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Theoretical analysis for the heterogeneous decomposition of hydrogen sulfide to hydrogen on an iron-metallic plate in a laminar stagnation-point flow

机译:层状滞流中铁-金属板上硫化氢非均相分解为氢的理论分析

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In this work, we have theoretically analyzed the conversion process of hydrogen sulfide, H2S, to atomic hydrogen, H-0, in a planar stagnation-point flow over an iron-metallic surface. We assume that a binary mixture of hydrogen sulfide and methane composes the laminar stagnation flow. In order to characterize this complex phenomenon with very specific chemical activities on the surface of the metallic plate, we propose a heterogeneous reaction scheme based on four reactions: two electrochemical, one adsorption and an additional exothermic reaction needed to complete the direct conversion of hydrogen sulfide to hydrogen on the surface of the iron. The nondimensional governing equations, which include the mass species and momentum conservation of the mixture and the molecular diffusion of hydrogen into the iron plate, are numerically solved by conventional finite-difference methods. The numerical results show the critical conditions of the H2S decomposition as functions of the involved nondimensional parameters of the present model. In particular, we show parametrically the influence that has the initial concentration of H2S on the surface coverage of the chemical products HS- H+ and H-0 derived from the chemical and electrochemical reactions. (c) 2006 Elsevier B.V. All rights reserved.
机译:在这项工作中,我们从理论上分析了在铁金属表面上的平面停滞点流中,硫化氢H2S转换为原子氢H-0的过程。我们假设硫化氢和甲烷的二元混合物组成了层流停滞流。为了用金属板表面上非常特殊的化学活性来表征这种复杂现象,我们提出了一种基于四个反应的非均相反应方案:两个电化学反应,一个吸附反应和一个额外的放热反应,需要完成硫化氢的直接转化铁表面的氢。通过常规的有限差分方法可以求解无量纲控制方程,其中包括混合物的质量种类和动量守恒以及氢分子在铁板上的分子扩散。数值结果表明,硫化氢分解的临界条件是本模型涉及的无量纲参数的函数。特别是,我们从参数上显示了硫化氢初始浓度对源自化学和电化学反应的化学产物HS- H +和H-0的表面覆盖率的影响。 (c)2006 Elsevier B.V.保留所有权利。

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