Degradation of the antibiotic oxolinic acid by photocatalysis with TiO2 in suspension

被引:169
作者
Giraldo, Ana L. [1 ,2 ]
Penuela, Gustavo A. [1 ]
Torres-Palma, Ricardo A. [1 ,3 ]
Pino, Nancy J. [1 ,2 ]
Palominos, Rodrigo A. [4 ]
Mansilla, Hector D. [4 ]
机构
[1] Univ Antioquia, Fac Ingn, Grp Diagnost & Control Contaminac, SIU, Medellin 1226, Colombia
[2] Univ Antioquia, Corp Acad Ambiental, Medellin 1226, Colombia
[3] Univ Antioquia, Fac Ciencias Exactas & Nat, Inst Quim, Grp Electroquim, Medellin 1226, Colombia
[4] Univ Concepcion, Fac Ciencias Quim, Concepcion, Chile
关键词
Advanced oxidation; Antibiotic; Oxolinic acid; Pharmaceuticals; TiO2; photocatalysis; Water treatment; WASTE-WATER; TITANIUM-DIOXIDE; AQUEOUS-SOLUTION; PHARMACEUTICALS; OXIDATION; REMOVAL; MECHANISM; UV; PHOTOTRANSFORMATION; PHOTODEGRADATION;
D O I
10.1016/j.watres.2010.05.011
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In the work presented here, a photocatalytic system using titanium Degussa P-25 in suspension was used to evaluate the degradation of 20 mg L-1 of antibiotic oxolinic acid (OA). The effects of catalyst load (0.2-1.5 g L-1) and pH (7.5-11) were evaluated and optimized using the surface response methodology and the Pareto diagram. In the range of variables studied, low pH values and 1.0 g L-1 of TiO2 favoured the efficiency of the process. Under optimal conditions the evolution of the substrate, chemical oxygen demand, dissolved organic carbon, toxicity and antimicrobial activity on Escherichia coli cultures were evaluated. The results indicate that, under optimal conditions, after 30 min, the TiO2 photocatalytic system is able to eliminate both the substrate and the antimicrobial activity, and to reduce the toxicity of the solution by 60%. However, at the same time, similar to 53% of both initial DOC and COD remain in solution. Thus, the photocatalytical system is able to transform the target compound into more oxidized by-products without antimicrobial activity and with a low toxicity. The study of OA by-products using liquid chromatography coupled with mass spectrometry, as well as the evaluation of OA degradation in acetonitrile media as solvent or in the presence of isopropanol and iodide suggest that the reaction is initiated by the photo-Kolbe reaction. Adsorption isotherm experiments in the dark indicated that under pH 7.5, adsorption corresponded to the Langmuir adsorption model, indicating the dependence of the reaction on an initial adsorption step. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5158 / 5167
页数:10
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