Photo-reduction of hexavalent chromium in aqueous solution in the presence of zinc oxide as semiconductor catalyst

被引:128
作者
Chakrabarti, Sampa [1 ]
Chaudhuri, Basab [1 ]
Bhattacharjee, Sekhar [1 ]
Ray, Ajay K. [2 ]
Dutta, Binay K. [3 ]
机构
[1] Univ Calcutta, Dept Chem Engn, Kolkata 700009, W Bengal, India
[2] Univ Western Ontario, Dept Chem & Biochem Engn, London, ON N6A 5B9, Canada
[3] Petr Inst, Chem Engn Program, Abu Dhabi, U Arab Emirates
关键词
Hexavalent chromium; Photocatalytic reduction; ZnO; UV radiation; Initial rate; Kinetic model; PHOTOCATALYTIC REDUCTION; CR(VI) REDUCTION; PHOTOCHEMICAL REDUCTION; WASTE-WATER; TIO2; LIGHT; PHOTOREDUCTION; OXIDATION; REMOVAL; ZNO;
D O I
10.1016/j.cej.2009.06.021
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Common sources of chromium in wastewater are electroplating and leather industries. Hexavalent chromium is more toxic and carcinogenic compared to its trivalent counterpart. Conversion of Cr(VI) to Cr(III) in an aqueous medium by photocatalytic reduction using UV radiation and ZnO semiconductor catalyst has been investigated using potassium dichromate as the model Compound. Effects of the process parameters such as ZnO loading (0-3 g/L) and intensity of UV radiation (0-125 W medium pressure Hg vapour lamp) on photocatalytic reduction were investigated. Initial concentration Of Substrate solution was varied from 40 to 120 mg/L. A comparison of the performance of the ZnO photocatalyst achieved in this Study with that reported in the literature for photocatalytic and conventional processes is presented. The initial rate of the photochemical method was found to be independent of the concentration of potassium dichromate. Methanol was added as a hole scavenger for enhancement of the photo-reduction. Initial rate of photo-reduction was found to be independent of the concentration of methanol above a particular value. A probable mechanism and the corresponding kinetic model have been proposed for the photo-reduction and tested by experimental results. An alternative rate equation based on the LHHW model compares well with the mechanistic rate equation. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:86 / 93
页数:8
相关论文
共 39 条
[1]   Comparative study of methanol, butyrate, and hydrogen as electron donors for long-term dechlorination of tetrachloroethene in mixed anerobic cultures [J].
Aulenta, F ;
Gossett, JM ;
Papini, MP ;
Rossetti, S ;
Majone, M .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 91 (06) :743-753
[2]   Photocatalytic degradation for environmental applications - a review [J].
Bhatkhande, DS ;
Pangarkar, VG ;
Beenackers, AACM .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2002, 77 (01) :102-116
[3]  
Bowers A.R., 1980, Progress in Water Technology, V12, P629
[4]   Photocatalytic degradation of model textile dyes in wastewater using ZnO as semiconductor catalyst [J].
Chakrabarti, S ;
Dutta, BK .
JOURNAL OF HAZARDOUS MATERIALS, 2004, 112 (03) :269-278
[5]   Reduction of chromate from electroplating wastewater from pH 1 to 2 using fluidized zero valent iron process [J].
Chen, Shiao-Shing ;
Cheng, Chih-Yu ;
Li, Chi-Wang ;
Chai, Pao-Hsuan ;
Chang, Yu-Min .
JOURNAL OF HAZARDOUS MATERIALS, 2007, 142 (1-2) :362-367
[6]   Visible light activity of TiO2 for the photoreduction of CCl4 and Cr(VI) in the presence of nonionic surfactant (Brij) [J].
Cho, YM ;
Kyung, H ;
Choi, W .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 52 (01) :23-32
[7]   Homogeneous photocatalysis by transition metal complexes in the environment [J].
Ciesla, P ;
Kocot, P ;
Mytych, P ;
Stasicka, Z .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2004, 224 (1-2) :17-33
[8]   LIGHT-INDUCED H-2 EVOLUTION IN A HYDROGENASE-TIO2 PARTICLE SYSTEM BY DIRECT ELECTRON-TRANSFER OR VIA RHODIUM COMPLEXES [J].
CUENDET, P ;
RAO, KK ;
GRATZEL, M ;
HALL, DO .
BIOCHIMIE, 1986, 68 (01) :217-221
[9]   Photoreduction of chromium(VI) in the presence of algae, Chlorella vulgaris [J].
Deng, Lin ;
Wang, Hongli ;
Deng, Nansheng .
JOURNAL OF HAZARDOUS MATERIALS, 2006, 138 (02) :288-292
[10]   PHOTOCATALYTICAL REDUCTION OF CR(VI) OVER ZNO POWDER [J].
DOMENECH, J ;
MUNOZ, J .
ELECTROCHIMICA ACTA, 1987, 32 (09) :1383-1386