Catalytic Behavior of Brønsted Acid Sites In MWW and MFI Zeolites

Tuesday, November 9, 2010: 1:33 PM
254 C Room (Salt Palace Convention Center)
Dongxia Liu1, Aditya Bhan1, Michael Tsapatsis1 and Saleh H. Al Hashimi2, (1)Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN, (2)Chemical Engineering Program, The Petroleum Institute, Abu Dhabi, United Arab Emirates

Zeolites possessing micro- and meso-porosity couple the catalytic features of micropores and the improved access and transport consequence of mesopores in a single material. The catalytic behavior of Brønsted acid sites in three acidic meso-/micro-porous zeolite materials (pillared MWW, pillared MFI, and 3DOm MFI) was studied using ethanol dehydration and monomolecular conversion of propane and isobutane as probe reactions. The pillared MWW (or MCM-36) consists of a zeolitic layer structure, with independent microporosity and mesoporosity within the layers and between the layers, respectively. Pillared MFI zeolite also contains a zeolitic layer structure, but with interconnected micropore and mesopore systems. 3DOm MFI contains nanometer-sized spherical elements forming an opaline structure, with highly interconnected meso- and micro-pores. The rate and apparent activation energy of the catalytic probe reactions in zeolites possessing dual micro- and meso-porosity was comparable to conventional microporous MCM-22 (MWW) and MFI materials. This similarity in kinetic behavior between materials possessing dual meso-/micro-porosity and their microporous analogues when assessed under conditions of strict kinetic control, implies that the catalytic behavior of Brønsted acid sites in materials with dual meso-/micro-porosity is preferentially dominated by the microporous environment possibly because it provides a better fit for adsorption of small alkane or alcohol reactant molecules.

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