The thermodynamics of micelle formation by a polystyrene-b-polyisoprene block copolymer in n-hexadecane, which is a selectively bad solvent for polystyrene, has been investigated. The temperature dependence of the critical micelle concentration (c.m.c.) was determined from measurements of scattering
A calorimetric study of the enthalpy of micelle formation by a polystyrene-b-polyisoprene block copolymer in n-hexadecane
β Scribed by C. Price; E.K.M. Chan; G. Pilcher; R.B. Stubbersfield
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 182 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
Abstraet--A calorimetric study was made of micelle formation by a polystyrene-b-polyisoprene block copolymer in n-hexadecane which is a selectively bad solvent for polystyrene. A value of -44.0 + 4.0 kJ mol-~ was obtained for the enthalpy of micellisation, in good agreement with a value of -40.7 +2.2kJmol -~ determined for this system in an earlier study from measurements of the temperature dependence of the critical micelle concentration. The agreement between the results supports the use of a simple mass-action model in accounting for the thermodynamics of micellisation of block copolymers in organic solvents.
π SIMILAR VOLUMES
The diblock copolymer poly(styrene-b~limethyl siloxane) (PS-PDMS) in n-dodecane forms multimolecular micelles in which insoluble PS blocks associate in a core surrounded by a shell of solvated PDMS blocks. Small angle X-ray scattering data have been obtained for PS-PDMS concentrations in the range 0
The dynamic structure of micelles formed by a polystyrene-b-poly(ethylene/propylene) block copolymer in paraffinic solvents has been studied by electron microscopy, photon correlation spectroscopy and LH and 13C-nuclear magnetic resonance. In n-octane below 50 Β°, the polystyrene core has two compone