Spectral properties of nuclear matter

We review self-consistent spectral methods for nuclear matter calculations. The in-medium T-matrix approach is conserving and thermodynamically consistent. It gives both the global and the single-particle properties the system. The T-matrix approximation allows to address the pairing phenomenon in cold nuclear matter. A generalization of nuclear matter calculations to the superfluid phase is discussed and numerical results are presented for this case. The linear response of a correlated system going beyond the Hartree-Fock+Random-Phase-Approximation scheme is studied. The polarization is obtained by solving a consistent Bethe-Salpeter equation for the coupling of dressed nucleons to an external field. We find that multipair contributions are important for the spin(isospin) response when the interaction is spin(isospin) dependent.Comment: Talk given at the workshop "Progress in Nonequilibrium Green's Functions III" 22-26 August 2005, Kie

Multiscale Modeling of Damage Processes in Aluminum Alloys: Grain-Scale Mechanisms

This paper has two goals related to the development of a physically-grounded methodology for modeling the initial stages of fatigue crack growth in an aluminum alloy. The aluminum alloy, AA 7075-T651, is susceptible to fatigue cracking that nucleates from cracked second phase iron-bearing particles. Thus, the first goal of the paper is to validate an existing framework for the prediction of the conditions under which the particles crack. The observed statistics of particle cracking (defined as incubation for this alloy) must be accurately predicted to simulate the stochastic nature of microstructurally small fatigue crack (MSFC) formation. Also, only by simulating incubation of damage in a statistically accurate manner can subsequent stages of crack growth be accurately predicted. To maintain fidelity and computational efficiency, a filtering procedure was developed to eliminate particles that were unlikely to crack. The particle filter considers the distributions of particle sizes and shapes, grain texture, and the configuration of the surrounding grains. This filter helps substantially reduce the number of particles that need to be included in the microstructural models and forms the basis of the future work on the subsequent stages of MSFC, crack nucleation and microstructurally small crack propagation. A physics-based approach to simulating fracture should ultimately begin at nanometer length scale, in which atomistic simulation is used to predict the fundamental damage mechanisms of MSFC. These mechanisms include dislocation formation and interaction, interstitial void formation, and atomic diffusion. However, atomistic simulations quickly become computationally intractable as the system size increases, especially when directly linking to the already large microstructural models. Therefore, the second goal of this paper is to propose a method that will incorporate atomistic simulation and small-scale experimental characterization into the existing multiscale framework. At the microscale, the nanoscale mechanics are represented within cohesive zones where appropriate, i.e. where the mechanics observed at the nanoscale can be represented as occurring on a plane such as at grain boundaries or slip planes at a crack front. Important advancements that are yet to be made include: 1. an increased fidelity in cohesive zone modeling; 2. a means to understand how atomistic simulation scales with time; 3. a new experimental methodology for generating empirical models for CZMs and emerging materials; and 4. a validation of simulations of the damage processes at the nano-micro scale. With ever-increasing computer power, the long-term ability to employ atomistic simulation for the prognosis of structural components will not be limited by computation power, but by our lack of knowledge in incorporating atomistic models into simulations of MSFC into a multiscale framework

Angle-resolved two-dimensional mapping of electron emission from the inner-shell 2p excitations in Cl₂

Angle-resolved Auger and valence photoelectron spectra were measured over a 14-eV photon energy range across the Cl2 2p ionization thresholds. The measurements were carried out using highly efficient time-of-flight spectrometers coupled with photons from the Atomic and Molecular undulator beamline of the Advanced Light Source and an advanced data-acquisition system. Auger-electron spectra of 2→pσ* and 2→pnl resonances were analyzed and the evolution of the resonant Auger to the normal Auger decay distorted by postcollision interaction was examined. We find that valence photoionization channels do not resonate strongly at the photon energies of the core-to-Rydberg excitation, in contrast to the strongly resonating ones observed in the HCl molecule. Auger decay spectra of the 2p−1σ* resonances showed no evidence of atomic transitions in Cl*, also in contrast to HCl. In addition, angular distribution of the photoelectron and Auger-electron lines was derived

Hydrodynamic modeling of deconfinement phase transition in nuclear collisions

The (3+1)-dimensional ideal hydrodynamics is used to simulate collisions of gold nuclei with bombarding energies from 1 to 160 GeV per nucleon. The initial state is represented by two cold Lorentz-boosted nuclei. Two equations of state: with and without the deconfinement phase transition are used. We have investigated dynamical trajectories of compressed baryon-rich matter as functions of various thermodynamical variables. The parameters of collective flow and hadronic spectra are calculated. It is shown that presence of the deconfinement phase transition leads to increase of the elliptic flow and to flattening of proton rapidity distributions.Comment: 11 pages, 6 figure

Angular Momentum Partitioning in the Dissociation of Diatomic Molecules

We discuss recent experiments that study the transfer of angular momentum from a projectile to the residual target in collisions between the simple diatomic molecules H2 and N2 and spin-polarized electrons or circularly-polarized photons. We observe the fluorescence of both the atomic fragments and excited molecular states, and measure the circular polarization fraction of this light, P3. The incident electron energies range from 10 to 100 eV; the incident photon energies from 33 to 38 eV

A Geometric Approach to Modeling Microstructurally Small Fatigue Crack Formation

The objective of this paper is to develop further a framework for computationally modeling microstructurally small fatigue crack growth in AA 7075-T651 [1]. The focus is on the nucleation event, when a crack extends from within a second-phase particle into a surrounding grain, since this has been observed to be an initiating mechanism for fatigue crack growth in this alloy. It is hypothesized that nucleation can be predicted by computing a non-local nucleation metric near the crack front. The hypothesis is tested by employing a combination of experimentation and nite element modeling in which various slip-based and energy-based nucleation metrics are tested for validity, where each metric is derived from a continuum crystal plasticity formulation. To investigate each metric, a non-local procedure is developed for the calculation of nucleation metrics in the neighborhood of a crack front. Initially, an idealized baseline model consisting of a single grain containing a semi-ellipsoidal surface particle is studied to investigate the dependence of each nucleation metric on lattice orientation, number of load cycles, and non-local regularization method. This is followed by a comparison of experimental observations and computational results for microstructural models constructed by replicating the observed microstructural geometry near second-phase particles in fatigue specimens. It is found that orientation strongly influences the direction of slip localization and, as a result, in uences the nucleation mechanism. Also, the baseline models, replication models, and past experimental observation consistently suggest that a set of particular grain orientations is most likely to nucleate fatigue cracks. It is found that a continuum crystal plasticity model and a non-local nucleation metric can be used to predict the nucleation event in AA 7075-T651. However, nucleation metric threshold values that correspond to various nucleation governing mechanisms must be calibrated

Experimental Verification of the Chemical Sensitivity of Two-Site Double Core-Hole States Formed by an X-ray FEL

We have performed X-ray two-photon photoelectron spectroscopy (XTPPS) using the Linac Coherent Light Source (LCLS) X-ray free-electron laser (FEL) in order to study double core-hole (DCH) states of CO2, N2O and N2. The experiment verifies the theory behind the chemical sensitivity of two-site (ts) DCH states by comparing a set of small molecules with respect to the energy shift of the tsDCH state and by extracting the relevant parameters from this shift.Comment: 11 pages, 2 figure