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dc.contributor.authorWang, Wei
dc.contributor.authorSaperdi, Angelo
dc.contributor.authorDodero, Andrea
dc.contributor.authorCastellano, Maila
dc.contributor.authorMüller Sánchez, Alejandro Jesús ORCID
dc.contributor.authorDong, Xia
dc.contributor.authorWang, Dujin
dc.contributor.authorCavallo, Dario
dc.date.accessioned2021-11-18T08:45:40Z
dc.date.available2021-11-18T08:45:40Z
dc.date.issued2021-09-01
dc.identifier.citationCrystal Growth and Design 21(10) : 5880-5888 (2021)es_ES
dc.identifier.issn1528-7483
dc.identifier.issn1528-7505
dc.identifier.urihttp://hdl.handle.net/10810/53805
dc.description.abstract[EN]In the present work, crystallization of a soluble nucleator N, N′, N″-tricyclohexyl-1,3,5-benzenetricarboxylamide (TMC-328) in a poly(l-lactic acid) (PLLA) matrix has been studied at different temperatures. Based on the change in solubility with temperature, different levels of supersaturation of TMC-328 in a PLLA matrix can be obtained. This nucleator presents a fibrous structure produced via self-assembling and develops into an interconnected network when the temperature is lowered. The TMC-328 crystal nuclei density is quantified via optical microscopy, using the average distance of the adjacent fibrillar structure, which shows a steady decrease with the decrease in temperature. The crystallization rates of TMC-328 were assessed through rheological measurements of network formation. Both fibrils’ density and crystallization kinetics display a power law dependence on supersaturation. For the first time, the solid–melt interfacial energy, the size of the critical nucleus, and the number of molecules making up the critical nucleus of the nucleator TMC-328 in the PLLA matrix have been determined by adopting the classical nucleation theory. The subsequent crystallization of PLLA induced by this nucleator was investigated as a function of the fibrils’ spatial density. The crystallization rate of PLLA is enhanced with the increase in the TMC-328 fibrils’ density because of the availability of a larger nucleating surface. The self-assembled fibril of TMC-328 can serve as shish to form a hybrid shish-kebab structure after the crystallization of PLLA, regardless of the number of nucleation sites.es_ES
dc.description.sponsorshipW.W. thanks the China Scholarship Council (CSC) for funding his Ph.D. scholarship. We would like to thank the financial support provided by the BIODEST project; this project has received funding from the European Union’s Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement no. 778092.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/778092es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectcrystal morphologyes_ES
dc.subjecttailoring crystallizationes_ES
dc.subjectmechanical-propertieses_ES
dc.subjectphase-behaviores_ES
dc.subjectkineticses_ES
dc.subjectagentes_ES
dc.subjectacides_ES
dc.subjectperformancees_ES
dc.subjectpolylactidees_ES
dc.subjectPLLAes_ES
dc.titleCrystallization of a Self-Assembling Nucleator in Poly(L-lactide) Meltes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2021 The Authors. Attribution 4.0 International (CC BY 4.0)es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acs.cgd.1c00750es_ES
dc.identifier.doi10.1021/acs.cgd.1c00750
dc.contributor.funderEuropean Commission
dc.departamentoesPolímeros y Materiales Avanzados: Física, Química y Tecnologíaes_ES
dc.departamentoeuPolimero eta Material Aurreratuak: Fisika, Kimika eta Teknologiaes_ES


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© 2021 The Authors. Attribution 4.0 International (CC BY 4.0)
Except where otherwise noted, this item's license is described as © 2021 The Authors. Attribution 4.0 International (CC BY 4.0)