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Thermal resistance effect on methanol-steam reforming performance in micro-scale reformers

机译:热阻对微型重整器中甲醇-蒸汽重整性能的影响

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We numerically investigate hydrogen production based on methanol-steam reforming (MSR) using a micro-scale cylindrical packed bed reformer. The reformer wall is included in the physical model. The heat required for the reforming reaction is supplied either internally using a heating rod placed along the center of the reformer or externally by a heat flux applied at the reformer outer wall. Our results show that the thermal resistance from the heat source to the reformer environment plays an important role in the reformer performance. This thermal resistance depends on the reformer geometry, wall material and heat transfer coefficients inside the catalyst bed and outside the reformer. Based on our numerical results, it is suggested that better methanol conversion and hydrogen yield can be obtained using reformer wall material with low thermal conductivity and thin thickness. For both internal and external heating under the same heat rate supply, no significant difference in reformer performance was found. A water gas shift (WGS) reaction model was included in the present numerical model. In the reformer low-temperature zone the forward WGS reaction was clearly demonstrated, resulting in a decrease in carbon monoxide (CO) selectivity. In the high temperature zone the backward WGS reaction was also clearly demonstrated in which CO selectivity increases with the increase in temperature. For both internal and external heating under the same heat rate supply, our results indicated that CO selectivity is about thirty times lower when the WGS reaction is neglected.
机译:我们使用小型圆柱形填充床重整器,对基于甲醇-蒸汽重整(MSR)的氢气生产进行了数值研究。重整器壁包含在物理模型中。重整反应所需的热量可以使用沿着重整器中心放置的加热棒在内部提供,也可以通过施加在重整器外壁的热通量从外部提供。我们的结果表明,从热源到重整器环境的热阻在重整器性能中起着重要作用。该热阻取决于重整器的几何形状,壁材料和催化剂床内部和重整器外部的传热系数。根据我们的数值结果,建议使用导热系数低且厚度薄的重整炉壁材料可以获得更好的甲醇转化率和氢气产率。对于在相同热速率供应下的内部和外部加热,重整器性能没有发现显着差异。本数值模型包括水煤气变换(WGS)反应模型。在重整器的低温区中,可以清楚地证明正向WGS反应,导致一氧化碳(CO)选择性降低。在高温区,还清楚地证明了反向WGS反应,其中CO选择性随温度的升高而增加。对于在相同加热速率下的内部和外部加热,我们的结果表明,当忽略WGS反应时,CO的选择性低约30倍。

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