7,463 research outputs found

    Massive spinor fields in flat spacetimes with non-trivial topology

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    The vacuum expectation value of the stress-energy tensor is calculated for spin 121\over 2 massive fields in several multiply connected flat spacetimes. We examine the physical effects of topology on manifolds such as R3×S1R^3 \times S^1, R2×T2R^2\times T^2, R1×T3R^1 \times T^3, the Mobius strip and the Klein bottle. We find that the spinor vacuum stress tensor has the opposite sign to, and twice the magnitude of, the scalar tensor in orientable manifolds. Extending the above considerations to the case of Misner spacetime, we calculate the vacuum expectation value of spinor stress-energy tensor in this space and discuss its implications for the chronology protection conjecture.Comment: 18 pages, Some of the equations in section VI as well as typographical errors corrected, 5 figures, Revtex

    Oxidation of Zr-2.5 Nb Nuclear Reactor Pressure Tubes A New Model

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    The corrosion and associated deuterium (D) uptake of Zr alloy nuclear reactor pressure tubes have been studied for over 40 years. Zircaloy tubes exhibit rapid D ingress after a period of in-reactor exposure, and have been replaced with tubes fabricated from the more resistant Zr-2.5 wt % Nb alloy. Recently, however, a small percentage of Zr-2.5 Nb tubes have been found to contain high D contents. There is currently no clear understanding of the mechanism for this increased D uptake, and concern exists that an increasing number of high-D tubes will develop with time. A new model for Zr-2.5 Nb corrosion is presented in this paper. The rate of corrosion is shown to be dependent on the rate of transformation of the protective inner oxide layer (closer to the metal) to a porous outer layer. The mechanism of this transformation is not known and should be the subject of future investigations. It is assumed in the model that zirconia chemically dissolves into the solution at the pore bottom. The rate of this dissolution reaction depends on the local pH, which increases if there is a buildup of deuteroxyl ions generated in the cathodic part of the Zr corrosion reaction. A mathematical description of this model, containing several parameters with unknown values, is presented. Assigning certain values to these parameters results in predictions of oxide formation (and thus D buildup) that correspond well with observations.Support of this work by the Atomic Energy Control Board under AECB project no. 2.349.1 is gratefully acknowledged

    Electromagnetic wormholes and virtual magnetic monopoles

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    We describe new configurations of electromagnetic (EM) material parameters, the electric permittivity ϵ\epsilon and magnetic permeability μ\mu, that allow one to construct from metamaterials objects that function as invisible tunnels. These allow EM wave propagation between two points, but the tunnels and the regions they enclose are not detectable to EM observations. Such devices function as wormholes with respect to Maxwell's equations and effectively change the topology of space vis-a-vis EM wave propagation. We suggest several applications, including devices behaving as virtual magnetic monopoles.Comment: 4 pages, 3 figure

    Pitting in Aluminum Thin Films Supersaturation and Effects of Dichromate Ions

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    The growth of pits in 209 nm thick Al films in chloride solutions with and without dichromate ions was examined using image analysis of the growing pits to determine pit current density. In pure chloride solutions, the pit current density decreased at high potentials after reaching a maximum value, and then was almost independent of applied potential. A hysteresis in the pit current density-potential behavior was observed during downward stepping of the potential from high values. This is a result of a combination of supersaturation of the pit electrolyte followed by salt film formation, and changes in mass transport from hydrogen bubbles that increase convection and lift the remnant passive film away from the dissolving surface. In solutions containing dichromate ions, the corrosion and repassivation potentials shifted in the noble direction, and rather large metastable pits formed at the open circuit. A large concentration of dichromate ions was needed to inhibit pit growth. In dichromate solutions, subsequent pit growth at higher potentials often initiated at the edge of the open-circuit pits. The rate of pit growth was lower for these pits because the remnant passive film layer was not easily lifted up at these sites, and thus created a barrier for mass transport away from the dissolving pit edge.This work was supported by Major H. DeLong at the United States Air Force Office of Scientific Research under contract F49620-96-0042

    Pit Growth Study in Al Alloys by the Foil Penetration Technique

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    The foil penetration technique was used to study pit growth in AA1100-O and AA2024-T3. Preliminary work on AA1100-O foils of different thicknesses indicated that the pit growth rate increased with increasing applied potential, suggesting that pit growth was not under transport control. Foil penetration experiments were also carried out on AA2024-T3 foils of a given thickness, at open circuit as well as anodic potentials. Dichromate ions and other oxidizing agents were added to some test solutions. Dichromate ions were shown to have little influence on the pit growth rate at controlled anodic potentials, even when added in large concentrations. However, dichromate ions effectively inhibited pitting at open circuit when present in very small amounts. Polarization curves of AA2024-T3 in 1 M NaCl with various additives show a large effect of dichromate ions in the cathodic region and no effect in the anodic region. These observations suggest that chromate (or its reduction product) acts as a cathodic inhibitor. Examination of penetrated samples was performed by optical and scanning electron microscopies, as well as by microradiography.This work was supported by Major H. DeLong at the Air Force Office of Scientific Research, under contract F49620-96-0042

    Taylor dispersion of gyrotactic swimming micro-organisms in a linear flow

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    The theory of generalized Taylor dispersion for suspensions of Brownian particles is developed to study the dispersion of gyrotactic swimming micro-organisms in a linear shear flow. Such creatures are bottom-heavy and experience a gravitational torque which acts to right them when they are tipped away from the vertical. They also suffer a net viscous torque in the presence of a local vorticity field. The orientation of the cells is intrinsically random but the balance of the two torques results in a bias toward a preferred swimming direction. The micro-organisms are sufficiently large that Brownian motion is negligible but their random swimming across streamlines results in a mean velocity together with diffusion. As an example, we consider the case of vertical shear flow and calculate the diffusion coefficients for a suspension of the alga <i>Chlamydomonas nivalis</i>. This rational derivation is compared with earlier approximations for the diffusivity

    Nuclear transparencies for nucleons, knocked-out under various semi-inclusive conditions

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    Using hadron dynamics we calculate nuclear transparencies for protons, knocked-out in high-Q2Q^2, semi-inclusive reactions. Predicted transparencies are, roughly half a standard deviation above the NE18 data. The latter contain the effects of binned proton missing momenta and mass, and of finite detector acceptances. In order to test sensitivity we compare computed transparencies without restrictions and the same with maximal cuts for missing momenta and the electron energy loss. We find hardly any variation, enabling a meaningful comparison with data and predictions based on hadron dynamics. Should discrepancies persist in high-statistics data, the above may with greater confidence be attributed to exotic components in the description of the outgoing proton.Comment: 13 pages + 3 figsin appended PS file, report # WIS-94/43/Oct-P

    Coupling nonpolar and polar solvation free energies in implicit solvent models

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    Recent studies on the solvation of atomistic and nanoscale solutes indicate that a strong coupling exists between the hydrophobic, dispersion, and electrostatic contributions to the solvation free energy, a facet not considered in current implicit solvent models. We suggest a theoretical formalism which accounts for coupling by minimizing the Gibbs free energy of the solvent with respect to a solvent volume exclusion function. The resulting differential equation is similar to the Laplace-Young equation for the geometrical description of capillary interfaces, but is extended to microscopic scales by explicitly considering curvature corrections as well as dispersion and electrostatic contributions. Unlike existing implicit solvent approaches, the solvent accessible surface is an output of our model. The presented formalism is illustrated on spherically or cylindrically symmetrical systems of neutral or charged solutes on different length scales. The results are in agreement with computer simulations and, most importantly, demonstrate that our method captures the strong sensitivity of solvent expulsion and dewetting to the particular form of the solvent-solute interactions.Comment: accpted in J. Chem. Phy

    Influence of Dichromate Ions on Corrosion Processes on Pure Magnesium

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    The corrosion behavior of Mg is of interest because of its growing use as an alloy in the transportation industry and also because it is a major component of some intermetallic phases in Al alloys, such as the deleterious S (Al2CuMg)-phase found in AA2024-T3. Pure Mg corrodes rapidly in a chloride-containing solution and even dissolves in water if the surface hydroxide is damaged by scratching the surface, for example. Uniform dissolution is drastically reduced in NaCl solutions (from 0.01 to 0.5 M) with the addition of very dilute concentrations of dichromate (10-4 M). However, it is replaced by a strong localized attack in the form of fast filiform-like attack. On a large-grained sample with a defined defect structure, the attack can be seen to propagate at twin boundaries. Orientation imaging microscopy analysis found that corrosion was limited to planes near {0001} orientations with propagation being in prismatic directions. Auger electron spectroscopy analysis shows that interaction of chromate with the Mg hydroxide results in incorporation of reduced chromium ions in the hydroxide surface layer. Formation of a more resistant surface film could explain the very local nature of the corrosion in this case. The interaction between dichromate ions and Mg hydroxide can also explain the higher corrosion resistance of S-phase particles in chloride solutions containing dilute dichromate, although differences in the surface film formed compared to pure Mg are observed. Sputter-etching of the surface in order to assess the depth of the attack revealed that very hard or isolating corrosion products difficult to sputter are produced along the filiform path and that chromium compounds are not integrated in the corrosion products. Focused ion beam sectioning followed by scanning electron microscopy investigation of the sectioned area, demonstrates the presence of a continuous protective surface film. Adhesion between the Mg hydroxide and the metal is lost at the location of the corrosion filament, suggesting that the mechanism of propagation is similar to filiform corrosion under a coating. The depth of attack is a couple of micrometers with large cracks present within the corroded area that could induce severe surface damage.This work was supported by the Air Force Office of Scientific Research under contract no. F49620-96-1-0479
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