Increased conversion and selectivity of 4-nitrostyrene hydrogenation to 4-aminostyrene on Pt nanoparticles supported on titanium-tungsten mixed oxides

FANTAUZZI, MARZIA;ROSSI, ANTONELLA;
2016-01-01

Abstract

A catalyst series consisting in platinum nanoparticles photodeposited on pure titania and on W/Ti mixed oxides, these latter prepared by the sol-gel method, were tested in the hydrogenation of 4-nitrostyrene. A remarkable increase in the reaction rate occurred when the catalyst support contained tungsten, with a parallel boosting in the selective reduction of the nitro group. With the selective W-containing catalysts, the reaction proceeded at constant rate (zero order rate law), while the tungsten-free catalyst showed a rate-dependence on the 4-nitrostyrene concentration (positive order reaction). The presence of tungsten in the support is beneficial not only because a higher surface area is obtained, thanks to the anatase stabilization of tungsten in titania, but also because it allows the photodeposition of smaller, better dispersed platinum particles, on which the adsorption of the aromatic part of 4-nitrostyrene is less favored. Tungsten not only substitutes titanium in the titania lattice, as revealed by HAAF-STEM analysis, but it is also present as WOx species partly covering the Pt nanoparticles photodeposited on the mixed oxide support, as revealed by an in depth distribution XPS analysis. This accounts for the progressively lower performance observed with increasing tungsten content in the catalysts, the highest conversion and selective hydrogenation of the 4-nitrostyrene nitro group having been achieved on the catalyst with a 1% W/Ti molar ratio
2016
Selective hydrogenation, Reduction of nitro group, Supported Pt, W-doped TiO2, X-ray photoelectron spectroscopy (XPS), Surface analysis, Surface chemistry
Files in This Item:
File Size Format  
Increased conversion and selectivity.pdf

Solo gestori archivio

Type: versione editoriale
Size 2.62 MB
Format Adobe PDF
2.62 MB Adobe PDF & nbsp; View / Open   Request a copy

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Questionnaire and social

Share on:
Impostazioni cookie