Dependence of Hertzian fracture angle on Poissons ratio and indentation techniques

Sub-parallel concentric conic fractures can be produced consecutively in Perspex by liquid indentation. There is a linear relationshp between the conic angle, , of Hertzian fracture and the Poisson's ratio, , of the material. This angle is about 10 higher than the calculated path of the principal stress trajectory for a given . decreases with the increase of stress application rate. This dependence of is very marked in materials with high Poisson's ratios.     

Structure of unidimensional temperature stresses

Using the structural approach, the temperature stresses are examined in a semiinfinite rod, insulated on the lateral faces and rigidly fixed at the end. A comparative analysis is made for three heat-transfer models.Notation k(t) heat flux relaxation function - (t) internal energy relaxation function - T rod temperature - ambient temperature - t time - x coordinate along the rod - _xx(x, t) stress - u(x, t) displacement - (x, t) deformation - c₀=(E/)^1/2 speed of sound in the rod under isothermal conditions - E elasticity modulus - density of the material - _t coefficient of thermal expansion - thermal-conductivity coefficient - a thermal-diffusivity coefficient - b thermal-activity coefficient - c_q=(a/_r)^1/2 velocity of heat propagation - _r heat flux relaxation time - (t) unique Heaviside function Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 33, No. 5, pp. 912–921, November, 1977.     

Effects of dimensionality and crystal structure on bound states of point defects in quantum solids

The effects of dimensionality and crystal structure on the bound states of point defects in quantum crystals are investigated. It is shown that tightly bound states tunnel slowly in some lattices (e.g., bcc) while they tunnel quickly through other lattices (e.g., hcp). Explicit band calculations are made for ( ³ He) ₂ impurity molecules in solid host ⁴ He crystals. These illustrate the qualitative differences present in various molecular tunneling modes.     

Universality and the scaling laws in the superfluid phase transition of3He-4He mixtures

From the second-sound velocityU ₂ near the superfluid transition point, the superfluid densities in³He-⁴He mixtures, _s (X) and _s (), were deduced along the paths of constant³He concentrationX and of constant chemical potential difference of³He and⁴He. The following critical exponents of _s are determined: (a) =XX for _s (X) in the(X, T) plane,(b) X for _s (X) in the(, T) plane, and(c) for _s () in the(, T) plane. It is found that and _X change by about 4–6% relative to with increasing³He concentration up toX=0.4 and by 8–10% up toX=0.53. It seems that, belowX=0.53, universality hold for . Values of have been found to be in good agreement with the critical exponent of _s in pure⁴He under constant pressure. The values of and _X forX0.53 are also found to be consistent with the scaling relations in the (,T) plane of³He-⁴He mixture.Work performed in part while at the Electrotechnical Laboratory.     

Susceptibility and Pressure Study of 3He nano-Clusters

Simultaneous measurements of pressure and magnetic susceptibility have been made in ³ He nano-clusters embedded in a ⁴ He matrix, following phase separation of the mixture. Susceptibility measurements extend from 0.5 mK to 10 mK for three different samples, which either undergo partial melting upon further cooling, or separate with liquid already present. The magnetic behavior of the clusters indicates solid fractions of 77, 54, and 19%, respectively, for pressures of 3.36 MPa, 3.06 MPa, and 2.88 MPa. The susceptibility of the 3.36 MPa sample follows a Curie law to the lowest temperature. For 3.06 MPa, we observe a kink in at 1.1 mK, which is approximately the ordering temperature T_N of the pure bulk ³ He if it existed at this pressure. However is almost constant down to 0.6 mK, with no drop at 1.1 mK, and no frequency shift, within our resolution of 10 Hz. Thus if there is magnetic ordering at 1.1 mK it is quite different than for bulk ³ He, not the U2D2 phase. For 2.88 MPa, follows a Curie-Weiss law with a positive Weiss =140 K, indicative of a ferromagnetic tendency, similar to that seen in 2D films.     

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.     

An Interpretation of Dispersionless Modes in Neutron Diffraction Experiments on Helium Films

We analyze the dynamic structure function S(q, ) for neutron scattering off helium films in the direction perpendicular to the substrate. Dispersionlessmodes that have been found in neutron diffraction experiments on helium films adsorbed on graphite powder (H. J. Lauter, H. Godfrin, and H. Wiechert, Excitations in ⁴ He films, in Proceedings of the Second International Conference on Phonon Physics, World Scientific, 1985) are interpreted as standing waves or resonances of the helium liquid perpendicular to the substrate. Our interpretation is supported by microscopic calculations of the ⁴He dynamic structure function.     

Equation of state of3He near its liquid-vapor critical point

We report high-resolution measurements of the pressure coefficient (P/T) for³He in both the one-phase and two-phase regions close to the critical point. These include data on 40 isochores over the intervals–0.1t+0.1 and–0.2+0.2, wheret=(T–T _c )/T _c and =(– _c )/ _c . We have determined the discontinuity (P/T) of (P/T) between the one-phase and the two-phase regions along the coexistence curve as a function of . The asymptotic behavior of (1/) (P/T) versus near the critical point gives a power law with an exponent (+–1)^–1=1.39±0.02 for0.010.2 or–1×10 ^–2t–10 ^–6 , from which we deduce =1.14±0.01, using =0.361 determined from the shape of the coexistence curve. An analysis of the discontinuity (P/T) with a correction-to-scaling term gives =1.17±0.02. The quoted errors are fromstatistics alone. Furthermore, we combine our data with heat capacity results by Brown and Meyer to calculate (/T) _c as a function oft. In the two-phase region the slope (²/T ²)_c is different from that in the one-phase region. These findings are discussed in the light of the predictions from simple scaling and more refined theories and model calculations. For the isochores 0 we form a scaling plot to test whether the data follow simple scaling, which assumes antisymmetry of – ( _c ,t) as a function of on both sides of the critical isochore. We find that indeed this plot shows that the assumption of simple scaling holds reasonably well for our data over the ranget0.1. A fit of our data to the linear model approximation is obtained for0.10 andt0.02, giving a value of =1.16±0.02. Beyond this range, deviations between the fit and the data are greater than the experimental scatter. Finally we discuss the (P/T) data analysis for ⁴ He by Kierstead. A power law plot of (1/) P/T) versus belowT _c leads to =1.13±0.10. An analysis with a correction-to-scaling term gives =1.06±0.02. In contrast to ³ He, the slopes (²/T ²)_c above and belowT _c are only marginally different.Work supported by a grant from the National Science Foundation.     

A transmission electron microscopic study of the Bethany iron meteorite

The Bethany iron meteorite which is a part of the Gibeon shower is a fine octahedrite with zoned plessite fields of various sizes. The optically irresolvable microstructural details inside the plessitic fields have been studied by transmission electron microscopy, and the crystallographic relationships between the primary kamacite () and the parent taenite (), and between the and particles in the coarse plessite, have been examined using electron diffraction. In the case of primary kamacite the orientation-relationship with was close to the Nishiyama-Wasserman relationship, whereas, for the plessitic , the orientation-relationship with was close to Kurdjumov-Sachs. It was also found that the (111) and (110) planes were not strictly parallel. Additionally, measurements of the composition profile through the zoned plessite have been made using STEM microanalysis technique, and related to microstructure.     

Velocity of second sound and superfluid density near the superfluid transition in3He-4He mixtures

Using superleak condenser transducers, the velocity of second soundU ₂ has been measured near the superfluid transition temperature T in³He-⁴He mixtures with molar concentrationsX of³He of 0.0, 0.038, 0.122, 0.297, and 0.440. We have obtained the superfluid density _s/ fromU ₂ on the basis of linearized two-fluid hydrodynamics. The results for _s/ are consistent with those obtained from the oscillating disk method, as expected from two-fluid hydrodynamics. The value of _s/ at eachX could be expressed by a single power law, _s/=k, where =1-T/R, with the experimental uncertainty. It is found that the exponent is independent of concentration forX0.44 within the experimental uncertainty. This concentration independence of is in agreement with the universality concept. From the conclusion that the values of are universal forX0.44, the concentration dependence of the superfluid component _s is expressed by an empirical equation _s(X, )=²_s(0, ). It is found that corresponds to the volume fraction of⁴He in the superfluid³He-⁴He mixture. The value of is in agreement with that obtained from the measurement of the molar volume by others.This paper is based on a thesis submitted to Tokyo University of Education in partial fulfillment of the requirements for the Ph.D. degree.     

Zero Sound Attenuation Near the Quantum Limit in Normal Liquid 3He Close to the Superfluid Transition

The zero sound attenuation of normal liquid ³He has been studied over a range of temperatures from slightly above the superfluid transition temperature, T _c, to approximately 10mK at the constant pressures of 1 and 5bar. Using longitudinal LiNbO₃ transducers, operating both on and off resonance, the experiment was performed at 15 discrete frequencies located in several broadband frequency windows, including 16–25, 60–70, and 105–111MHz. The results are compared to Landau's prediction for the attenuation of zero sound in the quantum limit, (k _B Tk _B T _F), where ₀(P,T, )= (P) T ²{1+(/2k _B T)²}. Calibration of the received zero sound signals was performed by measuring the temperature dependence of the first sound attenuation from 30 to 800mK at those same frequencies and pressures. The data are compared to previous results.     

The transverse acoustic impedance of dilute solutions of3He in superfluid4He

The transverse acoustic impedanceZ=R–iX of dilute solutions of³He in superfluid⁴He has been measured at a frequency (/2) of 20.5 MHz at temperaturesT from 30 mK to the transition at T. The³He concentrations studied werec=0.014, 0.031, 0.053, 0.060, and 0.092 below 1 K, thoughc decreased slightly near the point. The impedance was found from the temperature dependence of the quality factor and the resonant frequency of anAT-cut quartz crystal resonator immersed in the liquid. Below 1 K,Z is due to the Fermi gas of³He quasiparticles, and in the collisionless limit, 1 ( is a relaxation time),R remains constant whileX goes to zero. Measurements ofR(c, T) andX(c, T) were analyzed to determine the momentum accommodation coefficient (c, T) and (c, T). The relaxation times were in good agreement with previous work, while (c, T) was independent ofc, but increased from 0.29±0.03 below 0.1 K to 1.0±0.1 above 0.8 K. Various mechanisms are suggested to explain this. Between 1.0 and 1.5 K the³He quasiparticles and the thermally excited rotons are in the hydrodynamic region, 1. Values of the total viscosity (c, T) were obtained and analyzed to give the³He gas viscosity and the³He-³He and roton-³He scattering rates, both of which were energy-dependent. The superfluid healing length a was also measured. Near the point we founda=(0.1±0.03)^–2/3 nm, where =1–T/T, proportional to the phase coherence length . Our data are consistent with the hypothesis that _s/T is a universal constant for superfluid dilute solutions, where _s is the superfluid density. Between 1.0 and 1.8 K we found thata(c, T) was comparable to measurements in³He-⁴He films.     

Temperature-, concentration- and pressure-dependence of the viscosity of liquid3He-4He mixtures at low temperatures

We have investigated the viscosity of liquid³He-⁴He mixtures at various³He - concentrations (0.98%x9.5%) in the temperature range1 mK T 100 mK and at pressures 0 bar P 20 bar. At T10 mK the Fermi-liquid behaviour T² = const. as well as x^4/3 could be confirmed. However, there are significant deviations from theoretical predictions for the magnitude of the viscosity as well as for its pressure dependence.     

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.     

Spatial Evolution of High Frequency Phonons in Superfluid 4He from a Pulse-Heated Metal Film

An almost monochromatic spectrum of high frequency (/k _B 10 K) phonons in superfluid ⁴ He is created by a short ( 0.1s) pulse of Joule-heating in a metal film submerged in the liquid at saturated vapour pressure (svp). These phonons have lifetimes that tend to infinity as T 0, and are the ones effective in quantum evaporation experiments. Most of these high frequency (hf) phonons are not injected into the liquid ⁴ He across the metal—liquid interface, but are created in the liquid by energy-increasing interactions which begin with the injected phonons of much lower energy (/k _B 1 K). These hf phonons are created up to 5 millimetres in front of the heater, hence the time of flight from a heater to a detector only gives an approximate value (lower bound) of their energies. Here we present measurements at svp of phonon energy fluxes in liquid ⁴ He at various distances from a pulse-heated metal film. Analysis of these signals gives an improved determination of the hf phonon spectrum (peaked at 10.20 ± 0.05 K with HWHM 0.2 K on the high energy side).     

Shear viscosity measurements of liquid 4He and 3He-4He mixtures near the tricritical point

A torsional oscillator cell is described, by means of which simultaneous precision measurements of () and of the molar volume can be made in liquid ⁴He-⁴He mixtures over the temperature range between 0.5 and 3 K. Here is the mass density, the shear viscosity and in the superfluid phase they become the contributions _n and _n of the normal component. The results of for ⁴He near the superfluid transition are compared with the predictions by Schloms, Pankert and Dohm, and by Ferrell. Measurements of () are reported for mixtures with 0.64X0.74, where X is the ³He mole fraction. Those for X = 0.67 and 0.70 are compared with data by Lai and Kitchens. The viscosity experiments show no evidence of a weak singularity at the tricritical point.     

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.     

Analytical Theory of DC SQUIDS Operating in the Presence of Thermal Fluctuations

A comprehensive analytical theory of symmetric DC SQUIDs is presented taking into account the effects of thermal fluctuations. The SQUID has a reduced inductance < 1/ where = 2LI_c/₀, L is the loop inductance, ₀ is the flux quantum, and I_c is the critical current of the identical Josephson junctions which are assumed to be overdamped. The analysis, based on the two dimensional Fokker–Planck equation, has been successfully performed in first order approximation with considered a small parameter. All important SQUID characteristics (circulating current, current-voltage curves, transfer function, and energy sensitivity) are obtained. In the limit 1( = 2k_BT/I_c0 is the noise parameter, k_B is the Boltzmann constant, and T is the absolute temperature) the theory reproduces the results of numerical simulations performed for the case of small thermal fluctuations. It was found that for < 1 the SQUID energy sensitivity is optimum when is higher than 1/, i.e., outside the range for which the present analysis is valid. However, for 1 the energy sensitivity has a minimum at L = L_F , where L_F = ( ₀ /2) ²/k_B , and therefore, in this case, the optimal reduced DC SQUID inductance is _opt = 1/, i.e., within the range for which the present analysis is valid. In contrast to the case of an RF SQUID, for a DC SQUID the transfer function decreases not only with increasing L/L_F but also with increasing (as 1/). As a consequence, the energy sensitivity of a DC SQUID with < 1/ degrades more rapidly (as ⁴ ) with the increase of than that of an RF SQUID does (as ² ).     

Superfluid density near the lambda point of4He under pressure

The superfluid density in ⁴ He was determined near T from the second-sound velocity as a function of T–T and pressure. The critical exponent of the superfluid density was found to depend, even slightly, on the pressure. Furthermore, the fundamental length ₀ in the coherence length = ₀ [1–(T/T)]^–' seemed to be proportional to the mean interatomic distance. The implications of the results are also discussed.This work was partly supported by The Ito Science Foundation and by The Nishina Memorial Foundation.     

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.