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HERO ID
1949027
Reference Type
Journal Article
Title
OXIDE CATALYZED-REACTIONS OF ETHYLENE-OXIDE UNDER CONDITIONS RELEVANT TO ETHYLENE EPOXIDATION OVER SUPPORTED SILVER
Author(s)
Yong, YS; Kennedy, EM; Cant, NW
Year
1991
Is Peer Reviewed?
Yes
Journal
Applied Catalysis
ISSN:
0166-9834
Publisher
Elsevier
Volume
76
Issue
1
Page Numbers
31-48
DOI
10.1016/0166-9834(91)80003-F
Web of Science Id
WOS:A1991GE55500003
URL
https://linkinghub.elsevier.com/retrieve/pii/016698349180003F
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Abstract
Further reactions of ethylene oxide over oxide supports have been investigated in the context of the oxidation of ethylene to ethylene oxide using supported silver. As noted by others, high area aerosil type silicas have low activity for the isomerisation of ethylene oxide to acetaldehyde and silver supported on such materials exhibits good selectivity for ethylene epoxidation. By contrast silver supported on TiO2 and gamma-Al2O3 shows zero selectivity and this correlates with the high activity of these supports for further reactions of ethylene oxide. In the case of gamma-Al2O3 there is complete conversion of ethylene oxide at 239-degrees-C in the presence or absence of oxygen. Acetaldehyde is the major organic product in both cases but dioxane and small amounts of 2,3-butanedione, ethyl acetate and an unidentified compound, probably an unstable C4, are also observed. With oxygen present some carbon oxides are seen. In the absence of oxygen the amount of the unknown is greater and the gaseous mass balance is incomplete. With TiO2 the distribution amongst the major products is similar to that for gamma-Al2O3 but the conversion of ethylene oxide is much less. In situ infrared measurements with TiO2 show that ethylene oxide reacts instantaneously with surface hydroxyl groups to form a glycol like species. Reaction of acetaldehyde over TiO2 and gamma-Al2O3 occurs at a much slower rate than that of ethylene oxide under the same conditions. The dominant product is 2-butenal. Thus the C4 products formed when using ethylene oxide do not arise by further reaction of acetaldehyde. Formation of the major organics from both ethylene oxide and acetaldehyde can be accounted for in terms of catalysis by weak Bronsted acid sites. Silicas have little activity for the further reaction of acetaldehyde but silver supported on them induce oxidation of it. It is concluded that the zero selectivity of silver supported on TiO2 and gamma-Al2O3 for ethylene epoxidation is due to isomerisation of ethylene oxide to acetaldehyde on the support followed by complete oxidation on the silver.
Keywords
ACID SITES; CATALYST CHARACTERIZATION (INSITU IR); ETHYLENE OXIDATION; ETHYLENE OXIDE; SILVER ALUMINA; SILVER SILICA; SILVER TITANIA
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OPPT REs
•
OPPT_1,4-Dioxane_D. Exposure
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