I’m not experienced enough to know what vac/temp you can safely go to…I’m a redneck in the woods…which is why I specified -29hg.
I am interested now though…I was unaware I can pull a vac on my tank with solvent in it, given the temp is low and the vac level isn’t too low. So if I’ve got my tank in dry ice and acetone, I could safely pull -10 to 15hg safely after venting?
Ran a couple pounds of material over the weekend. Pulled vac in my solvent tank instead of just burping, but only to about -15hg. I can absolutely fucking rip on recovery now…holy fucking shit. I know I’m uneducated on this shit…having only learned from reading online and my own experience…but that right there is a break through for me. Massive time savings. Thank you for that piece to my puzzle homie. You’ve taught me so much with everything you post. Much respect.
At that temp and pressure. The only thing you were taking out was the nitrogen. You’re very welcome, man. I’m glad you are doing better with that little tid bit.
this needs to be connected to an air compressor to pull vacuum on a chilled solvent tank correct?
is that safe not doubting you just clarifying before i do something dumb?
There is also other models that pull less of a vacuum. Needing less cfm to push them.
Any other processes that you can think of that need pull a vacuum, not a hard one, or a full one?And also need a pump that doesn’t have moving parts to get damaged by vapors…
Like a roto evaporator, or a buchner/hochstrom filtration setup. You can put a couple of these around your lab instead of buying a bunch of expensive diaphragm pumps, which don’t have a strong vacuum, anyway.
The husky compressor that I am going to get for this (I’m using a smaller one currently) is more than powerful enough.
Bro, I wish I read this tread before investing in a 20k pump over a year ago. Here’s our ünique passive design with a hot-loop by pass. It’s been a evolution. Hope this makes sense to some of you.