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Kelly Hebert

Publications and source records attributed to Kelly Hebert.

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Reversing strain deformations probe mechanisms for enhanced segmental mobility of polymer glasses

Optical probe reorientation measurements were performed to monitor changes in segmental dynamics resulting from the nonlinear deformation of a polymer glass. Segmental dynamics were monitored in a poly(methyl methacrylate) glass near Tg before and after a series of reversing deformations in which the sample was extended at constant strain rate and then allowed to retract back to zero stress at constant strain rate. Evidence of a rejuvenation mechanism, as quantified by a departure of the segmental dynamics from the quiescent aging dynamics after the reversing deformation, is observed for deformations which reach 60% of the yield strain or greater. By this measure, a saturation of the rejuvenation mechanism is not observed until at least five times the yield strain. For comparison, purely mechanical measurements of rejuvenation, based upon the reduction of the yield stress in a subsequent deformation, were also performed. These purely mechanical experiments show broad qualitative agreement with the probe reorientation experiments, but quantitatively differ in the pre-yield regime. The results are discussed in the context of recent theoretical approaches and simulations which provide a molecular-level description of polymer glass deformation.

cond-mat.soft

A molecular perspective on the yield and flow of polymer glasses: The role of enhanced segmental dynamics during active deformation

The mechanical properties of polymer glasses are often critical in determining the best material for a particular application. Extremely stiff materials (high modulus) may be important for some applications while avoiding catastrophic failure due to fracture (high toughness) may be more important for others. The mechanical properties of a polymer glass will depend upon both molecular structure and many experimental variables, including temperature and the mode of deformation (tension, compression, or shear). In this chapter we discuss the mechanical response of polymer glasses from a molecular perspective. In particular, we consider how deformation changes the rate at which polymer segments rearrange and how this in turn influences the mechanical response of the material. It will be shown that this focus on the changes in dynamics provides an understanding of many important features of polymer glass deformation. Of course, it is also true that the structure of a polymer glass must be altered by nonlinear deformation. Although not a major focus, we will make some comments about these structural changes at the end of this chapter.

cond-mat.soft