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dc.creatorDžunuzović, Enis S.
dc.creatorTasic, S
dc.creatorBozic, B
dc.creatorBabić, Dragan
dc.creatorDunjic, B
dc.date.accessioned2018-03-01T19:28:52Z
dc.date.available2018-03-01T19:28:52Z
dc.date.issued2004
dc.identifier.issn0352-5139
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/2780
dc.description.abstractA series of acrylate functionalized samples based on hyperbranched hydroxy-terminated polyesters with different molecular weights and different degrees of acrylation were synthesized. The obtained urethane acrylates were slightly yellow viscose liquids. Their composition characterized by FTIR and H-1-NMR spectroscopy and their molecular weights were measured by GPC. All the synthesized samples were diluted with 25 wt.% 1.4-butanediol dimethacrylate (BDDM). The rheological properties of the uncured samples and the dynamic mechanical properties of the UV cured samples were examined. All the samples exhibit Newtonian behavior, which indicates the absence of physical entanglements in these polymers. The viscosity increases with increasing number of acrylic groups per molecule. The glass transition temperature of the UV cured samples increases with increasing the number of acrylic groups per molecule. The value of the storage modulus in the rubber-elastic plateau and the cross-link density increase with increasing number of acrylic groups per molecule. The formed networks are inhomogeneous and the residual unsaturation is the highest in the samples with the largest number of acrylic groups per molecule.en
dc.rightsopenAccessen
dc.sourceJournal of the Serbian Chemical Societyen
dc.subjecturethane acrylateen
dc.subjecthyperbranched hydroxy-terminated polyesteren
dc.subjectFTIRen
dc.subjectH-1-NMRen
dc.subjectGPCen
dc.subjectrheologyen
dc.subjectUV curingen
dc.subjectdynamic mechanical propertiesen
dc.titleDynamical mechanical analysis of photocrosslinked hyperbranched urethane acrylatesen
dc.typearticleen
dcterms.abstractДуњиц, Б; Дзунузовиц, Е; Тасиц, С; Бозиц, Б; Бабиц, Д;
dc.citation.volume69
dc.citation.issue6
dc.citation.spage441
dc.citation.epage453
dc.identifier.wos000222393300004
dc.identifier.doi10.2298/JSC0406441D
dc.citation.rankM23
dc.identifier.scopus2-s2.0-4143145226
dc.identifier.fulltexthttps://vinar.vin.bg.ac.rs//bitstream/id/12317/2776.pdf


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