The Role of Lewis Acid Sites in γ‐Al2O3 Oligomerization

Author:

Breckner Christian J.1,Pham Hien N.2,Dempsey Michael G.1,Perez‐Ahuatl Michelle A.1,Kohl Alyssa C.1,Lytle Corryn N.1,Datye Abhaya K.2ORCID,Miller Jeffrey T.1ORCID

Affiliation:

1. Davidson School of Chemical Engineering Purdue University West Lafayette IN 47907 USA

2. Department of Chemical and Biological Engineering and Center for Microengineered Materials University of New Mexico Albuquerque NM, 87137 USA

Abstract

AbstractOlefin oligomerization by γ‐Al2O3 has recently been reported, and it was suggested that Lewis acid sites are catalytic. The goal of this study is to determine the number of active sites per gram of alumina to confirm that Lewis acid sites are indeed catalytic. Addition of an inorganic Sr oxide base resulted in a linear decrease in the propylene oligomerization conversion at loadings up to 0.3 wt %; while, there is a >95 % loss in conversion above 1 wt % Sr. Additionally, there was a linear decrease in the intensity of the Lewis acid peaks of absorbed pyridine in the IR spectra with an increase in Sr loading, which correlates with the loss in propylene conversion, suggesting that Lewis acid sites are catalytic. Characterization of the Sr structure by XAS and STEM indicates that single Sr2+ ions are bound to the γ‐Al2O3 surface and poison one catalytic site per Sr ion. The maximum loading needed to poison all catalytic sites, assuming uniform surface coverage, was ∼0.4 wt % Sr, giving an acid site density of ∼0.2 sites per nm2 of γ‐Al2O3, or approximately 3 % of the alumina surface.

Funder

National Science Foundation

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,Atomic and Molecular Physics, and Optics

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