Greets all:
In preperation for SWIK's first LWR, he decided that there's no such thing as too-clean pseudo.
SWIK had about 20 grams of "clean" psuedo. He had extracting a bunch of generic 120s via the tetra trap method. He had also done 3 x NaOH and 1 x distilled H2O washes of the pseudo (and removed a grey emulsion, thanks Geez!). But being the paranoid type and not wanting *any* emulsions or GAKK-related post-workup problems, he decided that he'd expose the freebase crystals to the Japan Drier thingy.
SWIK took a 200ml solution of Japan Drier/Tetra (20ml/180ml), warmed it, and threw his 20g of freebase crystals in a waited an hour or so. He then filtered out the crystals and washed them with acetone until they were pristinely white once again.
Well, SWIK's got nice white pseudo crystals, but only about 5 grams worth!! Surely the other 15g of what SWIK thought was psuedo isn't all GAAK?!
So how does SWIK recover his other 15g of psuedo? He's got a 750ml solution consisting of about 550ml acetone, 20ml of Japan Drier and 180ml of tetra. SWIK knows he could just evapoate the whole mess, but he's concerned about the napthalic (sp?) salts. Aren't heavy metal salts of cobalt, etc., poisonous? Wouldn't evaporating the entire solution result in some heavy metal salts? How could SWIK possibly seperate the psuedo from the heavy metal salts?
SWIK tried putting the solution in the freezer for a couple of hours hoping the psuedo would crystalize, but no such luck.
SWIK thinks, though, that the Japan Drier migrates towards the bottom of the solution if left undisturbed for a couple of hours. He can see what appears to be two layers, the bottom 1/8" of his beaker appears to be a different color (almost white) than the rest of the solution (purplish brown) when left in the freezer for a couple of hours.
Advice anyone??
TIA,
--KidClean.