纳滤
膜
限制电流
聚酰胺
电渗析
界面聚合
化学工程
选择性
Zeta电位
聚合
化学
表面电荷
锂(药物)
材料科学
色谱法
分析化学(期刊)
聚合物
高分子化学
单体
电化学
有机化学
电极
物理化学
催化作用
纳米颗粒
内分泌学
工程类
医学
生物化学
作者
Jia-Shuai Chen,Jing Wang,Zhiyong Ji,Zhiyuan Guo,Panpan Zhang,Zhihui Huang
出处
期刊:Desalination
[Elsevier]
日期:2022-12-20
卷期号:549: 116312-116312
被引量:14
标识
DOI:10.1016/j.desal.2022.116312
摘要
With the rapid development of batteries and other industries, the demand for lithium has exploded. As about 70 wt% of the lithium resources exist in brines, the extraction of lithium by selective electrodialysis (S-ED) has attracted extensive attention. However, the similar hydrated ionic radius of Li+ and Mg2+ caused many challenges. Herein, a simple sequential interfacial polymerization (SIP) method was developed to adjust the surface charge and pore size of the electro-nanofiltration membranes (ENFMs), and the ENFMs were endowed with excellent selectivity due to the electrostatic repulsion and pore-size sieving effect. Polyethyleneimine (PEI) with different molecular weights was used for the SIP process based on the nascent polyamide separation layer prepared by interfacial polymerization. With the increase of the PEI molecular weight, the zeta potential of the membrane surface changed from negative to positive, while the pore size of the membranes also decreased. The optimal ENFMs achieved outstanding selectivity for Li+/Mg2+ (16.55) and high Li+ flux (3.08 × 10−8 mol·cm−2·s−1) at a current density of 10 mA·cm−2. Moreover, the optimal ENFMs exhibited high limiting current density (50.6 mA·cm−2) and low membrane electrical resistance (2.42 Ω·cm2), which has a great potential to be used for practical applications.
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