A hybridization approach to efficient TiO2 photodegradation of aqueous benzalkonium chloride

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TiO2 get positively charged upon UV-irradiation and repel the cationic pollutants away from the surface. Hybridization of AC onto TiO2 (ACT) tends catalyst surface negatively charged besides providing highly favorable adsorptions sites for cationic pollutants. The photodegradation of benzalkonium chloride (BKC), a quaternary ammonium surfactant and a pharmaceutical, is investigated with ACT. The surface charge of the catalyst in surfactant and non-surfactant aqueous dispersion under UV-irradiation is investigated and explained. The anomalous increase in COD values at the beginning of BKC-photodegradation is explained. The intermediate products formed are identified in both solution and solid phase. Trace amount of dodecane remained adsorbed on the catalyst surface after 1 h UV-irradiation, but complete mineralization of BKC is achieved with 2 h UV-irradiation. We propose that BKC photodegradation starts by central fission of benzyl C-N bond followed by dealkylation, and demethylation steps. (C) 2015 Elsevier B.V. All rights reserved.
Publisher
ELSEVIER SCIENCE BV
Issue Date
2015-08
Language
English
Article Type
Article
Citation

JOURNAL OF HAZARDOUS MATERIALS, v.293, pp.122 - 130

ISSN
0304-3894
DOI
10.1016/j.jhazmat.2015.03.011
URI
http://hdl.handle.net/10203/303726
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