Surface modification of polypropylene macroporous membrane by marrying RAFT polymerization with click chemistry

被引:44
作者
Wu, Xiu-Min [1 ]
Wang, Li-Li [1 ]
Wang, Yun [1 ]
Gu, Jia-Shan [1 ]
Yu, Hai-Yin [1 ]
机构
[1] Anhui Normal Univ, Lab Funct Mol Solids, Coll Chem & Mat Sci, Minist Educ,Anhui Key Lab Mol Based Mat, Wuhu 241000, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Click chemistry; Membrane surface modification; Polypropylene macroporous membrane; Protein rejection; Reversible addition-fragmentation chain transfer radical polymerization; RADICAL POLYMERIZATION; NANOPARTICLES; COMBINATION; ACRYLAMIDE; BRUSHES;
D O I
10.1016/j.memsci.2012.06.033
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The grafting-to approach is experimentally simple and can provide better control of the grafted polymer, but it usually suffers from a lower grafting density. In the present work, a novel three-step method for polyacrylamide grafting-to the polypropylene macroporous membrane was carried out by marrying click chemistry with reversible addition-fragmentation chain transfer radical polymerization. First, the membrane was brominated via a gas phase free radical photochemical pathway, followed by S(N)2 nucleophilic exchange of bromine atoms in the brominated membrane with azide groups in NaN3; second, alkyne-terminated polyacrylamide with determined structure was synthesized by using reversible addition-fragmentation transfer radical polymerization method; third, alkyne-terminated polyacrylamide was coupled onto the azide-functionalized membrane surface by the Cu-I-catalyzed azide-alkyne cycloaddition click reaction. The permeation performances of the modified membranes were tested by the filtration of a protein dispersion. The protein filtration experiments show that, in comparison with the unmodified membrane, the modified membrane can effectively reject proteins due to the densely grafted polymer chains. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 68
页数:9
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