A kinetic and mechanistic study of the chromium (VI) reduction by hydrogen peroxide in acidic aqueous solutions

• Published in: Water S. A. Vol. 33; no. 5; pp. 619 - 626
• Main Authors: Lachmann, G., Van Eldik, R., Hamza, M., Van Niekerk, W., Pienaar, J.J.
• Format: Journal Article
• Language: English
• Published: Pretoria Water Research Commission (WRC) 01.10.2007; Water Research Commision
• Subjects: Activation parameters; Biological and medical sciences; Chromium (VI); Earth sciences; Earth, ocean, space; Exact sciences and technology; Fundamental and applied biological sciences. Psychology; Hydrogen peroxide; Hydrology; Hydrology. Hydrogeology; Kinetics; Mechanism; Reduction; chromium; Hydrogen peroxide; strength; aqueous solutions; concentration; pressure; enthalpy; Radical scavenger; acids; entropy; pH; temperature; kinetics
• ISSN: 0378-4738

The reduction of hexavalent chromium, Cr(VI), by hydrogen peroxide in both buffered and non-buffered aqueous solutions was investigated as a function of concentration, pH, ionic strength, effect of radical scavengers, temperature and pressure. The rate of the reaction between Cr(VI) and hydrogen peroxide exhibited a strong dependence on the pH of the reaction mixture, viz. a decrease in reaction rate with increasing pH from 1.0 to 7.0. For a 2.5 x 10-4 mol·dm-3 Cr(VI) solution, a H2O2 concentration of at least 10 times the initial Cr(VI) concentration was required for complete reduction in this pH range. Neither the ionic strength of the reaction mixture, nor the presence of a radical scavenger had an effect on the rate of the rate-determining step. From the temperature dependence of the reaction the activation enthalpy (∆H≠) was calculated to be 10.4 ± 0.5 kJ·mol-1 and the activation entropy (∆S≠) to be -186 ± 3 J K-1·mol-1 for the rate-determining step. The volume of activation (∆V≠) was found to be -6.1 ± 0.5 cm3·mol-1 from the pressure dependence of the reaction rate. The empirical data could be fitted to : kobs = k[H+][H2O2]/(Ka + [H+]), with k = (48.4 ± 1.4) x 103 dm3·mol-1·s-1 and Ka the acid dissociation constant of H2CrO4. A reaction mechanism in which a Cr(VI)/H2O2 adduct is formed in the rate determining step, is proposed. The theoretical rate law that can be derived from this mechanism is in agreement with the empirical rate law.