gotcha. yep, letting your fresh material thaw while/before solvent washing is certainly on the list of ways to get your solvent wet.
it is generally avoidable. which is the preferred method.
going back for that second pass during R&D qualifies as due diligence imo, so don’t beat yourself up. You’ve learned something. possibly a couple of things.
you’ve also shared that learning so that the rest of the gang doesn’t have to try it for themselves.
we have been extracting fresh frozen biomass, around -25c, ethanol for solvent.
we have been buying new ethanol. after so many extractions the proof was down to 140. reproofing would suck
That’s a bad idea for a lot of reasons. First, even if it does remove the water the sieves get very hot when they work. Certainly hot enough to to decarb. Second, they are very prone to creating a silty dust that will contaminate your oil. I’ve never tried it, but I don’t think I ever will.