PeterM said:
because of the Se, and Te present.
What would the chances be, that the Selenium in this ore, could have become selenic acid? It'll dissolve gold also (gold III selenate), and is there a chance that this could be holding it in solution? https://en.wikipedia.org/wiki/Selenic_acid
Edit - This may be of some interest also, and added page numbers.
The Chemical News and Journal of Physical Science, Volume 86
Action of Tellurium and Selenium on Gold and Silver salts
Pages 309-311
https://books.google.com/books?id=8xlLAAAAYAAJ&pg=PA309&lpg=PA309&dq=selenium+aqua+regia+gold&source=bl&ots=5MTHGIKr2A&sig=S8O-XOlWSxC0GiN3I42awNe9KxI&hl=en&sa=X&ved=0ahUKEwiamaCTuqbKAhUGLyYKHQzGB24Q6AEILDAD#v=onepage&q=selenium%20aqua%20regia%20gold&f=false
Another edit - reworded
PeterM said:
Fellas, I am dealing with a very concentrated solution keep that in mind.
Gold (III) Selenate
Properties - small yellow cryst; decomposes in light
solubility - i, H2O, s H2SO4, HNO3
Look at the very first post, picture 2, spoon on the right. if you zoom in, it looks like yellow crystals. Did you get rid of the extra nitric?