Abstract: Hydrolytic degradation of the herbicide diclofop-methyl was
investigated in the multi-pH deionized water, natural aquatic systems and soil
suspensions. Resulting data indicated that the herbicide was stable in the
acidic and nearly neutral solutions for at least 15 d. The herbicide
diclofop-methyl rapidly dissipated in the natural aquatic systems and soil
suspensions with half-lives less than 4 d. Methyl-CD (partially methylated
β-cyclodextrin) improved its hydrolytic degradation in the pH 8 deionized
water and natural aquatic systems while humic acid inhibited its hydrolytic
degradation at the same conditions. But dissolved organic matter in the natural
aquatic systems and soil suspensions increased its hydrolysis. Two catalysis
mechanisms were introduced to describe the effects of cyclodextrin and organic
matter on its hydrolytic metabolism. Though inorganic ions maybe improved its
hydrolysis reaction in the natural aquatic systems, Fe^{2+}
and Cu^{2+} did not form complexes with the herbicide and
had poor influences on its hydrolytic degradation whether cyclodextrin was
added or not.