Platinum recycling through electroless dissolution under mild conditions using a surface activation assisted Pt-complexing approach
High industrial demand and limited global abundance of precious metals (PMs) make their recycling essential for industrial and societal sustainability. Owing to their high surface-to-volume ratio, recycling of nanoparticulate precious metals through dissolution in dilute acids at room temperature is quite relevant. However, their dissolution by approaches such as the cyclic oxidation-reduction of metal surfaces through surface potential manipulation may not be suitable for large-scale production. Here, we demonstrate fast dissolution of Pt-nanoparticles under mild conditions (normal temperature and pressure) in Cl- containing dilute acidic/neutral baths without using cyclic oxidation-reduction. We demonstrate that the dissolution of Pt nanoparticles through [PtClx]2- complexing is hindered by blockage of the Pt surface due to adsorption of non-oxide species (impurities), a phenomenon termed herein as non-oxide passivation (NOP). The nanoparticles can be kept active for the [PtClx]2- complexing through removal of the adsorbed species by surface activation, a process to remove the NOP layer by application of cyclic/continuous perturbation. As an example, average % dissolution rate (calculated on initial Pt loading) increases from ∼10% per h (∼30% dissolution in 3 h) for dissolution without NOP removal to ∼19% per h (∼55% dissolution in 3 h) for dissolution through cyclic activation of the Pt surface by HCl-water cycling. The approach may be implemented with a range of cost-efficient and non-toxic reagents for industrial-scale and environmentally friendly recycling of Pt.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2020 |
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Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:22 |
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Enthalten in: |
Physical chemistry chemical physics : PCCP - 22(2020), 23 vom: 17. Juni, Seite 13030-13040 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Sharma, Raghunandan [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Revised 19.06.2020 published: Print Citation Status PubMed-not-MEDLINE |
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doi: |
10.1039/c9cp06066a |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM310587735 |
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520 | |a High industrial demand and limited global abundance of precious metals (PMs) make their recycling essential for industrial and societal sustainability. Owing to their high surface-to-volume ratio, recycling of nanoparticulate precious metals through dissolution in dilute acids at room temperature is quite relevant. However, their dissolution by approaches such as the cyclic oxidation-reduction of metal surfaces through surface potential manipulation may not be suitable for large-scale production. Here, we demonstrate fast dissolution of Pt-nanoparticles under mild conditions (normal temperature and pressure) in Cl- containing dilute acidic/neutral baths without using cyclic oxidation-reduction. We demonstrate that the dissolution of Pt nanoparticles through [PtClx]2- complexing is hindered by blockage of the Pt surface due to adsorption of non-oxide species (impurities), a phenomenon termed herein as non-oxide passivation (NOP). The nanoparticles can be kept active for the [PtClx]2- complexing through removal of the adsorbed species by surface activation, a process to remove the NOP layer by application of cyclic/continuous perturbation. As an example, average % dissolution rate (calculated on initial Pt loading) increases from ∼10% per h (∼30% dissolution in 3 h) for dissolution without NOP removal to ∼19% per h (∼55% dissolution in 3 h) for dissolution through cyclic activation of the Pt surface by HCl-water cycling. The approach may be implemented with a range of cost-efficient and non-toxic reagents for industrial-scale and environmentally friendly recycling of Pt | ||
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