Design and Assembly of MiniFuel Targets for Characterization of High Burnup UO2 Specimens Irradiated in the High Flux Isotope Reactor
Explore the source record for details and available documents.
11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
Engineering topics
Kercher, Andrew
Publications and source records attributed to Kercher, Andrew.
Phase Field Sintering Simulations of Tagged UO 2
Isotopic taggants are being considered as an additive for UO 2 manufacturing to improve nuclear security. Before taggants can be adopted, it must be determined whether taggants have any effect on the fuel microstructure or performance. As part of this effort, a grand potential formulation of the phase field method was used to model untagged, Cr-tagged, and Fe-tagged UO 2 . The simulations were compared to determine whether the taggants had any effect on fuel density or grain size. The results suggest that the taggants will not affect the density or grain size, but these findings may not be reliable because of high uncertainty. Causes of the uncertainty were discussed, and future work is proposed to reduce the model uncertainty.
11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
Nuclear fuel irradiation testbed for nuclear security applications
The nuclear security community has long been interested in the identification and quantification of nuclear material signatures to understand a material’s provenance, use, and ultimate application. New forensics signatures and methods intended for non-traditional or advanced nuclear fuel applications require fuel irradiation experiments to demonstrate viability and validity. Integral fuel irradiations have historically required significant costs and long timelines to design, irradiate, and characterize. This paper describes how a recently developed nuclear fuel irradiation testbed can be used to provide a low cost, rapid turnaround, modular test environment for irradiation and evaluation of nuclear fuel specimens for nuclear security applications. The irradiation testbed houses six small ‘MiniFuel’ samples within hermetically sealed capsules inside targets that can be removed in between each ∼25-day operating cycle of the High Flux Isotope Reactor (HFIR). As many as nine targets can be irradiated using a single irradiation position (reflector region) in HFIR, allowing for varying irradiation temperatures and burnups. A suite of hot cell capabilities have been established to perform post-irradiation examination for measuring performance (e.g., fuel swelling, fission gas release) and facilitating experiment disassembly for subsequent property measurements, microstructural analysis, or chemical assay. This new testbed allows fuel irradiations to be conducted on an accelerated timeframe to enable rapid proof of concept testing and to provide reference material for nuclear fuel security applications. Recent applications using this testbed include the testing of isotopic taggants in UO 2 fuel (intentional forensics), testing of U-10Mo fuel for down-conversion of highly enriched uranium–fueled reactors, and the production of irradiated UO 2 fuel material for signature analysis of its isotopic composition (plutonium, fission gases, etc.).
98 NUCLEAR DISARMAMENT, SAFEGUARDS, AND PHYSICAL P↗
Correlative electron and ion beam analysis of the electrochemical performances of LiV 3 O 8 cathode films as a function of microstructures
Degradation mechanisms in LiV 3 O 8 cathode films (~500 nm) with different initial microstructures i.e., globular nanocrystals in amorphous matrix and needle-like nanocrystals, synthesized by annealing the cathodes at 150 °C and 300 °C for 6 h are studied by Transmission Electron Microscopy (TEM) and Auger Electron Spectroscopy (AES). In addition, a unique in-situ combination of TEM and Secondary Ion Mass Spectrometry (SIMS) imaging techniques, namely Parallel Ion and Electron beam Spectrometry (PIES) is carried out to measure the 3D distribution of V and Li with nanoscale resolution. These characterization studies focus on correlating the pre- and post-cycling microstructure to observed electrochemical performance. The LiV 3 O 8 cathode film with needle-like nanocrystals (300 °C) shows a higher initial capacity but it degrades rapidly compared to the film with globular nanocrystals embedded in amorphous matrix (150 °C). We observed that LiV 3 O 8 films with needle-like nanocrystals are more susceptible to cathode decohesion and vanadium dissolution than the films with globular nanocrystals embedded in amorphous matrix, explaining the differences in their electrochemical performance. The findings from this study have relevance to the development of thin film electrode microstructures for high capacity and cyclic stability.
25 ENERGY STORAGE↗