Separation and analysis of lanthanides by isotachophoresis coupled with inductively coupled plasma mass spectrometry

被引:27
作者
Vio, Laurent [1 ,4 ]
Cretier, Gerard [4 ]
Chartier, Frederic [2 ]
Geertsen, Valerie [3 ]
Gourgiotis, Alkiviadis [1 ]
Isnard, Helene [1 ]
Rocca, Jean-Louis [4 ]
机构
[1] CEA Saclay, DEN DPC SEARS LANIE, F-91191 Gif Sur Yvette, France
[2] CEA Saclay, DEN DPC, F-91191 Gif Sur Yvette, France
[3] CEA Saclay, DSM IRAMIS SIS2M LIONS, F-91191 Gif Sur Yvette, France
[4] Univ Lyon, Inst Sci Analyt UMR CNRS 5280, Villeurbanne, France
关键词
Isotachophoresis; Inductively coupled plasma mass spectrometry; Coupled techniques; Lanthanides; Fission products; Nuclear industry; SPENT NUCLEAR-FUELS; PERFORMANCE LIQUID-CHROMATOGRAPHY; CAPILLARY-ZONE-ELECTROPHORESIS; RARE-EARTH IONS; ICP-MS; SPALLATION REACTIONS; FISSION-PRODUCTS; ACTINIDES; SAMPLES; COMPLEXES;
D O I
10.1016/j.talanta.2012.06.041
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This study is a large project initiated by the French Nuclear Agency, and concerns the development of a new electrolyte system for the separation of lanthanides by isotachophoresis. This new system is based on a leading electrolyte that incorporates 2-hydroxy-2-methylbutyric acid as complexing agent. The optimization of separation conditions (complexing agent concentration, pH, capillary dimensions, injection conditions, and current intensity) performed by experiments on a commercial capillary instrument with contactless conductivity detection, which allows to improve the separation of 13 lanthanides (La to Lu, except Pm and Ho). We have also directly coupled the isotachophoresis to an inductively coupled plasma mass spectrometer to visualize the mono-elementary elution bands and demonstrate the potentiality of the method for isotope ratio measurements. The application to a simulated solution representative of a fraction of fission products present in a MOX spent fuel is presented in this paper to demonstrate the possible application in future on nuclear fuel samples. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:586 / 593
页数:8
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