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1.
Iron filling and iron filling–cement mixture were used to improve the shear strength characteristics of Irbid clayey soil. For this purpose, five types of Irbid clay soils were obtained and mixed with iron filling and iron filling–cement mixture at different percentages. Two sets of prepared samples were mixed with the admixture. The first set was prepared by mixing the soil samples with iron filling alone at 2.5, 5.0, 7.5, and 10% by dry weight of the soil. The second set was prepared by mixing with iron filling–cement mixture at equal ratio of the same percentages of the first set. An unconfined compression test was performed in this study to measure the shear strength properties of the soils. The test results showed that the increase in the percentages of the iron filling and iron filling–cement mixture up to 10% will result in increasing the maximum dry density of the soil and increase the unconfined compressive strength and the secant of modulus of elasticity of the clayey soil. Also, the addition of iron filling–cement mixture increased the unconfined compressive strength and secant modulus of elasticity of the clayey soil higher than the addition of iron filling alone.  相似文献   

2.
Abundant iron oxide deposits including banded iron formations, apatite iron oxide ores, and enigmatic marble/skarn-hosted magnetite deposits occur in the Palaeoproterozoic Bergslagen region, southern Sweden. During the last 100 years, the latter deposit class has been interpreted as contact metasomatic skarn deposits, metamorphosed iron formations, or metamorphosed carbonate replacement deposits. Their origin is still incompletely understood. At the Smältarmossen mine, magnetite was mined from a ca. 50-m-thick calcic skarn zone at the contact between rhyolite and stratigraphically overlying limestone. A syn-volcanic dacite porphyry which intruded the footwall has numerous apophyses that extend into the mineralized zone. Whole-rock lithogeochemical and mineral chemical analyses combined with textural analysis suggests that the skarns formed by veining and replacement of the dacite porphyry and rhyolite. These rocks were added substantial Ca and Fe, minor Mg, Mn, and LREE, as well as trace Co, Sn, U, As, and Sr. In contrast, massive magnetite formed by pervasive replacement of limestone. Tectonic fabrics in magnetite and skarn are consistent with ore formation before or early during Svecokarelian ductile deformation. Whereas a syngenetic–exhalative model has previously been suggested, our results are more compatible with magnetite formation at ca. 1.89 Ga in a contact metasomatic skarn setting associated with the dacite porphyry.  相似文献   

3.
The inner nebula out to ~3 A.U. was depleted in volatile elements that included potassium and manganese at a very early stage of solar-system history. The inner planets and many meteorites inherited this element signature, the cause of which probably was early violent solar activity. Because of this evidence for elemental depletions correlated with volatility, one might also expect to find examples of fractionation, particularly among lower mass elements. Here we discuss the search for such effects among the isotopes of K, Mg, Si, and Ca in a wide variety of terrestrial, lunar, and meteoritic samples. We examine examples of vaporization without isotope fractionation, and a comparison of the effects expected between distillation and condensation. Effects attributable both to evaporation and condensation are observed in refractory inclusions (CAIs) in meteorites and reflect localized events in the early nebula. However, the lack of isotopic fractionation that is observed among a wider variety of presolar-system materials rules out the general operation of Rayleigh-type fractionation on primitive solar-nebular material. We conclude with a discussion of volatileelement behavior during the giant Moon-forming impact that shows that the material in the Moon was not subjected to Rayleigh-type distillation.  相似文献   

4.
5.
Immobilization of trace elements in contaminated soils by zero-valent iron (ZVI) is a promising remediation method, but questions about its long-term performance remain unanswered. To quantify immobilization and predict possible contaminant remobilization on long timescales detailed knowledge about immobilization mechanisms is needed. This study aimed at assessing the long-term effect of ZVI amendments on dissolved copper and arsenic in contaminated soils, at exploring the immobilization mechanism(s), and at setting up a geochemical model able to estimate dissolved copper and arsenic under different scenarios. Samples from untreated and ZVI-treated plots in two field experiments where ZVI had been added 6 and 15 years ago were investigated by a combination of batch experiments, geochemical modeling and extended X-ray absorption fine structure (EXAFS) spectroscopy. Dissolved copper and arsenic concentrations were described by a multisurface geochemical model with surface complexation reactions, verified by EXAFS. The ZVI remained “reactive” after 6–15 years, i.e. the dissolved concentrations of copper and arsenic were lower in the ZVI-treated than in the untreated soils. There was a shift in copper speciation from organic matter complexes in the untreated soil to surface complexes with iron (hydr)oxides in the ZVI-treated soil. The pH value was important for copper immobilization and ZVI did not have a stabilizing effect if pH was lower than about 6. Immobilization of arsenic was slightly pH-dependent and sensitive to the competition with phosphate. If phosphate was ignored in the modeling, the dissolution of arsenate was greatly underestimated.  相似文献   

6.
The phase relations of Fe-6.4 wt% Si and Fe-9.9 wt% Si have been investigated up to 130 GPa and 2,600 K based on in situ synchrotron X-ray diffraction measurements in a laser-heated diamond-anvil cell along with chemical analysis of the quenched samples using a field-emission electron probe microanalyzer. We found that the maximum solubility of silicon in solid hcp-iron increases with increasing pressure. Linear extrapolation of the phase boundary between hcp + B2 and hcp phases for Fe-9.9 wt% Si suggests that the solid hcp-iron can include more than 9.9 wt% Si at the Earth’s inner-core conditions. If silicon is a major light element in the outer core, a substantial amount of silicon may be incorporated into the inner core during inner-core solidification.  相似文献   

7.
8.
In consideration of the poor correlation between soil and plant nutrient levels, biogeochemists often focus on nutrient stoichiometry, which is mostly used in ecology to indicate the limitation of nutrients in environments. The previous work indicated that the studies of nutrient cycles must go beyond linkage between environmental conditions and plant nutrient concentrations to consider plant internal processes such as growth and nutrient stoichiometry. The plant species composition in calcareous soils with higher pH, generally to be considered P-limited conditions, is expected to differ from that in acidic soils. Many vascular plant species are unable to colonize limestone soils. Thus, floristic composition and soil properties of adjacent limestone and sandstone altitudinal gradients differ greatly in Southwest China. Until now, mechanisms regulating this differing ability of plants to colonize limestone sites have not been elucidated. It is reported that the inability of many plants to establish in limestone sites seems to be related to a low capacity of such plants to solubilize phosphate from these soils. It is reported that the toxicity of manganese and the deficiency of iron were also closely correlated with floristic compositions. We focus on whether similar trends of nutrient distributions occur across different experimental plots during legume growing,  相似文献   

9.
The Dahongshan iron deposit is hosted in the Paleoproterozoic submarine metavolcanic rocks of the Dahongshan Group in the Yangtze Block, South China. LA-ICP-MS dating of hydrothermal zircon grains from the genetically associated albitite and dolomite albitite show ca. 2008 Ma ages that are consistent with the zircon ages from the host metavolcanic rocks (ca. 2012 Ma), and postdated the post-ore diabase dike (ca. 1724 Ma), marking the Dahongshan iron deposit as the oldest submarine volcanic-hosted deposit so far as known. The ore-hosting metavolcanic rocks in the Dahongshan deposit have low Ni (9.1–77.4 ppm), Cr (1.0–63.0 ppm) and Co contents (5.6–62.9 ppm), suggesting the fractionation of olivine, clinopyroxene and plagioclase within the magma chamber. The major and trace element features of the alkaline to tholeiitic metavolcanic rocks are consistent with high-degree partial melting of the mantle wedge metasomatized by melts enriched in high field strength elements (HFSEs), which were derived from the subducted slab in volcanic arc setting. Based on an evaluation of the morphology of orebody, ore fabrics, petrology and melt-fluid inclusions, as well as the geochemical characteristics of the major ore mineral (magnetite), we correlate the iron mineralization in the Dahongshan deposit with hydrothermal process induced by the high-temperature, high-salinity and Fe-rich brines derived through magmatic exsolution. The similar characteristic of Ce and Eu anomalies of the Dahongshan iron deposit and banded iron formations (BIFs) suggest that the Dahongshan deposit was formed in reducing environment, although the two types of iron ores were generated through distinct processes with hydrothermal processes dominating for the submarine volcanic-hosted iron deposits whereas the BIFs were formed through chemical precipitation.  相似文献   

10.
Although nitrogen in the Earth’s interior has attracted significant attention recently,it remains the most enigmatic of the light elements in the Earth’s core.In this work,synchrotron X-ray diffraction(XRD)and electrical conductivity experiments were conducted on iron nitrides(Fe2N and Fe4N)in diamond anvil cells(DACs)up to about 70 GPa at ambient temperature.These results show that iron nitrides are stable up to at least 70 GPa.From the equation of state(EOS)parameters,iron nitrides are more compressible than iron carbides.Moreover,using the van der Pauw method and Wiedemann-Franz law,the electrical and thermal conductivity of samples were determined to be much lower than that of iron carbides.The conductivities of Fe2N and Fe4N were similar at 20–70 GPa,suggesting no evident effects by varying the N stoichiometries in iron nitrides.Iron nitrides are less dense and conductive but more compressible than carbides at 0–70 GPa.This study indicates that less nitrogen than carbon can explain geophysical phenomena in the deep Earth,such as the density deficit.  相似文献   

11.
Several major iron deposits occur in the Quadrilátero Ferrífero (QF), southeastern region of Brazil, where metamorphosed and heterogeneously deformed banded iron formation (BIF) of the Cauê Formation, regionally called itabirite, was transformed into high- (Fe >64%) and low-grade (30%?2O3, with a higher amount of detrimental impurities, especially MnO, in the soft ore. Both hard and soft ores are depleted in trace elements. The high-grade ores at the Águas Claras Mine have at least a dual origin, involving hypogene and supergene processes. The occurrence of the hard, massive high-grade ore within “fresh” dolomitic itabirite is evidence of its hypogene origin. Despite the contention about the origin of the dolomitic itabirite (if this rock is a carbonate-rich facies of the Cauê Formation or a hematite–carbonate precursor of the soft high-grade ore), mineralogical and geochemical features of the soft high-grade ore indicate that it was formed by leaching of dolomite from the dolomitic itabirite by meteoric water. The comparison of the Águas Claras, Capão Xavier and Tamanduá orebodies shows that the original composition of the itabiritic protore plays a major role in the genesis of high- and low-grade soft ores in the QF. Under the same weathering and structural conditions, the dolomitic itabirite is the more favorable to form high-grade deposits than siliceous itabirite. Field relations at the Águas Claras and Capão Xavier deposits suggest that it is not possible to form huge soft high-grade supergene deposits from siliceous itabirite, unless another control, such as impermeable barriers, had played an important role. The occurrence in the Tamanduá Mine of a large, soft, high-grade orebody formed from siliceous itabirite and closely associated with hypogene hard ore suggests that large, soft, high-grade orebodies of the Quadrilátero Ferrífero, which occur within siliceous itabirite, have a hypogene contribution in their formation.  相似文献   

12.
Biological iron and manganese removal utilizing indigenous iron and manganese oxidizing bacteria (IRB hereafter) in groundwater can also be applied to arsenic removal according to our pilot-scale test. The arsenic removal probably occurred through sorption and complexation of arsenic to iron and manganese oxides formed by enzymic action of IRB. We investigated the chemical properties of iron and manganese oxides in IRB floc and the valence state of arsenic sorbed to the floc to clarify the mechanisms of the arsenic [especially As (Ⅲ)] removal. The floc samples were collected from two drinking water plants using IRB (Jyoyo and Yamatokoriyama, Japan), and our pilot - scale test site where arsenic and iron removal using IRB is under way (Mukoh, Japan). The Jyoyo and Yamatokoriyama IRB floc samples were subjected to As (Ⅲ) and As(Ⅴ) sorption experiments. The elemental composition of the floc samples was measured. XANES spectra were collected on As, Fe and Mn K-edges at synchrotron radiation facility Spring 8 (Hyogo, Japan). FT-IR and the X-ray diffraction spectra of the samples were also obtained. The IRB floc contained ca. 35 % Fe, 0.3%-3.5% Mn and 2%-6% P. The samples were highly amorphous and contained ferrihidrites and hydrated iron phosphate. According to XANES analyses of IRB, As associated with IRB was in +5 valence state when As (Ⅲ) (or As (Ⅴ)) was added in laboratory sorption test, Fe in +3 valence state, and Mn a mixture of+3 and +4 valence states. Small shift was observed in the XANES spectra of IRB on As K-edge as the equilibration time of the sorption experiment was increased. Gradual oxidation of a small amount of As (Ⅲ) associated with IRB or change in arsenic binding with sorption site were the probable mechanism.  相似文献   

13.
The role of siderite in Phanerozoic and Precambrian iron formations is discussed. Various types of iron formations are characterized, and their place in the evolution of sedimentary iron ore deposition is outlined. In Precambrian iron ore deposition, siderite is a primary mineral, whereas in Phanerozoic iron formations it becomes a secondary mineral and is commonly related to diagenetic and catagenetic processes.  相似文献   

14.
Hematite is an important iron oxide mineral in loess-paleosol sequences in central China. Investigation of the mineralogical characteristics, genetic mechanism and relationship of hematite with other iron oxides and Fe-bearing minerals will help understand the geochemical process before and after eolian deposit, paleocliamte significance of magnetic susceptibility and reconstruct paleoclimate in central China. So, hematite and related minerals of the loess and paleosol units from Chinese Loess Plateau were investigated using optical microscope, X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission microscopy (HRTEM). The results show that there are five genetic types of hematite in loess-paleosol sequences of central China: (1) weathering of Fe-bearing silicate minerals, for instance, chlorite, will release iron that is precipitated as aggregates of hematite nano-crystals on mineral surfaces; (2) hematite combined with eolian magnetite grains that resulted from partial oxidation of magnetite, even though the partial oxidation may occur in the original area; (3) phase transformation from eolian goethite to hematite; (4) hematite formed on the edge and surface of maghemite because of dissolution and hematite recrystallization; and (5) eolian detrial hematite. The hematite formed from chemical weathering of Fe-bearing silicates with nanoporous texture because of dehydration from iron hydroxide is the most important genetic mechanism. It is proposed that the fact that hematite was formed from chemical weathering of Fe-bearing silicates is a main reason for the redness in paleosol units. However, too intense pedogenesis and high amounts of precipitation will promote oxidation of eolian magnetite and maghemite dissolution, which may result in the decreasing of magnetic susceptibility.  相似文献   

15.
The advent of iron metallurgy changed the course of prehistoric Thailand. There is, however, little information on the nature of iron production and the extent to which locally abundant and easily quarried lateritic iron may have been the ore source. For northeast Thailand archaeological sites, the presence of both iron slag and laterite iron nodules within and surrounding these sites has widely been assumed to represent localized smelting using locally sourced iron ore. This interpretation is, however, based on untested laterite‐equals‐ore and slag‐equals‐smelting equations. This paper tests these assumptions by examining the chemistry of the lateritic iron nodules from two archaeological sites. At one site, the laterite is not a credible ore source and iron working probably comprised only smithing. Local laterite at the other site may be a usable ore. We conclude that, in northeast Thailand, the use of local laterite as an ore source cannot be assumed and that presence of both laterite and slag is not necessarily evidence for prehistoric smelting. © 2010 Wiley Periodicals, Inc.  相似文献   

16.
Mineralogy and Petrology - Uranium–lead isotopes and trace elements of titanite from the Chengchao iron skarn deposit (Daye district, Eastern China), located along the contact zones between...  相似文献   

17.
Archaean–Paleoproterozoic foliated amphibole-gneisses and migmatites interstratified with amphibolites, pyroxeno-amphibolites and REE-rich banded-iron formations outcrop at Mafé, Ndikinimeki area. The foliation is nearly vertical due to tight folds. Flat-lying quartz-rich mica schists and quartzites, likely of Pan-African age, partly cover the formations. Among the Mafé BIFs, the oxide BIF facies shows white layers of quartz and black layers of magnetite and accessory hematite, whereas the silicate BIF facies is made up of thin discontinuous quartz layers alternating with larger garnet (almandine–spessartine) + chamosite + ilmenite ± Fe-talc layers. REE-rich oxide BIFs compositions are close to the East Pacific Rise (EPR) hydrothermal deposit; silicate BIFs plot midway between EPR and the associated amphibolite, accounting for a contamination by volcanic materials, in addition to the hydrothermal influence during their oceanic deposition. The association of an oceanic setting with alkaline and tholeiitic magmatism is typical of the Algoma-type BIF deposit. The REE-rich BIFs indices recorded at Mafé are interpreted as resulting from an Archaean–Paleoproterozoic mineralization.  相似文献   

18.
Spectra of the REE distribution in the Quaternary–Recent peat bog ore of southern Karelia and Leningrad region are characterized by LaN/YbN < 1.0, presence of positive Eu and negative Ce anomalies, and higher Y enrichment (relative to Ho and Dy) because of the REE sorption by Fe-bearing minerals in acid boggy waters. The 87Sr/86Sr ratio is 0.7175 in iron oxyhydroxides of the Somino deposit (Leningrad region) and 0.7283 in the Polovinkino ore (southern Karelia). The 143Nd/144Nd ratio in them is 0.511844 and 0.511617, respectively.  相似文献   

19.
Manganese and iron are essential nutrients at low doses. However, long-term exposure in high doses may be harmful. Human activities and natural sources are responsible for manganese and iron contamination in water. This study aimed to investigate the source of high manganese and iron contents in shallow groundwater, where the groundwater is used for drinking purpose, and to decrease the excess manganese and iron from shallow groundwater. Based on the on-site analytical results taken from the wells in the study area, iron contents in water samples varied between 30 and 200 μg/L, which were under the allowable limits of Turkish Drinking Water Standards (TDWS) (Water intended for human consumption, http://rega.basbakanlik.gov.tr/eskiler/2005/02/20050217-3.htm, 2005). However, manganese levels varied from 30 to 248 μg/L, which some of them are higher than the allowable limits of TDWS (Water intended for human consumption, http://rega.basbakanlik.gov.tr/eskiler/2005/02/20050217-3.htm, 2005) (50 μg/L), and EPA (http://water.epa.gov/drink/contaminants/index.cfm, 2006) (50 μg/L). The source of excess manganese is originated mainly from geogenic source besides Porsuk River interaction in shallow aquifer in the specific section of the study area. To decrease high manganese content from the well water and reservoir water, laboratory and in situ treatment tests were applied. Among these tests, chlorination, associated with filtration (by fine sand, active carbon and zeolite) and the use of different filtration procedures by cation exchange resin were determined as the most effective methods, which was not previously applied on-site as a combinative approaches to reduce the excess manganese in water.  相似文献   

20.
Rietveld refinement of X-ray synchrotron data was performed for two synthetic tetrahedrite samples, with 0.61 and 1.83 Fe atoms, and two synthetic tennantite samples with 0.10 and 1.23 Fe atoms p.f.u. M12(Sb,As)4S13. Measurements were performed at 25 and 250°C. For both the phases, increased Fe substitution is reflected in the increased tetrahedral ‘Cu1’–S distance (‘Cu1’ is a site of Fe substitution) and Cu2–S distances. Cu2 was refined as a split position; the Cu2–Cu2 split about the plane of the S12S2 triangle is about 0.56 and 0.65 Å for tetrahedrite and tennantite, respectively. Cu2–Cu2 distances in the structure cavity are 2.8–2.9 Å. Between 25 and 250°C, the lattice parameter a increased by 0.02–0.04 Å and the interatomic distances by 0.01 Å on an average. Thermal expansion coefficients of little-substituted samples are similar to those of unsubstituted samples, whereas thermal expansion appears to decrease with increasing substitution by Fe. The Cu2–Cu2 split increases at 250°C by about 0.1 Å for tetrahedrite and by more than 0.15 Å for tennantite but the cage expansion is minimal so that the Cu2–Cu2 distances in the cavity decrease with temperature. Difference Fourier maps indicate that there is little residual electron density left between the two Cu2 half-sites in tetrahedrite but this inter-site density is substantially higher in tennantite. It increases with temperature, especially in the little-substituted tennantite sample.  相似文献   

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