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leHAI

New member
Joined
Oct 7, 2024
Messages
3
Location
vietnam
I new in this indduusstry, just learning, seeing video on Youtube, and faild 2 times, :)
I'm here hope to find what I miss, please support
 
I new in this indduusstry, just learning, seeing video on Youtube, and faild 2 times, :)
I'm here hope to find what I miss, please support
Welcome to us.
Point 1 Youtube is not a good teacher.
Point 2 We need more information, what have you tried to do.
Point 3 you need to study more obviously.

Give us some more information and we can start helping you.

In the mean time study these links:

We ask our new members to do 3 things.
1. Read C.M. Hokes book on refining jewelers scrap, it gives an easy introduction to the most important chemistry regarding refining.
It is free here on the forum: https://goldrefiningforum.com/phpBB3/viewtopic.php?f=54&t=19798
2. Then read the safety section of the forum: https://goldrefiningforum.com/forums/safety.47/
3. And then read about "Dealing with waste" in the forum: https://goldrefiningforum.com/threads/dealing-with-waste.10539/

Suggested reading:
https://goldrefiningforum.com/forums/the-library.101/
https://goldrefiningforum.com/threads/when-in-doubt-cement-it-out.30236/
https://goldrefiningforum.com/threa...le-read-this-before-you-post-about-ore.33333/


Forum rules is here.
https://goldrefiningforum.com/threads/gold-refining-forum-rules.31182/
 
Hi,
I'm happy to share my issue:
I have plates with 3 layer: gold, Niken and Copper and I start refining gold step by step as below:
Step 1: Immerse in a solution of nitric acid and water to separate the gold layers. After seeing that the gold layer has completely separated from the plate, I filter it through absorbent paper and obtain the gold-plated layer.
Step 2: I put the filter paper with the gold layer into the aqua regia solution (3HCL + HNO3) with heat, I tried to add as little HNO3 as possible by dropping until the metal was completely dissolved. After the metal was completely dissolved, I filtered the dissolved solution.
Step 3: I add in the same amount of water as the solution and boil until the water level returns to normal then let it cool, my purpose is to remove the HNO3
Step 4: I add SMB the solution, it turn to dark colour
After time, the solution appears precipitate but it stays cloudy and muddy, very soluble, i have attached a picture for you, i tested the water with stannous chloride and it turned black
Should I filter out this precipitate, boil the solution and continue adding SMB until I see a yellow precipitate or is there any other solution? Please advise.
 

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Hi,
I'm happy to share my issue:
I have plates with 3 layer: gold, Niken and Copper and I start refining gold step by step as below:
Step 1: Immerse in a solution of nitric acid and water to separate the gold layers. After seeing that the gold layer has completely separated from the plate, I filter it through absorbent paper and obtain the gold-plated layer.
Step 2: I put the filter paper with the gold layer into the aqua regia solution (3HCL + HNO3) with heat, I tried to add as little HNO3 as possible by dropping until the metal was completely dissolved. After the metal was completely dissolved, I filtered the dissolved solution.
Step 3: I add in the same amount of water as the solution and boil until the water level returns to normal then let it cool, my purpose is to remove the HNO3
Step 4: I add SMB the solution, it turn to dark colour
After time, the solution appears precipitate but it stays cloudy and muddy, very soluble, i have attached a picture for you, i tested the water with stannous chloride and it turned black
Should I filter out this precipitate, boil the solution and continue adding SMB until I see a yellow precipitate or is there any other solution? Please advise.
Well you can start reading the links I gave you.
In Step 3 this do not work at all.
If you are going to do it by evaporation.
You need to evaporate to a thick syrupy consistence.
Then add HCl.
Brown funes should evolve if there still is Nitric in there.
If so do it again.
Whan the Nitric and NOx is driven off.
Add HCl until all is dissolved and filter until crystal clear.

Then add SMB and the Gold should drop just fine. Then test with Stannous.
If it test negative you can set it aside until next day. Test it again then if it is still negative, decant the liquid and collect the powder on the bottom.
If needed refine again.
 
Well you can start reading the links I gave you.
In Step 3 this do not work at all.
If you are going to do it by evaporation.
You need to evaporate to a thick syrupy consistence.
Then add HCl.
Brown funes should evolve if there still is Nitric in there.
If so do it again.
Whan the Nitric and NOx is driven off.
Add HCl until all is dissolved and filter until crystal clear.

Then add SMB and the Gold should drop just fine. Then test with Stannous.
If it test negative you can set it aside until next day. Test it again then if it is still negative, decant the liquid and collect the powder on the bottom.
If needed refine again.
Sure I will read all the link,
But in this case, could you advise me now I should filter the brown precipitate,then start HCL process OR leave them there and start HCL process?
thank you for your respone
 
Sure I will read all the link,
But in this case, could you advise me now I should filter the brown precipitate,then start HCL process OR leave them there and start HCL process?
thank you for your respone
Have you tested with Stannous?
Have you tested the pH?
 

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