October 1, 2009
Journal Article

Separation and Quantification of Chemically Diverse Analytes in Neutron Irradiated Fissile Materials

Abstract

Quantitative measurement of fission and activation products resulting from neutron irradiation of fissile materials is of interest for applications in environmental monitoring, nuclear waste management, and national security. To overcome mass and spectral interferences, and the relative small quantities of some target analytes, an extensive series of chemical separations is necessary. Based on established separations processes involving co-precipitation, solvent extraction, and ion-exchange and extraction chromatography, we have been evaluating and optimizing a proposed sequence of separation steps to allow for the timely quantification of analytes of interest. For simplicity, much of the chemical separation development work has been performed using stable elements as surrogates for the radioactive material. We have recently evaluated the optimized procedures using an irradiated sample to examine the adequacy of separations for measurement of desired analytes by gamma spectrometry. Here we present the results of this evaluation and describe the radiochemical separations utilized.

Revised: June 23, 2010 | Published: October 1, 2009

Citation

Douglas M., J.I. Friese, L.R. Greenwood, O.T. Farmer, L. Thomas, T.C. Maiti, and E.C. Finn, et al. 2009. Separation and Quantification of Chemically Diverse Analytes in Neutron Irradiated Fissile Materials. Journal of Radioanalytical and Nuclear Chemistry 282, no. 1:63-68. PNNL-SA-66026.