The Green Team
Active member
I have experiment with the shor aka Poor Mans A/R. I was able to make it work, but it is very slow and the volume of material I had to use made a it a nightmare when time comes to filter.
For on going I am jumping through the hoops to buy real nitric and hcl.
I am a business so I might have a slight advantage here, but I must say I am going to be reviewed on paper and have a physical site inspection
prior to delivery of Nitric. I guess I am ok with that. I am a patriot after all
Overview:
I am working with brazing on metals. I reduce the content of base metal (410 ss most of the time) and then I digest the base and all pm's. Using
Poor mans I had to use a lot of muriatic and SubZero (doesn't seem
cheap enough to be considered poor mans) I have tried heating, and other methods to assist. Heating helps, but hard to control temp in my environment for long periods of time (I am using a turkey deep fryer to submerge a 5 gallon bucket in) The Turkey Fryer works well and is a stable platform.
The A/R hybrid seems to become saturated because of the amount of base metals. I increase the volume to thin it out, and still get it done, but the amount of a/r for 3 oz of Au gets up to 7 gallons, and I still think I have too much Au in filter sediments which leads me to washing it down to flush the Au into the A/r increasing the fluid amount. I have an XRF analyzer from Nitton with PM program which I use to check the fluid. AU is picked up in every filter (trace amounts if I rinse)
I tried a selective sample of 3.69 grams of mixed metal (base and braze) in a solution of 30 ml h202 (3%) and 30 ml of hcl (31.45%) This went to work on the base metals and the braze alloy got thin (estimated 82-90 percent au and balance nickel) I felt this approach might reduce the base metal leave the brazing and some base metal leaving me with less A/R to contend with for the final round. Looks like the gold becomes small flakes, and breaks off. Doesn't seem to dissolve, but will likely becomes lost at some percentage
The hcl alone seems to also do the same thing as the 1:1 hcl and h202
Sulfuric acid theoritically won't work on the Martnestic SS very quickly. I thing the nickel in the gold braze weakens the gold enough to liberate solids in tiny amounts. If I could do this with confidence and recover 100% of the Au then transfer into A/R that would be fine, but not comfortable with that prospect based on what I see.
I considered experimenting with dissolving only the AU and Nickel by Ionic interference with Chrome and Iron. A little advanced for right now. I am not a chemist, but I wish I were.
I also have fears that the filter content of Au sludge is from premature precipitation due to hi iron content in the A/R digestion process.
I do know it is worth getting good at this because I have already achieved better recoveries than what I normally get from my favorite professional refiner.
Bottom line is it seems I am different than the average person on this site because currently my feedstock is not electronics (do plan on doing some though)
Does anyone have any help they could offer?
I have locations in Mississippi, and California. I do this process in Mississippi though. I might be able to redistribute the Nitric Acid (I will have to buy bulk and I will be getting 63% conc.) to someone who can help.
I specifically would like help on ratios of total metals weight to volume of A/R.
Is the traditional 3:1 ratio good for this type of metal?
Are the ideal conc. level?
Temps seem to be best at 140 to 150f is this true?
I have studied patents which have a lot of data regarding these methods, and this leads me to questions on PH.
Should I adjust the PH to 2- 4 preferably 3 prior to percipitant?
have used storm (I am thinking Shor is not my future supplier of choice)
Ferrous Sulphate? or SMB? anything else?
Should I use an emulsifying agent like Butyl Stearate? I think this lends itself to making a finer gold sponge. I don't need finer I wont easy material to melt.
I am also curious about mol measuring. I wish I could quantify the gold content in fluid samples over a period of time to see when the Au is peaked.
I have also considered salts and electrolytic. I feel the surface area of my Au is mostly trapped and this technique may or may not work well.
I appreciate any response, and look forward to working with this forum.
I specialize in recycling exotic metals, and can sale metals (even gold) at real low margins. If I can help anyone out in this manner let me know.
I know this was lengthy, but it is my first post. It is a serious matter that I get competent with this procedure quickly so I thought I would spill most of my story intitially.
The Green Team
Levi Bradford
714-852-1300
[email protected]
For on going I am jumping through the hoops to buy real nitric and hcl.
I am a business so I might have a slight advantage here, but I must say I am going to be reviewed on paper and have a physical site inspection
prior to delivery of Nitric. I guess I am ok with that. I am a patriot after all
Overview:
I am working with brazing on metals. I reduce the content of base metal (410 ss most of the time) and then I digest the base and all pm's. Using
Poor mans I had to use a lot of muriatic and SubZero (doesn't seem
cheap enough to be considered poor mans) I have tried heating, and other methods to assist. Heating helps, but hard to control temp in my environment for long periods of time (I am using a turkey deep fryer to submerge a 5 gallon bucket in) The Turkey Fryer works well and is a stable platform.
The A/R hybrid seems to become saturated because of the amount of base metals. I increase the volume to thin it out, and still get it done, but the amount of a/r for 3 oz of Au gets up to 7 gallons, and I still think I have too much Au in filter sediments which leads me to washing it down to flush the Au into the A/r increasing the fluid amount. I have an XRF analyzer from Nitton with PM program which I use to check the fluid. AU is picked up in every filter (trace amounts if I rinse)
I tried a selective sample of 3.69 grams of mixed metal (base and braze) in a solution of 30 ml h202 (3%) and 30 ml of hcl (31.45%) This went to work on the base metals and the braze alloy got thin (estimated 82-90 percent au and balance nickel) I felt this approach might reduce the base metal leave the brazing and some base metal leaving me with less A/R to contend with for the final round. Looks like the gold becomes small flakes, and breaks off. Doesn't seem to dissolve, but will likely becomes lost at some percentage
The hcl alone seems to also do the same thing as the 1:1 hcl and h202
Sulfuric acid theoritically won't work on the Martnestic SS very quickly. I thing the nickel in the gold braze weakens the gold enough to liberate solids in tiny amounts. If I could do this with confidence and recover 100% of the Au then transfer into A/R that would be fine, but not comfortable with that prospect based on what I see.
I considered experimenting with dissolving only the AU and Nickel by Ionic interference with Chrome and Iron. A little advanced for right now. I am not a chemist, but I wish I were.
I also have fears that the filter content of Au sludge is from premature precipitation due to hi iron content in the A/R digestion process.
I do know it is worth getting good at this because I have already achieved better recoveries than what I normally get from my favorite professional refiner.
Bottom line is it seems I am different than the average person on this site because currently my feedstock is not electronics (do plan on doing some though)
Does anyone have any help they could offer?
I have locations in Mississippi, and California. I do this process in Mississippi though. I might be able to redistribute the Nitric Acid (I will have to buy bulk and I will be getting 63% conc.) to someone who can help.
I specifically would like help on ratios of total metals weight to volume of A/R.
Is the traditional 3:1 ratio good for this type of metal?
Are the ideal conc. level?
Temps seem to be best at 140 to 150f is this true?
I have studied patents which have a lot of data regarding these methods, and this leads me to questions on PH.
Should I adjust the PH to 2- 4 preferably 3 prior to percipitant?
have used storm (I am thinking Shor is not my future supplier of choice)
Ferrous Sulphate? or SMB? anything else?
Should I use an emulsifying agent like Butyl Stearate? I think this lends itself to making a finer gold sponge. I don't need finer I wont easy material to melt.
I am also curious about mol measuring. I wish I could quantify the gold content in fluid samples over a period of time to see when the Au is peaked.
I have also considered salts and electrolytic. I feel the surface area of my Au is mostly trapped and this technique may or may not work well.
I appreciate any response, and look forward to working with this forum.
I specialize in recycling exotic metals, and can sale metals (even gold) at real low margins. If I can help anyone out in this manner let me know.
I know this was lengthy, but it is my first post. It is a serious matter that I get competent with this procedure quickly so I thought I would spill most of my story intitially.
The Green Team
Levi Bradford
714-852-1300
[email protected]