I'm totally overstepping my real world knowledge here, but the freeze time and temp seems to be up to experimentation. The balance is to maximize time for the tricomes to dissolve in the etoh, while minimizing time for undesirable plant matter, wax, etc to also dissolve. What I'm thinking of doing is that 5-10minute soak first, filter, then add more etoh and do a longer soak to get more off. evaporate separately and see what I get.
vacuum heater seems to be the choice. I haven't found a cheap one yet, so I'm going to try no vacuum longer exposure to low heat. Like, 24 hours in my dehydrator at 100-150F. see what I get.
It'd be rad to hear your experimental designs when trying this yourself. Please share with results if you want.
AFA running the extract again through the Source...yes it can drive the etoh content further down, but what I read is that it becomes really crappy to get out of the reaction vessel that way. They say it's best to remove the extract while it's still bubbling and soupy, pour it on a silicone mat or glass baking plate, then finish the etoh removal via time, wind, heat, vacuum, or a combo of. If the extract was or gets decarbed, shatter can form. if not decarbed, a pull-n-snap or perhaps a sugar forms. the soup can also be agitated/whipped to make a peanut butter looking thing.