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Enhanced removal of dichloroacetonitrile from drinking water by the combination of solar-photocatalysis and ozonation

Authors
Shin, DonghoonJang, MinCui, MingcanNa, SeungminKhim, Jeehyeong
Issue Date
Nov-2013
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Dichloroacetonitrile; Oxidation; Solar; Photocatalysis; Ozonation
Citation
CHEMOSPHERE, v.93, no.11, pp.2901 - 2908
Indexed
SCIE
SCOPUS
Journal Title
CHEMOSPHERE
Volume
93
Number
11
Start Page
2901
End Page
2908
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/101718
DOI
10.1016/j.chemosphere.2013.09.042
ISSN
0045-6535
Abstract
In this study, the photocatalytic ozonation process using either UV lamps with a wavelength close to a solar wavelength (UVsolar) or natural solar light was established to study the effects of the major operating parameters on the removal of a toxic disinfection by-product (DBP), dichloroacetonitrile (DCAN), from drinking water. Based on the test results of a bench system, the UVsolar/TiO2/O-3 process had the highest DCAN-removal rate among the advanced oxidation processes (AOPs). The optimal TiO2 and ozone doses were 1 g L-1 and 1.13 g L-1 h(-1), respectively, while room temperature (20 degrees C) produced the highest rate constant in the kinetic tests. The kinetic rate constants linearly increased when the UVsolar intensity increased in the range 4.6-25 W m(-2); however, it increased less at intensities higher than 25W m(-2). The test results of the outdoor system showed that the solar/TiO2/O-3 process provided complete removal of DCAN that was two times faster and had about 4.6 times higher energy efficiency than with solar/TiO2. As a green oxidation technique, solar photocatalytic ozonation could be a good alternative for treating recalcitrant and toxic organic pollutants, because it has high oxidation potential and low energy consumption compared to conventional AOPs. (C) 2013 Elsevier Ltd. All rights reserved.
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