where D0 is in µm2/s, X is mole fraction of H2Ot on a single oxygen basis, T is temperature in K, and P is pressure in GPa.H2Ot diffusivities (DH2Ot, in µm2/s) can be calculated from H2Om diffusivity, or directly from the following expression:
At low H2Ot content (up to 2 wt.% if an error of a factor of 2 is allowed), H2Ot diffusivity is approximately proportional to H2Ot content:
where C is H2Ot content in wt.% and C0 is 1 wt.%. The new expressions for H2O diffusion not only reproduce our own data, but also match data in literature from different laboratories and using different methods, indicating good inter-laboratory and multi-method consistency. The new expressions cover a wide range of geological conditions, and can be applied to H2O diffusion in rhyolitic melts in various volcanic and magmatic processes.  相似文献   

18.
Strength and stability of frictional sliding of gabbro gouge at elevated temperatures   总被引：7，自引：1，他引：7  
Changrong He  Wenming Yao  Zeli Wang  Yongsheng Zhou   《Tectonophysics》2006,427(1-4):217
To investigate the strength of frictional sliding and stability of mafic lower crust, we conducted experiments on oven-dried gabbro gouge of 1 mm thick sandwiched between country rock pieces (with gouge inclined 35° to the sample axis) at slip rates of 1.22 × 10− 3 mm/s and 1.22 × 10− 4 mm/s and elevated temperatures up to 615 °C. Special attention has been paid to whether transition from velocity weakening to velocity strengthening occurs due to the elevation of temperature.Two series of experiments were conducted with normal stresses of 200 MPa and 300 MPa, respectively. For both normal stresses, the friction strengths are comparable at least up to 510 °C, with no significant weakening effect of increasing temperature. Comparison of our results with Byerlee's rule on a strike slip fault with a specific temperature profile in the Zhangbei region of North China shows that the strength given by experiments are around that given by Byerlee's rule and a little greater in the high temperature range.At 200 MPa normal stress, the steady-state rate dependence a − b shows only positive values, probably still in the “run-in” process where velocity strengthening is a common feature. With a normal stress of 300 MPa, the values of steady-state rate dependence decreases systematically with increasing temperature, and stick-slip occurred at 615 °C. Considering the limited displacement, limited normal stress applied and the effect of normal stress for the temperatures above 420 °C, it is inferred here that velocity weakening may be the typical behaviour at higher normal stress for temperature above 420 °C and at least up to 615 °C, which covers most of the temperature range in the lower crust of geologically stable continental interior. For a dry mafic lower crust in cool continental interiors where frictional sliding prevails over plastic flow, unstable slip nucleation may occur to generate earthquakes.  相似文献   

19.
Dissolution kinetics of probertite in boric acid solution     
A. Mergen  M.H. Demirhan 《International Journal of Mineral Processing》2009,90(1-4):16-20
Probertite (NaCaB5O9·5H2O) and ulexite (NaCaB5O9·8H2O) posses identical chemical formula except for their water content. In this study, the dissolution of probertite in boric acid solution was investigated as a function of temperature and time. As the boric acid concentration increased, the dissolution of probertite also increased. However, the boric acid concentrations above 5 wt.% at 60 °C and 80 °C did not significantly affect the dissolution of probertite. The stirring speed had almost no effect on the dissolution of probertite. The dissolution kinetics of probertite in boric acid solution was controlled by first order pseudo homogeneous reaction. The activation energies for different probertite particle sizes varied from 25.25 kJ/mol K to 28.25 kJ/mol K, indicating that particle size had minor effect on the dissolution of probertite.  相似文献   

20.
Large-strain deformation and strain partitioning in polyphase rocks: Dislocation creep of olivine–magnesiowüstite aggregates     
Misha Bystricky  Florian Heidelbach  Steve Mackwell   《Tectonophysics》2006,427(1-4):115
Aggregates composed of olivine and magnesiowüstite have been deformed to large strains at high pressure and temperature to investigate stress and strain partitioning, phase segregation and possible localization of deformation in a polyphase material. Samples with 20 vol.% of natural olivine and 80 vol.% of (Mg0.7Fe0.3)O were synthesized and deformed in a gas-medium torsion apparatus at temperatures of 1127 °C and 1250 °C, a confining pressure of 300 MPa and constant angular displacement rates equivalent to constant shear strain rates of 1–3.3 × 10− 4 s− 1. The samples deformed homogeneously to total shear strains of up to γ  15. During constant strain rate measurements the flow stress remained approximately stable at 1250 °C while it progressively decreased after the initial yield stress at the lower temperature. Mechanical data, microstructures and textures indicate that both phases were deforming in the dislocation creep regime. The weaker component, magnesiowüstite, controlled the rheological behavior of the bulk material and accommodated most of the strain. Deformation and dynamic recrystallization lead to grain refinement and to textures that were not previously observed in pure magnesiowüstite and may have developed due to the presence of the second phase. At 1127 °C, olivine grains behaved as semi-rigid inclusions rotating in a viscous matrix. At 1250 °C, some olivine grains remained largely undeformed while deformation and recrystallization of other grains oriented for a-slip on (010) resulted in a weak foliation and a texture typical for pure dry olivine aggregates. Both a-slip and c-slip on (010) were activated in olivine even though the nominal stresses were up to 2 orders of magnitude lower than those needed to activate these slip systems in pure olivine at the same conditions.  相似文献   

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1.
The recovery of magnesium from magnesite tailings in aqueous hydrochloric acid solutions by acid leaching was studied in a batch reactor using hydrochloric acid solutions. Subsequent, production of magnesium chloride hexahydrate (MgCl2.6H2O) from leaching solution was also investigated. The effects of temperature, acid concentration, solid-to-liquid ratio, particle size and stirring speed on the leaching process were investigated. The pseudo-second-order reaction model seemed to be appropriate for the magnesium leaching. The activation energy of the leaching process was estimated to be 62.4 kJ mol− 1. Finally, MgCl2.6H2O in a purity of 91% was produced by evaporation of leaching solution obtained at a temperature of 40 °C, 1.0 M acid, solid-to-liquid ratio of 10 g/L, particle size of 100 µm, stirring speed of 1250 rpm and leaching time of 60 min.  相似文献   

2.
Ilmenite separated from beach sands of Bangladesh was oxidized for 1 h at 950 °C and then reduced in charcoal for 4 h at 1050 °C. This was followed by leaching in 5% to 15% hydrochloric acid solution in temperature range of 30 to 75 °C for periods of up to 2 h. The results were compared with those obtained by leaching of ilmenite reduced without oxidizing. Oxidation prior to reduction of the ilmenite was found to increase both the extent and the rate of leaching. The residual iron contents after leaching were also found to be lower than that obtained for non-oxidized samples. The kinetic data of leaching of ilmenite reduced after oxidation was found to follow first order reaction model, i.e., G(α) = − ln(1 − α) up to an α value of 0.5 (i.e. up to 50% reduction) and then changed to spherical model, i.e., G(α) = [1 − (1 − α)]3. On the other hand, leaching of ilmenite reduced without oxidizing was found to follow the Ginstling-Brounshtein reaction, i.e., G(α) = 1 − (2/3)α − (1 − α)2/3 throughout the leaching process. Oxidation of ilmenite prior to reduction was also found to have decreased the activation energy of leaching from 43 kJ/mol, found for samples leached after reduction without oxidizing, to 30 kJ/mol.  相似文献   

3.
Twenty-eight samples of peat, peaty lignites and lignites (of both matrix and xylite-rich lithotypes) and subbituminous coals have been physically activated by pyrolysis. The results show that the surface area of the activated coal samples increases substantially and the higher the carbon content of the samples the higher the surface area.The adsorption capacity of the activated coals for NO, SO2, C3H6 and a mixture of light hydrocarbons (CH4, C2H6, C3H8 and C4H10) at various temperatures was measured on selected samples. The result shows a positive correlation between the surface area and the gas adsorption. In contrast, the gas adsorption is inversely correlated with the temperature. The maximum recorded adsorption values are: NO = 8.22 × 10− 5 mol/g at 35 °C; SO2 = 38.65 × 10− 5 mol/g at 60 °C; C3H6 = 38.9 × 10− 5 mol/g at 35 °C; and light hydrocarbons = 19.24 × 10− 5 mol/g at 35 °C. Adsorption of C3H6 cannot be correlated with either NO or SO2. However, there is a significant positive correlation between NO and SO2 adsorptions. The long chain hydrocarbons are preferentially adsorbed on activated lignites as compared to the short chain hydrocarbons.The results also suggest a positive correlation between surface area and the content of telohuminite maceral sub-group above the level of 45%.  相似文献   

4.
A simple process to produce fine and low soda α-alumina (α-Al2O3) from a commercial grade aluminium trihydroxide (gibbsite, Al(OH)3) produced by KC Corporation Ltd was developed. There are two options for this process with the first one producing low soda α-alumina (< 0.05% Na2O) having a mean particle size of 50 μm. The second option yields a fine product with a mean size of less than 10 μm. In the first option, a plant aluminium trihydroxide containing 0.20% Na2O was first fluidized with nitrogen at 400–600 °C to yield an amorphous activated alumina. This intermediate product was then treated with acetic or oxalic acid, washed with water and heated to 1200 °C to form calcined α-alumina, having a Na2O content of less than 0.05%. A 20 min leaching using 0.2 M acetic or oxalic acid could yield an alumina product containing 0.04% Na2O. In the second option, a new technique for the preparation of fine and low soda α-alumina was evaluated using an attrition mill working also as a leaching vessel at 80 °C. Fine (< 10 μm in mean particle size) and low soda (< 0.04% Na2O) alumina was produced by a 20 min leaching step with 0.2 M acetic acid and concurrent attrition milling.  相似文献   

5.
We have studied the paleomagnetism of the middle Cretaceous Iritono granite of the Abukuma massif in northeast Japan together with 40Ar–39Ar dating. Paleomagnetic samples were collected from ten sites of the Iritono granite (102 Ma 40Ar–39Ar age) and two sites of its associated gabbroic dikes. The samples were carefully subjected to alternating field and thermal demagnetizations and to rock magnetic analyses. Most of natural remanent magnetizations show mixtures of two components: (1) H component, high coercivity (Bc > 50–90 mT) or high blocking temperature (Tb > 350–560 °C) component and (2) L component, relatively low Bc or low Tb component. H component was obtained from all the 12 sites to give a mean direction of shallow inclination and northwesterly declination (I = 29.9°, D = 311.0°, α95 = 2.7°, N = 12). This direction is different from the geocentric axial dipole field at the present latitude (I = 56.5°) and the typical direction of the Cenozoic remagnetization in northeast Japan. Since rock magnetic properties indicate that the H component of the Iritono granite is carried mainly by magnetite inclusions in plagioclase, this component probably retains a primary one. Thus the shallow inclination indicates that the Abukuma massif was located at a low latitude (16.1 ± 1.6°N) about 100 Ma and then drifted northward by about 20° in latitude. The northwesterly deflection is attributed mostly to the counterclockwise rotation of northeast Japan due to Miocene opening of the Japan Sea. According to this model, the low-pressure and high-temperature (low-P/high-T) metamorphism of the Abukuma massif, which has been well known as a typical location, would have not occurred in the present location. On the other hand, the L component is carried mainly by pyrrhotite and its mean direction shows a moderate inclination and a northwesterly declination (I = 42.8°, D = 311.5°, α95 = 3.3°, N = 9). Since this direction is intermediate between the H component and early Cenozoic remagnetization in northeast Japan, some thermal event would have occurred at lower temperature than pyrrhotite Curie point ( 320 °C) during the middle Cretaceous to early Cenozoic time to have resulted in partial remagnetization.  相似文献   

6.
Metamorphic decarbonation reactions and volcanic degassing lead to significant influx of CO2, a major greenhouse gas, into the ocean-atmosphere system from the solid Earth. Here we present quantitative estimates on CO2 derived through metamorphic degassing during ultrahigh-temperature (UHT) metamorphism in the Neoproterozoic through the mineralogical and geological analyses of the UHT decarbonation. Our computations show that an extra flux of CO2 was added to the atmosphere through a Himalayan scale UHT metamorphism to the extent of 6 × 1016 to 3.0 × 1018 mol/my, for a duration of 10 my. A calculation of the impact of the extra CO2 influx to the global mean temperature in the context of carbon cycle and greenhouse effect of CO2 shows that at the peak influx stage, the steady state temperature would be raised by 4 °C from 15 °C and by 13 °C from 4 °C. Our results have important bearing in evaluating the mechanism of melting and the duration of the Snowball Earth. Our estimate of the maximum degassing rate during UHT metamorphism suggests that the duration of the Marinoan snowball Earth was probably shorter, and the recovery from an ice-covered Earth to ocean-covered Earth was faster than previous estimates.  相似文献   

7.
Cantilever torque magnetometry is utilized widely in physics and material science for the determination of magnetic properties of thin films and semiconductors. Here, we report on its first application in rock magnetism, namely the determination of K1 and K2 of single crystal octahedra of natural magnetite. The design of cantilever magnetometers allows optimization for the specific research question at hand. For the present study, a cantilever magnetometer was used that enables measurement of samples with a volume up to 64 mm3. It can be inserted into an electromagnet with a maximum field of 2 T. The cantilever spring is suitable for torque values ranging from 7.5 × 10− 7 N·m to 5 × 10− 6 N·m. The torque is detected capacitively; the measured capacitance is converted into torque by using a calibrated feedback coil. The magnetometer allows in-situ rotation of the sample in both directions and is, therefore, also suitable to analyze rotational hysteresis effects.The evaluation of the magnetite anisotropy constants involved Fourier analysis of the torque signal on the magnetite crystals' (001) and (110) planes. The absolute anisotropy constant has been computed using the extrapolation-to-infinite-field method. The value of K1 at room temperature is determined at − 1.28 × 104 [J m− 3] (± 0.13, i.e. 10%) and that of K2 at − 2.8 × 103 [J m− 3] (± 0.1, i.e. 2%). These values concur with earlier determinations that could not provide an instrumental error, in contrast with this work.The cantilever magnetometer performs four times faster than other torque magnetometers used for rock magnetic studies. This makes the instrument also suitable for magnetic fabric analysis.  相似文献   

8.
Heat flow and lithospheric thermal regime in the Northeast German Basin   总被引：3，自引：0，他引：3  
New values of surface heat flow are reported for 13 deep borehole locations in the Northeast German Basin (NEGB) ranging from 68 to 91 mW m− 2 with a mean of 77 ± 3 mW m− 2. The values are derived from continuous temperature logs, measured thermal conductivity, and log-derived radiogenic heat production. The heat-flow values are supposed free of effects from surface palaeoclimatic temperature variations, from regional as well as local fluid flow and from thermal refraction in the vicinity of salt structures and thus represent unperturbed crustal heat flow. Two-D numerical lithospheric thermal models are developed for a 500 km section along the DEKORP-BASIN 9601 deep seismic line across the basin with a north-eastward extension across the Tornquist Zone. A detailed conceptual model of crustal structure and composition, thermal conductivity, and heat production distribution is developed. Different boundary conditions for the thickness of thermal lithosphere were used to fit surface heat flow. The best fit is achieved with a thickness of thermal lithosphere of about 75 km beneath the NEGB. This estimate is corroborated by seismological studies and somewhat less than typical for stabilized Phanerozoic lithosphere. Modelled Moho temperatures in the basin are about 800 °C; heat flow from the mantle is about 35 to 40 mW m− 2. In the southernmost part of the section, beneath the Harz Mountains, higher Moho temperatures up to 900 to 1000 °C are shown. While the relatively high level of surface heat flow in the NEGB obviously is of longer wave length and related to lithosphere thickness, changes in crustal structure and composition are responsible for short-wave-length anomalies.  相似文献   

9.
Glide systems of hematite single crystals in deformation experiments   总被引：1，自引：0，他引：1  
The critical resolved shear stresses (CRSSs) of hematite crystals were determined in compression tests for r-twinning, c-twinning and {a}<m>-slip in the temperature range 25 °C to 400 °C, at 400 MPa confining pressure, and a strain rate of 10− 5 s− 1 by Hennig-Michaeli, Ch., Siemes, H., 1982. Experimental deformation of hematile crstals betwen 25 °C and 400 °C at 400 MPa confining pressure. In: Schreyer, W. (Ed.) High Pressure Research in Geoscience, Schweizerbart'sche Verlagsbuchhandlung, Stuttgart, p. 133–150. In the present contribution newly performed experiments on hematite single crystals at temperatures up to 800 °C at strain rates of 10− 5 s− 1 and 300 MPa confining pressure extends the knowledge about the CRSS of twin and slip modes. Optical observations, neutron diffraction goniometry, SEM forescatter electron images and electron backscatter diffraction are applied in order to identify the glide modes. Both twinning systems and {a}<m>-slip were confirmed by these methods. Besides the known glide systems the existence of the (c)<a>-slip system could be stated. Mechanical data establish that the CRSS of r-twinning decreases from 140 MPa at 25 °C to  5 MPa at 800 °C and for {a}<m>-slip from > 560 MPa at 25 °C to  40 MPa at 700 °C. At room temperature the CRSS for c-twinning is around 90 MPa and at 600 °C  60 MPa. The data indicate that the CRSSs above 200 °C seem to be between the values for r-twinning and {a}<m>-slip. For (c)<a>-slip only the CRSS at 600 °C could be evaluated to  60 MPa. Exact values are difficult to determine because other glide systems are always simultaneously activated.  相似文献   

10.
A novel one-step hydrothermal synthesis of 11 Å tobermorite, a cation exchanger, from a unique combination of waste materials is reported. 11 Å tobermorite was prepared from stoicheiometric quantities of cement bypass dust and waste container glass at 100 °C in water. The product also comprised 10 wt.% calcite and trace quartz as residual parent phases from the cement bypass dust. In a batch sorption study at 20 °C the uptakes of Cd2+ and Pb2+ by the waste-derived tobermorite product were found to be 171 mg g− 1 and 467 mg g− 1, respectively, and in both cases the removal process could be described using a simple pseudo-second-order rate model (k2 = 2.30 × 10− 5 g mg− 1 min− 1 and 5.09 × 10− 5 g mg− 1 min− 1, respectively). The sorption characteristics of the 11 Å tobermorite are compared with those of other waste-derived sorbents and potential applications are discussed.  相似文献   

11.
The objective of the study was to characterize changes of reflectance, reflectance anisotropy and reflectance indicating surface (RIS) shape of vitrinite, sporinite and semifusinite subjected to thermal treatment under inert conditions. Examination was performed on vitrinite, liptinite and inertinite concentrates prepared from channel samples of steam coal (Rr = 0.70%) and coking coal (Rr = 1.25%), collected from seam 405 of the Upper Silesian Coal Basin. The concentrates were heated at temperatures of 400–1200 °C for 1 h time in an argon atmosphere.All components examined in this study: vitrinite, sporinite and semifusinite as well as matrix of vitrinite and liptinite cokes, despite of rank of their parent coal, show, in general, the most important changes of reflectance value and optical anisotropy when heated at 500 °C, 800 °C (with the exception of bireflectance value of sporinite) and 1200 °C.After heating the steam coal at 1200 °C, the vitrinite and the semifusinite reveal similar reflectances, whereas the latter a slightly stronger anisotropy. Sporinite and matrix of liptinite coke have lower reflectances but anisotropy (Rbi and Ram values) similar to those observed for vitrinite and semifusinite. However, at 1000 °C sporinite and matrix of liptinite coke have the highest reflectivity of the studied components. The RIS at 1200 °C is the same for all components.The optical properties of the three macerals in the coking coal become similar after heating at 1000 °C. Coke obtained at 1200 °C did not contain distinguishable vitrinite grains. At 1200 °C semifusinite and vitrinite coke matrix have highest Rr values among the examined components. Maximum reflectance (Rmax) reach similar values for vitrinite and sporinite, slightly lower for semifusinite. Matrix of liptinite coke and matrix of vitrinite coke have considerably stronger anisotropy (Rbi and Ram values) than other components. RIS at 1200 °C is also similar for all components.  相似文献   

12.
Multi-equilibrium thermobarometry shows that low-grade metapelites (Cubito-Moura schists) from the Ossa–Morena Zone underwent HP–LT metamorphism from 340–370 °C at 1.0–0.9 GPa to 400–450 °C at 0.8–0.7 GPa. These HP–LT equilibriums were reached by parageneses including white K mica, chlorite and chloritoid, which define the earliest schistosity (S1) in these rocks. The main foliation in the schists is a crenulation cleavage (S2), which developed during decompression from 0.8–0.7 to 0.4–0.3 GPa at increasing temperatures from 400–450 °C to 440–465 °C. Fe3+ in chlorite decreased greatly during prograde metamorphism from molar fractions of 0.4 determined in syn-S1 chlorites down to 0.1 in syn-S2 chlorites. These new data add to previous findings of eclogites in the Moura schists indicating that a pile of allochtonous rocks situated next to the Beja-Acebuches oceanic amphibolites underwent HP–LT metamorphism during the Variscan orogeny. To cite this article: G. Booth-Rea et al., C. R. Geoscience 338 (2006).  相似文献   

13.
Two sets of cooling experiments were run at atmospheric conditions for two anhydrous starting latitic and trachytic melts: 1) five cooling rates (25, 12.5, 3, 0.5, and 0.125 °C/min) between 1300° and 800 °C, and 2) a 0.5 °C/min cooling rate from 1300 °C with quench temperatures at 1200°, 1100°, 1000° and 900 °C. Trachytic run-products are invariably glassy. Nucleation is also suppressed in the latitic run-products at the three highest cooling rates. Conversely, in the 0.5 and 0.125 °C/min runs, latites have a crystal content of  90 vol.%. The phases are: plagioclase, clinopyroxene, glass and iron-bearing oxide (in order of abundance). The variable quench temperatures, investigated by coupling experiments with Pt wire and Pt capsule sample containers in set 2, again did not produce crystallization of trachyte, whereas latitic samples are characterized by  10 vol.% of oxides, pyroxenes and plagioclase (in order of appearance), at temperature < 1000 °C. Effects of (preferential) heterogeneous nucleation on sample holders, of superheating degree, and chemical species loss during cooling are absent for both melt compositions. The difference of solidification paths between these two silicate melts can be ascribed only to their small chemical differences. In comparison with calculated equilibrium conditions all the experimental latitic and trachytic run-products revealed strong kinetic effects, interpretable in the light of the nucleation theory. The glass-forming ability (GFA) of trachyte is higher, whereas their critical cooling rate (Rc) is lower (< 0.125 °C/min), in comparison to latitic melts (Rc > 0.5 °C/min). The experimental results carried out in this study can be applied to lava flows and domes; trachytic lavas are able to flow for longer period with respect to latitic ones in a metastable condition. Glass-rich terrestrial lavas, i.e. obsidians, can be the result of sluggish nucleation kinetics due to the relative high polymerisation of evolved silicate melts.  相似文献   

14.
The western Pacific region has been refrigerated by the subducting cold oceanic plates since 450 Ma. However, the region is also characterized by the presence of many oceanic microplates less than 1300 km across, as well as active magmatism; the Philippine Sea plate is representative. We have compiled and examined petrochemical characters of drilled basalts of DSDP from the Philippine Sea plate, and conclude that the source mantle for oceanic basalts is rich in water ca. 0.2 wt.%, and is 50–60 °C lower than that for MORB. The extensive melting is due to the high water content in the source mantle.It is well known that some marginal basins apparently have greater depths than the major oceans. We calculated the age–depth correlation based on a model of transient half-space cooling at given parameters of temperatures of mantle and surface, 1280 and 0 °C, and the thermal diffusivity, 1 mm2 s− 1. The calculation shows the correlation of age-residual depth from a mid-oceanic ridge is 367 for the Philippine Sea, consistent with the bathymetric data. Moreover, the mid-oceanic ridge may be relatively deep because this region is underlain by the cooler mantle.Addition of water to the mantle peridotite lowers the solidus temperature and viscosity. Melting experiments of hydrous peridotite show that addition of 0.2 wt.% H2O content lowers the solidus temperature by 150 °C. As a result, the mantle under the region may practically correspond to a ca. 90 °C hotter mantle than normal MORB-source mantle in terms of magmatism and rheology. Numerical simulation for a hotter mantle suggests that many small plates should be formed because of extensive heat release by active magmatism, consistent with many microplates in this region. The presence of many oceanic microplates may be analogous to Archean plate tectonics, characterized by a hotter mantle.  相似文献   

15.
Hydrometallurgical processing of spent hydrodesulphurisation (HDS) catalyst for the recovery of molybdenum using sodium carbonate and hydrogen peroxide mixtures was investigated. The results indicated that the recovery of molybdenum was largely dependent on the concentrations of Na2CO3 and H2O2 in the reaction medium, which controls the acidity of the leach liquor and carry over of impurities such as Al, Ni, P, Si and V. Leaching process was exothermic and leaching efficiency of molybdenum decreased with increasing solid to liquid ratio. Large scale leaching of spent catalyst, under optimum conditions: 20% pulp density, 85 g/L Na2CO3, 10 vol.% H2O2 and 1 h reaction, resulted a leaching efficiency of 84% Mo. The obtained leach liquor contained (g/L): Mo — 22.0, Ni — 0.015 and Al — 0.82, P — 1.1, Si — 0.094 and minor quantities of V — 8 mg/L, As and Co — < 1 mg/L. Recovery of Mo from leach solution as MoO3 of 97.30% purity was achieved by ammonium molybdate precipitation method.  相似文献   

16.
The 1.27 Ga old Ivigtut (Ivittuut) intrusion in South Greenland is world-famous for its hydrothermal cryolite deposit [Na3AlF6] situated within a strongly metasomatised A-type granite stock. This detailed fluid inclusion study characterises the fluid present during the formation of the cryolite deposit and thermodynamic modelling allows to constrain its formation conditions.Microthermometry revealed three different types of inclusions: (1) pure CO2, (2) aqueous-carbonic and (3) saline-aqueous inclusions. Melting temperatures range between − 23 and − 15 °C for type 2 and from − 15 to − 10 °C for type 3 inclusions. Most inclusions homogenise between 110 and 150 °C into the liquid.Stable isotope compositions of CO2 and H2O were measured from crushed inclusions in quartz, cryolite, fluorite and siderite. The δ13C values of about − 5‰ PDB are typical of mantle-derived magmas. The differences between δ18O of CO2 (+ 21 to + 42‰ VSMOW) and δ18O of H2O (− 1 to − 21.7‰ VSMOW) suggest low-temperature isotope exchange. δD (H2O) ranges from − 19 to − 144‰ VSMOW. The isotopic composition of inclusion water closely follows the meteoric water line and is comparable to Canadian Shield brines. Ion chromatography revealed the fluid's predominance in Na, Cl and F. Cl/Br ratios range between 56 and 110 and may imply intensive fluid–rock interaction with the host granite.Isochores deduced from microthermometry in conjunction with estimates for the solidification of the Ivigtut granite suggest a formation pressure of approximately 1–1.5 kbar for the fluid inclusions. Formation temperatures of different types of fluid inclusions vary between 100 and 400 °C. Thermodynamic modelling of phase assemblages and the extraordinary high concentration in F (and Na) may indicate that the cryolite body and its associated fluid inclusions could have formed during the continuous transition from a volatile-rich melt to a solute-rich fluid.  相似文献   

17.
Huaiwei Ni  Youxue Zhang   《Chemical Geology》2008,250(1-4):68-78
Water diffusion in silicate melts is important for understanding bubble growth in magma, magma degassing and eruption dynamics of volcanos. Previous studies have made significant progress on water diffusion in silicate melts, especially rhyolitic melt. However, the pressure dependence of H2O diffusion is not constrained satisfactorily. We investigated H2O diffusion in rhyolitic melt at 0.95–1.9 GPa and 407–1629 °C, and 0.2–5.2 wt.% total water (H2Ot) content with the diffusion-couple method in a piston-cylinder apparatus. Compared to previous data at 0.1–500 MPa, H2O diffusivity is smaller at higher pressures, indicating a negative pressure effect. This pressure effect is more pronounced at low temperatures. Assuming H2O diffusion in rhyolitic melt is controlled by the mobility of molecular H2O (H2Om), the diffusivity of H2Om (DH2Om) at H2Ot ≤ 7.7 wt.%, 403–1629 °C, and ≤ 1.9 GPa is given by
DH2Om=D0exp(aX),
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