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

机译:通过时间分辨的EXAFS测量研究纯铁表面的温度驱动的氧化行为

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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:通过时间分辨地研究铁的表面前氧化机理,在200-700℃的各种氧化温度下测量荧光渗透荧光Exafs测量。根据氧化物层的深度选择瞥眼,大约1500-2000 A.使用快速溢出测量比较快速加热(在10分钟内最多600℃)的氧化行为进行比较。在缓慢加热的过程中,Fe_3O_4最初是相对低温(300-400℃)的主导相。然而,在相对较高的温度(高于600℃),Fe_2O_3和FeO结晶相随着涉及侵入性氧的连续氧化过程而逐渐富集。显着的在600℃以上的延长热处理中,在深层界面结构和Fe_2O_3相中存在的稳定Feo相最终主导了厚的前表面结构。然而,在快速加热的过程中,Fe_3O_4相位较少,这与普通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EXAFS结果。

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