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In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol

The missing-linker defects of UiO-66 were exploited to covalently anchor Cu nanoclusters (Cu/UiO-66). The molecular interactions between the metals and oxides as copper-zirconia interfaces in Cu/UiO-66 are essential for heterogeneous catalysis, leading to remarkable synergistic impacts on activity a...

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Autor principal: Farrag, Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287755/
https://www.ncbi.nlm.nih.gov/pubmed/37349346
http://dx.doi.org/10.1038/s41598-023-36627-x
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author Farrag, Mostafa
author_facet Farrag, Mostafa
author_sort Farrag, Mostafa
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description The missing-linker defects of UiO-66 were exploited to covalently anchor Cu nanoclusters (Cu/UiO-66). The molecular interactions between the metals and oxides as copper-zirconia interfaces in Cu/UiO-66 are essential for heterogeneous catalysis, leading to remarkable synergistic impacts on activity and selectivity. Homogeneously distributed carbonaceous mixed metal oxides (CuO/ZrO(2)@C) nanocomposite was prepared via carbonization of the Cu/UiO-66 at 600 °C for 3 h in air. To enhance the acidity properties of the CuO/ZrO(2)@C nanocomposite, a small amount of sulfuric acid was added and heated at 150 °C under an N(2) atmosphere (CuO/ZrO(2)-SO(3)H@C). The synthesised Cu/UiO-66 and CuO/ZrO(2)-SO(3)H@C catalysts were used as novel catalysts in the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). The Cu/UiO-66 and CuO/ZrO(2)-SO(3)H@C catalysts displayed complete conversion of the 4-NP solution during (4 and 2 min) stirring at room temperature, respectively. These two catalysts exhibited a high reduction rate of 8.61 × 10(–3) s(−1), and 18.3 × 10(–3) s(−1), respectively. The X-ray photoelectron spectroscopic (XPS) analysis showed the charge of copper atoms in the Cu/UiO-66 catalyst was Cu(0)/Cu(II) and in the CuO/ZrO(2)-SO(3)H@C catalyst was Cu(I)/Cu(II) with nearly the same ratio (65/35). The particle size and the elemental composition of the CuO/ZrO(2)-SO(3)H@C catalyst were analysed by using high resolution transmission electron microscopy (HR-TEM), and energy-dispersive X-ray spectroscopy (EDS), and elemental mapping, respectively. The key point beyond the high catalytic activity and selectivity of the CuO/ZrO(2)-SO(3)H@C catalyst is both the carbon–metal oxides heterojunction structure that leads to good dispersion of the CuO and ZrO(2) over the carbon sheets, and the high acidity properties that come from the combination between the Brønsted acid sites from sulfuric acid and Lewis acid sites from the UiO-66. The catalysts exhibited good recyclability efficiency without significant loss in activity, indicating their good potential for industrial applications.
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spelling pubmed-102877552023-06-24 In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol Farrag, Mostafa Sci Rep Article The missing-linker defects of UiO-66 were exploited to covalently anchor Cu nanoclusters (Cu/UiO-66). The molecular interactions between the metals and oxides as copper-zirconia interfaces in Cu/UiO-66 are essential for heterogeneous catalysis, leading to remarkable synergistic impacts on activity and selectivity. Homogeneously distributed carbonaceous mixed metal oxides (CuO/ZrO(2)@C) nanocomposite was prepared via carbonization of the Cu/UiO-66 at 600 °C for 3 h in air. To enhance the acidity properties of the CuO/ZrO(2)@C nanocomposite, a small amount of sulfuric acid was added and heated at 150 °C under an N(2) atmosphere (CuO/ZrO(2)-SO(3)H@C). The synthesised Cu/UiO-66 and CuO/ZrO(2)-SO(3)H@C catalysts were used as novel catalysts in the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). The Cu/UiO-66 and CuO/ZrO(2)-SO(3)H@C catalysts displayed complete conversion of the 4-NP solution during (4 and 2 min) stirring at room temperature, respectively. These two catalysts exhibited a high reduction rate of 8.61 × 10(–3) s(−1), and 18.3 × 10(–3) s(−1), respectively. The X-ray photoelectron spectroscopic (XPS) analysis showed the charge of copper atoms in the Cu/UiO-66 catalyst was Cu(0)/Cu(II) and in the CuO/ZrO(2)-SO(3)H@C catalyst was Cu(I)/Cu(II) with nearly the same ratio (65/35). The particle size and the elemental composition of the CuO/ZrO(2)-SO(3)H@C catalyst were analysed by using high resolution transmission electron microscopy (HR-TEM), and energy-dispersive X-ray spectroscopy (EDS), and elemental mapping, respectively. The key point beyond the high catalytic activity and selectivity of the CuO/ZrO(2)-SO(3)H@C catalyst is both the carbon–metal oxides heterojunction structure that leads to good dispersion of the CuO and ZrO(2) over the carbon sheets, and the high acidity properties that come from the combination between the Brønsted acid sites from sulfuric acid and Lewis acid sites from the UiO-66. The catalysts exhibited good recyclability efficiency without significant loss in activity, indicating their good potential for industrial applications. Nature Publishing Group UK 2023-06-22 /pmc/articles/PMC10287755/ /pubmed/37349346 http://dx.doi.org/10.1038/s41598-023-36627-x 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Farrag, Mostafa
In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol
title In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol
title_full In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol
title_fullStr In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol
title_full_unstemmed In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol
title_short In-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol
title_sort in-situ preparation of sulfonated carbonaceous copper oxide-zirconia nanocomposite as a novel and recyclable solid acid catalyst for reduction of 4-nitrophenol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287755/
https://www.ncbi.nlm.nih.gov/pubmed/37349346
http://dx.doi.org/10.1038/s41598-023-36627-x
work_keys_str_mv AT farragmostafa insitupreparationofsulfonatedcarbonaceouscopperoxidezirconiananocompositeasanovelandrecyclablesolidacidcatalystforreductionof4nitrophenol