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In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose Microspheres as Recyclable and Biodegradable Catalysts
[Image: see text] The preparation of reusable and eco-friendly materials from renewable biomass resources such as cellulose is an inevitable choice for sustainable development. In this work, cellulose was dissolved in 7 wt % NaOH/12 wt % urea aqueous solution at −12 °C with rapid stirring. Cellulose...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178767/ https://www.ncbi.nlm.nih.gov/pubmed/32337446 http://dx.doi.org/10.1021/acsomega.0c00437 |
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author | Wang, Guozhen Li, Fei Li, Lan Zhao, Jiayu Ruan, Xinxuan Ding, Wenping Cai, Jie Lu, Ang Pei, Ying |
author_facet | Wang, Guozhen Li, Fei Li, Lan Zhao, Jiayu Ruan, Xinxuan Ding, Wenping Cai, Jie Lu, Ang Pei, Ying |
author_sort | Wang, Guozhen |
collection | PubMed |
description | [Image: see text] The preparation of reusable and eco-friendly materials from renewable biomass resources such as cellulose is an inevitable choice for sustainable development. In this work, cellulose was dissolved in 7 wt % NaOH/12 wt % urea aqueous solution at −12 °C with rapid stirring. Cellulose microspheres (Cels) were fabricated by a sol–gel transition method. Subsequently, novel magnetic Ag–Fe(3)O(4) nanoparticles (NPs) supported on cellulose microspheres were successfully constructed by an in situ one-pot synthesis. The magnetic cellulose microspheres (MCels) displayed a spherical shape with mesoporous structure and had a narrow particle size distribution (10–20 μm). Many nanopores with a pore diameter of 5–40 nm were observed in MCels. The Ag–Fe(3)O(4) NPs were immobilized by anchoring with the hydroxyl groups on the surface of Cels. MCels were applied as a microreactor to evaluate their catalytic activities. 4-Nitrophenol (4-NP) could be reduced to 4-aminophenol (4-AP) in 5 min, catalyzed by MCels. Moreover, the magnetic microspheres exhibited a small hysteresis loop and low coercivity. Thus, MCels could be quickly gathered in water under a magnetic field in 10 s, as well as almost 9 cycle times, maintaining relatively high catalytic activity. In this work, cellulose matrix as the catalyst support could be biodegraded completely in the environment. It provided a green process for the utilization of biomass in nanocatalytic applications. |
format | Online Article Text |
id | pubmed-7178767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71787672020-04-24 In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose Microspheres as Recyclable and Biodegradable Catalysts Wang, Guozhen Li, Fei Li, Lan Zhao, Jiayu Ruan, Xinxuan Ding, Wenping Cai, Jie Lu, Ang Pei, Ying ACS Omega [Image: see text] The preparation of reusable and eco-friendly materials from renewable biomass resources such as cellulose is an inevitable choice for sustainable development. In this work, cellulose was dissolved in 7 wt % NaOH/12 wt % urea aqueous solution at −12 °C with rapid stirring. Cellulose microspheres (Cels) were fabricated by a sol–gel transition method. Subsequently, novel magnetic Ag–Fe(3)O(4) nanoparticles (NPs) supported on cellulose microspheres were successfully constructed by an in situ one-pot synthesis. The magnetic cellulose microspheres (MCels) displayed a spherical shape with mesoporous structure and had a narrow particle size distribution (10–20 μm). Many nanopores with a pore diameter of 5–40 nm were observed in MCels. The Ag–Fe(3)O(4) NPs were immobilized by anchoring with the hydroxyl groups on the surface of Cels. MCels were applied as a microreactor to evaluate their catalytic activities. 4-Nitrophenol (4-NP) could be reduced to 4-aminophenol (4-AP) in 5 min, catalyzed by MCels. Moreover, the magnetic microspheres exhibited a small hysteresis loop and low coercivity. Thus, MCels could be quickly gathered in water under a magnetic field in 10 s, as well as almost 9 cycle times, maintaining relatively high catalytic activity. In this work, cellulose matrix as the catalyst support could be biodegraded completely in the environment. It provided a green process for the utilization of biomass in nanocatalytic applications. American Chemical Society 2020-04-10 /pmc/articles/PMC7178767/ /pubmed/32337446 http://dx.doi.org/10.1021/acsomega.0c00437 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wang, Guozhen Li, Fei Li, Lan Zhao, Jiayu Ruan, Xinxuan Ding, Wenping Cai, Jie Lu, Ang Pei, Ying In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose Microspheres as Recyclable and Biodegradable Catalysts |
title | In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose
Microspheres as Recyclable and Biodegradable Catalysts |
title_full | In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose
Microspheres as Recyclable and Biodegradable Catalysts |
title_fullStr | In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose
Microspheres as Recyclable and Biodegradable Catalysts |
title_full_unstemmed | In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose
Microspheres as Recyclable and Biodegradable Catalysts |
title_short | In Situ Synthesis of Ag–Fe(3)O(4) Nanoparticles Immobilized on Pure Cellulose
Microspheres as Recyclable and Biodegradable Catalysts |
title_sort | in situ synthesis of ag–fe(3)o(4) nanoparticles immobilized on pure cellulose
microspheres as recyclable and biodegradable catalysts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178767/ https://www.ncbi.nlm.nih.gov/pubmed/32337446 http://dx.doi.org/10.1021/acsomega.0c00437 |
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