I have a scenario… when it comes to steps of cryo (2days -70c or lower), then evaporation to 1/3 of jar then cap (all at room temp, lets say 75f)
- Pour extract from collection pot to pint wide mouth mason jar (473ml whole jar), fills to about 250ml then loosely place lid and band on jar, and set in crushed dryice filled yeti chest for 2 day.
Now here is where it can go in a couple direction’s. 7-8 out of 10 times, there will be thca bloom, and other times there will just be a layer of (what looks like sand like) crash all at the bottom of the jar.
I can say when there is a full bloom the crystalized end results are way better then the sand like layered bottom bloom.
After reading other testimonies on here and OTSS tek forum, ive come to a mixed conclusion…
BTW the material is not a factor, like others state it can be done with sugar trim and larf. This was done with mix of trim/larf nugs
Solution was at proper solvent evaporated to extract ratio parameters. (Full bloom), proper saturation levels for bloom occurring.
There was more solvent then neccessary for a proper thca full bloom, thus forced the crash to bottom of jar and (layered like sand bloom)…
Improper solution level for bloom to occur…
-With this explanation (2.) Would the solution need more of the solvent to evaporate and lowering solution level in mason jar then putting back into cryo?