So, I'm Assuming Lye Does Not Come Through

[brokedownpalace10]

In the STB extractions, an excess of lye is used. To break up the rootbark and it also makes things easier since a PH checker is not needed.

I'm assuming the excess lye does not come through into the solvent? What if the Naptha is evaporated? What if a different solvent is used (like Xylene)?
Importantly, what if you do an A/B? Just use a big excess of lye to take the PH from acid to very basic? Nothing comes through in the final Product?

 

[fractals4life]

The lye won't dissolve in the solvent as such, but tiny bits may be *suspended* in there, and so end up in your end product.

The fix is easy, just water wash your solvent before the freeze precipitation stage so the lye gets dissolved in the water.

I just squirt my solvent into a measuring cylinder with a few cms of water in the bottom, then pipette it off into my precipitation dish after it settles again.

Make sure the water isn't too cold, otherwise some of the end product might crash out into the water, use water at least as warm as your solvent. Even if you do get cloudy water after, you can just add it back to your soup for recovery on the next pull.

 

[brokedownpalace10]

The lye won't dissolve in the solvent as such, but tiny bits may be *suspended* in there, and so end up in your end product.

The fix is easy, just water wash your solvent before the freeze precipitation stage so the lye gets dissolved in the water.

I just squirt my solvent into a measuring cylinder with a few cms of water in the bottom, then pipette it off into my precipitation dish after it settles again.

Make sure the water isn't too cold, otherwise some of the end product might crash out into the water, use water at least as warm as your solvent. Even if you do get cloudy water after, you can just add it back to your soup for recovery on the next pull.

Thanks. I did not know the temperature matters on that step.

 

[Anuc24]

The lye won't dissolve in the solvent as such, but tiny bits may be *suspended* in there, and so end up in your end product.

The fix is easy, just water wash your solvent before the freeze precipitation stage so the lye gets dissolved in the water.

I just squirt my solvent into a measuring cylinder with a few cms of water in the bottom, then pipette it off into my precipitation dish after it settles again.

Make sure the water isn't too cold, otherwise some of the end product might crash out into the water, use water at least as warm as your solvent. Even if you do get cloudy water after, you can just add it back to your soup for recovery on the next pull.

Hello. I know your post is old but it's somewhat the kind of info in looking for. You said you can just throw it back in the soup for next pull. So what if pull is complete but final result is sparkly, but way to dark. If it gets dumped back in soup, will it extract again, or should it just be a loss?