Highly selective lanthanide-doped ion sieves for lithium recovery from aqueous solutions

Lukang Zheng, Jin Chen, Jianke Sun, Min Liu, Yuyu Gao, Zhifeng Guo
{"title":"Highly selective lanthanide-doped ion sieves for lithium recovery from aqueous solutions","authors":"Lukang Zheng, Jin Chen, Jianke Sun, Min Liu, Yuyu Gao, Zhifeng Guo","doi":"10.1177/17475198231159051","DOIUrl":null,"url":null,"abstract":"The increased global demand for lithium is rapidly depleting the lithium ore reserves. Therefore, attention has turned to the recovery of lithium from aqueous solutions, such as lithium-containing brine. Compared with other methods of lithium recovery, adsorption is energy efficient and simple to implement, increasing demand for selective lithium adsorbents. In this study, a selective lithium-ion adsorbent, H4Ti5–xLa x O12, was synthesized via the sol–gel method, followed by heat treatment and acid washing. The effects of the temperature and degree of lanthanum doping (x) on the crystalline phase, morphology, lithium-ion adsorption capacity, and lithium-ion selectivity of the ion sieve were investigated, and the optimal synthetic conditions were determined. We found that doping with La3+ cations (x = 0.01) increased the lithium-ion adsorption capacity (23.96 mg g−1 at 25 °C at pH = 12; 8.2% higher than before doping), rate, and selectivity. In addition, the ion sieve could be used over multiple adsorption–desorption cycles with only a minor reduction in the lithium-ion adsorption capacity (22.88 mg g−1). Overall, these results suggest that doping with La3+ cations stabilized the H4Ti5–xLa x O12 crystal structure, alleviated particle agglomeration, expanded the lithium-ion channels, and decreased the resistance to lithium-ion migration, thus improving adsorption performance. The findings suggest that the proposed ion sieve has practical applications in the selective recovery of lithium from aqueous solutions containing a mixture of metal ions.","PeriodicalId":15318,"journal":{"name":"Journal of Chemical Research-s","volume":"23 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Research-s","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/17475198231159051","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

The increased global demand for lithium is rapidly depleting the lithium ore reserves. Therefore, attention has turned to the recovery of lithium from aqueous solutions, such as lithium-containing brine. Compared with other methods of lithium recovery, adsorption is energy efficient and simple to implement, increasing demand for selective lithium adsorbents. In this study, a selective lithium-ion adsorbent, H4Ti5–xLa x O12, was synthesized via the sol–gel method, followed by heat treatment and acid washing. The effects of the temperature and degree of lanthanum doping (x) on the crystalline phase, morphology, lithium-ion adsorption capacity, and lithium-ion selectivity of the ion sieve were investigated, and the optimal synthetic conditions were determined. We found that doping with La3+ cations (x = 0.01) increased the lithium-ion adsorption capacity (23.96 mg g−1 at 25 °C at pH = 12; 8.2% higher than before doping), rate, and selectivity. In addition, the ion sieve could be used over multiple adsorption–desorption cycles with only a minor reduction in the lithium-ion adsorption capacity (22.88 mg g−1). Overall, these results suggest that doping with La3+ cations stabilized the H4Ti5–xLa x O12 crystal structure, alleviated particle agglomeration, expanded the lithium-ion channels, and decreased the resistance to lithium-ion migration, thus improving adsorption performance. The findings suggest that the proposed ion sieve has practical applications in the selective recovery of lithium from aqueous solutions containing a mixture of metal ions.
用于从水溶液中回收锂的高选择性掺杂镧离子筛
全球对锂需求的增加正在迅速消耗锂矿储量。因此,人们的注意力转向了从含锂盐水等水溶液中回收锂。与其他锂回收方法相比,吸附法节能且易于实施,这增加了对选择性锂吸附剂的需求。本研究采用溶胶-凝胶法制备了一种选择性锂离子吸附剂H4Ti5-xLa x O12,并对其进行了热处理和酸洗。考察了镧掺杂温度和程度(x)对离子筛晶相、形貌、锂离子吸附能力和锂离子选择性的影响,确定了最佳合成条件。我们发现掺杂La3+阳离子(x = 0.01)增加了锂离子的吸附量(在25°C, pH = 12时为23.96 mg g - 1;比掺杂前高8.2%),速率和选择性。此外,离子筛可以在多次吸附-解吸循环中使用,而锂离子的吸附容量仅略有下降(22.88 mg g−1)。综上所述,La3+阳离子的掺杂稳定了H4Ti5-xLa x O12的晶体结构,减轻了颗粒团聚,扩大了锂离子通道,降低了锂离子的迁移阻力,从而提高了吸附性能。研究结果表明,所提出的离子筛在从含有金属离子混合物的水溶液中选择性回收锂方面具有实际应用价值。
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
Journal of Chemical Research-s
Journal of Chemical Research-s 化学科学, 有机化学, 有机合成
自引率
0.00%
发文量
0
审稿时长
1 months
期刊介绍: The Journal of Chemical Research is a peer reviewed journal that publishes full-length review and research papers in all branches of experimental chemistry. The journal fills a niche by also publishing short papers, a format which favours particular types of work, e.g. the scope of new reagents or methodology, and the elucidation of the structure of novel compounds. Though welcome, short papers should not result in fragmentation of publication, they should describe a completed piece of work. The Journal is not intended as a vehicle for preliminary publications. The work must meet all the normal criteria for acceptance as regards scientific standards. Papers that contain extensive biological results or material relating to other areas of science may be diverted to more appropriate specialist journals. Areas of coverage include: Organic Chemistry; Inorganic Chemistry; Materials Chemistry; Crystallography; Computational Chemistry.
×
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:481959085
Book学术官方微信