Linear thermoviscoelasticity and characterization of noncrystalline EPDM rubber networks

An experimental study has been made to specify how the time‐temperature superposition and the linear viscoelastic characteristics vary with the degree of crosslinking for a broad class of noncrystalline peroxide‐cured EPDM networks. A new, very sensitive method is applied to determine the horizontal and vertical shift functions in an independent way. All uncrosslinked samples are thermoelasticoviscously simple with horizontal shift functions a T of the WLF type and vertical shift functions almost independent of temperature, in agreement with recent theoretical understanding. Upon crosslinking, these materials become thermoviscoelastically complex networks, but superposition can still be accomplished by assuming different temperature dependences for the relaxational strength and the equilibrium modulus. The a T functions can be taken independent of the degree of crosslinking. The vertical shift functions b T for the relaxational strength vary with the degree of crosslinking between theoretical predictions for uncrosslinked and perfectly crosslinked EPDM networks. The equilibrium moduli of the lightly cured networks decreases with increasing temperature, which is ascribed to the presence of interchain associations between ethylene sequences in the trans state. Upon further crosslinking, these effects gradually vanish and eventually the networks can be described as viscoelastically simple with an energy elastic contribution due to the ethylene trans‐gauche transitions. The linear viscoelastic characteristics, namely the storage and loss moduli and compliances and phase‐angle master curves and the relaxation and retardation spectra are discussed as a function of the degree of crosslinking. A sol/gel analysis and equilibrium swelling measurements complete the experimental characterization of three familes of five EPDM networks each.