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Simulations show nichrome microstructure could impact corrosion
Researchers at Pennsylvania State University have reported evidence that small adjustments to a material’s atomic-level ordering can significantly affect the rate and extent of corrosion, even with identical baseline chemical compositions.
For the study, published recently in Corrosion Science, the team ran simulations for nichrome-based alloys, which have excellent strength, creep resistance, and tolerance to radiation-induced degradation, making them top candidates for use in molten salt reactors and other advanced energy systems.
Ian J. Hastings, Elio Mizzan, Alan M. Ross, John R. Kelm, Real J. Chenier, D. H. Rose, J. Novak
Nuclear Technology | Volume 68 | Number 1 | January 1985 | Pages 40-47
Technical Paper | Nuclear Fuel | doi.org/10.13182/NT85-A33565
Articles are hosted by Taylor and Francis Online.
Fragments of UO2 fuel pellets extracted from irradiated elements were heated in air at 175 to 275 °C for times up to 800 h. Unirradiated pellets and fragments were studied for comparison. Pretest burnup of the irradiated fuel was typically 190 MW-h/kgU (7900 MWd per tonne of uranium) at a maximum linear power of 45 kW/m. The fuel had been discharged for 1 to 3 yr. The maximum weight gain was at 275 °C, ∼4% in 70 h, indicating 100% conversion to U3O8. The activation energy for the oxidation process at 175 to 275 °C was 130 ± 10 kJ/mol. There was a strong effect of prior irradiation on oxidation rate; the weight gain at 250 °C was about a factor of 6 greater in irradiated compared with unirradiated fuel. There was also an effect of fragment size on oxidation rate. Also, weight gains of fragments from a naturally defected element were less than those for fragments from intact fuel, consistent with prior oxidation in the defected state.