http://www.cnr.it/ontology/cnr/individuo/prodotto/ID230904
Pulsed 1H NMR Relaxation in Crystalline Syndiotactic Polystyrene (Articolo in rivista)
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- Label
- Pulsed 1H NMR Relaxation in Crystalline Syndiotactic Polystyrene (Articolo in rivista) (literal)
- Anno
- 1991-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ma00002a046 (literal)
- Alternative label
D. Capitani, A.L. Segre, A. Grassi, S. Sykora (1991)
Pulsed 1H NMR Relaxation in Crystalline Syndiotactic Polystyrene
in Macromolecules (Online); American Chemical Society, Washington (Stati Uniti d'America)
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- D. Capitani, A.L. Segre, A. Grassi, S. Sykora (literal)
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- http://dx.doi.org/10.1021/ma00002a046 (literal)
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- Istituto di Metodologie Chimiche
Dipartimento di Fisica Università di Salerno
Stelar snc, Via E. Fermi 4, Mede (PV) (literal)
- Titolo
- Pulsed 1H NMR Relaxation in Crystalline Syndiotactic Polystyrene (literal)
- Abstract
- A marked shortening of T1 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 ?, ?, and ? polymorph modifications were studied by pulse 1H 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 relaxation: three for ? and ? s-PS and two for ? 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 to 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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