Ohh..i got it.It will dissolve easier as a powder, what I meant was to take a pinch of the powder and melt for testing.
Knowing what is there may point to better ways to refine.
I'll apply this onwards
Ohh..i got it.It will dissolve easier as a powder, what I meant was to take a pinch of the powder and melt for testing.
Knowing what is there may point to better ways to refine.
Did you read what I replied to you??Thanks for details
I usually weight the sludge and same quantity 1 part Nitric and 3 parts HCL
Above ratio is okay for sludge?
I didn't understand..the concept of "if it stops before nitric has been used, add a bit more HCL."
Update on my AR process __
Filtered solution twice still solution colour deep dark yellow colour (looks nearly blackish)
Used distilled water to washout filter but salt formed instantly. They block filtration
After filtering solution added SMB into solution and another trouble is all the solution looks like creamy mud type.
So i added boiling water and it helped me to separate gold mud.(repeated 3-4 times)
I also tried one small batch( for trial purpose) with HCL bath. And after hot water bath to washout chemical.
Then dried mud in sand bath.
Before melting added little copper with gold dust to soften alloy
Also borax in crucible as well as in gold dust.
While melting some impurities came
Finally process completed after lots of barriers
I checked link.. thanks for the very useful informationDid you read what I replied to you??
And the link I sent you?
Read it all before you continue, we do not recommend using set ratios.
Sometimes you end up using 1:10 other 1:8 and do on, no batch is similar.
But i need to clean all the stuff now.
See comments in bold in the quote.Why in the world don't you use line shifts and proper sentences, its very hard to read and comment.
So, i were trying to dissolve base metal on some plated silverware and decided to quit mid way i ended up getting first blue, then green solution, it eventually became so dark i couldn't see the bottom, i started adding bicarbonate, ended up adding 3 whole kilos till i stopped seing bubbling now the solution is clear blue.
What did you use to dissolve the base metals? Did you test for PMs? Why did you add bicarbonate?
I wasted a lot of acid and forgot to get better peroxide and try to finish the reaction, idk what to do with it, this is what i'm left with.
This depends on what acid you used.
I'd like to cement whatever the base metal is. Why are you going to cement the base metals? Is this a part of your waste management?
The disgusting blue solution is what i ended up with, added amonia after forgot it exists.
Why did you add Ammonia?
I recommend you to set your chemicals aside until you have studied enough to understand what you are doing.
A small newsflash, it will never pay to process plated silverware with chemicals.
Here are some PCB goodies too for future processes.
View attachment 55789
Before melting added little copper with gold dust to soften alloy
I'm not sure I'm comfortable unless I urge you to put the chemicals away and start studying again, if you ever have studied at all.Anyhow, any idea of what i could use to cement whatever is inside there? I know i could use aluminium but I'd rather not just swap metal for metal, anything upper in the reactivity table? I remember reading what i need but forgot in the while.
I got a bucket of iron oxide and dissolved iron solution, would it cement the blue thing? I forgot i could do this since i initially thought i have chromium in solution (was light green for the first while and bluish) now i believe i have nickel in solution.
Edit: eh the solution is crystal clear and i got a blue sediment, i guess it was a success but i wish i had completed the reaction i had plenty of acid there, enough to eat 3kg of bicarbonate, just missed the 9% peroxide.
Comment in BoldEdit: eh the solution is crystal clear and i got a blue sediment, i guess it was a success but i wish i had completed the reaction i had plenty of acid there, enough to eat 3kg of bicarbonate, just missed the 9% peroxide. What do you mean with this, what should the 9% peroxide been doing?
I have used a tiny bit of 5% peroxide oxy water and a couple bottles of 3% peroxide to get a mild reaction upon heating the water of the bucket that initially contained the smaller bottle, so instead of getting better and more hydrogen peroxide i quit to soon and neutralized the solution, thing I regret as i wish i had finished it. I used 3 kg of sodium bicarbonate to neutralize about 5l of solution then tossed about 500ml of ammonia to make sure i don't leave a acidic solution behind, today, upon stirring the "grease" film (probably bicarbonate) from the top i noticed the solution is crystal clear and with a fresh smell of perfume from the ammonia. The green solution turned blue by when i were done neutralizing and a blue precipitate came, which, i think it's either nickel either chromium oxide, quite beautiful, tomorrow i'll clean it up and save it.I'm not sure I'm comfortable unless I urge you to put the chemicals away and start studying again, if you ever have studied at all.
You have been a member for 3 years and have not read much yet if I understand your comment correct.
Obviously you do not understand much of this.
No oxide or other salts of metals will cement another metal, it can precipitate a metal as when Ferrous Sulfate precipitates Gold.
And there is no such "thing" as a blue thing in Chemistry.
Mixing random Chemicals on a whim like this, may injure you or worse.
Next time you plan to do something, I'll recommend that you post your plan here so we can correct errors or adjust procedures.
Comment in Bold
I'm still confused regarding what you did.I have used a tiny bit of 5% peroxide oxy water and a couple bottles of 3% peroxide to get a mild reaction upon heating the water of the bucket that initially contained the smaller bottle, so instead of getting better and more hydrogen peroxide i quit to soon and neutralized the solution, thing I regret as i wish i had finished it. I used 3 kg of sodium bicarbonate to neutralize about 5l of solution then tossed about 500ml of ammonia to make sure i don't leave a acidic solution behind, today, upon stirring the "grease" film (probably bicarbonate) from the top i noticed the solution is crystal clear and with a fresh smell of perfume from the ammonia. The green solution turned blue by when i were done neutralizing and a blue precipitate came, which, i think it's either nickel either chromium oxide, quite beautiful, tomorrow i'll clean it up and save it.
I trained a bit my pulse with these things for when I start dealing with my electronic scrap, which given my hobbist level is quite a bit.
I will read enough by when I start doing this and will post my plans here, i'm currently having a good overview over hook's book.
I seen a lot of sreetips but he only deals in precious metals.
Seems i had forgotten to stir, there was a lot, and i mean a lot of bicarbonate down there, there were indeed two different metals besides the silver plating, and not that much had dissolved.
How about studying?I added about 1,2 kg of plated silverware 3x 1l bottles of 26-32% hcl and 2.5x bottles of oxygenated water, which is water, 3% hydrogen peroxide and a bit of citric acid. I did add this somewhat slow.
The peroxide was consumed really fast, if i keept adding i would of had all the base metal dissolved pretty fast but i didn't have any at hand.
I were close of buying some 9% HP and finish getting the base metal, filter the silver and cement the base metals but i didn't and will make a ingot off leftover with a tiny bit less of base metal. But honestly, at 9% I already start having my doubts on if silver could dissolve or not.
I basically wasted a good bunch of HCL, luckily, it is still fairly cheap.
Today I will finish cleaning up the silverware, the copper oxidation bucket attempt and the iron oxide bucket, next time i start pouring solutions it will be in where i have some actual space to get this going.
I'm very excited about my electronic scrap, i nailed one of the first CRT tv's and the boards supposedly filled with palladium hehe. I have about 20-40 kg of boards I raised from incalculable amount of devices, 3 kg of ram/IDE cards and these new batches of really thick gold plating cards, i'll try to get as many of these as possible. Pretty well for a hobbist first batch imo .
I been pondering, for a good while now, about the perfect way to extract lithium from batteries, my lithium battery stash is fairly small but annoys me.
So my idea was having a big enough container, atleast 1000l, and have the lithium perhaps even burn down there, I read lithium oxide is very water soluble, if one could manage to contain it under water while it burns would have a safe means to extract the lithium and then separate the copper from the inside and the inox/nickel from the outer cover. I'm still amazed people discharges them in water without catching on fire.
There is just pennies worth of Silver in the plating.I studied for past years, but only about precious metals, as said, this is small scale and only cost me a few euros, or the equivalent of three beers at the bar.
Started this because boredom mostly, I would love myself a electrolitic cell but i definetly not have the space yet for one.
I'm pretty sure I could of completed this reaction fairly fast if i had the right, and enough peroxide.
I'm definetly not touching any PGM and will leave it all in a bucket till i get more experience, I don't mind have a silver or gold ingot with all the PGM as impurity, feels also safer.
I also don't plan on selling any metal.
If i really looked after money, and got this reaction till the end, silver would get out of the equation and the oxide/reactants of the chromium/nickel would of paid off for all I spent in acids.
Thank you all for the assistance and the worries!
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