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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12128/23585
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dc.contributor.authorTu, Wenkang-
dc.contributor.authorDzienia, Andrzej-
dc.contributor.authorMaksym, Paulina-
dc.contributor.authorDuarte, Daniel-
dc.contributor.authorBeena Unni, Aparna-
dc.contributor.authorChat, Katarzyna-
dc.contributor.authorKamiński, Kamil-
dc.contributor.authorAdrjanowicz, Karolina-
dc.date.accessioned2022-07-04T07:06:20Z-
dc.date.available2022-07-04T07:06:20Z-
dc.date.issued2022-
dc.identifier.citationPolymer, Vol. 254, (2022), art. no 125085pl_PL
dc.identifier.issn0032-3861-
dc.identifier.issn1873-2291-
dc.identifier.urihttp://hdl.handle.net/20.500.12128/23585-
dc.description.abstractThis work demonstrates the effect of a high dc bias field (up to 160 kV/cm) on the polyaddition reaction of the modeled epoxy resin system. Polymerization of bisphenol A diglycidyl ether (DGEBA) supported by high electric field results in obtaining epoxides with significantly increased molecular weight, which is seven-fold higher than the zero-field reference (Mn = 4.7 kg/mol). We also found a markedly reduced dispersity (Ð = 1.52 at 0 kV/cm, Đ = 1.21 at 160 kV/cm). The molecular weight and dispersity of obtained polymers change almost linearly with the reaction time. By following polymerization kinetics in the real-time of the experiment, via dielectric spectroscopy, we observe slowing down the reaction progress at dc fields of E = 160 kV/cm, compared to the zero-field case, E = 0 kV/cm. The polymer materials obtained in the presence/absence of static electric fields exhibit distinctly different glass transition temperatures. Our study highlights a better control over the reaction and product properties attained by using only the magnitude of the applied field as the control variable. Thus, a high electric field could provide an alternative pathway in synthesizing and developing advanced polymer materials using simpler, “green”, less-expensive, and technologically demanding approaches.pl_PL
dc.language.isoenpl_PL
dc.rightsUznanie autorstwa 3.0 Polska*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/pl/*
dc.subjectStep-growth polymerizationpl_PL
dc.subjectReaction kineticspl_PL
dc.subjectExternal electric fieldpl_PL
dc.subjectDispersitypl_PL
dc.subjectGlass transitionpl_PL
dc.subjectDielectric spectroscopypl_PL
dc.titleElectric-field assisted ring-opening polymerization: On the kinetics and product properties of DGEBA/aniline model systempl_PL
dc.typeinfo:eu-repo/semantics/articlepl_PL
dc.identifier.doi10.1016/j.polymer.2022.125085-
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Uznanie Autorstwa 3.0 Polska Creative Commons License Creative Commons