Experimental study of the boundary between single-phase convection and boiling in underheated cryogenic liquids

The effect of pressure and underheating on the position of the boundary between heat-transfer regimes in liquid helium and hydrogen is investigated.Notation q heat flux - p pressure - =T_s–T underheating - T_s saturation temperature - T temperature of liquid - T=T_wa – T T_s=T_wa – T_s - T_wa temperature of heat-emitting surface - A,a, B, b, C constants - m, n indices - Nu Nusselt number - Ra Rayleigh number - thermal conductivity - coefficient of cubical expansion - kinematic viscosity - g acceleration - standard deviation Indices 01 conditions of convection-boiling transition - 02 conditions of boiling-convection transition Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 42, No. 1, pp. 5–11, January, 1982.     

Flux motion in anisotropic type-II superconductors nearH c 2 with arbitrary vortex orientation

Flux motion in anisotropic type-II superconductors near H_{c 2} is studied in the framework of the time-dependent Ginzburg-Landau (TDGL) theory for the case that the average flux densityB is oriented in an arbitrary direction relative to the principal axes of the sample. The linearized TDGL equation for a uniformly translating order parameter is solved and expressions for all elements of the flux-flow resistivity tensor _ij (including the off-diagonal Hall elements) are obtained. The diagonal elements _ii show the angular scaling property that _ii(B) = _ii(B/H_{c 2}(, ø)), whereas the Hall elements _ij (i j) have additional angular dependences that are not contained in H_c2. For the case that the normal state Hall elements _ij ⁽ⁿ⁾ B _k with i j k, the ratios _ij/ _ij ⁽ⁿ⁾ are functions of B/H_c2 (, ) only.     

Thermal conductivity of hydrocarbons in the naphthene group under high pressures

The thermal conductivity of hydrocarbons in the naphthene group has been experimentally determined. An equation is now proposed for calculating the thermal conductivity over the given temperature and pressure ranges.Notation thermal conductivity - ₂₀ and ₃₀ values of the thermal conductivity at 20 and 30°C, respectively - t₀,P₀ thermal conductivity at t₀, p₀ - _t p thermal conductivity at temperature t and under pressure P - change in thermal conductivity - P pressure - P_melt melting pressure - P₀ atmospheric pressure - t₀ 20°C temperature - T, t temperature - T_cr critical temperature - temperature coefficient of thermal conductivity - ₂₀ temperature coefficient of density - density - ₂₀ density at 20°C - _cr critical density - M molar mass - =T/T_cr referred temperature - v specific volume - v₀ specific volume at 20°C - v change in specific volume - _{3 0} a coefficient - B (t) a function of the temperature - S a quadratic functional - W_i, weight of the i-th experimental point - _i error of the i-th experimental value of thermal conductivity - B _{y, =0.6} value of B (t) at T = 0.6T_cr - B = B (t)/B_{, =0.6} referred value of coefficient B (t) Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 41, No. 3, pp. 491–499, September, 1981.     

Temperature field in a plate containing a system of heat sources

The temperature field is determined in a circular plate with a system of thin extrinsic heat sources.Notation T temperature in the plate with the inclusions - r polar radius - polar angle - time - (r,) coefficient of thermal conductivity - (r,) heat transfer coefficient - C(r,) volume heat capacity - W(r,, ) specific intensity of the heat sources - half thickness of the plate - (x) Dirac's delta function - ¯T finite Fourier cosine transform of the temperature - p parameter for this transformation - T Laplace transform of the temperature - s its parameter - Iv(x) Bessel function with imaginary argument of order - K _v (x) the MacDonald function of order - and dimensionless temperature - Po Pomerantz number - Bi Biot number - Fo Fourier's number - dimensionless polar radius - b₁ ^* dimensionless radius of the circle on which the inclusions are placed - R^* dimensionless radius of the plate Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 40, No. 3, pp. 495–502, March, 1981.     

Analysis of the effect of the decomposition of char-forming heat-insulating materials on the free discharge of a gas mixture

The article presents results of a numerical solution of a nonsteady problem on the free discharge of a mixture of gases from a hemispherical volume with allowance for thermal decomposition of heat-insulating materials.Notation V volume - S area - t - P p - T - u v - Q q, dimensional and dimensionless time, pressure, temperature, TIM decomposition rate, and heat flux - adiabatic exponent - R gas constant - density - H specific enthalpy - c specific heat - thermal conductivity - , , _s dimensionless complexes - coefficient expressing the radiative properties of the gas medium and the heat-transfer surface - Stefan-Boltzmann constant Indices 0 initial state and scale factors - s surface - coke - M TIM material - P pyrolysis front - A ablation front - v volatile degradation products - adiabatic conditions - c completion of discharge Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 54, No. 5, pp. 787–793, May, 1988.     

Universal simulation of degenerating homogeneous turbulence

The problem of universal simulation of the dynamics of a turbulent velocity field (universal in the sense of arbitrary values of the Reynolds turbulence number) is treated on the basis of the moment model in the second approximation.Notation ¯q² _i ² double the kinetic turbulence energy - _u ² =5v¯q²/_u Taylor turbulence scale squared - _u=v1/x_k)²> kinetic-energy dissipation function - N_Re,=¯q²_u / Reynolds turbulence number Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 42, No. 1, pp. 46–52, January, 1982.     

Mössbauer studies of α″-Fe16N2 and α′-Fe8N films

Conversion-electron Mössbauer spectra of epitaxial -Fe₁₆N₂ and -Fe₈N films have been studied and their differences are discussed in detail. The Mössbauer spectrum of -Fe₁₆N₂ can be decomposed into three subspectra, which correspond to the 4d, 8h and 4c sites. The Mössbauer spectrum of -Fe₈N can be fitted using four spectra based on a nitrogen-atom-random-distribution model. The average hyperfine field is larger (3%) for -Fe₁₆N₂ than for -Fe₈N, which is approximately consistent with a 4.1% enhancement of the magnetic moments for -Fe₁₆N₂. The iron moments tend to locate in the film plane for -Fe₁₆N₂ and to arrange perpendicularly to the film plane for -Fe₈N.     

An extension of the theory of oscillating cup viscometers

The theory of the fluid motion in the interior of an oscillating or rotating cup is reexamined. The quantity of interest in viscometry is the torque exerted by the fluis on the sides and rims of the cup. In this paper expressions for the torque are obtained for geometries for which the cup height approaches a fluid boundary layer thickness. Interest in such geometries is due to viscosity measurements made in mixtures in the critical region where cups of small height are used in order to minimize gravity effects.Nomenclature D() Torque on the cup, Eq. (5) - E() Truncation error term, Eq. (24) - h Internal half-height of a filled cup or the height of the liquid in a partially filled cup - I Moment of inertia of cup and suspension system - I Moment of inertia of fluid inside cup - I _n Modified Bessel function of order n - J _{i, n} Defined in Eq. (13) - R Radius of the cup - S _n Defined in Eq. (7) - S _n Defined in Eq. (10) - x Variable 2 ₀/ - z Variable 2 ₀^1/2 - () Angular displacement of the cup - Boundary layer thickness - Logrithmic decrement - Laplace transform variable - ₀ Dimensionless height h/ - Frequency ratio / ₀ - Kinematic viscosity - ₀ Dimensionless radius R/ - Density of liquid - Dimensionless time ₀ t - Phase angle of oscillation - Angular frequency of oscillation with liquid present in cup - ₀ Angular frequency of oscillation in a vacuum     

Response of a spinning liquid column to pitch excitation

Summary The response of a solidly rotating liquid bridge consisting of inviscid liquid is determined for pitch excitation about its undisturbed center of mass. Free liquid surface displacement and velocity distribution has been determined in the elliptic (>2₀) and hyperbolic (<2₀) excitation frequency range.List of symbols a radius of liquid column - h length of column - I ₁ modified Besselfunction of first kind and first order - J ₁ Besselfunction of first kind and first order - r, ,z cylindrical coordinates - t time - u, v, w velocity distribution in radial-, circumferential-and axial direction resp. - mass density of liquid - free surface displacement - velocity potential - ₀ rotational excitation angle - ₀ velocity of spin - forcing frequency - _1n natural frequency - surface tension - acceleration potential - for elliptic range >2₀ - for hyperbolic range >2₀     

Interface shapes in a torsionally oscillating,layered medium of viscoelastic liquids

Summary The free surface motion of a layered medium of liquids in a gravitationally stable configuration, resting on top of a layer of mercury, driven by a torsionally oscillating, cylindrical outer wall is investigated. The non-linear problem in the unknown physical domain is expressed as a series of linear problems in the rest state by means of a domain perturbation method. The flow variables and the stress are expanded into series in terms of the amplitude of the oscillation of the cylinder. The shapes in the mean of the interfaces between layers and the flow field are determined up to second order in the perturbation parameter, the amplitude of the oscillation.Nomenclature Density - Modified pressure field - Amplitude of the oscillation - Frequency of the oscillation - Interfacial value of the surface tension - Dynamic viscosity - , , Material functions - Complex viscosity - Stream function - Position vector at timet= - ₁, ₂ The first two Rivlin-Ericksen constants - Quadratic shear relaxation modulus - ,t Time - u Velocity vector - u,v,w Velocity components - S Extra stress tensor - h Interface elevation - D Stretching tensor - G Strain history tensor - A ₁ The first Rivlin-Ericksen tensor - J Mean curvature - p Pressure - t Unit tangent vector - n Unit normal vector - G Shear relaxation modulus - X Position vector in the rest stateD ₀ - r, ,z Rest state coordinates - x Position vector in the physical spaceD - R, ,Z Physical space coordinates - r ₀ Radius of the oscillating cylinder - e _r ,e ,e _z Physical basis vectors inD ₀ - e _R ,e ,e _Z Physical basis vectors inD - Indicates the jump in the enclosed quantity across an interface With 1 FigurePresented at the Xth Canadian Congress of Applied Mechanics, The University of Western Ontario, London, Ontario, Canada, June 2–7, 1985.     

A dilatometric method to measure the thermal diffusivity of nonmetallic liquids

A new method to measure the thermal diffusivity of liquids is presented. It requires determination of the time dependence of the thermal expansion of the liquid when it is subjected to a heat source at the top of the cell containing the liquid. The high accuracy of the method (about 3%) is due to an essential reduction of convective currents and also to the absence of temperature detectors, which generally introduce unwanted perturbations on the thermal Field.Nomenclature Thermal conductivity - c Specific heat - Density - c = specific heat x density - h Newton coefficient - Thermal diffusivity - T, 0 Temperature - tV Electric signal - Calibration coefficient - _exp, _th Volume change of the liquid     

Conventional Electronic Structure of MgB2 and ZrB2: LDA vs. de Haas-v. Alphen & ARPES Data

We compare full potential LDA band calculations of the Fermi surfaces areas and band masses of MgB₂ and ZrB₂ previously reported and new dHvA data. Discrepancies in areas in MgB₂ can be removed by a small shift of bands relative to bands. Comparison of effective masses lead to orbit averaged el-ph coupling constants =1.3 and =0.5, whereas for ZrB₂ only weak el-ph coupling with <0.3 is found. The ARPES data can be also well described by the LDA showing the presence of surface states.     

Energy loss distribution of charged particles in thin absorbers

Conclusions 1. For thin absorbers, the Landau theory incorporating certain above-listed corrections is a general-purpose one and is in good agreement with experiment both for heavy and light charged particles 0.01. 2. For intermediate layers (0.01 1 and 1), exact solutions are provided by the Vavilov theory [11]. 3. The numerical-analytic method of plotting the energy loss distribution function proposed in [13] is suitable for very thin ( 0.01) absorbers.Translated from Izmeritel'naya Tekhnika, No. 3, pp. 60–62, March, 1970.     

Non-Newtonian properties of emulsions in solutions of surface-active agents

The adsorption of surface-active agents (surfactants) on channels changes the effective viscosity of an emulsion and gives it non-Newtonian properties.Notation a drop radius - C and C° concentration of surfactant near a drop and averaged over the medium - D diffusion coefficient of the surfactant - I second-rank unit tensor - n_i components of the unit normal vector to the drop surface - r radius vector directed from the center of the drop - s surface area of the drop occupied by one molecule of surfactant - t_j and T characteristic times - and sorption and desorption constants - gG and ° true and equilibrium surface concentrations of surfactant - , , and gh₁ effective viscosity and the viscosities of the disperse phase and dispersion medium - volume concentration of the disperse phase - surface tension of the drop - T_j, and characteristic times Indices + and * quantities near and inside the drop - t tangential components of vectors and tensors. The operators div_s and grad_s have the same meaning as the ordinary divergence and gradient operators, but with fixed values of the radius vector ra Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 56, No. 5, pp. 787–793, May, 1989.     

Dielectric Dispersion in Yttrium and Erbium Formate Dihydrate Crystals

The dielectric properties of Y(HCOO)₃ · 2H₂O and Er(HCOO)₃ · 2H₂O are studied. The frequency dependences (0.01 Hz to 20 kHz) of the real () and imaginary () parts of dielectric permittivity ( = – i) are shown to follow a fractal scaling law for the dielectric response of solids. In the tan versus temperature curves, a number of maxima are revealed in a narrow temperature range. The experimental data are used to evaluate the activation energies of relaxation processes. The observed anomalies are assumed to be associated with changes in the dynamics of protons in hydrogen bonds.     

Nonlinear asymptotic theory of hypersonic flow past a circular cone

Summary The hypersonic small-disturbance theory is reexamined in this study. A systematic and rigorous approach is proposed to obtain the nonlinear asymptotic equation from the Taylor-Maccoll equation for hypersonic flow past a circular cone. Using this approach, consideration is made of a general asymptotic expansion of the unified supersonic-hypersonic similarity parameter together with the stretched coordinate. Moreover, the successive approximate solutions of the nonlinear hypersonic smalldisturbance equation are solved by iteration. Both of these approximations provide a closed-form solution, which is suitable for the analysis of various related flow problems. Besides the velocity components, the shock location and other thermodynamic properties are presented. Comparisons are also made of the zeroth-order with first-order approximations for shock location and pressure coefficient on the cone surface, respectively. The latter (including the nonlinear effects) demonstrates better correlation with exact solution than the zeroth-order approximation. This approach offers further insight into the fundamental features of hypersonic small-disturbance theory.Notation a speed of sound - H unified supersonic-hypersonic similarity parameter, - K hypersonic similarity parameter, M - M freestream Mach number - P pressure - T temperature - S entropy - u, v radial, polar velocities - V freestream velocity - shock angle - cone angle - density - density ratio, /() - ratio of specific heats - polar angle - stretched polar angle, / - (), (), () gage functions     

Response of a spinning liquid column to axial excitation

Summary The response of a solidly rotating finite liquid column consisting of frictionless liquid is subjected to axial harmonic excitation. The response of the free liquid surface elevation and velocity distribution has been determined in the elliptic (>2 ₀) and hyperbolic frequency range (>2 ₀).Notation a radius of liquid bridge - h length of liquid bridge - I ₀,I ₁ modified Besselfunctions - J ₀,J ₁ Besselfunctions - P liquid pressure - r, ,z cylindrical polar coordinates - t time - u, v, w velocity distribution in rotating liquid - axial excitation amplitude - elliptic case (>2 ₀) - hyperbolic case (>2 ₀) - liquid density - surface tension - liquid surface displacement - acceleration potential - ₀ rotational speed - axial forcing frequency - natural frequency of rotating system - _02n –1 natural frequency of harmonic axial response With 8 Figures     

Study on the α2/γ interfacial structures in a two-phase (α2?+?γ) alloy deformed at elevated temperature

The details of structure modification on ₂/ interface induced by deformation in a hot-deformed Ti-45Al-10Nb alloy were investigated by conventional and high-resolution transmission electron microscopy. A new type of dislocation ledge containing 1/3[111] partials was identified. The Burgers vectors of these dislocation ledges were determined to be 1/2[110] or 1/2101]. The formation mechanism of this new type of dislocation ledge is discussed. Also, two types of hot deformation induced ₂/ interfaces, coherent interfaces with high density of ledges and misoriented semi-coherent ₂/ interfacial boundaries were observed. For the misoriented semi-coherent ₂ interfaces, the density of dislocation ledges in these interfaces increases with the misoriented angle between the (111) and (0001) planes, and 1/3[111] partial dislocations were involved in all the dislocation ledges. The formation mechanism of these deformation-induced ₂/ interfaces were discussed related to the role of ₂/ interfaces adjusting the deformation as a dislocation sink absorbing the slipping dislocations in the phase. Moreover, misoriented semi-coherent ₂ interface related deformation twinning and structure transformation induced by deformation were analyzed and discussed related to the role of ₂/ interfaces as a dislocation source during deformation.     

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.     

On internal stress and activation volume in polymers

The two-site model is developed for the analysis of stress relaxation data. It is shown that the product of d In (– )/d and (- _i) is constant where is the applied stress, _i is the (deformation-induced) internal stress and = d/dt. The quantity d In ( )/d is often presented in the literature as the (experimental) activation volume, and there are many examples in which the above relationship with (- _i) holds true. This is in apparent contradiction to the arguments that lead to the association of the quantity d In (– )/d with the activation volume, since these normally start with the premise that the activation volume is independent of stress. In the modified theory presented here the source of this anomaly is apparent. Similar anomalies arise in the estimation of activation volume from creep or constant strain rate tests and these are also examined from the standpoint of the site model theory. In the derivation presented here full account is taken of the site population distribution and this is the major difference compared to most other analyses. The predicted behaviour is identical to that obtained with the standard linear solid. Consideration is also given to the orientation-dependence of stress-aided activation.