Dynamics of polycarbonate far below the glass transition temperature:: A positron annihilation lifetime study -: art. no. 134206

被引:38
作者
Cangialosi, D
Wübbenhorst, M
Schut, H
van Veen, A
Picken, SJ
机构
[1] Delft Univ Technol, Dept Polymer Mat & Engn, NL-2628 BL Delft, Netherlands
[2] Dutch Polymer Inst, NL-5600 AX Eindhoven, Netherlands
[3] Delft Univ Technol, Interfac Reactor Inst, NL-2629 JB Delft, Netherlands
关键词
D O I
10.1103/PhysRevB.69.134206
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this study, we have extended the knowledge of the dynamics of polycarbonate (PC) far below T-g by means of positron annihilation lifetime spectroscopy (PALS), which is able to detect the isothermal relaxation of the free volume after rejuvenation above T-g. The free volume relaxation patterns at different temperatures below T-g were modeled according to a phenomenological model presented by Struik to obtain the equilibrium relaxation times of the process at each aging temperature. The dynamics of supercooled liquids above the glass transition temperature (T-g) is usually described by the Williams-Landel-Ferry (WLF) or Vogel-Fulcher-Tammann (VFT) equation. Recently, deviations from this behavior were found below T-g. In contrast, an Arrhenius-type temperature dependence was found. Our results suggest that, far below T-g, two possible scenarios can hold: (a) the relaxation process of PC is dominated by the beta process, though the fast modes of the alpha process still manifest even at the lowest investigated temperature; (b) an Arrhenius-type process, deriving from the coupling of few beta events, drives aging far below T-g. Finally, the aging process was related to a diffusion mechanism and a coupling parameter was introduced as a measure of the efficiency of the beta process in producing appreciable changes in the density. The magnitude of the coupling parameter suggests a weak coupling between the beta relaxation and the physical aging process.
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页码:134206 / 1
页数:9
相关论文
共 68 条
[1]   ON TEMPERATURE DEPENDENCE OF COOPERATIVE RELAXATION PROPERTIES IN GLASS-FORMING LIQUIDS [J].
ADAM, G ;
GIBBS, JH .
JOURNAL OF CHEMICAL PHYSICS, 1965, 43 (01) :139-&
[2]   NON-DEBYE DIELECTRIC-RELAXATION AROUND THE LIQUID-GLASS TRANSITION OF A GLASS-FORMING POLYMER [J].
ALEGRIA, A ;
GUERRICAECHEVARRIA, E ;
TELLERIA, I ;
COLMENERO, J .
PHYSICAL REVIEW B, 1993, 47 (22) :14857-14865
[3]  
Angell C., 1985, RELAXATIONS COMPLEX
[4]   Entropy and fragility in supercooling liquids [J].
Angell, CA .
JOURNAL OF RESEARCH OF THE NATIONAL INSTITUTE OF STANDARDS AND TECHNOLOGY, 1997, 102 (02) :171-185
[5]   FORMATION OF GLASSES FROM LIQUIDS AND BIOPOLYMERS [J].
ANGELL, CA .
SCIENCE, 1995, 267 (5206) :1924-1935
[6]   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
[7]   Dynamics of glass-forming polymers: "Homogeneous" versus "heterogeneous" scenario [J].
Arbe, A ;
Colmenero, J ;
Monkenbusch, M ;
Richter, D .
PHYSICAL REVIEW LETTERS, 1998, 81 (03) :590-593
[8]   NONEXPONENTIAL RELAXATIONS IN STRONG AND FRAGILE GLASS FORMERS [J].
BOHMER, R ;
NGAI, KL ;
ANGELL, CA ;
PLAZEK, DJ .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (05) :4201-4209
[9]   Accumulation of charges in polycarbonate due to positron irradiation [J].
Cangialosi, D ;
Schut, H ;
Wübbenhorst, M ;
van Turnhout, J ;
van Veen, A .
RADIATION PHYSICS AND CHEMISTRY, 2003, 68 (3-4) :507-510
[10]   Positron annihilation lifetime spectroscopy for measuring free volume during physical aging of polycarbonate [J].
Cangialosi, D ;
Schut, H ;
van Veen, A ;
Picken, SJ .
MACROMOLECULES, 2003, 36 (01) :142-147