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HERO ID
1958957
Reference Type
Journal Article
Title
Bimetallic Au-Pd catalysts for selective hydrogenation of butadiene: Influence of the preparation method on catalytic properties
Author(s)
El Kolli, N; Delannoy, L; Louis, C
Year
2013
Is Peer Reviewed?
Yes
Journal
Journal of Catalysis
ISSN:
0021-9517
EISSN:
1090-2694
Volume
297
Page Numbers
79-92
DOI
10.1016/j.jcat.2012.09.022
Web of Science Id
WOS:000314136500009
Abstract
Supported Au catalysts modified by the addition of small amount of Pd (Au/Pd atomic ratio (10) were prepared according to three different methods, co-deposition-precipitation with urea (DPU), deposition of colloids stabilised either by polyvinyl alcohol (PVA) or by tetrakis (hydroxypropyl) phosphonium chloride (THPC) on two oxide supports, alumina and titania. In all cases, after thermal treatments (under H-2 at 300 degrees C for DPU samples and under air then H-2 at 500 degrees C for PVA and THPC samples), the metal particles were smaller than 5 nm. Characterisation by DRIFTS coupled with CO adsorption revealed that the particles are bimetallic and that Pd is present on the particle surface as isolated Pd by Au atoms and as Pd dimers. In addition, the surface composition depends on the preparation method and the Au/Pd ratio and evolves under CO exposure towards a gradual enrichment in palladium.
AuPd catalysts showed improved catalytic properties compared to Au catalysts in selective hydrogenation of butadiene in presence of excess of propene. Activity was higher and directly related to the Pd content. The nature of the support has no influence on the catalytic properties. An optimised selectivity to butenes with poor formation of alkanes (propane and butane) could be achieved for an atomic Au/Pd ratio of 20. THPC-based catalysts showed higher activity than DPU samples in spite of slightly larger metal particles, and this was attributed to the presence of residual phosphorus after catalyst activation. PVA-based catalysts, which contained slightly larger metal particles, were slightly less active, but were more selective to butenes. This was related to the absence of Pd dimers, responsible for overhydrogenation. (c) 2012 Elsevier Inc. All rights reserved.
Keywords
AuPd bimetallic nanoparticles; Preparation; Surface segregation; Selective hydrogenation; Hydrogenation of butadiene; CO adsorption; FTIR; DRIFTS
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