Michael Krachler, Zsolt Varga, Adrian Nicholl, Klaus Mayer
{"title":"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","authors":"Michael Krachler, Zsolt Varga, Adrian Nicholl, Klaus Mayer","doi":"10.1016/j.acax.2019.100018","DOIUrl":null,"url":null,"abstract":"<div><p>Validated analytical measurement protocols for the fast and accurate determination of the uranium (U) isotopic composition (<sup>234</sup>U, <sup>235</sup>U, <sup>236</sup>U, <sup>238</sup>U) 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 (<em>n</em> = 65) analysis of a pressed pellet of certified isotopic reference material CRM U-030 (∼3 wt% <sup>235</sup>U). The expanded uncertainty (<em>k</em> = 2) for the <em>n</em>(<sup>235</sup>U)/<em>n</em>(<sup>238</sup>U) ratio was as low as 0.05%, rising to 0.62% and 1.09% for <em>n</em>(<sup>234</sup>U)/<em>n</em>(<sup>238</sup>U) and <em>n</em>(<sup>236</sup>U)/<em>n</em>(<sup>238</sup>U) ratios, respectively. LA-MC-ICP-MS measurements of a pressed pellet of certified isotopic reference material CRM U-020 (∼2 wt% <sup>235</sup>U) 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 <em>n</em>(<sup>234</sup>U)/<em>n</em>(<sup>238</sup>U), <em>n</em>(<sup>235</sup>U)/<em>n</em>(<sup>238</sup>U), and <em>n</em>(<sup>236</sup>U)/<em>n</em>(<sup>238</sup>U) ratios in two low-enriched UO<sub>2</sub> pellets from the fourth Collaborative Materials Exercise (CMX-4), four seized low-enriched UO<sub>2</sub> 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 UO<sub>2</sub> pellets, revealing straightforwardly their (in˗)homogeneity on the μm-scale. Calculating skewness and half width of the frequency distributions of the <em>n</em>(<sup>235</sup>U)/<em>n</em>(<sup>238</sup>U) 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.</p></div>","PeriodicalId":241,"journal":{"name":"Analytica Chimica Acta: X","volume":"2 ","pages":"Article 100018"},"PeriodicalIF":2.5000,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.acax.2019.100018","citationCount":"12","resultStr":"{\"title\":\"Analytical considerations in the determination of uranium isotope ratios in solid uranium materials using laser ablation multi-collector ICP-MS\",\"authors\":\"Michael Krachler, Zsolt Varga, Adrian Nicholl, Klaus Mayer\",\"doi\":\"10.1016/j.acax.2019.100018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Validated analytical measurement protocols for the fast and accurate determination of the uranium (U) isotopic composition (<sup>234</sup>U, <sup>235</sup>U, <sup>236</sup>U, <sup>238</sup>U) 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 (<em>n</em> = 65) analysis of a pressed pellet of certified isotopic reference material CRM U-030 (∼3 wt% <sup>235</sup>U). The expanded uncertainty (<em>k</em> = 2) for the <em>n</em>(<sup>235</sup>U)/<em>n</em>(<sup>238</sup>U) ratio was as low as 0.05%, rising to 0.62% and 1.09% for <em>n</em>(<sup>234</sup>U)/<em>n</em>(<sup>238</sup>U) and <em>n</em>(<sup>236</sup>U)/<em>n</em>(<sup>238</sup>U) ratios, respectively. LA-MC-ICP-MS measurements of a pressed pellet of certified isotopic reference material CRM U-020 (∼2 wt% <sup>235</sup>U) 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 <em>n</em>(<sup>234</sup>U)/<em>n</em>(<sup>238</sup>U), <em>n</em>(<sup>235</sup>U)/<em>n</em>(<sup>238</sup>U), and <em>n</em>(<sup>236</sup>U)/<em>n</em>(<sup>238</sup>U) ratios in two low-enriched UO<sub>2</sub> pellets from the fourth Collaborative Materials Exercise (CMX-4), four seized low-enriched UO<sub>2</sub> 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 UO<sub>2</sub> pellets, revealing straightforwardly their (in˗)homogeneity on the μm-scale. Calculating skewness and half width of the frequency distributions of the <em>n</em>(<sup>235</sup>U)/<em>n</em>(<sup>238</sup>U) 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.</p></div>\",\"PeriodicalId\":241,\"journal\":{\"name\":\"Analytica Chimica Acta: X\",\"volume\":\"2 \",\"pages\":\"Article 100018\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2019-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.acax.2019.100018\",\"citationCount\":\"12\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytica Chimica Acta: X\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2590134619300143\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytica Chimica Acta: X","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590134619300143","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Chemistry","Score":null,"Total":0}
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.