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Role of Catalyst Domain Size in the Hydrogenation of CO2 to Aromatics over ZnZrO x /ZSM‑5 Catalysts

The direct conversion of carbon dioxide into aromatic compounds may provide an environmentally friendly resource for a family of chemical building blocks with high global demandaromatic chemicals. An array of bifunctional catalysts composed of ZnZrO x for the conversion of CO2 to methanol and ZSM-5...

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Bibliographic Details
Published in:Journal of physical chemistry. C 2023-04, Vol.127 (13), p.6356-6370
Main Authors: Nezam, Iman, Zhou, Wei, Shah, Dhrumil R., Bukhovko, Maxim P., Ball, Madelyn R., Gusmão, Gabriel S., Medford, Andrew J., Jones, Christopher W.
Format: Article
Language:English
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Summary:The direct conversion of carbon dioxide into aromatic compounds may provide an environmentally friendly resource for a family of chemical building blocks with high global demandaromatic chemicals. An array of bifunctional catalysts composed of ZnZrO x for the conversion of CO2 to methanol and ZSM-5 for methanol aromatization is evaluated considering multiple operational and catalytic parameters, with a focus on the particle size of each catalyst functionality. Aromatic yields generally increase as the ZSM-5 domain size decreases for different configurations of catalyst domainsmixed powders, mixed pellets, and separate beds. However, for a physical mixture of the catalyst components prior to pelletization (mixed powder case), varying the ZSM-5 crystal size inversely impacts the particle size of ZnZrO x , leading to enlarged metal oxide domains and enhanced intermediate diffusion barriers for very small crystals of ZSM-5. Larger crystals of ZSM-5 can be employed to obtain a higher concentration of benzene, toluene, and xylene (BTX) among aromatics. Upon employing a physical mixture of the ZnZrO x /ZSM-5 catalyst with a Si/Al ratio of 300 and a ZSM-5 crystal size of 300 nm, a total aromatics selectivity of 44% at CO2 conversion of 6% was obtained at 320 °C, WHSV of 7200 mL gcatalyst –1 h–1, and H2/CO2 ratio of 3.
ISSN:1932-7447
1932-7455
DOI:10.1021/acs.jpcc.3c01306