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dc.contributor.authorMaría, Nicolás
dc.contributor.authorLe Goupil, Florian
dc.contributor.authorCavallo, Dario
dc.contributor.authorMaiz, Jon
dc.contributor.authorMüller Sánchez, Alejandro Jesús ORCID
dc.date.accessioned2022-09-29T16:38:46Z
dc.date.available2022-09-29T16:38:46Z
dc.date.issued2022-09-08
dc.identifier.citationInternational Journal of Molecular Sciences 23(18) : (2022) // Article ID 10365es_ES
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/10810/57873
dc.description.abstractIn this contribution, we study the effect of trifluoro ethylene (TrFE) comonomer content (samples with 80/20, 75/25, and 70/30 VDF/TrFE molar ratios were used) on the crystallization in P(VDF-co-TrFE) in comparison with a PVDF (Poly(vinylidene fluoride)) homopolymer. Employing Polarized Light Optical Microscopy (PLOM), the growth rates of spherulites or axialites were determined. Differential Scanning Calorimetry (DSC) was used to determine overall crystallization rates, self-nucleation, and Successive Self-nucleation and Annealing (SSA) thermal fractionation. The ferroelectric character of the samples was explored by polarization measurements. The results indicate that TrFE inclusion can limit the overall crystallization of the copolymer samples, especially for the ones with 20 and 25% TrFE. Self-nucleation measurements in PVDF indicate that the homopolymer can be self-nucleated, exhibiting the classic three Domains. However, the increased nucleation capacity in the copolymers provokes the absence of the self-nucleation Domain II. The PVDF displays a monomodal distribution of thermal fractions after SSA, but the P(VDF-co-TrFE) copolymers do not experience thermal fractionation, apparently due to TrFE incorporation in the PVDF crystals. Finally, the maximum and remnant polarization increases with increasing TrFE content up to a maximum of 25% TrFE content, after which it starts to decrease due to the lower dipole moment of the TrFE defect inclusion within the PVDF crystals.es_ES
dc.description.sponsorshipThis research was funded by the Basque Government, grant number IT 1503-22. J.M. acknowledges the Grant PID2021-123438NB-I00 funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”. J.M. also acknowledges the financial support of Eusko Jaurlaritza, code: IT-1566-22.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2021-123438NB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectP(VDF-co-TrFE)es_ES
dc.subjectcrystallization kineticses_ES
dc.subjectself-nucleationes_ES
dc.subjectSSA fractionationes_ES
dc.subjectcomonomer inclusiones_ES
dc.titleEffect of the TrFE Content on the Crystallization and SSA Thermal Fractionation of P(VDF-co-TrFE) Copolymerses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2022-09-22T12:04:41Z
dc.rights.holder© 2022 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 (https://creativecommons.org/licenses/by/ 4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/23/18/10365es_ES
dc.identifier.doi10.3390/ijms231810365
dc.departamentoesPolímeros y Materiales Avanzados: Física, Química y Tecnología
dc.departamentoeuPolimero eta Material Aurreratuak: Fisika, Kimika eta Teknologia


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© 2022 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 (https://creativecommons.org/licenses/by/ 4.0/).
Except where otherwise noted, this item's license is described as © 2022 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 (https://creativecommons.org/licenses/by/ 4.0/).