patnor1011
Well-known member
Depending on type of chip it can be a lot of copper and I would go for nitric leach first. That do have some other advantages, some chips contain Ag/Pd brazing, Ag will be dissolved in this leach along with copper.
Phillip Barrett said:Thanks a bunch guys for the fast answer !!! I just joined the forum less than a week ago and all i want to do is get on and read, read,read, I thought i knew a little about this but find out i know nothing !!! Just love it, so much to learn. I just ran across a bunch (lucient 1674ct48 chips). Is there any way of finding out from the number if they have any gold content without running a sample first? Again, Thanks for answers !!! Pillip
Obviously that isn't gold, just a lot of trash. It could have some gold hidden though.Stowmaster said:I made a better quality photo
https://www.dropbox.com/s/ji17gur5rv6935f/3.1.1.JPG
g_axelsson said:Obviously that isn't gold, just a lot of trash. It could have some gold hidden though.Stowmaster said:I made a better quality photo
https://www.dropbox.com/s/ji17gur5rv6935f/3.1.1.JPG
I would add some AR (Cover it in HCl and add a few drops of HNO3) and then test the solution with stannous. 1.7g of material wouldn't need any more than 1.7 ml HNO3 at the most if it was pure gold. If you get gold in solution, then filter it and either save it or drop it with a little bit of SMB.
What do you mean with "3) dissolved base metals and held flotation"? Gold can easily float on surface tension. What acid did you use for dissolving base metals?
Göran
Stowmaster said:Maybe I'm incorrectly to use the term flotation. Maybe somewhere error interpreter.
Sequence of my actions:
1) 500 grams of chips I filled 23% nitric acid for 2 days.
2) Brushing I cleaned the remains of tin acid.
3) I manually separated useless phragments of chips.
4) Chips I burned. Chips burned very well.
5) I burned chip grind in a coffee grinder.
6) I milled chip on 2 days filled 23% nitric acid. Several times a day mixed. Purpose - the dissolution of base metals.
7) I poured the contents of the jar onto the filter. Powder on the photo stayed at the bottom jar. I do not know how it happened. I did not plan this event. But I remember the technique of mixing in paragraph 6. I made a circular motion relatively the plane of the earth, holding the jar in hand. I think that there was a natural gravity separation.
8. The filtrate is washed with water and i added SSN - 30 ml of 70% nitric acid, 60 g of crystalline NaCl for 2 days. Several times a day mixed.
9) I added water, dissolved salt residue and the mixture was filtered. Then I washed several times with the filtrate.
Geo said:Here is where your gold is hidden. Do you still have the SSN from step 8? Did you test the SSN with stannous chloride for the presence of gold?
Everything solid after step 8 should be trash and there should be no solid gold after step 8.
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