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Versatility of Supported Gold Nanoparticles on Hydrotalcites used for Oxidation and Reduction Reactions

Authors :
Drault, Fabien
Snoussi, Youssef
Ferraz, Camila
Thuriot-Roukos, Joelle
Heyte, Svetlana
Junior, Ivaldo
Marinova, Maya
Paul, Sébastien
Wojcieszak, Robert
Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS)
Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)
Universidade Federal do Rio de Janeiro (UFRJ)
Institut Michel Eugène Chevreul - FR 2638 (IMEC)
Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
Source :
Catalysis Research, Catalysis Research, 2022, 2 (1), pp.1001. ⟨10.21926/cr.2201001⟩
Publication Year :
2022
Publisher :
HAL CCSD, 2022.

Abstract

Regardless of their size, supported gold nanoparticles are largely used for liquid-phase oxidation reactions. Small gold nanoparticles exhibit good performance during the reduction of organic compounds. The direct reduction of carboxylic acid to aldehyde is a famous and familiar reaction in the field of organic chemistry and is considered as one of the fundamental chemical transformations. Herein, we present Au/hydrotalcite, Au/MgO, and Au/Al2O3 systems as heterogeneous versatile catalysts to realize the oxidation of furfural (FF) to furoic acid (FA) and realize the reduction of FA to FF. Experiments showed that in standard aqueous conditions under air, FF can be easily oxidized to FA. When DMSO was used as a solvent to conduct the experiments under an atmosphere of CO2, FA was reduced to FF. The Au/HT series of catalysts was found to be active in both transformations, pointing out the versatility of the gold-based catalysts. The activity significantly depends on the acid-base properties of the catalyst.

Details

Language :
English
ISSN :
2771490X
Database :
OpenAIRE
Journal :
Catalysis Research, Catalysis Research, 2022, 2 (1), pp.1001. ⟨10.21926/cr.2201001⟩
Accession number :
edsair.doi.dedup.....c9490d7cc3ac75862d13d8948296f3c7