English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/27461
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

Title

Photocatalytic oxidation of aromatic alcohols to aldehydes in aqueous suspension of home prepared titanium dioxide: 2. Intrinsic and surface features of catalysts

AuthorsAugugliaro, Vincenzo; Kisch, Horst; Loddo, Vittorio; López-Muñoz, María José; Márquez Álvarez, Carlos ; Palmisano, Giovanni; Palmisano, Leonardo; Parrino, Francesco; Yurdakal, Sedat
KeywordsPhotocatalysis
TiO2
In situ ATR-FTIR analysis
Aromatic alcohols
Selective oxidation
Aliphatic alcohol
Issue Date31-Oct-2008
PublisherElsevier
CitationApplied Catalysis A - General
AbstractSome intrinsic electronic properties of home prepared (HP) TiO2 catalysts were investigated by diffuse reflectance spectroscopy and quasi-Fermi level measurements. These powders were used for carrying out the photocatalytic oxidation of benzyl alcohol to benzaldehyde and CO2 in water; the selectivity for aldehyde formation was enhanced by the addition of small amounts of ethanol, a typical hole trap. The values of band gap, valence band and conduction band edges are almost identical for all the HP samples in which anatase phase is predominant, whereas appreciable differences can be noticed for an HP sample containing high amount of rutile phase. A comparative ATR-FTIR study of the HP catalyst showing the highest selectivity and the commercial titania showing the highest activity towards benzyl alcohol oxidation (Degussa P25 TiO2) was carried out. The ATR-FTIR results indicate that HP and Degussa P25 surfaces show a very dissimilar hydrophilicity and different ability for adsorbing the organic compounds deriving from benzyl alcohol photocatalytic oxidation. Results show moreover that the improved selectivity to aldehyde by adding ethanol is due to competition between the substrate and the hole trap for adsorption on reactive sites.
Publisher version (URL)http://dx.doi.org/10.1016/j.apcata.2008.07.038
URIhttp://hdl.handle.net/10261/27461
DOI10.1016/j.apcata.2008.07.038
ISSN0926-860X
Appears in Collections:(ICP) Artículos
Files in This Item:
File Description SizeFormat 
ApplCatalA_2008_349_189_OA.pdf1,05 MBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.