High-performing stable green replacements for ammonium perchlorate

Patent metadata

Field	Value
Publication number	US-9309266-B2
Application number	US-201414284929-A
Country	US
Kind code	B2
Filing date	May 22, 2014
Priority date	May 22, 2013
Publication date	Apr 12, 2016
Grant date	Apr 12, 2016

Abstract

A highly energetic, high-oxygen carrier suitable as high-performing green replacement for ammonium perchlorate includes halogen-free ionic salts consisting of fuel cations and over-oxidized anions containing multiple nitro- or nitromethyl-substituted azolyl ligands. The over-oxidized anions include a central atom selected from the group consisting of boron, aluminum, or gallium. Characteristically, the carrier has sufficient amounts of oxygen for complete or near complete combustion of the over-oxidized anions, the fuel cations, metal additives and binders.

First claim

What is claimed is:

1. A highly energetic, high-oxygen carrier suitable as high-performing green replacement for ammonium perchlorate, the high-oxygen carrier comprising:
a halogen-free ionic salt having a fuel cation and an over-oxidized anion described by formula I:

wherein:
X 1 , X 2 , X 3 , X 4 are each independently C—R or N;
R is H, NO 2 or —C(NO 2 ) 3 with the proviso that 0, 1, 2, or 3 of X 1 , X 2 , X 3 , X 4 are N and at least one of X 1 , X 2 , X 3 , X 4 includes NO 2 or C(NO 2 ) 3 ; and
M is boron, aluminum, or gallium, the carrier having sufficient amounts of oxygen for complete or near complete combustion of the over-oxidized anion, the fuel cation, metal additives and binders.

2. The high-oxygen carrier of claim 1 wherein M is boron.

3. The high-oxygen carrier of claim 1 wherein the M is aluminum.

4. The high-oxygen carrier of claim 1 wherein the over-oxidized anion includes a nitro-substituted azolyl ligand selected from the group consisting of 3,5-dinitro-1H-1,2,4-triazolyl, 5-nitro-3-(trinitromethyl)-1H-1,2,4-triazolyl, 5-(trinitromethyl)-2H-tetrazolyl, 5-nitro-2H-tetrazolyl, 3,4,5-trinitro-1H-pyrazolyl, 2,4,5-trinitro-1H-imidazolyl, and combinations thereof.

5. The high-oxygen carrier of claim 1 wherein the cation is selected from the group consisting of NH 4 + , N 2 H 5 + , N 2 H 6 2+ , NH 3 OH + , and H 2 NC(NH 2 )NH 2 + .

6. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(3,5-dinitro-1H-1,2,4-triazolyl)borate.

7. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-nitro-3-(trinitromethyl)-1H-1,2,4-triazolyl)borate.

8. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-(trinitromethyl)-2H-tetrazolyl)borate.

9. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-nitro-2H-tetrazolyl)borate.

10. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(3,4,5-trinitro-1H-pyrazolyl)borate.

11. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(2,4,5-trinitro-1H-imidazolyl)borate.

12. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-nitro-2H-tetrazolyl)borate.

13. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-(trinitromethyl)-2H-tetrazolyl)borate.

14. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(3,5-dinitro-1H-1,2,4-triazolyl)aluminate.

15. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-nitro-3-(trinitromethyl)-1H-1,2,4-triazolyl)aluminate.

16. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-(trinitromethyl)-2H-tetrazolyl)aluminate.

17. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-nitro-2H-tetrazolyl)aluminate.

18. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(3,4,5-trinitro-1H-pyrazolyl)aluminate.

19. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(2,4,5-trinitro-1H-imidazolyl)aluminate.

20. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-nitro-2H-tetrazolyl)aluminate.

21. The high-oxygen carrier of claim 5 wherein the anion is tetrakis(5-(trinitromethyl)-2H-tetrazolyl)aluminate.

22. A method of preparing highly energetic, high-oxygen carriers, the method comprising:
reacting a metal or semimetal compound including a moiety having formula ML n with a nitro-substituted azole having formula II

to form a first salt having a first cation and an over-oxidized anion described by formula I such that molecular hydrogen or a C 1-12 alkane is evolved:

wherein:
X 1 , X 2 , X 3 , X 4 are each independently C—R or N;
R is H, NO 2 or —C(NO 2 ) 3 with the proviso that 0, 1, 2, or 3 of X 1 , X 2 , X 3 , X 4 are N and at least one of X 1 , X 2 , X 3 , X 4 includes NO 2 or C(NO 2 ) 3 ;
M is boron, aluminum, or gallium;
L are independently a hydrogen atom or a C 1-12 alkyl ligand; and
n is 1 to 4.

23. The method of claim 22 wherein the metal or semi-metal compound includes boron or aluminum.

24. The method of claim 22 wherein the metal or semi-metal compound includes boron.

25. The method of claim 22 wherein the metal or semi-metal compound includes aluminum.

26. The method of claim 22 wherein the metal or semi-metal compound includes BH 4 − .

27. The method of claim 26 wherein the metal or semi-metal compound is an alkali metal BH 4 − salt.

28. The method of claim 27 wherein the alkali metal BH 4 − salt includes an alkali metal selected from the group consisting of lithium, sodium, potassium.

29. The method of claim 22 wherein the metal or semi-metal compound is ammonia borane.

30. The method of claim 22 wherein the metal or semi-metal compound is reacted with the nitro-substituted azoles in a solvent that includes alkyl ethers.

31. The method of claim 30 wherein the solvent is 1-methoxy-2-(2-methoxyethoxy)ethane (diglyme).

32. The method of claim 31 wherein the metal or semi-metal compound is an alkali metal borohydride.

33. The method of claim 22 wherein the metal or semi-metal compound is an alkali metal borohydride.

34. The method of claim 22 wherein the first salt is an alkali metal tetrakis-nitroazolylborate salt.

35. The method of claim 34 wherein the alkali metal tetrakis-nitroazolylborate salt is contacted with an ion-exchange resin to form an ammonium salt.

36. The method of claim 34 wherein the alkali metal tetrakis-nitroazolylborate salt is reacted by double ion-exchange metathesis to form an ammonium salt.

37. The method of claim 22 wherein ammonia borane is reacted with acidic hydrogen atoms of nitroazoles under dihydrogen evolution to form an ammonium tetrakis-nitroazolylborate salt.

38. A method for forming an ammonium tetrakis-nitroazolylborate salt comprising reacting a tris-nitroazolyl borane having formula III with an ammonium nitroazolate salt having formula IV:

wherein:
X 1 , X 2 , X 3 , X 4 are each independently C—R or N;
R is H, NO 2 or —C(NO 2 ) 3 with the proviso that 0, 1, 2, or 3 of X 1 , X 2 , X 3 , X 4 are N and at least of X 1 , X 2 , X 3 , X 4 includes NO 2 or C(NO 2 ) 3 ; and
M 1 + is an ammonium cation or a substituted ammonium cation.

Assignees

• Univ Southern California

Inventors

• Haiges Ralf
• Christe Karl O
• Jones Cj Bigler

Classifications

• C07F5/069

  without C-aluminium linkages · CPC title

• C06B49/00 Primary

  Use of single substances as explosives · CPC title

• C06B47/10

  a component containing free boron, an organic borane or a binary compound of boron, except with oxygen · CPC title

• C07F5/022 Primary

  without C-boron linkages · CPC title

• C06B41/00

  Compositions containing a nitrated metallo-organic compound · CPC title