Controlled preparation and characterization of Pt-Rh/Al2O3 bimetallic catalysts for reactions in reducing conditions

[Display omitted] •Pt and Rh bimetallic catalysts were prepared by various techniques.•Characterization by CO-FTIR showed the presence of alloyed species.•Characterization by NO-CO FTIR permits to quantify Rh and Pt at the surface.•Strong Pt-Rh interactions enhance the activity and selectivity for M...

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Bibliographic Details
Published in:Applied catalysis. A, General General, 2016-05, Vol.517, p.81-90
Main Authors: Hérault, Nelly, Olivet, Lilian, Pirault-Roy, Laurence, Especel, Catherine, Vicerich, María A., Pieck, Carlos L., Epron, Florence
Format: Article
Language:English
Subjects:
Bimetallic supported catalysts
Catalysis
Chemical Sciences
Cyclohexane dehydrogenation
FTIR of CO
FTIR of NO-CO
Organic chemistry
Pt-Rh
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Summary:[Display omitted] •Pt and Rh bimetallic catalysts were prepared by various techniques.•Characterization by CO-FTIR showed the presence of alloyed species.•Characterization by NO-CO FTIR permits to quantify Rh and Pt at the surface.•Strong Pt-Rh interactions enhance the activity and selectivity for MCP ring-opening. Pt-Rh bimetallic catalysts on alumina support were prepared according to three different techniques, one leading to random deposition of the two metals at the support’s surface, the two others, namely the organometallic grafting and the colloidal route, favoring the formation of bimetallic particles with strong Pt-Rh interactions. Catalysts were characterized by ICP, H2 chemisorption, TPR, FTIR of chemisorbed CO and NO-CO. Then they were evaluated in cyclohexane dehydrogenation and methylcyclopentane hydrogenolysis reactions. Strong interaction between Pt and Rh was demonstrated for catalysts prepared by controlled preparation method, which leads to a strong synergetic effect for methylcyclopentane ring-opening, in terms of activity and selectivity, whereas these interactions do not play a role in cyclohexane dehydrogenation.
ISSN:0926-860X
1873-3875
DOI:10.1016/j.apcata.2016.02.024