IP Library Granted Patent US 7,307,117
Granted Patent B2
US 7,307,117 · App. 10/462,437 · Granted Dec 11, 2007

High strength reactive materials and methods of making

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Quick Facts
Patent No.
US 7,307,117
App. No.
10/462,437
Granted
Dec 11, 2007
Kind
B2
Abstract

In this method for making a sintered reactive material, fuel particles are blended with a polymer matrix comprising at least one fluoropolymer in an inert organic media to disperse the fuel particles in the polymer matrix and form a reactive material. The reactive material is dried and pressed to obtain a shaped preform, which is sintered in an inert atmosphere to form the sintered reactive material. By sintering in an inert atmosphere, the sintered reactive material may include reactive metals and/or metalloids in a nonoxidized state. The resulting sintered reactive material preferably has a tensile strength in excess of 1800 psi and an elongation at break in excess of 30%.

Claims (52)

1. A method of making a sintered reactive material, comprising:

blending fuel particles and a polymer matrix comprising at least one fluoropolymer in a medium that consists essentially of an inert organic medium to form a reactive material;

drying the reactive material;

pressing the reactive material to obtain a shaped preform; and

sintering the shaped preform in an inert atmosphere to form a sintered reactive material.

2. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises blending fuel particles comprising at least one member selected from the group consisting of aluminum, zirconium, titanium, and magnesium with the polymer matrix.

3. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises blending fuel particles comprising at least one member selected from the group consisting of reactive nonoxidized metals and reactive nonoxidized metalloids with the polymer matrix.

4. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises blending fuel particles having an average particle size of less than about 500 microns with the polymer matrix.

5. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises providing the fuel particles in an amount sufficient to account for up to approximately 35 weight percent of a total weight of the sintered reactive material.

6. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises providing the fuel particles in an amount sufficient to account for from approximately 15 weight percent to approximately 35 weight percent of a total weight of the sintered reactive material.

7. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises providing the fuel particles in an amount sufficient to account for from approximately 25 weight percent to approximately 30 weight percent of a total weight of the sintered reactive material.

8. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises blending fuel particles having an average particle size of not greater than about 250 microns with the polymer matrix.

9. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises blending fuel particles having an average particle size in a range of from approximately 1 micron to approximately 10 microns with the polymer matrix.

10. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprises blending aluminum with the polymer matrix.

11. The method of claim 1 , wherein pressing the reactive material to obtain a shaped preform comprises pressing the reactive material at a pressure ranging from approximately 3000 psi to approximately 10000 psi.

12. The method of claim 1 , wherein sintering the shaped preform in an inert atmosphere comprises avoiding oxidization of the fuel particles.

13. The method of claim 1 , wherein sintering the shaped preform in an inert atmosphere comprises heating the shaped preform in the inert atmosphere at a temperature that ranges from 350° C. to 385° C.

14. The method of claim 1 , wherein sintering the shaped preform in an inert atmosphere to form the sintered reactive material comprises forming the sintered reactive material having a tensile strength greater than about 1800 psi and a strain greater than about 30% elongation at break.

15. The method of claim 1 , wherein blending fuel particles and a polymer matrix comprising at least one fluoropolymer in a medium that consists essentially of an inert organic medium comprises blending the fuel particles and the polymer matrix in an environment that at least essentially excludes oxygen.

16. The method of claim 1 , wherein drying the reactive material comprises drying the reactive material in an environment that at least essentially excludes oxygen.

17. The method of claim 1 , wherein pressing the reactive material to obtain a shaped preform comprises pressing the reactive material in an environment that at least essentially excludes oxygen.

18. A method of making a sintered reactive material, comprising:

blending fuel particles and a polymer matrix comprising at least one fluoropolymer in a medium that consists essentially of an inert organic medium to form a reactive material;

drying the reactive material;

pressing the reactive material to obtain a shaped preform; and

sintering the shaped preform in an inert atmosphere to form a sintered reactive material, the sintered reactive material having a tensile strength greater than about 1800 psi and a strain greater than about 30% elongation at break.

19. The method of claim 18 , wherein blending fuel particles and a polymer matrix comprises blending fuel particles having an average particle size of less than 500 microns with the polymer matrix.

20. The method of claim 18 , wherein blending fuel particles and a polymer matrix comprises blending fuel particles comprising at least one reactive nonoxidized metal selected from the group consisting of aluminum, zirconium, titanium, and magnesium with the polymer matrix.

21. The method of claim 18 , wherein blending fuel particles and a polymer matrix comprises providing the fuel particles to account for from approximately 15 weight percent to approximately 35 weight percent of a total weight of the sintered reactive material.

22. The method of claim 18 , wherein blending fuel particles and a polymer matrix comprises blending aluminum particles and the polymer matrix.

23. The method of claim 18 , wherein blending fuel particles and a polymer matrix comprising at least one fluoropolymer in a medium that consists essentially of an inert organic medium comprises blending the fuel particles and the polymer matrix in an environment that at least essentially excludes oxygen.

24. The method of claim 18 , wherein drying the reactive material comprises drying the reactive material in an environment that at least essentially excludes oxygen.

25. The method of claim 18 , wherein pressing the reactive material to obtain a shaped preform comprises pressing the reactive material in an environment that at least essentially excludes oxygen.

26. A reactive material, comprising:

a polymeric matrix comprising at least one fluoropolymer; and

energetic fuel particles dispersed in the polymemic matrix, the energetic fuel particles comprising at least one nonoxidized metal selected from the group consisting of aluminum, zirconium, titanium, and magnesium, wherein the energetic fuel particles and polymeric matrix are sintered.

27. The reactive material of claim 26 , wherein the energetic fuel particles account for from approximately 15 weight percent to approximately 35 weight percent of a total weight of the reactive material.

28. The reactive material of claim 26 , wherein the energetic fuel particles have an average particle size of less than about 500 microns.

29. The reactive material of claim 26 , wherein an average particle size of the energetic fuel particles is not greater than about 250 microns.

30. The reactive material of claim 26 , wherein an average particle size of the energetic fuel particles is in a range of from approximately 1 micron to approximately 10 microns.

31. The reactive material of claim 26 , wherein the energetic fuel particles comprise aluminum.

32. The reactive material of claim 26 , wherein the reactive material has a tensile strength greater than about 1800 psi and a strain greater than about 30% elongation at break.

33. A warhead, comprising:

a liner comprising a sintered reactive material, the sintered reactive material comprising a polymeric matrix comprising at least one fluoropolymer and energetic fuel particles dispersed in the polymeric matrix, the energetic fuel particles comprising at least one nonoxidized metal selected from the group consisting of aluminum, zirconium, titanium, and magnesium.

34. The warhead of claim 33 , wherein the energetic fuel particles have an average particle size of less than about 500 microns.

35. The warhead of claim 33 , wherein an average particle size of the energetic fuel particles is not greater than about 250 microns.

36. The warhead of claim 33 , wherein an average particle size of the energetic fuel particles is in a range of from approximately 1 micron to approximately 10 microns.

37. The warhead of claim 33 , wherein the energetic fuel particles comprise aluminum.

38. The warhead of claim 33 , wherein the reactive material has a tensile strength greater than about 1800 psi and a strain greater than about 30% elongation at break.

39. The warhead of claim 33 , wherein the liner is continuous.

40. The warhead of claim 33 , wherein the liner is noncontinuous.

41. The warhead of claim 33 , wherein the energetic fuel particles account for from approximately 15 weight percent to approximately 35 weight percent of a total weight of the sintered reactive material.

Assignments (9)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2021
From: NORTHROP GRUMMAN INNOVATION SYSTEMS LLC
To: NORTHROP GRUMMAN SYSTEMS CORPORATION
Reel/Frame 055256/0892 →
CHANGE OF NAME Recorded Feb 4, 2021
From: NORTHROP GRUMMAN INNOVATION SYSTEMS, INC.
To: NORTHROP GRUMMAN INNOVATION SYSTEMS LLC
Reel/Frame 055223/0425 →
CHANGE OF NAME Recorded Nov 1, 2018
From: ORBITAL ATK, INC.
To: NORTHROP GRUMMAN INNOVATION SYSTEMS, INC.
Reel/Frame 047400/0381 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jun 6, 2018
From: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
To: ORBITAL ATK, INC.
Reel/Frame 046477/0874 →
CHANGE OF NAME Recorded Nov 28, 2017
From: ALLIANT TECHSYSTEMS INC.
To: ORBITAL ATK, INC.
Reel/Frame 044824/0466 →
RELEASE OF SECURITY INTEREST Recorded Oct 8, 2015
From: BANK OF AMERICA, N.A.
To: ALLIANT TECHSYSTEMS INC.; FEDERAL CARTRIDGE CO.; EAGLE INDUSTRIES UNLIMITED, INC.; AMMUNITION ACCESSORIES, INC.; ORBITAL ATK, INC. (F/K/A ALLIANT TECHSYSTEMS INC.)
Reel/Frame 036816/0624 →
RELEASE OF SECURITY INTEREST Recorded Oct 6, 2015
From: BANK OF AMERICA, N.A.
To: ALLIANT TECHSYSTEMS INC.
Reel/Frame 036734/0701 →
SECURITY AGREEMENT Recorded Sep 30, 2015
From: ORBITAL ATK, INC.; ORBITAL SCIENCES CORPORATION
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 036732/0170 →
SECURITY AGREEMENT Recorded Nov 26, 2013
From: ALLIANT TECHSYSTEMS INC.; CALIBER COMPANY; EAGLE INDUSTRIES UNLIMITED, INC.; FEDERAL CARTRIDGE COMPANY; SAVAGE ARMS, INC.; SAVAGE RANGE SYSTEMS, INC.; SAVAGE SPORTS CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 031731/0281 →