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Microscopic behavior and metallic iron morphology from reduction of iron oxide by CO/H-2 in a fluidized bed

机译:通过CO / H-2在流化床中减少氧化铁的微观行为和金属铁形态

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摘要

Fe2O3 particles reduced by CO or H-2 exhibit different metallic iron morphology. To determine the mechanism of metallic iron formation during the reduction of iron oxide particles by CO/H-2 in a fluidized bed, an innovative multiscale method was used. This method was validated by experimental results. Density functional theory calculations demonstrate that the CO molecule has a strong stretching effect on the iron ion of wustite in the vertical direction, but the H-2 molecule has no directional force on the structure of wustite. The energy released from CO reduction is used to overcome the energy barrier of iron ion diffusion. However, H-2 addition will hinder iron ion diffusion by consuming energy. By analysis of the thermogravimetric curves of Fe2O3 reduction, it was found that the adsorption ability of H-2 on the surface of FeO is weaker than that of CO. However, the reduction rate is higher under H-2 atmosphere, according to Langmuir adsorption isotherm theory. The morphology of metallic iron during the reduction of iron oxide particles by CO/H-2 was observed with a scanning electron microscope equipped with an energy dispersive X-ray spectroscopy detector
机译:通过CO或H-2减少Fe2O3颗粒表现出不同的金属铁形态。为了确定在流化床中通过CO / H-2减少铁氧化物颗粒期间金属铁形成的机制,使用了一种创新的多尺度方法。通过实验结果验证该方法。密度函数理论计算表明CO分子对垂直方向上硅铁的铁离子具有强烈的拉伸效果,但H-2分子在硅铁的结构上没有方向性。从CO减少释放的能量用于克服铁离子扩散的能量屏障。然而,H-2添加将通过消耗能量阻碍铁离子扩散。通过分析Fe2O3还原的热量曲线,发现H-2在FeO表面上的吸附能力弱于CO的表面。然而,根据Langmuir吸附的说法,在H-2气氛下减少率高等温本理论。通过配备有能量分散X射线光谱检测器的扫描电子显微镜观察金属铁在减少氧化铁颗粒期间的金属铁形态

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