Abstract

AbstractKinetics of the alkaline hydrolysis of isoproturon has been studied in the absence and presence of cetyltrimethylammonium bromide (CTAB) and sodium lauryl sulfate (NaLS) micelles. CTAB micelles were found to enhance the rate of reaction, while NaLS micelles inhibited the reaction rate. The reaction obeyed first‐order kinetics in [isoproturon] and was linearly dependent on [NaOH] at lower concentration. The rate of reaction became independent at higher [NaOH]. At lower [NaOH] the reaction proceeded via formation of hydroxide ion addition complex, while at higher [NaOH] the reaction occurred via deprotonation of NH, leading to the formation of isocyanate. The values of kw, km, and Ks were determined by considering the pseudophase ion exchange model. The activation parameters have also been reported. The effect of added salts (NaCl and KNO3) on the reaction rate has also been studied. © 2006 Wiley Periodicals, Inc. Int J Chem Kinet 39: 39–45, 2007

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