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The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium

The primary objective of this research is to investigate the reduction of 4‐nitroaniline (4‐NA) and 2‐nitroaniline (2‐NA) using synthesized copper ferrite nanoparticles (NPs) via facile one‐step hydrothermal method as a heterogeneous nano‐catalyst. Nitroanilines were reduced in the presence and with...

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Autores principales: Naghash‐Hamed, Samin, Arsalani, Nasser, Mousavi, Seyed Borhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633289/
https://www.ncbi.nlm.nih.gov/pubmed/36328769
http://dx.doi.org/10.1002/open.202200156
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author Naghash‐Hamed, Samin
Arsalani, Nasser
Mousavi, Seyed Borhan
author_facet Naghash‐Hamed, Samin
Arsalani, Nasser
Mousavi, Seyed Borhan
author_sort Naghash‐Hamed, Samin
collection PubMed
description The primary objective of this research is to investigate the reduction of 4‐nitroaniline (4‐NA) and 2‐nitroaniline (2‐NA) using synthesized copper ferrite nanoparticles (NPs) via facile one‐step hydrothermal method as a heterogeneous nano‐catalyst. Nitroanilines were reduced in the presence and without the catalyst with a constant amount (100 mg) of reducing agent of sodium borohydride (NaBH(4)) at room temperature in water to amino compounds. To characterize the functional groups, size, structure, and morphology of as‐prepared magnetic NPs, FTIR, XRD, SEM, and TEM were employed. The UV‐Vis spectrum was utilized to explore the catalytic effect of CuFe(2)O(4). The outcomes revealed that the synthesized CuFe(2)O(4) as a heterogeneous magnetic nano‐catalyst catalyzed the reduction of 4‐NA and 2‐NA significantly faster than other candidate catalysts. The outcomes demonstrated that the catalyst catalyzed 4‐nitroaniline to para‐phenylenediamine (p‐PDA) and 2‐nitroaniline to ortho‐phenylenediamine (o‐PDA) with a constant rate of 7.49×10(−2) s(−1) and 3.19×10(−2) s(−1), and conversion percentage of 96.5 and 95.6, in 40 s and 90 s, sequentially. Furthermore, the nanoparticles could be recovered by a magnetic separation method and reused for six consecutive cycles without remarkable loss of catalytic ability.
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spelling pubmed-96332892022-11-07 The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium Naghash‐Hamed, Samin Arsalani, Nasser Mousavi, Seyed Borhan ChemistryOpen Research Articles The primary objective of this research is to investigate the reduction of 4‐nitroaniline (4‐NA) and 2‐nitroaniline (2‐NA) using synthesized copper ferrite nanoparticles (NPs) via facile one‐step hydrothermal method as a heterogeneous nano‐catalyst. Nitroanilines were reduced in the presence and without the catalyst with a constant amount (100 mg) of reducing agent of sodium borohydride (NaBH(4)) at room temperature in water to amino compounds. To characterize the functional groups, size, structure, and morphology of as‐prepared magnetic NPs, FTIR, XRD, SEM, and TEM were employed. The UV‐Vis spectrum was utilized to explore the catalytic effect of CuFe(2)O(4). The outcomes revealed that the synthesized CuFe(2)O(4) as a heterogeneous magnetic nano‐catalyst catalyzed the reduction of 4‐NA and 2‐NA significantly faster than other candidate catalysts. The outcomes demonstrated that the catalyst catalyzed 4‐nitroaniline to para‐phenylenediamine (p‐PDA) and 2‐nitroaniline to ortho‐phenylenediamine (o‐PDA) with a constant rate of 7.49×10(−2) s(−1) and 3.19×10(−2) s(−1), and conversion percentage of 96.5 and 95.6, in 40 s and 90 s, sequentially. Furthermore, the nanoparticles could be recovered by a magnetic separation method and reused for six consecutive cycles without remarkable loss of catalytic ability. John Wiley and Sons Inc. 2022-11-03 /pmc/articles/PMC9633289/ /pubmed/36328769 http://dx.doi.org/10.1002/open.202200156 Text en © 2022 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Naghash‐Hamed, Samin
Arsalani, Nasser
Mousavi, Seyed Borhan
The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium
title The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium
title_full The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium
title_fullStr The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium
title_full_unstemmed The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium
title_short The Catalytic Reduction of Nitroanilines Using Synthesized CuFe(2)O(4) Nanoparticles in an Aqueous Medium
title_sort catalytic reduction of nitroanilines using synthesized cufe(2)o(4) nanoparticles in an aqueous medium
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633289/
https://www.ncbi.nlm.nih.gov/pubmed/36328769
http://dx.doi.org/10.1002/open.202200156
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