but we do edit's very well, we've got your back!And I don’t do technical very well.
but we do edit's very well, we've got your back!And I don’t do technical very well.
I would love to hear about this! I thank everyone for the wonderful input!It isn’t something I want to type up on a cell phone, . I will try to get on the computer and try it in the next few days. And I don’t do technical very well.
Yes! I get all my PMs out by using steel/iron. Is there something i might be missing?Read and follow the dealing with waste thread, it explains it all. Your plan is a bit off from what we usually do. you precios metals should be out before yo go to cementing and waste treatment.
Thank you! I didnt realize urea could be used to neutralize. HCl, i thought that was more of an excess Nitric removal for AR. regarding the scale of my hobbby. I think im just really lucky finding free stuff since I have almost 30-45 pounds of circuit boards. But I just process like 5-6 in cut up pieces at a time.Unless you live somewhere you CAN'T buy Nitric, don't bother trying to make it.
But - for PCB's - the 1st step should be a long (like 1 month long) soak in equal parts Distilled H20 + HCL + Hydrogen Peroxide until you get a reaction. Keep it covered and in direct sunlight if possible to keep it warm. As the mixture evaporates off (leave it OUTSIDE!!! add more of each to keep the reaction going.) This will flake the gold sputtering off of the boards without dissolving too much junk material. (PCB's have mostly copper in them, which makes AR tricky IMHO.) Especially if they are populated boards, going straight to AR introduces all sorts of other stuff from the other components on the board - specifically a lot of nickel, lead and copper.
Once everything has flaked off, you can wash the boards down with water and take them to a recycler or rubbish.
Now you have a bunch of flake in the bucket - wash this well with water, and filter. Pick out as many of the big components that may have flaked off the board along with the gold, but don't drive yourself crazy.
Filter it a few times, then into a glass beaker and add AR to start the normal process. Starting with raw PCB's means using a lot of nitric ($$$) and even more waste solution - where the HCL + HyPerox can be easily neutralized with Urea
Don't expect much - PCB's - even good ones - yield <1% by weight
Most people do a first cementing on copper because it will only cement precious metals and mercury if it is present. Iron will cement a host of base metals along with your values. See When In Doubt, Cement It Out.Yes! I get all my PMs out by using steel/iron. Is there something i might be missing?
This is a very good point. Theoretically, wouldnt HCl bath prior to ap/ar treatment dissolve most of the base metals? Ive beej reading Hokes book and this also has been mentioned. I have been doing HCl baths before anything else. Ive cemented copper and it looks to be relatively pure. If i ever get around to melting it to a bar of some sort, id probably give it another hcl bath.Most people do a first cementing on copper because it will only cement precious metals and mercury if it is present. Iron will cement a host of base metals along with your values. See When In Doubt, Cement It Out.
Dave
HCl does not dissolve copper or other base metals from brass or bronze.This is a very good point. Theoretically, wouldnt HCl bath prior to ap/ar treatment dissolve most of the base metals? Ive beej reading Hokes book and this also has been mentioned. I have been doing HCl baths before anything else. Ive cemented copper and it looks to be relatively pure. If i ever get around to melting it to a bar of some sort, id probably give it another hcl bath.
True and valid. This is all the copper i spent in actually practicing to cement my PMs when i was practicing using very low grade boards and multiple practice on a few small batches (as i am still new). This copper product in the photo is from the chemical by product of recovering silver. Ive used iron to cement out the copper in photo.HCl does not dissolve copper or other base metals from brass or bronze.
And you just spent a lot of time to put copper in solution to separate it from the pm's. Cementing it all back out sets you back to having a mix of copper, base metals and pm's.
Which is a waste of time and chemicals.
I'm trying to make sense of this, but i don't understand what you're saying here.For the copper image (if i ever wanted to refine it and reuse to recover PMs) I was hoping to add hcl to remove other base metals and reuse solution in h202 and hcl bath (for a long time).
I am so sorry! I meant HCL. H2O2 is to create the AP (i understand just a bottle cap first to start it.I'm trying to make sense of this, but i don't understand what you're saying here.
AP does not need H2O2 by the way.
Keep the Peroxide out. HCl alone do not touch Copper.True and valid. This is all the copper i spent in actually practicing to cement my PMs when i was practicing using very low grade boards and multiple practice on a few small batches (as i am still new). This copper product in the photo is from the chemical by product of recovering silver. Ive used iron to cement out the copper in photo.
For the copper image (if i ever wanted to refine it and reuse to recover PMs) I was hoping to add hcl to remove other base metals and reuse solution in h202 and hcl bath (for a long time).
How does that sound? or still inefficient (honest question and wanted to pick your brain)
This thread will be most informative if you do all of your current stash and collect the foils before you process the foils in aqua regia. Hopefully if you are patient we can get through the entire process and have an informative thread.I think im just really lucky finding free stuff since I have almost 30-45 pounds of circuit boards. But I just process like 5-6 in cut up pieces at a time.
This is the most important point in the long run. The more ways we know, the better chance of being successful.5. Next comes separation of the foils but let's get these first steps first and allow for comments from other AP users
Do we want to try and tackle all of these steps in one thread? That will cover a lot of ground and some points alone could become very long if we can get the silent majority to pitch in. Sad to say, but too many just sit and take but seldom, if ever pitch in.I think we are coming into this piecemeal which only adds to confusion. If I were new to this process and starting out we should start at the beginning.
1. I have acquired a few laptops or desktop computers and I want to recover the gold. I disassemble the units to end up with the circuit boards and that is where we should start.
2. The chips and switches fans and IC's on the board need to be removed first. What are a few basic scenario's for removing these items to leave me with bare boards?
3. Most boards are coated with a solder mask that is applied by the manufacturer to prevent solder bridging on close circuits when the boards are manufactured. They also will prevent the chemistry from reaching the parts it needs to interact with so it needs to be removed. How is this done?
4. Now we are at the point of adding the chemistry. If I have enough pieces to fill a 5 gallon pail, how do I proceed? What percentage of water to Hydrochloric Acid and (if any) peroxide? Is an air bubbler preferred? Does this reaction rise, if so I need to leave space to prevent overflows? Finally how long should I allow this to react? Should I cover it loosely? Is it OK standing outside without a hood?
5. Next comes separation of the foils but let's get these first steps first and allow for comments from other AP users.
I agree.In my personal opinion, I would probably discourage number 3. Yes, I know there's a bit of gold there, but if we want a comprehensive, common sense thread, I don't think I would encourage anyone to process depopulated boards. In my opinion, that should be part of this discussion. When to recognize the value of time and chemicals versus any tiny amount of values. Maybe I'm wrong because I've never processed depopulated boards, but from everything I've read here on the forum, there just doesn't seem to be enought left there to make it worth while.
It's kind of like chasing the last few PPM of values in a solution. Yes, you can do it, but is it worth the effort?
Dave
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