Physical ageing studied by a device allowing for rapid thermal equilibration
arXiv:0811.0994 · doi:10.1063/1.3487646
Abstract
Ageing of organic glasses to the equilibrium liquid state is studied by measuring the dielectric loss utilizing a microregulator where 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 ageing times. Data for five organic glass-forming liquids are presented. The existence of an "inner clock" is confirmed by a model-free test showing that the ageing of structure is controlled by the same material time that controls the dielectric properties. At long times relaxation is not stretched, but simple exponential, and there is no "expansion gap" between the limits of the relaxation rates following up and down jumps to the same temperature.
References in corpus (6)
- Glassy Aging Dynamics
- Prevalence of approximate square root t relaxation for the dielectric alpha process in viscous organic liquids
- Approximate square-root-time relaxation in glass-forming liquids
- Dielectric spectroscopy on aging glasses
- Broadband dielectric spectroscopy and aging of glass formers
- Aging in a free-energy landscape model for glassy relaxation
Cited by in corpus (28)
- Atomic-scale relaxation dynamics and aging in a metallic glass probed by X-ray photon correlation spectroscopy
- Compressed correlation functions and fast aging dynamics in metallic glasses
- Predicting nonlinear physical aging of glasses from equilibrium relaxation via the material time
- Identical temperature dependence of the time scales of several linear-response functions of two glass-forming liquids
- Evidence of growing spatial correlations during the aging of glassy glycerol
- Spatial heterogeneities in structural temperature cause Kovacs expansion gap paradox in aging of glasses
- Direct tests of single-parameter aging
- Equilibration and aging of dense soft-sphere glass-forming liquids
- Time reversibility during the ageing of materials
- Measuring the dynamic thermal expansivity of molecular liquids near the glass transition
- Narayanaswamy's 1971 aging theory and material time
- Generalized single-parameter aging tests and their application to glycerol
- Isomorph theory of physical aging
- From sub-aging to hyper-aging in structural glasses
- A simple nonlinear equation for structural relaxation in glasses
- Kovacs Effect in Glass with Material Memory Revealed in Non-Equilibrium Particle Interactions
- A pragmatical access to the viscous flow
- Aging of CKN: Modulus versus conductivity analysis
- The structural relaxation time of a polymer glass during deformation
- Single-parameter aging in a binary Lennard-Jones system
- High pressure specific heat spectroscopy reveals simple relaxation behavior of glass forming molecular liquid
- Non-linear physical aging of supercooled glycerol induced by large upward ideal temperature steps monitored through cooling experiments
- Structural relaxation, dynamical arrest and aging in soft-sphere liquids
- Structural relaxation and highly viscous flow
- Physical aging of glasses of an organic semiconductor
- Aging of glass-forming materials following a temperature jump
- Single-parameter aging in the weakly nonlinear limit
- Large temperature-up-jump simulations of a binary Lennard-Jones system