Simultaneous photoreductive removal of copper (II) and selenium (IV) under visible light over spherical binary oxide photocatalyst

被引:48
作者
Aman, Noor [1 ]
Mishra, T. [1 ]
Hait, J. [1 ]
Jana, R. K. [1 ]
机构
[1] CSIR, Natl Met Lab, ACC Div, Jamshedpur 831007, Bihar, India
关键词
Copper (II); Selenium (IV); Photoreduction; EDTA; Formic acid; Visible light; DIFFERENT TIO2 PHOTOCATALYSTS; DIOXIDE AQUEOUS SUSPENSIONS; TITANIUM-DIOXIDE; UV/TIO2; SYSTEM; REDUCTION; IONS; OXIDATION; CADMIUM; DEPOSITION; CR(VI);
D O I
10.1016/j.jhazmat.2010.11.001
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Waste water of copper mines and copper processing plant contains both copper and selenium ions with other contaminants. In this paper simultaneous photoreductive removal of copper (II) and selenium (IV) is studied for the first time using spherical binary oxide photocatalysts under visible light. All the synthesized materials are found to be mesoporous in nature with reasonably high surface area. Among a range of hole scavengers, only EDTA (ethylene diamine tetraacetic acid) and formic acid are found to be the most active for the reduction reaction. A comparative study is carried out using both the hole scavengers varying reaction time. concentration. pH etc. For a single contaminant, EDTA is found to be the best for Cu(II) reduction whereas formic acid is the best for Se(IV) reduction. In a mixed solution both EDTA and formic acid perform very well under visible light irradiation. Highest photocatalytic reduction in a mixed solution is observed at pH 3. Among all the synthesized materials. TiZr-10 performs as the best photocatalyst for both Cu(II) and Se(IV) reduction. However under UV light, Degussa P25 performs slightly better than TiZr-10. Present study shows that 100 ppm of mixed solution can be removed under visible light in 40 min of reaction using TiZr-10 as catalyst. Photodeposited material is found to be copper selenide rather than pure copper and selenium metal. This indicates that the waste water containing copper and selenium ions can be efficiently treated under visible or solar light. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:360 / 366
页数:7
相关论文
共 36 条
[1]   Features of the transformation of HgII by heterogeneous photocatalysis over TiO2 [J].
Botta, SG ;
Rodríguez, DJ ;
Leyva, AG ;
Litter, MI .
CATALYSIS TODAY, 2002, 76 (2-4) :247-258
[2]   Heterogeneous photocatalytic reduction of Cr(VI) in UV-irradiated titania suspensions: Effect of protons, ammonium ions, and other interfacial aspects [J].
Chenthamarakshan, CR ;
Rajeshwar, K .
LANGMUIR, 2000, 16 (06) :2715-2721
[3]   Photocatalytic reduction of divalent zinc and cadmium ions in aqueous TiO2 suspensions:: an interfacial induced adsorption-reduction pathway mediated by formate ions [J].
Chenthamarakshan, CR ;
Rajeshwar, K .
ELECTROCHEMISTRY COMMUNICATIONS, 2000, 2 (07) :527-530
[4]   CHARACTERIZATION OF PLUTONIUM IN MAXEY FLATS RADIOACTIVE TRENCH LEACHATES [J].
CLEVELAND, JM ;
REES, TF .
SCIENCE, 1981, 212 (4502) :1506-1509
[5]   Photocatalytic oxidation of cadmium-EDTA with titanium dioxide [J].
Davis, AP ;
Green, DL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (04) :609-617
[6]   REVERSIBLE PHOTOREDUCTIVE DEPOSITION AND OXIDATIVE DISSOLUTION OF COPPER IONS IN TITANIUM-DIOXIDE AQUEOUS SUSPENSIONS [J].
FOSTER, NS ;
NOBLE, RD ;
KOVAL, CA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (02) :350-356
[7]   EFFECT OF ORGANICS ON THE PHOTODEPOSITION OF COPPER IN TITANIUM-DIOXIDE AQUEOUS SUSPENSIONS [J].
FOSTER, NS ;
LANCASTER, AN ;
NOBLE, RD ;
KOVAL, CA .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1995, 34 (11) :3865-3871
[8]   Photocatalytic reduction and recovery of mercury by polyoxometalates [J].
Gkika, E ;
Troupis, A ;
Hiskia, A ;
Papaconstantinou, E .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (11) :4242-4248
[9]   Photocatalytic reduction and deposition of metallic ions in aqueous phase [J].
Kanki, T ;
Yoneda, H ;
Sano, N ;
Toyoda, A ;
Nagai, C .
CHEMICAL ENGINEERING JOURNAL, 2004, 97 (01) :77-81
[10]   Photocatalytic reduction of environmental pollutant Cr(VI) over some semiconductors under UV/visible light illumination [J].
Khalil, LB ;
Mourad, WE ;
Rophael, MW .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 17 (03) :267-273