101. Influence of Channel, Construction and Brønsted Acid Sites on the Catalytic Conversion Pathways of Isobutane Over MFI, TON and RFE Zeolites.
- Author
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Hou, Yibin, Zhang, Rongxin, Wang, Zijian, Lu, Bin, and Wang, Jieguang
- Abstract
Despite thorough exploration of the acidity properties and pore structure effects of zeolite catalysts on catalytic conversion, a comprehensive understanding of how these factors influence reaction pathways is still lacking. Herein, three common zeolites (ZSM-5, ZSM-22 and ZSM-48) of different shapes and size dimensions were introduced into catalytic conversion of isobutane, with combination of X-ray diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption and desorption, solid-state 29Si and 27Al MAS NMR, ammonia temperature programmed desorption (NH3-TPD) and pyridine adsorption infrared spectroscopy (Py-FTIR) to characterize their structure and acidity. And channels and topologies were associated with stability and catalytic activity. ZSM-5 performed best, showing the most active sites. Furthermore, ZSM-48 led to an increase in the propene yield by suppressing inhibitory secondary reactions in the monomolecular reaction pathway. Moreover, the amount of Brønsted acid sites (BASs) of ZSM-22 were a key factor in promoting light alkene formation. However, 1D channels contributed to the deactivation of ZSM-22 and ZSM-48. The detailed reaction pathways of zeolite catalysts with diverse pore structures and acidities are crucial for optimizing their catalytic performance. [ABSTRACT FROM AUTHOR]
- Published
- 2025
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