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Catalytic ozonation of organic pollutants in the presence of cerium oxide–carbon composites

Paper ID Volume ID Publish Year Pages File Format Full-Text
47120 46459 2011 8 PDF Available
Title
Catalytic ozonation of organic pollutants in the presence of cerium oxide–carbon composites
Abstract

Cerium oxide–carbon composites were prepared and tested as ozonation catalysts for the removal of two selected carboxylic acids, oxalic and oxamic, and one textile dye (C.I. Reactive Blue 5). The results were compared with those obtained in non-catalytic ozonation and ozonation catalysed by cerium oxide and carbon materials (activated carbon, carbon xerogel). With the exception of cerium oxide, a total degradation of oxalic acid was obtained in approximately 90 min for all prepared catalysts and the catalytic activity increases with the amount of carbon present in the composites. Despite of oxamic acid be more refractory to ozonation than oxalic acid, 75% of oxamic acid removal was achieved after 10 h of reaction in the presence of the ceria-activated carbon composite with 90% of carbon material. In the mineralization of the textile dye, the catalytic activity of the composites increases with the amount of activated carbon introduced.

Graphical abstractActivated carbon–ceria composite as ozonation catalysts.Figure optionsDownload full-size imageDownload as PowerPoint slideResearch highlights▶ A synergic effect occurs when ceria–carbon composites are used as ozonation catalysts. ▶ Catalytic activity increases with the amount of carbon present in the composites. ▶ Total degradation of oxalic acid was obtained in less than 90 min for all catalysts. ▶ Surface reactions are predominant over liquid bulk reactions involving HO radicals.

Keywords
Catalytic ozonation; Cerium oxide; Carbon materials; Carboxylic acids; Textile dye
First Page Preview
Catalytic ozonation of organic pollutants in the presence of cerium oxide–carbon composites
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis B: Environmental - Volume 102, Issues 3–4, 22 February 2011, Pages 539–546
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis