DVap's the real chemist, I'm just filling in...
actually all that is written wrongly, did that a bit quickly,
it's not really Nic-hydoxide as such, should have been:
Nic.H(+) + OH(-) --> Nic (freebase) + H2O
same principal and equilibrium though.
Yes it's different dried, cos the equilibrium only really applies to the soluble-ised & mobile molecules.
So more stable dried then, but the act of heating for drying could well
cause a high speed action of the excess hydroxide on the organic matter (?)
Would have to test that in practice, ie measure pH before drying & pH after re-wetting,
maybe for different drying regimes.
But any amount of re-adsorbed moisture would allow some chemical action.
I'm still plodding through my (originally) pH9 mint rustica, not going as quick as I thought
it might cos it's not as palatable as TF.
Edit:
Actually, about that 'organic counter-ion' form of nicotine thing...
in tobacco nic. apparently is a mixture of citrate & malate,
and probably 'every other organic solute present'-ate,
so wondering if free-basing is so important after all (assuming the
organic forms do actually cause faster/easier tissue adsorption).