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dc.contributor.authorFelix, Leibetseder-
dc.contributor.authorJulia, Bičvić-
dc.contributor.authorKlaus, Bretterbauer-
dc.date.accessioned2023-04-20T08:07:41Z-
dc.date.available2023-04-20T08:07:41Z-
dc.date.issued2023-
dc.identifier.urihttps://link.springer.com/article/10.1007/s00706-023-03037-8-
dc.identifier.urihttps://dlib.phenikaa-uni.edu.vn/handle/PNK/8162-
dc.descriptionCC BYvi
dc.description.abstractCommon linear polymers are known to undergo phase changes at the glass-transition temperature (Tg) and the melting point (Tm). In recent years, it has also been shown that molecules with long aliphatic side chains can give rise to a backbone-independent melting phenomenon, known as nanophase separation. This effect describes the self-assembly — independent of the polymer backbone — of alkyl side chains into semi-crystalline nanostructures. This work presents optimized, gram scale synthesis routes for dodecyl and octadecyl acrylamide and their respective homopolymers. Differential scanning calorimetry (DSC) experiments detected a broad endothermal signal for poly(n-dodecyl acrylamide) at − 29 °C and a narrower, more intense signal for poly(n-octadecyl acrylamide) at 34 °C. These signals indicate the nanophase separation TM of the alkyl side chains.vi
dc.language.isoenvi
dc.publisherSpringervi
dc.subjectDSCvi
dc.subjectglass-transition temperaturevi
dc.titleSynthesis of poly(n-alkyl acrylamides) and evaluation of nanophase separation effects by temperature-dependent infrared spectroscopyvi
dc.typeBookvi
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