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
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页数:9
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