聚酰胺
薄膜复合膜
界面聚合
膜
纳滤
材料科学
化学工程
聚合
聚合物
高分子化学
复合材料
反渗透
化学
单体
工程类
生物化学
作者
Liang Shen,Wei‐Song Hung,Jian‐Min Zuo,Xuan Zhang,Juin‐Yih Lai,Yan Wang
标识
DOI:10.1016/j.memsci.2018.10.014
摘要
Thin-film composite polyamide (TFC-PA) membranes prepared via interfacial polymerization (IP) are widely reported in water treatment applications, but the inefficient mixing of reactive monomers in the traditional IP process may cause the diffusion-limited growth of PA layer and the incomplete IP reaction, resulting in limited control over the morphology and microstructure of PA layer, and thus the membrane performance. Various strategies to address above issues have been explored via different chemical modifications. In this work, a "green" ultrasound-assisted interfacial polymerization approach is employed for the first time to fabricate TFC membranes for forward osmosis and nanofiltration applications. Ultrasound in IP process enlarges the mixing area of reactive monomers, facilitates the mass transport of the amine monomer, therefore contributing to an efficient monomer mixing and the resultant higher IP reaction degree. Additionally, the disrupted PA chain packing, more penetrated amine monomers and generated nanovoids contribute to a relative loose PA layer. Effects of ultrasound power on the microstructure (crosslinking degree and free volume) and morphology (roughness and thickness) of the resultant TFC membranes are also investigated systematically. In comparison with the control membrane, TFC membranes formed via ultrasound-assisted IP exhibit much superior separation performance.
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