Bad news. The assay came back with no significant pm's. Small amounts of Ag and PGM's
showed up, but no Au. There was 85% Mn and 15% Fe leaving only traces of other metals.
I don't know if there were sulfides, since the ICP assay only reports back metals.
On friday I ordered an omega OS524E IR pyrometer
The temperature of the furnace can be controlled several ways in order to stay in a needed range.
Any PM volatization will be captured in the exhaust system or furnace wall.
The material shown in the earlier posted slag/button photos was supposed to be an orecons and we did
not get it assayed before processing it so we flew blind into it. Is it possible that there are pm's help
up in the slag? Or volatized off? There were after all traces of Ag in it. The boiling temp of Mn is 2061 C
and it seems that we would be boiling off that base metal instead of the PM's if any metals were in fact boiling off.
We were running a reduced furnace. Any ideas on where the PM's may have gone?
I ordered the book "Chemistry of Gold Extraction" by John O.Marsden
http://www.smenet.org/store/mining-books.cfm/Chemistry-of-Gold-Extraction,-Second-Edition/240-8
At this time we are faced with needing to be able to reduce the base metal content of our buttons in order
for the refiner to accept them. We are getting a 2.6% PM button with an orecon with a reduced furnace
extraction. We are considering approaching better concentration by running smelts in an oxidized
furnace to fuse as much base metals into the flux slag as possible and then use wet chemistry acid to
dissolve the base metals and collect the PM particles. I'm wondering what the technical issues will be
with getting the PM's to settle to the bottom of the crucible while we are oxidizing the base metals.
Is this where a getter metal like silver would be employed to wash the PM's out of suspension?
PS