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I love my 5L but hate being limited to 3.5L for my reactions as that's my limit for safety. I've went bigger a few times and it gets VERY sketchy and I've foamed over, loosing 1/3 of it a few times.
Transition from 5 L beaker to reactors (proper, expensive way of executing larger reactions) or plastic barrels is always sobering :) It does not seem like a big deal to do say AR dissolution in cut HDPE canister, but it is very different. Once you tackle down the main problem - how to heat the contents without destruction of temperature sensitive HDPE - you practically won.

Biggest reaction I ever watched was in 220 L HDPE barrel. Foam over on this scale is something vastly different comparing to 5 L beaker. By the time you realize that you sometimes even need some sort of blower or vacuum suction tube to suck NOx-es from the space in the barrel unoccupied by liquid - because they are so dense that you can leave it open in hood for one hour and still see just brown... :)
And also, pouring solution with 100 ozt of gold or palladium by hand from relatively fragile 22L glass round bottom... That can result in horrible financial disaster if you somehow manage to screw up :)
Yeah, it is very different.

PS: Never lift HDPE vessel with hot contents :) always let it cool properly and after two or three dissolutions, replace it with new one. AR can do extraordinary damage, even to HDPE. Siphoning or pumping is preferred over pouring.
 
By the time you realize that you sometimes even need some sort of blower or vacuum suction tube to suck NOx-es from the space in the barrel

One of my memories from bucket refining is watching a reaction rise and saying to myself “big bubbles, big bubbles” as if the solution understood me! When the bubbles get big the rise slows down, it’s the small bubble foam that rises with a vengeance. When I saw that coming I was there with a suction receiver and a wand to prevent a disaster. (This is a little trick you learn the hard way!)
 
Nice chemistry set. Be careful and please share photos of some of your setups. Happy New Year.
Here is one for HCl production from waste H2SO4 and NaCl. Double backflow trap. Connections still need to be lubricated with molykote and fixed with clamps.
Hose to the funnel is still loose and I will put the beaker in an ice dish.
Setup to fill, empty and refill without taking it apart.

Not sure if the thermometer is needed, but i will first go for 2Molar in 500ml by converting 60grams of salt.
Tritation will tell how well I did.
Edited to add the picture.
20250112_173139.jpg
 
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