Local and Average Glass Transitions in Polymer Thin Films

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 tra...

Full description

Saved in:
Bibliographic Details
Published in:Macromolecules 2010-12, Vol.43 (23), p.9874-9880
Main Authors: Lipson, Jane E. G, Milner, Scott T
Format: Article
Language:English
Subjects:
Applied sciences
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
Properties and characterization
Thermal and thermodynamic properties
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary: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.
ISSN:0024-9297
1520-5835
DOI:10.1021/ma101099n