Catalytic oxidation of toluene over CuNaHY zeolites - Coke formation and removal

被引:88
作者
Antunes, AP
Ribeiro, MF
Silva, JM
Ribeiro, FR
Magnoux, P
Guisnet, M
机构
[1] Inst Super Tecn, Dept Engn Quim, P-1049001 Lisbon, Portugal
[2] Inst Super Engn Lisboa, Dept Engn Quim, P-1949014 Lisbon, Portugal
[3] Univ Poitiers, CNRS, UMR 6503, F-86022 Poitiers, France
关键词
volatile organic compounds; copper zeolite catalysts; toluene oxidation; coke;
D O I
10.1016/S0926-3373(01)00174-6
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
Catalytic deep oxidation of toluene at low concentration in air, has been studied over CuNaHY zeolites with different copper contents. The reaction has been investigated in the course of time-on-stream, at temperatures between 150 and 500 degreesC. The effect of copper content on the conversion of toluene into CO2 and on the formation of carbonaceous deposits (coke) retained inside the zeolite pores has been analyzed as a function of the reaction temperature. The analysis of the coke extracted from the catalysts showed that it is mainly composed of aromatic hydrocarbons and oxygenated aromatic compounds, the latter being predominant at low temperature and preferentially formed on the catalysts containing more copper. A bifunctional mechanism was proposed to explain the formation of coke over CuNaHY catalysts. Based on the differences of the nature of coke formed on NaHY and CuNaHY catalysts, and on a discussion about the coke formation and location, it was possible to conclude that copper sites are involved in both toluene and coke oxidation reactions. The increase of copper content from 1 to 8 wt.% promotes the oxidation of toluene and facilitates the removal of coke formed in the course of reaction. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 164
页数:16
相关论文
共 26 条
  • [1] RETAINED PRODUCTS FROM THE REACTION OF BENZENE AND TOLUENE OVER H-ZSM5 ZEOLITE
    ANDERSON, JR
    DONG, QN
    CHANG, YF
    WESTERN, RJ
    [J]. JOURNAL OF CATALYSIS, 1991, 127 (01) : 113 - 127
  • [2] REACTION NETWORKS IN THE CATALYTIC VAPOR-PHASE OXIDATION OF TOLUENE AND XYLENES
    ANDERSSON, SLT
    [J]. JOURNAL OF CATALYSIS, 1986, 98 (01) : 138 - 149
  • [3] ENVIRONMENTAL CATALYSIS
    ARMOR, JN
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 1992, 1 (04) : 221 - 256
  • [4] Investigations of coke deposits formed during deep oxidation of benzene over Pd and Cu exchanged Y-type zeolites
    Becker, L
    Forster, H
    [J]. APPLIED CATALYSIS A-GENERAL, 1997, 153 (1-2) : 31 - 41
  • [5] COKE FORMATION IN HIGH-SILICA ZEOLITES
    BIBBY, DM
    HOWE, RF
    MCLELLAN, GD
    [J]. APPLIED CATALYSIS A-GENERAL, 1992, 93 (01) : 1 - 34
  • [6] COMPARISON OF MODIFIED TRANSITION METAL-EXCHANGED ZEOLITE CATALYSTS FOR OXIDATION OF CHLORINATED HYDROCARBONS
    CHATTERJEE, S
    GREENE, HL
    PARK, YJ
    [J]. JOURNAL OF CATALYSIS, 1992, 138 (01) : 179 - 194
  • [7] Catalytic oxidation of volatile organic compounds II.: Influence of the physicochemical characteristics of Pd/HFAU catalysts on the oxidation of o-xylene
    Dégé, P
    Pinard, L
    Magnoux, P
    Guisnet, M
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2000, 27 (01) : 17 - 26
  • [8] Derouane E.G., 1985, Stud. Surf. Sci. Catal, V20, P221
  • [9] REACTION OF BENZENE AND TOLUENE IN THE PRESENCE OF OXYGEN OVER H-ZSM5 ZEOLITE - AROMATIC OXYGENATES IN THE PRODUCT
    DONG, QN
    ANDERSON, JR
    MOLE, T
    CHANG, YF
    WESTERN, RJ
    [J]. APPLIED CATALYSIS, 1991, 72 (01): : 99 - 107
  • [10] TEMPERATURE PROGRAMMED REDUCTION OF COPPER IONS IN ZEOLITES
    GENTRY, SJ
    HURST, NW
    JONES, A
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1979, 75 : 1688 - 1699