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1.
To investigate the potential for the geologic storage of CO2 in saline sedimentary aquifers, 1600 ton of CO2 were injected at 1500 m depth into a 24-m sandstone section of the Frio Formation — a regional reservoir in the US Gulf Coast. Fluid samples obtained from the injection and observation wells before, during and after CO2 injection show a Na–Ca–Cl type brine with 93,000 mg/L TDS and near saturation of CH4 at reservoir conditions. As injected CO2 gas reached the observation well, results showed sharp drops in pH (6.5 to 5.7), pronounced increases in alkalinity (100 to 3000 mg/L as HCO3) and Fe (30 to 1100 mg/L), and significant shifts in the isotopic compositions of H2O and DIC. Geochemical modeling indicates that brine pH would have dropped lower, but for buffering by dissolution of calcite and Fe oxyhydroxides. Post-injection results show the brine gradually returning to its pre-injection composition.  相似文献   

2.
Extraction of molybdenum and vanadium from ammonia leaching residue (main chemical composition: 2.05% Mo, 0.42% V, 65.6% Al2O3 and 10.7% SiO2) of spent catalyst was investigated by roasting the residue with soda carbonate, followed by hydrometallurgical treatment of the roasted products. In the roasting process, over 91.3% of molybdenum and 90.1% of vanadium could be extracted when a charge containing a sodium carbonate to spent catalyst ratio of 0.15 was roasted at 750 °C for 45 min and the roasted mass was leached with water (liquid to solid ratio of 2) at 80–90 °C for 15 min. After the purification of leach liquor, an extraction solvent consisting of 20 vol.% trialkylamine (N235, commercialized in China) and 10 vol.% secondary octyl alcohol (phase modifier) dissolved in sulfonated kerosene was used to extract molybdenum and vanadium in leach liquor. 10 wt.% ammonia water was used as stripping agent. Adding 30 g/l NH4NO3 to the stripping solution and adjusting the pH to 7–8.5, over 99% of vanadium can be crystallized as ammonium metavanadate. Over 98% of molybdenum can be crystallized as ammonium polymolybdate when pH is between 1.5 and 2.5 (pH is adjusted by HNO3). Ammonium metavanadate and ammonium polymolybdate were calcinated at 500–550 °C, the purity of MoO3 and V2O5 was 99.08% and 98.06% respectively. In the whole process, 88.2% of molybdenum and 87.1% of vanadium could be achieved. The proposed roasting, leaching and separation steps give a feasible alternative for the processing of ammonia leaching residue of spent catalyst and can be applied in the comprehensive utilization of low grade molybdenum ores.  相似文献   

3.
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   

4.
Between 1996 and 2001 an experimental set up in a chaparral community near San Diego, CA, examined various plant and ecosystem responses to CO2 concentrations ranging from 250 to 750 μl l− 1. These experiments indicated a significant increase in soil C sequestration as CO2 rose above the ambient levels. In 2003, two years after the cessation of the CO2 treatments, we returned to this site to examine soil C dynamics with a particular emphasis on stability of specific pools of C. We found that in as little as two years, C content in the surface soils (0–15 cm) of previously CO2 enriched plots had dropped to levels below those of the ambient and pretreatment soils. In contrast, C retained in response to CO2 enrichment was more durable in the deeper soil layers (> 25 cm deep) where both organic and inorganic C were on average 26% and 55% greater, respectively, than C content of ambient plots. Using stable isotope tracers, we found that treatment C represented 25% of total soil C and contributed to 55% of soil CO2 efflux, suggesting that most of treatment C is readily accessible to decomposers. We also found that, C present before CO2 fumigation was decomposed at a faster rate in the plots that were exposed to elevated CO2 than in those exposed to ambient CO2 levels. To our knowledge, this is the first report that allows for a detail accounting of soil C after ceasing CO2 treatments. Our study provides a unique insight to how stable the accrued soil C is as CO2 increases in the atmosphere.  相似文献   

5.
Supercritical gas sorption on moist coals   总被引：2，自引：1，他引：1  
The effect of moisture on the CO2 and CH4 sorption capacity of three bituminous coals from Australia and China was investigated at 55 °C and at pressures up to 20 MPa. A gravimetric apparatus was used to measure the gas adsorption isotherms of coal with moisture contents ranging from 0 to about 8%. A modified Dubinin–Radushkevich (DR) adsorption model was found to fit the experimental data under all conditions. Moisture adsorption isotherms of these coals were measured at 21 °C. The Guggenheim–Anderson–de Boer (GAB) model was capable of accurately representing the moisture isotherms over the full range of relative pressures.Moist coal had a significantly lower maximum sorption capacity for both CO2 and CH4 than dry coal. However, the extent to which the capacity was reduced was dependent upon the rank of the coal. Higher rank coals were less affected by the presence of moisture than low rank coals. All coals exhibited a certain moisture content beyond which further moisture did not affect the sorption capacity. This limiting moisture content was dependent on the rank of the coal and the sorbate gas and, for these coals, corresponded approximately to the equilibrium moisture content that would be attained by exposing the coal to about 40–80% relative humidity. The experimental results indicate that the loss of sorption capacity by the coal in the presence of water can be simply explained by volumetric displacement of the CO2 and CH4 by the water. Below the limiting moisture content, the CO2 sorption capacity reduced by about 7.3 kg t− 1 for each 1% increase in moisture. For CH4, sorption capacity was reduced by about 1.8 kg t− 1 for each 1% increase in moisture.The heat of sorption calculated from the DR model decreased slightly on addition of moisture. One explanation is that water is preferentially attracted to high energy adsorption sites (that have high energy by virtue of their electrostatic nature), expelling CO2 and CH4 molecules.  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.
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   

8.
A detailed geochemical study on river waters of the Australian Victorian Alps was carried out to determine: (i) the relative significance of silicate, carbonate, evaporite and sulfide weathering in controlling the major ion composition and; (ii) the factors regulating seasonal and spatial variations of CO2 consumption via silicate weathering in the catchments. Major ion chemistry implies that solutes are largely derived from evaporation of precipitation and chemical weathering of carbonate and silicate lithologies. The input of solutes from rock weathering was determined by calculating the contribution of halite dissolution and atmospheric inputs using local rain and snow samples. Despite the lack of carbonate outcrops in the study area and waters being undersaturated with respect to calcite, the dissolution of vein calcite accounts for up to 67% of the total dissolved cations, generating up to 90% of dissolved Ca and 97% of Mg. Dissolved sulfate has δ34S values of 16 to 20‰CDT, indicating that it is derived predominantly from atmospheric deposition and minor gypsum weathering and not from bacterial reduction of FeS2. This militates against sulphuric acid weathering in Victorian rivers. Ratios of Si vs. the atmospheric corrected Na and K concentrations range from ~ 1.1 to ~ 4.3, suggesting incongruent weathering from plagioclase to smectite, kaolinite and gibbsite.Estimated long-term average CO2 fluxes from silicate weathering range from ~ 0.012 × 106 to 0.039 × 106 mol/km2/yr with the highest values in rivers draining the basement outcrops rather than sedimentary rocks. This is about one order of magnitude below the global average which is due to low relief, and the arid climate in that region. Time series measurements show that exposure to lithology, high physical erosion and long water–rock contact times dominate CO2 consumption fluxes via silicate weathering, while variations in water temperature are not overriding parameters controlling chemical weathering. Because the atmospheric corrected concentrations of Na, K and Mg act non-conservative in Victorian rivers the parameterizations of weathering processes, and net CO2 consumption rates in particular, based on major ion abundances, should be treated with skepticism.  相似文献   

9.
The rise of large vascular plants during the mid-Paleozoic brought about a major increase in the rates of weathering of silicate minerals that induced a drop in the level of atmospheric CO2 and contributed, via the atmospheric greenhouse effect, to global cooling and the initiation of the most long lived and a really extensive glaciation of the past 550 million years. Sedimentary burial of the microbiologically resistant remains of the plants resulted during the Permo-Carboniferous in both further lowering of CO2 and in elevation of atmospheric O2. Evidence of changes in CO2 and O2 are provided by mathematical models, studies of paleosols, fossil plants, fossil insects, and the effects of modern plants on silicate weathering, and by laboratory studies of the effects of changes in O2 on plants and insects. To cite this article: R.A. Berner, C. R. Geoscience 335 (2003).  相似文献   

10.
Interpretation of carbon dioxide diffusion behavior in coals   总被引：3，自引：1，他引：3  
Storage of carbon dioxide in geological formations is for many countries one of the options to reduce greenhouse gas emissions and thus to satisfy the Kyoto agreements. The CO2 storage in unminable coal seams has the advantage that it stores CO2 emissions from industrial processes and can be used to enhance coalbed methane recovery (CO2-ECBM). For this purpose, the storage capacity of coal is an important reservoir parameter. While the amount of CO2 sorption data on various natural coals has increased in recent years, only few measurements have been performed to estimate the rate of CO2 sorption under reservoir conditions. An understanding of gas transport is crucial for processes associated with CO2 injection, storage and enhanced coalbed methane (ECBM) production.A volumetric experimental set-up has been used to determine the rate of sorption of carbon dioxide in coal particles at various pressures and various grain size fractions. The pressure history during each pressure step was measured. The measurements are interpreted in terms of temperature relaxation and transport/sorption processes within the coal particles. The characteristic times of sorption increase with increasing pressure. No clear dependence of the characteristic time with respect to the particle size was found. At low pressures (below 1 MPa) fast gas diffusion is the prevailing mechanism for sorption, whereas at higher pressures, the slow diffusion process controls the gas uptake by the coal.  相似文献   

11.
Torsion experiments were performed on the Al2SiO5 polymorphs in the sillimanite stability field to determine basic rheological characteristics and the effect of deformation on polymorphic transformation. The experiments resulted in extensive transformation of andalusite and kyanite to sillimanite. No transformation occurred during the hot-press (no deformation) stage of sample preparation, which was carried out at similar P–T conditions and duration as the torsion experiments. Experiments were conducted on fine-grained (< 15 µm) aggregates of natural andalusite, kyanite and sillimanite at 1250 °C, 300 MPa, and a constant shear strain rate of 2 × 10− 4/s to a maximum shear strain of 400%. Electron back-scattered diffraction (EBSD) analysis of the experiments revealed development of lattice-preferred orientations, with alignment of sillimanite and andalusite [001] slightly oblique to the shear plane. The kyanite experiment could not be analyzed using EBSD because of near complete transformation to sillimanite. Very little strain ( 30%) is required to produce widespread transformation in kyanite and andalusite. Polymorphic transformation in andalusite and kyanite experiments occurred primarily along 500 µm wide shear bands oriented slightly oblique and antithetic to the shear plane and dominated by sub-µm (100–150 nm) fibrolitic sillimanite. Shear bands are observed across the entire strain field preserved in the torsion samples. Scanning transmission electron microscope imaging shows evidence for transformation away from shear bands; e.g. fibrolitic rims on relict andalusite or kyanite. Relict grains typically have an asymmetry that is consistent with shear direction. These experimental results show that sillimanite is by far the weakest of the polymorphs, but no distinction can yet be made on the relative strengths of kyanite and andalusite. These observations also suggest that attaining high bulk strain energy in strong materials such as the Al2SiO5 polymorphs is not necessary for triggering transformation. Strain energy is concentrated along grain boundaries, and transformation occurs by a dynamic recrystallization type process. These experiments also illustrate the importance of grain-size sensitive creep at high strains in a system with simultaneous reaction and deformation.  相似文献   

12.
Using a recently developed petrogenetic grid for MORB + H2O, we propose a new model for the transportation of water from the subducting slab into the mantle transition zone. Depending on the geothermal gradient, two contrasting water-transportation mechanisms operate at depth in a subduction zone. If the geothermal gradient is low, lawsonite carries H2O into mantle depths of 300 km; with further subduction down to the mantle transition depth (approximately 400 km) lawsonite is no longer stable and thereafter H2O is once migrated upward to the mantle wedge then again carried down to the transition zone due to the induced convection. At this depth, hydrous β-phase olivine is stable and plays a role as a huge water reservoir. In contrast, if the geothermal gradient is high, the subducted slab may melt at 700–900 °C at depths shallower than 80 km to form felsic melt, into which water is dissolved. In this case, H2O cannot be transported into the mantle below 80 km. Between these two end-member mechanisms, two intermediate types are present. In the high-pressure intermediate type, the hydrous phase A plays an important role to carry water into the mantle transition zone. Water liberated by the lawsonite-consuming continuous reaction moves upward to form hydrous phase A in the hanging wall, which transports water into deeper mantle. This is due to a unique character of the reaction, because Phase A can become stable through the hydration reaction of olivine. In the case of low-pressure intermediate type, the presence of a dry mantle wedge below 100 km acts as a barrier to prevent H2O from entering into deeper mantle.  相似文献   

13.
The change in groundwater chemistry along the groundwater flow path in the Matsumoto tunnel vicinity was studied, and the origin of the groundwater and dissoluted substances was determined. The relationship between the concentration of HCO3 –, Ca2+, and Na+, and CO2 gas pressure in the groundwater indicated that the HCO3 –, Ca2+, and Na+ were produced by the reaction of the CO2 gas in the groundwater and feldspar in the rocks. The relationship between the concentration of NO3 – and the Eh and pH values in the groundwater indicated that in an oxidative condition, ammonia-oxidizing and nitriteoxidizing bacteria used NH4 + and produced NO3 – and H+, and in a reductive condition, denitrifying bacteria used NO3 – and produced N2 gas and OH–. The stable hydrogen and oxygen isotopic ratio in the groundwater and precipitation indicated that the groundwater originated from precipitation that had fallen on the area. The concentration of3H and the stable hydrogen and oxygen isotopic ratios in the groundwater suggested that it has been getting warmer climatically for more than 60 years. The stable carbon isotopic ratio indicated that the HCO3 – in the groundwater, excluding deep well water, originated from CO2 gas produced by organic matter in the soil. The deep well water, which had a higher concentration of HCO3 – than the other groundwater sampled, was thought to have acquired HCO3 – though contact with rocks. The36Cl/Cl ratio indicated the recharge age of the deep well water sampled at a depth of 760 m at the foot of the plateau was recent.  相似文献   

14.
Geological sequestration of CO2 is one of the options studied to reduce greenhouse gas emissions. Although the feasibility of this concept is proven, apart from literature data on modelling still little is known about the CO2–water–rock interactions induced by CO2-injection.To evaluate the effect of CO2–water–rock interactions on three sandstone aquifers in NE-Belgium an experimental setup was built. Eighteen experiments were performed in which sandstones were exposed to supercritical CO2. CO2–water–rock interactions were deduced from the evolution of aqueous concentrations of 25 species and a thorough characterisation of the sandstones before and after treatment. The results show that dissolution of ankerite/dolomite and Al-silicates could enhance porosity/permeability. The observed precipitation of end-member carbonates could increase storage capacity if it exceeds carbonate dissolution. Precipitation of the latter and of K-rich clays as observed, however, can hamper the injection.  相似文献   

15.
A continuously operated gas monitoring station was emplaced within the epicentral area of the NW Bohemian swarm earthquakes overlying directly the active Mariánské Lázně fault. The recordings of 8-month continuous monitoring period are presented. The variations in radon concentrations are similarly to variations in CO2, i.e. CO2 is considered to be the carrier gas for radon. Very small diurnal variations in gas concentration are caused by the earth tides, as daily variations in meteorological conditions cannot explain a short daily minimum at midday times. Sudden changes in gas concentration, which clearly exceed these diurnal variations occur and are always linked with seismic activities. Decreased gas concentration may indicate compression resulting in reduced fault permeability as is implied by negative peaks following local earthquake swarms. A sudden increase in CO2 and Rn concentration may indicate an increased fault permeability caused by stress redistribution, giving rise to opening of migration pathways. This implies a repeatedly sudden rise in gas concentration before local earthquake swarms. Several variations in gas concentration were monitored linked with remote earthquakes of ground motion amplitudes  >1 μm. These seismic events are accompanied by an interference of the diurnal gas concentration–stress-cycle along the Mariánské Lázně fault. However, if shocks of remote earthquake can alter properties of the migrating fluids or the fault properties it can be suggested that these are able to trigger local seismicity, as indicated in the case of the Slovenia earthquake on 12th July 2004.  相似文献   

16.
27Al,29Si MAS NMR studies of kaolinite and its thermal transformation products show that in the kaolinite-mullite reaction series there is an extensive segregation of Al2O3 and SiO2 and the reaction of Al2O3 with SiO2 to form mullite is the main path of mullite formation. At about 850° C, the peak intensity of A1(V) reaches its maximum and with the further rise of temperature the A1(V) signal completely disappears. At about 950°C, γ-Al2O3 accounts for about 71% of the material phases containing Al atoms. In the series there is no obvious presence of Al-Si spinel. The27Al and29Si MAS NMR spectra show that there is an obvious difference between the temperature points for Al-O2(OH)4 octahedral sheet collapsing and Si-O4 tetrahedral sheet breaking down.  相似文献   

17.
Geological sequestration of CO2 is an option for significantly reducing emissions into the atmosphere. Various hydrocarbon companies in western Canada are currently injecting acid-gas (CO2 and H2S) into deep subsurface formations. At West Stoddart, in northeast British Columbia, acid-gas has been injected since 1998 at 1600 m depth into sandstones of the Triassic Halfway Formation, which forms a regional aquifer. A comprehensive subsurface characterization was conducted of the regional and local-scale geology, reservoir characteristics, mineralogy, in situ fluid properties, and hydrogeology. Preliminary results from geochemical and numerical multi-phase flow modelling suggest that the majority of the injected acid-gas will dissolve in the formation water and remain within a radius of a few kilometres of the injection well. The experience with the acid-gas injection at West Stoddart and other operations in the Alberta Basin has shown that the process of large-scale CO2-injection into deep aquifers is technically feasible.  相似文献   

18.
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   

19.
研究了电感耦合等离子体发射光谱同时测定地质样品中次量钨、锡、钼的方法。为了避免基体干扰,采用氢氟酸低温分解试样,蒸干除硅,硅以四氟化硅的形式挥发除去。为了减小盐分,用少量过氧化钠熔融未被分解完全的试样残渣,热水提取,盐酸酸化,电感耦合等离子体发射光谱法同时测定钨、锡、钼。方法相对标准偏差(RSD,n=12)为钨10.80%,锡6.67%,钼8.33%。标准曲线线性浓度上限为:三氧化钨30.0 mg/L,锡40.0 mg/L,钼40.0 mg/L。方法经国家一级标准物质验证,分析结果与标准值相符。  相似文献   

20.
The chemical interaction between fluorine and highly polymerized sodium aluminosilicate melts [Al/(Al+Si)= 0.125–0.250 on the join NaAlO2-SiO2] has been studied with Raman spectroscopy. Fluorine is dissolved to form F– ions that are electrically neutralized with Na+ or Al3+. There is no evidence for association of fluorine with either Si4+ or Al3+ in four-fold coordination and no evidence of fluorine in six-fold coordination with Si4+ in these melt compositions. Upon solution of fluorine nonbridging oxygens are formed and are a part of structural units with nonbridging oxygen per tetrahedral cations (NBO/T) about 2 and 1. The proportions of these two depolymerized units in the melts increase systematically with increasing F/(F+O) at constant Al/(Al+Si) and with decreasing Al/(Al+Si) at constant F/(F+O). Depolymerization (increasing NBO/T) of silicate melts results from a fraction of aluminum and alkalies (in the present study; Na+) reacting to form fluoride complexes. In this process an equivalent amount of Na+ (orginally required for Al-3+charge-balance) or Al3+ (originally required Na+ to exist in tetrahedral coordination) become network-modifiers.The structural data have been used to develop a method for calculating the viscosity of fluorine-bearing sodium aluminosilicate melts at 1 atm. Where experimental viscosity data are available, the calculated and measured values are within 5% of each other.A method is also suggested by which the liquidus phase equilibria of fluorine-bearing aluminosilicate melts may be predicted. In accord with published experimental data it is suggested, for example, that — on the basis of the determined solubility mechanism of fluorine in aluminosilicate melts — with increasing fluorine content of feldspar-quartz systems, the liquidus boundaries between aluminosilicate minerals (e.g., feldspars) and quartz shift away from silica.  相似文献   

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