Failures

Great idea for an amusing thread, @anon93688! I wish I had room in my brain for all the fails in detail, but I usually just do things the right way with vague but strong semi-conscious alerts to pause right before I make a mistake. I could definitely say what NOT to do if I were explaining a specific procedure, though!

Ooh! I know! Do NOT add a stoichiometric equivalent of cannabinoids as MgO to a distillation flask of crude! Less than a teaspoon per liter of crude is plenty! More than that will turn into concrete with the resin, fucking up the distillation mechanics, making you want to push the temperature way too high just to save it, which can generate an imploding fireball if you vent air into it while hot! Yes, you can reach the actual flash point of cannabis resin in a distillation process! If there is high CBD content, any incoming air will make the condensing vapor turn bright purple, too, but don’t risk it!

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Oh I love this one :joy::rofl: we all been there. Eyes wide, excitement , this is gonna be greee… bang crash pow awww shit. I had a pressure filter looks so pretty slurry layer after layer… and foomp sinter disc imploded sucked shit in my shit awww shit

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Ran 4.5lbs of fresh frozen with 500 grams of Activated Alumina in the extraction column and 500g T-5 in the CRC. Ran cold butane and cold column (-78°C) and what I got out contained no cannabinoids.

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Opening the valve to an unknowingly pressurized keg of etoh and getting blasted in the face with like 2gal of -80 crude.

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Growing cannabis/dating a female wook

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Open blast crc
Open blast at high altitude

Prv (rubber stopper) nailed me in the face and once again Cannabis hair gel. I expected it to happen on the crc and was wearing goggles

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Haha I had to shave my beard once after getting sprayed with bho to the face.

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Made a huge batch and put my vacuum chamber lower then my vacuum pump. Gravity took its course and ruined the whole batch. Didn’t have any way to remediate vac pump oil at the time. Total loss

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Um I think that’s every guy every field of work :joy::rofl:

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Yeah, but not everyone has the skills to fail as spectacularly as I did

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:rofl::joy: oh man I love threads like this. Give her the ol kb. Aka kick box ha

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Probably my favorites from my early days were:

  1. Using a shop vac to empty a biomass column without checking to see if there was a filter in the vac. Covered the entire extraction lab in a film of dust, we found bits of it here and there for 2 years after

  2. Accidently let a heat gun power cord rest against a 170c thermal fluid line which turn ruptured and pissed hot fluid all over a WFE, luckily it did not get on me.

  3. Classic over ramping of vacuum and temp on undecarbed/degased crude causing rapid expansion through the distillation head and distribution head on an SPD

  4. Using the wrong PRV on a SFE system being run autonomously overnight, causing a large amount of crude to needlessly be splattered on the lab floor, also cooling and hardening overnight.

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Ooof. That sounds rough…rough stuff

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  1. Don’t microwave wash bottles to heat solvent, blew up a microwave like that… surprisingly enough it was from super heated acetone that super boiled all at once.

  2. When back filling your vac oven with inert gas don’t forget about it… I did and it blew the seal off the oven and killed the vac gauge.Oven still “worked” after but was not great.

  3. Always have a backup pump on your vacuum mantifold, I had a pump that electrically failed right as the head fraction was coming across.

  4. Gaskets … gaskets will leak from time to time from damage, improper torque, or simply worn out. Vigilance, a few room air meters, and a A/C sniffer will keep you safe. I have seen leaks form and had to deal with some situations that otherwise would have been an emergency if I had not dealt with them.

  5. valves… they can leak too, make sure you have all the tools you need to work on your extractor near by.

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MAKE SURE YOU USE A THERMO WELL.

One of my first big boy runs in a 5L i did not have a thermo well and was using a normal threaded coupler, at about 150c it failed and boom, ruined run, everything was volcanic rock.

Also be careful who you buy crude from! one of my clients got sold 10 gallons of wiper poop.

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Had all my heat exchangers freeze up, off grid mind you. It was quite a nightmare had to dump 12 columns into the collecrion. Then bleed and let det thaw over night

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Started vacuuming a jar with the lid resting on top of it (not screwed on, just resting on top) after the jar had been in the freezer for 24 hours. As soon as the vacuum depth in the oven reached a deeper vac depth than was inside the jar the whole thing exploded, covering my oven with a thick film of Tangie. Now every time I open the oven I get smacked in the face with orange peels

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Refluxung d9 with d10 contaminated material with T41 in the pot doesn’t get you anywhere good. You get d8 and d6a-10a. Maybe that’s good?!?

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Using supercritical CO2 extracted crude in hopes of making diamonds in alkane is not worth anyone’s time.

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What if you winterize co2 extracted crude then try to crystalize in an alkane? All without decarbing

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