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Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors

[Image: see text] In this work, a photocatalytic process was carried out to recover gold (Au) from the simulated non-cyanide plating bath solution. Effects of semiconductor types (TiO(2), WO(3), Nb(2)O(3), CeO(2), and Bi(2)O(3)), initial pH of the solution (3–10), and type of complexing agents (Na(2...

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Autores principales: Kunthakudee, Naphaphan, Puangpetch, Tarawipa, Ramakul, Prakorn, Hunsom, Mali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908523/
https://www.ncbi.nlm.nih.gov/pubmed/35284747
http://dx.doi.org/10.1021/acsomega.1c06362
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author Kunthakudee, Naphaphan
Puangpetch, Tarawipa
Ramakul, Prakorn
Hunsom, Mali
author_facet Kunthakudee, Naphaphan
Puangpetch, Tarawipa
Ramakul, Prakorn
Hunsom, Mali
author_sort Kunthakudee, Naphaphan
collection PubMed
description [Image: see text] In this work, a photocatalytic process was carried out to recover gold (Au) from the simulated non-cyanide plating bath solution. Effects of semiconductor types (TiO(2), WO(3), Nb(2)O(3), CeO(2), and Bi(2)O(3)), initial pH of the solution (3–10), and type of complexing agents (Na(2)S(2)O(3) and Na(2)SO(3)) and their concentrations (1–4 mM each) on Au recovery were explored. Among all employed semiconductors, TiO(2) exhibited the highest photocatalytic activity to recover Au from the simulated spent plating bath solution both in the absence and presence of complexing agents, in which Au was completely recovered within 15 min at a pH of 6.5. The presence of complexing agents remarkably affected the size of deposited Au on the TiO(2) surface, the localized surface plasmon effect (LSPR) behavior, and the valence band (VB) edge position of the obtained Au/TiO(2), without a significant change in the textural properties or the band gap energy. The photocatalytic activity of the obtained Au/TiO(2) tested via two photocatalytic processes depended on the common reduction mechanism rather than the textural or optical properties. As a result, the Au/TiO(2) NPs obtained from the proposed recovery process are recommended for use as a photocatalyst for the reactions occurring at the conduction band rather than at the valence band. Notably, they exhibited good stability after the fifth photocatalytic cycle for Au recovery from the actual cyanide plating bath solution.
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spelling pubmed-89085232022-03-11 Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors Kunthakudee, Naphaphan Puangpetch, Tarawipa Ramakul, Prakorn Hunsom, Mali ACS Omega [Image: see text] In this work, a photocatalytic process was carried out to recover gold (Au) from the simulated non-cyanide plating bath solution. Effects of semiconductor types (TiO(2), WO(3), Nb(2)O(3), CeO(2), and Bi(2)O(3)), initial pH of the solution (3–10), and type of complexing agents (Na(2)S(2)O(3) and Na(2)SO(3)) and their concentrations (1–4 mM each) on Au recovery were explored. Among all employed semiconductors, TiO(2) exhibited the highest photocatalytic activity to recover Au from the simulated spent plating bath solution both in the absence and presence of complexing agents, in which Au was completely recovered within 15 min at a pH of 6.5. The presence of complexing agents remarkably affected the size of deposited Au on the TiO(2) surface, the localized surface plasmon effect (LSPR) behavior, and the valence band (VB) edge position of the obtained Au/TiO(2), without a significant change in the textural properties or the band gap energy. The photocatalytic activity of the obtained Au/TiO(2) tested via two photocatalytic processes depended on the common reduction mechanism rather than the textural or optical properties. As a result, the Au/TiO(2) NPs obtained from the proposed recovery process are recommended for use as a photocatalyst for the reactions occurring at the conduction band rather than at the valence band. Notably, they exhibited good stability after the fifth photocatalytic cycle for Au recovery from the actual cyanide plating bath solution. American Chemical Society 2022-02-21 /pmc/articles/PMC8908523/ /pubmed/35284747 http://dx.doi.org/10.1021/acsomega.1c06362 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Kunthakudee, Naphaphan
Puangpetch, Tarawipa
Ramakul, Prakorn
Hunsom, Mali
Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors
title Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors
title_full Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors
title_fullStr Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors
title_full_unstemmed Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors
title_short Photocatalytic Recovery of Gold from a Non-Cyanide Gold Plating Solution as Au Nanoparticle-Decorated Semiconductors
title_sort photocatalytic recovery of gold from a non-cyanide gold plating solution as au nanoparticle-decorated semiconductors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908523/
https://www.ncbi.nlm.nih.gov/pubmed/35284747
http://dx.doi.org/10.1021/acsomega.1c06362
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