1. Colloidlike behaviour of a polystyrene- b -poly(ethylene- co -propylene) diblock copolymer dissolved in n -decane investigated by pulsed field gradient nuclear magnetic resonance
- Author
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Gerald Fleischer, A. Puhlmann, Frank Rittig, and Čestmír Koňák
- Subjects
Hydrodynamic radius ,Polymers and Plastics ,Diffusion ,Analytical chemistry ,Decane ,Micelle ,law.invention ,chemistry.chemical_compound ,Colloid and Surface Chemistry ,chemistry ,law ,Polymer chemistry ,Materials Chemistry ,Copolymer ,Polystyrene ,Physical and Theoretical Chemistry ,Crystallization ,Pulsed field gradient - Abstract
The self-diffusion of a polystyrene-b-poly(ethylene-co-propylene) diblock copolymer dissolved in a preferential solvent for the aliphatic block, n-decane, was investigated by pulsed field gradient NMR. The diblock copolymer forms micelles in solution, the structure of the solid polymer being preserved in the native solution because the polystyrene is in the glassy state. The equilibrium state is attained upon heating which again freezes in upon cooling to room temperature. The hydrodynamic radius of the micelles decreases by about 50% during this heating–cooling process. The concentration dependence of the self-diffusivity shows typical colloidlike behaviour, and it can be described by a Vogel–Fulcher–Tammann-like equation. No indications of crystallization at higher concentrations are observed in the micellar solution because the micellar sizes are slightly polydisperse. The self-diffusivity was measured up to the glasslike state, where in-cage- diffusion and dynamic heterogeneities could be detected.
- Published
- 1999
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