Synthesis, characterization and UV curing kinetics of hyperbranched polysiloxysilanes from A2 and CB2 type monomers

被引:27
|
作者
Wang, Sheng-Jie [1 ,2 ]
Fan, Xiao-Dong [2 ]
Kong, Jie [2 ]
Lu, Jian-Ren [3 ]
机构
[1] China Univ Petr, Ctr Bioengn & Biotechnol, Qingdao 266555, Peoples R China
[2] Northwestern Polytech Univ, Dept Appl Chem, Sch Sci, Xian 710072, Peoples R China
[3] Univ Manchester, Biol Phys Grp, Sch Phys & Astron, Manchester M13 9JP, Lancs, England
基金
中国国家自然科学基金;
关键词
Hyperbranched polysiloxysilanes; A(2) and CB2 type monomers; UV curing kinetics; PHOTOINITIATED POLYMERIZATION; PHOTOPOLYMERIZATION KINETICS; POLYMERS; DENDRIMERS; COMPOSITES; VISCOSITY;
D O I
10.1016/j.polymer.2009.05.049
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 controllable approach to synthesize UV curable hyperbranched polysiloxysilanes from A(2) (1,1,3,3-tetramethyldisiloxane) and CB2 type monomers (methyl(vinyl)silanediylbis(oxy)bis(ethane-2,1-diyl) diacrylate and methyl(vinyl) silanediylbis(oxy)bis(ethane-2,1-diyl)bis(2-methylacrylate)) was developed in the presented paper. The polymerization was monitored using FTIR, where a two-step polyaddition mode was observed. Vinyl silane group preferentially reacted with hydride silane, resulting in the formation of AB(2) type intermediates containing one hydride silane and two acrylate (or methacrylate) groups, at the same time, there may be low quantity of B-4 type intermediates. The intermediates further polymerized to form hyperbranched polymers. The UV curing kinetics of the hyperbranched polymers, especially the effects of atmosphere, content of photoinitiator and light intensity on UV curing behavior were studied in detail. The results indicated that the hyperbranched polymers could be cured rapidly under UV irradiation. The curing rates increased with the enhancement of light intensity, and the inhibition effect of oxygen could be restrained by increasing light intensity. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3587 / 3594
页数:8
相关论文
共 50 条
  • [1] Preparation of hyperbranched poly (urea-urethane) with hydroxyl end-groups from A2 and CB2 type monomers
    Gao, C
    Yan, DY
    [J]. CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 2002, 23 (11): : 2202 - 2204
  • [2] Sequential click synthesis of hyperbranched polymers via the A2 + CB2 approach
    Han, Jin
    Zhao, Bo
    Gao, Yanqin
    Tang, Aijin
    Gao, Chao
    [J]. POLYMER CHEMISTRY, 2011, 2 (10) : 2175 - 2178
  • [3] Synthesis and properties of a novel hyperbranched polyphosphoramidate using an A2 + CB2 approach
    Liu, Yuhong
    Yan, Ni
    Li, Feng
    Chen, Ping
    [J]. POLYMER INTERNATIONAL, 2013, 62 (03) : 390 - 396
  • [4] Synthesis, characterization, and UV curing kinetics of hyperbranched polycarbosilane
    Wang, Sheng-Jie
    Fan, Xiao-Dong
    Kong, Jie
    Liu, Yu-Yang
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2008, 107 (06): : 3812 - 3822
  • [5] An A2 + CB2 approach to the synthesis of hyperbranched polyester polyol and application in PU coatings
    Patil, Amardip M.
    Shirale, Dhammanand J.
    Jirimali, Harishchandra D.
    Jagtap, Ramanad N.
    [J]. JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, 2024, 21 (03) : 1085 - 1095
  • [6] Synthesis of hyperbranched polymers from commercially available A2 and BB′2 type monomers
    Gao, C
    Yan, DY
    [J]. CHEMICAL COMMUNICATIONS, 2001, (01) : 107 - 108
  • [7] Kinetic treatment for the copolycondensation of A2 and CB2 monomers with non-equal reactivity
    Zhou, Zhiping
    Yan, Deyue
    [J]. POLYMER, 2011, 52 (23) : 5387 - 5392
  • [8] Theoretical investigation on the polyaddition of A2 and CB2 monomers with non-equal reactivity
    Zhou, Zhiping
    Jia, Zhengwei
    Yan, Deyue
    [J]. POLYMER, 2009, 50 (23) : 5608 - 5612
  • [9] Synthesis of Arenesulfonated Hyperbranched Polyimide from A2 + B3 Monomers
    Huan Chen
    Jie Yin
    Hongjie Xu
    [J]. Polymer Journal, 2003, 35 : 280 - 285
  • [10] Synthesis, end-functionalization and characterization of hyperbranched polysiloxysilanes from AB3 type monomer
    Yoshihito Ishida
    Kazutoshi Yokomachi
    Makoto Seino
    Teruaki Hayakawa
    Masa-aki Kakimoto
    [J]. Macromolecular Research, 2007, 15 : 147 - 153