Fabrication of a novel acrylate polymer bearing chalcone and amide groups and investigation of its thermal and isoconversional kinetic analysis

MakaleAçık ErişimScopus SJRQ2

Özet

The aim of the article was to examine the thermal degradation, thermal decomposition kinetics and dielectric behavior of novel poly(APHP-Am–Ac). For this purpose, the novel monomer, 4-(3-(4-acetamidophenyl)-3-oxoprop-1-en-1-yl)phenyl acrylate (APHP-Am–Ac), was synthesized from 1-(4-aminophenyl)-3-(4-hydroxyphenyl) prop-2-en-1-one (APHP) and acetic anhydride reaction. The homopolymer P(APHP-Am–Ac) was prepared by free radical polymerization within dimethylformamide at 80 °C. The presence of rigid and bulky chalcone units in polymer side chains significantly improved the solubility of polyamides, giving them an amorphous nature and good thermal stability. The structural characterization of homopolymer was accomplished using FT-IR and NMR techniques. The thermal stability and degradation features of homopolymer have been performed by using TG analysis and FT-IR during partial degradation at different temperatures. The glass transition temperature of homopolymer was determined by DSC analysis. For thermal decomposition kinetics of poly(APHP-Am–Ac), Flynn–Wall–Ozawa and Kissinger methods were applied to thermogravimetric curves and apparent activation energies (Ea) calculated from these two methods. According to FWO, the activation energy (Ea) of the first step and the second step was found as: 157.78 kJ mol−1 and 151.81 kJ mol−1, respectively. For Kissinger’s model, Ea was calculated as 154.3 kJ mol−1 and 142.83 kJ mol−1, respectively. The dielectric and conductivity measurements of homopolymer were investigated by impedance analyzer technique in a range of 10 Hz–20 kHz frequency at different temperatures (from 25 to 120 °C). The results have been plotted as a function of frequency and temperatures. The values increased significantly with temperature.

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https://rdlopen.rawdatalibrary.net/r/munzur/3704Resmi atıflarda kullanılan kalıcı adres
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https://doi.org/10.1007/s10973-019-09243-zYayıncı resmi DOI adresi
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18
WoS
17
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorBiryan, Fatih
dc.contributor.authorPihtili, Güzin
dc.date.accessioned2026-10-28T14:56:59.794214651Z
dc.date.available2026-10-28T14:56:59.794214651Z
dc.date.issued2020
dc.description.abstractThe aim of the article was to examine the thermal degradation, thermal decomposition kinetics and dielectric behavior of novel poly(APHP-Am–Ac). For this purpose, the novel monomer, 4-(3-(4-acetamidophenyl)-3-oxoprop-1-en-1-yl)phenyl acrylate (APHP-Am–Ac), was synthesized from 1-(4-aminophenyl)-3-(4-hydroxyphenyl) prop-2-en-1-one (APHP) and acetic anhydride reaction. The homopolymer P(APHP-Am–Ac) was prepared by free radical polymerization within dimethylformamide at 80 °C. The presence of rigid and bulky chalcone units in polymer side chains significantly improved the solubility of polyamides, giving them an amorphous nature and good thermal stability. The structural characterization of homopolymer was accomplished using FT-IR and NMR techniques. The thermal stability and degradation features of homopolymer have been performed by using TG analysis and FT-IR during partial degradation at different temperatures. The glass transition temperature of homopolymer was determined by DSC analysis. For thermal decomposition kinetics of poly(APHP-Am–Ac), Flynn–Wall–Ozawa and Kissinger methods were applied to thermogravimetric curves and apparent activation energies (Ea) calculated from these two methods. According to FWO, the activation energy (Ea) of the first step and the second step was found as: 157.78 kJ mol−1 and 151.81 kJ mol−1, respectively. For Kissinger’s model, Ea was calculated as 154.3 kJ mol−1 and 142.83 kJ mol−1, respectively. The dielectric and conductivity measurements of homopolymer were investigated by impedance analyzer technique in a range of 10 Hz–20 kHz frequency at different temperatures (from 25 to 120 °C). The results have been plotted as a function of frequency and temperatures. The values increased significantly with temperature.
dc.identifier.doi10.1007/s10973-019-09243-z
dc.identifier.eissn1588-2926
dc.identifier.endpage3870
dc.identifier.issn1388-6150
dc.identifier.issue6
dc.identifier.scopus2-s2.0-85078620080
dc.identifier.startpage3857
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/3704
dc.identifier.volume139
dc.identifier.wosWOS:000507708000004
dc.language.isoen
dc.publisherSpringer Science and Business Media B.V.
dc.relation.conference2nd International Conference on Physical Chemistry and Functional Materials (PCFM)
dc.relation.ispartofJournal of Thermal Analysis and Calorimetry
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectActivation energy
dc.subjectChalcone
dc.subjectNon-isothermal thermogravimetric analysis
dc.subjectThermal study
dc.subject.classificationThermodynamics
dc.subject.classificationChemistry, Analytical
dc.subject.classificationChemistry, Physical
dc.subject.classificationChemistry
dc.subject.otherActivation analysis
dc.subject.otherDimethylformamide
dc.subject.otherFree radical polymerization
dc.subject.otherFree radicals
dc.subject.otherGlass transition
dc.subject.otherKinetics
dc.subject.otherThermodynamic stability
dc.subject.otherThermogravimetric analysis
dc.subject.otherThermolysis
dc.subject.otherAcrylate polymers
dc.subject.otherActivation energy E
dc.subject.otherChalcone groups
dc.subject.otherChalcones
dc.subject.otherIsothermal thermo-gravimetric analysis
dc.subject.otherNon-isothermal thermogravimetric analyse
dc.subject.otherNonisothermal
dc.subject.otherPolymer bearings
dc.subject.otherThermal decomposition kinetics
dc.subject.otherThermal study
dc.subject.otherActivation energy
dc.titleFabrication of a novel acrylate polymer bearing chalcone and amide groups and investigation of its thermal and isoconversional kinetic analysis
dc.typeArticle
rdl.citation.openalex18
rdl.citation.scopus18
rdl.citation.wos17
rdl.conference.dateJUN 25-27, 2019
rdl.conference.placeCappadocia, TURKEY
rdl.oa.statusgreen
rdl.oa.statuspreprint
rdl.oa.urlhttps://hdl.handle.net/11508/57449
rdl.scopus.quartileQ2
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)
rdl.wos.indexConference Proceedings Citation Index - Science (CPCI-S)