催化动力学分光光度法测定天然泉水和茶叶样品中痕量硒

R. Gürkan, Nevalnur Zeynep Gürkan
{"title":"催化动力学分光光度法测定天然泉水和茶叶样品中痕量硒","authors":"R. Gürkan, Nevalnur Zeynep Gürkan","doi":"10.26850/1678-4618eqj.v44.4.2019.p57-72","DOIUrl":null,"url":null,"abstract":"In this work, a new kinetic method is described for the determination of trace Se(IV) in natural spring waters and commercial tea samples. The method is based on the activation of Se(IV) onto the indicator reaction in acidic medium. The reaction was monitored using a fixed time approach of 20 min at 680 nm. The variables affecting the reaction rate were evaluated and optimized. The method allows the determination of Se(IV) in the range of 0.0125-1.0 mg L-1 with a detection limit of 3.6 µg L-1. The precision was in range of 0.63-3.15% (as RSD %) with a higher recovery than 98.6%. The method has been found to be selective against matrix effect. The method was applied to the speciation analysis of inorganic Se species present in the selected samples. The method was statistically validated by analysis of two certified samples and comparing the obtained results to those of HG-AAS analysis. Also, the total Se levels of the samples were determined by using both methods after conversion of Se(VI) into Se(IV) in ultrasonic bath in acidic medium for 30 min at 85-90 °C. The results were in good agreement with those of HG-AAS. The Se(VI) level of the samples was calculated from the difference between amounts of total Se and Se(IV).","PeriodicalId":11506,"journal":{"name":"Eclética Química Journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Determination of trace amounts of selenium in natural spring waters and tea samples by catalytic kinetic spectrophotometry\",\"authors\":\"R. Gürkan, Nevalnur Zeynep Gürkan\",\"doi\":\"10.26850/1678-4618eqj.v44.4.2019.p57-72\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this work, a new kinetic method is described for the determination of trace Se(IV) in natural spring waters and commercial tea samples. The method is based on the activation of Se(IV) onto the indicator reaction in acidic medium. The reaction was monitored using a fixed time approach of 20 min at 680 nm. The variables affecting the reaction rate were evaluated and optimized. The method allows the determination of Se(IV) in the range of 0.0125-1.0 mg L-1 with a detection limit of 3.6 µg L-1. The precision was in range of 0.63-3.15% (as RSD %) with a higher recovery than 98.6%. The method has been found to be selective against matrix effect. The method was applied to the speciation analysis of inorganic Se species present in the selected samples. The method was statistically validated by analysis of two certified samples and comparing the obtained results to those of HG-AAS analysis. Also, the total Se levels of the samples were determined by using both methods after conversion of Se(VI) into Se(IV) in ultrasonic bath in acidic medium for 30 min at 85-90 °C. The results were in good agreement with those of HG-AAS. The Se(VI) level of the samples was calculated from the difference between amounts of total Se and Se(IV).\",\"PeriodicalId\":11506,\"journal\":{\"name\":\"Eclética Química Journal\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Eclética Química Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.26850/1678-4618eqj.v44.4.2019.p57-72\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Eclética Química Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26850/1678-4618eqj.v44.4.2019.p57-72","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

本文建立了一种新的测定天然泉水和商品茶叶样品中痕量硒(IV)的动力学方法。该方法是基于Se(IV)在酸性介质中对指示剂反应的活化。采用固定时间方法监测反应,时间为20 min,波长为680 nm。对影响反应速率的因素进行了评价和优化。本方法对硒(IV)的测定范围为0.0125 ~ 1.0 mg L-1,检出限为3.6µg L-1。精密度为0.63 ~ 3.15% (RSD %),回收率高于98.6%。该方法对基体效应具有选择性。将该方法应用于所选样品中无机硒的形态分析。通过对两个认证样品的分析,并将所得结果与HG-AAS分析结果进行比较,对该方法进行了统计验证。将Se(VI)转化为Se(IV),在85 ~ 90℃的酸性介质中超声浴30 min后,用两种方法测定样品的总Se水平。结果与HG-AAS相吻合。根据样品中总硒量与硒(IV)量之差计算样品中的硒(VI)水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Determination of trace amounts of selenium in natural spring waters and tea samples by catalytic kinetic spectrophotometry
In this work, a new kinetic method is described for the determination of trace Se(IV) in natural spring waters and commercial tea samples. The method is based on the activation of Se(IV) onto the indicator reaction in acidic medium. The reaction was monitored using a fixed time approach of 20 min at 680 nm. The variables affecting the reaction rate were evaluated and optimized. The method allows the determination of Se(IV) in the range of 0.0125-1.0 mg L-1 with a detection limit of 3.6 µg L-1. The precision was in range of 0.63-3.15% (as RSD %) with a higher recovery than 98.6%. The method has been found to be selective against matrix effect. The method was applied to the speciation analysis of inorganic Se species present in the selected samples. The method was statistically validated by analysis of two certified samples and comparing the obtained results to those of HG-AAS analysis. Also, the total Se levels of the samples were determined by using both methods after conversion of Se(VI) into Se(IV) in ultrasonic bath in acidic medium for 30 min at 85-90 °C. The results were in good agreement with those of HG-AAS. The Se(VI) level of the samples was calculated from the difference between amounts of total Se and Se(IV).
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Estrogenic mycotoxins in surface waters of the Rico Stream micro-basin, São Paulo, Brazil: occurrence and potential estrogenic contribution Chemically modified cellulose as a potential oil adsorbent of contaminated marine ecosystems Determination of trace amounts of selenium in natural spring waters and tea samples by catalytic kinetic spectrophotometry Rapid and selective extraction of trace amount of Pb(II) in aqueous samples using a magnetic ion-imprinted polymer and detection by flame atomic absorption spectrometry Occurrence of caffeine in wastewater and sewage and applied techniques for analysis: a review
×
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