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PVDF ultrafiltration membranes of controlled performance via blending PVDF-g-PEGMA copolymer synthesized under different reaction times
Authors:Shuai Wang  Tong Li  Chen Chen  Baicang Liu  John C Crittenden
Institution:1.College of Architecture and Environment,Sichuan University,Chengdu,China;2.Institute of New Energy and Low Carbon Technology,Sichuan University,Chengdu,China;3.Research Center for Eco-Environmental Sciences,Chinese Academy of Sciences,Beijing,China;4.Litree Purifying Technology Co., Ltd,Haikou,China;5.Brook Byers Institute for Sustainable Systems, School of Civil and Environmental Engineering,Georgia Institute of Technology,Atlanta,USA
Abstract: PVDF blended different graft ratio of PVDF-g-PEGMA were systematically studied. Tuning the amphiphilic copolymer synthesis time to control membrane performance. The PVDF membrane with PVDF-g-PEGMA at 19 h possesses most surface oxygen content. The synthesis time of PVDF-g-PEGMA at 9 h is good for high flux UF membrane. Polyvinylidene fluoride grafted with poly(ethylene glycol) methyl ether methacrylate (PVDF-g-PEGMA) was synthesized using atomic transfer radical polymerization (ATRP) at different reaction times (9 h, 19 h, and 29 h). The corresponding conversion rates were 10%, 20% and 30%, respectively. PVDF was blended with the copolymer mixture containing PVDF-g-PEGMA, solvent and residual PEGMA under different reaction times. In this study, we explored the effect of the copolymer mixture additives with different synthesis times on cast membrane performance. Increasing the reaction time of PVDF-g-PEGMA causes more PVDF-g-PEGMA and less residual PEGMA to be found in the casting solution. Incremental PVDF-g-PEGMA can dramatically increase the viscosity of the casting solution. An overly high viscosity led to a delayed phase inversion, thus hindering PEGMA segments in PVDF-g-PEGMA from migrating to the membrane surface. However, more residual PEGMA contributed to helping more PEGMA segments migrate to the membrane surface. The pure water fluxes of the blended membrane with reaction times of 9 h, 19 h, and 29 h are 5445 L·m−2·h−1, 1068 L·m−2·h−1and 1179 L·m−2·h−1, respectively, at 0.07 MPa. Delayed phase inversion can form smaller surface pore size distributions, thus decreasing the water flux for the membranes with PVDF-g-PEGMA at 19 h and 29 h. Therefore, we can control the membrane pore size distribution by decreasing the reaction time of PVDF-g-PEGMA to obtain a better flux performance. The membrane with PVDF-g-PEGMA at 19 h exhibits the best foulant rejection and cleaning recovery due to its narrow pore size distribution and high surface oxygen content.
Keywords:Polyvinylidene fluoride ultrafiltration membrane  Amphiphilic copolymer  Blended modification  High flux  Atomic transfer radical polymerization  
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