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Effect of support acidity during selective hydrogenolysis of glycerol over supported palladium-ruthenium catalysts.
Guadix-Montero, Susana; Santos-Hernandez, Alba; Folli, Andrea; Sankar, Meenakshisundaram.
Afiliação
  • Guadix-Montero S; Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Cardiff CF10 3AT, UK.
  • Santos-Hernandez A; Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Cardiff CF10 3AT, UK.
  • Folli A; School of Chemistry, Cardiff University, Cardiff CF10 3AT, UK.
  • Sankar M; Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Cardiff CF10 3AT, UK.
Philos Trans A Math Phys Eng Sci ; 378(2176): 20200055, 2020 Jul 24.
Article em En | MEDLINE | ID: mdl-32623993
We report the role of the acidity of support during the selectivity hydrogenolysis of glycerol over supported bimetallic palladium-ruthenium (PdRu) catalysts. The PdRu nanoparticles were supported on a series of metal oxides and zeolitic supports via the modified impregnation method and tested for the liquid-phase hydrogenolysis of glycerol using gaseous hydrogen. The relative acid site densities of selected catalysts were determined by ammonia temperature-programmed desorption and pyridine desorption experiments. Based on these studies, we report a direct correlation between the catalytic activity (conversion and 1,2 propane diol yield) and two different acid sites (strong acid sites and very strong acid sites). Besides zeolite-supported catalysts, TiO2 supported PdRu nanoparticles exhibit moderate catalytic activity; however, this catalyst shows high selectivity for the desired C-O bond cleavage to produce C3 products over the undesired C-C bond cleavage to produce < C3 products. This article is part of a discussion meeting issue 'Science to enable the circular economy'.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article