Polymer pendant ligand chemistry, 4. Recovery of precious metal ions from strongly acidic solution with a polymer-supported o-phenylenediamine hydrochloride ligand

Abstract

We report on the synthesis and reactivity of a polymer-supported o-phenylenediamine hydrochloride ligand, PS-PDHC, using macroporous 6% crosslinked polystyrene-divinylbenzene beads. The PS-PDHC ligand was found to be highly selective to AuCl 4 − ions in strongly acidic solutions in the presence of other precious metal ions, PdCl 4 2−, PtCl 4 2−, RhCl 6 3−, and RuCl 5 2− (selectivity values: 2.5, Au/Pd; 7.5, Au Pt ; 7, Au Rh ; 2.2, Au Ru ) as well as other transition metal ions, Fe 3+, Cr 3+, CU 2+, Nit+, and Mn 2+. The sorption capacity, selectivity, kinetics of removal and recovery, and solution isotherms have been determined for AuCl 4 − ions in competition with the above-mentioned metal ions. The relative ease of formation of the anionic complex in 0.5 M HCI, AuCl 4 − was thought to be the primary reason for its selective ability to bind to the PS-PDHC ligand by an anion-exchange mechanism. Therefore, the effect of the HCI concentration on the kinetics of AuCl 4 − ion removal from solution was also investigated to clearly show that raising the pH from 0 to 5 caused a dramatic decrease in rate. The AuCl 4 − ion can be recovered quantitatively from the PS-PDHC beads using a 5% thiourea solution in 0.1 M HCl, allowing the polymer-supported ligand to be reused.