Zhenzhen Yao, Bingru Li, Zhihong Ma and Beihong Wang
{"title":"Determination of ultra-trace level Cr(vi) in seawater using large-volume direct injection by LC-ICP-MS with in-line matrix elimination","authors":"Zhenzhen Yao, Bingru Li, Zhihong Ma and Beihong Wang","doi":"10.1039/D3JA00191A","DOIUrl":null,"url":null,"abstract":"<p >In this study, we aimed to improve the detection of hexavalent chromium (Cr(<small>VI</small>)) in seawater by using large volume injection and in-line matrix elimination device in conjunction with LC-ICP-MS. Firstly, the sample solution was introduced into the chromatographic separation system through a 1000 μL quantitative loop. Then, the chromatographically separated solution was precisely introduced into the ICP-MS for analysis at the time of the Cr(<small>VI</small>) peak (2.8–4.2 min) by the valve switch in the in-line matrix elimination. And the separation of Cr(<small>VI</small>) was performed on a Dionex IonPac AG7 analytical column (50 mm × 4 mm, 10 μm) with 60 mmol L<small><sup>−1</sup></small> NH<small><sub>4</sub></small>NO<small><sub>3</sub></small> as the mobile phase at a flow rate of 1.0 mL min<small><sup>−1</sup></small> for 5 min. The detection limits (LOD) and limit of quantitation (LOQ) were found to be 0.002 and 0.007 μg L<small><sup>−1</sup></small>, respectively. Method precision and accuracy were satisfactory at 3.5% relative standard deviations (RSDs) for 0.1 μg L<small><sup>−1</sup></small> of Cr(<small>VI</small>), and 90% ∼ 105% recoveries for real samples. The developed method was successfully applied for the analysis of Cr(<small>VI</small>) in environmental seawater samples.</p>","PeriodicalId":81,"journal":{"name":"Journal of Analytical Atomic Spectrometry","volume":" 3","pages":" 954-961"},"PeriodicalIF":3.1000,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical Atomic Spectrometry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ja/d3ja00191a","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, we aimed to improve the detection of hexavalent chromium (Cr(VI)) in seawater by using large volume injection and in-line matrix elimination device in conjunction with LC-ICP-MS. Firstly, the sample solution was introduced into the chromatographic separation system through a 1000 μL quantitative loop. Then, the chromatographically separated solution was precisely introduced into the ICP-MS for analysis at the time of the Cr(VI) peak (2.8–4.2 min) by the valve switch in the in-line matrix elimination. And the separation of Cr(VI) was performed on a Dionex IonPac AG7 analytical column (50 mm × 4 mm, 10 μm) with 60 mmol L−1 NH4NO3 as the mobile phase at a flow rate of 1.0 mL min−1 for 5 min. The detection limits (LOD) and limit of quantitation (LOQ) were found to be 0.002 and 0.007 μg L−1, respectively. Method precision and accuracy were satisfactory at 3.5% relative standard deviations (RSDs) for 0.1 μg L−1 of Cr(VI), and 90% ∼ 105% recoveries for real samples. The developed method was successfully applied for the analysis of Cr(VI) in environmental seawater samples.