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Three models for chain conformation of block copolymers in solution and in solid state
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1996
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EngineeringPolymer NanocompositesChain ConformationSolid StatePolymersBlock CopolymersPolymer ProcessingPolymer PhysicSame ConformationPolymer ChemistryEthylene OxideMaterials ScienceSegregated ConformationBlock Co-polymersPolymer SolutionSelf-assemblyPolymer ScienceApplied PhysicsPolymer CharacterizationPolymer PropertyPolymer Modeling
Solution properties of polystyrene-poly(methyl methacrylate) (PS-PMMA) diblock copolymer, polystyrene-poly(tertiobutyl methacrylate) (PS-PtBuMA) diblock copolymer, and poly(ethylene oxide)-polystyrene-poly(ethylene oxide) (PEO-PS-PEO) triblock copolymer have been measured by viscometry. The PEO-PS-PEO copolymer has been studied also in solid state by differential scanning calorimetry and by optical microscopy. All the block copolymers present a conformational transition in solution at a given temperature region which is relatively narrow. If below this transition temperature a copolymer adopts a segregated conformation (dumb-bell model), above this transition adopts a nonsegregated or pseudo-gaussian conformation, and vice versa. In the transition temperature region the copolymer adopts a compressed segregated conformation (core and shell model). If the passage from the solution to the solid state is performed in a given constant temperature in which the copolymer presents a segregated or nonsegregated conformation the same conformation is observed in the solid state (memory effect). © 1996 John Wiley & Sons, Inc.