Jiang-yi Zhang , Wen-jing Liu , Di Liu , Guang-liang Wu , Zhi-fang Xu
{"title":"使用 ICP-MS/MS 快速测定水样中的 87Sr/86Sr 比率,无需浓度匹配和基质匹配","authors":"Jiang-yi Zhang , Wen-jing Liu , Di Liu , Guang-liang Wu , Zhi-fang Xu","doi":"10.1016/j.sab.2024.107046","DOIUrl":null,"url":null,"abstract":"<div><p>We present a rapid method for determining the <sup><strong>87</strong></sup><strong>Sr/</strong><sup><strong>86</strong></sup><strong>Sr ratio</strong> in water samples using <strong>inductively coupled plasma tandem mass spectrometry (ICP-MS/MS)</strong> in the oxygen reaction mode, thus eliminating the need for Sr purification. With <strong>O</strong><sub><strong>2</strong></sub> as the reaction gas, <strong>Sr</strong><sup><strong>+</strong></sup> ions undergo a mass shift, measured at <strong><em>m/z</em> 102 and 103</strong>. Our investigation into the interference elimination, concentration effects, and matrix effects revealed that the <sup><strong>87</strong></sup><strong>Sr/</strong><sup><strong>86</strong></sup><strong>Sr</strong> determination method is robust, yielding a value of <strong>0.7101 ± 0.0010 (2SD)</strong> for the <strong>NIST SRM 987</strong> standard, consistent with the reference value of <strong>0.71034 ± 0.00026 (2SD)</strong>. This accuracy was maintained even with a <strong>Rb/Sr</strong> ratio of <strong>100</strong>. Further, this method was insensitive to the concentration ratio of Sr in the sample and standard (from 0.1 to 10) and exhibited negligible sample matrix effects, as shown by the average values for an IAPSO seawater standard, calibrated with pure Sr and matrix-matched Sr standard solutions, yielding <sup><strong>87</strong></sup><strong>Sr/</strong><sup><strong>86</strong></sup><strong>Sr</strong> ratios of 0.7091 ± 0.0006 (2SD) and 0.7092 ± 0.0008 (2SD) respectively, which were consistent with the literature values. Subsequently, real water samples were analyzed using the proposed method, yielding good results.</p></div>","PeriodicalId":21890,"journal":{"name":"Spectrochimica Acta Part B: Atomic Spectroscopy","volume":"221 ","pages":"Article 107046"},"PeriodicalIF":3.2000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rapid determination of the 87Sr/86Sr ratio in water samples using ICP-MS/MS without concentration matching and matrix matching\",\"authors\":\"Jiang-yi Zhang , Wen-jing Liu , Di Liu , Guang-liang Wu , Zhi-fang Xu\",\"doi\":\"10.1016/j.sab.2024.107046\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We present a rapid method for determining the <sup><strong>87</strong></sup><strong>Sr/</strong><sup><strong>86</strong></sup><strong>Sr ratio</strong> in water samples using <strong>inductively coupled plasma tandem mass spectrometry (ICP-MS/MS)</strong> in the oxygen reaction mode, thus eliminating the need for Sr purification. With <strong>O</strong><sub><strong>2</strong></sub> as the reaction gas, <strong>Sr</strong><sup><strong>+</strong></sup> ions undergo a mass shift, measured at <strong><em>m/z</em> 102 and 103</strong>. Our investigation into the interference elimination, concentration effects, and matrix effects revealed that the <sup><strong>87</strong></sup><strong>Sr/</strong><sup><strong>86</strong></sup><strong>Sr</strong> determination method is robust, yielding a value of <strong>0.7101 ± 0.0010 (2SD)</strong> for the <strong>NIST SRM 987</strong> standard, consistent with the reference value of <strong>0.71034 ± 0.00026 (2SD)</strong>. This accuracy was maintained even with a <strong>Rb/Sr</strong> ratio of <strong>100</strong>. Further, this method was insensitive to the concentration ratio of Sr in the sample and standard (from 0.1 to 10) and exhibited negligible sample matrix effects, as shown by the average values for an IAPSO seawater standard, calibrated with pure Sr and matrix-matched Sr standard solutions, yielding <sup><strong>87</strong></sup><strong>Sr/</strong><sup><strong>86</strong></sup><strong>Sr</strong> ratios of 0.7091 ± 0.0006 (2SD) and 0.7092 ± 0.0008 (2SD) respectively, which were consistent with the literature values. Subsequently, real water samples were analyzed using the proposed method, yielding good results.</p></div>\",\"PeriodicalId\":21890,\"journal\":{\"name\":\"Spectrochimica Acta Part B: Atomic Spectroscopy\",\"volume\":\"221 \",\"pages\":\"Article 107046\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-09-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Spectrochimica Acta Part B: Atomic Spectroscopy\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0584854724001903\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"SPECTROSCOPY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Spectrochimica Acta Part B: Atomic Spectroscopy","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0584854724001903","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SPECTROSCOPY","Score":null,"Total":0}
Rapid determination of the 87Sr/86Sr ratio in water samples using ICP-MS/MS without concentration matching and matrix matching
We present a rapid method for determining the 87Sr/86Sr ratio in water samples using inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) in the oxygen reaction mode, thus eliminating the need for Sr purification. With O2 as the reaction gas, Sr+ ions undergo a mass shift, measured at m/z 102 and 103. Our investigation into the interference elimination, concentration effects, and matrix effects revealed that the 87Sr/86Sr determination method is robust, yielding a value of 0.7101 ± 0.0010 (2SD) for the NIST SRM 987 standard, consistent with the reference value of 0.71034 ± 0.00026 (2SD). This accuracy was maintained even with a Rb/Sr ratio of 100. Further, this method was insensitive to the concentration ratio of Sr in the sample and standard (from 0.1 to 10) and exhibited negligible sample matrix effects, as shown by the average values for an IAPSO seawater standard, calibrated with pure Sr and matrix-matched Sr standard solutions, yielding 87Sr/86Sr ratios of 0.7091 ± 0.0006 (2SD) and 0.7092 ± 0.0008 (2SD) respectively, which were consistent with the literature values. Subsequently, real water samples were analyzed using the proposed method, yielding good results.
期刊介绍:
Spectrochimica Acta Part B: Atomic Spectroscopy, is intended for the rapid publication of both original work and reviews in the following fields:
Atomic Emission (AES), Atomic Absorption (AAS) and Atomic Fluorescence (AFS) spectroscopy;
Mass Spectrometry (MS) for inorganic analysis covering Spark Source (SS-MS), Inductively Coupled Plasma (ICP-MS), Glow Discharge (GD-MS), and Secondary Ion Mass Spectrometry (SIMS).
Laser induced atomic spectroscopy for inorganic analysis, including non-linear optical laser spectroscopy, covering Laser Enhanced Ionization (LEI), Laser Induced Fluorescence (LIF), Resonance Ionization Spectroscopy (RIS) and Resonance Ionization Mass Spectrometry (RIMS); Laser Induced Breakdown Spectroscopy (LIBS); Cavity Ringdown Spectroscopy (CRDS), Laser Ablation Inductively Coupled Plasma Atomic Emission Spectroscopy (LA-ICP-AES) and Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS).
X-ray spectrometry, X-ray Optics and Microanalysis, including X-ray fluorescence spectrometry (XRF) and related techniques, in particular Total-reflection X-ray Fluorescence Spectrometry (TXRF), and Synchrotron Radiation-excited Total reflection XRF (SR-TXRF).
Manuscripts dealing with (i) fundamentals, (ii) methodology development, (iii)instrumentation, and (iv) applications, can be submitted for publication.