Or at least it did so for us.
Hello DMT-Nexus,
We have tried to extract an useable product from Phal. Arund. in 3 tries. MHRB is not easily available where I live so we needed something else, but luckily we managed to pin down the location of the best wild flowering phalaris strains in our area with the help of a botanic professor in the end. It only took us 3 days and one false identification.
For everyone who is on the lookout for Phalaris Arundinacea: Be warned about it's similarities with "Honey Gras"
In our first extraction we managed to get a white, crystal powdery .120g and oily yellow .150g after drying the goo.
In our second one, I believe we have rushed the extraction pulls a little bit too much and thus ended up with almost no residue after naphtha evaporation.
Now I need to pose a Question to the DMT-Nexus about the extraction tek, that should be used.
We decided to adapt a tek that has been specifically designed for Phalaris by a member of this forum "on processing phalaris.pdf".
(We used this slightly different tek in our second extraction.)
1. Put fresh Material through a Wheat Juicer.
2. (optional: we took the dejuiced plant material, mixed it with minimal amounts of water and put it in the mixer, after it has blended, it can be strained through a cloth to gain green solution in the same shade as the dejuiced)
3. We slowly boiled the chlorophyll out of the solution and after it has seperated we filtered it through the cloth again.
4. we added 100g of NaOH again with minimal amount of water to the solution, and stirred it thorougly.
5. After our Naphtha had been heated we combined it with the solution and stirred it again.
6. We used roughly 100ml and 150ml Naphtha in two pulls and stored it in glass petri dishes
Then we put our extract into the freezer for 45 minutes to see if anything precipitates out, but it did not seem like it, so we evaporated it.
Attached are the Pictures from the evaporated petri dish.
I know now, that patience definetely is a key component in the whole procedure and if we would have let the naphtha sit for 10-20 minutes, didnt rush the freeze precipitate and did more pulls we might have yielded around the same as in our first extraction.
But I have been wondering why almost all other teks, and many people use them also for Phalaris, include Acidifying the solution, like in the basic A/B extraction teks and so on.
At this point I am basically fearing that our extraction is not usable but only an Internet-Rumor (we did not achieve breakthrough from smoking our first product, so tension is building up) and that only A/B and STB teks are sufficiant.
So... Does any kind member of this forum know where the difference in using Acid/Base or STB to the Method that we used is, and which one did you find to be the best?
(Since we are using wild Phalaris for our research we do not want to waste too much of it)
Happy Middle of the week to everyone
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