Effect of positive charge concentration on TG of completely amorphous salt-polyether solutions

Hitoshi Masui, Mary Elizabeth Williams, Jeffrey W. Long, Matt Troutman, Royce W. Murray

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Solutions of salts in amorphous polyethers and charged species derivatized with polyethers have been found to both adhere to a common plot of glass transition temperature, TG, against cationic charge per polyether oxygen. It is proposed that the TG increase is mainly due to the (ion-dipole) solvation of cations, which increases the barriers to segmental motions. The salt induced shrinkage of the polymer only partially contributes to the increase and coordinative crosslinking by the cations has been ruled out as a principal cause.

Original languageEnglish (US)
Pages (from-to)175-184
Number of pages10
JournalSolid State Ionics
Volume107
Issue number3-4
StatePublished - Apr 1 1998

Fingerprint

Polyethers
Salts
salts
cations
Cations
crosslinking
Positive ions
shrinkage
glass transition temperature
solvation
plots
Solvation
dipoles
Crosslinking
causes
Polymers
polymers
oxygen
Ions
Oxygen

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Materials Science(all)
  • Condensed Matter Physics

Cite this

Masui, Hitoshi ; Williams, Mary Elizabeth ; Long, Jeffrey W. ; Troutman, Matt ; Murray, Royce W. / Effect of positive charge concentration on TG of completely amorphous salt-polyether solutions. In: Solid State Ionics. 1998 ; Vol. 107, No. 3-4. pp. 175-184.
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Masui, H, Williams, ME, Long, JW, Troutman, M & Murray, RW 1998, 'Effect of positive charge concentration on TG of completely amorphous salt-polyether solutions', Solid State Ionics, vol. 107, no. 3-4, pp. 175-184.

Effect of positive charge concentration on TG of completely amorphous salt-polyether solutions. / Masui, Hitoshi; Williams, Mary Elizabeth; Long, Jeffrey W.; Troutman, Matt; Murray, Royce W.

In: Solid State Ionics, Vol. 107, No. 3-4, 01.04.1998, p. 175-184.

Research output: Contribution to journalArticle

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