Abstract

Kinetic analysis of experimental data for 2-methylhexane cracking demonstrates that trends in activity and selectivity are well simulated by adjusting a single parameter that represents the acid strength of a Y-based FCC catalyst. This acid strength may be modified via steam deactivation, and we have experimentally corroborated acidity changes using ammonia microcalorimetry and infrared spectroscopy. Increased severity of steam treatment reduces the number and strength of catalyst acid sites, and it leads to a reduction in the turnover frequency of all surface processes and a decrease in overall site time yield. Steaming of the catalyst does not change the fundamental chemistry involved in catalytic cracking. However, change in acidity caused by steaming alters product selectivity by changing relative rates of various catalytic cycles in the cracking process. For example, steam treatment increases olefin selectivity by favoring catalytic cycles that produce olefins.

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