Framework materials such as zeolites and mesoporous silicas are commonly used for many applications, especially catalysis and separation. Here zeolite-mesoporous silica composite catalysts (employing zeolite Y, ZSM-5, KIT-6, SBA-15 and MCM-41 mesoporous silica) were prepared (with different weight percent of zeolite Y and ZSM-5) and assessed for catalytic cracking (using n-heptane, as the model compound at 550 °C) with the aim to improve the selectivity/yield of light olefins of ethylene and propylene from n-heptane. Physicochemical properties of the parent zeolites and the prepared composites were characterized comprehensively using several techniques including X-ray diffraction, nitrogen physisorption, scanning electron microscopy, fourier transform infrared spectroscopy, pulsed-field gradient nuclear magnetic resonance and thermogravimetric analysis. Catalytic cracking results showed that the ZY/ZSM-5/KIT-6 composite (20:20:60 wt %) achieved a high n-heptane conversion of 85% with approximately 6% selectivity to ethylene/propylene. In contrast, the ZY/ZSM-5/SBA-15 composite achieved a higher conversion of 95% and an ethylene/propylene ratio of 8%, indicating a more efficient process in terms of both conversion and selectivity. Magnetic resonance relaxation analysis of the ZY/ZSM-5/KIT-6 (20:20:60) catalyst confirmed a micro-mesoporous environment that influences n-heptane diffusion and mass transfer. As zeolite Y and ZSM-5 have micropores, n-heptane can move and undergo hydrogen transfer reactions, whereas KIT-6 has mesopores that facilitate n-heptane’s accessibility to the active sites of zeolite Y and ZSM-5. (Figure presented.)

Alhassawi H., Asuquo E., Zainal S., Zhang Y., Alhelali A., Qie Z., et al. (2024). Formulation of zeolite-mesoporous silica composite catalysts for light olefin production from catalytic cracking. FRONTIERS OF CHEMICAL SCIENCE AND ENGINEERING, 18(11), 1-12 [10.1007/s11705-024-2480-7].

Formulation of zeolite-mesoporous silica composite catalysts for light olefin production from catalytic cracking

D'Agostino C.;
2024

Abstract

Framework materials such as zeolites and mesoporous silicas are commonly used for many applications, especially catalysis and separation. Here zeolite-mesoporous silica composite catalysts (employing zeolite Y, ZSM-5, KIT-6, SBA-15 and MCM-41 mesoporous silica) were prepared (with different weight percent of zeolite Y and ZSM-5) and assessed for catalytic cracking (using n-heptane, as the model compound at 550 °C) with the aim to improve the selectivity/yield of light olefins of ethylene and propylene from n-heptane. Physicochemical properties of the parent zeolites and the prepared composites were characterized comprehensively using several techniques including X-ray diffraction, nitrogen physisorption, scanning electron microscopy, fourier transform infrared spectroscopy, pulsed-field gradient nuclear magnetic resonance and thermogravimetric analysis. Catalytic cracking results showed that the ZY/ZSM-5/KIT-6 composite (20:20:60 wt %) achieved a high n-heptane conversion of 85% with approximately 6% selectivity to ethylene/propylene. In contrast, the ZY/ZSM-5/SBA-15 composite achieved a higher conversion of 95% and an ethylene/propylene ratio of 8%, indicating a more efficient process in terms of both conversion and selectivity. Magnetic resonance relaxation analysis of the ZY/ZSM-5/KIT-6 (20:20:60) catalyst confirmed a micro-mesoporous environment that influences n-heptane diffusion and mass transfer. As zeolite Y and ZSM-5 have micropores, n-heptane can move and undergo hydrogen transfer reactions, whereas KIT-6 has mesopores that facilitate n-heptane’s accessibility to the active sites of zeolite Y and ZSM-5. (Figure presented.)
2024
Alhassawi H., Asuquo E., Zainal S., Zhang Y., Alhelali A., Qie Z., et al. (2024). Formulation of zeolite-mesoporous silica composite catalysts for light olefin production from catalytic cracking. FRONTIERS OF CHEMICAL SCIENCE AND ENGINEERING, 18(11), 1-12 [10.1007/s11705-024-2480-7].
Alhassawi H.; Asuquo E.; Zainal S.; Zhang Y.; Alhelali A.; Qie Z.; Parlett C.M.A.; D'Agostino C.; Fan X.; Garforth A.A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/994838
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