Mechanism of tetralin ring opening and ring contraction over bifunctional Ir/SiO2-Al2O3 catalysts

Autor: Guy Toussaint, Laurent Piccolo, Salim Nassreddine, Christophe Geantet
Přispěvatelé: Institut de recherches sur la catalyse et l'environnement de Lyon (IRCELYON), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Zdroj: ChemSusChem
ChemSusChem, ChemPubSoc Europe/Wiley, 2012, 5, pp.1717-1723. ⟨10.1002/cssc.201200080⟩
ISSN: 1864-5631
1864-564X
DOI: 10.1002/cssc.201200080⟩
Popis: The development of cleaner fuels from conventional resources requires the finding of new hydrotreatment processes able to improve the combustion performances of fuels and limit undesirable emissions. In the context of gas oil upgrading by selective ring opening, we have investigated the hydroconversion of tetralin over iridium nanoparticles supported on amorphous silica-alumina. The conversion of tetralin leads to hydrogenation, ring-contraction, and ring-opening products. The selectivity to ring-opening/-contraction products (ROCPs) increases linearly with the acid-metal site ratio and can be tuned by modifying the metal loading, the metal nanoparticle size, or the support composition. From the combination of catalytic tests at variable conversion and the products identification by two-dimensional gas chromatography, a mechanistic reaction scheme has been established. Aromatic ROCPs are formed through purely acidic steps, whereas the formation of saturated ROCPs mostly involves bifunctional reaction steps. Iridium-catalyzed hydrogenolysis appears to be a minor pathway with respect to iridium-catalyzed hydrogenation and Bronsted acid catalyzed isomerization.
Databáze: OpenAIRE