Solvent‐Free Aerobic Oxidative Cleavage of Methyl Oleate to Biobased Aldehydes over Mechanochemically Synthesized Supported AgAu Nanoparticles

Author:

da Silva Rafael T. P.1,Silva Dagoberto O.1,de Oliveira Paulo F. M.1ORCID,Bellabarba Ronan2ORCID,Johnston Peter2ORCID,Smit Joost2ORCID,Holt Jarle2,Betham Michael2,Rossi Liane M.1ORCID

Affiliation:

1. Instituto de Química Universidade de São Paulo 05508-000 São Paulo, SP Brazil

2. Johnson Matthey plc Billingham Cleveland TS23 4EA UK

Abstract

AbstractThe performance of mechanochemically synthesized supported bimetallic AgAu nanoalloy catalysts was evaluated in the oxidative cleavage of methyl oleate, a commonly available unsaturated bio‐derived raw material. An extensive screening of supports (SiO2, C, ZrO2, Al2O3), metallic ratios (Ag : Au), reaction times, temperatures, and use of solvents was carried out. The performance was optimized towards productivity and selectivity for the primary cleavage products (aldehydes and oxoesters). The optimal conditions were achieved in the absence of solvent, using Ag8Au92/SiO2 as catalyst, at 80 °C, reaction time of 1 h, substrate to catalyst=555 and 10 bar of molecular oxygen. A strong support effect was observed: the selectivity to aldehydes was best with silica as support, and to esters was best using zirconia. This shows not only that mechanochemical preparation of bimetallic catalysts is a powerful tool to generate useful catalyst compositions, but also that a safe, green, solventless synthesis of bio‐derived products can be achieved by aerobic oxidative cleavage.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Johnson Matthey

Publisher

Wiley

Subject

General Chemistry

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