A prominent driving force for the spallation of thermal barrier coatings: Chemistry dependent phase transformation of the bond coat

被引:18
作者
Wu, L. T. [1 ]
Wu, R. T. [1 ]
Xiao, P. [2 ]
Osada, T. [1 ]
Lee, K. I. [2 ]
Bai, M. [2 ]
机构
[1] Natl Inst Mat Sci, Tsukuba, Ibaraki, Japan
[2] Univ Manchester, Sch Mat, Manchester M1 7HS, Lancs, England
关键词
Phase transformation; Platinum aluminide; Interfacial adhesion; Rumpling; NICKEL-ALUMINIDE COATINGS; MARTENSITIC-TRANSFORMATION; MECHANICAL-BEHAVIOR; RUMPLING MECHANISM; DEFORMATION; SUPERALLOYS; OXIDATION; SYSTEMS;
D O I
10.1016/j.actamat.2017.06.037
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The influence of substrate and bond coat chemistry on the degradation mechanism leading to the early spallation of thermal barrier coatings (TBCs) has not been well understood despite years of research effort. This is largely due to the sheer number of factors (i.e. interfacial rumpling and oxide growth kinetics) that all seem to contribute to the degradation of TBCs. To clarify the chemical effect, extensive characterizations and in-depth analysis near the oxide-bond coat interface, were carried out on the isothermally exposed TBC specimens. It is evident that the formation of gamma' along the grain boundaries can significantly enhance rumpling, while martensitic transformation during cooling creates out-of-plane stresses and causes crack nucleation at the oxide-bond coat interface. These partial phase transformations in the beta bond coat system were determined to be a prominent driving force for the TBC spallation. To prevent the early spallation of TBCs, it is necessary to minimize the formation rate of gamma' and martensitic phases, which can be achieved by tailoring the inherent substrate/bond coat composition as elucidated in this paper. (C) 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:22 / 35
页数:14
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