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1.
Gold-bearing quartz lodes from the Egat gold mine, South Eastern Desert of Egypt, are associated with pervasively silicified, highly sheared ophiolitic metagabbro and island-arc metavolcanic rocks. The mineralized quartz veins and related alteration haloes are controlled by NNW-trending shear/fault zones. Microscopic and electron probe microanalyses (EPMA) data of the ore and gangue minerals reveal that fine-grained auriferous sulfarsenides represent early high-temperature (355–382 °C) phases, with formation conditions as (fS2?=??10, and fO2 around ?31). A late, low-temperature (302–333 °C) assemblage includes coarse pyrite, arsenopyrite, and free-milling gold grains (88–91 wt.% Au), with formation conditions as (fS2?=??8 and fO2 around ?30). Gold was impounded within early sulfarsenides, while free-milling gold blebs occur along microfractures in quartz veins and as inclusions in late sulfides. Infiltration of hydrothermal fluids under brittle–ductile shear conditions led to mobilization of refractory Au from early sulfarsenide phases and reprecipitated free gold, simultaneous with silicification of the host rocks. The positive correlation between Au and As favors and verifies the use of As as the best pathfinder for gold targets, along the NNW-trending shear zones.  相似文献   

2.
The new synthetic phase Mg2Al3O[BO4]2(OH) provisionally named “pseudosinhalite” is optically, chemically, and structurally similar to the mineral sinhalite, MgAl[BO4], isostructural with forsterite. It grows hydrothermally from appropriate bulk compositions in the range 4–40?kbar at temperatures that increase with pressure (～650?→?900?°C), and it breaks down at higher temperatures to sinhalite?+?corundum?+?H2O. At P?≥?20?kbar single-phase products of euhedral twinned crystals could often be obtained. Pseudosinhalite is monoclinic with a?=?7.455 (1) Å, b?=?4.330 (1) Å, c?=?9.825 (2) Å, β?=?110.68 (1)°, and space group P21/c. Crystal structure analysis reveals that pseudosinhalite is also based on hexagonal close packing (hcp) of oxygen atoms with Mg and Al in octahedral and B in tetrahedral coordination. In pseudosinhalite the winged octahedral chains in the plane of hcp are not straight as in sinhalite but have a zigzag, 3-repeat period (Dreierkette), and only 1/10 instead of 1/8 of all tetrahedral sites are filled by boron. Hydrogen is located at a split position between two oxygen atoms O5—O5, which are only 2.550 Å apart and thus generate strong hydrogen bonding. This may be responsible for the absence of an hydroxyl absorption band between 2800?cm?1 and 3500?cm?1 in the powder IR spectrum. The equilibrium breakdown curve of pseudosinhalite to form sinhalite, corundum, and water was determined by bracketing experiments to pass through 10?kbar, 745?°C and 35?kbar, 950?°C, giving a slope of about 8?°C/kbar, similar to dehydration curves of some silicates at high pressure. In nature pseudosinhalite could have been misidentified as sinhalite. A possible appearance, like sinhalite in boron-rich skarns, would require more aluminous bulk compositions than for sinhalite at relatively low temperatures. However, pseudosinhalite might also form as a hydrous alteration product of sinhalite at low temperatures, perhaps in association with szaibelyite, MgBO2(OH).  相似文献   

3.
The Dongping gold deposit hosted in syenites is one of the largest hydrothermal gold deposits in China and composed of ore veins in the upper parts and altered zones in the lower parts of the ore bodies. Pervasive potassic alteration and silicification overprint the wall rocks of the ore deposit. The alteration minerals include orthoclase, microcline, perthite, quartz, sericite, epidote, calcite, hematite and pyrite, with the quartz, pyrite and hematite assemblages closely associated with gold mineralization. The phases of hydrothermal alteration include: (i) potassic alteration, (ii) potassic alteration - silicification, (iii) silicification - epidotization - hematitization, (iv) silicification - sericitization - pyritization and (v) carbonation. Mass-balance calculations in potassic altered and silicified rocks reveal the gain of K2O, Na2O, SiO2, HFSEs and transition elements (TEs) and the loss of REEs. Most major elements were affected by intense mineral reactions, and the REE patterns of the ore are consistent with those of the syenites. Gold, silver and tellurium show positive correlation and close association with silicification. Fluid inclusion homogenization temperatures in quartz veins range from 154 °C to 382 °C (peak at 275 °C–325 °C), with salinities of 4–9 wt.% NaCl equiv. At temperatures of 325 °C the fluid is estimated to have pH = 3.70–5.86, log fO2 = − 32.4 to − 28.1, with Au and Te transported as Au (HS)2− and Te22 − complexes. The ore forming fluids evolved from high pH and fO2 at moderate temperatures into moderate-low pH, low fO2 and low temperature conditions. The fineness of the precipitated native gold and the contents of the oxide minerals (e.g., magnetite and hematite) decreased, followed by precipitation of Au- and Ag-bearing tellurides. The hydrothermal system was derived from an alkaline magma and the deposit is defined as an alkaline rock-hosted hydrothermal gold deposit.  相似文献   

4.
Previously studied thermosequences of wood (chestnut) and grass (rice straw) biochar were subjected to hydrogen pyrolysis (hypy) to evaluate the efficacy of the technique for determining pyrogenic carbon (CP) abundance. As expected, biochar from both wood and grass produced at higher temperature had higher CP amount. However, the trend was not linear, but more sigmoidal. CP/CT ratio values (CT = total organic carbon) for the wood thermosequence were ⩽0.03 at biochar production temperature (TCHAR) ⩽ 300 °C. They increased dramatically until 600 °C and remained relatively constant and near unity at higher biochar production temperature. Grass biochar was similar in profile, but CP/CT values rose dramatically after 400 °C. The findings are consistent with the hypothesis that hypy residues contain polycyclic aromatic hydrocarbons (PAHs) with a degree of condensation above at least 7–14 fused rings, with labile organic matter and pyrogenic PAHs below this degree of condensation removed by hypy.Both wood and grass thermosequences displayed δ13CP values that decreased with increased TCHAR, indicating that recalcitrant carbon compounds (pyrogenic aromatic PAHs with a relatively high degree of condensation) were first formed from structural components with relatively high δ13C values (e.g. cellulose). Relatively constant δ13C values at TCHAR ⩾ 500 °C suggested the dominant pyrolysis reaction was condensation of PAHs with no additional fractionation. Comparison of hypy with benzene polycarboxylic acid (BPCA), ‘ring current’ NMR and pyrolysis gas chromatography–mass spectrometry (GC–MS) results from the same suite of samples indicated a consistent overview of the structure of CP, but provided unique and complimentary information.  相似文献   

5.
湖南常宁县康家湾铅锌金矿硅化角砾岩岩石地球化学特征   总被引：8，自引：0，他引：8  
许德如  刘静  陈广浩 《地质科学》2002,37(3):356-364
湖南常宁县康家湾铅锌金矿床硅化角砾岩带由未硅化角砾岩—极弱硅化角砾岩—硅化角砾岩—强硅化角砾岩(似硅质岩)组成,产于侏罗系与下伏二叠系间的不整合面附近,角砾成份复杂,充填物和胶结物类型多样。随着硅化程度的加强,硅化角砾岩带SiO2含量变化大,最高可达95.34%,而Al2O3、MgO、FeO、K2O、Na2O、CaO、CO2和P2O5含量特别是MgO、CaO、CO2和P2O5含量明显降低,且K2O>Na2O,TiO2的含量显著偏低。硅化角砾岩带LREE/HREE比值为1.95～4.93,Ce(δCe=0.44～0.81)和Eu(δEu=0.58～0.89)均为弱负异常,属轻稀土富集型,但随硅化程度增高稀土元素含量显著减少:未硅化和弱硅化角砾岩稀土元素总量较高,为(176.82～318.93)×10-10,与当冲组泥质岩配分曲线相似;硅化强烈的角砾岩稀土元素总量低,为(7.71～65.95)×10-10,与下伏栖霞组灰岩稀土元素配分曲线极为相似。结合微量元素F、Ba、Cl、Cr、Ni、Sr、V研究结果及硅化角砾岩带自底部至顶部特有的下粗上细的韵律性层理构造,认为康家湾铅锌金矿床硅化角砾岩带是在地台体制向地洼体制转变期的大地构造环境下,由于地壳快速隆升,二叠纪灰岩、泥质岩、石英砂岩等岩石剥蚀,在古河流环境下搬运、沉积形成的。此  相似文献   

6.
We discuss the nature of the ore-forming hydrothermal fluid in the Noya gold-bearing calcite-quartz-adularia veins of central Kyushu, Japan on the basis of oxygen, carbon, and strontium isotope ratios, and aqueous speciation calculations for the present-day geothermal fluid. The isotopic values of the Noya ore-forming fluid were estimated to be −6.5‰ for δ13C and −7.5‰ for δ18O. The oxygen isotopic equilibrium temperatures for vein calcite are more than 180°C at the bottom of the Noya mineralization zone, and decrease with increasing elevation. As the temperature decreased, the dominant carbon species in the fluid changed from H2CO3 to HCO3- at about 120°C. The equilibrium temperatures for vein quartz are consistent with the calcite calculations. The carbon and oxygen isotope trends of the Noya vein calcite and the isotope ratios of strontium suggest that the fluids that precipitated the Noya veins were controlled by an andesite-dominated geology. Chondrite-normalized REE patterns for the white-colored veins from wells 51-WT-1 and 51-WT-2 displayed a light REE-rich pattern with positive Eu anomalies, suggesting the existence of a reducing environment for the fluid. The pyrite-rich gray-colored veins and a silicified rock from well 51-WT-2 showed higher REE concentrations than did the white veins. Altered host andesitic rocks have similar REE patterns to that of the silicified rock, and have higher REE contents than the others in the drill cores. Aqueous speciation calculations showed that the fluid in the hydrothermal reservoir is currently in muscovite stability. The fluid at the ore-mineralization stage may have contained more potassium or have had a higher pH, so that adularia precipitated with calcite and quartz, as well as gold. Fluid boiling at depth in the system produced the gold-bearing calcite-quartz-adularia veins.  相似文献   

7.
The effects on the ferric-ferrous ratio of varying individual components in a dry basaltic liquid have been determined at atmospheric pressure and constant oxygen fugacity (fO2). Experiments were conducted by suspending 100 mg samples from pt loops at 1200°C (fO2 = 10?8atm) and 1360°C (fO2 = 10?6atm) in an atmosphere controlled by mixtures of CO2 and H2. A microanalytical wetchemical technique and the electron microprobe were used to determine the composition of the resulting basaltic glasses. In order of decreasing significance, the addition of oxides of K, Na, Si, Al, or Ca produces an increase in the ferric-ferrous ratio of the melt at 1200°C. The change in the ferric-ferrous ratio produced by component addition is less at 1360°C than at 1200°C.  相似文献   

8.
The electrical conductivity of calcite cleavage fragments was measured using direct current. Five temperature intervals, characterized by different activation energies of conduction, were established — T 1: (300°)–500° C, T 2: 500–725° C, T 3: 725°–800° C, T 4: 800°–985° C and T 5: 985°–(1,200)° C. The data above 600° C indicate various intrinsic conduction mechanisms which are likely to be related to disorder in the CO3-sublattice of calcite. The transitions between the temperature intervals T 2-T 3-T 4 and T 4-T 5 are probably correlated with high-temperature transitions of calcite at 800° and 985° C. Measurement of the thermoelectric voltage indicates a conductivity dominated by negatively charged carriers.  相似文献   

9.
The thermal phase transition of K2SO4 has been investigated by high temperature polarized light microscopy. K2SO4 undergoes a first-order transition at 587° C where the orthorhombic low temperature form (Pmcn) transforms into a hexagonal high temperature modification (P63/mmc). Prior to the beginning of the phase transition, K2SO4 shows an anomalous optical behavior. The crystal apparently becomes optically uniaxial twice at 338° and 425° C, respectively, and truly optically uniaxial at 587° C. The phase transition propagates through an intermediate temperature form, which is sandwiched between the low and the high temperature forms and moves in a definite direction, 〈130〉 (orthorhombic indices), in the vicinity of the phase transition. Passing through the phase transition point on cooling, dark belts crossing each other are observed which are a result of the transformation twins parallel to {110} and {130}.  相似文献   

10.
A fossil wood cell texture with pitchblende and coffinite found at a sandstone-hosted roll-type uranium deposit, Xinjiang, NW China, is first reported here for the country. In the mineralized sandstone, detrital grains consisting of quartz, feldspar, rock fragments, carbonaceous trashes, mica and accessory minerals were deposited in early Turassic time and were cemented by clays and minor authigenic calcite and quartz. Pitchblende and minor coffinite are principal ore minerals at the deposit, and selectively replaced carbonized fossil wood remnants or filled fossil wood cells. An excellent fossil wood cell texture with primary uranium minerals formed. Replacement of organic debris by primary uranium minerals may be due to a local reducing environment resulting from the production of CH4, H2S or H2SO3 in its decomposition, and a biochemical reaction indicated by the common presence of framboidal pyrite.  相似文献   

11.
The influences of temperature and environmental hypoxia on the growth rates of two California anadromous fishes, white sturgeon (Acipenser transmontanus) and striped bass (Morone saxatilis) were examined. Fish (0.5–0.6 g initial weight) were fedad libitum rations ofArtemia in flow-through aquaria regulated for temperature (15, 20, and 25°C) and oxygen tension (130 and 90 torr Po 2). Growth of sturgeon was significantly greater at 20 °C compared with 15 °C, but there was no difference between 20 and 25 °C. Striped bass growth increased with each 5° increment of temeprature elevation to 3.2% body weight per d at 25 °C, the fastest growth rate measured. The temperature of maximum growth reflected the temperature of the native estuarine rearing area. Environmental hypoxia (90 torr Po 2) reduced growth of sturgeon within each temperature level, whereas striped bass growth was reduced by hypoxia only at the upper two temperatures. Sturgeon were much more active in the growth chambers than striped bass. Sturgeon activity increased with each 5 °C temperature increase under normoxia and hypoxia, except at 25 °C (hypoxia) where activity was insignificantly different from that at 20 °C (hypoxia).  相似文献   

12.
The orthorhombic-hexagonal phase transition of K2SO4 has been investigated by measurements of the temperature dependencies of the specific heat, expansion, and X-ray intensity of superstructure reflections, correlated with the structural point of view. The values of the net enthalpy and entropy changes are ΔH=4.28 KJ/mol and ΔS=4.98 J/mol·K at the phase transition temperature (587°C), respectively. The thermal expansion along the c axis shows strong anisotropic character above about 300°C and exhibits a very large discontinuous increase at 587°C, whereas those along the a and b axes increase linearly and exhibit small discontinuous decreases at 587°C. The X-ray intensity of superstructure reflections in the low-temperature form gradually decrease with increasing temperature, and come to extinction at 587°C, exhibiting a discontinuity. The observed entropy change and pressure dependence of the phase transition temperature were explained successfully by the use of results of the structural analysis and measured physical properties. The temperature dependencies of the spontaneous strain, X-ray intensity of superstructure reflection, and birefringence were consistently described by introducing a transition parameter on the basis of an instability at the M point in the Brillouin zone of the hexagonal phase.  相似文献   

13.
Speciation of aqueous calcium chloride and the solubility of wollastonite represented by the reaction wollastonite + 2HCl° → CaCl2° + quartz + H2O were experimentally investigated at 1 and 2 kbar in the range 425–600°C using rapid-quench hydrothermal techniques and a modified Ag + AgCl buffer technique (Frantz and Popp, 1979). Variation in the measured concentration in HCl° as a function of total dissolved calcium was used to identify associated aqueous CaCl2° as the predominant calcium species in the fluid at temperatures above 500°C at 2 kbar. The data were used to calculate the equilibrium constant for the above reaction as a function of temperature and pressure, from which the difference in Gibbs free energy of formation between CaCl2° and HCl° at 1 and 2 kbar, 450°–600°C was calculated. Solubility constants for minerals in the system MgO-CaO-SiO2-H2O-HCl-CO2 were calculated using the data from this study and from Frantz and Popp (1979). Calculated mineral solubilities were used to calculate the solution compositions and solid alteration products resulting from interactions of a Ca-Mg silicate mineral (diopside) with hydrothermal solutions containing a range of different total chloride concentrations. High total chloride (2.0 m) in the solution results in Si-Mg enrichment in the solids and Ca enrichment in the fluid, whereas low total chloride (0.008 m) results in Mg enrichment in the solids and Ca-Si enrichment in the fluid.  相似文献   

14.
Crystallization experiments of basaltic andesite mafic endmember from the 24 ka Lower Pollara eruption (Salina, Aeolian Islands, Italy) were investigated at 200 MPa, 950–1100 °C, in the H2O activity (aH2O) range ~0.3 to 1, and at two ranges of oxygen fugacity (fO2) between ~FMQ to FMQ+1 and ~FMQ+2 to FMQ+3.3 (log bars, FMQ is fayalite-magnetite-quartz). Comparison of the produced phase assemblages and phase compositions with the natural sample reveals that the storage conditions were ~1050 °C, ~2.8 wt% H2O in the melt (aH2O ~0.5), and relatively oxidizing (~FMQ+2.5). The composition of plagioclase in the groundmass indicates a period of cooling to ≤950 °C. The overall differentiation trends of the Salina volcanics can be explained by fractional crystallization close to H2O saturated conditions (~5 wt% H2O in the melt at 200 MPa) and most likely by accumulation of plagioclase, i.e., in basaltic andesites, and by various degree of mixing–mingling between the corresponding differentiates. The slightly elevated K2O contents of the most mafic basaltic andesites that can be found in the lowermost unit of the Lower Pollara pyroclastics reveal earlier processes of moderately hydrous fractional crystallization at higher temperature (>~1050 °C). Fractional crystallization with decreasing influence of H2O causes a moderate decrease of MgO and a significant increase of K2O relative to SiO2 in the residual liquids. It is exemplarily shown that the crystallization of SiO2-rich phases at high temperature and low aH2O of only moderately K2O-rich calc-alkaline basalts can produce shoshonitic and high potassic rocks similar to those of Stromboli and Volcano. This suggests that the observed transition from calc-alkaline to shoshonitic and high potassic volcanism at the Aeolian Arc over time can be initiated by a general increase of magmatic temperatures and a decrease of aH2O in response to the extensional tectonics and related increase of heat flow and declining influence of slab-derived fluids.  相似文献   

15.
Subsolidus and melting relations for the CaCO3-MgCO3 join at 30 kb have been determined using piston-cylinder apparatus. Data are also presented for the melting curve of CaCO3 to 30 kb, the decomposition and melting curves of MgCO3 to 36 kb, and the calcite-aragonite transition at 800°C, 950°C and 1100°C. At 30kb, the melting loop for the CaCO3-MgCO3 join extends from 1610°C (CaCO3) to 1585°C (MgCO3) through a liquidus minimum at 1290°C (near 42 mole% MgCO3). The dolomite-magnesite solvus barely intersects the 30 kb melting loop to produce a peritectic reaction at 1385°C. Integration of the new experimental data with other published data permits construction of a complete P-T projection and a sequence of isobars for the CaCO3-MgCO3 join for pressures between 5 and 30 kb. The phase relations for this join provide part of the essential framework of the model peridotite system CaO-MgO-SiO8-CO2-H2O, which has particular application to the origin of carbonatitic and kimberlitic magmas. In light of the accumulating evidence for CO2 in various forms within the upper mantle and of its effect on magmatic processes, analysis of the melting relations in this system is of considerable importance.  相似文献   

16.
The thermal response of the natural ferroan phlogopite-1M, K2(Mg4.46Fe0.83Al0. 34Ti0.22)(Si5.51Al2. 49)O20[OH3.59F0.41] from Quebec, Canada, was studied with an in situ neutron powder diffraction. The in situ temperature conditions were set up at ?263, 25, 100°C and thereafter at a 100°C intervals up to 900°C. The crystal structure was refined by the Rietveld method (R p=2.35–2.78%, R wp=3.01–3.52%). The orientation of the O–H vector of the sample was determined by the refinement of the diffraction pattern. With increasing temperature, the angle of the OH bond to the (001) plane decreased from 87.3 to 72.5°. At room temperature, a = 5.13 Å, b = 9.20 Å, c = 10.21 Å, β = 100.06° and V(volume) = 491.69 Å3. The expansion rate of the unit cell dimensions varied discontinuously with a break at 500°C. The shape of the M-octahedron underwent some significant changes such as flattening at 500°C. At temperatures above 500°C, the octahedral thickness and mean distance was decreased, while the octahedral flattening angle increased. Those results were attributed to the Fe oxidation and dehydroxylation processes. The dehydroxylation mechanism of the ferroan phlogopite was studied by the Fourier transform infrared spectroscopy (FTIR) after heated at temperatures ranging from 25 to 800°C with an electric furnace in a vacuum. In the OH stretching region, the intensity of the OH band associated with Fe2+(N B-band) begun to decrease outstandingly at 500°C. The changes of the IR spectra confirmed that dehydroxylation was closely related to the oxidation in the vacuum of the ferrous iron in the M-octahedron. The decrease in the angle of the OH bond to the (001) plane, with increasing temperature, might be related to the imbalance of charge in the M-octahedra due to Fe oxidation.  相似文献   

17.
Partial melting and retrogression have been recognized in high-grade metapelites of the Tatra Mountains, Western Carpathians (Slovakia) related to exhumation during Variscan orogeny. Reaction textures and phase equilibria define a clockwise P-T path. The prograde metamorphism from ca 600 °C and 9–10 kbar to >700 °C at 11–12 kbar resulted in muscovite dehydration-melting in the kyanite stability field. Further heating at decreasing pressure led to the dehydration-melting of biotite at >750 °C in the sillimanite stability field. This was followed by nearly isothermal decompression down to 4–5 kbar, producing cordierite and some additional melt. Later nearly isobaric cooling led to melt crystallization and sub-solidus retrogression. CO2-N2 fluids (5–30 mol. % N2) were generated at pressures <6 kbar by interaction between the melt-derived water and graphite at oxidizing conditions.  相似文献   

18.
In Mesozoic metacarbonates of the Tethyan Himalayas (Shiar Khola area, Central Nepal) two characteristic remanent magnetisations (ChRM1 and ChRM2) were identified by their unblocking temperature spectra. The ChRM1 is carried by pyrrhotite (unblocking temperature: 270–360°C) and the ChRM2 by magnetite (unblocking temperature spectra: 430–580°C). The temperature-related formation of pyrrhotite at the expense of primary magnetite during low-grade metamorphism in marly carbonates allows the determination of thermal gradients by the pyrrhotite/magnetite ratio. This new method can be used as a geothermometer for T≤300°C in low-grade metamorphic carbonates, where other methods are not available. This method is applied for the first time in the Tethyan Himalayas of Central Nepal.In the Shiar Khola valley, systematic variations in the ferrimagnetic content of the metacarbonates along an E–W profile were detected by the ratio of remanence intensity of pyrrhotite to magnetite, derived from natural remanent magnetisation (RPYR/MAG) and saturation magnetisation (SPYR/MAG). Over a stretch of 10 km the RPYR/MAG and SPYR/MAG increase from W to E from ~0.42 to ~0.91 and ~0.48 to ~1.0, respectively. Based on temperature estimates, the eastern part experienced upper anchizone–epizone (~250–300°C) conditions, while the western part underwent only diagenesis (~200°C). The temperature gradient and the temperature ranges suggested are consistent with the findings of the calcite twin lamellae geothermometry which is a non-magnetic method.  相似文献   

19.
The temperature tolerance and resistance times of postlarval (<25 mm SL) and small juvenile spot,Leiostomus xanthurus, from the Cape Fear Estuary, North Carolina were tested in the laboratory. Critical thermal maximum techniques were used to determine first equilibrium loss (FEL) and critical thermal maximum (CTM) end points and thermal shock methods were used to determine 96-h upper incipient lethal temperatures (LT50). Acclimation temperatures ranged from 10 to 35°C and acclimation salinities were 10, 20 and 30‰. A quadratics model was fit to the CTM and FEL data; r2 values were 0.924 and 0.928 respectively. Acclimation salinity, estimated weight, acclimation salinity by acclimation temperature interaction and acclimation temperature by estimated weight interaction were the significant components of the CTM model. Predicted CTM values ranged from 30°C at 10 °C and 30‰ acclimation to just over 40°C at 30 °C and 30‰ acclimation. Acclimation temperature, acclimation temperature squared, estimated weight and acclimation temperatures by estimated weight interaction were the significant components of the FEL model. Predicted FEL values ranged from around 28°C at 10°C and 10‰ acclimation to about 39°C at 30°C and 30‰ acclimation. The 96-h LT50 values of spot acclimated to 20‰ increased linearly with acclimation temperature to 25°C. From about 25 to 35°C, LT50 values increased very little with acclimation temperature. The ultimate upper incipient lethal temperature of postlarval and small juvenile spot was estimated at 35.2°C. Increased salinity increased resistance time but decreased LT50 estimates. Thermal shock tests were better for predicting the effects of thermal addition than were CTM tests.  相似文献   

20.
Experimental studies in the Fe3C–SiO2–MgO system (P = 6.3 GPa, T = 1100–1500°C, t = 20–40 h) have been carried out. It has been established that carbide-oxide interaction resulted in the formation of Fe-orthopyroxene, graphite, wustite, and cohenite (1100 and 1200°C), as well as a Fe–C–O melt (1300–1500°C). The main processes occurring in the system at 1100 and 1200°C are the oxidation of cohenite, the extraction of carbon from carbide, and the crystallization of metastable graphite, as well as the formation of ferrosilicates. At T ≥ 1300°C, graphite crystallization and diamond growth occur as a result of the redox interaction of a predominantly metallic melt (Fe–C–O) with oxides and silicates. The carbide–oxide interaction studied can be considered as the basis for modeling a number of carbon-producing processes in the lithospheric mantle at fO2 values near the iron–wustite buffer.  相似文献   

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