stationdragon
Rising Star
Hi there, me again with another STB question relating to recent extractions.
Bear with me, I will get to the main point but let me lay the setting first.
I'm following almost the same tek as usual, I stick closely to Nomans tek because it is the most doable of teks in my circumstances.
This time I have used pre-powdered bark (MHRB)and I asked a question on here recently regarding water content when using pre=powdered bark. Nomans tek says to double the water content and a fellow Nexian said that I can use double the bark I've been previously using.
So I set up my two 1 litre mason jars and into each I have begun a 100g extraction.
I used 750ml water, 100g lye and 100g salt (not in Nomans but seems effective in boosting yield). I was previously working with 1.5g lye per gram of bark because it seemed to have an effect on yield for one particular Nexian in the past but I read also that once the water reaches a certain PH it really doesn't make any difference how much more lye you add, so I brought that down to save my supplies.
I decided to do a side by side coleman (UK version without blue chemical) and zippo premium.
I used 40ml/50ml of each per pull after gently warming the naphtha in a water bath and after collecting I put them in separate jars labelled appropriately. I did four pulls of this size, evaporated at least two thirds overnight and put into a very cold and frosty freezer.
The zippo evaporated far quicker than the coleman, by morning the zippo was very low and turned extra milky when I blew on it. Coleman took a further 8 hours to reduce down enough (this is with two fans running).
Before I put the zippo jar in the freezer it was already forming crystals and they grew during their time in the freezer but despite reducing down to barely anything, the naphtha remained very milky still and after a couple of days hadn't crashed out any more crystals but I could see that the naphtha was still very saturated because of it's opacity.
I decided my best move was to take it out, break off the crystals and pour it through a filter and catch the drips in a glass baking dish to evaporate completely.
The naphtha filtered VERY slowly through the filter and what came out the other side was clear. After drying the crystals I got 140mg from the freeze precip and the resulting naphtha is still evaporating but not showing any signs of crystal growth yet despite it being just a dribble.
I noticed that there is a noticeable stain left on the filter which I haven't yet seen with zippo premium so I wondered if I'd been ripped off and sold another solvent in zippo premium cans but I thought this very unlikely. So instead I held a lighter beneath the filter paper and let the heat warm it up, and hey presto, DMT vapours.
So my conclusion is all that milky DMT suspended in the naphtha got caught up in the fibres of the filter paper. So...that's lost, I'm not balling up filter paper and stuffing them into my machine for a blastoff.
The coleman on the other hand is producing some very white cystals and the solution is totally clear so this has crashed all it has to give I think, but still, this when weighed is not going to add up to the numbers I'm expecting.
I have other pulls sitting at the moment, I didn't have time to warm the naphtha so I'm leaving it for a day or so before collecting.
I've had a lot of extraction fails in recent attempts and it's been blowing my mind, because my very first attempt was absolutely priceless. We poured out the naphtha and wow, there was so much straight away. I've not managed to achieve that since the second extraction. I've had very, very low yields and trouble getting it to crash.
I much prefer the idea of freeze precip because of time, smell, saving naphtha for reuse, convenience and I'm concerned about any leftover residue from solvents. Coleman seems to evaporate ultra clean but takes forever and zippo seems pretty clean too, leaving just an almost invisible outer line where it dries.
I just can't seem to get the same results as the first two times recently despite changing either nothing or very little in our method and it's bugging me so much.
I am going to keep pulling these jars until there's nothing to pull just because I need accurate figures, I need to know what I'm dealing with weight wise.
Unfortunately the place we got the bark from first time around seems to have vanished and we've had two different sources recently. It's hard to say whether it's bark quality, it's hard to settle on any one cause really but we're just going to keep pushing on and hope for the best.
I did read somewhere that pre-powdered has the habit of yielding less DMT but I really don't know about that kind of thing.
Of course, the places we buy from aren't always legit in their own country and therefore might not be legit in their sourcing, storage and honesty if pressed on the subject so it's so hard to tell.
If anybody has any ideas then great, if not I'll just keep pushing on until I get it right. Just wish I hadn't started on such a high note only to be disappointed since. It's such a simple process with so few steps and very little chance to get something wrong I'm absolutely baffled as to how I can get such varying results from unchanging methods.
Bear with me, I will get to the main point but let me lay the setting first.
I'm following almost the same tek as usual, I stick closely to Nomans tek because it is the most doable of teks in my circumstances.
This time I have used pre-powdered bark (MHRB)and I asked a question on here recently regarding water content when using pre=powdered bark. Nomans tek says to double the water content and a fellow Nexian said that I can use double the bark I've been previously using.
So I set up my two 1 litre mason jars and into each I have begun a 100g extraction.
I used 750ml water, 100g lye and 100g salt (not in Nomans but seems effective in boosting yield). I was previously working with 1.5g lye per gram of bark because it seemed to have an effect on yield for one particular Nexian in the past but I read also that once the water reaches a certain PH it really doesn't make any difference how much more lye you add, so I brought that down to save my supplies.
I decided to do a side by side coleman (UK version without blue chemical) and zippo premium.
I used 40ml/50ml of each per pull after gently warming the naphtha in a water bath and after collecting I put them in separate jars labelled appropriately. I did four pulls of this size, evaporated at least two thirds overnight and put into a very cold and frosty freezer.
The zippo evaporated far quicker than the coleman, by morning the zippo was very low and turned extra milky when I blew on it. Coleman took a further 8 hours to reduce down enough (this is with two fans running).
Before I put the zippo jar in the freezer it was already forming crystals and they grew during their time in the freezer but despite reducing down to barely anything, the naphtha remained very milky still and after a couple of days hadn't crashed out any more crystals but I could see that the naphtha was still very saturated because of it's opacity.
I decided my best move was to take it out, break off the crystals and pour it through a filter and catch the drips in a glass baking dish to evaporate completely.
The naphtha filtered VERY slowly through the filter and what came out the other side was clear. After drying the crystals I got 140mg from the freeze precip and the resulting naphtha is still evaporating but not showing any signs of crystal growth yet despite it being just a dribble.
I noticed that there is a noticeable stain left on the filter which I haven't yet seen with zippo premium so I wondered if I'd been ripped off and sold another solvent in zippo premium cans but I thought this very unlikely. So instead I held a lighter beneath the filter paper and let the heat warm it up, and hey presto, DMT vapours.
So my conclusion is all that milky DMT suspended in the naphtha got caught up in the fibres of the filter paper. So...that's lost, I'm not balling up filter paper and stuffing them into my machine for a blastoff.
The coleman on the other hand is producing some very white cystals and the solution is totally clear so this has crashed all it has to give I think, but still, this when weighed is not going to add up to the numbers I'm expecting.
I have other pulls sitting at the moment, I didn't have time to warm the naphtha so I'm leaving it for a day or so before collecting.
I've had a lot of extraction fails in recent attempts and it's been blowing my mind, because my very first attempt was absolutely priceless. We poured out the naphtha and wow, there was so much straight away. I've not managed to achieve that since the second extraction. I've had very, very low yields and trouble getting it to crash.
I much prefer the idea of freeze precip because of time, smell, saving naphtha for reuse, convenience and I'm concerned about any leftover residue from solvents. Coleman seems to evaporate ultra clean but takes forever and zippo seems pretty clean too, leaving just an almost invisible outer line where it dries.
I just can't seem to get the same results as the first two times recently despite changing either nothing or very little in our method and it's bugging me so much.
I am going to keep pulling these jars until there's nothing to pull just because I need accurate figures, I need to know what I'm dealing with weight wise.
Unfortunately the place we got the bark from first time around seems to have vanished and we've had two different sources recently. It's hard to say whether it's bark quality, it's hard to settle on any one cause really but we're just going to keep pushing on and hope for the best.
I did read somewhere that pre-powdered has the habit of yielding less DMT but I really don't know about that kind of thing.
Of course, the places we buy from aren't always legit in their own country and therefore might not be legit in their sourcing, storage and honesty if pressed on the subject so it's so hard to tell.
If anybody has any ideas then great, if not I'll just keep pushing on until I get it right. Just wish I hadn't started on such a high note only to be disappointed since. It's such a simple process with so few steps and very little chance to get something wrong I'm absolutely baffled as to how I can get such varying results from unchanging methods.