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Microtek
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[*] posted on 10-2-2022 at 06:03


Acting on a suggestion from MineMan, I tested a mix of 85% UZP and 15% Al-powder (nominally 3 um). In my standard setup it gave a dent of 3.71 mm (picric acid 3.53 mm and RDX 4.13 mm). This is still considerably lower than would be expected from the calculated VOD and Pcj data, but much better than my previous test with pure UZP which gave 2.92 mm.
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Laboratory of Liptakov
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[*] posted on 10-2-2022 at 13:29


It are very good results. Powerful than picric acid. Aluminium usually decrease brisancion, but here is it conversely. And the UZP works in your cavity as primary - secondary ?....:cool:...... Was tested? I know, you use for start aminoguanidine some perchlorate + PETN 300 mg for maximal kick of examined compoud. 300 mg PETN is too much. This can affect the result. It's a huge blow to the test substance. It would make a small dent in aluminum, even if the place of the substance under investigation was pressed sand. Just my opinion, nothing more.

[Edited on 10-2-2022 by Laboratory of Liptakov]




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[*] posted on 10-2-2022 at 23:39


I think there is a very high likelihood of it being able to DDT reliably under strong confinement. When heated in folded Al-foil, it tends to "pop" like flash powder. It is not extremely flame sensitive, but I think it is likely that transition metal complexes might be.

Regarding the use of 300 mg PETN, you are correct that it is enough to slightly dent the Al block even if the base charge is completely inert. However, since I have plans to also test some things that are very insensitive, and since the experimental setup should be identical in order to compare the results, I settled on this amount of booster. The point in being careful to use the exact same amount of PETN every time, is to make sure that it adds the same amount to the dent in all experiments.
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[*] posted on 11-2-2022 at 03:26


Yes, that makes sense. Promising materials that could be capable of DDT as a stand-alone monopropelant can be tested later.



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[*] posted on 11-2-2022 at 14:50


Microtek and LL. Yes it should DDT in strong cavity. That’s has been a thought I have had, although where we want it to shine is the detonation pressure. From this set up I would have expected a dent of over 4.5mm. Since the Al helped significantly I think this proves your original theory microtek. Despise the sensitivity it behaves as a non ideal explosive. Unless somehow the detonation wave is dead pressing the UZP ahead of it. But, the wave should move far faster then the speed of sound in UZP obviously.

I suppose the only other thing to try is compressing it to a density of 1.85-1.9 instead of over 2 or try larger quantity such as 5-10 grams. What do you think (LL and microtek)
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[*] posted on 12-2-2022 at 00:36


The last couple of tests I have done with UZP (with and without Al) have been just hand pressed precisely to avoid the likelyhood of dead pressing, so I'm afraid there's not much to gain there. However, another thing is that since UZP is so dense, 1 gram of it in a 7mm coloumn is just 13mm long (at 2 g/cc). It may be that the detonation doesn't have time to accelerate to its max velocity in such a short run. After all, when making shaped charges we make sure to have a certain head height above the apex of the cone. So, I will have to do an experiment with a longer charge. Then I will also have to do identical experiments with some of the other energetics, to establish a new baseline. To do these, I will have to construct a larger test chamber (since a longer charge with same diameter will obviously involve more material).
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[*] posted on 12-2-2022 at 01:36


Of course, that bigger amount will give more exact results and exact measurement of density. I estimate that 5g will enough. Diameter of high pressed EM of cylinder should by in this cause 12 - 15 mm at 5 g.
However alu brick must be a lot bigger. Which can be expensive. For 5g I reccomend using lead block of diameter 70 mm and 60 mm high.
Which is possible use repeatedly after casting. And measurement can be on 0,1 mm. Not on 0,01 mm.
Lead block is possible use also for measurement longer charge in cavity 7 mm / 5g. With less exact results. Advantage of lead is his huge dynamic resistance of entire block.
But 5g require testing chamber minimal 70 x 70 x 70 cm with wet sawdust.

[Edited on 12-2-2022 by Laboratory of Liptakov]




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[*] posted on 12-2-2022 at 02:21


Quote: Originally posted by Laboratory of Liptakov  
Of course, that bigger amount will give more exact results and exact measurement of density. I estimate that 5g will enough. Diameter of high pressed EM of cylinder should by in this cause 12 - 15 mm at 5 g.
However alu brick must be a lot bigger. Which can be expensive. For 5g I reccomend using lead block of diameter 70 mm and 60 mm high.
Which is possible use repeatedly after casting. And measurement can be on 0,1 mm. Not on 0,01 mm.
Lead block is possible use also for measurement longer charge in cavity 7 mm / 5g. With less exact results. Advantage of lead is his huge dynamic resistance of entire block.
But 5g require testing chamber minimal 70 x 70 x 70 cm with wet sawdust.

[Edited on 12-2-2022 by Laboratory of Liptakov]


What do you mean dynamic resistance of lead is huge?
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[*] posted on 12-2-2022 at 04:43


Lead is heavy. Test not need any solid pad for same repeatedly results. Lead block can be in any position at the test in chamber or sand pit. And "swim" there. Other on picture. For funny is there production special spoon for slow eating of soup.....:cool:

lead block.JPG - 1.1MB




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[*] posted on 12-2-2022 at 17:13


Quote: Originally posted by Laboratory of Liptakov  
Lead is heavy. Test not need any solid pad for same repeatedly results. Lead block can be in any position at the test in chamber or sand pit. And "swim" there. Other on picture. For funny is there production special spoon for slow eating of soup.....:cool:



That’s the only way I eat my soup. But I got a patent pal and my lawyer is gonna give you a call
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[*] posted on 13-2-2022 at 03:31


Feel free to patent the hole spoon . By your advice (for UZP) was tested Lithex with 10% aluminium powder bright. Interesting is, the deep is exact same as without aluminium. 7,5 mm exactly. Complete energy of detonation was bigger according flying sawdust and other flying parts of testing chamber. Aluminium can provide advantage used less amount of Lithex for a same brizancion. And also for somes application, where is total energy importantly, than maximal brizantion. For example EFP not require maximal brizantion, there is more importatly maximal energy for better shaping of slug. Was observed also more easy filling - pressing behavior, resoectively pull of rod. If is Aluminium not critical compound, he provide clear advantage in mixture Lithex. Interestling...:cool:



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[*] posted on 13-2-2022 at 18:52


Quote: Originally posted by Laboratory of Liptakov  
Feel free to patent the hole spoon . By your advice (for UZP) was tested Lithex with 10% aluminium powder bright. Interesting is, the deep is exact same as without aluminium. 7,5 mm exactly. Complete energy of detonation was bigger according flying sawdust and other flying parts of testing chamber. Aluminium can provide advantage used less amount of Lithex for a same brizancion. And also for somes application, where is total energy importantly, than maximal brizantion. For example EFP not require maximal brizantion, there is more importatly maximal energy for better shaping of slug. Was observed also more easy filling - pressing behavior, resoectively pull of rod. If is Aluminium not critical compound, he provide clear advantage in mixture Lithex. Interestling...:cool:


Interesting test indeed! I am not surprised. Al always helps DDT . Now if you can source nano 100nm Al you will find your Lithex will DDT in 50-100mg, perfect for micro detonators.
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[*] posted on 22-2-2022 at 06:35


In case someone wants to experiment with urazine for themselves, I'm attaching the relevant pages from Inorganic Synthesis vol 4 here:

Attachment: Urazine pages.pdf (332kB)
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[*] posted on 22-2-2022 at 14:07


Thank you Microtek! Any updates on the application of Urazine?
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[*] posted on 22-2-2022 at 23:12


I did a quick test of the use of urazine as a ligand in a Ni2+ complex with perchlorate anions. I dissolved Ni(NH3)6(ClO4)2 in hot water, added a little extra HClO4, and then gradually added two equivalents of urazine. This produces a very insoluble precipitate, that is only very slightly energetic. Wrapping it in Al foil and heating in a flame gives only a minute expansion of the foil package.
My hypothesis is that the precipitate is maybe nickel urazinate and not a complex at all.
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[*] posted on 23-2-2022 at 01:28


Lithex is in a similar situation. Enclosed in foil during heating, in the end it always just burns. And still quite reluctantly.



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[*] posted on 8-3-2022 at 01:18


Recently, I have devoted my spare time to developing test methodology for measuring VOD using an oscilloscope. I can now report my preliminary findings:



PETN_d1.57_15mm.png - 32kB

This is a screencapture from a test on pure PETN with probe placement 15 mm apart. The probes are ionisation probes, with each probe simply consisting of two square cut copper leads inserted (the picture shows a single probe point):

Sleeve.jpg - 2.3MB

The test sleeve is resin 3d printed and the flaring base is just to have a secure attachment to the print plate. It also allows me to glue it onto a witness plate if I want to test brisance along with VOD (the axial hole goes all the way through). The picture doesn't do it justice, but the probe holes are very cleanly printed at exactly 5mm center distance.
The principle of this testing method is that the reaction zone just behind the detonation front is conductive since it is a high density plasma. Therefore, it can act as a switch to close a circuit. I have then constructed a simple circuit with the probes acting as switches in parallel and included a voltage divider setup to allow the change in signal to be detected, even if the conduction zone hasn't completely faded at one probe before triggering the next. The circuit is powered by a 9V battery, which provides the signal.

In the screen capture above, you can clearly see the very sharp rise in the signal as the detonation reaches the probe, followed by a gradual fall as the conductive zone attenuates. The time between the leading edges is very close to 2.5 us which, with probes 15mm apart, corresponds to a VOD of 6.0 km/s. It is difficult to assess this value since I don't know the exact density of the charge. Also, litterature values are often the result of tests on much larger charges, so even if I did know the density, the VOD of my charge would be less than most litterature values at the same value.
Nevertheless, I find the results encouraging.

I still have much work to do, examining the reproducibility of the setup and trying more than two probes to see if I can map the velocity profile. I also have to examine many different explosives to see if the detonation zone is similarly conductive for others.

[Edited on 8-3-2022 by Microtek]
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[*] posted on 16-3-2022 at 18:39


Attachment: BCHMX.pdf (1MB)
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Attachment: BCHMX2.pdf (750kB)
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Attachment: BCHMX3.pdf (1.2MB)
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[*] posted on 19-3-2022 at 14:42


I think BCHMX is mainly interesting for thos who don't have access to acetic anhydride. If you can get just a small amount of Ac2O and P2O5, you can go the DADN -> SOLEX -> HMX route. All of the steps are easy, and gives essentially 100% yield. Look for the patents by Lukasavage.
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[*] posted on 22-3-2022 at 17:08


Glyoxal + (Amino)-Guanidine + Tetrazole... ???
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[*] posted on 24-3-2022 at 00:46


Take a look at this paper. The perchlorate salt is especially interesting IMO: d=1.99 (measured), VOD=9500 m/s and Pcj=45.7 GPa (Explo 5), Tdec=275C, IS=24J, FS=90N.

The friction sensitivity is perhaps a little high, but other than that, it is almost perfect. The question is if it is hygroscopic like so many other promising perchlorate salts.

Attachment: azotriazole salts.pdf (539kB)
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[*] posted on 24-3-2022 at 01:20


Quote: Originally posted by Microtek  
Take a look at this paper. The perchlorate salt is especially interesting IMO: d=1.99 (measured), VOD=9500 m/s and Pcj=45.7 GPa (Explo 5), Tdec=275C, IS=24J, FS=90N.

The friction sensitivity is perhaps a little high, but other than that, it is almost perfect. The question is if it is hygroscopic like so many other promising perchlorate salts.


What is the synth like? Seems expensive involving silver?
Any update on the Urazine?
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[*] posted on 24-3-2022 at 07:48


The silver is not really necessary, just convenient, and would be recycleable anyway. The synthesis involves oxidative coupling using sodium dichloroisocyanurate (ordinary pool chem) and then reaction with triphenylphosphine which I need to buy.
Lately I have been working on The VOD measurements, so I haven't experimented further with urazine.
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[*] posted on 24-3-2022 at 23:29


Thank you Microtek!
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[*] posted on 29-3-2022 at 00:34


Full-nitro-nitroamino cooperative action: Climbing the energy peak of benzenes with enhanced chemical stability:

https://www.science.org/doi/10.1126/sciadv.abn3176


Here's the paper with the actual synthesis notes for TNTNB if interested:

Attachment: sciadv.abn3176.pdf (1.6MB)
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[Edited on 29-3-2022 by greenlight]




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