CHINESE JOURNAL OF ENERGETIC MATERIALS
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丙烯酸-2,4,6-三硝基苯乙酯的合成及热分解
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作者单位:

西南科技大学,西南科技大学,西南科技大学,中物院化材所,西南科技大学,中物院化材所

作者简介:

刘强强(1987-),男,硕士在读,主要从事火箭推进剂催化剂研究。e-mail: 6070831@163.com

通讯作者:

金波(1982-),男,博士,主要从事含能材料和富勒烯化学方面的研究。e-mail: jinbo@swust.edu.cn; 彭汝芳(1967-),女,教授,主要从事含能材料和富勒烯化学方面的研究。e-mail: pengrufang@swust.edu.cn

基金项目:

国家自然科学基金资助(批准号: 11076002),碳纳米材料四川省青年科技创新研究团队(批准号:2011JTD0017)


Synthesis and Thermal Decomposition Performance of Acrylic 2,4,6-Trinitrophenethyl Ester
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suthwest university of science and technology,southwest university of science and technology,southwest of science and technology,CAEP,southwest university of science and technology,CAEP

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    摘要:

    以TNT、甲醛为原料,在弱碱性条件下反应合成得到2,4,6-三硝基苯乙醇(PicCH2CH2OH); PicCH2CH2OH在浓硫酸催化下和丙烯酸在甲苯中回流反应24 h,合成得到丙烯酸-2,4,6-三硝基苯乙酯,产率为62%。采用紫外可见光谱(UV-Vis)、核磁共振氢谱(1H NMR)、红外光谱(FTIR)、质谱(MS)以及元素分析等对产物结构进行了表征。利用热重分析(TG)对产物热稳定性进行了研究, 采用Kissinger方法和Ozawa方法计算其热分解活化能Ea分别为99.8,2.96 kJ·mol-1。 

    Abstract:

    Trinitrophenyl ethanol (PicCH2CH2OH) was prepared through the reaction of TNT and formaldehyde used as starting materials under the weak base condition, and the target product acrylic 2,4,6-trinitrophenethyl ester with a yield of 62% was synthesized through the reaction of acrylic acid and PicCH2CH2OH under the conditions of concentrated sulfuric acid as catalyst, toluene as solvent and reflux for 24 h. The product was characterized by 1H NMR, FTIR, UV-Vis, MS and elemental analysis. The thermal stability of the product was studied by thermogravimetric analysis (TG), and the kinetic parameters (activation energy and pre-exponential factor) for decomposition reaction were obtained by Kissinger′s method and Ozawa′s method. 

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刘强强,金波,彭汝芳,等.丙烯酸-2,4,6-三硝基苯乙酯的合成及热分解[J].含能材料, 2012, 20(5):579-582. DOI:10.3969/j. issn.1006-9941.2012.05.013.
LIU Qiang-qiang, JIN Bo, PENG Ru-fang, et al. Synthesis and Thermal Decomposition Performance of Acrylic 2,4,6-Trinitrophenethyl Ester[J]. Chinese Journal of Energetic Materials, 2012, 20(5):579-582. DOI:10.3969/j. issn.1006-9941.2012.05.013.

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  • 收稿日期: 2012-07-06
  • 最后修改日期: 2012-07-20
  • 录用日期: 2012-07-20
  • 在线发布日期: 2012-09-26
  • 出版日期: