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季铵化改性制备荷正电纳滤膜用于锂镁分离

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Mg2+和Li+的有效分离是从盐湖卤水中提取锂资源的主要挑战。本工作基于接枝改性的方法,先在聚合反应中引入1-(2-吡啶基)哌嗪(PDP),构筑含吡啶基团的聚酰胺复合纳滤膜,再用溴乙胺(BEA)对吡啶基团进行季铵化反应,使吡啶基团转化为季铵盐基团,得到荷正电的季铵盐类纳滤膜(TFC-PDP-BEA膜)。通过考察PDP浓度、BEA浓度、反应温度和反应时间等参数对膜结构和性能的影响,探究最佳的改性制备条件。TFC-PDP-BEA膜在最优条件下MgCl2、LiCl截留率分别达到90。21%、40。78%,分离因子为6。05,水渗透通量为37。27 L/(m2·h)。本工作建立了一种新的聚酰胺复合纳滤膜表面荷正电改性的方法,从而提升膜的锂镁分离性能,为纳滤膜在锂镁离子分离领域提供技术参考。
Preparation of Quaternary Modified Positive Charge Nanofiltration Membrane for Li+/Mg2+Separation
The effective separation of Mg2+and Li+is a major challenge for the extraction of lithium resources from salt-lake brines.In this work,the surface grafting method was applied to fabricate the nanofiltration membrane,which introduced 1-(2-pyridyl)piperazine(PDP)into the interfacial polymerization reaction to construct a polyamide membrane with pyridine groups.Then quaternization reaction of bromethylamine(BEA)with the pyridine group on the membrane surface transformed the pyridine group into a quaternary ammonium group,which produced a positively charged quaternary ammonium salt nanofiltration membrane(TFC-PDP-BEA membrane).The optimal reaction conditions were investigated by examining the effects of PDP concentration,BEA concentration,reaction temperature and reaction time on the membrane structure and performance.The prepared TFC-PDP-BEA membrane showed rejections of 90.21% for MgCl2 and 40.78% for LiCl under the optimal conditions,with a separation factor of 6.05 and a water permeation flux of 37.27 L/(m2·h).This work established a method to modify the surface of a polyamide composite nanofiltration membrane with a positive charge,and improved the lithium-magnesium separation performance,which provides a technical reference for the separation of Li+/Mg2+by nanofiltration membrane.

membrane separationquaternary ammonium saltlithium extraction from salt lakesubstitution reactionhalogenated hydrocarbons

王雨、付红燕、陈莹莹、胡丹、冯旭东

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北京工商大学 轻工科学与工程学院

中国轻工业清洁生产和资源综合利用重点实验室:北京 100048

膜分离 季铵盐 盐湖提锂 取代反应 卤代烃

2025

水处理技术
杭州水处理技术研究开发中心有限公司

水处理技术

北大核心
影响因子:0.731
ISSN:1000-3770
年,卷(期):2025.51(1)