膜
聚酰胺
纳米复合材料
化学工程
共价有机骨架
材料科学
胺气处理
共价键
高分子化学
界面聚合
纳滤
聚合物
有机化学
化学
复合材料
单体
生物化学
工程类
作者
Li Chen,Cailong Zhou,Luxi Tan,Wei Zhou,Huizhen Shen,Chenyang Lu,Lichun Dong
标识
DOI:10.1016/j.memsci.2022.120590
摘要
A key challenge in polyamide (PA) based nanocomposite membranes is to achieve non-accumulation filler and defect-free features, based on proper compatibility and great dispersion between the particles in the matrix. To address this issue, herein, an interfacial bridging strategy was introduced to fabricate the nanocomposite membrane. A covalent organic framework (COF), TAPB-BPTA (TAPB = 1,3,5-tris(4-aminophenyl)benzene and BPTA = 1,4-benzenedicarboxaldehyde), containing alkynyl was synthesized by a microwave-assisted solvothermal route and preliminarily grafted with the cysteine (CYS) bridge via a click reaction. Furthermore, the short chain of amine moieties in TAPB-BPTA not only makes more amine groups and carboxy groups in the COF pore wall, thereby elevating its hydrophilicity and improving its dispersion in the polyethyleneimine coating solution, but also presumably brings further free motion for amine groups to react with acyl functions in trimesoyl chloride (TMC). The COF was copolymerized using TMC to finally obtain the crosslinked top skin layer without the defect formation between filler and polymer during the interfacial reaction. The pure water permeance of the optimized nanocomposite membrane is higher than that of the pristine PA membrane. Accordingly, the optimized membrane exhibited good permeability and competitive selectivity for dyes and antibiotics. Meanwhile, it had a highly rejection of 92% for methylene blue after multi-cycle separation test, showing excellent industrial wastewater treating capability.
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