JesseSShaw
Active member
This time I kept heat applied just below the boiling point so that I could monitor the reaction. I eventually had to call it a day so I let it cool and corked it so I could continue the process the next day with heat again. I noticed that when the solution cools down, it becomes very dark. After applying heat again, the solution reverts back to a semi-opaque state. I kept adding HCL as needed while keeping heat applied so as not to remove the iron chloride and disturb the reaction. Now I am thrilled to say that the contaminant metals are continuing to dissolve. Maybe another day of applying heat should complete the dissolution. Considering this was my first time attempting this procedure, I made mistakes and used a tremendous amount of HCL. I am not sure how much HCL would actually be consumed for this procedure if done correctly. That will have to wait for the next time I attempt it.
I am not sure if this question was already asked somewhere on this forum. Forgive me if it was answered already. But does anyone know where I can find filters under 1micron pore size? I found some on amazon.com but they are unbelievably expensive. I would like to filter out as much of the gold as I can before storing the solution for later processing.
Thanks for sharing information and the help. It is much appreciated.
I am not sure if this question was already asked somewhere on this forum. Forgive me if it was answered already. But does anyone know where I can find filters under 1micron pore size? I found some on amazon.com but they are unbelievably expensive. I would like to filter out as much of the gold as I can before storing the solution for later processing.
Thanks for sharing information and the help. It is much appreciated.