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Method for atomically transferring radical polymerization grafting polymer on surface of explosive

A technology of atom transfer and free radicals, applied in the direction of aromatic nitration composition, etc., can solve the problem that the surface structure is difficult to be effectively adjusted, and achieve the effect that the surface structure can be adjusted and the surface properties are easy

Active Publication Date: 2019-08-02
INST OF CHEM MATERIAL CHINA ACADEMY OF ENG PHYSICS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] However, the use of interface enhancer coating is a physical effect, and the coating strength needs to be further improved. It is difficult to effectively control the surface structure, but there are few reports on the surface structure control of explosive materials.

Method used

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  • Method for atomically transferring radical polymerization grafting polymer on surface of explosive

Examples

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Effect test

Embodiment 1

[0029] (1) Functional group pre-modification: Add 100.0 g of explosives to 2 L of dopamine hydrochloride aqueous solution with a concentration of 2.5 g / L and a pH of 9.0, stir at a rate of 350 rpm for 3 h, then suction filter and dry in vacuum;

[0030] (2) Initiator reaction: Add 50.0 g of the explosive obtained in step (1) to 100 mL of a mixture of n-hexane and pyridine at a volume ratio of 1:1, disperse by ultrasonication for 2 minutes, stir at a rate of 450 rpm, and slowly add 5.0 g of atomic Transfer the free radical polymerization initiator bromoisobutyryl bromide, pass through dry Ar, stir at room temperature for 2h, filter with suction, and rinse with ethanol / water with a volume ratio of 1:1, and dry with Ar purging;

[0031] (3) Catalyst solution preparation: After adding 10.0 g of catalyst ligand PMDETA to 20.0 g of absolute ethanol and mixing, pass through Ar purge, under the protection of Ar, add 0.1 g of catalyst CuBr, and ultrasonically obtain a catalyst solution;...

Embodiment 2

[0034] (1) Functional group pre-modification: add 100 g of explosives to 2 L of dopamine hydrochloride aqueous solution with a concentration of 2.5 g / L and a pH of about 9.0, stir at a rate of 450 rpm for 3 h, then suction filter and dry in vacuum;

[0035] (2) Initiator reaction: Add 100.0 g of the explosive obtained in step (1) to 100 mL of a mixture of n-hexane and pyridine with a volume ratio of 1:1, disperse by ultrasonication for 1 min, stir at a rate of 450 rpm, and slowly add 2.0 g of atomic Transfer the free radical polymerization initiator bromoisobutyryl bromide, pass through dry Ar, stir at room temperature for 1 h, filter with suction, and rinse with ethanol / water with a volume ratio of 1:1, and dry with Ar purging;

[0036] (3) Catalyst solution preparation: After adding 5.0 g of catalyst ligand PMDETA to 50.0 g of absolute ethanol and mixing, pass through Ar purge, under the protection of Ar, add 0.1 g of catalyst CuBr, and sonicate to obtain a catalyst solution;...

Embodiment 3

[0039] (1) Functional group pre-modification: add 100.0 g of explosives to 2 L of dopamine hydrochloride aqueous solution with a concentration of 2.5 g / L and a pH of about 9.0, stir at a rate of 450 rpm for 3 h, filter with suction, and dry in vacuum;

[0040] (2) Initiator reaction: Add 100.0 g of the explosive obtained in step (1) to 100 mL of a mixture of n-hexane and pyridine at a volume ratio of 1:1, disperse by ultrasonication for 1 min, stir at a rate of 450 rpm, and slowly add 5.0 g of atomic Transfer the free radical polymerization initiator bromopropylacyl bromide, pass through dry Ar, stir at room temperature for 1 h, filter with suction, and rinse with ethanol / water with a volume ratio of 1:1, and dry with Ar purging;

[0041] (3) Catalyst solution preparation: After adding 37.5g of catalyst ligand PMDETA to 150.0g of absolute ethanol and mixing, pass through Ar to purge, under the protection of Ar, add 0.5g of catalyst CuBr, and ultrasonically obtain the catalyst s...

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Abstract

The invention discloses a method for atomically transferring a radical polymerization grafting polymer on the surface of an explosive, and belongs to the technical field of energy-containing compositematerials. The method comprises the following steps: (1) functional group pre-modification: pre-coating the surface of an explosive crystal with a hydroxyl functional group; (2) initiator reaction: introducing an initiator for atomically transferring the radical polymerization on the surface of the explosive; (3) preparation of a catalyst liquid: introducing Ar, adding a catalyst ligand into anhydrous ethanol, mixing, then adding CuBr, and performing ultrasonic treatment to obtain the catalyst solution; and (4) atomically transferring of radical polymerization grafting on the surface: completing the grafting of the polymer on the surface of the explosive by an atom transfer radical polymerization grafting reaction. The invention has the significance of providing a novel technology for surface control over new explosive crystals, which can provide technical support for the application of explosives in composite explosives.

Description

technical field [0001] The invention relates to the technical field of energetic composite materials, in particular to a method for atom transfer free radical polymerization grafted macromolecules on the surface of explosives. Background technique [0002] Explosives are widely used in equipment, propellant, civil blasting and other fields. Most explosives are organic small molecule crystals. In the process of preparation, molding and use, due to the weak interface between the explosive crystals and the polymer binder, the explosive crystals will be incompletely coated or bonded weakly. One of the effective ways to improve the adhesive properties of explosives is to modify the surface of explosives. [0003] For example, through the modification of the interface enhancer, the surface adhesion of the explosive can be increased, and the interface between the explosive and the polymer binder can be improved. U.S. Patent No. 4,350,542 uses different coupling agents to prepare ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08F20/54C08F20/20C08F4/50C08F2/38C06B25/04
CPCC06B25/04C08F2/38C08F4/50C08F20/20C08F20/54C08F2438/01
Inventor 巩飞艳曾诚成林聪妹潘丽萍杨志剑
Owner INST OF CHEM MATERIAL CHINA ACADEMY OF ENG PHYSICS