Simultaneous Determination Of Cd And Ni In Salvia Yunnanensis By Deep Eutectic Solvent-Based Rapidly Synergistic Cloud Point Extraction And ICP-OES Analysis

IF 3.4 2区 化学 Q1 SPECTROSCOPY
Wen Wen
{"title":"Simultaneous Determination Of Cd And Ni In Salvia Yunnanensis By Deep Eutectic Solvent-Based Rapidly Synergistic Cloud Point Extraction And ICP-OES Analysis","authors":"Wen Wen","doi":"10.46770/as.2022.100","DOIUrl":null,"url":null,"abstract":": In this study, a deep eutectic solvent (DES)-based rapid synergistic cloud point extraction (RS-CPE) was coupled with inductively coupled plasma optical emission spectrometry (ICP-OES). This unprecedented method was used for the simultaneous determination of Cd and Ni in the medicinal plant Salvia yunnanensis C. H. Wright ( S. yunnanensis ). Compared with traditional CPE, RS-CPE was accomplished rapidly at room temperature. In this study, DES was used as an environmentally friendly cloud point and synergic reagent to decrease the cloud point temperature (CPT) of Triton X-114 (TX-114) and assist the subsequent rapid extraction process, thereby replacing toxic organic reagents. The experimental parameters affecting extraction efficiency were investigated and optimized. Using this combined extraction method and analytical technique, the analytical performance of ICP-OES was notably improved. Under the optimal conditions, the limits of detection (LOD) of Cd and Ni were 0.01 and 0.05 μg L -1 , and the limits of quantification (LOQ) were 0.04 and 0.16 μg L -1 , respectively. The enhancement factors (EFs) of Cd and Ni were 33 and 30; the spiked recoveries were 96.1–105% and 90.3–106%, respectively. The established method was applied to analyze S. yunnanensis samples with satisfactory results and provided a simple, rapid, sensitive, and green method for the determination of potentially toxic elements in medicinal herbs. reagent. results showed that there was no statistical difference between the results obtained for the real samples, as determined by the established method, compared with those obtained using ICP-MS. These results indicate that the proposed method is accurate and reliable.","PeriodicalId":8642,"journal":{"name":"Atomic Spectroscopy","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2022-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atomic Spectroscopy","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.46770/as.2022.100","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SPECTROSCOPY","Score":null,"Total":0}
引用次数: 8

Abstract

: In this study, a deep eutectic solvent (DES)-based rapid synergistic cloud point extraction (RS-CPE) was coupled with inductively coupled plasma optical emission spectrometry (ICP-OES). This unprecedented method was used for the simultaneous determination of Cd and Ni in the medicinal plant Salvia yunnanensis C. H. Wright ( S. yunnanensis ). Compared with traditional CPE, RS-CPE was accomplished rapidly at room temperature. In this study, DES was used as an environmentally friendly cloud point and synergic reagent to decrease the cloud point temperature (CPT) of Triton X-114 (TX-114) and assist the subsequent rapid extraction process, thereby replacing toxic organic reagents. The experimental parameters affecting extraction efficiency were investigated and optimized. Using this combined extraction method and analytical technique, the analytical performance of ICP-OES was notably improved. Under the optimal conditions, the limits of detection (LOD) of Cd and Ni were 0.01 and 0.05 μg L -1 , and the limits of quantification (LOQ) were 0.04 and 0.16 μg L -1 , respectively. The enhancement factors (EFs) of Cd and Ni were 33 and 30; the spiked recoveries were 96.1–105% and 90.3–106%, respectively. The established method was applied to analyze S. yunnanensis samples with satisfactory results and provided a simple, rapid, sensitive, and green method for the determination of potentially toxic elements in medicinal herbs. reagent. results showed that there was no statistical difference between the results obtained for the real samples, as determined by the established method, compared with those obtained using ICP-MS. These results indicate that the proposed method is accurate and reliable.
深共晶溶剂基快速协同云点萃取- ICP-OES同时测定云南丹参中Cd和Ni
本研究将基于深共晶溶剂(DES)的快速协同云点萃取(RS-CPE)与电感耦合等离子体发射光谱(ICP-OES)相结合。本方法首次应用于云南丹参中镉和镍的同时测定。与传统CPE相比,RS-CPE在室温下快速完成。本研究采用DES作为环保型云点和协同试剂,降低Triton X-114 (TX-114)的云点温度(CPT),辅助后续的快速提取过程,从而取代有毒的有机试剂。对影响提取效率的实验参数进行了研究和优化。采用该萃取方法与分析技术相结合,ICP-OES的分析性能明显提高。在最佳条件下,Cd和Ni的检出限分别为0.01和0.05 μg L -1,定量限分别为0.04和0.16 μg L -1。Cd和Ni的增强因子(EFs)分别为33和30;加标回收率分别为96.1 ~ 105%和90.3 ~ 106%。将所建立的方法应用于云南石竹样品的分析,结果令人满意,为中药材中潜在有毒元素的检测提供了一种简便、快速、灵敏、绿色的方法。试剂结果表明,用所建立的方法测定的真实样品的结果与用ICP-MS测定的结果没有统计学差异。结果表明,该方法准确可靠。
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
Atomic Spectroscopy
Atomic Spectroscopy 物理-光谱学
CiteScore
5.30
自引率
14.70%
发文量
42
审稿时长
4.5 months
期刊介绍: The ATOMIC SPECTROSCOPY is a peer-reviewed international journal started in 1962 by Dr. Walter Slavin and now is published by Atomic Spectroscopy Press Limited (ASPL). It is intended for the rapid publication of both original articles and review articles in the fields of AAS, AFS, ICP-OES, ICP-MS, GD-MS, TIMS, SIMS, AMS, LIBS, XRF and related techniques. Manuscripts dealing with (i) instrumentation & fundamentals, (ii) methodology development & applications, and (iii) standard reference materials (SRMs) development can be submitted for publication.
×
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