(327c) The Role of External Acidity of Meso-/Microporous Zeolites in Determining Selectivity for Acid-Catalyzed Reactions of Benzyl Alcohol

Authors: 
Emdadi, L., Univeristy of Maryland
Oh, S. C., University of Maryland
Wu, Y., Univeristy of Maryland
Liu, D., University of Maryland

A comparison of selectivity in catalytic conversion of benzyl alcohol in mesitylene on hybrid lamellar-bulk MFI (HLBM) zeolite materials containing dual meso-/microporosity showed that the external Brønsted acidity in meso-/microporous MFI zeolites effectively impact on selectivity of the parallel alkylation and etherification reactions. HLBM zeolites, consisting of crystalline bulk microporous core and lamellar mesoporous shell, not only catalyzed the parallel reactions on the external environments (external surface and mesopore) but also etherification reaction in the internal environment (micropore) as illustrated by the completely suppressed alkylation and retained residual etherification reactions after 2,6-di-tert-butylpyridine (DTBP) poisoning. A systematic study of HLBM zeolites with tunable meso-/microporous domains achieved by a dual template assisted synthesis revealed that parallel alkylation and etherification reactions are tailored by the tunable external acidity and external surface area of the HLBM zeolites upon tuning the ratio of dual templates in the synthesis. The external alkylation and etherification reaction rates as a function of cumulative DTBP addition suggested Brønsted acid sites with different strengths on external environments of the HLBM zeolites, which influenced the alkylation reaction, but irrelevant to the external etherification reaction. The evidence shown here for the involvement of external acidity in catalyzing parallel reactions and for the role of external acidity with variable strengths in HLBM zeolite materials extends the scope of observed catalytic behaviors of meso-/microporous zeolite materials beyond those reflecting transport effects and accessibility of acid sites.