Ran into the Medusa at a new job, quickly was able to come up with a solid work around!

I have jars to prove it, I just like being in the sideline observing and soaking in knowledge.
I first noticed this worked on march of this year. I was post processing like I normally do to separate my isolate and terps and I noticed that the diamonds that formed in my terp jars were normal and not rectangular in shape. Also they did not “Medusa” after being out of mother liquor. I actually enjoy re xing in pentane so I never really got into this discussion. I’m glad others have found the compound that’s causing the problem. Now just adjust old SOPs thy worked for years to new SOPs thy need a bit more refining.

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:pray::heart: Keep crushing brudda

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Nah it’s definitely the soapy water. I need to put in an order for soapy water. I’m not sure if I’m qualified to use soapy water though. I better check the MSDS, i haven’t handled the substance in years.

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can you explain fractioning your oil please

You could ask @Swet254k for clarification and look @murphymurri’s Instagram.

They’re not doing quite the same thing, and I don’t have time to try explain two tek I don’t perform.

Murphy does chromatography and literally fractionates her pour(s).

Some exploration over here: Color remediation chromatography

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Thank you, your info was very helpful in referencing her crc chroma,

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@Swet254k I would love to hear your input on why your fractioning alleviates this issue

Crc and chroma should be regarded as two separate things. One is a hammer and one is a scalpel.

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I hate to say it, but I am here again to say after discarding my gas and changing it after who knows how long it’s last been done, my work around is no longer working. I’ve distilled at 170F and closed everything off to allow solvent to reach 165f (verified with thermal C’s) burped a few times hoping to have released any contaminates and the new solvent just won’t allow my work around to work.

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Thank you for coming back and sharing the update with us!!

Sorry it’s being more persistent than before.

What’s changed since your last successful remediations?

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I discarded the old gas in the solvent tank because no one could tell me the last time it was changed and right when I put fresh gas in, it’s been unstoppable. I’m assuming the old solvent was just ran through sieve so many times we slowly got a big portion cleaned up.

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And ofcourse, it’s never easy but it’s something that will help us all out before spending days trying to distill hot

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Did you clean the solvent tank or just discard the contents?

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Soap and watered it big time. Jk haha I did definitely do a quick etho wipe down

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How do you clean your gas before hand? I don’t have consistent results yet, but everything I’m reading about DEA and MeOH are pointing towards carbon working, though apparently coal works better than hardwood/coconut/etc.

If I can get the parts together I’m going to rig up a 4"x24" column or taller and fill a couple socks with carbon and alumina, respectively, and pass thru that. If it works consistently it would be the simplest fix, because it also remediates the other contaminants that popped up this year. I think it’s down to figuring out the best source of carbon (not brand, but the material it was sourced from)

I don’t have alumina yet, but so far the carbon seems to be working if I use enough during the cleaning. Just gonna keep playing around until I can say for sure.

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I was telling you it helps but it can’t fix a really bad tank. No sop can other than crashing sugar and ripening it into bigger rocks.
That clean and brand new gas has humbled me a few times

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I’m gonna get this shit fixed. Mark my words. It’s been such a fun “welcome back to extracting” gift hahahaha

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Sounds like first time it was methanol for you and this time maybe you got amines. Much higher boiling point.

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Hey man, I hear Whole Foods has a killer deal on their carbon rn :sweat_smile::joy:

Sorry lol.

Anyways, multistage it with AA and potentially 13x beads or 4a beads.

Carbon first, then alumina, then the beads.

Powdered/pulverized carbon is what I would recommend, not larger aggregate. Source of carbon isn’t too important, more so available surface area. (Powderized)

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