Local and average glass transitions in polymer thin films

Jane E G Lipson, Scott Thomas Milner

Research output: Contribution to journalArticle

46 Citations (Scopus)

Abstract

In the companion paper (DOI 10.1021/ma101098d), we presented a quantitative theory for the suppression of the glass transition in a thin polymer film. Our delayed glassification (DG) model follows a proposal by de Gennes that free volume can be transmitted from surface to film interior via kinks transported along molecular strands or loops. In this paper, we use the DG model to predict the effects of molecular weight and film thickness on the film-averaged glass transition for a polystyrene sample. Our predictions for both freestanding and supported films of polystyrene illustrate that the DG model is able to account for some, but not all, of the experimental trends. This leads us to confront a number of issues, including how to average local glass transitions to yield a sample value as well as how to rationalize the nature of the molecular weight dependence for transitions in the thinnest freestanding films.

Original languageEnglish (US)
Pages (from-to)9874-9880
Number of pages7
JournalMacromolecules
Volume43
Issue number23
DOIs
StatePublished - Dec 14 2010

Fingerprint

Polymer films
Glass transition
Polystyrenes
Thin films
Molecular weight
Free volume
Film thickness

All Science Journal Classification (ASJC) codes

  • Organic Chemistry
  • Materials Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry

Cite this

Lipson, Jane E G ; Milner, Scott Thomas. / Local and average glass transitions in polymer thin films. In: Macromolecules. 2010 ; Vol. 43, No. 23. pp. 9874-9880.
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Local and average glass transitions in polymer thin films. / Lipson, Jane E G; Milner, Scott Thomas.

In: Macromolecules, Vol. 43, No. 23, 14.12.2010, p. 9874-9880.

Research output: Contribution to journalArticle

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