The formation of radical species during ozonation of phenols in water
was investigated with ESR spectroscopy. Ozonation of 2,3-, 2,5- and 2,
6-dichlorophenol gave ESR spectra with a triplet of lines whose peaks
have a height ratio of 1:2:1. The ESR parameters of the triplet were s
imilar to those of the corresponding dichloro-p-semiquinone radical. O
zonation of 2,4,5- and 2,4,6-trichlorophenol gave the same spectra tha
t resulted from the ozonation of 2,5- and 2,6-dichlorophenol, respecti
vely, indicating the replacement of the chlorine in the p-position by
a hydroxyl group during ozonation. The amount of the radical increased
with increasing ozone concentration and was inhibited by two hydroxyl
radical scavengers, mannitol and uric acid. The Fenton system, howeve
r, produced no radicals from phenols. These results indicate that an a
ctive species in addition to the hydroxyl radical participates in the
formation of the p-semiquinone radical from chlorophenols during ozona
tion. (C) 1998 Elsevier Science Ltd. All rights reserved.