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a Dep. of Soils and Agricultural Chemistry, Alexandria Univ., Alexandria, Egypt
b Dep. of Soils and Waters, Tanta Univ.,Egypt
* Corresponding author (aelprince{at}gmail.com).
Peroxide application has been proposed as a method to control soil aeration. The objectives of this study were to formulate the rate law, identify the inorganic catalyst, identify preferred active centers, and hypothesize a mechanism for the H2O2 decomposition reaction in Torrifluvents. The rate of decomposition of H2O2(aq) by Torrifluvents (10 locations in the Nile Delta) and synthetic Mn oxides was determined by measuring with a gas burette the volume of O2(g) given off. Heat pretreatment showed that the catalytic activity of the air-dried soil is essentially nonenzymatic on the time scale of the reaction. Pretreatment of the soil samples by NH2OH–HCl (pH 2), designed for selectively dissolving MnO2(s), completely deactivated their catalytic capacity. The pseudo-first-order rate coefficient, k*, for Torrifluvents was expressed by the equation: k* = ko[MnO2(s)](10–pH/4), where ko is a constant. Contrary to cryptomelane and pyrolusite, values of k* for birnessite satisfied the above equation, indicating that pedogenic birnessite was the active catalyst in Torrifluvents. Diethylenetriamine pentaacetic acid (DTPA) was found to be a more effective inhibitor than ethylenediamine tetraacetic acid (EDTA). A high value of the activation energy (E) was connected with a high value of the pre-exponential factor (A) of the Arrhenius equation. It was suggested that the birnessite surface has two kinds of active centers: MnIII/MnII and MnIV/MnIII. While the former is less numerous (lnA = 37 ± 4) with low activation energy (E = 75 ± 4 kJ mol–1), the latter is numerous (lnA = 62 ± 3) and of high activation energy (E = 144 ± 17 kJ mol–1). The Habes and Weiss mechanism explained the experimental results obtained.
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