Highly Efficient Selective Hydrogenation of Cinnamaldehyde to Cinnamyl Alcohol over Gold Supported on Zinc Oxide Materials

Hangning Chen, David A. Cullen, J. Z. Larese

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41 Scopus citations

Abstract

Au/ZnO catalysts have been used for liquid-phase selective hydrogenation of cinnamaldehyde to cinnamyl alcohol and compared with Au/Fe2O3 catalysts. To investigate the influence of the support on the hydrogenation activity and selectivity, three different Au/ZnO catalysts were synthesized, including Au/rod-tetrapod ZnO, Au/porous ZnO, and Au/ZnO-CP prepared using a coprecipitation method. The influence of calcination temperature was also systematically investigated in this study. The characterization of Au/ZnO catalysts was performed using ICP, N2 adsorption/desorption isotherms, X-ray diffraction, scanning transmission electron microscopy, and X-ray photoelectron spectroscopy. Among all the supported Au catalysts prepared in this study, Au/ZnO-CP exhibits both the highest hydrogenation activity and selectivity. Using a 1.5% Au/ZnO-CP catalyst, 100% selectivity could be achieved with 94.9% conversion. We find that the Au particle (size and shape), the ZnO support (size and surface texture) and the interaction between Au and ZnO are three important parameters for achieving a highly efficient Au/ZnO catalyst.

Original languageEnglish
Pages (from-to)28885-28894
Number of pages10
JournalJournal of Physical Chemistry C
Volume119
Issue number52
DOIs
StatePublished - Dec 31 2015

Funding

We would like to express our thanks to Paige Landry, Ben Estes, Harry Meyers, and Nathaniel Bass for useful discussions, comments, and assistance. We would especially like to acknowledge the efforts of Nicholas Strange who provided substantial assistance in improving the graphics in the revised manuscript. This research has benefitted from the technical expertise and instrumentation access made possible by a user project supported by ORNL’s Center for Nanophase Materials Sciences (CNMS), which is a DOE Office of Science User Facility. JZL received partial support for the initial stages of this work from the DOE BES.

FundersFunder number
CNMS
ORNL’s Center for Nanophase Materials Sciences
Office of Science
Basic Energy Sciences

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