甲烷化
硫化
化学
微通道
热力学
稳态(化学)
近程
推流式反应器模型
催化作用
微型反应器
连续搅拌釜式反应器
物理化学
一氧化碳
物理
有机化学
作者
В. А. Данилов,M. Wichert,Gunther Kolb
标识
DOI:10.1016/j.cej.2022.137863
摘要
• A dynamic two-dimensional model has been developed for CO 2 methanation. • A simplified reaction mechanism with deactivation and sulfidation submodel. • The model describes transient and steady-state behavior of the reactor. • A simplified mechanism of the methanation agrees well with experimental data. • The multi-step reaction simplification technique is suitable for various catalysts. A dynamic two-dimensional model was developed for transfer processes in a microchannel reactor in an innovative plant concept for CO 2 methanation. The model is based on balance equations together with deactivation and sulfidation submodels taking into account the chemisorption of impurity (H 2 S). The deactivation of the catalyst is described by Levenspiel's deactivation kinetic model (LDKM). Sulfidation is defined by the shrinking core model (SCM) equation. Following the rate-determining step assumption, a simplified mechanism is derived for CO 2 and CO methanation in a microchannel reactor with kinetic rate expressions. The developed 2D model adequately describes transient and steady-state behavior of the microchannel methanation reactor following the trend in experimental profiles available in the literature.
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