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Silver is a metal widely applied in renewable energy applications and therefore subject to resource scarcity. The paper presents a new approach for recovering silver from zinc-containing solutions mimicking hydrometallurgical base metal process solution. By nature, silver present in ores or concentrates is more noble than zinc and not effectively leached into the sulfate media during zinc hydrometallurgical processing. This paper presents a novel approach for concentrating and recovering silver present in minor amounts in zinc sulfate media. The electrodeposition–redox replacement (EDRR) method was investigated in synthetic zinc sulfate solutions ([Zn] = 60 g/L, [Ag] = 1 ppb–250 ppm, [H2SO4] = 10 g/L) containing silver as low as 1 ppb. The deposited metal coating was analyzed by electrochemical techniques and SEM-EDS. As a result, an enrichment of silver as nano- and microparticles on electrodes was evident. With the application of multiple EDRR steps (n = 160), the method was shown to result in a high purity Ag layer (Ag/Zn ratio ≈ 1500 in the product) from solution with minor Ag content (Ag/Zn ratio ≈ 0.0017 in solution). Moreover, at the concentration levels studied, the EDRR method was shown to outperform conventional electrowinning (EW).

Site-specific assembly of gold nanoparticles on a polysaccharide surface was accomplished via a straightforward method exploiting interfacial polymer blends, selective protein adsorption and electrostatic interaction. The method could be useful in further applications due to the universal nature of the utilized phenomena.

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In the current study, platinum—present as a negligible component (below 1 ppb, the detection limit of the HR-ICP-MS at the dilutions used) in real industrial hydrometallurgical process solutions—was recovered by an electrodeposition–redox replacement (EDRR) method on pyrolyzed carbon (PyC) electrode, a method not earlier applied to metal recovery. The recovery parameters of the EDRR process were initially investigated using a synthetic nickel electrolyte solution ([Ni] = 60 g/L, [Ag] = 10 ppm, [Pt] = 20 ppm, [H2SO4] = 10 g/L), and the results demonstrated an extraordinary increase of 3 × 105 in the [Pt]/[Ni] on the electrode surface cf. synthetic solution. EDRR recovery of platinum on PyC was also tested with two real industrial process solutions that contained a complex multimetal solution matrix: Ni as the major component (>140 g/L) and very low contents of Pt, Pd, and Ag (i.e., <1 ppb, 117 and 4 ppb, respectively). The selectivity of Pt recovery by EDRR on the PyC electrode was found to be significant—nanoparticles deposited on the electrode surface comprised on average of 90 wt % platinum and a [Pt]/[Ni] enrichment ratio of 1011 compared to the industrial hydrometallurgical solution. Furthermore, other precious metallic elements like Pd and Ag could also be enriched on the PyC electrode surface using the same methodology. This paper demonstrates a remarkable advancement in the recovery of trace amounts of platinum from real industrial solutions that are not currently considered as a source of Pt metal.

The electrochemical method for gold extraction from multi-metal industrial solutions in an environmentally benign and energy efficient manner is explained in detail.

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