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dc.contributor.authorFernández Fernández, María Dolores ORCID
dc.contributor.authorGuzmán, Dailyn J.
dc.contributor.authorRamos, Johnny R.
dc.contributor.authorFernández Fernández, María Jesús ORCID
dc.date.accessioned2020-01-15T09:02:50Z
dc.date.available2020-01-15T09:02:50Z
dc.date.issued2019-10-19
dc.identifier.citationPolymers 11(10) : (2019) // Article ID 1719es_ES
dc.identifier.issn2073-4360
dc.identifier.urihttp://hdl.handle.net/10810/38472
dc.descriptionThis article belongs to the Special Issue Thermal Analysis of Polymer Materialses_ES
dc.description.abstractThe study of the non-isothermal crystallization behavior of polymers is of great importance due to the effect of degree of crystallinity and crystallization process on the polymer properties. The effect of aminopropylisobutyl polyhedral oligomeric silsesquioxane (APIBPOSS) and aminopropylisooctyl polyhedral oligomeric silsesquioxane (APIOPOSS) on poly(epsilon-caprolactone) (PCL) crystallization is studied by differential scanning calorimetry (DSC) under non-isothermal conditions and polarized optical microscopy (POM). The crystallization kinetics is analyzed using the Avrami and Mo models, and effective activation energies are evaluated by the Friedman isoconversional method. The results show that the compatibility between polyhedral oligomeric silsesquioxanes (POSS) and PCL and POSS loading affect the crystallization process. A higher crystallization temperature, a narrower size distribution of crystallite, and a faster crystallization rate are obtained in the presence of all the studied contents of APIBPOSS and at lower contents of APIOPOSS. At APIOPOSS contents higher than 2 wt %, the crystallization temperature is lowered, the size distribution of crystallite is broadened, and the crystallization process is retarded. The presence of POSS leads to an increase in the number of nucleation sites, and a reduction in the size of the crystallite and the overall degree of crystallinity, as a result of the confinement of PCL chains caused by POSS nanoparticles.es_ES
dc.description.sponsorshipThis research was funded by the Basque Government (SAIOTEK 2012 S-PE12UN006) and the University of the Basque Country (UFI11/56).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectpoly(epsilon-caprolactone) nanocompositeses_ES
dc.subjectposs nanoparticleses_ES
dc.subjectdsces_ES
dc.subjectnonisothermal crystallizationes_ES
dc.subjectkinetices_ES
dc.subjectmechanical-propertieses_ES
dc.subjectoligomeric silsesquioxanees_ES
dc.subjectthermal-degradationes_ES
dc.subjectkineticses_ES
dc.subjectpolypropylenees_ES
dc.subjectmorphologyes_ES
dc.subjectpolyethylenees_ES
dc.subjectchemistryes_ES
dc.subjectbarrieres_ES
dc.subjectblendses_ES
dc.titleEffect of Alkyl Chain Length in POSS Nanocage on Non-Isothermal Crystallization Behavior of PCL/Amino-POSS Nanocompositeses_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.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.mdpi.com/2073-4360/11/10/1719es_ES
dc.identifier.doi10.3390/polym11101719
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/).