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Fe rich Fe-Al alloys single crystals, determining three dimensional order and atomic displacements coefficients by X ray diffuse scattering
An experimental study of wall static pressure distributions and mean velocity profiles along a duct and diffuser downstream of wall-jet injection was conducted over a range of diffuser total angles from 15 to 40 deg at injection to core flow mass flux ratios from 0 to 6. Pressure recovery in the diffuser increased with injection ratio and decreased with diffuser total angle. Peak velocities in the wall-jet decayed along the flow and the inner shear layer and outer mixing region grew in thickness along the flow. The inner layer was near similarity condition, but non-similar variations were found in the outer layer. Estimated wall shear stresses depended upon injection mass fluxes, downstream distance and diffuser total angle. Greater decay of peak velocity and larger friction coefficients were found in the diffuser than indicated by correlations from data for a wall-jet without a pressure gradient. At the largest diffuser total angle and the highest injection ratio flow reversal occurred in the core region.
Gas-phase chemistry in the steady state is reviewed. The chemistries of C and O, and the reactions for the formation of CO, D-bearing, and N-bearing molecules are discussed. Consideration is given to the column density of H3(+) in diffuse clouds, the rate coefficient, abundances of H3(+), and the steady-state models of van Dishoeck and Black (1986). The varying lifetime of H2, from 1000 years at the boundary to 5,000,000 years or more at the center of diffuse clouds, and changes in the H2/H abundance ratio in dense clouds are studied, and the nonequilibrium chemistry that occurs in shock-heated gas is analyzed. The estimation of photo rates and the radiation field; models of molecular formations on grains; and the synthesis of molecules in clouds are examined.
A layered canopy model was used to analyze the effects of diffuse light on canopy gross photosynthesis in controlled environment plant growth chambers, where, in contrast to the field, highly diffuse light can occur at high irradiance. The model suggests that high diffuse light fractions (approximately 0.7) and irradiance (1400 micromoles m-2 s-1) may enhance crop life-cycle canopy gross photosynthesis for hydroponic wheat by about 20% compared to direct light at the same irradiance. Our simulations suggest that high accuracy is not needed in specifying diffuse light fractions in chambers between approximately 0.7 and 1, because simulated photosynthesis for closed canopies plateau in this range. We also examined the effect of leaf angle distribution on canopy photosynthesis under growth chamber conditions, as these distributions determine canopy extinction coefficients for direct and diffuse light. We show that the spherical leaf angle distribution is not suitable for modeling photosynthesis of planophile canopies (e.g., soybean and peanut) in growth chambers. Also, the absorption of the light reflected from the surface below the canopy should generally be included in model simulations, as the corresponding albedo values in the photosynthetically active range may be quite high in growth chambers (e.g., approximately 0.5). In addition to the modeling implications, our results suggest that diffuse light conditions should be considered when drawing conclusions from experiments in controlled environments.
A model which explains the nonresonant waves which produce the diffuse resonance observed near 3/2 f(H) by the Alouette and Isis topside sounders, where f(H) is the ambient electron cyclotron frequency, is presented. These waves are the result of plasma wave instabilities driven by anisotropic electron velocity distributions initiated by the high-power short-duration sounder pulse. Calculations of the nonlinear wave-particle coupling coefficients show that the diffuse resonance wave can be maintained by nonlinear Landau damping of the sounder-stimulated 2f(H) wave which is observed with a time duration longer than that of the diffuse resonance wave. The time duration of the diffuse resonance is determined by the transit time of the instability-generated and nonlinearly maintained diffuse resonance wave from the remote short-lived hot region back to the antenna. The model is consistent with the Alouette/Isis observations and it demonstrates the existence of nonlinear wave-particle interactions in the ionosphere.
Polymer matrix composites are increasingly used in demanding structural applications in which they may be exposed to harsh environments. The durability of such materials is a major concern, potentially limiting both the integrity of the structures and their useful lifetimes. The goal of the current investigation is to develop a mechanism-based model of the chemical degradation which occurs, such that given the external chemical environment and temperatures throughout the laminate, laminate geometry, and ply and/or constituent material properties, we can calculate the concentration of diffusing substances and extent of chemical degradation as functions of time and position throughout the laminate. This objective is met through the development and use of analytical models, coupled to an analysis-driven experimental program which offers both quantitative and qualitative information on the degradation mechanism. Preliminary analyses using coupled diffusion/reaction model are used to gain insight into the physics of the degradation mechanisms and to identify crucial material parameters. An experimental program is defined based on the results of the preliminary analysis which allows the determination of the necessary material coefficients. Thermogravimetric analyses are carried out in nitrogen, air, and oxygen to provide quantitative information on thermal and oxidative reactions. Powdered samples are used to eliminate diffusion effects. Tests in both inert and oxidative environments allow the separation of thermal and oxidative contributions to specimen mass loss. The concentration dependency of the oxidative reactions is determined from the tests in pure oxygen. Short term isothermal tests at different temperatures are carried out on neat resin and unidirectional macroscopic specimens to identify diffusion effects. Mass loss, specimen shrinkage, the formation of degraded surface layers and surface cracking are recorded as functions of exposure time. Geometry effects in the neat resin, and anisotropic diffusion effects in the composites, are identified through the use of specimens with different aspect ratios. The data is used with the model to determine reaction coefficients and effective diffusion coefficients. The empirical and analytical correlations confirm the preliminary model results which suggest that mass loss at lower temperatures is dominated by oxidative reactions and that these reaction are limited by diffusion of oxygen from the surface. The mechanism-based model is able to successfully capture the basic physics of the degradation phenomena under a wide range of test conditions. The analysis-based test design is successful in separating out oxidative, thermal, and diffusion effects to allow the determination of material coefficients. This success confirms the basic picture of the process; however, a more complete understanding of some aspects of the physics are required before truly predictive capability can be achieved.
Polymer matrix composites are increasingly used in demanding structural applications in which they may be exposed to harsh environments. The durability of such materials is a major concern, potentially limiting both the integrity of the structures and their useful lifetimes. The goal of the current investigation is to develop a mechanism-based model of the chemical degradation which occurs, such that given the external chemical environment and temperatures throughout the laminate, laminate geometry, and ply and/or constituent material properties, we can calculate the concentration of diffusing substances and extent of chemical degradation as functions of time and position throughout the laminate. This objective is met through the development and use of analytical models, coupled to an analysis-driven experimental program which offers both quantitative and qualitative information on the degradation mechanism. Preliminary analyses using a coupled diffusion/reaction model are used to gain insight into the physics of the degradation mechanisms and to identify crucial material parameters. An experimental program is defined based on the results of the preliminary analysis which allows the determination of the necessary material coefficients. Thermogravimetric analyses are carried out in nitrogen, air, and oxygen to provide quantitative information on thermal and oxidative reactions. Powdered samples are used to eliminate diffusion effects. Tests in both inert and oxidative environments allow the separation of thermal and oxidative contributions to specimen mass loss. The concentration dependency of the oxidative reactions is determined from the tests in pure oxygen. Short term isothermal tests at different temperatures are carried out on neat resin and unidirectional macroscopic specimens to identify diffusion effects. Mass loss, specimen shrinkage, the formation of degraded surface layers and surface cracking are recorded as functions of exposure time. Geometry effects in the neat resin, and anisotropic diffusion effects in the composites, are identified through the use of specimens with different aspect ratios. The data is used with the model to determine reaction coefficients and effective diffusion coefficients. The empirical and analytical correlations confirm the preliminary model results which suggest that mass loss at lower temperatures is dominated by oxidative reactions and that these reaction are limited by diffusion of oxygen from the surface. The mechanism-based model is able to successfully capture the basic physics of the degradation phenomena under a wide range of test conditions. The analysis-based test design is successful in separating out oxidative, thermal, and diffusion effects to allow the determination of material coefficients. This success confirms the basic picture of the process; however, a more complete understanding of some aspects of the physics are required before truly predictive capability can be achieved.
A time-dependent diffusion equation with velocity-dependent diffusion and energy-loss coefficients was solved for the case where energetic solar particles are injected into a coronal loop and then diffuse out the ends of the loop into the lower corona/chromosphere. The solution yields for the case of relativistic electrons, precipitation rates and populations which are necessary for calculating thick and thin target X-ray emission. It follows that the thick target emission is necessarily delayed with respect to the particle acceleration on injection by more than the mere travel time of the particle over the loop length. In addition the time-dependent electron population at the top of the loop is calculated. This is useful in estimating the resulting micron-wave emission. The results show relative timing differences in the different emission processes which are functions of particle species, energy and the point of injection of the particles into the loop. Equivalent quantities are calculated for non-relativistic protons.
Diffuse reflection and transmission coefficients computed for radiative transfer in homogeneous slabs of finite thickness with isotropic scattering
A new technique of high-temperature thermal-conductivity measurement is described. A CO2 gas laser is used to generate a low-frequency temperature wave at one face of a small disk-shaped sample, and an infrared detector views the opposite face to detect the phase of the emerging radiation. A mathematical expression is derived which enables phase data at several frequencies to be used for the simultaneous determination of thermal diffusivity and mean extinction coefficient. Lattice and radiative thermal conductivities are then calculated. Test results for sintered aluminum oxide at temperatures from 530 to 1924 K are within the range of error of previously existing data.
The first part of the present theory is devoted to the derivation of a Fokker-Planck equation. The eddies smaller than the hydrodynamic scale of the diffusion cloud form a diffusivity, while the inhomogeneous, bigger eddies give rise to a nonuniform migratory drift. This introduces an eddy-induced shear which reflects on the large-scale diffusion. The eddy-induced shear does not require the presence of a permanent wind shear and is intrinsic to the diffusion. Secondly, a transport theory of diffusivity is developed by the method of repeated-cascade and is based upon a relaxation of a chain of memories with decreasing information. The full range of diffusion consists of inertia, composite, and shear subranges, for which variance and eddy diffusivities are predicted. The coefficients are evaluated. Comparison with experiments in the upper atmosphere and oceans is made.
A knowledge of the structure of the rocket exhaust plumes is necessary to solve problems involving plume signatures, base heating, plume/surface interactions, etc. An algorithm is presented which treats the viscous flow of multiphase chemically reacting fluids in a two-dimensional or axisymmetric supersonic flow field. The gas-particle flow solution is fully coupled with the chemical kinetics calculated using an implicit scheme to calculate chemical production rates. Viscous effects include chemical species diffusion with the viscosity coefficient calculated using a two-equation turbulent kinetic energy model.
The effect of solid-liquid interface shape on lateral solute segregation during steady-state unidirectional solidification of a binary mixture is calculated under the assumption of no convection in the liquid. A finite element technique is employed to compute the concentration field in the liquid and the lateral segregation in the solid with a curved boundary between the liquid and solid phases. The computational model is constructed assuming knowledge of the solid-liquid interface shape; no attempt is made to relate this shape to the thermal field. The influence of interface curvature on the lateral compositional variation is investigated over a range of system parameters including diffusivity, growth speed, distribution coefficient, and geometric factors of the system. In the limiting case of a slightly nonplanar interface, numerical results from the finite element technique are in good agreement with the analytical solutions of Coriell and Sekerka obtained by using linear theory. For the general case of highly non-planar interface shapes, the linear theory fails and the concentration field in the liquid as well as the lateral solute segregation in the solid can be calculated by using the finite element method.
Energetic solar flare particles, both electrons and protons, must survive the turbulent environment of a flaring loop and propogate to the lower corona or chromosphere in order to produce hard X-ray and gamma ray bursts. This plasma turbulence, often observed in soft X-ray line widths to be in excess of 100 km/s, is presumably capable of efficiently scattering the fast flare particles. This prevents to some degree the free streaming of accelerated particles and depending on the amplitude of the turbulence, restricts the particles to diffusive propagation along the length of the loop to the target chromosphere. In addition this turbulence is capable of performing additional acceleration of the fast particles by the second order Fermi mechanism. For compact flares with rise times 10s, the acceleration effect is small and the propagation of the particles is governed by spatial diffusion and energy loss in the ambient medium. The solution of the time dependent diffusion equation with velocity dependent diffusion and energy loss coefficients yields for the case of nonrelativistic protons particle precipitation rates which are necessary for calculating thick target gamma ray emission and also yields the total thin target emissivity.
An approximate analytical technique for extracting the concentration dependence of the interdiffusion coefficient was derived from diffusion measurements carried out with the diaphragm cell. The systematic error incurred in using the technique was estimated and found to be no greater than the random error ordinarily encountered in these experiments.
An examination of the ages and sizes of 114 terrestrial impact craters shows that their aging kinetics can be described by the diffusion laws. The macrodiffusion coefficient which determines random displacements of mineral masses on the Earth has a mean value of 0.02 sq m/year. The amount of matter in a crater that contains information about the impact event decreases with time according to the 1/T law. The basic characteristic parameter of a crater is its initial area, inasmuch as sufficiently large craters are nearly surficial formations. The relaxation time of a crater is proportional to its initial area.
To illustrate the effect of the viscous and inertial terms on the structure of cosmic-ray-modified shocks, an analysis of a time-independent 1D shock is presented in which the pressure of the background fluid and the magnetic-field energy density are negligible compared with the cosmic-ray pressure. The effect of the magnetic field on cosmic-ray transport coefficients is retained. The diffusion, viscous and inertial terms work to 'thicken' the shock. When the average magnetic field is negligible and the cosmic-ray transport is isotropic, diffusion is the dominant effect unless the parameters are such that the scattering time becomes comparable to the characteristic times for velocity change in the fluid frame. For a perpendicular shock, where the diffusion is strongly reduced by the magnetic field, the relative magnitude of the viscous effect is increased by a factor about (omega tau) exp 2, leading to the conclusion that cosmic-ray viscosity can be important to the structure of collisionless MHD shocks. In both cases considered, the viscous and inertial terms become important for those parameter ranges where the diffusion approximation begins to break down.
Self-, N2-, O2-, H2-, Ar-, and He-broadening coefficients, pressure shifts, and integrated intensities have been measured for most transitions in the Q branch of the nu3 fundamental band of methane using a difference-frequency laser spectrometer. A systematic dependence of the broadening coefficients on the tetrahedral symmetry species and order index is observed with striking similarities for N2, O2, and Ar and for H2 and He buffer gases. Comparison with earlier measurements on other bands and branches of methane indicates very little vibrational, branch, or carbon isotope dependence. Dicke narrowing is evident at intermediate pressures, yielding an average narrowing coefficient and an optical diffusion constant for each gas mixture.