Transient analysis of oxygen storage capacity of Pt/CeO2-ZrO2 materials with millisecond- and second-time resolution

被引:18
作者
Kondratenko, Evgenii V. [1 ]
Sakamoto, Yoshiyuki [2 ]
Okumura, Kohei [2 ]
Shinjoh, Hirofumi [2 ]
机构
[1] Univ Rostock, Leibniz Inst Catalysis, Branch Berlin, D-12489 Berlin, Germany
[2] Toyota Cent Res & Dev Labs Inc, Nagakute, Aichi 4801192, Japan
关键词
Oxygen storage capacity; Mechanism; TAP; Platinum; Ceria; CEO2-ZRO2 MIXED OXIDES; SURFACE-AREA; REDOX BEHAVIOR; PARTIAL OXIDATION; 3-WAY CATALYSTS; SYNTHESIS GAS; CO OXIDATION; METHANE; TEMPERATURE; MECHANISM;
D O I
10.1016/j.apcatb.2009.01.006
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
A simple method for determining the speed of oxygen release from Pt/CeO2-ZrO2 materials is proposed. We determined the speed of oxygen release from three differently prepared Pt(1 wt%)/CeO-ZrO2 catalysts by two methods: the method employing temporal analysis of products (TAP) reactor with CO, O-2, and CO2 pulsed gases, and a conventional method with CO and O-2 switch gases. Strong CO2 adsorption precluded correct analysis of oxygen release speed, when it was determined from the amount Of CO2 formed. Therefore, instead Of the amount of CO2. formed, we suggested the t(max) value, defined as the position of maximal intensity Of CO2 transient responses obtained Upon low-intensity (10(15)-10(16) molecules) CO pulsing ill the TAP reactor. Shorter the t(max) Value, higher the rate of oxygen release, because the temperature dependence of the t(max) determined in the present Study resembles the previous results of oxygen release analysis [T. Tanabe, A. Suda, C. Descorme, D. Duprez. H. Shinjoh, M. Sugiura, Stud. Surf. Sci. Catal. 138 (2001) 135]. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:476 / 483
页数:8
相关论文
共 30 条
  • [11] Interactions of CO with Pt/ceria catalysts
    Holmgren, A
    Andersson, B
    Duprez, D
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 1999, 22 (03) : 215 - 230
  • [12] Studies of the oxygen release reaction in the platinum-ceria-zirconia system
    Hori, CE
    Brenner, A
    Ng, KYS
    Rahmoeller, KM
    Belton, D
    [J]. CATALYSIS TODAY, 1999, 50 (02) : 299 - 308
  • [13] Preparation of CeO2/ZrO2 modified by MgO: Roles of MgO for upgrading redox property
    Kakuta, Noriyoshi
    Kudo, Yosuke
    Eguchi, Tsuyoshi
    Ohkita, Hironobu
    Mizushima, Takanori
    Yamomoto, Takashi
    Yasuda, Mitsunobu
    [J]. SCIENTIFIC BASES FOR THE PREPARATION OF HETEROGENEOUS CATALYSTS, PROCEEDINGS OF THE 9TH INTERNATIONAL SYMPOSIUM, 2006, 162 : 777 - 784
  • [14] Mechanistic origin of the different activity of Rh-ZSM-5 and Fe-ZSM-5 in N2O decomposition
    Kondratenko, Evgenii V.
    Kondratenko, Vita A.
    Santiago, Marta
    Perez-Ramirez, Javier
    [J]. JOURNAL OF CATALYSIS, 2008, 256 (02) : 248 - 258
  • [15] Oxygen mobility in CeO2 and CexZr(1-x)O2 compounds:: Study by CO transient oxidation and 18O/16O isotopic exchange
    Madier, Y
    Descorme, C
    Le Govic, AM
    Duprez, D
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (50) : 10999 - 11006
  • [16] MATSUMOTO S, 1991, CAT SCI TEC, V1, P335
  • [17] Matsumoto S, 2008, ADV CHEM ENG, V33, P1, DOI 10.1016/S0065-2377(07)33001-9
  • [18] MONTERRA C, 1995, SPECTROCHIM ACTA A, V55, P95
  • [19] Direct conversion of methane to synthesis gas through gas-solid reaction using CeO2-ZrO2 solid solution at moderate temperature
    Otsuka, K
    Wang, Y
    Nakamura, M
    [J]. APPLIED CATALYSIS A-GENERAL, 1999, 183 (02) : 317 - 324
  • [20] PARTIAL OXIDATION OF METHANE USING THE REDOX OF CERIUM OXIDE
    OTSUKA, K
    USHIYAMA, T
    YAMANAKA, I
    [J]. CHEMISTRY LETTERS, 1993, (09) : 1517 - 1520