Fe3+ ions induced rapid co-deposition of polydopamine-polyethyleneimine for monovalent selective cation exchange membrane fabrication

Zeta电位 选择性 化学工程 沉积(地质) 化学 离子交换 基质(水族馆) 涂层 表面改性 降水 离子 无机化学 纳米颗粒 有机化学 催化作用 海洋学 物理 地质学 工程类 古生物学 气象学 生物 生物化学 沉积物
作者
Wangrui Zhao,Wei Zhang,Yan Liu,George Q. Chen,Ronald Halim,Huining Deng
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:300: 121802-121802 被引量:31
标识
DOI:10.1016/j.seppur.2022.121802
摘要

Selective monovalent cation transport is crucial for the concentration of target ion(s) using electro-membrane processes prior to precipitation. Co-deposition of biomimetic adhesive polydopamine (PDA) and the positively charged polyethyleneimine (PEI) has emerged as an effective approach for building monovalent perm-selectivity functional coatings for cation exchange membranes (CEMs). Here we report a facile strategy to fabricate monovalent selective cation exchange membranes through quick co-deposition of PDA-PEI induced by ferric (Fe3+) ions. With CEM substrate ion exchanged with Fe3+ ions, the polymerization of DA on the membrane surface was accelerated. The mechanism of the promoting effect of Fe3+ ions on the PDA-PEI co-deposition was explored by UV spectroscopy, SEM, AFM, zeta potential and area resistance measurements. In this approach, the characteristics of the membrane surface were easily manipulated by varying the Fe3+ concentration. The selective CEM fabricated through 0.0001 M FeCl3 pretreatment and only 30-min PDA-PEI deposition showed remarkably enhanced Na+/Mg2+ selectivity of 8.3, low electrical resistance and excellent stability. This study provides a simple and scalable technique for time-saving and environmentally friendly construction of PDA based coating for membrane modifications.
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