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author:

Li, X.Z. (Li, X.Z..) [1] | Yuan, B.L. (Yuan, B.L..) [2] | Graham, N. (Graham, N..) [3]

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Abstract:

The aim of the present work was to study the interaction of ferrate oxidation and photocatalytic oxidation in terms of dibutyl phthalate (DBP) degradation in aqueous solution, in which three sets of experiments were carried out, including (1) ferrate oxidation alone, (2) photocatalytic oxidation alone, and (3) the combination of ferrate oxidation and photocatalytic oxidation. Laboratory experiments demonstrated that ferrate oxidation and phtotocatalytic oxidation of DBP in aqueous solution are relatively slow processes. However, the presence of TiO2 and ferrate together under UV illumination accelerated the DBP degradation significantly. Since ferrate was reduced quickly due to the presence of TiO2 and UV irradiation, the DBP degradation reaction can be divided into two phases. During the first 30 min (Phase 1) the DBP was degraded by both photocatalytic oxidation and ferrate oxidation, and by interactive reactions. After 30 min (Phase 2), the ferrate residual had declined to a very low level and the photocatalytic reaction was the dominant mechanism of further DBP degradation. The influence of three main factors, ferrate dosage, TiO2 dosage and pH, on the DBP degradation were investigated in order to understand the reaction mechanism and kinetics. © 2008 American Chemical Society.

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  • [ 1 ] [Li, X.Z.]Department of Civil and Structural Engineering, Hong Kong Polytechnic University, Hong Kong
  • [ 2 ] [Yuan, B.L.]Department of Civil and Structural Engineering, Hong Kong Polytechnic University, Hong Kong
  • [ 3 ] [Yuan, B.L.]Department of Environmental Science and Engineering, Fuzhou University, Fuzhou, China
  • [ 4 ] [Graham, N.]Department of Civil and Environmental Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, United Kingdom

Reprint 's Address:

  • [Li, X.Z.]Department of Civil and Structural Engineering, Hong Kong Polytechnic UniversityHong Kong

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Source :

ACS Symposium Series

ISSN: 0097-6156

Year: 2008

Volume: 985

Page: 364-377

Language: English

0 . 5 6 6

JCR@2005

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 5

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 2

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