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Influence of fusion temperature on nonisothermal crystallization kinetics of polyamide 6

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dc.title Influence of fusion temperature on nonisothermal crystallization kinetics of polyamide 6 en
dc.contributor.author Nasr, Ahmed Mostafa Alazab Aly
dc.contributor.author Svoboda (FT), Petr
dc.relation.ispartof Polymers
dc.identifier.issn 2073-4360 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2023
utb.relation.volume 15
utb.relation.issue 8
dc.type article
dc.language.iso en
dc.publisher MDPI
dc.identifier.doi 10.3390/polym15081952
dc.relation.uri https://www.mdpi.com/2073-4360/15/8/1952
dc.subject polyamide 6 en
dc.subject DSC en
dc.subject optical microscope en
dc.subject nonisothermal crystallization en
dc.subject fusion temperature en
dc.subject cooling function en
dc.description.abstract The effect of fusion temperature and duration on the nonisothermal crystallization kinetics of polyamide 6 (PA6) was investigated using differential scanning calorimetry (DSC) and a polarized optical microscope (OM). The rapid cooling method involved heating the polymer above its melting point, holding it at this temperature to ensure complete melting, and then rapidly cooling it to the crystallization temperature. By monitoring the heat flow during cooling, the crystallization kinetics of PA6 were characterized, including the degree of crystallinity, crystallization temperature, and crystallization rate. The study found that changing the fusion temperature and duration significantly impacted the crystallization kinetics of PA6. Increasing the fusion temperature decreased the degree of crystallinity, with smaller nucleation centers requiring a higher degree of supercooling for crystallization. The crystallization temperature shifted towards lower temperatures, and the crystallization kinetics slowed down. The study also found that lengthening the fusion time raised the relative crystallinity, but any further increase did not result in a significant change. The study showed that an increase in fusion temperature led to a longer time needed to reach a given level of crystallinity, reducing the crystallization rate. This can be explained by the thermodynamics of the crystallization process, where higher temperatures promote molecular mobility and crystal growth. Moreover, the study revealed that decreasing a polymer's fusion temperature can lead to a greater degree of nucleation and faster growth of the crystalline phase, which can significantly impact the values of the Avrami parameters used to characterize the crystallization kinetics. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1011522
utb.identifier.obdid 43884806
utb.identifier.scopus 2-s2.0-85154027288
utb.identifier.wok 000977374100001
utb.identifier.pubmed 37112099
utb.source j-scopus
dc.date.accessioned 2023-05-24T13:10:16Z
dc.date.available 2023-05-24T13:10:16Z
dc.description.sponsorship Tomas Bata University in Zlin, TBU: IGA/FT/2023/008
dc.description.sponsorship Tomas Bata University in Zlin [IGA/FT/2023/008]
dc.rights Attribution 4.0 International
dc.rights.uri http://creativecommons.org/licenses/by/4.0/
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 This research was funded by the Internal Grant Agency of the Faculty of Technology, Tomas Bata University in Zlin, ref. No: IGA/FT/2023/008.
utb.fulltext.sponsorship The authors thank Tomas Bata University in Zlin for supporting this research through its Internal Grant Agency (IGA/FT/2023/008).
utb.wos.affiliation [Nasr, Ahmed; Svoboda, Petr] Univ Zlin, Fac Technol, Dept Polymer Engn, Tomas Bata, 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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Attribution 4.0 International Kromě případů, kde je uvedeno jinak, licence tohoto záznamu je Attribution 4.0 International