Well, since I was the biggest derail-ER...let me see if I can act my age for a change!
I need some help from folks who know the concentrates better than I - I have only RSO in my arsenal for experience, and I looked extensively through some posts but got very confused.
I want to run a test of the "new" thing I have been hearing about - running cannabis oil through a distillation-type setup, and could use some assistance. The temp needs to be 300-400F.
In my mind, I would use my fondue pot (which can go up to 450F) containing high-heat saffron oil (which can handle over 500F before hitting its smoke point).
I thought about using something like a high-school student chemistry set, with a beaker to hold the oil sitting in the fondue pot/oil bath. And then...
That's where I am lacking. I have ideas - there seem to be various glass pipes and fittings that might work. One has an air-cooling swirly tube inside another one, etc.
I am interested in looking at this because I want to see WHY the resulting oil would be so reportedly more potent than any other. My gut actually said, and still kind of says, "Are you NUTS? You'll blow out most of the other cannabinoids and all of the terps!".
So far, the folks I have seen working on this (saw it on skunk pharm site, and Rick Simpson's website) haven't emerged with specifics - just a constant "wow this is the most awesomest ever". And they swear (being who I am, I want to see data data data) that they are preserving *more* testable terps in the final product. (Of course, I did find cases where some folks just added terps back in, but that was the exception not the rule).
I considered that if it DID have some merit, then maybe the clue was on the decarb chart we all have seen (will include it below) and many of us have used.
I originally was looking to the RIGHT side of the chart to see how LOW I could go with heat and still get a decent result. And I think the answer might be there on the chart already, but on the LEFT side.
If faster/higher heat leads to better THCA-to-THC conversion, but the drawback is that then at 70% decarb or so (according to skunk pharm) THC-to-CBN conversion begins to outpace THCA-to-THC conversion, then MAYBE there is something about taking it to the temps they are talking about with this new method - 300 to 400F - that BYPASSES that "rule" and actually allows THCA-to-THC conversion to continue outpacing THC-to-CBN conversion. Or maybe creates a ceiling for the THC-to-CBN conversion, etc. A different action on the "A" part of "THCA" at those temps that doesn't effect "THC" stripped of the "A" the same? Or something completely different.
And I want to try to know the answer to that question, and of course will offer what I find back to FC.
:-)
I saw some stuff for folks who make BHO that looked somewhat similar, though not in glass, but that's okay. And I need to not break the bank on this, since I don't know if I will run it more than once that way.
Anyway, here's the chart. And any assistance is really appreciated.
Peace and healing to us all!