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Highly Efficient and Reusable Denitrogenation Adsorbent Obtained by the Fluorination of PMA-MIL-101
[Image: see text] A simple but efficient strategy to improve the ability of adsorptive denitrogenation (ADN) of MIL-101(M101) was studied by the in situ encapsulation of phosphomolybdic acid (PMA) and the subsequent purification of the as-synthesized product by the NH(4)F solution. After the NH(4)F...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468879/ https://www.ncbi.nlm.nih.gov/pubmed/37663508 http://dx.doi.org/10.1021/acsomega.3c04670 |
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author | Zhao, Zhe Yang, Qing-He Li, Hui-Feng Zong, Meng-Ya Wang, Dan-Hong |
author_facet | Zhao, Zhe Yang, Qing-He Li, Hui-Feng Zong, Meng-Ya Wang, Dan-Hong |
author_sort | Zhao, Zhe |
collection | PubMed |
description | [Image: see text] A simple but efficient strategy to improve the ability of adsorptive denitrogenation (ADN) of MIL-101(M101) was studied by the in situ encapsulation of phosphomolybdic acid (PMA) and the subsequent purification of the as-synthesized product by the NH(4)F solution. After the NH(4)F treatment, the vast majority of PMA was removed, loss of organic ligand (BDC) was observed, and the fluorination of the hydroxyl group in the M101 structure occurred. The ADN activities of the Cr-MOF matrix composites before and after fluorination were studied in detail. The rest of PMA interacts strongly with M101 and assists the ADN activity. Coordination unsaturated metal sites (CUS) in M101 are formed after fluorination and also contribute to ADN activity. Further, fluoride anions replace most of the hydroxide groups in M101, which can promote the ADN of quinoline (QUI) and indole (IND) through an acid–base interaction and N-atom coordination with the CUS in M101. P-M101-F 5% exhibits the highest adsorptive capacity and excellent regeneration ability. Special emphasis in this work is placed on structure modulation (including PMA doping, CUS creation, and fluorination) of M101 for enhancing ADN activity, which provides a useful scaffold for future research in the rational design of MOF-based ADN catalysts. |
format | Online Article Text |
id | pubmed-10468879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104688792023-09-01 Highly Efficient and Reusable Denitrogenation Adsorbent Obtained by the Fluorination of PMA-MIL-101 Zhao, Zhe Yang, Qing-He Li, Hui-Feng Zong, Meng-Ya Wang, Dan-Hong ACS Omega [Image: see text] A simple but efficient strategy to improve the ability of adsorptive denitrogenation (ADN) of MIL-101(M101) was studied by the in situ encapsulation of phosphomolybdic acid (PMA) and the subsequent purification of the as-synthesized product by the NH(4)F solution. After the NH(4)F treatment, the vast majority of PMA was removed, loss of organic ligand (BDC) was observed, and the fluorination of the hydroxyl group in the M101 structure occurred. The ADN activities of the Cr-MOF matrix composites before and after fluorination were studied in detail. The rest of PMA interacts strongly with M101 and assists the ADN activity. Coordination unsaturated metal sites (CUS) in M101 are formed after fluorination and also contribute to ADN activity. Further, fluoride anions replace most of the hydroxide groups in M101, which can promote the ADN of quinoline (QUI) and indole (IND) through an acid–base interaction and N-atom coordination with the CUS in M101. P-M101-F 5% exhibits the highest adsorptive capacity and excellent regeneration ability. Special emphasis in this work is placed on structure modulation (including PMA doping, CUS creation, and fluorination) of M101 for enhancing ADN activity, which provides a useful scaffold for future research in the rational design of MOF-based ADN catalysts. American Chemical Society 2023-08-19 /pmc/articles/PMC10468879/ /pubmed/37663508 http://dx.doi.org/10.1021/acsomega.3c04670 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Zhao, Zhe Yang, Qing-He Li, Hui-Feng Zong, Meng-Ya Wang, Dan-Hong Highly Efficient and Reusable Denitrogenation Adsorbent Obtained by the Fluorination of PMA-MIL-101 |
title | Highly Efficient
and Reusable Denitrogenation Adsorbent
Obtained by the Fluorination of PMA-MIL-101 |
title_full | Highly Efficient
and Reusable Denitrogenation Adsorbent
Obtained by the Fluorination of PMA-MIL-101 |
title_fullStr | Highly Efficient
and Reusable Denitrogenation Adsorbent
Obtained by the Fluorination of PMA-MIL-101 |
title_full_unstemmed | Highly Efficient
and Reusable Denitrogenation Adsorbent
Obtained by the Fluorination of PMA-MIL-101 |
title_short | Highly Efficient
and Reusable Denitrogenation Adsorbent
Obtained by the Fluorination of PMA-MIL-101 |
title_sort | highly efficient
and reusable denitrogenation adsorbent
obtained by the fluorination of pma-mil-101 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468879/ https://www.ncbi.nlm.nih.gov/pubmed/37663508 http://dx.doi.org/10.1021/acsomega.3c04670 |
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