Phase transformation and bond coat oxidation behavior of plasma-sprayed zirconia thermal barrier coating

• Published in: Surface & coatings technology Vol. 124; no. 1; pp. 1 - 12
• Main Authors: Lee, C.H., Kim, H.K., Choi, H.S., Ahn, H.S.
• Format: Journal Article
• Language: English
• Published: Lausanne Elsevier B.V 01.02.2000; Elsevier
• Subjects: Bond coat oxidation; Composition and phase identification; Condensed matter: structure, mechanical and thermal properties; Exact sciences and technology; Phase transformation; Physics; Surfaces and interfaces; thin films and whiskers (structure and nonelectronic properties); Thermal barrier effect; Thermal expansion mismatch; Thin film structure and morphology; Phase transformation; Thermal barrier effect; Thermal expansion mismatch; Bond coat oxidation; Thin films; Zirconia; Thermal expansion; Phase transformations; Thermal accommodation; Thermal barriers; Plasma arc spraying; Oxidation; Experimental study; Coatings
• ISSN: 0257-8972; 1879-3347
• DOI: 10.1016/S0257-8972(99)00517-4

ZrO 2–CeO 2–Y 2O 3 and ZrO 2–Y 2O 3 thermal barrier coatings were prepared using the air plasma spray process. Phase transformation in the ceramic top coating, bond coat oxidation and thermal barrier properties were investigated to compare ZrO 2–CeO 2–Y 2O 3 with ZrO 2–Y 2O 3 at 1300°C under high temperature thermal cycles. In the as-sprayed condition, both coatings showed a 7∼11% porosity fraction and typical lamellar structures formed by continuous wetting by liquid droplets. In the ZrO 2–CeO 2–Y 2O 3 coating, the phase ratio of tetragonal to cubic phase was 75:25 and ZrO 2–Y 2O 3 coating had a 100% non-transformable tetragonal phase. There was no monoclinic phase in either coating. However, the phase ratio of the coatings was changed after 1300°C thermal cycles. In the ZrO 2–CeO 2–Y 2O 3 coating, the ratio of tetragonal to cubic was changed to 88:12 and a monoclinic phase was still not detected, but a 10∼19% monoclinic phase had formed in the ZrO 2–Y 2O 3 coating. The life of the coatings was found to be strongly dependent on the temperature which the bond coat experienced during exposure to a peak temperature of 1300°C. When the bond coat experienced a temperature higher than 1100°C, the useful life of both thermal barrier coatings was decreased drastically and this was related to the oxidation behavior of the bond coat. Al 2O 3 formed preferentially along the bond and top coat interface and the other oxides such as NiO and Ni(Cr,Al) 2O 4 spinel, which were believed to decrease the coating life by oxide growth stress, formed rapidly at the top coat side of the interface at temperature higher than 1100°C. The thermally shocked ZrO 2–Y 2O 3 coating exhibited a non-linear thermal expansion curve which was probably due to a reversible tetragonal–monoclinic transformation. The ZrO 2–CeO 2–Y 2O 3 coating was found to have better thermal cycling behavior than the ZrO 2–Y 2O 3 coating. The reason for this could be that there was no phase transformation from tetragonal to monoclinic phase, which induces volume expansion. The thermal expansion mismatch is smaller and the effect of oxide growth stress is relatively small because of better thermal insulation.