Models for Adhesion at Weak Polymer Interfaces

被引:9
|
作者
Zhang, Jianbin [2 ]
Lodge, Timothy P. [1 ,2 ]
Macosko, Christopher W. [2 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
adhesion; blends; block copolymers; interfaces; FRACTURE ENERGY; IMMISCIBLE POLYMERS; FAILURE MECHANISMS; DIBLOCK COPOLYMER; 1ST-PRINCIPLES; ENTANGLEMENTS; POLYSTYRENE; PROMOTION; SLIP;
D O I
10.1002/polb.21827
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 weak interfaces between immiscible polymer pairs typically fail through chain scission. The critical facture toughness for such interfaces is closely related to the density of intermolecular entanglements at the interface. From scaling analysis, a simple correlation between facture toughness and chain entanglement was developed. It predicts well the interfacial adhesion for many immiscible polymer pairs found in the literature. For an interface with block copolymer reinforcement, its critical fracture toughness comes from both intermolecular entanglements of homopolymers and copolymer bridges. In the chain scission regime (low copolymer coverage), the block copolymer contribution is found proportional to copolymer interfacial coverage, with the coefficient being the energy to stretch and break a copolymer chain. The chain-breaking energy for different copolymers was evaluated and compared to literature data. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 2313-2319, 2009
引用
收藏
页码:2313 / 2319
页数:7
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