The water-gas-shift reaction at short contact times

被引:168
|
作者
Wheeler, C [1 ]
Jhalani, A [1 ]
Klein, EJ [1 ]
Tummala, S [1 ]
Schmidt, LD [1 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
water-gas shifts; short contact times; Pt; ceria; elementary-step mechanism; noble metals; methanation; first-order kinetics;
D O I
10.1016/j.jcat.2004.01.002
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
We have examined the water-gas-shift reaction over noble metals and metals with ceria for catalyst contact times between 0.008 and 0.05 s for temperatures from 300 to 1000 degreesC. With reactants of CO, H-2, and H2O at a 1/2/4 composition, the reaction approached equilibrium at these contact times for temperatures as low as 380degreesC, which corresponds to a 5011 H-2/CO ratio. All results follow the equilibrium conversion versus temperature curve at high temperatures and then the rate decreases rapidly as temperature decreases. All metals show considerable promotion upon ceria addition, with Pt/ceria showing the most promise in terms of promotion, stability, and lack of methanation activity. A simple kinetic model that assumes first-order reversible reaction in all species fits all data at all temperatures from equilibrium to low conversions. The rate is nearly independent of surface area over a wide variation of parameters, and rates indicate that mass-transfer limitations are not dominant. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:191 / 199
页数:9
相关论文
共 50 条
  • [1] Water-gas-shift reaction on metal nanoparticles and surfaces
    Liu, Ping
    Rodriguez, Jose A.
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2007, 126 (16):
  • [2] Combination of autothermal reforming with water-gas-shift reaction - small-scale testing of different water-gas-shift catalysts
    Pasel, J
    Cremer, P
    Wegner, B
    Peters, R
    Stolten, D
    [J]. JOURNAL OF POWER SOURCES, 2004, 126 (1-2) : 112 - 118
  • [3] Mechanisms of the water-gas-shift reaction by iron pentacarbonyl in the gas phase
    Rozanska, Xavier
    Vuilleumier, Rodolphe
    [J]. INORGANIC CHEMISTRY, 2008, 47 (19) : 8635 - 8640
  • [4] Perovskite-type catalysts for the water-gas-shift reaction\
    Basile, Francesco
    Brenna, Giuseppe
    Fornasari, Giuseppe
    Del Gallo, Pascal
    Gary, Daniel
    Vaccari, Angelo
    [J]. SCIENTIFIC BASES FOR THE PREPARATION OF HETEROGENEOUS CATALYSTS: PROCEEDINGS OF THE 10TH INTERNATIONAL SYMPOSIUM, 2010, 175 : 471 - 474
  • [5] On the reaction mechanism of methanol synthesis and water-gas-shift on Cu
    Grabow, Lars C.
    Mavrikakis, Manos
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2010, 240
  • [6] Mechanistic Studies of Water-Gas-Shift Reaction on Transition Metals
    Lin, Chia-Hao
    Chen, Chung-Liang
    Wang, Jeng-Han
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (38): : 18582 - 18588
  • [7] Water-gas-shift reaction: A reaction network analysis of the microkinetic model.
    Callaghan, C
    Fishtik, I
    Datta, R
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 226 : U558 - U558
  • [8] A Study of Support Effects for the Water-Gas-Shift Reaction over Cu
    Chang, Jian
    Feng, Zhuoming
    Vohs, John M.
    Gorte, Raymond J.
    [J]. CATALYSTS, 2022, 12 (11)
  • [9] Progress in water-gas-shift catalysts
    Liu, QS
    Zhang, QC
    Ma, WP
    He, RX
    Kou, LJ
    Mou, ZJ
    [J]. PROGRESS IN CHEMISTRY, 2005, 17 (03) : 389 - 398
  • [10] Deactivation mechanisms for Pd/ceria during the water-gas-shift reaction
    Wang, X
    Gorte, RJ
    Wagner, JP
    [J]. JOURNAL OF CATALYSIS, 2002, 212 (02) : 225 - 230