alexcycling
Bluelighter
- Joined
- Feb 25, 2024
- Messages
- 20
After searching, I concluded discussing extraction is legit here. If not, please inform me.
I follow noman's tek (and yes I have some experience with chemistry and know how to handle NaOH and acids etc.).
I need to start from chunked stuff, and 'treated' it with a high-speed mixer which resulted in powder and fibers. I tried to run the fibers through a decent coffee grinder, but it gets stuck (as I expected), so I'm left with powder/fiber mix.
The text (addendum 1) also comments on the pre-powdered stuff: it has at least a part of the fibers also powdered, which leads to a sludge which won't release the naphta. From this I conclude we should probably not have the fibers in the solution? But I guess that keeping the fibers there might extract extra good (or bad?) stuff. And: separation of the powder from the fiber is impossible; so getting rid of the fibers in dry state would mean to also remove lots of powder.
So the question is how to proceed?
Having fibrous stuff in the solution makes it hard to separate the phases later on using a separation funnel. Getting rid of it from the lye phase before adding naphta is nasty (e.g. filtrating the alkaline stuff adds extra complexity / dangers).
So would one leave it all in and go for an Erlenmeyer flask / pipette approach?
Another question is:
I'm thinking about using some water in the mixer, as this might help braking down even further. Then decanting everything into the actual mixing jar and carfully adding NaOH.
Any thoughts?
I follow noman's tek (and yes I have some experience with chemistry and know how to handle NaOH and acids etc.).
I need to start from chunked stuff, and 'treated' it with a high-speed mixer which resulted in powder and fibers. I tried to run the fibers through a decent coffee grinder, but it gets stuck (as I expected), so I'm left with powder/fiber mix.
The text (addendum 1) also comments on the pre-powdered stuff: it has at least a part of the fibers also powdered, which leads to a sludge which won't release the naphta. From this I conclude we should probably not have the fibers in the solution? But I guess that keeping the fibers there might extract extra good (or bad?) stuff. And: separation of the powder from the fiber is impossible; so getting rid of the fibers in dry state would mean to also remove lots of powder.
So the question is how to proceed?
Having fibrous stuff in the solution makes it hard to separate the phases later on using a separation funnel. Getting rid of it from the lye phase before adding naphta is nasty (e.g. filtrating the alkaline stuff adds extra complexity / dangers).
So would one leave it all in and go for an Erlenmeyer flask / pipette approach?
Another question is:
I'm thinking about using some water in the mixer, as this might help braking down even further. Then decanting everything into the actual mixing jar and carfully adding NaOH.
Any thoughts?