Organic chemistry of coke formation

被引:677
作者
Guisnet, M [1 ]
Magnoux, P [1 ]
机构
[1] Univ Poitiers, Catalyse Chim Organ Lab, UMR CNRS 6503, Fac Sci, F-86022 Poitiers, France
关键词
coke formation; bifunctional catalysts; acid catalysts;
D O I
10.1016/S0926-860X(00)00845-0
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 modes of formation of carbonaceous deposits ("coke") during the transformation of organic compounds over acid and over bifunctional noble metal-acid catalysts are described. At low reaction temperatures, (< 200 degreesC) "coke" formation involves mainly condensation and rearrangement steps. Therefore, the deposits are not polyaromatic and their composition depends very much on the reactant. The retention of the "coke" molecules on the catalysts is mainly due to their strong adsorption and to their low volatility (gas-phase reactions) or to their low solubility (liquid-phase reactions). At high temperatures (> 350 degreesC), the coke components are polyaromatic. Their formation involves hydrogen transfer (acid catalysts) and dehydrogenation (bifunctional catalysts) steps in addition to condensation and rearrangement steps. On microporous catalysts, the retention of coke molecules is due to their steric blockage within the micropores. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:83 / 96
页数:14
相关论文
共 59 条
  • [1] RETAINED AND DESORBED PRODUCTS FROM REACTION OF 1-HEXENE OVER H-ZSM5 ZEOLITE - ROUTES TO COKE PRECURSORS
    ANDERSON, JR
    CHANG, YF
    WESTERN, RJ
    [J]. JOURNAL OF CATALYSIS, 1989, 118 (02) : 466 - 482
  • [2] ANDERSON JR, 1991, STUD SURF SCI CATAL, V68, P745
  • [3] 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
  • [4] Skeletal isomerization of n-butenes - II. Composition, mode of formation, and influence of coke deposits on the reaction mechanism
    Andy, P
    Gnep, NS
    Guisnet, M
    Benazzi, E
    Travers, C
    [J]. JOURNAL OF CATALYSIS, 1998, 173 (02) : 322 - 332
  • [5] [Anonymous], STUD SURF SCI CATAL
  • [6] [Anonymous], CHEM CATALYTIC PROCE
  • [7] APPLEBY WG, 1962, IND ENG CHEM PROC DD, V2, P106
  • [8] BAKER RTK, 1991, STUD SURF SCI CATAL, V68, P1
  • [9] DEACTIVATION OF REFORMING CATALYSTS BY COKING - A REVIEW
    BARBIER, J
    [J]. APPLIED CATALYSIS, 1986, 23 (02): : 225 - 243
  • [10] BARBIER J, 1987, B SOC CHIM FR, P910