Journal article

Crystallization-induced aggregation of block copolymer micelles: influence of crystallization kinetics on morphology

  • Mihut, Adriana M. Physical Chemistry I, University Bayreuth, Germany
  • Crassous, Jérôme J. Adolphe Merkle Institute, University Fribourg, Switzerland
  • Schmalz, Holger Macromolecular Chemistry II, University Bayreuth, Germany
  • Ballauff, Matthias Soft Matter and Functional Materials, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Berlin, Germany - Department of Physics, Humboldt University Berlin, Germany
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    04.02.2010
Published in:
  • Colloid & Polymer Science. - 2010, vol. 288, no. 5, p. 573-578
English We present a systematic investigation of the crystallization and aggregation behavior of a poly(1,2-butadiene)-block-poly(ethylene oxide) diblock copolymer (PB-b-PEO) in n-heptane. n-Heptane is a poor solvent for PEO and at 70°C the block copolymer self-assembles into spherical micelles composed of a liquid PEO core and a soluble PB corona. Time- and temperature-dependent light scattering experiments revealed that when crystallization of the PEO cores is induced by cooling, the crystal morphology depends on the crystallization temperature (T c ): Below 30°C, the high nucleation rate of the PEO core dictates the growth of the crystals by a fast aggregation of the micelles into meander-like (branched) structures due to a depletion of the micelles at the growth front. Above 30°C the nucleation rate is diminished and a relatively small crystal growth rate leads to the formation of twisted lamellae as imaged by scanning force microscopy. All data demonstrate that the formation mechanism of the crystals through micellar aggregation is dictated by two competitive effects, namely, by the nucleation and growth of the PEO core.
Faculty
Faculté des sciences
Department
Adolphe Merkle Institute
Language
  • English
Classification
Physics
License
License undefined
Identifiers
Persistent URL
https://folia.unifr.ch/unifr/documents/301482
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