The huge amount of methane hydrate deposits identified in deep marine sediments is considered as the new resource for future energy. Since carbonates are one of the major components of marine sediments, in the present study, an investigation has been made to study methane hydrate stability and kinetics in the presence of CaCO3 and MgCO3. Effect of the presence of carbonates on the solubility of methane in the system has also been examined as it directly affects the hydrate formation process. It has been observed that in presence of CaCO3 and MgCO3, the hydrate formation is inhibited. Comparative studies have also been done in the presence of artificial seawater to consider the effect of presence of different salts. Mole consumption of methane gas during hydrate formation in different carbonate samples was measured using real gas equation and found to be minimum in CaCO3 in seawater sample due to the combined effect of the presence of CaCO3 and different salts of seawater. An increase in nucleation and induction time was also observed demonstrating the inhibition of hydrate formation in the presence of these components. Further, the decrease in hydrate formation rate also confirmed the inhibition effect of CaCO3 and MgCO3 on hydrate formation. 相似文献
Orange precipitate was collected at the mouth of groundwater drainage tubes from the Kumanashi Landslide slip zone in Toyama prefecture, Northwest Japan. Data from XRF, X-ray diffraction, and Mössbauer spectroscopy determined the precipitate as hydrous ferric oxide (HFO) bearing multi-elements such as phosphorous, silica, calcium, etc. The occurrence of HFO may indicate an oxidation of ferrous iron in the percolated groundwater from the slip zone. Moreover, the precipitate iron should be mobilized with groundwater circulation from the slip zone, whose reducing condition was determined by the iron speciation on the same type of landslide profiles within the study area in previous studies. The HFO precipitate may be considered as a secondary reliable indicator to locate the seepage of a slip zone on surface, especially for a landslide newly investigated under wet-warm climate. 相似文献
A 2-D periodic ab initio Hartree–Fock LCAO study was performed on Fe-substituted 1:1 sheet silicate, lizardite. The atomic
orbitals were described by large-core pseudopotentials (Fe atoms) and a sp basis set (the other atoms). Calculated atomic
charges and the results of bond population analysis indicate that the Fe-O bond was as ionic as the Mg-O. This hypothesis
was supported by calculated density of states and electron density maps. Increasing Fe for Mg substitution changed the shape
of projected density of states (PDOS) of O(p) orbitals.
Received: 27 January 2000 / Accepted: 21 May 2000 相似文献
Simple model calculations show that the reversible temperature effects reported for broad OH-stretching bands in infrared
spectra of silica, aluminosilicate, and similar glasses can be explained, in essentials, by homogeneous thermal broadening
of the ν(OH) envelope constituents and a decrease in intensity with increasing temperature taking place uniformly across the
band. This means that these effects are reasonably consistent with the temperature behaviour of narrow ν(OH) bands of crystalline
OH-bearing minerals. These findings leave little room for the previously agreed interpretation in terms of a change in hydrogen-bonding
strength, although the dependence of integrated intensity on temperature still remains to be understood.
Received: 16 April 1999 / Accepted: 4 April 2000 相似文献
Trace element partition coefficients (D's) for up to 13 REE, Nb, Ta, Zr, Hf, Sr and Y have been determined by SIMS analysis of seven garnets, four clinopyroxenes, one orthopyroxene and one phlogopite crystallized from an undoped basanite and a lightly doped (200 ppm Nb, Ta and Hf) quartz tholeiite. Experiments were conducted at 2–7.5 GPa, achieving near-liquidus crystallization at relatively low temperatures of 1080–1200°C under strongly hydrous conditions (5–27 wt.% added water). Garnet and pyroxene DREE show a parabolic pattern when plotted against ionic radius, and conform closely to the lattice strain model of Blundy and Wood (Blundy, J.D., Wood, B.J., 1994. Prediction of crystal–melt partition coefficients from elastic moduli. Nature 372, 452–454). Comparison, at constant pressure, between hydrous and anhydrous values of the strain-free partition coefficient (D0) for the large cation sites of garnet and clinopyroxene reveals the relative importance of temperature and melt water content on partitioning. In the case of garnet, the effect of lower temperature, which serves to increase D0, and higher water content, which serves to decrease D0, counteract each other to the extent that water has little effect on garnet–melt D0 values. In contrast, the effect of water on clinopyroxene–melt D0 overwhelms the effect of temperature, such that D0 is significantly lower under hydrous conditions. For both minerals, however, the lower temperature of the hydrous experiments tends to tighten the partitioning parabolas, increasing fractionation of light from heavy REE compared to anhydrous experiments.
Three sets of near-liquidus clinopyroxene–garnet two-mineral D values increase the range of published experimental determinations, but show significant differences from natural two-mineral D's determined for subsolidus mineral pairs. Similar behaviour is observed for the first experimental data for orthopyroxene–clinopyroxene two-mineral D's when compared with natural data. These differences are in large part of a consequence of the subsolidus equilibration temperatures and compositions of natural mineral pairs. Great care should therefore be taken when using natural mineral–mineral partition coefficients to interpret magmatic processes.
The new data for strongly hydrous compositions suggest that fractionation of Zr–Hf–Sm by garnet decreases with increasing depth. Thus, melts leaving a garnet-dominated residuum at depths of about 200 km or greater may preserve source Zr/Hf and Hf/Sm. This contrasts with melting at shallower depths where both garnet and clinopyroxene will cause Zr–Hf–Sm fractionation. Also, at shallower depths, clinopyroxene-dominated fractionation may produce a positive Sr spike in melts from spinel lherzolite, but for garnet lherzolite melting, no Sr spike will result. Conversely, clinopyroxene megacrysts with negative Sr spikes may crystallize from magmas without anomalous Sr contents when plotted on mantle compatibility diagrams. Because the characteristics of strongly hydrous silicate melt and solute-rich aqueous fluid converge at high pressure, the hydrous data presented here are particularly pertinent to modelling processes in subduction zones, where aqueous fluids may have an important metasomatic role. 相似文献
A new installation for the analysis of picomole quantities of nitrogen has been designed and constructed. It permits the simultaneous analysis of N and rare gases extracted from silicates by heating. The extraction procedure involves the use of a CO2 laser as a heater, and the analysis is made by static mass spectrometry using a high sensitivity, high resolution mass spectrometer. Procedural blanks of 2 picomoles N2 (60 picogram N) allow us to analyse routinely N in mg-sized samples such as mantle-derived and meteoritic minerals, and Lunar soil grains. 相似文献