Graphene oxide membranes with a confined mass transfer effect for Li+/Mg2+ separation: a molecular dynamics study

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Jinman Wu, Nan Li, Shengkai Liu, Wenxiong Shi, Chunying Min, Bo Zhu, Ruiqi Shao, Xiaoyuan Pei, Zhijiang Cai and Zhiwei Xu
{"title":"Graphene oxide membranes with a confined mass transfer effect for Li+/Mg2+ separation: a molecular dynamics study","authors":"Jinman Wu, Nan Li, Shengkai Liu, Wenxiong Shi, Chunying Min, Bo Zhu, Ruiqi Shao, Xiaoyuan Pei, Zhijiang Cai and Zhiwei Xu","doi":"10.1039/D2CP03542A","DOIUrl":null,"url":null,"abstract":"<p >Membrane separation technology represented by graphene oxide (GO) membranes has been widely used in lithium extraction from salt lakes. It is extraordinary to study the extraction of Li<small><sup>+</sup></small> by GO membranes from the perspective of the confined mass transfer effect. This study establishes a GO channel model with the confined mass transfer effect to closely fit the actual mass transfer process. Meanwhile, this study investigates the dynamic fluid characteristics in the separation of Li<small><sup>+</sup></small>/Mg<small><sup>2+</sup></small> by GO membranes using molecular dynamics simulations. The results showed that the Li<small><sup>+</sup></small>/Mg<small><sup>2+</sup></small> separation ratio is maximum at 1.0 nm layer spacing and 10% oxidation degree of the GO membrane. Water molecules form a bilayer within the channel at the appropriate interlayer channel (1 nm) and oxidation level (10%), which accelerates the ion transport rate. Furthermore, the GO oxidation group has the weakest hydrogen bonding effect on water which promotes the passage of water. Finally, the maximum separation ratio is reached due to the fact that the binding force of Li<small><sup>+</sup></small> to water molecules in the channel is lower than that of Mg<small><sup>2+</sup></small>. The results of this study will provide theoretical consideration for the design of high-performance Li<small><sup>+</sup></small>/Mg<small><sup>2+</sup></small> separation membranes.</p>","PeriodicalId":99,"journal":{"name":"Physical Chemistry Chemical Physics","volume":" 42","pages":" 26011-26022"},"PeriodicalIF":2.9000,"publicationDate":"2022-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical Chemistry Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2022/cp/d2cp03542a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 3

Abstract

Membrane separation technology represented by graphene oxide (GO) membranes has been widely used in lithium extraction from salt lakes. It is extraordinary to study the extraction of Li+ by GO membranes from the perspective of the confined mass transfer effect. This study establishes a GO channel model with the confined mass transfer effect to closely fit the actual mass transfer process. Meanwhile, this study investigates the dynamic fluid characteristics in the separation of Li+/Mg2+ by GO membranes using molecular dynamics simulations. The results showed that the Li+/Mg2+ separation ratio is maximum at 1.0 nm layer spacing and 10% oxidation degree of the GO membrane. Water molecules form a bilayer within the channel at the appropriate interlayer channel (1 nm) and oxidation level (10%), which accelerates the ion transport rate. Furthermore, the GO oxidation group has the weakest hydrogen bonding effect on water which promotes the passage of water. Finally, the maximum separation ratio is reached due to the fact that the binding force of Li+ to water molecules in the channel is lower than that of Mg2+. The results of this study will provide theoretical consideration for the design of high-performance Li+/Mg2+ separation membranes.

Abstract Image

具有有限传质效应的氧化石墨烯膜用于Li+/Mg2+分离:分子动力学研究
以氧化石墨烯膜为代表的膜分离技术在盐湖提锂中得到了广泛的应用。从受限传质效应的角度研究氧化石墨烯膜对Li+的萃取是一项非常有意义的研究。本研究建立了一个具有有限传质效应的氧化石墨烯通道模型,以贴近实际传质过程。同时,本研究利用分子动力学模拟研究了氧化石墨烯膜分离Li+/Mg2+过程中的动态流体特性。结果表明,在层间距为1.0 nm、氧化程度为10%时,氧化石墨烯膜的Li+/Mg2+分离比最大;在适当的层间通道(1nm)和氧化水平(10%)下,水分子在通道内形成双分子层,加速了离子传输速率。此外,氧化石墨烯氧化基对水的氢键作用最弱,促进水的通过。最后,由于通道中Li+与水分子的结合力低于Mg2+,使得分离比达到最大。本研究结果将为高性能Li+/Mg2+分离膜的设计提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信