Rapid determination of the 87Sr/86Sr ratio in water samples using ICP-MS/MS without concentration matching and matrix matching

IF 3.2 2区 化学 Q1 SPECTROSCOPY
Jiang-yi Zhang , Wen-jing Liu , Di Liu , Guang-liang Wu , Zhi-fang Xu
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Abstract

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.

Abstract Image

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
我们介绍了一种在氧反应模式下使用电感耦合等离子体串联质谱法(ICP-MS/MS)测定水样中 87Sr/86Sr 比率的快速方法,因此无需进行 Sr 净化。以氧气作为反应气体时,Sr+ 离子会发生质量移动,在 m/z 102 和 103 处测得。我们对干扰消除、浓度效应和基质效应的研究表明,87Sr/86Sr 测定方法是可靠的,NIST SRM 987 标准的测定值为 0.7101 ± 0.0010(2SD),与参考值 0.71034 ± 0.00026(2SD)一致。即使在铷/锶比值为 100 的情况下,也能保持这一精度。此外,该方法对样品和标准品中 Sr 的浓度比(从 0.1 到 10)并不敏感,样品基质效应也可忽略不计,如用纯 Sr 和基质匹配 Sr 标准溶液校准的 IAPSO 海水标准品的平均值所示,87Sr/86Sr 比值分别为 0.7091 ± 0.0006 (2SD) 和 0.7092 ± 0.0008 (2SD),与文献值一致。随后,使用所提议的方法对真实水样进行了分析,结果良好。
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来源期刊
CiteScore
6.10
自引率
12.10%
发文量
173
审稿时长
81 days
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.
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