Sorption of cadmium ions from saline waters onto Fe(III)-zeolite

The sorption of Cd2+ from natural seawater, artificial seawater, distilled water and NaCl solution of the same ionic strength as the seawater onto zeolite modified by iron(III) oxide (Fe(III)-zeolite) was investigated. The sorption was found to be time, concentration and pH dependent. The sorption c...

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Veröffentlicht in:Hemijska industrija 2015-01, Vol.69 (3), p.253-260
Hauptverfasser: Ahribesh, Aysha, Lazarevic, Slavica, Potkonjak, Branislav, Bjelajac, Andjelika, Janackovic, Djordje, Petrovic, Rada
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Sprache:eng
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Zusammenfassung:The sorption of Cd2+ from natural seawater, artificial seawater, distilled water and NaCl solution of the same ionic strength as the seawater onto zeolite modified by iron(III) oxide (Fe(III)-zeolite) was investigated. The sorption was found to be time, concentration and pH dependent. The sorption capacity at the initial pH = 7 decreased in the following order: distilled water > NaCl solution > artificial seawater > natural seawater. The isotherm study showed that Langmuir isotherm model could be adequately applied for the sorption in distilled water, indicating the homogeneous monolayer coverage at Fe(III)-zeolite surface, while the Freundlich isotherm model showed a better fit than the Langmuir model of the sorption data in saline waters, indicating multilayer heterogeneous coverage at the sorbent surface. The values of Freundlich parameter n suggested that the sorption was a favorable process and bonds between Cd2+ and Fe(III)-zeolite surface were stronger in NaCl solution than in natural and artificial seawater. Kinetics analyzes showed that the mechanism of Cd2+ sorption from natural seawater differed from the sorption mechanism out of distilled water, NaCl solution and artificial seawater. The intra-particle diffusion kinetic model indicated that both boundary layer diffusion and intra-particle diffusion influenced the rate of sorption.
ISSN:0367-598X
2217-7426
DOI:10.2298/HEMIND140122038A