Whats the theory behind alcohole extraction. I mean PG seems a much stronger solvent. Is this an attempt to create a cleaner burning NET?
In my situation, having already completed a month long room temperature extraction in PG, the secondary vodka extraction is more of a final wash of the tobacco used in the PG soak method. The vodka certainly has removed a majority of the PG that I was unable to remove via pressing.
I feel confident at this point that in order to extract the very highest percentage of usable extract the following steps should be considered.
1) Reduce tobacco size by chopping (10-16 mesh seems sufficient).
2) Soak tobacco in PG, VG, or PGA the quantity must be sufficient to completely cover the fully saturated tobacco for 30 days.
3) Remove liquids from tobacco by pressing.
4) Soak the pressed tobacco in PGA for (4 hours PG and VG method), (I'm not sure for the PGA method).
5) Remove PGA wash from tobacco by pressing.
6) Filter liquids to your desired level of clarity (do not mix the PG/VG extract with the PGA wash at this time).
7) Reduce PGA wash liquid level to 10% of its original volume by heating to 140degF.
8) Combine extract and reduced PGA wash.
The PGA soak and wash steps are purely optional, and to some extent may be less effective if your method of pressing the PG/VG soaked tobacco is exceptionally more efficient than mine. In my experience the additional PGA soak and wash were highly effective in removing additional usable extract.
It should go without saying that the more uniform your methods are the more uniform your results will be. By way of example in step 1) you are chopping the tobacco product into smaller particles, passing your chopped tobacco through a wire colander will sort the larger sizes out that need more chopping. This will give you a more uniform product on the back end of the project.
Maurice