Premium
Hot Corrosion of Stabilized Zirconia Thermal Barrier Coatings and the Role of Mg Inhibitor
Author(s) -
Bajpai Preeti,
Das Amit,
Bhattacharya Prajina,
Madayi Shimjith,
Kulkarni Kaustubh,
Omar Shobit
Publication year - 2015
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/jace.13631
Subject(s) - yttria stabilized zirconia , materials science , cubic zirconia , thermal barrier coating , coating , corrosion , sulfur , porosity , phase (matter) , metallurgy , chemical engineering , microporous material , monoclinic crystal system , layer (electronics) , composite material , chemistry , crystallography , crystal structure , ceramic , organic chemistry , engineering
The 3–4 mol% yttria‐stabilized zirconia ( YSZ ) is widely used as a material for thermal barrier coating; however, the corrosive constituents present in fuel typically result in mechanical disintegration of YSZ coatings. The 3–4 mol% YSZ coatings with respective porosity of ~3% and ~22% have been undertaken with the objective to compare the hot corrosion behavior in air and sulfur‐rich atmospheres. The coatings are kept in contact with V 2 O 5 + MgO powder mixture at 750°C for different dwell times of 24 and 76 h. The samples kept in air have shown intact YSZ layer for both the coatings, whereas a delamination of YSZ layer is observed for high porosity sample kept in sulfur‐rich atmosphere. XRD patterns of all the samples treated in sulfur‐rich atmosphere have indicated a phase transformation in YSZ from tetragonal to monoclinic. However, no such phase transformation has been found for samples treated in air. The V 2 O 5 ‐induced hot corrosion attack on YSZ coating in air has been successfully inhibited by MgO, which forms a thermally stable Mg 3 V 2 O 8 compound. However, in sulfur‐rich atmosphere, MgO is partially consumed to form sulfates, which allows certain fraction of V 2 O 5 to react with Y 2 O 3 causing the degradation of top coat.