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Temperature-Driven Oxidation Behavior of Pure Iron Surface Investigated by time-resolved EXAFS Measurements

机译:时间分辨EXAFS测量研究纯铁表面的温度驱动氧化行为

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The surface-front oxidation mechanism of iron was investigated by time-resolved, glancing-alngle Fe K-edge fluorescence EXAFS measurements at various oxidation temperatures of 200-700 deg C. The glancing angle was chosen according to the depth of the oxide layer, roughly 1500-2000 A. The oxidation behavior under rapid heating(up to 600 deg C within 10 minutes) was compared with the slowly heated oxidation process using the Quick-EXAFS measurements. In the slowly heated process, Fe_3O_4 was the dominating phase at a relatively low temperature (300-400 deg C) initially. However, at a relatively high temperature (above 600 deg C), the Fe_2O_3 and FeO crystalline phases are gradually enriched as the successive oxidation process involving intrusive oxygen proceeded. Remarkably under a prolonged heat treatment above 600 deg C, the stable FeO phase that exists in a deep-lying interface structure and Fe_2O_3 phase eventually dominates the thick front-surface structure. In a quickly heated process, however, Fe_3O_4 phase is less dominating, which is contradictory to the commonly accepted oxidation models. The EXAFS results are discussed in conjunction with the x-ray diffraction features under the same heat treatment conditions.
机译:通过在200-700摄氏度的各种氧化温度下进行时间分辨的掠射角Fe K边缘荧光EXAFS测量,研究了铁的表面氧化机理。掠射角是根据氧化物层的深度选择的,大约1500-2000A。使用Quick-EXAFS测量,将快速加热(在10分钟内达到600摄氏度)下的氧化行为与缓慢加热的氧化过程进行了比较。在缓慢加热的过程中,Fe_3O_4最初是在相对较低的温度(300-400摄氏度)下的主要相。但是,在相对较高的温度下(600摄氏度以上),随着涉及侵入性氧的连续氧化过程的进行,Fe_2O_3和FeO晶相逐渐富集。显着地,在超过600摄氏度的长时间热处理下,稳定的FeO相存在于较深的界面结构中,而Fe_2O_3相最终占据了较厚的前表面结构。但是,在快速加热的过程中,Fe_3O_4相的控制较少,这与通常接受的氧化模型相矛盾。在相同的热处理条件下,结合X射线衍射特征讨论了EXAFS结果。

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