Ubiquitous nature of the three-layered structure formation in the asymmetric phase separation of the epoxy/thermoplastic blends

被引:5
|
作者
Zhang, Yan [1 ,2 ]
Chen, Fenghua [1 ]
Li, Zhiyong [1 ,2 ]
Han, Charles C. [1 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Joint Lab Polymer Sci & Mat, State Key Lab Polymer Phys & Chem,Inst Chem, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Three-layered structure; Dynamic asymmetry; Hydrodynamic flow; DIAMINE THERMOSET/THERMOPLASTIC BLENDS; EPOXY-RESIN; CURE KINETICS; FRACTURE-TOUGHNESS; ETHER KETONE; MORPHOLOGY; POLYMERIZATION; NETWORK; TEMPERATURE; MIXTURES;
D O I
10.1016/j.polymer.2011.11.051
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 reaction induced phase separation behavior was investigated in various epoxy/thermoplastic (TP) blends. Several morphological structures, including the sea-island, dual morphological (epoxy-rich particles may disperse in the TP-rich domains, while TP-rich particles can also have some dispersions in the epoxy-rich phase) or three-layered (TP-rich continuous domains mainly located in the middle part of the sample while outer layers are mostly composed of epoxy-rich matrix) and nodular structure, were observed with the increase of the TP concentrations. In the middle TP concentration ranges, when the TP with low glass transition temperature (T-g) was used, dual morphological structures were formed. While for the epoxy/TP blends with high T-g thermoplastics, three-layered structures were observed. High T-g and the large molecular weight of the TP was considered to cause the dynamic asymmetry, which dominated the phase separation mechanism and formed such an unusual structure. Through the in-situ investigation on time evolution of phase separation process, ubiquitous nature of this formation mechanism of the three-layered structure were discussed, which may have some important implications on the applications of the epoxy/TP blends. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:588 / 594
页数:7
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