| Pages:
1
..
19
20
21
22
23 |
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
Alright. Very interesting. Everyday I check to see an update from you. I hope you can post more frequently because your updates are a treat
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
So, I found another chinese paper (attached). It's about modifying HMX by dissolving it in DMSO along with triaminoguanidine nitrate, and then in
situ polymerizing the TAGN with glyoxal (this polymeric material is named TAGP in the paper). Supposedly, this traps the HMX molecules between
layers of the high nitrogen 2D polymer. Because of the pi-interactions between the TAGP layers, the HMX is forced into a less favoured conformation,
thereby introducing strain in the molecule, and also increasing the density.
The HMX to TAGP ratio can be adjusted via the amounts of TAGN and glyoxal. I aimed for the one they call HT-4 in the paper. The authors measured the
crystal density to be 2.04 g/cc for this variant. The synthesis proceeded as described in the SI, except that I would describe the colour as tan
rather than grey. This may simply be a translational error, since the colour of my material closely matches the pictures in the paper.
I then pressed the material at high pressure (about 50 MPa), which gave me a very hard and tough pellet of about 2.0 g/cc. In my first attempt, the
casing deformed from the pressure, so I had to remove the material from the casing. The pressed material is mechanically similar to hard candy, and
can be (carefully) machined if required.
In my standard plate dent test it gave 4.52 mm, corresponding to 104.8% of HMX(95)/viton(5).
Attachment: HMX-TAGP.pdf (1.2MB)
This file has been downloaded 394 times
Attachment: HMX-TAGP_SI.pdf (4.6MB)
This file has been downloaded 361 times
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
Quote: Originally posted by Microtek  | So, I found another chinese paper (attached). It's about modifying HMX by dissolving it in DMSO along with triaminoguanidine nitrate, and then in
situ polymerizing the TAGN with glyoxal (this polymeric material is named TAGP in the paper). Supposedly, this traps the HMX molecules between
layers of the high nitrogen 2D polymer. Because of the pi-interactions between the TAGP layers, the HMX is forced into a less favoured conformation,
thereby introducing strain in the molecule, and also increasing the density.
The HMX to TAGP ratio can be adjusted via the amounts of TAGN and glyoxal. I aimed for the one they call HT-4 in the paper. The authors measured the
crystal density to be 2.04 g/cc for this variant. The synthesis proceeded as described in the SI, except that I would describe the colour as tan
rather than grey. This may simply be a translational error, since the colour of my material closely matches the pictures in the paper.
I then pressed the material at high pressure (about 50 MPa), which gave me a very hard and tough pellet of about 2.0 g/cc. In my first attempt, the
casing deformed from the pressure, so I had to remove the material from the casing. The pressed material is mechanically similar to hard candy, and
can be (carefully) machined if required.
In my standard plate dent test it gave 4.52 mm, corresponding to 104.8% of HMX(95)/viton(5). |
I read that paper as well and was very excited about it… however I thought there was so issues so as large inconsistency’s that precluded it from
being practical. You duplicating it obviously gives it a second wind.
My big question, can this be done with UZP or the other perchlorate mentioned earlier in this threat with a VOD of 9500m/s and a density of 2.0. If it
can be done with UZP
We are looking at 2.3 density.
I can’t remember the name of that other promising perchlorate you linked the paper too, but it was less sensitive than UZP
With a VOD of 9500m/s
Well done! Impressive! Still crazy the UZP has a larger dent…
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Microtek | So, I found another chinese paper (attached). It's about modifying HMX by dissolving it in DMSO along with triaminoguanidine nitrate, and then in
situ polymerizing the TAGN with glyoxal (this polymeric material is named TAGP in the paper). Supposedly, this traps the HMX molecules between
layers of the high nitrogen 2D polymer. Because of the pi-interactions between the TAGP layers, the HMX is forced into a less favoured conformation,
thereby introducing strain in the molecule, and also increasing the density.
The HMX to TAGP ratio can be adjusted via the amounts of TAGN and glyoxal. I aimed for the one they call HT-4 in the paper. The authors measured the
crystal density to be 2.04 g/cc for this variant. The synthesis proceeded as described in the SI, except that I would describe the colour as tan
rather than grey. This may simply be a translational error, since the colour of my material closely matches the pictures in the paper.
I then pressed the material at high pressure (about 50 MPa), which gave me a very hard and tough pellet of about 2.0 g/cc. In my first attempt, the
casing deformed from the pressure, so I had to remove the material from the casing. The pressed material is mechanically similar to hard candy, and
can be (carefully) machined if required.
In my standard plate dent test it gave 4.52 mm, corresponding to 104.8% of HMX(95)/viton(5). |
How did you prepare and cure the HMX Viton? I have searched for uncured viton but have not been able to find any… there are many many grades of
fluroelastomers and viton… which one did you use?
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
A kind member on this forum had obtained a large amount of unvulcanized Viton and donated some to me. It is very easy to use since it is quite soluble
in acetone, so I just added 5 parts Viton and 95 parts HMX to enough acetone to dissolve the Viton. Then evaporated the solvent while stirring. When
it contains just a trace of acetone, it presses very well.
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
Regarding the idea of using the TAGP (triaminoguanidine polymer) to modify UZP, I did consider it, and this is what I have come up with:
If UZP is sufficiently soluble in DMSO, then we have to find an anti-solvent which can precipitate the UZP-TAGP material. In the chinese paper they
use water, but that won't work with UZP. Maybe an alcohol or a non-polar solvent such as gasoline could work.
If it can be made to work, the question remains what effect it will have on the properties of UZP. UZP is inherently different from HMX in that it is
a salt, and I am not sure what that will do in this system. The reason that the density of HMX is enhanced is that normal HMX is an eight-membered
ring which, due to the bond angles in the molecule, can't be packed very closely (the "ring" is kinked). The TAGP layers act by squeezing the
molecule, thus flattening it to a degree, which allows it to pack qin more dense crystals (according to the paper).
UZP is a five-membered ring system which is planar, so I don't think we will see much enhancement of the density, but we won't know for sure until we
try.
Also, if the TAGP-system can work as an anti-hygroscopic barrier, that would easily be worth it. If the sensitivity is decreased, even more so.
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Microtek | Regarding the idea of using the TAGP (triaminoguanidine polymer) to modify UZP, I did consider it, and this is what I have come up with:
If UZP is sufficiently soluble in DMSO, then we have to find an anti-solvent which can precipitate the UZP-TAGP material. In the chinese paper they
use water, but that won't work with UZP. Maybe an alcohol or a non-polar solvent such as gasoline could work.
If it can be made to work, the question remains what effect it will have on the properties of UZP. UZP is inherently different from HMX in that it is
a salt, and I am not sure what that will do in this system. The reason that the density of HMX is enhanced is that normal HMX is an eight-membered
ring which, due to the bond angles in the molecule, can't be packed very closely (the "ring" is kinked). The TAGP layers act by squeezing the
molecule, thus flattening it to a degree, which allows it to pack qin more dense crystals (according to the paper).
UZP is a five-membered ring system which is planar, so I don't think we will see much enhancement of the density, but we won't know for sure until we
try.
Also, if the TAGP-system can work as an anti-hygroscopic barrier, that would easily be worth it. If the sensitivity is decreased, even more so.
|
I see! Would there be any other way to apply inter molecular pressure to increase the crystal density?
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
None that I can think of just now.
Some people have speculated that it might be possible to nest one energetic molecule inside another. This kind of structure can be seen in zeolites,
and there was a report of a composite of nanoporous silicon and liquid oxygen some years ago. It was reportedly very powerful, but of course
completely impractical. The problem with experimenting with this kind of thing from my perspective, is that I have no access to the required
analytical equipment, so I would be shooting in the dark.
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Microtek | None that I can think of just now.
Some people have speculated that it might be possible to nest one energetic molecule inside another. This kind of structure can be seen in zeolites,
and there was a report of a composite of nanoporous silicon and liquid oxygen some years ago. It was reportedly very powerful, but of course
completely impractical. The problem with experimenting with this kind of thing from my perspective, is that I have no access to the required
analytical equipment, so I would be shooting in the dark. |
The silicon and liquid oxygen was a sensational headline in my opinion. Some Russian guy claimed CL-20 type power but… look at the reaction. SiO2 is
the product. That does not fit detonation theory of being a good explosive.
Any updates with the UZP or higher concentrations like the H7 with more TAG binder? Microtek man, your one of the only ones keeping this place alive.
We love your updates. I do. If you get this, successfully I will build a shrine of you. Ok
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
I did some experiments with UZP and DMSO to determine the viability of using in situ synthesized TAG-polymer to improve some of the properties of UZP.
It seems that DMSO does dissolve UZP, forming a clear solution. However, when I tried reprecipitating it by adding an antisolvent (isopropanol), only
unprotonated urazine was recovered. I also tried detergent gasoline (a mixture of alkanes), but it doesn't mix with DMSO. The possibility remains
that the presence of TAGP might change this behavior, but I'm not very hopeful.
I also think it likely that the glyoxal might react with the amino group of urazine which would alter the composition of the polymer. This could be a
good or a bad thing.
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Microtek | I did some experiments with UZP and DMSO to determine the viability of using in situ synthesized TAG-polymer to improve some of the properties of UZP.
It seems that DMSO does dissolve UZP, forming a clear solution. However, when I tried reprecipitating it by adding an antisolvent (isopropanol), only
unprotonated urazine was recovered. I also tried detergent gasoline (a mixture of alkanes), but it doesn't mix with DMSO. The possibility remains
that the presence of TAGP might change this behavior, but I'm not very hopeful.
I also think it likely that the glyoxal might react with the amino group of urazine which would alter the composition of the polymer. This could be a
good or a bad thing. |
Ahh. Darn!
Would you be willing to try a debt test on the H-7… the one that contains more TAGP?
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
Yes, I plan on doing that at some point. I may need to prepare some more HMX first though.
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
Microtek any updates? Why not try H-7 with K6… easier and more powerful than HMx
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
I am exploring some ideas with the TAGP system. I tried preparing a TAGP-UZP material using an aqueous system and the simply heating to drive the
water off. It seemed to work, but of course, I don't know if the same kind of intercalated compound was formed. The product was much less sensitive to
impact, but unfortunately still quite hygroscopic. I didn't test energetic properties, and now I've run out of urazine. In the mean time, I'm working
on something else which may have some potential. I will reveal more when I have something to report.
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Microtek | | I am exploring some ideas with the TAGP system. I tried preparing a TAGP-UZP material using an aqueous system and the simply heating to drive the
water off. It seemed to work, but of course, I don't know if the same kind of intercalated compound was formed. The product was much less sensitive to
impact, but unfortunately still quite hygroscopic. I didn't test energetic properties, and now I've run out of urazine. In the mean time, I'm working
on something else which may have some potential. I will reveal more when I have something to report. |
Ok microtek. Amazing it worked with the UZP. Any ideas on density? I am curious what your current project is!
|
|
|
katyushaslab
Hazard to Self
Posts: 81
Registered: 19-1-2021
Member Is Offline
Mood: precipitating
|
|
Previously in the thread, during discussions of semicarbazide/carbohydrazide as routes to urazine, I came across an old post by Microtek about NTO
(nitrotriazolone), made by nitrating triazolone (formed by the condensation of semicarbazide hydrochloride and formic acid) on another, now defunct
forum.
Yesterday I started pulling that thread again, and came up with a few things of note that I will just leave here.
While looking up some papers, I came across [1].
This paper is the source of the condensation of semicarbazide and formic acid route to triazolone, and also mentions that the best yields for NTO
seems to be with nitric acid of around 65% - noting that fuming mineral acids cause carbonization of the starting material, which seems delicate. This
is rather interesting, as azeotropic nitric acid is a lot less expensive to produce.
NTO itself is an insensitive high explosive, but practical applications suffer somewhat due to being water soluble.
The patent [2] mentions that crystal/particle size has an impact on critical diameter and sensitivity of the material. A further paper, [3], mentions
that it forms hydrates - and that water can make the material more sensitive.
Its performance seems to be in the 7-8km/s range of velocity of detonation,
Notable things from this paper [1] include:
- Nitrotriazolone is water soluble and is also a relatively strong acid, forming salts. A potassium, and a mercury salt are mentioned - but their
energetic properties aren't really explored. Potentially an avenue for research? Apparently the sodium and potassium salts are sparingly soluble, but
the lithium salt is soluble. Barium and Silver salts are mentioned. I'd guess a lead or copper salt is possible also.
- There are two forms of aminotriazolone, one of which can be formed by melting together aminoguanidine hydrochloride and urea, the other is formed by
reduction (HCl/Zn) of nitrotriazolone.
- Both forms of aminotriazolone can be isolated as picrates, and both form salts with silver with different properties - one is a red, the other is a
white colour. Nothing is mentioned about their energetic properties either. Other salts are likely to be possible.
I need to chase down more references on this, but this could be a potentially promising thread to pull on to find interesting materials to explore.
Especially given semicarbazide and aminoguanidine are already well-trodden areas of research for the SM community.
Edit:
A search lead me to more angles on this, see the thread/post in [4], pointing at patent [5], referring to hydrazine and aminoguanidine salts of
nitrotriazolone, among other things. Some properties are elaborated upon in the patent, but as with all patents, take with a pinch of salt.
[1]: https://sci-hub.se/https://doi.org/10.1007/BF00955602
[2]: https://patents.google.com/patent/WO1994006779A1/en
[3]: https://sci-hub.se/https://doi.org/10.1016/j.molliq.2021.116...
[4]: https://www.sciencemadness.org/whisper/viewthread.php?tid=10...
[5]: https://patents.google.com/patent/US5256792
[Edited on 30-5-2022 by katyushaslab]
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
Interesting. I haven't done very much experimentation with NTO due to the critical diameter. At the time, I felt that it would require too large
charges for my experimental scale. It is certainly interesting if a particle size reduction can lower the critical diameter similarly to UZP. Also, I
would think a hydroxylammonium salt might be worth exploring.
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
Alright, I have been extremely busy at work, but now I have a little time to report some of my findings:
I explored an ETN/TAGP compound produced similarly to the HMX/TAGP reported earlier. My thinking was that if ETN could be flattened between sheets of
TAGP as with HMX, some strain must be induced in the molecule (otherwise the "un-flattened" conformation would not represent an energetically stable
minimum). This would lead to a higher heat of formation and if the density was also increased, performance would almost have to improve also.
I prepared the compound in a similar manner to HMX/TAGP since the ETN molecule is almost the same mass as HMX. The preparation was uncomplicated, and
the density was measured to about 1.85 g/cc (at room temp). Diverging values of ETN density are found online (1.72 and also 1.83). As far as I can
tell the higher value is measured at cryogenic temperatures, so if that is true, it seems that the density is indeed improved. I tested the brisance
of the compound and found a dent depth of 4.60 mm (HMX95/viton5 4.31, UZP 4.64).
I then thought about PETN, which should also have a lot of potential for flattening. PETN/TAGP gave a dent of 4.70 mm, though the density didn't
increase noticeably. Then I tested unmodified PETN for comparison, and got exactly the same dent 4.70 mm. I don't have enough ETN to test that
unmodified just now.
My preliminary conclusion is that the sensitive nitric esters are quite hard to beat at the very small scale, at least in this kind of test. I may
have to look into CNC machining SC liners to see if the faster energetics are better in those applications at the ~1 g scale.
|
|
|
dettoo456
Hazard to Others
Posts: 243
Registered: 12-9-2021
Member Is Online
|
|
I’m guessing that brisance levels (although there’s no real defined measurement calc for it) and by-proxy, critical diameter, relate more at the
<1g scale. I don’t think that det pressure necessarily takes into effect for the munroe effect but as a product of propagation and
density-packing of the material as it’s initiated, the rate at which the EM ‘gets going’ is more important at low masses. Also, I haven’t been
able to test it yet but incorporating plane wave lenses into the shape charge design may help to boost performance aswell.
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
I have used lenses in my SCs in the past, and they do indeed help with the performance at the very small scale as well. However, my reason for
considering SCs in this context is not to get as much performance as possible, but simply to compare the performance of different HEs. The idea is to
device tests that are on the one hand standardized at the scale I work at, and on the other hand simulates some of the applications of such materials.
VOD and Pcj is only indirectly interesting to me; it is the ability of the energetic to do useful work that I find to be the real criterion.
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
Any update on UZP microtek?
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
No, I haven't worked on UZP since I ran out of urazine. However, I came across some papers on derivatives of 5,5'-Diamino-3,3'-bis-1,2,4-triazole. The
parent heterocycle is produced very simply and in decent yield by the reaction of aminoguanidine*HCO3 with oxalic acid. The product can then be
treated with nitrous acid and ionic nitrite to give the dinitro derivative, or nitrated with mixed acid to give the dinitramine. Both can form salts
with anions such as hydrazine, ammonia, diaminourea, hydroxylamine and others. Many of the seem to have promising properties, such as high density and
VOD, low sensitivity and high thermal stability.
The reactants and apparatus requirements seem to be within reach, although the dinitro derivative requires a LOT of nitrite. I think I may try some of
these reactions when I am done with the guanazole derivatives I am working on at present.
[Edited on 16-12-2022 by Microtek]
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Microtek | No, I haven't worked on UZP since I ran out of urazine. However, I came across some papers on derivatives of 5,5'-Diamino-3,3'-bis-1,2,4-triazole. The
parent heterocycle is produced very simply and in decent yield by the reaction of aminoguanidine*HCO3 with oxalic acid. The product can then be
treated with nitrous acid and ionic nitrite to give the dinitro derivative, or nitrated with mixed acid to give the dinitramine. Both can form salts
with anions such as hydrazine, ammonia, diaminourea, hydroxylamine and others. Many of the seem to have promising properties, such as high density and
VOD, low sensitivity and high thermal stability.
The reactants and apparatus requirements seem to be within reach, although the dinitro derivative requires a LOT of nitrite. I think I may try some of
these reactions when I am done with the guanazole derivatives I am working on at present.
[Edited on 16-12-2022 by Microtek] |
Any of them with VODs above 9500m/s? Or that outperform ANQN?
Can you link the paper?
|
|
|
Microtek
National Hazard
Posts: 869
Registered: 23-9-2002
Member Is Offline
Mood: No Mood
|
|
I don't think any of them outperform ANQN (on paper at least), but in my opinion, high performance coupled with low stability is not that valuable.
For performance, you could just nitrate 5-aminotetrazole to get nitraminotetrazole. The product has density 2.06 g/cc, Pcj of 48.5 GPa and a VOD above
10 km/s according to one of the attached papers. Nevertheless, I would prefer reacting it with an organic high-nitrogen base to improve stability and
lower the sensitivity.
Attachment: Energetic Salts of 3-Nitro-1,2,4-triazole-5-one and 5-Nitroaminotetrazole.pdf (166kB)
This file has been downloaded 288 times
Attachment: Bis(nitrimino-1,2,4-triazole)salts.pdf (111kB)
This file has been downloaded 229 times
Attachment: phpzaBYwu (909kB)
This file has been downloaded 266 times
|
|
|
MineMan
International Hazard
Posts: 1004
Registered: 29-3-2015
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Microtek | I don't think any of them outperform ANQN (on paper at least), but in my opinion, high performance coupled with low stability is not that valuable.
For performance, you could just nitrate 5-aminotetrazole to get nitraminotetrazole. The product has density 2.06 g/cc, Pcj of 48.5 GPa and a VOD above
10 km/s according to one of the attached papers. Nevertheless, I would prefer reacting it with an organic high-nitrogen base to improve stability and
lower the sensitivity.
Thank you microtek!!
|
|
|
|
| Pages:
1
..
19
20
21
22
23 |
![[*]](images/xpblue/default_icon.gif){kind=icon}
