UV-VIS photocatalytic degradation of nitrobenzene from water using heavy metal doped titania

被引:30
作者
Nitoi, Ines [1 ]
Oancea, Petruta [2 ]
Raileanu, Malina [3 ]
Crisan, Maria [3 ]
Constantin, Lucian [1 ,4 ]
Cristea, Ionut [1 ]
机构
[1] Natl Res & Dev Inst Ind Ecol ECOIND, Bucharest 060652, Romania
[2] Univ Bucharest, Fac Chem, Dept Phys Chem, Bucharest 030016, Romania
[3] Romanian Acad, Iife Murgulescu Inst Phys Chem, Bucharest, Romania
[4] Univ Politehn Bucuresti, Fac Appl Chem & Mat Sci, Bucharest 011061, Romania
关键词
Photocatalysis; Doped TiO2 catalyst; Heavy metals; Nitrobenzene degradation; TIO2; DIOXIDE; TRANSFORMATION; DICHLORVOS; SUSPENSION;
D O I
10.1016/j.jiec.2014.03.036
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The photocatalytic degradation of nitrobenzene (NB) under UV-VIS irradiation with un-doped TiO2 and various heavy metals doped TiO2 powders were studied for aerated solutions. The dopant type (Fe, Co, Ni) and its concentration (0.5-5 wt.% TiO2) influence on pollutant degradation efficiency were investigated. The photocatalyst with lowest Fe content (0.5 wt.%) showed a considerable better behaviour in respect to pollutant degradation than catalyst with higher Fe content and Co and Ni doped titania catalysts. The experiments were carried out for solutions with (0.37-8.45) x 10(-4) M NB initial content, using 50-250 mg/L catalyst dose, at various pHs (4-10) and irradiation time between 30 and 240 min. The kinetics of NB degradation and organic nitrogen mineralization was assessed and pseudo-first order rate constants were calculated. For optimum working conditions (0.5 wt.% Fe doped-TiO2 loading of 250 mg/L, 2.52 x 10(-4) M pollutant initial concentration, pH = 7 and 240 min irradiation time) NB removal and organic nitrogen mineralization efficiencies were 99% and 85%, respectively. It was also demonstrated that degradation process occurs on catalyst surface, so experimental results are in accordance with Langmuir-Hinshalwood model. (C) 2014 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:677 / 682
页数:6
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