I have processed 2 times an out put of Silver Crystals in an Electrolyte Silver Nitrate Cell.
I just had 50 ounces of crystals analyzed at a high end reputable gold / silver dealer in Houston recommend by the host of syndicated radio show of Michael Berry.
I understand that PGM metals can follow silver which I assume even in the elecgtrolysis process.
What I am uncertain how the other metals ended up in mu silver crystals.
Here is a breakdown of the XRF read out:
In - .671
Ag - 96.120
Ru - 1.262
Co - .638
Fe - .936
Mn - .310
Cr - .039
The Ru, I understand some PGM metal must have been in the feed stock I used to create the Silver Nitrate and is below in thee scale of metals that follow metals above.
The other metals as listed in The Metal Reactivity Series are a puzzle to me>
Fe & Mn are common to each other but above Ag. So thinking out loud here I am going to throw it out here that these metals might have been in the feed stock as well as the PGN contamination.
The In, Co, & Cr followed too I guess.
The question or uncertainty I have is, if any metal that is in the Silver Nitrate solution will they always follow the ion exchange from the anode to the cathode?
Next question is there a test I can conduct on the Silver Nitrate solution for other metals?
I know I can test for PGM and precipate with DMG but other metals I am unclear how to test and even remove before I start the cell.
On the bright side I did not have any Cu follow so I am pleased with that result.
My thought of how to proceed from this point is to start completely over.
re-Acid dissolution of the crystals, Silver shot, Anode bar and drop the silver out with copper in the 6 gallons of silver nitrate after I drop out any PGM metals it may contain.
last question or clarification is if I am correct with my deduction that the contamination is in the silver nitrate if these metals or similar metals listed are contained in the anode silver shot is is likely they will follow the ION exchange. I am of the opinion they would remain in the slimes filter basket yet at this point I am obviously uncertain.
Once again guidance is appreciated.
I just had 50 ounces of crystals analyzed at a high end reputable gold / silver dealer in Houston recommend by the host of syndicated radio show of Michael Berry.
I understand that PGM metals can follow silver which I assume even in the elecgtrolysis process.
What I am uncertain how the other metals ended up in mu silver crystals.
Here is a breakdown of the XRF read out:
In - .671
Ag - 96.120
Ru - 1.262
Co - .638
Fe - .936
Mn - .310
Cr - .039
The Ru, I understand some PGM metal must have been in the feed stock I used to create the Silver Nitrate and is below in thee scale of metals that follow metals above.
The other metals as listed in The Metal Reactivity Series are a puzzle to me>
Fe & Mn are common to each other but above Ag. So thinking out loud here I am going to throw it out here that these metals might have been in the feed stock as well as the PGN contamination.
The In, Co, & Cr followed too I guess.
The question or uncertainty I have is, if any metal that is in the Silver Nitrate solution will they always follow the ion exchange from the anode to the cathode?
Next question is there a test I can conduct on the Silver Nitrate solution for other metals?
I know I can test for PGM and precipate with DMG but other metals I am unclear how to test and even remove before I start the cell.
On the bright side I did not have any Cu follow so I am pleased with that result.
My thought of how to proceed from this point is to start completely over.
re-Acid dissolution of the crystals, Silver shot, Anode bar and drop the silver out with copper in the 6 gallons of silver nitrate after I drop out any PGM metals it may contain.
last question or clarification is if I am correct with my deduction that the contamination is in the silver nitrate if these metals or similar metals listed are contained in the anode silver shot is is likely they will follow the ION exchange. I am of the opinion they would remain in the slimes filter basket yet at this point I am obviously uncertain.
Once again guidance is appreciated.