CHINESE JOURNAL OF ENERGETIC MATERIALS
+高级检索
偶氮四唑胍盐的热分解机理
作者:
作者单位:

(西安近代化学研究所, 陕西 西安 710065)

作者简介:

王琼(1985-),男,硕士,主要从事火炸药热分析及环境适应性等相关研究。e-mail: 0304140125@163.com

通讯作者:

基金项目:


Mechanism of Thermal Decomposition of Guanidinium Azotetrazolate
Author:
Affiliation:

(Xi′an Modern Chemistry Research Institute, Xi′an 710065, China)

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
    摘要:

    采用热重分析(TG), 差示扫描量热法(DSC), 固体原位池/红外和质谱(直接进样和热裂解-色谱-质谱联用方式)研究了偶氮四唑胍(GZT)的热分解行为, 凝聚相产物和气相产物的变化, 提出了GZT的热分解机理。结果表明, GZT分解失重的第一阶段由偶氮四唑的放热分解反应和胍分解的吸热过程构成。在单独热作用下, GZT首先发生质子转移形成偶氮四唑和胍, 然后分别分解。偶氮四唑的四唑环经过开环反应, 可能形成中间产物叠氮四唑(CHN7), 最终生成三聚氰胺和叠氮铵等高沸点物质。在离子源轰击作用下除了四唑环开环解离外, C—Nazo也会发生断裂, 进而裂解。

    Abstract:

    The thermal behavior of guanidinium azotetrazolate (GZT) was studied using the thermogravimetry and differential scanning calorimetry. The thermal decomposition mechanism of GZT was proposed based on the investigation of products in condensed and gas phases by the combination techniques of solid in situ cell with the rapid-scan Fourier transform infrared spectroscopy and pyrolysis-gas-chromatography-mass-spectrometry (Py-GC-MS). Results show the first mass loss process of GTZ includes the exothermic decomposition reaction of azotetrazolate and the endothermic decomposition reaction of guanidinium. Under heating, the intermediate product tetrazoleazide (CHN7) may forme through the ring-opening reaction of tetrazole on the azotetrazolate molecular and the ultimate products are high boiling point materials: melamine and ammonium azide. Under the bombardment of ion source, the bond C—Nazo on azotetrazolate molecular also split and dissociate in sequence.

    参考文献
    相似文献
    引证文献
文章指标
  • PDF下载次数:
  • HTML阅读次数:
  • 摘要点击次数:
  • 引用次数:
引用本文

王琼,安亭,潘清,等.偶氮四唑胍盐的热分解机理[J].含能材料, 2014, 22(1):36-42. DOI:10.3969/j. issn.1006-9941.2014.01.008.
WANG Qiong, AN Ting, PAN Qing, et al. Mechanism of Thermal Decomposition of Guanidinium Azotetrazolate[J]. Chinese Journal of Energetic Materials, 2014, 22(1):36-42. DOI:10.3969/j. issn.1006-9941.2014.01.008.

复制
历史
  • 收稿日期: 2013-05-04
  • 最后修改日期: 2013-09-02
  • 录用日期: 2013-09-12
  • 在线发布日期: 2014-01-23
  • 出版日期: 2014-02-25