Issue 7, 2013

High catalytic performance of palladium nanoparticles supported on multiwalled carbon nanotubes in alkene hydrogenation reactions

Abstract

The synthesis of Pd nanoparticles (Pd-NPs) supported on multi-walled carbon nanotubes (MWCNTs) and the cataytic performance of the resulting material (Pd-NPs/MWCNTs) in hydrogenation reactions are presented. Facile preparation approaches based on the decomposition of Pd precursors in the presence of MWCNTs lead to homogeneous dispersions of supported Pd-NPs with an average size of 4 nm and Pd loads of about 12%. The catalytic performance of this material was evaluated in hydrogenation reactions of α,β-unsaturated ketones, alkenes, cyclic di-, tri- and tetraenes, aromatic compounds, terpenes and terpenoids, resulting in very high activity offering short reaction times, high conversion rates, notable selectivity, and acceptable recyclability under mild conditions.

Graphical abstract: High catalytic performance of palladium nanoparticles supported on multiwalled carbon nanotubes in alkene hydrogenation reactions

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2013
Accepted
24 Mar 2013
First published
26 Apr 2013

New J. Chem., 2013,37, 1968-1972

High catalytic performance of palladium nanoparticles supported on multiwalled carbon nanotubes in alkene hydrogenation reactions

M. Cano, A. M. Benito, W. K. Maser and E. P. Urriolabeitia, New J. Chem., 2013, 37, 1968 DOI: 10.1039/C3NJ00183K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements