首页> 外文期刊>Journal of Applied Polymer Science >Modification of Electrospun Poly(vinylidene fluoride-co-hexafluoropropylene) Membranes Through the Introduction of Poly(ethylene glycol) Dimethacrylate
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Modification of Electrospun Poly(vinylidene fluoride-co-hexafluoropropylene) Membranes Through the Introduction of Poly(ethylene glycol) Dimethacrylate

机译:通过引入聚乙二醇二甲基丙烯酸酯对电纺聚偏二氟乙烯-共-六氟丙烯膜的改性

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摘要

For the modification of an electrospun poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) membrane for its potential use as an electrolyte or separator in lithium batteries, poly(ethylene glycol) dimethacrylate (PEGDMA) was introduced into a polymer solution for electrospinning. A post heat treatment of the as-electro-spun membrane at an elevated temperature was performed for PEGDMA polymerization, and this was verified by Fourier transform infrared spectroscopy. The results showed that no significant variations in the membrane morphology were detected when a small amount of PEGDMA (PVDF-HFP/PEGDMA mass ratio = 4/1) was incorporated. This electrospun membrane after heat treatment at 130 degrees C for 2 h exhibited a significantly higher tensile strength (6.26 +/- 0.22 MPa) than that of an electrospun PVDF-HFP membrane (3.28 +/- 0.35 MPa) without PEGDMA. The porosity and liquid absorption of the electrospun PVDF-HFP/PEGDMA (4/1) membrane were 70.0 +/- 1.6% and 267 +/- 11%, respectively, lower than those of the electrospun PVDF-HFP membrane (76.5 +/- 0.3% and 352 +/- 15%) because of the introduction of PEGDMA. (C) 2008 Wiley Periodicals, Inc. J Appl Polym Sci III: 3104-3112, 2009
机译:为了修饰电纺聚(偏二氟乙烯-共-六氟丙烯)(PVDF-HFP)膜以潜在地用作锂电池中的电解质或隔板,将聚乙二醇二甲基丙烯酸酯(PEGDMA)引入到聚合物溶液中静电纺丝。对于PEGDMA聚合,在升高的温度下对电纺丝膜进行后热处理,这通过傅里叶变换红外光谱法得到证实。结果表明,当掺入少量PEGDMA(PVDF-HFP / PEGDMA质量比= 4/1)时,未检测到膜形态的显着变化。与没有PEGDMA的电纺PVDF-HFP膜(3.28 +/- 0.35 MPa)相比,该电纺膜在130℃热处理2小时后表现出显着更高的拉伸强度(6.26 +/- 0.22 MPa)。电纺PVDF-HFP / PEGDMA(4/1)膜的孔隙率和液体吸收率分别比电纺PVDF-HFP膜(76.5 + /)低70.0 +/- 1.6%和267 +/- 11% -0.3%和352 +/- 15%),因为引入了PEGDMA。 (C)2008 Wiley Periodicals,Inc. J Appl Polym Sci III:3104-3112,2009

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