期刊
CHEMOSPHERE
卷 66, 期 11, 页码 2106-2113出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2006.09.027
关键词
TiO2; o-chloroaniline; photodecay; radicals; mineralization; oxyhalogens
Photodecay of o-chloroaniline (o-CIA) in various combinations of UV sources, TiO2, and oxylialogens was investigated. To improve the conventional photocatalytic process by using UV/TiO2, the addition of oxyhalogens (ClO3-, BrO3- and IO3-) into UV/TiO2 system was studied and the effect in such addition is very encouraging for all the selected additives. Oxyhalogens are capable of deferring the electron-hole recombination of TiO2 which significantly improved its catalytic performance. The presence of IO3- in UV/TiO2 resulted in the fastest o-CIA decay among three oxhalogens at the same dosage. The decay of o-CIA in UV/TiO2/oxyhalogen process is characterized by a two-stage pseudo-kinetics, where a faster initial decay was followed by a retardation state. A mathematics model was successfully established for the prediction of the two-stage decay of o-CIA in UV/TiO2/IO3- with any designed [IO3-] concentration. (c) 2006 Elsevier Ltd. All rights reserved.
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