I like coffee.
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Have you ever had the kind of coffee that is made from beans that have been shit out of an animal? Bucket list for me. So far I’ve only eaten gummy worms from a strippers ass.
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2I am curious what in the coffee beans might be extracted by mammalian digestion… Or what in gummy worms may be extracted by dancer derrier…
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2Have you ever made cannabis smell and look like coffee grounds?
there is a way… not pleasant one… but it's possible
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Shit…… I took that as he likes to eat shit. To answer your question, he’s extraction shit from the dancers derrier.
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Pay me $1,000,000,000
It's pronounced
LEMON-NINE
But i've squeezed a lemon or two once.
got kicked out of the store but i'd say the extraction was a success
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1Seeing that for the first time really gave me an idea of the solvent potential of terps in relation to rosin
My brother brought that to my attention and it just sent me down a rabbit hole…
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When you recover your limonene solvent all of your Pinene terpinolene terpenine and all the limonene isomers are going with it
So maybe for crude
And don't push with CO2
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And everything with a lower boiling point and slightly higher as well since we always overshoot a bit
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Limonene is really hard to remove the last amount, it has a high BP. I had some people who I worked for like 6-7 years ago that tried it. They left it being vacuumed over night pulling on multiple other ovens that had shatter in em. Next morning everything had turned to goop and auto buddered. I couldn't stand them, it made me laugh because I had nothing to do with it. I was only there to make crumble, because they couldn't "figure it out".
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get some. Mix ~1g in 40mL of etOH. Then you can put a drop of your disty onto a paper plate and then a drop of the KOH onto the disty. If it turns as purple as Barney’s Dick, you still have CBD in there.
I’ll send you the writeup. But I think there could be some CBD remaining in there. Do you use an adsorbents on your first pass?
23,000g 99.9 cbd iso to 450g t-41
15% by weight
was doing 10% previous a d someone suggested bumping to 15% to make sure all CBD has isomerized
so i gave it a go and now im left with pink in high volumes… crystal water clear in small volumes. i highly doubt its just chromatic aberration
someone told me previously that it could be oxidation because my SPD unit wasnt running inert??
my argument would be that i would develop a ring not an entire hue change of the flask but my knowledge and experience is very limited
I have found that too much adsorbents can definitely yield a pink/red hue when distilling. I have never attempted a bf RXN as I have always followed the reactor SOP. We use 1.5% adsorbents and we generally get a very neutral color
2Makes sense. Heads looked clear, and then the rest of the oil had time and temp to change color with the presence of too much adsorbents.
2It could be a possible culprit tbh, there’s a few factors meaning you have either powders left over which if your filtration after lle is good I don’t see why you should. Then second, water content being present & not dealt with can cause unwanted color change to happen as well. I suggest sodium sulfate to pull the rest of the moisture some will suggest mgso4. You can pour the powder into what you’ve collected the organic layer in(flask) and watch the salt absorb the water content then filter it all out over a 25um filter or lower. Then roto & spd.
No brine washes won’t pull all of it from the organic layer, you’ll still have a minuscule amount.
1You're not cutting right
1That's the beginning of your heads
And if you run with powder, when it hits dryness you're going to send powder through you system
You'll run through clear then purple then pink then clear almost yellow tint
You can start at the yellow
You also might be going too fast through your heads to catch your main
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Wow, i dig the new layout. Okkayyyy
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@c0dean i think you should spend some time reading here on the alkaline beam test. First you need to ensure that you are getting complete conversion. If not, your color will not be right. After you ensure complete conversion, you need to spend time dialing in your adsorbents. On first (and only for us) pass, we are using around 1.5-3% adsorbents. Everytime we have used too much adsorbents, we get distillate that looks like yours.
3thanks my man @MedicineManHempCo i appreciate it
hey @MedicineManHempCo i used 5% and its turning out MUCH better thanks for the spoon dude
1Nice job brotha! Feels good to be able to contribute back with what I’ve learned so far
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So start sad thread…
said
Was just checking to see if there was one first…search results are terp heavy but didn't see a specific allocation thus far 
I shall kick it off
Curious if there's an obvious difference between the lower and higher testing strains. Do the higher testing varieties generally always have louder profiles?
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