Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study

Detalhes bibliográficos
Autor(a) principal: Besnard, M.
Data de Publicação: 2013
Outros Autores: Cabao, M. I., Coutinho, J. A. P., Danten, Y.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/19620
Resumo: The dense phase of CO2-CS2 mixtures has been analysed by Raman spectroscopy as a function of the CO2 concentration (0.02-0.95 mole fractions) by varying the pressure (0.5 MPa up to 7.7 MPa) at constant temperature (313 K). The polarised and depolarised spectra of the induced (nu(2), nu(3)) modes of CS2 and of the nu(1)-2 nu(2) Fermi resonance dyad of both CO2 and CS2 have been measured. Upon dilution with CO2, the evolution of the spectroscopic observables of all these modes displays a \"plateau-like\" region in the CO2 mole fraction 0.3-0.7 never previously observed in CO2-organic liquids mixtures. The bandshape and intensity of the induced modes of CS2 are similar to those of pure CS2 up to equimolar concentration, after which variations occur. The preservation of the local ordering from pure CS2 to equimolar concentration together with the non-linear evolution of the spectroscopic observables allows inferring that two solvation regimes exist with a transition occurring in the plateau domain. In the first regime, corresponding to CS2 concentrated mixtures, the liquid phase is segregated with dominant CS2 clusters, whereas, in the second one, CO2 monomers and dimers and CO2-CS2 hetero-dimers coexist dynamically on a picosecond time-scale. It is demonstrated that the subtle interplay between attractive and repulsive interactions which provides a molecular interpretation of the non-ideality of the CO2-CS2 mixture allows rationalizing the volume expansion and the existence of the plateau-like region observed in the pressure-composition diagram previously ascribed to the proximity of an upper critical solution temperature at lower temperatures. (C) 2013 AIP Publishing LLC.
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spelling Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering studyINTERACTION-INDUCED SPECTRALIQUID CARBON-DISULFIDEDOT-O INTERACTIONSIONIC LIQUIDSVIBRATIONAL-SPECTRAFERMI RESONANCEBINARY-MIXTURESAB-INITIOHARD SPHEROCYLINDERSCOMPUTER-SIMULATIONThe dense phase of CO2-CS2 mixtures has been analysed by Raman spectroscopy as a function of the CO2 concentration (0.02-0.95 mole fractions) by varying the pressure (0.5 MPa up to 7.7 MPa) at constant temperature (313 K). The polarised and depolarised spectra of the induced (nu(2), nu(3)) modes of CS2 and of the nu(1)-2 nu(2) Fermi resonance dyad of both CO2 and CS2 have been measured. Upon dilution with CO2, the evolution of the spectroscopic observables of all these modes displays a \"plateau-like\" region in the CO2 mole fraction 0.3-0.7 never previously observed in CO2-organic liquids mixtures. The bandshape and intensity of the induced modes of CS2 are similar to those of pure CS2 up to equimolar concentration, after which variations occur. The preservation of the local ordering from pure CS2 to equimolar concentration together with the non-linear evolution of the spectroscopic observables allows inferring that two solvation regimes exist with a transition occurring in the plateau domain. In the first regime, corresponding to CS2 concentrated mixtures, the liquid phase is segregated with dominant CS2 clusters, whereas, in the second one, CO2 monomers and dimers and CO2-CS2 hetero-dimers coexist dynamically on a picosecond time-scale. It is demonstrated that the subtle interplay between attractive and repulsive interactions which provides a molecular interpretation of the non-ideality of the CO2-CS2 mixture allows rationalizing the volume expansion and the existence of the plateau-like region observed in the pressure-composition diagram previously ascribed to the proximity of an upper critical solution temperature at lower temperatures. (C) 2013 AIP Publishing LLC.AMER INST PHYSICS2017-12-07T19:19:01Z2013-01-01T00:00:00Z2013info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/19620eng0021-960610.1063/1.4821593Besnard, M.Cabao, M. I.Coutinho, J. A. P.Danten, Y.info: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:RCAAP2024-02-22T11:38:11Zoai:ria.ua.pt:10773/19620Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:54:22.900396Repositório 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 Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
title Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
spellingShingle Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
Besnard, M.
INTERACTION-INDUCED SPECTRA
LIQUID CARBON-DISULFIDE
DOT-O INTERACTIONS
IONIC LIQUIDS
VIBRATIONAL-SPECTRA
FERMI RESONANCE
BINARY-MIXTURES
AB-INITIO
HARD SPHEROCYLINDERS
COMPUTER-SIMULATION
title_short Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
title_full Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
title_fullStr Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
title_full_unstemmed Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
title_sort Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
author Besnard, M.
author_facet Besnard, M.
Cabao, M. I.
Coutinho, J. A. P.
Danten, Y.
author_role author
author2 Cabao, M. I.
Coutinho, J. A. P.
Danten, Y.
author2_role author
author
author
dc.contributor.author.fl_str_mv Besnard, M.
Cabao, M. I.
Coutinho, J. A. P.
Danten, Y.
dc.subject.por.fl_str_mv INTERACTION-INDUCED SPECTRA
LIQUID CARBON-DISULFIDE
DOT-O INTERACTIONS
IONIC LIQUIDS
VIBRATIONAL-SPECTRA
FERMI RESONANCE
BINARY-MIXTURES
AB-INITIO
HARD SPHEROCYLINDERS
COMPUTER-SIMULATION
topic INTERACTION-INDUCED SPECTRA
LIQUID CARBON-DISULFIDE
DOT-O INTERACTIONS
IONIC LIQUIDS
VIBRATIONAL-SPECTRA
FERMI RESONANCE
BINARY-MIXTURES
AB-INITIO
HARD SPHEROCYLINDERS
COMPUTER-SIMULATION
description The dense phase of CO2-CS2 mixtures has been analysed by Raman spectroscopy as a function of the CO2 concentration (0.02-0.95 mole fractions) by varying the pressure (0.5 MPa up to 7.7 MPa) at constant temperature (313 K). The polarised and depolarised spectra of the induced (nu(2), nu(3)) modes of CS2 and of the nu(1)-2 nu(2) Fermi resonance dyad of both CO2 and CS2 have been measured. Upon dilution with CO2, the evolution of the spectroscopic observables of all these modes displays a \"plateau-like\" region in the CO2 mole fraction 0.3-0.7 never previously observed in CO2-organic liquids mixtures. The bandshape and intensity of the induced modes of CS2 are similar to those of pure CS2 up to equimolar concentration, after which variations occur. The preservation of the local ordering from pure CS2 to equimolar concentration together with the non-linear evolution of the spectroscopic observables allows inferring that two solvation regimes exist with a transition occurring in the plateau domain. In the first regime, corresponding to CS2 concentrated mixtures, the liquid phase is segregated with dominant CS2 clusters, whereas, in the second one, CO2 monomers and dimers and CO2-CS2 hetero-dimers coexist dynamically on a picosecond time-scale. It is demonstrated that the subtle interplay between attractive and repulsive interactions which provides a molecular interpretation of the non-ideality of the CO2-CS2 mixture allows rationalizing the volume expansion and the existence of the plateau-like region observed in the pressure-composition diagram previously ascribed to the proximity of an upper critical solution temperature at lower temperatures. (C) 2013 AIP Publishing LLC.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-01T00:00:00Z
2013
2017-12-07T19:19:01Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/19620
url http://hdl.handle.net/10773/19620
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0021-9606
10.1063/1.4821593
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dc.publisher.none.fl_str_mv AMER INST PHYSICS
publisher.none.fl_str_mv AMER INST PHYSICS
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
instacron:RCAAP
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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