Highly selective and stable alkylation of benzene with ethane into ethylbenzene over bifunctional PtH-MFI catalysts

• Published in: Journal of molecular catalysis. A, Chemical Vol. 279; no. 1; pp. 128 - 132
• Main Authors: Lukyanov, Dmitry B., Vazhnova, Tanya
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 02.01.2008; Elsevier
• Subjects: Alkylation; Bifunctional catalysis; Catalysis; Chemistry; Dehydrogenation; Ethylbenzene; Exact sciences and technology; General and physical chemistry; Ion-exchange; Surface physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Zeolites; Zeolites: preparations and properties; Ethylbenzene; Bifunctional catalysis; Dehydrogenation; Zeolites; Alkylation; Catalytic reaction; Bifunctional catalyst; Hydrocarbon; Zeolite; Ethane; Molecular sieve; Heterogeneous catalysis; Platinum; Benzene; Benzenic compound; Catalysis; Modified material
• ISSN: 1381-1169; 1873-314X
• DOI: 10.1016/j.molcata.2007.10.016

This paper demonstrates for the first time the feasibility of the highly selective and stable benzene alkylation with ethane into ethylbenzene over bifunctional zeolite catalysts and indicates the reaction conditions and catalysts for further research into this interesting and potentially important reaction. ▪ Benzene alkylation with ethane into ethylbenzene (EB) was studied at 370 °C over two Pt-containing MFI catalysts with the Si/Al ratios of 36 and 140, and the reaction temperature and catalysts were selected based on the analysis of the thermodynamic and kinetic limitations associated with this reaction. The experimental results suggest that EB formation proceeds via ethane dehydrogenation into ethene over Pt sites and subsequent benzene alkylation with ethene over acid sites. Under selected reaction conditions the whole process of EB formation is driven by the alkylation reaction and many side reactions (including coke formation) are suppressed due to the inherently low ethene concentration at 370 °C. Also, the low and moderate acidity of the catalysts allows decoupling of EB formation steps and the steps of its subsequent transformation into side products. As a consequence, both catalysts demonstrate a remarkably stable performance (during 45–49 h on stream) with EB selectivity in the aromatic products in the range between 92.6 and 95.3 mol%, with the highest (benzene-based) EB yield of 10.7%. These observed EB selectivities and yield are essentially higher than those reported previously both for the zeolite and superacidic catalytic systems.