• DOI:10.1063/1.3487646
• Corpus ID: 38546037

Physical aging of molecular glasses studied by a device allowing for rapid thermal equilibration.

@article{Hecksher2008PhysicalAO,
  title={Physical aging of molecular glasses studied by a device allowing for rapid thermal equilibration.},
  author={Tina Hecksher and Niels Boye Olsen and Kristine Niss and Jeppe C. Dyre},
  journal={The Journal of chemical physics},
  year={2008},
  volume={133 17},
  pages={
          174514
        }
}

• T. Hecksher, N. B. Olsen, +1 author J. Dyre
• Published 6 November 2008
• Materials Science, Physics
• The Journal of chemical physics

Aging to the equilibrium liquid state of organic glasses is studied. The glasses were prepared by cooling the liquid to temperatures just below the glass transition. Aging following a temperature jump was studied by measuring the dielectric loss at a fixed frequency using a microregulator in which temperature is controlled by means of a Peltier element. Compared to conventional equipment, the new device adds almost two orders of magnitude to the span of observable aging times. Data for the following five glass-forming liquids are presented: dibutyl phthalate, diethyl phthalate, 2,3-epoxy propyl-phenyl-ether, 5-polyphenyl-ether, and triphenyl phosphite. The aging data were analyzed using the Tool-Narayanaswamy formalism. The following features are found for all five liquids: (1) The liquid has an "internal clock," a fact that is established by showing that aging is controlled by the same material time that controls the dielectric properties. (2) There are no so-called expansion gaps between the long-time limits of the relaxation rates following up and down jumps to the same temperature. (3) At long times, the structural relaxation appears to follow a simple exponential decay. (4) For small temperature steps, the rate of the long-time exponential structural relaxation is identical to that of the long-time decay of the dipole autocorrelation function.