Iron-nickel bimetallic nanoparticles for reductive degradation of azo dye Orange G in aqueous solution

被引:302
作者
Bokare, Alok D. [1 ]
Chikate, Rajeev C. [2 ]
Rode, Chandrashekhar V. [3 ]
Paknikar, Kishore M. [1 ]
机构
[1] Agharkar Res Inst, Ctr Nanobiosci, Pune 411004, Maharashtra, India
[2] MES Abasaheb Garware Coll, Dept Chem, Pune 411004, Maharashtra, India
[3] Natl Chem Lab, Chem Engn & Proc Dev Div, Pune 411008, Maharashtra, India
关键词
iron; nickel; nanoparticles; azo dye; degradation;
D O I
10.1016/j.apcatb.2007.10.033
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 degradation of Orange G, a monoazo dye, in aqueous solutions was investigated using Fe-Ni bimetallic nanoparticles. Transmission electron microscopy (TEM) of as-synthesized nanoparticles showed the presence of spherical particles having a size of 20-40 nm. X-ray photoelectron spectroscopy (XPS) did not detect the presence of nickel on the nanoparticle surface, which suggested a uniform distribution of both metals inside the particle core. Batch experiments with a minimum nanocatalyst loading of 3 g/L showed complete dye degradation after 10 min of reaction time. The degradation efficiency was linearly dependent on the initial dye concentration, pH of the solution and total Fe-Ni catalyst concentration. The efficiency increased with increasing Fe-Ni concentration and decreasing pH of the solution, but decreased with an increase in the dye concentration. The degradation rate followed first order reaction kinetics with respect to the dye concentration. High performance liquid chromatography-mass spectrometry (HPLC-MS) analysis of the degradation products revealed that the degradation mechanism proceeds through a reductive cleavage of the azo linkage resulting in the formation of aniline and surface-adsorbed naphthol amine derivatives. The latter are subsequently hydroxylated through an oxidative process. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:270 / 278
页数:9
相关论文
共 30 条
[1]   Reducing degradation of azo dye by zero-valent iron in aqueous solution [J].
Cao, JS ;
Wei, LP ;
Huang, QG ;
Wang, LS ;
Han, SK .
CHEMOSPHERE, 1999, 38 (03) :565-571
[2]   The enhancement methods for the degradation of TCE by zero-valent metals [J].
Cheng, SF ;
Wu, SC .
CHEMOSPHERE, 2000, 41 (08) :1263-1270
[3]   Photocatalytic degradation of azo dyes by organic-capped anatase TiO2 nanocrystals immobilized onto substrates [J].
Comparelli, R ;
Fanizza, E ;
Curri, ML ;
Cozzoli, PD ;
Mascolo, G ;
Passino, R ;
Agostiano, A .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 55 (02) :81-91
[4]   On the nonlinear relationship between kobs and reductant mass loading in iron batch systems [J].
Cwiertny, DM ;
Roberts, AL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (22) :8948-8957
[5]   Carcinogenicity of azo colorants: influence of solubility and bioavailability [J].
Golka, K ;
Kopps, S ;
Myslak, ZW .
TOXICOLOGY LETTERS, 2004, 151 (01) :203-210
[6]   Reduction of N-nitrosodimethylamine with granular iron and nickel enhanced iron.: 1.: Pathways and kinetics [J].
Gui, L ;
Gillham, RW ;
Odziemkowski, MS .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (16) :3489-3494
[7]   Catalytic combustion of Orange II on hematite Surface species responsible for the dye degradation [J].
Herrera, F ;
Lopez, A ;
Mascolo, G ;
Albers, E ;
Kiwi, J .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2001, 29 (02) :147-162
[8]   ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[9]   New method of improving photocatalytic activity of commercial Degussa P25 for azo dyes, decomposition [J].
Janus, M. ;
Morawski, A. W. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 75 (1-2) :118-123
[10]   Kinetics of halogenated organic compound degradation by iron metal [J].
Johnson, TL ;
Scherer, MM ;
Tratnyek, PG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (08) :2634-2640