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.
Original language | English (US) |
---|---|
Journal | Ceramics International |
DOIs | |
State | Accepted/In press - 2024 |
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Process Chemistry and Technology
- Surfaces, Coatings and Films
- Materials Chemistry
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Konnik, M. T., Oldham, T., Panerai, F. (Accepted/In press). The effect of nitrogen on the isothermal oxidation of substoichiometric zirconium carbide: Microstructural and spectroscopic investigations. Ceramics International. https://doi.org/10.1016/j.ceramint.2024.04.387
The effect of nitrogen on the isothermal oxidation of substoichiometric zirconium carbide: Microstructural and spectroscopic investigations. / Konnik, Matthew T.; Oldham, Trey; Panerai, Francesco et al.
In: Ceramics International, 2024.
Research output: Contribution to journal › Article › peer-review
Konnik, MT, Oldham, T, Panerai, F 2024, 'The effect of nitrogen on the isothermal oxidation of substoichiometric zirconium carbide: Microstructural and spectroscopic investigations', Ceramics International. https://doi.org/10.1016/j.ceramint.2024.04.387
Konnik MT, Oldham T, Panerai F, Stephani KA. The effect of nitrogen on the isothermal oxidation of substoichiometric zirconium carbide: Microstructural and spectroscopic investigations. Ceramics International. 2024. doi: 10.1016/j.ceramint.2024.04.387
Konnik, Matthew T. ; Oldham, Trey ; Panerai, Francesco et al. / The effect of nitrogen on the isothermal oxidation of substoichiometric zirconium carbide : Microstructural and spectroscopic investigations. In: Ceramics International. 2024.
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title = "The effect of nitrogen on the isothermal oxidation of substoichiometric zirconium carbide: Microstructural and spectroscopic investigations",
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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T2 - Microstructural and spectroscopic investigations
AU - Konnik, Matthew T.
AU - Oldham, Trey
AU - Panerai, Francesco
AU - Stephani, Kelly A.
N1 - Publisher Copyright:© 2024 The Authors
PY - 2024
Y1 - 2024
N2 - 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.
AB - 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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