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Tannerite
[quote][i]Originally posted by 12AX7[/i]
Axt detonated some CuO/Al (magnalium or magnesium would wo ... |
27-12-2005 at 06:58
by: Axt |
Unconventional Shaped Charges
[quote][i]Originally posted by Deceitful_Frank[/i]
One question, Do you think that because of the d ... |
27-12-2005 at 06:52
by: Axt |
Unconventional Shaped Charges
[quote][i]Originally posted by PHILOU Zrealone[/i]
I think he meant that but without the lower half ... |
21-12-2005 at 06:04
by: Axt |
Iodoso & Iodoxy compounds
[quote][i]Originally posted by PHILOU Zrealone[/i]
So I meaned has someone eard about diaminodiiody ... |
21-12-2005 at 06:01
by: Axt |
Exotic Primaries - Complex Salts
[quote][i]Originally posted by PHILOU Zrealone[/i]
What was the exact procedure you used?
[/quote] ... |
21-12-2005 at 05:35
by: Axt |
Unconventional Shaped Charges
[quote][i]Originally posted by MephistosMinion[/i]
Is copper half pipe availiable or do I have to c ... |
20-12-2005 at 02:52
by: Axt |
Exotic Primaries - Complex Salts
You'll need a reducing agent to get silvering, I silvered a beaker trying to precipitate the chlorit ... |
20-12-2005 at 02:19
by: Axt |
Unconventional Shaped Charges
[quote][i]Originally posted by MephistosMinion[/i]
Hypothetically, if someone was pissed off at the ... |
19-12-2005 at 20:50
by: Axt |
Iodoso & Iodoxy compounds
[quote][i]Originally posted by PHILOU Zrealone[/i]
I wonder if trans diiodoxylethylene exists[/quot ... |
19-12-2005 at 05:37
by: Axt |
Exotic Primaries - Complex Salts
[quote][i]Originally posted by Rosco Bodine[/i]
and " oxiamines " ?[/quote]
Oxiamines would be ... |
19-12-2005 at 04:42
by: Axt |
silver salts
I've tried to form some silver salts, the only success was ethylenediaminesilver (I) bromate. Which ... |
14-12-2005 at 23:13
by: Axt |
Iodoso & Iodoxy compounds
[quote]Bubbling acethylene through I2 in Ethanol will provide more certainly diiodoacethylene...wich ... |
14-12-2005 at 22:36
by: Axt |
Iodoso & Iodoxy compounds
Attaching a couple references of interest, first gives the synthesis of the explosive iodylvinyl chl ... |
13-12-2005 at 18:38
by: Axt |
Lead Perchlorate
[quote][i]Originally posted by SAM4CH[/i]
The amount I used = 20-25 grams
Please I need more about ... |
11-12-2005 at 18:33
by: Axt |
Unconventional Shaped Charges
Heres some of the same .45 colt/.357 mag shaped charges as shown on page 3. This time into 6 3mm pla ... |
11-12-2005 at 17:34
by: Axt |
Mem. des Poudres
I dont think they were scanned, pdb put me onto those those 1882-1900 volumes a while ago through ga ... |
10-12-2005 at 11:30
by: Axt |
Ethylenedinitramine
[quote][i]Originally posted by Axt[/i]
I found the reason we don't hear much of the -N(NO2)2 group ... |
9-12-2005 at 03:21
by: Axt |
Diiodoacetylene
I stuck a movie of diiodoacetylene deflag up. You can see why it didn't earn a spot in the energetic ... |
6-12-2005 at 13:44
by: Axt |
Diiodoacetylene
I left a "2" out of the first equation. H2O should be 2H2O.
Still reckon the name needs a new lin ... |
6-12-2005 at 05:20
by: Axt |
Diiodoacetylene
Never thought to look in war gasses. It states that you can produce diiodoacetylene via C2H2 + KI + ... |
5-12-2005 at 12:22
by: Axt |
Diiodoacetylene
No, I havn't tested sensitivity. (yet)
The other documented procedures for diiodoacetylene are no ... |
5-12-2005 at 10:07
by: Axt |
Self-made reflux
[quote][i]Originally posted by Polverone[/i]
How does this look? I want the look to be clean, stand ... |
5-12-2005 at 08:53
by: Axt |
Diiodoacetylene
Preperation of Diiodoacetylene.
WARNING: Diiodoacetylene is extremely toxic (ref. 2) and a shock, ... |
5-12-2005 at 08:43
by: Axt |
nitropropene via nitromethane?
General nitroalkane-aldehyde condensation is below. Know nothing on dehydrating it.
[quote]To a s ... |
4-12-2005 at 14:25
by: Axt |
C.T.M.T.N.A (R-salt)
OK, you scared me there for a while. Punching buttons on the calculator scratching my head  You fo ... |
4-12-2005 at 10:43
by: Axt |
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