Bowb Aandweeve
New member
New to them,never had anybody else' concentrates, so I have no benchmarks and I'll be honest, with all the designations, I don't know what to call what I've been making but I do have a question. My process is freezing partially dried crushed bud in a thermos, adding 4x butane to cover plus an inch, then returning to the freezer for a 60 minute soak. I strain through a unbleached coffee filter, into a white Corningware casserole dish. I then put that into a water bath for initial decarb. After major solvent is gone, I put it on a heat mat at 100F , in a thing film method until ALL bubbles are gone. I then scrape it, ball it and let it sit again until it spreads out flat, then it's cooled and good to go.
Now the question-ish thing: I've found that if I leave the cover off the dish during the violent initial decarb, water vapor seems to mix in with my product and it never gets a nice clear color and stays a very moist consistency but if I cover the dish I get pure honey colored hard candy. So, is leaving the cover on, doing me good by keeping water vapor out or bad because even though I have absolutely no bubble in my product, it's somehow still saturated with some type of byproduct?
Side note: Sure tastes good.
Now the question-ish thing: I've found that if I leave the cover off the dish during the violent initial decarb, water vapor seems to mix in with my product and it never gets a nice clear color and stays a very moist consistency but if I cover the dish I get pure honey colored hard candy. So, is leaving the cover on, doing me good by keeping water vapor out or bad because even though I have absolutely no bubble in my product, it's somehow still saturated with some type of byproduct?
Side note: Sure tastes good.