Selective Observation of the Interface of Heterogeneous Polycarbonate/Polystyrene Blends by Dynamic Nuclear Polarization C-13 NMR

Abstract

Heterogeneous blends of polycarbonate and polystyrene were formed by serial film casting. The polystyrene phase of each blend was homogeneously doped with 2% by weight of a bisdiphenylenephenylallyl free radical complex with benzene. Proton polarization enhanced by dynamic nuclear polarization was generated in the polycarbonate phase by dipolar coupling to electrons in the polystyrene phase under 39-GHz microwave irradiation at the difference of the electron and proton Larmor frequencies. Proton magnetization was then transferred to carbons under matched, spin lock conditions for detection with chemical shift selectivity by magic-angle spinning 13C NMR. The 13C signal from polycarbonate arises exclusively from chains which are at the polycarbonate polystyrene interface. Signals from bulk polycarbonate were suppressed by differencing techniques. Attempts at direct polarization transfers from electrons in the polystyrene phase to carbons in the polycarbonate phase failed.

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Document Details

Document Type
Technical Report
Publication Date
Nov 14, 1991
Accession Number
ADA242574

Entities

People

  • Jacob Schaefer
  • Mobae Afeworki
  • Robert A. Mckay

Organizations

  • University of Washington

Tags

Communities of Interest

  • Advanced Electronics
  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Alkenes
  • Chemical Shifts
  • Chemistry
  • Cross Polarization
  • Dielectric Polymers
  • Free Radicals
  • Frequency
  • Magnetic Fields
  • Magnetic Resonance
  • Materials
  • Microscopes
  • Nuclear Magnetic Resonance
  • Nuclear Spins
  • Polymers
  • Quantum Properties
  • Resonance
  • Thin Films

Readers

  • Polymer Science and Technology
  • Quantum spin resonance or Electron Paramagnetic Resonance spectroscopy.

Technology Areas

  • Microelectronics
  • Microelectronics - Graphene