Photocatalytic degradation of various dyes by combustion synthesized nano anatase TiO2

被引:372
作者
Sivalingam, G
Nagaveni, K
Hegde, MS
Madras, G [1 ]
机构
[1] Indian Inst Sci, Dept Chem Engn, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
关键词
nano-size anatase TiO2; solution combustion method; photocatalysis; transition metal doping; Langmuir-Hinshelwood model;
D O I
10.1016/S0926-3373(03)00124-3
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 8-10 nm pure anatase phase titania with 156 m(2)/g BET surface area was prepared by solution combustion method and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and BET surface area. This catalyst was used for the photocatalytic degradation of various dyes such as heteropolyaromatic dye (Methylene blue), anthraquinonic dye (Alizarin S), and azoic dyes (Methyl red, Congo red, and Orange G). The effect of catalyst loading, initial concentrations of the dyes, pH, and transition metal doping on TiO2 was investigated. Substitution of TiO2 with transition metal had a detrimental effect on the photocatalytic activity. However, this inhibition effect was not observed with Pt impregnated TiO2. This was attributed to the metals being in ionic state in metal substituted TiO2 synthesized by combustion method, and zero state of metal in impregnated catalysts as evidenced by XPS study. The degradation of dyes was also investigated in solar exposure. The photoactivity of the combustion synthesized titania was higher than commercial TiO2 (Degussa P-25) for both UV and solar exposure. The experimental data followed Langmuir-Hinshelwood (L-H) rate form and the kinetic parameters were obtained. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:23 / 38
页数:16
相关论文
共 34 条
[1]  
AKHTAR MK, 1994, NANOSTRUCT MATER, V4, P537, DOI 10.1016/0965-9773(94)90061-2
[2]  
Aruna ST., 1996, J Mater Synth Process, V4, P175
[3]   THE ROLE OF THE SURFACE INTERMEDIATES IN THE PHOTOELECTROCHEMICAL BEHAVIOR OF ANATASE AND RUTILE TIO2 [J].
AUGUSTYNSKI, J .
ELECTROCHIMICA ACTA, 1993, 38 (01) :43-46
[4]  
BARD A, 1974, ENCY ELECTROCHEMISTR, V2, P192
[5]   A STRUCTURAL INVESTIGATION OF TITANIUM-DIOXIDE PHOTOCATALYSTS [J].
BICKLEY, RI ;
GONZALEZCARRENO, T ;
LEES, JS ;
PALMISANO, L ;
TILLEY, RJD .
JOURNAL OF SOLID STATE CHEMISTRY, 1991, 92 (01) :178-190
[6]   Pathways of phenol and benzene photooxidation using TiO2 supported on a zeolite [J].
Chen, J ;
Eberlein, L ;
Langford, CH .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2002, 148 (1-3) :183-189
[7]   THE EFFECT OF WO3 ON THE PHOTOCATALYTIC ACTIVITY OF TIO2 [J].
DO, YR ;
LEE, W ;
DWIGHT, K ;
WOLD, A .
JOURNAL OF SOLID STATE CHEMISTRY, 1994, 108 (01) :198-201
[8]   TITANIUM-DIOXIDE PHOTOSENSITIZED REACTIONS STUDIED BY DIFFUSE REFLECTANCE FLASH-PHOTOLYSIS IN AQUEOUS SUSPENSIONS OF TIO2 POWDER [J].
DRAPER, RB ;
FOX, MA .
LANGMUIR, 1990, 6 (08) :1396-1402
[9]   HETEROGENEOUS PHOTOCATALYSIS [J].
FOX, MA ;
DULAY, MT .
CHEMICAL REVIEWS, 1993, 93 (01) :341-357
[10]   Photooxidation of the phenylazonaphthol AO20 on TIO2:: kinetic and mechanistic investigations [J].
Galindo, C ;
Jacques, P ;
Kalt, A .
CHEMOSPHERE, 2001, 45 (6-7) :997-1005