Dissolution of Corundum and Andalusite in H2O-Saturated Haplogranitic Melts at 800{degrees}C and 200 MPa: Constraints on Diffusivities and the Generation of Peraluminous Melts

The mechanisms and kinetics of equilibration between peraluminousminerals and granitic melt were investigated experimentallyby the dissolution of corundum and andalusite into H₂O-saturatedmetaluminous haplogranitic melt at 800°C and 200 MPa. Mineraland haplogranitic glass rods were juxtaposed inside platinumcapsules, and then subjected to experimental conditions fortimes ranging from 12 to 2900 h. Upon melting, the mineral –meltinterface retreats with the square root of time. The compositionof the melt at the interface changes with time, but its ASI[aluminum saturation index = molar Al₂O₃/(CaO + Na₂O + K₂O)]remains constant at     

A coupled,dynamical and chemical model for the prestellar core L1544: Comparison of modeled and observed C<Superscript>18</Superscript>O,HCO<Superscript>+</Superscript>, and CS emission spectra

We consider radiative transfer in C¹⁸O, HCO⁺, and CS molecular lines in a spherically symmetrical, coupled, dynamical and chemical model of a prestellar core whose evolution is determined by ambipolar diffusion. Theoretical and observed line profiles are compared for the well-studied core L1544, which may be a collapsing protostellar cloud. We study the relationship between the line shapes and model parameters. The structure of the envelope and kinematic parameters of the cloud are the most important factors determining the shape of the lines. Varying the input model parameters for the radiative transfer—the kinetic temperature and microturbulent velocity—within the limits imposed by observations does not result in any substantial variations of the line profiles. The comparison between the model and observed spectra indicates that L1544 displays a flattened structure, and is viewed at an oblique angle. A two-dimensional model is needed to reproduce this structure.     

Scientific problems addressed by the Spektr-UV space project (world space Observatory—Ultraviolet)

The article presents a review of scientific problems and methods of ultraviolet astronomy, focusing on perspective scientific problems (directions) whose solution requires UV space observatories. These include reionization and the history of star formation in the Universe, searches for dark baryonic matter, physical and chemical processes in the interstellar medium and protoplanetary disks, the physics of accretion and outflows in astrophysical objects, from Active Galactic Nuclei to close binary stars, stellar activity (for both low-mass and high-mass stars), and processes occurring in the atmospheres of both planets in the solar system and exoplanets. Technological progress in UV astronomy achieved in recent years is also considered. The well advanced, international, Russian-led Spektr-UV (World Space Observatory—Ultraviolet) project is described in more detail. This project is directed at creating a major space observatory operational in the ultraviolet (115–310 nm). This observatory will provide an effective, and possibly the only, powerful means of observing in this spectral range over the next ten years, and will be an powerful tool for resolving many topical scientific problems.     

Neutral atmosphere near the icy surface of Jupiter’s moon Ganymede

The paper discusses the formation and dynamics of the rarefied gas envelope near the icy surface of Jupiter’s moon Ganymede. Being the most massive icy moon, Ganymede can form a rarefied exosphere with a relatively dense near-surface layer. The main parent component of the gas shell is water vapor, which enters the atmosphere due to thermal degassing, nonthermal radiolysis, and other active processes and phenomena on the moon’s icy surface. A numerical kinetic simulation is performed to investigate, at the molecular level, the formation, chemical evolution, and dynamics of the mainly H₂O- and O₂-dominant rarefied gas envelopes. The ionization processes in these rarefied gas envelopes are due to exposure to ultraviolet radiation from the Sun and the magnetospheric plasma. The chemical diversity of the icy moon’s gas envelope is attributed to the primary action of ultraviolet solar photons and plasma electrons on the rarefied gas in the H₂O- or O₂-dominant atmosphere. The model is used to calculate the formation and development of the chemical diversity in the relatively dense near-surface envelope of Ganymede, where an important contribution comes from collisions between parent molecules and the products of their photolysis and radiolysis.     

Surface-bounded atmosphere of Europa

A 1-D collisional Monte Carlo model of Europa's atmosphere is described in which the sublimation and sputtering sources of H₂O molecules and their molecular fragments are accounted for as well as the radiolytically produced O₂. Dissociation and ionization of H₂O and O₂ by magnetospheric electron, solar UV-photon and photo-electron impact, and collisional ejection from the atmosphere by the low-energy plasma are taken into account. Reactions with the surface are discussed, but only adsorption and atomic oxygen recombination are included in this model. The size of the surface-bounded oxygen atmosphere of Europa is primarily determined by a balance between atmospheric sources from irradiation of the satellite's icy surface by the high-energy magnetospheric charged particles and atmospheric losses from collisional ejection by the low-energy plasma, photo- and electron-impact dissociation, and ionization and pick-up from the surface-bounded atmosphere. A range of sources rates for O₂ to H₂O are used with a larger oxygen-to-water ratio than suggested by laboratory measurements in order to account for differences in adsorption onto grains in the regolith. These calculations show that the atmospheric composition is determined by both the water and oxygen photochemistry in the near-surface region, escape of suprathermal oxygen and water into the jovian system, and the exchange of radiolytic water products with the porous regolith. For the electron impact ionization rates used, pick-up ionization is the dominant oxygen loss process, whereas photo-dissociation and atmospheric sputtering are the dominant sources of neutral oxygen for Europa's neutral torus. Including desorption and loss of water enhances the supply of oxygen species to the neutral torus, but hydrogen produced by radiolysis is the dominant source of neutrals for Europa's torus in these models.     

Contrasting interactions of sodium and potassium with H<Subscript>2</Subscript>O in haplogranitic liquids and glasses at 200 MPa from hydration–diffusion experiments

This study examines hydration–diffusion in the metaluminous haplogranite system at 200 MPa H₂O and 800–300°C. At 800°C hydration is accompanied by melting and uphill diffusion of sodium from anhydrous glass toward the region of hydration and melting, whereas potassium diffuses away from the hydration front and into anhydrous glass. Silicon and aluminum are simply diluted upon hydration. There is no change in molecular Al/(Na + K) throughout the entire hydration-diffusion aureole and, therefore, (1) there is no loss of alkalis to the vapor, and (2) K migrates to replace Na in order to maintain local charge balance required by ^IVAl. Alkali diffusion occurs over a viscosity contrast from 10^4.1 Pa s in hydrous liquid to 10^11.8–10^13.5 Pa s in anhydrous glass. From these results, we interpret that: (1) Na is structurally or energetically favored over K as a charge-balancing cation for ^IVAl in hydrous granitic liquids, whereas the opposite behavior has been observed for anhydrous melts, and (2) the diffusion of alkalis through silicate melts is largely independent of viscosity. Results from 600°C are similar to those at 800°C, but hydration at 300°C involves a loss of Na and concomitant increase in molar Al/(Na + K) in the hydration zone due to hydrogen-alkali exchange between fluid and glass. Hydration behavior at 400°C is transitional between those at 300°C and 600°C, suggesting that the change in hydration mechanism occurs near the glass transition.     

Stochastic models of hot planetary and satellite coronas: A hot oxygen corona of Mars

The processes of the kinetics and transport of hot oxygen atoms in the transition (between thermosphere and exosphere) region of the upper atmosphere of Mars are studied. The reaction of dissociative recombination of the main ionospheric ion O ₂ ⁺ with thermal electrons in the ionosphere of Mars is considered as a source of hot oxygen atoms. The distribution of suprathermal oxygen atoms by kinetic energy is calculated. It is shown that the exosphere is populated by a considerable number of suprathermal oxygen atoms with kinetic energies just below the escape energy of 2 eV; that is, a hot oxygen corona of Mars is formed.     

Stochastic models of hot planetary and satellite coronas: Atomic oxygen in Europa’s corona

This paper analyzes the formation, kinetics, and transport of hot oxygen atoms in the atmosphere of the Jovian satellite Europa. Atmospheric sources of suprathermal oxygen atoms are assumed to be represented by the processes of dissociation of molecular oxygen, which is the main component of the atmosphere, by solar UV radiation and electron fluxes from the inner magnetosphere of Jupiter, as well as by the reaction of dissociative recombination of the main ionospheric ion O ₂ ⁺ which thermal electrons. It is shown that dissociation in Europa’s near-surface atmosphere is balanced by the processes of the loss of atomic oxygen due to the effective escape of suprathermal oxygen atoms into the inner magnetosphere of Jupiter along the orbit of Europa and due to ionization by magnetospheric electrons and catalytic recombination of oxygen atoms on the icy surface of the satellite. It thus follows that atomic oxygen is only a small admixture to the main atmospheric component—molecular oxygen—in the near-surface part of the atmosphere. However, the outer exospheric layers of Europa’s atmosphere are populated mostly by suprathermal oxygen atoms. The near-surface molecular envelope of Europa is therefore surrounded by a tenuous extended corona of hot atomic oxygen.     

Kinetic Monte Carlo method for simulating astrochemical kinetics: Test calculations of molecular hydrogen formation on interstellar dust particles

Molecular hydrogen formation on the surfaces of interstellar dust grains has been studied numerically. Different stochastic methods (analogue Monte Carlo methods, direct solutions of the chemical master equation, continuous-time random-walk simulations, etc.) have been recently applied to the astrochemistry of hydrogen formation; however, the computational efficiency of these approaches is usually low because they are extremely time consuming (Herbst and Shematovich, 2003). A kinetic version of the Monte Carlo method based on splitting by physical processes is presented in the study. Each of the basic physical processes—adsorption of atomic hydrogen on the surface, thermal diffusion, formation of molecular hydrogen, and hydrogen desorption from the surface-are considered as independent random Markovian-type processes and are simulated using stochastic algorithms. The suggested numerical model is computationally efficient allowing calculations to be held on model surfaces with up to 10⁶ active centers, which corresponds to interstellar grains of up to 0.4 μm in diameter. Test calculations of the efficiency of molecular hydrogen formation were held for the two models of the surfaces of interplanetary grains, namely, for the homogeneous surfaces of olivine and amorphous carbon. It was confirmed that the effective formation of molecular hydrogen in diffuse molecular clouds is possible only within a narrow range of dust-particle temperatures. A comparison with the numerical results of other authors is presented.     

Formation of complex chemical species in astrochemistry (a review)

In recent years, a rapid growth in a new area of space studies??astrochemistry??has been observed. Its subject is the chemical evolution and chemical diversity of interstellar matter. Molecules yield unique information concerning physical conditions in the interstellar medium and, in particular, in the star-formation regions, through spectral observations of the matter in the gas-phase and dust fractions via rotational and vibrational transitions of interstellar molecules. Moreover, an understanding of the chemistry of molecules can tell us about the lifetime and history of the observed objects. Such an understanding, however, requires detailed chemical knowledge of the gas-phase reactions and grain-surface chemical processes that very often take place under rather exotic conditions strongly differing from those for chemical reactions in the laboratory. Note that the interests of chemists and astronomers in this new area are different: chemists are more likely to be interested in chemical diversity throughout the Universe, whereas astronomers are more likely to use molecules as probes of physical processes.