纳滤
膜
聚酰胺
界面聚合
化学工程
二价
渗透
化学
电负性
共价键
高分子化学
渗透
有机化学
聚合物
单体
生物化学
工程类
作者
Guangzhe Wang,Jinqiu Yuan,Junhui Zhao,Yafei Li,Runnan Zhang,Jianliang Shen,Xiaoyao Wang,Hong Wu,Ayman El–Gendi,Yanlei Su,Zhongyi Jiang
标识
DOI:10.1016/j.memsci.2022.120451
摘要
Porous framework materials hold great promise in tuning the chemical and physical structure of polyamide membranes for efficient nanofiltration. In this work, anionic covalent organic framework (aCOF) with abundant sulfonic acid groups was embedded into polyamide matrix via interfacial polymerization to modulate both membrane charge property and thickness for the removal of divalent ions. Benefiting from the high negative charged density, aCOF not only enhanced the membrane electronegativity from −25.6 mV to −71.5 mV but also slowed down the diffusion rate of piperazine by electrostatic interaction to decrease the membrane thickness from 93 nm to 18 nm. The enhanced electronegativity can intensify the charge exclusion to divalent anions (Na2SO4 rejection above 97%), while the ultrathin structure endows membrane with high water permeance of up to 39 L m−2 h−1 bar−1, about 2.4 times higher than that of pristine PA membrane. Our membranes provide a new path to rational design and controllable construction of high-performance nanofiltration membranes.
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