Parametric study of propene oxidation over Pt and Au catalysts supported on sulphated and unsulphated titania

被引:28
作者
Baylet, Alexandre [1 ,2 ]
Capdeillayre, Chloe [1 ,2 ]
Retailleau, Laurence [1 ,2 ]
Luis Valverde, Jose [3 ]
Vernoux, Philippe [1 ,2 ]
Giroir-Fendler, Anne [1 ,2 ]
机构
[1] Univ Lyon 1, CNRS, IRCELYON, UMR 5256, F-69622 Villeurbanne, France
[2] Univ Lyon, F-69003 Lyon, France
[3] Univ Castilla La Mancha, Dept Ingn Quim, Fac Quim, E-13071 Ciudad Real, Spain
关键词
Platinum; Gold; Titania; Sulphate; Partial pressure order; Propene; Oxygen; VOLATILE ORGANIC-COMPOUNDS; NOBLE-METAL CATALYSTS; PHOTOCATALYTIC ACTIVITY; OXIDE CATALYSTS; CO OXIDATION; COMBUSTION; PLATINUM; HYDROCARBONS; AU/TIO2; STABILIZATION;
D O I
10.1016/j.apcatb.2010.11.040
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The influence of the experimental parameters such as total flow rate, partial pressure of O-2 and C3H6, the nature of the metal, platinum or gold, and the surface treatment of the titania support, sulphated or not, have been investigated on the reaction of propene oxidation. Analysis including XPS, ICP and TEM were carried out in order to characterize the platinum and gold particles and sulphate compounds (oxidation degree, content, morphology). The XPS analysis revealed the presence of Pt2+ and Au degrees species at the catalyst surface. The TEM micrographs indicated Pt particles less than 5 nm and Au particle size composed between 6 and 15 nm with a heterogeneous dispersion. For the Pt catalyst, catalytical testing displayed that the presence of sulphate compounds at the support surface did not influence the partial pressure order of O-2 and C3H6, 1.5 and 0, respectively. For the Au catalyst, the acidity of the support modified the kinetics by decreasing the partial pressure order from 0.5 to 0.7 for O-2 and from 0 to 0.7 for C3H6. In the steady state conditions, a simple power rate law model was adopted to determine the rate constant and the activation energy; Ea varying between 20 and 50 kJ mol(-1). For the Pt catalysts, the rate determining step was oxygen adsorption whereas for the Au catalysts the limiting step was concluded to be the propene dissociation. The catalytic activity was not linked to the specific surface area or the metal content but could be attributed to the nature of the metal, the sulphated support and to the particle oxidation degree and, to a less extent, the particle size. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:180 / 189
页数:10
相关论文
共 48 条
[31]   REGULARITY IN CATALYTIC PROPERTIES OF METAL OXIDES IN HYDROCARBON OXIDATION [J].
MOROOKA, Y ;
MORIKAWA, Y ;
OZAKI, A .
JOURNAL OF CATALYSIS, 1967, 7 (01) :23-&
[32]   Performance of nano-sized Au/TiO2 for selective catalytic reduction of NOx by propene [J].
Nguyen, Long Q. ;
Salim, Chris ;
Hinode, Hirofumi .
APPLIED CATALYSIS A-GENERAL, 2008, 347 (01) :94-99
[33]   Mechanistic study into the direct epoxidation of propene over gold/titania catalysts [J].
Nijhuis, TA ;
Visser, T ;
Weckhuysen, BM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (41) :19309-19319
[34]   ROLE OF ANIONS IN THE SURFACE-AREA STABILIZATION OF ZIRCONIA [J].
NORMAN, CJ ;
GOULDING, PA ;
MCALPINE, I .
CATALYSIS TODAY, 1994, 20 (02) :313-322
[35]   The influence of volatile organic compound structure on conditions required for total oxidation [J].
O'Malley, A ;
Hodnett, BK .
CATALYSIS TODAY, 1999, 54 (01) :31-38
[36]   The relation between surface state and reactivity in the DeNOx mechanism on platinum-based catalysts [J].
Pitchon, V ;
Fritz, A .
JOURNAL OF CATALYSIS, 1999, 186 (01) :64-74
[37]   Kinetics of deep oxidation of n-hexane and toluene over Pt/Al2O3 catalysts -: Platinum crystallite size effect [J].
Radic, N ;
Grbic, B ;
Terlecki-Baricevic, A .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 50 (03) :153-159
[38]   THE RATE-LIMITING STEP FOR OLEFIN COMBUSTION ON SILVER - EXPERIMENT COMPARED TO THEORY [J].
ROBERTS, JT ;
MADIX, RJ ;
CREW, WW .
JOURNAL OF CATALYSIS, 1993, 141 (01) :300-307
[39]   The extended Eyring kinetic equation and the compensation effect in catalysis [J].
Rooney, JJ .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1998, 129 (2-3) :131-134
[40]   Pt/ZrO2/TiO2 catalysts for selective hydrogenation of crotonaldehyde:: Tuning the SMSI effect for optimum performance [J].
Ruppert, A. M. ;
Paryjczak, T. .
APPLIED CATALYSIS A-GENERAL, 2007, 320 :80-90