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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.
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页数:9
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