Hydrophobic/hydrophilic P(VDF-TrFE)/PHEA polymer blend membranes

被引:4
作者
Tamano-Machiavello, Maria N. [1 ]
Bracke, Benjamin [1 ]
Costa, Carlos M. [2 ]
Lanceros-Mendez, Senentxu [2 ]
Sabater i Serra, Roser [1 ,3 ]
Gomez Ribelles, Jose Luis [1 ,3 ]
机构
[1] Univ Politecn Valencia, Ctr Biomat & Tissue Engn CBIT, E-46022 Valencia, Spain
[2] Univ Minho, Ctr Dept Fis, P-4710057 Braga, Portugal
[3] CIBER BBN, Biomed Res Networking Ctr Bioengn Biomat & Nanome, Valencia, Spain
关键词
hydrophilic; hydrophobic; P(VDF-TrFE); PHEA hydrogel; porous membrane; PVDF MEMBRANES; SURFACE MODIFICATION; ACRYLATE) HYDROGELS; OXIDE); CRYSTALLIZATION; METHANOL;
D O I
10.1002/polb.23959
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymer blend membranes have been obtained consisting of a hydrophilic and a hydrophobic polymers distributed in co-continuous phases. In order to obtain stable membranes in aqueous environments, the hydrophilic phase is formed by a poly(hydrohyethyl acrylate), PHEA, network while the hydrophobic phase is formed by poly(vinylidene fluoride-co-trifluoroethylene) P(VDF-TrFE). To obtain the composites, in a first stage, P(VDF-TrFE) is blended with poly(ethylene oxyde) (PEO), the latter used as sacrificial porogen. P(VDF-TrFE)/PEO blend membranes were prepared by solvent casting at 70 degrees C followed by cooling to room temperature. Then PEO is removed from the membrane by immersion in water obtaining a P(VDF-TrFE) porous membrane. After removing of the PEO polymer, a P(VDF-TrFE) membrane results in which pores are collapsed. Nevertheless the pores reopen when a mixture of hydroxethyl acrylate (HEA) monomer, ethyleneglycol dimethacrylate (as crosslinker) and ethanol (as diluent) is absorbed in the membrane and subsequent polymerization yields hybrid hydrophilic/hydrophobic membranes with controlled porosity. The membranes are thus suitable for lithium-ion battery separator membranes and/or biostable supports for cell culture in biomedical applications. (c) 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 672-679
引用
收藏
页码:672 / 679
页数:8
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