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
收藏
页数:14
相关论文
共 60 条
[1]   Salient properties of glassforming liquids close to the glass transition [J].
Alba-Simionesco, C .
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE IV PHYSIQUE ASTROPHYSIQUE, 2001, 2 (02) :203-216
[2]   ALPHA-RELAXATION IN THE GLASS-TRANSITION RANGE OF AMORPHOUS POLYMERS .1. TEMPERATURE BEHAVIOR ACROSS THE GLASS-TRANSITION [J].
ALEGRIA, A ;
GUERRICAECHEVARRIA, E ;
GOITIANDIA, L ;
TELLERIA, I ;
COLMENERO, J .
MACROMOLECULES, 1995, 28 (05) :1516-1527
[3]   alpha-Relaxation in the glass-transition range of amorphous polymers .2. Influence of physical aging on the dielectric relaxation [J].
Alegria, A ;
Goitiandia, L ;
Telleria, I ;
Colmenero, J .
MACROMOLECULES, 1997, 30 (13) :3881-3887
[4]   Relaxation in glassforming liquids and amorphous solids [J].
Angell, CA ;
Ngai, KL ;
McKenna, GB ;
McMillan, PF ;
Martin, SW .
JOURNAL OF APPLIED PHYSICS, 2000, 88 (06) :3113-3157
[5]  
ANGELO PD, 2007, J APPL PHYS, V101
[6]   Kinetics of structural relaxation of glass-forming melts [J].
Avramov, I .
THERMOCHIMICA ACTA, 1996, 280 :363-382
[7]   Physical aging kinetics of syndiotactic polystyrene as determined from creep behavior [J].
Beckmann, J ;
McKenna, GB ;
Landes, BG ;
Bank, DH ;
Bubeck, RA .
POLYMER ENGINEERING AND SCIENCE, 1997, 37 (09) :1459-1468
[8]   Physical aging in polymers and polymer composites: An analysis and method for time-aging time superposition [J].
Bradshaw, RD ;
Brinson, LC .
POLYMER ENGINEERING AND SCIENCE, 1997, 37 (01) :31-44
[9]   Diffusion mechanism for physical aging of polycarbonate far below the glass transition temperature studied by means of dielectric spectroscopy [J].
Cangialosi, D ;
Wübbenhorst, M ;
Groenewold, J ;
Mendes, E ;
Picken, SJ .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 2005, 351 (33-36) :2605-2610
[10]  
Debenedetti PG, 1996, Metastable liquids: concepts and principles