Aislin_the_Dreamer
Rising Star
Most of the teks I've come across seem to aim for pure white crystals and/or use non-food-grade chemicals. There are a handful of food-grade teks which I have read and tried to understand as well. My goal is to extract jungle spice since I believe that would provide a more full and robust experience. It also seems to require less time and resources even if it's a touch more work. Before I experiment with acacia this weekend, I'm just trying to get my comparisons, thoughts, and understanding on paper. I wouldn't mind any affirmations or "that's nonsense."
Acid Step
A lot of folk heat this step which makes sense. A variety of acids can be used but to me, vinegar seems like an excellent choice with a pH of about 2.4. This converts the spice to the salt form, making it polar so I can understand the addition of ethanol and/or water here. I might give that a try as well. I guess here are the questions:
1) How fast is conversion?
2a) Is it really worthwhile to have several heat steps with new vinegar/ethanol/water?
2b) are yield differences negligible or worthwhile from this?
2c) Or does the repeated heat treatment simply pull more unwanted tannins?
Defat Step
I don't view this as necessary since I'm aiming for jungle spice. I'm still researching all the the other compounds and just recently found a detailed post about it.
Base Step
I've seen methods where the acid is left on the material and others where it's taken off. I suppose if you take the acid off the material before you add base, you can then have the material to start again if something went amiss. My attempts with Q21Q21's tek (using MHRB) where the base was added to the material worked successfully so I may try the other method this time around and see what happens. Calcium Hydroxide will be the key player here with a pH of about 11 so that should convert about 99.9% of the spice.
Nonpolar Pulls
This will be the first time I'll be using limonene. Since the spice is now in the freebase form, it should be soluble in this nonpolar solvent. Xylene or naptha could be used and evaporated or freeze precipitated but going to the next step seems less time consuming albeit more work.
Vinegar/water Pull
Using a separatory funnel I just recently acquired and am very excited to use, I will pull out the spice by adding vinegar to the limonene. This should convert the freebase back into a salt. I will do a few water pulls as well to ensure I've got most of it.
All that would remain is reducing the acid/water mixture to a manageable level, quantifying the tincture, and pat myself on the back for putting my chemistry minor to good use. Many thanks.
PS. Unrelated curiosity: What happens to ancient posts that seem forgotten and lost in time?
Acid Step
A lot of folk heat this step which makes sense. A variety of acids can be used but to me, vinegar seems like an excellent choice with a pH of about 2.4. This converts the spice to the salt form, making it polar so I can understand the addition of ethanol and/or water here. I might give that a try as well. I guess here are the questions:
1) How fast is conversion?
2a) Is it really worthwhile to have several heat steps with new vinegar/ethanol/water?
2b) are yield differences negligible or worthwhile from this?
2c) Or does the repeated heat treatment simply pull more unwanted tannins?
Defat Step
I don't view this as necessary since I'm aiming for jungle spice. I'm still researching all the the other compounds and just recently found a detailed post about it.
Base Step
I've seen methods where the acid is left on the material and others where it's taken off. I suppose if you take the acid off the material before you add base, you can then have the material to start again if something went amiss. My attempts with Q21Q21's tek (using MHRB) where the base was added to the material worked successfully so I may try the other method this time around and see what happens. Calcium Hydroxide will be the key player here with a pH of about 11 so that should convert about 99.9% of the spice.
Nonpolar Pulls
This will be the first time I'll be using limonene. Since the spice is now in the freebase form, it should be soluble in this nonpolar solvent. Xylene or naptha could be used and evaporated or freeze precipitated but going to the next step seems less time consuming albeit more work.
Vinegar/water Pull
Using a separatory funnel I just recently acquired and am very excited to use, I will pull out the spice by adding vinegar to the limonene. This should convert the freebase back into a salt. I will do a few water pulls as well to ensure I've got most of it.
All that would remain is reducing the acid/water mixture to a manageable level, quantifying the tincture, and pat myself on the back for putting my chemistry minor to good use. Many thanks.
PS. Unrelated curiosity: What happens to ancient posts that seem forgotten and lost in time?
