腐蚀
材料科学
降级(电信)
熔盐
相(物质)
四方晶系
陶瓷
矿化(土壤科学)
盐(化学)
冶金
无机化学
化学
有机化学
计算机科学
电信
氮气
作者
Jinshuang Wang,Yinghui Wang,Mengdi Chen,Chen Wang,Yongsheng Yu,Yongshang Tian,Bing Liu,Qiangshan Jing
标识
DOI:10.1016/j.surfcoat.2022.128352
摘要
In this study, (Ce 0.15 Ti 0.05 )Zr 0.80 O 2 (CTZ) with the tetragonal (t) phase was fabricated by solid-state reaction, and the destabilization resistance of CTZ ceramic was investigated in V 2 O 5 , and Na 2 SO 4 + V 2 O 5 molten salts , respectively. After CTZ was corroded in V 2 O 5 molten salt at 700 °C for 2 h, ZrV 2 O 7 and CeVO 4 were formed, and the t phase was the main crystalline phase on the CTZ surface. After CTZ was corroded in V 2 O 5 molten salt at 800 °C or 900 °C for 2 h, the amount of CeVO 4 increased significantly, and CTZ surface underwent a more corrosion degradation than at 700 °C. After CTZ was corroded in Na 2 SO 4 + V 2 O 5 molten salts at 700 °C or 800 °C for 2 h, the hot corroded products were m-ZrO 2 and CeVO 4 . However, after CTZ was corroded in Na 2 SO 4 + V 2 O 5 molten salts at 800 °C for 10 h or 900 °C for 2 h or 10 h, a new phase of CeO 2 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. • The destabilization of CTZ ceramic was mainly caused by the chemical interaction and phase transformation. • Corrosion products and corrosion degree are closely related to the type of corrosion salts, the corrosion temperature and heat duration. • The morphologies of CeVO 4 exhibited significant difference. It evolved from the V 2 O 5 corrosion environment is polyhedral, while it was rod-like in the Na 2 SO 4 +V 2 O 5 corrosion environment.
科研通智能强力驱动
Strongly Powered by AbleSci AI