Abstract
In the reported experiments, thermally stimulated discharge has been used in the past to diagnose and estimate the magnitude of electrical polarization in polymers. Nevertheless, molecular characterization of operative phenomena by this technique alone is often a difficult task. In the present work, IR attenuated total reflection spectroscopy has been used to investigate the origin of thermally stimulated discharge currents near 200 degree C in externally unpolarized films of polyacrylonitrile (PAN). Spectroscopic analysis of thermally degraded films reveals some unsaturation of the PAN backbone and possibly the generation of cyanide ions. Opposite surfaces in a solvent-cast film give different spectra, indicating a gradient in chemical degradation products across the film thickness. Data suggest that nonuniform generation of charged species and unsaturated bonds gives rise to internal potentials in PAN. The origin of thermally stimulated currents in PAN near 200 degree C is thus believed to be associated with the onset of chemical degradation.
| Original language | English |
|---|---|
| Title of host publication | J Polym Sci Polym Phys Ed |
| Pages | 485-499 |
| Number of pages | 15 |
| Volume | 15 |
| Edition | 3 |
| Publication status | Published - Mar 1977 |
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ASJC Scopus subject areas
- Engineering(all)
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CHEMICAL ORIGIN OF THERMALLY STIMULATED DISCHARGE CURRENTS IN POLYACRYLONITRILE. / Stupp, Samuel I; Carr, S. H.
J Polym Sci Polym Phys Ed. Vol. 15 3. ed. 1977. p. 485-499.Research output: Chapter in Book/Report/Conference proceeding › Chapter
}
TY - CHAP
T1 - CHEMICAL ORIGIN OF THERMALLY STIMULATED DISCHARGE CURRENTS IN POLYACRYLONITRILE
AU - Stupp, Samuel I
AU - Carr, S. H.
PY - 1977/3
Y1 - 1977/3
N2 - In the reported experiments, thermally stimulated discharge has been used in the past to diagnose and estimate the magnitude of electrical polarization in polymers. Nevertheless, molecular characterization of operative phenomena by this technique alone is often a difficult task. In the present work, IR attenuated total reflection spectroscopy has been used to investigate the origin of thermally stimulated discharge currents near 200 degree C in externally unpolarized films of polyacrylonitrile (PAN). Spectroscopic analysis of thermally degraded films reveals some unsaturation of the PAN backbone and possibly the generation of cyanide ions. Opposite surfaces in a solvent-cast film give different spectra, indicating a gradient in chemical degradation products across the film thickness. Data suggest that nonuniform generation of charged species and unsaturated bonds gives rise to internal potentials in PAN. The origin of thermally stimulated currents in PAN near 200 degree C is thus believed to be associated with the onset of chemical degradation.
AB - In the reported experiments, thermally stimulated discharge has been used in the past to diagnose and estimate the magnitude of electrical polarization in polymers. Nevertheless, molecular characterization of operative phenomena by this technique alone is often a difficult task. In the present work, IR attenuated total reflection spectroscopy has been used to investigate the origin of thermally stimulated discharge currents near 200 degree C in externally unpolarized films of polyacrylonitrile (PAN). Spectroscopic analysis of thermally degraded films reveals some unsaturation of the PAN backbone and possibly the generation of cyanide ions. Opposite surfaces in a solvent-cast film give different spectra, indicating a gradient in chemical degradation products across the film thickness. Data suggest that nonuniform generation of charged species and unsaturated bonds gives rise to internal potentials in PAN. The origin of thermally stimulated currents in PAN near 200 degree C is thus believed to be associated with the onset of chemical degradation.
UR - http://www.scopus.com/inward/record.url?scp=0017471836&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0017471836&partnerID=8YFLogxK
M3 - Chapter
AN - SCOPUS:0017471836
VL - 15
SP - 485
EP - 499
BT - J Polym Sci Polym Phys Ed
ER -