Solid explosive and propellant compositions containing a polyurethane polyacetal elastomer binder and method for the preparation thereof

• US 4,925,503 A
• Filed: 02/17/1988
• Issued: 05/15/1990
• Est. Priority Date: 02/17/1988
• Status: Expired due to Fees

• Current Assignee: OLIN Corporation
• Original Assignee: OLIN Corporation
• Inventors: Katz, Lawrence E., Canterberry, J. B.
• Primary Examiner(s): Miller, Edward A.
• Application Number:
  US07/156,689
• Time in Patent Office: 818 Days
• Field of Search: 149/19.4, 149/19.6
• US Class Current: 149/19.4
• CPC Class Codes: C06B 45/10 the organic component containing a resin

Abstract

A high energy solid explosive or propellant composition having low vulnerability to unplanned stimuli and desired mechanical properties, including a desired degree of hardness. Also claimed is a process for producing this composition.

Claims

1. A solid explosive or propellant composition characterized by low vulnerability to unplanned stimuli and having desired mechanical properties, including a desired degree of hardness, said composition comprising between 51 and 99 weight percent of a high energy material and between 1 and 50 weight percent of a binder, said binder being a chain-extended polyurethane polyacetal elastomer made by a process of:

(a) reacting a dihydroxy-terminated polyacetal homopolymer with an alkylene diisocyanate in the presence of a urethane-forming catalyst in a reaction to produce an isocyanate-terminated prepolymer, said homopolymer having a weight average molecular weight of between about, 1,000 and about 60,000 as measured against a polystyrene standard by gel permeation chromatography and being produced by polymerizing a 4-lower alkyl substituted-1,3-dioxolane, said reaction employing between about 50 mole percent and about 70 mole percent of said alkylene diisocyanate based upon the total amount of said alkylene diisocyanate and said homopolymer employed,

(b) reacting said isocyanate-terminated prepolymer with a dihydroxy-terminated polyacetal copolymer in the presence of a solvent and a urethane forming catalyst to provide a polyurethane polyacetal elastomer, said copolymer having a weight average molecular weight of between about 1,000 and about 200,000 as measured against a polystyrene standard by gel permeation chromatography and being the reaction product of a formaldehyde-providing compound and 1,3-dioxolane, said copolymer being employed in an amount of between about 30 and about 50 mole percent based upon the total amount of said copolymer and said isocyanate-terminated prepolymer employed, and

(c) reacting said elastomer at an elevated temperature with an organic polyisocyanate to provide a chain-extended polyurethane polyacetal elastomer.

2. The composition of claim 1 which preferably has a decomposition temperature peak of within about 20°

C. of the decomposition temperature of said high energy material.

3. The composition of claim 1 which is further characterized by having a decomposition temperature peak of within about 5°

C. of the decomposition temperature of said high energy material.

4. The composition of claim 1 wherein said high energy material is selected from the group consisting of RDX, NTO, TNT, HMX, TAGN, nitroguanidine, ammonium nitrate, diethylene glycol dinitrate, butane triol trinitrate, trimetriol trinitrate, or 2(2,4-dinitrophenoxy)ethanol.

5. The composition of claim 1 wherein the reaction of step (a) additionally employs a solvent.

6. The composition of claim 1 wherein said solvent is a halohydrocarbon.

7. The composition of claim 6 wherein said halohydrocarbon is selected from the group consisting of tetrachloroethane, chloroform, trichloroethane, and mixtures thereof.

8. The composition of claim 1 wherein said urethane-forming catalyst is dibutyltin dilaurate.

9. The composition of claim 1 wherein said urethane-forming catalyst is employed in an amount of between about 0.1 weight percent and about 5 weight percent, based on the total amount of said polyacetal homopolymer or polyacetal copolymer employed.

10. The composition of claim 1 wherein the reactions of step (a) and step (b) are individually conducted within a temperature range of between 25°

C. and 90°

C.

11. The composition of claim 1 wherein the reactions of step (a) and step (b) are carried out essentially simultaneously in an in situ reaction.

12. An explosive or propellant composition characterized by low vulnerability to unwanted detonation, said composition comprising between 51 and 99 weight percent of a high energy material and between 1 and 50 weight percent of a binder, said binder being a polyurethane polyacetal elastomer made by a process of:

(a) reacting a dihydroxy-terminated polyacetal copolymer with an alkylene diisocyanate in the presence of a urethane-forming catalyst in a reaction to produce an isocyanate-terminated prepolymer, said copolymer having a weight average molecular weight of between about 1,000 and about 200,000 as measured against a polystyrene standard by gel permeation chromatography and being the reaction product of a formaldehyde-providing compound and 1,3-dioxolane, said, reaction employing between about 50 mole percent and about 70 mole percent of said alkylene diisocyanate based upon the total amount of said alkylene diisocyanate and said copolymer employed, and

(b) reacting said isocyanate-terminated prepolymer with a dihydroxy-terminated polyacetal homopolymer in the presence of a solvent and a urethaneforming catalyst to provide said elastomer, said homopolymer having a weight average molecular weight of between about 1,000 and about 60,000, as measured against a polystyrene standard by gel permeation chromatography and being produced by polymerizing a 4-lower alkyl substituted-1,3-dioxolane, said homopolymer being employed in an amount of between about 30 and about 50 mole percent based upon the total amount of said homopolymer and said isocyanateterminated prepolymer employed, and

(c) reacting said elastomer at an elevated temperature with an organic polyisocyanate to provide a chain-extended polyurethane polyacetal elastomer.

13. The composition of claim 12 which is further characterized by having a decomposition temperature peak of within about 20°

C. of the decomposition temperature of said high energy material.

14. The composition of claim 12 which is further characterized by having a decomposition temperature peak of within about 5°

C. of the decomposition temperature of said high energy material.

15. The composition of claim 12 wherein said high energy material is selected from the group consisting of RDX, NTO, TNT, HMX, TAGN, nitroguanidine, ammonium nitrate, diethylene glycol dinitrate, butane triol trinitrate, trimetriol trinitrate, or (2,4-dinitrophenoxy)ethanol.

16. The composition of claim 12 wherein the reactions of step (a) and step (b) are carried out essentially simultaneously in an in situ reaction.