Continuous supercritical iC4/C4= alkylation over H-Beta and H-USY Influence of the zeolite structure

• Published in: Applied catalysis. A, General General, 2008-03, Vol.336 (1-2), p.61-71
• Main Authors: MOTA SALINAS, A. L, SAPALY, G, BEN TAARIT, Y, VEDRINE, J. C, ESSAYEM, N
• Format: Article
• Language: English
• Subjects: Catalysis; Chemistry; 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: preparations and properties
• ISSN: 0926-860X; 1873-3875
• DOI: 10.1016/j.apcata.2007.09.020

This study presents a comparison of the catalytic performances and stabilities of H-Beta and H-USY zeolites for iC4/C4= alkylation in supercritical isobutane phase. The experimental results clearly show that the zeolite structure strongly influences the performance and deactivation behavior of the zeolite in iC4/C4= alkylation performed in SC conditions. H-Beta outperformed H-USY zeolite as regards to its lower deactivation and the stable quality of the alkylate, composed mainly of isoparaffins while olefin di-/oligomerization was shown to be responsible of the H-USY deactivation with time-on-stream. Characterization of the spent catalysts gave clues to the differentiated performance of the two zeolites. The stable activity of H-Beta was attributed to the effective extractive effect of the supercritical iC4 media to 'clean'the acid sites located on the external surface of the small crystallites of H-Beta or located at the pore mouth. By contrast, the deactivation observed for H-USY was caused by olefin oligomerization inside the zeolite supercages. The supercritical isobutane media was shown to be unable to prevent the oligomers formation inside the zeolite supercages and/or to in situ extract these oligomers located in the supercages of the large crystals of the H-USY zeolite.