I asked about pushing w compressor before I found nitro…
Was met w LARGE RESOUNDING NO by couple Highly reputable members here but I really don’t understand what’s going on here anyways w the scrubbing. Isnt solvent still present? Don’t throw rocks just trying to understand.
Oxygen makes the butane more readily ignited. As long as you’re doing passive, using at the very end just to scrub and using a mol sieve right after it shouldnt be much of a problem. I’ll try it as soon as my stone gets here. I’ve buchner funneled butane with a regular vac pump for like 3-4yrs daily over 4hrs of use. Thank god I didnt blow up but seems like this situation will be much more safe and controlled
Thus the reason not to put air into your extractor.
Sorry this won’t save you.
Mol seive will remove h20 and is pretty standard on most cls, This does nothing for the o2.
Why a vacuum pump? pressure filtration would be safer, and have the benefit of not boiling your solvent.
Don’t give dangerous advice, that’s bad all around.
I’ve noticed different results from vac and pressure. This is only for research and yes the mol is only meant for the h20. What I meant for passive was I wont be using anything that could ignite it once its mixed with the air. The only problem would be removing the oxygen afterwards. I’m not recommending anybody to try it im pointing out that back before I knew any of this I would winterize with an open pot and the ambient air seemed to help somehow. I’m sure theres some literature out there that explains what is going on and that’s what I’m looking for but I dont know the terms to google. So here I go experimenting
The simple fact is that your are creating a fuel air mixture, depending on the total volume of the system, amount of air injected, and amount of fuel you may stumble onto the upper or lower explosive limit of the fuel.Ignition sources can be electrostatic, fluids rushing through hoses will accumulate static charge, and can build if the system isn’t properly grounded.If you want to play with adding fuel and air together I would suggest a shit ton of fire sprinklers.
you need to understand that people can read things on here and kill themselves with bad advice.For the good of harm reduction and sullying this industry name we must present good information.
I’ve done a couple osha classes when I used to do plumbing for the union I’m so well aware of the dangers when mixing gases. I’m just very curious about this. My slabs that I exposed to.ambient air wouldnt oxidize but inline they do. Idk if it was the ambient air oxidizing prior to scrub, or the dry ice subliminating into the solution.
I was thinking of a way it send tane through the powders to prewet them while its inline under negative pressure, prior to sending my tane/oil through them. Shouldnt be to hard to do just need the parts to implement it
I dont recomend anybody trying it but for research purposes I want to state the conditions in which I made these observations to see if anybody out there with more knowledge can help explain what’s going on
I meant slabs that were made inline would oxidize over time sitting in the oven. But I remeber back then when I used to funnel they wouldnt. So how could we get it to oxidize prior to scrubbing in a safe manner?
I highly doubt waxplug is telling anyone to do this. I have done similar stuff but i dont recommend anyone to do it. One of those do as i say not as i do things
I’m just saying my slabs inline look fine and still fire but the funnel tek produced a higher quality that no matter how hard i try I cant replicate inline…they even muffin different
I’ve tried carbon chemistrys products and still the same. I’m also thinking it could be pressure filtration is pushing things through that wouldnt make it through with vacuumn