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The WLF equation is a consequence of time–temperature superposition (TTSP), which mathematically is an application of Boltzmann's superposition principle. It is TTSP, not WLF, that allows the assembly of a compliance master curve that spans more time, or frequency, than afforded by the time available for experimentation or the frequency range ...
An alternative model suggested by Arrhenius is also used. The WLF model is related to macroscopic motion of the bulk material, while the Arrhenius model considers local motion of polymer chains. Some materials, polymers in particular, show a strong dependence of viscoelastic properties on the temperature at which they are measured.
This is the average length a polymer molecule must diffuse to escape from its particular tube, and so the characteristic time for this to happen can be calculated using diffusive equations. A classical derivation gives the reptation time t {\displaystyle t} :
Flory–Huggins solution theory is a lattice model of the thermodynamics of polymer solutions which takes account of the great dissimilarity in molecular sizes in adapting the usual expression for the entropy of mixing. The result is an equation for the Gibbs free energy change for mixing a polymer with a solvent. Although it makes simplifying ...
Polymer physics is the field of physics that studies polymers, their fluctuations, mechanical properties, as well as the kinetics of reactions involving degradation of polymers and polymerisation of monomers.
FENE-P is one of few polymer models that can be used in computational fluid dynamics simulations since it removes the need of statistical averaging at each grid point at any instant in time. It is demonstrated to be able to capture some of the most important polymeric flow behaviors such as polymer turbulence drag reduction and shear thinning.
The Deborah number (De) is a dimensionless number, often used in rheology to characterize the fluidity of materials under specific flow conditions. It quantifies the observation that given enough time even a solid-like material might flow, or a fluid-like material can act solid when it is deformed rapidly enough.
Flory–Stockmayer theory is a theory governing the cross-linking and gelation of step-growth polymers. [1] The Flory–Stockmayer theory represents an advancement from the Carothers equation, allowing for the identification of the gel point for polymer synthesis not at stoichiometric balance. [1]