Yea I ran a couple runs anyway by just pumping the total solvent over the biomass and I’m going to test it but I have a feeling it is inadequate.
Once I get the results back I’ll hook up a recirculating system and just recirculate through and then do a quick wash with fresh ethanol for the final minute to pull off all the residual I think.
As others have mentioned, that is really what gave us the best efficiency doing traditional ethanol soak in a centrifuge was during the spin dry cycle, we would rinse the biomass with fresh ethanol from the CIP spray ball for 2-3 20-30s intervals. It brought us down to <0.3% THC remaining in the biomass post extraction, often times much lower.
This is definitely a thought I’ve had, but my concern is always the balance of time:color. I do believe that cusomers want a light colored oil, but in my areas they almost exclusively shop based on potency… which is silly.
This rotovap is already the incorrect tool for our scale and I feel as though if I run it much cooler it’ll take days. I will probably try it just to do it.
We use a welch pump on rotovap and usually hover around -25"Hg (digial gauge/bullseye used elsewhere). Should we compensate for the cooler temps by pulling the deepest vac possible? Or will that leaves us back at square one?
Oh that’s a fools gambit! People telling me “You can do X, if you’re determined” is a fantastic way for me to waste a whole bunch of time. Usually resulting in me doing it, but hating every second of it.
I’m not super confident in the little welch that could being able to go deep enough to prevent excessive run times. If my lab partner wants to go for it we will though.
It’s actually decent quality biomass. It was harvest less than 3 months ago, hand trimmed, some smalls/larf, and obviously completely cured. We’ve had different growers biomass produce a much more magnificent yellow color, but our in-house biomass has almost always produced this color.
Hmm. I’m not really sure then. I admit i don’t have a ton of different biomasses I’ve run by this method. I definitely did observe some browning when the temp was up and had to keep below 40 to stay golden.
I am quite familiar with DOE but we haven’t invested in any DOE based software to assist with this and if I’m going to model DOE and run statistical analysis I would much rather leverage software than trying to do it all manually or with excel :).
I mean really the best way to give anyone advice from nanoemulsion formulation to experimental extraction can all be told to use a DOE type methodology.
Either way I’ll definitely end up sharing the results I get with or without applying DOE methodology.