| Author |
Topic: Takin' a break |
Android Member |
posted 12-23-1999 02:23 AM
My dreamin' sumtimes includes pictures. It looks so real,
doesn't it? Set up a hotbath with a pyrex boiling pot. 1 gram of
pure soody was placed in an 8" test tube @ 8:30 pm dreamtiime. Then added
7ml GAA. Temperature was kept on low on the old BettyCrocker hotplate($15
Raley's). After 30 min. or so, 5 drops of H2SO4 was added, test tube was
lightly plugged #3, and the heat was turned up to near boiling. During
the next hour and a half, the ACU-RITE (walmart $12.98) showed old Betty
was holdin' steady at 97.4 degrees C. Then I noticed the beautiful
clear, watery, homogenized (as UF describes it) was slightly golding up on
me, so I stopped dreaming to reflect on the possibles. Unable to EVER not
be busy, I decided to post the dream picture of the happy moments before
this (whatever, it's only a gram, anyway) curve came up. Kodak photo
GAA. Napa battery acid. H2SO4 listed as only ingredient. Superclean
P.E. I figure battery acid isn't concentrated enough. But I was bored
and I got a lifetime of stash so wutdafuk?
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CHEMMAN Member |
posted 12-23-1999 04:47 AM
Oh shit Dont leave us .Well miss you real badddd
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Android Member |
posted 12-23-1999 04:54 AM
Where ya goin', Chemman? I'll miss you, too! Hurry back, though! Wonder
why he wanted to tell me he was leaving? Trying to think of anything I
could've said, that would inspire this obvious crush he has on me.  Hope he didn't do
anything stupid. Well, anything more stupid than tryin' to flame me that
is!
------------------ "ARROGANT &
CYNICAL" (Ticklish,too!)
|
CHEMMAN Member |
posted 12-23-1999 05:20 AM
I aint flamin ya man your OK .A sense of humor is good around here
sometimes.Things are bad here at present , buts lets try to keep a
|
Android Member |
posted 12-23-1999 07:14 AM
How come you're not flaming me? Don't ya like me no more?
Anyway, due to the different color, I decided what it needed
was a good bath!
What looks like a
little wad a gum in there is a stir bar I fashioned to fit in that tiny
area. The little mag/stirrer is homemade, too! My stirring hotplate is the
size of a television, so too big, bra! After chargin' it up for 20
min., I poured the solution into the hydrogenator and began stirring. That
remindes me, better return to dream and check on that sucka. Would want
goldenboy to drown. This method's been
around a long time, I know, but it's kinda fun and normally gives ya good
microstash.
|
Android Member |
posted 12-23-1999 08:55 AM
After loggin' 3000 coulombs (And the fact that the steady flow of bubbles
mysteriously decided they'd had enough and left without sayin' goodbye
'bout a minute before I stopped the party), I shut 'er down and setup
vaccuum filtration using a simple aeriator, 600ml buchner funnel with a
porous insert and a single coffee filter(just to keep stains off the
porous insert) with a 2L polylab sidearm flask, and poured the reacted
(hopefully) solution through just to remove the metallic powder that the
silverdollars leave. Guess I'll go back
to the dream and do the last step now. Wish me luck.
|
Android Member |
posted 12-23-1999 09:49 AM
Poured the clear filtered solution into 1L Sep Funnel. Unfortunately, the phone
woke me from the dream. My wife left to go pick her mother at the train
station. I'll finish the dream as soon as her mom goes shoppin' er
whatever.  I'm
always the last one to know in this house!
|
aqua-girl Member |
posted 12-23-1999 12:08 PM
Thanks for the Christmas pictures
Whats the power source in this dream? I just can't figure out a good
OTC power supply for this electrogizmo stuff. Keep hearing different
reports....
|
Hematite Member |
posted 12-23-1999 12:44 PM
Hey did someone forget your maintenance schedule for the likes of disc
defragmenting and temp file cleaning etc.? I ask cause you have to be
the slowest and most patient person ever not to be human !!! The wife
left to go to the train station for goodness sake!!!!! I usually get
knocked about the head for finding shit like that out tomorroww ! Just
finish the damn thing and the hell with this teasing baiting shit ok
tinman ?
------------------ Regards,Hematite.
|
Huffalump Member |
posted 12-23-1999 01:00 PM
Are you saying that you used a silver dollar rather than palladium for the
cathode?
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Android Member |
posted 12-23-1999 07:36 PM
I'm sorry, but my missuses mum is hovering around like a fruitfly! I feel like I'm
trapped in a bad episode of Leave to Beaver. Huff: I don't have any
palladium. Would be nice! Never dedicated any enough time & effort
into lectrosynth to find a sources. Shit! There she is!
Later! Promise! I'm as anxious as you!
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Huffalump Member |
posted 12-23-1999 07:48 PM
Complain about a headache, cart everything into the bathroom, and then
tell them you're going to take a nice long hot bath until you feel
better.
|
Android Member |
posted 12-23-1999 10:40 PM
Actually, that's a more conservative suggestion than I would expect from
you, Huff. Chloroform and duct tape is more Huffianlike.  I did manage to
sneak away long enough to neutrallize it, though. I'm out of pre-gassed
solvent, so I'll have to wait til dear mum retires to set up a gas
generator. Nothing short of an apocalypse will keep me from completing my
little dream. I fail to see any significant contribution for anyone
outside of entertainment from this, but I've alway been a little naive.
 Sweet mum is a
couple of feet to my left poring over a crossword puzzle at this very
moment whilst I post this.  Wonder what the
grieving duration is on accidental mother-n-law terminations?Hmmmmmmmm.
Grieving wives are
so distracting.
Ain't I a stinker?
------------------ "ARROGANT &
CYNICAL" (Ticklish,too!)
|
Android Member |
posted 12-23-1999 11:42 PM
Slipped away again and added 100ml of solvent to the base. I chose xylene over
toluene mainly because it's been my experience that toluene tends to
attract alot of emulsion. Please don't bother to flood me with chemical
facts on the two solvents. If you're not happy with the above reason, then
just call it "personal preference".  I'm thinking of
scrapping the generator for acid drops, what with the present mum
situation. It'll fudge the product percentage(if any) calculation, though,
since I set aside a portion of the base solvent just in case I go too far
on the low side of pH.
|
Android Member |
posted 12-24-1999 12:06 AM
Oh, aqua girl! Ya never did thank me fer helpin' ya out with your post,
but in answer to your question, straight from the battery of my wife's
jeep cherokee, baby! I fucked around a few months ago with different power
sources and mA DC variators, but an hour of straight 12 from a car battery
was the only thing that kept the party going long enough to see results.
Probably due my okie old lamp cords and clips from long dead motorcycle
battery chargers that keep the amperage around 300DC V mA. But then, I
know as little about electronics as I do about chemistry.
Remember: Regardless of real or imagined or dreamed results, this is
purely for entertainment purposes only. That's my job at the
Hive. Entertainment.(Plus my dreams provide kick-ass go-go for me) 
|
Android Member |
posted 12-24-1999 04:17 AM
With a pH reading that didn't change the pH strip's color,(that's good)I
separated the lower layer into a small visionware bowl. That's a small
portable heater on the left, a 60 watt light bulb above right, and it's
resting on a heating pad. The piece of paper is for photograghic purposes
only. I'm not worried about time at this point. I didn't come this far to
be distracted from the hotplate, and have my labor go up in
smoke.(Although it does end up in my glass pipe anyway!)  I'll check back
soon with the yea or nay. I saved everything, so if this pull produces
nothing, I won't bore you with the search which will ensue,(unless ya
wanna be) just know that an extensive search will be conducted.
|
Xtract Junior
Member |
posted 12-24-1999 08:55 AM
Droid bestus pics ever.......man yo da man ..with youre mom in law there
even...can yoiu tell us a little more about da shit ....? would a 15 volt
unregulated power source bee OK? What is GAA? And how do you hide all that
shit while youre inlaws are a few feet away ??? Yo da man!!!
menotX
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aqua-girl Member |
posted 12-24-1999 09:04 AM
great, thanks. I thought I was gonna have to send you nudie pics of myself
to get the answer.
Fuckit, I'll send one anyway ... I used to model for
Matrix hair shit ya know!
Mebbe I can whore myself out for precursors... LOL!
|
Huffalump Member |
posted 12-24-1999 09:58 AM
A picture of Android?
|
Android Member |
posted 12-24-1999 12:18 PM
I know Xcrement, maybe you should read this again.  aqua girl, you
bitch! My
computer's cryin' about not being about to read MIME! Shit!  Huff, thank you for
post one of my better pics. Handsome devil, aren't I?
Anyhow, awoke this morning after a rare occurence of 'sleep',(think it
had something to do with bout of monkey lust with the wife)I found the
drying bowl still in a state of evaporation. I was happy to see the layer
of almost transparent crystal formation, though. No celebration yet,
though. that could be unwashed base salt, or the solution could've flown
south on me after checking it's pH. That happens sometimes when doin' the
acid drops method.  Hard to photogragh
them. Especially
after jostling the liquid into them when I moved it for the shot. Back
in a bit with word of the shit.
|
Android Member |
posted 12-24-1999 01:43 PM
Drying is at last complete! This thick layer of
almost transparent precipitation is all that one would expect from only a
gram of starting material. The question now is, is it still just starting
material? Or worse, is it one or both of the aforementioned byproducts?
 I think a
fresh razorblade is now the tool of choice to further investigate this,
followed by a wash with a splash of acetone. I shall return!
|
dextram Member |
posted 12-24-1999 03:01 PM
Best of the best there Android, um are them plates in the picture???
Is there any membrane upon them plates.... was/is there any electro
film on either of them plates I understand that anodization should free up
some of the metal catalyst into the solution this is the metodology,
right? THANKS
very good Mery X-mas to you 
|
Android Member |
posted 12-24-1999 03:18 PM
As for yield,
.235gm is less than sad. Most likely a
combination of reasons including: my obsessive behavior syndrome with
washing the solvent with DH20, the acid drops method of crystalization,
the portion I reserved in case I brought the pH too low, inexperience with
delicate procedures involved with batches below 1 ounce, inexperience
period, etc. That's why I save everything! Because judging by the fact
that I am soaring like Fuck Thighlicker just from my unconcious habit of
licking the razorblade, the reduction was incredibly successful! What you
see before you is a high quality pharmaceutical grade product. And
thus, bringing this entertainment piece to an end. I hope you enjoyed the
show. There's gold in them there save jars, and by god, this miner's gonna
get busy!  Feel
free to ask questions about setup, my sanity, etc. Or just publicly
ridicule or flame me! I always enjoy hearing from the Hive membership. I
love you all!  Yes, even you,
Worlock.
------------------ "ARROGANT &
CYNICAL" (Ticklish,too!)
|
Huffalump Member |
posted 12-24-1999 05:02 PM
I've got a question:
Is there an indicator that can be used to distinguish between eph and
meth? If so, determining if one actually had product could be done before
extract & x-tal.
Huffalump
|
Android Member |
posted 12-24-1999 06:24 PM
That's true, Huff, and there probably is. I'm my only indicator, but I
prefer to wait til AFTER crystallization!  This procedure is
of not much worth until it can be made large scale at low cost. For me,
it's just something to do when I'm in the mood for something to
do. todolu!
|
CHEMMAN Member |
posted 12-24-1999 07:31 PM
Very nice pics.Very entertaining.Yes I find the consumption method the
best indicator. Test it a few times to be sure  Happy Xmas
|
mrr
pyrex Member |
posted 12-24-1999 09:12 PM
Well from the appearance, I can say without ANY doubt andriod that was as
pure as pure gets. I have seen mixtures, and mixtures will leave those
nasty pinwheel lookin creations. When you get plates like that, well I be
willing to bet Andriod is spinnin like a 78 record, unless andriods get
spun from E and not Meth ;-) Me not knowing andriods physiology(sp?) and
all. But regarding telling the difference there is Marquis Reagent and it
does give definte results---Orange is E or Pfed//Brown to darkening
brown/black is Meth. If it stays orange your SOL, otherwise your doing
somethin right. Pyrex clause P.S.-nice write up driod
|
mrr
pyrex Member |
posted 12-24-1999 09:31 PM
Huffy, took me three times of rollin past it before I saw it but HOLY
FUC*ING SHI*....RRRRRROOOOOFFFFLLLLL!! gessss those blinkin eyesss
bbbhaaawwaaaa
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Huffalump Member |
posted 12-24-1999 10:20 PM
I've got a friend, and he's thinking:
Low yeilds aside, I think this is the method for me. I've got 72g of
clean pfed and have been waiting for an opportunity to dispose of it...
dispose meaning that I no longer have any pfed, whatever it may become. I
was going to use iodine and rp, but a recent post here made me a bit
nervous, and I also feel very wary about ordering any pyrochem right now
because of the general insanity surrounding the millenium. I was going to
do electro, but Pd isn't cheap, and although I'm not fundless, the $405 (a
coin, not an ingot) I was quoted would take quite a chunk out of my
playtime. As things are, I don't sell drugs, and although I still use them
quite a bit(more than I'd like), they aren't so much of a lifestyle. I
work for my money now, which ain't bad (even if it does suck), but there's
no quick money schemes like there used to be... so saving is slow. But,
back to the point, I did consider using silver, and was going to try it
out, silver being a noble metal and all... and no, I never searched to see
if it would work. I'm rambling a little bit, but let me just say that this
thread is inspiring. Using silver rather than Pd--not to mention the low
overhead and scavenge-a-bility of all the other equipment--really puts
this in my right-about-now range. And, since I don't plan on selling any
of it, I really don't care about yeilds anyways... which probably wouldn't
be too great for a first time methsynth no matter what path I chose to
take.
That's what he said, that crazy drunk fuck, I've got no affiliation
with him whatsoever. Nice work Android,
Huffalump
|
Huffalump Member |
posted 12-24-1999 10:29 PM
Two more questions:
1. Did you get your wife a digital camera for christmas? The turnover
and candidness of those photos makes me wonder.
2. You had monkey-sex with your wife while her mother was in the house?
You're one sick bitch.
Huffalump
|
dextram Member |
posted 12-24-1999 11:57 PM
I gues homade from nicle plate and stuff from coins ans a plate if need be
of not CO but lead Co in the glaze old blue plate, this lead patr of the
gizmo is hooded with a gas extraction port and likewise not shown the
hydrogen is bubbled inthrough to cause addational hydrogenation and
catalytic activity upon the electrode of interest I like that little nudge
at the bottom, tell us more??? Is a tiny amount of quantitary mathyamine
added to get things going or have ya siply follwed directions?
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dextram Member |
posted 12-25-1999 12:13 AM
second gueese the picture is of an ashtray of covered in some kinda
membrane it looks though like a speaker? It is a lead glazed Cobalt
colored ashtray with a protective covering prally with attacjed a spread
array of multiple attaching small wire leads from the bundel ussing most
proally some kinda lead soder? possibly a rubber glove? the other one
looks like it is a doual pound silver dollar assortment
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dextram Member |
posted 12-25-1999 12:16 AM
pantyhose humm interesting methodology
|
dextram Member |
posted 12-25-1999 12:19 AM
I bet you drink alot of coffe? more than any normal consumer.
|
Android Member |
posted 12-25-1999 01:22 AM
If you're finished, Dex, I'd like to squeeze in here for a brief chat with
Huff. Huff: Make sure you do the research. I don't want to be
responsible for any failures or loses of supplies you or any other member
might suffer. One of the main reasons I stress that this dream pictorial
is for entertainment purposes only. Now, if you pursue this for your
own reasons only, then I wish you great success!  To the
others: There are two silver dollars. The flattened out one visible,
and the one that's tucked neatly into a same-shaped piece of pottery.(It's
a lid off one of those decorative little candles which I swiped from my
wife's knick-knack shelf) A lid from a bottle of H2SO4 snaps perfectly
into the back of it after inserting the coin. A tiny hole was drilled in
the coin to attach the wire. A tiny hole was drilled into the lid to allow
for the wire. Near this hole, a larger hole was drilled for filler
port.(for the acid/water mix) This, of course, is the top, and kept above
the level of acid/water in the main chamber. Some of the questions must
be translated from chem-jargonese. I'm happy to say, I speak common-man
American only.
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dextram Member |
posted 12-25-1999 03:23 AM
My eyes are burning but yes I will bemoth back to my lair for a while it
seems.....
|
mrr
pyrex Member |
posted 12-25-1999 03:35 AM
GAA=Glacial Acetic Acid Pyrex out
|
chencho Member |
posted 12-25-1999 01:16 PM
Android, Well I guess this pretty much supports the opinion that pfed
works as well as ephed. Thanks for sharing.
|
Android Member |
posted 12-25-1999 02:41 PM
Clencho: But of course!
Huff. I have an old G.E. full-size camcorder. I also have Snappy
software installed on my computer. Between the two. . well, you see the
results.  Isn't
this thread testiment enough to my being sick? In fact, I'm crazy to the
point sanity! Kinda like drinkin' yerself sober.
My writing skills are about the only thing I retained from college.
They're weak, at best. Oh, yeah, liver damage. Can't get through college
without liver damage.
Merry Christmas!
------------------ "ARROGANT &
CYNICAL" (Ticklish,too!)
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