Photooxidation of Fe(II) at acidic pH occurs in photocatalytic processes of Fe(III) species, but its reaction mechanism is not well understood. The kinetics of Fe(II) oxidation in irradiated aqueous solutions at pH 3.0 have been investigated in terms of kinetic modeling approach, rate constant estimation and the significance of various oxidation pathways. Fe(II) oxidation kinetics strongly rely on the availability of UV light, Fe(III) ions and oxygen. The presence of a portion of Fe(III) in Fe(II)-containing solutions favors the rapid oxidation of Fe(II). At high concentration of Fe(II), excitation of Fe(III) species may be quenched by Fe(II) in deaerated systems or may sensitize Fe(II) oxygenation under oxic conditions. By incorporation of this photosensitization pathway, the established model in this study is shown to be able to adequately describe the oxidation of Fe(II) at pH 3.0. Sensitivity analysis indicates that photolysis of Fe(III) species is critically important for overall Fe(II) oxidation kinetics. Fe(III)-catalyzed oxygenation of Fe(II), and oxidation of Fe(II) by HO2 center dot and center dot OH also exerts a marked impact on the oxidation of Fe(II). Therefore, Fe(III)-catalyzed oxygen activation and their secondary reactive oxygen species (ROS) account for the oxidation kinetics of Fe(II) at acidic pH. (C) 2013 Elsevier B.V. All rights reserved.