Ester Reduction with H2 on Bifunctional Metal-Acid Catalysts: Implications of Metal Identity on Rates and Selectivities |
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Authors: | Dr Claudia E Berdugo-Díaz Melissa T Manetsch Dr Yang Sik Yun Jieun Lee Dr Jing Luo Dr Xue Chen Prof Dr David W Flaherty |
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Institution: | 1. Department of Chemical and Biomolecular Engineering, University of Illinois Urbana-Champaign, Urbana, IL 61801 USA;2. Core R&D, The Dow Chemical Company, Midland, MI 48674 USA;3. Dow Industrial Solutions, The Dow Chemical Company, Freeport, TX 77566 USA |
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Abstract: | Esters reduce to form ethers and alcohols on contact with metal nanoparticles supported on Brønsted acidic faujasite (M-FAU) that cleave C−O bonds by hydrogenation and hydrogenolysis pathways. Rates and selectivities for each pathway depend on the metal identity (M=Co, Ni, Cu, Ru, Rh, Pd, and Pt). Pt-FAU gives propyl acetate consumption rates up to 100 times greater than other M-FAU catalysts and provides an ethyl propyl ether selectivity of 34 %. Measured formation rates, kinetic isotope effects, and site titrations suggest that ester reduction involves a bifunctional mechanism that implicates the stepwise addition of H* atoms to the carbonyl to form hemiacetals on the metal sites, followed by hemiacetal diffusion to a nearby Brønsted acid site to dehydrate to ethers or decompose to alcohol and aldehyde. The rates of reduction of propyl acetate appear to be determined by the H* addition to the carbonyl and by the C−O cleavage of hemiacetal. |
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Keywords: | Bifunctional Catalysis Hydrogenation Hydrogenolysis Transition Metals Zeolites |
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