Rheology and structure of a butadiene-styrene diblock copolymer in dibutyl phthalate: Role of concentration fluctuation in disruption and reformation of micellar lattice

Hiroshi Watanabe, Yumi Matsumiya, Toshiji Kanaya, Yoshiaki Takahashi

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Rheological properties were examined for a butadiene-styrene (BS) diblock copolymer dissolved in an S-selective solvent, dibutyl phthalate (DBP). This copolymer was composed of a deuterated B block (MB = 13.3 × 103) and a protonated S block (MS = 53.9 × 103), and the microdomain structure in the quiescent state as well as under steady shear was detected with small-angle neutron scattering (SANS). At 25 °C, a quiescently equilibrated BS/DBP system of the BS concentration = 28 wt % exhibited elastic behavior under slow, small-amplitude oscillatory shear. This elasticity reflected a bcc lattice of BS micelles with B cores and S corona. Although the B cores were in the liquid state, the thermodynamic power of segregation from the S/DBP phase forced these cores to be arranged on the lattice at equilibrium. Under steady shear, the BS/DBP system exhibited significantly non-Newtonian flow behavior. At low shear rates (γ̇), the steady state was attained after a significant stress overshoot followed by a thixotropic stress decay, and the viscosity η in this state was proportional to γ̇-1. This plastic behavior reflected mild disruption of the micellar lattice (decrease of the grain size) under slow shear. In contrast, at higher γ̇, the lattice was massively disrupted to exhibit weaker γ̇ dependence of η. Corresponding to this massive disruption, the BS/DBP system just after cessation of the fast pre-shear exhibited full relaxation (with no equilibrium elasticity) attributed to the B/S concentration fluctuation. This pre-sheared system reformed the micellar lattice to recover its elasticity when kept quiescently, and the slowest reformation/recovery was observed at the pre-shear rate being comparable to the frequency ωf of the concentration fluctuation. Thus, the pre-shear at γ̇ ≅ ωf disrupted the lattice most efficiently (thereby resulting in the slowest lattice reformation). These rheological features and structures of the BS/DBP system were discussed in relation to the softness of the micellar B cores.

Original languageEnglish
Pages (from-to)6742-6755
Number of pages14
JournalMacromolecules
Volume34
Issue number19
DOIs
Publication statusPublished - Sep 11 2001
Externally publishedYes

Fingerprint

Dibutyl Phthalate
Styrene
Butadiene
Rheology
Block copolymers
Elasticity
Shear deformation
Non Newtonian flow
Micelles
Neutron scattering
1,3-butadiene
Copolymers
Thermodynamics
Viscosity
Plastics
Recovery
Liquids

All Science Journal Classification (ASJC) codes

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

Cite this

Rheology and structure of a butadiene-styrene diblock copolymer in dibutyl phthalate : Role of concentration fluctuation in disruption and reformation of micellar lattice. / Watanabe, Hiroshi; Matsumiya, Yumi; Kanaya, Toshiji; Takahashi, Yoshiaki.

In: Macromolecules, Vol. 34, No. 19, 11.09.2001, p. 6742-6755.

Research output: Contribution to journalArticle

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abstract = "Rheological properties were examined for a butadiene-styrene (BS) diblock copolymer dissolved in an S-selective solvent, dibutyl phthalate (DBP). This copolymer was composed of a deuterated B block (MB = 13.3 × 103) and a protonated S block (MS = 53.9 × 103), and the microdomain structure in the quiescent state as well as under steady shear was detected with small-angle neutron scattering (SANS). At 25 °C, a quiescently equilibrated BS/DBP system of the BS concentration = 28 wt {\%} exhibited elastic behavior under slow, small-amplitude oscillatory shear. This elasticity reflected a bcc lattice of BS micelles with B cores and S corona. Although the B cores were in the liquid state, the thermodynamic power of segregation from the S/DBP phase forced these cores to be arranged on the lattice at equilibrium. Under steady shear, the BS/DBP system exhibited significantly non-Newtonian flow behavior. At low shear rates (γ̇), the steady state was attained after a significant stress overshoot followed by a thixotropic stress decay, and the viscosity η in this state was proportional to γ̇-1. This plastic behavior reflected mild disruption of the micellar lattice (decrease of the grain size) under slow shear. In contrast, at higher γ̇, the lattice was massively disrupted to exhibit weaker γ̇ dependence of η. Corresponding to this massive disruption, the BS/DBP system just after cessation of the fast pre-shear exhibited full relaxation (with no equilibrium elasticity) attributed to the B/S concentration fluctuation. This pre-sheared system reformed the micellar lattice to recover its elasticity when kept quiescently, and the slowest reformation/recovery was observed at the pre-shear rate being comparable to the frequency ωf of the concentration fluctuation. Thus, the pre-shear at γ̇ ≅ ωf disrupted the lattice most efficiently (thereby resulting in the slowest lattice reformation). These rheological features and structures of the BS/DBP system were discussed in relation to the softness of the micellar B cores.",
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