Cathodic Fenton degradation of 4,6-dinitro-o-cresol with nano-magnetite

被引:26
作者
Zeng, Xia [1 ]
Hanna, Khalil [2 ]
Lemley, Ann T. [1 ]
机构
[1] Cornell Univ, FSAD, Grad Field Environm Toxicol, Ithaca, NY 14853 USA
[2] Univ Henri Poincare, CNRS, UMR 7564, LCPME, F-54600 Villers Les Nancy, France
关键词
Nano-magnetite; DNOC; Cathodic Fenton degradation; Kinetic model; ELECTRO-FENTON; AQUEOUS-MEDIUM; PHOTOELECTRO-FENTON; ANODIC-OXIDATION; IRON-OXIDES; REAGENT; WATER; ACID; 2,4-DICHLOROPHENOL; MINERALIZATION;
D O I
10.1016/j.molcata.2011.03.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The successful removal of 4,6-dinitro-o-cresol (DNOC) is reported using nano-magnetite (Fe3O4) as the iron source and cathodic Fenton generation of hydrogen peroxide. Operating conditions were optimized by varying the electrolyte concentration, electric current, and O-2 flow. The effects of different DNOC initial concentrations, pH values and nano-magnetite quantities on the degradation rate of DNOC were also examined. The results showed that a lower DNOC initial concentration and a lower pH led to faster degradation of DNOC. It was also observed that the amount of nano-magnetite affected the degradation rate at lower pH while having no influence at neutral pH. Both homogeneous and heterogeneous reactions in the system were investigated. The homogeneous reaction dominated at a lower pH; direct electrolysis appears to take place at neutral pH; and a contribution from a heterogeneous reaction was not obvious under the experimental conditions studied. A model was developed to describe the degradation mechanism at low pH conditions, and the model matched experimental data very well. The combination of nano-magnetite and cathodic Fenton provides a fast way to degrade organic contaminants with readily available materials. Furthermore, magnetite is more stable, reusable and easy to separate compared to ferrous salt and other iron rich minerals. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 34 条
[1]   Electro-Fenton Process and Related Electrochemical Technologies Based on Fenton's Reaction Chemistry [J].
Brillas, Enric ;
Sires, Ignasi ;
Oturan, Mehmet A. .
CHEMICAL REVIEWS, 2009, 109 (12) :6570-6631
[2]   Anodic oxidation and electro-Fenton treatment of rotenone [J].
Dhaouadi, Anissa ;
Monser, Lotfi ;
Adhoum, Nafaa .
ELECTROCHIMICA ACTA, 2009, 54 (19) :4473-4480
[3]   Mineral iron oxides as iron source in electro-Fenton and photoelectro-fenton mineralization processes [J].
Exposito, Eduardo ;
Sanchez-Sanchez, Carlos M. ;
Montiel, Vicente .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2007, 154 (08) :E116-E122
[4]   Degradation of 4,6-dinitro-o-cresol from water by anodic oxidation with a boron-doped diamond electrode [J].
Flox, C ;
Garrido, JA ;
Rodríguez, RM ;
Centellas, F ;
Cabot, PL ;
Arias, C ;
Brillas, E .
ELECTROCHIMICA ACTA, 2005, 50 (18) :3685-3692
[5]  
Franson M.A.H., 1998, STANDARD METHODS EXA, V20
[6]  
GETOFF N, 1971, J PHYS CHEM-US, V75, P749
[7]   Hydrogen peroxide photolysis, Fenton reagent and photo-Fenton for the degradation of nitrophenols: a comparative study [J].
Goi, A ;
Trapido, M .
CHEMOSPHERE, 2002, 46 (06) :913-922
[8]   ENVIRONMENTAL-HAZARD OF 8 CHEMICALS PRESENT IN THE RHINE RIVER [J].
HALFON, E ;
BRUGGEMANN, R .
WATER SCIENCE AND TECHNOLOGY, 1989, 21 (8-9) :815-820
[9]   Synthesis of the mixed oxides of iron and quartz and their catalytic activities for the Fenton-like oxidation [J].
Hanna, K. ;
Kone, T. ;
Medjahdi, G. .
CATALYSIS COMMUNICATIONS, 2008, 9 (05) :955-959
[10]   Sorption of 1-hydroxy-2-naphthoic acid to goethite, lepidocrocite and ferrihydrite: Batch experiments and infrared study [J].
Hanna, K. ;
Carteret, C. .
CHEMOSPHERE, 2007, 70 (02) :178-186