Customizing the surface charge of thin-film composite membranes by surface plasma thin film polymerization

等离子体聚合 聚合 化学工程 界面聚合 薄膜复合膜 表面电荷 高分子化学 渗透 表面改性 马来酸酐 化学 材料科学 反渗透 单体 聚合物 有机化学 共聚物 生物化学 工程类 物理化学
作者
Rackel Reis,Mikel Duke,Andrea Merenda,Bjørn Winther‐Jensen,Ljiljana Puškar,Mark J. Tobin,John D. Orbell,Ludovic F. Dumée
出处
期刊:Journal of Membrane Science [Elsevier BV]
卷期号:537: 1-10 被引量:37
标识
DOI:10.1016/j.memsci.2017.05.013
摘要

Solute-surface interactions are critical in membrane science and dominate a number of diffusion and selectivity parameters. In water treatment particularly, the charge on the membrane has been shown to affect ion transport selectivity as well as fouling mechanisms. The development of advanced surface technologies that allow for potential customization of the surface charge for specific applications, without compromising the essential performance of the membrane, is therefore desirable. In this paper, a novel plasma polymerization strategy was applied to commercial reverse osmosis membrane in order to tune the surface charge. Two monomers, maleic anhydride and vinylimidazole, were plasma polymerized onto the membrane resulting in a modification of the surface energy with resultant isoelectric points of approximately pH 3 and pH 7 respectively. This required only a short 5 min plasma polymerization treatment in each case. Thus, in addition to enhancing the water permeation by up to 10%, in comparison to the reference membranes, the overall charge of the membranes was shifted from highly negatively charged upon maleic anhydride polymerization to highly positively charged upon vinylimidazole polymerization. A comprehensive morphological and chemical analysis was performed to correlate the changes to the presence of functional groups and the alteration of the surface texture. Short treatments were found to smooth the surface whilst enriching the surface with either carboxylic or amine/amide groups. This work opens new avenues to engineer advanced membranes with improved performance and selectivity.
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