电渗析
膜
阳离子聚合
选择性
亚苯基
离子交换
化学
二价
化学工程
无机化学
高分子化学
离子
聚合物
有机化学
催化作用
工程类
生物化学
作者
Noor Ul Afsar,Muhammad Aamir Shehzad,Muhammad Irfan,Kamana Emmanuel,Fangmeng Sheng,Tingting Xu,Xuemei Ren,Liang Ge,Tongwen Xu
出处
期刊:Desalination
[Elsevier BV]
日期:2019-02-15
卷期号:458: 25-33
被引量:68
标识
DOI:10.1016/j.desal.2019.02.004
摘要
The advances of electrodialysis (ED) have been restricted by the trade-off between perm-selectivity and ion flux of ion exchange membranes. This article lucidly explains the fabrication of novel PVA-based hybrid membranes modified with cationic and anionic layers. Cationic layer is composed of quaternized poly (2, 6-dimethyl-1, 4-phenylene oxide), while anionic layer is sulfonated poly (2, 6-dimethyl-1, 4-phenylene oxide). Interestingly, the perm-selectivity of Li+/Mg2+ via ED was observed up to 5.16 with a feed concentration of 0.1 mol L−1 LiCl/MgCl2 at 2.12 mA cm−2 current density. Electrochemical impedance spectroscopy was used to get further insight about the membrane and solution interfaces such as the influence of a base membrane and the deposited layers, which showed the perm-selective behavior of the modified membranes. The observed high perm-selectivity of modified membranes will step forward the ED applications for production of salts and treatment of saline water comprising monovalent and divalent cations.
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