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Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes

Authors :
Catherine Especel
Florence Epron
Maria Ana Vicerich
Carlos Luis Pieck
V. M. Benitez
Instituto de Investigaciones en Catálisis y Petroquímica 'Ing. José Miguel Parera' [Santa Fe] (INCAPE)
Consejo Nacional de Investigaciones Científicas y Técnicas [Buenos Aires] (CONICET)-Universidad Nacional del Litoral [Santa Fe] (UNL)
Du site actif au matériau catalytique (E3) (SAMCat )
Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP)
Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Poitiers-Institut de Chimie du CNRS (INC)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Poitiers-Institut de Chimie du CNRS (INC)
Université de Poitiers-Centre National de la Recherche Scientifique (CNRS)-Université de Poitiers-Centre National de la Recherche Scientifique (CNRS)
Source :
Applied Catalysis A : General, Applied Catalysis A : General, Elsevier, 2013, 453, pp.167-174. ⟨10.1016/j.apcata.2012.12.015⟩
Publication Year :
2013
Publisher :
HAL CCSD, 2013.

Abstract

The influence of Ir content on the properties of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes was studied. It was found that these catalysts display a strong Pt–Ir interaction but only a weak metal–support interaction. Catalyst acidities depend on the metal loading, but opposite effects were observed on alumina (decrease) or titania (increase) as the metal loading increased. The results obtained from test reactions (cyclohexane dehydrogenation and cyclopentane hydrogenolysis) showed that titania supported catalysts were less active than their alumina supported counterparts. This behavior could be due to the partial blockage of metallic sites by migrated TiOx species and the sinterization of metallic phase during the reduction step. The methylcyclopentane ring opening reaction was found to occur through a partially selective mechanism, and an increase in activity as the Ir loading increased was observed. The selective mechanism was favored by higher total metal loadings, possibly due to an increase in the size of metallic aggregates. Alumina supported catalysts present higher ring opening selectivities. The activity for decalin ring opening increased both with metal loading and reaction temperature level. Fil: Vicerich, Maria Ana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina Fil: Benitez, Bibiana M.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina Fil: Especel, Catherine. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; Francia Fil: Epron, Florence. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; Francia Fil: Pieck, Carlos Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina

Details

Language :
English
ISSN :
0926860X
Database :
OpenAIRE
Journal :
Applied Catalysis A : General, Applied Catalysis A : General, Elsevier, 2013, 453, pp.167-174. ⟨10.1016/j.apcata.2012.12.015⟩
Accession number :
edsair.doi.dedup.....7bf3b76e2a1e04717d38e4edef70212e
Full Text :
https://doi.org/10.1016/j.apcata.2012.12.015⟩