Degradation of chloro-organics in bleach plant E-1 effluents by ultras
ound sonication was investigated to evaluate the effects of ultrasonic
treatment on the dechlorination. On sonolysis, ca. 65mol% of 4-chloro
phenol (1) at concentration of 1.0 x 10(-4)M in aqueous solution was d
ecomposed and 35mol% of chlorine in the substrate was released as chlo
ride ions (Cl-) after 80min at room temperature under atmospheric pres
sure. By contrast, under the same reaction conditions, only ca. 1.1 mo
l% and 3 mol % of 1 were decomposed at the concentrations of 1.0 x 10(
-3)M and 1.0 x 10(-2)M with the release of ca. 5 and 1mol% of Cl-, res
pectively. Although the kinetics for the disappearance of 1 fits a fir
st-order law, the rate constant decreases with increasing initial conc
entration of the substrate. This suggests that the disappearance rate
of 1 does not followed the first order law and the reaction mechanism
involved is rather complex. When hydrogen peroxide was added to the so
lution in the molar ratio of substrate to hydrogen peroxide 1 : 10, bo
th the rates of degradation and dechlorination were not affected. Howe
ver, an addition of a smaller amount of hydrogen peroxide to the solut
ion resulted in a decrease in the rate of the degradation. In the pres
ence of hydrogen peroxide, the kinetics for the decomposition of I als
o follows the same pattern for that without hydrogen peroxide. On sono
lysis, polychlorinated oxylignins (PCOLs) isolated from E-1 effluent r
eleased chloride ions. The high relative mass PCOL released larger amo
unts of chloride ions than the low relative mass PCOL. The sonolysis b
rought about a very small decrease in the relative mass of PCOLs, and
no significant degradation of PCOLs except for release of chloride ion
s. This result suggests that an acoustic cavitation by ultrasonic trea
tment plays a important role in cleavage of C-Cl bonds, but not C-C bo
nds.