What is this mess?

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zamistro

Well-known member
Joined
Sep 29, 2009
Messages
52
I tried to use AP to remove the gold plating from pins on some cpus. The gold left, but seems to have gone into solution. Couldn't get it out. Mainly out of curiosity I boiled it dry and got this:

003eg.jpg


Do you suppose the yellow stuff has gold content?
 
If there's one thing I've learned from looking at buckets of dried crud laying around refineries is that you can never make a determination based on color alone. Well you can.....and a lot of guys do...... you'll probably just be wrong.
 
Not trying to get your hopes up, but I've seen contaminated dried gold powder that looked like that. I guess it could be an iron compound, but it looks heavier than that. Scrape some up with a spoon. How much does a level teaspoon weigh? It it's gold powder, it would be heavy.
 
If that was AP and CPUs that powder will contain everything and tiny bit of gold. Certainly the biggest part of that powder is copper and iron.
 
I agree. There should be gold content, the gold had to go somewhere, but most of this is crud. This being a small batch I was fooling around with it. It started out as AP then I added sodium nitrate over heat to see if it would become AR. Later, I threw in some urea and SMB. Y'know, just to see.

Any ideas on trying to get the gold out of this mess?
 
zamistro said:
Any ideas on trying to get the gold out of this mess?
Simple!
Incinerate to a dull red heat, but DO NOT MELT. Heat in an old stainless fry pan.

Place the remaining solids in a heat resistant glass container, and heat to a low boil using dilute nitric acid. Heat until upon the addition of a small amount more of acid causes no reaction. Dilute well with water (tap water is perfectly acceptable in this case). Siphon after the solids have settled. Repeat, until the rinse water is clear of color.

Get the solids back in the fry pan and heat to dull red once again. Afterwards, repeat the above washing process, but instead of nitric, use HCl. Repeat the rinse cycles.

Leaving the solids in the same container, after you decant the solution, heat VERY slowly over a low heat source, evaporating the remaining traces of liquid. Shake the remaining solids occasionally to insure that they do not stick to the vessel. As they dry, they should clump up, assuming the gold is fairly clean.

The end result should be gold of reasonably high quality.

DO NOT OVERLOOK THE INCINERATION PROCESSES MENTIONED. Otherwise you risk dissolving values along with the base metals.

I would recommend the resulting gold be re-refined at some time in the future if quality is an issue.

An alternate to the second incineration. Rinse the solids with ammonium hydroxide, then rinse well with tap water. It is important that no nitric remain before introducing HCl for the second recommended wash.

Harold
 
Well I am probably stepping into it here.

Harold_V said:
Dilute well with water (tap water is perfectly acceptable in this case). Siphon after the solids have settled.

Why would tap water be acceptable here if you are possibly removing silver with the nitric and perhaps creating silver chloride solids? Lead should also be considered.

Harold_V said:
An alternate to the second incineration. Rinse the solids with ammonium hydroxide, then rinse well with tap water. It is important that no nitric remain before introducing HCl for the second recommended wash

This ammonium hydroxide wash would solve the silver chloride problem if it indeed developed but if tap water was used in the first step it would have to be chloride free in order to skip this later step and have clean gold.

Always acidify hydroxide solutions that may contain silver.
 
Oz said:
Well I am probably stepping into it here.

Harold_V said:
Dilute well with water (tap water is perfectly acceptable in this case). Siphon after the solids have settled.
Why would tap water be acceptable here if you are possibly removing silver with the nitric and perhaps creating silver chloride solids? Lead should also be considered.
In this instance, I am considering the recovery of gold, and nothing more. The process I recommended will solve all of the problems, and if traces of silver may be present (but likely are not), the silver would be recovered at some time in the future. My logic is that only a fool will spend premium time trying to recover a few cents worth of silver that may or may not be present. That which may have followed the rinse solution would be recovered with copper, so what we're talking about is nothing short of a miniscule trace.

Regards addressing the presence of lead, the rinses that follow the nitric digest should be with hot water, with decanting taking place prior to any lead nitrate self precipitating upon cooling of the solution. Hot water will generally facilitate rapid settlement, keeping any lead that may be present in solution.

Assuming there is a small amount of silver present, so what? No harm is done by creating a trace of silver chloride, nor is it lost so long as the solids (filter and contents) are not discarded. As Kenny Rogers said in his song, The Gambler, you have to know when to hold 'em, and know when to fold 'em.

Harold_V said:
An alternate to the second incineration. Rinse the solids with ammonium hydroxide, then rinse well with tap water. It is important that no nitric remain before introducing HCl for the second recommended wash
This ammonium hydroxide wash would solve the silver chloride problem if it indeed developed but if tap water was used in the first step it would have to be chloride free in order to skip this later step and have clean gold. [/quote]
It has nothing to do with silver chloride. It has to do with insuring that all of the nitric has been eliminated.
I refined for more than 20 years, using tap water for all of my operations aside from running my silver cell. In all that time, I never had a problem in dissolving gold because of the use of chlorinated tap water, and ours was heavily chlorinated. It was obvious by the smell, by the taste and by the traces of silver chloride that were precipitated from silver nitrate solutions. Again, so what? The silver chloride, to me, was a desirable byproduct. I processed all of my waste materials by furnace, relying on the presence of silver chloride to act as a collector for the greater values, The concept proved to be an excellent solution to harvesting greater values. I recommend it highly.

Always acidify hydroxide solutions that may contain silver.
Even if there was traces of silver present, in this particular application, the end result would not yield any problems having introduced ammonium hydroxide. I agree, otherwise, that the solution should be acidified if there is any chance there would be silver present. Remember, he was advised to rinse until the solution was free of color. At that point, so little of ANYTHING but the solids remains that the material could likely be then processed directly without incineration. The miniscule traces of silver chloride that may have resulted from the use of tap water would require that the entire ammonium hydroxide wash solution and rinse water be dried----which, in my opinion, is highly unlikely. I do agree that the hazards should be well understood, however.

The incineration, or the addition of the ammonium hydroxide (in place of the second incineration, as I advised) could in all likelihood be eliminated. It was suggested so the that those that read the comments gain knowledge that can, in the future, keep them out of trouble in the way of losing values.

Consider that my final advise would be to re-refine the yield if quality was an issue. I expect it would be, but his question was one of bailing out from a mess.

I stand 100% by the instructions I posted. They will guarantee success.

When it's all said and done, I rely on the picture that has been seen countless times. Proof positive that my method of refining yielded exception results.

Harold

edit: corrected spelling----no change in content otherwise
 
In defence of OZ we all step in it now and then, I will have to go clean my shoe's now.
I would think that nitric in first part would remove most lead oxide & silver, I would also think that the small amount of silver chloride would not precipitate easily in the acidic hot HCl solution, and would also be removed with the decanting and rince's. and this mess will have to be re-refined if purity was the desire, that would get anything that survived,
no wonder Harold's gold shines, well he probably has clean shoe's too :lol:
 

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