Viscoelasticity, linear time-temperature superposition

Time-temperature superposition [10] increases the accessible frequency window of the linear viscoelastic experiments. It applies to stable material states where the extent of reaction is fixed ( stopped samples ). Winter and Chambon [6] and Izuka et al. [121] showed that the relaxation exponent n is independent of temperature and that the front factor (gel stiffness) shifts with temperature... 

In Eq. (4.13) NT is the total number of internal degrees of freedom per unit volume which relax by simple diffusion (NT — 3vN for dilute solutions), and t, is the relaxation time of the ith normal mode (/ = 1,2,3NT) for small disturbances. Equation (4.13), together with a stipulation that all relaxation times have the same temperature coefficient, provides, in fact, the molecular basis of time-temperature superposition in linear viscoelasticity. It also reduces to the expression for the equilibrium shear modulus in the kinetic theory of rubber elasticity when tj = oo for some of the modes. 

Time-temperature superposition was first suggested by H. Leaderman who discovered that creep data can be shifted on the horizontal time scale in order to extrapolate beyond the experimentally measured time frame (9-10). The procedure was shown to be valid for any of the viscoelastic functions measured within the linear viscoelastic range of the polymer. The time-temperature superposition procedure was first explicitly applied to experimental data by... 

Linear Viscoelasticity of Unfractionated Samples. The BP6L and BP6H samples were found to give reproducible data at temperatures below 120°C if first exposed to 150°C for 5 minutes. After such a heat treatment measurements were made on these samples at T = 35, 41, 50, 60, 70, 80, 90, 101, and 120°C. The empirical time-temperature superposition principle (13) was found to be valid for BP6L between 60°C and 120°C and for BP6H between 40°C and 120°C, and was used to make master curves at a reference temperature of 101°C (Figs. 4 and 5). The modulus scale... 

The second important consequence of the relaxation times of all modes having the same temperature dependence is the expectation that it should -bp possible to superimpose linear viscoelastic data taken at different temperatures. This is commonly known as the time-temperature superposition principle. Stress relaxation modulus data at any given temperature Tcan be superimposed on data at a reference temperature Tq using a time scale multiplicative shift factor uj- and a much smaller modulus scale multiplicative shift factor hf. 

Time-temperature superposition also applies to other linear viscoelastic data, with the same shift factors. Two examples are the complex modulus in oscillatory shear,... 

It is now easy to understand why the viscoelastic behavior of filled vulcanizates at large strains is so complex and why it is so difficult to investigate in definitive manner. None of the processes responsible for stress-softening occur instantaneously (16,182), nor can they generally be expected to obey the time-temperature relationships of linear viscoelasticity. Since time-temperature superposition is no longer applicable,... 

Another interesting aspect of linear viscoelasticity is that it can be extended to enable predictions at different temperatures. The basis for this approach is based on a time-temperature superposition principle.This approach has been shown to work well in a restricted temperature range, but does not change the requirement of small strains. 

Validity of Eqs 7.81 and 7.82 was examined for mixtures of entangled, nearly monodispersed blends of poly(ethylene-a/r-propylene) with head-to-head PP [Gell et al., 1997]. The viscoelastic properties compared at constant distance from the glass transition temperature of each system were found to obey the time-temperature superposition principle. The data agreed better with the predictions of Eq 7.82 than Eq 7.81. However, for blends of linear and branched PE the relations 7.82 were found valid only when MW and rheological properties of the two components were similar [Groves et al., 1996]. 

In the following sections we discuss the two superposition principles that are important in the theory of viscoelasticity. The first is the Boltzmann superposition principle, which is concerned with linear viscoelasticity, and the second is time-temperature superposition, which deals with the time-temperature equivalence. 

Fortunately for linear amorphous polymers, modulus is a function of time and temperature only (not of load history). Modulus-time and modulus-temperature curves for these polymers have identieal shapes they show the same regions of viscoelastic behavior, and in each region the modulus values vary only within an order of magnitude. Thus, it is reasonable to assume from such similarity in behavior that time and temperature have an equivalent effect on modulus. Such indeed has been found to be the case. Viscoelastic properties of linear amorphous polymers show time-temperature equivalence. This constitutes the basis for the time-temperature superposition principle. The equivalence of time and temperature permits the extrapolation of short-term test data to several decades of time by carrying out experiments at different temperatures. 

This time-temperature superposition of linear viscoelastic data means that all the retardation times t, of the linear viscoelastic model have a common temperature shift factor a(T)... 

In linear viscoelasticity the stress relaxation test is often used, along with the time-temperature superposition principle and the Boltzmann superposition principle,... 

Non-linear mechanical properties were observed for rubber eomposites and referred to as the Payne effect. The Payne effeet was interpreted as due to filler agglomeration where the filler clusters formed eontained adsorbed rubber. The occluded rubber molecules within filler elusters eould not eontribute to overall elastic properties. The composites behaved similarly to rubber composites with higher filler loading. Uniform and stable filler dispersion is required for rubber composites to exhibit linear viscoelastic behaviour. Payne performed dielectric measurements on SBR vulcanizates containing silica or carbon black. The dielectric data were used to construct time-temperature superposition master curves. The reference temperature increased with crosslinking but not significantly with filler. Comparison of dynamic mechanical and dielectric results for the SBR blended with NR was made and interpreted. ... 

Yu et al. (2011) studied rheology and phase separation of polymer blends with weak dynamic asymmetry ((poly(Me methacrylate)/poly(styrene-co-maleic anhydride)). They showed that the failure of methods, such as the time-temperature superposition principle in isothermal experiments or the deviation of the storage modulus from the apparent extrapolation of modulus in the miscible regime in non-isothermal tests, to predict the binodal temperature is not always applicable in systems with weak dynamic asymmetry. Therefore, they proposed a rheological model, which is an integration of the double reptation model and the selfconcentration model to describe the linear viscoelasticity of miscible blends. Then, the deviatirMi of experimental data from the model predictions for miscible... 

General Regimes of Response. The nonlinear viscoelastic response of polymers, of course, follows some of the same classifications as does the linear response. Hence, the behavior above the glass temperature and into the terminal zone is fluid behavior, and often follows time-temperature superposition. The phenomenology of polymer melts and solutions is commonly described by... 

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