Combination of Nitrogen-Rich Skeleton and Coordination Group: Synthesis of a High-Energy Primary Explosive Based on 1H-Tetrazole-5-Carbohydrazide

被引:11
|
作者
Wang, Tingwei [1 ]
Lu, Zujia [1 ]
Bu, Shu [3 ]
Kuang, Baolong [1 ]
Zhang, Lu [1 ]
Yi, Zhenxin [2 ]
Wang, Kun [3 ]
Zhu, Shunguan [2 ]
Zhang, Jianguo [1 ]
机构
[1] Beijing Inst Technol, State Key Lab Explos Sci & Technol, Beijing 100081, Peoples R China
[2] Nanjing Univ Sci & Technol, Sch Chem Engn, 200 Xiaolingwei St, Xuanwu, Nanjing 210094, Peoples R China
[3] Anhui Univ, Dept Chem, Lab Struct & Funct Regulat Hybrid Mat, Minist Educ, Hefei 230601, Peoples R China
来源
DEFENCE TECHNOLOGY | 2024年 / 31卷
基金
中国国家自然科学基金;
关键词
1H-tetrazole-5-carbohydrazide; Primary explosive; Decomposition mechanism; Coordination polymers; Laser; TRANSITION-METAL-COMPLEXES; CRYSTAL-STRUCTURES; MONOTETRAZOLES; PERFORMANCE; STABILITY; POLYMERS; SILVER;
D O I
10.1016/j.dt.2023.02.014
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The high energy coordination compounds Cu(TZCA)2(ClO4)2 (ECCs-1) was prepared by 1H-tetrazole-5- carbohydrazide (TZCA) with a high energy skeleton and a strong coordination ability group. At the same time, the reaction activity of the ligand was explored, and the single crystal structure of it and intermediate were obtained. The structures of all substances were characterized by IR and EA. And the structure and composition of ECCs-1 are confirmed by ESP, AC, SEM and ICP-OES. Physical and chemical properties tests show that ECCs-1 has an acceptable thermal stability (Td = 177 degrees C) and extremely sensitive mechanical stimulation (IS =1 J, FS = 5 N). The comprehensive performance test results show that ECCs-1 has excellent initiation ability. In addition, the decomposition mechanism of ECCs-1 is explored from two aspects of experiment and theoretical calculation. (c) 2023 China Ordnance Society. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页码:271 / 277
页数:7
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