Abstract

In this study, the Ag+-imprinted chitosan gel beads were synthesized to selectively adsorb Ag+ from bimetallic aqueous solutions containing the same molar concentration of Ag+ and Cu2+. The Ag+-imprinting not only helps to achieve extremely high selectivity of Ag+, but also enhances the uptake capacity of the target Ag+ by protecting some amine groups, the primary binding sites of metal ions from cross-linking. The maximum uptake of Ag+ by the ion-imprinted chitosan beads was found to be 89.20mgg−1 at 25.0°C with an initial Ag+ concentration of 352.95mgL−1 and the biosorbent dosage of 1.0gL−1. The adsorption equilibrium and kinetics of Ag+ by the ion-imprinted chitosan beads can be better described by Langmuir isotherm and the intraparticle diffusion model. FTIR and XPS analyses suggested that amine functional groups involve the binding of Ag+ via complexation at higher solution pH (3.0≤pH≤5.0) and ion exchange at lower solution pH (1.0≤pH<3.0).

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