posted 05-25-99 06:45 AM         

one question, two actually, kinda three...

do you know when you've added enough NaOH by when it smells like urine/ammonia? is there another way to tell?

and, how many layers are there in the last gatorade jug, 2 or 3? is the water layer also the acid layer, or does the acid go into the coleman layer, or is the coleman layer seperate from the acid and the water layer?

thanks for the info dude...

posted 05-28-99 07:08 AM         

what about ordering ephedrine or pseudoephedrine overseas? anyone have any experience with this?

or extraction from ma huang?

posted 05-28-99 08:17 AM         

http://members.xoom.com/_lysergic/pushpull.html

posted 05-29-99 03:46 AM         

this is my first time posting to the hive, pretty fuckin cool place.

posted 05-30-99 05:03 PM         

then centrifuge or filter

now evaporate in oven slightly agar or with desicant inside

scrap off from pyrex cutting board ya melt this yourself slightly concave or has a grid thrown on the top for fun Make the water pool into little droplets, called cappilary action

Anyhow yes rinse product in MeOH three COLD

Filter centrifuge or fucking cook????
Are you crazy?????????????????????????

Any how filter ????????
What off???????

Wash shit away with Meoh while it is still an acid

Put into water or meoh dont really mater rereally

Unless you basify the stuff and salt out, this causes the H2S04 and HCL it aint hcl

Anyways do not basify

Strip Meoh for reuse filter it if necessary or pur down drain or burn it off

I used to burn it off kinda gets ya off to

Anyways do please centrifuge the meoh off add water and centrifuge the goodies

Now crystalize the good stuff

Mix some suggar in various amounts get a bouey you know a fish float!

Ok noew check the boyancy of the suggar make the booey.

Now mix your stuff in whatever it is ya are gona crystalize in, tempature solvent mixture compuonding is important to this procedure and nobody has it posted

Ok so make your own suggesting battery with a nicrome wire immersed into fluid cold seems that crystal can be controled as far as growth is concerned.

Anyways the crystals are evaporated from the solvent and allowed to settle out on the platform,[nicrome needle] or another dangling crystal fron an invisible string

Hopefully you are getting the idea by now!

Ok so the evaporate has some stuff in there and as it cools down ya want to keep the gasses moving some is gona not collect and falls off into the swimming pool it is recycled later, it the lost crystal does eventually fall to the bottom of the sugar solution if properly boyant and maintained from evaporation, ever had a B-52?

Well anyways the gas is ignited in a controled manner [previously discussed]and allowed to flow up to the platform, here here it make a large and beautiful Ice

posted 05-30-99 05:55 PM         

http://www.alfa.com/

posted 06-27-99 09:10 AM         

http://www.labx.com/v2/adsearch/Detail3.CFM?adnumb=24273&adtype=LabAuction

posted 06-28-99 01:08 AM         

http://www.labx.com/v2/adsearch/Detail3.CFM?adnumb=23741&adtype=LabAuction

They're 4L *and* have top hose attachment for 25 bucks. Pretty cool for push/pull I'd say...

Quick question for push/pull xperts - methhead/fzr96/toast (I know I've seen this discussed before but I can't seem to find the thread it was in, I swear) - anybody have successful push/pull dreams on the 1/2 oz (14g) level? Say, for instance, you only have a couple a bottle of Polar Pure left (totaling 1/2 oz of I), would you proceed? Just curious.

posted 07-07-99 09:52 PM         

Hope you can help out on some questions.

The questions are as follows:

1. In the Hive message post, "Crystal Meth, where did i go wrong "
Worlock responds:
Your dreaming about purifying the pills to obtain sudo. This is not necessarily a difficult process, and does not require the acid / base extraction in most situations.-------
You want the dream that goes
Weigh out sudo, phosphorus, and Iodine, in a ratio of 3 : 1 : 3 respectively.

Question: What would the ratio be if one needs to do A/B extraction to clean shitty sudo befores P/P reaction? Icannot obtain cleaner pills unless I mail order.

Question: When using a smaller reaction vessel to react 1 ounce or lower of sudo, would it be advisable to reduce the volume of water in the gas container, thereby reducing the pressure?

Question: What is the hose inside diameter and length from reaction vessel to cans?

Question: When using angel hair to filter sudo, what brand do you use? This pasta thing really gums things up!!!!!!! (never mind)

Thanks.

posted 07-08-99 12:35 AM         

Slow down boy.

The question pertaining to Worlock was for clarification. In the attempt for finding out the perfect measures if using a sudo shit, or perfecting to a freebase or a salt. Why not try for 80% return.

The same would apply to the question pertaining to the water level in the gas cans if a smaller vessel is used for reaction.

No were is hose diameter mentioned. I've looked.

And the angel hair one was a joke.
And you responded to it. Oh man what a droid!
I didn't think anyone would respond to that one. Have you become our new Crystal Moderator?
Nay, just a droid.
Goodnight girls

posted 07-08-99 05:50 PM         

As for the sudo I hope I can A/B it clean before reacting and not screw up the results.
Will announce results soon.
Thanks again.