Evaluation of the photoelectrocatalytic method for oxidizing chloride and simultaneous removal of microcystin toxins in surface waters

被引:48
作者
Fraga, Luciano E. [1 ]
Anderson, Marc A. [2 ]
Beatriz, Maria L. P. M. A. [3 ]
Paschoal, Fabiana M. M. [1 ]
Romao, Luciane P. [3 ]
Zanoni, Maria Valnice B. [1 ]
机构
[1] Univ Estadual Paulista, Dept Quim Analit, Inst Quim, BR-14801970 Araraquara, SP, Brazil
[2] Univ Wisconsin, Environm Chem & Technol Program, Madison, WI 53706 USA
[3] Univ Fed Sergipe, Dept Quim, Aracaju, Sergipe, Brazil
基金
美国国家科学基金会; 巴西圣保罗研究基金会;
关键词
Chlorine generation; Photoelectrocatalytic oxidation; Ti/TiO2; electrodes; Microcystin degradation; Water disinfections; PHOTOCATALYTIC OXIDATION; CYANOBACTERIAL TOXINS; ACTIVE CHLORINE; BY-PRODUCTS; DOPED TIO2; DEGRADATION; DISINFECTION; DYE; DESTRUCTION; HEPATOTOXINS;
D O I
10.1016/j.electacta.2008.08.060
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The production of chlorine was investigated in the photoelectrocatalytic oxidation of a chloride-containing solution using a TiO2 thin-film electrode biased at current density from 5 to 50 mA cm(-2) and illuminated by UV light. Such parameters as chloride concentrations from 0.001 to 0.10 mol L-1, pH 2-12, and interfering salts were varied in this study in order to determine their effect on this oxidation process. At an optimum condition this photoelectrocatalytic method can produce active chlorine at levels compatible to water disinfections processes using a chloride concentration higher than 0.010 mol L-1 at a pH of 4 and a current density of 30 mA cm(-2). The method was successfully applied to treat surface water collected from a Brazilian river. After 150 min of photoelectrocatalytic oxidation, we obtained a 90% reduction in total organic carbon removal, a 100% removal of turbidity, a 93% decrease in colour and a chemical oxygen demand (COD) removal of around 96% (N=3). The proposed technology based on photoelectrocatalytic oxidation was also tested in treating 250 mL of a solution containing 0.05 mol L-1 NaCl and 50 mu g L-1 of Microcystin aeruginosa. The bacteria is completely removed after 5 min of photoelectrocatalysis following an initial rate constant removal of -0.260 min(-1), suggesting that the present method could be considered as a promising alternative to chlorine-based disinfections. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2069 / 2076
页数:8
相关论文
共 49 条
[1]   Kinetics of reactions between chlorine and the cyanobacterial toxins microcystins [J].
Acero, JL ;
Rodriguez, E ;
Meriluoto, J .
WATER RESEARCH, 2005, 39 (08) :1628-1638
[2]  
ANTONIOU MG, 2005, J ENV ENG, V9, P1239
[3]  
APHA/AWWA/WEF, 2017, Standard Methods for the Examination of Water and Wastewater, V23rd
[4]   Product and by-product formation in laboratory studies on disinfection electrolysis of water using boron-doped diamond anodes [J].
Bergmann, M. E. Henry ;
Rollin, Johanna .
CATALYSIS TODAY, 2007, 124 (3-4) :198-203
[5]   Studies on electrochemical disinfectant production using anodes containing RuO2 [J].
Bergmann, MEH ;
Koparal, AS .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2005, 35 (12) :1321-1329
[6]  
CALLAWAY JO, 1989, STANDARD METHODS EXA, P62
[7]  
Candal R.J., 1998, J ADV OXID TECHNOL, V3, P270
[8]   CYANOBACTERIA SECONDARY METABOLITES - THE CYANOTOXINS [J].
CARMICHAEL, WW .
JOURNAL OF APPLIED BACTERIOLOGY, 1992, 72 (06) :445-459
[9]   Evaluation of color removal and degradation of a reactive textile azo dye on nanoporous TiO2 thin-film electrodes [J].
Carneiro, PA ;
Osugi, ME ;
Sene, JJ ;
Anderson, MA ;
Zanoni, MVB .
ELECTROCHIMICA ACTA, 2004, 49 (22-23) :3807-3820
[10]  
CASSON LW, 2003, CONVERTION ON SITE S