Direct Catalytic Conversion of Ethanol to C5+ Ketones: Role of Pd–Zn Alloy on Catalytic Activity and Stability

Author:

Subramaniam Senthil12,Guo Mond F.12ORCID,Bathena Tanmayi3,Gray Michel1,Zhang Xiao12,Martinez Abraham1,Kovarik Libor1,Goulas Konstantinos A.3,Ramasamy Karthikeyan K.1ORCID

Affiliation:

1. Chemical and Biological Processing Group Pacific Northwest National Laboratory Richland WA 99354 USA

2. The Gene and Linda Voiland School of Chemical Engineering and Bioengineering Washington State University Pullman WA 99164 USA

3. Chemical, Biological, and Environmental Engineering Oregon State University Corvallis OR 97331 USA

Abstract

AbstractEthanol can be used as a platform molecule for synthesizing valuable chemicals and fuel precursors. Direct synthesis of C5+ ketones, building blocks for lubricants and hydrocarbon fuels, from ethanol was achieved over a stable Pd‐promoted ZnO‐ZrO2 catalyst. The sequence of reaction steps involved in the C5+ ketone formation from ethanol was determined. The key reaction steps were found to be the in situ generation of the acetone intermediate and the cross‐aldol condensation between the reaction intermediates acetaldehyde and acetone. The formation of a Pd–Zn alloy in situ was identified to be the critical factor in maintaining high yield to the C5+ ketones and the stability of the catalyst. A yield of >70 % to C5+ ketones was achieved over a 0.1 % Pd‐ZnO‐ZrO2 mixed oxide catalyst, and the catalyst was demonstrated to be stable beyond 2000 hours on stream without any catalyst deactivation.

Funder

Office of Energy Efficiency and Renewable Energy

Publisher

Wiley

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