Degradation of polycyclic aromatic hydrocarbons by ultrasonic irradiation

被引:24
作者
Park, JK
Hong, SW
Chang, WS
机构
[1] Korea Inst Sci & Technol, Seoul 130650, South Korea
[2] LG Inst Environm Safety & Hlth, Seoul 130650, South Korea
关键词
polycyclic aromatic hydrocarbon (PAH); ultrasonic irradiation; hydroxyl radical (OH center dot); ring cleavage;
D O I
10.1080/09593332108618162
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polycyclic aromatic hydrocarbons (PAHs) are known to be hazardous compounds with life threatening effects as some of them are proven to be environmentally obnoxious carcinogenic compounds. Ultrasonic irradiation was investigated as a method of attacking the chemical structure of PAH compounds for a complete breakdown. This method produced very promising results with formation of hydroxyl radical (OH .), which is known as a less selective oxidant and very reactive with carbon-chlorine bonds and carbon-carbon double bonds making them capable of generating aromatic ring cleavage. Ultrasonic irradiation resulted in a decrease of PAHs with time and the dominant free radical reaction became a controlling factor. Further, hydrogen peroxide and argon gas markedly enhanced the degradation efficiency during sonolysis. With these agents, more than 30% of additional degradation efficiencies were achieved for all PAHs used in this experiment. Higher degradation efficiencies of PAHs were observed with lowering organic solvent/water ratios and pH range (acidic condition, pH 2). The apparent kinetics were first-order, with the observed rates ranging from 1.60 to 2.81 x 10(-2) min(-1) depending on types of PAHs and presence/absence of hydrogen peroxide and argon gas.
引用
收藏
页码:1317 / 1323
页数:7
相关论文
共 11 条
[1]   ISOTOPIC TECHNIQUES IN THE STUDY OF THE SONOCHEMICAL FORMATION OF HYDROGEN PEROXIDE [J].
DELDUCA, M ;
YEAGER, E ;
DAVIES, MO ;
HOVORKA, F .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1958, 30 (04) :301-307
[2]   STANDARD GIBBS ENERGY OF FORMATION OF THE HYDROXYL RADICAL IN AQUEOUS-SOLUTION - RATE CONSTANTS FOR THE REACTION CLO2- + O3 REVIRSIBLE O3- + CLO2 [J].
KLANING, UK ;
SEHESTED, K ;
HOLCMAN, J .
JOURNAL OF PHYSICAL CHEMISTRY, 1985, 89 (05) :760-763
[3]  
KOTRONAROU A, 1992, THESIS CALTECH
[4]   CHEMICAL EFFECTS OF ULTRASOUND ON AQUEOUS-SOLUTIONS - FORMATION OF HYDROXYL RADICALS AND HYDROGEN-ATOMS [J].
MAKINO, K ;
MOSSOBA, MM ;
RIESZ, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (08) :1369-1377
[5]  
Mason T., 1981, ULTRASOUND THEORY AP
[6]  
Mason T.J., 1991, Practical Sonochemistry: User's Guide To Applications
[7]  
MORRISON RH, 1975, ORGANIC CHEM
[8]   USE OF 2,2-DIPHENYL-1-PICRYLHYDRAZYL TO INVESTIGATE THE CHEMICAL BEHAVIOR OF FREE-RADICALS INDUCED BY ULTRASONIC CAVITATION [J].
SEHGAL, C ;
YU, TJ ;
SUTHERLAND, RG ;
VERRALL, RE .
JOURNAL OF PHYSICAL CHEMISTRY, 1982, 86 (15) :2982-2986
[9]  
SHUTILOV VA, 1988, FUNDAMENTAL PHYSICS
[10]  
Suslick K. S., 1988, ULTRASOUND ITS CHEM