Uranium isotope analysis by MC-ICP-MS in sub-ng sized samplesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ja00238b

This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions. The used Neptune Plus™ MC...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Boulyga, Sergei F, Koepf, Andreas, Konegger-Kappel, Stefanie, Macsik, Zsuzsanna, Stadelmann, Guillaume
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2284
container_issue 11
container_start_page 2272
container_title
container_volume 31
creator Boulyga, Sergei F
Koepf, Andreas
Konegger-Kappel, Stefanie
Macsik, Zsuzsanna
Stadelmann, Guillaume
description This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions. The used Neptune Plus™ MC-ICP-MS is equipped with the so-called "Jet Interface", which comprises a high capacity interface pump and specially designed sample and skimmer cones. Together with a high-efficiency sample introduction system (Aridus II™, Cetac Technologies, NE, USA), absolute U registration efficiencies of typically 1.5% to 2.5% can be achieved under routine operation. A mass bias correction, background/memory effect correction, hydride formation correction, yield and dead time correction of the multi-collector ion counters, and peak-tailing correction are performed for isotope ratio measurements. The effect of potential molecular interferences is assessed by the screening of concentrations of interfering elements in uranium fractions. The new MC-ICP-MS makes possible the determination of n ( 235 U)/ n ( 238 U) with relative expanded uncertainties ( k = 2) lower than 0.2% and allows achieving detection limits of 1 × 10 −7 for n ( 233 U)/ n ( 238 U) and 6 × 10 −8 for n ( 236 U)/ n ( 238 U) in solution aliquots containing 0.4 ng to 0.6 ng uranium. The relative expanded uncertainties ( k = 2) of n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) ratios (>10 −5 ) are below 1% and the absolute accuracy for minor isotope ratios n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) measured in CRMs is below the 1 ppm level. The developed method has been validated by comparative measurements with the previously used thermal ionisation mass spectrometry (TIMS) method by analysing test samples from an inter-laboratory comparison exercise. The MC-ICP-MS method has been applied for analysis of U isotope ratios in U fractions obtained from cotton swipe samples. This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions.
doi_str_mv 10.1039/c6ja00238b
format Article
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c6ja00238b</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c6ja00238b</sourcerecordid><originalsourceid>FETCH-rsc_primary_c6ja00238b3</originalsourceid><addsrcrecordid>eNqFjj1LxEAURQdRMK429sKz02LWybdrGyObYlGI1uElO5FZZibDvKwQf4S_2RSCheBWF-49HC5jl6FYhiJe3XXZDoWI4vv2iAVhnCU8TZPkmAUiynK-SvL8lJ0R7YQQSRqlAft682jV3oCiYRycBLSoJ1IE7QSbglfFC9_UoCzQvuX2HUh9yi0QGqcllVp2ox-s6ubZzY2RdkQ_zXw_eIOjGizclHV1C_iBSmOr5RJqKeHxuXqAv6_P2UmPmuTFTy7Y1VP5Wqy5p65xXplZ3vzi8YJd_7c3btvHhxzf29Re8g</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Uranium isotope analysis by MC-ICP-MS in sub-ng sized samplesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ja00238b</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Boulyga, Sergei F ; Koepf, Andreas ; Konegger-Kappel, Stefanie ; Macsik, Zsuzsanna ; Stadelmann, Guillaume</creator><creatorcontrib>Boulyga, Sergei F ; Koepf, Andreas ; Konegger-Kappel, Stefanie ; Macsik, Zsuzsanna ; Stadelmann, Guillaume</creatorcontrib><description>This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions. The used Neptune Plus™ MC-ICP-MS is equipped with the so-called "Jet Interface", which comprises a high capacity interface pump and specially designed sample and skimmer cones. Together with a high-efficiency sample introduction system (Aridus II™, Cetac Technologies, NE, USA), absolute U registration efficiencies of typically 1.5% to 2.5% can be achieved under routine operation. A mass bias correction, background/memory effect correction, hydride formation correction, yield and dead time correction of the multi-collector ion counters, and peak-tailing correction are performed for isotope ratio measurements. The effect of potential molecular interferences is assessed by the screening of concentrations of interfering elements in uranium fractions. The new MC-ICP-MS makes possible the determination of n ( 235 U)/ n ( 238 U) with relative expanded uncertainties ( k = 2) lower than 0.2% and allows achieving detection limits of 1 × 10 −7 for n ( 233 U)/ n ( 238 U) and 6 × 10 −8 for n ( 236 U)/ n ( 238 U) in solution aliquots containing 0.4 ng to 0.6 ng uranium. The relative expanded uncertainties ( k = 2) of n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) ratios (&gt;10 −5 ) are below 1% and the absolute accuracy for minor isotope ratios n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) measured in CRMs is below the 1 ppm level. The developed method has been validated by comparative measurements with the previously used thermal ionisation mass spectrometry (TIMS) method by analysing test samples from an inter-laboratory comparison exercise. The MC-ICP-MS method has been applied for analysis of U isotope ratios in U fractions obtained from cotton swipe samples. This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions.</description><identifier>ISSN: 0267-9477</identifier><identifier>EISSN: 1364-5544</identifier><identifier>DOI: 10.1039/c6ja00238b</identifier><language>eng</language><creationdate>2016-10</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Boulyga, Sergei F</creatorcontrib><creatorcontrib>Koepf, Andreas</creatorcontrib><creatorcontrib>Konegger-Kappel, Stefanie</creatorcontrib><creatorcontrib>Macsik, Zsuzsanna</creatorcontrib><creatorcontrib>Stadelmann, Guillaume</creatorcontrib><title>Uranium isotope analysis by MC-ICP-MS in sub-ng sized samplesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ja00238b</title><description>This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions. The used Neptune Plus™ MC-ICP-MS is equipped with the so-called "Jet Interface", which comprises a high capacity interface pump and specially designed sample and skimmer cones. Together with a high-efficiency sample introduction system (Aridus II™, Cetac Technologies, NE, USA), absolute U registration efficiencies of typically 1.5% to 2.5% can be achieved under routine operation. A mass bias correction, background/memory effect correction, hydride formation correction, yield and dead time correction of the multi-collector ion counters, and peak-tailing correction are performed for isotope ratio measurements. The effect of potential molecular interferences is assessed by the screening of concentrations of interfering elements in uranium fractions. The new MC-ICP-MS makes possible the determination of n ( 235 U)/ n ( 238 U) with relative expanded uncertainties ( k = 2) lower than 0.2% and allows achieving detection limits of 1 × 10 −7 for n ( 233 U)/ n ( 238 U) and 6 × 10 −8 for n ( 236 U)/ n ( 238 U) in solution aliquots containing 0.4 ng to 0.6 ng uranium. The relative expanded uncertainties ( k = 2) of n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) ratios (&gt;10 −5 ) are below 1% and the absolute accuracy for minor isotope ratios n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) measured in CRMs is below the 1 ppm level. The developed method has been validated by comparative measurements with the previously used thermal ionisation mass spectrometry (TIMS) method by analysing test samples from an inter-laboratory comparison exercise. The MC-ICP-MS method has been applied for analysis of U isotope ratios in U fractions obtained from cotton swipe samples. This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions.</description><issn>0267-9477</issn><issn>1364-5544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFjj1LxEAURQdRMK429sKz02LWybdrGyObYlGI1uElO5FZZibDvKwQf4S_2RSCheBWF-49HC5jl6FYhiJe3XXZDoWI4vv2iAVhnCU8TZPkmAUiynK-SvL8lJ0R7YQQSRqlAft682jV3oCiYRycBLSoJ1IE7QSbglfFC9_UoCzQvuX2HUh9yi0QGqcllVp2ox-s6ubZzY2RdkQ_zXw_eIOjGizclHV1C_iBSmOr5RJqKeHxuXqAv6_P2UmPmuTFTy7Y1VP5Wqy5p65xXplZ3vzi8YJd_7c3btvHhxzf29Re8g</recordid><startdate>20161026</startdate><enddate>20161026</enddate><creator>Boulyga, Sergei F</creator><creator>Koepf, Andreas</creator><creator>Konegger-Kappel, Stefanie</creator><creator>Macsik, Zsuzsanna</creator><creator>Stadelmann, Guillaume</creator><scope/></search><sort><creationdate>20161026</creationdate><title>Uranium isotope analysis by MC-ICP-MS in sub-ng sized samplesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ja00238b</title><author>Boulyga, Sergei F ; Koepf, Andreas ; Konegger-Kappel, Stefanie ; Macsik, Zsuzsanna ; Stadelmann, Guillaume</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c6ja00238b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boulyga, Sergei F</creatorcontrib><creatorcontrib>Koepf, Andreas</creatorcontrib><creatorcontrib>Konegger-Kappel, Stefanie</creatorcontrib><creatorcontrib>Macsik, Zsuzsanna</creatorcontrib><creatorcontrib>Stadelmann, Guillaume</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boulyga, Sergei F</au><au>Koepf, Andreas</au><au>Konegger-Kappel, Stefanie</au><au>Macsik, Zsuzsanna</au><au>Stadelmann, Guillaume</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Uranium isotope analysis by MC-ICP-MS in sub-ng sized samplesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ja00238b</atitle><date>2016-10-26</date><risdate>2016</risdate><volume>31</volume><issue>11</issue><spage>2272</spage><epage>2284</epage><pages>2272-2284</pages><issn>0267-9477</issn><eissn>1364-5544</eissn><abstract>This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions. The used Neptune Plus™ MC-ICP-MS is equipped with the so-called "Jet Interface", which comprises a high capacity interface pump and specially designed sample and skimmer cones. Together with a high-efficiency sample introduction system (Aridus II™, Cetac Technologies, NE, USA), absolute U registration efficiencies of typically 1.5% to 2.5% can be achieved under routine operation. A mass bias correction, background/memory effect correction, hydride formation correction, yield and dead time correction of the multi-collector ion counters, and peak-tailing correction are performed for isotope ratio measurements. The effect of potential molecular interferences is assessed by the screening of concentrations of interfering elements in uranium fractions. The new MC-ICP-MS makes possible the determination of n ( 235 U)/ n ( 238 U) with relative expanded uncertainties ( k = 2) lower than 0.2% and allows achieving detection limits of 1 × 10 −7 for n ( 233 U)/ n ( 238 U) and 6 × 10 −8 for n ( 236 U)/ n ( 238 U) in solution aliquots containing 0.4 ng to 0.6 ng uranium. The relative expanded uncertainties ( k = 2) of n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) ratios (&gt;10 −5 ) are below 1% and the absolute accuracy for minor isotope ratios n ( 234 U)/ n ( 238 U) and n ( 236 U)/ n ( 238 U) measured in CRMs is below the 1 ppm level. The developed method has been validated by comparative measurements with the previously used thermal ionisation mass spectrometry (TIMS) method by analysing test samples from an inter-laboratory comparison exercise. The MC-ICP-MS method has been applied for analysis of U isotope ratios in U fractions obtained from cotton swipe samples. This study describes the multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) method for the determination of n ( 233 U)/ n ( 238 U), n ( 234 U)/ n ( 238 U), n ( 235 U)/ n ( 238 U), and n ( 236 U)/ n ( 238 U) isotope ratios in purified uranium solutions.</abstract><doi>10.1039/c6ja00238b</doi><tpages>13</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0267-9477
ispartof
issn 0267-9477
1364-5544
language eng
recordid cdi_rsc_primary_c6ja00238b
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Uranium isotope analysis by MC-ICP-MS in sub-ng sized samplesElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ja00238b
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T18%3A26%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Uranium%20isotope%20analysis%20by%20MC-ICP-MS%20in%20sub-ng%20sized%20samplesElectronic%20supplementary%20information%20(ESI)%20available.%20See%20DOI:%2010.1039/c6ja00238b&rft.au=Boulyga,%20Sergei%20F&rft.date=2016-10-26&rft.volume=31&rft.issue=11&rft.spage=2272&rft.epage=2284&rft.pages=2272-2284&rft.issn=0267-9477&rft.eissn=1364-5544&rft_id=info:doi/10.1039/c6ja00238b&rft_dat=%3Crsc%3Ec6ja00238b%3C/rsc%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true