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Abstract
A project has been undertaken at Pacific Northwest National Laboratory (PNNL) to tailor a series of efficient chemical separations to allow the rapid quantification of gamma-ray emitting isotopes in mixed fission product (MFP) samples. In support of that goal, modeling of singles and coincident gamma-ray spectra that would result from various chemical separation strategies has been performed. These simulated spectra have identified likely instances of spectral interference and have provided an estimate of the time window available for the detection of radionuclides following various chemical separation schemes. A description of results to date is presented here, demonstrating the utility of this approach for improved processing and analysis of fission product samples.
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