Degradation of CeO2 and TiO2 co-stabilized ZrO2 by the V2O5 molten salts and Na2SO4 + V2O5 molten salts

被引:6
|
作者
Wang, Jinshuang [1 ]
Wang, Yinghui [1 ]
Chen, Mengdi [1 ]
Wang, Chen [1 ]
Yu, Yongsheng [1 ]
Tian, Yongshang [1 ]
Liu, Bing [2 ]
Jing, Qiangshan [1 ]
机构
[1] Xinyang Normal Univ, Henan Prov key Lab Utilizat Nonmet Mineral south H, Xinyang 464000, Peoples R China
[2] Inst Dev & Applicat Shangtianti Nonmet Min Technol, Xinyang 464117, Peoples R China
基金
中国国家自然科学基金;
关键词
TBCs; ZrO2; Chemical interaction; Mineralization effect; HOT CORROSION BEHAVIOR; THERMAL BARRIER COATINGS; MICROSTRUCTURE EVOLUTION; PHYSICAL PROPERTIES; TETRAGONAL PHASE; ZIRCONIA; YTTRIA; CERIA; CERAMICS; SYSTEM;
D O I
10.1016/j.surfcoat.2022.128352
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this study, (Ce0.15Ti0.05)Zr0.80O2 (CTZ) with the tetragonal (t) phase was fabricated by solid-state reaction, and the destabilization resistance of CTZ ceramic was investigated in V2O5, and Na2SO4 + V2O5 molten salts, respectively. After CTZ was corroded in V2O5 molten salt at 700 degrees C for 2 h, ZrV2O7 and CeVO4 were formed, and the t phase was the main crystalline phase on the CTZ surface. After CTZ was corroded in V2O5 molten salt at 800 degrees C or 900 degrees C for 2 h, the amount of CeVO4 increased significantly, and CTZ surface underwent a more corrosion degradation than at 700 degrees C. After CTZ was corroded in Na2SO4 + V2O5 molten salts at 700 degrees C or 800 degrees C for 2 h, the hot corroded products were m-ZrO2 and CeVO4. However, after CTZ was corroded in Na2SO4 + V2O5 molten salts at 800 degrees C for 10 h or 900 degrees C for 2 h or 10 h, a new phase of CeO2 was formed due to the mineralization effect. The destabilization of CTZ ceramic under hot corrosion was mainly caused by the chemical interaction and phase transformation.
引用
收藏
页数:9
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