http://www.cnr.it/ontology/cnr/individuo/prodotto/ID230943
Polymorphism in Syndiotactic Polystyrene: An 1H NMR Relaxation Study (Articolo in rivista)
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- Label
- Polymorphism in Syndiotactic Polystyrene: An 1H NMR Relaxation Study (Articolo in rivista) (literal)
- Anno
- 1992-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ma00041a008 (literal)
- Alternative label
D. Capitani, C. De Rosa, A. Ferrando, A. Grassi, A.L. Segre (1992)
Polymorphism in Syndiotactic Polystyrene: An 1H NMR Relaxation Study
in Macromolecules (Online); American Chemical Society, Washington (Stati Uniti d'America)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- D. Capitani, C. De Rosa, A. Ferrando, A. Grassi, A.L. Segre (literal)
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- http://dx.doi.org/10.1021/ma00041a008 (literal)
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- Istituto di Metodologie Chimiche
Dipartimento di Chimica, Università di Napoli
Montedipe, Via Taliercio 14, 46100 Mantova
Dipartimento di Fisica, Università di Salerno (literal)
- Titolo
- Polymorphism in Syndiotactic Polystyrene: An 1H NMR Relaxation Study (literal)
- Abstract
- A marked shortening of T, relaxations in solid aromatic polymers can be attributed to O2 adsorbed on the aromatic rings. This effect, observed as a function of temperature, is modulated by the amount of adsorbed O2, Which, in turn, varies according to the molecular packing and crystalline/amorphous ratio. Within the temperature range 77-400 K, semicrystalline syndiotactic polystyrenes (s-PS) in the alpha, beta, and gamma-polymorph modifications were studied by pulse H-1 NMR at 30 MHz. Due to the presence of many relaxation components, 1,2,2-trideuterio-s-PS was synthesized, crystallized, and characterized by X-ray powder diffraction. At low temperature, when both the O2 diffusion and the spin-diffusion processes are slow enough, the backbone-deuteriated polymers exhibit multiple T1 relaxations: three for alpha and beta s-PS and two for gamma s-PS. These T1 components are attributed to crystalline and amorphous phases. From the study of these components as a function of temperature and from direct comparison of T1 values in the different phases, the following conclusions were drawn: (i) Clear differentiation was possible between different s-PS polymorphs. (ii) Determination of the crystalline vs amorphous ratio fully consistent with X-ray diffraction data was achieved. (iii) The amorphous component of different semicrystalline s-PS polymorphs could be distinguished. (literal)
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