Hi members,
I accidentally mixed an acacia extract (A. obtusifolia and A. maidenii phyllodes and branch bark) with a mimosa hostilis acidic solution (mhrb had been already acid-boiled and filtered). The extraction leading to the acacia extract went just fine, was using acetic acid.
I realized too late that the acid used in the mhrb extraction was hydrochloric acid and when continuing to extract, basing the mix with naoh, a strange massive precipitation of big needles occured. I knew not to use hcl with acacia but i just forgot about the hcl in the mhrb mix
:?:
It is almost impossible to pull with d-limonene, magnetic stiring the mix as well. The whole solution gets very thick and needles can be seen throughout.
Can anybody tell me, from a chemically stand point of view, what those needles might be (Besides DMT and other goodies
) i.e. what kind of chemical reaction occured (might have occured) (acacia+hcl) and how one could/should proceed? Might there maybe be a trick to reverse that negative reaction and save the extraction?
Also, even within the salted solution there already has occured some precipitation which kind of looks like the same as the before mentioned. But these can of course just be filtered away, though
Here are some photos of the precipitations:
Thanks, nexians
I accidentally mixed an acacia extract (A. obtusifolia and A. maidenii phyllodes and branch bark) with a mimosa hostilis acidic solution (mhrb had been already acid-boiled and filtered). The extraction leading to the acacia extract went just fine, was using acetic acid.
I realized too late that the acid used in the mhrb extraction was hydrochloric acid and when continuing to extract, basing the mix with naoh, a strange massive precipitation of big needles occured. I knew not to use hcl with acacia but i just forgot about the hcl in the mhrb mix
:?: It is almost impossible to pull with d-limonene, magnetic stiring the mix as well. The whole solution gets very thick and needles can be seen throughout.
Can anybody tell me, from a chemically stand point of view, what those needles might be (Besides DMT and other goodies
) i.e. what kind of chemical reaction occured (might have occured) (acacia+hcl) and how one could/should proceed? Might there maybe be a trick to reverse that negative reaction and save the extraction?Also, even within the salted solution there already has occured some precipitation which kind of looks like the same as the before mentioned. But these can of course just be filtered away, though
Here are some photos of the precipitations:
Thanks, nexians

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I guess it was due to a logistic thought, because I had different unfinished extractions and wanted to make myself less work. If I remember correctly I planned a zinc reduction. In the end I got more work, got a mess :x