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Porous aromatic framework epaf-1 material and cl-20@epaf-1 composite energetic material and preparation method

An EPAF-1, porous aromatic skeleton technology, used in nitroalkane compositions, explosives, etc., can solve the problems of complex synthesis steps, increased research work on the stability of dispersed uniform materials, etc., and achieve good detonation performance, high Effects of energy density, mild preparation conditions

Active Publication Date: 2022-04-12
BEIJING INSTITUTE OF TECHNOLOGYGY
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the acquisition of the target energetic product not only requires the support of previous theoretical calculation simulation data, but also complex synthesis steps, yield and cost considerations, difficulty in cultivating crystallization, uniformity of dispersion, and stability of materials. The process of designing and synthesizing materials has added great difficulty to the research work of researchers

Method used

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  • Porous aromatic framework epaf-1 material and cl-20@epaf-1 composite energetic material and preparation method
  • Porous aromatic framework epaf-1 material and cl-20@epaf-1 composite energetic material and preparation method
  • Porous aromatic framework epaf-1 material and cl-20@epaf-1 composite energetic material and preparation method

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Experimental program
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Embodiment 1

[0026] The present invention uses energy-containing monomer cyanuric chloride and 5,5'-diamino-3,3'-bi-1,2,4-triazole (DABT) as raw materials to polymerize the energy-containing porous aromatic skeleton EPAF- 1 Synthetic route and structural diagram of the material:

[0027]

[0028] Weigh 92.5mg of cyanuric chloride (0.5mmol) and 124.5mg of DABT (0.75mmol) into a 10mL pyrex glass tube, add 2mL of mesitylene and 0.3mL of N,N diisopropylethylamine (DIPEA) , sonicate the mixed solution for 5 min. The freezing and pumping operation was carried out under the protection of nitrogen and liquid nitrogen, and three cycles of freezing-vacuumizing-thawing were performed, and then the tube was sealed under a butane / oxygen flame under vacuum conditions. When the glass tube containing the mixed solution rose to room temperature, it was placed in an oven at 180° C. for 3 days to react. The glass tube was removed from the oven to cool to room temperature, and the product was filtered. ...

Embodiment 2

[0036] Weigh 92.5mg of cyanuric chloride (0.5mmol) and 124.5mg of DABT (0.75mmol) in a 10mL pyrex glass tube, add 2mL of o-dichlorobenzene and 0.3mL of N,N diisopropylethylamine (DIPEA ), the mixed solution was ultrasonicated for 5 min. The freezing and pumping operation was carried out under the protection of nitrogen and liquid nitrogen, and three cycles of freezing-vacuumizing-thawing were performed, and then the tube was sealed under a butane / oxygen flame under vacuum conditions. When the glass tube containing the mixed solution rose to room temperature, it was placed in an oven at 180° C. for 3 days to react. The glass tube was removed from the oven to cool to room temperature, and the product was filtered. Then wash with ethanol, boiling water, and ethanol respectively, and vacuum-dry overnight at 80° C. to obtain the porous aromatic skeleton EPAF-1 material. Weigh 600mg of CL-20 into a glass bottle, add 5mL of acetone and 5mL of n-hexane mixed solvent to fully dissolv...

Embodiment 3

[0038] Weigh 925mg of cyanuric chloride (5mmol) and 1.25g of DABT (7.5mmol) in a 100mL two-necked bottle, add 20mL of mesitylene and 3mL of N,N diisopropylethylamine (DIPEA), and ultrasonicate the mixed solution for a period of time. time. Under the protection of nitrogen, the reaction was stirred in an oil bath at 180°C for 3 days, and the product was filtered. Wash with ethanol and boiling water respectively, and dry under vacuum at 80°C overnight to obtain the porous aromatic skeleton EPAF-1 material. Weigh 600mg of CL-20 into a glass bottle, add 5mL of acetone and 5mL of n-hexane mixed solvent to fully dissolve it, and then add 200mg of EPAF-1 material. Put the glass bottle in an oil bath at 50°C, and keep stirring with the open door open (stirring rate is 200r / min) until a dry solid powder is obtained, and then the CL-20@EPAF-1 composite with 75wt% CL-20 doping amount can be obtained Energetic materials.

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Abstract

The present invention relates to a porous aromatic skeleton EPAF‑1 material and CL‑20@EPAF‑1 composite energetic material and a preparation method thereof, which use low-cost energetic monomers cyanuric chloride and DABT as raw materials to synthesize nitrogen-enriched The energetic porous aromatic framework EPAF‑1 material with the heterocycle as the skeleton is then combined with the high-energy elemental explosive CL‑20 to obtain the CL‑20@EPAF‑1 energetic composite material with both high energy and low sensitivity, which is a new type of high energy and low sensitivity The development of energetic materials provides a new research strategy.

Description

technical field [0001] The invention belongs to the field of energetic materials, and relates to a porous aromatic framework EPAF-1 material and a CL-20@EPAF-1 composite energetic material and a preparation method, aiming to invent a new type of high-energy and low-sensitivity energetic material with practical application prospects . Background technique [0002] The development of Energetic materials (EMs) technology is not only the embodiment of a country's military combat capability, but also one of the core strategies related to national security, economic construction and technological development. After being excited by a specific stimulus, energetic materials will quickly release a large amount of energy to damage the surrounding objects, and are widely used in military and civilian fields such as weapons and ammunition, aerospace propellants, mining engineering, and pyrotechnics. However, high-energy substances are often accompanied by poor safety performance, such ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08G73/06C06B43/00C06B25/40
CPCC08G73/0644C08G73/065C06B43/00C06B25/40
Inventor 束庆海宋健吕席卷吴启才邹浩明王俊峰杜君宜
Owner BEIJING INSTITUTE OF TECHNOLOGYGY