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An Automated SeaFAST ICP-DRC-MS Method for the Determination of 90Sr in Spent Nuclear Fuel Leachates.
Vicente Vilas, Víctor; Millet, Sylvain; Sandow, Miguel; Iglesias Pérez, Luis; Serrano-Purroy, Daniel; Van Winckel, Stefaan; Aldave de Las Heras, Laura.
Affiliation
  • Vicente Vilas V; European Commission, Joint Research Centre, Directorate for Nuclear Safety and Security, D-76125 Karlsruhe, Germany.
  • Millet S; European Commission, Joint Research Centre, Directorate for Nuclear Safety and Security, D-76125 Karlsruhe, Germany.
  • Sandow M; European Commission, Joint Research Centre, Directorate for Nuclear Safety and Security, D-76125 Karlsruhe, Germany.
  • Iglesias Pérez L; Karlsruhe Institute for Technology, Institute for Nuclear Waste Disposal, D-76021 Karlsruhe, Germany.
  • Serrano-Purroy D; European Commission, Joint Research Centre, Directorate for Nuclear Safety and Security, D-76125 Karlsruhe, Germany.
  • Van Winckel S; European Commission, Joint Research Centre, Directorate for Nuclear Safety and Security, D-76125 Karlsruhe, Germany.
  • Aldave de Las Heras L; European Commission, Joint Research Centre, Directorate for Nuclear Safety and Security, D-76125 Karlsruhe, Germany.
Molecules ; 25(6)2020 Mar 21.
Article in En | MEDLINE | ID: mdl-32245155
ABSTRACT
To reduce uncertainties in determining the source term and evolving condition of spent nuclear fuel is fundamental to the safety assessment. ß-emitting nuclides pose a challenging task for reliable, quantitative determination because both radiometric and mass spectrometric methodologies require prior chemical purification for the removal of interfering activity and isobars, respectively. A method for the determination of 90Sr at trace levels in nuclear spent fuel leachate samples without sophisticated and time-consuming procedures has been established. The analytical approach uses a commercially available automated pre-concentration device (SeaFAST) coupled to an ICP-DRC-MS. The method shows good performances with regard to reproducibility, precision, and LOD reducing the total time of analysis for each sample to 12.5 min. The comparison between the developed method and the classical radiochemical method shows a good agreement when taking into account the associated uncertainties.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spectrophotometry, Atomic / Mass Spectrometry / Strontium Radioisotopes / Radioactive Waste Type of study: Prognostic_studies Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2020 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spectrophotometry, Atomic / Mass Spectrometry / Strontium Radioisotopes / Radioactive Waste Type of study: Prognostic_studies Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2020 Document type: Article Affiliation country: Germany