Measurement of ultra-trace level 237Np in soil and sediment by triple-quadrupole inductively coupled plasma-mass spectrometry with different mass modes combined with chemical separation

IF 3.2 2区 化学 Q1 SPECTROSCOPY Spectrochimica Acta Part B: Atomic Spectroscopy Pub Date : 2024-05-31 DOI:10.1016/j.sab.2024.106956
Weichao Zhang , Chuan Lu , Yihong Xu , Jianfeng Lin , Jia Zhan , Haitao Zhang , Xiaowei Yi , Ning Chen , Xiaolin Hou , Dongjin Wan , Haijun Dang
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Abstract

Long-lived trans‑uranium nuclides such as 237Np, may reside in the environment for long period and result in ecological impact and human health threat. Accurate measurement of 237Np in the environment is important for the risk assessment and ecological evaluation. However, the spectral peak tailing and polyatomic ions interference greatly limit the measurement of 237Np with triple quadrupole ICP-MS (ICP-MS/MS), which have been successfully used for analysis of ultra-trace level 239,240Pu and 241Am. The novel methods for 237Np measurement with ICP-MS/MS in both on-mass and mass-shift modes were examined in this paper. When helium was used as the collision gas for the ICP-MS/MS measurement with on-mass mode, the interference contribution to the counts for 237Np (at m/z 237) as low as 4 × 10−8 was observed only from Hg, while no measurable interference from Tl and Pb was observed. Moreover, when the mass-shift mode is employed with O2/He and He as the collision/reaction gas, the interference contributions from Hg, Tl and Pb were all negligible. The detection limit of 237Np was reduced to 0.014 fg/g and 0.019 fg/g for on-mass and mass-shift mode, respectively. The novel methods were demonstrated to enable accurate determination of 1.0 fg/g level 237Np in the emulated sample solutions with a 237Np/238U atomic ratio as low as 10−9. Combined with appropriate chemical separation procedure, the developed methods were verified with certified reference materials and soil samples.

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采用不同质量模式的三重四极杆电感耦合等离子体质谱结合化学分离法测量土壤和沉积物中的超痕量 237Np
237Np 等长寿命反式铀核素可能长期存在于环境中,对生态环境和人类健康造成影响。精确测量环境中的 237Np 对风险评估和生态评价非常重要。然而,光谱峰尾和多原子离子干扰极大地限制了三重四极杆 ICP-MS (ICP-MS/MS)对 237Np 的测量,ICP-MS/MS 已成功用于分析超痕量水平的 239、240Pu 和 241Am。本文研究了利用 ICP-MS/MS 在质谱模式和质量位移模式下测量 237Np 的新方法。当使用氦气作为碰撞气体进行质谱模式下的 ICP-MS/MS 测量时,只观察到汞对 237Np(在 m/z 237 处)计数的干扰贡献低至 4 × 10-8,而没有观察到 Tl 和 Pb 的可测量干扰。此外,在使用 O2/He 和 He 作为碰撞/反应气体的质量偏移模式时,来自 Hg、Tl 和 Pb 的干扰均可忽略不计。在质谱和质移模式下,237Np 的检出限分别降至 0.014 fg/g 和 0.019 fg/g。实验证明,新方法可以在 237Np/238U 原子比低至 10-9 的模拟样品溶液中准确测定 1.0 fg/g 水平的 237Np。结合适当的化学分离程序,用经认证的参考材料和土壤样品对所开发的方法进行了验证。
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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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