Mesoscale distribution of adsorbates in ZSM-5 zeolite
Autor: | Li-Xiong Wen, Jian Zhou, Jinghai Li, Wen Lai Huang, Chao Ma, Zhicheng Liu |
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Rok vydání: | 2019 |
Předmět: |
Materials science
Applied Mathematics General Chemical Engineering Diffusion 02 engineering and technology General Chemistry 021001 nanoscience & nanotechnology Heterogeneous catalysis Industrial and Manufacturing Engineering Catalysis Adsorption 020401 chemical engineering Chemical physics Desorption Particle Kinetic Monte Carlo 0204 chemical engineering 0210 nano-technology Zeolite |
Zdroj: | Chemical Engineering Science. 198:253-259 |
ISSN: | 0009-2509 |
Popis: | Complex distribution of adsorbates can emerge in heterogeneous catalysis due to the compromise among different mechanisms (showing different tendencies of structural evolution) associated with different processes. On two-dimensional catalyst surfaces, all the surfaces are exposed to the gas reservoir (and thus adsorption and desorption processes are accessible to all the surfaces), and we have investigated the effects of adsorption, desorption, diffusion, and reactions on the adlayer structure, and revealed the mechanisms (Huang and Li, 2016). However, in zeolites, only the entrances (or exits) of the pore channels are exposed to the gas reservoir (and thus adsorption and desorption processes are limited there), so the mesoscale behavior might be somewhat different. In this work we explore the influence of adsorption, desorption, diffusion, and reactions on the adsorbate distribution in the ZSM-5 zeolite using kinetic Monte Carlo simulations. Complex distributions of adsorbates (nonlinearly gradient, showing apparent adsorbate shells in some cases) have been revealed, and the channel utilization has been evaluated. The approach and results might be useful to catalyst design, especially determining the optimal thickness of zeolite on a catalyst particle (pellet), since the channel utilization is a measure of effective fraction of the catalyst and is correlated with the practical efficiency of catalysis. |
Databáze: | OpenAIRE |
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