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There is no hole, but the result is good.

Awesome man

Looks like some cool scientific experiment you got here

Man, that is dope

You can use acetone as a solvent to dissolve PETN and ETN, which will increase the power.

Nice, good work!

Anybody has notice that etn increase its powerfull when gets older? It is not the same a batch 3 month old, than 1 or 2 years old batch. I have achieved this fact

Interesting..

you are alive?

Hello, very nice. But if you want a piercing, you must put the steel plate onto a wood plank2'5cm thick directly on the floor. Guaranteed piercing, even onto 10mm .

Next video try 100g of Uranium Bomb, I really want to see it.

Now do 1,000,000kiloton of uranium.

Is it Etn ?

Cool

nice

Cool

Nice sound

Nice

Hi

Chemistry king💯

never seen uranium ore before. looks cool

Would love it If you could put some subtitles explaining roughly the chemical basics of what is going on. Like what are you putting in and at which degree to get what in the destination and such.

Dunno which kind of camera you're using but if you could invest in some zoom lenses. It would make it a lot more cool. Still pretty banger though. I Love explosions

no water cooling :/, typically I found that heating does drive some NOx off from the acid but not much, the acid just becomes blood red when hot, I have tried an air bubbler and it works somewhat but not very much. I haven't tried adding urea (probably just gonna form urea nitrate anyways) but ammonium nitrate didn't do much either, so I think the best way so far is vacuum distillation, or using a 2 neck flask and keeping the pot temp below 120C, above that it seems not only decomp is more significant but also the nitric being distilled has water (typically I dry my acid by distilling with sulfuric again anyways). I think it may be possible to deNOx it by adding peroxide with vigorous stirring and then distilling over sulfuric acid, I have noticed when adding nitric to sulfuric, the nitric goes clear so I suspect the sulfuric could possibly be removing some NOx but I haven't done any very conclusive tests yet. It could be possible to use ozone, but I mean like who's gonna bother using ozone for it. I have had somewhat more success by fractionally distilling the acid as the reflux causes more NO2 to leave the acid and the NO2 collects in the first bit of distillate, however strangely the almost clear nitric I get becomes dilute after a few days of storage (however this was months back and at the time I stored it in a jointed bottle that didn't seal properly so it could just be hygroscopicity). I think the best chance is still to control the pot temp carefully and or do under vacuum, which both I plan on trying when my new glassware arrives since I uh broke the jointed flasks I had (typical)

You didn't fail you just grossly underestimated the amount of nitrogen oxides you needed to dissolve in the peroxide, and over estimated the amount of peroxide you would need. You need something like 400 volumes of gas to get 1 volume of acid. The rate of reaction is also problematic it can take several hours to fully dissolve the gas so a lot of it is lost into the air. An aquarium bubble stone helps a lot with that, especially if you get the ceramic ones designed for CO2 which have smaller holes.

The problem is the tube. It is too long, so the NO2 has problems with getting through it.

Are you refreshing the solution with H2O2 between each treatment?

it's okay to wear gloves

8H+ 2+NO3- +3CU--->2NO +4H2O+ 3CU2+ NO+O2(AIR)---->NO2 . H2O2 +2 NO2--->2 HNO3(COLD) .

mantap.....

The beginning of world war 3.

Ammonia nitrate .put in a acedic liquid and boom you have some HNO

idk if this is right but i think the problem is that the reaction vessels contents are too dilute. if the nitric acid that forms is cold/dilute it reacts with copper to make NO, not directly NO2. at first this is fine bc there’s oxygen in the system to oxidize it to no2, but i think it runs out. you can see when you open up the container in the end that the gas inside is colorless as first but it turns brown upon exposure to air, indicating its NO not no2. i think what you can do to improve the concentration of reactants is use a stoichiometric excess of your nitrate salt compared to hcl, keep the reaction on heat.

Great demo to show why you don't wear gloves (Nitrile ones) when working with fuming nitric acid.