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Role of acidity in catalytic cracking of n-decane over supported Pt-based catalysts

[Display omitted] •Acidity of catalyst can be adjusted by combination of different acidic-basic oxide.•Catalytic activity is closely related to amount and distribution of acid sites.•30 wt% SiO2-modified Al2O3 owns proper amount and distribution of acid sites.•Pt/SiO2-Al2O3 catalyst exhibited the hi...

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Published in:Applied surface science 2020-03, Vol.507, p.145113, Article 145113
Main Authors: Zhang, Jun, Chen, Ting, Jiao, Yi, Wang, Linlin, Wang, Jianli, Chen, Yaoqiang, Zhu, Quan, Li, Xiangyuan
Format: Article
Language:English
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Summary:[Display omitted] •Acidity of catalyst can be adjusted by combination of different acidic-basic oxide.•Catalytic activity is closely related to amount and distribution of acid sites.•30 wt% SiO2-modified Al2O3 owns proper amount and distribution of acid sites.•Pt/SiO2-Al2O3 catalyst exhibited the highest heat sink of 3.920 MJ/kg.•Coverage of active sites is one of the main factors to catalyst deactivation. Different acidic-basic oxides, Al2O3, SiO2, MgO, MgO-SiO2, MgO-Al2O3 and SiO2-Al2O3, were employed as supports of Pt-based catalysts for n-decane cracking, aiming to investigate the effect of acidity on cracking activity and coking behaviors. The as-prepared catalysts were characterized by the techniques of N2 absorption-desorption, X-ray diffraction (XRD), CO chemisorption, temperature programmed desorption of ammonia (NH3-TPD) and Fourier transform infrared spectroscopy (FTIR) of adsorbed pyridine. The results showed that acidic support catalysts are more suitable for catalytic cracking reaction of n-decane than alkaline support catalyst. Particularly, Pt/SiO2-Al2O3 catalyst exhibited the optimal catalytic activity, leading to heat sink of 3.920 MJ/kg and n-decane conversion of 85.5% at 750 °C. Meanwhile, excellent cracking activity over Pt/SiO2-Al2O3 catalyst is due to large ratio of strong to total acid sites and large amount of Lewis acid sites. Additionally, stability and regeneration experiments of Pt/SiO2-Al2O3 showed that coverage of active sites due to coke deposition is main factor to catalyst deactivation, and carburization of Pt metals will lead to the reduction of catalytic activity.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2019.145113