膜
乙二醇
相位反转
甲基丙烯酸酯
共聚物
聚苯乙烯
化学工程
生物污染
高分子化学
材料科学
聚偏氟乙烯
牛血清白蛋白
两亲性
化学
色谱法
聚合物
复合材料
工程类
生物化学
作者
Antoine Venault,Yi‐Hung Liu,Jia-Ru Wu,Hui-Shan Yang,Yung Chang,Juin‐Yih Lai,Pierre Aimar
标识
DOI:10.1016/j.memsci.2013.09.004
摘要
In the present work, the focus is laid on the formation, and low-biofouling properties of polyvinylidene fluoride (PVDF) membranes modified using an amphiphilic copolymer additive: polystyrene-b-poly (ethylene glycol) methacrylate (PS-b-PEGMA). PVDF was blended with PS-b-PEGMA and membranes were prepared by liquid-induced phase separation. The additive played a significant role on membrane formation, slightly decreasing surface porosity, reducing the shrinkage during phase separation, and increasing both the size and porosity of macrovoids. Owing to its numerous hydrophilic moieties, the copolymer was believed to promote solvent and nonsolvent exchanges during phase inversion. In addition, it significantly enhanced surface hydrophilicity and matrix hydration capability. Indeed, water was easily trapped by the PEGylated chains spread onto the surface and within the matrix, and then stored in the larger macrovoids. It led to an important reduction of protein adsorption, including bovine serum albumin (65%) and lysozyme (89%). Bacterial attachment tests revealed that adhesion of Escherichia coli and Staphylococcus epidermidis was almost totally prevented (over 99% reduction of attachment), which demonstrates the excellent efficiency of PS-b-PEGMA copolymer to provide PVDF membranes with low-biofouling properties.
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