Abstract
Consideration is given to the stress-strain and ultimate tensile properties of an unplasticized and a plasticized styrene-butadiene-styrene triblock polymer at temperatures from −40 to 60°C. It is concluded that the time dependence of their mechanical properties and also their high tensile strengths result from energy dissipation associated with the plastic deformation, and eventual disruption, of the colloidal polystyrene domains. A similar mechanism is undoubtedly responsible for the high strength of segmented diisocyanate-linked (polyurethane) elastomers and also styrene-butadiene rubber vulcanizates filled with colloidal polystyrene spheres. It is further concluded that a non-crystallizable elastomer will exhibit high strength provided it contains about 25% of colloidal plastic particles, uniformly dispersed. For optimum reinforcement, the particles should deform plastically to dissipate stored elastic energy, thus relieving unfavorable stress concentrations in the vicinity of slowly growing, or incipient, cracks.
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References
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Smith, T.L. (1970). Time-Dependent Mechanical Properties of Elastomeric Block Polymers in Large Tensile Deformations. In: Aggarwal, S.L. (eds) Block Polymers. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-1842-2_10
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DOI: https://doi.org/10.1007/978-1-4684-1842-2_10
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