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1.
This study was aimed at evaluating the mechanical and pH-dependent leaching performance of a mixed contaminated soil treated with a mixture of Portland cement (CEMI) and pulverised fuel ash (PFA). It also sought to develop operating envelopes, which define the range(s) of operating variables that result in acceptable performance. A real site soil with low contaminant concentrations, spiked with 3000 mg/kg each of Cd, Cu, Pb, Ni and Zn, and 10,000 mg/kg of diesel, was treated with one part CEMI and four parts PFA (CEMI:PFA = 1:4) using different binder and water contents. The performance was assessed over time using unconfined compressive strength (UCS), hydraulic conductivity, acid neutralisation capacity (ANC) and pH-dependent leachability of contaminants. With binder dosages ranging from 5% to 20% and water contents ranging from 14% to 21% dry weight, the 28-day UCS was up to 500 kPa and hydraulic conductivity was around 10−8 m/s. With leachant pH extremes of 7.2 and 0.85, leachability of the contaminants was in the range: 0.02–3500 mg/kg for Cd, 0.35–1550 mg/kg for Cu, 0.03–92 mg/kg for Pb, 0.01–3300 mg/kg for Ni, 0.02–4010 mg/kg for Zn, and 7–4884 mg/kg for total petroleum hydrocarbons (TPHs), over time. Design charts were produced from the results of the study, which show the water and/or binder proportions that could be used to achieve relevant performance criteria. The charts would be useful for the scale-up and design of stabilisation/solidification (S/S) treatment of similar soil types impacted with the same types of contaminants. 相似文献
2.
《Chemie der Erde / Geochemistry》2016,76(4):597-604
The objective of this study is to understand cement alteration processes with the evolution of porosity and hardness under geologic CO2 storage conditions. For this study, the cylindrical cement cores (class G) were reacted with CO2–saturated water in a vessel (40 °C and 8 MPa) for 10 and 100 days. After the experiment, the CO2 concentration and Vickers hardness were measured in the hydrated cement core to estimate the carbonation depth and to identify the change in hardness, respectively. Diffusive-reactive transport modeling was also performed to trace the alteration processes and subsequent porosity changes. The results show that cement alteration mainly results from carbonation. With alteration processes, four different reaction zones are developed: degradation zone, carbonation zone, portlandite depletion zone, and unreacted zone. In the degradation zone, the re-dissolution of calcite formed in the carbonation zone leads to the increase of porosity. In contrast, the carbonation zone is characterized by calcite formation resulting mainly from the dissolution of portlandite. The carbonation zone acts as a barrier to CO2 intrusion by consuming dissolved CO2. Especially in this zone, although the porosity decreases, the Vickers hardness increases. Our results show that cement alteration processes can affect the physical and hydrological properties of the hydrated cement under CO2-saturated conditions. Further long-term observation is required to confirm our results under in-situ fluid chemistry of a CO2 storage reservoir. Nonetheless, this study would be helpful to understand alteration processes of wellbore cements under CO2 storage conditions. 相似文献
3.
Cementitious materials will be used for the construction of the engineered barrier of the planned repositories for radioactive waste in Switzerland. Superplasticizers (SPs) are commonly used to improve the workability of concretes and, along with a set accelerator (Acc), to produce shotcrete. In this study the influence of a polycarboxylate- (PCE) and a polynaphthalene-sulphonate-based (PNS) SP on the hydration process, mineral composition and the sorption behaviour of metal cations has been investigated using an ordinary Portland cement (OPC), a low-alkali cement mix (LAC) consisting of CEM III-type cement and nanosilica, and a shotcrete-type cement mix (ESDRED) consisting of a CEM I-type cement and silica fume prepared in the presence of an alkali-free set accelerator.Both the PCE and PNS SP do not significantly influence the amount and quantity of hydrates formed during hydration. The concentration of both SPs decreased rapidly in the early stage of the hydration process for all cements due to sorption onto cement phases. After 28 days of hydration and longer, the concentration of the PNS SP in the pore fluids of all cements was generally lower than that of the PCE SP, indicating stronger uptake of the PNS SP. The formate present in the Acc sorbs only weakly onto the cement phases, which led to higher aqueous concentration of organics in the ESDRED cement than in OPC and LAC.Sorption experiments with 63Ni, 152Eu and 228Th on a cation exchange resin indicate that, at concentrations above 0.1 g L−1, the two SPs could reduce sorption of metal cations. Thermodynamic modelling further indicates that radionuclide complexation by formate at the concentration level in Acc can be excluded, suggesting that the apparent effect of Acc in the sorption measurements on the resin can be attributed to colloids formed owing to the high concentrations of Al and S in Acc. Sorption studies with the same radionuclides on hardened cement paste (HCP) in the presence of concrete admixture solutions and pore fluids squeezed from cement pastes further revealed no significant effect on sorption by either the concrete admixtures or their degradation products that were potentially present in the pore fluids. This finding suggests that the investigated concrete admixtures (PNS, PCE, Acc) and their degradation products have no significant impact on radionuclide mobilisation. 相似文献
4.
Composite Portland cement–basalt caprock cores with fractures, as well as neat Portland cement columns, were prepared to understand the geochemical and geomechanical effects on the integrity of wellbores with defects during geologic carbon sequestration. The samples were reacted with CO2–saturated groundwater at 50 °C and 10 MPa for 3 months under static conditions, while one cement–basalt core was subjected to mechanical stress at 2.7 MPa before the CO2 reaction. Micro-XRD and SEM–EDS data collected along the cement–basalt interface after 3-month reaction with CO2–saturated groundwater indicate that carbonation of cement matrix was extensive with the precipitation of calcite, aragonite, and vaterite, whereas the alteration of basalt caprock was minor. X-ray microtomography (XMT) provided three-dimensional (3-D) visualization of the opening and interconnection of cement fractures due to mechanical stress. Computational fluid dynamics (CFD) modeling further revealed that this stress led to the increase in fluid flow and hence permeability. After the CO2-reaction, XMT images displayed that calcium carbonate precipitation occurred extensively within the fractures in the cement matrix, but only partially along the fracture located at the cement–basalt interface. The 3-D visualization and CFD modeling also showed that the precipitation of calcium carbonate within the cement fractures after the CO2-reaction resulted in the disconnection of cement fractures and permeability decrease. The permeability calculated based on CFD modeling was in agreement with the experimentally determined permeability. This study demonstrates that XMT imaging coupled with CFD modeling represent a powerful tool to visualize and quantify fracture evolution and permeability change in geologic materials and to predict their behavior during geologic carbon sequestration or hydraulic fracturing for shale gas production and enhanced geothermal systems. 相似文献
5.
《Sedimentary Geology》2001,139(3-4):285-317
Petrographic and geochemical data from five localities in the Ziz Valley of Morocco indicate that Jurassic limestones have undergone early diagenesis that varied with location from shelf to basinal settings, burial diagenesis that was most pronounced in basinal settings, and late diagenesis caused by compression and uplift of the High Atlas Mountains.Marine cements occur at all five localities from shelf-to-basin center, although cement types vary from peloidal microcrystalline cements updip on the shelf-to-equant calcite in basinal settings. Presence of moldic grains and/or Mg-poor, Fe-poor blocky cements suggest that meteoric waters influenced early diagenesis at all shelf localities and on an upturned fault block in the basinal region, leaving only one locality unaffected by early meteoric processes. 87Sr/86Sr ratios of 0.70810–0.70895 (greater than 87Sr/86Sr of coeval limestones), Mg contents that decrease upward from 47.5 to 43.0 mol% MgCO3, presence of dolomitized marine cements, and dolomite cements that postdate marine cements but predate meteoric-to-burial cements suggest that dolomitization and dolomite cementation at two shelf localities took place in mixed meteoric and marine waters early in diagenesis. However, poorer preservation of depositional fabrics, lower δ18O values, and larger and more anhedral crystals suggest that dolostones downdip underwent later modification during burial, whereas those updip did not.Compaction during diagenesis generated numerous concavo–convex and sutured intergranular contacts at updip shelf, downdip shelf, and basinal localities where earlier meteoric cementation was not extensive. Compaction was insignificant in more extensively cemented mid-shelf settings. High Sr (1200–3800 ppm) and Fe (1000–2300 ppm) contents in brachiopod grains suggest that LMC components underwent some modification during burial in basinal settings in Sr-rich reducing waters. Fe contents of late intergranular cements increase from 2000 ppm at the basin's edge to as much as 6000 ppm in the basin's center. Bedding-parallel stylolites occur at all localities.The most negative δ18O values of sparry dolomites near the Tizi n'Firest fault (−6.2‰ vs. PDB) imply diagenetic temperatures of 65–85°C assuming water δ18O values of 0.0–2.0‰ vs. SMOW. Those temperatures are much less than previous estimates of burial temperatures in the High Atlas basin. An isotopic gradient extrapolating to roughly 5‰/km in diagenetically modified dolostones likewise suggests a geothermal gradient less than gradients previously proposed for at least parts of the area.Comparison of morphologies of transverse stylolites, which are found at all localities, with morphologies of bedding parallel stylolites suggests that transverse stylolites formed due to compression during late diagenesis. Uplift accompanying that compression allowed influx of low-Mg waters that, along with other factors, caused calcitization of dolomites. The Fe concentration of calcite that fills late fractures increases from less than 2000 ppm at the basin center to values in excess of 3000 ppm at the basin edge, opposite trends in earlier cements and reflecting uplift of the High Atlas Mountains and resultant changes in patterns of groundwater flow. 相似文献
6.
The Upper Paleozoic section contains a tight gas sandstone reservoir (of 2.75 × 1012 m3) in the Ordos Basin, central China. The measured porosities (< 10%) and permeabilities (generally < 1 mD) are the result of significant mechanical and chemical compaction and precipitation of carbonate, quartz and authigenic clay cements. Fluid inclusion geochemistry and kinetic modeling (generation of gaseous components and δ13C1) were integrated to constrain the timing of gas charge into the tight reservoir. The modeling results indicate that the natural gases in the present reservoir are similar to gases liberated from quartz inclusions in both composition and stable carbon isotope values and also similar to gas generated from Upper Paleozoic coal. The similar geochemistry suggests that an important phase of quartz cementation must have occurred after gas emplacement in the reservoirs during regional uplift at the end of the Cretaceous. The latest carbonate cement, postdating quartz cementation, consumed most of the late CO2 generated from coal at high maturity (RO > 1.7%) and reduced the reservoir quality dramatically. On the contrary, tight sandstones from non-producing areas have fluid inclusions that were trapped in quartz cements much earlier. These data indicate that natural gas migrated into the Upper Paleozoic reservoir when it still retained high porosity and permeability. The reservoir continued to experience porosity and permeability reduction from continued quartz and carbonate cementation after gas charging due to low gas saturation. Comparison of the relative timing of gas charging with that of sandstone cementation can help to predict areas of risk during tight gas exploration and development. 相似文献
7.
Trace element contents and distributions in authigenic quartz cement in deeply buried (2500–4000 m) Haushi Group sandstones from wells in Oman have been investigated in order to determine the factors that control trace element uptake during precipitation.Scanning electron microscope-cathodoluminescence images show well developed growth zones within the quartz cement, which correlate with chemical zonations observed in electron microprobe Al distribution maps. The most abundant trace elements are Al (50–3000 μg g?1), Li (1–100 μg g?1), Na (1–40 μg g?1), and Ge (0.3–5 μg g?1) with a strong linear correlation between Li and Al and a weaker one between Ge and Al. The molar concentration of Li (+ Na) accounts only for ~ 15% of the charge compensation for Al3+ substitution of Si4+. Though H was not measured in this study, these data indicate a major role of H in charge balancing Al3+. The samples belong to the same stratigraphic unit and have similar petrography, but show considerable variability in absolute trace element concentrations between different wells. This variability does not correlate with either sample depth or temperature and shows no regional pattern, but seems to reflect petrophysical and tectonic differences within the sedimentary basin.Petrographic observations of the cogenetic mineral assemblages and hydrochemical modelling indicate that a change from the equilibrium assemblage quartz–kaolinite (–dolomite) to quartz–illite (–dolomite) reflects a decrease in the CO2 concentration and concurrent variations of the Al concentration. It is concluded that changes in the CO2 concentrations are responsible for fluctuations in fluid Al concentrations and thus likely also in the investigated quartz cements. 相似文献
8.
With the continuous development of science and technology and the human understanding of the moon, many scientists have planned the creation of a space station on the moon using lunar building materials. Environmental factors mainly include large temperature differentials, and the presence of a hard vacuum on the surface of the moon is a huge challenge for the performance of lunar building materials. Geopolymer materials have the following properties: approximately zero water consumption, resistance to high- and low-temperature cycling, vacuum stability and good mechanical properties. Additionally, they meet most of the requirements for use in the lunar environment. Here, we present a potential lunar cement material that was fabricated using volcanic ash and sodium hydroxide solution as activator, based on geopolymer technology. The compressive strengths of the volcanic ash geopolymer specimens processed for 24 h under vacuum conditions and 30 freeze-thaw cycles in liquid nitrogen are 45.53 and 44.95 MPa, respectively. Additionally, 98.61% of water could be recycled, in consistence with the water recycling-simulated lunar environment in the lab. Although volcanic ash is not equivalent to the lunar soil, we speculate that the alkali activation of lunar soil could be very close to that of volcanic ash because of their similar chemical and mineralogical composition. In summary, this study provides a feasible approach for the development of near-zero water consumption lunar cement materials based on geopolymer technology. 相似文献
9.
The Han-Xing region is located in the south Taihang Mountains (TM) in the central part of the North China Craton, and is an important iron producing area. The iron deposits in this region are of skarn type, related to an Early Cretaceous high-Mg diorite complex, including gabbro diorite, hornblende diorite, diorite, diorite porphyrite, and monzonite. In this study we report the detailed mineral chemistry of the high-Mg diorites and skarn rocks. The olivine in the gabbro diorite shows chemical composition similar to that in mantle peridotite xenoliths. Clinopyroxene in the gabbro diorite is dominantly augite, with only minor diopside, whereas the clinopyroxenes in the diorite and monzonite are diopside. Amphiboles in the high-Mg diorites show compositional range from magnesiohornblende to magnesiohastingsite, with minor pargasite and tschermakite. Most plagioclase in the high-Mg diorite is andesine and oligoclase. The magnesio-biotite in gabbro diorites shows chemical characteristics of re-equilibrated primary biotites and those in calc-alkaline rocks. In the diorite and diorite porphyrite, plagioclase shows complex chemical zoning. Clinopyroxene and garnet in skarn rocks show varying FeO contents, the former containing low FeO (< 9 wt.%) and occurring as the major skarn mineral in large-scale iron deposits, and the latter within small-scale iron deposits with high FeO (mostly > 25 wt.%) content. We computed the pressure, temperature, oxygen fugacity and water contents based on the mineral chemistry of amphibole and biotite. Based on the results, the magma crystallization can be divided into two stages, one within the deep magma chamber, forming clinopyroxene, amphibole and plagioclase phenocrysts; the other after emplacement, forming the rim of phenocrysts and matrix minerals. The magma during the early stage shows high temperature (~ 900 °C–950 °C), pressure (~ 300 MPa–500 MPa), relatively high logfO2 (NNO–NNO + 2), and H2O content in melt (4%–8%). During the late stage, the magma temperature dropped to about 750 °C, and pressure came down to less than 100 MPa, with the logfO2 rising to NNO + 1–NNO + 2.The zoning of amphibole and plagioclase records the process of magma mixing and crystallization, with injection of mafic magma into the felsic magma chamber. The relatively high logfO2 and H2O content inhibited partitioning of iron into mafic minerals and favored concentration of Fe in the melt. Iron ore precipitation occurred when the magma was emplaced at shallow level, and was principally controlled by the chemical composition of carbonate wall rocks. The high logfO2, Fe3 + rich ore-forming fluid generated andradite and clinopyroxene when it reacted with limestone and dolomitic limestone respectively. 相似文献
10.
The relatively stable concentrations of calcium (42.2–122.3 mg/l) and magnesium (48.9–88.1 mg/l) between 2012 and 2013 and their possible weathering paths identified by mass balance models for both soil solutions and stream water from a small salted (regular applications of winter road deicing salt) watershed in New Jersey, USA indicate that the weathering of feldspars and dissolution of carbonates are the primary sources for these cations. However, the relatively stable and lower concentrations of sodium and chloride in soil solutions (19.6–46.1 mg/l for Na and 12.7–88.3 mg/l for Cl) and their fluctuating and higher concentrations in stream water (14.6–103.1 mg/l for Na and 15.2–260.4 mg/l)) from the same watershed during the same period also indicate that road deicing salt is the primary source for sodium and chloride in stream water. Furthermore, positive correlations between calcium and sulfur concentrations (correlation coefficient r = 0.77) and magnesium and sulfur concentrations (r = 0.73) in stream water between 2009 and 2013, as well as positive correlations between sulfur and iron concentrations in soil compositions (r = 0.27), indicate that both the dissolution of gypsum and the oxidation of pyrite into hematite might be the primary sources of sulfate in the watershed. Analyses of water chemistry from the related and much larger Delaware River Watershed (DRW) show that sodium and chloride concentrations have increased steadily (2.7 times for Na and 4.56 times for Cl for 10-year average) due to the regular application of winter deicing salt from 1944 to 2011 for which data are available. The greater increase of stream water chloride concentrations compared with sodium concentrations also results in the steady decline of Na+/Cl− molar ratios from 1.51 to 0.92 for the 10-year average during that time in the DRW and approximately 78% of the chloride in the DRW now being anthropogenic. In addition, the decline of sulfate concentration from 22.08 to 14.59 mg/l (∼34%) for the 10-year average from 1980 to 2011 in the DRW stream water may be attributed to the decline of sulfate levels in atmospheric deposition resulting from enhanced national and state environmental regulations and a shift in local economic activities. There also are more periods of low silica stream water concentrations in the DRW than in the past, perhaps as a result of recent increases in summer stream temperatures combined with an increase of impervious surface area in the region. Warmer stream water might cause the temporary bloom of biota requiring silica, particularly plankton, increasing its uptake from stream water, while an expanded impervious surface area increases the contribution of low-silica runoff water to total stream discharge, thereby lowering the silica concentration in stream water. The combined results of this study illustrate the possible changing anthropogenic factors that can control stream water chemistry in salted watersheds and that these factors need to be taken into account when future water quality regulations and policy are considered. 相似文献
11.
Narraguinnep Reservoir in southwestern Colorado is one of several water bodies in Colorado with a mercury (Hg) advisory as Hg in fish tissue exceed the 0.3 μg/g guideline to protect human health recommended by the State of Colorado. Concentrations of Hg and methyl-Hg were measured in reservoir bottom sediment and pore water extracted from this sediment. Rates of Hg methylation and methyl-Hg demethylation were also measured in reservoir bottom sediment. The objective of this study was to evaluate potential sources of Hg in the region and evaluate the potential of reservoir sediment to generate methyl-Hg, a human neurotoxin and the dominant form of Hg in fish. Concentrations of Hg (ranged from 1.1 to 5.8 ng/L, n = 15) and methyl-Hg (ranged from 0.05 to 0.14 ng/L, n = 15) in pore water generally were highest at the sediment/water interface, and overall, Hg correlated with methyl-Hg in pore water (R2 = 0.60, p = 0007, n = 15). Net Hg methylation flux in the top 3 cm of reservoir bottom sediment varied from 0.08 to 0.56 ng/m2/day (mean = 0.28 ng/m2/day, n = 5), which corresponded to an overall methyl-Hg production for the entire reservoir of 0.53 g/year. No significant point sources of Hg contamination are known to this reservoir or its supply waters, although several coal-fired power plants in the region emit Hg-bearing particulates. Narraguinnep Reservoir is located about 80 km downwind from two of the largest power plants, which together emit about 950 kg-Hg/year. Magnetic minerals separated from reservoir sediment contained spherical magnetite-bearing particles characteristic of coal-fired electric power plant fly ash. The presence of fly-ash magnetite in post-1970 sediment from Narraguinnep Reservoir indicates that the likely source of Hg to the catchment basin for this reservoir has been from airborne emissions from power plants, most of which began operation in the late-1960s and early 1970s in this region. 相似文献
12.
Wildfires transform the landscape, leading to changes in surface cover and, potentially, in water quality. The purpose of this study was to assess changes in the chemical composition of soils and surface water as a result of a wildfire that burned in 2006 in the Marão Mountains, NE Portugal, by comparing pre- and post-fire hydrochemical data and burned/unburned soil data, and to examine the recovery of vegetation over time using Landsat TM imagery. Studies that have access to pre-fire data are rare and even fewer studies document changes in biomass as a result of fire and during the postfire recovery period. Samples of ash, soil and water, from within and outside the burned area, were collected 5 months, and one year after the fire, for chemical analyses. Landsat TM Images were downloaded and transformed into a vegetation index, in order to analyze landcover dynamics and to calculate biomass. The wildfire effects on the Marão River water quality, resulted in an increase in the total mineralization of water. Five months after the wildfire the electrical conductivity (E.C.) at the mainstem was about 56% higher than pre-fire values (E.C. increased from 25 to 39 μS/cm) and still higher one year after (36 μS/cm). Cations of Ca, Na, Mg and Mn showed the greatest increase. This increase was probably triggered by the movement of ash to the watercourses. This disturbance had already attenuated one year after wildfire to values closer to pre-fire data except for manganese. Manganese had anomalous concentrations in the water within the burned area. The concentration of Mn in ash samples reached values up to 5 times more than values found in underlying soils. One year after the wildfire, almost all the burned area had recovered with herbaceous vegetation and patches of shrub vegetation. The wildfire burned 1194.7 dry tons of biomass which means, on average, 4.9 dry ton/ha. Based on the mass of burned biomass, we calculated approximately 350 g/ha of Mn were released as a result of the fire. We suggest that this type of calculation can be conducted before a fire to help resource managers understand worst-case scenarios for changes in water quality that have the potential to affect aquatic biotic and the suitability of water for drinking water purposes and agriculture. 相似文献
13.
Crnac is an intermediate sulfidation Pb–Zn–Ag epithermal deposit located within the Vardar suture zone of the Central Balkan Peninsula. The epithermal Pb–Zn–Ag mineralization consists of (i) a series of steeply-dipping veins hosted within the Jurassic amphibolites, and (ii) overlying hydrothermal-explosive breccia with angular (level IV) or rounded fragments of listwanite (surface) cemented by epithermal mineralization. The mineralization is related to the Oligocene quartz latite dykes that crosscut the Crnac antiform. Quartz latite rocks predominantly display a shoshonitic character. The obtained 40Ar/39Ar age of fresh quartz latite is 28.9 ± 0.3 Ma. Fine-grained sericite from altered quartz latite is dated at 28.6 ± 0.5 Ma. Early, alteration related fluid inclusions within quartz latite show coexistence of high-density brine and a low-density vapor-saturated phase that homogenized at 280–405 °C. Phase separation occurs at a paleodepth of 0.6 to 0.9 km.Epithermal mineralization developed in three stages: (i) early pyrite–arsenopyrite–pyrrhotite–quartz–kaolinite; (ii) main sphalerite–galena–tetrahedrite–chalcopyrite and (iii) late carbonate–pyrite–arsenopyrite assemblage. The onset of mineral deposition within epithermal veins was initiated by boiling of Na–Cl ± K ± Ca ± Mg fluid at a paleodepth of 0.6 to 0.9 km. Coexisting vapor and liquid-rich inclusions display salinities and trapping temperatures of 4 wt.% NaCl equiv., 280–370 °C and 2–27 wt.% NaCl equiv., 230–375 °C, respectively. Boiling continued throughout the deposition of the sphalerite-galena-tetrahedrite-chalcopyrite assemblage. Late stage carbonate was deposited from diluted, non-boiling, low-temperature Na–Ca–Mg–Cl ± CO2 fluid (0.2 to 4.8 wt.% NaCl equiv., 115–280 °C).About 100–150 m higher in the system, precipitation of listwanite breccia cement began as a result of boiling Na–Cl ± Ca ± Mg ± K fluid of medium salinities (2.6 to 12.1 wt.% NaCl equiv.) at temperatures of 245–370 °C. Boiling and dilution of fluids continue throughout the precipitation of the main sphalerite-galena-tetrahedrite and late, mainly carbonate assemblage. Surface listwanite breccia contain quartz phenocrysts deposited from a homogeneous fluid with a medium salinity (8–10 wt.% NaCl equiv.) and high temperatures (Th = 295–315 °C), whereas the early and main stage of a surface listwanite breccia cement precipitated from a boiling fluid of decreasing salinity and temperature. Aqueous ± CO2, high salinity (16 to 18 wt.% NaCl equiv.), low temperature (120 °C), homogeneously trapped fluid that precipitated late stage carbonates, is most likely a remnant of boiled off fluid. The epithermal assemblage of the surface listwanites precipitated at a paleodepth of 0.4 to 0.6 km.The δ13C values of the late stage ankerite range from − 4.2 to 4.1‰, whereas δ18O range from 9.6 to 17.5‰. The calculated δ18O of fluid that precipitated carbonates within epithermal veins, and listwanite breccia cement range from 6.3 to 11.3‰, indicating a contribution of magmatic water.Deposition of all mineralization types was initiated by neutralization of primary acidic magmatic fluid by water-rock reactions that caused widespread propylitization and sericitization. Extensive and long-lasting boiling combined with dilution by meteoric water increased the pH towards the final stage of hydrothermal activity. 相似文献
14.
《Russian Geology and Geophysics》2015,56(6):885-892
Based on the analysis of experimental data on the viscosity of mafic to ultramafic magmatic melts with the use of our structure-chemical model for the calculation and prediction of the viscosity of magmas, we have first predicted that diamond-carryihg kimberlite magma must ascend from mantle to crust with considerable acceleration. The viscosity of kimberlite magma decreases by more than three times during its genesis, evolution, and ascent from mantle to crust despite the significant decrease in the temperature of the ascending kimberlite magma (~ 150 °C) and its partial crystallization and degassing. In the case of partial melting (< 1 wt.%) of carbonated peridotite in the mantle at depths of 250-350 km, high-viscosity (~ 35 Pas) kimberlite melts can be generated at ~ 8.5 GPa and ~ 1350 °C, the water content in the melt being up to ~ 8 wt.%, C(OH-) = 0-2 wt.%, and C(H2O) = 0-6 wt.%. On the other hand, during the formation of kimberlite pipes, dikes, and sills, the viscosity of near-surface kimberlite melts is much lower (~ 10 Pa s) at ~ 50 MPa and 1200 °C, the volume contents of crystals (Vcr) and the fluid phase (bubbles) (Vfl) are 35 and 5 vol.%, respectively, and the water content in magma, C(OH-), is 0.5 wt.%. On the contrary, the viscosity of basaltic magmas increases by more than two orders of magnitude during their ascent from mantle to crust. The basaltic magmas which can be generated in the asthenosphere at depths of ~ 100 km have the minimum viscosity (up to ~ 2.3 Pas) at ~ 4.0 GPa, 1350 °C, C(OH-) - 3 wt.%, and C(H2O) - 5 wt.%. However, at the final stage of evolution (e.g., during volcanic eruptions), the viscosity of basaltic magma is considerably higher (600 Pa s) at ~ 10 MPa, 1180 °C, Vcr - 30 vol.%, Vf - 15 vol.%, and C(OH-) - 0.5 wt.%. 相似文献
15.
Hydrated Portland cement was reacted with CO2 in supercritical, gaseous and aqueous phases to understand the potential cement alteration processes along the length of a wellbore, extending from a deep CO2 storage reservoir to the shallow subsurface during geologic carbon sequestration. The 3-D X-ray microtomography (XMT) images showed that the cement alteration was significantly more extensive with CO2-saturated synthetic groundwater than dry or wet supercritical CO2 at high P (10 MPa)-T (50 °C) conditions. Scanning electron microscopy with energy dispersive spectroscopy (SEM–EDS) analysis also exhibited a systematic Ca depletion and C enrichment in cement matrix exposed to CO2-saturated groundwater. Integrated XMT, XRD and SEM–EDS analyses identified the formation of an extensive carbonated zone filled with CaCO3(s), as well as a porous degradation front and an outermost silica-rich zone in cement after exposure to CO2-saturated groundwater. Cement alteration by CO2-saturated groundwater for 2–8 months overall decreased the porosity from 31% to 22% and the permeability by an order of magnitude. Cement alteration by dry or wet supercritical CO2 was slow and minor compared to CO2-saturated groundwater. A thin single carbonation zone was formed in cement after exposure to wet supercritical CO2 for 8 months or dry supercritical CO2 for 15 months. An extensive calcite coating was formed on the outside surface of a cement sample after exposure to wet gaseous CO2 for 1–3 months. The chemical–physical characterization of hydrated Portland cement after exposure to various phases of CO2 indicates that the extent of cement carbonation can be significantly heterogeneous depending on the CO2 phase present in the wellbore environment. Both experimental and geochemical modeling results suggest that wellbore cement exposure to supercritical, gaseous and aqueous phases of CO2 during geologic C sequestration is unlikely to damage the wellbore integrity because cement alteration by all phases of CO2 is dominated by carbonation reactions. This is consistent with previous field studies of wellbore cement with extensive carbonation after exposure to CO2 for three decades. However, XMT imaging indicates that preferential cement alteration by supercritical CO2 or CO2-saturated groundwater can occur along the cement–steel or cement–rock interfaces. This highlights the importance of further investigation of cement degradation along the interfaces of wellbore materials to ensure permanent geologic carbon storage. 相似文献
16.
《Proceedings of the Geologists' Association. Geologists' Association》2017,128(2):173-179
The concept that Rannoch Moor, the centre of the Younger Dryas (YD), West Highland Icefield, was deglaciated as early as 12.5 cal ka BP is discussed in the light of radiocarbon dates and varve sequences from outlet glaciers of this icefield, and climate change during the YD. The maximum positions of three YD glaciers were reached after 11.6–11.8 cal ka BP (Lomond), and after 11.8–11.9 cal ka BP (Spean and Treig) indicating that ice remained on Rannoch Moor until long after c.12.5 cal ka BP, and possibly until the YD/Holocene transition at c.11.7 cal ka BP. Further, the Spean glacier dammed a proglacial lake in Lochaber for at least 495 varve years over a period that included the deposition of the Vedde Ash (c.12.1 cal ka BP) and a late YD ash layer (c. 11.7–11.2 cal ka BP), a thesis at variance with supposed early YD deglaciation. Recent examination of this issue using 10Be exposure age determinations from Rannoch Moor is equivocal. In view of the presence of hard water algae at the sampling site on Rannoch Moor it is recommended that the ‘early’ 14C dates from Rannoch Moor need to be further reassessed using chronological constraints provided by dated microtephra, and a collaborative radiocarbon dating programme. 相似文献
17.
《Chemical Geology》2007,236(1-2):1-12
The nucleation of H2O bubbles in magmas has been proposed as a trigger for volcanic eruptions. To determine how bubbles nucleate heterogeneously in silicate melts, experiments were carried out in which high-silica rhyolitic melts were hydrated at 800 °C and either 50 or 125 MPa, and then decompressed by 20–91 MPa at temperatures that ranged between 550 and 700 °C, and held at the lower pressures for 10–720 s before being quenched. Bubbles nucleated in number densities (NB) that vary between 3 × 107 and 2 × 108 cm− 3. Blocky shaped magnetite or the ends of needle-shaped hematite acted as sites for nucleation, but only if a minimum super-saturation was exceeded, which increases with increasing melt viscosity. Bubbles did not nucleate along the lengths of hematite needles nor on plagioclase. Both the beginning and ending times of the nucleation event increases with increasing melt viscosity. Using nucleation theory predictions, neither the slower nucleation rates nor the changing activation of nucleation sites can be adequately explained by the differences in temperature, water diffusivity, or viscosity. Instead, the variations in nucleation kinetics are best explained by changes in surface tension between melt and vapor, resulting from the increasing polymerization of the melt at lower temperatures and water contents. Because only ∼ 108 bubbles cm− 3 nucleate on magnetite in the rhyolite melt used, almost regardless of experimental conditions, results from this study may not be directly comparable to vesicle numbers in volcanic pumice of different compositions. 相似文献
18.
The Duolong district in central Tibet hosts a number of porphyry as well as high sulfidation epithermal copper–gold deposits and prospects, associated with voluminous calc-alkaline volcanism and plutonism. In this study, we present new geochronological, geochemical, isotopic and mineralogical data for both economically mineralized and barren porphyritic intrusions from the Duobuza and Naruo porphyry Cu–Au deposits. Zircon U–Pb analyses suggest the emplacement of economically mineralized granodiorite porphyry and barren granodiorite porphyry at Naruo deposit took place at 119.8 ± 1.4 Ma and 117.2 ± 0.5 Ma, respectively. Four molybdenite samples from the Naruo deposit yield an isochron Re–Os age of 119.5 ± 3.2 Ma, indicating mineralization occurred synchronously with the emplacement of the early granodiorite porphyry. At Duobuza deposit, the barren quartz diorite porphyry intruded at 119.5 ± 0.7 Ma, and two economically mineralized intrusions intruded at 118.5 ± 1.2 Ma (granodiorite porphyry) and 117.5 ± 1.2 Ma (quartz diorite porphyry), respectively. Petrographic investigations and geochemical data indicate that all of the porphyritic intrusions were oxidized, water rich, and subduction-related calc-alkaline magmas. Zircons from the porphyritic intrusions have a wide range in the εHf (0–11.1) indicating that they were sourced from mixing of mantle-derived mafic, and crust-derived felsic melts. Moreover, the variation of trace element content of plagioclase phenocrysts indicates that the magma chambers were recharged by mafic magmas.Comparison of the composition of amphibole phenocrysts indicates the porphyry copper–gold mineralization at Duolong was generated in magma chambers at low crystallization temperatures and pressures (754° to 791 °C, 59 M to 73 MPa, n = 8), and under highly oxidizing conditions (ΔNNO 2.2 to 2.7, n = 8). In contrast, barren intrusions were sourced from the magma chambers with higher crystallization temperatures and pressures (816° to 892 °C, 111 to 232 MPa, n = 22) that were less oxidizing (ΔNNO 0.6 to 1.6, n = 22). The requirement for a thermal contrast is supported by the declining of Ti content in magnetite crystals in barren intrusions (12,550 to 34,200 ppm) versus those from economically mineralized intrusions (600 to 3400 ppm). Moreover, the V content in magnetite crystals from economically mineralized intrusions (990 to 2510 ppm) is lower than those recorded from barren intrusions (2610 to 3510 ppm), which might reflect the variation in oxidation state of the magma. The calculated water solubility of the magma forming the economically mineralized intrusions (3.2–3.7 wt%) is lower than that of magma forming the barren intrusions (4.6–6.4 wt%). Based on the chemical–physical characteristics of economically mineralized magma, our study suggests that the development of porphyry Cu–Au mineralization at Duolong was initiated by shallow-level emplacement of a magma that crystallized at lower temperatures and pressures. Experimental studies show that copper and water solubilities in silicate melts decrease with falling temperatures and pressures, indicating metals and ore-forming fluids are more likely to be released from a magma reservoir emplaced at shallow crustal levels. We propose the magnetite might be a convenient exploration tool in the search for porphyry copper mineralization because the variations in Ti and V content of mineral concentrates and rock samples are indicative of barren versus mineralized intrusions. 相似文献
19.
A.C. Rocha-Campos M.A. Basei A.P. Nutman Laura E. Kleiman R. Varela E. Llambias F.M. Canile O. de C.R. da Rosa 《Gondwana Research》2011,19(2):509-523
We present four SHRIMP U–Pb zircon ages for the Choiyoi igneous province from the San Rafael Block, central–western Argentina. Dated samples come from the Yacimiento Los Reyunos Formation (281.4 ± 2.5 Ma) of the Cochicó Group (Lower Choiyoi section: andesitic breccias, dacitic to rhyolitic ignimbrites and continental conglomerates), Agua de los Burros Formation (264.8 ± 2.3 Ma and 264.5 ± 3.0 Ma) and Cerro Carrizalito Formation (251.9 ± 2.7 Ma Upper Choiyoi section: rhyolitic ignimbrites and pyroclastic flows) spanning the entire Permian succession of the Choiyoi igneous province. A single zircon from the El Imperial Formation, that is overlain unconformably by the Choiyoi succession, yielded an early Permian age (297.2 ± 5.3 Ma), while the main detrital zircon population indicated an Ordovician age (453.7 ± 8.1 Ma). The new data establishes a more precise Permian age (Artinskian–Lopingian) for the section studied spanning 30 Ma of volcanic activity. Volcanological observations for the Choiyoi succession support the occurrence of explosive eruptions of plinian to ultraplinian magnitudes, capable of injecting enormous volumes of tephra in the troposphere–stratosphere. The new SHRIMP ages indicate contemporaneity between the Choyoi succession and the upper part of the Paraná Basin late Paleozoic section, from the Irati up to the Rio do Rasto formations, encompassing about 24 Ma. Geochemical data show a general congruence in compositional and tectonic settings between the volcanics and Paraná Basin Permian ash fall derived layers of bentonites. Thickness and granulometry of ash fall layers broadly fit into the depletion curve versus distance from the remote source vent of ultraplinian eruptions. Thus, we consider that the Choiyoi igneous province was the source of ash fall deposits in the upper Permian section of the Paraná Basin. Data presented here allow a more consistent correlation between tectono-volcanic Permian events along the paleo-Pacific margin of southwestern Gondwana and the geological evolution of neighboring Paleozoic foreland basins in South America and Africa. 相似文献
20.
H.T.B.M. Petrus Tsuyoshi Hirajima Yuji Oosako Moriyasu Nonaka Keiko Sasaki Takashi Ando 《International Journal of Mineral Processing》2011,98(1-2):15-23
Cenospheres recovery is one of the coal fly ash beneficiations, providing economic as well as environmental benefits. Current techniques, such as lagoon or other wet-separation processes, consume large amounts of water and add to water pollution due to leaching of toxic materials from fly ash. The other possible disadvantage is the need for a wide operational area, which is unsuitable for densely populated countries. As wet-separation processes have some disadvantages, an improved and/or sustainable alternative recovery technique is required. An air classifier is one of the alternative techniques. In this study, two types of air classifiers, namely a closed-type pneumatic separator and a micron separator, have been investigated. In terms of separation efficiency, it was found that the micron separator has the potential to be applied in cenospheres recovery from coal fly ash, giving a Newton's efficiency of 0.44, as compared to a value of about 0.26 for the closed-type pneumatic separator. The cenospheres recoveries of both pieces of equipment at their optimum Newton's efficiencies were similar at over 60 wt.%. The separation performance was further assessed from the particle distributions of the overflow and underflow products obtained from both pieces of equipment, as well as from SEM images. It was found that the lower Newton's efficiency of the closed-type pneumatic separator was due to the re-concentration of fine particles in the underflow product at air-flow rates higher than 2.2 m/s (the underflow product yield was about 55 wt.%).In order to further confirm the applicability of this technique, the micron separator, which had provided higher separation efficiency and cenospheres recovery, was deployed in a cenospheres recovery unit prior to the use of a wet-separation process (float and sink tank). About 80% of the cenospheres was recovered, with an 87.8% reduction in the total mass of fly ash to be separated in the float and sink tank. Consequently, much less water was needed for the process of cenospheres recovery. Moreover, it was also confirmed that the micron separator could yield higher quality fly ashes, that is, fly ash types I and II, from lower feed quality of fly ash type IV, which is the lowest category in commercial classification of fly ash according to JIS A6201. 相似文献