Comparison of Gel Relaxation Times and End-Block Pullout Times in ABA Triblock Copolymer Networks

被引:28
|
作者
Peters, Andrew J. [1 ]
Lodge, Timothy P. [1 ,2 ]
机构
[1] Univ Minnesota, Dept Chem, 207 Pleasant St SE, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem Engn & Mat Sci, 421 Washington Ave SE, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
SPHERICAL DOMAIN-STRUCTURE; ORDER-DISORDER TRANSITION; ASSOCIATING POLYMERS; VISCOELASTIC PROPERTIES; ASYMMETRIC DIBLOCK; MOLECULAR-EXCHANGE; PHYSICAL GELATION; SELECTIVE SOLVENT; SELF-DIFFUSION; PHASE-BEHAVIOR;
D O I
10.1021/acs.macromol.6b01921
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The gel relaxation times of two different poly[styrene-b-(ethylene-altpropylene)-b-styrene] (SEPS) ABA triblock copolymers in squalane at various concentrations has been measured by Theology. These relaxation times were compared with the results of previous time-resolved small-angle neutron scattering (TR-SANS) experiments, which measured chain exchange kinetics in SEP diblock and SEPS triblock micelles in squalane. The gels relaxed up to four orders of magnitude faster than expected based on the chain exchange measurements of equivalent diblock polymers. By accounting for two factors a bias toward shorter end-block lengths in the gel relaxation, and a reduction in the energy barrier to chain pullout caused by the triblock architecture a model is constructed that reconciles the surprisingly short gel relaxation times with the chain exchange times measured via TR-SANS.
引用
收藏
页码:7340 / 7349
页数:10
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