Ozonation of benzothiazole saturated-activated carbons: Influence of carbon chemical surface properties

Valdes, H.; Zaror, CA

Abstract

The combined or sequential use of ozone and activated carbon to treat toxic effluents has increased in recent years. However, little is known about the influence of carbon surface active sites on ozonation of organic adsorbed pollutants. This paper presents experimental results on the effect of metal oxides and oxygenated surface groups on gaseous ozonation of spent activated carbons. Benzothiazole (BT) was selected as a target organic compound in this study due to its environmental concern. Activated carbons with different chemical surface composition were prepared from a Filtrasorb-400 activated carbon. Pre-treatment included: ozonation, demineralisation, and deoxygenation of activated carbon. Ozonation experiments of BT saturated-activated carbons were conducted in a fixed bed reactor loaded with 2 g of carbon samples. The reactor was fed with an O 2/O 3 gas mixture (2 dm 3/min, 5 g O 3/h), for a given exposure time, in the range 10-120 min, at 298 K and 1 atm. Results show that extended gaseous ozonation of activated carbon saturated with BT led to the effective destruction of the adsorbate by oxidation reactions. Oxidation of BT adsorbed on activated carbon seemed to occur via both direct reaction with ozone molecules, and by oxygen radical species generated by catalytic ozone decomposition on metallic surface sites. © 2006 Elsevier B.V. All rights reserved.

Más información

Título según WOS: Ozonation of benzothiazole saturated-activated carbons: Influence of carbon chemical surface properties
Título según SCOPUS: Ozonation of benzothiazole saturated-activated carbons: Influence of carbon chemical surface properties
Título de la Revista: JOURNAL OF HAZARDOUS MATERIALS
Volumen: 137
Número: 2
Editorial: Elsevier
Fecha de publicación: 2006
Página de inicio: 1042
Página final: 1048
Idioma: English
URL: http://linkinghub.elsevier.com/retrieve/pii/S0304389406002664
DOI:

10.1016/j.jhazmat.2006.03.025

Notas: ISI, SCOPUS