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HeinzBeans
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Thanks for the response Axt and dettoo456, and you where pretty much right in regards to your question about the method of production, I’ll be
following this synthesis;
http://www.sciencemadness.org/talk/viewthread.php?tid=12966
Only difference is that I’ll use potassium nitrate instead. Also vacuum and cryocooling are a little overkill and optional. N2O4 forms at about -10c
so no need for liquid nitrogen temps lol
I have been thinking though, and what do you think about the idea of using Dinitrogen tetroxide + Sulfuric acid as a nitration mix instead of just
N2O4 alone.
Perhaps the Sulfuric acid will act like it does with nitric acid to help form the nitronium ion?
Will also bind to any residual water, though the N2O4 should be anhydrous anyways from this method.
[Edited on 14-5-2025 by HeinzBeans]
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dettoo456
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I’d only recommend vacuum and strong cooling since I’d be worried that some NO2 would decompose at the high temps involved in the thermal
decomposition. If no vacuum is used, I’d at least try to heavily agitate the melt somehow to ensure the NO2 is stripped and cooled as quickly as
possible. Leading O2 into the off-gas is overkill but could also work if you had a O2 concentrator lying around.
N2O5/H2SO4 is overkill, anhydrous N2O5 will nitrate basically anything.
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HeinzBeans
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Ok, thank you for the input 
Also when I referred to using Sulfuric acid I meant with the tetroxide not the pentoxide, little spelling mistake on my part.
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dettoo456
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N2O4 will not nitrate anything really, it’ll nitrosate instead. Like Axt mentioned, you need the NO2- species in solution.
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dettoo456
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I have seen differing procedural methods, mainly depending on availability, but does anyone here nitrate with <98% H2SO4? Basically in the range of
93-98%? I figure it shouldnt complicate reaction conditions that drastically, but I dont have any practical experience with anything less than 98%. I
mean to use AN with the H2SO4 directly, not with azeo HNO3.
I have a decent amount of 98% from Duda along with some 93% industrial grade stuff, and if blended, Ill end up with approx 95.5%, which to me seems
fine. Id prefer not to distill it if possible.
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Microtek
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I have only ever used 96% and that has worked fine for everything from nitric esters to TNT.
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dettoo456
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Alright, thanks. Ill blend what I have up and just use that.
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BoroNar
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have problem making
Silver Azide directly via Hydrazine Sulfate/HNO3
Tried this reaction:
http://www.sciencemadness.org/talk/viewthread.php?tid=1987&a...
Same from Astral Chemistry’s video:
“Preparation of hydrazoic acid (azoimid) and silver azide” https://www.youtube.com/watch?v=53BvufurXKA
exactly 1:1 no point to re-write all my steps,
even heating very gently, runaway happens and Noxes are polluting nitrate solution, once I managed to redirect noxes to scrubber but precipitate is
still unusable.
Precipitate is snow white color, powderly. After drying it will not ddt, as shown in video, I use torch and it will just melt that powder and metal
(silver) droplets are formed.
Any ideas or variations of this method are welcome. Sodium nitrite and therefore IPN is not available to me, so I have only this route to have azide.
Thanks
[Edited on 3-8-2025 by BoroNar]
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Axt
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I don't know why it's not working for you nor have i tried HNO3 oxidation in this setup. But if you check early in that megathread pg. 3 or 4 I did
test persulphate/H2SO4 and successfully caught HN3 as lead azide. It was of questionable safety so I didn't experiment any further. I posted that H2O2
seems to do the same thing but I cannot remember any of that now.
Silver nitrite has low solubility, if you are passing NO/NO2 into solution this is your likely precipitate.
[Edited on 4-8-2025 by Axt]
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UndermineBriarEverglade
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Dense nitroguanidine?
Quote: Originally posted by dettoo456  | | NQ is far and away the best option for mixing with ETN, as it’s very powerful on its own, insensitive, and very stable. The only issue is obtaining
the right crystal morphology to select for small particle size and rounded crystal shape. Even so, UN is just too weak and finnicky IMO.
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What are the usual ways to get high-density nitroguanidine? Are there suitable melt-cast carriers? Can the crystals be wet-ground in a blender? Are
there any solvents that result in better crystals?
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Axt
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This is the Chinese method
1 eq NQ
14 eq water with 0.01-0.10 % PVA (poly ~1750)
Boil to dissolve
Adjust pH to 8 with ammonia solution
Under stirring cool 0.1-0.5C per minute to 50C
Rapidly cool from 50C to 20C
Filter, rinse and dry at 65C.
Nominal density increased from 0.16 to 0.8-0.9g/cm3.
[Edited on 29-8-2025 by Axt]
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UndermineBriarEverglade
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Thanks. I read about antisolvent recrystallization which promises .94-.97g/cm3 but calls for NMP and more precision. PVA and water looks accessible to the
amateur. Do you have a link to this Chinese paper? I'm not sure how well I can control the rate of cooling with a simple ice bath.
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Axt
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It's all in Chinese.
You won't need an ice bath for that slow cooling, you'll need a larger or insulated thermal mass bath. It'd take some experimentation but 1L or 2L
bath heated to boiling then place beaker in it and let it all cool slowly more mass more insulation slower the cooling.
Attachment: High bulk density nitroguanidine (chinese).pdf (1.9MB)
This file has been downloaded 81 times
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BoroNar
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I have aminoguanidine bicarb batches prepared via reducing nitroguanidine with zinc powder. Synth done exactly per dug's video "Aminoguanidine [small
batch]" all carefully scripted and executed.
One batch I have is white and another is yellow
only difference is that at the end after adding bicarb, accidentally left stirring for hour or so, when came back very fine white precipitate was in
beaker. "Yellow batch" was left overnight to slowly form precipitate.
questions are:
what is "fast white" precipitate, if not AQB then what?
how do amateur can test AQB? what are options for testing and confirmation
Tried burning on alu foil, both "fast white" and "slow yellow" burn with yellow residue. Burn was same for both, same fizzling, fumes and speed.
any idea where that "yellow" comes from? what may be the cause? wanted to recryst, but even in boiling water so tiny powder dissolved, gave up.
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Axt
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Aminoguanidine bicarb wont "burn" it'll fizz and decompose with considerable white smoke leaving yellow residue but not in a self-sustaining reaction.
If yours is self sustaining its likely partial reduction to nitrosoguanindine, which happens to be yellow. Aminoguanidine will yellow over time
though, even lab acquired will produce a yellow solution.
Attached is my sample of nitrosoguanidine, its recrystallisable from boiling water. Soluble in dilute NaOH which precipitates an energetic silver salt
from AgNO3.
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BoroNar
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Axt
Thanks for reply,
yes, there was no burn with flames, only fizzing and smoke and foil was heated from bottom with torch.
But residue left is quite large, color is same yellow as on your picture. if nitrosoguanidine was there, it would dissolve in water when I tried to
recryst AQB. I always try to confirm results one way or another, melting point, water solubility, color, etc.. so sad I have no practical way for AQB.
will report back results if these AQB batches have any success in further reactions down the line.
[Edited on 19-10-2025 by BoroNar]
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Axt
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Note that nitrosoguanidine wont "burn" with a flame either, just that it's a rapid self-sustaining reaction when touched with a flame. If what you
have is only decomposing when heat is applied, it's likely the bicarb. Just sit a bit underwater and add HCl and see if it fizzes and goes into
solution. Just don't add H2SO4 out of water as that'll make nitrosoguanidine fizz off as well.
The above was made via zinc-NH4Cl reduction of nitroguanidine.
[Edited on 19-10-2025 by Axt]
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