Degradation pathways of ethyl violet by photocatalytic reaction with ZnO dispersions

被引:120
作者
Chen, Chiing-Chang [1 ]
机构
[1] Natl Taichung Nursing Coll, Dept Gen Educ, Taichung 403, Taiwan
关键词
ethyl violet; N-de-ethylation; ZnO; photocatalytic; dyes;
D O I
10.1016/j.molcata.2006.09.013
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photodegradation of ethyl violet (EV; N,N,N',N',N',N'-hexaethyl-pararosaniline; C.I. 42600) dye was examined in aqueous ZnO dispersions under UV light irradiation. The techniques of HPLC-ESI-MS have been used to identify the various intermediates and to investigate the photocatalytic mechanism of the dye after low watt irradiation. The degradation progresses through competitive reactions such as N-de-ethylation and oxidative degradation. Twenty-six intermediates have been detected by HPLC-ESI-MS. The N-de-ethylation took place in a stepwise manner to yield mono-, di, tri-, tetra-, penta-, and hexa-ethylated EV species while the oxidative degradation yielded 4-diethylaminophenol (DAP), 4-diethylamino-4'-diethylaminobenzophenone (DDBP) and their N-de-ethylated products, which were found for the first time in the ZnO-mediated photocatalysis process. Moreover, the hydroxyethylated intermediates formed in the N-de-ethylated EV, DDBP, and DAP processes were also separated and identified for the first time. For decolorization of dyes, the possible photodegradation pathways were proposed and discussed. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:82 / 92
页数:11
相关论文
共 29 条
[21]   PHOTOCATALYSIS ON TIO2 SURFACES - PRINCIPLES, MECHANISMS, AND SELECTED RESULTS [J].
LINSEBIGLER, AL ;
LU, GQ ;
YATES, JT .
CHEMICAL REVIEWS, 1995, 95 (03) :735-758
[22]   Photooxidation pathway of sulforhodamine-B.: Dependence on the adsorption mode on TiO2 exposed to visible light radiation [J].
Liu, GM ;
Li, XZ ;
Zhao, JC ;
Hidaka, H ;
Serpone, N .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (18) :3982-3990
[23]   Kinetic studies of photocatalytic degradation in a TiO2 slurry system:: Distinguishing working regimes and determining rate dependences [J].
Mehrotra, K ;
Yablonsky, GS ;
Ray, AK .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (11) :2273-2281
[24]   Photocatalytic degradation of atrazine using suspended and supported TiO2 [J].
Parra, S ;
Stanca, SE ;
Guasaquillo, I ;
Thampi, KR .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 51 (02) :107-116
[25]  
SHAEFER FC, 1970, J ORG CHEM, V35, P2165
[26]  
SILVA CG, 2003, J PHOTOCH PHOTOBIO A, V155, P133, DOI DOI 10.1016/S1010-6030(02)00374-X
[27]   Comparison of azo dye degradation efficiency using UV/single semiconductor and UV/coupled semiconductor systems [J].
Wu, CH .
CHEMOSPHERE, 2004, 57 (07) :601-608
[28]   Studies on the photodegradation of Rhodamine dyes on nanometer-sized zinc oxide [J].
Yu, DZ ;
Cai, RX ;
Liu, ZH .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2004, 60 (07) :1617-1624
[29]   Photoassisted degradation of dye pollutants.: 3.: Degradation of the cationic dye rhodamine B in aqueous anionic surfactant/TiO2 dispersions under visible light irradiation:: Evidence for the need of substrate adsorption on TiO2 particles [J].
Zhao, JC ;
Wu, TX ;
Wu, KQ ;
Oikawa, K ;
Hidaka, H ;
Serpone, N .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (16) :2394-2400