Phase behavior of styrene-isoprene diblock derivatives with varying conformational asymmetry

Chiajen Lai, William B. Russel, Richard Alan Register, Gary R. Marchand, Douglas H. Adamson

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

At present, diblock copolymer phase behavior in the long-chain limit is considered to be governed by three factors: the volume fraction of one block, φ; the segregation strength of the diblock, χN; and the conformational asymmetry parameter, ε. This implies that the phase diagrams for polymers of different chemistry but similar molecular weight should evolve simply and smoothly as ε is varied. We present here partial phase diagrams (covering the cylinder-gyroid-lamella region) for two derivatives of the well-known styrene-isoprene diblocks: styrene-(ethylene-alt-propylene) and vinylcyclohexane-(ethylene-alt-propylene), all of similar molecular weights. Comparison of the S/I, VCH/EP, and S/EP phase diagrams reveals that the phase behavior does not vary simply with ε. In particular, the shape and extent of the gyroid region differ greatly between the three chemistries; in the S/EP system, this region disappears into a cusp at moderate segregation strengths (χN≈24). Our findings indicate that factors other than φ, χN, and ε do influence the free energy of diblock copolymer mesophases and their regions of stability.

Original languageEnglish (US)
Pages (from-to)3461-3466
Number of pages6
JournalMacromolecules
Volume33
Issue number9
DOIs
StatePublished - May 2 2000

All Science Journal Classification (ASJC) codes

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

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