Sk. Han et al., QUANTITATIVE-ANALYSIS FOR THE ENHANCEMENT OF HYDROXYL RADICAL GENERATION BY PHENOLS DURING OZONATION OF WATER, Water research (Oxford), 32(11), 1998, pp. 3261-3266
Generation of hydroxy] radical, one of the major reactive species in t
he ozonation of water, was directly and quantitatively measured with t
he combination technique of spin-trapping, stopped-flow and electron s
pin resonance (ESR) spectroscopy. Hydroxyl radical in ozonated water w
as trapped with 5,5-dimethyl-pyrrolidine-1-oxyl (DMPO) as a stable rad
ical, DMPO-OH, and the amount of DMPO-OH was quantitatively measured w
ith an ESR spectrometer. The ESR signal of DMPO-OH increased linearly
with increasing ozone and 1 M ozone produced 0.011 M DMPO-OH, if one m
olecule of ozone produces one molecule of (OH)-O-.. The kinetics of DM
PO-OH generation was determined with a stopped-flow/ESR method and ana
lyzed by two different methods. The logarithmic plot of the initial ve
locity of DMPO-OH generation vs the ozone concentration gave a linear
relationship, which was expressed as v(o) (M s(-1)) = 8.7 x 10(1) x[O-
3 (M)](2.25). The rate constant of DMPO-OH generation, 8.7 x 10(1) M-1
.25 s(-1) is close to the reaction constant of ozone with an hydroxide
ion. The decomposition rate of ozone to (OH)-O-. was estimated to be
0.026 s(-1) at 40 mu M aqueous ozone from the semilogarithmic plot of
the amount of DMPO-OH against reaction time. The presence of phenol de
rivatives increased both the generation rate and the final amount of D
MPO-OH in a dose dependent manner. The enhancing effect of phenols on
(OH)-O-. generation was also analyzed with the above two methods the d
ecomposition of ozone and the generation of DMPO-OH. The effect depend
ed on the kind, position and number of substituents of phenol. The chl
orine substitution of phenol had a more enhancing effect than that of
methyl substitution and the ortho-substitution by chlorine showed a st
ronger enhancement. 2,4-Dichlorophenol showed the strongest enhancing
effect on (OH)-O-. generation among phenols examined, followed by 2-ch
lorophenol. (C) 1998 Elsevier Science Ltd. All rights reserved.