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Chain Conformations and Phase Behavior in Confined Polymer Blends

In: High Performance Computing in Science and Engineering’ 04

Author

Listed:
  • A. Cavallo

    (Johannes Gutenberg Universität, Institut für Physik, WA331)

  • M. Müller

    (Johannes Gutenberg Universität, Institut für Physik, WA331)

  • K. Binder

    (Johannes Gutenberg Universität, Institut für Physik, WA331)

Abstract

We investigate the chain conformations and phase separation in binary polymer blends. Using large scale semi-grandcanonical Monte Carlo simulations and finite size scaling, we investigate the molecular extension and the intermolecular paircorrelation function in thin films with hard, non-preferentially adsorbing surfaces. The interplay between chain conformations, demixing and the validity of mean field theory is investigated for a large variation of chain lengths 16 ≤ N ≤ 512. Three regimes of film thickness D can be distinguished: (i) For film thicknesses much larger than the unperturbed chain extension R e, bulk behavior is observed, i.e., the critical temperature of demixing T c increases linearly with chain length, and the mean field theory becomes asymptotically correct for large N. (ii) For D ∼ R e, the critical temperature scales linearly, T c ∼ N, but the mean field theory overestimates the prefactor even in the limit N → ∞ (iii) For ultrathin films, the chain conformations are quasi-two-dimensional, T c ∼ √N and mean field theory completely fails.

Suggested Citation

  • A. Cavallo & M. Müller & K. Binder, 2005. "Chain Conformations and Phase Behavior in Confined Polymer Blends," Springer Books, in: Egon Krause & Willi Jäger & Michael Resch (ed.), High Performance Computing in Science and Engineering’ 04, pages 3-15, Springer.
  • Handle: RePEc:spr:sprchp:978-3-540-26589-4_2
    DOI: 10.1007/3-540-26589-9_2
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