Spatial Organization of Homopolymer Chains Inside Spherical Polybutadiene Domains of SB Diblock Copolymers.

Abstract

Blends of perdeuterated polybutadiene homopolymer and a polystyrene-polybutadiene diblock copolymer were prepared by solution casting techniques. Small angle neutron scattering and transmission electron microscopy experiments on blends containing homopolymer with chain length smaller than the corresponding block sequence showed that homopolymer chains are solubilized by the spherical microdomains up to a homopolymer content of about 15 mole percent. The solubilized homopolymer is distributed in a spatially uniform manner throughout the domain volume and the homopolymer radius of gyration is only slightly larger than that of an unperturbed chain in bulk. At about 18 mole percent pools, of homopolymer appear outside the microdomains; the change in scattering intensities indicate that pool formation is a kinetic phenomenon rather than a thermodynamically controlled event. Experiments on blends containing longer homopolymer chains revealed a lower concentration, between 3 and 6 mole percent, for the onset of homopolymer pool formation.

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Document Details

Document Type
Technical Report
Publication Date
Mar 16, 1988
Accession Number
ADA193390

Entities

People

  • C. V. Berney
  • Peifu Cheng
  • Robert E. Cohen

Organizations

  • Massachusetts Institute of Technology

Tags

DTIC Thesaurus Topics

  • Block Copolymers
  • Copolymers
  • Dielectric Polymers
  • Electron Microscopes
  • Electron Microscopy
  • Electrons
  • Intensity
  • Materials
  • Microscopy
  • Molecular Weight
  • Neutron Scattering
  • Polybutadiene
  • Polymers
  • Polystyrenes
  • Scattering
  • Synthetic Rubber
  • Transmission Electron Microscopy

Readers

  • Atmospheric Science / Meteorology, specifically Wind Wave Turbulence.
  • Polymer Science and Technology

Technology Areas

  • Microelectronics