A kinetic study of enhancing effect by phenolic compounds on the hydroxyl radical generation during ozonation

2004 ◽  
Vol 50 (8) ◽  
pp. 97-102 ◽  
Author(s):  
Y.-H. Han ◽  
K. Ichikawa ◽  
H. Utsumi

Ozone decomposition in aqueous solution proceeds through a radical type chain mechanism. These reactions involve the very reactive and catalytic intermediates O2- radical, OH radical, HO2 radical, OH-, H2O2, etc. OH radical is proposed as an important factor in the ozonation of water among them. In the present study, the enhancing effects of several phenolic compounds; phenol, 2-, 3-, 4-monochloro, 2,4-dichloro, 2,4,6-trichlorophenol on OH radical generation were mathematically evaluated using the electron spin resonance (ESR)/spin-trapping technique. OH radical was trapped with a 5,5-dimethyl-1-pyrroline-Noxide (DMPO) as a stable adduct, DMPO-OH. The initial velocities of DMPO-OH generation in ozonated water containing phenolic compounds were quantitatively measured using a combined system of ESR spectroscopy with stopped-flow apparatus, which was controlled by homemade software. The initial velocities of DMPO-OH generation increased as a function of the ozone concentration. The relation among ozone concentration, amount of phenolic compounds and the initial velocity (ν0) of DMPO-OH generation was mathematically analyzed and the following equation was obtained, ν0 (10-6 M/s) = (A′ × [PhOHs (10-9M)] + 0.0005) exp (60 × [ozone (10-9 M)]). The equation fitted very well with the experimental results, and the correlation coefficient was larger than 0.98.

2004 ◽  
Vol 4 (5-6) ◽  
pp. 305-311
Author(s):  
Y.-H. Han ◽  
I. Koshiishi ◽  
H. Utsumi

Ozone decomposition in aqueous solution proceeds through a radical type chain mechanism. These reactions involve the very reactive and catalytic intermediates hydroxyl (OH) radical, O2− radical, HO2 radical, OH−, H2O2, etc. OH radical is proposed as an important factor in the ozonation of water. In the previous study, generation of OH radical in the ozonation of water containing 3-chlorophenol was mathematically evaluated. In this study, we estimated the kinetic equation for the effect of 3-chlorophenol on OH radical generation during ozonation using the power law equation, in order to analyze it more correctly. The OH radical was trapped with a 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) as a stable adduct, DMPO-OH. The relationship between the ozone concentration, 3-chlorophenol content, and the initial velocity (ν0) of DMPO-OH generation was analyzed mathematically, and the following equation was obtained: ν0 (10−6 M/s)=(1.58×10−5)×[3-chlorophenol (10−6 M)]×[ozone (10−6 M)]2.40+(3.09×10−5)×[ozone (10−6 M)]1.72. The equation fitted very well with the experimental results, and square of the correlation coefficient was larger than 0.9.


2017 ◽  
Vol 43 (1) ◽  
pp. 65-72 ◽  
Author(s):  
Hossein Ebrahimi ◽  
Farshid Ghorbani Shahna ◽  
Abdulrahman Bahrami ◽  
Babak Jaleh ◽  
Kamal ad-Din Abedi

Abstract The decomposition of hydrocarbons using combined advanced oxidation methods is largely considered owing to abundant production of OH radicals and the potential economic advantages. In this study, the synergetic effect of ozonation on photocatalytic oxidation of chloroform and chlorobenzene over expanded graphite-TiO2&ZnO Nano composite was investigated. The effect of introduced ozone concentration and residence time was also examined on removal efficiency. The results showed that the removal efficiency was significantly enhanced by the combined system resulting from the additional oxidation process causing active species to be increased. Increasing the introduced ozone concentration which generates more reactive compounds had a greater effect on the removal efficiency than that of residence time. However, from the mineralization point of view, the residence time had a dominant effect, and the selectivity towards CO2 was dramatically declined when the flow rate increased. Based on these results, the combined system is preferred due to higher removal efficiency and complete mineralization.


2013 ◽  
Vol 20 (4) ◽  
pp. 1092-1097 ◽  
Author(s):  
Kazuaki Ninomiya ◽  
Hiromi Takamatsu ◽  
Ayaka Onishi ◽  
Kenji Takahashi ◽  
Nobuaki Shimizu

1994 ◽  
Vol 28 (1-3) ◽  
pp. 175-186 ◽  
Author(s):  
Louis Strong ◽  
Lu Xiao-Ming ◽  
Ronald G. Tompkins ◽  
Martin L. Yarmush

2006 ◽  
Vol 124 (2) ◽  
pp. 024305 ◽  
Author(s):  
Sumana SenGupta ◽  
Hari P. Upadhyaya ◽  
Awadhesh Kumar ◽  
Prakash D. Naik ◽  
Parmanand Bajaj
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