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。

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Talanta Pub Date : 2025-01-01 Epub Date: 2024-09-25 DOI:10.1016/j.talanta.2024.126932
Wenshan Ni, Tiantian Wang, Xiangju Mao, Liping Zhang, Xiaorui Guo, Lei Fan, Hongli Zhang, Fang Xiao
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引用次数: 0

摘要

本研究建立了锑火法富集结合激光烧蚀ICP-MS(LA-ICP-MS)测定地质样品中超痕量铂族元素(PGEs)的新方法。提出了超洁净高纯度火试收集器 Sb2O3 的提纯和回收技术,并研制了高纯度石英坩埚以替代常用的粘土坩埚,使 PGEs 的空白值低至 0.0007-0.0028 ng g-1(20 g 样品)。采用 190Os 同位素稀释剂作为内标(IS),定量添加到火法化验配料中,并通过高温熔化、杯装、坩埚和皿水平旋转等方法与实际样品中的 PGEs 充分混合和平衡。真实样品中的 190Os 和 PGEs 都预先浓缩在微克级的 Sb 颗粒(100 毫克)中。经过研磨和抛光后,用 LA-ICP-MS 测定了 Sb 切片中的 195Pt、105Pd、101Ru、103Rh、193Ir、总 189Os 和富集的 190Os,用同位素稀释方程计算了内标物中的 190Os。用同样的方法处理 PGEs 的标准物质(CRMs),得到基质完全匹配的 Sb 切片,以解决没有国际公认的统一 PGEs 标准物质用于 LA-ICP-MS 测定的问题。由于LA-ICP-MS成像发现不同PGEs在Sb切片中的分布趋势相似,因此采用基质匹配的内标校正策略来降低元素分馏效应,提高LA-ICP-MS的测定精度和准确度。对激光频率、能量密度、去核直径和停留时间进行了优化。在优化条件下,采用经验系数法对标准曲线进行拟合,得到了极好的 PGEs 曲线拟合结果,相关系数在 0.9990 和 0.9999 之间。PGEs的方法检出限为0.00042~0.010 ng g-1。所建立的方法成功地应用于实际地球化学样品和各种基体的国内外标准物质的分析,其测定值与Sb-FA ICP-MS的结果和标准值吻合良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
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.
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