RELATION BETWEEN CATALYTIC PROPERTIES AND STRUCTURE OF METAL FILMS .I. DEUTERIUM EXCHANGE OF METHANE ETHANE AND PROPANE OVER NICKEL

被引:34
作者
ANDERSON, JR
MACDONAL.RJ
机构
[1] School of Physical Sciences, Flinders University, Adelaide, SA
基金
澳大利亚研究理事会;
关键词
D O I
10.1016/0021-9517(69)90443-6
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
To assess the influence of surface structure on the mode of adsorption of saturated hydrocarbons, deuterium exchange reactions with propane, ethane, and methane were studied over various ultra-high-vacuum-deposited nickel films. Reactions were studied over {111} and {100} surfaces, prepared by nickel evaporation onto mica and sodium chloride, respectively, at elevated substrate temperatures, as well as over sintered and unsintered random polycrystal films. Reactions with propane and ethane gave initial product distributions from which the following conclusions are drawn: (i) at exchange temperatures, it is very unlikely that a monoadsorbed hydrocarbon residue will be retained on {111} or {100} surfaces because of the ready formation of a double bond between the carbon and the metal; (ii) surface sites for the retention of a monoadsorbed hydrocarbon residue are present on lowtemperature random polycrystal films, but they are thermally unstable in that they are much reduced by sintering, and are completely absent in {111} or {100} surfaces; (iii) exchange by a process of rapid interconversion between monoadsorbed and α,β-diadsorbed surface species does not occur on {111} or {100} surfaces and, ipso facto, is unlikely on sintered surfaces; (iv) multiple exchange occurs mainly by desorption from extensively dehydrogenated surface residues. It is suggested that the thermally unstable sites suitable for monoadsorption are associated with atomically rough areas of surface, either as high index planes or facets, or at quasimacroscopic features such as steps and terrace edges. Although the product distributions were sensitive to surface structure, activation energies and frequency factors were not. Methane exchange did not show discrimination with respect to surface structure, and reasons for this are discussed. The possible unreliability of exchange data obtained under conditions of poor surface cleanliness is emphasized. © 1969.
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页码:345 / &
相关论文
共 40 条
[1]   REACTION OF DEUTERIUM WITH CYCLOPROPANE AND METHYLCYCLOPROPANE OVER EVAPORATED METAL FILMS [J].
ANDERSON, JR ;
AVERY, NR .
JOURNAL OF CATALYSIS, 1967, 8 (01) :48-&
[2]   ISOMERIZATION OF ALIPHATIC HYDROCARBONS OVER EVAPORATED FILMS OF PLATINUM AND PALLADIUM [J].
ANDERSON, JR ;
AVERY, NR .
JOURNAL OF CATALYSIS, 1966, 5 (03) :446-&
[3]   HYDROCRACKING OF SATURATED HYDROCARBONS OVER EVAPORATED METAL FILMS [J].
ANDERSON, JR ;
BAKER, BG .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1963, 271 (1344) :402-+
[4]   STRUCTURE AND PROPERTIES OF EVAPORATED METAL FILMS [J].
ANDERSON, JR ;
BAKER, BG ;
SANDERS, JV .
JOURNAL OF CATALYSIS, 1962, 1 (05) :443-457
[5]   CATALYSIS ON EVAPORATED METAL FILMS .3. THE EFFICIENCY OF DIFFERENT METALS FOR THE REACTION BETWEEN ETHANE AND DEUTERIUM [J].
ANDERSON, JR ;
KEMBALL, C .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1954, 223 (1154) :361-377
[6]  
ANDERSON JR, 1966, P RADIO RESEARCH BOA, P38
[7]   THE INFLUENCE OF DEFECTS AND SURFACE STRUCTURE ON THE CATALYTIC ACTIVITY OF SILVER FILMS [J].
BAGG, J ;
JAEGER, H ;
SANDERS, JV .
JOURNAL OF CATALYSIS, 1963, 2 (06) :449-464
[8]   ADSORPTION OF XENON ON NICKEL FILMS EPITAXED ON SODIUM CHLORIDE [J].
BAKER, BG ;
BRUCE, LA .
TRANSACTIONS OF THE FARADAY SOCIETY, 1968, 64 (549P) :2533-&
[9]  
BAKER BG, PRIVATE COMMUNICATIO
[10]  
BOUDART J, 1966, J CATALYSIS, V6, P92