Abstract
Relaxation properties of linear and network polymers are analyzed on the basis of physical networks.
Two approaches are proposed: a) taking into account the equilibrium concentration of physical crosslinks; b) taking into account the concentration of nonequilibrium physical crosslinks reflecting the nonequilibrium chain conformation and kinetics of their transformation to equilibrium ones. The modulus changing with time and/or temperature is shown to connect with integral function of molar mass distribution of polymer chains.
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© 1996 Dr. Dietrich Steinkopff Verlag GmbH & Co. KG
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Irzhak, V.I., Varyukhin, S.E., Irzhak, T.F. (1996). Relaxation properties of polymer gels and concept of physical networks. In: ZrÃnyi, M. (eds) Gels. Progress in Colloid & Polymer Science, vol 102. Steinkopff. https://doi.org/10.1007/BFb0114379
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DOI: https://doi.org/10.1007/BFb0114379
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