The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic Pollutants

Practical photocatalysis for degradation of organic pollutants must take into account the influence of other chemicals. Significant Al deposition on titania can occur at naturally occurring concentrations of dissolved Al. This paper reviews the author’s work on the influence of deliberately deposite...

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Main Author: Terry A. Egerton
Format: Article
Language:English
Published: MDPI AG 2013-03-01
Series:Catalysts
Subjects:
Online Access:http://www.mdpi.com/2073-4344/3/1/338
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spelling doaj-1338304c4dc94701bfeed915f045ce412020-11-24T21:27:26ZengMDPI AGCatalysts2073-43442013-03-013133836210.3390/catal3010338The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic PollutantsTerry A. EgertonPractical photocatalysis for degradation of organic pollutants must take into account the influence of other chemicals. Significant Al deposition on titania can occur at naturally occurring concentrations of dissolved Al. This paper reviews the author’s work on the influence of deliberately deposited hydrous oxides of aluminium on the behavior of a ~130 m2 g−1 rutile TiO2, and then compares the behavior of deposited alumina with that of deposited silica. On rutile some adsorbed nitrogen is infrared-active. Alumina and silica deposited on the rutile reduce, and ultimately eliminate, this infrared-active species. They also reduce photocatalytic oxidation of both propan-2-ol and dichloroacetate ion and the photocatalytic reduction of diphenyl picryl hydrazine. The surface oxides suppress charge transfer and may also reduce reactant adsorption. Quantitative measurement of TiO2 photogreying shows that the adsorbed inorganics also reduce photogreying, attributed to the capture of photogenerated conduction band electrons by Ti4+ to form Ti3+. The influence of adsorbed phosphate on photocatalysis is briefly considered, since phosphate reduces photocatalytic disinfection. In the context of classical colloid studies, it is concluded that inorganic species in water can significantly reduce photoactivity from the levels that measured in pure water.http://www.mdpi.com/2073-4344/3/1/338photocatalysisrutilesilicaaluminacoatingoxidationreductionphotogreying
collection DOAJ
language English
format Article
sources DOAJ
author Terry A. Egerton
spellingShingle Terry A. Egerton
The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic Pollutants
Catalysts
photocatalysis
rutile
silica
alumina
coating
oxidation
reduction
photogreying
author_facet Terry A. Egerton
author_sort Terry A. Egerton
title The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic Pollutants
title_short The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic Pollutants
title_full The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic Pollutants
title_fullStr The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic Pollutants
title_full_unstemmed The Influence of Surface Alumina and Silica on the Photocatalytic Degradation of Organic Pollutants
title_sort influence of surface alumina and silica on the photocatalytic degradation of organic pollutants
publisher MDPI AG
series Catalysts
issn 2073-4344
publishDate 2013-03-01
description Practical photocatalysis for degradation of organic pollutants must take into account the influence of other chemicals. Significant Al deposition on titania can occur at naturally occurring concentrations of dissolved Al. This paper reviews the author’s work on the influence of deliberately deposited hydrous oxides of aluminium on the behavior of a ~130 m2 g−1 rutile TiO2, and then compares the behavior of deposited alumina with that of deposited silica. On rutile some adsorbed nitrogen is infrared-active. Alumina and silica deposited on the rutile reduce, and ultimately eliminate, this infrared-active species. They also reduce photocatalytic oxidation of both propan-2-ol and dichloroacetate ion and the photocatalytic reduction of diphenyl picryl hydrazine. The surface oxides suppress charge transfer and may also reduce reactant adsorption. Quantitative measurement of TiO2 photogreying shows that the adsorbed inorganics also reduce photogreying, attributed to the capture of photogenerated conduction band electrons by Ti4+ to form Ti3+. The influence of adsorbed phosphate on photocatalysis is briefly considered, since phosphate reduces photocatalytic disinfection. In the context of classical colloid studies, it is concluded that inorganic species in water can significantly reduce photoactivity from the levels that measured in pure water.
topic photocatalysis
rutile
silica
alumina
coating
oxidation
reduction
photogreying
url http://www.mdpi.com/2073-4344/3/1/338
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