Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale

Detalhes bibliográficos
Autor(a) principal: Sardo, Mariana
Data de Publicação: 2021
Outros Autores: Afonso, Rui, Juźków, Joanna, Pacheco, Marlene, Bordonhos, Marta, Pinto, Moisés L., Gomes, José R. B., Mafra, Luís
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/31593
Resumo: This work entails a comprehensive solid-state NMR and computational study of the influence of water and CO2 partial pressures on the CO2-adducts formed in amine-grafted silica sorbents. Our approach provides atomic level insights on hypothesised mechanisms for CO2 capture under dry and wet conditions in a tightly controlled atmosphere. The method used for sample preparation avoids the use of liquid water slurries, as performed in previous studies, enabling a molecular level understanding, by NMR, of the influence of controlled amounts of water vapor (down to ca. 0.7 kPa) in CO2 chemisorption processes. Details on the formation mechanism of moisture-induced CO2 species are provided aiming to study CO2 :H2O binary mixtures in amine-grafted silica sorbents. The interconversion between distinct chemisorbed CO2 species was quantitatively monitored by NMR under wet and dry conditions in silica sorbents grafted with amines possessing distinct bulkiness (primary and tertiary). Particular attention was given to two distinct carbonyl environments resonating at dC ?161 and 155 ppm, as their presence and relative intensities are greatly affected by moisture depending on the experimental conditions. 1D and 2D NMR spectral assignments of both these 13C resonances were assisted by density functional theory calculations of 1H and 13C chemical shifts on model structures of alkylamines grafted onto the silica surface that validated various hydrogen-bonded CO2 species that may occur upon formation of bicarbonate, carbamic acid and alkylammonium carbamate ion pairs. Water is a key component in flue gas streams, playing a major role in CO2 speciation, and this work extends the current knowledge on chemisorbed CO2 structures and their stabilities under dry/wet conditions, on amine-modified solid surfaces.
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spelling Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scaleCO2 captureChemisorptionSolid-state NMRMesoporous materialsThis work entails a comprehensive solid-state NMR and computational study of the influence of water and CO2 partial pressures on the CO2-adducts formed in amine-grafted silica sorbents. Our approach provides atomic level insights on hypothesised mechanisms for CO2 capture under dry and wet conditions in a tightly controlled atmosphere. The method used for sample preparation avoids the use of liquid water slurries, as performed in previous studies, enabling a molecular level understanding, by NMR, of the influence of controlled amounts of water vapor (down to ca. 0.7 kPa) in CO2 chemisorption processes. Details on the formation mechanism of moisture-induced CO2 species are provided aiming to study CO2 :H2O binary mixtures in amine-grafted silica sorbents. The interconversion between distinct chemisorbed CO2 species was quantitatively monitored by NMR under wet and dry conditions in silica sorbents grafted with amines possessing distinct bulkiness (primary and tertiary). Particular attention was given to two distinct carbonyl environments resonating at dC ?161 and 155 ppm, as their presence and relative intensities are greatly affected by moisture depending on the experimental conditions. 1D and 2D NMR spectral assignments of both these 13C resonances were assisted by density functional theory calculations of 1H and 13C chemical shifts on model structures of alkylamines grafted onto the silica surface that validated various hydrogen-bonded CO2 species that may occur upon formation of bicarbonate, carbamic acid and alkylammonium carbamate ion pairs. Water is a key component in flue gas streams, playing a major role in CO2 speciation, and this work extends the current knowledge on chemisorbed CO2 structures and their stabilities under dry/wet conditions, on amine-modified solid surfaces.Royal Society of Chemistry2021-03-072021-03-07T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/31593eng2050-748810.1039/D0TA09808FSardo, MarianaAfonso, RuiJuźków, JoannaPacheco, MarleneBordonhos, MartaPinto, Moisés L.Gomes, José R. B.Mafra, Luísinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:00:51Zoai:ria.ua.pt:10773/31593Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:03:23.149077Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
title Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
spellingShingle Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
Sardo, Mariana
CO2 capture
Chemisorption
Solid-state NMR
Mesoporous materials
title_short Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
title_full Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
title_fullStr Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
title_full_unstemmed Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
title_sort Unravelling moisture-induced CO2 chemisorption mechanisms in amine-modified sorbents at the molecular scale
author Sardo, Mariana
author_facet Sardo, Mariana
Afonso, Rui
Juźków, Joanna
Pacheco, Marlene
Bordonhos, Marta
Pinto, Moisés L.
Gomes, José R. B.
Mafra, Luís
author_role author
author2 Afonso, Rui
Juźków, Joanna
Pacheco, Marlene
Bordonhos, Marta
Pinto, Moisés L.
Gomes, José R. B.
Mafra, Luís
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sardo, Mariana
Afonso, Rui
Juźków, Joanna
Pacheco, Marlene
Bordonhos, Marta
Pinto, Moisés L.
Gomes, José R. B.
Mafra, Luís
dc.subject.por.fl_str_mv CO2 capture
Chemisorption
Solid-state NMR
Mesoporous materials
topic CO2 capture
Chemisorption
Solid-state NMR
Mesoporous materials
description This work entails a comprehensive solid-state NMR and computational study of the influence of water and CO2 partial pressures on the CO2-adducts formed in amine-grafted silica sorbents. Our approach provides atomic level insights on hypothesised mechanisms for CO2 capture under dry and wet conditions in a tightly controlled atmosphere. The method used for sample preparation avoids the use of liquid water slurries, as performed in previous studies, enabling a molecular level understanding, by NMR, of the influence of controlled amounts of water vapor (down to ca. 0.7 kPa) in CO2 chemisorption processes. Details on the formation mechanism of moisture-induced CO2 species are provided aiming to study CO2 :H2O binary mixtures in amine-grafted silica sorbents. The interconversion between distinct chemisorbed CO2 species was quantitatively monitored by NMR under wet and dry conditions in silica sorbents grafted with amines possessing distinct bulkiness (primary and tertiary). Particular attention was given to two distinct carbonyl environments resonating at dC ?161 and 155 ppm, as their presence and relative intensities are greatly affected by moisture depending on the experimental conditions. 1D and 2D NMR spectral assignments of both these 13C resonances were assisted by density functional theory calculations of 1H and 13C chemical shifts on model structures of alkylamines grafted onto the silica surface that validated various hydrogen-bonded CO2 species that may occur upon formation of bicarbonate, carbamic acid and alkylammonium carbamate ion pairs. Water is a key component in flue gas streams, playing a major role in CO2 speciation, and this work extends the current knowledge on chemisorbed CO2 structures and their stabilities under dry/wet conditions, on amine-modified solid surfaces.
publishDate 2021
dc.date.none.fl_str_mv 2021-03-07
2021-03-07T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/31593
url http://hdl.handle.net/10773/31593
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2050-7488
10.1039/D0TA09808F
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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