聚砜
膜
纳滤
聚酰胺
界面聚合
薄膜复合膜
材料科学
化学工程
锌
纳米复合材料
聚合
咪唑
高分子化学
反渗透
聚合物
单体
纳米技术
化学
有机化学
复合材料
冶金
工程类
生物化学
作者
Wenjie Yang,Yaoyao Zhu,Zhijuan Sun,Congjie Gao,Lixin Xue
标识
DOI:10.1002/admi.201901482
摘要
Abstract Polyamide (PA) thin‐film composite (TFC) nanofiltration (NF) membranes with superior water permeating nanoscale Turing type networks are formed using preloaded zinc(II) cations as diffusion slower during the interfacial polymerization on polysulfone support. Large nanopores in the size of about 4.3–8.0 Å formed during the interfacial polymerization process are self‐sealed by in situ grown zinc imidazole framework (ZIF) nanocrystals in a counterdiffusion polymerization reaction of Zn(II) cations with imidazole ligands. PA/ZIF mixed matrix NF membranes with superior water permeating networks are formed. Such novel membranes show not only 3–4 fold higher water flux than TFC membranes, but also retain comparably high salt rejection and antifouling resistance capability. The impact of Zn(II) loading levels, counterdiffusion reaction times, and structures of imidazole ligands on the structures and properties of formed TFN‐ZIF membranes are studied.
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