Photocatalytic reduction of Hg(II) on TiO2 and Ag/TiO2 prepared by the sol-gel and impregnation methods

被引:83
作者
Lenzi, G. G. [1 ]
Favero, C. V. B. [1 ]
Colpini, L. M. S. [2 ]
Bernabe, H. [3 ]
Baesso, M. L. [3 ]
Specchia, S. [4 ]
Santos, O. A. A. [1 ]
机构
[1] Univ Estadual Maringa, Dept Engn Quim, BR-87020900 Maringa, Parana, Brazil
[2] Univ Fed Parana, Curso Super Tecnol Biocombustiveis, BR-85950000 Palotina, Parana, Brazil
[3] Univ Estadual Maringa, Dept Fis, BR-87020900 Maringa, Parana, Brazil
[4] Politecn Torino, Dept Mat Sci & Chem Engn, I-10138 Turin, Italy
关键词
Photocatalytic reduction; Mercury; Sol-gel catalyst; HETEROGENEOUS PHOTOCATALYSIS; AQUEOUS-SOLUTIONS; OXIDATION; COMPLEXATION; DEGRADATION; KINETICS; TITANIA; REMOVAL; PHENOL; NICKEL;
D O I
10.1016/j.desal.2010.11.051
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Heterogeneous photocatalysis is a convenient tool for mercury(II) reduction, because it uses inexpensive chemicals and near-UV light. However, structural features of titania (band gap at 3.2 eV) make extending its optical absorption in the visible region difficult. This key factor results in low photocatalytic efficiency, as about only 5% of the solar spectrum is used. This study focuses on the characterization and evaluation of the photocatalytic activity of TiO2. The titania preparation method (commercial and sol-gel), the presence of metal on the surface of the oxide (2% wt. Ag), and the calcination temperature (350 and 500 degrees C) were evaluated. The characterization techniques used were: temperature-programmed reduction (TPR), determination of specific surface area (BET method), X-ray diffraction (XRD), scanning electron microscopy (SEM), and photoacoustic spectroscopy. The photocatalytic reduction of Hg2+ to Hg-0 was performed by aqueous solution containing formic acid. The results showed that the presence of Ag on the surface of TiO2 (commercial and sol-gel) decreased the band gap energy and increased the photoactivity efficiency, i.e., all the Hg2+ in the solution was reduced to Hg-0. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:241 / 247
页数:7
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