tseuq
Rising Star
Simply_Me said:Why the edit and the change to cold Nap in warm Solution?
The result of my first pull (warm N in warm S) wasn't that clean as I was looking for, but cold N in warm S did the job for me.
Happy extracting, tseuq
Simply_Me said:Why the edit and the change to cold Nap in warm Solution?
Alev-Kev said:JefFlux said:Hi Alex-Kev,
First attempt at an STB (Cyb's hybrid salt tek) yielded exactly %3. Have been looking to see if it is possible to improve on this, as using 'max ion' bore no discernible increase.
As one more familiar with A-B on acacia, I have often wondered if the acidic heat bath stage of Cyb's teks could be improved by simmering the acidic bark-solution in a pot over an element on low heat (60 degrees Celsius) avoiding evaporation ..rather than the standard heat bath method?
Or even just 3 acidic boils and then discarding the bark as one would do for ACRB.
FLux
Hey, Flux
Thx for taking the time... I do, almost boil the whole time, simmering for reduction with water,and then white vinegar. I did strain a cal times, but I noticed that by removing/straining bark that my yields went down. When I leave it in, yields increase. So, I guess moving to the basing of the solution, some alkaloids are still trapped in the bar. I, also, go under the 1:1 ratio for lye, but I don't have a pH meter. The trial n error method produced a seeming 'sweet spot' for enough to keep emulsions to next to nothing, while releasing & binding all the D effectively. I should probably get a tester just for accuracy sake, but all $ has been put into good glass for my experiments, at this point. Thanks again for stopping thru...
A-K









