A model which treats spin diffusion and spin-lattice relaxation in multiphase polymers on the same footing is proposed. This new approach allows for more accurate determination of domain sizes and interfacial thickness in the probed polymers. In a poly(styrene-b-isoprene) copolymer example a significant improvement in the agreement between the NMR measurements and the simulated results can be obtained with the incorporation of a spin-lattice relaxation term into the spin diffusion process. The obtained microphase structural parameters are similar to the small angle X-ray scattering results. In addition, the spin-lattice relaxation times (T1) in different domains can be predicted reasonably well based on T1s of the component homopolymers and...
Solid-state NMR techniques were used to evaluate the sizes of the dispersed domains and the interfac...
The Mori-Zwanzig projection operator technique was employed to derive the effective Hamiltonian for ...
The spin-lattice relaxation times in polymer melts with the molecular weight above the critical valu...
H-1 spin diffusion and small-angle X-ray scattering (SAXS) measurements were carried out for a serie...
A formalism is presented permitting the evaluation of the relative mean-squared displacement of mole...
The universal features of polymer dynamics are specifically represented by laws for (anomalous) segm...
The theory of spin-lattice relaxation is constructed for melts of polymers with Mw values that excee...
The theory of spin-lattice relaxation is constructed for melts of polymers with Mw values that excee...
© 2017 Elsevier B.V.Field-cycling NMR relaxometry is a well-established technique for probing molecu...
The dynamics of polymer chains in model tubes of variable diameter and varying chain and wall potent...
An alternative and general formalism for the frequency dependence of the spin-lattice relaxation tim...
The microphase structure of polyisoprene-block-poly(methyl methacrylate) diblock copolymers was stud...
abstractWe have performed NMR spin?lattice relaxation experiments and molecular dynamics (MD) comput...
The domain sizes of a range of diblock polymers have been measured using solid-state NMR spin diffus...
A formalism for polymer melts was derived linking the spin-lattice relaxation time T1, the correlati...
Solid-state NMR techniques were used to evaluate the sizes of the dispersed domains and the interfac...
The Mori-Zwanzig projection operator technique was employed to derive the effective Hamiltonian for ...
The spin-lattice relaxation times in polymer melts with the molecular weight above the critical valu...
H-1 spin diffusion and small-angle X-ray scattering (SAXS) measurements were carried out for a serie...
A formalism is presented permitting the evaluation of the relative mean-squared displacement of mole...
The universal features of polymer dynamics are specifically represented by laws for (anomalous) segm...
The theory of spin-lattice relaxation is constructed for melts of polymers with Mw values that excee...
The theory of spin-lattice relaxation is constructed for melts of polymers with Mw values that excee...
© 2017 Elsevier B.V.Field-cycling NMR relaxometry is a well-established technique for probing molecu...
The dynamics of polymer chains in model tubes of variable diameter and varying chain and wall potent...
An alternative and general formalism for the frequency dependence of the spin-lattice relaxation tim...
The microphase structure of polyisoprene-block-poly(methyl methacrylate) diblock copolymers was stud...
abstractWe have performed NMR spin?lattice relaxation experiments and molecular dynamics (MD) comput...
The domain sizes of a range of diblock polymers have been measured using solid-state NMR spin diffus...
A formalism for polymer melts was derived linking the spin-lattice relaxation time T1, the correlati...
Solid-state NMR techniques were used to evaluate the sizes of the dispersed domains and the interfac...
The Mori-Zwanzig projection operator technique was employed to derive the effective Hamiltonian for ...
The spin-lattice relaxation times in polymer melts with the molecular weight above the critical valu...