Vanadium species supported on inorganic oxides as catalysts for propene epoxidation in the presence of N2 O as an oxidant
Authors:
- Agnieszka Mariola Held,
- Jolanta Kowalska-Kuś,
- A. Łapiński,
- Krystyna Nowińska
Abstract
The surface structure of vanadium species supported on SiO2, Al2O3, TiO2, and MgO and the effect of these supports on the activity of vanadium catalysts for propylene to propylene oxide oxidation with N2O as an oxidant were studied using ultraviolet visible diffuse reflectance spectroscopy and Raman spectroscopy, infrared spectra (IR) of adsorbed reagents, and the measurements of catalytic activity. The acidity of the samples was estimated from temperature-programmed desorption of ammonia and from IR spectra of adsorbed pyridine. On the basis of spectroscopic measurements, it was concluded that positively charged V 5+ ions formed on silica support are responsible for N2O adsorption through nitrogen with the formation of weakly electronegative oxygen capable of interacting with a double CC bond with the formation of epoxide. Analysis of different vanadium bonds present on the V/(oxide support) system indicates that mainly VOSi groups are responsible for activity in propylene epoxidation. © 2013 Elsevier Inc. All rights reserved.
- Record ID
- UAM3c78ed1d4eb747fabc7bcf2da1d5617b
- Author
- Journal series
- Journal of Catalysis, ISSN 0021-9517
- Issue year
- 2013
- Vol
- 306
- Pages
- 1-10
- ASJC Classification
- ;
- DOI
- DOI:10.1016/j.jcat.2013.06.001 Opening in a new tab
- Language
- (en) English
- Score (nominal)
- 45
- Score source
- journalList
- Score
- Publication indicators
- = 15; = 15; : 2013 = 2.078; : 2013 (2 years) = 6.073 - 2013 (5 years) =6.423
- Uniform Resource Identifier
- https://researchportal.amu.edu.pl/info/article/UAM3c78ed1d4eb747fabc7bcf2da1d5617b/
- URN
urn:amu-prod:UAM3c78ed1d4eb747fabc7bcf2da1d5617b
* presented citation count is obtained through Internet information analysis and it is close to the number calculated by the Publish or PerishOpening in a new tab system.