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Nuclear Criticality Safety
NCSD provides communication among nuclear criticality safety professionals through the development of standards, the evolution of training methods and materials, the presentation of technical data and procedures, and the creation of specialty publications. In these ways, the division furthers the exchange of technical information on nuclear criticality safety with the ultimate goal of promoting the safe handling of fissionable materials outside reactors.
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Chicago, IL|Chicago Marriott Downtown
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Smarter waste strategies: Helping deliver on the promise of advanced nuclear
At COP28, held in Dubai in 2023, a clear consensus emerged: Nuclear energy must be a cornerstone of the global clean energy transition. With electricity demand projected to soar as we decarbonize not just power but also industry, transport, and heat, the case for new nuclear is compelling. More than 20 countries committed to tripling global nuclear capacity by 2050. In the United States alone, the Department of Energy forecasts that the country’s current nuclear capacity could more than triple, adding 200 GW of new nuclear to the existing 95 GW by mid-century.
Mathew W. Swinney, Charles M. Folden III, Ronald J. Ellis, Sunil S. Chirayath
Nuclear Technology | Volume 197 | Number 1 | January 2017 | Pages 1-11
Technical Paper | doi.org/10.13182/NT16-76
Articles are hosted by Taylor and Francis Online.
A terrorist attack using an improvised nuclear device is one of the most serious dangers facing the United States. The work presented here is part of an effort to improve nuclear deterrence by developing a methodology to attribute weapons-grade plutonium to a source reactor by measuring the intrinsic physical characteristics of the interdicted plutonium. In order to demonstrate the developed methodology, plutonium samples were produced from depleted uranium dioxide (DUO2) surrogates irradiated in a fast-neutron environment. In order to replicate the neutron flux in a fast-neutron-spectrum reactor and obtain experimental samples emulating weapons-grade plutonium produced in the blanket of a fast breeder reactor, DUO2 samples were placed in a gadolinium sheath and irradiated in the High Flux Isotope Reactor (HFIR) at Oak Ridge National Laboratory. Previous computational work on this topic identified several fission products that could be used to distinguish between reactor types (fast and thermal reactors), specifically: 137Cs, 134Cs, 154Eu, 125Sb, 144Ce, 85Rb, 147Pm, and 150Sm along with the plutonium isotopes. Simulations of the fast neutron irradiation of the DUO2 fuel surrogates in the HFIR were carried out using the Monte Carlo radiation transport code MCNPX 2.7. Comparisons of the predicted values of plutonium and fission product concentrations to destructive and nondestructive assay measurements of neutron-irradiated DUO2 surrogates are presented here. The agreement between the predictions and gamma spectroscopic measurements in general were within 10% for 134Cs, 137Cs, 154Eu, and 144Ce. Additional experimental results (mass spectroscopy) agreed to within 5% for the following isotopes: 85Rb, 147Pm, 150Sm, 154Eu, 148Nd, 144Ce, and 239Pu. Two indicator isotopes previously suggested to differentiate between the reactor types were ruled out for use in the attribution methodology; 125Sb was ruled out due to the difficulty in accurately predicting its concentration, and 242Pu was ruled out because of its low content in weapons-grade plutonium.