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1.
In recent years, most of domestic and foreign researches about heavy metal pollutions of metal mine mainly focus on water, soil and plants on the surface. There is lack of researches about heavy metal pollution in groundwater of metal mine. In this research, a certain antimony mine area is selected as a typical study area. Also, the study about statistical characteristics of heavy metals in groundwater has been carried out. Furthermore, the interrelationships have been preliminarily discussed through related analysis, such as relevant analysis, cluster analysis and principle component analysis. The results show that: the excessive elements in groundwater of study area are Sb, As, Pb, Se, and Ni. The average mass concentration of Sb, As, and Pb is higher than that of drinking water standards (GB5749-2006). The concentration of most heavy metals in dry season is lower than or equal to that in wet season for groundwater. Zn is the only metal in groundwater showing a different pattern, the concentration of which in dry season is higher than that in wet season. Under the impacts of stratum leaching and absorption effect, the concentration of heavy metals (except Pb and Ba) in groundwater are lower than or equal to that in surface water. As and Se, the two heavy metals have a significant positive correlation, which shows the two elements might have gone through similar environmental geochemical effect. Also, the connection among Zn, Hg, Pb, and Mn is not obvious; therefore, the sources of those elements are quite different. In addition, the elements of Se and As have obvious positive interrelationship with elements of CO32- and F-. Also, the Pb has significant positive correlation with PO43-, H2SiO3 and oxygen consumption. The results of cluster analysis show that 9 different heavy metals in the study area can be divided into 3 categories: Zn, Cd, Mn, Hg, Cu, and Cr belong to the first category, Se and As belong to the second one, and the last category is Pb. Also, the principle component analysis divides 6 heavy metals (Zn, As, Hg, Pb, Mn, and Se) into 4 different principle components, which can be utilized to assess heavy metals pollution situations in groundwater. The reliability of this method is higher than 91%. Moreover, the research provides theory basis and models for establishing evaluation index system and exploring the evaluation method of heavy mental pollution in groundwater. 相似文献
2.
Authigenic pyrite grains from a section of the Lower Toarcian Posidonia Shale were analysed for their trace‐element contents and sulphur‐isotope compositions. The resulting data are used to evaluate the relationship between depositional conditions and pyrite trace‐element composition. By using factor analysis, trace‐elements in pyrite may be assigned to four groups: (i) heavy metals (including Cu, Ni, Co, Pb, Bi and Tl); (ii) oxyanionic elements (As, Mo and Sb); (iii) elements partitioned in sub‐microscopic sphalerite inclusions (Zn and Cd); and (iv) elements related to organic or silicate impurities (Ga and V). Results indicate that trace‐element contents in pyrite depend on the site and mechanism of pyrite formation, with characteristic features being observed for diagenetic and syngenetic pyrites. Diagenetic pyrite formed within anoxic sediments generally has a high heavy metals content, and the degree of pyritization of these elements increases with increasing oxygen deficiency, similar to the degree of pyritization of reactive Fe. The highest gradient in the increase of the degree of trace element pyritization with bottom‐water oxygenation was found for the elements Ni < Cu < Mo = As < Tl. In contrast, syngenetic pyrite formed within a euxinic water column typically is enriched in As, Mo and Sb, but is low in heavy metals, and the geochemical variation reflects changes in sea water composition. 相似文献
3.
云浮黄铁矿利用过程中微量毒害元素的环境化学活动性 总被引：13，自引：3，他引：13
为了解云浮黄铁矿利用过程中微量毒害元素的环境地球化学行为，客观评价它们对环境质量的影响，利用元素结合形态的连续提取实验方法，分析了云浮黄铁矿及其工业废渣中Co,Ni,Cu,Zn,As,Se,Cd,Sn,Sb,Pb和Tl等11种毒害元素的形态及化学活动性。结果表明，黄铁矿中大部分微量毒害元素都有着极强的化学活动性，各元素活动态浸出比例依次为Co96.3%,Se91.9%,Cu90.3%,Cd90.0%,Pb89.7%,Zn88.6%,Sb82.5%,Ni80.6%，Sn70%,Tl55.1%和As31.9％，元素As和Tl主要赋存于硫化物和硅酸盐矿物相中，另有少量的Cu,Pb和Sb可能赋存于碳酸盐矿物相中，其他元素则主要赋存于硫化物矿物相中。与黄铁矿相比，飞灰和灰渣中各元素可交换态和碳酸盐结合态所占的比例明显减少。废渣中各元素的化学活动性表现出很大的差别，其中Cu,Zn和Cd的化学活动性最强，活性态浸出比例在90％以上；其次是Co,Ni,Se,Pb和Tl，浸出比例在50％左右；Sb,As和Sn的稳定性较高，浸出比例分别为1％、5％和14％左右；飞灰中微量毒害元素的活动性均高于灰渣。 相似文献
4.
《Ore Geology Reviews》2011,43(1):32-46
Hydrothermal pyrite contains significant amounts of minor and trace elements including As, Pb, Sb, Bi, Cu, Co, Ni, Zn, Au, Ag, Se and Te, which can be incorporated into nanoparticles (NPs). NP-bearing pyrite is most common in hydrothermal ore deposits that contain a wide range of trace elements, especially deposits that formed at low temperatures. In this study, we have characterized the chemical composition and structure of these NPs and their host pyrite with high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), analytical electron microscopy (AEM), and electron microprobe analysis (EMPA). Pyrite containing the NPs comes from two types of common low-temperature deposits, Carlin-type (Lone Tree, Screamer, Deep Star (Nevada, USA)), and epithermal (Pueblo Viejo (Dominican Republic) and Porgera (Papua New-Guinea)).EMPA analyses of the pyrite show maximum concentrations of As (11.2), Ni (3.04), Cu (2.99), Sb (2.24), Pb (0.99), Co (0.58), Se (0.2), Au (0.19), Hg (0.19), Ag (0.16), Zn (0.04), and Te (0.04) (in wt.%). Three types of pyrite have been investigated: “pure” or “barren” pyrite, Cu-rich pyrite and As-rich pyrite. Arsenic in pyrite from Carlin-type deposits and the Porgera epithermal deposit is negatively correlated with S, whereas some (colloform) pyrite from Pueblo Viejo shows a negative correlation between As + Cu and Fe. HRTEM observations and SAED patterns confirm that almost all NPs are crystalline and that their size varies from 5 to 100 nm (except for NPs of galena, which have diameters of up to 500 nm). NPs can be divided into three groups on the basis of their chemical composition: (i) native metals: Au, Ag, Ag–Au (electrum); (ii) sulfides and sulfosalts: PbS (galena), HgS (cinnabar), Pb–Sb–S, Ag–Pb–S, Pb–Ag–Sb–S, Pb–Sb–Bi–Ag–Te–S, Pb–Te–Sb–Au–Ag–Bi–S, Cu–Fe–S NPs, and Au–Ag–As–Ni–S; and (iii) Fe-bearing NPs: Fe–As–Ag–Ni–S, Fe–As–Sb–Pb–Ni–Au–S, all of which are in a matrix of distorted and polycrystalline pyrite. TEM-EDX spectra collected from the NPs and pyrite matrix document preferential partitioning of trace metals including Pb, Bi, Sb, Au, Ag, Ni, Te, and As into the NPs. The NPs formed due to exsolution from the pyrite matrix, most commonly for NPs less than 10 nm in size, and direct precipitation from the hydrothermal fluid and deposition into the growing pyrite, most commonly for those > 20 nm in size. NPs containing numerous heavy metals are likely to be found in pyrite and/or other sulfides in various hydrothermal, diagenetic and groundwater systems dominated by reducing conditions. 相似文献
5.
Bo Peng Xiaoyan Tang Changxun Yu Shurong Xie Meilian Xiao Zhi Song Xianglin Tu 《Environmental Geology》2009,57(2):421-434
The acid mine drainage (AMD) discharged from the Hejiacun uranium mine in central Hunan (China) was sampled and analyzed using
ICP-MS techniques. The analyzing results show that the AMD is characterized by the major ions FeTotal, Mn, Al and Si, and is concentrated with heavy metals and metalloids including Cd, Co, Ni, Zn, U, Cu, Pb, Tl, V, Cr, Se,
As and Sb. During the AMD flowing downstream, the dissolved heavy metals were removed from the AMD waters through adsorption
onto and co-precipitation with metal-oxhydroxides coated on the streambed. Among these metals, Cd, Co, Ni, Zn, U, Cu, Pb and
Tl are negatively correlated to pH values, and positively correlated to major ions Fe, Al, Si, Mn, Mg, Ca and K. The metals/metalloids
V, Cr, Se, As and Sb are conservative in the AMD solution, and negatively-correlated to major ions Na, Ca and Mg. Due to the
above different behaviors of these chemical elements, the pH-negatively related metals (PM) and the conservative metals (CM)
are identified; the PM metals include Cd, Co, Ni, Zn, U, Cu, Pb and Tl, and the CM metals V, Cr, Se, As and Sb. Based on understanding
the geochemistry of PM and CM metals in the AMD waters, a new equation: EXT = (Acidity + PM)/pH + CM × pH, is proposed to
estimate and evaluate extent of heavy-metal pollution (EXT) of AMD. The evaluation results show that the AMD and surface waters
of the mine area have high EXT values, and they could be the potential source of heavy-metal contamination of the surrounding
environment. Therefore, it is suggested that both the AMD and surface waters should be treated before they are drained out
of the mine district, for which the traditional dilution and neutralization methods can be applied to remove the PM metals
from the AMD waters, and new techniques through reducing the pH value of the downstream AMD waters should be developed for
removal of the CM metals. 相似文献
6.
The Bent Hill massive sulfide deposit and ODP Mound deposit in Middle Valley at the northernmost end of the Juan de Fuca Ridge are two of the largest modern seafloor hydrothermal deposits yet explored. Trace metal concentrations of sulfide minerals, determined by laser-ablation ICP-MS, were used in conjunction with mineral paragenetic studies and thermodynamic calculations to deduce the history of fluid-mineral reactions during sulfide deposition. Detailed analyses of the distribution of metals in sulfides indicate significant shifts in the physical and chemical conditions responsible for the trace element variability observed in these sulfide deposits. Trace elements (Mn, Co, Ni, As, Se, Ag, Cd, Sb, Pb, and Bi) analyzed in a representative suite of 10 thin sections from these deposits suggest differences in conditions and processes of hydrothermal alteration resulting in mass transfer of metals from the center of the deposits to the margins. Enrichments of some trace metals (Pb, Sb, Cd, Ag) in sphalerite at the margins of the deposits are best explained by dissolution/reprecipitation processes consistent with secondary remineralization. Results of reaction-path models clarify mechanisms of mass transfer during remineralization of sulfide deposits due to mixing of hydrothermal fluids with seawater. Model results are consistent with patterns of observed mineral paragenesis and help to identify conditions (pH, redox, temperature) that may be responsible for variations in trace metal concentrations in primary and secondary minerals. Differences in trace metal distributions throughout a single deposit and between nearby deposits at Middle Valley can be linked to the history of metal mobilization within this active hydrothermal system that may have broad implications for sulfide ore formation in other sedimented and unsedimented ridge systems. 相似文献
7.
Smart C. Obiora Anthony Chukwu Sadrack F. Toteu Theophilus C. Davies 《Journal of the Geological Society of India》2016,87(4):453-462
Mining activities have been undertaken for over 95 years in Enyigba area of southeastern Nigeria. In this area, thirty-six (36) trace metals including those that are essential for plant and animal nutrition have been analyzed from forty-nine (49) soil samples that were collected from three Pb-Zn mines. The aim of the analysis is to assess the level of contamination of the soils caused by mining activities. Potentially harmful elements which are commonly associated with Pb-Zn mines were of special interest. Such elements included Pb, Zn, As, Cd, Mn, Fe, Se, Sb, Cu and Bi. Generally, the samples analyzed showed elevated concentrations of Pb, Zn, Cd, Cu and Cr when compared with concentrations documented in the international agricultural soil standards. Geo-accumulation indices of soils that occur closer to the mines indicate moderate to extreme level of contamination in Pb and moderate levels in Cd. Enrichment factor (EF) showed very high enrichment to extremely high enrichment in Pb. Cd and Zn enrichment were found to be significant and moderate respectively. Conversely, the geo-accumulation indices for soil samples located away from the mines indicate moderate to heavy contamination in Pb but had moderate to significant enrichment in Cd and moderate in Bi and Cr. In general, soil quality all around the mines were found to have deteriorated as revealed by the pollution load index. Thus the results of this study call for immediate remedial measures to be initiated. In addition, miners and local communities living around the mines need to be enlightened about the dangers of exposure to these heavy metal contaminants. 相似文献
8.
珠江三角洲污灌区地下水重金属含量及其相互关系 总被引：7，自引：0，他引：7
为了解污灌区地下水重金属含量特征,采集地表水样5组、地下水样14组进行化学组分定量分析。结果表明：污灌区地下水8种重金属元素中,仅有Ni和As两种元素超标,超标率分别为14.3％和42.9％。8种重金属含量在污灌区地表水、工厂废水以及地下水中存在明显的对应关系。Ni、Zn、Se、Cd这4种元素间存在显著或极显著的正相关关系,Cu与Pb和Cd分别呈极显著和显著的正相关关系,Cr仅与Ni呈显著的正相关关系,As与其它7种元素的相关性均不明显。聚类分析结果显示8种重金属可分为4类：Pb和Cu一类,Se、Cd、Ni、Zn一类,Cr和As均单独一类。Pb和Cu与Fe的相似性最好,Se、Cd、Ni、Zn与Mg2+存在较好的相似性,Cr与HCO－3的相似性最好,As与SO2－4存在一定的相似性。 相似文献
9.
Heavy meals in urban roadside soils, part 1: effect of particle size fractions on heavy metals partitioning 总被引：8，自引：0，他引：8
Urban roadside soils are important environmental media for assessing heavy metal concentrations in urban environment. However, among other things, heavy metal concentrations are controlled by soil particle grain size fractions. In this study, two roadside sites were chosen within the city of Xuzhou (China) to reflect differences in land use. Bulk soil samples were collected and then divided by particle diameter into five physical size fractions, 500–250, 250–125, 125–74, 74–45, < 45 μm. Concentrations of metals (Ti, Cr, Al, Ga, Pb, Ba, Cd, Co, Cu, Mn, Ni, V, Zn, Mo, As, Sb, Se, Hg, Bi, Ag) were determined for each individual fraction. These metals could be roughly classified into two groups: anthropogenic element (Pb, Ba, Cd, Cu, Zn, Mo, As, Sb, Se, Hg, Bi, Ag) and lithophile element (Ti, Cr, Al, Ga, Co, Mn, Ni, V) in terms of values of enrichment factor. As expected, higher concentrations of anthropogenic heavy metals (Cu, Zn, Mo, As, Hg, Bi, Ag) are observed in the finest particle grain size fraction (i.e. < 45 μm). However, heavy metals Se, Sb and Ba behave independently of selected grain size fractions. From the viewpoint of mass loading, more than 30% of the concentrations for all anthropogenic heavy metals are contributed by the particle grain size fractions of 45–74 μm at site 1 and more than 70% of the concentrations for all heavy metals are contributed by the particle grain size fractions of 45–74 and 74–125 μm at site 2. These results are important for transport of soil-bound heavy metals and pollution control by various remedial options. 相似文献
10.
This paper investigates the role played by the fumarolic plume of a passive degassing volcano in the genesis of rock coatings
(RC) and in the introduction and re-distribution of metals and trace elements in the surficial environment. At La Fossa active
volcano (Vulcano Island) and in the surrounding environment RC develop owing to exposure of the ground surface to the volcanic
acid plume produced by the passive degassing of La Fossa. Significant positive anomalies of a wide variety of metals and trace
elements (including Bi, Ag, Se, Te, Sb, Pb, As, Cu, Tl and Cd) were observed either in distal and proximal RC. Most of these
anomalies are interpreted to be the result of the transport and subsequent deposition of trace elements, likely to form volatile
compounds, in the fumarolic plume. Two main processes seem to control the geochemistry of RC: one is represented by the leaching
and subsequent deposition of elements from the proximal toward the distal RC; the other is the direct input of trace elements
carried by the emitted volcanic aerosol. The fact that most of the trace elements (particularly Pb, As, Tl, Bi, Te, Se, Cd)
enriched in the RC of Vulcano are highly toxic and potentially dangerous to health in high concentration, indicates that the
atmospheric metal injection by the quiescently degassing La Fossa volcano together with the subsequent deposition and remobilization
by means of surficial waters may represent an environmental hazard that should be taken into account in evaluating the potential
impact of volcanic air pollution on human health. 相似文献
11.
In the old mining area of Rodalquilar, mine wastes, soil and sediments were characterized and the results revealed high concentration
of Au, Ag, As, Bi, Cu, Fe, Mn, Pb, Se, Sb and Zn in tailings and sediments. The contaminant of greatest environmental concern
is As. The mean concentration in the tailings was 679.9, and 345 mg/kg in the sediments of Playazo creek. The groundwater
samples from the alluvial aquifer showed high concentration of Al, As, Cd, Fe, Hg, Mn, Ni, Pb, Se, Sb and Zn and very high
concentration of chloride and sulfate, which were above the concentration defined in the European standards for drinking water.
The presence of As in groundwater may be caused by the oxidation of arsenian pyrite, the possible As desorption from goethite
and ferrihydrite and the jarosite dissolution. Groundwater concentrations of Cd, Fe, Mn, and possibly Cu, were associated
with low values of Eh, indicating the possible dissolution of oxy-hydroxides of Fe and Mn. The mobility of metals in the column
experiments show the release of Al, Fe, Mn, Cr, Cu, Ni, V and Zn in significant concentrations but below the detected values
in groundwater. However, As, Cd, Sb, Se Pb and Au, are generally mobilized in concentrations above the detected values in
groundwater. The possible mass transfer processes that could explain the presence of the contaminants in the aquifer and the
leachates was simulated with the PHREEQC numerical code and revealed the possible dissolution of the following mineral phases:
jarosite, natrojarosite, arsenian pyrite, alunite, chlorite, kaolinite and calcite. 相似文献
12.
山西高凡银金矿床黄铁矿的微量元素标型特征及其应用 总被引：2，自引：0，他引：2
高凡银金矿床黄铁矿的微量元素研究发现富Au、Ag、Pb、Zn、As、Sb,贫Co、Ni、Se,且S/Se较大,S/As和Fe/(Pb+Zn)较小,As/(Co+Ni)、(Pb+Zn)/(Co+Ni)>10。同时高凡矿田中的滩上铜钼矿化点的黄铁矿则显示相反的特征。总结出一套区分两类矿化黄铁矿微量元素的标型特征,对高凡矿田和五台地区各矿化点的判别和评价中显示了一定的适用性,可作为本区寻找同类金银矿床的找矿标型特征。 相似文献
13.
The ash yield and concentrations of twenty-four minor and trace elements, including twelve potentially hazardous trace elements were determined in Mukah coal from Sarawak, Malaysia. Comparisons made to the Clarke values show that Mukah coal is depleted in Ag, Ba, Be, Cd, Co, Mn, Ni, Se, U, and V. On the other hand, it is enriched in As, Cr, Cu, Pb, Sb, Th, and Zn. Among the trace elements studied, V and Ba are associated predominantly with the clay minerals. Manganese, Cr, Cu, Th, and Ni are mostly bound within the aluminosilicate, sulphide and/or carbonate minerals in varying proportions, though a portion of these elements are also organically bound. Arsenic, Pb and Sb are mostly organically bound, though some of these elements are also associated with the sulphide minerals. Zinc is associated with both the organic and inorganic contents of the coal. Among the potentially hazardous trace elements, Be, Cd, Co, Mn, Ni, Se, and U may be of little or no health and environmental concerns, whereas As, Cr, Pb, Sb and Th require further examination for their potential health and environmental concerns. Of particular concern are the elements As, Pb and Sb, which are mostly organically bound and hence cannot be removed by physical cleaning technologies. They escape during coal combustion, either released as vapours to the atmosphere or are adsorbed onto the fine fly ash particles. 相似文献
14.
Chunye Lin Mengchang He Xitao Liu Wei Guo Shaoqing Liu 《Environmental Earth Sciences》2013,70(7):3163-3173
The Daliao River System (DRS) is one of the major river systems in the northeastern China and receives substantial discharges from industrial, municipal, and agricultural effluents. In this study, the contents and partition of toxic trace elements in the DRS sediments were evaluated in terms of contamination levels and ecological risks using geoaccumulation index (Igeo), relative enrichment factor (REF), sediment pollution index (SPI), and potential effect concentration quotient (PECQ). Fourteen samples were collected and measured for trace and major elements and sediment properties. The following concentration ranges (mg kg?1) of toxic trace elements were found: As, 1.6–18.0; Cd 0.1–0.9; Co 3.8–23.4; Cr 12.9–151.6; Cu 4.6–86.1; Hg 0.01–0.35; Ni 8.4–64.4; Pb 11.6–67.1; Sb 0.13–1.77; V 18.5–153.3; and Zn 20.4–211.3. The proportions of soluble and exchangeable trace metals were less than 1 %, while the proportions of trace metals bound to carbonate, amorphous oxides, organic matter, and crystalline oxides were usually each <10 %. However, 28.8 % of Cd, on average, was associated with carbonate. The average proportions of trace metals in the residual fraction ranged 57.3 % for Cd to 85.4 % for Cr, indicating low mobility and bioavailability. Cr, Ni, V, and Co in the sediments mainly originated from natural sources, while Cd, As, Pb, Sb, and Hg partially originated from anthropogenic sources. The Igeo, REF, SPI, and PECQ values of the heavy metals in the sediment were not in agreement with each another. The average REF values of Cd and As were higher than those of the other metals. However, the average PECQ value was higher for Cr and Ni than for the other metals, indicating that these two metals would cause higher adverse biological effects than the other metals. In addition, the sediments located adjacent to cities were more contaminated. Therefore, it is suggested that future management and pollution control within the DRS might focus on As, Cd, Cr, and Ni in the sediments, particularly in the sediments adjacent to cities. 相似文献
15.
为了解酸性矿山排水（AMD）影响下水库沉积物中微量元素的质量分数水平及其分布特征,对常年受酸性废水影响的贵州兴仁猫石头水库沉积物中26种微量元素的质量分数、相关性及控制因素进行了分析。结果表明：猫石头水库沉积物柱中Sr、Ba、Zr、V、Cr和As质量分数平均值超过了100 μg/g,其中As质量分数最高,平均值超过800 μg/g;Be、Ta、Co、Ag、Cd、Sn和Se质量分数的平均值都在5 μg/g以下;其他元素质量分数平均值则在10~60 μg/g之间。相较未受AMD影响的水系沉积物,研究区水库沉积物具有明显的As和Sb富集特征。水库沉积物中Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th之间存在显著正相关关系,而As与这些元素之间存在显著负相关关系。元素相关分析、因子分析及微量元素图解表明,Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th、Cr、Sb等元素受控于流域岩石化学风化和土壤物理侵蚀,这也是控制研究区元素分布最重要的因素,而Cu、Cd等重金属元素则与AMD对地层中元素的溶蚀析出和有机质等细颗粒物的吸附有关。另外,研究区重金属元素中,Cd、Cu、Pb、Cr、Zn的生态风险轻微,而As和Sb则具有很强的潜在生态风险。 相似文献
16.
Coal gangue with/without wild puff balls growing on or covering up were analyzed by means of inductively coupled plasma atomic emission spectrometry （ICP-AES） and atomic fluorescence spectrometry （AFS） to detect the contents of heavy metal elements in the plants. Seven heavy metals were chosen to do the experiments, which showed that the puffballs have strong enrichment capacity for heavy metals （As, Pb, Mn and Ni）. The highest enrichment level was Mn, 220.3 mg/kg （dry weight） for puffball fruiting bodies, and the highest As, Cr and Pb enrichment levels for puffball mycelium were 111,265.3 and 86 mg/kg, respectively. Cd, Mn and Ni could transfer from puffball mycelium to its fruiting bodies, while As, Cr, Pb and Co mainly accumulated in the mycelium. The contents of five organic acids （tartaric acid, glycolic acid, lactic acid, citric acid and malic acid） in puffballs were determined with high performance liquid chromatography. With water, ethanol and ethyl acetate as solvents, the puffball extracts performed dissolution reactions with coal gangue, in which the water extract （containing a large amount of organic acids） was most effective in releasing heavy metals, especially As, Pb, Cr, Mn, Co and Ni from coal gangue. As a pioneer species, puff balls absorbed the hazardous trace elements in coal gangue matrix to reduce its eco-toxicity, on the other hand, it raised the pH value of coal gangue, improving the vegetation growing conditions for coal gangue matrix to a certain extent and laying the foundation for ecological restoration of coal gangue dumps. 相似文献
17.
A routine method for the direct determination of Au and associated trace metals in sulfides has been developed for use with a low-flux nuclear reactor (SLOWPOKE II Reactor Facility, University of Toronto). Small samples (100–200 mg) are analysed simultaneously for Au, Ag, As, Sb, Mo, Co, Se, Cd, Fe, and Zn. Sulfides containing finely divided gold can be analysed with a high degree of precision and yield results which agree closely with commercial fire assay-atomic absorption analyses for Au. Favourable comparisons with other analytical techniques (flameless atomic absorption and emission spectrometry) are also indicated for Ag, As, and Sb. Neutron activation has the advantage of providing precise and accurate results for these elements without chemical separation or preconcentration. Analyses of 10 sulfide-bearing reference materials from CANMET, Ottawa are compared with published best values for selected trace metals including Au. 相似文献
18.
Gülbin Gürdal 《International Journal of Coal Geology》2011,87(2):157-173
This study presents the concentrations and modes of occurrence of trace elements in 81 coal samples from the Çan basin of northwestern Turkey. The concentration of trace elements in coal were determined by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry. Additionally, traditional coal parameters were studied by proximate, ultimate, X-ray diffraction, and petrographic analyses. Twenty trace elements, including As, B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se Sn, Th, Tl, U, V, and Zn, receive much attention due to their related environmental and human health concerns. The Çan coals investigated in this study are lignite to sub-bituminous coal, with a broad range of ash yields and sulphur contents. The trace element concentrations show variety within the coal seams in the basin, and the affinities vary among locations. The concentrations of B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se, Sn, Tl, and Zn in Çan coals are within the Swaine's worldwide concentration range, with the exception of As, Th, U, and V. On the other hand, compared with world coals, the Çan basin coals have higher contents of As, B, Cu, Co, Mo, Pb, Th, U, V, and Zn. Based on statistical analyses, most of the trace elements, except for U, show an affinity to ash yield. Elements including As, Cd, Hg, Se, Cu, Mo, Ni, and Zn, show a possible association with pyrite; however, the elements Se, B, and Mo can be have both organic and inorganic associations. 相似文献
19.
Saday Azadoglu ALIYEV Ali SARI Bahadir KTEN Ankara University Faculty of Engineering Department of Geological Engineering Tandogan Ankara Turkey 《《地质学报》英文版》2008,82(6)
Concentrations of some heavy metals and trace elements such as Cr,Ga,Ni,Zn,Mo,Cu, Pb,Yb,Y,Nb,Ti,Sr,Ba,Mn,Sc,Co,V,Zr,Fe,Al,W,Se,Bi,Sb,As,Cd in recent mollusk shells and factors affecting their distribution and deposits collected from various depths in the southern and southwestern parts of the Marmara Sea are investigated.The distribution of the elements in the shells is categorized into four groups.Of these,concentrations of 12 elements(As,Bi,Cd,Co,Ga,Mo,Nb, Sb,Se,Sc,W and Yb)are below zero [(0.053-0.79)×10~(-6)];concentrations of seven elements(Cr,Ni, Pb,V,Y,Zr and Cu)are(1.0-6.0)×10~(-6);concentrations of four elements(Ti,Mn,Ba and Zn)are 10- 20×10~(-6);and concentrations of five elements(Si,Al,Fe,Mg and Sr)are(47.44-268.11)×10~(-6).The taxonomic characteristics of the 29 elements were studied separately in mollusk shells such as Chamalea gallina(Linné),Pitar-rudis(Poll),Nassarius reticulatus(Linné),Venerupis senescens (Coocconi),Mytilus galloprovincialis(Lamarck),Mytilaster lineatus(Gemelin in Linné)and Chlamys glabra.It was found that,in mollusk taxonomy,the elements have unique values.In other words, element concentrations in various mollusk shells depend mainly on the taxonomic characteristics of mollusks.In various bionomic environments different element distributions of the same species are attributed to the different geochemical characters of the each environment.Data obtained in this study indicate that the organisms are the most active and deterministic factors of the environment. 相似文献