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Robust Hydrogen-Bonded Organic Framework with Four-Fold Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr
[Image: see text] Hydrogen-bonded organic frameworks (HOFs) are an emerging class of porous materials that hold promise for the adsorptive separation of industrially relevant gas mixtures. However, developing HOFs with high thermal stability and resistance to water remains a daunting challenge. We r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
University of Science and Technology of China and American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685716/ https://www.ncbi.nlm.nih.gov/pubmed/38037594 http://dx.doi.org/10.1021/prechem.3c00040 |
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author | Guo, Fu-An Zhou, Kang Liu, Jiaqi Wang, Hao Li, Jing |
author_facet | Guo, Fu-An Zhou, Kang Liu, Jiaqi Wang, Hao Li, Jing |
author_sort | Guo, Fu-An |
collection | PubMed |
description | [Image: see text] Hydrogen-bonded organic frameworks (HOFs) are an emerging class of porous materials that hold promise for the adsorptive separation of industrially relevant gas mixtures. However, developing HOFs with high thermal stability and resistance to water remains a daunting challenge. We report here a microporous HOF (HIAM-103) assembled from a hexacarboxylate linker (2,4,6-trimethylbenzene-1,3,5-triylisophthalic acid, H(6)TMBTI). The compound crystallizes in the trigonal crystal system, and its structure is a four-fold interpenetrated network. Upon thermal activation, the single crystals remain intact, allowing for precise determination of the activated structure. HIAM-103 exhibits remarkable thermal and hydrothermal stability. Its microporous channels demonstrate selective adsorption of C(2)H(6) over C(2)H(4) and Xe over Kr, and its separation capability toward mixed gases has been validated by column breakthrough experiments under dry and humid conditions. The preferential gas adsorption sites and separation mechanisms have been uncovered through DFT analysis, which suggests that the methyl group decorated 1D channels are the primary reason for the selective adsorption. |
format | Online Article Text |
id | pubmed-10685716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | University of Science and Technology of China and American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106857162023-11-30 Robust Hydrogen-Bonded Organic Framework with Four-Fold Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr Guo, Fu-An Zhou, Kang Liu, Jiaqi Wang, Hao Li, Jing Precis Chem [Image: see text] Hydrogen-bonded organic frameworks (HOFs) are an emerging class of porous materials that hold promise for the adsorptive separation of industrially relevant gas mixtures. However, developing HOFs with high thermal stability and resistance to water remains a daunting challenge. We report here a microporous HOF (HIAM-103) assembled from a hexacarboxylate linker (2,4,6-trimethylbenzene-1,3,5-triylisophthalic acid, H(6)TMBTI). The compound crystallizes in the trigonal crystal system, and its structure is a four-fold interpenetrated network. Upon thermal activation, the single crystals remain intact, allowing for precise determination of the activated structure. HIAM-103 exhibits remarkable thermal and hydrothermal stability. Its microporous channels demonstrate selective adsorption of C(2)H(6) over C(2)H(4) and Xe over Kr, and its separation capability toward mixed gases has been validated by column breakthrough experiments under dry and humid conditions. The preferential gas adsorption sites and separation mechanisms have been uncovered through DFT analysis, which suggests that the methyl group decorated 1D channels are the primary reason for the selective adsorption. University of Science and Technology of China and American Chemical Society 2023-06-29 /pmc/articles/PMC10685716/ /pubmed/38037594 http://dx.doi.org/10.1021/prechem.3c00040 Text en © 2023 The Authors. Co-published by University of Science and Technology of China and American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Guo, Fu-An Zhou, Kang Liu, Jiaqi Wang, Hao Li, Jing Robust Hydrogen-Bonded Organic Framework with Four-Fold Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr |
title | Robust Hydrogen-Bonded
Organic Framework with Four-Fold
Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr |
title_full | Robust Hydrogen-Bonded
Organic Framework with Four-Fold
Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr |
title_fullStr | Robust Hydrogen-Bonded
Organic Framework with Four-Fold
Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr |
title_full_unstemmed | Robust Hydrogen-Bonded
Organic Framework with Four-Fold
Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr |
title_short | Robust Hydrogen-Bonded
Organic Framework with Four-Fold
Interpenetration for Adsorptive Separation of C(2)H(6)/C(2)H(4) and Xe/Kr |
title_sort | robust hydrogen-bonded
organic framework with four-fold
interpenetration for adsorptive separation of c(2)h(6)/c(2)h(4) and xe/kr |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685716/ https://www.ncbi.nlm.nih.gov/pubmed/38037594 http://dx.doi.org/10.1021/prechem.3c00040 |
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