Decolourization and COD removal from reactive dye-containing wastewater using sonophotocatalytic technology

被引:43
作者
An, TC [1 ]
Gu, HF
Xiong, Y
Chen, WG
Zhu, XH
Sheng, GY
Fu, JM
机构
[1] Chinese Acad Sci, Guangzhou Inst Geochem, State Key Lab Organ Geochem, Guangzhou 510640, Peoples R China
[2] Zhongshan Univ, Sch Chem & Chem Engn, Guangzhou 510275, Peoples R China
关键词
sonophotocatalysis; photocatalysis; ultrasound; dye decolourization; COD removal; synergetic effect;
D O I
10.1002/jctb.915
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Decolourization and COD removal from synthetic wastewater containing Reactive Brilliant Orange K-R (RBOKR) dye using sonophotocatalytic technology was investigated. Experimental results showed that this hybrid technology could efficiently remove the colour and reduce COD from the synthetic dye-containing wastewater, and that both processes followed pseudo first-order kinetics. At the condition of 0.1 m(3) h(-1) airflow, 0.75 g dm(-3) titanium dioxide and 0.5 mmol dm(-3) RBOKR solution, the rate constants of decolourization and COD removal were 0.0750 and 0.0143 min(-1) respectively for the sonophotocatalytic process; 0.0197 and 0.0046 min(-1) respectively for the photocatalytic process and 0.0005 and 0.0001 min(-1) respectively for the sonochemical process. The rate constants of sonophotocatalysis were greater than that of both the photocatalytic and sonochemical processes either in isolation or as a sum of the individual process, indicating an apparent synergetic effect between the photo- and sono-processes. (C) 2003 Society of Chemical Industry.
引用
收藏
页码:1142 / 1148
页数:7
相关论文
共 40 条
[21]   Photocatalytic degradation rate of oxalic acid on the semiconductive layer of n-TiO2 particles in the batch mode plate reactor -: Part I:: Mass transfer limits [J].
Kulas, J ;
Rousar, I ;
Krysa, J ;
Jirkovsky, J .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1998, 28 (08) :843-853
[22]  
Leng WH, 2000, J PHOTOCH PHOTOBIO A, V131, P125
[23]   Synergy effect in the photocatalytic degradation of phenol on a suspended mixture of titania and activated carbon [J].
Matos, J ;
Laine, J ;
Herrmann, JM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (3-4) :281-291
[24]   Association of activated carbons of different origins with titania in the photocatalytic purification of water [J].
Matos, J ;
Laine, J ;
Herrmann, JM .
CARBON, 1999, 37 (11) :1870-1872
[25]   PHOTOOXIDATIVE DEGRADATION OF COLORED ORGANICS IN WATER USING SUPPORTED CATALYSTS - TIO2 ON SAND [J].
MATTHEWS, RW .
WATER RESEARCH, 1991, 25 (10) :1169-1176
[26]   Iron-doped titania powders prepared by a sol-gel method.: Part II:: Photocatalytic properties [J].
Navío, JA ;
Testa, JJ ;
Djedjeian, P ;
Padrón, JR ;
Rodríguez, D ;
Litter, MI .
APPLIED CATALYSIS A-GENERAL, 1999, 178 (02) :191-203
[27]  
PELAGRINI R, 1999, APPL CATAL B-ENVIRON, V22, P83
[28]   A new photocatalytic reactor for destruction of toxic water pollutants by advanced oxidation process [J].
Ray, AK .
CATALYSIS TODAY, 1998, 44 (1-4) :357-368
[29]  
SHENG HL, 1993, WATER RES, V27, P1743
[30]   Sonophotochemical destruction of aqueous solution of 2,4,6-trichlorophenol [J].
Shirgaonkar, IZ ;
Pandit, AB .
ULTRASONICS SONOCHEMISTRY, 1998, 5 (02) :53-61