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Indict Evolution
Добавлен 13 июл 2018
Видео
40 grams melt cast ETN vs steel bar
Просмотров 1,4 тыс.Месяц назад
40 grams melt cast ETN vs steel bar
35g Melt Cast ETN
Просмотров 463Месяц назад
Next video will be 50g melt cast ETN vs 3/4 inch (19mm) steel plate (railroad tie plate).
X-Ray Tube Camera Interference
Просмотров 505 месяцев назад
#xray #radiation #xrays X-Rays causing pixels in my phone's CMOS sensor to activate. You should see it as a static in the video when the tube powers up.
Hot fused silica glass tube in cold water
Просмотров 1256 месяцев назад
One end of this tube was already broken from falling, so I decided to test if it would break from thermal shock out of curiosity.
M80 Buried In Sand
Просмотров 1682 года назад
Probably would have looked better zoomed out more, but I wasn't quite expecting this.
Flash Powder 20 Grams (1x, 8x, 32x slow)
Просмотров 2692 года назад
20 grams PP AL (60/40) in thick cardboard tube. Epoxied end caps.
Nitric Acid Distillation Timelapse
Просмотров 1732 года назад
You'll notice the distillate starts out yellow, then turns clear at about 0:20, and then yellow again at 0:47. I believe this is because the temperature of the distillate reached a high enough temperature to decompose the dissolved nitrogen oxides, but when I then reduce the heat, the distillate turns yellow again. I will do a test in the future to see if heating contaminated nitric acid will r...
Making uranium ore fluoresce with nitric acid
Просмотров 1562 года назад
Making uranium ore fluoresce with nitric acid
Thorite from thorium mine
Просмотров 4742 года назад
NOTE: I said the thorite in this rock was reddish orange, I think that is wrong. I believe the thorite is the black specs, obvious in the rock at 1:30. Not the dark gray, but the black specs. Also found some other cool things like a big piece of blue chrysocolla with thorite and purple fluorite crystals on it. Inside of the mine was not too interesting. Just a very short tunnel with no bends.
Reacting fuming nitric acid with copper & nitrile glove
Просмотров 2674 года назад
I distilled about 20ml of fuming nitric acid (greater than 80%) obtained via a reaction between sulfuric acid and potassium nitrate, and reacted it with copper and a nitrile glove. When adding the nitric acid to the test tube with copper, the copper was passivated by the nitric acid. I add a few drops of water to allow the copper nitrate layer formed via passivation to dissolve, which is why th...
Peroxymonosulfuric Acid (Piranha Solution)
Просмотров 9854 года назад
Mixed ~93% sulfuric acid with ~12% hydrogen peroxide to oxidize the H2SO4 to H2SO5. I then react some organic matter with it.
Making dilute nitric acid (Unsuccessful)
Просмотров 11 тыс.4 года назад
Making dilute nitric acid (Unsuccessful)
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.
Just need to figure out how to enrich my uranium ore. Can't be that hard right? Just some finely tuned laser.
@@IndictEvolution Yeah, Have you ever done thermobaric?, I want to see!
Is it Etn ?
I thing anfo...
Because Etn smokeless
@@Myhandgonebro..maybe had aluminium
@@user-lh2qr9wz6f Yes little flash
Cool
nice
Cool
bad
@@tuffycalcitelol
@@tuffycalcite Wut da u mean bad?
@@Myhandgonebro.. it is literally in your name
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)
$20? Thats a bit overpriced, I got mine for 16 off ebay, better than putting NO2 through a proper rotary vane though!
Yeah yours is definitely better, 16 kpa absolute while mine is round 89kpa absolute, my fridge comp can go lower but it has some issues with vibration and also the fact the vacuum line feeds into the shell of the compressor so if anything gets it in get murdered, I could probably get some WFNA with my vacuum pump but idk bout how much decomp
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.....
Mantap bgt
The beginning of world war 3.
Ammonia nitrate .put in a acedic liquid and boom you have some HNO
You would have to then distil off the nitric acid, and not all acidic conditions would work
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.
And mixing concentrated Cl- NO3- H+ will form NOCl too.
Exactly man
If you pay attention he used hydrogen peroxide in the collection vessel. (This video is basically a duplication of the nurd rage video.) There's plenty of oxygen available in the collector to make nitric acid. The problem is simply time he needed to do 7 to 9 more batches of the reactants to be able to make enough gas to get a decent concentration of nitric acid.
Great demo to show why you don't wear gloves (Nitrile ones) when working with fuming nitric acid.