AI Article Synopsis

  • The study focuses on the molecular diffusion of triblock copolymers in water, using Pulsed Field Gradient NMR to analyze a range of polymer weight fractions.
  • The amphiphilic nature of these copolymers leads to their ability to self-organize, forming micelles and distinct liquid crystalline structures, including cubic, hexagonal, and lamellar phases at room temperature.
  • The research highlights that self-assembly creates "pore-like" diffusion effects, resulting in anisotropic diffusion patterns, where diffusion is quasi one-dimensional in the hexagonal phase and quasi two-dimensional in the lamellar phase, due to the ordered molecular arrangement.

Article Abstract

Molecular diffusion of triblock copolymers poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) in water was studied with the help of Pulsed Field Gradient NMR in the broad range of polymer weight fractions from 0.09 to 0.8. Owing to amphiphilic nature of the molecules, these block copolymers exhibit rich self-organization properties when mixed with water. In particular, at ambient temperatures they form micelles and three liquid crystalline mesophases: cubic, hexagonal, and lamellar. The corresponding super-molecular structure formations were studied with the same block copolymer and at the same temperature. Self-assembly of molecules was shown to produce "pore-like" effects on their self-diffusion properties by imposing severe constraints on the dimensionality of propagation. Diffusion in the hexagonal phase was shown to be quasi one-dimensional in the direction parallel to the long axis of the ordered molecular rods. In the lamellar phase, diffusion was found to be quasi two-dimensional, in the plane of the lamellar structures. The observed diffusion anisotropy was attributed to the effects of the specific molecular ordering on the mesoscopic length scale.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458975PMC
http://dx.doi.org/10.3390/ma5050966DOI Listing

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