Interfacial spring model for ultrasonic interactions with imperfect interfaces: Theory of oblique incidence and application to diffusion-bonded butt joints

The quasi-static distributed spring model is used to derive the ultrasonic reflectivity of an imperfectly-bonded interface as a function of frequency and angle of incidence. The results are then incorporated in a model for the corner reflection from a diffusion-bonded joint between two abutting plates, the corner being defined by the bond plane and the common lower surface plane of the plates. An immersion-inspection geometry is assumed, and seven categories of corner reflections are identified and examined in detail. These fall into two classes: those having parallel incident and exiting rays in water (=), and those having nonparallel water rays ( ). The = categories are suitable for single probe (pulse-echo) inspections of the joint. Based on the amplitude of the outgoing corner-reflected signal, two = geometries appear promising. These employ, respectively, a corner reflection involving only longitudinal waves with the interface illuminated at near-grazing incidence (LLL), and a corner reflection involving only transverse waves with the interface illuminated at near 45° incidence (TTT). In addition, two practical geometries are indicated; these both involve mode conversion upon reflection from the interface, with the incident or outgoing longitudinal wave traveling nearly parallel to the interface. Model predictions for LLL and TTT reflections are compared to measurements on diffusion-bonded Inconel specimens, and techniques for applying the model results to more complicated bond geometries are discussed.     

Influence of stabilizers on Na-β′′-Al2O3 phase formation in Li2O(MgO)-Na2O-Al2O3 ternary systems

The influences of stabilizers on - and -Al2O3 phase formations in Li2O(MgO)-Na2O-Al2O3 systems were investigated. When stabilized with 4MgCO3Mg(OH)25H2O, most of the -Al2O3 phase formed below 1200°C and further - to -Al2O3 transformation with an increase of temperature was not observed. On the other hand, when stabilized with Li2CO3,-Al2O3 formation occurred by two steps. First, -Al2O3 was partly formed below 1200°C, and, second, noticeable transformation from -Al2O3 to -Al2O3 occurred at higher temperature ranges. It was shown that transient eutectic liquid in the Li2O-Na2O-Al2O3 system promoted the - to -Al2O3 transformation at higher temperatures. Uniform distribution of both Mg2+ and Li+ stabilizing ions enhanced -Al2O3 formation at low temperatures. In the Li-stabilized systems, however, homogeneous distribution of Li+ ions hindered both the formation of transient eutectic liquid and the second - to -Al2O3 phase transformation at high temperatures.     

Effect of elastic interaction energy on coarsening of γ′ precipitates in a mechanically alloyed ODS Ni-base superalloy

The coarsening behavior of precipitates with a uniform size distribution and with a bimodal size distribution in a mechanically alloyed ODS Ni-base superalloy were investigated to clarify the effect of elastic interaction energy on the coarsening behavior of precipitates. The coarsening rate decreased with increasing size of precipitates with a uniform size distribution, contrary to the classical LSW theory, and the coarsening behavior of precipitates with a bimodal size distribution exhibited Ostwald ripening in which the larger precipitates grow at the expense of smaller precipitates. The driving force for coarsening of precipitates was analyzed based on the two-particle model, considering the effect of elastic interaction energy in addition to the effect of interfacial energy. The contribution of elastic interaction energy on the total energy was found to increase with increasing size of precipitates, and the decelerated coarsening of precipitates was attributed to the decrease in the driving force for coarsening with increasing size of precipitates.     

Microstructure and mechanical properties of rapidly quenched L20 and L20+L12 alloys in Ni-Al-Fe and Ni-Al-Co systems

Ductile L2₀-type wires and+L1₂-type duplex wires with high strengths and large elongation in the Ni-Al-Fe and Ni-Al-Co ternary systems have been manufactured directly from the liquid state by an in-rotating-water spinning method. The wire diameter was in the range 80 to 180m and the average grain size was 2 to 4m for the wires and 0.2 to 1.0m for the+ wires. _y, _f and _p of the wires were found to be about 360 to 760 MPa, 560 to 960 MPa, and 0.2 to 5.5%, respectively, for the Ni-Al-Fe system, those of the+ wires were about 395 to 660 MPa, 670 to 1285 MPa, and 3.5 to 17%, respectively, for the Ni-Al-Fe system, and about 260 to 365 MPa, 600 to 870 MPa, and 4.0 to 7.0%, respectively, for the Ni-Al-Co system. Cold-drawing caused a significant increase in _y and _f and the values attained were about 1850 and 2500 MPa, respectively, for Ni-20Al-30Fe and Ni-25Al-30Co wires drawn to about 90% reduction in area. The high strengths, large elongation and good cold-workability of the melt-quenched and+ compound wires have been inferred to be due to the structural change into a low-degree ordered state containing a high density of phase boundaries, suppression of grain-boundary segregation and refinement of grain size.     

Elevated temperature deformation behaviour of multi-phase Ni-20 at % Al-30 at % Fe and its constituent phases

The mechanical behaviour of the multi-phase ( + /) alloy Ni-20 at % Al-30 at % Fe and alloys similar to its constituent and / phases, Ni-30 at % Al-20 at % Fe and Ni-12 at % Al-40 at % Fe, respectively, were investigated. When tested in tension at 300 K, the alloys exhibited 20%, 2% and 28% elongation, respectively. At elevated test temperatures (700, 900 and 1100 K), the multi-phase alloy exhibited increased ductility, reaching an elongation in excess of 70% at 1100 K without necking or fracture. Similarly, the alloy demonstrated increased ductility with increasing test temperatures. In contrast, the / alloy showed greatly reduced ductility with increasing temperature and was quite brittle both at 900 and 1100 K. Thus, whilst at room temperature the / phase improved the ductility of the + / aggregate, at elevated temperatures the phase alleviated the brittleness of the / phase, thereby preventing any embrittlement of the multi-phase alloy over the temperature range 300–1100 K. Also, whilst the phase improved the room-temperature strength of the multi-phase alloy, at elevated temperatures where the phase is known to be weak, the / phase improved the strength of the multi-phase alloy up to 900 K, beyond which the strength deteriorated due to disordering and lack of anomalous strengthening in the / component.     

Phase relationship between β′- and O′-sialon at 1623 K

-sialon whiskers and co-products of synthesis, such as -sialon powders and O-sialon powders, were annealed at 1623 K for 8 h in a closed graphite reaction tube under 1 atm nitrogen. Phase stabilities, Si/Al ratios, and crystallographic features were investigated. The O-sialon phase, which formed in the early stage of synthesis when oxygen partial pressure was relatively high, became less stable in the present annealing condition and decomposed. The majority of released aluminium and possibly oxygen from the decomposed O-powder was incorporated into -sialon whiskers with little change in its lattice parameters, when the -sialon whiskers were included in annealing. The aluminium contents were always lower in the -whiskers than in the powders even after increasing its aluminium content during 8 h annealing. The lattice parameters of both -whiskers and powders increased with increasing aluminium content and became closer after annealing. The lattice parameters of -whiskers remained the same before and after annealing despite the increased aluminium content, while the lattice parameters of -powders decreased despite its aluminium content remaining unchanged. The lattice parameters of O-sialon increased with increasing aluminium content, and the increase in thea direction is the largest when compared with other parameters.     

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.     

The Ni3Al-Ni3Cr-Ni3Ru section of the Ni-Cr-Al-Ru system

An investigation is reported of the 75 at% nickel section of the Ni-Cr-Al-Ru system at 1523 and 1273 K. Constitutional data obtained by electron probe microanalysis, X-ray diffraction and microscopical examination are presented as partial isothermal sections. At 1523 K, the major part of the section consists of phase, while the aluminium-rich region contains a and+ region; the extent of the solid solution of chromium and ruthenium in totals ~ 4 at%. The ruthenium-rich corner of the section shows a two-phase region consisting of + ruthenium-rich solid solution. At 1273 K the,+ and + ruthenium regions increase in extent. The/ mismatch values in the equilibrated alloys studied lie in the range ~ –0.08 to –0.39%. Constitutional features of as-cast alloys are also reported.     

Determination of the local angular radiation coefficients in certain two-body systems

A method is shown and formulas are derived by which local angular radiation coefficients can be determined in certain two-body systems where the configuration is arbitrary but one of the bodies is either a cylinder or a rectangular plate.Notation _int radiation vector of body 1 - _E ^int intrinsic radiation intensity of body 1 - _x, _y, _z components of the geometrical radiation vector along rectangular coordinates - r₀=x²+z² shortest distance from point M(x, y, z) to linear radiator - ₀ , ₀ ^' angles subtending the two segments of the linear radiator from point M(x, y, z) on area element 2 of irradiated surface - l length of the cylinders - x, y, z space coordinates of point M Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 22, No. 6, pp. 1080–1088, June, 1972.     

Kondo Impurity in a Mesoscopic Ring: Charge Persistent Current

We study the influence of a magnetic impurity or ultrasmallquantum dot on the charge persistent current of a mesoscopicring. The system consists of electrons in a one-dimensionalring threaded by spin-dependent Aharonov–Bohm/Casher fluxes,coupled via an antiferromagnetic exchange interaction to alocalized electron. By passing to a basis of electron stateswith definite parities, the problem is mapped onto a Kondomodel for the even-parity channel plus free electrons in theodd-parity channel. The twisted boundary conditionsrepresenting the fluxes couple states of opposite parityunless the twist angles satisfy =f,where f are integers, with spin index=, . For these special values of, the model is solved exactly by a Bethe ansatz.Special cases are investigated in detail. In particular weshow that the charge stiffness in the case= is insensitive to the presenceof the magnetic impurity/quantum dot.     

IN-713C characteristic properties optimized through different heat treatments

The strength of a nickel-based superalloy hardened through precipitation is related to the volume fraction, particle size and distribution of the precipitated phase, . These parameters may vary as a result of heat treatment, or high-temperatures service. The information obtained, describing the influence of time and temperature on the precipitated phase, , is of special importance owing to its technological application at high temperatures. Dissolution or precipitation kinetics are such that the volume-fraction balance of the phase is quickly established at an ageing temperature given by successive changes due only to the particle growth. The results of the present study describe heat-treatment effects on size and distribution of the phase, and precipitated carbides ageing of a nickel-based superalloy (IN-713C). These on ageing studies at a certain temperature show that the kinetic growth of particles by controlled diffusion follows that r t ^1/3 law.     

The effect of Ag additions on the microstructure of aluminium–lithium alloys

Minor quantities of Ag have been added to Al–Li–Cu–Mg–Zr alloys. Their microstructure has been studied by means of optical metallography, transmission electron microscopy and X-ray diffraction. In the high Li, low Cu:Mg ratio alloys the main phases found were , , S and T1, while fewer T2 and Al7Cu2Fe precipitates were also observed. The addition of up to 0.5 wt% Ag diminishes the and T1 precipitates size. This is attributed to a small increase of Li solubility in the matrix. In the low Li, high Cu:Mg ratio alloy the addition of 0.2 wt% Ag resulted in the precipitation of phase simultaneously with , , S and T1 phases. Due to the low Li concentration an unusual growth of the / precipitates at the expense of the precipitates was also observed. © 1998 Kluwer Academic Publishers     

Fabrication of β- and β′′-Al2O3 tubes by pressureless powder packing forming and salt infiltration

A new forming method, pressureless powder packing (PLPP), was studied to fabricate the - and -Al2O3 tubes. Alkali sources were infiltrated into the pores of -Al2O3 tube preforms that had been prepared by the PLPP forming method. The composition for the synthesis of -Al2O3 phase was Na2O · 0. 138Li2 · 4.4Al2O3. The -Al2O3 fraction of calcined and sintered bodies was increased with the increase of calcination temperature, and phase formation was largely affected by the type of starting -Al2O3. Large particle size and narrow size distribution of fused -Al2O3 resulted in uniform green microstructure that enhanced the homogeneity of alkali salts after infiltration, which was very important for the -Al2O3 formation. Sintered microstructure was uniform in all specimens but further development was required for density improvement.     

The influence of neutron irradiation on the thermal conductivity of aluminum in the range 5–50 K

Measurements of thermal conductivity of 6N to 3N pure aluminum in the temperature range 5–50 K subjected to fast neutron irradiation, with exposures of 10¹³ and 10¹⁶ n · cm^–2, are reported. The thermal conductivity maximum was found to shift towards higher temperatures with an increase in the fast neutron irradiation exposure. At high temperatures, a departure from Wilson's theory was observed, which may be attributed to the existence of additional electron scattering mechanisms. An increase in both ideal and residual thermal resistivity components with an increase in the radiation exposure was noted.Nomenclature I ₅ (/t) Debye integral of the fifth order - –m slope of the straight line that crosses maximum thermal conductivity values - n exponent in ideal thermal resistivity component - T _m temperature corresponding to maximum thermal conductivity - W _e total electronic thermal resistivity - W _i ideal thermal resistivity - W ₀ residual thermal resistivity - ideal thermal resistivity coefficient in Eq. (4) - ideal thermal resistivity coefficient in Eq. (1) - constant related to the ideal part of thermal resistivity in Eq. (2) - () ideal thermal resistivity coefficient depending on irradiation exposure - () residual thermal resistivity coefficient depending on irradiation exposure - thermal conductivity - _m maximum thermal conductivity - Debye characteristic temperature - irradiation exposure     

The constitution of the Ni-Al-Ru system

The constitution of the Ni-Al-Ru system has been investigated in the range 0 to 50 at% Al. Isothermal sections at 1523 and 1273 K have been determined using microstructural observations, electron probe microanalysis and X-ray diffraction. The phases present were: nickel-based solid solution (); (based on Ni₃Al); solid solutions based on NiAl and RuAl, respectively (designated ₁ and ₂), and ruthenium-based solid solution (Ru). The maximum solubility of Ru in was 5 at%. ₁, and ₂ show extensive range of solubilities, namely up to 20at% Ru in ₁ and up to 25 to 35 at% Ni in ₂. Three-phase equilibrium between , ₂ and (Ru) existed at 1523 and 1273 K. Also at 1523 K, three-phase equilibria existed between , and ₁ and ,₁ and ₂, while at 1273 K, the equilibria were between , ₁,₂ and , , ₂ indicating the occurrence of a reaction +₁, +₂ at a temperature between 1523 and 1273 K. Liquidus features have been deduced from data on as-solidified structures. Lattice parameter data and hardnesses are also reported.     

Differential-flow-induced instability in a cubic autocatalator system

The formation of spatio-temporal stable patterns is considered for a reaction-diffusion-convection system based upon the cubic autocatalator, A + 2B 3B, B C, with the reactant A being replenished by the slow decay of some precursor P via the simple step P A. The reaction is considered in a differential-flow reactor in the form of a ring. It is assumed that the reactant A is immobilised within the reactor and the autocatalyst B is allowed to flow through the reactor with a constant velocity as well as being able to diffuse. The linear stability of the spatially uniform steady state (a, b) = (µ^–1, µ), where a and b are the dimensionless concentrations of the reactant A and autocatalyst B, and µ is a parameter reflecting the initial concentration of the precursor P, is discussed first. It is shown that a necessary condition for the bifurcation of this steady state to stable, spatially non-uniform, flow-generated patterns is that the flow parameter > _c(µ, ) where _c(µ,) is a (strictly positive) critical value of and is the dimensionless diffusion coefficient of the species B and also reflects the size of the system. Values of _c at which these bifurcations occur are derived in terms of µ and . Further information about the nature of the bifurcating branches (close to their bifurcation points) is obtained from a weakly nonlinear analysis. This reveals that both supercritical and subcritical Hopf bifurcations are possible. The bifurcating branches are then followed numerically by means of a path-following method, with the parameter as a bifurcation parameter, for representatives values of µ and . It is found that multiple stable patterns can exist and that it is also possible that any of these can lose stability through secondary Hopf bifurcations. This typically gives rise to spatio-temporal quasiperiodic transients through which the system is ultimately attracted to one of the remaining available stable patterns.     

A high-resolution-electron-microscopy study of a γ/γ′-α directionally solidified eutectic alloy

The microstructure of a /- directionally solidified (DS) eutectic alloy with a nominal composition of Ni-30.26Mo-6.08Al-1.43V (wt%) was investigated by means of high-resolution electron microscopy (HREM) and analytical electron microscopy. The -fibres exhibited a typical morphology with a rectangular cross-section and they displayed the Bain orientation relationship (OR) with the / matrix; that is, [001][001] and (110)(010). Misfit dislocations and lattice strain fields existed at the / interface for different habit planes; that is, (110)(010) and (100)(110) were analysed. EDAX (Energy dispersive X-ray) analysis showed that the composition of the -phase was approximately Ni₄(Mo, Al, V); it contained 90° rotational domains of Ni₃(Mo, Al, V) with a DO₂₂ structure and Ni₂(Mo, Al, V) with a Pt₂Mo structure.     

Instability of the self-similar front of a phase transition

The stability of self-similar diffusional processes with respect to small disturbances of plane, cylindrical, and spherical phase interfaces is investigated.Notation c weight concentration in solution - D coefficient of diffusion - K curvature - n angular number - R radius of cylinder or sphere - r, r radial coordinate and disturbance of the surface r=R - t time - u velocity of front - x, y, z linear coordinates - X coordinate of front - x disturbance of a plane front - parameter of growth rate - coefficient of surface tension - parameter introduced in (8) or (21) - , dimensionless disturbance of surface of the front and its amplitude - , , , dimensionless coordinates - , angular coordinates - H dimensionless wave number - wavelength of disturbance - concentration in solid - dimensionless time - (), amplitudes of disturbances of concentration - dimensionless concentration - dimensionless growth increment of disturbances Indices 0 and states at a plane front and in the solution far from the front - anasterisk state at a curved front - m fastest growing disturbances - a degree sign pertains to self-similar variables Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 40, No. 5, pp. 818–827, May, 1981.     

The Possibility of Reproducing the Units of Complex Permittivity at High Frequencies

The results of theoretical investigations of the reproduction of the units of the components of complex permittivity and by a method based on the use of the wave properties of a coaxial line are presented. The errors in reproducing and are analyzed.     

Effect of crystalline phase, orientation and temperature on the dielectric properties of poly (vinylidene fluoride) (PVDF)

The effect of crystalline phase, uniaxial drawing and temperature on the real () and imaginary () parts of the relative complex permittivity of poly (vinylidene fluoride) (PVDF) was studied in the frequency range between 10² and 10⁶ Hz. Samples containing predominantly and phases, or a mixture of these, were obtained by crystallization from a DMF solution at different temperatures. phase samples were also obtained from melt crystallization and from commercial films supplied by Bemberg Folien. Different molecular orientations were obtained by uniaxial drawing of and phase samples. The results showed that the crystalline phase exerts strong influence on the values of and , indicating that the _a relaxation process, associated with the glass transition of PVDF, is not exclsively related to the amorphous region of the polymer. An interphase region, which maintains the conformational characteristics of the crystalline regions, should influence the process decisively. The molecular orientation increased the values of for both PVDF phases and modified its dependence with temperature over the whole frequency range studied. The influence of the crystallization and molecular orientation conditions on the dc electric conductivity (_dc) were also verified. The value of _dc was slightly higher for samples crystallized from solution at the lowest temperature and decreased with draw ratio.