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hello, greetings with x-tals

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CozmoChemist

Rising Star
Merits
42
hello, swim is brand new to this site, swim has a deep intrest in spice as do lots of you here. For being new swim thought he might greet you with photos of
x-tals swim has just finished growing.
swim used naptha for this re-x and plans on using bestine for the next re-x.
the x-tal on the right( bigger one) weights about 0.1
the method used was stb
does anyone know how swim would grow a more solid crystal?

I apologize if i posted in the wrong area

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Icon said:
Could you continue re-growing those as large as you pleased?

Are they more dense/strong and less waxxy than the flat, needle crystals?
Is there a noticeable difference in effect? I would imagine the rocks packing a bigger punch.

-I believe if one performed repeated re-x's and slowed temperature decrease even further then the resulting crystals would be bigger and clearer each time. Haven't tried this yet, I've still got lots to learn.

-Yes they are more dense (Bigger ones weigh around 60mg) and are not sticky at all compared to the snowflake type crystals. They are easy to handle and feel almost rocklike; best of all they don't stick to every damn thing they touch haha.

-As far as effect goes, I don't know for Sure if the effects are different from shard type crystals because I haven't ever tried these. I'd say no though; its the same dmt content no matter what form it's in. 50mg of spice crystal should have the same effect as 50mg of the powder it started as.
 
Cosmo: Are you able to get crystals that large consistently. This is one thing I've had trouble with. I've never had much success with evaporation techniques but would love if I could grow gem type crystals as large as yours. Can you tell me the measurements of your materials i.e. starting weight of spice, mL of solvent etc?

Nvm I see where you posted that info. But if you used 1g surely those arent the only crystals you produced?
 
VIII said:
Here is the thread I was referring to earlier.

Geometry of DMT crystals and a follow-up thread of sorts, Significance of DMT Crystalline Geometries and Our Experiences?

Very interesting, I read quite a bit from the first thread you posted. So are the crystals I have been getting considered uncommon? I only ask because I have only been doing this for a couple months and it seems like these gem/diamond type crystals are formed by slow temperature drops and using more solvent than recommended in most re-x teks I've seen. There may be some key during my process I'm unaware of but I get these everytime I try for them. I wish I could post outside of the new members forum...haha I have so many questions.
 
So essentially the slower the cool down process, and longer period of time the bigger the crystals.. Very cool. I did the opposite and tried to get my crystals out of the nap asap. next time I will use hep, and I will do a time lapse with my nice camera.😁

Although I don't see we are able to put videos here on the Nexus. And I wouldn't want to dumb down the quality and create a gif. I don't know if Youtube is the answer either. Maybe I will title it "Brown Sugar Crystal Formation" haha, and put it on Youtube and post a link here.

Question, after you've freeze prepped and collected your crystal, what do you do with your remaining solvent? I was only able to get a gooey substance out of it.. Should I throw it out? (assuming I've pulled as much from my mhrb) or use it in a zippo or something like that?
 
Digest Yourself said:
. Question, after you've freeze prepped and collected your crystal, what do you do with your remaining solvent? I was only able to get a gooey substance out of it.. Should I throw it out? (assuming I've pulled as much from my mhrb) or use it in a zippo or something like that?

It will be depleted of spice so save it in a jar for next time..or zippo..or Re-x
 
Nmk8743 said:
Cosmo: Are you able to get crystals that large consistently. This is one thing I've had trouble with. I've never had much success with evaporation techniques but would love if I could grow gem type crystals as large as yours. Can you tell me the measurements of your materials i.e. starting weight of spice, mL of solvent etc?

Nvm I see where you posted that info. But if you used 1g surely those arent the only crystals you produced?

it depends if I work at it enough, if I dont like what I see after 2- 3 hours ill re disolve the spice and slowly cool again till I get the formation I want
and your right, there was more from re-xing the gram, just smaller x-tals not woth taking pictures of


yes your crystals are uncommon and what most desire to make I would think, I know I do
so what ever you do !! you do it right and well!!
 
Digest Yourself said:
So essentially the slower the cool down process, and longer period of time the bigger the crystals.. Very cool. I did the opposite and tried to get my crystals out of the nap asap. next time I will use hep, and I will do a time lapse with my nice camera.😁

-That would be incredibly cool; almost like watching art grow.

Digest Yourself said:
Question, after you've freeze prepped and collected your crystal, what do you do with your remaining solvent? I was only able to get a gooey substance out of it .. Should I throw it out? (assuming I've pulled as much from my mhrb) or use it in a zippo or something like that?

-I always let it evaporate at room temp to get any remaining spice. If it's excessively waxy/gooey I just recrystallize it again. Some of the goo is likely dmt n-oxide and I haven't experimented with converting it to freebase. Never throw anything out unless you have to; there's always more spice that gets stuck somewhere during the process ha.
 
CozmoChemist said:
it depends if I work at it enough, if I dont like what I see after 2- 3 hours ill re disolve the spice and slowly cool again till I get the formation I want
and your right, there was more from re-xing the gram, just smaller x-tals not woth taking pictures of


yes your crystals are uncommon and what most desire to make I would think, I know I do
so what ever you do !! you do it right and well!!

-I see, so you are essentially letting crystals form at room temp and then redissolving until desired size is reached? That would make sense.

-I will gladly post a write up for re-x'ing 1g of spice to yield gem-type crystals with pictures if anyone would like. I'm interested to see if others will have success with my methods. I wouldn't post that in this thread though right?

-I apologize cozmo. Swear I'm not trying to hijack your thread haha.
 
Kash said:
That would be awsome. Im sure it would help out many nexus members. :thumb_up:

-Ok, I will begin to work on this then. Be warned I am a busy individual with a family and this is going to take a while. But when I get it done I'll post a link in this thread for sure.
 
Hello again!
swim has recently re-xed and crystalized spice using the quick notes
that nmk8743 left back a few post ,thanks again nmk8743
the only thing different is that swim used naphtha instead of heptane, heptane doesnt seem to work AT ALL. no matter how slowly you cool the solvent it only produces tiny tiny flakes of x-tals in clusters, you cant pick the cluster up with out it all flaking away.
So naphtha seems to be the best solvent for growing large x-tals and heptane is only good for obtaining an ultra pure spice

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that big chunk is exactly 0.1

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you know, this whole ordeal is quite rightly pissing me off now( the whole crystalization)

before the x-tal would come out like the first post swim posted. swim was letting it cool only to room temp in about 2 hours with just the beaker in a glass of water.

then I tried your method nmk8743.
I used a thermos that was supose to retain heat up to 6 hours (with out the cooler step)
I left it for a day and put it in the fridge over night the next morning I put in in the frezzer and what came out is pictured above, so it worked!

Now to answer your question nmk8743, the big one is like layered and kinda brittle
the other pieces are like little rocks, but still no where near the quality of yours.

heres where EVERYTHING goes to shit.

before swim had only used naphtha, swim decided to try using heptane. this time swim did add the cooler step to allow a much slower cool down time. what swim has is a foam thermal chest not to big not to small. swim did everything the same except thoes 2 changes.

end result are tiny tiny slivers of x-tals in clusters and when you go to pick it up its like slush cause the x-tals are so fine.

now Ive tried everthing I can think of

added cooling time
reduced cooling time
not using the thermal chest
using the thermal chest
different amounts of solvent where tried to no luck
starting the cooling process from different temps

and heres where chemistry decides its fun to mess with me

swim decided to go back to start and use naphtha again.
to his suprize !.....tiny tiny x-tals

I literally cant get anything to grow larger then the thickness of a human hair
all of a sudden.

so I did some reading about crystalization in general


supposedly, there are zillions of factors such as the content of the air in the environment
and thats not something swim can change all to easily

I can't for the life of me figure out what variable changed

perhapse my beaker is shot?

some info on general crystal growing

 
That is interesting. Are your containers clean? I mean acetone wash clean? Dust particles will affect growth significantly. But you're right there are tons of variables and by no means is there a step by step to absolutely get what you want.
 
Oh and here's the ratios I use of spice:heptane that have produced crystals like I pictured pretty consistently.

1g spice: 25ml heptane

You can adjust to fit the amount of spice you're re-xing.
 
usually I clean my glass pretty well , but you never know.
I shall look in to that as a suspected variable change
and try the acetone wash

thanks for the ratio of spice to heptane
I was doing 1g to 30ml just a bit different but it counts

I will get back to you with the results
after a retry with such
 
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