Assessing the non-ideality of the CO2-CS2 system at molecular level: A Raman scattering study
Autor(a) principal: | |
---|---|
Data de Publicação: | 2013 |
Outros Autores: | , , |
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. |
id |
RCAP_135e3e9a6c5d1b43b178a12a441fedba |
---|---|
oai_identifier_str |
oai:ria.ua.pt:10773/19620 |
network_acronym_str |
RCAP |
network_name_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository_id_str |
7160 |
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 |
format |
article |
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 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
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 |
repository.mail.fl_str_mv |
|
_version_ |
1799137596626960384 |