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dc.contributor.authorCaputo, Maria Rosaria
dc.contributor.authorTang, Xiaoyan
dc.contributor.authorWestlie, Andrea H.
dc.contributor.authorSardon Muguruza, Haritz
dc.contributor.authorChen, Eugene Y.-X.
dc.contributor.authorMüller Sánchez, Alejandro Jesús ORCID
dc.date.accessioned2022-11-08T16:31:34Z
dc.date.available2022-11-08T16:31:34Z
dc.date.issued2022-08
dc.identifier.citationBiomacromolecules 23(9) : 3847-3859 (2022)es_ES
dc.identifier.issn1525-7797
dc.identifier.issn1526-4602
dc.identifier.urihttp://hdl.handle.net/10810/58279
dc.description.abstractPoly(3-hydroxybutyrate) (PHB) is naturally accumulated by bacteria but can also be synthesized chemically. Its processability is limited, as it tends to degrade at temperatures above its melting temperature; hence, investigation into crystallization kinetics and morphology of PHB materials of both natural and synthetic origins is of great need and interest to get a better understanding of structure-property relationship. Accordingly, this contribution reports a first study of the crystallization and morphology of synthetic PHB materials of different molecular weights. These synthetic PHBs are racemic mixtures (50/50 mol %) of R and S chain configurations and are compared with an enantiopure bacterial R-PHB. Nonisothermal and isothermal crystallization studies show that R and S chains of PHB can cocrystallize in the same unit cell as the R-PHB. Most significantly, the results show that the presence of S chains decreases the overall crystallization rate, which could enhance the processability and industrialization of PHB-based materials.es_ES
dc.description.sponsorshipThe work performed at CSU was supported by the U.S. National Science Foundation (NSF-1955482) to E.Y.C. W e would like to acknowledge the financial support from the BIODEST project; this project has received funding from the European Union's Horizon 2020 Research and Innovation Programme under the Marie Sklodowska-Curie Grant Agreement No. 778092. We acknowledge funding from the Basque Government through Grant IT1503-22. We also thank the ALBA synchrotron for funding (Granted Proposal 2021085253) , facilities, and staff support.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.subjectring opening polymerizationes_ES
dc.subjectbeta-butyrolactonees_ES
dc.subjectthermal behaviores_ES
dc.subjectmorphologyes_ES
dc.subjectpolyhydroxyalkanoateses_ES
dc.subjecthydroxybutyratees_ES
dc.subjectmicrostructurees_ES
dc.subjectdegradationes_ES
dc.subjectgrowthes_ES
dc.titleEffect of Chain Stereoconfiguration on Poly(3-hydroxybutyrate) Crystallization Kineticses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022 The Authors. Published by American Chemical Society under a Creative Commons license 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.biomac.2c00682es_ES
dc.identifier.doi10.1021/acs.biomac.2c00682
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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© 2022 The Authors. Published by American Chemical Society under a Creative Commons license Attribution 4.0 International (CC BY 4.0)
Except where otherwise noted, this item's license is described as © 2022 The Authors. Published by American Chemical Society under a Creative Commons license Attribution 4.0 International (CC BY 4.0)