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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 6972-6981 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Rouse model for dilute polymer solutions undergoing homogeneous flows has been generalized to include the inertia of the beads in the equations of motion. To obtain the correct "diffusion equation'' for the probability density distribution function in phase space, we generalize the diffusion equation derived by Murphy and Aguirre [J. Chem. Phys. 57, 2098 (1972)] from Hamilton's equations of motion for an arbitrary number of interacting Brownian particles at equilibrium. Material functions are found, and the noninertial case is seen to be obtained as the zero mass limit in all steps of the development. In particular, the steady-state shear results are unaffected by the inclusion of inertia. It is also shown how two assumptions, "equilibration in momentum space,'' and the neglect of acceleration, made independently by Curtiss, Bird, and Hassager in their phase-space kinetic theory, are actually the result of assuming zero mass.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 4917-4927 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Curtiss–Bird model of polymer melts has been extended to include polydisperse mixtures. The formula for the stress tensor derived in the last paper is used here to give explicit expressions for material functions in shear and elongational flow. Predictions are shown for viscosity, first normal stress coefficient, elongational stress growth viscosity, and steady elongational viscosity for Flory–Schulz and log–normal molecular weight distributions. It is also shown how generalizations that are observed experimentally for viscosity are predicted by the Curtiss–Bird model. In the next paper, these calculations are compared with experimental data.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 4928-4936 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The modification to the Curtiss–Bird model to account for polydispersity is used to compare predictions of several material functions to experimental data. The data were taken from samples of polymer melts and concentrated solutions with two types of molecular weight distributions, log-normal and Flory–Schulz. The Curtiss–Bird model is also compared to predictions of the Doi–Edwards model for viscosity of polydisperse samples. Experimental data for first normal stress coefficient, elongational stress growth viscosity, and steady elongational viscosity were also compared to the predictions of the Curtiss–Bird model. In all cases, the best fit to the experimental data were found for nonzero values of the link tension coefficient ε. It is found that HDPE η¯ data (and η¯+ data) can be fit by ε(approximately-equal-to)0.05, a value of ε that is low enough to predict rod dipping for this material.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 6965-6969 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Anisotropic thermal diffusivity is examined in a cross-linked silicone elastomer deformed in simple elongation. Thermal diffusivity both parallel and perpendicular to the stretch direction is measured using an optical technique called forced Rayleigh scattering. The thermal diffusivity is found to increase linearly with stretch ratio to a value 10% larger than the equilibrium value for a stretch ratio of two. Measurements of the birefringence and tensile stress were used to evaluate the stress-optic rule, which was found to be valid. The difference between measured thermal diffusivities parallel and perpendicular to the stretch direction and tensile stress data were used to show the thermal conductivity and stress tensors are linearly related. These data appear to be the first direct evaluation of the stress-thermal rule in a deformed polymeric material. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-1528
    Keywords: Key words Reptation model ; stochastic simulations ; full chain dynamics ; independent alignment approximation ; linear response ; theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract A reptation model for the primitive chain that does not assume independent alignment or consistent-averaging for the retraction process, or equilibrium relaxation for the reptation process is proposed and compared to the analytical expressions of Doi and Edwards in single-step, double-step strains and steady-state shear flow. The Doi and Edwards model with independent alignment approximation underpredicts the magnitude of the relaxation modulus by 25%, and consistently overpredicts the magnitude of the damping function; for steady shear flow, it predicts the correct shape for the steady-state viscosity and the first normal stress difference coefficient, although the magnitude is incorrect. The analytical expressions of Doi and Edwards without independent alignment approximation are excellent approximations to the damping function. In double-step strains, the expressions of Doi assuming consistent averaging, but no independent alignment, predict well the stress decay following the second strain. Linear response theory is found to be invalid for describing the stress relaxation following single-step strain for the models considered. Similar to the Doi and Edwards model, no overshoot for the first normal stress difference is observed for the simulation model. Unlike the Doi equation derived without the independent alignment approximation but restricted to double-step strains, the simulation model proposed here can be easily generalized to complex flow fields. No contour length fluctuation or constraint release is considered in this model, and chain retraction is assumed to be instantaneous.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1401-1417 
    ISSN: 0887-6266
    Keywords: polyelectrolytes ; Brownian dynamics ; shear flow ; extensional flow ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The conformational and rheological dynamics of dilute solutions of polyelectrolyte macromolecules undergoing shear and extensional flow are modeled using Nonequilibrium Brownian Dynamics (NEBD) and Configuration-Biased Monte Carlo (CBMC) simulations. The mathematical model utilizes a bead-spring chain with charged beads that interact through a screened Debye-Hückel potential, and that also interact through stretching and bending forces. The diffusion (or Fokker-Planck) equation for the probability density of the positions of the beads of the chain is converted to a Stochastic Differential Equation (SDE), from which the simulation algorithm for the NEBD is obtained. The CBMC is used in the initial chain generation and in determining steady-state properties in elongational flows. Various conformational and rheological quantities, such as the stress and birefringence, are monitored, under both steady-state and transient conditions, with the primary independent variable being the salt concentration (parametrized through the Debye length) and the strength of interaction q, related to the degree of ionization of the chain. It is found that this model is able to describe qualitatively many of the experimentally observed features in such systems. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1401-1417, 1998
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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