Viscoelasticity Newtonian

On some time scale, all liquids display viscoelasticity. Newtonian liquids like water have viscosity independent of shear rate over ordinary ranges of measurement (10 s < 7 < 10 s ). Dielectric spectroscopy reveals that water molecules respond to an oscillating electric field at a frequency of 17 GHz at room temperature. Hence, at shear rates of order 10 s water would be expected to be viscoelastic, and have a shear thinning apparent viscosity. 

Polymers owe much of their attractiveness to their ease of processing. In many important teclmiques, such as injection moulding, fibre spinning and film fonnation, polymers are processed in the melt, so that their flow behaviour is of paramount importance. Because of the viscoelastic properties of polymers, their flow behaviour is much more complex than that of Newtonian liquids for which the viscosity is the only essential parameter. In polymer melts, the recoverable shear compliance, which relates to the elastic forces, is used in addition to the viscosity in the description of flow [48]. 

Material parameters defined by Equations (1.11) and (1.12) arise from anisotropy (i.e. direction dependency) of the microstructure of long-chain polymers subjected to liigh shear deformations. Generalized Newtonian constitutive equations cannot predict any normal stress acting along the direction perpendicular to the shearing surface in a viscometric flow. Thus the primary and secondary normal stress coefficients are only used in conjunction with viscoelastic constitutive models. 

All of the described differential viscoelastic constitutive equations are implicit relations between the extra stress and the rate of deformation tensors. Therefore, unlike the generalized Newtonian flows, these equations cannot be used to eliminate the extra stress in the equation of motion and should be solved simultaneously with the governing flow equations. 

The practical and computational complications encountered in obtaining solutions for the described differential or integral viscoelastic equations sometimes justifies using a heuristic approach based on an equation proposed by Criminale, Ericksen and Filbey (1958) to model polymer flows. Similar to the generalized Newtonian approach, under steady-state viscometric flow conditions components of the extra stress in the (CEF) model are given a.s explicit relationships in terms of the components of the rate of deformation tensor. However, in the (CEF) model stress components are corrected to take into account the influence of normal stresses in non-Newtonian flow behaviour. For example, in a two-dimensional planar coordinate system the components of extra stress in the (CEF) model are written as... 

Johnson, M. W. and Segalman, D., 1977. A model for viscoelastic fluid behaviour which allows non-affine deformation. J. Non-Newtonian Fluid Mech. 2, 255-270. 

As already discussed, in general, polymer flow models consist of the equations of continuity, motion, constitutive and energy. The constitutive equation in generalized Newtonian models is incorporated into the equation of motion and only in the modelling of viscoelastic flows is a separate scheme for its solution reqixired. 

Application of the weighted residual method to the solution of incompressible non-Newtonian equations of continuity and motion can be based on a variety of different schemes. Tn what follows general outlines and the formulation of the working equations of these schemes are explained. In these formulations Cauchy s equation of motion, which includes the extra stress derivatives (Equation (1.4)), is used to preseiwe the generality of the derivations. However, velocity and pressure are the only field unknowns which are obtainable from the solution of the equations of continuity and motion. The extra stress in Cauchy s equation of motion is either substituted in terms of velocity gradients or calculated via a viscoelastic constitutive equation in a separate step. 

Luo, X. L, and Tanner, R. L, 1989. A decoupled finite element streamline-upwind scheme for viscoelastic flow problems. J. Non-Newtonian Fluid Mech. 31, 143-162. 

Marchal, J. M. and Crochet, M.J., 1987. A new mixed finite element for calculating viscoelastic flow. J. Non-Newtonian Pluid Mech. 20, 77-114. 

In generalized Newtonian fluids, before derivation of the final set of the working equations, the extra stress in the expanded equations should be replaced using the components of the rate of strain tensor (note that the viscosity should also be normalized as fj = rj/p). In contrast, in the modelling of viscoelastic fluids, stress components are found at a separate step through the solution of a constitutive equation. This allows the development of a robust Taylor Galerkin/ U-V-P scheme on the basis of the described procedure in which the stress components are all found at time level n. The final working equation of this scheme can be expressed as... 

For some materials the linear constitutive relation of Newtonian fluids is not accurate. Either stress depends on strain in a more complex way, or variables other than the instantaneous rate of strain must be taken into account. Such fluids are known collectively as non-Newtonian. Many different types of behavior have been observed, ranging from fluids for which the viscosity in the Navier-Stokes equation is a simple function of the shear rate to the so-called viscoelastic fluids, for which the constitutive equation is so different that the normal stresses can cause the fluid to flow in a manner opposite to that predicted for a Newtonian fluid. 

Viscous Hquids are classified based on their rheological behavior characterized by the relationship of shear stress with shear rate. Eor Newtonian Hquids, the viscosity represented by the ratio of shear stress to shear rate is independent of shear rate, whereas non-Newtonian Hquid viscosity changes with shear rate. Non-Newtonian Hquids are further divided into three categories time-independent, time-dependent, and viscoelastic. A detailed discussion of these rheologically complex Hquids is given elsewhere (see Rheological measurements). 

The mechanical properties of LDPE fall somewhere between rigid polymers such as polystyrene and limp or soft polymers such as polyvinyls. LDPE exhibits good toughness and pHabiUty over a moderately wide temperature range. It is a viscoelastic material that displays non-Newtonian flow behavior, and the polymer is ductile at temperatures well below 0°C. Table 1 fists typical properties. 

Colloidal State. The principal outcome of many of the composition studies has been the delineation of the asphalt system as a colloidal system at ambient or normal service conditions. This particular concept was proposed in 1924 and described the system as an oil medium in which the asphaltene fraction was dispersed. The transition from a coUoid to a Newtonian Hquid is dependent on temperature, hardness, shear rate, chemical nature, etc. At normal service temperatures asphalt is viscoelastic, and viscous at higher temperatures. The disperse phase is a micelle composed of the molecular species that make up the asphaltenes and the higher molecular weight aromatic components of the petrolenes or the maltenes (ie, the nonasphaltene components). Complete peptization of the micelle seems probable if the system contains sufficient aromatic constituents, in relation to the concentration of asphaltenes, to allow the asphaltenes to remain in the dispersed phase. 

Rheological Properties. Materials must have suitable flow properties in order to be used in production. Both Newtonian and non-Newtonian fluids and their viscoelasticity properties play a critical role in the performance of the embedding materials. 

Eig. 7. Viscoelastic behavior of encapsulant materials (a) Newtonian fluid (b) non-Newtonian fluid. 

Though experimental data on suspensions of fibers in Newtonian dispersion media give more or less regular picture, a transition to non-Newtonian viscoelastic liquids, as Metzner noted [21], makes the whole picture far or less clear. Probably, the possibility to make somewhat general conclusions on a longitudinal flow of suspensions in polymer melts requires first of all establishing clear rules of behavior of pure melts at uniaxial extension this problem by itself has no solution as yet. 

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