Nanofiltration membranes based on poly(vinylidene fluoride-co-chlorotrifluoroethylene)-graft-poly(styrene sulfonic acid)

被引:20
作者
Koh, Joo Hwan [1 ]
Kim, Yong Woo [1 ]
Park, Jung Tae [1 ]
Min, Byoung Ryul [1 ]
Kim, Jong Hak [1 ]
机构
[1] Yonsei Univ, Dept Chem Engn, Seoul 120749, South Korea
关键词
atom transfer radical polymerization (ATRP); graft copolymer; composite membrane; nanofiltration;
D O I
10.1002/pat.1182
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Graft copolymers comprising poly(vinylidene fluoride-co-chlorotrifluoroethylene) backbone and poly(styrene sulfonic acid) side chains, i.e. P(VDF-co-CTFE)-g-PSSA were synthesized using atom transfer radical polymerization (ATRP) for composite nanofiltration (NF) membranes. Direct initiation of the secondary chlorinated site of CTFE units facilitates grafting of PSSA, as revealed by FT-IR spectroscopy. The successful "grafting from" method and the microphase-separated structure of the graft copolymer were confirmed by transmission electron microscopy (TEM). Wide angle X-ray scattering (WAXS) also showed the decrease in the crystallinity of P(VDF-co-CTFE) upon graft copolymerization. Composite NF membranes were prepared from P(VDF-co-CTFE)-g-PSSA as a top layer coated onto P(VDF-co-CTFE) ultrafiltration support membrane. Both the rejections and the flux of composite membranes increased with increasing PSSA concentration due to the increase in SO3H groups and membrane hydrophilicity, as supported by contact angle measurement. The rejections of NF membranes containing 47 wt% of PSSA were 83% for Na2SO4 and 28% for NaCl, and the solution flux were 18 and 32 L/m(2) hr, respectively, at 0.3 MPa pressure. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:1643 / 1648
页数:6
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