Lol. Yes i didnt put a proper relieve valve on the vessel i was using and got impatient.
Reading along iT Sting to mind would iT make sense to collect globes of fat and
Clean them up real good and Ad back to sapy shatters that don t want to stiff up
Anyone dooing this ?
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This happened to me one day. Holy chit, i really made a mess that day. 
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Bad part is it was for a client
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Dirty 
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Yep thats coming out of pocket ffs.
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Start material
Finish but not purged all the way
Dissolved in isotane
Put in freezer
Filter through 25um filter paper
Filled a dewax column half full of isotane, dewaxed for 2hr with 99.9 isopropyl and dry ice
Sent through 50g t5, 100g t41, 50 silica, with 25um paper, 5um disc, 5um screen, 6um paper, 2 um screen, 2.5 um paper, 2um screen.( i know my order is a bit off with sizes) .
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Isotane ? Whats that ? Iso butane i guess with iso propanol ?
Yes isobutane
99.9 Isopropyl alcohol/dry ice to chill dewax column
Ok so dissolved in iso butane inside a sleaved jacket Wich was cooled by isopropyl and dry ice
I read ithe first time like WTF this Guy is mad iso butane iso propanol and dry ice inside the dewax colum
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I disolved with isobutane in a 6 inch site glass and put into a household freezer.
Then filtered through 25um paper filter. Second dewax chilled with isopropyl alcohol and dry ice
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Do you have to worry about thca crashing out?
No i didnt, was multistage dewax
So, when everyone is complaining about this happening. Let’s say, maybe, you dewax 15 grams of fats. 20-25% potential thc. So you are concerned with an ⅛ when you would be dumping a half lb of oil.
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I think maybe you misunderstood. I’m not concerned about losing thc in the lost fat I’m wondering if doing that could cause the cold crash bloom type things you see when making thca diamond and maybe screw something up not allowing it to turn into shatter.
Ah. I get what you mean now.
Are you slabs solid? Majority of my slabs that come out looking like this are very maluable.