Viscoelastic properties of blends of styrene-butadiene diblock copolymer and low molecular weight homopolybutadiene

1983 ◽  
Vol 16 (5) ◽  
pp. 769-774 ◽  
Author(s):  
Hiroshi Watanabe ◽  
Tadao Kotaka
Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 973 ◽  
Author(s):  
Zhi-Chao Yan ◽  
Md. Hossain ◽  
Michael Monteiro ◽  
Dimitris Vlassopoulos

We report on the viscoelastic properties of linear, monocyclic, and multicyclic polystyrenes with the same low molecular weight. All polymers investigated were found to exhibit unentangled dynamics. For monocyclic polymers without inner loops, a cyclic-Rouse model complemented by the contribution of unlinked chains (whose fraction was determined experimentally) captured the observed rheological response. On the other hand, multicyclic polymers with inner loops were shown to follow a hierarchical cyclic-Rouse relaxation with the outer loops relaxing first, followed by the inner loop relaxation. The influence of unlinked linear chains was less significant in multicyclic polymers with inner loops. The isofrictional zero-shear viscosity decreased with increasing number of constrained segments on the coupling sites, which was attributed to the decreasing loop size and the dilution effect due to the hierarchical relaxation.


1994 ◽  
Vol 272 (11) ◽  
pp. 1430-1438 ◽  
Author(s):  
D. J. Plazek ◽  
C. A. Bero ◽  
S. Neumeister ◽  
G. Floudas ◽  
G. Fytas ◽  
...  

1996 ◽  
Vol 461 ◽  
Author(s):  
S. Kim ◽  
C. C. Han

ABSTRACTThe effect of diblock copolymer on the phase-separation process of polymer blends has been investigated by using light scattering and optical microscopic observations. To quench the system into the two phase region, a shear-jump technique is employed instead of the conventional temperature-jump technique. The samples studied are blends of low-molecular-weight polystyrene and polybutadiene with and without added styrene-butadiene block copolymer as a compatibilizer. It was observed that the addition of diblock copolymers could accelerate the phase separation kinetics depending on the shear history. As the concentration of diblock copolymer increases, the distribution of domain sizes becomes narrower and the growth rate slows down. The extent of slowing-down depends on the molecular weight and concentration of the copolymer. The time dependence of domain growth is clearly observed with optical microscopy.


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