Self-diffusion of multiarm star polymers in solution far from and near the ordering transition

被引:28
作者
Fleischer, G
Fytas, G
Vlassopoulos, D
Roovers, J
Hadjichristidis, N
机构
[1] FORTH, IESL, Heraklion 71110, Crete, Greece
[2] Univ Leipzig, Fak Phys & Geowissensch, D-04103 Leipzig, Germany
[3] Natl Res Council Canada, Inst Chem Proc & Environm Technol, Ottawa, ON K1A 0R6, Canada
[4] Univ Athens, Dept Chem, Athens 15771, Greece
[5] Max Planck Inst Polymerforsch, D-6500 Mainz, Germany
来源
PHYSICA A | 2000年 / 280卷 / 3-4期
关键词
hyper star polymers; non-dilute solutions; self-diffusion; colloidal behavior;
D O I
10.1016/S0378-4371(99)00604-4
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The self-diffusion of three 128-arm polybutadiene star solutions in toluene was investigated over a broad concentration range from dilute to the ordering region with pulsed field gradient NMR (PFG-NMR). The strong concentration dependence of the self-diffusion coefficient in the fluid state is distinguished clearly from that of linear chains and can be described by a non-Arrhenius VFT-like equation with the concentration playing the role of inverse temperature. In the concentrated regime, the observation of two dynamic phases reflects the coexistence of crystalline and liquid phases over a limited concentration region. The concentration dependences of both the ordinary (fluid-like) diffusion and the completely restricted in-cage motion of these hyper stars are in agreement with the behavior of concentrated colloidal suspensions. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:266 / 278
页数:13
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