Synthesis and characterization of isotopically barcoded nickel, molybdenum, and tungsten taggants for intentional nuclear forensics.

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL Talanta Pub Date : 2025-04-01 Epub Date: 2024-12-18 DOI:10.1016/j.talanta.2024.127425
Rachel Bergin, Kyle Samperton, Michael Bronikowski, Eric Hoar, John Rolison, Quinn Shollenberger, Naomi Marks, Matthew Wellons, Spencer Scott
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Abstract

Intentional nuclear forensics is a concept wherein the deliberate addition of benign and persistent material signatures to nuclear material can be used to reduce the time between the discovery of material outside of regulatory control and determination of its original provenance. One concept within intentional nuclear forensics involves the use of perturbed stable isotopes to generate unique isotope ratio "barcodes" to encode information (e.g., production batch, location, etc.) and track material throughout the nuclear fuel cycle. Synthesis of taggant species of nickel (Ni), molybdenum (Mo), and tungsten (W) was undertaken via a double-spike mechanism, wherein two highly enriched isotopes of interest per elemental taggant were mixed to form an enriched "double-spike" which was subsequently isotopically diluted with bulk material having a natural isotopic composition. Two taggant species perturbing isotopic ratios, alpha (α) and beta (β), for each of Ni, Mo, and W were synthesized. Independent measurements of double spikes and alpha and beta taggant species agreed within uncertainty and are clearly resolvable from natural compositions. High-precision analyses were independently performed by MC-ICP-MS at two U.S. National Laboratories, with consensus values and uncertainties calculated for all samples. Observed isotopic perturbations in the final taggant species measured on the order of hundreds to thousands of permille (‰) with respect to natural for isotope ratios of interest (e.g., 60Ni/58Ni, 100Mo/98Mo, 186 W/183W). Discrepancies between modeled and measured isotopic compositions were observed and are largely attributed to imprecise vendor assay values for starting materials. Using measured starting material compositions as inputs for the mixing model improved the level of agreement between predicted and measured α and β taggant isotope ratios. Overall, characterization of all taggant species demonstrates that this "barcode" concept could have viability for use in nuclear forensics. It is expected that for any two-isotope mixing array dozens of isotopic barcodes could be encoded into a material system and subsequently resolved utilizing modern mass spectrometric methods.

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用于核取证的同位素条形码镍、钼和钨标记物的合成和表征。
故意核取证是一个概念,其中故意在核材料上添加良性和持久的材料特征,可用于缩短发现监管控制之外的材料与确定其原始来源之间的时间。故意核取证中的一个概念涉及使用扰动稳定同位素生成独特的同位素比率“条形码”来编码信息(例如,生产批次、位置等)并在整个核燃料循环中跟踪材料。镍(Ni)、钼(Mo)和钨(W)标记物的合成是通过双尖刺机制进行的,其中每个元素标记物的两种高富集同位素混合形成富集的“双尖刺”,随后用具有天然同位素组成的大块材料进行同位素稀释。对Ni、Mo和W分别合成了干扰同位素比值的α (α)和β (β)两种标记物。双尖刺和α和β标记物的独立测量结果在不确定范围内一致,并且可以从自然成分中清楚地分辨出来。在两个美国国家实验室,MC-ICP-MS独立进行高精度分析,计算所有样品的一致值和不确定度。与自然同位素比值(例如,60Ni/58Ni, 100Mo/98Mo, 186w /183W)相比,在最终诱变物种中观测到的同位素扰动在数百至数千permille(‰)量级。观察到模拟和测量的同位素组成之间存在差异,这在很大程度上归因于供应商对起始材料的测定值不精确。使用测量的起始物质成分作为混合模型的输入,提高了预测和测量的α和β标记物同位素比率之间的一致性。总的来说,所有标记物种的特征表明,这种“条形码”概念可以在核取证中使用。对于任何双同位素混合阵列,可以将数十个同位素条形码编码到材料系统中,然后利用现代质谱方法进行解析。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
期刊最新文献
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