{"title":"光化学蒸汽发生-电感耦合等离子体质谱法测定地质样品中痕量硒和碲","authors":"Yonghai Yuan, Zhixuan Han, Feng Yang, Hongxia Yu, Yinhui Zhang, Meilan Wen","doi":"10.1111/ggr.12539","DOIUrl":null,"url":null,"abstract":"<p>An analytical method to accurately determine trace levels of Se and Te is essential to meet the growing importance of these elements to Earth science research. Herein, an in-house assembled photochemical vapour generation (PVG) unit, instead of normal sample nebulisation, with inductively coupled plasma-mass spectrometry (ICP-MS), was developed for the detection of Se and Te in geological samples. The major parameters that might potentially influence the PVG efficiencies of Se(IV) and Te(IV) were investigated. The unit could fully generate volatile species under 30 s of ultraviolet irradiation in the presence of 15% <i>v</i>/<i>v</i> formic acid, 15% <i>v</i>/<i>v</i> acetic acid and 50 mg l<sup>-1</sup> of Co<sup>2+</sup>. Under optimised conditions, the limit of detections (LODs, 3<i>s</i>, <i>n</i> = 11) of the proposed method were 0.5 ng l<sup>-1</sup> for Se and 0.6 ng l<sup>-1</sup> for Te. The RSDs of Se and Te were 2.0% and 2.3% (1 μg l<sup>-1</sup>, <i>n</i> = 7), respectively. Interference experiments showed that Fe, Ti, V and Cu have certain negative effects, so the standard addition method was used for real sample analysis. Measurement results for eleven CRMs, including soils (GSS-4, GSS-7), sediments (GSD-9, GSD-10) and rocks (GSR-1, GSR-2, GSR-3, GSR-5, AGV-2, GSP-2 and W-2a), were consistent with literature values, and showed better precision, indicating the feasibility of the proposed method for determination of trace Se and Te in geological samples.</p>","PeriodicalId":12631,"journal":{"name":"Geostandards and Geoanalytical Research","volume":"48 1","pages":"133-143"},"PeriodicalIF":2.7000,"publicationDate":"2023-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Determination of Trace Se and Te in Geological Samples by Photochemical Vapour Generation Combined with Inductively Coupled Plasma-Mass Spectrometry\",\"authors\":\"Yonghai Yuan, Zhixuan Han, Feng Yang, Hongxia Yu, Yinhui Zhang, Meilan Wen\",\"doi\":\"10.1111/ggr.12539\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>An analytical method to accurately determine trace levels of Se and Te is essential to meet the growing importance of these elements to Earth science research. Herein, an in-house assembled photochemical vapour generation (PVG) unit, instead of normal sample nebulisation, with inductively coupled plasma-mass spectrometry (ICP-MS), was developed for the detection of Se and Te in geological samples. The major parameters that might potentially influence the PVG efficiencies of Se(IV) and Te(IV) were investigated. The unit could fully generate volatile species under 30 s of ultraviolet irradiation in the presence of 15% <i>v</i>/<i>v</i> formic acid, 15% <i>v</i>/<i>v</i> acetic acid and 50 mg l<sup>-1</sup> of Co<sup>2+</sup>. Under optimised conditions, the limit of detections (LODs, 3<i>s</i>, <i>n</i> = 11) of the proposed method were 0.5 ng l<sup>-1</sup> for Se and 0.6 ng l<sup>-1</sup> for Te. The RSDs of Se and Te were 2.0% and 2.3% (1 μg l<sup>-1</sup>, <i>n</i> = 7), respectively. Interference experiments showed that Fe, Ti, V and Cu have certain negative effects, so the standard addition method was used for real sample analysis. Measurement results for eleven CRMs, including soils (GSS-4, GSS-7), sediments (GSD-9, GSD-10) and rocks (GSR-1, GSR-2, GSR-3, GSR-5, AGV-2, GSP-2 and W-2a), were consistent with literature values, and showed better precision, indicating the feasibility of the proposed method for determination of trace Se and Te in geological samples.</p>\",\"PeriodicalId\":12631,\"journal\":{\"name\":\"Geostandards and Geoanalytical Research\",\"volume\":\"48 1\",\"pages\":\"133-143\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2023-11-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Geostandards and Geoanalytical Research\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/ggr.12539\",\"RegionNum\":2,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GEOCHEMISTRY & GEOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geostandards and Geoanalytical Research","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ggr.12539","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
引用次数: 0
摘要
一种准确测定硒和碲痕量水平的分析方法对于满足这些元素在地球科学中日益增长的重要性至关重要。本文利用电感耦合等离子体质谱(ICP-MS)技术,开发了一种自组装的光化学蒸汽产生(PVG)装置,代替了常规的样品雾化,用于检测地质样品中的Se和Te。研究了可能影响Se(IV)和Te(IV) PVG效率的主要参数。在15% v/v甲酸、15% v/v乙酸和50 mg l-1 Co2+的存在下,在30 s的紫外照射下,该装置能充分生成挥发种。在优化条件下,该方法的检出限(lod, 3s, n = 11)分别为Se 0.5 ng l-1和Te 0.6 ng l-1。Se和Te的rsd分别为2.0%和2.3% (1 μg -1, n = 7)。干涉实验表明,Fe、Ti、V、Cu均有一定的负面影响。因此,实际样品分析采用标准添加法。土壤(GSS-4、GSS-7)、沉积物(GSD-9、GSD-10)和岩石(GSR-1、GSR-2、GSR-3、GSR-5、AGV-2、GSP-2和W-2a) 11个样品的测定结果与文献值一致,精度较高,表明该方法可用于地质样品中痕量硒和碲的测定。
Determination of Trace Se and Te in Geological Samples by Photochemical Vapour Generation Combined with Inductively Coupled Plasma-Mass Spectrometry
An analytical method to accurately determine trace levels of Se and Te is essential to meet the growing importance of these elements to Earth science research. Herein, an in-house assembled photochemical vapour generation (PVG) unit, instead of normal sample nebulisation, with inductively coupled plasma-mass spectrometry (ICP-MS), was developed for the detection of Se and Te in geological samples. The major parameters that might potentially influence the PVG efficiencies of Se(IV) and Te(IV) were investigated. The unit could fully generate volatile species under 30 s of ultraviolet irradiation in the presence of 15% v/v formic acid, 15% v/v acetic acid and 50 mg l-1 of Co2+. Under optimised conditions, the limit of detections (LODs, 3s, n = 11) of the proposed method were 0.5 ng l-1 for Se and 0.6 ng l-1 for Te. The RSDs of Se and Te were 2.0% and 2.3% (1 μg l-1, n = 7), respectively. Interference experiments showed that Fe, Ti, V and Cu have certain negative effects, so the standard addition method was used for real sample analysis. Measurement results for eleven CRMs, including soils (GSS-4, GSS-7), sediments (GSD-9, GSD-10) and rocks (GSR-1, GSR-2, GSR-3, GSR-5, AGV-2, GSP-2 and W-2a), were consistent with literature values, and showed better precision, indicating the feasibility of the proposed method for determination of trace Se and Te in geological samples.
期刊介绍:
Geostandards & Geoanalytical Research is an international journal dedicated to advancing the science of reference materials, analytical techniques and data quality relevant to the chemical analysis of geological and environmental samples. Papers are accepted for publication following peer review.