Ok so I think most of the Teks kind of skim over the wash and re-x you do after the first freeze precipitation…I’d like to really refine my techique in this and a few other areas like decanting or separating…I’m pretty much committed to doing both the wash and re-crystallizing, at least once. I can’t imagine needing more than 1 re-x, I may not even waste my time doing multiple re-x…
One problem I’m having right now is that my freeze precip is not really sticking to the glass anymore, thus I am no longer able to simply pour out the remaining NPS and put the jar upside down to dry. I’m watching tons of goodies flowing right out, like it wasn’t all crystals stuck to the glass it was more like a half inch of sludge at the bottom. So I’ve got a Büchner funnel but it’s so damn slow the spice just reabsorbs into the solvent, or is getting stuck absorbed into the filter.
Does anybody have a technique u like for removing the solvent after the freeze precip? Is filtering really necessary? Or maybe I have to clean my solvent somehow? I’m still within my first kg of bark, maybe just over halfway thru the bag
Also the wash, do I do the sodium carbonate wash by shaking it up so the water cleans the dmt-loaded naphtha solution (before freezer?), or should I wash the dried crystals after they dry? Or should I redissolve it in a minimum amount of NPS before shaking it up with the wash?
Also I tried redissolving in clean naphtha for re-x and another freeze precip, and a surprising amount of junk remains that wouldn’t redissolve in warm naphtha, like a bunch of grains of sand mixed in with the water after I decanted the solvent for freeze precip. Idk if that is significant, and is there anything I can do with this stuff that’s supposed to be plant oils etc but it smells like dmt but idk if I want to even put it in my pipe and junk up the choreboy u know what I mean