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thetruth707
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After removing the ethanol, we run it through either a Kugelrohr, or a Trommel molecular still to produce Clear.would a good way of making this be
Buy a 100L ethanol extractor like Eden labs makes
Then put that product through the clear machines?
I have a legal lab in CA and we can't use butane.
I'm imagining this would work great.
Thoughts?
Greywolf thanks for chiming in.
Quick Q for you.
If you weren't using butane what would you use to extract as much as possible to then make into the clear.
I was assuming a large 100L ethanol extractor from Eden labs.
Then continue through the clear process.
Thanks for your guidance
My second choice of solvent would be 190 proof Ethanol.Greywolf thanks for chiming in.
Quick Q for you.
If you weren't using butane what would you use to extract as much as possible to then make into the clear.
I was assuming a large 100L ethanol extractor from Eden labs.
Then continue through the clear process.
Thanks for your guidance
I think Eden Lab's unit is alcohol recovery, versus alcohol extraction.Ps I don't know anyone using. Large ethanol extractor like this.
I saw Eden labs us one for about $50k.
My assumption was this would be a great start to industrial size clear extraction.
has anyone tried takeing your oil winterizing it then doing this
ive also heard the terps have hold alot of the color in them which makes the me wonder about the terps in general like how this would effect the different sized chain terps or how this method of removeing color would affect the terp yield or quality in general being afterwards ran through a short path setup?Yes, Pharmer Joe mixes bleaching clays and chromatography beads, which works well and which he offers at Oregonmedicalgrowers@gmail.com.
ive also heard the terps have hold alot of the color in them which makes the me wonder about the terps in general like how this would effect the different sized chain terps or how this method of removeing color would affect the terp yield or quality in general being afterwards ran through a short path setup?
dude thankyou so much you are the only person i can find that knows about this stuff i have one final question (id ask more but dont want to be annoying) when i re condense my vapor in the shortpath its my understanding that the bumpy glass piece is designed to re condense my vapor to liquid because of surface space of the glass and density of vapor then its re condensed further and this part is where i am a little iffy i want to get the best re condescension without use of explosive gases or chemicals ive heard acetone and dryice works great together but like i said im anti explosive so i was wondering would dryice work alone or would that not touch enough surface area or would i be better off if i use water and dryice or water and regular ice? and would one compared to the other have a huge difference in the re condensing yield? ive also read about the dryice and acetone condensing oxygen which is also explosive so im a little scared of that one being i am not a chemist thankyou very much for answering all my questions i really appreciate the knowledge being shared :)Most of the monoterpenes are colorless or close to it. The triterpenes are where most of the color resides.
I use methanol alcohol and dry ice. While it is flammable, not much vapor at those temperatures and they are clouded in CO2, excluding oxygen. It is important to have good ventilation with open containers of Methanol.
would a good way of making this be
Buy a 100L ethanol extractor like Eden labs makes
Then put that product through the clear machines?
I have a legal lab in CA and we can't use butane.
I'm imagining this would work great.
Thoughts?
do you think regular ice and water is a bad choice for this? maybe i could get a longer tube for more of a opportunity to re-condense the vapor maybe? or not??
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