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dc.contributor.authorPérez Camargo, Ricardo Arpad
dc.contributor.authorLiu, Guoming
dc.contributor.authorCavallo, Dario
dc.contributor.authorWang, Dujin
dc.contributor.authorMüller Sánchez, Alejandro Jesús ORCID
dc.date.accessioned2021-03-26T19:31:33Z
dc.date.available2021-03-26T19:31:33Z
dc.date.issued2020-07-14
dc.identifier.citationBiomacromolecules 21(8,) :3420-3435 (2020)es_ES
dc.identifier.issn1525-7797
dc.identifier.issn1526-4602
dc.identifier.urihttp://hdl.handle.net/10810/50792
dc.descriptionUnformatted post-print version of the accepted articlees_ES
dc.description.abstractBiomedical applications of polymers require precise control of the solid-state structure, which is of particular interest for biodegradable copolymers. In this work, we evaluated the influence of crystallization conditions on the comonomer exclusion/inclusion balance of biodegradable poly (butylene succinate-ran-butylene adipate) (PBSA) isodimorphic random copolymers. Regardless of the crystallization conditions, the copolymers retain their isodimorphic character displaying a pseudo-eutectic behavior with crystallization in the entire composition range. This illustrates the thermodynamic nature of the isodimorphic behavior for PBSA random copolymers. However, depending on the composition, the crystallization conditions affect the exclusion/inclusion balance of the comonomers. Fast cooling favors BA inclusion inside the PBS crystals, whereas isothermal crystallization strongly limits it. PBA rich compositions behave differently. Both fast and slow crystallization formed the β-phase, whereas BS unit inclusion is favored independently of the cooling conditions. During Successive Self-nucleation and Annealing (SSA), the BA inclusion is intermediate between non-isothermal and isothermal conditions, while the crystalline structure of the PBA phase changes from β-phase to the more stable α-phase. We propose a simple crystallographic model to explain the changes in the unit cell dimension of the copolymers.es_ES
dc.description.sponsorshipThis work is supported by the National Key R&D Program of China (2017YFE0117800) and the National Natural Science Foundation of China (51820105005). R.A.P-C is supported by PIFI of the Chinese Academy of Science for international postdoctoral researchers (2019PE0004). This project has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement No 778092. This work has also received funding from MINECO through project MAT2017-83014-C2-1-P and from the Basque Government through grant IT1309-19. We also thank Thibaud Debuissy and Luc Averous for providing us with the PBSA samples, whose synthesis has been reported in previous publications.19, 91, 92 The support of the European Synchrotron Radiation Facility (ESRF) and the ALBA synchrotron facility is gratefully acknowledged.es_ES
dc.language.isoenges_ES
dc.publisherACSes_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.subjectIsodimorphic biodegradable random copolyesterses_ES
dc.subjectsuccessive-self-nucleation and annealing (SSA)es_ES
dc.subjectcrystallizationes_ES
dc.subjectexclusion/inclusion balancees_ES
dc.subjectpolymorphismes_ES
dc.subjectcrystalses_ES
dc.subjectmeltinges_ES
dc.subjectcopolymerses_ES
dc.subjectdifferential scanning calorimetryes_ES
dc.titleEffect of the crystallization conditions on the exclusion/inclusion balance in biodegradable poly(butylene succinate-ran-butylene adipate) copolymerses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2020 American Chemical Societyes_ES
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acs.biomac.0c00847es_ES
dc.identifier.doi10.1021/acs.biomac.0c00847
dc.contributor.funderEuropean Commission
dc.departamentoesCiencia y tecnología de polímeroses_ES
dc.departamentoeuPolimeroen zientzia eta teknologiaes_ES


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