Abstract

Abstract This paper presents the results of the propylene epoxidation in co-presence of hydrogen and oxygen on both dried and calcined Au catalysts, which were prepared by liquid grafting method using Me 2 Au(acac) as a precursor and trimethylsilylated Ti-MCM-48 as a support. The calcined catalyst shows PO activity at temperatures much higher and wider than the dried one. Addition of inorganic salts greatly modified the catalytic behaviors. CsNO 3 could be a promising promoter whereas KBr led to the production of propionaldehyde instead of propylene oxide.

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