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Research on the existence and stability of interfacial tetragonal zirconia formed on zirconium alloys

机译:在锆合金中形成界面四方氧化锆的存在性和稳定性研究

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摘要

Corrosion of zirconium claddings is one of the key properties that must be considered when designing new zirconium alloys. Tetragonal phase is formed on the zirconium matrix during high temperature corrosion and is mainly stabilized near the metal/oxide interface. This phase has a tremendous influence on the corrosion behavior of zirconium alloys. T-ZrO2 phase formed on Zr-0.5Sn-0.15Nb-0.5Fe-0.2 V (N2) and Zr-1.0Sn-1.0Nb-0.3Fe (N36) claddings corroded in 773 K/10.3 MPa steam were studied. A Micro Raman spectrometer was used to analyze the existence and stability of oxide phase before and after dissolution of the zirconium matrix. The result indicates that interfacial t-ZrO2 is not transformed after the removal of the zirconium matrix. Even though most of the stress in m-ZrO2 is released, the lattice distortion in t-ZrO2 still exists, causing this phase to deviate from normal state and maintain its stability. We suggest that the possible reason for stabilizing t-ZrO2 is not the released macroscopic compressive stress, but the existence of small tetragonal grains or large amount of vacancies which can also introduce lattice distortions. The results highlight the important role of oxygen vacancies. Therefore, the stability of t-ZrO2 after matrix dissolution provides us with a chance to observe the microscopic evolution of tetragonal phase at the inner face. T-ZrO2 grows with increasing corrosion time and its intensity drops down after transition. Its microscopic distribution seems to be related to oxide particles and interfacial waviness. (C) 2019 Elsevier B.V. All rights reserved.
机译:锆覆层的腐蚀是设计新的锆合金时必须考虑的关键特性之一。在高温腐蚀期间,在锆基质上形成四边形相,主要稳定在金属/氧化物界面附近。该阶段对锆合金的腐蚀行为有巨大影响。研究了在773k / 103MPa蒸汽中腐蚀的Zr-0.5Sn-0.15Nb-0.5Fe-0.2V(N2)和Zr-1.0Sn-1.0NB-0.3Fe(N36)包层上形成的T- ZrO2相。微拉曼光谱仪用于分析氧化锆基质溶解前后氧化物相的存在和稳定性。结果表明在除去锆基质之后不会改变界面T-ZrO2。尽管M-ZrO2中的大部分应力被释放,但T-ZrO2中的晶格变形仍然存在,导致该相位偏离正常状态并保持其稳定性。我们建议稳定T-ZrO2的可能原因不是释放的宏观压缩应力,而是存在小四方谷物或大量空位,其也可以引入晶格畸变。结果突出了氧气职位空缺的重要作用。因此,基质溶解后T-ZrO2的稳定性为我们提供了有机会观察内表面处四方相的微观演变。 T-ZrO2随着腐蚀时间的增加而增长,其强度在过渡后下降。其显微镜分布似乎与氧化物颗粒和界面波纹有关。 (c)2019 Elsevier B.v.保留所有权利。

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