Mixed-valence molybdenum oxide as a recyclable sorbent for silver removal and recovery from wastewater
Penghui Shao,
Ziwen Chang,
Min Li (),
Xiang Lu,
Wenli Jiang,
Kai Zhang,
Xubiao Luo and
Liming Yang ()
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Penghui Shao: Nanchang Hangkong University
Ziwen Chang: Nanchang Hangkong University
Min Li: Chongqing University of Science and Technology
Xiang Lu: Nanchang Hangkong University
Wenli Jiang: Chinese Academy of Sciences
Kai Zhang: Nanchang Hangkong University
Xubiao Luo: Nanchang Hangkong University
Liming Yang: Nanchang Hangkong University
Nature Communications, 2023, vol. 14, issue 1, 1-10
Abstract:
Abstract Silver ions in wastewater streams are a major pollutant and a threat to human health. Given the increasing demand and relative scarcity of silver, these streams could be a lucrative source to extract metallic silver. Wastewater is a complex mixture of many different metal salts, and developing recyclable sorbents with high specificity towards silver ions remains a major challenge. Here we report that molybdenum oxide (MoOx) adsorbent with mixed-valence (Mo(V) and Mo(VI)) demonstrates high selectivity (distribution coefficient of 6437.40 mL g−1) for Ag+ and an uptake capacity of 2605.91 mg g−1. Our experimental results and density functional theory calculations illustrate the mechanism behind Ag+ adsorption and reduction. Our results show that Mo(V) species reduce Ag+ to metallic Ag, which decreases the energy barrier for subsequent Ag+ reductions, accounting for the high uptake of Ag+ from wastewater. Due to its high selectivity, MoOx favorably adsorbs Ag+ even in the presence of interfering ions. High selective recovery of Ag+ from wastewater (recovery efficiency = 97.9%) further supports the practical applications of the sorbent. Finally, MoOx can be recycled following silver recovery while maintaining a recovery efficiency of 97.1% after five cycles. The method is expected to provide a viable strategy to recover silver from wastewater.
Date: 2023
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37143-2
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DOI: 10.1038/s41467-023-37143-2
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