Thermo-responsive polyacrylonitrile membranes prepared with poly(acrylonitrile-g-isopropylacrylamide) as an additive

被引:29
作者
Fei, Zheng-Dong [1 ,2 ]
Wan, Ling-Shu [1 ]
Wang, Wu-Min [2 ]
Zhong, Ming-Qiang [2 ]
Xu, Zhi-Kang [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ Technol, Coll Chem Engn & Mat Sci, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Thermo-responsive membrane; Polyacrylonitrile; Amphiphilic graft polymer; Surface segregation; Immersion precipitation phase inversion; TRANSFER RADICAL POLYMERIZATION; UNSYMMETRICAL DIVINYL COMPOUNDS; CROSS-LINKING POLYMERIZATION; PH-RESPONSIVE POLYMERS; ALLYL METHACRYLATE; SURFACE SEGREGATION; GRAFT-COPOLYMERIZATION; ENE; POLY(N-ISOPROPYLACRYLAMIDE); THIOL;
D O I
10.1016/j.memsci.2013.01.008
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Thermo-responsive polyacrylonitrile (PAN) membranes were prepared by the immersion precipitation phase inversion process using poly(acrylonitrile-graft-isopropylacrylamide) [P(AN-g-NIPAAm)] as an additive. This additive was synthesized by a facile approach based on the combination of reversible addition-fragmentation chain transfer and thiol-ene click chemistry followed by radical copolymerization. The graft copolymer was characterized by Fourier transform infrared spectroscopy and proton nuclear magnetic resonance. Its side chains thermo-responsibility was determined by ultraviolet analysis and water contact angle measurement. Effects of P(AN-g-NIPAAm) addition on the morphologies of PAN membranes were investigated by scanning electron microscope. X-ray photoelectron spectroscopy was conducted at different take-off angles to elucidate the surface segregation of the amphiphilic graft copolymer in the prepared membranes. Results show that the hydrophilic PNIPAAm chains greatly segregate at the membrane surface, which endows these PAN membranes with obvious thermo-responsibility for water permeation. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 49
页数:8
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