Psychedelia.dk

Desuden er kviksølv ikke så slemt. Folk der var børn i 70'erne stod med det i hænderne.

Desuden er kviksølv ikke så slemt. Folk der var børn i 70'erne stod med det i hænderne.

Desuden er kviksølv ikke så slemt. Folk der var børn i 70'erne stod med det i hænderne.

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EXTRACTION -

1. Pulverize the grass cuttings as much as you can. You must
do this to rupture the cellular structure the plant. A good
way is to put the plant material in the freezer overnight,
remove the next day, thaw it, put it in the freezer again, and
then remove and thaw it again. After two or three such cycles
it will usually be mushy and easily minced in a blender. Place
the phalaris in the blender when it is frozed and the blender
will chop it easier.
2. Next add enough water to the much to make a pourable soup.
3. Now you must add an acid. Just enough to bring the PH down to
about 5. You can use white vinegar, lemon juice, or acetic acid.
Check the PH with PH paper, it is usually sold at most drug
stores. The acid reacts with the alkaloids in the plant
material and converts them into a salt. A good way to
facilitate this reaction is to simmer the acidified soup in a
slow cooker overnight; leave the lid on, as we don't want any
liquid to evaporate.
4. Strain the plant matter through cheesecloth, then through a
paper coffee filter. The bulk roughage may now be discarded
because the alkaloids we seek have migrated into the aqueous
solution.
5. Add a small percentage of a defatting solvent such as methylene
chloride, ether, chloroform, or naphtha. Naptha is easily
available in the form of Coleman fuel or lighter fluid. The
reason we do this procedure is to remove the oils and fats
which are in the solution - they will migrate into the solvent.
Shake up the mixture and put it aside long enough to seperate
into two layers, one aqueous, the other solvent. If you've ever
made vinegar and oil salad dressing then you've seen this done.
6. A separatory funnel is useful for this next operation. This is
a simple lab tool consisting of a tapered glass container
with a tap at the bottom and a stoppered opening at the top.
The two liquids are poured in the top (the bottom faucet is
closed, of course); The container is corked and shaken about
to mix its contents. It is then set aside until the fluids
seperate into 2 layers. Then a tap is opened to allow the lower
stratum to drain into a container. Just before the descending
upper fraction reaches the faucet, it is closed off. You can
also do the above separation procedure with a turkey baster
Discard the solvent (along with the unwanted oils and fats) and
now the remaining aqueous solution contains the alkaloids.
7. The next step is to add a base to our solution. One often used
in extraction formulas is ammonium hydroxide, a liquid. If this
is unobtainable you can substitute regular lye crystals. This
is sold as drain cleaner and is also called sodium hydroxide.
Dissolve this is water to a high concentration. This fluid is
added in small increments to the aqueous solution, shaking the
mixture each time, then testing it until eventually the pH
reaches 9 or 10. Be patient. It usually takes a while to
get it just right. Now you have 'unhooked' the salt and
transformed the alkaloids into their freebase form. They are
now no longer a salt, and hence no longer soluble in water...
So now the are accessable to extraction by one of the organic
solvents mentioned above. Using coleman starting fuel is best
and easy to obtain.
8. A ratio of 10 percent of the aqueous solution should be enough
solvent for each extraction. The easiest way to estimate this
is to visualize where the 10% line is on your container of
aqueous solution, then add that amount of solvent to the whole,
increasing the volume to 110% (A super accurate measurement is
not necessary) The container must be kept closed tightly so
that the solvent won't evaporate from the solution.
9. Four extractions are made to make SURE that all of the alkaloids
are removed. These are done at one 24-hour, and then at three
weekly intervals. The solvent layer will soon take on a darker
tint, usually yellowish or reddish-brown. This indicates the
presence of alkaloids as they slowly move out of the aqueous
solution. It will take almost a month to get most of them, and
the mixture should be shaken at least twice a day to ensure
that all of the alkaloid molecules come into contact with the
solvent. At each weekly extraction carefully separate this from
the aqeous solution be either of the methods mentioned above.
Save these solvent fractions and combine them in one container.
each time add fresh solvent to the aqeous solution until the
extraction series is complete.
10. The last step is to pour the combined solvent fractions into a
shallow baking dish or pan and allow it all to evaporate in an
open space free from flame or sparks. The residue remaining
after the evaporation contains the alkaloids, and may be put
into gelatin capsules. If it is unduly gummy, one may add
small amounts of ordinary flour to the gum until it thickens.

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Desuden er kviksølv ikke så slemt. Folk der var børn i 70'erne stod med det i hænderne.

Desuden er kviksølv ikke så slemt. Folk der var børn i 70'erne stod med det i hænderne.

Hvor meget DMT kan man ende op med hvis man bruger 1kg frisk græs?

Desuden er kviksølv ikke så slemt. Folk der var børn i 70'erne stod med det i hænderne.

Desuden er kviksølv ikke så slemt. Folk der var børn i 70'erne stod med det i hænderne.