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  • Generalized hydrodynamics  (1)
  • Rheological equation  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 27 (1988), S. 241-254 
    ISSN: 1435-1528
    Keywords: Rheological equation ; dilute polymersolution ; polyelectrolyte ; shear thickening ; polyacrylamide solution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract A mathematical model based on the diffusion-convection equations is used to describe the rheological properties of dilute polymer solutions. The model uses a second-order conformation tensor as a measure of the internal strain; this avoids the mathematical complexity resulting from the use of a more detailed description of the macromolecules and also avoids the necessity of introducing additional ad-hoc assumptions (closure approximations) commonly used in other molecular theories. The rheological equation is obtained in terms of the rate-of-deformation tensor $$\dot \gamma $$ and a scalar functionf(σ) relating the extra stress tensorσ to the internal strain tensorc. The functionf(σ) depends on the physical insight introduced in the Helmholtz free energyA(c) of the solvent-polymer system. This approach is illustrated for an intra-molecular potential of a “FENE-charged” type. The concept of an isotropic, but conformation-dependent, friction coefficient, is also introduced to account for the “coil-stretch” transformation of macromolecules in solution. Viscosity and first normal-stress data, of partially hydrolyzed polyacrylamide solutions, (polyelectrolytes) are analyzed and compared to the model predictions in steady shear and elongational flows.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 21 (1982), S. 1-14 
    ISSN: 1435-1528
    Keywords: Generalized hydrodynamics ; entropy principle ; polymeric liquid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Three generalizations of classical hydrodynamic theories that are compatible with equilibrium thermodynamics and that are suitable for an appropriate macroscopic dynamical theory of polymeric liquids are considered. The strain tensor, the stress tensor and the chain segment distribution function (introduced in the network theory of polymeric liquids) are accepted as new state variables. We find that the generalized hydrodynamic equations are compatible with equilibrium thermodynamics provided certain conditions restricting the freedom of choice of constitutive relations are satisfied. In some particular cases the conditions are known from other considerations. We say that a dynamical theory is compatible with equilibrium thermodynamics, or equivalently, that it obeys the entropy principle if the properties listed in section 2.1 are satisfied.
    Type of Medium: Electronic Resource
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