Mechanism of the enhanced degradation of pentachlorophenol by ultrasound in the presence of elemental iron

被引:90
作者
Dai, Youzhi [1 ]
Li, Fenfang [1 ]
Ge, Fei [1 ]
Zhu, Fei [1 ]
Wu, Lanyan [1 ]
Yang, Xiangzheng [1 ]
机构
[1] Xiangtan Univ, Dept Environm Engn, Xiangtan 411105, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
ultrasound; iron; hydroxyl radical; synergistic mechanism;
D O I
10.1016/j.jhazmat.2006.04.025
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ultrasound combined with elemental iron (US/Fe-0) is effective in oxidizing organic contaminants in water. The sonolysis degradation of pentachlorophenol (PCP) was significantly enhanced by a factor of 4.2 with the addition of elemental iron, mainly via reaction with hydroxyl radicals ((OH)-O-center dot radicals), and the synergistic mechanism of the enhancement in the combined system was investigated. Experiments were performed with (1) sole ultrasonic treatment; (2) ultrasound in presence of iron; (3) ultrasound combined with copper powder as the same particle size as iron powder; (4) ultrasound in presence of Fe(II). It was observed that PCP degradation and (OH)-O-center dot radicals production were both enhanced in these combined methods, and the pitting on the sonicated iron surface was apparent. These results indicated that the rate enhancements in US/Fe-0 system were attributed to (1) the iron solid effect and the catalysis of Fe(II) produced from corroded-iron with promoting the production of (OH)-O-center dot radicals; (2) the increased surface area of iron particles by acoustic cavitation with promoting the adsorption process. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1424 / 1429
页数:6
相关论文
共 26 条
[1]   Iron(II)-catalyzed enhancement of ultrasonic-induced degradation of diethylstilbestrol (DES) [J].
Ben Abderrazik, N ;
Azmani, A ;
R'kiek, C ;
Song, WH ;
O'Shea, KE .
CATALYSIS TODAY, 2005, 101 (3-4) :369-373
[2]  
[戴友芝 Dai Youzhi], 2005, [环境污染治理技术与设备, Techniques and equipment for environmental pollution control], V6, P19
[3]   Kinetic model for the sonochemical degradation of monocyclic aromatic compounds is aqueous solution [J].
DeVisscher, A ;
VanEenoo, P ;
Drijvers, D ;
VanLangenhove, H .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (28) :11636-11642
[4]   Ultrasonic degradation of trichloroethylene and chlorobenzene at micromolar concentrations: kinetics and modelling [J].
Dewulf, J ;
Van Langenhove, H ;
De Visscher, A ;
Sabbe, S .
ULTRASONICS SONOCHEMISTRY, 2001, 8 (02) :143-150
[5]   Hot spot conditions during cavitation in water [J].
Didenko, YT ;
McNamara, WB ;
Suslick, KS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (24) :5817-5818
[6]   Decomposition of phenol and trichloroethylene by the ultrasound/H2O2/CuO process [J].
Drijvers, D ;
van Langenhove, H ;
Beckers, M .
WATER RESEARCH, 1999, 33 (05) :1187-1194
[7]   A combination of ultrasound and a bio-catalyst: removal of 2-chlorophenol from aqueous solution [J].
Entezari, MH ;
Mostafai, M ;
Sarafraz-yazdi, A .
ULTRASONICS SONOCHEMISTRY, 2006, 13 (01) :37-41
[8]   A combination of ultrasound and inorganic catalyst: removal of 2-chlorophenol from aqueous solution [J].
Entezari, MH ;
Heshmati, A ;
Sarafraz-yazdi, A .
ULTRASONICS SONOCHEMISTRY, 2005, 12 (1-2) :137-141
[9]   A combination of ultrasound and oxidative enzyme:: sono-enzyme degradation of phenols in a mixture [J].
Entezari, MH ;
Pétrier, C .
ULTRASONICS SONOCHEMISTRY, 2005, 12 (04) :283-288
[10]   Sonochemical degradation of phenol in water:: a comparison of classical equipment with a new cylindrical reactor [J].
Entezari, MH ;
Pétrier, C ;
Devidal, P .
ULTRASONICS SONOCHEMISTRY, 2003, 10 (02) :103-108