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首页> 外文期刊>Desalination: The International Journal on the Science and Technology of Desalting and Water Purification >Low fouling and improved chlorine resistant thin film composite reverse osmosis membranes by cerium(IV)/polyvinyl alcohol mediated surface modification
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Low fouling and improved chlorine resistant thin film composite reverse osmosis membranes by cerium(IV)/polyvinyl alcohol mediated surface modification

机译:铈(IV)/聚乙烯醇介导的表面改性的低结垢性和改进的耐氯薄膜复合反渗透膜

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We report the Ce(IV)/polyvinyl alcohol (PVA) redox system mediated rapid surface modification of polyamide thin film composite (TFC) reverse osmosis (RO) membrane for the improvement of both antifouling and chlorine resistant properties. Copolymerization of 3-sulphopropyl methacrylate (SPMA) and methylene-bis-acrylarnide (MBA) in the presence of Ce(IV)/PVA on premade TFC membrane provided surface modified membranes. The successful surface modification of TFC membranes was evident from attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), contact angle (theta), scanning electron microscope (SEM) and atomic force microscope (AFM). Based on IR, SEM, AFM and theta, it is concluded that a soft hydrophilic polymer layer of a complex mixture of PVA-g-poly(SPMA-co-MBA), polyamide-g-poly(SPMA) and polyamide-g-poly(SPMA-co-MBA)-g-PVA like structures was generated on membrane surface. The modified membranes exhibited much enhanced antifouling property during desalination of water in the presence of scale forming salt and protein compared to that of the unmodified membrane. The chlorine stability test at accelerated conditions clearly indicated enhanced chlorine resistance by the modified membranes compared to unmodified membrane. The enhanced antifouling and chlorine stability of the modified membranes might be the result of the formation of a complex polymeric protective layer on top of polyamide barrier layer. (C) 2014 Elsevier B.V. All rights reserved.
机译:我们报告了铈(IV)/聚乙烯醇(PVA)氧化还原系统介导的聚酰胺薄膜复合材料(TFC)反渗透(RO)膜的快速表面改性,以提高防污性和耐氯性。在预制的TFC膜上,在Ce(IV)/ PVA存在下,甲基丙烯酸3-磺丙基丙基酯(SPMA)和亚甲基双丙烯酰胺(MBA)进行共聚,以提供表面改性膜。通过衰减全反射傅里叶变换红外光谱(ATR-FTIR),接触角(θ),扫描电子显微镜(SEM)和原子力显微镜(AFM)可以明显地证明TFC膜的成功表面改性。基于IR,SEM,AFM和θ,得出结论是PVA-g-poly(SPMA-co-MBA),聚酰胺-g-poly(SPMA)和聚酰胺-g-g-的复杂混合物的柔软亲水性聚合物层膜表面产生了聚(SPMA-co-MBA)-g-PVA样结构。与未改性的膜相比,在存在水垢形成盐和蛋白质的情况下,在水脱盐期间,改性的膜表现出大大增强的防污性能。在加速条件下的氯稳定性测试清楚地表明,与未改性的膜相比,改性膜增强了耐氯性。改性膜增强的防污和氯稳定性可能是在聚酰胺阻隔层顶部形成复杂的聚合物保护层的结果。 (C)2014 Elsevier B.V.保留所有权利。

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