The adsorption of ethylene oxide on Ag(110) and Pt(111): Relevance to selective olefin oxidation

• Published in: Surface science 1986-12, Vol.177 (2), p.417-430
• Main Authors: Campbell, Charles T., Paffett, M.T.
• Format: Article
• Language: English
• Subjects: Chemistry; Exact sciences and technology; General and physical chemistry; Solid-gas interface; Surface physical chemistry
• ISSN: 0039-6028; 1879-2758
• DOI: 10.1016/0039-6028(86)90149-4

The interactions of ethylene oxide (EtO) with the Ag(110) and Pt(111) surfaces have been studied using XPS, TDS, AES and EELS. On Ag(110), the interaction is very weak, with only molecular desorption observable. The heat of adsorption is ≈ 10.1 kcal mole −1. In contrast, decomposition reactions strongly predominate on Pt(111) at low coverage. Molecular desorption is only seen at high coverages. The heat of adsorption decreases from > 11.9 to 10 kcal mole −1 with increasing coverage. Condensed multilayers desorb at ≈ 140 K. Ultimate decomposition products on Pt(111) include H 2 and CO gas, and carbon residue on the surface. Evidence suggests that adsorbed decomposition intermediates may include atomic hydrogen, CO, acetyl and ethylidyne species, with at least one other, yet unidentified, species. These results imply that, if produced, adsorbed ethylene oxide would be unlikely to escape a reactor containing Pt catalyst without further decomposition reactions. This may help explain the uniqueness of Ag catalysts in ethylene epoxidation.