus
Question 1. Can I let it settle, remove all acid I can and filter, thus saving the gold powder and then add 3 parts Borax and melt? If rinsing is needed, what do I rinse with?
Question 2. Should I use carbon and lead for the anode and cathode or is the copper and lead fine? I am trying to avoid contaminating the solution.
Here are my questions. What is the next step in my final goal of getting the gold. I am confused as I believe I am to let it settle then maybe rinse? I think I am trying to avoid using the auqa-regina method but I am mixed up as what the next step is due to reading about the ar methods. I keep referring back to Hooke and the handbook but my thinking is contaminated by trying to absorb the different methods at one time. I thought it better to ask then cause a castropy. Thank you in advance.-Aptus
Question 1. Can I let it settle, remove all acid I can and filter, thus saving the gold powder and then add 3 parts Borax and melt? If rinsing is needed, what do I rinse with?
Question 2. Should I use carbon and lead for the anode and cathode or is the copper and lead fine? I am trying to avoid contaminating the solution.