A workflow-optimized protocol for accelerated sample preparation and automated Sr separation from natural waters for 87Sr/86Sr determination†

IF 3.1 2区 化学 Q2 CHEMISTRY, ANALYTICAL
Grace N. Manestar, Hilary M. K. Lewis, Alex McCoy-West, Nishen Naidoo, Stefan Makart, Ondrea Thompson and Brandon Mahan
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Abstract

Radiogenic strontium (87Sr/86Sr) is a powerful tool for characterizing and differentiating water reservoirs (among many other applications). The development and improvement of high-precision analytical platforms (namely MC-ICP-MS) has enhanced throughput for isotope ratio determination. However, analyte purification—needed to remove isobaric interferences—continues to occur largely via conventional manual gravity-driven ion exchange chromatography (hereafter: manual IEC), which generally cannot match instrument throughput. This has created a persistent throughput gap that encumbers use and proliferation, emphasizing the need for rapid separation of Sr, and of comprehensive, end-to-end high throughput workflows and analytical approaches that are fit-for-purpose. Here we have developed a workflow-optimized protocol for sample preparation and separation of Sr from natural water samples using both workflow-optimized manual IEC and automated high pressure ion chromatography (HPIC), for subsequent analysis via MC-ICP-MS. These methods have been designed to seamlessly integrate with common international practice for water sample collection. The automated HPIC technique accommodates introduction of water samples filtered with standard 0.45 μm membranes and acidified with ultra-high purity nitric acid (HNO3, to pH of 1–2, approximated as 0.09 mol per L HNO3). Filtered and acidified samples are directly introduced into the HPIC system where Sr is separated from other cations (namely Ca) and collected as an isolate in a specific volume of ultrapure water. Strontium isolates, with no further preparation (e.g. dry-down and reflux), are then directly acidified to 0.5 mol per L HNO3 and analyzed by MC-ICP-MS. This technique can process 40–50 samples in a 24 hour period with mitigated potential for human error, matching current MC-ICP-MS analytical capacity, and achieving analytical precision sufficient to distinguish the variability observed in natural samples across many applications.

Abstract Image

一种工作流程优化的方案,用于加速样品制备和自动从自然水中分离锶,用于87Sr/86Sr测定†
放射性成因锶(87Sr/86Sr)是表征和区分水库(以及许多其他应用)的有力工具。高精度分析平台(即MC-ICP-MS)的发展和改进提高了同位素比测定的通量。然而,分析物纯化-需要消除等压干扰-仍然主要通过传统的手动重力驱动离子交换色谱(以下简称:手动IEC)进行,通常无法匹配仪器吞吐量。这造成了持续的吞吐量差距,阻碍了使用和扩展,强调了对Sr的快速分离,以及全面的,端到端高吞吐量工作流和适合用途的分析方法的需求。在这里,我们开发了一种工作流程优化的方案,用于样品制备和天然水样中Sr的分离,使用工作流程优化的手动IEC和自动化高压离子色谱(HPIC),随后通过MC-ICP-MS进行分析。这些方法的设计与水样采集的国际惯例无缝结合。自动化HPIC技术适用于引入用标准0.45 μm膜过滤并用超高纯度硝酸(HNO3, pH为1-2,近似为0.09 mol / L HNO3)酸化的水样。过滤和酸化后的样品直接导入HPIC系统,其中Sr与其他阳离子(即Ca)分离,并在特定体积的超纯水中作为分离物收集。分离的锶,无需进一步制备(如干燥和回流),然后直接酸化至0.5 mol / L HNO3,并通过MC-ICP-MS进行分析。该技术可以在24小时内处理40-50个样品,减少人为错误的可能性,匹配当前MC-ICP-MS的分析能力,并达到足够的分析精度,以区分在许多应用中自然样品中观察到的可变性。
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来源期刊
CiteScore
6.20
自引率
26.50%
发文量
228
审稿时长
1.7 months
期刊介绍: Innovative research on the fundamental theory and application of spectrometric techniques.
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