自然科学版
陕西师范大学学报(自然科学版)
化学与材料科学
多硝基吡啶酮类高氮含能盐的合成、结构表征及热分解行为
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蔡美玉,张国防*,周海波,景萍,何冲
(应用表面与胶体化学教育部重点实验室; 陕西师范大学 化学与材料科学学院, 陕西 西安 710062)
蔡美玉,女,硕士,主要研究方向为含能材料合成及结构.* 通信作者:张国防, 男, 副教授,博士.E-mail:gfzhang@snnu.edu.cn.
摘要:
基于多硝基吡啶酮类化合物的较强酸性,设计并在水相中合成了12种新颖的高氮含能盐.利用熔点测定、元素分析、1H NMR、FT-IR、粉末XRD分析技术及单晶X射线衍射分析对其进行了结构表征,证实是目标产物.化合物5的晶体属三斜晶系,空间群P1-;化合物6的晶体属单斜晶系,空间群C2/c.用DSC和TG-DTG技术分析了化合物5和8的热分解行为,研究发现化合物5经历两个峰温为183℃和214℃的吸热过程和一个峰温为278℃的放热过程,而化合物8只有一个峰温为319℃的强放热过程.两个化合物放热过程的焓变分别为-181.37 kJ/mol和-382.6 kJ/mol.
关键词:
高氮含能盐; 多硝基吡啶酮; 合成; 晶体结构; 热分解行为
收稿日期:
2009-05-15
中图分类号:
O626.23
文献标识码:
A
文章编号:
1672-4291(2010)03-0043-07
基金项目:
兵器工业总公司国防燃烧重点实验室基金资助项目(2004);陕西师范大学大学生开放基金资助项目(2008).
Doi:
Preparation, characterization and thermodecomposition behaviors of high-nitrogen energetic salts derived from polynitropyridone
CAI Mei-yu, ZHANG Guo-fang*, ZHOU Hai-bo, JING Ping, HE Chong
(Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education; College of Chemistry and Materials Science, Shaanxi Normal University, Xi′an 710062, Shaanxi, China)
Abstract:
Based on the relatively stronger acidity of polynitropyridone(DNP), we designed and synthesized twelve novel high-nitrogen energetic salts in aqueous phase. The products were confirmed by melting point determinations, element analysis, 1H NMR, FT-IR, powder XRD analyses and X-ray single-crystal diffraction analyses. The single crystals data of NH4(4DNP) and (C2H5)2NH2(4DNP) indicated that the former belonged to a Triclinic, P1- space group and the latter to a monoclinic, C2/c space group. The thermal decomposition analyses studied by using DSC and TG-DTG techniques revealed that NH4(4DNP) experienced two endothermic processes with peak temperatures of 183℃ and 214℃ and one exothermal process with peak temperature of 278℃ and CN2H4NH2(4DNP) only one intense exothermal process with peak temperature of 319℃. The exothermic enthalpy changes for NH4(4DNP) and CN2H4NH2(4DNP) are -183.37 kJ/mol and -382.6 kJ/mol, respectively.
KeyWords:
high-nitrogen energetic salt; polynitropyridone; synthesis; crystal structure; thermodecom position behavior