Self-Acceleration of Nucleation and Formation of Shish in Extension-Induced Crystallization with Strain Beyond Fracture

被引:79
作者
Cui, Kunpeng
Meng, Lingpu
Tian, Nan
Zhou, Weiqing
Liu, Yanping
Wang, Zhen
He, Jie
Li, Liangbin [1 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
FLOW-INDUCED CRYSTALLIZATION; SHEAR-INDUCED CRYSTALLIZATION; ISOTACTIC POLYPROPYLENE CRYSTALLIZATION; MOLECULAR-WEIGHT POLYETHYLENE; HIGH-DENSITY POLYETHYLENE; X-RAY-SCATTERING; SITU RHEO-SAXS; POLYMER CRYSTALLIZATION; KEBAB FORMATION; POLY(ETHYLENE OXIDE);
D O I
10.1021/ma300338c
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Extension flow induced crystallization of isotatic polypropylene (iPP) has been studied with a combination of extension rheological and in situ small-angle X-ray scattering (SAXS) measurements at 140 degrees C. Rheological data of step extension on iPP melt are divided into before and beyond fracture strain zones in strain-strain rate space, where intermediate strains between them lead to fracture of samples. Coincidently, weak and strong accelerations of nucleation are observed in the before and beyond fracture strain zones respectively, where distinctly different features of crystallization kinetics and nucleation form occur in these two zones. The microrheological model explains the acceleration of nucleation in the "before fracture strain zone" well, while a "ghost nucleation" mechanism is proposed to interpret the strong acceleration of nucleation in the "beyond fracture strain zone". The "ghost nucleation" is due to the displacement of initial parent point nuclei, where daughter nuclei are induced along the trails. This new mechanism explains well the acceleration of nucleation in orders of magnitude and the formation of shish in iPP melt.
引用
收藏
页码:5477 / 5486
页数:10
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