Thermal transport properties of helium near the superfluid transition. II. Dilute3He-4He mixtures in the superfluid phase

Measurements of the average thermal conductivity _exp hQ/T and of the thermal relaxation time to reach steady-state equilibrium conditions are reported in the superfluid phase for dilute mixtures of³He in⁴He. Hereh is the cell height,Q is the heat flux, andT is the temperature difference across the fluid layer. The measurements were made over the impurity range 2×10^–9<X(³He)<3×10^–2 and with heat fluxes 0.3<Q<160 µW/cm². Assuming the boundary resistanceR _b , measured forX<10^–5, to be independent ofX over the whole range ofX, a calculation is given for _exp. ForQ smaller than a well-defined critical heat fluxQ _c (X) X ^0.9, _exp is independent of Q and can be identified with the local conductivity _eff, which is found to be independent of the reduced temperature = (T–T)/T for –10^–2. Its extrapolated value at T is found to depart forX10^–3 from the prediction X ^–1 , tending instead to a weaker divergence X ^–a witha0.08. A finite conductivity asX tends to zero is not excluded by the data, however. ForQ >Q _c (X), a nonlinear regime is entered. ForX10^–6, the measurements with the available temperature resolution are limited to the nonlinear conditions, but can be extrapolated into the linear regime forX2×10^–7. The results for _exp(Q),Q _c (X), and _eff(XX) are found to be internally consistent, as shown by comparison with a theory by Behringer based on Khalatnikov's transport equations. Furthermore, the observed relaxation times (X) in the linear regime are found to be consistent forX>10^–5 with the hydrodynamic calculations using the measured _eff(X). ForX<10^–5, a faster relaxation mechanism than predicted seems to dominate. The transport properties in the nonlinear regimes are presented and unexplained observations are discussed.     

Ultrasonic dispersion and attenuation near the liquid-gas critical point of 3He

We report ultrasonic dispersion and attenuation measurements near the liquid-gas critical point of ³He at frequencies from 0.5 to 5.0 MHz and densities from 0.89 _c to 1.15 _c . The singular part of the sound attenuation and the dispersion on the critical isochore _c = 0.0414 g/cm³ are analyzed in terms of the Kawasaki-Mistura theory. If the Ornstein-Zernike order parameter correlation function is assumed in the analysis, good agreement with our data is achieved, except close to the critical temperature T _cin the high-frequency region, where ^* = /_D 1. Here _D is the characteristic relaxation rate of the critical fluctuations. From a fit of the theory to our data, and assuming the inverse correlation length is expressed by = ₀, where = (T–T_c)/T_c with = 0.63, we obtain ₀ = (3.9 ± 0.4) × 10⁹ m^–1. It is found that a more realistic form of the correlation function, as proposed by Fisher and Langer and calculated by Bray, yields even poorer agreement with out data than does the classical Ornstein-Zernike form for ^* > 10. The same difficulties appear in the analysis of the available data for xenon. Thus, the present mode coupling theory is unable to satisfactorily describe the acoustic experiments on fluids near the liquid-vapor critical point over a large range of reduced frequencies ^*. In the appendix, we reanalyze previously reported ultrasonic data in ⁴He, taking into account the nonsingular term of the thermal conductivity. Using = 0.63, we obtain a good fit of the experiment to the theory in the hydrodynamic region with ₀ = (5.5 ± 1) × 10⁹ m^–1.Supported by a grant from the National Science Foundation.     

Hydrodynamic heat flow in very dilute superfluid3He-4He mixtures

The superfluid hydrodynamics of heat flow is examined for very small mass concentrationsc of³He in⁴He in an effort to better understand recent results for the effective heat conductivity _eff, which appear to be in conflict with predictions. The full hydrodynamics contains a thermal boundary layer; within this layer the temperature and concentration gradients differ from those in the bulk fluid. An examination of finite heating effects based on the ansatz _eff c ^–p for smallc shows distinctly different behavior for experimental determinations of _eff whenp<1,p=1, andp>1. Thus, finite heating can be used as a probe to evaluate the exponentp.     

Thermal response of a3He-superfluid-4He mixture

The response of a layer of superfluid mixture to an ac heat source,Q(t)=Q ₀ exp(it), is determined. In the low-frequency regime, the temperature response at the heated side of a superfluid layer is essentially identical to that of an ordinary fluid having a thermal conductivity _eff and a thermal diffusion coefficient ₀ /2. Here _eff is the effective conductivity of Khalatnikov, and ₀ is the diffusion coefficient of Griffin. At much higher frequencies, the results are more complicated. The low-frequency regime is defined in terms of the second sound velocityu ₂ by u ₂ ² / ₀ . The ac response function is valuable in a number of ways. It can be used to obtain the system response to more complicated time-dependent variations inQ such as step changes inQ. A knowledge of the response function in the low-frequency regime provides a mechanism for directly determining the Kapitza resistance in mixtures. Finally, a knowledge of the response function provides an additional opportunity to test two-fluid hydrodynamics. Alternative tests of superfluid hydrodynamics are of particular interest in light of recent experiments that show anomalous values for _eff in the low ³ He concentration limit     

Thermal Conductivity of the Four-Leg Spin-Ladder System La2Cu2O5 Single Crystal

We have investigated the magnetic susceptibility, , and the thermal conductivity, , in magnetic fields for the four-leg spin-ladder system La₂Cu₂O₅ single crystal. The in a magnetic field parallel to the ladder exhibits a kink at 130 K in correspondence to the magnetic ordering. The along the ladder exhibits a peak at 25 K and a shoulder at 14 K, which are probably related to the thermal conductivity due to magnons, _magnon, and that due to phonons, _phonon, respectively. The perpendicular to the ladder, on the other hand, exhibits only one broad peak related to _phonon. The observed large anisotropy of has been explained based upon the anisotropy of _magnon.     

Thermal transport properties in helium near the superfluid transition. III. Dilute3He-4He mixtures in the normal phase

An experimental study is presented for the thermal conductivity and the thermal relaxation for dilute mixtures of³He in⁴He with concentration 9×10^–4X(³He)5×10^–2 at saturated vapor pressure and in the normal phase near the superfluid transition. The conductivity results for are compared with predictions by Dohm and Folk from field-theoretic renormalization group(RG) theory. The conductivity _s =[^–1(T)–^–1(T)]^–1, is compared with Ahlers' phenomenological arguments, and also with predictions by Dohm and Folk and by Onuki. The temperature difference transient T(t) across the fluid, measured as a function of timet after switching on and off the heat current, is analyzed. The thermal diffusion ratiok _T and the mass diffusion coefficientD are obtained by fitting the calculated transient to the experimental one. The results are compared with the predictions that follow from the RG approach by Dohm and Folk. Very good agreement is obtained fork _T. The transient is not very sensitive toD, and hence the determination is not accurate. Yet within the uncertainty, the deducedD also agrees with predictions. Appendices give (1) the corrections to from finite heat effects, (2) the calculation of the concentration susceptibility (X/) _T,P , and (3) the calculation procedure for ,k _T, andD using the RG approach of Dohm and Folk.     

Impulse approximation in solid helium

The incoherent dynamic form factorS _i(Q, ) is evaluated in solid helium for comparison with the impulse approximation (IA). The purpose is to determine theQ values for which the IA is valid for systems such as helium where the atoms interact via a potential having a steeply repulsive but not infinite hard core. For³He,S _i(Q, ) is evaluated from first principles, beginning with the pair potential. The density of statesg() is evaluated using the self-consistent phonon theory andS _i(Q, ) is expressed in terms ofg(). For solid⁴He reasonable models ofg() using observed input parameters are used to evaluateS _i(Q, ). In both casesS _i(Q, ) is found to approach the impulse approximationS _IA(Q, ) closely for wave vector transfersQ20 Å^–1. The difference betweenS _i andS _IA, which is due to final state interactions of the scattering atom with the remainder of the atoms in the solid, is also predominantly antisymmetric in (–_R), where _R is the recoil frequency. This suggests that the symmetrization procedure proposed by Sears to eliminate final state contributions should work well in solid helium.     

Grain growth in the two-phase Al-Cu alloys

Grain and phase growth in the two-phase Al-Cu alloys containing 6, 11, 1 7, 24 and 33 wt % Cu were investigated by annealing at 535 °C for 0.5–100 h. The grain and phase sizes of the phase are seen to be larger than that of the phase. The size of phase decreases whereas the size of phase increases with increasing copper content in the alloy. As such, the phase- and grain-size distributions are broader than the phase- and grain-size distributions, but the size range depends on annealing time and alloy composition. The grain sizes of the ,d , and ,d , phases can be related to the volume fraction of the phase,f , according to the equationd = 0.497d /f .     

Transport properties for a dilute solution of3He in two-dimensional liquid4He

The temperature variations of the diffusion coefficientD(T), thermal diffusion ratio k _T (T) and thermal conductivity (T) in a dilute solution of³He atom in two-dimensional liquid helium are evaluated explicitly by solving the kinetic equations via phonon-phonon, phonon-roton, roton-roton, impurityelementary excitation and impurity-impurity scatterings. In the low-temperature region, the main contributions toD(T) and (T) come from the interactions between phonons and impurities, while in the high-temperature region the interactions between impurities and whole elementary excitations contribute more strongly toD(T) and (T) than those of only elementary excitations. For a dilute solution, the thermal diffusion ratio k _T (T), neglecting the internal mass counterflow, is much smaller than the effective thermal diffusion ratio k _T ^* (T), which is a function of thermostatic properties. The effective thermal conductivity _eff is much larger than the thermal conductivity and has different temperature dependence from the thermal conductivity. The behaviors of the two-dimensional diffusion coefficient and thermal conductivity are much like the bulk case, where they exhibit exponential decay with increasing temperature, although they are much smaller than those of the bulk case.     

Transport properties in the superfluid phase of dilute3He-4He mixtures nearT λ

A cell for the simultaneous measurements of temperature and³He concentration gradients, induced by a heat currentQ across a fluid helium layer is described. This cell is operated over the temperature range 1.7T<2.5 K. Measurement of the anomalous boundary resistance R_b in superfluid⁴He(X(³He)2 ppb) near T for heat currents between 8 and 47 µW/cm² are described. The results for both the weakly divergent and the heat-dependent, more strongly divergent contributions to R _b are presented. The observed amplitude of the linear part is found to be larger than predictions by Onuki, by Ginzburg and Sobaynin and by Frank and Dohm, and also larger than recent data by Duncan and Ahlers (DA). These discrepancies are discussed in the light of the effective boundary area in the cell. The nonlinear part of R _b is consistent with the data by DA. It is found that the maximum observed R _b at the superfluid transition is independent ofQ. Analysis of the conductivity data of mixtures leads to the conjecture that R _b will decrease will the addition of³He. Our measurement of both the effective thermal diffusion ratiok _T ^* and of the thermal conductivity _eff over the range 10^–6<X<5×10^–2 show departures from the predictions by Khalatnikov. In particular forX<10^–3,k _T ^* is found to be a function of X, and _eff deviates from the predicted _effX ^–1. This last result confirms measurements with a previous cell. In the appendices, determinations and tabulations of auxiliary thermodynamic derivatives, such as (V/X)_T,P and (S/X)_T,P are presented.     

Sound propagation in 3He-4He mixtures near the superfluid transition

Measurements of the acoustic attenuation and dispersion in liquid ³He-⁴He mixtures near the superfluid transition T (x) are reported. The frequency range is /2gp=1–45 MHz and the ³He mole fraction X of the mixtures is 0.007, 0.05, 0.15, and 0.36. Comparisons are made with the measurements of Buchal and Pobell for similar mixtures obtained in the kHz region, and on the whole, the consistency between the two experiments is very satisfactory. An analysis is then performed using both the kHz and MHz data. In the normal phase, where the energy dissipation is caused by order parameter fluctuations having a lifetime _F , the attenuation data can all be scaled according to the expression = (T )f(_F. Here (T )^1+y, with y being a function of the mole fraction X and _F(T–T )^–x, with x increasing weakly with X. In the superfluid phase, we attempt a similar scaling representation, which is found to be fairly successful, but where x(T\s-T ) is roughly 15% larger than x(T>T ). In the superfluid phase we also analyze the attenuation data, assuming the additivity of relaxation and fluctuation-dissipation mechanism, and discuss the relaxation times so derived. In contrast to the attenuation, the dispersion data cannot be brought satisfactorily into a scaling representation. However, at T , we find U()-U(0)^y as predicted by Kawasaki, where y is in good agreement with the values from attenuation experiments.Supported by a grant from the National Science Foundation.     

Thermodynamics of the quasiequilibrial growth of crazes

By comparing the morphology and physical properties (averaged over the scale of 1 to 10m) of a crazed and uncrazed polymer, it can be concluded that crazing is a new phase development in the initially homogeneous material. The present study is based on recent work on the general thermodynamic explanation of the development of a damaged layer of material. The treatment generalizes the model of a crack-cut in mechanics. The complete system of equations for the quasiequilibrial craze growth follows from the conditions of local and global phase equilibrium, mechanical equilibrium and a kinematic condition. Constitutive equations of craze growth-equations are proposed that are between the geometric characteristics of a craze and generalized forces. It is shown that these forces, conjugated with the geometric characteristics of a craze, can be expressed through the known path independent integrals (J, L, M,). The criterion of craze growth is developed from the condition of global phase equilibrium. F Helmholtz's free energy - G Gibb's free energy (thermodynamic potential) - f density ofF - g density ofG - T absolute temperature - S density of entropy - strain tensor - components of - stress tensor - components of - _y stress along the boundary of an active zone (yield stress) - _b stress along the boundary of an inert zone - applied stress - value of at the moment of craze initiation - K stress intensity factor - C tensor of elastic moduli - C ^–1 tensor of compliance - internal tensorial product - V volume occupied by sample - V ₁ volume occupied by original material - V ₂ volume occupied by crazed material - V boundary ofV - (V) vector-function localized on V - (x) characteristic function of an area - (x) variation of(x) - (x) a finite function - tensor of alternation - components of the boundary displacement vector - l components of the vector of translation - n components of the normal to a boundary - _k components of the vector of rotation - e symmetric tensor of deviatoric deformation of an active zone - expansion of an active zone - J ⁽ⁱ⁾ ,L _k ⁽ⁱ⁾ ,M ⁽ⁱ⁾,N ⁽ⁱ⁾ partial derivatives ofG ⁽ⁱ⁾ with respect tol , _k, ande , respectively - [ ] jump of the parameter inside the brackets - thickness of a craze - 2l length of a craze - 2b length of an active zone - l _c distance between the geometrical centres of the active zone and the craze - ^* craze thickness on the boundary of an active and the inert zone - l ^* craze parameter (length dimension) - A craze parameter (dimensionless) - ^* extension of craze material     

Residual thermal stresses in the pull-out specimen: A finite element calculation

The residual thermal stress field in the pull-out specimen is calculated in the case of a high properties thermoset system (carbon-bismaleimide). The calculation is performed within the framework of the linear theory of elasticity by means of a finite element method. The specimen is modelled as a three-phase composite (holder-fibre-matrix). The meniscus which forms at the fibre entry is taken into account in order to provide a realistic stress concentration. The latter is far higher than the matrix strength. Evidence that fibre debonding propagates from the fibre end during cooling is then produced.Nomenclature T thermal load - L _e embedded length - r _f fibre radius - _c curvature radius of the meniscus (fibre entry) - r _c radial dimension of the finite element mesh - E _m,E _h matrix and holder moduli - E _A,E _T fibre axial and transverse moduli - _m, _h matrix and holder thermal expansion coefficients - _A, _T fibre axial and transverse thermal expansion coefficients - _rr, , _zz, _rz non-zero components of the residual stress field - _rr ⁱ , ^im , _zz ^im , _rz ⁱ stresses at the interface in the matrix (r=r _f + ) - _rr ⁱ , ^if , _zz ^if , _rz ⁱ stresses at the interface in the fibre (r=r _f–) - _p1 maximum principal stress - _zz ^f mean axial stress over the fibre section - _rupt ^m matrix strength - u _r ,u _z non-zero components of the displacement field     

Bounding-surface plasticity: Stress space versus strain space

Summary A bounding-surface plasticity model is formulated in stress space in a general enough manner to accommodate a considerable range of hardening mechanisms. Conditions are then established under which this formulation can be made equivalent to its strain-space analogue. Special cases of the hardening law are discussed next, followed by a new criterion to ensure nesting. Finally, correlations with experimental data are investigated.Notation (a) centre of the stress-space (strain-space) loading surface; i.e., backstress (backstrain) - ^* (a ^*) centre of the stress-space (strain-space) bounding surface - (a ) target toward which the centre of the stress-space (strain-space) loading surface moves under purely image-point hardening - (b) parameter to describe how close the loading surface is to nesting with the bounding surface in stress (strain) space; see (H10) - (c) elastic compliance (stiffness) tensor - (d) parameter to describe how close the stress (strain) lies to its image point on the bounding surface; see (H10) - (D) generalised plastic modulus (plastic compliance); see (1) - function expressing the dependence of the generalised plastic modulus on (plastic complianceD ond) - ^* (D ^*) analogue to (D) for the bounding surface - function expressing the dependence of ^* on (D ^* ond) - () strain (stress) - ' (') deviatoric strain (stress) - ^P ( ^R ) plastic strain (stress relaxation); see Fig. 1 - () image point on the bounding surface corresponding to the current strain (stress) - _iso (f _iso) at the point of invoking consistency, the fraction of local loading-surface motion arising from a change of radius; i.e., fraction of isotropic hardening in the stress-space theory - _kin (f _kin) at the point of invoking consistency, the fraction of local loading-surface motion arising from a change in the backstress (backstrain); i.e., fraction of kinematic hardening in the stress-space theory - _nor (f _nor) at the point of invoking consistency, the fraction of backstress (backstrain) motion directed toward the image stress (strain); i.e., the image-point fraction of the kinematic hardening in the stress-space theory - _ima (f _ima) at the point of invoking consistency, the fraction of backstress (backstrain) motion directed toward the image stress (strain); i.e., the image-point fraction of the kinematic hardening in the stress-space theory - function relating _iso to , , and (f _iso tob,d, andl) - function relating _kin to , , and (f _kin onb,d, andl) - function relating _nor to , , and (f _nor onb,d, andl) - function relating _ima to , , and (f _ima onb,d, andl) - the fraction of outwardly normal bounding-surface motion at the Mróz image point which arises from a change of radius - the fraction of outwardly normal bounding-surface motion at the Mróz image point which arises from a change in the centre - function relating _iso ^* to (f _iso ^* tod) - function relating _kin ^* to (f _kin ^* tod) - (l) parameter to describe the full extent of plastic loading up to the present, giving the arc length of plastic strain (stress relaxation) trajectory; see (H10) - function relating the direction for image-point translation of the loading surface to various other tensorial directions associated with the current state; see (H5). With 6 Figures     

Dependence of the flux flow viscosity coefficient on the Ginzburg-Landau parameter κ in superconducting indium films

The flux flow viscosity coefficient b ^–1 (in units of ₀ H _{c n} ^–1 c ^–2) of vacuum-deposited indium thin films with low values (1.0–2.8) is measured at temperatures between 0.5T _cand 0.98T _cin the weak magnetic field region. At each temperature, b ^–1 decreases as increases for larger than 1.7. The decrease of b ^–1 with increasing is more rapid as the temperature increases. From an analysis of the present results as well as the existing data on intermediate- and high- superconducting alloys, the relation between b ^–1 and is established over a wide range of . The dependence of b ^–1 on is qualitatively explained by taking into account the contribution of the normal electron dissipation to the viscosity coefficient in the Bardeen-Stephen model.Financial support provided by the Fonds National Suisse de la Recherche Scientifique.On leave from the Department of Electronic Engineering, Faculty of Engineering, Kyushu Industrial University, Fukuoka, Japan.     

Thermal conductivity and quantum diffusion in solid H2

The thermal conductivity of solid H₂ and the NMR absorption signal of isolated o-H₂ were measured simultaneously along isotherms 0.07<T<1.5 K as a function of time after a rapid cooldown from 2 K. The o-H₂ concentration ranged from 3.4% to 0.4%, and the pressure was 90 atm. During the measurements, clustering of o-H₂ particles occurred as seen from the changes both of the NMR signal amplitude and of with time t. The difference ^–1 = ^–1 ()– ^–1(0) between the thermal resistivity ^–1 (t=0) just after cool down and in equilibrium, ^–1 (), was found to change sign near 0.23 K, and this result is discussed with respect to previous experiments. The equilibrium resistivity attributed to the o-H₂ impurities, , is derived and is compared with previous determinations and with predictions. An analysis of the equilibration process for ^–1 and for the NMR signal amplitude is presented. It shows that the characteristic times are of comparable but not equal magnitude. Comparison of the derived from NMR data atP=90 and 0 atm favors resonant ortho-para conversion over quantum tunneling as the leading mechanism for quantum diffusion.     

The Interplay of Electronic and Nuclear Magnetism in PtFe x at Milli-, Micro-, and Nanokelvin Temperatures

We have measured ac susceptibility, nuclear magnetic resonance, and nuclear heat capacity of two PtFe _x samples with concentrations of magnetic impurities x = 11 ppm and 41 ppm at magnetic fields (0 ± 0.05) mTB248 mT. The susceptibility data have been measured at temperatures of 0.3 KT100 mK, no hint for nuclear magnetic ordering could be detected to a temperature of 0.3 K. The nuclear heat capacity data taken at 1.4 KT10 mK show enhanced values which scale with x at low polarization. This effect is described by a model assuming an internal magnetic field caused by the impurities. No indication for nuclear magnetic ordering could be detected to 1.4 K. The nuclear magnetic resonance experiments have been performed on these samples at 0.8 KT0.5 mK and 2.5 mTB22.8 mT as well as on three other samples with x = 5, 10, 31 ppm in a different setup at 40 KT0.5 mK and at 5.4 mTB200 mT. Spin-lattice and effective spin-spin relaxation times ₁and ₂ ^* of ¹⁹⁵ Pt strongly depend on x and on the external magnetic field. No temperature dependence of ₁and ₂ ^* could be detected and the NMR data, too, give no hint for nuclear magnetic ordering to 0.8 K.     

Transport property and battery discharge characteristic studies on 1−x(0.75Agl∶0.25AgCl)∶ xAl2O3 composite electrolyte system

Various experimental studies on a new fast Ag⁺ ion-conducting composite electrolyte system: (1–x) (0.75Agl0.25AgCl)xAl₂O₃ are reported. Undried Al₂O₃ particles of size <10 m were used. The conventional matrix material Agl has been replaced by a new mixed 0.75Agl0.25AgCl quenched and/or annealed host compound. Conductivity enhancements 10 from the annealed host and 3 times from the quenched host obtained for the composition 0.7(0.75Agl0.25AgCl)0.3Al₂O₃, can be explained on the basis of the space charge interface mechanism. Direct measurements of ionic mobility as function of temperature together with the conductivity were carried out for the best composition. Subsequently, the mobile ion concentration n values were calculated from and a data. The value of heat of ion transport q* obtained from the plot of thermoelectric power versus 1/T supports Rice and Roth's free ion theory for superionic conductors. Using the best composition as an electrolyte various solid state batteries were fabricated and studied at room temperature with different cathode preparations and load conditions.     

Singular behavior of the mass conductivity of liquid4He in a superleak at the superfluid transition

From measurements of the damping of sound in liquid ⁴ He caused by fluid penetration into a porous medium at the superfluid transitionT _s, we have deduced a critical temperature dependence of the mass conductivity of the form (T–T _s ) ^{–0.31±0.03}      

Standard Gibbs' energies of formation of BaCuO2, Y2Cu2O5 and Y2BaCuO5

The Gibbs' energies of formation of BaCuO₂, Y₂Cu₂O₅ and Y₂BaCuO₅ from component oxides have been measured using solid state galvanic cells incorporating CaF₂ as the solid electrolyte under pure oxygen at a pressure of 1.01×10⁵ Pa BaO + CuO BaCuO₂ G _f,ox ^o (± 0.3) (kJ mol^–1)=–63.4–0.0525T(K) Y₂O₃ + 2CuO Y₂Cu₂O₂ G _f,ox ^o (± 0.3) (kJ mol^–1)=18.47–0.0219T(K) Y₂O₃ + BaO + CuO Y₂BaCuO₅ G _f,ox ^o (± 0.7) (kJ mol^–1)=–72.5–0.0793T(K) Because the superconducting compound YBa₂Cu₃O_7– coexists with any two of the phases CuO, BaCuO₂ and Y₂BaCuO₅, the data on BaCuO₂ and Y₂BaCuO₅ obtained in this study provide the basis for the evaluation of the Gibbs' energy of formation of the 1-2-3 compound at high temperatures.