EFFECT OF THE REDUCTION TREATMENT ON THE STRUCTURE AND REACTIVITY OF SILICA-SUPPORTED COPPER PARTICLES

被引:220
|
作者
VANDERGRIFT, CJG [1 ]
WIELERS, AFH [1 ]
JOGHI, BPJ [1 ]
VANBEIJNUM, J [1 ]
DEBOER, M [1 ]
VERSLUIJSHELDER, M [1 ]
GEUS, JW [1 ]
机构
[1] STATE UNIV UTRECHT,DEPT INORGAN CHEM,3522 AD UTRECHT,NETHERLANDS
关键词
D O I
10.1016/0021-9517(91)90334-Z
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
Silica-supported copper particles of high thermostability have been subjected to oxidation-reduction treatments after which the metal particle size, the surface structure, and the catalytic hydrogenolysis of methyl acetate were investigated. The metal particle size was assessed from the dissociative adsorption of nitrous oxide, X-ray line broadening, and transmission electron microscopy. The surface structure of the copper particles was derived from infrared spectra of adsorbed carbon monoxide. The hydrogenolysis of methyl acetate was used as a structure-sensitive test reaction to illustrate the effect of the surface structure on the activity of the catalyst. The copper particle size is not affected by reduction treatments up to 873 K, whereas the surface structure of the copper particles and thereby the oxygen uptake during dissociative adsorption of nitrous oxide and the activity of the catalyst in the hydrogenolysis of methyl acetate strongly depend upon the temperature and duration of the reduction treatment. Without a change of the copper particle size, prolonged reduction of the catalyst results in more densely packed copper surfaces that are more susceptible to penetration of oxygen during passivation with nitrous oxide and less active in the hydrogenolysis of methyl acetate. The rearrangement of the surface structure of the copper particles is reversible upon repeated oxidation-reduction cycles. © 1991.
引用
收藏
页码:178 / 189
页数:12
相关论文
共 50 条
  • [31] THE EFFECT OF IMPREGNATION CONDITIONS ON THE SURFACE-STRUCTURE OF SILICA-SUPPORTED CUO CATALYSTS
    SELIM, SA
    HASSAN, HA
    ABDELKHALIK, M
    MIKHAIL, RS
    [J]. THERMOCHIMICA ACTA, 1981, 45 (03) : 349 - 360
  • [32] A silica-supported copper(I) catalyzed Sonogashira coupling reaction
    Zhang, LY
    Li, PH
    Wang, L
    [J]. LETTERS IN ORGANIC CHEMISTRY, 2006, 3 (04) : 282 - 285
  • [33] Environmentally friendly silica-supported copper phenanthroline catalysts.
    Bowman, SC
    Watton, SP
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 220 : U436 - U436
  • [34] Mono- and dinuclear silica-supported titanium(IV) complexes and the effect of TiOTi connectivity on reactivity
    Bouh, AO
    Rice, GL
    Scott, SL
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (31) : 7201 - 7210
  • [35] Transformations of cyclohexene over silica-supported copper in the presence of deuterium
    Fasi, A
    Palinko, I
    Katona, T
    Bartok, M
    [J]. JOURNAL OF CATALYSIS, 1997, 167 (01) : 215 - 223
  • [36] Silica-supported copper phenanthroline complexes as functional metallooxygenase mimics
    Bowman, SC
    Moore, CM
    Cosel, JD
    Watton, SP
    [J]. JOURNAL OF INORGANIC BIOCHEMISTRY, 2001, 86 (01) : 156 - 156
  • [37] FORMATION OF METALLIC PARTICLES DURING TEMPERATURE-PROGRAMMED REDUCTION OF SILICA-SUPPORTED PLATINUM AND NICKEL CHLORIDES
    JENTYS, A
    HALLER, GL
    LERCHER, JA
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (02): : 484 - 488
  • [38] Copper Nitrate Redispersion To Arrive at Highly Active Silica-Supported Copper Catalysts
    Munnik, P.
    Wolters, M.
    Gabrielsson, A.
    Pollington, S. D.
    Headdock, G.
    Bitter, J. H.
    de Jongh, P. E.
    de Jong, K. P.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (30): : 14698 - 14706
  • [39] PHOTOINDUCED REDUCTION OF SILICA-SUPPORTED CUO DURING XPS IRRADIATION
    DICASTRO, V
    PIREDDA, G
    [J]. CHEMICAL PHYSICS LETTERS, 1985, 114 (01) : 109 - 113
  • [40] Mesoporous silica-supported metal oxides: Synthesis and catalytic reactivity.
    Nieweg, JA
    Woldegiorgis, KL
    Lin, VSY
    Bakac, A
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 229 : U983 - U983