Sean R. Scott, Kirby P. Hobbs, Amanda D. French, Isaac J. Arnquist, Sonia Alcantar Anguiano, Daniel L. Sullivan and Staci M. Herman
{"title":"利用 ICP-MS 对未净化溶液中的铀进行同位素分析","authors":"Sean R. Scott, Kirby P. Hobbs, Amanda D. French, Isaac J. Arnquist, Sonia Alcantar Anguiano, Daniel L. Sullivan and Staci M. Herman","doi":"10.1039/D4JA00130C","DOIUrl":null,"url":null,"abstract":"<p >Mass spectrometry is a widely used tool for analysis of uranium isotopic composition. For solution based inductively coupled plasma mass spectrometry, uranium isotopes are typically analyzed after purification from complex matrices. In this work, we tested the ability of three mass spectrometers (ThermoScientific iCAP TQ, ThermoScientific Neoma, and Agilent 8900) to analyze uranium isotopes in an unpurified NIST reference material (SRM2780a, Hard Rock Mine Waste) digest solution. Results indicate that <small><sup>235</sup></small>U/<small><sup>238</sup></small>U can be analyzed within 1% of the true value. <small><sup>234</sup></small>U/<small><sup>238</sup></small>U is a more challenging analysis due to low count rates and potential isobar interferences, but strategies to mitigate these effects, such as the use of reaction gases in a collision cell and desolvating nebulizer introduction system, are effective for the triple quadrupole instruments. However, the use of the Neoma MS/MS in reaction mode using O<small><sub>2</sub></small> gas was problematic. Nevertheless, analysis of unpurified solutions for quick assessment of uranium isotope compositions is practical, especially when high precision is not required.</p>","PeriodicalId":81,"journal":{"name":"Journal of Analytical Atomic Spectrometry","volume":" 8","pages":" 2106-2115"},"PeriodicalIF":3.1000,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ja/d4ja00130c?page=search","citationCount":"0","resultStr":"{\"title\":\"Uranium isotopic analysis in unpurified solutions by ICP-MS†\",\"authors\":\"Sean R. Scott, Kirby P. Hobbs, Amanda D. French, Isaac J. Arnquist, Sonia Alcantar Anguiano, Daniel L. Sullivan and Staci M. Herman\",\"doi\":\"10.1039/D4JA00130C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Mass spectrometry is a widely used tool for analysis of uranium isotopic composition. For solution based inductively coupled plasma mass spectrometry, uranium isotopes are typically analyzed after purification from complex matrices. In this work, we tested the ability of three mass spectrometers (ThermoScientific iCAP TQ, ThermoScientific Neoma, and Agilent 8900) to analyze uranium isotopes in an unpurified NIST reference material (SRM2780a, Hard Rock Mine Waste) digest solution. Results indicate that <small><sup>235</sup></small>U/<small><sup>238</sup></small>U can be analyzed within 1% of the true value. <small><sup>234</sup></small>U/<small><sup>238</sup></small>U is a more challenging analysis due to low count rates and potential isobar interferences, but strategies to mitigate these effects, such as the use of reaction gases in a collision cell and desolvating nebulizer introduction system, are effective for the triple quadrupole instruments. However, the use of the Neoma MS/MS in reaction mode using O<small><sub>2</sub></small> gas was problematic. Nevertheless, analysis of unpurified solutions for quick assessment of uranium isotope compositions is practical, especially when high precision is not required.</p>\",\"PeriodicalId\":81,\"journal\":{\"name\":\"Journal of Analytical Atomic Spectrometry\",\"volume\":\" 8\",\"pages\":\" 2106-2115\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2024-06-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ja/d4ja00130c?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Analytical Atomic Spectrometry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ja/d4ja00130c\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical Atomic Spectrometry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ja/d4ja00130c","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Uranium isotopic analysis in unpurified solutions by ICP-MS†
Mass spectrometry is a widely used tool for analysis of uranium isotopic composition. For solution based inductively coupled plasma mass spectrometry, uranium isotopes are typically analyzed after purification from complex matrices. In this work, we tested the ability of three mass spectrometers (ThermoScientific iCAP TQ, ThermoScientific Neoma, and Agilent 8900) to analyze uranium isotopes in an unpurified NIST reference material (SRM2780a, Hard Rock Mine Waste) digest solution. Results indicate that 235U/238U can be analyzed within 1% of the true value. 234U/238U is a more challenging analysis due to low count rates and potential isobar interferences, but strategies to mitigate these effects, such as the use of reaction gases in a collision cell and desolvating nebulizer introduction system, are effective for the triple quadrupole instruments. However, the use of the Neoma MS/MS in reaction mode using O2 gas was problematic. Nevertheless, analysis of unpurified solutions for quick assessment of uranium isotope compositions is practical, especially when high precision is not required.