Novel embedded Pd@CeO2 catalysts: a way to active and stable catalysts (Articolo in rivista)

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  • Novel embedded Pd@CeO2 catalysts: a way to active and stable catalysts (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1039/b916035c (literal)
Alternative label
  • Cargnello Matteo; Montini Tiziano; Polizzi Stefano; Wieder Noah L.; Gorte Raymond J.; Graziani Mauro; Fornasiero Paolo (2010)
    Novel embedded Pd@CeO2 catalysts: a way to active and stable catalysts
    in Dalton transactions (2003. Print); ROYAL SOC CHEMISTRY, THOMAS GRAHAM HOUSE,, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND (Regno Unito)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Cargnello Matteo; Montini Tiziano; Polizzi Stefano; Wieder Noah L.; Gorte Raymond J.; Graziani Mauro; Fornasiero Paolo (literal)
Pagina inizio
  • 2122 (literal)
Pagina fine
  • 2127 (literal)
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  • international co-authors (literal)
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  • http://pubs.rsc.org/en/Content/ArticleLanding/2010/DT/b916035c (literal)
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  • 39 (literal)
Rivista
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  • 6 (literal)
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  • 8 (literal)
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  • ISI Web of Science (WOS) (literal)
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  • Univ Trieste, Dept Chem, Trieste Res Unit, ICCOM,CNR,CENMAT, I-34127 Trieste, Italy Univ Trieste, INSTM, Trieste Res Unit, I-34127 Trieste, Italy Univ Venice, Venice Res Unit, INSTM, Dept Phys Chem, I-30172 Venice, Italy Univ Penn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA (literal)
Titolo
  • Novel embedded Pd@CeO2 catalysts: a way to active and stable catalysts (literal)
Abstract
  • 1-wt% Pd-CeO2 catalysts were prepared by co-precipitation of Pd nanoparticles with ceria (Pd@CeO2-CP), by a microemulsion procedure (Pd@CeO2-ME), and by normal impregnation of Pd salts (Pd/CeO2-IMP) in order to test the concept that Pd-CeO2 catalysts could be more stable for the water-gas-shift (WGS) reaction when the Pd is embedded in CeO2. Initial WGS rates measured at 250 degrees C were similar for the Pd@CeO2-CP and Pd/CeO2-IMP, indicating that Pd was accessible for gas-phase reactions on both catalysts. Pd@CeO2-CP exhibited better stability for WGS than did Pd/CeO2-IMP but exposure to the WGS environment at 400 degrees C still caused a decrease in activity. Physical characterization of the Pd@CeO2-ME implied that the core-shell nanoparticles underwent condensation that resulted in a low surface area and poor Pd accessibility. However, the Pd@CeO2-ME sample exhibited good stability for WGS, suggesting that more effective encapsulation of Pd can limit the sintering of the metal phase, thus resulting in stable catalysts under high temperature reaction conditions. (literal)
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