The molecular mobility in PEG-PVP blends as a function of the time of system storage and the PVP molecular mass is studied by the pulsed-field gradient NMR method. The distribution of PEG molecules over their mobilities is found in a blend containing 36 vol % of PEG with the molecular mass of 400 g/mol. As the storage time of the system increases, the spectrum of diffusion coefficient values varies, thereby indicating the redistribution of PEG400 molecules in the blend with PVP. An anomalous (partly restricted) diffusion of PEG400 molecules is discovered, reflecting the influence of PVP macromolecules on the motion of short PEG chains. It is shown that, during the redistribution of PEG molecules in the blend, they are involved in a complex ...
A formalism is presented permitting the evaluation of the relative mean-squared displacement of mole...
The translational motion of polymers is a complex process and has a big impact on polymer structure ...
[[abstract]]The effect of the repeated unit length on the substantially increasing molecular motion ...
The molecular mobility in PEG-PVP blends as a function of the time of system storage and the PVP mol...
The concentration and molecular mass dependencies of the self-diffusion coefficients were obtained f...
The Pulsed Field Gradient (PFG) NMR spectroscopy was uesd to determine, via the diffusion coefficien...
The translational mobility of linear macromolecules of poly(ethylene glycol) (PEG) within a weakly c...
Pulse NMR has been used to study the self-diffusion of the macromolecules of fractionated PS in solu...
Macromolecule self-diffusion in poly(ethylene glycol)s with Mn = 3 × 102 to 4 × 104 and Mw Mn ≈ 1.1 ...
The diffusion coefficients of oligomeric radicals in monomer-polymer systems have a major influence ...
The self diffusion of phthalate molecules and macromolecules has been investigated in PVC and PS sol...
The aim of this study has been to investigate the self-diffusion behaviour in polymer solutions and ...
This work consists of two topics. The first part deals with deuterium nuclear magnetic resonance (²H...
Molecular mobility in polyblock regular alternating block copolymers has been investigated by pulsed...
PEG self-diffusion coefficients of poly(ethylene glycol)s (PEGs) (1080, 8500, and 82 250 g/mol) were...
A formalism is presented permitting the evaluation of the relative mean-squared displacement of mole...
The translational motion of polymers is a complex process and has a big impact on polymer structure ...
[[abstract]]The effect of the repeated unit length on the substantially increasing molecular motion ...
The molecular mobility in PEG-PVP blends as a function of the time of system storage and the PVP mol...
The concentration and molecular mass dependencies of the self-diffusion coefficients were obtained f...
The Pulsed Field Gradient (PFG) NMR spectroscopy was uesd to determine, via the diffusion coefficien...
The translational mobility of linear macromolecules of poly(ethylene glycol) (PEG) within a weakly c...
Pulse NMR has been used to study the self-diffusion of the macromolecules of fractionated PS in solu...
Macromolecule self-diffusion in poly(ethylene glycol)s with Mn = 3 × 102 to 4 × 104 and Mw Mn ≈ 1.1 ...
The diffusion coefficients of oligomeric radicals in monomer-polymer systems have a major influence ...
The self diffusion of phthalate molecules and macromolecules has been investigated in PVC and PS sol...
The aim of this study has been to investigate the self-diffusion behaviour in polymer solutions and ...
This work consists of two topics. The first part deals with deuterium nuclear magnetic resonance (²H...
Molecular mobility in polyblock regular alternating block copolymers has been investigated by pulsed...
PEG self-diffusion coefficients of poly(ethylene glycol)s (PEGs) (1080, 8500, and 82 250 g/mol) were...
A formalism is presented permitting the evaluation of the relative mean-squared displacement of mole...
The translational motion of polymers is a complex process and has a big impact on polymer structure ...
[[abstract]]The effect of the repeated unit length on the substantially increasing molecular motion ...