Kinetics and mechanism of the enhanced reductive degradation of nitrobenzene by elemental iron in the presence of ultrasound

被引:165
作者
Hung, HM [1 ]
Ling, FH [1 ]
Hoffmann, MR [1 ]
机构
[1] CALTECH, WM Keck Labs, Pasadena, CA 91125 USA
关键词
D O I
10.1021/es990385p
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Sonolysis, reduction by elemental iron (Fe-0), and a combination of the two processes were used to facilitate the degradation of nitrobenzene (NB) and aniline (AN) in water. The rates of reduction of nitrobenzene by Fe-0 are enhanced in the presence of ultrasound. The first-order rate constant, k(US),for nitrobenzene degradation by ultrasound is 1.8 x 10(-3) min(-1), while in the presence of Fe-0, the rate was found to be substantially faster. The observation of similar degradation rates for aniline in each system suggests that the sonication process was not affected by the presence of Fe-0. The observed rate enhancements for the degradation of nitrobenzene can be attributed primarily to the continuous cleaning and chemical activation of the Fe-0 surfaces by acoustic cavitation and to accelerated mass transport rates of reactants, intermediates, and products between the solution phase and the Fe-0 surface. The relative concentrations of nitrosobenzene and aniline, the principal reaction intermediates generated by Fe-0 reduction, are altered substantially in the presence of ultrasound.
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收藏
页码:1758 / 1763
页数:6
相关论文
共 22 条
[1]   Reduction of nitro aromatic compounds by zero-valent iron metal [J].
Agrawal, A ;
Tratnyek, PG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (01) :153-160
[2]   Monitoring of the ultrasonic irradiation effect on the extraction of airborne particulate matter by ion chromatography [J].
Carvalho, LRF ;
Souza, SR ;
Martinis, BS ;
Korn, M .
ANALYTICA CHIMICA ACTA, 1995, 317 (1-3) :171-179
[3]   SONOCHEMICAL DESTRUCTION OF CHLORINATED HYDROCARBONS IN DILUTE AQUEOUS-SOLUTION [J].
CHEUNG, HM ;
BHATNAGAR, A ;
JANSEN, G .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1991, 25 (08) :1510-1512
[4]  
Fennelly JP, 1998, ENVIRON SCI TECHNOL, V32, P1980, DOI 10.1021/es970784p
[5]   ENHANCED DEGRADATION OF HALOGENATED ALIPHATICS BY ZERO-VALENT IRON [J].
GILLHAM, RW ;
OHANNESIN, SF .
GROUND WATER, 1994, 32 (06) :958-967
[6]   Kinetics and mechanism of the sonolytic degradation of CCl4: Intermediates and byproducts [J].
Hua, I ;
Hoffmann, MR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (03) :864-871
[7]   Optimization of ultrasonic irradiation as an advanced oxidation technology [J].
Hua, I ;
Hoffmann, MR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (08) :2237-2243
[8]   Kinetics and mechanism of the enhanced reductive degradation of CCl4 by elemental iron in the presence of ultrasound [J].
Hung, HM ;
Hoffmann, MR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (19) :3011-3016
[9]   Kinetics of halogenated organic compound degradation by iron metal [J].
Johnson, TL ;
Scherer, MM ;
Tratnyek, PG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (08) :2634-2640
[10]   Degradation of carbon tetrachloride by iron metal: Complexation effects on the oxide surface [J].
Johnson, TL ;
Fish, W ;
Gorby, YA ;
Tratnyek, PG .
JOURNAL OF CONTAMINANT HYDROLOGY, 1998, 29 (04) :379-398