Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling
- Autores
- Puig, Julieta; Zucchi, Ileana Alicia; Ceolin, Marcelo Raul; Schroeder, Walter Fabian; Williams, Roberto Juan Jose
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Polymerization-induced nanostructuration combined with crystallization-driven self-assembly was used to generate complex nanostructures in an epoxy network. A PE-b-PEO block copolymer (Mn = 1400; 50 wt% PEO), was dispersed in diglycidylether of bisphenol A (DGEBA) and homopolymerization initiated by a tertiary amine was carried out at 120°C (above the melting temperature of PE). The plasticization produced by the miscible PEO blocks decreased the Tg of the cured matrix to values located below the crystallization temperature of PE. Therefore, crystallization-driven self-assembly of PE blocks took place during the cooling step through the rubbery region of the epoxy network. Depending on the initial amount of PE-b-PEO dispersed in DGEBA, a variety of nanostructures could be generated, such as a dispersion of disk-like micelles (6.7 nm in thickness), a concentrated dispersion of short nanoribbons (50-200 nm in length and 6.7 nm in thickness), partially stacked and oriented in space, and complex spherulitic structures composed of large stacked nanoribbons. The thickness of micellar objects was close to the theoretical value of fully extended PE chains of the block copolymer. IR spectroscopy confirmed the all-trans conformation of PE chains. Therefore, crystals were formed by interdigitated PE chains, with PEO blocks tethered at both planar interfaces in an alternating way. The way in which these complex nanostructures affect the fracture resistance or functional properties (such as shape memory) of the resulting epoxy networks has yet to be analyzed.
Fil: Puig, Julieta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina
Fil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina
Fil: Ceolin, Marcelo Raul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Schroeder, Walter Fabian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina
Fil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina - Materia
-
Block Copolymer
Epoxy
Self-Assembly
Crystallization-Driven Self-Assembly - 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:11336/40149
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Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during coolingPuig, JulietaZucchi, Ileana AliciaCeolin, Marcelo RaulSchroeder, Walter FabianWilliams, Roberto Juan JoseBlock CopolymerEpoxySelf-AssemblyCrystallization-Driven Self-Assemblyhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Polymerization-induced nanostructuration combined with crystallization-driven self-assembly was used to generate complex nanostructures in an epoxy network. A PE-b-PEO block copolymer (Mn = 1400; 50 wt% PEO), was dispersed in diglycidylether of bisphenol A (DGEBA) and homopolymerization initiated by a tertiary amine was carried out at 120°C (above the melting temperature of PE). The plasticization produced by the miscible PEO blocks decreased the Tg of the cured matrix to values located below the crystallization temperature of PE. Therefore, crystallization-driven self-assembly of PE blocks took place during the cooling step through the rubbery region of the epoxy network. Depending on the initial amount of PE-b-PEO dispersed in DGEBA, a variety of nanostructures could be generated, such as a dispersion of disk-like micelles (6.7 nm in thickness), a concentrated dispersion of short nanoribbons (50-200 nm in length and 6.7 nm in thickness), partially stacked and oriented in space, and complex spherulitic structures composed of large stacked nanoribbons. The thickness of micellar objects was close to the theoretical value of fully extended PE chains of the block copolymer. IR spectroscopy confirmed the all-trans conformation of PE chains. Therefore, crystals were formed by interdigitated PE chains, with PEO blocks tethered at both planar interfaces in an alternating way. The way in which these complex nanostructures affect the fracture resistance or functional properties (such as shape memory) of the resulting epoxy networks has yet to be analyzed.Fil: Puig, Julieta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Ceolin, Marcelo Raul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Schroeder, Walter Fabian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaRoyal Society of Chemistry2016-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/40149Puig, Julieta; Zucchi, Ileana Alicia; Ceolin, Marcelo Raul; Schroeder, Walter Fabian; Williams, Roberto Juan Jose; Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling; Royal Society of Chemistry; RSC Advances; 6; 41; 3-2016; 34903-349122046-2069CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/c6ra03019jinfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C6RA03019Jinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:26:14Zoai:ri.conicet.gov.ar:11336/40149instacron: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:34982025-10-15 14:26:14.861CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling |
title |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling |
spellingShingle |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling Puig, Julieta Block Copolymer Epoxy Self-Assembly Crystallization-Driven Self-Assembly |
title_short |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling |
title_full |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling |
title_fullStr |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling |
title_full_unstemmed |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling |
title_sort |
Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling |
dc.creator.none.fl_str_mv |
Puig, Julieta Zucchi, Ileana Alicia Ceolin, Marcelo Raul Schroeder, Walter Fabian Williams, Roberto Juan Jose |
author |
Puig, Julieta |
author_facet |
Puig, Julieta Zucchi, Ileana Alicia Ceolin, Marcelo Raul Schroeder, Walter Fabian Williams, Roberto Juan Jose |
author_role |
author |
author2 |
Zucchi, Ileana Alicia Ceolin, Marcelo Raul Schroeder, Walter Fabian Williams, Roberto Juan Jose |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Block Copolymer Epoxy Self-Assembly Crystallization-Driven Self-Assembly |
topic |
Block Copolymer Epoxy Self-Assembly Crystallization-Driven Self-Assembly |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Polymerization-induced nanostructuration combined with crystallization-driven self-assembly was used to generate complex nanostructures in an epoxy network. A PE-b-PEO block copolymer (Mn = 1400; 50 wt% PEO), was dispersed in diglycidylether of bisphenol A (DGEBA) and homopolymerization initiated by a tertiary amine was carried out at 120°C (above the melting temperature of PE). The plasticization produced by the miscible PEO blocks decreased the Tg of the cured matrix to values located below the crystallization temperature of PE. Therefore, crystallization-driven self-assembly of PE blocks took place during the cooling step through the rubbery region of the epoxy network. Depending on the initial amount of PE-b-PEO dispersed in DGEBA, a variety of nanostructures could be generated, such as a dispersion of disk-like micelles (6.7 nm in thickness), a concentrated dispersion of short nanoribbons (50-200 nm in length and 6.7 nm in thickness), partially stacked and oriented in space, and complex spherulitic structures composed of large stacked nanoribbons. The thickness of micellar objects was close to the theoretical value of fully extended PE chains of the block copolymer. IR spectroscopy confirmed the all-trans conformation of PE chains. Therefore, crystals were formed by interdigitated PE chains, with PEO blocks tethered at both planar interfaces in an alternating way. The way in which these complex nanostructures affect the fracture resistance or functional properties (such as shape memory) of the resulting epoxy networks has yet to be analyzed. Fil: Puig, Julieta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina Fil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina Fil: Ceolin, Marcelo Raul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina Fil: Schroeder, Walter Fabian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina Fil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina |
description |
Polymerization-induced nanostructuration combined with crystallization-driven self-assembly was used to generate complex nanostructures in an epoxy network. A PE-b-PEO block copolymer (Mn = 1400; 50 wt% PEO), was dispersed in diglycidylether of bisphenol A (DGEBA) and homopolymerization initiated by a tertiary amine was carried out at 120°C (above the melting temperature of PE). The plasticization produced by the miscible PEO blocks decreased the Tg of the cured matrix to values located below the crystallization temperature of PE. Therefore, crystallization-driven self-assembly of PE blocks took place during the cooling step through the rubbery region of the epoxy network. Depending on the initial amount of PE-b-PEO dispersed in DGEBA, a variety of nanostructures could be generated, such as a dispersion of disk-like micelles (6.7 nm in thickness), a concentrated dispersion of short nanoribbons (50-200 nm in length and 6.7 nm in thickness), partially stacked and oriented in space, and complex spherulitic structures composed of large stacked nanoribbons. The thickness of micellar objects was close to the theoretical value of fully extended PE chains of the block copolymer. IR spectroscopy confirmed the all-trans conformation of PE chains. Therefore, crystals were formed by interdigitated PE chains, with PEO blocks tethered at both planar interfaces in an alternating way. The way in which these complex nanostructures affect the fracture resistance or functional properties (such as shape memory) of the resulting epoxy networks has yet to be analyzed. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-03 |
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/11336/40149 Puig, Julieta; Zucchi, Ileana Alicia; Ceolin, Marcelo Raul; Schroeder, Walter Fabian; Williams, Roberto Juan Jose; Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling; Royal Society of Chemistry; RSC Advances; 6; 41; 3-2016; 34903-34912 2046-2069 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/40149 |
identifier_str_mv |
Puig, Julieta; Zucchi, Ileana Alicia; Ceolin, Marcelo Raul; Schroeder, Walter Fabian; Williams, Roberto Juan Jose; Evolution of morphologies of a PE-b-PEO block copolymer in an epoxy solvent induced by polymerization followed by crystallization-driven self-assembly of PE blocks during cooling; Royal Society of Chemistry; RSC Advances; 6; 41; 3-2016; 34903-34912 2046-2069 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1039/c6ra03019j info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C6RA03019J |
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 application/pdf application/pdf application/pdf 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 |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
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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1846082705735811072 |
score |
13.22299 |