膜
电渗析
反向电渗析
化学
选择性
离子
化学工程
共价键
浓差极化
膜技术
色谱法
渗透(战争)
无机化学
有机化学
催化作用
运筹学
生物化学
工程类
作者
Xiaojun Sun,Mengting Di,Gao Li,Lei Hu,Wenji Zheng,Xuehua Ruan,Xiaoming Yan,Gaohong He
出处
期刊:Desalination
[Elsevier]
日期:2022-11-01
卷期号:542: 115976-115976
被引量:8
标识
DOI:10.1016/j.desal.2022.115976
摘要
Reverse electrodialysis (RED) is a promising membrane-based technology for salinity gradient power while it faces the challenge of the energy loss caused by the insufficient monovalent/multivalent ion selectivity of the membranes (such as Na+/Mg2+). Here, covalent organic frameworks (COFs) with nanometre-scale pores (pore size of ~8 Å) are designed as composite membranes to selectively conduct monovalent ion (Na+ ~7.1 Å vs Mg2+ ~8.6 Å) by size sieving. Compared with the commercial Neosepta CMX membrane, the COF composite membrane effectively inhibits the penetration of Mg2+ without sacrificing Na+ penetration flux in RED, which to a large extent reduces the energy loss in RED caused by the penetration of Mg2+. Even for Mg2+ solution with high molar fraction of 30 %, the maximum power density (Pd, max) of CCM only shows a slight decrease of 1.7 %. In contrast, the Pd, max of the commercial Neosepta CMX membrane severely decreases by 35.8 %. This study highlights the prospects of COFs as the significant material for designing monovalent ion selective membranes which can improve energy efficiency in RED.
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