Significant glass-transition-temperature increase through hydrogen-bonded copolymers

被引:49
作者
Kuo, SW
Xu, HY
Huang, CF
Chang, FC [1 ]
机构
[1] Natl Chiao Tung Univ, Inst Appl Chem, Hsinchu, Taiwan
[2] Anhui Univ, Dept Chem, Hefei 230039, Peoples R China
关键词
glass transition; hydrogen bonding; copolymerization; association;
D O I
10.1002/polb.10292
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The role of hydrogen bonding in promoting intermolecular cohesion and higher glass-transition temperatures of polymer is a subject of longstanding interest. A series of poly(vinylphenol-co-vinylpyrrolidone) copolymers were prepared by the free-radical copolymerization of acetoxystyrene and vinylpyrrolidone; this was followed by the selective removal of the acetyl protective group, with corresponding and significant glass-transition-temperature increases after this procedure. The incorporation of acetoxystyrene into poly(vinylpyrrolidone) resulted in lower glass-transition temperatures because of the reduced dipole interactions in its homopolymers. However, the deacetylation of acetoxystyrene to transform the poly(vinylphenol-co-vinylpyrrolidone) copolymer enhanced the higher glass-transition temperature because of the strong hydrogen bonding in the copolymer chain. The thermal properties and hydrogen bonding of these two copolymers were investigated with differential scanning calorimetry and Fourier transform infrared spectroscopy, and good correlations between the thermal behaviors and IR results were observed. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:2313 / 2323
页数:11
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