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The influence of bond coat surface roughness on chemical failure and delamination in TBC systems
Author(s) -
Taylor M. P.,
Pragnell W. M.,
Evans H. E.
Publication year - 2008
Publication title -
materials and corrosion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.487
H-Index - 55
eISSN - 1521-4176
pISSN - 0947-5117
DOI - 10.1002/maco.200804135
Subject(s) - materials science , aluminium , delamination (geology) , asperity (geotechnical engineering) , composite material , nucleation , oxide , coating , metallurgy , surface roughness , thermal barrier coating , surface finish , isothermal process , forensic engineering , subduction , paleontology , thermodynamics , physics , biology , tectonics , chemistry , organic chemistry , engineering
Localised loss of aluminium from the bond coat within thermal barrier coating (TBC) systems is a critical factor determining the lifetime of these coatings. In this paper, it will be demonstrated that electroplated MCrAlY bond coats with asperities of high aspect ratios can experience premature chemical failure during isothermal exposures at 1100 °C in air. This can result in the rapid conversion of the asperity into Co‐ and Cr‐rich oxides. The enhanced aluminium depletion within these asperities, which leads to chemical failure, is a consequence of their increased surface area coupled with a limited physical access to the reservoir of aluminium in the bulk of the bond coat. This process has been demonstrated using the 2‐D finite‐difference model ODIN which predicts a depletion to less than 1 at% aluminium within a typical asperity after 1 h exposure at 1100 °C. The results also show that the aluminium content of the bulk of the bond coat is sufficient to enable the formation of a continuous protective alumina underneath these regions, as observed experimentally. It is suggested that the volume increase associated with the conversion of the bond coat asperities into breakaway oxide results in out‐of‐plane tensile stress development at the oxidation temperature. These stresses are anticipated to be at a maximum between the oxide asperities and are thought to nucleate small, sub‐critical cracks at these locations at temperature. Further delamination will occur during cooling both by the extension of these cracks and by the growth of crack‐like defects within the porous breakaway oxides.