Form of presentation | Articles in international journals and collections |
Year of publication | 2018 |
Язык | английский |
|
Fatkullin Nail Fidaievich, author
|
Bibliographic description in the original language |
Mohamed F., Flaemig M., Hofmann M., Scaling analysis of the viscoelastic response of linear polymers//JOURNAL OF CHEMICAL PHYSICS. - 2018. - Vol.149, Is.4. - Art. №44902. |
Annotation |
Viscoelastic response in terms of the complex shear modulus G*(ω) of the linear polymers poly(ethylene-alt-propylene), poly(isoprene), and poly(butadiene) is studied for molar masses (M) from 3k up to 1000k and over a wide temperature range starting from the glass transition temperature Tg (174 K–373 K). Master curves G'(ωτα) and G«(ωτα) are constructed for the polymer-specific relaxation. Segmental relaxation occurring close to Tg is independently addressed by single spectra. Altogether, viscoelastic response is effectively studied over 14 decades in frequency. The structural relaxation time τα used for scaling is taken from dielectric spectra. We suggest a derivative method for identifying the different power-law regimes and their exponents along G«(ωτα) ∝ ωε«. The exponent ε« = ε«(ωτα) ≡ d ln G«(ωτα)/d ln(ωτα) reveals more details compared to conventional analyses and displays high similarity among the polymers. Within a simple scaling model, the original tube-reptation model is |
Keywords |
polymer melts viscoelastivity |
The name of the journal |
Journal of Chemical Physics
|
URL |
https://doi.org/10.1063/1.5038643 |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=185221&p_lang=2 |
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Fatkullin Nail Fidaievich |
ru_RU |
dc.date.accessioned |
2018-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2018-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2018 |
ru_RU |
dc.identifier.citation |
Mohamed F., Flaemig M., Hofmann M., Scaling analysis of the viscoelastic response of linear polymers//JOURNAL OF CHEMICAL PHYSICS. - 2018. - Vol.149, Is.4. - Art. №44902. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=185221&p_lang=2 |
ru_RU |
dc.description.abstract |
Journal of Chemical Physics |
ru_RU |
dc.description.abstract |
Viscoelastic response in terms of the complex shear modulus G*(ω) of the linear polymers poly(ethylene-alt-propylene), poly(isoprene), and poly(butadiene) is studied for molar masses (M) from 3k up to 1000k and over a wide temperature range starting from the glass transition temperature Tg (174 K–373 K). Master curves G'(ωτα) and G«(ωτα) are constructed for the polymer-specific relaxation. Segmental relaxation occurring close to Tg is independently addressed by single spectra. Altogether, viscoelastic response is effectively studied over 14 decades in frequency. The structural relaxation time τα used for scaling is taken from dielectric spectra. We suggest a derivative method for identifying the different power-law regimes and their exponents along G«(ωτα) ∝ ωε«. The exponent ε« = ε«(ωτα) ≡ d ln G«(ωτα)/d ln(ωτα) reveals more details compared to conventional analyses and displays high similarity among the polymers. Within a simple scaling model, the original tube-reptation model is |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
|
ru_RU |
dc.title |
Scaling analysis of the viscoelastic response of linear polymers |
ru_RU |
dc.type |
Articles in international journals and collections |
ru_RU |
|