Activity and selectivity differences of external Brønsted acid sites of single-unit-cell thick and conventional MFI and MWW zeolites

• Published in: Microporous and mesoporous materials Vol. 200; pp. 287 - 290
• Main Authors: Liu, Dongxia, Zhang, Xueyi, Bhan, Aditya, Tsapatsis, Michael
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 01-12-2014; Elsevier
• Subjects: Alkylation; Brønsted acid site; Catalysis; Chemistry; Colloidal state and disperse state; Exact sciences and technology; General and physical chemistry; Hierarchical materials; Ion-exchange; Meso-/microporous; Porous materials; Surface physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Unit-cell thick zeolite; Zeolites: preparations and properties; Brønsted acid site; Hierarchical materials; Meso-/microporous; Unit-cell thick zeolite; Alkylation; Acidic site; Selectivity; Benzyl alcohol; Zeolite; Bronsted site; Porous material; Heterogeneous catalysis; Microporosity; Brönsted acid; Mesitylene
• ISSN: 1387-1811; 1873-3093
• DOI: 10.1016/j.micromeso.2014.06.029

•Activity and selectivity of external Brønsted acid sites in zeolites were examined.•Catalytic conversion of benzyl alcohol in mesitylene was used as probe reaction.•External surface of MWW zeolites favors the alkylation reaction.•Etherification takes place with similar reaction rates on MFI and MWW zeolites.•Catalytic reaction rate per external Brønsted acid site is higher for MWW than MFI.
A comparison of activity and selectivity of external Brønsted acid sites in catalytic conversion of benzyl alcohol in mesitylene over unit-cell thick zeolite materials (MCM36 or pillared MWW, pillared MFI, and self-pillared pentasil (SPP)) showed that the external surface of MWW and MFI zeolites influences drastically the activity and selectivity of the parallel alkylation and etherification reactions. Pillared MWW, containing independent (not-interconnected) micropores and mesopores, catalyzed both of the parallel reactions only in the mesopores as evidenced by complete loss of the activity upon 2,6-di-tert-butylpyridine (DTBP) titration. Pillared MFI and SPP, consisting of highly interconnected micropores and mesopores, catalyzed both of the parallel reactions in the mesopores. Pillared MFI and SPP catalyzed only the etherification reaction in the micropores as illustrated by the complete suppression of alkylation and retention of residual etherification activity after DTBP titration. Moreover, it was found that the external surface of MWW zeolites favors the alkylation reaction, while the etherification reaction takes place with similar reaction rates on MFI and MWW external surfaces. The evidence shown here for the assessment of external acid sites in catalyzing parallel reactions extends the scope of observed catalytic performances in these materials beyond those reflecting transport effects and accessibility of acid sites and highlights the importance of external surface structure.