WIZZARD
Well-known member
Sunlight, UV, radical atoms, protons, ect
Sunlight
I've had the following events take place when dealing with complex solutions of Noble Metals and sunlight exposure. Yes I'm using ore concentrate, and assay's show a good amount of Au, PGM's present, along with all the other elements that can be in ore, Cr, Ti, Fe, ect. Using HCL and non nitric oxidizer boiled, the minus 1,000 mesh ore for two hours, the filtered solutions range from yellow, orange to burgundy.
Ammonium Chloride
The solution was deluded with 4 time h2o, and added saturated ammonium chloride to the solutions, and placed in the sunlight. Text book yellow salts drop takes place in few days, next orange salts drop, next a red salts drop, then large salts a deep ruby red. The remaining solution is black with a lot of golden glitter that will not filter. When I forgo the sunlight, and just boil with ammonium chloride, the next day the salts are mixed colors, but mostly ruby red.
Sponge ignition and gold?
When the salts are ignited to PM sponge, close to end point of the sponge going gray, a brown fume begins to develop. Stopping the heat and examining the sponge residue, under the microscope , it appears to have velvet brown golden mossy looking deposit on top of the gray sponge. Not brown nitric fumes as none was used. After cooling and continuing to heat the velvet brown looks like Au micro crystals, mixed through out the gray sponge.
Question:
Has the exposure to sunlight with all those radical electrons, and protons, UV, ect, created some AuCl to be mixed with ammonium Pt/Cl salts? Hoke stated; some go for Au first while others go for the PM first? What conditions dictates, which one first? Also a science explanation of what might be going on with 5 day exposure to the sunlight, would be very helpful.
Wiz
Sunlight
I've had the following events take place when dealing with complex solutions of Noble Metals and sunlight exposure. Yes I'm using ore concentrate, and assay's show a good amount of Au, PGM's present, along with all the other elements that can be in ore, Cr, Ti, Fe, ect. Using HCL and non nitric oxidizer boiled, the minus 1,000 mesh ore for two hours, the filtered solutions range from yellow, orange to burgundy.
Ammonium Chloride
The solution was deluded with 4 time h2o, and added saturated ammonium chloride to the solutions, and placed in the sunlight. Text book yellow salts drop takes place in few days, next orange salts drop, next a red salts drop, then large salts a deep ruby red. The remaining solution is black with a lot of golden glitter that will not filter. When I forgo the sunlight, and just boil with ammonium chloride, the next day the salts are mixed colors, but mostly ruby red.
Sponge ignition and gold?
When the salts are ignited to PM sponge, close to end point of the sponge going gray, a brown fume begins to develop. Stopping the heat and examining the sponge residue, under the microscope , it appears to have velvet brown golden mossy looking deposit on top of the gray sponge. Not brown nitric fumes as none was used. After cooling and continuing to heat the velvet brown looks like Au micro crystals, mixed through out the gray sponge.
Question:
Has the exposure to sunlight with all those radical electrons, and protons, UV, ect, created some AuCl to be mixed with ammonium Pt/Cl salts? Hoke stated; some go for Au first while others go for the PM first? What conditions dictates, which one first? Also a science explanation of what might be going on with 5 day exposure to the sunlight, would be very helpful.
Wiz