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Title Platinum Recovery from Industrial Process Solutions by Electrodeposition-Redox Replacement
ID_Doc 25662
Authors Halli, P; Heikkinen, JJ; Elomaa, H; Wilson, BP; Jokinen, V; Yliniemi, K; Franssila, S; Lundström, M
Title Platinum Recovery from Industrial Process Solutions by Electrodeposition-Redox Replacement
Year 2018
Published Acs Sustainable Chemistry & Engineering, 6, 11
DOI 10.1021/acssuschemeng.8b03224
Abstract 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 x 10(5) 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 10(11) 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.
Author Keywords Circular economy; Critical precious metals; Electrochemistry; Green chemistry; Electrochemically assisted cementation
Index Keywords Index Keywords
Document Type Other
Open Access Open Access
Source Science Citation Index Expanded (SCI-EXPANDED)
EID WOS:000449577200111
WoS Category Chemistry, Multidisciplinary; Green & Sustainable Science & Technology; Engineering, Chemical
Research Area Chemistry; Science & Technology - Other Topics; Engineering
PDF https://pubs.acs.org/doi/pdf/10.1021/acssuschemeng.8b03224
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