Roth C B, Dutcher J R
Department of Physics and the Guelph-Waterloo Physics Institute, University of Guelph, Guelph, Ontario, Canada N1G 2W1.
Phys Rev E Stat Nonlin Soft Matter Phys. 2005 Aug;72(2 Pt 1):021803. doi: 10.1103/PhysRevE.72.021803. Epub 2005 Aug 10.
We have probed the whole chain mobility of polymer molecules confined to freely standing films by measuring the flow of gas through holes growing in the films at elevated temperatures using a differential pressure experiment. Freely standing polystyrene films were measured for the temperature range 92 degrees C<T<105 degrees C for films with two different molecular weights Mw=717 x 10(3) and 2240 x 10(3) , with thicknesses 51 nm<h<97 nm . This range of film thicknesses is of particular interest because large reductions in the glass transition temperature Tg have been measured previously for freely standing PS films in this thickness range. We find that hole formation and growth, and therefore substantial chain mobility, does not occur until temperatures close to the bulk value of the glass transition temperature T(bulk)g. The characteristic growth times tau for the thinnest films, which have reduced values of Tg, are not substantially less than those for thicker films, and we find that these small differences in tau can be understood in terms of the bulk phenomenon of shear thinning. We also show that the viscosity at the edge of the hole inferred from the characteristic growth times obtained in this and previous studies exhibit shear thinning with reduced shear strain rates beta that span twelve orders of magnitude.