Modeling of flow-induced crystallization in blends of isotactic polypropylene and poly(ethylene-co-octene)

被引:10
|
作者
Yu, Fengyuan [1 ]
Zhang, Zinan [1 ]
Yu, Wei [1 ]
Zhou, Chixing [1 ]
Zhang, Hongbin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Technol, Dept Polymer Sci & Engn, Adv Rheol Inst, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
polypropylene; flow-induced crystallization; model; blend; crystallization kinetics; SHEAR-INDUCED CRYSTALLIZATION; POLYMER MELTS; CONTINUUM MODEL; INTERNAL STRUCTURE; MOLECULAR-WEIGHT; KINETICS; MORPHOLOGY; BEHAVIOR; POLYETHYLENE; QUIESCENT;
D O I
10.1002/pi.4220
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(ethylene-co-octene) (PEOc) has been shown to provide a high toughening contribution to isotactic polypropylene (iPP). The theoretical modeling of flow-induced crystallization (FIC) of blends of iPP and PEOc is not much reported in the literature. The aim of the present work is to clarify the FIC of iPP upon addition of PEOc in terms of theoretical modeling. The crystallization of iPP and PEOc blends in flow is simulated by a modified FIC model based on the conformation tensor theory. Two kinds of flow fields, shear flow and elongational flow, are considered in the prediction to analyze the influence of flow field on the crystallization kinetics of the polymer. The simulation results show that the elongation flow is much more effective than shear flow in reducing the dimensionless induction time of polymer crystallization. In addition, the induction time of crystallization in the blends is sensitive to the change of shear rate. In comparison with experimental data, the modified model shows its validity for the prediction of the induction time of crystallization of iPP in the blends. Moreover, the simulated relaxation time for the blends becomes longer with increasing percentage of PEOc in the blends. Copyright (c) 2012 Society of Chemical Industry
引用
收藏
页码:1389 / 1393
页数:5
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