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Post SWIM's Yeilds !

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So let me get this straight I’m a little confused , they did the pulls on the acidified purple liquid before adding lye then did more pulls
You'll have to link to the post you're asking about - there's a 'reply' option underneath every post - otherwise it's hard to make sense of what you're asking about in a fourteen-page thread.
 
0,81 g (0,81%) yield from 100 g MHRB (Brazil), via ATB Max Ion Tek, 6x naphta heated pulls, than freeze precip. 95% white cristals. Some bigger chunks remained after shredding the bark. Next time I will shred with a milkshake blender, after soaking. I hope it helps make it way smaller, rising the result.
After pulls I did one extra pull with xilol. The evaporation is in progress, so more goodies (some red colored jungle spice) I expect. My plan is making a solution with citric acid, so will be consumable via oral route. I wont know how much actives will be in this extra product. I tried once like a pharma and it has a decent effect!
 
Just shy of 4.5g from 200g MHRB using some variation of the max ion Tek. Some small portion of that could have been carry over from previous failed attempts at ACRB. Hardest .3g ever pulled let me tell you.

Currently running another batch of 200g of the same MHRB loosely following max ion, except this time I used 0.2 M HCL (vinegar previously) as the acid soak (similar to method 2 in this paper), followed by vacuum filtration through a Buchner filter, and a 3x shake and settle naphtha defat step. Salted tonight and I'll base and pull tomorrow. Curious to see if it'll make any difference in yield, crystal quality or ease of pulling, mostly just fooling around as it keeps me busy. I want to make some ejuice and also some different enhanced leafs, so grams go quick down that road.
 
Just shy of 4.5g from 200g MHRB using some variation of the max ion Tek. Some small portion of that could have been carry over from previous failed attempts at ACRB. Hardest .3g ever pulled let me tell you.

Currently running another batch of 200g of the same MHRB loosely following max ion, except this time I used 0.2 M HCL (vinegar previously) as the acid soak (similar to method 2 in this paper), followed by vacuum filtration through a Buchner filter, and a 3x shake and settle naphtha defat step. Salted tonight and I'll base and pull tomorrow. Curious to see if it'll make any difference in yield, crystal quality or ease of pulling, mostly just fooling around as it keeps me busy. I want to make some ejuice and also some different enhanced leafs, so grams go quick down that road.
Where are the pics!!!!!????

One love
 
The way to go in what regard?

One love
For crystallization. Trying to scrape those jars was pretty bad. I ended up just getting most of it and just hit it with a little more NPS to redissolve it. I've tried the glass food containers with plastic lids with silicone seals, they seem fine, but the plastic is probably warping.
 
So I finished evaporating my first three pulls from the above and beyond method above (filter, defat, 0.2 M HCL). Just under 2 grams. But boy is it clean and powdery. All in all seems like it will be less of a yield weight wise. Not sure how much of the difference is going to be DMT vs other stuff. Haven't tried the new batch to compare, probably too subjective to draw any conclusions. But if you want nice clean crystals, and have a Buchner filter, give it a roll.

IMG_7431.jpg
 
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