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High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin
Developing an eco-friendly, efficient, and highly selective gold-recovery technology is urgently needed in order to maintain sustainable environments and improve the utilization of resources. Here we report an additive-induced gold recovery paradigm based on precisely controlling the reciprocal tran...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998620/ https://www.ncbi.nlm.nih.gov/pubmed/36894545 http://dx.doi.org/10.1038/s41467-023-36591-0 |
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author | Wu, Huang Wang, Yu Tang, Chun Jones, Leighton O. Song, Bo Chen, Xiao-Yang Zhang, Long Wu, Yong Stern, Charlotte L. Schatz, George C. Liu, Wenqi Stoddart, J. Fraser |
author_facet | Wu, Huang Wang, Yu Tang, Chun Jones, Leighton O. Song, Bo Chen, Xiao-Yang Zhang, Long Wu, Yong Stern, Charlotte L. Schatz, George C. Liu, Wenqi Stoddart, J. Fraser |
author_sort | Wu, Huang |
collection | PubMed |
description | Developing an eco-friendly, efficient, and highly selective gold-recovery technology is urgently needed in order to maintain sustainable environments and improve the utilization of resources. Here we report an additive-induced gold recovery paradigm based on precisely controlling the reciprocal transformation and instantaneous assembly of the second-sphere coordinated adducts formed between β-cyclodextrin and tetrabromoaurate anions. The additives initiate a rapid assembly process by co-occupying the binding cavity of β-cyclodextrin along with the tetrabromoaurate anions, leading to the formation of supramolecular polymers that precipitate from aqueous solutions as cocrystals. The efficiency of gold recovery reaches 99.8% when dibutyl carbitol is deployed as the additive. This cocrystallization is highly selective for square-planar tetrabromoaurate anions. In a laboratory-scale gold-recovery protocol, over 94% of gold in electronic waste was recovered at gold concentrations as low as 9.3 ppm. This simple protocol constitutes a promising paradigm for the sustainable recovery of gold, featuring reduced energy consumption, low cost inputs, and the avoidance of environmental pollution. |
format | Online Article Text |
id | pubmed-9998620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99986202023-03-11 High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin Wu, Huang Wang, Yu Tang, Chun Jones, Leighton O. Song, Bo Chen, Xiao-Yang Zhang, Long Wu, Yong Stern, Charlotte L. Schatz, George C. Liu, Wenqi Stoddart, J. Fraser Nat Commun Article Developing an eco-friendly, efficient, and highly selective gold-recovery technology is urgently needed in order to maintain sustainable environments and improve the utilization of resources. Here we report an additive-induced gold recovery paradigm based on precisely controlling the reciprocal transformation and instantaneous assembly of the second-sphere coordinated adducts formed between β-cyclodextrin and tetrabromoaurate anions. The additives initiate a rapid assembly process by co-occupying the binding cavity of β-cyclodextrin along with the tetrabromoaurate anions, leading to the formation of supramolecular polymers that precipitate from aqueous solutions as cocrystals. The efficiency of gold recovery reaches 99.8% when dibutyl carbitol is deployed as the additive. This cocrystallization is highly selective for square-planar tetrabromoaurate anions. In a laboratory-scale gold-recovery protocol, over 94% of gold in electronic waste was recovered at gold concentrations as low as 9.3 ppm. This simple protocol constitutes a promising paradigm for the sustainable recovery of gold, featuring reduced energy consumption, low cost inputs, and the avoidance of environmental pollution. Nature Publishing Group UK 2023-03-09 /pmc/articles/PMC9998620/ /pubmed/36894545 http://dx.doi.org/10.1038/s41467-023-36591-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Huang Wang, Yu Tang, Chun Jones, Leighton O. Song, Bo Chen, Xiao-Yang Zhang, Long Wu, Yong Stern, Charlotte L. Schatz, George C. Liu, Wenqi Stoddart, J. Fraser High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin |
title | High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin |
title_full | High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin |
title_fullStr | High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin |
title_full_unstemmed | High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin |
title_short | High-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin |
title_sort | high-efficiency gold recovery by additive-induced supramolecular polymerization of β-cyclodextrin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998620/ https://www.ncbi.nlm.nih.gov/pubmed/36894545 http://dx.doi.org/10.1038/s41467-023-36591-0 |
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