Abstract
The oxidation behavior of hot-pressed sub-stoichiometric zirconium carbide was investigated through isothermal flow-tube furnace experiments at temperatures ranging from 1000 to 1600 °C. Auxiliary gas composition influence on the oxidation of ZrC0.63 was studied by introducing oxygen to substrates held under either pure argon or nitrogen environments. During furnace ramp-up, prior to isothermal oxygen exposure, nitrogen flow was found to infiltrate the substrate resulting in ZrCxNy formation which provided superior oxidation resistance to the as-received ZrC0.63. Ex situ investigation of ceramic-oxide interfacial regions revealed the presence of carbon precipitate in both material sets at treatment temperatures of up to 1400 °C, along with the presence of the ZrCxOy system. At sufficiently high test temperatures, resulting scale formations for the N2/O2 systems were found to be less porous than the Ar/O2 counterparts, with a higher degree of c-/t-ZrO2 crystallites present at room temperature attributed to nitrogen incorporation into the anion sublattice of ZrO2.
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