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1.
Abstract— Films condensed from vapors containing SiO, Fe, or Mg showed an amorphous structure. Infrared (IR) spectra and electron microscopic characterization have been carried out on these films. After the heat treatment of these films in air, IR peaks at approximately 18–23 μm appeared, in addition to peaks attributable to SiO2. These peaks can be attributed to metallic oxides such as FeO, Fe2O3, and MgO. It can be concluded that Fe‐ or Mg‐bearing silicate minerals cannot be produced by the rapid cooling of SiO, Fe, or Mg vapors. Although IR spectra of FeO have been discussed in order to match some spectra obtained with the Infrared Space Observatory, the identification of FeO as the impurity would be very important because the IR spectra of FeO grains are very dependent on the shape and size of the grains. These impurities can also influence the IR spectral feature of SiO2.  相似文献   

2.
Abstract— Thermochemical equilibria are calculated in the multicomponent gas‐solution‐rock system in order to evaluate the formation conditions of fayalite, (Fe0.88–1.0Mg0.12–0)2SiO4, Fa88–100, in unequilibrated chondrites. Effects of temperature, pressure, water/rock ratio, rock composition, and progress of alteration are evaluated. The modeling shows that fayalite can form as a minor secondary and transient phase with and without aqueous solution. Fayalite can form at temperatures below ?350 °C, but only in a narrow range of water/rock ratios that designates a transition between aqueous and metamorphic conditions. Pure fayalite forms at lower temperatures, higher water/rock ratios, and elevated pressures that correspond to higher H2/H2O ratios. Lower pressure and water/rock ratios and higher temperatures favor higher Mg content in olivine. In equilibrium assemblages, fayalite usually coexists with troilite, kamacite, magnetite, chromite, Ca‐Fe pyroxene, and phyllosilicates. Formation of fayalite can be driven by changes in temperature, pressure, H2/H2O, and water/rock ratios. However, in fayalite‐bearing ordinary and CV3 carbonaceous chondrites, the mineral could have formed during the aqueous‐to‐metamorphic transition. Dissolution of amorphous silicates in matrices and/or silica grains, as well as low activities of Mg solutes, favored aqueous precipitation of fayalite. During subsequent metamorphism, fayalite could have formed through the reduction of magnetite and/or dehydration of ferrous serpentine. Further metamorphism should have caused reductive transformation of fayalite to Ca‐Fe pyroxene and secondary metal, which is consistent with observations in metamorphosed chondrites. Although bulk compositions of matrices/chondrites have only a minor effect on fayalite stability, specific alteration paths led to different occurrences, quantities, and compositions of fayalite in chondrites.  相似文献   

3.
Abstract— Experimental studies of coalescence between Mg grains and SiO grains in smoke reveal the direct production of crystalline forsterite grains. The present results also show that different materials can be produced by grain‐grain collisions, which have been considered one of the models of grain formation in the interstellar medium. The fundamentals of coalescence growth in smoke, which have been developed in our series of experiments, are presented in this paper. Mg2Si polyhedral grains were obtained in a Mg grain‐rich atmosphere. Mg2SiO4 polyhedral grains were obtained in a SiO grain‐rich atmosphere. The IR spectra of the resultant grains showed the characteristics of crystalline forsterite.  相似文献   

4.
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Cover: A FESEM image of the border of a shock meltpocket in Tissint (section from the collection of the University of Tennessee). One sees ahrensite (Fe2SiO4-spinel) as solid state transformation product of fayalite at the rim of the pocket, closer to the pocket, ahrensite has desintegrated into ferrous bridgmanite and wuestite (bright mall grains), in addition there is troillite.  相似文献   

5.
Pulsed‐laser irradiation causes the visible‐near‐infrared spectral slope of olivine (Fo90 and Fo99+) and SiO2 to increase (redden), while the olivine samples darken and the SiO2 samples brighten slightly. XPS analysis shows that irradiation of Fo90 produces metallic Fe. Analytical SEM and TEM measurements confirm that reddening in the Fo90 olivine samples correlates with the production of “nanophase” metallic Fe (npFe0) grains, 20–50 nm in size. The reddening observed in the SiO2 sample is consistent with the formation of SiO or other SiOx species that absorb in the visible. The weak spectral brightening induced by laser irradiation of SiO2 is consistent with a change in surface topography of the sample. The darkening observed in the olivine samples is likely caused by the formation of larger npFe0 particles, such as the 100–400 nm diameter npFe0 identified during our TEM analysis of Fo90 samples. The Fo90 reflectance spectra are qualitatively similar to those in previous experiments suggesting that in all cases formation of npFe0 is causing the spectral alteration. Finally, we find that the accumulation of successive laser pulses cause continued sample darkening in the Vis‐NIR, which suggests that repeated surface impacts are an efficient way to darken airless body surfaces.  相似文献   

6.
The chemistry leading to the formation of solid aerosols (tholins) in Titan's atmosphere is simulated by a capacitively coupled plasma in a N2-CH4 gas mixture. The solid grains are produced in volume directly in the gas phase and studied ex-situ by SEM imaging and by light scattering on clouds of particles. The scattered light properties depend on the physical properties of the particles (morphologies, size distribution), as well as on the phase angle and the wavelength of the light. The particles may be aggregated or agglomerated grains. The grains size distribution is studied as a function of plasma parameters such as initial methane concentration introduced into the discharge, gas flow, absorbed RF power and plasma duration. The average grain size increases when the amount of CH4 increases, when the gas flow decreases, and when the plasma duration increases up to a limit for each production condition.For all the samples, the absorption decreases with increasing wavelength in the visible domain. As usually found for irregular particles, the polarization phase curves have a bell-shaped positive branch and a shallow negative branch. The maximum of polarization (Pmax) increases when the average grain size decreases (sub-μm-sized grains). To obtain Pmax values within the range of those measured in Titan's atmosphere; the average grains diameter has to be smaller than 100 nm, in agreement with the space observations results. In the light-scattering experiment, the size of the agglomerates in the clouds is in the 40-80 μm range in equivalent diameter. As a consequence Pmax increases with decreasing wavelength due to the increasing absorption, in agreement with observations of Titan from outside the atmosphere.  相似文献   

7.
Identification of astronomical dust composition rests on comparison of Infrared (IR) spectra with standard laboratory spectra; frequently, however, a single mineralogical composition is assumed for spectral matching. Advances in laboratory instrumentation have enabled very precise IR spectra to be measured on single grains and zones within grains; with a more complete set of spectral data for planetary dust, better compositional matches will be achieved for astronomical dust. We have compared several FT-IR spectroscopy techniques (open path transmission spectroscopy and diffuse reflectance spectroscopy of powders; microspectroscopy of single grains and powders and ATR spectroscopy of thin sections) to determine their utility for the direct measurement of the mid-IR spectra of small amounts of extraterrestrial grains. We have focussed our investigation on the spectra of the olivine series of silicates, (Mg,Fe)2SiO4, a species frequently identified as one of the major constituents of interstellar dust. The positions of three characteristic SiO4 stretching bands at ∼10.4, 11.3 and 12 μm were measured for comparison of the techniques. All methods gave satisfactory results, although care must be taken to guard against artefacts from sample thickness and orientation effects. Single grains hand-picked from meteorites can be analysed, but results are inaccurate if the grain size is too large (>1-10 μm). Spectra for single grains also show variations that arise from sample orientation effects. Once the analytical artefacts are taken into account, we found that measurement of powder with a diamond compression cell is best suited for the analysis of small amounts of materials.  相似文献   

8.
Mid- and far-infrared spectra from the Composite InfraRed Spectrometer (CIRS) have been used to determine volume mixing ratios of nitriles in Titan's atmosphere. HCN, HC3N, C2H2, and temperature were derived from 2.5 cm−1 spectral resolution mid-IR mapping sequences taken during three flybys, which provide almost complete global coverage of Titan for latitudes south of 60° N. Three 0.5 cm−1 spectral resolution far-IR observations were used to retrieve C2N2 and act as a check on the mid-IR results for HCN. Contribution functions peak at around 0.5-5 mbar for temperature and 0.1-10 mbar for the chemical species, well into the stratosphere. The retrieved mixing ratios of HCN, HC3N, and C2N2 show a marked increase in abundance towards the north, whereas C2H2 remains relatively constant. Variations with longitude were much smaller and are consistent with high zonal wind speeds. For 90°-20° S the retrieved HCN abundance is fairly constant with a volume mixing ratio of around 1 × 10−7 at 3 mbar. More northerly latitudes indicate a steady increase, reaching around 4 × 10−7 at 60° N, where the data coverage stops. This variation is consistent with previous measurements and suggests subsidence over the northern (winter) pole at approximately 2 × 10−4 m s−1. HC3N displays a very sharp increase towards the north pole, where it has a mixing ratio of around 4 × 10−8 at 60° N at the 0.1-mbar level. The difference in gradient for the HCN and HC3N latitude variations can be explained by HC3N's much shorter photochemical lifetime, which prevents it from mixing with air at lower latitude. It is also consistent with a polar vortex which inhibits mixing of volatile rich air inside the vortex with that at lower latitudes. Only one observation was far enough north to detect significant amounts of C2N2, giving a value of around 9 × 10−10 at 50° N at the 3-mbar level.  相似文献   

9.
Limb and nadir spectra acquired by Cassini/CIRS (Composite InfraRed Spectrometer) are analyzed in order to derive, for the first time, the meridional variations of diacetylene (C4H2) and methylacetylene (CH3C2H) mixing ratios in Saturn’s stratosphere, from 5 hPa up to 0.05 hPa and 80°S to 45°N. We find that the C4H2 and CH3C2H meridional distributions mimic that of acetylene (C2H2), exhibiting small-scale variations that are not present in photochemical model predictions. The most striking feature of the meridional distribution of both molecules is an asymmetry between mid-southern and mid-northern latitudes. The mid-southern latitudes are found depleted in hydrocarbons relative to their northern counterparts. In contrast, photochemical models predict similar abundances at north and south mid-latitudes. We favor a dynamical explanation for this asymmetry, with upwelling in the south and downwelling in the north, the latter coinciding with the region undergoing ring shadowing. The depletion in hydrocarbons at mid-southern latitudes could also result from chemical reactions with oxygen-bearing molecules.Poleward of 60°S, at 0.1 and 0.05 hPa, we find that the CH3C2H and C4H2 abundances increase dramatically. This behavior is in sharp contradiction with photochemical model predictions, which exhibit a strong decrease towards the south pole. Several processes could explain our observations, such as subsidence, a large vertical eddy diffusion coefficient at high altitudes, auroral chemistry that enhances CH3C2H and C4H2 production, or shielding from photolysis by aerosols or molecules produced from auroral chemistry. However, problems remain with all these hypotheses, including the lack of similar behavior at lower altitudes.Our derived mean mixing ratios at 0.5 hPa of (2.4 ± 0.3) × 10−10 for C4H2 and of (1.1 ± 0.3) × 10−9 for CH3C2H are compatible with the analysis of global-average ISO observations performed by Moses et al. (Moses, J.I., Bézard, B., Lellouch, E., Gladstone, G.R., Feuchtgruber, H., Allen, M. [2000a]. Icarus 143, 244-298). Finally, we provide values for the ratios [CH3C2H]/[C2H2] and [C4H2]/[C2H2] that can constrain the coupled chemistry of these hydrocarbons.  相似文献   

10.
Abstract— The CH carbonaceous chondrites contain a population of ferrous (Fe/(Fe + Mg) ? 0.1‐0.4) silicate spherules (chondrules), about 15–30 μm in apparent diameter, composed of cryptocrystalline olivinepyroxene normative material, ±SiO2‐rich glass, and rounded‐to‐euhedral Fe, Ni metal grains. The silicate portions of the spherules are highly depleted in refractory lithophile elements (CaO, Al2O3, and TiO2 <0.04 wt%) and enriched in FeO, MnO, Cr2O3, and Na2O relative to the dominant, volatile‐poor, magnesian chondrules from CH chondrites. The Fe/(Fe + Mg) ratio in the silicate portions of the spherules is positively correlated with Fe concentration in metal grains, which suggests that this correlation is not due to oxidation, reduction, or both of iron (FeOsil ? Femet) during melting of metal‐silicate solid precursors. Rather, we suggest that this is a condensation signature of the precursors formed under oxidizing conditions. Each metal grain is compositionally uniform, but there are significant intergrain compositional variations: about 8–18 wt% Ni, <0.09 wt% Cr, and a sub‐solar Co/Ni ratio. The precursor materials of these spherules were thus characterized by extreme elemental fractionations, which have not been observed in chondritic materials before. Particularly striking is the fractionation of Ni and Co in the rounded‐to‐euhedral metal grains, which has resulted in a Co/Ni ratio significantly below solar. The liquidus temperatures of the euhedral Fe, Ni metal grains are lower than those of the coexisting ferrous silicates, and we infer that the former crystallized in supercooled silicate melts. The metal grains are compositionally metastable; they are not decomposed into taenite and kamacite, which suggests fast postcrystallization cooling at temperatures below 970 K and lack of subsequent prolonged thermal metamorphism at temperatures above 400–500 K.  相似文献   

11.
Abstract— We report results of our investigation of the relationship between values of Is/FeO (relative concentration of nanophase Fe0 divided by total FeO content), glass abundance, total Fe content, and degree of digestion of <20 μm clasts for 22 individual agglutinates (250–1000 μm) from the mature Apollo 16 soil 61181 (Is/FeO = 82 units in the <250 μm fraction). Agglutinates are important products of space weathering on the Moon, and they influence spectral observations at visible and near-IR wavelengths. Values of Is/FeO for individual agglutinates (250–1000 μm) within this single soil span a range from 3 to 262 units which is larger than the range observed for all Apollo 16 bulk soils (～0 to 110 units). No correlation was observed between Is/FeO and glass abundance and FeO concentrations for either agglutinitic glass or whole agglutinate particles under investigation. Our results suggest that the variation in Is/FeO for agglutinates from a single soil may be in part a consequence of natural mixing processes on the Moon that produce highly-variable environments (with respect to surface exposure) for agglutinate formation and in part to variable kinetics of reactions in an agglutinate melt, which are influenced by a variety of factors including melt composition, temperature, impactor velocity, and quench rate. We cannot exclude but do not see evidence for other processes including addition of exotic agglutinates, micrometeoritic bombardment into compositionally-diverse microtargets, recycling of agglutinates, preferential melting of very fine soil particles, and production of nanophase Fe0 in amorphous rims of very fine irradiated lunar grains contributing to the observed variation of Is/FeO.  相似文献   

12.
Up to now, there has been no corroboration from Cassini CIRS of the Voyager IRIS-discovery of cyanoacetylene (HC3N) ice in Titan’s thermal infrared spectrum. We report the first compelling spectral evidence from CIRS for the ν6 HC3N ice feature at 506 cm−1 at latitudes 62°N and 70°N, from which we derive particle sizes and column abundances in Titan’s lower stratosphere. We find mean particle radii of 3.0 μm and 2.3 μm for condensed HC3N at 62°N and 70°N, respectively, and corresponding ice phase molecular column abundances in the range 1-10 × 1016 mol cm−2. Only upper limits for cloud abundances can be established at latitudes of 85°N, 55°N, 30°N, 10°N, and 15°S. Under the assumption that cloud tops coincide with the uppermost levels at which HC3N vapor saturates, we infer geometric thicknesses for the clouds equivalent to 10-20 km or so, with tops at 165 km and 150 km at 70°N and 62°N, respectively.  相似文献   

13.
Ryo Nakamura  Eiji Ohtani 《Icarus》2011,211(1):648-654
We have determined the phase relation of the MgSO4-H2O binary system using an externally heated diamond anvil cell in the compositional range of 0-30 wt.% MgSO4, and under temperature and pressure conditions from 298 to 500 K and up to 4.5 GPa. Using our experimental results, we were able to estimate the composition of the ice mantle of the large icy satellites of Jupiter, such as Ganymede.In our experiments, we identified the following phases in the MgSO4-H2O system up to 4 GPa at 298 K: Ices VI and VII, magnesium heptahydrate, MgSO4·7H2O, and a liquid phase. The present phase relations suggest that there may be a deep internal ocean down to a depth about 800 km in the interior of Ganymede.  相似文献   

14.
The unusual achondrite Shergotty resembles terrestrial diabases, and textural and chemical evidence indicates pre-settling and post-settling crystallization of zoned augite (En48Fs19Wo33-En25Fs47Wo28) and pigeonite (En61Fs26Wo13-En21Fs61Wo18) coupled with late crystallization of plagioclase (Ab43An56/Or1-Ab56An41Or3: now shocked to maskelynite), titanomagnetite-ilmenite composite grains, mesostasis (normative Qz34Ab21An5Or38Fs2, assuming Fe as ferrous), whitlockite, pyrrhotite (Fe0.94S), fayalite (Fo10), baddeleyite and chlorapatite. The oxide compositions (Usp62Mt38, Al2O3 2.4, Cr2O3 0.8 wt %; Ilm95Hm5) indicate ～ 850 °C and log oxygen fugacity ? 14, while the occurrence of fayalite rims on mesostasis next to ilmenite indicates 890 °C. Bearing in mind experimental uncertainties, these data are consistent with late-stage crystallization under relatively high oxygen fugacity, as indicated by coexistence of fayalite, Ti-magnetite and a silica glass. The high alkali content of the maskelynite and mesostasis, coupled with the redox state, indicates that the Shergotty meteorite resembles terrestrial basalts more than any other meteorites. Nevertheless the absence of H2O, as shown by the occurrence of phosphorus in whitlockite rather than in hydroxylapatite, distinguish the Shergotty achondrite from typical terrestrial diabases. Whereas the FeO/MnO ratios of pyroxenes from the Moon, Earth and several differentiated meteorites are independent of FeO, the ratio for Shergotty pyroxenes changes from 30 to 40 with increasing FeO, and the linear trend extrapolates to 0.2 MnO for zero iron. Hence caution is needed in using FeO/MnO as a planetary indicator. For pyroxenes, Na is almost independent of Fe/Mg while Ti increases and Cr decreases with increasing Fe/Mg. Maskelynite contains 0.5–0.25 wt % K2O, 0.6 wt % FeO, 0.04 TiO2, 0.04–0.07 MgO, ～ 0.01 BaO and 0.02–0.03 P2O5. A bulk analysis calculated from the mode and compositions of the minerals matches quite well with two bulk chemical analyses but not with a third.  相似文献   

15.
Abstract– We have used synchrotron Fe‐XANES, XRS, microRaman, and SEM‐TEM analyses of Stardust track 41 slice and track 121 terminal area slices to identify Fe oxide (magnetite‐hematite and amorphous oxide), Fe‐Ti oxide, and V‐rich chromite (Fe‐Cr‐V‐Ti‐Mn oxide) grains ranging in size from 200 nm to ～10 μm. They co‐exist with relict FeNi metal. Both Fe‐XANES and microRaman analyses suggest that the FeNi metal and magnetite (Fe2O3FeO) also contain some hematite (Fe2O3). The FeNi has been partially oxidized (probably during capture), but on the basis of our experimental work with a light‐gas gun and microRaman analyses, we believe that some of the magnetite‐hematite mixtures may have originated on Wild 2. The terminal samples from track 121 also contain traces of sulfide and Mg‐rich silicate minerals. Our results show an unequilibrated mixture of reduced and oxidized Fe‐bearing minerals in the Wild 2 samples in an analogous way to mineral assemblages seen in carbonaceous chondrites and interplanetary dust particles. The samples contain some evidence for terrestrial contamination, for example, occasional Zn‐bearing grains and amorphous Fe oxide in track 121 for which evidence of a cometary origin is lacking.  相似文献   

16.
Abstract— The lunar soil characterization consortium, a group of lunar‐sample and remote‐sensing scientists, has undertaken the extensive task of characterization of the finest fractions of lunar soils, with respect to their mineralogical and chemical makeup. These compositional data form the basis for integration and modeling with the reflectance spectra of these same soil fractions. This endeavor is aimed at deciphering the effects of space weathering of soils on airless bodies with quantification of the links between remotely sensed reflectance spectra and composition. A beneficial byproduct is an understanding of the complexities involved in the formation of lunar soil. Several significant findings have been documented in the study of the <45 μm size fractions of selected Apollo 17 mare soils. As grain size decreases, the abundance of agglutinitic glass increases, as does the plagioclase, whereas the other minerals decrease. The composition of the agglutinitic glass is relatively constant for all size fractions, being more feldspathic than any of the bulk compositions; notably, TiO2 is substantially depleted in the agglutinitic glass. However, as grain size decreases, the bulk composition of each size fraction continuously changes, becoming more Al‐rich and Fe‐poor, and approaches the composition of the agglutinitic glasses. Between the smallest grain sizes (10–20 and < 10 μm), the IS/FeO values (amount of total iron present as nanophase Fe0) increase by greater than 100% (>2x), whereas the abundance of agglutinitic glass increases by only 10–15%. This is evidence for a large contribution from surface‐correlated nanophase Fe0 to the IS/FeO values, particularly in the <10 μm size fraction. The surface nanophase Fe0 is present largely as vapor‐deposited patinas on the surfaces of almost every particle of the mature soils, and to a lesser degree for the immature soils (Keller et al., 1999a). It is reasoned that the vapor‐deposited patinas may have far greater effects upon reflectance spectra of mare soils than the agglutinitic Fe0.  相似文献   

17.
This thermal annealing experiment at 1000 K for up to 167 h used a physical mixture of vapor phase‐condensed magnesiosilica grains and metallic iron nanograins to test the hypothesis that a mixture of magnesiosilica grains and an Fe‐source would lead to the formation of ferromagnesiosilica grains. This exploratory study found that coagulation and thermal annealing of amorphous magnesiosilica and metallic grains yielded ferromagnesiosilica grains with the Fe/(Fe + Mg) ratios in interplanetary dust particles. Furthermore, decomposition of brucite present in the condensed magnesiosilica grains was the source for water and the cause of different iron oxidation states, and the formation of amorphous Fe3+‐ferrosilica, amorphous Fe3+‐Mg, Fe‐silicates, and magnesioferrite during thermal annealing. Fayalite and ferrosilite that formed from silica/FeO melts reacted with forsterite and enstatite to form Mg, Fe‐silicates. The presence of iron in different oxidation states in extraterrestrial materials almost certainly requires active asteroid‐like parent bodies. If so, the possible presence of trivalent Fe compounds in comet P/Halley suggests that Halley‐type comets are a mixture of preserved presolar and processed solar nebula dust. The results from this thermal annealing experiment further suggest that the Fe‐silicates detected in the impact‐induced ejecta from comet 9P/Temple 1 might be of secondary origin and related to the impact experiment or to processing in a regolith.  相似文献   

18.
Observations of the Composite InfraRed Spectrometer (CIRS) during the entire nominal Cassini mission (2004-2008) provide us with an accurate global view of composition and temperature in the middle atmosphere of Titan (between 100 and 500 km). We investigated limb spectra acquired at resolution at nine different latitudes between 56°S and 80°N, with a better sampling in the northern hemisphere where molecular abundances and temperature present strong latitudinal variations. From this limb data acquired between February 2005 and May 2008, we retrieved the vertical mixing ratio profiles of C2H2, C2H4, C2H6, C3H8, CH3C2H, C4H2, C6H6, HCN, HC3N and CO2. We present here for the first time, the latitudinal variations of the C2H6, C3H8, CO2, C2H4 and C6H6 vertical mixing ratios profiles. Some molecules, such as C2H6 or C3H8 present little variations above their condensation level. The other molecules (except CO2) show a significant enhancement of their mixing ratios poleward of 50°N. C2H4 is the only molecule whose mixing ratio decreases with height at latitudes below 46°N. Regions depleted in C2H2, HCN and C4H2 are observed around 400 km (0.01 mbar) and 55°N. We also inferred a region enriched in CO2 located between 30 and 40°N in the 2-0.7 mbar pressure range. At 80°N, almost all molecules studied here present a local minimum of their mixing ratio profiles near 300 km (∼0.07 mbar), which is in contradiction with Global Circulation Models that predict constant-with-height vertical profiles due to subsidence at the north pole.  相似文献   

19.
Visible and near-infrared spectroscopic properties have been measured on elemental iron experimentally weathered in simulated Martian atmosphere and correlated to mineralogical compositions determined by X-ray diffraction. Two main features are observed in the reflectance spectra, corresponding to two deep bands located at 0.9 and 3.1 μm, respectively the iron band and the hydration band. In early weathering stages both Fe2+ and Fe3+ bands are identified. In addition, whereas the water band position does not change with time, the Fe2+ band disappears, and the Fe3+ band shifts towards longer wavelength (from 0.88 to 0.92 μm) because of transition from Fe2+ phases (siderite) to Fe3+ phases (ferrihydrite and goethite). Apart from these spectral signatures, other bands more specific of each phase are not clearly evidenced, especially for siderite. This is due to relatively low abundance of siderite (<20 wt%), but also to the very small grain size of secondary phase as well as surface coatings of iron (oxy)hydroxides. Therefore, our results suggest that carbonates, even if not detected, could be present in the form of very small grains in the surface of Mars.  相似文献   

20.
This paper describes a new experimental method to synthesise metal silicate particles in the laboratory with compositions and structures which reflect those likely to form in planetary atmospheres and in relatively cool regions of oxygen-rich stellar outflows. Fe–Mg-silicate nanoparticles of olivine composition were produced by the photo-oxidation of a mixture of Fe(CO)5, Mg(OC2H5)2 and Si(OC2H5)4 vapours in the presence of O3 at room temperature and atmospheric pressure. Transmission electron microscope X-ray and electron energy loss analysis of the particles from a number of experiments run with different precursor vapour mixture ratios show that Mg2xFe2?2xSiO4 particles can be produced ranging from x = 0 to 1, where x is linearly proportional to the ratio of Mg(OC2H5)2/(Fe(CO)5 + Mg(OC2H5)2). Electronic structure calculations with hybrid density functional/Hartree–Fock theory are then used to explore the pathways involved in producing olivine particles from the FeO3, MgO3 and SiO2 produced from the photolysis of the organometallic precursors in O3. These calculations indicate that highly exothermic reactions lead to the formation of Mg2SiO4, MgFeSiO4 and Fe2SiO4 molecules, which then polymerize. An alternative pathway, also strongly favoured thermodynamically, is the polymerization of MgSiO3 and FeSiO3 to form pyroxenes, which then undergo structural rearrangement to olivine and silica phases. The implications for metal silicate formation in planetary atmosphere and stellar outflows are then discussed.  相似文献   

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