Macromolecules, 2018, vol 51, 23, pp. 9484-9493
DOI:10.1021/acs.macromol.8b01801
Abstract
The orientation of polymers under confinement is a basic, yet not fully understood phenomenon. In this work, the texture of poly(ethylene oxide) (PEO) infiltrated in nanoporous anodic alumina oxide (AAO) templates was investigated by X-ray pole figures. The influence of geometry and crystallization conditions, such as pore diameter, aspect ratio, and cooling rates, was systematically examined. All the samples exhibited a single, volume-dependent crystallization temperature (Tc) that is much lower than that exhibited by bulk PEO, indicating “clean” microdomains without detectable heterogeneous nucleation. An “orientation diagram” was established to account for the experimental observations. Under very high cooling rates (quenching), crystallization of PEO within AAO was nucleation-controlled, adopting a random distribution of crystallites. Under low cooling rates, growth kinetics played a decisive role in the crystal orientation. A relatively faster cooling rate (10 °C/min) and/or smaller pores lead to the ⟨120⟩*||pore axis (n⃗) mode (uniaxial orientation). When the cooling rate was lower (1 °C/min) and/or the pores were larger, a mixed orientation, with a coexistence of ⟨120⟩*||n⃗ and ⟨010⟩*∥n⃗, was observed. The results favor the kinetic model that the fastest growth direction tends to align parallel to the pore axis.
