ahmadbayoumi
Well-known member
Hello ALL,
Seems that things get better from one trail to another.
For my 2nd experiment for processing RAMs, I started with 2ks of normal PC RAMs.
Then, ended up with about 140g of closely trimmed fingers and 570 IC chips.
1st, I started to process the 140g of fingers using AP.
tired this time to be patient as much as I can and to avoid all my mistakes from the previous experiment.
I followed the steps exactly as it should be and got a quite good gold powder precipitated in the bottom of my flask.
I washed 2 times with plain water but I faced an issue that there was always some gold powder floating on the water surface and I was unable to decant the water.
So I decided to boil the flask with the water (150 ml) and gold.
But I believe it was a bad idea as once the water started to boil, the gold powder stared to boil also and after evaporating all water the remaining gold powder was attached to flak and got stuck and I was unable to collect it.
So, I decided to dissolve again using AR.
I did the AR and again tried to be patient as much as I can and added NHO3 in very small increments.
The workaround worked quite good and I got again Aucl2 ready to gold precipitating.
I used a little bit of sulfamic acid to make sure no free NHO3 in my solution.
The gold powder precipitated this time was quite shiny and looks really like gold (not brown powder) and looks like very fine gold particles (mash) making ride stones.
This time I was able to decant almost all water and the then evaporated the remaining water by putting the flask in low heat.
Then left the flask to coll and collected the gold and it was 0.5g of shinny gold.
My question now, why in the after re-dissolving the gold I got this shiny gold mash rather than brown gold powder ?
My 2nd question is 0.5g of gold is good yield out of 140g of trimmed finger ?
Thanks for your usual support.
Seems that things get better from one trail to another.
For my 2nd experiment for processing RAMs, I started with 2ks of normal PC RAMs.
Then, ended up with about 140g of closely trimmed fingers and 570 IC chips.
1st, I started to process the 140g of fingers using AP.
tired this time to be patient as much as I can and to avoid all my mistakes from the previous experiment.
I followed the steps exactly as it should be and got a quite good gold powder precipitated in the bottom of my flask.
I washed 2 times with plain water but I faced an issue that there was always some gold powder floating on the water surface and I was unable to decant the water.
So I decided to boil the flask with the water (150 ml) and gold.
But I believe it was a bad idea as once the water started to boil, the gold powder stared to boil also and after evaporating all water the remaining gold powder was attached to flak and got stuck and I was unable to collect it.
So, I decided to dissolve again using AR.
I did the AR and again tried to be patient as much as I can and added NHO3 in very small increments.
The workaround worked quite good and I got again Aucl2 ready to gold precipitating.
I used a little bit of sulfamic acid to make sure no free NHO3 in my solution.
The gold powder precipitated this time was quite shiny and looks really like gold (not brown powder) and looks like very fine gold particles (mash) making ride stones.
This time I was able to decant almost all water and the then evaporated the remaining water by putting the flask in low heat.
Then left the flask to coll and collected the gold and it was 0.5g of shinny gold.
My question now, why in the after re-dissolving the gold I got this shiny gold mash rather than brown gold powder ?
My 2nd question is 0.5g of gold is good yield out of 140g of trimmed finger ?
Thanks for your usual support.