Synthesis and Characterization of [60] Fullerene-Glycidyl Azide Polymer and Its Thermal Decomposition

被引:21
作者
Huang, Ting [1 ]
Jin, Bo [1 ,2 ]
Peng, Ru Fang [1 ]
Chen, Cong Di [1 ]
Zheng, Rong Zong [1 ]
He, Yi [2 ]
Chu, Shi Jin [1 ]
机构
[1] Southwest Univ Sci & Technol, State Key Lab Cultivat Base Nonmetal Composites &, Mianyang 621010, Sichuan, Peoples R China
[2] Southwest Univ Sci & Technol, Sch Natl Def Sci & Technol, Mianyang 621010, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
C-60; glycidyl azide polymer (GAP); thermal analysis; energetic material; DERIVATIVES; COMBUSTION; ESTERS; C-60;
D O I
10.3390/polym7050896
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A new functionalized [60]fullerene-glycidyl azide polymer (C-60-GAP) was synthesized for the first time using a modified Bingel reaction of [60]fullerene (C-60) and bromomalonic acid glycidyl azide polymer ester (BM-GAP). The product was characterized by Fourier transform infrared (FTIR), ultraviolet-visible (UV-Vis), and nuclear magnetic resonance spectroscopy (NMR) analyses. Results confirmed the successful preparation of C-60-GAP. Moreover, the thermal decomposition of C-60-GAP was analyzed by differential scanning calorimetry (DSC), thermogravimetric analysis coupled with infrared spectroscopy (TGA-IR), and in situ FTIR. C-60-GAP decomposition showed a three-step thermal process. The first step was due to the reaction of the azide group and fullerene at approximately 150 degrees C. The second step was ascribed to the remainder decomposition of the GAP main chain and N-heterocyclic at approximately 240 degrees C. The final step was attributed to the burning decomposition of amorphous carbon and carbon cage at around 600 degrees C.
引用
收藏
页码:896 / 908
页数:13
相关论文
共 40 条
  • [1] Analysis of C60-fullerene derivatives and pristine fullerenes in environmental samples by ultrahigh performance liquid chromatography-atmospheric pressure photoionization-mass spectrometry
    Astefanei, Alina
    Nunez, Oscar
    Teresa Galceran, Maria
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2014, 1365 : 61 - 71
  • [2] The preparation and structures of non-hydrocarbon functionalised fullerene-diamine adducts
    Butts, CP
    Jazdzyk, M
    [J]. CHEMICAL COMMUNICATIONS, 2003, (13) : 1530 - 1531
  • [3] Preparation of polynitrofullerene by the action of dinitrogen tetroxide on C-60.
    Cataldo, F
    [J]. FULLERENE SCIENCE AND TECHNOLOGY, 1997, 5 (01): : 257 - 265
  • [4] Synthesis and explosive decomposition of polynitro[60]fullerene
    Cataldo, Franco
    Ursini, Ornella
    Angelini, Giancarlo
    [J]. CARBON, 2013, 62 : 413 - 421
  • [5] Chaves C. W., 2014, AIP ADV, V9
  • [6] Efficient one-flask synthesis of water-soluble [60]fullerenols
    Chiang, LY
    Bhonsle, JB
    Wang, LY
    Shu, SF
    Chang, TM
    Hwu, JR
    [J]. TETRAHEDRON, 1996, 52 (14) : 4963 - 4972
  • [7] Structure and Mechanical Properties of Novel Composites Based on Glycidyl Azide Polymer and Propargyl-Terminated Polybutadiene as Potential Binder of Solid Propellant
    Ding, Youzhao
    Hu, Chong
    Guo, Xiang
    Che, Yuanyuan
    Huang, Jin
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2014, 131 (07)
  • [8] Dresselhaus M. S., 1996, Science of fullerenes and carbon nanotubes: their properties and applications
  • [9] Fazlioglu H, 2002, J MACROMOL SCI PURE, V39, P759
  • [10] Thermal decomposition of glycidyl azide polymer by direct insertion probe mass spectrometry
    Fazlioglu, H
    Hacaloglu, J
    [J]. JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2002, 63 (02) : 327 - 338