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CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol
In this work, we studied the CO(2) absorption mechanism by nonaqueous solvent comprising hindered amine 2-[(1,1-dimethylethyl)amino]ethanol (TBAE) and ethylene glycol (EG). The NMR and FTIR results indicated that CO(2) reacted with an -OH group of EG rather than the -OH of TBAE by producing hydroxye...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729447/ https://www.ncbi.nlm.nih.gov/pubmed/33291408 http://dx.doi.org/10.3390/molecules25235743 |
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author | Li, Ran Wu, Congyi Yang, Dezhong |
author_facet | Li, Ran Wu, Congyi Yang, Dezhong |
author_sort | Li, Ran |
collection | PubMed |
description | In this work, we studied the CO(2) absorption mechanism by nonaqueous solvent comprising hindered amine 2-[(1,1-dimethylethyl)amino]ethanol (TBAE) and ethylene glycol (EG). The NMR and FTIR results indicated that CO(2) reacted with an -OH group of EG rather than the -OH of TBAE by producing hydroxyethyl carbonate species. A possible reaction pathway was suggested, which involves two steps. In the first step, the acid–base reaction between TBAE and EG generated the anion HO-CH(2)-CH(2)-O-; in the second step, the O(−) of HO-CH(2)-CH(2)-O(−) attacked the C atom of CO(2), forming carbonate species. |
format | Online Article Text |
id | pubmed-7729447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77294472020-12-12 CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol Li, Ran Wu, Congyi Yang, Dezhong Molecules Article In this work, we studied the CO(2) absorption mechanism by nonaqueous solvent comprising hindered amine 2-[(1,1-dimethylethyl)amino]ethanol (TBAE) and ethylene glycol (EG). The NMR and FTIR results indicated that CO(2) reacted with an -OH group of EG rather than the -OH of TBAE by producing hydroxyethyl carbonate species. A possible reaction pathway was suggested, which involves two steps. In the first step, the acid–base reaction between TBAE and EG generated the anion HO-CH(2)-CH(2)-O-; in the second step, the O(−) of HO-CH(2)-CH(2)-O(−) attacked the C atom of CO(2), forming carbonate species. MDPI 2020-12-05 /pmc/articles/PMC7729447/ /pubmed/33291408 http://dx.doi.org/10.3390/molecules25235743 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Ran Wu, Congyi Yang, Dezhong CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol |
title | CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol |
title_full | CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol |
title_fullStr | CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol |
title_full_unstemmed | CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol |
title_short | CO(2) Absorption Mechanism by the Nonaqueous Solvent Consisting of Hindered Amine 2-[(1,1-dimethylethyl)amino]ethanol and Ethylene Glycol |
title_sort | co(2) absorption mechanism by the nonaqueous solvent consisting of hindered amine 2-[(1,1-dimethylethyl)amino]ethanol and ethylene glycol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729447/ https://www.ncbi.nlm.nih.gov/pubmed/33291408 http://dx.doi.org/10.3390/molecules25235743 |
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