It’s just scale brah……… I measured his on my phone screen and your on my phone screen. Same size brah. 3-5mm 
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Ima give it a shot I have a theory on how those are made
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Lol it’s only a saturation of weight of likely your smallest stone brother. Wasnt going for fast tek here. Just playing with the “loosie” stuff. Once I can get a situation to scale I’ll post photos/ video of that as well.
This scale was literally maybe 4g of input & under my view didn’t have only thca in there sadly, I filtered of some coagulation that wasn’t diluting.
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Wow 
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You got dreds down to yiur ass and no power at your house…. Walk around in full army fatigue with night vision shooting nothing.
Ok then. 
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I have ass dreds
When I forget to pay fpl
I have an old acu somewhere over here
I’m plenty inaccurate during the day, thank you
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Well this is him every day. Not a circumstantial wook…….
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Damn, I’m not dedicated enough to #wooklife and everyone can see it.
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Lol what? I have power…and I shoot at bugs…the AR gets them every time…no big deal.
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Also wooks don’t have $$ bills yall
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I thought you told me your were totally off the grid. My bad! He has power.
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thanks for the hints! i have been getting faster and faster, really appreciate these little knowledge drops!
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My 18 hour crystallization I started yesterday, getting closer every day @TheWillBilly strong text
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Looking great man!! nice work!
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Looking great, Keep it up man!
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There are additional steps if one were to go about them a seperate route for much cleaner product. Please read both completely before applying.
Hope these may help someone. 
(Later today I’ll post how to utilize the crystallized terpene(s) after purification processing).
There are 2 different style teks in this write up. So please READ IT COMPLETELY.
Loosie tek/ Fast tek(s)
(Optional steps are not needed but do help!)
- [ ] Use crc (T5/B80/AA/SILICA60A) inline of extraction & obtain a acidic ph range for crude solution. Extract at minimum -65c to -80 preferably to avoid as many impurities (lipids fats & waxes) as possible.
- [ ] Extract high THCA or CBD extract & recover oil to the point of being a solution suspension (+15psig to 0psig). You’ll have some solvent left.
(OPTIONAL STEPS)
- Recover all solvent at 65f-76f in vacuum oven.( don’t worry about decarb at this point)
- Then take thick crude & re-saturate with solvent (methanol or acetone preferably).
- Filter out coagulated impurities that did nothing dilute in solution over bed of B80/T5/AA/SILICA60A.
- Add solution to reactor under low vacuum as to not violently evaporate solvent.
- Ramp Rpms up to 450-550 & apply cold thermal transfer (-45c to -65c) intermittently ( on 10minutes of 15 & cycle till you see nucleation forming.
- Allow all acidic cannabinoid to drop out of solution ( it will be fine grain to sugar consistency).
- Remove mother liquor & set aside in separate vessel to repeat same steps above to make sure you got it all. (This can be done at later time if needed).
- Apply heat thermal transfer(68c to 76c)to reactor m/vessel under vacuum to remove majority of solvent left.
- Rinse solvate with cold heptane to not dissolve any acid cannabinoids & push remaining prior residuals off.
- Remove isolated acidic cannabinoid from vessel to weigh for first yield. Record weight, then add to reactor for LLE with heptane & distilled water at 6.5-7ph. (Additional base washes will be needed for balancing ph for all LLE steps.)
- Dissolve cannabinoid into heptane at 1:1 w:v add to reactor. No heat.
- Add 2:1 distilled water : solution by v:v to reactor.
- Begin LLE agitation for 15 minutes at high Rpms.
- Let settle for 30 to 45 minutes then discard of aqueous layer.
- Remove & filter organic layer over bed of SILICA60A/AA/B80/SODIUM SULFATE to remove additional moisture.
- Add solution to reactor.
- Recover solvent.
- Redissolve in pentane at 3:1 solvent: purified cannabinoid.
- Add acetic acid by .01% v:v & stir Rpms at 200 to 250rpms.
- Observe acidic cannabinoid reforming( it’ll look cloudy till you see nucleation forming [it will be noticeable]. (Do not oversaturate if you do you’ll have to LLE the acetic acid & restart & kill your yield).
- Allow acidic cannabinoid to form singular formations then LLE the acetic acid out at 25c with a 2:1 v:v of solution : distilled water (repeat 2 times).
- Discard of aqueous layer & run solution over bed of SILICA60A/AA/B80/SODIUM SULFATE to remove additional moisture.
- Remove solvent & collect high purity acidic cannabinoid crude & follow steps below after redissolving in terpene(s) or final crystallizing solvent/ terpene(s) blend. (I prefer acetone or pentane as it will allow for a low enough BP to preserve terpenes as well).
- Dissolve at 3:1 or 5:1 blend : cannabinoid then proceed.
(D-Limonene, A-pinene, bisabolol, camphene, terpineol, A-Humulene, & Borneol are terpenes that will be susceptible to higher crashing rates as well.) they will also likely co-crystallize within the crystalline lattice when in contact with the addition of acetic acid (or hcl I prefer hcl )or by themselves in mother liquor you can crystallize these terpene(s).
(Using 5% water gradient displacement to force crash faster with co-solvents
(END OF OPTIONAL STEPS)
CONTINUED STEPS:
- [ ] Pour out into sealable quart or smaller mason jar 2/3 the way full. (Cap with lid & leave band loose).
- [ ] Apply sonication 35hz-45hz (or modified overhead UL listed stirrer at 350-450rpms) to vessel with no heat applied for time being. (It will be experiencing a temperature & agitation dynamic to speed up nucleation).
- [ ] Allow jar to sit at room temp for 1 hour while in a dust free are in a c1d1 hood or vacuum oven that can be evacuated by vacuum as to not allow solvent in your immediate vicinity.
- [ ] Let sit at room temp under sonicator for up to 1 hour with lid on & band loose.
- [ ] Observe for nucleation sites forming individually & then remove sonicator.
- [ ] Set jar on heat in oven or on heat plate at 85f for 1.5-2 hours then remove from heat to sit at room temp for 15 minutes.
- [ ] At this point you’ll have good formation of growth & you can either add sonication again if singular formations aren’t stacking to tightly, or you can allow the pressure from the jar to release for a brief quick moment & it will “pop” the formations loose & then tilt your jar & give it a good patting on the bottom side & watch to observe them to see if they are adequate for your liking. Then seperate from solution & wash with cold pentane to cleanse stones & purge afterwards.
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Did I mess a word up ?(if so please point it out, thought I had gotten all misspellings).
No its just overly complex for a butane extraction to diamond sop
Only 3 simple steps to get this jar Triller
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