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Highly Hydrophilic Thin-Film Composite Forward Osmosis Membranes Functionalized with Surface-Tailored Nanoparticles

机译:表面修饰的纳米粒子功能化的高度亲水性薄膜复合正渗透膜

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摘要

Thin-film composite polyamide membranes are state-of-the-art materials for membrane-based water purification and desalination processes, which require both high rejection of contaminants and high water permeabilities. However, these membranes are prone to fouling when processing natural waters and wastewaters, because of the inherent surface physicochemical properties of polyamides. The present work demonstrates the fabrication of forward osmosis polyamide membranes with optimized surface properties via facile and scalable functionalization with fine-tuned nanoparticles. Silica nanoparticles are coated with superhydrophilic ligands possessing functional groups that impart stability to the nanoparticles and bind irreversibly to the native carboxyl moieties on the membrane selective layer. The tightly tethered layer of nanoparticles tailors the surface chemistry of the novel composite membrane without altering the morphology or water/ solute permeabilities of the membrane selective layer. Surface characterization and interfacial energy analysis confirm that highly hydrophilic and wettable membrane surfaces are successfully attained. Lower intermolecular adhesion forces are measured between the new membrane materials and model organic foulants, indicating the presence of a bound hydration layer at the polyamide membrane surface that creates a barrier for foulant adhesion.
机译:薄膜复合聚酰胺膜是用于基于膜的水净化和脱盐工艺的最先进材料,既需要污染物的高去除率又需要高的水渗透性。然而,由于聚酰胺固有的表面物理化学性质,当处理天然水和废水时,这些膜易于结垢。本工作展示了通过微调纳米粒子的便捷且可扩展的功能化,制备具有最佳表面性能的正渗透聚酰胺膜。二氧化硅纳米颗粒涂有具有亲水基团的超亲水性配体,这些官能团赋予纳米颗粒稳定性,并且不可逆地与膜选择层上的天然羧基部分结合。纳米颗粒的紧密束缚层可调整新型复合膜的表面化学性质,而不会改变膜选择层的形态或水/溶质渗透性。表面表征和界面能分析证实成功获得了高度亲水和可润湿的膜表面。在新的膜材料和模型有机污垢剂之间测得较低的分子间粘附力,表明聚酰胺膜表面存在结合的水合层,从而形成了污垢粘附的屏障。

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