Stable and selective catalysts for propane dehydrogenation operating at thermodynamic limit

Author:

Motagamwala Ali Hussain12ORCID,Almallahi Rawan12ORCID,Wortman James12ORCID,Igenegbai Valentina Omoze12ORCID,Linic Suljo12ORCID

Affiliation:

1. Department of Chemical Engineering, University of Michigan, Ann Arbor, MI, USA.

2. Catalysis Science and Technology Institute, University of Michigan, Ann Arbor, MI, USA.

Abstract

Hitting the limits on propene synthesis The greater abundance of propane from shale gas has spurred efforts to use it as a propylene feedstock. Direct dehydrogenation catalysts consisting of platinum–tin alloy nanoparticles supported on alumina often must run with hydrogen dilution to avoid carbon buildup and excess tin to avoid alloy segregation. Motagamwala et al. report that platinum–tin nanoparticles interact more weakly with a silica support and the metals thus do not segregate. The use of undiluted reactants allowed the reaction to run near the thermodynamically limit of about 67% conversion with a selectivity to propylene of more than 99%. This catalyst also does not build up carbon and could run up to 30 hours without deactivation. Science , abg7894, this issue p. 217

Funder

U.S. Department of Energy

Michigan Center for Materials Characterization, University of Michigan

US Department of Energy, Rapid

RAPID under Award Number

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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