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使用合成同位素混合物通过MC-ICP-MS准确测定钼同位素丰度比的质量相关效应研究。

Investigation of mass dependence effects for the accurate determination of molybdenum isotope amount ratios by MC-ICP-MS using synthetic isotope mixtures.

作者信息

Malinovsky Dmitry, Dunn Philip J H, Petrov Panayot, Goenaga-Infante Heidi

机构信息

LGC Limited, Queens Road, Teddington, Middlesex, TW11 0LY, UK,

出版信息

Anal Bioanal Chem. 2015 Jan;407(3):869-82. doi: 10.1007/s00216-014-8112-1. Epub 2014 Aug 29.

Abstract

Methodology for absolute Mo isotope amount ratio measurements by multicollector inductively coupled plasma-mass spectrometry (MC-ICP-MS) using calibration with synthetic isotope mixtures (SIMs) is presented. For the first time, synthetic isotope mixtures prepared from seven commercially available isotopically enriched molybdenum metal powders ((92)Mo, (94)Mo, (95)Mo, (96)Mo, (97)Mo, (98)Mo, and (100)Mo) are used to investigate whether instrumental mass discrimination of Mo isotopes in MC-ICP-MS is consistent with mass-dependent isotope distribution. The parent materials were dissolved and mixed as solutions to obtain mixtures with accurately known isotope amount ratios. The level of elemental impurities in the isotopically enriched molybdenum metal powders was quantified by ICP-MS by using both high-resolution and reaction cell instruments to completely resolve spectral interferences. The Mo isotope amount ratio values with expanded uncertainty (k = 2), determined by MC-ICP-MS for a high-purity Mo rod from Johnson Matthey, were as follows: (92)Mo/(95)Mo = 0.9235(9), (94)Mo/(95)Mo = 0.5785(8), (96)Mo/(95)Mo = 1.0503(9), (97)Mo/(95)Mo = 0.6033(6), (98)Mo/(95)Mo = 1.5291(20), and (100)Mo/(95)Mo = 0.6130(7). A full uncertainty budget for the measurements is presented which shows that the largest contribution to the uncertainty budget comes from correction for elemental impurities (∼51%), followed by the contribution from weighing operations (∼26 %). The atomic weight of molybdenum was calculated to be 95.947(2); the uncertainty in parentheses is expanded uncertainty with the coverage factor of 2. A particular advantage of the developed method is that calibration factors for all six Mo isotope amount ratios, involving the (95)Mo isotope, were experimentally determined. This allows avoiding any assumption on mass-dependent isotope fractions in MC-ICP-MS, inherent to the method of double spike previously used for Mo isotope amount ratio measurements. However, data obtained in this study show that instrumental mass discrimination in MC-ICP-MS is consistent with mass-dependent Mo isotope fractionation. This was demonstrated by a good agreement between experimentally obtained and theoretically expected values of the exponent of isotope fractionation, β, for each triad of Mo isotopes.

摘要

介绍了使用合成同位素混合物(SIMs)校准通过多接收电感耦合等离子体质谱法(MC-ICP-MS)测量钼同位素绝对量比的方法。首次使用由七种市售同位素富集钼金属粉末((92)Mo、(94)Mo、(95)Mo、(96)Mo、(97)Mo、(98)Mo和(100)Mo)制备的合成同位素混合物,来研究MC-ICP-MS中钼同位素的仪器质量歧视是否与质量依赖同位素分布一致。将母体材料溶解并作为溶液混合,以获得具有准确已知同位素量比的混合物。通过使用高分辨率和反应池仪器完全解决光谱干扰,通过ICP-MS对同位素富集钼金属粉末中的元素杂质水平进行了定量。由MC-ICP-MS测定的来自庄信万丰的高纯度钼棒的扩展不确定度(k = 2)下的钼同位素量比值如下:(92)Mo/(95)Mo = 0.9235(9),(94)Mo/(95)Mo = 0.5785(8),(96)Mo/(95)Mo = 1.0503(9),(97)Mo/(95)Mo = 0.6033(6),(98)Mo/(95)Mo = 1.5291(20),以及(100)Mo/(95)Mo = 0.6130(7)。给出了测量的完整不确定度预算,表明不确定度预算的最大贡献来自元素杂质校正(约51%),其次是称重操作的贡献(约26%)。计算得出钼的原子量为95.947(2);括号中的不确定度是覆盖因子为2的扩展不确定度。所开发方法的一个特别优点是,通过实验确定了涉及(95)Mo同位素的所有六个钼同位素量比的校准因子。这避免了MC-ICP-MS中对质量依赖同位素分数的任何假设,这是先前用于钼同位素量比测量的双尖峰方法所固有的。然而,本研究获得的数据表明,MC-ICP-MS中的仪器质量歧视与质量依赖的钼同位素分馏一致。这通过实验获得的和理论预期的每个钼同位素三元组的同位素分馏指数β值之间的良好一致性得到了证明。

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