downwardsfromzero
Boundary condition
So, were you pre-drying your mushrooms before putting them with the desiccant? It looks as though you might have been, I just don't see (or haven't seen) where you've explicitly stated this. This seems like one of those "too obvious" questions that no-one else asks - do forgive me!
I've used normal, retail calcium chloride - similar to the one you've pictured - as a desiccant for years. !!However, before placing the mushrooms in the tub with the desiccant, they will have been dried for maybe 24hrs with an airflow desiccator, like Northerner suggested. The mushrooms remain sealed in the tub atop the calcium chloride for between a few days to a few years - separated from direct contact with the desiccant with a couple of sheets of greaseproof paper.
While I haven't shown the dedication to ongoing comparison of mushroom potency that you have, my experiences have shown nonetheless that they remain amply potent. This comes with the caveat that the species concerned were (mostly, in order of frequency) P. semilanceata (wild), P. cyanescens (feral and cultivated) and P. ovoideocystidiata (cultivated) [this last one being quite phenomenal in its power to the extent that I considered embarking on a full legal process to complete an interspecies marriage between myself and the mushroom. Perhaps one day, in one of your churches?] P. sem and P. ovo at least show a lasting preponderance of the phosphorylated alkaloids which is considered to confer better air stability.
Anyhow, I digress somewhat. Silica gel I've used, as the little pouches one finds enclosed with various items of commerce, to place in jars of already desiccated mushrooms so that there is minimal chance of mould formation during storage. I suspect you already considered silica gel as potentially advantageous because it can be regenerated indefinitely. With that use case it's best to include at least some of the cobalt chloride doped material which turns from dark blue to pink once the silica has reached its capacity for water vapour adsorption.
I built my own airflow desiccator (as I have said before in various places) at minimal cost using a bucket, a computer fan and a low-wattage light bulb, plus whatever bits of mesh could be found. Pan splatter guards are pretty good. To protect sensitive material from excessive light, some kind of opaque, heat resistant material can be used. I used a pyrex bowl (not transparent, obviously!) It was a fun project which lends itself to further adaptations and improvements.
Just to make it clear for all readers, my hypothesis was that dehydrated chitin (or other cellular material) undergoes a structural change that makes it harder for the actives subsequently to be extracted from the intracellular space. A comparison of yields obtained using ultrasonic extraction would at least be a first step towards understanding what effect you may have noticed here.
I've used normal, retail calcium chloride - similar to the one you've pictured - as a desiccant for years. !!However, before placing the mushrooms in the tub with the desiccant, they will have been dried for maybe 24hrs with an airflow desiccator, like Northerner suggested. The mushrooms remain sealed in the tub atop the calcium chloride for between a few days to a few years - separated from direct contact with the desiccant with a couple of sheets of greaseproof paper.
While I haven't shown the dedication to ongoing comparison of mushroom potency that you have, my experiences have shown nonetheless that they remain amply potent. This comes with the caveat that the species concerned were (mostly, in order of frequency) P. semilanceata (wild), P. cyanescens (feral and cultivated) and P. ovoideocystidiata (cultivated) [this last one being quite phenomenal in its power to the extent that I considered embarking on a full legal process to complete an interspecies marriage between myself and the mushroom. Perhaps one day, in one of your churches?] P. sem and P. ovo at least show a lasting preponderance of the phosphorylated alkaloids which is considered to confer better air stability.
Anyhow, I digress somewhat. Silica gel I've used, as the little pouches one finds enclosed with various items of commerce, to place in jars of already desiccated mushrooms so that there is minimal chance of mould formation during storage. I suspect you already considered silica gel as potentially advantageous because it can be regenerated indefinitely. With that use case it's best to include at least some of the cobalt chloride doped material which turns from dark blue to pink once the silica has reached its capacity for water vapour adsorption.
What gets limited here - although I can see the benefits of alu foil - is airflow, airflow, airflow!I prefer alu foil.
I built my own airflow desiccator (as I have said before in various places) at minimal cost using a bucket, a computer fan and a low-wattage light bulb, plus whatever bits of mesh could be found. Pan splatter guards are pretty good. To protect sensitive material from excessive light, some kind of opaque, heat resistant material can be used. I used a pyrex bowl (not transparent, obviously!) It was a fun project which lends itself to further adaptations and improvements.
Similar but different. I certainly get what you're saying and it would be a worthwhile scientific experiment to compare degradation of mushroom material subjected to differing degrees of drying/desiccation. One nuance of your hypothesis would be that the strongly desiccated material, either spontaneously or during the powdering process, undergoes increased oxidation of the psilocin/baeocin™/norbaeocin™ because of cell wall destruction through increased brittleness of the dehydrated chitin.What I thought is similar. The cell membrane gets damaged, and the oxidation might kick in.
Just to make it clear for all readers, my hypothesis was that dehydrated chitin (or other cellular material) undergoes a structural change that makes it harder for the actives subsequently to be extracted from the intracellular space. A comparison of yields obtained using ultrasonic extraction would at least be a first step towards understanding what effect you may have noticed here.
