{"title":"以同位素尖峰 190Os 为内标,结合经验系数 LA-ICP-MS 和锑火法测定地球化学样品中的超痕量铂族元素。","authors":"Wenshan Ni, Tiantian Wang, Xiangju Mao, Liping Zhang, Xiaorui Guo, Lei Fan, Hongli Zhang, Fang Xiao","doi":"10.1016/j.talanta.2024.126932","DOIUrl":null,"url":null,"abstract":"<p><p>In this work, a novel method of antimony fire assay (Sb-FA) enrichment combined with laser ablation ICP-MS (LA-ICP-MS) for the determination of ultra-trace platinum group elements (PGEs) in geological samples was established. The purification and recycling technology of ultra-clean and high-purity fire assay collector Sb<sub>2</sub>O<sub>3</sub> was proposed, in addition, high-purity quartz crucible was developed to replace the usual clay crucible, then the blank values of PGEs were as low as 0.0007-0.0028 ng g<sup>-1</sup> (for 20 g sample). <sup>190</sup>Os isotopic diluent was used as internal standard (IS) and quantitatively added into the fire assay ingredients, and fully mixed and balanced with the PGEs in the real samples by means of high temperature melting, cupellation and horizontal rotation of crucible and dish. Both <sup>190</sup>Os and PGEs in the real sample were pre-concentrated in microgram level Sb granules (100 mg) through Sb-remaining cupellation. After grinding and polishing, <sup>195</sup>Pt, <sup>105</sup>Pd, <sup>101</sup>Ru, <sup>103</sup>Rh, <sup>193</sup>Ir, total <sup>189</sup>Os and <sup>190</sup>Os enriched in Sb slices were determined by LA-ICP-MS, <sup>190</sup>Os in the internal standard was calculated by isotope dilution equations. The Certified Reference Materials (CRMs) for PGEs were treated by the same procedure to obtain completely matrix matched Sb slices to solve the problem of no internationally recognized uniform PGEs standard materials for LA-ICP-MS determination. Due to the similar distribution trends of different PGEs in Sb slices by LA-ICP-MS imaging, then matrix-matched internal standard calibration strategy was used to reduce the element fractionation effect and improve the determination precision and accuracy of LA-ICP-MS. The laser frequency, energy density, denudation diameter and dwell times were optimized. Under the optimal conditions, empirical coefficient method was used to fit the standard curve and excellent curve fitting of PGEs were obtained with the correlation coefficient between 0.9990 and 0.9999. The method detection limits (LODs) for PGEs ranged from 0.00042 to 0.010 ng g<sup>-1</sup>. The established method was successfully applied to analyze real geochemical samples and various matrix Certified Reference Materials (CRMs) domestic and international, the determined values were in good agreement with the results of Sb-FA ICP-MS and the certified values.</p>","PeriodicalId":435,"journal":{"name":"Talanta","volume":"281 ","pages":"126932"},"PeriodicalIF":5.6000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isotopic spike <sup>190</sup>Os as internal standard and empirical coefficient LA-ICP-MS combined with Sb fire assay for the determination of ultra-trace platinum group elements in geochemical samples.\",\"authors\":\"Wenshan Ni, Tiantian Wang, Xiangju Mao, Liping Zhang, Xiaorui Guo, Lei Fan, Hongli Zhang, Fang Xiao\",\"doi\":\"10.1016/j.talanta.2024.126932\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In this work, a novel method of antimony fire assay (Sb-FA) enrichment combined with laser ablation ICP-MS (LA-ICP-MS) for the determination of ultra-trace platinum group elements (PGEs) in geological samples was established. The purification and recycling technology of ultra-clean and high-purity fire assay collector Sb<sub>2</sub>O<sub>3</sub> was proposed, in addition, high-purity quartz crucible was developed to replace the usual clay crucible, then the blank values of PGEs were as low as 0.0007-0.0028 ng g<sup>-1</sup> (for 20 g sample). <sup>190</sup>Os isotopic diluent was used as internal standard (IS) and quantitatively added into the fire assay ingredients, and fully mixed and balanced with the PGEs in the real samples by means of high temperature melting, cupellation and horizontal rotation of crucible and dish. Both <sup>190</sup>Os and PGEs in the real sample were pre-concentrated in microgram level Sb granules (100 mg) through Sb-remaining cupellation. After grinding and polishing, <sup>195</sup>Pt, <sup>105</sup>Pd, <sup>101</sup>Ru, <sup>103</sup>Rh, <sup>193</sup>Ir, total <sup>189</sup>Os and <sup>190</sup>Os enriched in Sb slices were determined by LA-ICP-MS, <sup>190</sup>Os in the internal standard was calculated by isotope dilution equations. The Certified Reference Materials (CRMs) for PGEs were treated by the same procedure to obtain completely matrix matched Sb slices to solve the problem of no internationally recognized uniform PGEs standard materials for LA-ICP-MS determination. Due to the similar distribution trends of different PGEs in Sb slices by LA-ICP-MS imaging, then matrix-matched internal standard calibration strategy was used to reduce the element fractionation effect and improve the determination precision and accuracy of LA-ICP-MS. The laser frequency, energy density, denudation diameter and dwell times were optimized. Under the optimal conditions, empirical coefficient method was used to fit the standard curve and excellent curve fitting of PGEs were obtained with the correlation coefficient between 0.9990 and 0.9999. The method detection limits (LODs) for PGEs ranged from 0.00042 to 0.010 ng g<sup>-1</sup>. The established method was successfully applied to analyze real geochemical samples and various matrix Certified Reference Materials (CRMs) domestic and international, the determined values were in good agreement with the results of Sb-FA ICP-MS and the certified values.</p>\",\"PeriodicalId\":435,\"journal\":{\"name\":\"Talanta\",\"volume\":\"281 \",\"pages\":\"126932\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Talanta\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1016/j.talanta.2024.126932\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/9/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Talanta","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.talanta.2024.126932","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/25 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Isotopic spike 190Os as internal standard and empirical coefficient LA-ICP-MS combined with Sb fire assay for the determination of ultra-trace platinum group elements in geochemical samples.
In this work, a novel method of antimony fire assay (Sb-FA) enrichment combined with laser ablation ICP-MS (LA-ICP-MS) for the determination of ultra-trace platinum group elements (PGEs) in geological samples was established. The purification and recycling technology of ultra-clean and high-purity fire assay collector Sb2O3 was proposed, in addition, high-purity quartz crucible was developed to replace the usual clay crucible, then the blank values of PGEs were as low as 0.0007-0.0028 ng g-1 (for 20 g sample). 190Os isotopic diluent was used as internal standard (IS) and quantitatively added into the fire assay ingredients, and fully mixed and balanced with the PGEs in the real samples by means of high temperature melting, cupellation and horizontal rotation of crucible and dish. Both 190Os and PGEs in the real sample were pre-concentrated in microgram level Sb granules (100 mg) through Sb-remaining cupellation. After grinding and polishing, 195Pt, 105Pd, 101Ru, 103Rh, 193Ir, total 189Os and 190Os enriched in Sb slices were determined by LA-ICP-MS, 190Os in the internal standard was calculated by isotope dilution equations. The Certified Reference Materials (CRMs) for PGEs were treated by the same procedure to obtain completely matrix matched Sb slices to solve the problem of no internationally recognized uniform PGEs standard materials for LA-ICP-MS determination. Due to the similar distribution trends of different PGEs in Sb slices by LA-ICP-MS imaging, then matrix-matched internal standard calibration strategy was used to reduce the element fractionation effect and improve the determination precision and accuracy of LA-ICP-MS. The laser frequency, energy density, denudation diameter and dwell times were optimized. Under the optimal conditions, empirical coefficient method was used to fit the standard curve and excellent curve fitting of PGEs were obtained with the correlation coefficient between 0.9990 and 0.9999. The method detection limits (LODs) for PGEs ranged from 0.00042 to 0.010 ng g-1. The established method was successfully applied to analyze real geochemical samples and various matrix Certified Reference Materials (CRMs) domestic and international, the determined values were in good agreement with the results of Sb-FA ICP-MS and the certified values.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.