that the same thing as italics? But country slang put in to it
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Eye-tal-ics
At least I think that’s how it’s spelled
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Check out .20 micron cartridges. They have fantastic flow rates compared to welded disks.
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Have you tried breaking a gram of the “diamonds” while it’s still in diamond form, and gotten it tested? Should definitely test a gram to see the % of thca present in the “diamond”. I assume it’d be in the high 90’s-99.99% range if it is in fact a pure diamond and not something else.
That’s some crazy shit.
I noticed bubbles too, what’s up with that?
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How long did it take to form and at what temp
I. Going w to fast forming it didn’t seal over…bc if u look close its sugared throughout the whole thing
Was this a cold formation formed?
U said this was reX of thca, then I’m going w u never got everything dissolved…u had microaugar forming this which was inclusion city
Take it outta the solvent,the evaporation all way through the stone causes auto sugar bc was never fully melted in the solvent
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Stored under atmosphere! Have had some stored in a closed space (mason jar) and some left out in the open in a pyrex dish with some press and seal. Both with the same reaction.
Had this guy change over the weekend!
This was 12 hours after separation :
After the weekend stored in a mason jar in the dark
This is what they look like broken up
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We run through a 5um disk---->1um disk---->0.5um ptfe felt
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Humidity of the booth/post processing room has been sitting around 30-55% recently
So it’s not just a surface effect, they transform the whole way through?
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What’s the yellow liquidy hollow dot in the middle where it was split? I’m no expert, but that makes me think you have a bit of solvent trapped that is eating it’s way out like a crack in a windshield.
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Explain ur growth method…are u taking a bunch washed crc thca? Melting it in butane,?
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The first image was a cryo run. Probably not lower than -20F for a couple of days. Pulled out until room temp then left open for half an hour. Capped then fully dissolved after about 3 hours. Diamond growth took around 3 week’s at 66°F after full dissolve.
The other images of the original post were not cryoed. We ran into an issue about a week or two after the first image where jars put into cryo would not re-dissolve after being taken out. Still have that issue. Jars currently crash like this from pour :
Usually we just pour and cap if we do not do cryo. Straight from biomass no washed crc thca; just filtered and poured.
The second and third image of the original post are re-dissolved thca. Separated from the mother liquor then melted down in butane and re-crashed (crashed like the video originally and attempted to re-crash into diamonds). They did crash into diamonds but then started chalking up like the rest
Yes they transform all the way through!
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Either it all hadn’t turned yet or there was a facet hiding on the inside Will keep an eye on it to see if this piece will turn as well. Seems the change occurs from the outside to the inside
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Its ur cold as growth probably…plus if ur using crc ur using way way to much powders
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oh
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Take a few grams & drop them into 10 ml of acetone, allow to fully “homogenize” then add 2 ml of distilled water, take a video & post it here please, it’ll may show you if you have a spore issue or moisture issue.
But I also do agree with the gas supplier statement above, there could very well be moisture within the hydrocarbon you’re extracting with especially if not running mol sieve or distilling your gas yourself, then utilizing it for extraction.
Hoping y’all don’t see no floaters once diluted into the “testing” solvent recommended above.
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Will get workin on that right now!
We have two 3"x2’ columns with mol sieve which we change daily/every other day and we do distill our solvent prior to use!
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How are you prepping the sieve beads before changing?
We leave it cooking in an oven at 225F with our clay