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1.
In a previous derivation of Darcy's law, the closure problem was presented in terms of an integro-differential equation for a second-order tensor. In this paper, we show that the closure problem can be transformed to a set of Stokes-like equations and we compare solutions of these equations with experimental data. The computational advantages of the transformed closure problem are considerable.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 e area of entrances and exits for the-phase contained within the averaging volume, m2 - B second-order tensor used to respresent the velocity deviation - b vector used to represent the pressure deviation, m–1 - C second-order tensor related to the permeability tensor, m–2 - D second-order tensor used to represent the velocity deviation, m2 - d vector used to represent the pressure deviation, m - g gravity vector, m/s2 - I unit tensor - K C –1,–D, Darcy's law permeability tensor, m2 - L characteristic length scale for volume averaged quantities, m - characteristic length scale for the-phase, m - l i i=1, 2, 3, lattice vectors, m - n unit normal vector pointing from the-phase toward the-phase - n e outwardly directed unit normal vector at the entrances and exits of the-phase - p pressure in the-phase, N/m 2 - p intrinsic phase average pressure, N/m2 - p p , spatial deviation of the pressure in the-phase, N/m2 - r position vector locating points in the-phase, m - r 0 radius of the averaging volume, m - t time, s - v velocity vector in the-phase, m/s - v intrinsic phase average velocity in the-phase, m/s - v phase average or Darcy velocity in the \-phase, m/s - v v , spatial deviation of the velocity in the-phase m/s - V averaging volume, m3 - V volume of the-phase contained in 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  相似文献   

2.
We give a necessary and sufficient condition for the existence of L 1-connections between equilibria of a semilinear parabolic equation. By an L 1-connection from an equilibrium to an equilibrium + we mean a function u(, t) which is a classical solution on the interval (–, T) for some T and blows up at t = T but continues to exist in the space L 1 for t [T, ) and satisfies u(, t) ± (in a suitable sense) as t ±. The main tool in our analysis is the zero number.  相似文献   

3.
McAdams  J. E.  Williams  M. C. 《Rheologica Acta》1986,25(2):102-109
Theta solvents for polystyrene are prepared from high-viscosity blends of styrene and low-molecular-weight polystyrene, and then used to make dilute solutions with monodisperse polystyrene solutes of high-M = 2.3, 6.0, 9.0, 18.0 · 105. A Weissenberg rheogoniometer is used to measure the non-Newtonian viscosity as a function of shear stress, for low values, and also the complex viscosity components and as functions of frequency. A capillary viscometer is used for high- measurements of(). Viscometric properties, at room temperature, are analyzed as functions of high-molecular-weight solute concentrationc with parameters of constant or to obtain [()], [ ()], and [ ()]. Such a collection of data has apparently not previously been available for polymers in theta solvents (in which Gaussian chain statistics prevail). Also unique is the achievement of high stress ( = 2 104 Pa) at low shear rate, by virtue of high solvent viscosity which is not characteristic of other known theta solvents.  相似文献   

4.
When analyzing stochastic steady flow, the hydraulic conductivity naturally appears logarithmically. Often the log conductivity is represented as the sum of an average plus a stochastic fluctuation. To make the problem tractable, the log conductivity fluctuation, f, about the mean log conductivity, lnK G, is assumed to have finite variance, f 2. Historically, perturbation schemes have involved the assumption that f 2<1. Here it is shown that f may not be the most judicious choice of perturbation parameters for steady flow. Instead, we posit that the variance of the gradient of the conductivity fluctuation, f 2, is more appropriate hoice. By solving the problem withthis parameter and studying the solution, this conjecture can be refined and an even more appropriate perturbation parameter, , defined. Since the processes f and f can often be considered independent, further assumptions on f are necessary. In particular, when the two point correlation function for the conductivity is assumed to be exponential or Gaussian, it is possible to estimate the magnitude of f in terms of f and various length scales. The ratio of the integral scale in the main direction of flow ( x ) to the total domain length (L*), x 2=x/L*, plays an important role in the convergence of the perturbation scheme. For x smaller than a critical value c, x < c, the scheme's perturbation parameter is =f/x for one- dimensional flow, and =f/x 2 for two-dimensional flow with mean flow in the x direction. For x > c, the parameter =f/x 3 may be thought as the perturbation parameter for two-dimensional flow. The shape of the log conductivity fluctuation two point correlation function, and boundary conditions influence the convergence of the perturbation scheme.  相似文献   

5.
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.  相似文献   

6.
Zusammenfassung Das instationÄre Temperaturfeld oberhalb einer waagerechten, mit konstanter Wärmestromdichte beheizten Platte in verschiedenen Flüssigkeiten wurde experimentell untersucht. —Die Versuche haben ergeben, da\ sich das Einsetzen der InstabilitÄt (Konvektionsbeginn) durch eine Kenngrö\eK=gq 0 kr 2 /c p beschreiben lÄ\t. Hierin istg die lokale Fallbeschleunigung, der isobare thermische Ausdehnungskoeffizient, die dynamische ViskositÄt,c p die isobare spezifische WärmekapazitÄt,q 0 die Wärmestromdichte und kr die kritische Zeit, das ist der Zeitabschnitt zwischen dem Einschalten der Heizung und dem ersten Einsetzen der Konvektion.
The onset of convection in a horizontal fluid layer heated from below
The unsteady temperature field on the upper side of a horizontal plate heated with constant heat flux is experimentally studied in different fluids. The beginning of the instability (onset of convection) can be described by a dimensionless number given asK=gq 0 kr 2 /c p whereg is the local gravitational acceleration, the expansion coefficient at constant pressure,q 0 the heat flux, kr the critical time, namely the time interval between the starting of heating and the onset of convection.
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7.
A numerical investigation has been made of the hypersonic flow of a rarefied monatomic gas past the windward part of the side surface of an infinite circular cylinder. The calculation was made by direct statistical Monte Carlo modeling for freestream Mach number Mt8=20, ratio of the surface temperature of the body to the stagnation temperature equal to ttw =T tw/T t0 = 0.03, sweep angle 75°, and Reynolds number Ret0 30.Translated from Izvestiya Rossiiskoi Akademii Nauk, Mekhanika Zhidkosti i Gaza, No. 1, pp. 146–154, January–February, 1992.  相似文献   

8.
Linear and nonlinear viscoelastic properties were examined for a 50 wt% suspension of spherical silica particles (with radius of 40 nm) in a viscous medium, 2.27/1 (wt/wt) ethylene glycol/glycerol mixture. The effective volume fraction of the particles evaluated from zero-shear viscosities of the suspension and medium was 0.53. At a quiescent state the particles had a liquid-like, isotropic spatial distribution in the medium. Dynamic moduli G* obtained for small oscillatory strain (in the linear viscoelastic regime) exhibited a relaxation process that reflected the equilibrium Brownian motion of those particles. In the stress relaxation experiments, the linear relaxation modulus G(t) was obtained for small step strain (0.2) while the nonlinear relaxation modulus G(t, ) characterizing strong stress damping behavior was obtained for large (>0.2). G(t, ) obeyed the time-strain separability at long time scales, and the damping function h() (–G(t, )/G(t)) was determined. Steady flow measurements revealed shear-thinning of the steady state viscosity () for small shear rates (< –1; = linear viscoelastic relaxation time) and shear-thickening for larger (>–1). Corresponding changes were observed also for the viscosity growth and decay functions on start up and cessation of flow, + (t, ) and (t, ). In the shear-thinning regime, the and dependence of +(t,) and (t,) as well as the dependence of () were well described by a BKZ-type constitutive equation using the G(t) and h() data. On the other hand, this equation completely failed in describing the behavior in the shear-thickening regime. These applicabilities of the BKZ equation were utilized to discuss the shearthinning and shear-thickening mechanisms in relation to shear effects on the structure (spatial distribution) and motion of the suspended particles.Dedicated to the memory of Prof. Dale S. Parson  相似文献   

9.
Zusammenfassung Zur Berechnung der dynamischen Idealviskosität Ideal (T) und der Idealwärmeleitfähigkeit ideal (T) benötigt man die kritische TemperaturT kr, das kritische spezifische Volum kr, die MolmasseM, den kritischen Parameter kr und die molare isochore WärmekapazitätC v(T). Sowohl das theoretisch, als auch das empirisch abgeleitete erweiterte Korrespondenzgesetz ergeben eine für praktische Zwecke ausreichende Genauigkeit für die Meßwertwiedergabe, die bei den assoziierenden Stoffen und den Quantenstoffen jedoch geringer ist als bei den Normalstoffen.
The extended correspondence law for the ideal dynamic viscosity and the ideal thermal conductivity of pure substances
For the calculation of the ideal dynamic viscosity Ideal (T) and the ideal thermal conductivity ideal (T) the critical temperatureT kr, the critical specific volumev kr, the molecular massM, the critical parameter kr, and the molar isochoric heat capacityC v(T) is needed. Not only the theoretically determined but also the empirically determined extended correspondence law gives for practical use a good representation of the measured data, which for the associating substances and the quantum substances is not so good as for the normal substances.
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10.
In this paper we develop the averaged form of the Stokes equations in terms of weighting functions. The analysis clearly indicates at what point one must choose a media-specific weighting function in order to achieve spatially smoothed transport equations. The form of the weighting function that produces the cellular average is derived, and some important geometrical theorems are presented.Roman Letters A interfacial area of the- interface associated with the local closure problem, m2 - A e area of entrances and exits for the-phase contained within the averaging system, m2 - A p surface area of a particle, m2 - d p 6V p/Ap, effective particle diameter, m - g gravity vector, m/s2 - I unit tensor - K m permeability tensor for the weighted average form of Darcy's law, m2 - L general characteristic length for volume averaged quantities, m - L p general characteristic length for volume averaged pressure, m - L characteristic length for the porosity, m - L v characteristic length for the volume averaged velocity, m - l characteristic length (pore scale) for the-phase - l i i=1, 2, 3 lattice vectors, m - (y) weighting function - m(–y) (y), convolution product weighting function - v special weighting function associated with the traditional averaging volume - m v special convolution product weighting function associated with the traditional averaging volume - m g general convolution product weighting function - m V unit cell convolution product weighting function - m C special convolution product weighting function for ordered media which produces the cellular average - m D special convolution product weighting function for disordered media - m M master convolution product weighting function for ordered and disordered media - n unit normal vector pointing from the-phase toward the-phase - p pressure in the-phase, N/m2 - pm superficial weighted average pressure, N/m2 - p m intrinsic weighted average pressure, N/m2 - p traditional intrinsic volume averaged pressure, N/m2 - p p p m , spatial deviation pressure, N/m2 - r 0 radius of a spherical averaging volume, m - r m support of the convolution product weighting function, m - r position vector, m - r position vector locating points in the-phase, m - V averaging volume, m3 - V volume of the-phase contained in the averaging volume, m3 - V cell volume of a unit cell, m3 - V velocity vector in the-phase, m/s - vm superficial weighted average velocity, m/s - v m intrinsic weighted average velocity, m/s - V volume of the-phase contained in the averaging volume, m3 - V p volume of a particle, m3 - v traditional superficial volume averaged velocity, m/s - v v p m spatial deviation velocity, m/s - x position vector locating the centroid of the averaging volume or the convolution product weighting function, m - y position vector relative to the centroid, m - y position vector locating points in the-phase relative to the centroid, m Greek Letters indicator function for the-phase - Dirac distribution associated with the- interface - V /V, volume average porosity - m m * . weighted average porosity - mass density of the-phase, kg/m3 - viscosity of the-phase, Ns/m2 - V /V, volume fraction of the-phase  相似文献   

11.
We prove the existence and uniqueness of entropy solutions of the Neumann problem for the quasilinear parabolic equation uta(u, Du), where a(z,)=f(z,), and f is a convex function of with linear growth as ||||, satisfying other additional assumptions. In particular, this class includes the case where f(z,)=(z)(), >0, and is a convex function with linear growth as ||||.  相似文献   

12.
In this work, we make use of numerical experiments to explore our original theoretical analysis of two-phase flow in heterogeneous porous media (Quintard and Whitaker, 1988). The calculations were carried out with a two-region model of a stratified system, and the parameters were chosen be consistent with practical problems associated with groundwater flows and petroleum reservoir recovery processes. The comparison between theory (the large-scaled averaged equations) and experiment (numerical solution of the local volume averaged equations) has allowed us to identify conditions for which the quasi-static theory is acceptable and conditions for which a dynamic theory must be used. Byquasi-static we mean the following: (1) The local capillary pressure,everywhere in the averaging volume, can be set equal to the large-scale capillary pressure evaluated at the centroid of the averaging volume and (2) the large-scale capillary pressure is given by the difference between the large-scale pressures in the two immiscible phases, and is therefore independent of gravitational effects, flow effects and transient effects. Bydynamic, we simply mean a significant departure from the quasi-static condition, thus dynamic effects can be associated with gravitational effects, flow effects and transient effects. To be more precise about the quasi-static condition we need to refer to the relation between the local capillary pressure and the large-scale capillary pressure derived in Part I (Quintard and Whitaker, 1990). Herep c ¦y represents the local capillary pressure evaluated at a positiony relative to the centroid of the large-scale averaging volume, and {p c x represents the large-scale capillary pressure evaluated at the centroid.In addition to{p c } c being evaluated at the centroid, all averaged terms on the right-hand side of Equation (1) are evaluated at the centroid. We can now write the equations describing the quasi-static condition as , , This means that the fluids within an averaging volume are distributed according to the capillary pressure-saturation relationwith the capillary pressure held constant. It also means that the large-scale capillary pressure is devoid of any dynamic effects. Both of these conditions represent approximations (see Section 6 in Part I) and one of our main objectives in this paper is to learn something about the efficacy of these approximations. As a secondary objective we want to explore the influence of dynamic effects in terms of our original theory. In that development only the first four terms on the right hand side of Equation (1) appeared in the representation for the local capillary pressure. However, those terms will provide an indication of the influence of dynamic effects on the large-scale capillary pressure and the large-scale permeability tensor, and that information provides valuable guidance for future studies based on the theory presented in Part I.Roman Letters A scalar that maps {}*/t onto - A scalar that maps {}*/t onto - A interfacial area between the -region and the -region contained within, m2 - A interfacial area between the -region and the -region contained within, m2 - A interfacial area between the -region and the -region contained within, m2 - a vector that maps ({}*/t) onto , m - a vector that maps ({}*/t) onto , m - b vector that maps ({p}– g) onto , m - b vector that maps ({p}– g) onto , m - B second order tensor that maps ({p}– g) onto , m2 - B second order tensor that maps ({p}– g) onto , m2 - c vector that maps ({}*/t) onto , m - c vector that maps ({}*/t) onto , m - C second order tensor that maps ({}*/t) onto , m2 - C second order tensor that maps ({}*/t) onto . m2 - D third order tensor that maps ( ) onto , m - D third order tensor that maps ( ) onto , m - D second order tensor that maps ( ) onto , m2 - D second order tensor that maps ( ) onto , m2 - E third order tensor that maps () onto , m - E third order tensor that maps () onto , m - E second order tensor that maps () onto - E second order tensor that maps () onto - p c =(), capillary pressure relationship in the-region - p c =(), capillary pressure relationship in the-region - g gravitational vector, m/s2 - largest of either or - - - i unit base vector in thex-direction - I unit tensor - K local volume-averaged-phase permeability, m2 - K local volume-averaged-phase permeability in the-region, m2 - K local volume-averaged-phase permeability in the-region, m2 - {K } large-scale intrinsic phase average permeability for the-phase, m2 - K –{K }, large-scale spatial deviation for the-phase permeability, m2 - K –{K }, large-scale spatial deviation for the-phase permeability in the-region, m2 - K –{K }, large-scale spatial deviation for the-phase permeability in the-region, m2 - K * large-scale permeability for the-phase, m2 - L characteristic length associated with local volume-averaged quantities, m - characteristic length associated with large-scale averaged quantities, m - I i i = 1, 2, 3, lattice vectors for a unit cell, m - l characteristic length associated with the-region, m - ; characteristic length associated with the-region, m - l H characteristic length associated with a local heterogeneity, m - - n unit normal vector pointing from the-region toward the-region (n =–n ) - n unit normal vector pointing from the-region toward the-region (n =–n ) - p pressure in the-phase, N/m2 - p local volume-averaged intrinsic phase average pressure in the-phase, N/m2 - {p } large-scale intrinsic phase average pressure in the capillary region of the-phase, N/m2 - p local volume-averaged intrinsic phase average pressure for the-phase in the-region, N/m2 - p local volume-averaged intrinsic phase average pressure for the-phase in the-region, N/m2 - p –{p }, large scale spatial deviation for the-phase pressure, N/m2 - p –{p }, large scale spatial deviation for the-phase pressure in the-region, N/m2 - p –{p }, large scale spatial deviation for the-phase pressure in the-region, N/m2 - P c p –{p }, capillary pressure, N/m2 - {pc}c large-scale capillary pressure, N/m2 - r 0 radius of the local averaging volume, m - R 0 radius of the large-scale averaging volume, m - r position vector, m - , m - S /, local volume-averaged saturation for the-phase - S * {}*{}*, large-scale average saturation for the-phaset time, s - t time, s - u , m - U , m2 - v -phase velocity vector, m/s - v local volume-averaged phase average velocity for the-phase in the-region, m/s - v local volume-averaged phase average velocity for the-phase in the-region, m/s - {v } large-scale intrinsic phase average velocity for the-phase in the capillary region of the-phase, m/s - {v } large-scale phase average velocity for the-phase in the capillary region of the-phase, m/s - v –{v }, large-scale spatial deviation for the-phase velocity, m/s - v –{v }, large-scale spatial deviation for the-phase velocity in the-region, m/s - v –{v }, large-scale spatial deviation for the-phase velocity in the-region, m/s - V local averaging volume, m3 - V volume of the-phase in, m3 - V large-scale averaging volume, m3 - V capillary region for the-phase within, m3 - V capillary region for the-phase within, m3 - V c intersection of m3 - V volume of the-region within, m3 - V volume of the-region within, m3 - V () capillary region for the-phase within the-region, m3 - V () capillary region for the-phase within the-region, m3 - V () , region in which the-phase is trapped at the irreducible saturation, m3 - y position vector relative to the centroid of the large-scale averaging volume, m Greek Letters local volume-averaged porosity - local volume-averaged volume fraction for the-phase - local volume-averaged volume fraction for the-phase in the-region - local volume-averaged volume fraction for the-phase in the-region - local volume-averaged volume fraction for the-phase in the-region (This is directly related to the irreducible saturation.) - {} large-scale intrinsic phase average volume fraction for the-phase - {} large-scale phase average volume fraction for the-phase - {}* large-scale spatial average volume fraction for the-phase - –{}, large-scale spatial deviation for the-phase volume fraction - –{}, large-scale spatial deviation for the-phase volume fraction in the-region - –{}, large-scale spatial deviation for the-phase volume fraction in the-region - a generic local volume-averaged quantity associated with the-phase - mass density of the-phase, kg/m3 - mass density of the-phase, kg/m3 - viscosity of the-phase, N s/m2 - viscosity of the-phase, N s/m2 - interfacial tension of the - phase system, N/m - , N/m - , volume fraction of the-phase capillary (active) region - , volume fraction of the-phase capillary (active) region - , volume fraction of the-region ( + =1) - , volume fraction of the-region ( + =1) - {p } g, N/m3 - {p } g, N/m3  相似文献   

13.
We consider a surface S = (), where 2 is a bounded, connected, open set with a smooth boundary and : 3 is a smooth map; let () denote the components of the two-dimensional linearized strain tensor of S and let 0 with length 0 > 0. We assume the the norm ,|| ()||0, in the space V0() = { H1() × H1() × L2(); = 0 on 0 } is equivalent to the usual product norm on this space. We then establish that this assumption implies that the surface S is uniformly elliptic and that we necessarily have 0 = .  相似文献   

14.
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, nk 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  相似文献   

15.
Since the temperature is not an additive function, the traditional thermodynamic point of view suggests that the volume integral of the temperature has no precise physical meaning. This observation conflicts with the customary analysis of non-isothermal catalytic reactors, heat pipes, driers, geothermal processes, etc., in which the volume averaged temperature plays a crucial role. In this paper we identify the thermodynamic significance of the volume averaged temperature in terms of a simple two-phase heat transfer process. Given the internal energy as a function of the point temperature and the density
we show that the volume averaged internal energy is represented by e = F(T , )when e is a linear function of T and , or when the traditional length-scale constraints associated with the method of volume averaging are satisfied. When these conditions are not met, higher order terms involving the temperature gradient and the density gradient appear in the representation for e .  相似文献   

16.
Zusammenfassung Es wird eine analytische Lösung für die Absorption in einem laminaren Rieselfilm mit homogener und heterogener chemischer Reaktion 1. Ordnung vorgestellt, wobei der Stofftransportwiderstand auf der Gasseite liegt. Die Lösung ist eine Funktion von drei dimensionslosen ParameternBi, und, welche die BiotZahl und einen homogenen bzw. heterogenen Reaktionsparameter darstellen. Es wird gezeigt, daß für feste Werte vonBi und die Absorptionsrate (bezogen auf die Breite 1 des Rieselfilms) über eine gewisse Länge (dimensionslos) des Rieselfilms unabhängig von ist, wenn, < 0,6 ist. Die laufende Länge wird von der Stelle aus gemessen, an der die Absorption beginnt. Für b 0,6 nimmt der FlußQ mit zu, erreicht aber einen Sättigungswert bei=10, wonachQ nurmehr sehr langsam anwächst. Jedoch für ein gegebenes und ohne Übergangswiderstand im Film (Bi ) nimmtQ mit für alle 0 zu.
Mass transfer with chemical reaction in a laminar falling film
An analytical solution is presented for gas absorption in a laminar falling film with first-order homogeneous and heterogeneous chemical reaction and external gas-phase mass transfer resistance. The solution depends on three dimensionless parametersBi, and, wich represent the Biot number, homogeneous and heterogeneous reaction parameters, respectively. It is shown that for fixed values ofBi and, the rate of gas absorption (per unit breadth) over a certain length; (dimensionless) along the falling film measured from the point where surface absorption begins is independent of if < 0.6. For 0.6, this fluxQ increases with but reaches a saturation value at=10 beyond whichQ increases very slowly. But for given and zero gas film resistance (Bi ),Q increases with for all 0.
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17.
An experimental study was done to quantify the effects of a variety of background particulates on the delayed laminar-turbulent transition of a thermally stabilized boundary layer in water. A Laser-Doppler Velocimeter system was used to measure the location of boundary layer transition on a 50 mm diameter, 9:1 fineness ratio ellipsoid. The ellipsoid had a 0.15 m RMS surface finish. Boundary layer transition locations were determined for length Reynolds numbers ranging from 3.0 × 106 to 7.5 × 106. The ellipsoid was tested in three different heating conditions in water seeded with particles of four distinct size ranges. For each level of boundary layer heating, measurements of transition were made for clean water and subsequently, water seeded with 12.5 m, 38.9 m, 85.5 m and 123.2 m particles, alternately. The three surface heating conditions tested were no heating, T = 10°C and T = 15°C where T is the difference between the inlet model heating water temperature, T i, and free stream water temperature, T . The effects of particle concentration were studied for 85.5 m and 123.2 m particulates.The results of the study can be summarized as follows. The 12.5 m and 38.9 m particles has no measurable effect on transition for any of the test conditions. However, transition was significantly affected by the 85.5 m and 123.2 m particles. Above a length Reynolds number of 4 × 106 the boundary layer transition location moved forward on the body due to the effect of the 85.5 m particles for all heating conditions. The largest percentage changes in transition location from clean water, were observed for 85.5 m particles seeded water.Transition measurements made with varied concentrations of background particulates indicated that the effect of the 85.5 m particles on the transition of the model reached a plateau between 2.65 particulates/ml concentration and 4.2 particles/ml. Measurements made with 123.3 m particles at concentrations up to 0.3 part/ml indicated no similar plateau.  相似文献   

18.
Shear softening and thixotropic properties of wheat flour doughs are demonstrated in dynamic testing with a constant stress rheometer. This behaviour appears beyond the strictly linear domain (strain amplitude 0 0.2%),G,G and |*| decreasing with 0, the strain response to a sine stress wave yet retaining a sinusoidal shape. It is also shown thatG recovers progressively in function of rest time. In this domain, as well as in the strictly linear domain, the Cox-Merz rule did not apply but() and | *())| may be superimposed by using a shift factor, its value decreasing in the former domain when 0 increases. Beyond a strain amplitude of about 10–20%, the strain response is progressively distorted and the shear softening effects become irreversible following rest.  相似文献   

19.
The molecular theory of Doi has been used as a framework to characterize the rheological behavior of polymeric liquid crystals at the low deformation rates for which it was derived, and an appropriate extension for high deformation rates is presented. The essential physics behind the Doi formulation has, however, been retained in its entirety. The resulting four-parameter equation enables prediction of the shearing behavior at low and high deformation rates, of the stress in extensional flows, of the isotropic-anisotropic phase transition and of the molecular orientation. Extensional data over nearly three decades of elongation rate (10–2–101) and shearing data over six decades of shear rate (10–2–104) have been correlated using this analysis. Experimental data are presented for both homogeneous and inhomogeneous shearing stress fields. For the latter, a 20-fold range of capillary tube diameters has been employed and no effects of system geometry or the inhomogeneity of the flow-field are observed. Such an independence of the rheological properties from these effects does not occur for low molecular weight liquid crystals and this is, perhaps, the first time this has been reported for polymeric lyotropic liquid crystals; the physical basis for this major difference is discussed briefly. A Semi-empirical constant in eq. (18), N/m2 - c rod concentration, rods/m3 - c * critical rod concentration at which the isotropic phase becomes unstable, rods/m3 - C interaction potential in the Doi theory defined in eq. (3) - d rod diameter, m - D semi-empirical constant in eq. (19), s–1 - D r lumped rotational diffusivity defined in eq. (4), s–1 - rotational diffusivity of rods in a concentrated (liquid crystalline) system, s–1 - D ro rotational diffusivity of a dilute solution of rods, s–1 - f distribution function defining rod orientation - F tensorial term in the Doi theory defined in eq. (7) (or eq. (19)), s–1 - G tensorial term in the Doi theory defined in eq. (8) - K B Boltzmann constant, 1.38 × 10–23 J/K-molecule - L rod length, m - S scalar order parameter - S tensor order parameter defined in eq. (5) - t time, s - T absolute temperature, K - u unit vector describing the orientation of an individual rod - rate of change ofu due to macroscopic flow, s–1 - v fluid velocity vector, m/s - v velocity gradient tensor defined in eq. (9), s–1 - V mean field (aligning) potential defined in eq. (2) - x coordinate direction, m - Kronecker delta (= 0 if = 1 if = ) - r ratio of viscosity of suspension to that of the solvent at the same shear stress - s solvent viscosity, Pa · s - * viscosity at the critical concentrationc *, Pa · s - v 1, v2 numerical factors in eqs. (3) and (4), respectively - deviatoric stress tensor, N/m2 - volume fraction of rods - 0 constant in eq. (16) - * volume fraction of rods at the critical concentrationc * - average over the distribution functionf(u, t) (= d 2u f(u, t)) - gradient operator - d 2u integral over the surface of the sphere (|u| = 1)  相似文献   

20.
An oscillating vortex embedded within a turbulent boundary layer was generated experimentally by forcing a periodic lateral translation of a half-delta wing vortex generator. The objective of the experiment was to investigate the possibility that a natural oscillation, or meander, might be responsible for flattened vortex cores observed in previous work, which could also have contaminated previous turbulence measurements. The effect of this forced oscillation was characterized by comparison of measurements of the mean velocities and Reynolds stresses at two streamwise stations, for cases with and without forcing. The Reynolds stresses, especially w, were affected significantly by the forced oscillation, mainly through contributions from the individual production terms, provided the vortex was not too diffuse.List of Symbols a amplitude of forced vortex motion - f frequency of forced vortex generator motion - l vortex generator root chord - L flow length scale - R Y , R Z vortex core radial dimensions in vertical and spanwise directions, respectively - Rr vortex circulation Reynolds number R = / - u, v, w instantaneous velocity components in X, Y, Z directions - U, V, W mean velocities; shorthand notation for u, , w - X, Y, Z right-hand Cartesian streamwise, vertical, and spanwise coordinate directions - boundary-layer thickness - overall circulation - air kinematic viscosity - x streamwise vorticity, X = W/Y–V/d+t6Z - ( )0 reference value (measured at X = 10 cm) - ( )c refers to vortex center - ( ) max maximum value for a particular crossflow plane - ( ) (overbar) time average - ( ) (prime) fluctuating component, e.g., u=U+u  相似文献   

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