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Conference Spotlight
Nuclear Energy Conference & Expo (NECX)
September 8–11, 2025
Atlanta, GA|Atlanta Marriott Marquis
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Powering the future: How the DOE is fueling nuclear fuel cycle research and development
As global interest in nuclear energy surges, the United States must remain at the forefront of research and development to ensure national energy security, advance nuclear technologies, and promote international cooperation on safety and nonproliferation. A crucial step in achieving this is analyzing how funding and resources are allocated to better understand how to direct future research and development. The Department of Energy has spearheaded this effort by funding hundreds of research projects across the country through the Nuclear Energy University Program (NEUP). This initiative has empowered dozens of universities to collaborate toward a nuclear-friendly future.
P. Mohanakrishnan, H. C. Huria
Nuclear Science and Engineering | Volume 68 | Number 2 | November 1978 | Pages 220-226
Technical Note | doi.org/10.13182/NSE78-A27294
Articles are hosted by Taylor and Francis Online.
A theoretical analysis of the reactivities of experimentally measured uniform light-water-moderated and -reflected PuO2 in UO2 lattices and Pu(NO3)4 solutions is presented here. The mixed-oxide single-rod lattices are homogenized by the use of multigroup integral transport theory, and diffusion theory is used for the cylindrical core calculations. The cross sections are derived from the WIMS library. The homogeneous spherical Pu(NO3)4 solutions are analyzed by discrete-ordinates transport theory. Due to the small size of these assemblies, it is necessary that one-dimensional core calculations also be performed with a cross-section energy-group structure that can accurately represent neutron slowing down and thermalization at the core-reflector interface. Due to the uncertainty present in the Battelle Northwest Laboratories analyses of the mixed-oxide lattices, the agreement of our predictions for these lattices with measurement is considered to be more satisfactory. Our reactivity predictions agree generally within +0.6% of measurements for the mixed-oxide lattices and within 1% for the solution systems.