Peessure intensification on the front of a shock wave propagating in a heterogeneous system

An increase in pressure in the wave front as compared to the pulse initiating the wave has been observed experimentally in a study of shock-wave propagation in aqueous suspensions of bentonite [1]. In suspensions in which the solid phase is in the form of colloidal size particles =10^–7–10^–8 m of the mineral montmorillonite with mass content c=6%, with multishock loading an intensification of this effect from experiment to experiment was observed [2]. In order to study the principles involved in this anomalous intensification of pressure on the shock wave front, as well as to clarify the effect of the nature of the material in the dispersed phase, experiments were performed with particles of another broad class of clay-like minerals — kaolinite.Translated from Zhurnal Prikladnoi Mekhaniki i Tekhnicheskoi Fiziki, No. 5, pp. 86–92, September–October, 1986.     

Some general rheological properties of dilute polymer solutions predicted from intrinsic viscosity measurements

Expressions for the rheological properties of dilute polymer solutions at low and moderate deformation rates are established through the computation and analysis of exact Zimm's eigenvalues. It is shown that they can be expressed in terms of measurable parameters from intrinsic viscosity data. Under moderate deformation rates one needs to introduce a slippage between the solvent and the smoothed polymer to be able to describe shear-thinning behaviour.     

Rheology of concentrated coagulating suspensions in non-aqueous media

The rheology of concentrated coagulating suspensions is analysed on the basis of the following model: (i) at low shear rates, the shear is not distributed homogeneously but limited to certain shear planes; (ii) the energy dissipation during steady flow is due primarily to the overcoming of viscous drag by the suspended particles during motion caused by encounters of particles in the shear planes. This model is called the giant floc model.With increasing shear rate the distance between successive shear planes diminishes, approaching the suspended particles' diameter at average shear stresses of 88–117 Pa in suspensions of 78 µm particles (glass ballotini coated by a hydrophobic layer) in glycerol — water mixtures, at solid volume fractions between 0.35 and 0.40. Smaller particles form a more persistent coagulation structure. The average force necessary to separate two touching 78 µm particles is too large to be accounted for by London-van der Waels forces; thus coagulation is attributed to bridging connections between polymer chains protruding from the hydrophobic coatings.The frictional ratio of the glass particles in these suspensions is of the order of 10. Coagulation leads to build-up of larger structural units at lower shear rates; on doubling the shear rate the average distance between the shear planes decreases by a factor of 0.81 to 0.88. A inter-shear plane distance - A Hamaker constant - b radius of primary particles - f frictional ratio - F _A attractive force between two particles - g acceleration due to gravity - H distance between the surfaces of two particles - K proportionality constant in power law - l fraction of distance by which a moving particle entrains its neighbours - l effective length of inner cylinder in the rheometer - M torque experienced by inner cylinder during measurements - n exponent in power law - n ₀ ,n ₁ ,n ₂ constants in extended power law - NC _hex number of contacts, per mm², between particles in adjacent layers with an average degree of occupation, assuming a hexagonal arrangement of the particles within the layers - NC _cub asNC _hex, but with a cubical arrangement - p () d increase of slippage probability when the shear stress increases from to + d - q average coordination number of a particle in a coagulate - R _i radius of inner cylinder of rheometer - R _u radius of outer cylinder of rheometer - t _i time during which particlei moves - t ₀ time during which a particle bordering a shear plane moves from its rectilinear course, on meeting another particle - u angle between the direction of motion, and the line connecting the centers of two successive particles bordering a shear plane - V _A attractive energy between two particles - x, y, z Cartesian coordinates:x — the direction of motion;y — the direction of the velocity gradient - y ₀ ,z ₀ y, z value of a particle meeting another particle, when both are far removed from each other - y ₀ spread iny ₀ values - —2/n - ₀ capture efficiency - shear rate - average shear rate calculated for a Newtonian liquid - _i distance by which particlei moves - ₀ distance by which a particle bordering a shear plane moves from its rectilinear course, when it encounters another particle - square root of area occupied by a particle bordering a shear plane, in this plane - _c energy dissipated during one encounter of two particles bordering a shear plane - _p energy dissipated by one particle - energy dissipated per unit of volume and time during steady flow - viscosity - _app calculated as if the liquid is Newtonian - ₀ viscosity of suspension medium - _PL lim - [] intrinsic viscosity - _diff - _{diff, rel diff}/ ₀ - standard deviation of distribution ofy ₀ values - shear stress - _n average shear stress at the highest values applied - mass average particle diameter - _n number average particle diameter - solid volume fraction - _eff effective solid volume fraction in Dougherty-Krieger relation - _max maximum solid volume fraction permitting flow - _i angular velocity of inner cylinder in rheometer during measurements     

On surface waves in generalized thermoelasticity

Knowles' representation theorem for harmonically time-dependent free surface waves on a homogeneous, isotropic elastic half-space is extended to include harmonically time-dependent free processes for thermoelastic surface waves in generalized thermoelasticity of Lord and Shulman and of Green and Lindsay.r , , r , , .This work was done when author was unemployed.     

A dynamic slip velocity model for molten polymers based on a network kinetic theory

In this paper the slip phenomenon is considered as a stochastic process where the polymer segments (taken as Hookean springs) break off the wall due to the excessive tension imposed by the bulk fluid motion. The convection equation arising in network theories is solved for the special case of a polymer/wall interface to determine the time evolution of the configuration distribution function (Q, t). The stress tensor and the slip velocity are calculated by averaging the proper relations over a large number of polymer segments. Due to the fact that the model is probabilistic and time dependent, dynamic slip velocity calculations become possible for the first time and therefore some new insight is gained on the slip phenomenon. Finally, the model predictions are found to match macroscopic experimental data satisfactorily.Nomenclature rate of creation of polymer segments - g(Q) constant of rate of creation of polymer segments - rate of loss of polymer segments - h(Q) constant of rate of loss of polymer segments - h(Q) constant of rate of loss of polymer segments due to destruction of its B-link - H Hookean spring constant - k Boltzmann's constant - n unit vector normal to the polymer/wall interface - n ₀ number density of polymer segments - n ₀ surface number density of polymer segments - Q vector defining the size and orientation of a polymer segment - Q ^* critical length of a segment beyond which the tension may overcome the W _adh - t time - t _h howering time of broken polymer segments - T absolute temperature - W _adh work of adhesion Greek Letters _n nominal strain - strain - _n nominal shear rate - shear rate - dimensionless constant in the expressions of h(Q), g(Q) - viscosity - ^T velocity gradient tensor - ₀ time constant - standard deviation of vectors Q at equilibrium - _w wall shear stress - stress tensor - ₀ equilibrium configuration distribution function of Q - configuration distribution function of Q     

The dynamic performance of the Weissenberg rheogoniometer III. Large amplitude oscillatory shearing — harmonic analysis

The harmonic content of the nonlinear dynamic behaviour of 1% polyacrylamide in 50% glycerol/water was studied using a standard Model R 18 Weissenberg Rheogoniometer. The Fourier analysis of the Oscillation Input and Torsion Head motions was performed using a Digital Transfer Function Analyser.In the absence of fluid inertia effects and when the amplitude of the (fundamental) Oscillation Input motion _I is much greater than the amplitudes of the Fourier components of the Torsion Head motion _Tn empirical nonlinear dynamic rheological propertiesG _n (, ⁰),G _n (, ⁰) and/or _n (, ⁰), _n (, ⁰) may be evaluated without a-priori-knowledge of a rheological constitutive equation. A detailed derivation of the basic equations involved is presented.Cone and plate data for the third harmonic storage modulus (dynamic rigidity)G ₃ (, ⁰), loss modulusG ₃ (, ⁰) and loss angle ₃ (, ⁰) are presented for the frequency range 3.14 × 10^–2 1.25 × 10² rad/s at two strain amplitudes, _CP ⁰ = 2.27 and 4.03. Composite cone and plate and parallel plates data for both the third and fifth harmonic dynamic viscosities ₃ (, ⁰), _S (, ⁰) and dynamic rigiditiesG ₃ (, ⁰),G ₅ (, ⁰) are presented for strain amplitudes in the ranges 1.10 _CP ⁰ 4.03 and 1.80 _PP ⁰ 36 for a single frequency, = 3.14 × 10^–1 rad/s. Good agreement was obtained between the results from both geometries and the absence of significant fluid inertia effects was confirmed by the superposition of the data for different gap widths.     

Determination of permeability tensors for two-phase flow in homogeneous porous media: Theory

In this paper we continue previous studies of the closure problem for two-phase flow in homogeneous porous media, and we show how the closure problem can be transformed to a pair of Stokes-like boundary-value problems in terms of pressures that have units of length and velocities that have units of length squared. These are essentially geometrical boundary value problems that are used to calculate the four permeability tensors that appear in the volume averaged Stokes' equations. To determine the geometry associated with the closure problem, one needs to solve the physical problem; however, the closure problem can be solved using the same algorithm used to solve the physical problem, thus the entire procedure can be accomplished with a single numerical code.Nomenclature a a vector that maps V onto , m^-1. - A a tensor that maps V onto . - A area of the - interface contained within the macroscopic region, m². - A area of the -phase entrances and exits contained within the macroscopic region, m². - A area of the - interface contained within the averaging volume, m². - A area of the -phase entrances and exits contained within the averaging volume, m². - Bo Bond number (= (=(–)g²/). - Ca capillary number (= v/). - g gravitational acceleration, m/s². - H mean curvature, m^-1. - I unit tensor. - permeability tensor for the -phase, m². - viscous drag tensor that maps V onto V. - ^* dominant permeability tensor that maps onto v , m². - ^* coupling permeability tensor that maps onto v , m². - characteristic length scale for the -phase, m. - l characteristic length scale representing both and , m. - L characteristic length scale for volume averaged quantities, m. - n unit normal vector directed from the -phase toward the -phase. - n unit normal vector representing both n and n . - n unit normal vector representing both n and n . - P pressure in the -phase, N/m². - p superficial average pressure in the -phase, N/m². - p intrinsic average pressure in the -phase, N/m². - p –p , spatial deviation pressure for the -phase, N/m². - r ₀ radius of the averaging volume, m. - r position vector, m. - t time, s. - v fluid velocity in the -phase, m/s. - v superficial average velocity in the -phase, m/s. - v intrinsic average velocity in the -phase, m/s. - v –v , spatial deviation velocity in the -phase, m/s. - V volume of the -phase contained within the averaging volmue, m³. - averaging volume, m³. Greek Symbols V /, volume fraction of the -phase. - viscosity of the -phase, Ns/m². - density of the -phase, kg/m³. - surface tension, N/m. - (v +v ^T ), viscous stress tensor for the -phase, N/m².     

Comparison of a new internal viscosity model with other constrained-connector theories of dilute polymer solution rheology

Complex viscosity ^* = -i predictions of the Dasbach-Manke-Williams (DMW) internal viscosity (IV) model for dilute polymer solutions, which employs a mathematically rigorous formulation of the IV forces, are examined in the limit of infinite IV over the full range of frequency number of submolecules N, and hydrodynamic interaction h ^*. Although the DMW model employs linear entropic spring forces, infinite IV makes the submolecules rigid by suppressing spring deformations, thereby emulating the dynamics of a freely jointed chain of rigid links. The DMW () and () predictions are in close agreement with results for true freely jointed chain models obtained by Hassager (1974) and Fixman and Kovac (1974 a, b) with far more complicated formalisms. The infinite-frequency dynamic viscosity predicted by the DMW infinite-IV model is also found to be in remarkable agreement with the calculations of Doi et al. (1975). In contrast to the other freely jointed chain models cited above, however, the DMW model yields a simple closed-form solution for complex viscosity expressed in terms of Rouse-Zimm relaxation times.     

Transport in ordered and disordered porous media V: Geometrical results for two-dimensional systems

In this paper we continue the geometrical studies of computer generated two-phase systems that were presented in Part IV. In order to reduce the computational time associated with the previous three-dimensional studies, the calculations presented in this work are restricted to two dimensions. This allows us to explore more thoroughly the influence of the size of the averaging volume and to learn something about the use of anon-representative region in the determination of averaged quantities.

Nomenclature

Roman Letters A interfacial area of the– interface associated with the local closure problem, m² - a _i i=1, 2, gaussian probability distribution used to locate the position of particles - l unit tensor - characteristic length for the-phase particles, m - ⁰ reference characteristic length for the-phase particles, m - characteristic length for the-phase, m - _i i=1,2,3 lattice vectors, m - m convolution product weighting function - m _V special convolution product weighting function associated with a unit cell - n _i i=1, 2 integers used to locate the position of particles - n unit normal vector pointing from the-phase toward the-phase - r _p position vector locating the centroid of a particle, m - r gaussian probability distribution used to determine the size of a particle, m - r ₀ characteristic length of an averaging region, m - V averaging volume, m³ - V volume of the-phase contained in the averaging volume,V, m³ - x position of the centroid of an averaging area, m - x ₀ reference position of the centroid of an averaging area, m - y position vector locating points in the-phase relative to the centroid, m Greek Letters V /V, volume average porosity - _{a i} standard deviation ofa _i - _r standard deviation ofr - intrinsic phase average of      

The rheology of suspensions of vinylon fibers in polymer liquids. II. Suspensions in polymer solutions

Summary The rheological properties of vinylon fiber suspensions in polymer solutions were studied in steady shear flow. Shear viscosity, first normal-stress difference, yield stress, relative viscosity, and other properties were discussed. Three kinds of flexible vinylon fibers of uniform length and three kinds of polymer solutions as mediums which exhibited remarkable non-Newtonian behaviors were employed. The shear viscosity and relative viscosity ( _r ) increased with the fiber content and the aspect ratio, and depended upon the shear rate. Shear rate dependence of _r was found only in the low shear rate region. This result was different from that of vinylon fiber suspensions in Newtonian fluids. The first normal-stress difference increased at first slightly with increasing fiber content but rather decreased and showed lower values for high content suspensions than that of the medium. A yield stress could be determined by using a modified equation of Casson type. The flow properties of the fiber suspensions depended on the viscosity of the medium in the suspensions under consideration.With 16 figures and 1 table     

Rheological behaviour of two-phase flow of solid particles in a gas

The present investigation was concerned with the rheological behaviour of dilute suspensions of solid particles in a gas in a vertical cocurrent flow moving upwards. Starting from the experimentally determined dependence of the pressure drop on the concentration of solid particles and the Reynolds number of the carrier medium in the steady flow region, the rheological parameters were estimated using pseudo-shear diagrams. Air was the carrier medium and the dispersed phase was one of six fractions of polypropylene powder and five fractions of glass ballotini. The results show that the investigated two-phase systems have pseudoplastic character which becomes more pronounced with increases in concentration, equivalent diameter and density of solid particles in the flowing suspension. C _d coefficient of particle resistance - d _e equivalent diameter of particles - D column diameter - Fr Froude number - g gravitational acceleration - K rheological parameter - L length - n rheological parameter - p _t pressure drop due to friction - p _m total pressure drop - p _ag pressure drop due to acceleration of the gas phase - p _as pressure drop due to acceleration of the solid phase - p _g hydrostatic pressure of the gas phase - p _s specific effective weight of the dispersed phase - r radius - Re Reynolds number - Re _p Reynolds number of a particle - Re _G generalized Reynolds number - Re _G1 generalized Reynolds number relating to the end of the laminar flow region - Re _G2 generalized Reynolds number relating to the beginning of the turbulent flow region - w _z axial component of velocity - u _t steady free-fall velocity of a single particle - w average velocity - w _g average velocity of the gas phase - w _s average velocity of the dispersed phase of solid particles - relative mass fraction of solid particles - x _s volume fraction of solid particles - _g coefficient of pressure drop due to friction - µ dynamic viscosity - _g density of the gas phase - _m density of the suspension - _s density of solid particles - _ds density of the dispersed phase - _w shear stress at the wall     

Hydrodynamic models as applied to the investigation of magnetic plasma stability

In the present paper magnetohydrodynamic models are employed to investigate the stability of an inhomogeneous magnetic plasma with respect to perturbations in which the electric field may be regarded as a potential field (rot E 0). A hydrodynamic model, actually an extension of the well-known Chew-Goldberg er-Low model [1], is used to investigate motions transverse to a strong magnetic field in a collisionless plasma. The total viscous stress tensor is given; this includes, together with magnetic viscosity, the so-called inertial viscosity.Ordinary two-fluid hydrodynamics is used in the case of strong collisions=. It is shown that the collisional viscosity leads to flute-type instability in the case when, collisions being neglected, the flute mode is stabilized by a finite Larmor radius. A treatment is also given of the case when epithermal high-frequency oscillations (not leading immediately to anomalous diffusion) cause instability in the low-frequency (drift) oscillations in a manner similar to the collisional electron viscosity, leading to anomalous diffusion.Notation f particle distribution function - E electric field component - H₀ magnetic field - density - V particle velocity - e charge - m, M electron and ion mass - _i, _e ion and electron cyclotron frequencies - viscous stress tensor - P pressure - r_i Larmor radius - P pressure tensor - t time - frequency - T temperature - collision frequency - collision time - j current density - _i, _e ion and electron drift frequencies - k_x, k_y, k_z wave-vector components - n₀ particle density - g acceleration due to gravity. The authors are grateful to A. A. Galeev for valuable discussion.     

Flow in porous media II: The governing equations for immiscible,two-phase flow

The Stokes flow of two immiscible fluids through a rigid porous medium is analyzed using the method of volume averaging. The volume-averaged momentum equations, in terms of averaged quantities and spatial deviations, are identical in form to that obtained for single phase flow; however, the solution of the closure problem gives rise to additional terms not found in the traditional treatment of two-phase flow. Qualitative arguments suggest that the nontraditional terms may be important when / is of order one, and order of magnitude analysis indicates that they may be significant in terms of the motion of a fluid at very low volume fractions. The theory contains features that could give rise to hysteresis effects, but in the present form it is restricted to static contact line phenomena.Roman Letters (, = , , and ) A interfacial area of the- interface contained within the macroscopic system, m² - A _e area of entrances and exits for the -phase contained within the macroscopic system, m² - A interfacial area of the- interface contained within the averaging volume, m² - A ^* interfacial area of the- interface contained within a unit cell, m² - A _e ^* area of entrances and exits for the-phase contained within a unit cell, m² - g gravity vector, m²/s - H mean curvature of the- interface, m^–1 - H area average of the mean curvature, m^–1 - H – H , deviation of the mean curvature, m^–1 - I unit tensor - K Darcy's law permeability tensor, m² - K permeability tensor for the-phase, m² - K viscous drag tensor for the-phase equation of motion - K viscous drag tensor for the-phase equation of motion - L characteristic length scale for volume averaged quantities, m - characteristic length scale for the-phase, m - n unit normal vector pointing from the-phase toward the-phase (n = –n ) - p _c p – P , capillary pressure, N/m² - p pressure in the-phase, N/m² - p intrinsic phase average pressure for the-phase, N/m² - p – p , spatial deviation of the pressure in the-phase, N/m² - r ₀ radius of the averaging volume, m - t time, s - v velocity vector for the-phase, m/s - v phase average velocity vector for the-phase, m/s - v intrinsic phase average velocity vector for the-phase, m/s - v – v , spatial deviation of the velocity vector for the-phase, m/s - V averaging volume, m³ - V volume of the-phase contained within the averaging volume, m³ Greek Letters V /V, volume fraction of the-phase - mass density of the-phase, kg/m³ - viscosity of the-phase, Nt/m² - surface tension of the- interface, N/m - viscous stress tensor for the-phase, N/m² - / kinematic viscosity, m²/s     

Flow in porous media I: A theoretical derivation of Darcy's law

Stokes flow through a rigid porous medium is analyzed in terms of the method of volume averaging. The traditional averaging procedure leads to an equation of motion and a continuity equation expressed in terms of the volume-averaged pressure and velocity. The equation of motion contains integrals involving spatial deviations of the pressure and velocity, the Brinkman correction, and other lower-order terms. The analysis clearly indicates why the Brinkman correction should not be used to accommodate ano slip condition at an interface between a porous medium and a bounding solid surface.The presence of spatial deviations of the pressure and velocity in the volume-averaged equations of motion gives rise to aclosure problem, and representations for the spatial deviations are derived that lead to Darcy's law. The theoretical development is not restricted to either homogeneous or spatially periodic porous media; however, the problem ofabrupt changes in the structure of a porous medium is not considered.Roman Letters A interfacial area of the - interface contained within the macroscopic system, m² - A _e area of entrances and exits for the -phase contained within the macroscopic system, m² - A interfacial area of the - interface contained within the averaging volume, m² - A ^* interfacial area of the - interface contained within a unit cell, m² - Ae area of entrances and exits for the -phase contained within a unit cell, m² - B second order tensor used to represent the velocity deviation (see Equation (3.30)) - b vector used to represent the pressure deviation (see Equation (3.31)), m^–1 - d distance between two points at which the pressure is measured, m - g gravity vector, m/s² - K Darcy's law permeability tensor, m² - L characteristic length scale for volume averaged quantities, m - characteristic length scale for the -phase (see Figure 2), m - characteristic length scale for the -phase (see Figure 2), m - n unit normal vector pointing from the -phase toward the -phase (n =–n ) - n _e unit normal vector for the entrances and exits of the -phase contained within a unit cell - p pressure in the -phase, N/m² - p intrinsic phase average pressure for the -phase, N/m² - p –p , spatial deviation of the pressure in the -phase, N/m² - r ₀ radius of the averaging volume and radius of a capillary tube, m - v velocity vector for the -phase, m/s - v phase average velocity vector for the -phase, m/s - v intrinsic phase average velocity vector for the -phase, m/s - v –v , spatial deviation of the velocity vector for the -phase, m/s - V averaging volume, m³ - V volume of the -phase contained within the averaging volume, m³ Greek Letters V/V, volume fraction of the -phase - mass density of the -phase, kg/m³ - viscosity of the -phase, Nt/m² - arbitrary function used in the representation of the velocity deviation (see Equations (3.11) and (B1)), m/s - arbitrary function used in the representation of the pressure deviation (see Equations (3.12) and (B2)), s^–1     

Fractal-time stochastic processes and dynamic functions of polymeric systems

Dynamic material functions of polymeric systems are calculated via a defect-diffusion model. The random motion of defects is modelled by a fractaltime stochastic process. It is shown that the dynamic functions of polymeric solutions can be approximated by the defect-diffusion process of the mixed type. The relaxation modulus of Kohlrausch type is obtained for a fractal-time defect-diffusion process, and it is shown that this modulus is capable of portraying the dynamic behavior of typical viscoelastic solutions.The Fourier transforms of the Kohlrausch function are calculated to obtain and. A three-parameter model for and is compared with the previous calculations. Experimental measurements for five polymer solutions are compared with model predictions. D rate of deformation tensor - G(t) mechanical relaxation modulus - H relaxation spectrum - I(t) flux of defects - P _n (s) probability of finding a walker ats aftern-steps - P generating function ofP _n (s) - s(t) fraction of surviving defects - , () gamma function (incomplete) - ₀ zero shear viscosity - ^* () complex viscosity - frequency - t _n n-th moment - F[] Fourier transform - f ^* (u) Laplace transform off(t) - , components of ^* - G _f, _f ^* fractional model - G ₃, ₃ ^* three parameter model - complex conjugate ofz - material time derivative ofD     

Temperature and concentration dependent viscosity and gelation temperature of ABA triblock copolymer solutions

In solutions of ABA-triblock copolymers in a poor solvent for A thermoreversible gelation can occur. A three-dimensional dynamic network may form and, given the polymer and the solvent, its structure will depend on temperature and polymer mass fraction. The zero-shear rate viscosity of solutions of the triblock-copolymer polystyrene-polyisoprene-polystyrene in n-tetradecane was measured as a function of temperature and polymer mass fraction, and analyzed; the polystyrene blocks contained about 100 monomers, the polyisoprene blocks about 2000 monomers. Empirically, in the viscosity at constant mass fraction plotted versus inverse temperature, two contributions could be discerned; one contribution dominating at high and the other one dominating at low temperatures. In a comparison with theory, the contribution dominating at low temperatures was identified with the Lodge transient network viscosity; some questions remain to be answered, however. An earlier proposal for defining the gelation temperature T _gel is specified for the systems considered, and leads to a gelation curve; T _gel as a function of polymer mass fraction.Mathematical symbols {} functional dependence; e.g., f{x} means f is a function of x - p _log logarithm to the base number p; e.g., ¹⁰log is the common logarithm - exp exponential function with base number e - sin trigonometric sine function - lim limit operation - – in integral sign: Cauchy Principal Value of integral, e.g., - derivative to x - partial derivative to x Latin symbols dimensionless constant - b constant with dimension of absolute temperature - constant with dimension of absolute temperature - B dimensionless constant - c mass fraction - dimensionless constant - constant with dimension of absolute temperature - d ^* dimensionless constant - D{0} constant with dimension of absolute temperature - e base number of natural (or Naperian) logarithm - g distribution function of inverse relaxation times - G relaxation strength relaxation function - h distribution function of relaxation times reaction constant enthalpy of a molecule - H Heaviside unit step function - i complex number defined by i ² = –1 - j{0} constant with dimension of viscosity - j index number - k Boltzmann's constant - k _H Huggins' coefficient - m mass of a molecule - n number - N number - p index number - s entropy of a molecule - t time - T absolute temperature Greek symbols as index: type of polymer molecule - as index: type of polymer molecule - shear as index: type of polymer molecule - shear rate - small variation; e.g. T is a small variation in T relative deviation Dirac delta distribution as index: type of polymer molecule - difference; e.g. is a difference in chemical potential - constant with dimension of absolute temperature - (complex) viscosity - constant with dimension of viscosity - [] intrinsic viscosity number - inverse of relaxation time - chemical potential - number pi; circle circumference divided by its diameter - mass per unit volume - relaxation time shear stress - angular frequency     

Comportement rhéologique de sols d'acide polysilicique.

Résumé Le comportement rhéologique de sols d'acide silicique a été examiné au cours du temps à des pH compris entre 6 et 8 à la concentration de 10 g 1^–1 de silice, et à pH = 8 à des concentrations variant entre 0,5 et 10 g 1^–1. Les courbes d'écoulement révélent un comportement rhéologique complexe. L'analyse des rhéogrammes en fonction du temps, du pH et de la concentration contribue à la connaissance de l'état structural du polymère au cours de la formation du gel. Il ressort que le comportement initialement rhéoépaississant aux faibles concentrations correspondant à l'état d'une solution colloïdale, laisse place à un écoulement rhéofluidifiant dans les conditions favorables á la polymérisation de l'acide silicique. La transition sol-gel est marquée par un breakpoint; en prolongeant les mesures on observe un comportement plastique dû à l'apparition d'agrégats sous l'effet du cisaillement. Tous les processus rhéologiques se trouvent exacerbées à pH = 8.

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The rheological behaviour of silicic acid in aqueous solutions was studied over a period of time for pH values between 6 and 8 at the concentration 10 g 1^–1, and at pH = 8 for different concentrations varying from 0.5 to 10 g 1^–1. The shear stress-shear rate curves indicate a very complex character of rheological behaviour. Its analysis with respect to the influence of time, pH and concentration contributes to the knowledge of the structure of the polymer during the process of gel formation. It is shown that the inital shear-thickening behaviour of the colloïdal sol at low concentrations is followed by a shear-thinning behaviour under conditions of polymerization of the silicic acid. The sol-gel transition is marked by a breakpoint. When measurements pass beyond this point, plastic flow behaviour is observed because of the shear induced formation of amorphous silicic aggregates. All rheological processes of silicic acid sols are intensified at pH = 8.

     

Asymptotics of the homogenized moduli for the elastic chess-board composite

We find the asymptotic behavior of the homogenized coefficients of elasticity for the chess-board structure. In the chess board white and black cells are isotropic and have Lamé constants (, ,) and (, ) respectively. We assume that the black cells are soft, so 0. It turns out that the Poisson ratio for this composite tends to zero with .     

Flocculation and rheology of kaolinite/quartz suspensions

Rheological properties of suspensions of Na-kaolinite and colloidal quartz (Min-U-Sil) at constant overall volume concentration of 2% are determined with a Weissenberg Rheogoniometer using a combined Couette and cone-and-plate geometry. The results are interpreted in terms of the flocculation behaviour of the constituent particles in the presence of high salt concentrations (0.1–0.75m NaCl) at pH 6, 7 and 8. In these chemical environments these suspensions are pseudoplastic for much of the range of mixture compositions becoming Newtonian for suspensions containing only quartz. These properties reflect the dominant influence of interactions between kaolinite particles on the flocculation behaviour of the mixture.Nomenclature a ₁, a₂ radii of spheres - A Hamaker constant - b radius of cylinder - C volumetric solids concentration - e ₀ electronic charge - H ₀ shortest distance between surfaces - I ionic strength - J collision frequency per unit volume - k Boltzmann constant - l length of cylinder - m number in eq. (2) - N particle number concentration - S (H ₀ + b)/b in eq. (4) - T absolute temperature - U electrophoretic mobility - V _A van der Waals attractive energy - V _R coulombic energy - V _T total energy of interaction - X H ₀/2a₁ in eq. (5) - Y a ₂/a₁ in eq. (5) - thickness of plate - shear rate - permittivity - zeta potential - k Debye-Hückel parameter - µ dynamic viscosity - µ _pl plastic viscosity - v valency of counter ion - shear stress - _B Bingham stress - ₁, ₂ dimensionless potentials - ₁, ₂ surface potentials     

Die swell of filled polymer melts

The Barus effect in polypropylene and polystyrene blended with a variety of fillers at various concentrations was investigated using a capillary extrusion rheometer. If the die swell is defined as the square of the ratio of the extrudate diameterd to the die diameterD, it is found to depend on the apparent shear stress _W . Below a certain value of _w the relation =B _B ^A applies. The die swell, _M , of a filled polymer depends on the type, size and volume fraction of the filler. In particular,A increases as the volume fraction increases and is largest for powders, smaller for flakes and smallest for fibres, whereasB shows the opposite trend but to a lesser extent.