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Synthesis, characterization and thermally activated curing of polysulfones with benzoxazine end groups

dc.contributor.authorAtes, Sahin
dc.contributor.authorDizman, Cemil
dc.contributor.authorAydogan, BİNNUR
dc.contributor.authorKISKAN, Bans
dc.contributor.authorTORUN, Lokman
dc.contributor.authorYağcı, Yusuf
dc.contributor.institutionauthorTEMEL, BİNNUR
dc.date.accessioned2020-10-30T00:23:48Z
dc.date.available2020-10-30T00:23:48Z
dc.date.issued2011-03-23T00:00:00Z
dc.description.abstractPolysulfones with benzoxazine end groups (PSU-B-a) were obtained using monomer synthesis method from the phenol terminated polysulfone (PSU-OH), aniline and paraformaldehyde as starting materials. For this purpose, the precursor PSU-OHs with different molecular weights were prepared by condensation of bisphenol-A and bis(p-chlorophenyl) sulfone in presence of potassium carbonate. The structure of the polymers before and after functionalization was confirmed by proton nuclear magnetic resonance spectroscopy (H-1 NMR) and Fourier transform infrared spectroscopy (FT-IR). Thermally activated crosslinking behavior of these polymers was investigated by differential scanning calorimetry (DSC). Thermal and tensile properties of the crosslinked polymers obtained from PSU-B-a alone or with low molar mass benzoxazine (P-a) were studied by thermal gravimetric analysis (TGA) and dynamic mechanical analysis (DMA). (C) 2011 Elsevier Ltd. All rights reserved.
dc.identifier.citationAtes S., Dizman C., Aydogan B., KISKAN B., TORUN L., Yağcı Y., -Synthesis, characterization and thermally activated curing of polysulfones with benzoxazine end groups-, POLYMER, cilt.52, ss.1504-1509, 2011
dc.identifier.doi10.1016/j.polymer.2011.01.051
dc.identifier.scopus79952619021
dc.identifier.urihttp://hdl.handle.net/20.500.12645/27219
dc.identifier.wosWOS:000288592000005
dc.titleSynthesis, characterization and thermally activated curing of polysulfones with benzoxazine end groups
dc.typeArticle
dspace.entity.typePublication
local.avesis.idf6198203-d171-4a8d-85b1-5526f5b7108e
local.publication.isinternational1
relation.isAuthorOfPublicationd73c61cc-93fa-4fce-a294-f68e807cd50a
relation.isAuthorOfPublication.latestForDiscoveryd73c61cc-93fa-4fce-a294-f68e807cd50a

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