LAUSR

The paper aims to present research results obtained at the study of equilibrium and kinetics of U(VI)aq sorption on in situ generated Fe2O3 x nH2O from model solutions. The studied systems represent U(VI) solutions with CU(VI) = 5-30 mg�L-1 for which maximum U(VI) removal efficiencies (%RU(VI) = 95.98) on in situ generated Fe2O3��nH2O were obtained in the following working conditions: pH = 8.75, tcontact = 30 min, [U(VI)] : [Fe(III)] =1:75 and stirring rate 250 RPM. The Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherm models were used to study U(VI) sorption equilibrium. Langmuir isotherm with the correlation coefficient R2 (0.9808) suggests that it involves physical interactions. Freundlich (R2 = 0.8349) and Temkin (R2 = 0.8715) models describe well the sorption process suggesting that there also exists a chemical component, complexing and/or co-precipitation. The kinetic modelling according to the pseudo-first and pseudo-second order models, respectively has demonstrated that the U(VI) sorption equilibrium follows the pseudo-second order equation suggesting a chemical component of the process.