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Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework
A greener route to synthesize mesoporous copper–gallic acid metal–organic framework (CuGA MOF) than the conventional method using harmful DMF solvent was proposed in this study. Various synthesis attempts were conducted by modifying the synthesis conditions to produce CuGA MOF with comparable physic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645746/ https://www.ncbi.nlm.nih.gov/pubmed/33154425 http://dx.doi.org/10.1038/s41598-020-75927-4 |
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author | Azhar, Badril Angkawijaya, Artik Elisa Santoso, Shella Permatasari Gunarto, Chintya Ayucitra, Aning Go, Alchris Woo Tran-Nguyen, Phuong Lan Ismadji, Suryadi Ju, Yi-Hsu |
author_facet | Azhar, Badril Angkawijaya, Artik Elisa Santoso, Shella Permatasari Gunarto, Chintya Ayucitra, Aning Go, Alchris Woo Tran-Nguyen, Phuong Lan Ismadji, Suryadi Ju, Yi-Hsu |
author_sort | Azhar, Badril |
collection | PubMed |
description | A greener route to synthesize mesoporous copper–gallic acid metal–organic framework (CuGA MOF) than the conventional method using harmful DMF solvent was proposed in this study. Various synthesis attempts were conducted by modifying the synthesis conditions to produce CuGA MOF with comparable physical properties to a reference material (DMF-synthesized CuGA NMOF). The independent variables investigated include the molar ratio of NaOH to GA (1.1 to 4.4) and the synthesis temperature (30, 60, 90 °C). It was found that proper NaOH addition was crucial for suppressing the generation of copper oxide while maximizing the formation of CuGA MOF. On the other hand, the reaction temperature mainly affected the stability and adsorption potential of CuGA MOF. Reacting Cu, GA, and NaOH at a molar ratio of 1:1:2.2 and a temperature of 90 °C, produced mesoporous MOF (CuGA 90–2.2) with a surface area of 198.22 m(2)/g, a pore diameter of 8.6 nm, and a thermal stability of 219 °C. This MOF exhibited an excellent adsorption capacity for the removal of methylene blue (124.64 mg/g) and congo red (344.54 mg/g). The potential usage of CuGA 90–2.2 as a reusable adsorbent was demonstrated by its high adsorption efficiency (> 90%) after 5 adsorption–desorption cycles. |
format | Online Article Text |
id | pubmed-7645746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76457462020-11-06 Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework Azhar, Badril Angkawijaya, Artik Elisa Santoso, Shella Permatasari Gunarto, Chintya Ayucitra, Aning Go, Alchris Woo Tran-Nguyen, Phuong Lan Ismadji, Suryadi Ju, Yi-Hsu Sci Rep Article A greener route to synthesize mesoporous copper–gallic acid metal–organic framework (CuGA MOF) than the conventional method using harmful DMF solvent was proposed in this study. Various synthesis attempts were conducted by modifying the synthesis conditions to produce CuGA MOF with comparable physical properties to a reference material (DMF-synthesized CuGA NMOF). The independent variables investigated include the molar ratio of NaOH to GA (1.1 to 4.4) and the synthesis temperature (30, 60, 90 °C). It was found that proper NaOH addition was crucial for suppressing the generation of copper oxide while maximizing the formation of CuGA MOF. On the other hand, the reaction temperature mainly affected the stability and adsorption potential of CuGA MOF. Reacting Cu, GA, and NaOH at a molar ratio of 1:1:2.2 and a temperature of 90 °C, produced mesoporous MOF (CuGA 90–2.2) with a surface area of 198.22 m(2)/g, a pore diameter of 8.6 nm, and a thermal stability of 219 °C. This MOF exhibited an excellent adsorption capacity for the removal of methylene blue (124.64 mg/g) and congo red (344.54 mg/g). The potential usage of CuGA 90–2.2 as a reusable adsorbent was demonstrated by its high adsorption efficiency (> 90%) after 5 adsorption–desorption cycles. Nature Publishing Group UK 2020-11-05 /pmc/articles/PMC7645746/ /pubmed/33154425 http://dx.doi.org/10.1038/s41598-020-75927-4 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Azhar, Badril Angkawijaya, Artik Elisa Santoso, Shella Permatasari Gunarto, Chintya Ayucitra, Aning Go, Alchris Woo Tran-Nguyen, Phuong Lan Ismadji, Suryadi Ju, Yi-Hsu Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework |
title | Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework |
title_full | Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework |
title_fullStr | Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework |
title_full_unstemmed | Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework |
title_short | Aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework |
title_sort | aqueous synthesis of highly adsorptive copper–gallic acid metal–organic framework |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645746/ https://www.ncbi.nlm.nih.gov/pubmed/33154425 http://dx.doi.org/10.1038/s41598-020-75927-4 |
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