Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers
- Autores
- Maestro, Armando; Bonales, Laura J.; Ritacco, Hernán Alejandro; Fischer, Thomas; Rubio, Ramón G.; Ortega, Francisco
- Año de publicación
- 2011
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- We have studied the surface shear viscoelasticity of poly(tert-butyl- acrylate) Langmuir monolayers spread at the air/water interface, by tracking the Brownian motion of tracer particles with different sizes and surface chemical nature, trapped at the same interface. Surface shear moduli have been extracted from the particles mean square displacements (MSD), using different approaches: hydrodynamic calculations of drag coefficients and direct inversion of the MSD by means of the generalized Stokes-Einstein equation. It has been found that these different theoretical approaches lead to comparable values of the shear interfacial viscosity independent of the polymer concentration and molecular weight. In addition, no effect of the size or chemical nature of the probe has been detected. The results have demonstrated the consistency of the microrheological techniques used, and confirm the existence of entanglements in PtBA monolayers, as recently deduced from dilational elasticity and viscosity measurements, [Maestro et al., Soft Matter, 2010, 6, 4407]. An unexpected result was that the interfacial viscosity values obtained from microrheology have been found to be several orders of magnitude lower than the ones obtained with macroscopic interfacial shear rheometers. At the moment there is no clear explanation for this disagreement, although it is not related to the probe size or their chemical nature. Furthermore, this discrepancy is not related to the analysis methodology used, including the calculation of the two-point correlation function used in 3D microrheology when there are heterogeneities present within the range of the probe size. © The Royal Society of Chemistry 2011.
Fil: Maestro, Armando. Universidad Complutense de Madrid; España
Fil: Bonales, Laura J.. Universidad Complutense de Madrid; España
Fil: Ritacco, Hernán Alejandro. Universidad Complutense de Madrid; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Física del Sur. Universidad Nacional del Sur. Departamento de Física. Instituto de Física del Sur; Argentina
Fil: Fischer, Thomas. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. University of Bayreuth; Alemania
Fil: Rubio, Ramón G.. Universidad Complutense de Madrid; España
Fil: Ortega, Francisco. Universidad Complutense de Madrid; España - Materia
-
Surface Rheology
Polymers
2d Glass Transitions
Particle Tracking - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/66429
Ver los metadatos del registro completo
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Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayersMaestro, ArmandoBonales, Laura J.Ritacco, Hernán AlejandroFischer, ThomasRubio, Ramón G.Ortega, FranciscoSurface RheologyPolymers2d Glass TransitionsParticle Trackinghttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1We have studied the surface shear viscoelasticity of poly(tert-butyl- acrylate) Langmuir monolayers spread at the air/water interface, by tracking the Brownian motion of tracer particles with different sizes and surface chemical nature, trapped at the same interface. Surface shear moduli have been extracted from the particles mean square displacements (MSD), using different approaches: hydrodynamic calculations of drag coefficients and direct inversion of the MSD by means of the generalized Stokes-Einstein equation. It has been found that these different theoretical approaches lead to comparable values of the shear interfacial viscosity independent of the polymer concentration and molecular weight. In addition, no effect of the size or chemical nature of the probe has been detected. The results have demonstrated the consistency of the microrheological techniques used, and confirm the existence of entanglements in PtBA monolayers, as recently deduced from dilational elasticity and viscosity measurements, [Maestro et al., Soft Matter, 2010, 6, 4407]. An unexpected result was that the interfacial viscosity values obtained from microrheology have been found to be several orders of magnitude lower than the ones obtained with macroscopic interfacial shear rheometers. At the moment there is no clear explanation for this disagreement, although it is not related to the probe size or their chemical nature. Furthermore, this discrepancy is not related to the analysis methodology used, including the calculation of the two-point correlation function used in 3D microrheology when there are heterogeneities present within the range of the probe size. © The Royal Society of Chemistry 2011.Fil: Maestro, Armando. Universidad Complutense de Madrid; EspañaFil: Bonales, Laura J.. Universidad Complutense de Madrid; EspañaFil: Ritacco, Hernán Alejandro. Universidad Complutense de Madrid; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Física del Sur. Universidad Nacional del Sur. Departamento de Física. Instituto de Física del Sur; ArgentinaFil: Fischer, Thomas. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. University of Bayreuth; AlemaniaFil: Rubio, Ramón G.. Universidad Complutense de Madrid; EspañaFil: Ortega, Francisco. Universidad Complutense de Madrid; EspañaRoyal Society of Chemistry2011-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/66429Maestro, Armando; Bonales, Laura J.; Ritacco, Hernán Alejandro; Fischer, Thomas; Rubio, Ramón G.; et al.; Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers; Royal Society of Chemistry; Soft Matter; 7; 17; 9-2011; 7761-77711744-683X1744-6848CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2011/sm/c1sm05225jinfo:eu-repo/semantics/altIdentifier/doi/10.1039/c1sm05225jinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:23:09Zoai:ri.conicet.gov.ar:11336/66429instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:23:09.332CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers |
title |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers |
spellingShingle |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers Maestro, Armando Surface Rheology Polymers 2d Glass Transitions Particle Tracking |
title_short |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers |
title_full |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers |
title_fullStr |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers |
title_full_unstemmed |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers |
title_sort |
Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers |
dc.creator.none.fl_str_mv |
Maestro, Armando Bonales, Laura J. Ritacco, Hernán Alejandro Fischer, Thomas Rubio, Ramón G. Ortega, Francisco |
author |
Maestro, Armando |
author_facet |
Maestro, Armando Bonales, Laura J. Ritacco, Hernán Alejandro Fischer, Thomas Rubio, Ramón G. Ortega, Francisco |
author_role |
author |
author2 |
Bonales, Laura J. Ritacco, Hernán Alejandro Fischer, Thomas Rubio, Ramón G. Ortega, Francisco |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Surface Rheology Polymers 2d Glass Transitions Particle Tracking |
topic |
Surface Rheology Polymers 2d Glass Transitions Particle Tracking |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
We have studied the surface shear viscoelasticity of poly(tert-butyl- acrylate) Langmuir monolayers spread at the air/water interface, by tracking the Brownian motion of tracer particles with different sizes and surface chemical nature, trapped at the same interface. Surface shear moduli have been extracted from the particles mean square displacements (MSD), using different approaches: hydrodynamic calculations of drag coefficients and direct inversion of the MSD by means of the generalized Stokes-Einstein equation. It has been found that these different theoretical approaches lead to comparable values of the shear interfacial viscosity independent of the polymer concentration and molecular weight. In addition, no effect of the size or chemical nature of the probe has been detected. The results have demonstrated the consistency of the microrheological techniques used, and confirm the existence of entanglements in PtBA monolayers, as recently deduced from dilational elasticity and viscosity measurements, [Maestro et al., Soft Matter, 2010, 6, 4407]. An unexpected result was that the interfacial viscosity values obtained from microrheology have been found to be several orders of magnitude lower than the ones obtained with macroscopic interfacial shear rheometers. At the moment there is no clear explanation for this disagreement, although it is not related to the probe size or their chemical nature. Furthermore, this discrepancy is not related to the analysis methodology used, including the calculation of the two-point correlation function used in 3D microrheology when there are heterogeneities present within the range of the probe size. © The Royal Society of Chemistry 2011. Fil: Maestro, Armando. Universidad Complutense de Madrid; España Fil: Bonales, Laura J.. Universidad Complutense de Madrid; España Fil: Ritacco, Hernán Alejandro. Universidad Complutense de Madrid; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Física del Sur. Universidad Nacional del Sur. Departamento de Física. Instituto de Física del Sur; Argentina Fil: Fischer, Thomas. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. University of Bayreuth; Alemania Fil: Rubio, Ramón G.. Universidad Complutense de Madrid; España Fil: Ortega, Francisco. Universidad Complutense de Madrid; España |
description |
We have studied the surface shear viscoelasticity of poly(tert-butyl- acrylate) Langmuir monolayers spread at the air/water interface, by tracking the Brownian motion of tracer particles with different sizes and surface chemical nature, trapped at the same interface. Surface shear moduli have been extracted from the particles mean square displacements (MSD), using different approaches: hydrodynamic calculations of drag coefficients and direct inversion of the MSD by means of the generalized Stokes-Einstein equation. It has been found that these different theoretical approaches lead to comparable values of the shear interfacial viscosity independent of the polymer concentration and molecular weight. In addition, no effect of the size or chemical nature of the probe has been detected. The results have demonstrated the consistency of the microrheological techniques used, and confirm the existence of entanglements in PtBA monolayers, as recently deduced from dilational elasticity and viscosity measurements, [Maestro et al., Soft Matter, 2010, 6, 4407]. An unexpected result was that the interfacial viscosity values obtained from microrheology have been found to be several orders of magnitude lower than the ones obtained with macroscopic interfacial shear rheometers. At the moment there is no clear explanation for this disagreement, although it is not related to the probe size or their chemical nature. Furthermore, this discrepancy is not related to the analysis methodology used, including the calculation of the two-point correlation function used in 3D microrheology when there are heterogeneities present within the range of the probe size. © The Royal Society of Chemistry 2011. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-09 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/66429 Maestro, Armando; Bonales, Laura J.; Ritacco, Hernán Alejandro; Fischer, Thomas; Rubio, Ramón G.; et al.; Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers; Royal Society of Chemistry; Soft Matter; 7; 17; 9-2011; 7761-7771 1744-683X 1744-6848 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/66429 |
identifier_str_mv |
Maestro, Armando; Bonales, Laura J.; Ritacco, Hernán Alejandro; Fischer, Thomas; Rubio, Ramón G.; et al.; Surface rheology: Macro- and microrheology of poly(tert-butyl acrylate) monolayers; Royal Society of Chemistry; Soft Matter; 7; 17; 9-2011; 7761-7771 1744-683X 1744-6848 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2011/sm/c1sm05225j info:eu-repo/semantics/altIdentifier/doi/10.1039/c1sm05225j |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf 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:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844614225315495936 |
score |
13.070432 |