Poly(ethylene oxide) Crystal Orientation Changes in an Inverse Hexagonal Cylindrical Phase Morphology Constructed by a Poly(ethylene oxide)-block-polystyrene Diblock Copolymer

Citations Over TimeTop 10% of 2007 papers

Abstract

A poly(ethylene oxide)-block-polystyrene (PEO-b-PS) diblock copolymer with number-average molecular weights of 7.7k g/mol for the PS block and 21.4k g/mol for the PEO block was used to study the PEO crystal orientation changes at different crystallization temperatures (Tx) via small- and wide-angle X-ray scattering techniques. For this diblock copolymer, an inverse hexagonal cylinder (IHC) phase morphology was identified with PS cylinders hexagonally packed within the PEO matrix. In this IHC morphology, the PEO blocks were tethered on the convex interfaces of the PS domains, and the crystallization of PEO blocks was outside of the cylinders. The crystal orientation of the PEO blocks (the c-axis of the PEO crystals) after crystallization among the PS cylinders was, for the first time, found to change with respect to the long cylinder axis, â, depending solely on Tx. At very low Tx's, when the samples were quenched into liquid nitrogen, the crystals possessed a random orientation. When −30 °C ≤ Tx ≤ 5 °C, PEO crystals had an orientation with their c-axis parallel to â. Within the temperature region of 10 °C ≤ Tx ≤ 20 °C, the c-axis crystal orientation changed to be tilted with respect to â (the tilting angle was defined to be between the c-axis of the PEO crystals and â). This tilting angle increased with increasing Tx. Finally, a major crystal orientation with the c-axes of PEO crystals perpendicular to â was observed when Tx reached 30 °C. Furthermore, it was particularly interesting that the PEO crystals in the IHC phase were oriented in two dimensions when Tx = 30 °C. Namely, the PEO crystal growth was specifically grown along the {101̄0} planes of the hexagonal PS cylinders. The crystallite sizes were estimated by the Scherrer equation. The PEO crystal sizes, at least along one dimension, were on the scale of the sizes limited by the distance between the neighboring glassy PS cylinders in the hexagonal lattice.

Related Papers

• → Catalytic degradation of polystyrene into styrene and a design of recyclable polystyrene with dispersed catalysts(2000)172 cited
• → Broadening of the Nematic Temperature Range by a Non-Mesogenic Solute in a Nematic Liquid Crystal(1976)37 cited
• → Twist walls in nematic liquid crystals(1974)12 cited
• → Influence of the smectic A-nematic transitional order on the formation of the smectic phases of 4-n-hexyloxybenzylidene-4′-n-butyIaniline and 4-n-butyloxybenzylidene-4′-n-octyIaniline from an electrically deformed nematic phase(1990)4 cited
• → Phase transitions in mixtures of a side-on-side chain liquid crystalline polymer and low molar mass nematic liquid crystals(1998)15 cited