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Influence of thermal degradation on the crystallization of poly(butylene terephthalate)

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dc.title Influence of thermal degradation on the crystallization of poly(butylene terephthalate) en
dc.contributor.author Nasr, Ahmed Mostafa Alazab Aly
dc.contributor.author Svoboda (FT), Petr
dc.relation.ispartof Express Polymer Letters
dc.identifier.issn 1788-618X Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2024
utb.relation.volume 18
utb.relation.issue 3
dc.citation.spage 309
dc.citation.epage 325
dc.type article
dc.language.iso en
dc.publisher BME-PT and GTE
dc.identifier.doi 10.3144/expresspolymlett.2024.22
dc.relation.uri http://expresspolymlett.com/issue.php?y=2024&n=3
dc.relation.uri doi.org/10.3144/expresspolymlett.2024.22
dc.subject degradation en
dc.subject kinetics en
dc.subject crystallization en
dc.subject crystallinity en
dc.subject aromatic polyesters en
dc.subject PBT en
dc.subject differential scanning calorimetry en
dc.subject X-ray en
dc.description.abstract Our work reveals a notable shift in the crystallization temperature (Tc) of poly(butylene terephthalate) (PBT) at which crystallization occurs due to exposure to prolonged thermal degradation at 270°C in an environment of nitrogen gas. The initial Tc of 193°C undergoes a marked decrease, settling at 133°C, which signifies a considerable 60°C shift towards lower temperature ranges. This transition is discernible across three distinct degradation stages: an initial phase of increase, an intermediate phase characterized by a sharp decline, and a subsequent late stage of the degradation phase characterized by a more moderate decrease in Tc. Both crystallinity and crystallization kinetics consistently mirror this pattern, demonstrating an initial rise, a rapid subsequent drop, and a gradual decline in the late-stage period. Evident from the presence of two melting peaks, the research implies differing lamellar thicknesses. As the degradation progresses, the melting points of these peaks, denoted as Tm1 and Tm2, decline at 38 and 41°C, respectively. Validation of the degradation-induced changes is provided by a small angle X-ray scattering (SAXS), which corroborates the observed decrease in the long period (L). A contextualization of the results against prior studies underscores analogous trends in the alteration of crystallization behaviour consequent to degradation. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1011793
utb.identifier.obdid 43885390
utb.identifier.scopus 2-s2.0-85182483391
utb.identifier.wok 001177645600003
utb.source j-scopus
dc.date.accessioned 2024-02-14T13:51:45Z
dc.date.available 2024-02-14T13:51:45Z
dc.description.sponsorship U niversity of Tomas Bata in Zlin, (IGA/FT/2023/008)
dc.rights.access openAccess
utb.ou Department of Polymer Engineering
utb.contributor.internalauthor Nasr, Ahmed Mostafa Alazab Aly
utb.contributor.internalauthor Svoboda (FT), Petr
utb.fulltext.sponsorship The University of Tomas Bata in Zlin funded this research through its internal grant agency (IGA/FT/2023/008).
utb.wos.affiliation [Nasr, Ahmed; Svoboda, Petr] Tomas Bata Univ Zlin, Fac Technol, Dept Polymer Engn, Vavreckova 5669, Zlin 76001, Czech Republic
utb.scopus.affiliation Department of Polymer Engineering, Faculty of Technology, Tomas Bata, University in Zlin, Vavreckova 5669, Zlin, 76001, Czech Republic
utb.fulltext.projects IGA/FT/2023/008
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