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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/40149

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network_name_str CONICET Digital (CONICET)
spelling 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
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dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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