Novel magnetic bimetallic AuCu catalyst for reduction of nitroarenes and degradation of organic dyes.
Autor: | Gholinejad M; Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), Gavazang, P. O. Box 45195-1159, Zanjan, 45137-66731, Iran. gholinejad@iasbs.ac.ir.; Research Center for Basic Sciences & Modern Technologies (RBST), Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan, 45137-66731, Iran. gholinejad@iasbs.ac.ir., Bashirimousavi S; Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), Gavazang, P. O. Box 45195-1159, Zanjan, 45137-66731, Iran., Sansano JM; Departamento de Química Orgánica, Instituto de Síntesis Orgánica, and Centro de Innovación en Química Avanzada (ORFEO-CINQA), Universidad de Alicante, 03690, Alicante, Spain. |
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Jazyk: | angličtina |
Zdroj: | Scientific reports [Sci Rep] 2024 Mar 11; Vol. 14 (1), pp. 5852. Date of Electronic Publication: 2024 Mar 11. |
DOI: | 10.1038/s41598-024-56559-4 |
Abstrakt: | Herein, core-shell magnetic nanoparticles are modified with imidazolium-tagged phosphine and propylene glycol moieties and used for the stabilization of bimetallic AuCu nanoparticles. The structure and morphology of the prepared material are identified with SEM, TEM, XRD, XPS, atomic absorption spectroscopy, Fourier translation infrared spectroscopy, and a vibrating sample magnetometer. This hydrophilic magnetic bimetallic catalyst is applied in the reduction of toxic nitroarenes and reductive degradation of hazardous organic dyes such as methyl orange (MO), methyl red (MR), and rhodamine B (RhB), as well as in the degradation of tetracycline (TC). This magnetic AuCu catalyst indicated superior activity in all three mentioned reactions in comparison with its single metal Au and Cu analogs. This catalyst is recycled for 17 consecutive runs in the reduction of 4-nitrophenol to 4-aminophenol without a significant decrease in catalytic activity and recycled catalyst is characterized. (© 2024. The Author(s).) |
Databáze: | MEDLINE |
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