Microphase separation in poly(isoprene-b-ethylene oxide) diblock copolymer melts. I. Phase state and kinetics of the order-to-order transitions

Abstract

The phase state and the kinetics of the order-to-order transitions have been studied in a series of poly(isoprene-b-ethylene oxide) (PI-PEO) diblock copolymers with a PI volume fraction in the range 0.25<fPI<0.92, using small angle x-ray scattering (SAXS), and rheology. The mean-field theory (MFT) structure factor is used to describe the SAXS profiles in the disordered phase and to extract the temperature dependence of the interaction parameter χ(T). In general, an agreement is found with the phase diagram proposed by an extended MFT, except at fPI=0.61 where the following sequence of phases was found: Lc→Hex→Gyroid→Dis (Lc is the crystalline lamellar phase, Hex signifies hexagonally packed cylinders, Gyroid is the bicontinuous cubic network with the Ia3̄d symmetry, and Dis is the disordered phase). We found that crystallization disrupts the amorphous ordered morphologies and imposes a layered structure (Lc). The study of the kinetics of the Hex to Lc and the Hex to Gyroid transitions is facilitated by the different viscoelastic contrast and the distinctly different scattering patterns of the three phases involved (Lc, Hex, Gyroid). Our studies show that it is possible to undercool and overheat ordered phases just as we can undercool the disordered phase. The transformation from the Hex to the Lc phase proceeds via a heterogeneous nucleation and growth process and results in the formation of a spherulitic superstructure composed from stacks of lamellar crystals. The transformation of the Hex to the Gyroid phase involves two steps. The first step—which is too fast to be picked up by rheology—involves fluctuations of the hexagonal phase. The second “slow” step involves a nucleation and growth process of elongated objects. The transformation proceeds nearly epitaxially and has an activation energy of 47 kcal/mol which is typical for a collective process.

Micro-vs.macro-phase separation in binary blends of poly(styrene)-poly(isoprene) and poly(isoprene)-poly(ethylene oxide) diblock copolymers

“…The phase boundary measurements and the resulting interaction parameter agree well with literature [10]. The interaction parameter of scattering experiments [10,11] is found to be different from phase boundary measurements, as discussed elsewhere [12]. However, the phase-boundaries-determined interaction parameter χ seems to be suitable for the purpose of predicting phase boundaries.…”

Unexpected Intermediate State for the Cylinder-to-Gyroid Transition in a Block Copolymer Solution

“…Floudas et al examined a polyisoprene-block-poly-(ethylene oxide) diblock copolymer that underwent transitions from crystalline lamellae to cylinder to gyroid phases upon heating. [8,9] The gyroid structure was observed to grow directly from a randomly oriented cylinder phase following various temperature increases. Vigild et al examined order-order transitions in a poly-(ethylene-alt-propylene)-block-polydimethylsiloxane diblock copolymer blend.…”

Tunable Mesoporous Bragg Reflectors Based on Block Copolymer Self-Assembly

“…Because of the stronger overall driving force for PI-PEO separation combined with their high mobility, PI-b-PEO self-assembly occurs orders of magnitudes faster compared to the widely used Pluronic polymers. 21,22 Utilising PI-b-PEO for TiO 2 synthesis, structural stability and fidelity during calcination can be maintained up to 700…”