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Absolute Amber from Banana Silver Ladyboys
- Thread starter jump117
- Start date
dope_roor
Member
ive been experimenting with spraying onto pre warmed dishes, still unsure whether or not the method is too abrupt for some of the more volatile components but it sure does cut down on purge time. floating the pyrex in water also conveniently ensures that the glass remains absolutely level during the spray, sometimes allowing for the butane to purge before it gets a chance to creep up the side wall/pool in a corner as it is less biased to flow to one side
Hello everyone, today i am finishing my final extraction and first try at amber. I left you last time when I put the EthO solution in the freezer, 30 hours later I have
Then I coffee filtered it by pouring the solution through a funnel with a coffee filter inside
the solution was then filtered, and I could see visible fats and waxes in my pyrex dish so i instantly poured it back into the funnel with 2 coffee filters this time. then the solution was very clear, and I poured it back into the pyrex and began the steam bath. I used a metal pan about 2' high and poured small amounts of water per time for maximum steam.
after the ethonal is disolved I have
then I scrape the amber into the centre of the pan and I have(sorry for the bad pic, I left my pyrex on the metal dish used for steaming bath, all that is there is what you see the yellow solution)
This is what I ended up with
I was unsure if those little bubbles were a solvent or something natural so I continued to heat it, eventually in the stove at 150 degrees, big mistake. the end product was still very clean and good tasting but almost no taste or smell and it is a 'Budder' style texture.
im wondering aproximatly how long it will take to remove all of the solvents VIA steam bath?
this was my 1st run so im not completely disapointed but im still somewhat upset.
I have 10LBs of medium fresh chopped material I am freezing and am going to keep trying till I get the results like you have jump.
let me know any ideas or thoughts on how long it will take to remove solvents via steam.. thanks alot guys
Then I coffee filtered it by pouring the solution through a funnel with a coffee filter inside
the solution was then filtered, and I could see visible fats and waxes in my pyrex dish so i instantly poured it back into the funnel with 2 coffee filters this time. then the solution was very clear, and I poured it back into the pyrex and began the steam bath. I used a metal pan about 2' high and poured small amounts of water per time for maximum steam.
after the ethonal is disolved I have
then I scrape the amber into the centre of the pan and I have(sorry for the bad pic, I left my pyrex on the metal dish used for steaming bath, all that is there is what you see the yellow solution)
This is what I ended up with
I was unsure if those little bubbles were a solvent or something natural so I continued to heat it, eventually in the stove at 150 degrees, big mistake. the end product was still very clean and good tasting but almost no taste or smell and it is a 'Budder' style texture.
im wondering aproximatly how long it will take to remove all of the solvents VIA steam bath?
this was my 1st run so im not completely disapointed but im still somewhat upset.
I have 10LBs of medium fresh chopped material I am freezing and am going to keep trying till I get the results like you have jump.
let me know any ideas or thoughts on how long it will take to remove solvents via steam.. thanks alot guys
Last edited:
Trichgnomes
Member
bump!
Some amber produced from royal kush:
Some amber produced from royal kush:
bump!
Some amber produced from royal kush:
Hee, hee, hee, nice art work!
Cool pic trichgnomes! Guys I'm doing another extraction tonight and this time I'm going to pool the liquid butane in my coffee pot and then soak the herb for 20 mins per 2 oz's, I'm just wondering after I filter the 1st 2 oz's of herb out of the liquid butane via coffee filters, can I reuse that same liquid in say another 2 ounces of then fresh material? And keep cycling the same liquid butane through in total possibly 1LB of fresh material? Or would that somehow degrade the oil or something? I'm fairly new to this style of butane extraction I've only ever used sprayer type extractors. Thanks
daheadies
poppin' outta control
check these threads out
https://www.icmag.com/ic/showthread.php?t=203067
https://www.icmag.com/ic/showthread.php?t=211453
https://www.icmag.com/ic/showthread.php?t=203067
https://www.icmag.com/ic/showthread.php?t=211453
Hey Tr
hgnomes 
for the gift!
Hey bukket!
I have not tried to use the same butane to flush with new downloads.
I think that this should take care to reduce losses from evaporation of butane.
Insulate the coffee pot or better use a thermos.
Temperature of the solvent and exposure time are critical parameters for extraction.
The warmer the solvent, the faster it dissolves and the wider the range of the solute.
Tamisium users say that at room temperature for butane in a few minutes begins lipophilic pollution of extract.
Long cold vs. short warm.
From a can, cooled to -20°C, ~ 0°F, liquid gas flows out calm laminar flow and fills the vessel, as an ordinary liquid.
Can with a temperature of 8°C, ~46°F, sprays like a fire extinguisher.
Part of the liquid gas evaporates and is wasted in cooling the loaded material,
and only then begins to work as a liquid solvent.
Pre-cooled material will save this part of the gas in liquid form for extraction.
for the gift!
Hey bukket!
I have not tried to use the same butane to flush with new downloads.
I think that this should take care to reduce losses from evaporation of butane.
Insulate the coffee pot or better use a thermos.
Temperature of the solvent and exposure time are critical parameters for extraction.
The warmer the solvent, the faster it dissolves and the wider the range of the solute.
Tamisium users say that at room temperature for butane in a few minutes begins lipophilic pollution of extract.
Long cold vs. short warm.
From a can, cooled to -20°C, ~ 0°F, liquid gas flows out calm laminar flow and fills the vessel, as an ordinary liquid.
Can with a temperature of 8°C, ~46°F, sprays like a fire extinguisher.
Part of the liquid gas evaporates and is wasted in cooling the loaded material,
and only then begins to work as a liquid solvent.
Pre-cooled material will save this part of the gas in liquid form for extraction.
Cool! thanks for the response jump.
Im just wondering about my last step in the last picture I posted in my last reply. there is the final turn out from 1 Oz dryed material, im sure you cant see it very well but there are small bubbles left in the resin, im just wondering if they were non harmful or if I should contiunue to steam bath untill all bubbles are gone or what do I do.. this is the one part where I messed up.. please help guys.. thanks again
Im just wondering about my last step in the last picture I posted in my last reply. there is the final turn out from 1 Oz dryed material, im sure you cant see it very well but there are small bubbles left in the resin, im just wondering if they were non harmful or if I should contiunue to steam bath untill all bubbles are gone or what do I do.. this is the one part where I messed up.. please help guys.. thanks again
daheadies
poppin' outta control
Hi!
Hope you get it Jump!! you deserve it!! like i said months ago, you deserve some sort of award!!
M
Mr. Mountain
This is by far my favorite hash making technique! I use the "Blow thru" method with my Butane. Then re-dissolve in 99% Iso or 95% Ethanol. I freeze the entire liquid alcohol/hash mixture overnight and place my filtering rig in the refrigerator.
I filter the alcohol/hash mixture a few ounces at a time, returning the bulk of the solution back to the freezer to keep the waxes out of solution.
When I am done with the filtering process, I have a white layer of lipids/wax on my filter.
The Absolute I make is BARELY semi-solid more of a viscous liquid really. I find that keeping everything cold during filtering helps prevent any wax from going back into solution, keeping it more liquid.
After purging for many days, this oil is still just that... AN OIL! I used a pipette to suck it up and place it in a vial for further use.
I will supplement this post with pictures as soon as possible. On my next run!
Until then,
Mr. M
I filter the alcohol/hash mixture a few ounces at a time, returning the bulk of the solution back to the freezer to keep the waxes out of solution.
When I am done with the filtering process, I have a white layer of lipids/wax on my filter.
The Absolute I make is BARELY semi-solid more of a viscous liquid really. I find that keeping everything cold during filtering helps prevent any wax from going back into solution, keeping it more liquid.
After purging for many days, this oil is still just that... AN OIL! I used a pipette to suck it up and place it in a vial for further use.
I will supplement this post with pictures as soon as possible. On my next run!
Until then,
Mr. M
Mr. Mountain, thank you for your report!
Evaporation of the cold ventilation is not sufficient for complete removal of ethanol. Especially if THCA/THC ratio is high.
Extract thickens and its viscosity keeps ethanol, and ethanol does not allow the resin to harden.
To completely remove residual ethanol, as well as to remove residual butane extract has heated up to melt or at least softening,
that is fatal to terpenes.
It should be noted that it is not bad for stealth use in public places where odors can attract unwanted attention.
For this purpose I made out thin stick of solid amber and insert it into the cigarette, where the pre-pierced channel for its placement.
The appearance of a cigarette is not changed.
Smoke resin with the first deep puff.
If you choose not to smoke the load of amber stick can be easily derived from cigarette without loss.
Try evaporate a few drops of your nectar on a plate over boiling water.
Steam bath provides a melt temperature THCA and more complete removal of ethanol.
If, however, this consistency is not solidified, it means that the ratio THCA / THC is small,
ie material mostly or completely decarboxylated and ready for orals.
As metrologist how do you assume pressure in the pipe during the "Blow thru" extraction?
The higher the pressure, the higher the temperature of liquid butane, the faster the extraction and shorter pure phase.
If, as in your situation, the gas is available and inexpensive, it might be worth a try cold butane extraction in an open thermos,
it will give a clear and consistent extract.
J
juicepuddle
Jump those last pics are BEAUTY'S!
This flower mass
in the storage room of my friend Tigerdream aka Summer,
after which it was granted for the experiments.Rinse part of them in Butane (-20C), in a thermos for one hour, evaporated and dissolved in ethanol.
Strange that weren’t flakes in ethanol in dissolution of first run BHO, but they fell in the second hour smaller ~10% run.
The color darkened to cherry-red, but it still holds the consistency, you can keep in fingers like 30 seconds, then it sticks.
It was the first life of this amber, then followed by two more.
