Magnetized Accretion Inside the Marginally Stable Orbit around a Black Hole

Qualitative arguments are presented to demonstrate that the energy density of magnetic fields in matter accreting onto a black hole inside the marginally stable orbit is automatically comparable to the rest-mass energy density of the accretion flow. Several consequences follow: magnetic effects must be dynamically significant, but cannot be so strong as to dominate; outward energy transport in Alfven waves may alter the effective efficiency of energy liberation; and vertical magnetic stresses in this region may contribute to "coronal" activity.Comment: to appear in Ap. J. Letter

WhiskyMHD: a new numerical code for general relativistic magnetohydrodynamics

The accurate modelling of astrophysical scenarios involving compact objects and magnetic fields, such as the collapse of rotating magnetized stars to black holes or the phenomenology of gamma-ray bursts, requires the solution of the Einstein equations together with those of general-relativistic magnetohydrodynamics. We present a new numerical code developed to solve the full set of general-relativistic magnetohydrodynamics equations in a dynamical and arbitrary spacetime with high-resolution shock-capturing techniques on domains with adaptive mesh refinements. After a discussion of the equations solved and of the techniques employed, we present a series of testbeds carried out to validate the code and assess its accuracy. Such tests range from the solution of relativistic Riemann problems in flat spacetime, over to the stationary accretion onto a Schwarzschild black hole and up to the evolution of oscillating magnetized stars in equilibrium and constructed as consistent solutions of the coupled Einstein-Maxwell equations.Comment: minor changes to match the published versio

Numerical 3+1 general relativistic magnetohydrodynamics: a local characteristic approach

We present a general procedure to solve numerically the general relativistic magnetohydrodynamics (GRMHD) equations within the framework of the 3+1 formalism. The work reported here extends our previous investigation in general relativistic hydrodynamics (Banyuls et al. 1997) where magnetic fields were not considered. The GRMHD equations are written in conservative form to exploit their hyperbolic character in the solution procedure. All theoretical ingredients necessary to build up high-resolution shock-capturing schemes based on the solution of local Riemann problems (i.e. Godunov-type schemes) are described. In particular, we use a renormalized set of regular eigenvectors of the flux Jacobians of the relativistic magnetohydrodynamics equations. In addition, the paper describes a procedure based on the equivalence principle of general relativity that allows the use of Riemann solvers designed for special relativistic magnetohydrodynamics in GRMHD. Our formulation and numerical methodology are assessed by performing various test simulations recently considered by different authors. These include magnetized shock tubes, spherical accretion onto a Schwarzschild black hole, equatorial accretion onto a Kerr black hole, and magnetized thick accretion disks around a black hole prone to the magnetorotational instability.Comment: 18 pages, 8 figures, submitted to Ap

U redox state and speciation of U in contact with magnetite nanoparticles : High resolution XANES, EXAFS, XPS and TEM study

Long-term storage of high-level radioactive waste is associated with potential radioecological hazards. One chemical element of high interest is uranium (U), which can mainly exists as a mobile U(VI) (oxidizing conditions) and sparingly soluble U(IV) (reducing conditions) species. It is expected that the main inorganic reducing agent for U(VI) in the environment are ferrous species in magnetite, formed on the steel canisters surface as an intermediate iron (Fe) corrosion product [1]. Results obtained from laboratory experiments for the interaction of U(VI) with magnetite nanoparticles point to partial reduction of U(VI) [2] or the formation of ~3 nm uranium dioxide (UO₂) particles on the surface layer [3]. The evidence for U(VI) reduction to intermediate U(V) state was found with no direct evidence of U(IV), which is in contradiction with thermodynamic calculations [4]. Continuous interaction and related phase dissolution/recrystallization processes can also lead to U redox changes and structural U incorporation into Fe oxides, resulting in U immobilization [5]. U redox state and speciation analyses are still very challenging due to simultaneous formation of several different species in such mineral systems. New advanced spectroscopic methods for characterization of such systems will provide more precise results from speciation studies. The main goal of our investigation is to assess the U M4 edge high energy resolution X-ray absorption near edge structure (HR-XANES) spectroscopy technique for detection of U(V) possibly co-existing with U(IV) and U(VI) under reducing conditions on/in Fe containing minerals. The U M4 edge HR-XANES has an advantage compared to the conventional U L3 edge XANES, as the measured spectra are less dominated by corehole lifetime broadening effects and therefore have narrower spectral features [6-8]. This technique facilitates the detection of minor contribution of one oxidation state in mixtures. We have investigated the U redox states and speciation in a set of samples where U coprecipitated with magnetite nanoparticles (~ 20 nm) with U concentrations varying in the 1000-10000 ppm range (1000, 3000, 6000 and 10000 ppm). In addition to U M4 edge HR-XANES, U L3 edge extended X-ray absorption fine structure (EXAFS), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) techniques have been applied. The studied system models the interaction of U(VI) with magnetite in aqueous solution, important for the understanding of the retarding effect of Fe corrosion products on U in the context of deep geological spent nuclear fuel disposal. These spectroscopic results can be compared with thermodynamic calculations and geochemical models describing this interaction. After 10 days U interaction with magnetite U M4 edge HR-XANES results indicate the formation of U(IV), U(V) and U(VI) mixtures in varying ratios, depending on the initial U loading. Going from 10000 to 3000 ppm, the U(VI) content decreases continuously and is no longer found in the 1000 ppm sample. At the same time the U(IV) and U(V) fractions increase. U(V) is stabilized as the main U redox state in the 1000 ppm sample along with a smaller U(IV) contribution. After 20 days of contact time XPS data show the predominance of U(IV) and U(V) species in the 6000 ppm sample. However, mostly U(V) and some U(IV) is found for the 1000 ppm sample. For all samples aged for 240 days U L3 XANES and EXAFS strongly suggest the formation of a UO₂ phase, UO₂ is the dominating species in the 10000 ppm sample with U-O bond distance 2.33. Å as determined by EXAFS. UO₂ crystalline clusters with about 5 nm size formed on the surface of the magnetite nanoparticles are also found by TEM in the 10000 and 3000 ppm samples. The major and minor contributions of U(V) and U(IV), respectively, for the 1000 ppm sample after 240 days confirm the assumption that the U redox kinetics has completed within less than 10 days at this U concentration. EXAFS analyses reveal U(V)-Fe interaction in the second U coordination sphere, which substantially increases from the 10000 to 1000 ppm sample and is the dominating species in the 1000 ppm sample

Nonlocal calculation for nonstrange dibaryons and tribaryons

We study the possible existence of nonstrange dibaryons and tribaryons by solving the bound-state problem of the two- and three-body systems composed of nucleons and deltas. The two-body systems are $NN$, $N\Delta$, and $\Delta\Delta$, while the three-body systems are $NNN$, $NN\Delta$, $N\Delta\Delta$, and $\Delta\Delta\Delta$. We use as input the nonlocal $NN$, $N\Delta$, and $\Delta\Delta$ potentials derived from the chiral quark cluster model by means of the resonating group method. We compare with previous results obtained from the local version based on the Born-Oppenheimer approximation.Comment: 19 pages. To be published in Physical Review

Investigation of the foil structure and corrosion mechanisms of modern Zwischgold using advanced analysis techniques

Zwischgold is a two-sided metal foil made by adhering a gold leaf over a silver leaf to present a gold surface while using less gold than gold foils. Corroded Zwischgold surfaces appear dark, accompanied by gloss loss and possible mechanical stability issues. Zwischgold applied artefacts are commonly found in museums and churches across Europe and they currently face an uncertain future as conservators have little knowledge to base conservation treatments on. We present a comprehensive material analysis of Zwischgold models through advanced characterization techniques including focused ion beam coupled with scanning electron microscopy (FIB-SEM), transmission electron microscopy (TEM), scanning transmission X-ray microscopy (STXM), time-of-flight secondary ion mass spectrometry (TOF-SIMS) and Rutherford backscattering spectrometry (RBS). Complementary information on the foil thickness, sharpness of the gold-silver interface, gold purity, and the formation as well as distribution of corrosion products on Zwischgold models have been obtained, representing a starting point for understanding the morphology and the long-term chemistry of Zwischgold artefacts. (C) 2017 The Authors. Published by Elsevier Masson SAS

Structural tale of two novel (Cr, Mn)C carbides in steel

Chromium (Cr), manganese (Mn) and carbon (C) are well known alloying elements used in technologically important alloy steels and advanced high strength steels. It is known that binary CrCx and MnCx carbides can be formed in steels, but in this study we reveal for the first time that Cr and Mn were found combined in novel ternary cementite type (Cr, Mn)C carbides. Electron diffraction experiments showed that Cr, Mn and C formed two distinct carbide phases possessing orthorhombic and monoclinic crystal structures. Density functional theory calculations were performed on these phases and excellent agreement was found between calculations and experiments on the lattice parameters and relative atomic positions. The calculations showed that the combination of Mn and Cr resulted in a very high thermodynamic stability of the (Cr, Mn)C carbides, and that local structural relaxations are associated with carbon additions. Possible implications of these ternary carbides for novel applications in steel design and manufacturing are discussed