激光烧蚀多收集器ICP-MS测定固体铀材料中铀同位素比值的分析考虑

IF 2.5 Q1 Chemistry
Michael Krachler, Zsolt Varga, Adrian Nicholl, Klaus Mayer
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引用次数: 12

摘要

采用激光烧蚀(LA)耦合多收集器ICP-MS,建立了快速、准确测定固体核材料中铀(U)同位素组成(234U、235U、236U、238U)的分析测量方法。通过频繁(n = 65)分析经认证的同位素标准物质CRM U-030(~ 3 wt% 235U)的压球,保证了分析过程的准确性。n(235U)/n(238U)的扩展不确定度(k = 2)低至0.05%,n(234U)/n(238U)和n(236U)/n(238U)的扩展不确定度分别上升至0.62%和1.09%。在分析每个样品之前,对经过认证的同位素参考物质CRM U-020(~ 2 wt% 235U)的压球进行LA-MC-ICP-MS测量,可以计算离子计数器增益和质量偏差校正。利用单个点分析和线扫描分析测量了来自第四次协同材料运动(CMX-4)的两个低富集UO2颗粒,四个从非法贩运中截获的低富集UO2颗粒和一个由贫铀组成的金属样品中的n(234U)/n(238U), n(235U)/n(238U)和n(236U)/n(238U)比率。所有调查样品的LA-MC-ICP-MS结果与热电离质谱(TIMS)获得的U同位素比率吻合良好。TIMS对LA-MC-ICP-MS结果的独立确认奠定了生成的高质量分析数据的基础。在几分钟的线扫描分析过程中,我们获取了数千个数据点,从而获得了所选UO2颗粒U同位素组成空间分布的详细信息,直接揭示了它们在μm尺度上的均匀性。计算n(235U)/n(238U)量比频率分布的偏度和半宽度,可以定量评估所调查样本的(in-)均匀性。这些信息可以得出用于生产颗粒的起始材料的结论。从核取证的角度来看,LA-MC-ICP-MS提供了关于主要和次要U同位素空间分布的快速,准确的结果,同时保留了样品,即证据,基本上完好无损。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Analytical considerations in the determination of uranium isotope ratios in solid uranium materials using laser ablation multi-collector ICP-MS

Analytical considerations in the determination of uranium isotope ratios in solid uranium materials using laser ablation multi-collector ICP-MS

Validated analytical measurement protocols for the fast and accurate determination of the uranium (U) isotopic composition (234U, 235U, 236U, 238U) of solid nuclear materials were developed employing ns-laser ablation (LA) coupled to multi-collector ICP-MS. The accuracy of the analytical procedure was assured by frequent (n = 65) analysis of a pressed pellet of certified isotopic reference material CRM U-030 (∼3 wt% 235U). The expanded uncertainty (k = 2) for the n(235U)/n(238U) ratio was as low as 0.05%, rising to 0.62% and 1.09% for n(234U)/n(238U) and n(236U)/n(238U) ratios, respectively. LA-MC-ICP-MS measurements of a pressed pellet of certified isotopic reference material CRM U-020 (∼2 wt% 235U) before analysis of each sample allowed calculation of the ion counter gains and mass bias correction. Both individual spot analysis and line scan analysis were used to measure n(234U)/n(238U), n(235U)/n(238U), and n(236U)/n(238U) ratios in two low-enriched UO2 pellets from the fourth Collaborative Materials Exercise (CMX-4), four seized low-enriched UO2 pellets intercepted from illicit trafficking and one metal sample consisting of depleted U. LA-MC-ICP-MS results of all investigated samples matched well with U isotope ratios obtained by thermal ionisation mass spectrometry (TIMS). This independent confirmation of the LA-MC-ICP-MS results by TIMS underpinned the high quality of generated analytical data. Acquisition of several thousand data points within a couple of minutes during line scan analysis yielded detailed information on the spatial distribution of the U isotopic composition of selected UO2 pellets, revealing straightforwardly their (in˗)homogeneity on the μm-scale. Calculating skewness and half width of the frequency distributions of the n(235U)/n(238U) amount ratio allowed the quantitative assessment of the (in-)homogeneity of the investigated samples. This information allows drawing conclusions on the starting materials used for the production of the pellets. From a nuclear forensics perspective, LA-MC-ICP-MS provides quick, accurate results on the spatial distribution of major and minor U isotopes while preserving the sample i.e. piece of evidence, essentially intact.

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来源期刊
Analytica Chimica Acta: X
Analytica Chimica Acta: X Chemistry-Analytical Chemistry
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