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991.
The Horní Slavkov–Krásno Sn–W ore district is hosted by strongly altered Variscan topaz–albite granite (Krudum granite body) on the northwestern margin of the Bohemian Massif. We studied the fluid inclusions on greisens, ore pockets, and ore veins from the Hub Stock, an apical expression of the Krudum granite. Fluid inclusions record almost continuously the post-magmatic cooling history of the granite body from ~500 to <50°C. Rarely observed highest-temperature (~500°C) highest-salinity (~30?wt.% NaCl eq.) fluid inclusions are probably the result of secondary boiling of fluids exsolved from the crystallizing magma during pressure release which followed hydraulic brecciation of the gneissic mantle above the granite cupola. The greisenization was related to near-critical low-salinity (0–7?wt.% NaCl eq.) aqueous fluids with low amount of CO2, CH4, and N2 (≤10?mol% in total) at temperatures of ~350–400°C and pressures of 300–530 bar. Crush-leach data display highly variable and negatively correlated I/Cl and Br/Cl values which are incompatible with both orthomagmatic and/or metamorphic origin of the fluid phase, but can be explained by infiltration of surficial and/or sedimentary fluids. Low fluid salinity indicates a substantial portion of meteoric waters in the fluid mixture that is in accordance with previous stable isotope data. The post-greisenization fluid activity associated with vein formation and argillitization is characterized by decreasing temperature (<350 to <50°C), decreasing pressure (down to ~50–100 bar), and mostly also decreasing salinity.  相似文献   
992.
Hydrothermal alteration and mineralization at the Wunugetu porphyry Cu–Mo deposit, China, include four stages, i.e., the early stage characterized by quartz, K-feldspar and minor mineralization, followed by a molybdenum mineralization stage associated with potassic alteration, copper mineralization associated with sericitization, and the last Pb–Zn mineralization stage associated with carbonation. Hydrothermal quartz contains three types of fluid inclusions, namely aqueous (W-type), daughter mineral-bearing (S-type) and CO2-rich (C-type) inclusion, with the latter two types absent in the late stage. Fluid inclusions in the early stage display homogenization temperatures above 510°C, with salinities up to 75.8 wt.% NaCl equivalent. The presence of S-type inclusions containing anhydrite and hematite daughter minerals and C-type inclusions indicates an oxidizing, CO2-bearing environment. Fluid inclusions in the Mo- and Cu-mineralization stages yield homogenization temperatures of 342–508°C and 241–336°C, and salinities of 8.6–49.4 and 6.3–35.7 wt.% NaCl equivalent, respectively. The presence of chalcopyrite instead of hematite and anhydrite daughter minerals in S-type inclusions indicates a decreasing of oxygen fugacity. In the late stage, fluid inclusions yield homogenization temperatures of 115–234°C and salinities lower than 12.4 wt.% NaCl equivalent. It is concluded that the early stage fluids were CO2 bearing, magmatic in origin, and characterized by high temperature, high salinity, and high oxygen fugacity. Phase separation occurred during the Mo- and Cu-mineralization stages, resulting in CO2 release, oxygen fugacity decrease and rapid precipitation of sulfides. The late-stage fluids were meteoric in origin and characterized by low temperature, low salinity, and CO2 poor.  相似文献   
993.
Relative humidity ( P\textH 2 \textO P_{{{\text{H}}_{ 2} {\text{O}}}} , partial pressure of water)-dependent dehydration and accompanying phase transitions in NAT-topology zeolites (natrolite, scolecite, and mesolite) were studied under controlled temperature and known P\textH 2 \textO P_{{{\text{H}}_{ 2} {\text{O}}}} conditions by in situ diffuse-reflectance infrared Fourier transform spectroscopy and parallel X-ray powder diffraction. Dehydration was characterized by the disappearance of internal H2O vibrational modes. The loss of H2O molecules caused a sequence of structural transitions in which the host framework transformation path was coupled primarily via the thermal motion of guest Na+/Ca2+ cations and H2O molecules. The observation of different interactions of H2O molecules and Na+/Ca2+ cations with host aluminosilicate frameworks under high- and low- P\textH 2 \textO P_{{{\text{H}}_{ 2} {\text{O}}}} conditions indicated the development of different local strain fields, arising from cation–H2O interactions in NAT-type channels. These strain fields influence the Si–O/Al–O bond strength and tilting angles within and between tetrahedra as the dehydration temperature is approached. The newly observed infrared bands (at 2,139 cm−1 in natrolite, 2,276 cm−1 in scolecite, and 2,176 and 2,259 cm−1 in mesolite) result from strong cation–H2O–Al–Si framework interactions in NAT-type channels, and these bands can be used to evaluate the energetic evolution of Na+/Ca2+ cations before and after phase transitions, especially for scolecite and mesolite. The 2,176 and 2,259 cm−1 absorption bands in mesolite also appear to be related to Na+/Ca2+ order–disorder that occur when mesolite loses its Ow4 H2O molecules.  相似文献   
994.
Vibrational density of states of the NaAlSi2O6 jadeite and NaAlSiO4 calcium ferrite (CF)-type, and SiO2 stishovite is calculated as a function of pressure up to 50 GPa using density functional perturbation theory. The calculated frequencies are used to determine the thermal contribution to the Helmholtz free energy within the quasi-harmonic approximation and to derive the equation of state and several thermodynamic properties of interest. A dissociation of jadeite into a mixture of a CF-type phase and stishovite is predicted to occur at 23.4 GPa and 1,800 K with a positive Clapeyron slope of 2.8 MPa/K. Elastic anisotropy for jadeite, the CF-type phase, and stishovite also computed clearly shows that stishovite and the CF-type phase are the most anisotropic and isotropic in these three phases, respectively.  相似文献   
995.
A set of raw industrial materials, that is, pure quartz and quartz-rich mixtures, were investigated through electron paramagnetic resonance and electron spin echo-envelope modulation spectroscopies, with the aim of evaluating the effective role played by defect centres and of assessing whether they can be used to monitor changes in the physical properties of quartz powders with reference to their health effects. The obtained results point to two interactions of the Al defect centres with H+, hosted in sites within the channels parallel and perpendicular to the c axis of quartz, respectively. These two Al/H+ (hAl) centres exhibit a weak chemical bond, and their relative amounts appear to be modified/controlled by the thermo-mechanical processes underwent by powders. Indeed, a mechanically promoted inter-conversion between the two kinds of site is suggested. As a consequence, the hAl centres are effective in monitoring even modest activations of powders, through thermal or mechanical processes, and they are also supposed to play a specific, relevant role in quartz reactivity during the considered industrial processes.  相似文献   
996.
Meridianiite, MgSO4·11H2O, is the most highly hydrated phase in the binary MgSO4–H2O system. Lower hydrates in the MgSO4–H2O system have end-member analogues containing alternative divalent metal cations (Ni2+, Zn2+, Mn2+, Cu2+, Fe2+, and Co2+) and exhibit extensive solid solution with MgSO4 and with one another, but no other undecahydrate is known. We have prepared aqueous MgSO4 solutions doped with these other cations in proportions up to and including the pure end-members. These liquids have been solidified into fine-grained polycrystalline blocks of metal sulfate hydrate + ice by rapid quenching in liquid nitrogen. The solid products have been characterised by X-ray powder diffraction, and the onset of partial melting has been quantified using a thermal probe. We have established that of the seven end-member metal sulfates studied, only MgSO4 forms an undecahydrate; ZnSO4 forms an orthorhombic heptahydrate (synthetic goslarite), MnSO4, FeSO4, and CoSO4 form monoclinic heptahydrates (syn. mallardite, melanterite, bieberite, respectively), and CuSO4 crystallises as the well-known triclinic pentahydrate (syn. chalcanthite). NiSO4 forms a new hydrate which has been indexed with a triclinic unit cell of dimensions a = 6.1275(1) Å, b = 6.8628(1) Å, c = 12.6318(2) Å, α = 92.904(2)°, β = 97.678(2)°, and γ = 96.618(2)°. The unit-cell volume of this crystal, V = 521.74(1) Å3, is consistent with it being an octahydrate, NiSO4·8H2O. Further analysis of doped specimens has shown that synthetic meridianiite is able to accommodate significant quantities of foreign cations in its structure; of the order 50 mol. % Co2+ or Mn2+, 20–30 mol. % Ni2+ or Zn2+, but less than 10 mol. % of Cu2+ or Fe2+. In three of the systems we examined, an ‘intermediate’ phase occurred that differed in hydration state both from the Mg-bearing meridianiite end-member and the pure dopant end-member hydrate. In the case of CuSO4, we observed a melanterite-structured heptahydrate at Cu/(Cu + Mg) = 0.5, which we identify as synthetic alpersite [(Mg0.5Cu0.5)SO4·7H2O)]. In the NiSO4- and ZnSO4-doped systems we characterised an entirely new hydrate which could also be identified to a lesser degree in the CuSO4- and the FeSO4-doped systems. The Ni-doped substance has been indexed with a monoclinic unit-cell of dimensions a = 6.7488(2) Å, b = 11.9613(4) Å, c = 14.6321(5) Å, and β = 95.047(3)°, systematic absences being indicative of space-group P21/c with Z = 4. The unit-cell volume, V = 1,176.59(5) Å3, is consistent with it being an enneahydrate [i.e. (Mg0.5Ni0.5)SO4·9H2O)]. Similarly, the new Zn-bearing enneahydrate has refined unit cell dimensions of a = 6.7555(3) Å, b = 11.9834(5) Å, c = 14.6666(8) Å, β = 95.020(4)°, V = 1,182.77(7) Å3, and the new Fe-bearing enneahydrate has refined unit cell dimensions of a = 6.7726(3) Å, b = 12.0077(3) Å, c = 14.6920(5) Å, β = 95.037(3)°, and V = 1,190.20(6) Å3. The observation that synthetic meridianiite can form in the presence of, and accommodate significant quantities of other ions increases the likelihood that this mineral will occur naturally on Mars—and elsewhere in the outer solar system—in metalliferous brines.  相似文献   
997.
The Indian Ocean Tsunami of December 2004 caused inundation of seawater along the Northern coast of Tamil Nadu, India, resulting in loss of 8,000 people with extensive damage to properties. The paper describes the inundation of seawater in two northern districts, namely Kancheepuram and Villupuram districts, which showed distinct patterns of inundation of seawater and run-up levels due to variations in geomorphic features. TUNAMI N2 model was used to predict the seawater inundation for earthquakes occurred in 1881 at Car Nicobar, Sumatra 2004 and a worst-case scenario. The coastal areas with beaches having gentle slope showed more inundation compared with coastal areas having varied slope and habited by sand dunes and coastal vegetation. Appreciable inundation of seawater with tsunami simulated for 1881 Car Nicobar indicated that proximity to the source plays a major role besides earthquake parameters in causing inundation. The worst-case scenario generated from subduction zone of Car Nicobar using Sumatra 2004 earthquake parameters revealed extreme vulnerability of coasts of both the districts to giant tsunamis.  相似文献   
998.
Two-dimensional dam break flooding simulation: a GIS-embedded approach   总被引:2,自引:2,他引:0  
In the twenty-first century, around 200 notable dam and reservoir failures happened worldwide causing massive fatalities and economic costs. In order to reduce the losses, managers usually define mitigation strategies identifying flooding area due to dam break by using standalone hydrodynamic models and then importing the results within a GIS to perform risk analysis. This two-step procedure is time expensive, error prone due to export/import requirements and not user friendly. For this reason with this work, a new numerical model for the solution of the two-dimensional dam break problem has been implemented in the GRASS GIS with a GIS-embedded approach. The model solves the conservative form of the 2D shallow water equations using a finite volume method; the intercell flux is computed by one-side upwind conservative scheme extended to a two-dimensional problem. The newly developed GIS module, among others outputs, allows to derive maximum intensity maps that can be directly used for risk assessment. Finally, the model has been (1) tested against two standard synthetic problems referenced in literature showing differences in estimated water depth of 2, 3 and 15% and (2) verified against official flooding map of an existing dam (Verzasca) detecting 75% of similarity. The problem formulation, the new GRASS module and its validation is presented.  相似文献   
999.
This paper presents a comparison of near-fault and far-fault ground motion effects on geometrically nonlinear earthquake behavior of suspension bridges. Bo?azi?i (The First Bosporus) and Fatih Sultan Mehmet (Second Bosporus) suspension bridges built in Istanbul, Turkey, are selected as numerical examples. Both bridges have almost the same span. While Bo?azi?i Suspension Bridge has inclined hangers, Fatih Sultan Mehmet Suspension Bridge has vertical hangers. Geometric nonlinearity including P-delta effects from self-weight of the bridges is taken into account in the determination of the dynamic behavior of the suspension bridges for near-fault and far-fault ground motions. Near-fault and far-fault strong ground motion records, which have approximately identical peak ground accelerations, of 1999 Chi-Chi, 1999 Kocaeli, and 1979 Imperial Valley earthquakes are selected for the analyses. Displacements and internal forces of the bridges are determined using the finite element method including geometric nonlinearity. The displacements and internal forces obtained from the dynamic analyses of suspension bridges subjected to each fault effect are compared with each other. It is clearly seen that near-fault ground motions are more effective than far-fault ground motion on the displacements and internal forces such as bending moment, shear force and axial forces of the suspension bridges.  相似文献   
1000.
In Europe, the Wide Wheel abrasion (WWA) test and the B?hme abrasion (BA) test are among the most widely used standard test methods for determining abrasion resistance of natural stones, the former being the reference test method in EN 14157 Standard. However, it is stated in the Annex-A (Informative) of EN 14157 Standard that very limited data are available to provide correlations between these two test methods. To be able to fill this gap, in this study, 25 different natural stones belonging to sedimentary, metamorphic and igneous groups were tested for their abrasion resistance as well as physico-mechanical properties. Also, for a better interpretation of abrasion resistance characteristics of the tested stone materials, relationships between abrasion resistance and physico-mechanical properties were statistically examined. A statistically significant linear correlation (R 2 = 0.85; P value = 0.000) was established between the WWA test and the BA test, which could be used in practice for converting the measured abrasion resistance values from one testing method to another. It was also found that the correlation between these two test methods improved significantly (R 2 = 0.93; P value = 0.001) when relatively high-porosity stone materials (porosity ≥1%) were separately evaluated. Both methods of abrasion resistance employed in the present study showed statistically significant linear correlations with uniaxial compressive strength and Brazilian tensile strength, the former proving to be a more influencing parameter on resistance to abrasion. Also, from the point view of representing actual abrasion mechanism of stone materials in practice, the necessity of simulating multi-directional foot traffic in abrasion testing methods was discussed. In this respect, the reference test method in the EN 14157 Standard was criticized for not fully meeting this requirement. It was also pointed out that the reference method could have some drawbacks when applied to coarse-grained granitic rocks having cleavable minerals such as plagioclase and orthoclase feldspars.  相似文献   
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