Model reactor for photocatalytic degradation of persistent chemicals in ponds and waste water

被引:78
作者
Franke, R
Franke, C
机构
[1] 12 249 Berlin
关键词
model reactor; photocatalysis; titanium dioxide; solar energy; persistent chemicals; degradation; waste water treatment;
D O I
10.1016/S0045-6535(99)00200-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 [工学]; 0830 [环境科学与工程];
摘要
A laboratory scale flow-through model reactor for the degradation of persistent chemicals using titanium dioxide (TiO2) as photocatalyst immobilized on glass beads is presented. In the test system with a volume of 18 L contaminated water is pumped to the upper part of the floating reactor and flows over the coated beads which are exposed to UV-radiation. The degradation of two dyes of different persistance was investigated. Primary degradation of methylene blue did not fit a first order kinetic due to coincident adsorption onto the photocatalyst and direct photolysis, resulting in a half-life of 6 h. A filtrate of a green algae suspension accelerated the colour removal. in contrast, reactive red 2 was degraded only by photocatalysis; neither adsorption nor direct photolysis led to a colour removal. The course of primary degradation followed a first order kinetic with a half-life of 18 h and a rate constant of 0.04 h(-1). Analysis of the degradation products indicated mineralization by detection of NO2- and NO3-, accompanied by a decrease of pH and an increase of conductivity. A successful adaptation of the model reactor (scale 1:10) to dimensions required for surface waters and waste water treatment plants would be a cost-efficient and environmentally sustainable application of photocatalysis for the treatment of industrially polluted water and could be of relevance for third world contries, particularly those favoured by high solar radiation. (C)1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2651 / 2659
页数:9
相关论文
共 12 条
[1]
SOLAR WASTE-WATER DECONTAMINATION [J].
BAHNEMANN, D .
NACHRICHTEN AUS CHEMIE TECHNIK UND LABORATORIUM, 1994, 42 (04) :378-&
[2]
Photocatalytic detoxification with the thin-film fixed-bed reactor (TFFBR): Clean-up of highly polluted landfill effluents using a novel TiO2-photocatalyst [J].
Bekbolet, M ;
Lindner, M ;
Weichgrebe, D ;
Bahnemann, DW .
SOLAR ENERGY, 1996, 56 (05) :455-469
[3]
GOSLICH R, 1996, P 8 INT S SOL THERM
[4]
ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[5]
Photocatalytic degradation of PCBs in TiO2 aqueous suspensions [J].
Huang, IW ;
Hong, CS ;
Bush, B .
CHEMOSPHERE, 1996, 32 (09) :1869-1881
[6]
Photochemical degradation of dicarboximide fungicides in the presence of soil constituents [J].
Hustert, K ;
Moza, PN .
CHEMOSPHERE, 1997, 35 (1-2) :33-37
[7]
On the photodegradation of some unsaturated triazine derivatives with herbicide and bactericide activity [J].
Korte, F ;
Konstantinova, T ;
Mansour, M ;
Ilieva, P ;
Bogdanova, A .
CHEMOSPHERE, 1997, 35 (1-2) :51-54
[8]
Experimental approaches to studying the photostability of selected pesticides in water and soil [J].
Mansour, M ;
Feicht, EA ;
Behechti, A ;
Scheunert, I .
CHEMOSPHERE, 1997, 35 (1-2) :39-50
[9]
LARGE SOLAR PLANT PHOTOCATALYTIC WATER DECONTAMINATION - DEGRADATION OF PENTACHLOROPHENOL [J].
MINERO, C ;
PELIZZETTI, E ;
MALATO, S ;
BLANCO, J .
CHEMOSPHERE, 1993, 26 (12) :2103-2119
[10]
Photocatalytic decolourization of reactive azo dye: A comparison between TiO2 and CdS photocatalysis [J].
Reutergardh, LB ;
Iangphasuk, M .
CHEMOSPHERE, 1997, 35 (03) :585-596