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U.S. Department of Energy
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CARBIDE FUEL DEVELOPMENT. Progress Report, April 1, 1963 to June 30, 1963

Technical Report ·
DOI:https://doi.org/10.2172/4055233· OSTI ID:4055233
Experiments were performed to synthesize carbon stabilized (UPu)O. The products were mixtures of dioxideand monoxide-type phases, and contained about 1 wt% carbon. Measurements of lattice parameters vs time indicated a change with (U/sub 0.8/Pu/sub 0.95/)C/sub 0.95/ which was not evident with (U/sub 0.95/Pu/sub 0.05/)C/sub 0.98/. Microprobe analyses of (U/sub 0.8/Pu/sub 0.2/)C/sub 0.95/ + 0.1% Ni concluded that the second-phase sesquicarbide had a higher Pu/U ratio than the monocarbide matrix. Compatibility tests between (U/sub 0.95/Pu/sub 0.05/ )C/sub 0.98/ and type 316 stainless steel, niobium, and niobium-- 1% zirconium alloy for 1000 hr at 816 deg C showed no reaction. Zircaloy-2 is believed to have reacted with the fuel at a temperature as low as 593 deg C, after 1000 hr. Examination of coefficient of expansion specimens after testing showed no change in chemical analysis or microstructure. All (U/sub 0.8/Pu/sub 0.2/)C/sub 0.95/ specimens operated in-pile, close to design conditions. Four specimens reached their target burnups of 4.9 x 10/sup 20/ fissions/cm/sup 3/, and were removed from the reactor for post-irradiation examination. (auth)
Research Organization:
United Nuclear Corp. Development Div., White Plains, N.Y.; Carborundum Co, Niagara Falls, N.Y.
NSA Number:
NSA-18-016426
OSTI ID:
4055233
Report Number(s):
UNC-5068
Country of Publication:
United States
Language:
English