Effect of Temperature on Stress-Optical Properties of Styrene Butadiene Block Copolymers

1967 ◽  
Vol 40 (5) ◽  
pp. 1373-1380 ◽  
Author(s):  
E. Fischer ◽  
J. F. Henderson

Abstract Stress, strain, and optical properties of three elastomeric styrene butadiene block copolymers containing 31, 40 and 49 wt per cent styrene were studied as a function of temperature. Mechanical and optical properties indicate that these materials are two phase systems in which the polybutadiene chains form an elastomeric phase and the polystyrene a glassy phase with the latter providing physical crosslinks. Birefringence measurements indicate that decreases in modulus and strength of these materials are associated with decrease in concentration of elastically effective network chains. Independence of stress-optical coefficient of temperature suggests that the decrease in concentration of elastically effective chains is not due to onset of rubberlike behavior or flow within the polystyrene regions themselves, at least for temperatures below about 70° C. Rather, the decrease seems to be associated with increased mobility of the polybutadiene chains at higher temperatures, which also leads to an increase in the rate of stress relaxation. Birefringence measured during extension and retraction showed that stress strain hysteresis is due to restricted mobility of polybutadiene chain segments rather than to permanent viscous flow or to change in the effective network structure of the block copolymers. The ultimate properties of these rubbers were well correlated with the effective network structure in undeformed specimens.

1995 ◽  
Vol 28 (10) ◽  
pp. 3597-3603 ◽  
Author(s):  
Maarten Svensson ◽  
Per Linse ◽  
Folke Tjerneld

1967 ◽  
Vol 40 (4) ◽  
pp. 1183-1199 ◽  
Author(s):  
C. W. Childers ◽  
G. Kraus

Abstract In butadiene styrene copolymers containing long block sequences chain segments associate with like segments to form a two phase structure. Properties of such polymers are dependent not only on composition and molecular weight but also on block sequence along the chain. Polymers containing two or more polystyrene blocks per molecule form networks and exhibit elastomeric properties in the uncured state resembling those of filler reinforced vulcanizates. This behavior is shown both by linear styrene-butadiene-styrene elastomers and multichain block copolymers branched in the polybutadiene blocks. A prominent loss tangent peak was observed around —40° C for the multichain polymers. Stress strain following prestretching and stress relaxation measurements indicate some shifting of polystyrene associations during stretching. Tensile strength is reduced by increasing temperature and addition of plasticizers. Reinforcement by polystyrene domains in vulcanized block copolymers is evident from tensile strength, dynamic modulus, and swelling measurements, but decreases with increased crosslinking. The number of styrene sequences in the primary molecules is less important after vulcanization as crosslinking destroys the individuality of the original polymer chains.


1999 ◽  
Vol 839 (1-2) ◽  
pp. 71-83 ◽  
Author(s):  
Mårten Svensson ◽  
Kristina Berggren ◽  
Andres Veide ◽  
Folke Tjerneld

1969 ◽  
Vol 42 (5) ◽  
pp. 1257-1276 ◽  
Author(s):  
T. L. Smith ◽  
R. A. Dickie

Abstract A study was made of the stress—strain and ultimate properties in simple tension of an elastomeric styrene—butadiene—styrene block copolymer (Kraton 101) and also of a similar material (Thermolastic 226) that contains about 35% plasticizer as well as inorganic pigments. Stress—strain data were obtained at crosshead speeds from 0.02 to 20 in./min at temperatures from − 40 to 60° C. The relaxation rate, derived from the data at constant extension rates, was about 8% per decade of time for both materials at temperatures from − 40 to about 40° C and at extensions from about 20% up to 400%. Above − 30° C, the shift factor log aT was found to vary linearly with temperature. These findings indicate that the time and temperature dependence of the mechanical properties results primarily from the plastic (or viscoelastic) characteristics of the styrene domains. The tensile strength for Kraton 101 below 40° C is somewhat greater than 4000 psi, sensibly independent of extension rate and temperature. For the highly plasticized Thermolastic 226, the tensile strength at an extension rate of 1.0 min−1 increases from 2200 psi at 0° C to 3600 psi at − 40° C. Above 40° C for Kraton 101 and above 0° C for Thermolastic 226, the tensile strengths are dependent on extension rate and temperature owing to the increased ductility of the styrene domains. The high strength of these materials results from the uniformly dispersed styrene domains of colloidal dimensions. To obtain a crack of sufficient size to satisfy an energetic criterion for self-sustained high-speed propagation, domains must be disrupted. The plastic characteristics of the domains have a controlling effect on crack growth and thus on the ultimate properties of the materials. The strength and extensibility of other elastomers are considered in relation to those of the block copolymers.


2015 ◽  
Vol 406 ◽  
pp. 70-76 ◽  
Author(s):  
Andrés Felipe Chamorro Rengifo ◽  
Gabriel Max Dias Ferreira ◽  
Guilherme Max Dias Ferreira ◽  
Maria C. Hespanhol da Silva ◽  
Luis Henrique Mendes da Silva

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