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naptha separation anxiety

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jbark

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Senior Member
OG Pioneer
This is the 1st time I post, so my apologies if I am posting in the wrong place/way. I am a self-professed newbie having a lot of problems separating Naptha. I have read extensively on this site from the FAQ & troubleshooting sections to forum posts concerning separation « anxiety » (couldn’t resist…) I am using « QT’s Extraction for students » (from erowid - I know, I know, but I am already in neck deep and just want to get out so I can start a simpler tech…), with muriatic acid, naptha (Coleman camp fuel) for a solvent and NaOH (lye acquired in a soap-making shop) as a base. I used 133 g pre-powdered MHRB split into 4 large mason jars.
Followed the tech as closely as possible (but a vague tech leads to vague technique…). Here is an abreviated version of my lab notes (sorry for the length and the details, but I really have no idea where I went wrong):

Day 1 acidified demineralized water to ph 2. Poured to cover MHRB in 4 jars and shook till mixed. Heated under 50 degrees C (122F) then let sit.
Day 2 48 hours later – filtered all through coffee filters 2 X.

Repeated day 1 & 2 twice more then discarded MHRB.

Day 7 defatted with about 100 ml naptha in each jar. Shook vigorously for 20 mins.
Day 8 24 hours later : removed naptha and pink cloudy guck. Filtered through coffee filters 2 X (still some mhrb residue.)

Repeated day 7 & 8 twice more. No more visible MHRB residue.

Day 13 Mixed NaOH to ph 12 in tap water (ran out of demineralized water – is this where I went wrong ?) This is where things get a little sloppy; Added teaspoon after teaspoon of base to defatted jars (tech called for about 10, but when I got to 30 in each jar (containing an extraction from an initial 33g MHRB in each) there was still no heat or change of colour or consistency. I added 2 tsp NaOH to my remaining (approx) 500ml of base. And added tsp after tsp – at 8 a reaction started (grey to black sludge, but curiously no temperature change…) and by 12 tsp I reached target ph (11 in my case – although very difficult to tell ph differences between 10 and 13 : green grey to grey green to grey, so I can’t really be sure of the exact ph…) Oh yeah, shook vigorously all the while (what can I say – I’m a noob! I won’t shake next time I promise…)

Day 14 Now things get strange: 24 hours later and the mixture seems to have separated into 3 distinct layers : a 2mm band of burgundy liquid sandwiched between two layers of grey sludge ! I remixed (this time by slowly overending jars for 10 mins each to avoid bubbles & emulsion…) then let sit for 48 hrs.

Day 15 Same 3 layers. Following the troubleshooting guide on this site, I added 25 ml naptha & remixed slowly and waited 5 hours . No change. Added 4 tsp of same NaOH preparation as before.

Day 16 24 hrs later. Some change : mixture has now separated into 2 layers -
the liquid has settled to deep burgundy (a grey silt like sediment has accumulated on the bottom) and the solvent has sort of separated into a distinct layer, although seems to be emulsified if I understand the term correctly (bubbles, not translucent and pinkish in colour). There is however, a thin film of clear solvent on the top (roughly ½ mm…). Added 5 tsp of NaOH mixture, mixed end over end, put in warm water, cooled and waited :

Day 17 no change… Added 2 tsp of salt into one jar as a test, then overended to mix (curiously, it thickened up, turned to black sludge and despite my efforts to the contrary, formed thick bubbles on the surface). 10 hours later, full circle : a thin burgundy layer sandwiched between 2 thick grey layers !

At a loss as to what to do next… only thing i haven’t tried is filtering through cotton. Doesn’t sound like it’ll work and I am dreading it, but if I’m told to, I’ll buckle up and hit it. Current status is 3 jars in 2 lyers as per day 16 and one in grey sandwich hell as per day 17.
I can send pictures if it’ll help, but my camera battery is charging at the moment. I have 2 (obvious) questions : What did I do wrong and what do I do next? thanks in advance, guys.
 
You fixed it! Looks good - pretty yellow compared to mine. From what I read I wasn't expecting it to be white after the precip - nor was I expecting crystals right off the bat. If no one else responds, I guess I'll go ahead and re-x juat to be safe.
cheers,
JBA
PS - what was your yield from that and what was the starting mass of MHRB?
 
SWIM hasn't finished the extraction yet, but she's at about 1.1g measured out from 150g MHRB. 50g of the bark came from a previous extraction that went poorly, so she doesn't think it's a good standard.
 
Here's the latest; I don't know how much is there because my scale isn't sensitive enough, but it's certainly more than I thought! Now to purify...
cheers,
JBA

ps - Questions:does one purify/re-x strictly for health reasons or does it actually improve and clean the experience itself?
 

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Can anyone out there recommend another, cheaper solvent? Coleman's costs 18$ for 3.8 l (1 us gallon). After 1 extraction including defatting 3x (133g of mhrb) i am down to 1 l...
Thanks,
JBA
 
Only if they're random! Thanks for the quick answer; i couldn't wait so i went ahead and smoked a little - wow!! Vermillion shards and orange jigsaw hunks hurtling toward me, cartoon faces filling the centre of my line of sight, a tingling in body i otherwise felt no more and, finally, buzzing in and out like some out of range broadcast, a B&W image as if from an old talkie: a woman waist down in a sparking argentine skirt walking what i mistook as a poodle on a leash until it stood up on its hind legs elongated into furry tubes and advanced, transformed into some sort of small biped! The broadcast flitted in and out, alternating with the barrage of multicoloured pieces until it subsided and there was nothing but the near darkness of my joined lids... (full reports of my first four journeys to follow in the appropriate forum). I am no stranger to tryptamines (or salvia for that matter), but that was the first real vision i haveever had, as brief as it was.
To return to this thread: i will definitely purify then, entropymaster. Do you have a limonene or non toxic tech to recommend? I was going to switch over anyway, but i have all this lye and muriatic acid kicking around now, so i though i would use tjem up before going "safe". Are the yields the same with limonene etc? How about time? This last extracyion took close to a month and will add another week minimum to purify... Not complaining -the wait is well worth it, even though i have yet to break through, but it would be nice to cut down the labour - i have busy career, too many hobbies/interests and a 14 month old little boy to boot!!
Thanks
JBA
 
Ecstatic to hear you had a good transition! SWIM has the same issue with toxic supplies still hanging out, going to try d-limo after (q21q21's probably) they run out. From what I understand, d-limo pulls better than naptha and you don't have to worry about purifying since you crash the crystals out and then convert to freebase.

A week doesn't seem like much to avoid any long-term issues.

Be cool, be well!
 
Always appreciate your comments & advice ragabr. I am at my chalet right now, so I am going to "launch" one more time with the "filthy" spice before i head back to town to purify. Unfortuately i have to eyeball quantities... ( for now)
cheers
JBArk
 
I am eager to see the results of your further purification/re-xing. SWIMS currently in a similiar problem and would like to hear from you the results of this. Have you smoked with any adverse effects?
 
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