Chain Dynamics on Crossing the Glass Transition: Nonequilibrium Effects and Recovery of the Temperature Dependence of the Structural Relaxation

被引:10
|
作者
Arrese-Igor, S. [1 ]
Alegria, A. [1 ,2 ]
Colmenero, J. [1 ,2 ,3 ]
机构
[1] Ctr Mixto CSIC UPV EHU, Ctr Fis Mat MPC, San Sebastian 20018, Spain
[2] Dept Fis Mat UPV EHU, San Sebastian 20080, Spain
[3] Donostia Int Phys Ctr, San Sebastian 20018, Spain
来源
ACS MACRO LETTERS | 2014年 / 3卷 / 11期
关键词
DIELECTRIC-SPECTROSCOPY; VISCOELASTIC BEHAVIOR; SEGMENTAL DYNAMICS; AMORPHOUS POLYMERS; CONSTRAINT RELEASE; ENTHALPY RECOVERY; MOLECULAR WEIGHT; CIS-POLYISOPRENE; ALPHA-RELAXATION; POLYSTYRENE;
D O I
10.1021/mz500508t
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this paper we report thermally stimulated depolarization current on the chain and segmental dynamics of two. monodisperse polyisoprenes accessing both dynamics at ultralow frequency range and exploring the relationship between segmental and chain time scales when crossing the glass transition. In this range, we have recorded experimental evidence of nonequilibrium effects on the slowest chain Mode dynamics. The nonequilibrium effects seem to occur simultaneously for both chain and alpha-relaxation. Moreover, detailed analysis strongly indicates the recovery of an even T-dependence for the chain and alpha-relaxation dynamics on crossing glass transition and in the glassy, state. The obtained results can be understood taking into account the different temperature dependences of the length scales involved in the segmental and chain relaxations.
引用
收藏
页码:1215 / 1219
页数:5
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