Efficient Separation of Pr(III) and Nd(III) via Shear-Induced Dissociation Coupling with Ultrafiltration: Insights from Experiments and Theory

IF 3.8 3区 工程技术 Q2 ENGINEERING, CHEMICAL Industrial & Engineering Chemistry Research Pub Date : 2024-12-17 DOI:10.1021/acs.iecr.4c03858
Min Zhou, Zhenglin Liu, Zilong Dai, Wenjing Tang, Yunren Qiu
{"title":"Efficient Separation of Pr(III) and Nd(III) via Shear-Induced Dissociation Coupling with Ultrafiltration: Insights from Experiments and Theory","authors":"Min Zhou, Zhenglin Liu, Zilong Dai, Wenjing Tang, Yunren Qiu","doi":"10.1021/acs.iecr.4c03858","DOIUrl":null,"url":null,"abstract":"The separation of Pr(III) and Nd(III) poses a significant challenge due to their similar physicochemical properties, including comparable ionic radii and coordination chemistry. In this study, acidic phosphoric chitosan (aPCS) was employed as a complexing agent in the shear-induced dissociation coupling with ultrafiltration (SID-UF) technique for the sequential separation of Pr(III) and Nd(III). SID-UF uses shear stress to reduce membrane contamination and enables efficient metal ion separation while allowing complexing agent recovery without acid decomplexation, simplifying the process and lowering costs. The complexation kinetics of Pr(III) and Nd(III) with aPCS were investigated for the first time, following a pseudo-first-order model. The SID-UF technique achieved over 97% removal efficiency under optimized conditions, with a separation factor β<sub>Pr/Nd</sub> of 12.01. DFT calculations showed greater electron transfer for Nd(III) (0.2218 e) compared to Pr(III) (0.2149 e), indicating stronger complexation with Nd(III). The interaction energies further confirmed this, with Nd(III) exhibiting a more favorable binding energy of −32.19 kcal mol<sup>–1</sup> compared to −31.09 kcal mol<sup>–1</sup> for Pr(III). These results highlight the high selectivity, efficiency, and environmental benefits of SID-UF, making it a promising alternative for industrial rare-earth separations.","PeriodicalId":39,"journal":{"name":"Industrial & Engineering Chemistry Research","volume":"20 1","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Research","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1021/acs.iecr.4c03858","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The separation of Pr(III) and Nd(III) poses a significant challenge due to their similar physicochemical properties, including comparable ionic radii and coordination chemistry. In this study, acidic phosphoric chitosan (aPCS) was employed as a complexing agent in the shear-induced dissociation coupling with ultrafiltration (SID-UF) technique for the sequential separation of Pr(III) and Nd(III). SID-UF uses shear stress to reduce membrane contamination and enables efficient metal ion separation while allowing complexing agent recovery without acid decomplexation, simplifying the process and lowering costs. The complexation kinetics of Pr(III) and Nd(III) with aPCS were investigated for the first time, following a pseudo-first-order model. The SID-UF technique achieved over 97% removal efficiency under optimized conditions, with a separation factor βPr/Nd of 12.01. DFT calculations showed greater electron transfer for Nd(III) (0.2218 e) compared to Pr(III) (0.2149 e), indicating stronger complexation with Nd(III). The interaction energies further confirmed this, with Nd(III) exhibiting a more favorable binding energy of −32.19 kcal mol–1 compared to −31.09 kcal mol–1 for Pr(III). These results highlight the high selectivity, efficiency, and environmental benefits of SID-UF, making it a promising alternative for industrial rare-earth separations.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
由于镨(III)和钕(III)具有相似的物理化学性质,包括可比的离子半径和配位化学性质,因此它们的分离是一项重大挑战。在本研究中,酸性磷酸壳聚糖(aPCS)被用作剪切力诱导解离耦合超滤(SID-UF)技术中的络合剂,用于依次分离 Pr(III)和 Nd(III)。SID-UF 利用剪切应力减少膜污染,实现高效的金属离子分离,同时无需酸解络合即可回收络合剂,从而简化了工艺并降低了成本。根据伪一阶模型,首次研究了 Pr(III) 和 Nd(III) 与 aPCS 的络合动力学。在优化条件下,SID-UF 技术的去除效率超过 97%,分离因子 βPr/Nd 为 12.01。DFT 计算显示,与 Pr(III) (0.2149 e) 相比,Nd(III) (0.2218 e) 的电子转移更大,表明与 Nd(III) 的络合更强。相互作用能进一步证实了这一点,Nd(III) 的结合能为 -32.19 kcal mol-1,而 Pr(III) 的结合能为 -31.09 kcal mol-1。这些结果凸显了 SID-UF 的高选择性、高效率和环境效益,使其成为工业稀土分离的一种有前途的替代方法。
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 去求助
来源期刊
Industrial & Engineering Chemistry Research
Industrial & Engineering Chemistry Research 工程技术-工程:化工
CiteScore
7.40
自引率
7.10%
发文量
1467
审稿时长
2.8 months
期刊介绍: ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.
期刊最新文献
Multifaceted Roles of Additives in Regulating Crystal Growth: A Case of Acephate Graph-Based Modeling and Molecular Dynamics for Ion Activity Coefficient Prediction in Polymeric Ion-Exchange Membranes Study on the Thermal Behavior of Mixtures of Ammonium Nitrate and Micronutrient Chelates with Potential toward Enhancing the Efficiency of Precision Agriculture Macro-microreactor-Based Process Intensification for Achievement of High-Mixing-Performance, Low-Pressure-Drop, and High-Throughput Liquid–Liquid Homogeneous Chemical Processes Enhancing Reactive Microemulsion Processes: Dynamic Optimization and Cyclic Semibatch Operation for the Reductive Amination of Undecanal in a Mini-Plant
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1