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The influence of surface morphology and oxide microstructure on the nucleation and growth of uranium hydride on alpha uranium

机译:表面形态和氧化物微观结构对氢化铀在α铀上成核和生长的影响

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While the bulk kinetics of the uranium-hydrogen reaction are well understood, the mechanisms underlying the initial nucleation of uranium hydride on uranium remain controversial. In this study we have employed environmental cell optical microscopy, Scanning Electron Microscopy (SEM) and Atomic Force Microscopy, (AFM) is an attempt to relate the structure of the surface and the microstructure of the subjstrate with the susceptibility and site of hydride nucleation. Samples have been investigated with varying grain size, inclusion (carbide) concentration, and thermal history. There is a clear correlationto heat treatment immediately prior to hydrogen exposure. Susceptibility to hydride formation also appears to be related to impurities in the uranium. The oxidized surface is very ocmplex, exhibiting wide variations in thickness and topography between samples, between grains in the same sample, and within individual grains. It is, however, very difficult to relate this fine scale variability to the relatively sparse hydride initiation sites. Therefore, the surface oxide layer itself does not appear to control the sites where hydride attack is initiated, although it must play a role in the induction period prior to hydride initiation.
机译:虽然铀-氢反应的整体动力学已广为人知,但氢化铀在铀上初始成核的机理仍存在争议。在这项研究中,我们采用了环境细胞光学显微镜,扫描电子显微镜(SEM)和原子力显微镜(AFM),试图将表面的结构和基质的微观结构与氢化物成核的敏感性和位置联系起来。研究了具有不同晶粒尺寸,夹杂物(碳化物)浓度和热历史的样品。暴露于氢之前的热处理与热处理之间存在明显的相关性。氢化物形成的敏感性似乎也与铀中的杂质有关。氧化的表面非常复杂,在样品之间,同一样品中的晶粒之间以及单个晶粒中,厚度和形貌表现出很大的差异。但是,很难将这种精细尺度的变化与相对稀疏的氢化物起始位点联系起来。因此,尽管表面氧化物层必须在氢化物引发之前的诱导期中发挥作用,但表面氧化物层本身似乎并不能控制引发氢化物侵蚀的部位。

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