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

被引:90
作者
Hecksher, Tina [1 ]
Olsen, Niels Boye [1 ]
Niss, Kristine [1 ]
Dyre, Jeppe C. [1 ]
机构
[1] Roskilde Univ, Dept Sci, DNRF Ctr Glass & Time, IMFUFA, DK-4000 Roskilde, Denmark
基金
新加坡国家研究基金会;
关键词
TAU-EFFECTIVE PARADOX; STRUCTURAL RELAXATION; ENTHALPY RELAXATION; TRANSITION TEMPERATURE; ALPHA-RELAXATION; VOLUME-RECOVERY; DIELECTRIC-SPECTROSCOPY; HETEROGENEOUS DYNAMICS; AMORPHOUS POLYMERS; TIME-TEMPERATURE;
D O I
10.1063/1.3487646
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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. (C) 2010 American Institute of Physics. [doi:10.1063/1.3487646]
引用
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页数:14
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