Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions
Autor(a) principal: | |
---|---|
Data de Publicação: | 2015 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.colsurfa.2015.01.086 http://hdl.handle.net/11449/160648 |
Resumo: | This work aims to delineate the single isotropic vesicle phase (Ves) in the binary didodecyldimethylammonium bromide (DDAB)/water system, limited by the critical vesicle concentrations, CVC1 approximate to 0.05 mM (2.3 x 10(-3) wt%) and CVC2 approximate to 0.7 mM (3.1 x 10(-2) wt%), as the onset of unilamellar vesicle formation and of two-phase separation into Ves + Lam (lamellar) phases, respectively. Isothermal titration calorimetry (ITC), turbidity, and crossed polaroids observations indicate that below CVC1 the dispersion is dominated by free monomers or micelles, but rich in uni- and multilamellar vesicles between CVC1 and CVC2, with CVC2 = 0.21 mM (9.5 x 10(-3) wt%) being the onset of multilamellar vesicle formation. Above CVC2, the volume of the Lam phase increases, while the volume for the Ves phase decreases to vanish around CVC3 approximate to 21 mM (0.95 wt%). Differential scanning calorimetry (DSC) data show that the gel-to-liquid crystalline transition at T-m approximate to 16 degrees C is highly cooperative (Delta T-1/2 approximate to 0.3 degrees C), and the melting enthalpy (Delta H-m) increases with DDAB concentration. Because of the remarkably slow liquid crystalline-to-gel kinetics, a cooling transition around T-m' approximate to 9.5 degrees C is reported here for the first time, we ascribe to the liquidcrystallineto-gel transition (thermal hysteresis Delta T-m approximate to 6.5 degrees C). Vesicle and lamellar structure formation is supported also by hydrodynamic diameter (D-H) data, being 100-140 and 800-1200 nm, respectively, at 25 degrees C. The zeta potential (zeta) increases with DDAB concentration but does not change much with temperature, indicating no pronounced structural change when temperature varies around T-m. (C) 2015 Elsevier B.V. All rights reserved. |
id |
UNSP_4d7347e88e8e17ae572a761bc7d5ace6 |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/160648 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersionsCationic vesiclesDDABDifferential scanning calorimetryDynamic light scatteringGel-liquid crystalline transitionsZeta potentialsThis work aims to delineate the single isotropic vesicle phase (Ves) in the binary didodecyldimethylammonium bromide (DDAB)/water system, limited by the critical vesicle concentrations, CVC1 approximate to 0.05 mM (2.3 x 10(-3) wt%) and CVC2 approximate to 0.7 mM (3.1 x 10(-2) wt%), as the onset of unilamellar vesicle formation and of two-phase separation into Ves + Lam (lamellar) phases, respectively. Isothermal titration calorimetry (ITC), turbidity, and crossed polaroids observations indicate that below CVC1 the dispersion is dominated by free monomers or micelles, but rich in uni- and multilamellar vesicles between CVC1 and CVC2, with CVC2 = 0.21 mM (9.5 x 10(-3) wt%) being the onset of multilamellar vesicle formation. Above CVC2, the volume of the Lam phase increases, while the volume for the Ves phase decreases to vanish around CVC3 approximate to 21 mM (0.95 wt%). Differential scanning calorimetry (DSC) data show that the gel-to-liquid crystalline transition at T-m approximate to 16 degrees C is highly cooperative (Delta T-1/2 approximate to 0.3 degrees C), and the melting enthalpy (Delta H-m) increases with DDAB concentration. Because of the remarkably slow liquid crystalline-to-gel kinetics, a cooling transition around T-m' approximate to 9.5 degrees C is reported here for the first time, we ascribe to the liquidcrystallineto-gel transition (thermal hysteresis Delta T-m approximate to 6.5 degrees C). Vesicle and lamellar structure formation is supported also by hydrodynamic diameter (D-H) data, being 100-140 and 800-1200 nm, respectively, at 25 degrees C. The zeta potential (zeta) increases with DDAB concentration but does not change much with temperature, indicating no pronounced structural change when temperature varies around T-m. (C) 2015 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Sao Paulo State Univ, Dept Phys, BR-15054000 Sao Jose Do Rio Preto, SP, BrazilUniv Sao Paulo, Inst Quim Sao Carlos, Sao Paulo, SP, BrazilSao Paulo State Univ, Dept Phys, BR-15054000 Sao Jose Do Rio Preto, SP, BrazilFAPESP: 2011/03566-0FAPESP: 2011/07414-0Elsevier B.V.Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Feitosa, Elosi [UNESP]Adati, Renata D. [UNESP]Alves, Fernanda R.2018-11-26T16:16:08Z2018-11-26T16:16:08Z2015-09-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article253-259application/pdfhttp://dx.doi.org/10.1016/j.colsurfa.2015.01.086Colloids And Surfaces A-physicochemical And Engineering Aspects. Amsterdam: Elsevier Science Bv, v. 480, p. 253-259, 2015.0927-7757http://hdl.handle.net/11449/16064810.1016/j.colsurfa.2015.01.086WOS:000356051200033WOS000356051200033.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengColloids And Surfaces A-physicochemical And Engineering Aspects0,753info:eu-repo/semantics/openAccess2023-11-15T06:12:21Zoai:repositorio.unesp.br:11449/160648Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:43:42.414084Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions |
title |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions |
spellingShingle |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions Feitosa, Elosi [UNESP] Cationic vesicles DDAB Differential scanning calorimetry Dynamic light scattering Gel-liquid crystalline transitions Zeta potentials |
title_short |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions |
title_full |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions |
title_fullStr |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions |
title_full_unstemmed |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions |
title_sort |
Thermal and phase behavior of didodecyldimethylammonium bromide aqueous dispersions |
author |
Feitosa, Elosi [UNESP] |
author_facet |
Feitosa, Elosi [UNESP] Adati, Renata D. [UNESP] Alves, Fernanda R. |
author_role |
author |
author2 |
Adati, Renata D. [UNESP] Alves, Fernanda R. |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Feitosa, Elosi [UNESP] Adati, Renata D. [UNESP] Alves, Fernanda R. |
dc.subject.por.fl_str_mv |
Cationic vesicles DDAB Differential scanning calorimetry Dynamic light scattering Gel-liquid crystalline transitions Zeta potentials |
topic |
Cationic vesicles DDAB Differential scanning calorimetry Dynamic light scattering Gel-liquid crystalline transitions Zeta potentials |
description |
This work aims to delineate the single isotropic vesicle phase (Ves) in the binary didodecyldimethylammonium bromide (DDAB)/water system, limited by the critical vesicle concentrations, CVC1 approximate to 0.05 mM (2.3 x 10(-3) wt%) and CVC2 approximate to 0.7 mM (3.1 x 10(-2) wt%), as the onset of unilamellar vesicle formation and of two-phase separation into Ves + Lam (lamellar) phases, respectively. Isothermal titration calorimetry (ITC), turbidity, and crossed polaroids observations indicate that below CVC1 the dispersion is dominated by free monomers or micelles, but rich in uni- and multilamellar vesicles between CVC1 and CVC2, with CVC2 = 0.21 mM (9.5 x 10(-3) wt%) being the onset of multilamellar vesicle formation. Above CVC2, the volume of the Lam phase increases, while the volume for the Ves phase decreases to vanish around CVC3 approximate to 21 mM (0.95 wt%). Differential scanning calorimetry (DSC) data show that the gel-to-liquid crystalline transition at T-m approximate to 16 degrees C is highly cooperative (Delta T-1/2 approximate to 0.3 degrees C), and the melting enthalpy (Delta H-m) increases with DDAB concentration. Because of the remarkably slow liquid crystalline-to-gel kinetics, a cooling transition around T-m' approximate to 9.5 degrees C is reported here for the first time, we ascribe to the liquidcrystallineto-gel transition (thermal hysteresis Delta T-m approximate to 6.5 degrees C). Vesicle and lamellar structure formation is supported also by hydrodynamic diameter (D-H) data, being 100-140 and 800-1200 nm, respectively, at 25 degrees C. The zeta potential (zeta) increases with DDAB concentration but does not change much with temperature, indicating no pronounced structural change when temperature varies around T-m. (C) 2015 Elsevier B.V. All rights reserved. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-09-05 2018-11-26T16:16:08Z 2018-11-26T16:16:08Z |
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://dx.doi.org/10.1016/j.colsurfa.2015.01.086 Colloids And Surfaces A-physicochemical And Engineering Aspects. Amsterdam: Elsevier Science Bv, v. 480, p. 253-259, 2015. 0927-7757 http://hdl.handle.net/11449/160648 10.1016/j.colsurfa.2015.01.086 WOS:000356051200033 WOS000356051200033.pdf |
url |
http://dx.doi.org/10.1016/j.colsurfa.2015.01.086 http://hdl.handle.net/11449/160648 |
identifier_str_mv |
Colloids And Surfaces A-physicochemical And Engineering Aspects. Amsterdam: Elsevier Science Bv, v. 480, p. 253-259, 2015. 0927-7757 10.1016/j.colsurfa.2015.01.086 WOS:000356051200033 WOS000356051200033.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Colloids And Surfaces A-physicochemical And Engineering Aspects 0,753 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
253-259 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128850765283328 |