Abstract

In this study, 1-octyl-2-(2′-pyridyl)imidazole (OPIM), along with dinonylnaphthalene sulfonic acid (DNNSA) as a synergist, was investigated as a potential selective extractant of Ni2+ from base metals in a solvent extraction system using 2-octanol/Shellsol 2325 (4:1) as a diluent and modifier, respectively. The separation of Ni2+ from the borderline and hard acids; Co2+, Cu2+, Zn2+, Fe2+, Fe3+, Mn2+, Mg2+ and Ca2+ was carried out at a pH range of 0.5–3.5 in sulfate and sulfate/chloride media. The separation of Ni2+ from Co2+ in 0.001M solutions was achieved with an optimised concentration of 0.025M OPIM along with 0.02M DNNSA to the tune of a ∆pH½≈1.6. The extraction system further proved the rejection of 0.001M Fe3+, Mn2+, Mg2+ and Ca2+. The absence of DNNSA resulted in very low extraction efficiencies of the Ni2+ metal ions in the pH range under investigation, thus highlighting the role of the synergist (DNNSA). The three-stage counter-current extraction of Ni2+, at the optimised pH of 1.89, from a synthetic mixture of Ni2+, Co2+ and Cu2+, yielded 99.01 (±1.79)%. The total co-extracted Cu2+ was 48.72 (±0.24)% of the original quantity in the mixture, and it was 19.85 (±0.28%) for Co2+. The co-extracted Cu2+ was scrubbed off from the loaded organic phase at pH≈8.5 by using an ammonium buffer, while co-extracted Co2+ was selectively and quantitatively stripped with H2SO4 at pH 1.64. The total recovery of Ni2+ by stripping at pH 0.32 was 94.05 (±1.70)%. The underlying chemistry in this extraction system was studied through solid state/solution studies for the complexation of the ligand with the base metals, and it is apparent from the qualitative/semi-quantitative data that the separations achieved are of kinetic origin rather than thermodynamic, nor are they being driven by stereochemical preferences. Therefore, 1-octyl-2-(2′-pyridyl)imidazole can be effectively utilized alongside DNNSA as a co-extractant in the separation of Ni2+ from base metals in acidic sulfate and sulfate/chloride media.

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