Heavy metals adsorption by novel EDTA-modified chitosan-silica hybrid materials.

J Colloid Interface Sci

Laboratory of Green Chemistry, Department of Energy and Environmental Technology, Faculty of Technology, Lappeenranta University of Technology, Mikkeli, Finland.

Published: June 2011

AI Article Synopsis

  • Novel adsorbents were created by combining chitosan and silica with EDTA ligands, enhancing their structural and functional properties.
  • The research focused on the adsorption of metals like Co(II), Ni(II), Cd(II), and Pb(II), exploring how factors like pH and contact time influenced the effectiveness of the adsorbents.
  • It was found that the adsorbents performed best at adsorbing Pb(II) and had varying capacities, with the most chitosan-rich adsorbent showing the highest adsorption efficiency.

Article Abstract

Novel adsorbents were synthesized by functionalizing chitosan-silica hybrid materials with (ethylenediaminetetraacetic acid) EDTA ligands. The synthesized adsorbents were found to combine the advantages of both silica gel (high surface area, porosity, rigid structure) and chitosan (surface functionality). The Adsorption potential of hybrid materials was investigated using Co(II), Ni(II), Cd(II), and Pb(II) as target metals by varying experimental conditions such as pH, contact time, and initial metal concentration. The kinetic results revealed that the pore diffusion process played a key role in adsorption kinetics, which might be attributed to the porous structure of synthesized adsorbents. The obtained maximum adsorption capacities of the hybrid materials for the metal ions ranged from 0.25 to 0.63 mmol/g under the studied experimental conditions. The adsorbent with the highest chitosan content showed the best adsorption efficiency. Bi-Langmuir and Sips isotherm model fitting to experimental data suggested the surface heterogeneity of the prepared adsorbents. In multimetal solutions, the hybrid adsorbents showed the highest affinity toward Pb(II).

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Source
http://dx.doi.org/10.1016/j.jcis.2011.02.059DOI Listing

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