Transient kinetics of carbon monoxide oxidation by oxygen over supported palladium/ceria/zirconia three-way catalysts in the absence and presence of water and carbon dioxide

被引:79
作者
Rajasree, R [1 ]
Hoebink, JHBJ [1 ]
Schouten, JC [1 ]
机构
[1] Eindhoven Univ Technol, Lab Chem Reactor Engn, NL-5600 MB Eindhoven, Netherlands
关键词
kinetics; modeling; diffusion CO oxidation; H2O; CO2; three-way catalysis;
D O I
10.1016/j.jcat.2003.12.014
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 transient kinetics of CO oxidation by O-2 over alumina-supported Pd/CeO2/ZrO2 three-way catalysts is described in the absence and presence of H2O and CO2 in the feed. Experiments were carried out in a laboratory fixed-bed reactor at 573 K, while periodically switching between a feed of 1 vol% CO in He and a feed of 0.5 vol% O-2 in He with a frequency Of 1/30 Hz. Separate experiments were performed with 14 vol% water in both feeds, and, as is the case with real engine exhaust gas, with 14 vol% water and 14 Vol% CO2 in both feeds. The presence of water largely enhanced the reaction rate, while it was inhibited by CO2. A transient kinetic model has been developed for this catalyst, based on the experimental data. It was found that the reaction in the absence of H2O and CO) proceeds via the same elementary steps as reported for a Pt/Rh/CeO2/gamma-Al2O3 catalyst (R.H. Nibbelke, AJ.L. Nievergeld, J.H.B.J. Hoebink, G.B. Marin, Appl. Catal. B 19 (1998) 245). Only the rate coefficient for CO desorption from I'd was significantly lower, in line with literature data. Additional elementary steps were combined with the above model in order to describe quantitatively the effect of water. The present study also shows that bulk diffusion of oxygen in ceria plays a major role, when the rate is enhanced by water. The inhibition effect Of CO2 could be described by a lower amount of oxygen-storage sites. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:36 / 43
页数:8
相关论文
共 38 条
  • [1] Surface and reduction energetics of the CeO2-ZrO2 catalysts
    Balducci, G
    Kaspar, J
    Fornasiero, P
    Graziani, M
    Islam, MS
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (03): : 557 - 561
  • [2] STEAM EFFECTS IN 3-WAY CATALYSIS
    BARBIER-JR, J
    DUPREZ, D
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 1994, 4 (2-3) : 105 - 140
  • [3] BEROWITZ PJ, 1988, J CHEM PHYS, V92, P5213
  • [4] CAMPMAN MAJ, 1996, THESIS EINDHOVEN U T
  • [5] SOLID-STATE H-1 MAS NMR CHARACTERIZATION OF GAMMA-ALUMINA AND MODIFIED GAMMA-ALUMINAS
    DECANIO, EC
    EDWARDS, JC
    BRUNO, JW
    [J]. JOURNAL OF CATALYSIS, 1994, 148 (01) : 76 - 83
  • [6] ENGEL T, 1979, ADV CATAL, V28, P1
  • [7] Engler BH, 1995, STUD SURF SCI CATAL, V96, P441
  • [8] RH-LOADED CEO2-ZRO2 SOLID-SOLUTIONS AS HIGHLY EFFICIENT OXYGEN EXCHANGERS - DEPENDENCE OF THE REDUCTION BEHAVIOR AND THE OXYGEN STORAGE CAPACITY ON THE STRUCTURAL-PROPERTIES
    FORNASIERO, P
    DIMONTE, R
    RAO, GR
    KASPAR, J
    MERIANI, S
    TROVARELLI, A
    GRAZIANI, M
    [J]. JOURNAL OF CATALYSIS, 1995, 151 (01) : 168 - 177
  • [9] Using a high-resolution magnetic sector mass spectrometer for fast analysis of transient reaction processes in automotive catalytic converters
    Harmsen, JMA
    Bijvoets, T
    Hoebink, JHBJ
    Hachiya, T
    Bassett, J
    Brooker, AD
    Schouten, JC
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (10) : 957 - 964
  • [10] NO reduction by CO over automotive exhaust gas catalysts in the presence of O2
    Harmsen, JMA
    Hoebink, JHBJ
    Schouten, JC
    [J]. CATALYSIS LETTERS, 2001, 71 (1-2) : 81 - 90