Result from acrb extraction...

[Travling Tommy]

Hi, i took out the result from my 4`th acrb x-traction from the freeze just now,the re-x that is.(Max ion tek)
I have mixed feelings about it: i dont think it yeilded enough, i made some misstakes,and it tok a long time(and im a fairly pationed guy).
But the spice turned out very good, and i learned some new things.

544mg pure white x-tals.
1062mg a little more sticky slightly coloured x-tals. Total 1606 mg and some black goo i didnt bother to weigh.

Posting some random pictures from the extraction, and i have a few questions as well.
1: The naphta was coloured pink/Purple when i pulled(same colour all 6 pulls) Whats going on or what is it?(wineglass Picture)
2:I got some black goo, what is it? (and can it be smoked?)

 

[ooo0ooo]

How many grams were you extracting from?

The "black" stuff looks like it's got ACRB powder in it. I'd collect and do a quick A/B on it to see what you get out of it.

0.

 

[starway6]

Looks good..!
Did you try it yet?
Does it feel like mostly DMT... or some NMT efects?

 

[Earthwalker]

How many grams were you extracting from?

The "black" stuff looks like it's got ACRB powder in it. I'd collect and do a quick A/B on it to see what you get out of it.

0.

I think from memory Traveling Tommy said it was 300gram Taiwanese ACRB !!

I'm doing same TEK ( max-ion ) later next week with so I've been advised ( nice fresh red pink inner bark ) so I'd like to compare notes when finished !

This latest learning curve , or hot topic , is encouraging news concerning confusa as many ppl are getting goo and goo only ( goo is good ) and with the sharing of info I think things are only going to get brighter , so let's put on the shades and lets get sharing !
8)

 

[Travling Tommy]

Yes, it was 300g(two vessels with 150g each). I was to quick to use it as a drain cleaner, i was so sure it was all good after the six pulls, should have waited to see the results first. Lesson learned.I did some misstakes, like i did not use enough water in the salting step-but there simply was not Space enough in the wessels,so the mixture was to thick and i used citric acid instead of HCl as i always did before(i dont really know it was a misstake to use citric acid but im going back to HCl anyway)...I only got +0,5% yeild. Use to get more.
Im sure it was much left.

TT

 

[Du57mi73]

There might still have been solvent in the jar that had not seperated yet from the basic mixture. I now know that I used to toss away lots of naptha that had not seperated from the basic soup but i couldnt tell. It wasnt until my friend shined a flashlight on my jars that i could see that there was still TONS of naptha still left in a jar that i would have otherwise just dumped.

 

[Earthwalker]

There might still have been solvent in the jar that had not seperated yet from the basic mixture. I now know that I used to toss away lots of naptha that had not seperated from the basic soup but i couldnt tell. It wasnt until my friend shined a flashlight on my jars that i could see that there was still TONS of naptha still left in a jar that i would have otherwise just dumped.

I no there's a few posts about how the acacia is slower to release the DMT , but using the flashlight " tip " . They should be shared I one place like here Sharing Various extraction results with CYB'S TEK(pics!) - STB - Welcome to the DMT-Nexus sorry I don't no how to hyper link yet ! Lol:wink: