Degradation of Dipyrone by Electrogenerated H2O2 Combined with Fe2+ Using a Modified Gas Diffusion Electrode

被引:9
作者
Barros, Willyam R. P. [1 ]
Borges, Michelle P. [1 ]
Steter, Juliana R. [1 ]
Forti, Juliane C. [2 ]
Rocha, Robson S. [1 ]
Lanza, Marcos R. V. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13566590 Sao Paulo, Brazil
[2] Univ Estadual Paulista, BR-17602496 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
PERSONAL CARE PRODUCTS; HYDROGEN-PEROXIDE; ELECTROCHEMICAL DEGRADATION; FENTON DEGRADATION; PILOT SURVEY; PHARMACEUTICALS; WATER; SEWAGE; METAMIZOLE; TOXICITY;
D O I
10.1149/2.0091414jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The aim of the present study was to investigate the electrochemical degradation of dipyrone in a single compartment electrochemical cell equipped with a gas diffusion electrode (GDE) modified with cobalt (II) phthalocyanine. Degradations were performed under conditions of anodic oxidation (GDE pressurized with N-2) and under conditions promoting the electrogeneration of H2O2 (GDE pressurized with O-2) both in the absence and presence of 1 mmol FeSO4.7H2O (electro-Fenton conditions). The efficiency of the electro-Fenton process was satisfactory at all studied potentials, and achieved a maximum reduction of 67% in electrolyte absorbance at 262 nm after 90 min electrolysis at -0.7 V (vs. Ag/ AgCl). The reduction in dipyrone concentration attained 95% after 90 min of reaction with electrogenerated H2O2 in the absence or presence of Fe2+ ions at all potentials except -0.5 V (vs. Ag/ AgCl). The removal of total organic carbon (TOC) was most efficient under electro-Fenton conditions with a decrease of 54.4% in organic load attained at -0.9 V (vs. Ag/AgCl) and energy consumption (EC) of 270 kWh per kg of TOC removed. (C) 2014 The Electrochemical Society. All rights reserved.
引用
收藏
页码:H867 / H873
页数:7
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