Partial hydrogenation reactions over Pd-containing hybrid inorganic / polymeric catalytic membranes (Articolo in rivista)

Type
Label
  • Partial hydrogenation reactions over Pd-containing hybrid inorganic / polymeric catalytic membranes (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.apcata.2013.03.040 (literal)
Alternative label
  • Liguori, Francesca; Barbaro, Pierluigi; Giordano, Cristiana; Sawa, Haruo (2013)
    Partial hydrogenation reactions over Pd-containing hybrid inorganic / polymeric catalytic membranes
    in Applied catalysis. A, General (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Liguori, Francesca; Barbaro, Pierluigi; Giordano, Cristiana; Sawa, Haruo (literal)
Pagina inizio
  • 81 (literal)
Pagina fine
  • 88 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 459 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di Chimica dei Composti Organo Metallici - Consiglio Nazionale delle Ricerche (ICCOM-CNR), Via Madonna del Piano 10, 50019 Sesto Fiorentino; Firenze, Italy. Centro di Microscopie Elettroniche - Consiglio Nazionale delle Ricerche (CeME), Via Madonna del Piano 10, 50019 Sesto Fiorentino; Firenze, Italy. Nippon Kodoshi Corporation, 648 Hirookakami, Haruno, Kochi, 781-0395, Japan. (literal)
Titolo
  • Partial hydrogenation reactions over Pd-containing hybrid inorganic / polymeric catalytic membranes (literal)
Abstract
  • Palladium nanoparticles (4.6 nm) were grown into a hybrid zirconia / polyvinyl alcohol matrix, to afford a contactor type catalytic membrane suitable for application to partial hydrogenation reactions in the liquid phase under smooth conditions. A Pd content as low as 0.3% weight allowed for the hydrogenation of C=C and C?C bonds within reasonable timeframes and satisfactory selectivity. Particularly, the partial hydrogenation reaction of 3-hexyn-1-ol to the cis-ene product could be achieved with no significant loss of catalytic performance over prolonged reaction period. The catalytic system showed significant benefits in terms of metal leaching, efficiency under mild reaction conditions, reusability, mechanical and chemical stability, use in hydrophilic solvents, with no need of regeneration steps. (literal)
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