The focus of this study was to investigate the use of advanced oxidati
on processes to oxidize a residual water in which chlorobenzenes were
found in the range of 1 mg/L to 10 mg/L and whose TOC was about 1,000
mg/L, and a solution of chlorobenzenes whose concentration was 0.03 mg
/L, which was prepared from stock solutions. Ozone in basic medium (pH
= 9) and ozone in the presence of hydrogen peroxide (H2O2) were compa
red. The carbonyl ozonation byproducts (Glaze, 1989) have been identif
ied as PFBOA [O-(2,3,4,5,6-pentafluorobenzyl) hydroxylamine] derivativ
es by gas chromatography/mass spectrometry (GC/MS). A quantitative ana
lysis by GC/ECD (gas chromatograph equipped with an Electron Capture D
etector) and by GC/FID (Flame Ionization Detector) was carried out on
the complete series of chlorobenzenes in order to determine the elimin
ation levels reached after treatment with ozone and ozone/hydrogen per
oxide. 2-Chlorophenol and 4-chlorophenol were identified as first oxid
ation byproducts of chlorobenzene.