An innovative ultrasound, Fe2+ and TiO2 photoassisted process for bisphenol a mineralization

被引:90
作者
Torres-Palma, Ricardo A. [1 ,2 ,3 ]
Nieto, Jessica I. [1 ]
Combet, Evelyne [3 ]
Petrier, Christian [4 ]
Pulgarin, Cesar [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Swiss Fed Inst Technol, GGEC, Inst Chem Sci & Engn, CH-1015 Lausanne, Switzerland
[2] Univ Antioquia, Fac Ciencias Exactas & Nat, Inst Quim, Grp Electroquim, Medellin 1226, Colombia
[3] Univ Savoie, LCME, F-73376 Le Bourget Du Lac, France
[4] Univ Grenoble 1, LEPMI, F-38402 St Martin Dheres, France
关键词
Sonochemical degradation; Photocatalysis; Photo-Fenton; Sonophotocatalysis; Endocrine-disrupting chemical; Bisphenol A elimination; Water treatment; Advanced oxidation; AQUEOUS-SOLUTIONS; PHOTOCATALYTIC DEGRADATION; WATER; CAVITATION; POLLUTANTS; ACID; SONOCHEMISTRY; DISINFECTION; CONTAMINANTS; PRETREATMENT;
D O I
10.1016/j.watres.2009.12.050
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This paper explores the degradation of a model pollutant, bisphenol A, by an advanced oxidation process that combines sonolysis, Fe2+, and TiO2 in a photoassisted process. Experiments were done under saturated oxygen conditions. The effect of different Fe2+ (0.56 and 5.6 mg/L) and TiO2 (10 and 50 mg/L) concentrations was investigated on both the elimination and mineralization of the pollutant. A pronounced synergistic effect that led to the complete and rapid elimination of dissolved organic carbon (DOC) was observed even at low catalyst loadings. In this system, almost a complete removal of DOC (93%) was observed after 4 h using 10 and 5.6 mg/L of TiO2 and Fe2+, respectively, whereas at the same time, only 5, 6, and 22% of DOC was removed by an individual process alone (TiO2 photocatalysis, ultrasound, and photo-Fenton, respectively). In this system, ultrasound has the principal role of eliminating the initial substrate and providing hydrogen peroxide for the photocatalytic systems, while photo-Fenton and TiO2 photocatalysis are mainly responsible for the transformation of the intermediates in CO2 and H2O. The role of H2O2 generated from the sonochemical process is also discussed. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2245 / 2252
页数:8
相关论文
共 35 条
[1]   Sonochemistry in environmental remediation. 1. Combinative and hybrid sonophotochemical oxidation processes for the treatment of pollutants in water [J].
Adewuyi, YG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (10) :3409-3420
[2]   Chemical(photo-activated) coupled biological homogeneous degradation of p-nitro-o-toluene-sulfonic acid in a flow reactor [J].
Bandara, J ;
Pulgarin, C ;
Peringer, P ;
Kiwi, J .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1997, 111 (1-3) :253-263
[3]   Sonolytic, photocatalytic and sonophotocatalytic degradation of malachite green in aqueous solutions [J].
Berberidou, C. ;
Poulios, I. ;
Xekoukoulotakis, N. P. ;
Mantzavinos, D. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 74 (1-2) :63-72
[4]   Photochemical mineralization of di-n-butyl phthalate with H2O2/Fe3+ [J].
Chiou, Chyow-San ;
Chen, Yi-Hung ;
Chang, Chang-Tang ;
Chang, Ching-Yuan ;
Shie, Je-Lueng ;
Li, Yuan-Shan .
JOURNAL OF HAZARDOUS MATERIALS, 2006, 135 (1-3) :344-349
[5]   Photocatalytic degradation of pesticide contaminants in water [J].
Devipriya, S ;
Yesodharan, S .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2005, 86 (03) :309-348
[6]   Photocatalytic degradation of short-chain organic diacids [J].
Franch, MI ;
Ayllón, JA ;
Peral, J ;
Domènech, X .
CATALYSIS TODAY, 2002, 76 (2-4) :221-233
[7]   Accelerated photo-oxidation of concentrated p-coumaric acid in homogeneous solution. Mechanistic studies, intermediates and precursors formed in the dark [J].
Herrara, F ;
Pulgarin, C ;
Nadtochenko, V ;
Kiwi, J .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 17 (1-2) :141-156
[8]   Kinetics and mechanisms of ultrasonic degradation of volatile chlorinated aromatics in aqueous solutions [J].
Jiang, Y ;
Pétrier, C ;
Waite, TD .
ULTRASONICS SONOCHEMISTRY, 2002, 9 (06) :317-323
[9]   Influence of particles on sonochemical reactions in aqueous solutions [J].
Keck, A ;
Gilbert, E ;
Köster, R .
ULTRASONICS, 2002, 40 (1-8) :661-665
[10]  
KIWI J, 1993, NEW J CHEM, V17, P487