Synthesis of poly(amido amine)-derived dendrimers with pendant benzoxazine groups and their thermal behavior

被引:11
作者
Lu, Yanbing [1 ]
Chen, Junren [1 ]
Lu, Yunlong [1 ]
Gai, Pengbo [1 ]
Zhong, Hailin [1 ]
机构
[1] Hunan Univ, Polymer Res Inst, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China
关键词
dendrimers; synthesis; kinetics; benzoxazine; differential scanning calorimetry; NETWORK STRUCTURE; KINETIC-ANALYSIS; NMR-SPECTROSCOPY; MODEL COMPOUNDS; EPOXY-RESIN; POLYBENZOXAZINES; POLYMERS; POLYMERIZATION; CHEMISTRY; BLENDS;
D O I
10.1002/app.37886
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two novel dendrimer-derived compounds with pendant benzoxazine, named 0G benzoxazine (0G BOZ) and 1G benzoxazine (1G BOZ), were prepared using 0G poly(amido amine) (PAMAM) and 1G PAMAM, phenol, and paraformaldehyde. Effects of different generations of PAMAM on curing kinetics and thermal properties were investigated. Differential scanning calorimetric (DSC) measurements of the 0G BOZ and 1G BOZ were carried out at different heating rates of 5, 10, 15, and 20 K/min. Kinetic analysis by Kissinger's and Ozawa's method revealed the activation energy (Ea) of 0G BOZ were 109.1 and 109.3 kJ mol-1, respectively, and those of 1G BOZ were 88.0 and 91.4 kJ mol-1. The autocatalytic kinetic model was found to be the best description of the investigated curing reactions. In addition, the predicted curves from our kinetic models fit well with the nonisothermal DSC thermograms. Thermogravimetrical analysis of cured resin of 0G BOZ and 1G BOZ showed that the char yields of 0G BOZ and 1G BOZ were 37.6 and 26.3%, respectively. (C) 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2012
引用
收藏
页码:282 / 288
页数:7
相关论文
共 36 条
  • [1] Synthesis and characterization of novel benzoxazine monomers containing allyl groups and their high performance thermosets
    Agag, T
    Takeichi, T
    [J]. MACROMOLECULES, 2003, 36 (16) : 6010 - 6017
  • [2] Polymerization of linear aliphatic diamine-based benzoxazine resins under inert and oxidative environments
    Allen, Douglas J.
    Ishida, Hatsuo
    [J]. POLYMER, 2007, 48 (23) : 6763 - 6772
  • [3] Physical and mechanical properties of flexible polybenzoxazine resins: Effect of aliphatic diamine chain length
    Allen, Douglas J.
    Ishida, Hatsuo
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2006, 101 (05) : 2798 - 2809
  • [4] Effect of phenol substitution on the network structure and properties of linear aliphatic diamine-based benzoxazines
    Allen, Douglas J.
    Ishida, Hatsuo
    [J]. POLYMER, 2009, 50 (02) : 613 - 626
  • [5] Synthesis of linear polymers containing benzoxazine moieties in the main chain with high molecular design versatility via click reaction
    Chernykh, Andrey
    Agag, Tarek
    Ishida, Hatsuo
    [J]. POLYMER, 2009, 50 (02) : 382 - 390
  • [6] 31P NMR spectroscopy in benzoxazine model compounds and benzoxazine chemistry - main chain and end group studies
    Chutayothin, Papinporn
    Ishida, Hatsuo
    [J]. EUROPEAN POLYMER JOURNAL, 2009, 45 (05) : 1493 - 1505
  • [7] Polybenzoxazines - New high performance thermosetting resins: Synthesis and properties
    Ghosh, N. N.
    Kiskan, B.
    Yagci, Y.
    [J]. PROGRESS IN POLYMER SCIENCE, 2007, 32 (11) : 1344 - 1391
  • [8] Benzoxazine oligomers: Evidence for a helical structure from solid-state NMR spectroscopy and DFT-based dynamics and chemical shift calculations
    Goward, GR
    Sebastiani, D
    Schnell, I
    Spiess, HW
    Kim, HD
    Ishida, H
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (19) : 5792 - 5800
  • [9] The curing reactions of ethynyl-functional benzoxazine
    Huang, Jianxiang
    Zhang, Jian
    Wang, Fan
    Huang, Farong
    Du, Lei
    [J]. REACTIVE & FUNCTIONAL POLYMERS, 2006, 66 (12) : 1395 - 1403
  • [10] Regioselectivity and network structure of difunctional alkyl-substituted aromatic amine-based polybenzoxazines
    Ishida, H
    Sanders, DP
    [J]. MACROMOLECULES, 2000, 33 (22) : 8149 - 8157