Thermal Properites and Thermal Shock Resistance of Liquid Phase Sintered ZrC-Mo Cermets
Abstract
The linear thermal expansion coefficient (CTE), heat capacity, and thermal conductivity, were investigated as a function of temperature for hot pressed ZrC and liquid phase sintered ZrC-Mo cermets. The ZrC and the ZrC-Mo cermets had the same CTE at 50 °C (not, vert, similar5.1-5.5 ppm °C−1), but the CTE of ZrC increased to not, vert, similar12.2 ppm °C−1 at 1000 °C compared to not, vert, similar7.2-8.5 ppm °C−1 for the ZrC-Mo cermets. Heat capacity was calculated using a rule of mixtures and previously reported thermodynamic data. Thermal diffusivity was measured with a laser flash method and was, in turn, used to calculate thermal conductivity. Thermal conductivity increased linearly with increasing temperature for all compositions and was affected by solid solution formation and carbon deficiency of the carbide phases. Hot pressed ZrC had the highest thermal conductivity (not, vert, similar30-37 W m−1 K−1). The nominally 20 and 30 vol% Mo compositions of the ZrC-Mo cermets had a lower thermal conductivity, but the thermal conductivity generally increased with increasing Mo content. Water quench thermal shock testing showed that ZrC-30 vol% Mo had a critical temperature difference of 350 °C, which was not, vert, similar120 °C higher than ZrC. This increase was due to the increased toughness of the cermet compared to ZrC.
Recommended Citation
S. E. Landwehr et al., "Thermal Properites and Thermal Shock Resistance of Liquid Phase Sintered ZrC-Mo Cermets," Materials Chemistry and Physics, Elsevier, Jun 2009.
The definitive version is available at https://doi.org/10.1016/j.matchemphys.2009.02.012
Department(s)
Materials Science and Engineering
Keywords and Phrases
Thermal Properties; Thermal Shock; Zirconium Carbide; Molybdenum
International Standard Serial Number (ISSN)
0254-0584
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2009 Elsevier, All rights reserved.
Publication Date
01 Jun 2009