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41.
Fabienne Delhaise Alessandro Morbidelli 《Celestial Mechanics and Dynamical Astronomy》1993,57(1-2):155-173
The luni-solar effects of a geosynchronous artificial satellite orbiting near the critical inclination is investigated. To tackle this four-degrees-of-freedom problem, a preliminary exploration separately analyzing each harmonic formed by a combination of the satellite longitude of the node and the Moon longitude of the node is opportune. This study demonstrates that the dynamics induced by these harmonics does not show resonance phenomena. In a second approach, the number of degrees of freedom is halved by averaging the total Hamiltonian over the two non-resonant angular variables. A semi-numerical method can now be applied as was done when considering solely the inhomogeneity of the geopotential (see Delhaise et Henrard, 1992). Approximate surfaces of section are constructed in the plane of the inclination and argument of perigee. The main effects of the Sun and Moon attractions compared to the terrestrial attraction alone are a strong increase in the amplitude of libration in inclination (from 0.6° to 3.2°) and a decrease of the corresponding libration period (from the order of 200 years to the order of 20 years).Research Assistant for the Belgian National Fund for Scientific Research 相似文献
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Frédéric Feder Fabienne Trolard Guilhem Bourrié 《Geochimica et cosmochimica acta》2005,69(18):4463-4483
A miniaturized Mössbauer spectrometer, adapted to the Earth’s conditions from the instrument developed for Mars space missions, has been used for the first time to study in situ variations with depth and transformations with time of iron minerals in a gleysol. The instrument is set into a PVC tube and can be moved up and down precisely (±1 mm) at the desired depth. Mössbauer spectra were obtained from 15 to 106 cm depth and repeated exactly at the same point at different times to follow mineralogical transformations with time. X-ray diffraction (XRD) and selective extraction techniques were performed on soil samples. The piezometric level of the water table was measured and the composition of the soil solution was monitored in situ and continuously, with a multiparametric and automatic probe. All the Mössbauer spectra obtained are characteristic of Fe(II)-Fe(III) green rust-fougerite, a natural mineral of the meixnerite group, that is, whose structural formula is: [Fe1 − xII Mgy FexIII (OH)2+2y]x+[xA, mH2O]x−, where x is the ratio Fe3+/Fetot. and A the intercalated anion. The name of fougerite has been formally approved by the Commission on New Minerals and Mineral Names of IMA (number 2003-057), on January 29, 2004. No other iron phases have been found by this way or by XRD. About 90% of total iron is extractible by dithionite-citrate-bicarbonate, and 60% by citratebicarbonate. In the horizons showing oximorphic properties that are in the upper part of the studied soil profile, x ratio in fougerite, deduced from Mössbauer spectra, is approximately 2/3. In the deepest horizons that show reductomorphic properties, x ratio is only 1/3. Fast mineralogical transformations were observed at well-defined points in soil, as evidenced by x ratio variations observed when Mössbauer spectra were acquired at different times at the same depth. Variations of the level of the water table and of pe and pH of the soil solution were simultaneously observed and could explain these mineralogical transformations. A ternary solid solution model previously proposed for OH-fougerite has been extended to chloride, sulphate, and carbonate green rusts to estimate the Gibbs free energies of formation of fougerite, providing for possible anions other than OH− in the interlayer and for Mg substitution. Soil solutions appear as largely oversaturated with respect to OH-fougerite, either oversaturated or undersaturated to “carbonate-fougerite” and “sulphate-fougerite”, and largely undersaturated with respect to “chloro-fougerite”. Fougerite forms most likely from oversaturated solutions by coprecipitation of Fe3+ with Fe2+ and Mg2+. Oxidation and reduction are driven by pH and pe variations, with both long timescale variations and short duration events. Exactly as synthetic green rusts are very reactive compounds in the laboratory, fougerite is thus a very reactive mineral and readily forms, dissolves, or evolves in soils. 相似文献
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This work compares the quantities of labile metals removed from the Vire River (Normandy) sediments by a sequential extraction procedure to those liberated by single leaches (Mg(NO3)2, HCl and EDTA). Compared to the other extractions, Mg(NO3)2 underestimated the mobility results. The sequential procedure was the most aggressive, except for Ca and Pb. The hypothetic correlation between quantities of an element removed by single leaches and its fractionation in the sediment according to the sequential procedure was not satisfying. Finally, it should be underlined that enrichments of Cd, Pb and Zn were noticed in the Vire sediments. To cite this article: L. Leleyter, F. Baraud, C. R. Geoscience 337 (2005). 相似文献
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Various iron-bearing primary phases and rocks have been weathered experimentally to simulate possible present and past weathering processes occurring on Mars. We used magnetite, monoclinic and hexagonal pyrrhotites, and metallic iron as it is suggested that meteoritic input to the martian surface may account for an important source of reduced iron. The phases were weathered in two different atmospheres: one composed of CO2 + H2O, to model the present and primary martian atmosphere, and a CO2 + H2O + H2O2 atmosphere to simulate the effect of strong oxidizing agents. Experiments were conducted at room temperature and a pressure of 0.75 atm. Magnetite is the only stable phase in the experiments and is thus likely to be released on the surface of Mars from primary rocks during weathering processes. Siderite, elemental sulfur, ferrous sulfates and ferric (oxy)hydroxides (goethite and lepidocrocite) are the main products in a water-bearing atmosphere, depending on the substrate. In the peroxide atmosphere, weathering products are dominated by ferric sulfates and goethite. A kinetic model was then developed for iron weathering in a water atmosphere, using the shrinking core model (SCM). This model includes competition between chemical reaction and diffusion of reactants through porous layers of secondary products. The results indicate that for short time scales, the mechanism is dominated by a chemical reaction with second order kinetics (k = 7.75 × 10−5 g−1/h), whereas for longer time scales, the mechanism is diffusion-controlled (DeA = 2.71 × 10−10 m2/h). The results indicate that a primary CO2- and H2O-rich atmosphere should favour sulfur, ferrous phases such as siderite or Fe2+-sulfates, associated with ferric (oxy)hydroxides (goethite and lepidocrocite). Further evolution to more oxidizing conditions may have forced these precursors to evolve into ferric sulfates and goethite/hematite. 相似文献
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Fougerite is a new iron oxide, a mixed M(II)–M(III) hydroxide, a member of the green rust group. Its structure consists of a brucitic layer of Fe(III)–Fe(II)–Mg(II), where the excess of the positive charge due to Fe3+ is compensated in the interlayer by anions. The limits of composition are structurally and geochemically constrained, and the stabilities of the mineral and green rusts are obtained by a thermodynamic model of a regular solid solution, for different compensating anions and for any allowed composition of the brucitic layer. 相似文献
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Nyameogo Gretta Fabienne Toudanaba Mbonimpa Mamert Bussière Bruno Awoh Akué-Sylvette 《Acta Geotechnica》2020,15(2):409-421
The efficiency of soil covers used as oxygen barriers to control the generation of acid drainage from sulfidic mine wastes can be evaluated in terms of the diffusive oxygen flux reaching the underlying wastes. Oxygen diffusion has been extensively investigated over the last few decades for unsaturated porous materials that are not frozen. However, little attention has been paid to materials that are fully or partially frozen, and thus, the diffusion of oxygen through soil covers during the winter freezing period has been generally neglected. This paper presents a laboratory method developed to evaluate the effective diffusion coefficient of oxygen (De) in frozen, inert materials. The method is a modified version of the conventional double-chamber cell in which the temperature and unfrozen volumetric water content of the sample are measured in addition to the more commonly monitored change in oxygen concentration. Several tests were conducted on non-reactive materials: that is, a sand at multiple degrees of saturation (Sr?=?20, 30, 39, and 42%), a silt (Sr?=?47%), and a mixture of the two (Sr?=?90%). Experimental data were interpreted using the POLLUTE code. Values of De for frozen materials were slightly lower than those obtained at ambient laboratory temperatures. In addition to the development of an empirical method for determining De, a preliminary model based on the model proposed by Aachib et al. (Water Air Soil Pollut 156:163–193, 2004) was created for the prediction of De in frozen materials by defining the involved parameters as temperature-dependent. The results indicate that predicated values of De are slightly higher than experimental values, suggesting that there remains room for improvement in the model.
相似文献48.
Philippe Blanc Hélène Gailhanou Jacques Rogez Georges Mikaelian Hitoshi Kawaji Fabienne Warmont Stéphane Gaboreau Sylvain Grangeon Jean-Marc Grenèche Philippe Vieillard Claire I. Fialips Eric Giffaut Eric C. Gaucher F. Claret 《Physics and Chemistry of Minerals》2014,41(8):603-615
In the context of the deep waste disposal, we have investigated the respective stabilities of two iron-bearing clay minerals: berthierine ISGS from Illinois [USA; (Al0.975FeIII0.182FeII1.422Mg0.157Li0.035Mn0.002)(Si1.332Al0.668)O5(OH)4] and chlorite CCa-2 from Flagstaff Hill, California [USA; (Si2.633Al1.367)(Al1.116FeIII0.215Mg2.952FeII1.712Mn0.012Ca0.011)O10(OH)8]. For berthierine, the complete thermodynamic dataset was determined at 1 bar and from 2 to 310 K, using calorimetric methods. The standard enthalpies of formation were obtained by solution-reaction calorimetry at 298.15 K, and the heat capacities were measured by heat-pulse calorimetry. For chlorite, the standard enthalpy of formation is measured by solution-reaction calorimetry at 298.15 K. This is completing the entropy and heat capacity obtained previously by Gailhanou et al. (Geochim Cosmochim Acta 73:4738–4749, 2009) between 2 and 520 K, by using low-temperature adiabatic calorimetry and differential scanning calorimetry. For both minerals, the standard entropies and the Gibbs free energies of formation at 298.15 K were then calculated. An assessment of the measured properties could be carried out with respect to literature data. Eventually, the thermodynamic dataset allowed realizing theoretical calculations concerning the berthierine to chlorite transition. The latter showed that, from a thermodynamic viewpoint, the main factor controlling this transition is probably the composition of the berthierine and chlorite minerals and the nature of the secondary minerals rather than temperature. 相似文献