Shear viscosity of liquid4He and3He-4He mixtures,especially near the superfluid transition

High-resolution measurements of are reported for liquid⁴He and³He-⁴He mixtures at saturated vapor pressures between 1.2 and 4.2 K with particular emphasis on the superfluid transition. Here is the mass density, the shear viscosity, and in the superfluid phase both and are the contributions from the normal component of the fluid ( _n and _n ). The experiments were performed with a torsional oscillator operating at 151 Hz. The mole fraction X of³He in the mixtures ranged from 0.03 to 0.65. New data for the total density and data for _n by various authors led to the calculation of . For⁴He, the results for are compared with published ones, both in the normal and superfluid phases, and also with predictions in the normal phase both over a broad range and close to T. The behavior of and of in mixtures if presented. The sloped/dT near T and its change at the superfluid transition are found to decrease with increasing³He concentration. Measurements at one temperature of versus pressure indicate a decreasing dependence of on molar volume asX(³He) increases. Comparison of at T, the minimum of _n in the superfluid phase and the temperature of this minimum is made with previous measurements. Thermal conductivity measurements in the mixtures, carried out simultaneously with those of , revealed no difference in the recorded superfluid transition, contrary to earlier work. In the appendices, we present data from new measurements of the total density for the same mixtures used in viscosity experiments. Furthermore, we discuss the data for _n determined for⁴He and for³He-⁴He mixtures, and which are used in the analysis of the data.     

Eta-conversion for the languages of explicit substitutions

Some new calculi [1,12,7], referred to by the collective name of - calculus, have been recently introduced to provide an explicit treatment of substitutions in the -calculus. They are term rewriting systems, with two sorts: substitution and term. The -terms are exactly the ground -terms of sort term containing no substitutions and the -reduction is decomposed in these calculi, into a starting reduction with a rule called (Beta) followed by a derivation computing explicitly the substitution. These calculi differ by their treatment of substitution. In this paper, we extend the -calculi with a conditional rewriting relation, called c. This relation coincides, on -terms, with the classical-reduction of -calculus. We prove that the confluent -calculus, augmented byc, remains confluent and that the ground confluent version [1], extended by c, is still ground confluent. The result extends readily to Categorical Combinatory Logic. The proof is done by the interpretation method introduced in [9].This work has been partially supported by the Eureka Software Factory project.     

A finite volume technique to simulate the flow of a viscoelastic fluid

Hydrodynamically developing flow of Oldroyd B fluid in the planar die entrance region has been investigated numerically using SIMPLER algorithm in a non-uniform staggered grid system. It has been shown that for constant values of the Reynolds number, the entrance length increases as the Weissenberg number increases. For small Reynolds number flows the center line velocity distribution exhibit overshoot near the inlet, which seems to be related to the occurrence of numerical breakdown at small values of the limiting Weissenberg number than those for large Reynolds number flows. The distributions of the first normal stress difference display clearly the development of the flow characteristics from extensional flow to shear flow.List of symbols D rate of strain tensor - L slit halfheight - P pressure, indeterminate part of the Cauchy stress tensor - R the Reynolds number - t time - U average velocity in the slit - u velocity vector - u,v velocity components - W the Weissenberg number based on the difference between stress relaxation time and retardation time - W ₁ the Weissenberg number based on stress relaxation time - x,y rectangular Cartesian coordinates - ratio of retardation time to stress relaxation time - zero-shear-rate viscosity, ₁ + ₂ - ₁ non-Newtonian contribution to - ₂ Newtonian contribution to - ₁ stress relaxation time - ₂ retardation time - density - (, , ) xx, yy and xy components of ₁, respectively - determinate part of the Cauchy stress tensor - ₁ non-Newtonian contribution to - ₂ Newtonian contribution to      

Phase decomposition in extruded Zn-Al based alloy

Ageing characteristics of an extruded eutectoid Zn-Al based alloy were investigated using X-ray diffraction and scanning electron microscopy techniques. The extruded alloy consisted of Al rich phase and Zn rich _E and phases. The original cast eutectoid Zn-Al alloy was extruded at 250 °C. Both supersaturated _s and _s phase decomposed during extrusion and appeared as fine and coarse lamellar structures. The _E and phases particles formed in the original interdendritic region. It was found that two Zn rich phases _E and decomposed sequentially during ageing at 170, 140 °C. The decomposition of the _E phase occurred as a discontinuous precipitation in the early stage of ageing and the decomposition of the phase took place in a four phase transformation: + T + in the prolonged ageing. Two typical morphologies of the decomposition of the Zn rich phases _E and were distinctive in back-scattered scanning electron microscopy.     

Dependence of the contact heat conductivity of granular systems on the external load

An examination has been made of the dependence of the contact heat conductivity of granular systems on the external load. The calculation formulas proposed for contact heat conduction are applicable over a wide range of materials.Notation s_a area of actual contact of two particles in a granular material - _c conductivity of the contact between two particles - h_r height of a micro-roughness - _s thermal conductivity of the material of the particles - d=2r particle diameter - _c contact thermal conductivity of the granular material - p porosity of the system - S_a1, S_a2 area of contact of two particles in the freely poured state and under the action of a load - f thermal conductivity of the granular system in the freely poured state - () portion of the thermal conductivity of a granular material that depends on the external load - relative area of contact - s_n nominal area of contact of the two particles - external specific load - E modulus of elasticity of the particle material - E₀ effective modulus of elasticity of the granular material - k₁, k₂, k₃, k_m, k_b empirical coefficients     

Shear viscosity measurements of liquid 3He-4He mixtures above 0.5 K

Simultaneous measurements of () and of the molar volume are reported for liquid mixtures of ³He in ⁴He over the temperature range between 0.5 and 2.5 K. Here is the shear viscosity and is the mass density. In the superfluid phase, the product of the normal components, _n and _n , is measured. The mixtures with ³He molefractions 0.30 < X < 0.80 are studied with emphasis on the region near the superfluid transition T and near the phase-separation curve. Along the latter, they are compared with data by Lai and Kitchens. For X > 0.5, the viscosity singularity near T becomes a faint peak, which however fades into the temperature-dependent background viscosity as X tends to the tricritical concentration X _t. Likewise, no singularity in is apparent when T _t is approached along the phase separation branches _– and ₊. Furthermore, viscosity data are reported for ³He and compared with previous work. Finally, for dilute mixtures with 0.01 X 0.05, the results for are compared with previous data and with predictions.     

Effect of phase fluctuations upon penetration depth

The temperature dependence of the static penetration (T) has been used as a guide to the nature of the superconducting state in high-T _c materials. It has been argued that an algebraic temperature dependence in the ratio (T)/(0) [(T) — (0)]/(0) at low temperature is evidence for d-wave pairing. This paper examines the effect of superconducting phase fluctuations upon (T) and finds an algebraic dependence over a broad range of temperature.     

Ageing characteristics of furnace cooled eutectoid Zn-Al based alloy

Phase transformations and microstructural changes of a furnace cooled eutectoid Zn-Al based alloy were studied during ageing at 100 and 170°C using X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. Three phase transformations occurred in the furnace cooled eutectoid Zn-Al alloy. The metastable _FC phase decomposed during isothermal ageing. The four-phase transformation, + T + followed the discontinuous decomposition of the _FC phase. Typical morphologies of the decomposition of the _FC and phases were observed in scanning electron microscopy. Decomposition of Al-rich phase was observed during the prolonged ageing by transmission electron microscopy. The different types of decomposition of the different metastable phases dominated at different stages of ageing.     

Separable functions in load separation for the ηpl and ηpl CMOD plastic factors estimation

The objective of this paper is to develop the load separation method for evaluating the _pl and _pl ^CMOD plastic factors used in the J estimation approach based on load versus displacement records. Appropriate forms for the geometry and deformation functions have been suggested from the EPRI Handbook solutions to produce the separable form for the load. The obtained functions are applied to evaluate the _pl and _pl ^CMOD plastic factors for center cracked tension specimen. The present load separation method gave results which are somewhat different from the estimated values of _pl given in the literature. For shallow cracks, the _pl and ^CMOD _pl plastic factors show considerable variation with crack size and the strain hardening exponent. For a deeply cracked CCT specimen, the ^CMOD _pl factor tends to the _pl factor and equals approximately unity. Abbreviations: CCT – center cracked specimen; CMOD – Crack Mouth Opening Displacement; EPRI – Electric Power Research Institute; FEM – Finite Element Method; LLD – Load Line Displacement.     

Transport in the low-temperature limit of a Landau Fermi liquid

The Boltzmann equation for Landau quasiparticles is solved for T 0 by a specialization of a method discussed by Sykes and Brooker. The quasiparticle distribution function is expanded in Legendre polynomials, assuming a boundary condition which imposes axial symmetry, and even-order terms are assumed to relax together with relaxation time _e , odd-order terms with relaxation time _o . By letting wavelength , with finite, one obtains a first-sound solution, and by lettingT 0, and then , one obtains a zero-sound solution. When these solutions are used to calculate the pressure, it is found that the first-sound solution is consistent with hydrodynamics, exhibiting viscosity = _s , while the zero-sound velocityc ₁=[^–1(B₁+4/3_s)]^1/2, so that phenomenologically zero-sound propagates like a longitudinal elastic wave in a glass. A higher zero-sound mode is also predicted, but is heavily damped. The heat flux is calculated and found to obey Vernotte's equation, which contains an intertial term, added to Fourier's law, that becomes significant asT 0.     

Viscoelastic and rheological behavior of concentrated colloidal suspensions

Molecular approaches are discussed to the density (), viscoeleastic (), and rheological () behavior of the viscosity(,,) of concentrated colloidal suspensions with 0.3 < < 0.6, where, is the volume fraction, the applied frequency, and ; the shear rate. These theories are based on the calculation of the pair distribution functionP ₂(r,,), wherer is the relative position of a pair of colloidal particles. The linear viscoelastic behavior(,,=0) follows from an equation forP ₂(r,,) derived from the Smoluchowski equation for small, generalized to large by introducing the spatial ordering and (cage) diffusion typical for concentrated suspensions. The rheological behavior(,,=0) follows from an equation forP ₂(r,) of a dense hard-sphere fluid derived from the Liouville equation. This leads to a hard-sphere viscosity^hs(,) which yields the colloidal one(,) by the scaling relation(,) ₀=^hs(,) _B, where ₀ is the solvent viscosity. _B is the dilute hard-sphere (Boltzmann ) viscosity and the's are appropriately scaled,(,) and(,) agree well with experiment. A unified theore for(,,) is clearly needed and pursued.Paper presented at the Twelfth Symposium on Thermophysical Properties, June 19–24, 1994. Boulder, Colorado, U.S.A.     

Relations Between Transport Coefficients in Lennard–Jones Fluids and in Liquid Metals

Several simple approximate hard-sphere relations for transport coefficients are compared with the results of molecular dynamics (MD) simulations performed on Lennard–Jones (LJ) fluids. Typically the individual transport coefficients: self-diffusion coefficients, D, shear viscosity, _s, bulk viscosity, _B, and thermal conductivity, , agree within a factor of two of the exact results over the fluid and liquid parts of the phase diagram, which seems reasonable in view of the approximations involved in the models. We have also considered the ratio, /_s, and the product, D_s, for which simple analytic expressions exist in the hardsphere models. These two quantities also agree within a factor of two of the simulation values and hard sphere analytic expressions. Using time correlation functions, Tankeshwar has recently related the ratio /D to thermodynamic quantities, in particular, to the differences in specific heats, C _p – C _V, and to the isothermal compressibility, T. Using D and thermodynamic values taken solely from LJ MD simulations, his relation was tested and found to give typically better than ~20% agreement at liquid densities, deteriorating somewhat as density decreases into the gas phase. Finally liquid metals are considered. In this case, is dominated by its electronic contribution, which is related approximately to the electrical conductivity by the Wiedemann–Franz Law. Some theoretical results for the electrical conductivity of Na are referenced, which allow a semiquantitative understanding of the measured thermal conductivity of the liquid metal. Shear viscosity is also discussed and, following the work of Tosi, is found to be dominated by ionic contributions; Nevertheless, at the melting temperature of Na, a relation emerges between thermal conductivity, electrical resistivity and shear viscosity.     

Cross-Correlated Dynamic Resistance of a Direct Current Superconducting Quantum Interference Device

This paper presents experimental data on a comparative study of a dc SQUID with voltage and current bias. We introduce a cross-correlated dynamic resistance of the device defined as a ratio R _dCV = _VC/_IV, where _VC = (V/) _A is the slope of the voltage-to-flux characteristics measured in the current bias mode and _IV = (I/) _A is the slope of the current-to-flux characteristics measured with voltage bias. It has been found that R _dCV may deviate strongly from the dynamic resistance observed in the current bias mode of operation. The intrinsic energy resolution of the SQUID remains unchanged for both modes of operation, but the current noise of the voltage biased device scales with the cross-correlated dynamic resistance. In our SQUID with the loop inductance L = 105 pH, is equal to 37 h in the white noise region at a temperature of 4.2 K.     

Secondary and tertiary dendrite arm spacing relationships in directionally solidified Al-Si alloys

Secondary, ₂, and tertiary, ₃, dendrite arm spacings have been measured from Al-Si alloys which were directionally solidified as functions of growth velocity,V, temperature gradient,G, and composition,C _o. Both ₂ and ₃ decreased as the imposed growth velocity and silicon concentrations were increased, and for each function a systematic variance in the rate was seen. Complications with measuring secondary arm spacings are shown and it was found that the tertiary arm data agree much better with coarsening theory, the implication being that ₃, when measurable, is a more representative and reliable measure of the solidification history than ₂.     

Effect of annealing upon decomposition of electrodeposited iron-zinc alloy coatings

As-deposited electrodeposited iron-zinc alloy coatings containing phase, decompose upon heating through a sequence of metastable phases. The h c p phase transforms to b c c G, or -like phase via a rapid diffusional phase transformation in the vicinity of 150 °C. For bulk iron contents of 8–13 wt%, transforms to 100% G phase. The G phase subsequently transforms at 240 °C to phase, which in turn transforms to or ₁ phase near 300 °C by depletion of iron from the surrounding matrix. The decomposition process may be driven by supersaturation of with iron.     

The behavior of the4He viscosity near the superfluid transition

Measurements of the shear viscosity at saturated vapor pressure through the lambda transition indicate a singular behavior of the form |1 – (/)|=A ^x , (where =|1–(T/T )|, with equal values for the critical exponent on both sides of the transition.Work sponsored by Consiglio Nazionale delle Ricerche, Rome (Italy).     

Ageing characteristics of cast Zn-Al based alloy (ZnAl7Cu3)

Microstructure and ageing characteristics of a cast Zn-Al based alloy (ZnAl7Cu3) were studied using X-ray diffraction, electron scanning microscopy and back-scattered diffraction techniques. Two stages of phase transformation, i.e., decomposition of zinc rich phase and four phase transformation, + T + , were detected during ageing at 150°C. Electron back-scattered diffraction technique was applied in distinguishing both zinc rich and phases.     

Branching of the Falkner-Skan solutions for λ<0

Summary The Falkner-Skan equation f+ff+(1-f²)=0,f(0)=f(0), is discussed for <0. Two types of problems, one with f()=1 and another with f()=-1, are considered. For =0^- a close relation between these two types is found. For <-1 both types of problem allow multiple solutions which may be distinguished by an integer N denoting the number of zeros of f-1. The numerical results indicate that the solution branches with f()=1 and those with f()=-1 tend towards a common limit curve as N increases indefinitely. Finally a periodic solution, existing for <-1, is presented.     

Analytic solutions of parabolic and hyperbolic heat-transfer equations for nonlinear media

New classes of analytic solutions are obtained which describe unsteady temperature distributions and take account of the temperature dependence of the thermophysical properties of the material. The concept of a solution of the boundary layer transition type is introduced for the generalized heat-transfer equation.Notation T temperature - x Cartesian coordinate - t time - c volumetric heat capacity - thermal conductivity of medium - heat-transfer (heat flux) relaxation period - q_v internal heat source strength - new argument - auxiliary function Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 40, No. 3, pp. 510–517, March, 1981.     

Correlation of dense fluid self-diffusion,shear viscosity,and thermal conductivity coefficients

A general procedure has been developed for simultaneously fitting any two of the self-diffusion coefficient, the viscosity (as the fluidity), and the thermal conductivity (as its reciprocal) as Dymond reduced coefficients, (D*,*,*), to a simple function of the volume and the temperature for dense fluids. For example,D*=₁+₂ V _r/(1+₃,/V _r), whereV _r=V[1-₁(T–T _r)-₂(T–T _r)²].T _r is any convenient temperature, here 273.15 K. AsV _r is common to the two properties, only eight coefficients, _j and _k are required. Such reduced transport-coefficient curves are geometrically similar for members of groups of closely related compounds. The procedure has been extended to give family curves for such groups by fitting a pair of transport properties for three substances from the group in a single regression. Overall, fewer coefficients are required than for other schemes in the literature, and the fitting functions used are simpler. The curves so constructed can be used for the correlation of data obtained from different sources, as well as interpolation and, to a limited extent, extrapolation. A comparison is made for a number of compotmd groups between simultaneous fits of the pairs (D– ), (D–), and (–)Paper presented at the Twelfth Symposium on Thermophysical Properties, June 19–24, 1994, Boulder, Colorado, U.S.A.