Acidic properties of nanolayered ZSM-5 zeolites

LeiLei Wu, P.C.M.M. Magusin, V. Degirmenci, M. Li, S.M.T. Almutairi, X. Zhu, B. Mezari, E.J.M. Hensen

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Abstract

The acidic properties of nanolayered ZSM-5 zeolites synthesized with the aid of multiquaternary ammonium surfactants were investigated in detail. A substantial fraction of Al is present in highly dispersed form at extraframework positions indicative of the defective nature of the calcined nanolayered zeolites. Acidity characterization reveals that the Brønsted acid sites are similar in strength to those in bulk HZSM-5. Nanolayered zeolites contain a higher amount of Brønsted acid sites (BAS) at their external (mesopore) surface. Unilamellar zeolites have a higher concentration of external BA and silanol sites than multilamellar ones. The number of BAS in the nanolayered zeolites is considerably lower than the tetrahedral Al content, the difference increasing with nanolayer thickness. Except for one particular sample (nanolayered ZSM-5 synthesized from C22-6-6OH2 template), the total turnover of methanol normalized per BAS trends inversely with the concentration of BAS. There is no correlation with the concentration of external BAS. Catalyst deactivation due to coke mainly depends on the BAS concentration. A unilamellar ZSM-5 zeolite prepared using C22-6-6OH2 displayed substantially improved performance in terms of a much lower rate of coke deactivation in line with earlier data Choi et al. [10]. Since the acidic and textural properties of this zeolite did not differ significantly from the others, it remains to be determined why this zeolite performs so much better.
Original languageEnglish
Pages (from-to)144-157
Number of pages14
JournalMicroporous and Mesoporous Materials
Volume189
DOIs
Publication statusPublished - 2014

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    Wu, L., Magusin, P. C. M. M., Degirmenci, V., Li, M., Almutairi, S. M. T., Zhu, X., Mezari, B., & Hensen, E. J. M. (2014). Acidic properties of nanolayered ZSM-5 zeolites. Microporous and Mesoporous Materials, 189, 144-157. https://doi.org/10.1016/j.micromeso.2013.08.042