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Adsorptive removal of 134Cs+, 60Co2 + and 152 + 154Eu3 + radionuclides from aqueous solutions using sepiolite: Single and multi-component systems.

Authors :
Mahmoud, Mamdoh R.
Rashad, Ghada M.
Metwally, Essam
Saad, Ebtissam A.
Elewa, Ahmed M.
Source :
Applied Clay Science. Jun2017, Vol. 141, p72-80. 9p.
Publication Year :
2017

Abstract

Single and multi-component adsorptive removal of 134 Cs + , 60 Co 2 + and 152 + 154 Eu 3 + from aqueous solutions onto sepiolite are studied in the present study. Removal of these radionuclides in single systems is found to be strongly dependent on the initial pH on the solution. Removals > 99% (for 60 Co 2 + and 152 + 154 Eu 3 + ) and of about 82% (for 134 Cs + ) are achieved at initial pH values higher than 4 and 5, respectively. The kinetic data and the equilibrium isotherms are modeled by two kinetic models, the pseudo-first-order and the pseudo-second-order, and two isotherm models, Langmuir and Freundlich, respectively. The effect of various coexisting cations, Na + , Ca 2 + and Al 3 + , at different concentrations on the adsorption processes of the concerned radionuclides in single systems was evaluated. Desorption studies of radionuclide-loaded sepiolite are studied using different concentrations of organic, EDTA and HA (strong complexing agents for radionuclides), and inorganic, HCl, NaCl, CaCl 2 , Mg(NO 3 ) 2 and AlCl 3 , desorbing agents. Adsorption mechanisms of radionuclides onto sepiolite are deeply discussed. Multi-component adsorptive removal of 134 Cs + , 60 Co 2 + and 152 + 154 Eu 3 + onto sepiolite as a function of adsorbent weight and time was also studied. The influence of the solution pH on co-removal efficiency of radionuclides was investigated in presence of EDTA. Furthermore, the present investigation evaluated the removal efficiency of radionuclides, in multi-systems, in presence of different concentrations either of NaCl or CaCl 2 . [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01691317
Volume :
141
Database :
Academic Search Index
Journal :
Applied Clay Science
Publication Type :
Academic Journal
Accession number :
121935677
Full Text :
https://doi.org/10.1016/j.clay.2016.12.021