Highly Selective Recovery of Gold by In Situ Magnetic Field‐Assisted Fe/Co‐MOF@PDA/NdFeB Double Network Gel
There are enormous economic benefits to conveniently increasing the selective recovery capacity of gold. Fe/Co‐MOF@PDA/NdFeB double‐network organogel (Fe/Co‐MOF@PDA NH) is synthesized by aggregation assembly strategy. The package of PDA provides a large number of nitrogen‐containing functional group...
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Veröffentlicht in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-11, Vol.20 (48), p.e2404241-n/a |
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Sprache: | eng |
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Zusammenfassung: | There are enormous economic benefits to conveniently increasing the selective recovery capacity of gold. Fe/Co‐MOF@PDA/NdFeB double‐network organogel (Fe/Co‐MOF@PDA NH) is synthesized by aggregation assembly strategy. The package of PDA provides a large number of nitrogen‐containing functional groups that can serve as adsorption sites for gold ions, resulting in a 21.8% increase in the ability of the material to recover gold. Fe/Co‐MOF@PDA NH possesses high gold recovery capacity (1478.87 mg g−1) and excellent gold selectivity (Kd = 5.71 mL g−1). With the assistance of an in situ magnetic field, the gold recovery capacity of Fe/Co‐MOF@PDA NH is increased from 1217.93 to 1478.87 mg g−1, and the recovery rate increased by 24.7%. The above excellent performance is attributed to the efficient reduction of gold by FDC/FC+, Co2+/Co3+ double reducing couple, and the optimization of the reduction reaction by the magnetic field. After the samples are calcined, high‐purity gold (95.6%, 22K gold) is recovered by magnetic separation. This study proposes a forward‐looking in situ energy field‐assisted strategy to enhance precious metal recovery, which has a guiding role in the development of low‐carbon industries.
With the assistance of an in situ magnetic field, the gold recovery capacity of Fe/Co‐MOF@PDA NH is increased from 1217.93 to 1478.87 mg g−1, and the recovery rate increased by 24.7%. This study proposes a forward‐looking in situ energy field‐assisted strategy to enhance precious metal recovery. |
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ISSN: | 1613-6810 1613-6829 1613-6829 |
DOI: | 10.1002/smll.202404241 |