NoIdea
Well-known member
Evening All – Cupellation? I have read what Hoke has to offer, spent hours reading all the forum posts I could find on this topic, assume stuff by the way, performed a real cool experiment and now it’s time to ask a few question, if I may. Bit of a description first.
I am having loads of fun, and wish for it to remain fun, in saying that you must keep in mind that I am using rudimentary/crude equipment, charcoal, coal, homemade incinerator/furnace/burning thingy, stainless steel bowls, lead from nail-heads and wheel weights, a spoon, safety wear, and a nice fresh breeze.
Ok, my starting material was pyrolized low and high grade boards, of which most of the components were removed, leaving some chips, surface mounted items, and fingers intact.
After pyrolysis, the material was ground, sieved (the larger bits, greater than 0.5mm are metal beads/ceramics/glass, saved for later), incinerated, boiled in caustic soda x2, washed with hot water x2, and again incinerated producing a fine powder.
The lead consisted of wheel balance weights and lead head nails; I had a small tin can filled with slag left over from melting lead for sale, with all of the iron removed from the lead.
I placed a quantity (?) of the material into a stainless steel bowl, this was placed on the incinerator and brought up to a dull red, at which point I added the lead/lead slag, which weighed (?), waited for it to melt and smoke, added old activated charcoal (from the homebrew Gin days), at this point I started to stir and swirl the mix.
The mixing and swirling caused puffs of brown dust (which stayed inside the bowl), I covered the bowl for a couple of minutes, removed lid, stirred and swirled, periodically adding more carbon when it stared to smoke, repeating this process until the melt started to stiffen, requiring more heat to regain a melt. At this point I stopped, took the bowl off the heat, gave it a few giggles, like you were gently panning for gold fines, and set the bowl on its edge to cool. The nugget so produced looked similar to the nugget to the right in the picture, which weighted 187g. I should note that at no stage after the lead had melted into the sample mix, was the lead visible but I could feel it moving along the bottom.
The nugget produced was reheated till completely melted, and then I skimmed off the oxide slag, which was a rainbow of colours, I stopped before the nugget got too small and cast, resulting in the nugget to the left of the picture.
The slag produced from the skimming was put back into the material left over from the formation of the first nugget, ground in my grinder along with more charcoal, producing the nugget to the right of the picture.
Ahh, now its question time:
1. How do you know when all the lead has been removed? No more oxide produced and is this temperature dependent?
2. Any idea as to the pretty colours produced during the skimming?
3. I read a post where an iron ladle was contaminated with gold, silver, and lead was advised as a mean to pull them out of the iron, at what stage will the silver content/concentration within the lead, prevent this pulling power?
4. Remembering my financial situation, I can not afford the more suitable equipment, so please advice, and comment away, please.
Thanks
Deano
I am having loads of fun, and wish for it to remain fun, in saying that you must keep in mind that I am using rudimentary/crude equipment, charcoal, coal, homemade incinerator/furnace/burning thingy, stainless steel bowls, lead from nail-heads and wheel weights, a spoon, safety wear, and a nice fresh breeze.
Ok, my starting material was pyrolized low and high grade boards, of which most of the components were removed, leaving some chips, surface mounted items, and fingers intact.
After pyrolysis, the material was ground, sieved (the larger bits, greater than 0.5mm are metal beads/ceramics/glass, saved for later), incinerated, boiled in caustic soda x2, washed with hot water x2, and again incinerated producing a fine powder.
The lead consisted of wheel balance weights and lead head nails; I had a small tin can filled with slag left over from melting lead for sale, with all of the iron removed from the lead.
I placed a quantity (?) of the material into a stainless steel bowl, this was placed on the incinerator and brought up to a dull red, at which point I added the lead/lead slag, which weighed (?), waited for it to melt and smoke, added old activated charcoal (from the homebrew Gin days), at this point I started to stir and swirl the mix.
The mixing and swirling caused puffs of brown dust (which stayed inside the bowl), I covered the bowl for a couple of minutes, removed lid, stirred and swirled, periodically adding more carbon when it stared to smoke, repeating this process until the melt started to stiffen, requiring more heat to regain a melt. At this point I stopped, took the bowl off the heat, gave it a few giggles, like you were gently panning for gold fines, and set the bowl on its edge to cool. The nugget so produced looked similar to the nugget to the right in the picture, which weighted 187g. I should note that at no stage after the lead had melted into the sample mix, was the lead visible but I could feel it moving along the bottom.
The nugget produced was reheated till completely melted, and then I skimmed off the oxide slag, which was a rainbow of colours, I stopped before the nugget got too small and cast, resulting in the nugget to the left of the picture.
The slag produced from the skimming was put back into the material left over from the formation of the first nugget, ground in my grinder along with more charcoal, producing the nugget to the right of the picture.
Ahh, now its question time:
1. How do you know when all the lead has been removed? No more oxide produced and is this temperature dependent?
2. Any idea as to the pretty colours produced during the skimming?
3. I read a post where an iron ladle was contaminated with gold, silver, and lead was advised as a mean to pull them out of the iron, at what stage will the silver content/concentration within the lead, prevent this pulling power?
4. Remembering my financial situation, I can not afford the more suitable equipment, so please advice, and comment away, please.
Thanks
Deano