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Determination of long-lived radionuclides in radioactive wastes from the IEA-R1 nuclear research reactor

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Abstract

Ion-exchange resins and activated charcoal beds are employed for purification of the cooling water that is pumped through the core of pool type nuclear research reactors. Once expended, these media are replaced and become radioactive wastes that contain low concentrations of long-lived fission and activation products, uranium isotopes and transuranium elements. Determination of the radioactive inventory is of paramount importance in the management of such radioactive wastes, which, besides high-energy photon emitters that can be identified and quantified directly by gamma-ray spectrometry, also contain pure alpha, pure beta and low-energy photon emitters whose quantitative determination require radiochemical separation. These later are collectively known as difficult to measure (DTM) radionuclides. A characterization program embracing the DTM radionuclides is currently in progress for spent ion-exchange resins and activated charcoal beds that were definitively withdrawn from the water cleanup system of the IEA-R1 nuclear research reactor. Radiochemical methods used in the characterization program include separations with specific anionic resins, chromatographic extractions and co-precipitation, which enabled the measurement of the activity concentrations of 90Sr, 234U, 235U, 238U, 238Pu, 239+240Pu, 241Pu, 241Am and 244Cm. An enhanced retention of uranium and transuranium elements was observed in the activated charcoal compared to the ion-exchange resins as a result of the tendency of actinides to undergo hydrolysis in aqueous solutions.

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Acknowledgments

The authors gratefully acknowledge support from the staff of the Radioactive Waste Management Department of IPEN/CNEN-SP in sampling the wastes.

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Correspondence to L. A. A. Terremoto.

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Taddei, M.H.T., Vicente, R., Marumo, J.T. et al. Determination of long-lived radionuclides in radioactive wastes from the IEA-R1 nuclear research reactor. J Radioanal Nucl Chem 295, 951–957 (2013). https://doi.org/10.1007/s10967-012-1865-0

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  • DOI: https://doi.org/10.1007/s10967-012-1865-0

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