Nonisothermal Crystallization Behavior and Mechanical Properties of Poly(butylene succinate)/Silica Nanocomposites

被引:42
|
作者
Bian, Junjia [1 ]
Han, Lijing [1 ]
Wang, Xuemei [1 ]
Wen, Xin [1 ]
Han, Changyu [1 ]
Wang, Shusheng [1 ]
Dong, Lisong [1 ]
机构
[1] Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
基金
美国国家科学基金会;
关键词
crystallization; mechanical properties; nanocomposites; GLASS-FORMING MELTS; CATALYZED NUCLEATION; CARBON NANOTUBE; KINETICS; COMPOSITES; SILICA;
D O I
10.1002/app.31617
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Silica nanoparticles and poly(butylene succinate) (PBS) nanocomposites were prepared by a melt-blending process. The influence of silica nanoparticles on the nonisothermal crystallization behavior, crystal structure, and mechanical properties of the PBS/silica nanocomposites was investigated. The crystallization peak temperature of the PBS/silica nanocomposites was higher than that of neat PBS at various cooling rates. The half-time of crystallization decreased with increasing silica loading; this indicated the nucleating role of silica nanoparticles. The nonisothermal crystallization data were analyzed by the Ozawa, Avrami, and Mo methods. The validity of kinetics models on the nonisothermal crystallization process of the PBS/silica nanocomposites is discussed. The approach developed by Mo successfully described the nonisothermal crystallization process of the PBS and its nanocomposites. A study of the nucleation activity revealed that the silica nanoparticles had a good nucleation effect on PBS. The crystallization activation energy calculated by Kissinger's method increased with increasing silica content. The modulus and yield strength were enhanced with the addition of silica nanoparticles into the PBS matrix. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sri 116: 902-912, 2010
引用
收藏
页码:902 / 912
页数:11
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