For the first time, polyketone (poly-3-oxotrimethylene, PK) has been employed as support for Pd nanoparticles. Three different approaches have been adopted: (i) reduction of Pd(OAc)(2) in EtOH under microwave irradiation, (ii) hydrothermal reduction of the same precursor in EtOH or n-BuOH employing traditional heating and (iii) vaporization of Pd metal through metal vapour synthesis. These supported systems have been characterized by solid state NMR, TEM, ICP, XPS, BET and tested in the selective hydrogenation of cinnamaldehyde (CAL) to hydrocinnamaldehyde (HCAL) as probe reaction. Their catalytic performances have been compared in relation to their preparation procedure and morphology. It is remarkable that these catalysts do not show significant leaching even after several catalytic recycles, thus indicating their high stability and recyclability, ascribed to a stabilizing capacity of this particular polymeric support. (c) 2012 Elsevier B.V. All rights reserved.
New palladium catalysts on polyketone prepared through different smart methodologies and their use in the hydrogenation of cinnamaldehyde
MARTRA, Gianmario;MANZOLI, Maela
2012-01-01
Abstract
For the first time, polyketone (poly-3-oxotrimethylene, PK) has been employed as support for Pd nanoparticles. Three different approaches have been adopted: (i) reduction of Pd(OAc)(2) in EtOH under microwave irradiation, (ii) hydrothermal reduction of the same precursor in EtOH or n-BuOH employing traditional heating and (iii) vaporization of Pd metal through metal vapour synthesis. These supported systems have been characterized by solid state NMR, TEM, ICP, XPS, BET and tested in the selective hydrogenation of cinnamaldehyde (CAL) to hydrocinnamaldehyde (HCAL) as probe reaction. Their catalytic performances have been compared in relation to their preparation procedure and morphology. It is remarkable that these catalysts do not show significant leaching even after several catalytic recycles, thus indicating their high stability and recyclability, ascribed to a stabilizing capacity of this particular polymeric support. (c) 2012 Elsevier B.V. All rights reserved.File | Dimensione | Formato | |
---|---|---|---|
PdKApplCatalA2012.pdf
Accesso riservato
Descrizione: Articolo principale
Tipo di file:
PDF EDITORIALE
Dimensione
1.37 MB
Formato
Adobe PDF
|
1.37 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
Erratum2013.pdf
Accesso riservato
Descrizione: Corrigendum dell'articolo principale
Tipo di file:
PDF EDITORIALE
Dimensione
151.35 kB
Formato
Adobe PDF
|
151.35 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.