I’ve got the secret to filtering acid solution down to a certain micron pretty well…then u could take it to Buckner a large one if u needed go passed 50micron or 25 can’t remember what my smallest one is but
Surface area is key and ny filter is gravity fed
But its my baby , a secret worth about 1000 to me.lol bc it pours it through the filter and it all trickles out
So what if a guy came into about 5 gallons of mhrb mother liquor of sorts. The original extraction was done, and simply reduced and crashed out in a freezer.
There is deems left in the naphtha, as well as all the fats. The dude didn’t defat at all.
I’m interested in defatting and reducing the solvent volume to get another crash.
I haven’t gone over to the Nexus yet to reread various methods to figure out how I’ll proceed…but that’s the plan. Kinda excited to play…but also have a full schedule and not much room for new projects.
Get the solution really hot like 170f and add mkre.naphtha. keep the naphtha…evaporate some.the naphtha then cold crash it…if nothing comes off then evaporate all the naphtha see if something left, if there is then reX in heptane to clean it up some
But most likely they did the main pulls and got it all
Btw u can’t defat once uve went to base ph
the yellow goo IS NOT FATS…I’ve did 3x defatting on mhrb and acrb it always has some yellow goo that will dry and depending on dmt.content crystal some
its nmt mainly and mhrb has less of it than acrb
The hardest part making deems is straining that powdered bark…glad I come up w a way much faster that doesn’t clog really
So as I’ve evaporated solvent, something has fallen out of solution into a goo on the bottom of the pan I was using. The solution turned from a clear yellow green pickle juice look, to a murky pickle juice. Something was wanting to come out. So I poured it off into a 64oz mason jar for later. Returning to it, it us clear with some sediment at the bottom of the jar.
The original extractor usually stops after a 1% yield. There’s probably something left.
Heat the jars up to melt it back into the solvent and start filling a glass pan…as more evaporate add to the pan…it’ll start falling out like crazy
Sounds like ur guy only takes the white pure dmt but I say it just like this
When u extract live resin…do u wanna dab just plain thca or thca and terps
Well both these ingredients are active alkaloids that will make u trip ur balls off and the yellow goo holds a bunch dmt in it usually
Pour the solvent into glass pans…put fan over it…as the pans evaporate down add them together…whatever sticks to bottom on the pour off scrap into next pan full solvent
Whens its done spread the goo out on parchment paper hit it w vacuum pump…then leave it out to dry…will become a badder look thats highly and I mean highly potent
My customers complain if I leave the yellow goo out and just send out dmt carts…they want a full spectrum…which ur passed bc he took majorities of dmt
But you still can be left w yellow crystalline powder or yellow badder like material
I can show u how to try and crystallize it once all evaporated out and u got all the goodies
So recently, my ex wife has been going through some issues, in her new marriage and life in general. It’s her normal way of existing. She had lots of trauma as a kid. So she was interested in these now legal ketamine treatments for her depression etc. I brought up DMT as an option. She was interested. I got her set up with a cart that as you say, had some goo. The next cart she got was with a very light yellow dmt…the shit that was pulled from my pickle juice. So anyway, the ex wife complained about the second cart, that it wasn’t as strong. This could be why?