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Proton conducting grafted/crosslinked membranes prepared from poly(vinylidene fluoride-co-chlorotrifluoroethylene) copolymer
被引:11
|作者:
Seo, Jin Ah
[1
]
Kim, Yong Woo
[1
]
Roh, Dong Kyu
[1
]
Shul, Yong Gun
[1
]
Kim, Jong Hak
[1
]
机构:
[1] Yonsei Univ, Dept Chem & Biomol Engn, Seoul 120749, South Korea
关键词:
atom transfer radical polymerization (ATRP);
polymer electrolyte membrane;
graft copolymers;
crosslinking;
proton conductivity;
TRANSFER RADICAL POLYMERIZATION;
FUEL-CELL APPLICATIONS;
EXCHANGE MEMBRANES;
GRAFT-COPOLYMERS;
FLUORIDE) FILMS;
METHANOL;
ELECTROLYTE;
TRANSPORT;
BRUSHES;
PVDF;
D O I:
10.1002/pat.1629
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
Poly(vinylidene fluoride-co-chlorotrifluoroethylene) (P(VDF-co-CTFE)) backbone was grafted with crosslinkable chains of poly(hydroxyl ethyl acrylate) (PHEA) and proton conducting chains of poly(styrene sulfonic acid) (PSSA) to produce amphiphilic P(VDF-co-CTFE)-g-P(HEA-co-SSA) graft copolymer via atom transfer radical polymerization (ATRP). Successful synthesis and microphase-separated structure of the copolymer were confirmed by (1)H NMR, FT-IR spectroscopy, and TEM analysis. Furthermore, this graft copolymer was thermally crosslinked with sulfosuccinic acid (SA) to produce grafted/crosslinked membranes. Ion exchange capacity (IEC) increased continuously with increasing SA contents but the water uptake increased up to 6wt% of SA concentration, above which it decreased monotonically. The membrane also exhibited a maximum proton conductivity of 0.062 S/cm at 6 wt% of SA concentration, resulting from competitive effect between the increase of ionic groups and the degree of crosslinking. XRD patterns also revealed that the crystalline structures of P(VDF-co-CTFE) disrupted upon graft polymerization and crosslinking. These membranes exhibited good thermal stability at least up to 250 degrees C, as revealed by TGA. Copyright (C) 2009 John Wiley & Sons, Ltd.
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页码:1434 / 1441
页数:8
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