A new method for determining 236U/238U isotope ratios in environmental samples by means OF ICP-MS/MS

被引:28
作者
Diez-Fernandez, Silvia [1 ]
Jaegler, Hugo [2 ]
Bresson, Carole [1 ]
Chartier, Frederic [3 ]
Evrard, Olivier [2 ]
Hubert, Amelie [4 ]
Nonell, Anthony [1 ]
Pointurier, Fabien [4 ]
Isnard, Helene [1 ]
机构
[1] Univ Paris Saclay, CEA, Den Serv Etud Analyt & React Surfaces SEARS, F-91191 Gif Sur Yvette, France
[2] Univ Paris Saclay, CEA, CNRS, LSCE,IPSL,UVSQ,UMR 8212, Gif Sur Yvette, France
[3] Univ Paris Saclay, CEA, Den Dept Physicochim DPC, F-91191 Gif Sur Yvette, France
[4] CEA, DAM, DIF, F-91297 Arpajon, France
关键词
Uranium-236; ICP-MS/MS; Spectral interferences; MC-ICP-MS; Pukushima; Environmental samples; INDUCTIVELY-COUPLED PLASMA; STANDARD DEVIATIONS; ANTHROPOGENIC U-236; REACTION CELL; URANIUM; SEPARATION; TRACER; SEA;
D O I
10.1016/j.talanta.2019.120221
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The U-236/U-238 isotope ratio is a widely used tracer, which provides information on source identification for safeguard purposes, nuclear forensic studies and environmental monitoring. This paper describes an original approach to determine U-236/U-239 ratios, below 10(-8), in environmental samples by combination of ICP-MS/MS for U-236/U-239 ratio and multiple collector ICPMS measurements for U-233/U-239 and U-234/U-235 isotope ratios. Since the hydride form of UO+ (UGH +) is less prone to occur than UH+, we were focused on the oxidised forms of uranium in order to reduce hydride based-interferences in ICP-MS/MS. Then, in-cell ion-molecule reactions with O-2 and CO2 were assessed to detect the uranium isotopes in mass-shift mode (Q1: U+ -> Q2: UO+). The performances in terms of UO+ sensitivity and minimisation of hydride form of UO+ were evaluated using five different desolvating systems. The best conditions, using an Apex Omega or an Aridus system, produced uranium oxide hydride rate ((UOH+)-U-235-O-160-H-1/(UO+)-U-235-O-16) of about 10(-7) with O-2 in the collision cell. The method was validated through measurements of two certified IRMM standards with U-236/U-239 isotope ratio of 1.245 x 10(-7) and 1.052 x 10(-8), giving results in agreement with certified reference values. The relative standard deviations on seven independent measurements for each standard were respectively of 1.5% and 6.2%. Finally, environmental samples corresponding to sediments from the radioactive contamination plume emitted by the Fukushima Daiichi Nuclear Power Plant accident were analysed after a well-established uranium chemical separation procedure. U-236/U-239 atomic ratios between 1.5 x 10(-8) and 7 x 10(-9) were obtained with a level accuracy lower than 20%.
引用
收藏
页数:8
相关论文
共 33 条
[1]   Inductively coupled plasma - Tandem mass spectrometry (ICP-MS/MS): A powerful and universal tool for the interference-free determination of (ultra) trace elements - A tutorial review [J].
Balcaen, Lieve ;
Bolea-Fernandez, Eduardo ;
Resano, Martin ;
Vanhaecke, Frank .
ANALYTICA CHIMICA ACTA, 2015, 894 :7-19
[2]   Determination of extremely low 236U/238U isotope ratios in environmental samples by sector-field inductively coupled plasma mass spectrometry using high-efficiency sample introduction [J].
Boulyga, SF ;
Heumann, KG .
JOURNAL OF ENVIRONMENTAL RADIOACTIVITY, 2006, 88 (01) :1-10
[3]   Determination of uranium isotopic composition and 236U content of soil samples and hot particles using inductively coupled plasma mass spectrometry [J].
Boulyga, SF ;
Becker, JS .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2001, 370 (05) :612-617
[4]   Isotope ratio measurements of spent reactor uranium in environmental samples by using inductively coupled plasma mass spectrometry [J].
Boulyga, SF ;
Becker, JS ;
Matusevitch, JL ;
Dietze, HJ .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2000, 203 (1-3) :143-154
[5]   Development and application of mass spectrometric techniques for ultra-trace determination of 236U in environmental samples-A review [J].
Bu, Wenting ;
Zheng, Jian ;
Ketterer, Michael E. ;
Hu, Sheng ;
Uchida, Shigeo ;
Wang, Xiaolin .
ANALYTICA CHIMICA ACTA, 2017, 995 :1-20
[6]   A first transect of 236U in the North Atlantic Ocean [J].
Casacuberta, N. ;
Christl, M. ;
Lachner, J. ;
van der Loeff, M. Rutgers ;
Masque, P. ;
Synal, H. -A. .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2014, 133 :34-46
[7]   A depth profile of uranium-236 in the Atlantic Ocean [J].
Christl, Marcus ;
Lachner, Johannes ;
Vockenhuber, Christof ;
Lechtenfeld, Oliver ;
Stimac, Ingrid ;
van der Loeff, Michiel Rutgers ;
Synal, Hans-Arno .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2012, 77 :98-107
[8]   Recent contributions to the rapid screening of radionuclides in emergency responses and nuclear forensics [J].
Croudace, Ian W. ;
Warwick, Phillip E. ;
Reading, David G. ;
Russell, Benjamin C. .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2016, 85 :120-129
[9]   236U/238U and 240Pu/239Pu isotopic ratios in small (2 L) sea and river water samples [J].
Eigl, R. ;
Srncik, M. ;
Steier, P. ;
Wanner, G. .
JOURNAL OF ENVIRONMENTAL RADIOACTIVITY, 2013, 116 :54-58
[10]   Simultaneous uranium/plutonium separation and direct isotope ratio measurements by using CO2 as the gas in a collision/reaction cell based MC-ICPMS [J].
Gourgiotis, A. ;
Granet, M. ;
Isnard, H. ;
Nonell, A. ;
Gautier, C. ;
Stadelmann, G. ;
Aubert, M. ;
Durand, D. ;
Legand, S. ;
Chartier, F. .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2010, 25 (12) :1939-1945