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C.T.M.T.N.A (R-salt)
Yes 60g 32% (actually checking bottle, its 32% not 35 as I previously said) HCl was added to 100ml H ... |
4-12-2005 at 09:57
by: Axt |
Gas combination that explodes upon light
Hydrogen + Chlorine. |
3-12-2005 at 08:17
by: Axt |
C.T.M.T.N.A (R-salt)
You will get HNO2 from water + N2O3, which then decomposes from the exotherm. You'll get some f ... |
28-11-2005 at 01:20
by: Axt |
Nitramide reactions
[quote][i]Originally posted by Chris The Great[/i]
A Study on the Condensation of Nitramide (NH2NO2 ... |
26-11-2005 at 23:57
by: Axt |
C.T.M.T.N.A (R-salt)
[quote][i]Originally posted by halogen[/i]
You bubbled N2O3 through hexamine/hydrochloric acid? Why ... |
26-11-2005 at 18:01
by: Axt |
W Process
The article I attached early in this thread is quite vague when it comes to the condensatiion of K-s ... |
21-11-2005 at 14:23
by: Axt |
Peroxide of Acetylacetone (2,4-pentandione) ??
A few months ago I mixed up some acetylacetone/H2O2/HCl, I didn't seperate so I extracted it wi ... |
19-11-2005 at 20:21
by: Axt |
Unconventional Shaped Charges
[quote][i]Originally posted by Axt[/i]
A mixture of latex and copper powder (~50:50 by volume)[/quo ... |
18-11-2005 at 23:20
by: Axt |
Mix of iodoform and hexamethylenetetramine
For what its worth, heres the Sorbe reference, the wording does seem to imply some vehemence to the ... |
16-11-2005 at 19:38
by: Axt |
Unconventional Shaped Charges
[quote][i]Originally posted by lacrimachemist[/i]
Is this tube used instead of the cone? [/quote]
... |
16-11-2005 at 02:52
by: Axt |
Ethylenedinitramine
8g cast EBCN was detonated against a 3mm plate. The expected performace of EBCN wasnt realised with ... |
14-11-2005 at 22:04
by: Axt |
Unconventional Shaped Charges
But it stands to reason that the transference of detonation pressure into the liner will be greatest ... |
14-11-2005 at 08:40
by: Axt |
ethanolamine
Anyone have info on the azeotrope's boiling point and %'s of ethanolamine/water ? (whats t ... |
13-11-2005 at 16:29
by: Axt |
ethanolamine
I guess diazotisation of excess ethylenediamine will get you it, but ethanolamine is common OTC.
... |
13-11-2005 at 11:18
by: Axt |
Large pictures destroying lay-out.
You can just use ms paint, its all I use. Open "image", "stretch & skew" cho ... |
12-11-2005 at 15:28
by: Axt |
Ethylenedinitramine
[quote]The H2O is at a huge molar excess, and, and reactivity of hydrogen bound to the N would have ... |
12-11-2005 at 14:02
by: Axt |
Ethylenedinitramine
[quote][i]Originally posted by simply RED[/i]
Simple electrolysis of aqueous HF can not give F2.
2 ... |
12-11-2005 at 06:14
by: Axt |
Unconventional Shaped Charges
I cant say with certainty, and can provide no direct references to liner "security", but m ... |
11-11-2005 at 09:35
by: Axt |
Iodoso & Iodoxy compounds
Yes, I should have said to take no notice of the bonding situation around the iodine. It was drawn t ... |
9-11-2005 at 11:12
by: Axt |
Iodoso & Iodoxy compounds
The chemical reviews articles above are quite lengthy (~100 pages all up) and detail the chlorinati ... |
9-11-2005 at 10:39
by: Axt |
Iodoso & Iodoxy compounds
Heres an interesting explosive group that I hadn't come across until recently. By oxidising an ... |
9-11-2005 at 08:50
by: Axt |
Neglected RDX Process
[quote][i]Originally posted by quicksilver[/i]
HN4 salt[/quote]
Dyslexia 
[quote][i]Origin ... |
8-11-2005 at 07:00
by: Axt |
Ethylenedinitramine
Not that I know what the hell I'm talking about when it comes to electrolysis, but I at least c ... |
7-11-2005 at 06:46
by: Axt |
simple HMX-synth without Ac2O
[quote][i]Originally posted by BASF[/i]
In the prepn. of dinitrosopentamethylenetetramine (I) from ... |
6-11-2005 at 15:10
by: Axt |
Ethylenedinitramine
I'm not sure what you mean by electrolysis of (aqueous?) HF without generating fluorine gas. Na ... |
6-11-2005 at 14:53
by: Axt |
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