Precise U and Pu Isotope Ratio Measurements in Nuclear Samples by Hyphenating Capillary Electrophoresis and MC-ICPMS
Author(s) -
Benoît Martelat,
Hélène Isnard,
Laurent Vio,
Erwan Dupuis,
Térence Cornet,
Anthony ll,
Fredéric Chartier
Publication year - 2018
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.8b01884
Subject(s) - chemistry , spent nuclear fuel , mass spectrometry , capillary electrophoresis , inductively coupled plasma mass spectrometry , analytical chemistry (journal) , radiochemistry , isotope , thermal ionization mass spectrometry , analyte , chromatography , ion source , nuclear chemistry , nuclear physics , ion , physics , organic chemistry
Precise isotopic and elemental characterization of spent nuclear fuel is a major concern for the validation of the neutronic calculation codes and waste management strategy in the nuclear industry. Generally, the elements of interest, particularly U and Pu which are the two major elements present in spent fuel, are purified by ion exchange or extractant resins before off-line measurements by thermal ionization mass spectrometry. The aim of the present work was to develop a new analytical approach based on capillary electrophoresis (CE) hyphenated to a multicollector inductively coupled plasma mass spectrometer (MC-ICPMS) for online isotope ratio measurements. An electrophoretic separation protocol of U, Pu, and the fraction containing fission products and minor actinides (Am and Cm) was developed using acetic acid as the electrolyte and complexing agent. The instrumentation for CE was designed to be used in a glovebox, and a laboratory-built interface was developed for hyphenation with MC-ICPMS. The separation was realized with only a few nL of a solution of spent nuclear fuel, and the reproducibilities obtained on the U and Pu isotope ratios were on the order of a few ‰ which is comparable to those obtained by thermal ionization mass spectrometry (TIMS). This innovative protocol allowed a tremendous reduction of the analyte masses from μg to ng and also a drastic reduction of the liquid waste production from mL to μL. In addition, the time of analysis was shorted by at least a factor of three. All of these improved parameters are of major interest for nuclear applications.
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