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Separation techniques for low-level determination of actinides in soil samples
Affiliation:1. Department of Earth and Planetary Sciences, Macquarie University, NSW 2109, Australia;2. Department of Earth Sciences, University of Oxford, South Parks Road, Oxford OX1 3AN, UK;3. Department of Nuclear Physics, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601, Australia
Abstract:The separation methods for soil samples applied at PSI are based on extraction chromatography and ion exchange. After sample leaching, the actinides are pre-concentrated via precipitation using oxalic acid. Besides the classical separation methods applying the extraction chromatographic resins U/TEVA™ (for U, Th), TRU™ (Pu, Am), new methods were recently implemented to increase the radiochemical recovery of particularly trivalent Am and Cm. These methods do not require initial reduction of Pu(IV) to Pu(III) but stabilize Pu on the tetravalent oxidation state using a mixture of NaNO2/H2O2 in strong acidic medium. The Pu-fraction is then fixed along with Th onto Dowex AG 1-X2 anion exchanger resin. Th is eluted via complexation with 10 M HCl, Pu via reduction with HI. The fractions of Am+Cm and U are loaded onto DGA™ resin. This resin shows extraordinary high distribution coefficients (k′-values) exceeding 104 (for Am) in strong nitric acid medium. The separation between U and Am is obtained quantitatively by decreasing the HNO3 concentration from 3 to 0.25 M (stripping of the U-fraction) while Am can be easily eluted thereafter using 0.25 M HCl as complexation compound.
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