Interfacial coupling between immiscible polymers: Reactive interface between polysulfone and amorphous polyamide

被引:33
作者
Oyama, HT
Ougizawa, T [1 ]
Inoue, T
Weber, M
Tamaru, K
机构
[1] Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
[2] Yamagata Univ, Dept Polymer Sci & Engn, Yonezawa, Yamagata 9928510, Japan
[3] BASF AG, Polymer Res Lab, D-67056 Ludwigshafen, Germany
[4] Univ Tokyo, Bunkyo Ku, Tokyo 1138654, Japan
关键词
D O I
10.1021/ma010668d
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 coupling reaction at the immiscible polymer-polymer interface formed between bilayer films composed of amorphous polyamide (aPA) and polysulfone (PSU) incorporating different functional groups was monitored by X-ray photoelectron spectroscopy (XPS). The overall coupling reaction was consistent with pseudo-first-order kinetics, and the process was controlled by the reaction between functional groups situated at the interface. Anhydride groups attached to PSU, both phthalic anhydride and maleic anhydride, showed significantly faster and higher reactivities than epoxide and triazine groups in the reaction with the primary amine end group of aPA. The saturation areal density of the copolymers at the interface, Sigma*, changed depending on the architecture of the resultant copolymers, which suggested that Sigma* would be determined by the interfacial area occupied by a single copolymer chain at saturation.
引用
收藏
页码:7017 / 7024
页数:8
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