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Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
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Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
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Road to disorder in smectic elastomers.

Evgeny P Obraztsov1, Adrian S Muresan, Boris I Ostrovskii

  • 1FOM Institute for Atomic and Molecular Physics, Kruislaan 407, Amsterdam, Netherlands.

Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|March 21, 2008
PubMed
Summary
This summary is machine-generated.

This study reveals how cross-linking affects order in smectic elastomers using X-ray analysis. Increased cross-linking concentration and stiffness disrupt the material's one-dimensional order, transitioning it towards disorder.

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Area of Science:

  • Materials Science
  • Polymer Physics
  • Condensed Matter Physics

Background:

  • Smectic elastomers exhibit one-dimensional translational order.
  • Random cross-linking can disrupt this order, leading to changes in material properties.
  • Understanding the relationship between cross-linking and order is crucial for designing novel materials.

Purpose of the Study:

  • To investigate the effects of random cross-linking on the order in side-chain smectic elastomers.
  • To quantify the influence of cross-linker concentration and stiffness on the disruption of one-dimensional translational order.
  • To analyze the transition from ordered to disordered states using X-ray scattering.

Main Methods:

  • High-resolution X-ray scattering experiments were performed.
  • Analysis of quasi-Bragg peak line shapes was used to probe structural order.
  • The Caillé correlation function convoluted with a stretched Gaussian was employed to model smectic line shapes.

Main Results:

  • A transition from algebraic decaying order to disorder was observed with increasing cross-linking.
  • The exponent of the stretched Gaussian factor changed from 1 to <0.5, indicating a transition from finite-size domains to short-range correlations.
  • Flexible cross-linkers induced disorder at higher concentrations (0.15-0.20) than stiff cross-linkers (<0.10).
  • X-ray peak broadening indicated strain and local deformations due to dislocations.

Conclusions:

  • The degree of disorder in smectic elastomers is controllable via cross-linker concentration and stiffness.
  • X-ray line shape analysis provides a sensitive method to characterize the order-disorder transition.
  • The findings offer insights into the structure-property relationships of cross-linked polymer systems.