Functionalized polymer film surfaces via surface-initiated atom transfer radical polymerization

被引:6
|
作者
Hu, Y. [1 ]
Li, J. S. [2 ]
Yang, W. T. [1 ]
Xu, F. J. [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Key Lab Carbon Fiber & Funct Polymers, Minist Educ,Coll Mat Sci & Engn, Beijing 100029, Peoples R China
[2] Sichuan Univ, Coll Polymer Sci & Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
Surface functionalization; Polymer; Thin film; Polyethylene; Nylon; Initiator; Atom transfer radical polymerization; TERMINATED SI(100) SURFACES; METHACRYLATE) BRUSHES; NYLON SURFACE; SI HYBRIDS; MEMBRANES; DENSITY; GRAFT; ATRP; IMMOBILIZATION; POLYPROPYLENE;
D O I
10.1016/j.tsf.2013.02.020
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The ability to manipulate and control the surface properties of polymer films, without altering the substrate properties, is crucial to their wide-spread applications. In this work, a simple one-stepmethod for the direct immobilization of benzyl chloride groups (as the effective atom transfer radical polymerization (ATRP) initiators) on the polymer films was developed via benzophenone-induced coupling of 4-vinylbenzyl chloride (VBC). Polyethylene (PE) and nylon films were selected as examples of polymer films to illustrate the functionalization of film surfaces via surface-initiated ATRP. Functional polymer brushes of (2-dimethylamino) ethyl methacrylate, sodium4-styrenesulfonate, 2-hydroxyethylmethacrylate and glycidyl methacrylate, as well as their block copolymer brushes, have been prepared via surface-initiated ATRP from the VBC-coupled PE or nylon film surfaces. With the development of a simple approach to the covalent immobilization of ATRP initiators on polymer film surfaces and the inherent versatility of surface-initiated ATRP, the surface functionality of polymer films can be precisely tailored. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:325 / 333
页数:9
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