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Title: FTIR spectroscopic study of thiophene, SO[sub 2], and CO adsorption on Cu/Al[sub 2]O[sub 3] catalysts

Journal Article · · Journal of Catalysis; (United States)
;  [1];  [2];  [3]
  1. The University, Dundee (United Kingdom)
  2. Liverpool Univ. (United Kingdom)
  3. ICI Katalco R T Group, Billingham (United Kingdom)

Infrared spectra are reported of copper-alumina catalysts in various states of oxidation or reduction and exposed to carbon monoxide, thiophene, sulphur dioxide, co-adsorbed carbon monoxide and thiophene, and co-adsorbed sites could be broadly divided into four groups: Cu[sup 2+], Cu[sup +] in a matrix of Cu[sup 2+], Cu[sup +] in a matrix of Cu[sup +], and Cu[sup 0]. Both site-blocking and electronic effects of thiophene on CO adsorption have been identified and are discussed in terms of the nature of the surface-adsorbate interactions, the oxidation state of the adsorption sites, and the specific effects of thiophene on the adsorption site for CO. Sulphur dioxide blocked CO adsorption on Cu[sup 2+] sites. Adsorption of CO on Cu[sup +] sites was non inhibited by adsorption of sulphur dioxide, the latter having an electronic effect on CO molecules at adjacent sites. Adsorption of sulphur dioxide on a reduced Cu[sup 0] surface caused surface oxidation giving Cu[sup +] sites which were available for the subsequent adsorption of CO. The pre-adsorption of CO impeded but did not prevent the oxidative effects of sulphur dioxide chemisorption. 81 refs., 15 figs., 1 tab.

OSTI ID:
6659583
Journal Information:
Journal of Catalysis; (United States), Vol. 148:2; ISSN 0021-9517
Country of Publication:
United States
Language:
English