Ultrasound can be used to oxidize aqueous pollutants; however, due to
economic reasons, higher oxidation/destruction rates are needed. This
study reports enhancements of reaction rates by the addition of sodium
chloride salt. Using 20 kHz ultrasound, large salt-induced enhancemen
ts are observed-6-fold for chlorobenzene, 7-fold for p-ethylphenol, an
d 3-fold for phenol oxidation. The reaction rate enhancements are prop
ortional to the diethyl ether-water partitioning coefficient of the po
llutants. It appears that the majority of oxidation reactions occur in
the bubble-bulk interface region. The addition of salt increases the
ionic strength of the aqueous phase which drives the organic pollutant
s toward the bubble-bulk interface. A first order reaction rate equati
on is proposed which can represent the observed enhancement with a goo
d accuracy. A new sonochemical-waste-oxidation process is proposed uti
lizing the salt-induced enhancement.