Solid-fluid transition in a granular shear flow

The rheology of a granular shear flow is studied in a quasi-2D rotating cylinder. Measurements are carried out near the midpoint along the length of the surface flowing layer where the flow is steady and nonaccelerating. Streakline photography and image analysis are used to obtain particle velocities and positions. Different particle sizes and rotational speeds are considered. We find a sharp transition in the apparent viscosity (eta) variation with rms velocity (u). Below the transition depth we find that the rms velocity decreases with depth and eta proportional to u(-1.5) for all the different cases studied. The material approaches an amorphous solidlike state deep in the layer. The velocity distribution is Maxwellian above the transition point and a Poisson velocity distribution is obtained deep in the layer. The results indicate a sharp transition from a fluid to a fluid + solid state with decreasing rms velocity.     

Self-organization in granular slurries

We report the existence of self-organization in wet granular media or slurries, mixtures of particles of different sizes dispersed in a lower density liquid. As in the case of dry granular mixtures, axial banding (alternating bands rich in small and large particles in a long rotating cylinder) and radial segregation (in quasi-2D containers) are observed in slurries. However, when compared with the dry counterpart axial segregation is significantly faster and the spectrum of outcomes is richer. Moreover, experiments with suitable fluids reveal, for the first time, the internal structure of axially segregated systems, something that up to now has been accessible only via magnetic resonance imaging experimentation.     

Mn site substitution of La0.67Ca0.33MnO3 with closed shell ions: Effect on magnetic transition temperature

Mn site is substituted with closed shell ions (Al, Ga, Ti, Zr and a certain combination of Zr and Al) and also with Fe and Ru ions carrying the magnetic moment (S=5/2 and 2 respectively) at a fixed concentration of 5 at %. Substitution did not change either the crystal symmetry or the oxygen stoichiometry. All substituents were found to suppress both the metal-insulator and ferromagnetic transition temperatures (T _p(ρ) and T _C, respectively) to varied extents. Two main contributions identified for the suppression are the lattice disorder arising due to difference in the ionic radii between the substituent (r _M) and the Mn³⁺ ion (r _Mn ³⁺) and in the case of the substituents carrying a magnetic moment, the type of magnetic coupling between the substituent and that of the neighboring Mn ion.     

Mixing and segregation of granular materials in chute flows

Mixing of granular solids is invariably accompanied by segregation, however, the fundamentals of the process are not well understood. We analyze density and size segregation in a chute flow of cohesionless spherical particles by means of computations and theory based on the transport equations for a mixture of nearly elastic particles. Computations for elastic particles (Monte Carlo simulations), nearly elastic particles, and inelastic, frictional particles (particle dynamics simulations) are carried out. General expressions for the segregation fluxes due to pressure gradients and temperature gradients are derived. Simplified equations are obtained for the limiting cases of low volume fractions (ideal gas limit) and equal sized particles. Theoretical predictions of equilibrium number density profiles are in good agreement with computations for mixtures of equal sized particles with different density for all solids volume fractions, and for mixtures of different sized particles at low volume fractions (nu<0.2), when the particles are elastic or nearly elastic. In the case of inelastic, frictional particles the theory gives reasonable predictions if an appropriate effective granular temperature is assumed. The relative importance of pressure diffusion and temperature diffusion for the cases considered is discussed. (c) 1999 American Institute of Physics.     

Numerical simulation of the sedimentation of a sphere in a sheared granular fluid: a granular Stokes experiment

We study, computationally, the sedimentation of a sphere of higher mass in a steady, gravity-driven granular flow of otherwise identical spheres, on a rough inclined plane. Taking a hydrodynamic approach at the scale of the particle, we find the drag force to be given by a modified Stokes law and the buoyancy force by the Archimedes principle, with excluded volume effects taken into account. We also find significant differences between the hydrodynamic case and the granular case, which are highlighted.     

Chaotic mixing of granular materials in two-dimensional tumbling mixers

We consider the mixing of similar, cohesionless granular materials in quasi-two-dimensional rotating containers by means of theory and experiment. A mathematical model is presented for the flow in containers of arbitrary shape but which are symmetric with respect to rotation by 180 degrees and half-filled with solids. The flow comprises a thin cascading layer at the flat free surface, and a fixed bed which rotates as a solid body. The layer thickness and length change slowly with mixer rotation, but the layer geometry remains similar at all orientations. Flow visualization experiments using glass beads in an elliptical mixer show good agreement with model predictions. Studies of mixing are presented for circular, elliptical, and square containers. The flow in circular containers is steady, and computations involving advection alone (no particle diffusion generated by interparticle collisions) show poor mixing. In contrast, the flow in elliptical and square mixers is time periodic and results in chaotic advection and rapid mixing. Computational evidence for chaos in noncircular mixers is presented in terms of Poincare sections and blob deformation. Poincare sections show regions of regular and chaotic motion, and blobs deform into homoclinic tendrils with an exponential growth of the perimeter length with time. In contrast, in circular mixers, the motion is regular everywhere and the perimeter length increases linearly with time. Including particle diffusion obliterates the typical chaotic structures formed on mixing; predictions of the mixing model including diffusion are in good qualitative and quantitative (in terms of the intensity of segregation variation with time) agreement with experimental results for mixing of an initially circular blob in elliptical and square mixers. Scaling analysis and computations show that mixing in noncircular mixers is faster than that in circular mixers, and the difference in mixing times increases with mixer size. (c) 1999 American Institute of Physics.     

Study of molecular motions in liquids by electron spin-lattice relaxation measurements,I: Semiquinone ions in hydrogen bonding solvents

The electron spin-lattice relaxation times (T ₁) of a variety of semiquinone ions in hydrogen bonding solvents have been measured by the pulsed saturation recovery technique as a function of temperature (T) and viscosity (η) of the solvent. Also linewidths (ΔH) have been measured in suitable cases in such solvents at low radical concentrations (～10^?4 M). It is observed that (i) the temperature and viscosity dependence ofT ₁ can be fitted to an equation of the form 1/T ₁=A(T/η)+Bexp(-ΔE/RT) whereA andB are constants and ΔE is an activation energy of the order of 1 kcal mole^?1 for these systems; (ii)T ₁ is essentially independent of the radical concentration within the range 10^?3 to 5×10^?2 M; (iii) the concentration independent part of the linewidth (ΔH) increases linearly with (η/T) at sufficiently low temperatures, and (iv) the (η/T) dependent part ofT ₁ is sensitive to the size of the semiquinone as well as that of the solvent molecule, whereas the linewidth which is proportional to (η/T) at high viscosity, low temperature region is not sensitive to the size of the semiquinone and that of the solvent. Based on these observations, it is postulated that in hydrogen bonding solvents, three types of motion contribute significantly to electron spin relaxation:

1. A restricted small step diffusional motion, not involving large changes in the orientation of the molecule, leading to the dominant viscosity dependent contributions toT ₁ and ΔH, due to spin rotation interaction;
2. a large amplitude reorientation of the semiquinone, coupled to translational diffusion, resulting in viscosity dependent contributions toT ₁ and ΔH, throughg-modulation;
3. a hindred rotation of the semiquinone within the solvent cage, contributing toT ₁ due to spin rotation interaction.

The fact thatT ₁ is not sensitive to the concentration of the radicals, is ascribed to the formation of the solvent cage that prevents the close approach of radicals, thereby rendering radical-radical interactions to be weak mechanisms for relaxation, even at relatively high radical concentrations.     

DSC analysis of Cu–Zn–Sn shape memory alloy fabricated via electrodeposition route

Cu–Zn–Sn shape memory alloy strips with composition range of 13.70–46.30 mass% Sn were fabricated by electrodepositing Sn on a shim brass surface and then subsequently annealed at a constant temperature of 400 °C for 120 min under flowing nitrogen. Subjecting the Sn-plated strips to differential scanning calorimetry (DSC) analysis revealed that the austenitic start (A _s) temperature was essentially constant at 225 °C while the martensite start (M _s) temperature was consistently within the 221.5–222 °C interval. Austenite to martensite phase transformation showed two distinct peaks on the DSC thermogram which can be attributed to the non-homogeneity of the bulk Cu–Zn–Sn ternary alloy. The latent heats of cooling and heating were found to increase with the mass% Sn plated on the shim brass. Effect of annealing temperature was also investigated wherein strips with an essentially constant composition of 26 mass% Sn were annealed at a temperature range of 350–420 °C for 120 min under flowing nitrogen. Varying the annealing temperature has no significant effect on the transformation temperatures of the ternary alloy.