Influence of Nucleation on the Brittle-Ductile Transition Temperature of Impact-Resistant Polypropylene Copolymer: From the Sight of Phase Morphology

被引:14
作者
Cheng, Dong [1 ,2 ]
Feng, Jiachun [1 ,2 ]
Yi, Jianjun [3 ]
机构
[1] Fudan Univ, Dept Macromol Sci, Minist Educ, Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[2] Fudan Univ, Adv Mat Lab, Shanghai 200433, Peoples R China
[3] China Natl Petr Corp, Inst Petrochem Technol, Key Lab Synthet Resin, Beijing 100083, Peoples R China
关键词
impact-resistant polypropylene copolymer; brittle-ductile transition temperature; crystallization; phase morphology; BINARY POLYMER MIXTURES; ISOTACTIC POLYPROPYLENE; SPHERULITIC CRYSTALLIZATION; MECHANICAL-PROPERTIES; SPINODAL DECOMPOSITION; SEPARATION; BLENDS; BEHAVIOR; GROWTH; MELT;
D O I
10.1002/app.34639
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Influence of alpha- and beta-nucleation on brittle-ductile transition temperature (BDTT) of impact-resistant polypropylene copolymers (IPCs) and their phase morphologies were comparatively investigated. Impact test showed that the BDTT of beta-nucleated IPC (beta-IPC) is similar to 24 degrees C lower than that of a-nucleated one (alpha-IPC). Structural characterizations including atomic force and scanning electron microscopic observations, small angle X-ray scattering examination, and dynamical mechanical analysis revealed that dispersion of the ethylene-propylene random copolymer-rich (EPR-rich) phase was finer in beta-IPC in comparison with that in alpha-IPC. For the reason of looser lamellar arrangement, the portion of EPR-rich components included in the interlamellar region of beta-IPC was higher than those of alpha-IPC, which led to improved mobility for the amorphous polypropylene chains. It was proposed that the finer distribution of EPR-rich phase, which might result from faster growth rate of the beta-crystal and looser lamellar arrangement of beta-spherulite, should be responsible for the improved impact-resistance and lower BDTT in beta-IPC samples. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci 123: 1784-1792, 2012
引用
收藏
页码:1784 / 1792
页数:9
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