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Author: Subject: Biuret ?
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[*] posted on 13-1-2014 at 01:03
Biuret ?


I saw this chemical from wikipedia and it looks interesting for nitration! Has anybody play with that ever ? It may have some good properties as an EM, Maybe some di/trinitrobiuret or whatever...

[Edited on 13-1-2014 by underground]
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Dany
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[*] posted on 13-1-2014 at 01:58


take a look on this PhD thesis (2005):

PhD thesis

search in the Pdf for biuret.

Dany.

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[*] posted on 13-1-2014 at 02:11


The link does not work for me. I can not open the pdf file
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[*] posted on 13-1-2014 at 02:27


download from here:

http://www45.zippyshare.com/v/34298528/file.html

Dany.

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[*] posted on 13-1-2014 at 03:18


Firstly a big thanks to Dany, a really good pdf file!

By the way,we have some good points here. Dinitrobiuret it looks like a little bit sensitive EM, i guess something close to ETN, but it looks stable in air, i guess it will be also stable in storge, with positive OB and with VoD of 8660, almost as RDX. The positive OB may also help to further increase the VoD with some addition fuel. Also, some salts can be formed. I bet that the ammonium salt of Dinitrobiuret shoud have a really high VoD !! Or even better the guanidine salt of Dinitrobiuret!!

[Edited on 13-1-2014 by underground]
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[*] posted on 13-1-2014 at 04:23


Biuret have a very high negative heat of formation, therefore its less advantages compared to some other similar compounds such as guanidine and carbohydrazide however, i believe biuret is more dense, and it can probably form salts such as biuret dinitrate.
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[*] posted on 13-1-2014 at 06:58


I bet biuret will form more stable and storage salts than those of guanidine and urea, a really big advantage...

[Edited on 13-1-2014 by underground]
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[*] posted on 13-1-2014 at 10:10


Dinitrobiuret seems like it does not have a high impact sensitivity. some links for more info on DNB

https://www.google.ae/url?sa=t&rct=j&q=&esrc=s&a...

http://www.dtic.mil/dtic/tr/fulltext/u2/a547366.pdf

I still wonder if nitro-guanidine cation exist.

http://www.chemspider.com/Chemical-Structure.16372117.html

such as one stated in this picture, it have similar OB with dinitrobiuret however it should be more energetic since the C=O group on dinitrobiuret causes high negative hof.
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[*] posted on 13-1-2014 at 10:58


Quote: Originally posted by DubaiAmateurRocketry  
Dinitrobiuret seems like it does not have a high impact sensitivity. some links for more info on DNB

https://www.google.ae/url?sa=t&rct=j&q=&esrc=s&a...



sweet....very interesting stuff

but how to make the MonoNitro-compound?
simple synthesis with, lets say, 65% HNO3 ?

8660m/s and 33.9GPa sounds preety interesting...
they wrote that the performace of it will be between PETN and HMX !!:o

:D
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[*] posted on 13-1-2014 at 13:06


Also how biuret can be formed from urea ? and how can we separate it ?

Update:
Biuret It is formed during urea production upon heating urea at 80 Degree C and higher, especially above its melting point according due to the following reaction release of ammonia:

2 CO(NH2)2 → H2N-CO-NH-CO-NH2 + NH3

[Edited on 13-1-2014 by underground]
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[*] posted on 14-1-2014 at 07:06


Umm.. I also think diamino guanidine, triamino guanidine, carbohydrazide competitive.

Elemental analysis of diamino guanidine compared to guanidine shows spectacular differences in its nitrogen content.

Diamino guanidine H2NNHC(NH)NHNH2, 13.5% Carbon, 78.6% Nitrogen, 7.9% Hydrogen,

Guanidine, CH5N3, 20.3% Carbon, 71.1% Nitrogen, 8.53% Hydrogen.

Carbohydrazide, CH6N4O, 13.3%Carbon, 6.7% Hydrogen, 62.2% Nitrogen, 17.7% Oxygen.

Biuret C2H5N3O2, 23.35%Carbon, 41% Nitrogen, 4.9% Hydrogen, 31% Oxygen

Urea, CH4N2O, 20% Carbon, 6.7% Hydrogen, 46.6% Nitrogen, 26.6% Oxygen.

Biuret has lowest nitrogen/highest carbon content with lowest heat of formation which is unfavorable to be used in EM which is most likely why its less investigated, I am interested in carbohydrazide and diamino guanidine salts. They both can form 2+ cation. Diamino guanidine dinitrate [CH8N4O]2+ 2[NO3]- (CH8N6O7) might have a good VoD.

Triamino guanidine nitrate (this mono nitrate version is not good)
http://www.explosia.cz/en/vupch/download/tagn.pdf

Dinitrate salts of above triamino, diamino, amino guanidine, and some others are mentioned in this patent. I still look forward to the didinitramide version
http://www.google.nl/patents/CA2342366A1?cl=en

Also wonder if Urea dinitramide is ever synthesized.

[Edited on 14-1-2014 by DubaiAmateurRocketry]
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[*] posted on 15-1-2014 at 07:49


Also there is triuret out there.... What about triuret dinitrate ?

And one more think, how can i form different tipes of salts with dinitrobiuret as an cation, like ammonium dinitrobiuret ?

[Edited on 15-1-2014 by underground]
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[*] posted on 2-2-2014 at 19:59


I was thinking .... How Di Nitro Urea is used in Keto-RDX synth ....
What impact would it have if it was to be replaced by Di Nitro Biuret ??
Keto-HMX perhaps ?




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[*] posted on 3-2-2014 at 05:03


Quote: Originally posted by Motherload  
I was thinking .... How Di Nitro Urea is used in Keto-RDX synth ....
What impact would it have if it was to be replaced by Di Nitro Biuret ??
Keto-HMX perhaps ?


maybe not exactly what you want to see, and not same structure with HMX, however this is also 8 membered fused ringed compound has 2 dinitrourea group(which include 2 keto and 4 NNO2, similar to that of HMX)

http://www.iloveexplosives.com/2008/10/sorguyl-aka-tgnu-synt...
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[*] posted on 5-2-2014 at 03:24


Here is a copy - paste message from a very good friend on this forum :)

From urea, biuret is obtainable via heating at a specific temperature (a little search in freepatents online should give you some hints...presence of biuret is observable because of the specific coloration it displays with copper salts complexation...the solution turns from the usual blue to pink-violet. Maybe there is an isolation process playing on that property; or fractionnal cristalization.
Once you have biuret...with diluted HNO3 you would get biuret dinitrate...allow to evaporate until dry and cristaline and finaly treat the dinitrate with >98% H2SO4 (like the system to make nitroguanidine from guanidine nitrate -or- nitrourea from urea nitrate) to get the dinitrobiuret.
The investigation of the salts of DNBiuret might lead to discovery of new primaries or propellants!
O2N-N(Z)-CO-NH-CO-N(Z)-NO2
Z being a metal (Na,K, Pb, Cu, Ag, Hg, ...)or an amine (NH4, N2H5, NH3OH)...
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[*] posted on 5-2-2014 at 08:42


Are you sure one would get Di nitrate and not just nitrate in one step via dil HNO3 ?



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[*] posted on 5-2-2014 at 10:19


Quote: Originally posted by Motherload  
Are you sure one would get Di nitrate and not just nitrate in one step via dil HNO3 ?


This is a message from an another member on this forum... he told me that and then i just copy-paste the message


Also i was thinking for something else, biuret has more oxygen and nitrogen content and it is denser than guanidine. Also aminonitroguanidine nitrate has a VoD 9750m/s calculated but unfortunately it is not so storage stable e.t.c. Ammonium Dinitroguanidine has a VoD 9055m/s calculated. So i was thinking for aminonitrobiuret nitrate and Ammonium Dinitrobiuret not only because their VoD i guess would be greater, but also for their chemical and storage stability.

[Edited on 5-2-2014 by underground]
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[*] posted on 5-2-2014 at 11:07


Quote: Originally posted by Motherload  
Are you sure one would get Di nitrate and not just nitrate in one step via dil HNO3 ?


i read alot about DNB last month and im pretty sure, that when taking diluted HNO3 at the first step, you get the mono-nitro compound....

i never read about (di)nitrate stuff when reacting biuret with HNO3

[Edited on 5-2-2014 by VladimirLem]
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[*] posted on 5-2-2014 at 14:58


Quote: Originally posted by VladimirLem  

i read alot about DNB last month and im pretty sure, that when taking diluted HNO3 at the first step, you get the mono-nitro compound....

i never read about (di)nitrate stuff when reacting biuret with HNO3

[Edited on 5-2-2014 by VladimirLem]


Can you share with us your sources about Dinitrobiuret ?
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[*] posted on 6-2-2014 at 10:55


Quote: Originally posted by underground  
Quote: Originally posted by VladimirLem  

i read alot about DNB last month and im pretty sure, that when taking diluted HNO3 at the first step, you get the mono-nitro compound....

i never read about (di)nitrate stuff when reacting biuret with HNO3

[Edited on 5-2-2014 by VladimirLem]


Can you share with us your sources about Dinitrobiuret ?


i searched the shit out of google and only found a few PDFs...

"High energy density materials based on tetrazole and nitramine compounds"
"Dinitrobiuret & its Salts"
"thermal decomposition of 1,5-DiNitroBiuret"

there are very rare informations out there :/ the VoD and performace seems pretty interesting...but no sources about exact density.
Solublity (Mono, Nitro) is anywhere in the PDFs.
DNB seems to be chemical instable to alkaline compounds.

i also found a source that said, making biuret out of urea will be a damn long and inefficient process (heating for days at the decomposition themerature of urea) so i dounbt i will ever make it and carry on with electroforming copper-lines for shaped charges (and testing some easier to make explosives of course^^)
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[*] posted on 7-2-2014 at 02:43


I though that biuret could easily be made out of urea,this thing change everything.
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[*] posted on 7-2-2014 at 07:49


Quote: Originally posted by underground  
I though that biuret could easily be made out of urea,this thing change everything.


well...this source says something about a few hours, but the yield seems to be not really good...

http://link.springer.com/article/10.1007%2Fs11814-009-0164-0...

the advantage is, that it seems to be very easy to wash the urea/biuret mixture with cold water and getting 95%< biuret, cause urea is very soluble in water and biuret just a little bit
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[*] posted on 8-2-2014 at 05:53


Quote: Originally posted by VladimirLem  

well...this source says something about a few hours, but the yield seems to be not really good...

http://link.springer.com/article/10.1007%2Fs11814-009-0164-0...

the advantage is, that it seems to be very easy to wash the urea/biuret mixture with cold water and getting 95%< biuret, cause urea is very soluble in water and biuret just a little bit


Those catalysts looks really dificult to find... Have you got any document about the temperature, the quantity of urea used, the time is needed and the final yelds of biuret ?
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[*] posted on 8-2-2014 at 08:45


Quote: Originally posted by underground  


Those catalysts looks really dificult to find... Have you got any document about the temperature, the quantity of urea used, the time is needed and the final yelds of biuret ?


i didnt read the complete text...and by the way, i see this link doesnt work correct...when browsing from google, a pdf opens (images below)

000.png - 100kB001.png - 113kB
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[*] posted on 9-2-2014 at 17:02


So it looks like the yelds are close to 22%, This is not so bad, urea is cheap and this reaction can be used with big quantities to get as much biuret as you like
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