Published October 2010 | Version v1
Journal article

Adsorption of uranium from aqueous solution on heat and acid treated sepiolites

  • 1. Istanbul University, Department of Chemistry, Avcilar, 34320 Istanbul (Turkey)

Description

In this work adsorption of uranium on natural, heat and acid treated sepiolite was studied. For acid treatment HCl and H2SO4 were used separately. Heat and acid treatment caused some changes in sepiolite such as surface area, micropore volume (cm3/g) and average pore diameter (A). Different amounts of Mg ions were extracted from the lattice depending on the type of acid. After acid treatment with HCl, the amount of Mg left in the sepiolite changed a little. During H2SO4 treatment the sepiolite structure was progressively transformed into amorphous silica. These heat and acid treatments changed adsorption capacity and mechanism of uranium on sepiolite. Data obtained from the adsorption experiments were applied to Langmuir and Dubinin-Radushkevich (D-R) adsorption isotherms. Using these isotherms different adsorption capacities were found for natural and treated sepiolite samples. The capacity values were 3.58x10-3, 3.14x10-3, 2.78x10-3 and 1.55x10-3 mol/g for HCl treated, heat treated, natural and H2SO4 treated sepiolite samples, respectively. In order to evaluate the adsorption mechanism adsorption energies were calculated by the D-R isotherm. According to the adsorption energy values uranium fixed to the natural and heat treated sepiolite surface with ion exchange (12.75 and 12.12 kJ/mol, respectively). Simple physical attractions were the driving force for adsorption on HCl and H2SO4 treated ones (6.62 and 6.87 kJ/mol, respectively).

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apradiso.2010.04.021

Additional details

Identifiers

DOI
10.1016/j.apradiso.2010.04.021;
PII
S0969-8043(10)00165-X;

Publishing Information

Journal Title
Applied Radiation and Isotopes
Journal Volume
68
Journal Issue
10
Journal Page Range
p. 2016-2019
ISSN
0969-8043
CODEN
ARISEF

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.