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Abstract

A reliable and fast procedure with minimum waste generation for plutonium determination in soils and sediments is proposed. The procedure combines microwave-assisted digestion for sample dissolution, extraction chromatography for chemical separation, and co-precipitation and alpha-spectrometry for activity measurement. The work is focused on optimisation of the attack and separation steps. The microwave-assisted pre-treatment with mixtures of HF-HNO(3) and HF-HClO(4) achieved total mineralisation of samples in 2h and 30min. For the separation step, the influence on actinide chemical recovery of several ions usually present in soil and sediment matrices, particularly trivalent iron, were studied. The potential reusability of the chromatographic resins was also evaluated and, in spite of the preservation of plutonium recovery and selectivity, some memory effects in consecutive analysis were noticed. The column obstructions during the separation process were solved by using a peristaltic pump. Good accuracy, long-term repeatability (CV 6-7%) and minimum detectable activity (0.11-0.35Bqkg) for the proposed procedure were obtained by analysing 238Pu and 239+240Pu in the sediment CRM IAEA-135.

Additional information

Authors: TORIBIO M, Departament de Química Analítica, Universitat de Barcelona (ES);GARCÍA J F, Departament de Química Analítica, Universitat de Barcelona (ES);RAURET G, Departament de Química Analítica, Universitat de Barcelona (ES);PILVIÖ R, European Commission, Joint Research Centre, Institute for Reference Materials and Measurements, Geel (BE);BICKEL M, European Commission, Joint Research Centre, Institute for Reference Materials and Measurements, Geel (BE);GARCIA J F, Departament de Quimica Analitica, Universitat de Barcelona (ES)
Bibliographic Reference: An article published in: Analytica Chimica Acta, Vol. 447 (1-2), (2001), pp. 179-189
Record Number: 200214489 / Last updated on: 2002-03-28
Category: PUBLICATION
Original language: en
Available languages: en