Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluent

Abstract A set of nCN/WO3 − x composites was synthesized through a simple thermal treatment for gold recovery from the simulated effluent of a non-cyanide-based plating bath. The obtained results exhibited that all nCN/WO3 − x composites demonstrated a higher photocatalytic activity for gold recover...

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Main Authors: Pimchanok Longchin, Tesfaye Tadesse Gebremariam, Naphaphan Kunthakudee, Auttawit Thoumrungroj, Thanapol Sutthiphong, Mali Hunsom
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-024-81928-4
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author Pimchanok Longchin
Tesfaye Tadesse Gebremariam
Naphaphan Kunthakudee
Auttawit Thoumrungroj
Thanapol Sutthiphong
Mali Hunsom
author_facet Pimchanok Longchin
Tesfaye Tadesse Gebremariam
Naphaphan Kunthakudee
Auttawit Thoumrungroj
Thanapol Sutthiphong
Mali Hunsom
author_sort Pimchanok Longchin
collection DOAJ
description Abstract A set of nCN/WO3 − x composites was synthesized through a simple thermal treatment for gold recovery from the simulated effluent of a non-cyanide-based plating bath. The obtained results exhibited that all nCN/WO3 − x composites demonstrated a higher photocatalytic activity for gold recovery than their pristine components due to the formation of nanocomposites which paved a convenient pathway for charge transfer. Among all synthesized composites, the 5.0CN/WO3 − x composite exhibited the highest photocatalytic activity, recovering around 69.4% of gold within 120 min under UV-vis light irradiation at an intensity of 3.45 mW/cm² and a catalyst loading of 1.0 g/L, in the absence of hole scavenger. This result can be ascribed to the presence of an optimal number of defects, which can act as electron trapping sites and thereby reduce the recombination rate of charge carriers. Gold recovery increased with repeated reuse, attributed to the decorated gold, which enhances light absorption and decreases the recombination rate of charge carriers. The feasible application of used CN/WO3 − x were also explored for H2 production, dye degradation and gold recovery. The obtained results provide a new insight about the photocatalytic recovery of gold from industrial wastewater and also shed light on the application of gold-decorated CN/WO3 − x as a catalyst for other photocatalytic applications.
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spelling doaj-art-6c969c55a15b4da787e3098d9d29b2ce2025-01-19T12:20:59ZengNature PortfolioScientific Reports2045-23222025-01-0115111510.1038/s41598-024-81928-4Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluentPimchanok Longchin0Tesfaye Tadesse Gebremariam1Naphaphan Kunthakudee2Auttawit Thoumrungroj3Thanapol Sutthiphong4Mali Hunsom5Department of Chemical Engineering, Faculty of Engineering, Mahidol UniversityDepartment of Chemical Engineering, Faculty of Engineering, Mahidol UniversityDepartment of Chemical Engineering, Faculty of Engineering, Mahidol UniversityDepartment of Chemical Engineering, Faculty of Engineering, Mahidol UniversityDepartment of Chemical Engineering, Faculty of Engineering, Mahidol UniversityDepartment of Chemical Engineering, Faculty of Engineering, Mahidol UniversityAbstract A set of nCN/WO3 − x composites was synthesized through a simple thermal treatment for gold recovery from the simulated effluent of a non-cyanide-based plating bath. The obtained results exhibited that all nCN/WO3 − x composites demonstrated a higher photocatalytic activity for gold recovery than their pristine components due to the formation of nanocomposites which paved a convenient pathway for charge transfer. Among all synthesized composites, the 5.0CN/WO3 − x composite exhibited the highest photocatalytic activity, recovering around 69.4% of gold within 120 min under UV-vis light irradiation at an intensity of 3.45 mW/cm² and a catalyst loading of 1.0 g/L, in the absence of hole scavenger. This result can be ascribed to the presence of an optimal number of defects, which can act as electron trapping sites and thereby reduce the recombination rate of charge carriers. Gold recovery increased with repeated reuse, attributed to the decorated gold, which enhances light absorption and decreases the recombination rate of charge carriers. The feasible application of used CN/WO3 − x were also explored for H2 production, dye degradation and gold recovery. The obtained results provide a new insight about the photocatalytic recovery of gold from industrial wastewater and also shed light on the application of gold-decorated CN/WO3 − x as a catalyst for other photocatalytic applications.https://doi.org/10.1038/s41598-024-81928-4g-C3N4/WO3 − x compositePhotocatalysisGold recoveryPlating effluent
spellingShingle Pimchanok Longchin
Tesfaye Tadesse Gebremariam
Naphaphan Kunthakudee
Auttawit Thoumrungroj
Thanapol Sutthiphong
Mali Hunsom
Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluent
Scientific Reports
g-C3N4/WO3 − x composite
Photocatalysis
Gold recovery
Plating effluent
title Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluent
title_full Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluent
title_fullStr Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluent
title_full_unstemmed Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluent
title_short Structural modification of defective WO3 by g-C3N4 for photocatalytic gold recovery from non-cyanide-based plating effluent
title_sort structural modification of defective wo3 by g c3n4 for photocatalytic gold recovery from non cyanide based plating effluent
topic g-C3N4/WO3 − x composite
Photocatalysis
Gold recovery
Plating effluent
url https://doi.org/10.1038/s41598-024-81928-4
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