OXIDATION OF SPENT FUEL IN AIR AT 175 TO 195-DEGREES-C

被引：42

作者：

EINZIGER, RE ^{[1
]}

THOMAS, LE ^{[1
]}

BUCHANAN, HC ^{[1
]}

STOUT, RB ^{[1
]}

机构：

[1] LAWRENCE LIVERMORE NATL LAB, LIVERMORE, CA 94550 USA

来源：

JOURNAL OF NUCLEAR MATERIALS | 1992年 / 190卷

关键词：

D O I：

10.1016/0022-3115(92)90075-V

中图分类号：

T [工业技术];

学科分类号：

08 ;

摘要：

Air oxidation tests were conducted on four LWR spent fuels at 175 and 195-degrees-C to determine the effects of variations in burnup, gas release, and grain size on oxidation of fuel in a potential repository. Weight gains were measured and samples were examined by XRD, ceramography, and TEM. The fuel characteristics were found to affect only the initial oxidation behavior. Following transient behavior related to differences in grain-boundary susceptibility to oxidation, all four fuels progressed toward a metastable state at an oxygen-to-metal (O/M) ratio near 2.4. Unlike nonirradiated UO2 under similar conditions, the fuels oxidized preferentially along grain boundaries and formed U4O9 rather than U3O7. Cubic U4O9, the sole oxidation product observed at times to approximately 38000 h, persisted to oxygen supersaturations as high as UO2.4 with no detectable U3O8 formation. Growth of the U4O9 into the UO2 grains followed parabolic kinetics with an activation energy of 26.6 kcal/mol. Based on reaction kinetics, the time to completely oxidize LWR spent fuel to U4O9 at 95-degrees-C would be greater than 2000 years.

引用

页码：53 / 60

页数：8

共 23 条

[1] SELF-DIFFUSION OF OXYGEN IN URANIUM DIOXIDE [J].