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dc.contributor.authorSafari, Maryam
dc.contributor.authorMugica Iztueta, Miren Agurtzane
dc.contributor.authorZubitur Soroa, María Manuela
dc.contributor.authorMartínez de Ilarduya, Antxon
dc.contributor.authorMuñoz-Guerra, Sebastián
dc.contributor.authorMüller Sánchez, Alejandro Jesús ORCID
dc.date.accessioned2023-04-18T15:31:43Z
dc.date.available2023-04-18T15:31:43Z
dc.date.issued2019-12-20
dc.identifier.citationPolymers 12(1) : (2020) // Artilce ID 17es_ES
dc.identifier.issn2073-4360
dc.identifier.urihttp://hdl.handle.net/10810/60795
dc.description.abstractIn this work, we study for the first time, the isothermal crystallization behavior of isodimorphic random poly(butylene succinate)-ran-poly(ε-caprolactone) copolyesters, PBS-ran-PCL, previously synthesized by us. We perform nucleation and spherulitic growth kinetics by polarized light optical microscopy (PLOM) and overall isothermal crystallization kinetics by differential scanning calorimetry (DSC). Selected samples were also studied by real-time wide angle X-ray diffraction (WAXS). Under isothermal conditions, only the PBS-rich phase or the PCL-rich phase could crystallize as long as the composition was away from the pseudo-eutectic point. In comparison with the parent homopolymers, as comonomer content increased, both PBS-rich and PCL-rich phases nucleated much faster, but their spherulitic growth rates were much slower. Therefore, the overall crystallization kinetics was a strong function of composition and supercooling. The only copolymer with the eutectic composition exhibited a remarkable behavior. By tuning the crystallization temperature, this copolyester could form either a single crystalline phase or both phases, with remarkably different thermal properties.es_ES
dc.description.sponsorshipFunding: This research was funded by (a) MINECO through project MAT2017-83014-C2-1-P, (b) ALBA synchrotron facility through granted proposal 2018082953 (c) the Basque Government through grant IT1309-19 and (d) European Union´s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 778092 Acknowledgments: MS gratefully acknowledges the award of a PhD fellowship by POLYMAT Basque Center for Macromolecular Design and Engineering.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/778092es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/MAT2017-83014-C2-1-Pes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectisodimorphismes_ES
dc.subjectrandom copolymerses_ES
dc.subjectcrystallizationes_ES
dc.subjectnucleationes_ES
dc.subjectgrowth ratees_ES
dc.titleControlling the Isothermal Crystallization of Isodimorphic PBS-ran-PCL Random Copolymers by Varying Composition and Supercoolinges_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2073-4360/12/1/17es_ES
dc.identifier.doi10.3390/polym12010017
dc.contributor.funderEuropean Commission
dc.departamentoesCiencia y tecnología de polímeroses_ES
dc.departamentoeuPolimeroen zientzia eta teknologiaes_ES


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© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).