A study on the melt viscosity of linear and branched poly(butyleneterephthalate)

Linear and branched PBTP samples were synthesized and characterized in terms of the intrinsic viscosity, the melt-flow-index and, for some, the melt viscosity over a range of shear rates at 250 °C.An exponent of 3.2 in the equation relating to was found for linear samples. Both linear and branched samples exhibited Newtonian behaviour over a wide range of shear rates, but for any given melt-viscosity the branched samples became shear thinning at lower shear rates than the linear ones. Correlation between a branching index,, and melt-visocity ratio (0,b/0,l) was in agreement with a previous theoretical study.     

Material functions generated by the complex viscosity

Based on the complex viscosity model various steady-state and transient material functions have been completed. The model is investigated in terms of a corotational frame reference. Also, BKZ-type integral constitutive equations have been studied. Some relations between material functions have been derived. C ^–1 Finger tensor - F[], (F ^–1[]) Fourier (inverse) transform - rate of deformation tensor in corotating frame - h(I, II) Wagner's damping function - J (x) Bessel function - m parameter inh (I, II) - m(s) memory function - m _k, n_k integers (powers in complex viscosity model) - P principal value of the integral - parameter in the complex viscosity model - rate of deformation tensor - shear rates - [], [] incomplete gamma function - (a) gamma function - steady-shear viscosity - ^* complex viscosity - , real and imaginary parts of ^* - ₀ zero shear viscosity - ⁺, ₁ ⁺ stress growth functions - ^–, ₁ ^- stress relaxation functions - (s) relaxation modulus - ₁(s) primary normal-stress coefficient - ø(a, b; z) degenerate hypergeometric function - ₁, ₂ time constants (parameters of ^*) - frequency - extra stress tensor     

Rheology of molten polymers

Summary TheCross equation describes the flow of pseudoplastic liquids in terms of an upper and a lower Newtonian viscosity corresponding to infinite and zero shear, and ₀, and of a third material constant related to the mechanism of rupture of linkages between particles in the intermediate, non-Newtonian flow regime, Calculation of of bulk polymers is important, since it cannot be determined experimentally. The equation was applied to the melt flow data of two low density polyethylenes at three temperatures.Using data in the non-Newtonian region covering 3 decades of shear rate to extrapolate to the zero-shear viscosity resulted in errors amounting to about onethird of the measured ₀ values. The extrapolated upper Newtonian viscosity was found to be independent of temperature within the precision of the data, indicating that it has a small activation energy.The ₀ values were from 100 to 1,400 times larger than the values at the corresponding temperatures.The values of were large compared to the values found for colloidal dispersions and polymer solutions, but decreased with increasing temperature. This shows that shear is the main factor in reducing chain entanglements, but that the contribution of Brownian motion becomes greater at higher temperatures.

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Zusammenfassung Die Gleichung vonCross beschreibt das Fließverhalten von pseudoplastischen Flüssigkeiten durch drei Konstante: Die obereNewtonsche Viskosität (bei sehr hohen Schergeschwindigkeiten), die untereNewtonsche Viskosität ₀ (bei Scherspannung Null), und eine Materialkonstante, die vom Brechen der Bindungen zwischen Partikeln im nicht-Newtonschen Fließbereich abhängt. Die Berechnung von ist wichtig für unverdünnte Polymere, wo man sie nicht messen kann.Die Gleichung wurde auf das Fließverhalten der Schmelzen von zwei handelsüblichen Hochdruckpolyäthylenen bei drei Temperaturen angewandt. Die Werte von ₀, durch Extrapolation von gemessenen scheinbaren Viskositäten im Schergeschwindigkeitsbereich von 10 bis 4000 sec^–1 errechnet, wichen bis 30% von den gemessenen ₀-Werten ab. Die Aktivierungsenergie der war so klein, daß die-Werte bei den drei Temperaturen innerhalb der Genauigkeit der Extrapolation anscheinend gleich waren. Die ₀-Werte waren 100 bis 1400 mal größer als die-Werte.Im Verhältnis zu kolloidalen Dispersionen und verdünnten Polymerlösungen war das der Schmelzen groß, nahm aber mit steigender Temperatur ab. Deshalb wird die Verhakung der Molekülketten hauptsächlich durch Scherbeanspruchung vermindert, aber der Beitrag derBrownschen Bewegung nimmt mit steigender Temperatur zu.

     

The contribution of internal degrees of freedom to the non-Newtonian rheology of model polymer fluids

We report non-equilibrium molecular dynamics simulations of rigid and non-rigid dumbbell fluids to determine the contribution of internal degrees of freedom to strain-rate-dependent shear viscosity. The model adopted for non-rigid molecules is a modification of the finitely extensible nonlinear elastic (FENE) dumbbell commonly used in kinetic theories of polymer solutions. We consider model polymer melts — that is, fluids composed of rigid dumbbells and of FENE dumbbells. We report the steady-state stress tensor and the transient stress response to an applied Couerte strain field for several strain rates. We find that the rheological properties of the rigid and FENE dumbbells are qualitatively and quantitatively similar. (The only exception to this is the zero strain rate shear viscosity.) Except at high strain rates, the average conformation of the FENE dumbbells in a Couette strain field is found to be very similar to that of FENE dumbbells in the absence of strain. The theological properties of the two dumbbell fluids are compared to those of a corresponding fluid of spheres which is shown to be the most non-Newtonian of the three fluids considered.Symbol Definition b dimensionless time constant relating vibration to other forms of motion - F force on center of mass of dumbbell - F _i force on bead i of dumbbell - F force between center of masses of dumbbells and - F _ij force between beads i and j - h vector connecting bead to center of mass of dumbbell - H dimensionless spring constant for dumbbells, in units of / ² - I moment of inertia of dumbbell - J general current induced by applied field - k _B Boltzmann's constant - L angular momentum - m mass of bead, (= m/2) - M mass of dumbbell, g - N number of dumbbells in simulation cell - P translational momentum of center of mass of dumbbell - P pressure tensor - P _xy xy component of pressure tensor - Q separation of beads in dumbbell - Q _eq equilibrium extension of FENE dumbbell and fixed extension of rigid dumbbell - Q ₀ maximum extension of dumbbell - r _ij vector connecting beads i and j - r position vector of center of mass dumbbell - R vector connecting centers of mass of two dumbbells - t time - t ^* dimensionless time, in units of m/ - T ^* dimensionless temperature, in units of /k - u potential energy - u velocity vector of flow field - u _x x component of velocity vector - V volume of simulation cell - X general applied field - strain rate, s^–1 - ^* dimensionless shear rate, in units of /m ² - general transport property - Lennard-Jones potential well depth - friction factor for Gaussian thermostat - shear viscosity, g/cms - ^* dimensionless shear viscosity, in units of m/ ² - ^* dimensionless number density, in units of ^–3 - Lennard-Jones separation of minimum energy - relaxation time of a fluid - angular velocity of dumbbell - orientation angle of dumbbell      

A three-parameter model describing the experimental relation between shear stress and shear rate for laminar flow of aqueous polymer solutions

Summary A three-parameter model is introduced to describe the shear rate — shear stress relation for dilute aqueous solutions of polyacrylamide (Separan AP-30) or polyethylenoxide (Polyox WSR-301) in the concentration range 50 wppm – 10,000 wppm. Solutions of both polymers show for a similar rheological behaviour. This behaviour can be described by an equation having three parameters i.e. zero-shear viscosity ₀, infinite-shear viscosity , and yield stress ₀, each depending on the polymer concentration. A good agreement is found between the values calculated with this three-parameter model and the experimental results obtained with a cone-and-plate rheogoniometer and those determined with a capillary-tube rheometer.

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Zusammenfassung Der Zusammenhang zwischen Schubspannung und Schergeschwindigkeit von strukturviskosen Flüssigkeiten wird durch ein Modell mit drei Parametern beschrieben. Mit verdünnten wäßrigen Polyacrylamid-(Separan AP-30) sowie Polyäthylenoxidlösungen (Polyox WSR-301) wird das Modell experimentell geprüft. Beide Polymerlösungen zeigen im untersuchten Schergeschwindigkeitsbereich von ein ähnliches rheologisches Verhalten. Dieses Verhalten kann mit drei konzentrationsabhängigen Größen, nämlich einer Null-Viskosität ₀, einer Grenz-Viskosität und einer Fließgrenze ₀ beschrieben werden. Die Ergebnisse von Experimenten mit einem Kegel-Platte-Rheogoniometer sowie einem Kapillarviskosimeter sind in guter Übereinstimmung mit den Werten, die mit dem Drei-Parameter-Modell berechnet worden sind.

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a Pa^–1 physical quantity defined by:a = {1 – ( / ₀)}/ ₀ - c l concentration (wppm) - D m capillary diameter - L m length of capillary tube - P Pa pressure drop - R m radius of capillary tube - u m s^–1 average velocity - v _r m s^–1 local axial velocity at a distancer from the axis of the tube - shear rate (–dv _r /dr) - local shear rate in capillary flow - s^–1 wall shear rate in capillary flow - Pa s dynamic viscosity - _a Pa s apparent viscosity defined by eq. [2] - ( _a ) Pa s apparent viscosity in capillary tube at a distanceR from the axis - ₀ Pa s zero-shear viscosity defined by eq. [4] - Pa s infinite-shear viscosity defined by eq. [5] - l ratior/R - kg m^– density - Pa shear stress - ₀ Pa yield stress - _r Pa local shear stress in capillary flow - _R Pa wall shear stress in capillary flow _R = (PR/2L) - _v m³ s^–1 volume rate of flow With 8 figures and 1 table     

An analytical solution for the velocity and shear rate distribution of non-ideal Bingham fluids in concentric cylinder viscometers

An analytical solution is presented for the calculation of the flow field in a concentric cylinder viscometer of non-ideal Bingham-fluids, described by the Worrall-Tuliani rheological model. The obtained shear rate distribution is a function of the a priori unknown rheological parameters. It is shown that by applying an iterative procedure experimental data can be processed in order to obtain the proper shear rate correction and the four rheological parameters of the Worrall-Tuliani model as well as the yield surface radius. A comparison with Krieger's correction method is made. Rheometrical data for dense cohesive sediment suspensions have been reviewed in the light of this new method. For these suspensions velocity profiles over the gap are computed and the shear layer thicknesses were found to be comparable to visual observations. It can be concluded that at low rotation speeds the actually sheared layer is too narrow to fullfill the gap width requirement for granular suspensions and slip appears to be unavoidable, even when the material is sheared within itself. The only way to obtain meaningfull measurements in a concentric cylinder viscometer at low shear rates seems to be by increasing the radii of the viscometer. Some dimensioning criteria are presented.Notation A, B Integration constants - C Dimensionless rotation speed = µ/_y - c = 2µ - d = ₀ ²–2c_y - f() = (–₀)²+2c(–_y) - r Radius - r _b Bob radius - r _c Cup radius - r _y Yield radius - r ₀ Stationary surface radius - r Rotating Stationary radius - Y ₀ Shear rate parameter = /µ Greek letters Shear rate - = (r _y /r _b )²– 1 - µ Bingham viscosity - µ₀ Initial differential viscosity - µ µ₀-µ - Rotation speed - Angular velocity - Shear stress - _b Bob shear stress - _B Bingham stress - _y (True) yield stress - ₀ Stress parameter = _B +µ Y ₀ - _B - _y      

A general model for the effective viscosity of pseudoplastic and dilatant fluids

Summary A new and very general expression is proposed for correlation of data for the effective viscosity of pseudoplastic and dilatant fluids as a function of the shear stress. Most of the models which have been proposed previously are shown to be special cases of this expression. A straightforward procedure is outlined for evaluation of the arbitrary constants.

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Zusammenfassung Eine neue und sehr allgemeine Formel wird für die Korrelation der Werte der effektiven Viskosität von strukturviskosen und dilatanten Flüssigkeiten in Abhängigkeit von der Schubspannung vorgeschlagen. Die meisten schon früher vorgeschlagenen Methoden werden hier als Spezialfälle dieser Gleichung gezeigt. Ein einfaches Verfahren für die Auswertung der willkürlichen Konstanten wird beschrieben.

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Nomenclature b arbitrary constant inSisko model (eq. [5]) - n arbitrary exponent in eq. [1] - x independent variable - y(x) dependent variable - y ₀(x) limiting behavior of dependent variable asx 0 - y(x) limiting behavior of dependent variable asx - z original dependent variable - arbitrary constant inSisko model (eq. [5]) andBird-Sisko model (eq. [6]) - arbitrary exponent in eqs. [2] and [8] - effective viscosity = shear stress/rate of shear - _A effective viscosity at = _A - _B empirical constant in eqs. [2] and [8] - ₀ limiting value of effective viscosity as 0 - ₀() limiting behavior of effective viscosity as 0 - limiting value of effective viscosity as - () limiting behavior of effective viscosity as - rate of shear - arbitrary constant inBird-Sisko model (eq.[6]) - shear stress - _A arbitrary constant in eqs. [2] and [8] - ₀ shear stress at inBingham model - _1/2 shear stress at = ( ₀ + )/2 With 8 figures     

Rheological models for gypsum plaster pastes

Shear stress and shear rate data obtained for gypsum plaster pastes were correlated by means of different rheological models. The pastes were prepared from a commercial calcium sulfate hemihydrate at various water/plaster ratios ranging from 100/150 to 100/190. The tests were performed at 25°C using a rotating coaxial cylinder viscosimeter. The measurements were accomplished by applying a step-wise decreasing shear rate sequence. Discrimination among the models was made: (1) on the basis of the fitting goodness; (2) by checking the physical meaning of the calculated parameters; (3) on the basis of the stability of the parameters and of their prediction capacity beyond the limits of the experimental data. In the light of above, the Casson model seemed to be most effective for application to gypsum plaster pastes. K Consistency - n Power-law index - N Number of experimental data - P Number of parameters - Shear rate (s^–1) - ₀ Viscosity (Pa · s) - _d Dispersing medium viscosity (Pa · s) - _p Plastic viscosity (Pa · s) - Viscosity at zero shear rate (Pa · s) - Viscosity at infinite shear rate (Pa · s) - [] Intrinsic viscosity - ² Variance - Shear stress (Pa) - ₀ Yield stress (Pa) - Solid volume fraction - _m Maximum solid volume fraction     

The steady shear viscosity of filled polymeric liquids described by a linear superposition of two relaxation mechanisms

Filled polymeric liquids often exhibit apparent yielding and shear thinning in steady shear flow. Yielding results from non-hydrodynamic particle—particle interactions, while shear thinning results from the non-Newtonian behavior of the polymer melt. A simple equation, based on the linear superposition of two relaxation mechanisms, is proposed to describe the viscosity of filled polymer melts over a wide range of shear rates and filler volume fraction.The viscosity is written as the sum of two generalized Newtonian liquid models. The resulting equation can describe a wide range of shear-thinning viscosity curves, and a hierarchy of equations is obtained by simplifying the general case. Some of the parameters in the equation can be related to the properties of the unfilled liquid and the solid volume fraction. One adjustable parameter, a yield stress, is necessary to describe the viscosity at low rates where non-hydrodynamic particle—particle interaction dominate. At high shear rates, where particle—particle interactions are dominated by interparticle hydrodynamics, no adjustable parameters are necessary. A single equation describes both the high and low shear rate regimes. Predictions of the equation closely fit published viscosity data of filled polymer melts. n power-law index - n ₁,n ₂ power-law index of first (second) term - shear rate - steady shear viscosity - ₀ zero-shear rate viscosity - _{0, 1}, _{0, 2} zero-shear rate viscosity of first (second) term - time constant - ₁, ₂ time constant of first (second) term - µ _r relative viscosity of filled Newtonian liquid - ₀ yield stress - ø solid volume fraction - ø _m maximum solid volume fraction     

Theory of oscillatory experiments with a coaxial cylinder viscometer

Equations are derived for the coaxial cylinder system in the combined oscillatory and steady-state shear mode. The limitations of the use of the various equations are presented. If the usual linear equations are used, the main limitation, in the case of oscillatory shear only, is that the frequency of measurement should be below 0.016 | ^*|/(r ₂ –r ₁ )². Here | ^*| is the modulus of the complex viscosity, is the density of the liquid andr ₁ andr ₂ are the radii of the cylinders. Furthermore it is shown that there is a small error in the numerical factor of the usually applied equations. The calculations are set up in such a way that extension to higher harmonics follows in a natural way. An experimental example illustrates the use of the derived equations.     

Rheo-NMR study of a non-flow-aligning side-chain liquid crystal polymer in nematic solution

The flow behavior of a highly concentrated solution of a nematic side-chain liquid crystal polymer in a low molecular mass nematic solvent is investigated by deuterium nuclear magnetic resonance with simultaneous measurement of the shear viscosity in a cone-and-plate NMR viscometer. The director orientation under shear in the magnetic field is determined from the quadrupole splitting of the NMR spectra. The orientation as a function of shear rate is analyzed in terms of the Ericksen-Leslie-Parodi theory, yielding the Leslie coefficients ₂ and ₃ and thus the flow alignment parameter . From the combined analysis of orientation and viscosity as a function of shear rate a total of four independent viscosity parameters is obtained for the nematic solution. The value determined for the flow-alignment parameter, 0.2, and the analysis of the data based on Brochard's theory show that the polymer is of the non-flow-aligning type and has a slightly prolate shape.     

Zur analytischen Beschreibung des Füllstoffeinflusses auf das Fließverhalten von Kunststoff-Schmelzen

From literature some representative equations have been compiled describing the influence of filler on the viscosity of polymer melts. By application of these on the experimental results obtained from GF-SAN it was found that the relative viscosity _R , i.e. the ratio of the viscosities of the filled and unfilled melt, shows a pronounced dependence on the shear rate but not on the shear stress. Defining _R with constant and not with constant (as it is usually done), an analytical approach is possible independent of Further the influence of pressure, temperature and filler content on the zero-shear viscosity of filled polymer melts may be expressed by a modified Arrhenius equation.

     

Laminar source flow between parallel porous disks with equal suction and injection

An analysis is presented for laminar source flow between parallel stationary porous disks with suction at one of the disks and equal injection at the other. The solution is in the form of an infinite series expansion about the solution at infinite radius, and is valid for all suction and injection rates. Expressions for the velocity, pressure, and shear stress are presented and the effect of the cross flow is discussed.Nomenclature a distance between disks - A, B, ..., J functions of R _w only - F static pressure - p dimensionless static pressure, p(a ²/ ²) - Q volumetric flow rate of the source - r radial coordinate - r dimensionless radial coordinate, r/a - R radial coordinate of a point in the flow region - R dimensionless radial coordinate of a point in the flow region, R - Re source Reynolds number, Q/2a - R _w wall Reynolds number, Va/ - reduced Reynolds number, Re/r ² - critical Reynolds number - velocity component in radial direction - u dimensionless velocity component in radial direction, a/ - average radial velocity, Q/2a - u dimensionless average radial velocity, Re/r - ratio of radial velocity to average radial velocity, u/u - velocity component in axial direction - v dimensionless velocity component in axial direction, v - V magnitude of suction or injection velocity - z axial coordinate - z dimensionless axial coordinate, z a - viscosity - density - kinematic viscosity, / - shear stress at lower disk - shear stress at upper disk - ₀ dimensionless shear stress at lower disk, - ₁ dimensionless shear stress at upper disk, - dimensionless stream function     

Laminar forced convection in elliptic ducts

The problem of laminar forced convection heat transfer in short elliptical ducts with (i) uniform wall temperature and (ii) prescribed wall heat flux is examined in detail with the well known Lévêque theory of linear velocity profile near the wall. Moreover, consideration is given to the variation of the slope of the linear velocity profile with the position on the duct wall. A correction factor for the temperature dependent viscosity is included. Expressions for the local and average Nusselt numbers and wall temperatures are obtained. For the case of constant heat flux the Nusselt numbers are higher than for constant wall temperature.The results corresponding to the classical Graetz and Purday problems are deduced as special cases.Nomenclature a, b semiaxes of ellipse, b Graetz number (average), Re Pr D _e/Z - h _i ^o local heat transfer coefficient - J _n(x) Bessel function of order n - K thermal conductivity of the fluid - [X] Laplace transform of X - N _u ^o local Nusselt number, h _i ^o D _e/K - perimeter average Nusselt number - overall average Nusselt number - Nu _w wall Nusselt number - Nu Nusselt number at large distance from the inlet - p Laplace transform parameter - Pr Prandtl number, C _a/K - Re Reynolds number, D _e / _a - T temperature of the fluid - T ₁, T _W inlet and wall temperatures, respectively - u _z local isothermal velocity along the axis of the duct - average fluid velocity - x, y, z Cartesian coordinates, z-axis parallel to the axis of the duct (z=0 at duct inlet) - Z length of the duct - thermal diffusivity, K/C - * correction factor for the temperature dependent viscosity - (x) gamma function - coordinate measured normal to the wall of the duct - _a, _w viscosity of fluid at average and wall temperatures - , , z elliptic cylindrical coordinates - density of fluid - (z) heat flux     

Uniqueness and the maximum principle for quasilinear elliptic equations with quadratic growth conditions

In this paper, we show that the maximum principle holds for quasilinear elliptic equations with quadratic growth under general structure conditions.Two typical particular cases of our results are the following. On one hand, we prove that the equation (1) {ie77-01} where {ie77-02} and {ie77-03} satisfies the maximum principle for solutions in H ¹()L(), i.e., that two solutions u ₁, u ₂H¹() L() of (1) such that u ₁u₂ on , satisfy u ₁u₂ in . This implies in particular the uniqueness of the solution of (1) in H ₀ ¹ ()L().On the other hand, we prove that the equation (2) {ie77-04} where fH^–1() and g(u)>0, g(0)=0, satisfies the maximum principle for solutions uH¹() such that g(u)¦Du|{²L¹(). Again this implies the uniqueness of the solution of (2) in the class uH ₀ ¹ () with g(u)¦Du|{²L¹().In both cases, the method of proof consists in making a certain change of function u=(v) in equation (1) or (2), and in proving that the transformed equation, which is of the form (3) {ie77-05}satisfies a certain structure condition, which using ((v₁ -v ₂)⁺)ⁿ for some n>0 as a test function, allows us to prove the maximum principle.     

Concentration-dependent behaviour of the shear viscosity of coal-fuel oil suspensions

A function correlating the relative viscosity of a suspension of solid particles in liquids to their concentration is derived here theoretically using only general thermodynamic ideas, with out any consideration of microscopic hydrodynamic models. This function ( _r = exp (1/2B ^* C ²)) has a great advantage over the many different functions proposed in literature, for it depends on a single parameter,B ^*, and is therefore concise. To test the validity of this function, a least-squares regression analysis was undertaken of available data on the viscosity and concentration of suspensions of coal particles in fuel oil, which promise to be a useful alternative to fuel oil in the near future. The proposed function was found to accurately describe the concentration-dependent behaviour of the relative viscosity of these suspensions. Furthermore, an attempt was made to obtain information about the factors affecting the value ofB ^*, however the results were only qualitative because of, among other things, the inaccuracy of the viscosity measurements in such highly viscous fluids. shear viscosity of the suspension - ₀ shear viscosity of the Newtonian suspending medium - _r = /₀ relative viscosity - solid volume concentration - c solid weight concentration - _m maximum attainable volume concentration of solids - solid volume concentration at which the relative viscosity of the suspension becomes infinite - c _m maximum attainable solid weight concentration - _s density of the solid phase - _l density of the liquid phase - _m density of the suspension - k _n coefficients of theø-power series expansion of _r - { _j } sets of parameters specifying the thermodynamic state of the solid phase of a suspension - T absolute temperature (K) - f (c, T, _j) formal expression for the relative variation of the viscosity with concentration = [1 / (/c)] _T,j - d median size of the granulometric distribution - _B plastic or Bingham viscosity - K consistency factor - n flow index - g ([c _m –c],T, _j ) function including an asymptotic divergence asc tends toc _m , formally describing the concentration dependent behaviour of the shear viscosity of a suspension - A (T, _j) regression analysis parameters - B (T, _j) regression analysis parameters - B ^* (T, _j ) regression analysis parameters     

Deformation to breaking of deep water gravity waves

The results of laboratory observations of the deformation of deep water gravity waves leading to wave breaking are reported. The specially developed visualization technique which was used is described. A preliminary analysis of the results has led to similar conclusions than recently developed theories. As a main fact, the observed wave breaking appears as the result of, first, a modulational instability which causes the local wave steepness to approach a maximum and, second, a rapidly growing instability leading directly to the breaking.List of symbols L total wave length - H total wave height - crest elevation above still water level - trough depression below still water level - wave steepness =H/L - crest steepness =/L - trough steepness =/L - F ₁ forward horizontal length from zero-upcross point (A) to wave crest - F ₂ backward horizontal length from wave crest to zero-downcross point (B) - crest front steepness =/F ₁ - crest rear steepness =/F ₂ - vertical asymmetry factor=F ₂/F ₁ (describing the wave asymmetry with respect to a vertical axis through the wave crest) - µ horizontal asymmetry factor=/H (describing the wave asymmetry with respect to a horizontal axis: SWL) - T ₀ wavemaker period - L ₀ theoretical wave length of a small amplitude sinusoïdal wave generated at T _inf0 ^sup–1 frequency - ₀ average wave height     

Viscosity of a Dilute Suspension in a High‐Frequency Electromagnetic Field

The action of a highfrequency electromagnetic field on a dilute suspension of spherical particles with a constant dipole moment is studied using statistical mechanics. An expression for effective viscosity is obtained. It is shown that the shear viscosity of the dilute suspension depends on the frequency, magnitude, and direction of the highfrequency electromagnetic field. Depending on the frequency of the highfrequency electromagnetic field, the rotation of the suspension particles is decelerated or accelerated, with the viscosity increasing or decreasing, respectively. It is shown that the acceleration of the suspension particles by a highfrequency electromagnetic field and, hence, the decrease in shear viscosity has a resonant nature.     

Similar solutions and the asymptotics of filtration equations

In this paper we consider the asymptotic behavior of solutions of the quasilinear equation of filtration as t. We prove that similar solutions of the equation u _t = (u )_xx asymptotically represent solutions of the Cauchy problem for the full equation u _t = [(u)]_xx if (u) is close to u for small u.     

Rheology/morphology/flow conditions relationships for polymethylmethacrylate/rubber blend

Viscoelastic behavior, phase morphology and flow conditions relationships in polymer/rubber blends have been investigated. The importance of such correlations is illustrated on polymethylmethacrylate (PMMA)/rubber blends subjected to different flow conditions both under small and large deformations. In small-amplitude oscillatory shear (the morphology does not change during the flow) the elastic modulus G of the concentrated blends shows a secondary plateau, G _p , in the low frequency region. This solid-like behavior appears for rubber particle contents beyond the percolation threshold concentration (15%). Morphological observations revealed that for concentrations higher than 15%, the particles are dispersed in a three-dimensional network-type structure.In capillary flow it was found that the network-type structure was destroyed and replaced by an alignment of particles in the flow direction. This morphological modification resulted in a decrease in both viscosity and post-extrusion swell of the blends. Morphological observations revealed that the ordered structure in the flow direction was concentrated only in the skin region of the extrudate, where the shear stress is higher than the secondary plateau, G _p . A simple kinetic mechanism is proposed to explain the observed morphology.Similarly, steady shear measurements performed in the cone-and-plate geometry revealed alignment of particles in the flow direction for shear stress values higher than G_p.Presented in part at the Symposium Recent Developments in Structured Continua Montréal (Canada) 26–28 May 1993 and at the 45th Canadian Chemical Engineering Conference, Quebec, October 15–18 (1995)