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1.
The gold mining process at Kolar gold field (KGF) mines has generated about 32 million tons of tailings. Gold was extracted from the mined ores using cyanidation technique that involved dissolution of gold in the ore by water soluble alkali metal cyanides (example, sodium cyanide or potassium cyanide). Of the several dumps that received the mine tailings only the Kennedy’s Line dump was active prior to closure of the KGF mines in the year 2000. The Kennedy’s Line dump received sulfide bearing tailings in slurry form that comprised of spent ore and process water bearing soluble alkali metal cyanide. Depending on the pH of the tailing slurry, the free cyanides may exist as aqueous hydrogen cyanide that can escape to the atmosphere as hydrogen cyanide gas or occur as soluble cyanide (CN−) ions that can be leached by infiltrating water to the sub-surface environment. Additionally, the presence of pyrite minerals in the Kennedy’s Line dump makes them susceptible to acid drainage. This study examines the potential of gold tailings of Kennedy’s Line dump to release cyanide ions (CN−) and acid drainage to the sub-surface environment by performing physico-chemical and leaching tests with tailing samples collected from various depths of the dump, sub-surface soil samples beneath the dump and groundwater samples from vicinity of Kennedy’s Line dump. The chemical mechanisms responsible for the ambient cyanide and pH levels of the tailing dump, sub-surface soil samples and groundwater are also inferred from the laboratory results.  相似文献   

2.
Farmlands and rivers have been seriously polluted by cyanide from a goldmine tailings dam that collapsed in early spring of 1995 in Yining County, Xinjiang Autonomous Region of China. The cyanide distribution in the polluted farmland and the abandoned tailings dam was studied, three and 4 years after the accident occurred. The results indicated that natural degradation of cyanide in soils is slower than in natural water bodies. The cyanide transport in the soil section is similar to freely soluble salts. In arid and semiarid areas, cyanide can be highly enriched in the salt crust in which the concentration is even higher than the fresh tailings debris though cyanide has decomposed for 4 years. In the polluted farmland, the sticky layer in the soil section can highly adsorb and enrich cyanide so it can partly prevent cyanide transfer to groundwater. According to the characteristics of cyanide natural degradation in soil, the measures for prevention and cure of soil polluted by goldmine tailing dam collapse have been discussed.  相似文献   

3.
地球化学模式程序的原理,分类与功能   总被引：15，自引：0，他引：15  
周文斌  史维浚 《铀矿地质》1995,11(4):217-222
地球化学模式是用化学反应式和数学公式来描述地球化学作用的一种概念化的模式，在这种概念化的模式基础上利用数学方法和计算机语言编制的软件便是地球化学模式程序。按照原理和复杂程度可把地球化学模式程序分为３大类，即质量平衡程序、物质转化程序和溶质迁移程序。地球化学模式程序的主要功能包括计算元素在水溶液中的存在形式，预测各类地球化学反应进行的方向，物质的溶解与沉淀，溶液的Ｅｈ、ｐＨ值，计算地球化学作用的反应速度和反应途径等。  相似文献   

4.
铁岭柴河1#尾矿坝数值模拟及其稳定性分析   总被引：1，自引：0，他引：1  
铁岭柴河1#尾矿坝位于辽宁省开原市靠山镇猴石社区的关门山沟内,由初期坝和尾矿堆积坝组成。本文在该尾矿坝现场勘察的基础上,将坝体实测主轴剖面进行合理地概化和延伸,建立有限差分数值模型,并以Duncan—Chang双曲线模型来反映尾矿坝岩土体应力—应变本构关系,对处于正常运行条件下的坝体进行数值分析,从而揭露坝体内部应力状态,同时在数值分析结果的基础上,采用基于极限平衡理论的条分法——Fellenius法和Biship法对尾矿坝的稳定性进行计算,从而实现对尾矿坝稳定性的定量分析,对尾矿库的安全生产具有重要指导意义。  相似文献   

5.
The use of cyanide (CN), which is characterized by volatility, toxicity and high odor, in gold mining is scarcely addressed in the literature and remain controversial. Environmentalists oppose CN usage as it potentially poses serious environmental threats, whereas economic and mining geologists are in favor of its usage for its extracting capacity and economic feasibility. The present study investigates the possible dispersion of CN into groundwater resources caused by a gold mine (ca. 15 years old) located in the arid area of Yanqul, North Oman. The gold is hosted in gossan deposits associated with ophiolitic rocks and sulfide deposits. Sodium cyanide is mixed with 0.5 m3 of water and then added to a tonne of crushed ore rock to extract 6 g of gold mineral. The final residues are dumped in engineered, lined and uncovered tailing dams. Subsequent to rainfall water draining the mine plateau flows along the wadies and percolates into the shallow Quaternary alluvium aquifer. Hence, groundwater samples were collected from 16 piezometers adjacent to and around the mine. The samples were analyzed for CN using the revised phenolphthalin method and they all show CN concentration below the detection limit (5 ppb). The samples were also analyzed for heavy metals to investigate the potential of CN complexation. Most of heavy metals indicated very trace concentration. The absence of CN in groundwater is attributed to volatilization of CN (converted to HCN), lined dam structure, high evapotranspiration rate and deeper water table. This finding is consistent with the historical CN analysis in the groundwater and solid wastes. It can be pointed out that within few years of operation well engineered tailing dams can provide safe structure preventing CN-groundwater pollution in arid areas. Potential threats to the air and soil are not addressed in this article.  相似文献   

6.

Background  

Proteins of various compositions are required by organisms inhabiting different environments. The energetic demands for protein formation are a function of the compositions of proteins as well as geochemical variables including temperature, pressure, oxygen fugacity and pH. The purpose of this study was to explore the dependence of metastable equilibrium states of protein systems on changes in the geochemical variables.  相似文献   

7.
Acid Mine Drainage (AMD) is a great concern in many abandoned mines because of its adverse effect on the environment. In mining processes, many kinds of wastes are produced. These wastes may become eventually sources of environmental degradation. The focus of this study is the geochemical characterization of the end-processed tailings generated by Akara Gold Mine, the biggest gold mine in Thailand. Tailing samples were systematically collected for analyses of chemical and mineralogical compositions. As a result, their quantitative chemical analyses are slightly different from place to place, but mineral components cannot be clearly differentiated. For instance, it may be assumed that the end-processed tailings, which were a mixture between high and low grade concentrates, would have similar mineral components. However, the little variation of chemical composition may be caused by the ore refining processes that are somehow varied in proportion to chemical additives, alkali cyanide and quick lime in particular. In addition, clay composition in ore-bearing layers may also influence alumina content of tailings, accordingly. Distribution of the tailings is not related to depth and distance of the tailing storage pond because the disposal has sped them over the pond during operation. Total heavy metals of the tailing samples were analyzed on the basis of the EPA 3052 method. Consequently, the most toxic elements (e.g., Co, Cu, Cd, Cr, Pb, Ni and Zn) were found falling within the standard of Thailand Soil Quality Standards for Habitat and Agriculture. Only Mn appears to have higher content than the standard. In addition, leaching tests proved that these tailings contain low metal concentrations. As a result, at pH 2, Mn can leach out exceeding the Thailand Surface Water Quality Standard for Agricultural (Mn <1 ppm) and the Thailand Industrial Effluent Standard (<5 ppm). Although leachate at pH 4 and neutral conditions contains lower Mn than the Industrial Effluent Standard it still exceeds the surface water quality standard. Interestingly, Pb can be leached out exceeding both standards (0.2 ppm for the industrial effluent standard and 0.05 ppm for the surface water quality standard). For Ni leaching, its concentration is lower than the Industrial Effluent Standard at all pH conditions but still exceeds the Surface Water Standard at pH 2 and 4. This information should be taken into consideration for further environmental monitoring. Acid generating potential of the tailings was estimated using acid–base accounting (ABA) and net acid generation (NAG) tests. The results of ABA and NAG tests show that the tailing samples contain a high amount of sulfur. However, they also contain high acid neutralization capacity. Consequently, these tailings may not have potential to generate acid drainage; in the other words, they can be classified as a non-acid forming (NAF) material. However, since these tailings contain some heavy metals (e.g., Ni, Mn and Pb) that are observed in leachates exceeding the standards at low pH, the AMD conditions may lead to heavy metal release. Therefore, prevention of oxidizing process and dissolution should be considered with great care. In addition, Mn and Pb can also be leached at neutral conditions. Barrier of air and water, clay layer for example, should be placed over the tailings pound before covering by topsoil for re-vegetation. Growing native grass is recommended for stabilization of the surface and reducing erosion rate. Monitoring of water quality should also be carried out annually.  相似文献   

8.
Three large-scale experimental waste rock piles (test piles) were constructed and instrumented at the Diavik Diamond Mine in the Northwest Territories, Canada, as part of an integrated field and laboratory study to measure and compare physical and geochemical characteristics of experimental, low sulfide waste rock piles at various scales. This paper describes the geochemical response during the first season from a test pile containing 0.053 wt.% S. Bulk drainage chemistry was measured at two sampling points for pH, Eh, alkalinity, dissolved cations and anions, and nutrients. The geochemical equilibrium model MINTEQA2 was used to interpret potential mineral solubility controls on water chemistry. The geochemical response characterizes the initial flushing response of blasting residues and oxidation products derived from sulfides in waste rock exposed to the atmosphere for less than 1 year. Sulfate concentrations reached 2000 mg L−1 when ambient temperatures were >10 °C, and decreased as ambient temperatures declined to <0 °C. The pH decreased to <5, concomitant with an alkalinity minimum of <1 mg L−1 (as total CaCO3), suggesting all available alkalinity is consumed by acid-neutralizing reactions. Concentrations of Al and Fe were <0.36 and <0.11 mg L−1, respectively. Trends of pH and alkalinity and the calculated saturation indices for Al and Fe (oxy)hydroxides suggest that dissolution of Al and Fe (oxy)hydroxide phases buffers the pH. The effluent water showed increased concentrations of dissolved Mn (<13 mg L−1), Ni (<7.0 mg L−1), Co (<1.5 mg L−1), Zn (<0.5 mg L−1), Cd (<0.008 mg L−1) and Cu (<0.05 mg L−1) as ambient temperatures increased. Manganese is released by aluminosilicate weathering, Ni and Co by pyrrhotite [Fe1−xS] oxidation, Zn and Cd by sphalerite oxidation, and Cu by chalcopyrite [CuFeS2] oxidation. No dissolved metals appear to have discrete secondary mineral controls. Changes in SO4, pH and metal concentrations indicate sulfide oxidation is occurring and effluent concentrations are influenced by ambient temperatures and, possibly, increasing flow path lengths that transport reaction products from previously unflushed waste rock.  相似文献   

9.
In this research, a new low cost and abundant biosorbent; Agave americna (L.) fibres has been investigated in order to remove metal dye (Alpacide yellow) from aqueous solutions. In order to optimize the biosorption process, the effect of pH, temperature, contact time and initial solution concentration was investigated in batch system. The results indicated that acidic pH=2 was favourable for metal dye removal. The increase of temperature increases the velocity of the biosorption reaction. The biosorption kinetics of alpacide yellow were closer to the pseudo-second order than to the first order model for all concentrations and temperature. The calculated thermodynamic parameters such as dGG°, dGH° and dGS° indicated a spontaneous and endothermic biosorption process of metal dye onto Agave americana fibres. The equilibrium data were analysed using the Langmuir and Freundlich isotherms and showed a good fit with Langmuir model at lower temperatures and with Freundlich model at 50 °C.  相似文献   

10.
The compositional characteristics of many geochemical systems which involve the interaction of natural aqueous solutions with minerals and gases are conveniently described using the following thermodynamic components: Cl?, SO4=, HS?, CO3=, H+, Na+, K+, Ca++, Mg++, Fe++, Zn++, Cu+, Al+++, SiO2 and H2O. A set of mass balance and mass action equations equal in number to the number of components plus the number of saturated minerals (and gases) is defined for a specified temperature, pressure and bulk composition. The mass balance equations include terms for minerals, gases and the molalities of aqueous complexes and dissociated species. This set of non-linear equations can be solved with the aid of a computer using'a Newton-Raphson technique. The calculation takes account of aqueous ion complexing, oxidation-reduction equilibria, activity coefficients, non-unit water activity and solid solutions. The use of H+, SO4=, HS? and H2O as components allows straightforward treatment of processes involving oxidation-reduction, evaporation, boiling and changes of total aqueous H+ due to hydrolysis, mineral reaction or temperature change. One product of this approach is a technique for calculating pH at high temperature from measurement of pH at room temperature.By linking a series of discrete overall heterogeneous equilibrium calculations in which incremental changes of bulk composition, temperature or pressure are made, dynamic geochemical processes can be modeled. Example calculations for two such processes are given. These are the heating of seawater from 25° to 300°C and the isothermal irreversible reaction of rhyolite with an aqueous solution at 250°C.  相似文献   

11.
《Applied Geochemistry》1998,13(7):893-904
The octanol–water partition coefficients (log Kow) of 2,4,6-trichlorophenol and pentachlorophenol were determined as functions of pH, ionic strength and aqueous metal content. For both chlorophenols, the log Kow exhibits pH dependence in the range pKa−1<pH<pKa+3. At lower and higher pH values, the behaviour of the chlorophenols is independent of pH. The present data, in conjunction with that of pre-existing data, indicate that a linear relationship exists between log Kow and log ionic strength of the aqueous solution for pentachlorophenol, and the data also suggest that aqueous metal–chlorophenolate complexation can significantly alter the partitioning behaviour. The data reported here was used to obtain an empirical model of the partitioning behaviour based on speciation of the aqueous chlorophenol. The model requires knowledge of the low pH partitioning behaviour, as well as the acidity constant for the particular chlorophenol of interest. Although Kow values have been measured as a function of pH and/or ionic strength for only pentachlorophenol, the input parameters for our empirical model are readily accessible in the literature for many chlorophenols. The model greatly expands our ability to quantify the hydrophobicity of chlorophenols, enabling accurate estimations of the pH and ionic strength dependencies of the partitioning behaviour over a wide range of pH and ionic strength values of environmental interest.  相似文献   

12.
Biosorption is an effective method to remove heavy metals from wastewater. In this work, the biosorption of Cd(II) onto Hydrilla verticillata was examined in aqueous solution with parameters of initial pH, adsorbent dosage, contact time, initial Cd(II) concentration, temperature, and co-existing ion. Linear Langmuir and Freundlich models were applied to describe the equilibrium isotherms, and both of the two models were fitted well. The monolayer adsorption capacity of Cd(II) was found to be 50 mg/g at pH 6 and 20°C. Dubinin–Radushkevich isotherm model was also applied to the equilibrium data. The mean free energy of adsorption (11.18 kJ/mol) indicated that the adsorption of Cd(II) onto H. verticillata might be carried out via chemical ion-exchange mechanism. Thermodynamic parameters, including free energy (∆G 0), enthalpy (∆H 0), and entropy (∆S 0) of adsorption, were also calculated. These results showed that the biosorption of Cd(II) onto H. verticillata was a feasible, spontaneous, and exothermic process in nature. Desorption experiments indicated that 0.01 mol/L EDTA and HNO3 were efficient desorbents for the recovery of Cd(II) from biomass. IR spectrum analysis suggested that amido, hydroxyl, C=O and C–O could combine strongly with Cd(II). EDX spectrum analysis suggested that an ion exchange mechanism might be involved.  相似文献   

13.
We have studied the hydrolytic behavior of Y3 + and trivalent ions of rare earth elements in aqueous solutions at 25 ºC. The stepwise stability constants of hydroxide complexes were measured by spectrophotometry, using m-cresol purple and 1-(2-pyridylazo)-2-naphthol as pH indicators at an ionic strength no more than 0.0005. The results showed that at pH ranging between 6.0 and 11.0 in freshly prepared solutions of REE trichlorides, lanthanides are presented as Ln3 +, Ln(OH)2 +, Ln(OH)2, and Ln(OH)3. The plots of the formation constants of + 0 monohydroxo complexes of 4f n ions M3 + versus atomic number Z deviate from smooth ones and consist of four convex curves. This phenomenon is also observed in normalized spectra of REE concentrations in natural objects and is known as the tetrad effect. The obtained data give an insight into the relationship between REE complex formation and REE fractionation in geochemical processes and can be used for physicochemical modeling of geochemical systems.  相似文献   

14.
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15.
The batch removal of hexavalent chromium from aqueous solutions using almond shell, activated sawdust, and activated carbon, which are low-cost biological wastes under different experimental conditions, was investigated in this study. The influences of initial concentration, adsorbent dose, adsorbent particle size, agitation speed, temperature, contact time, and pH of solution were investigated. The adsorption was solution pH dependent and the maximum adsorption was observed at a solution pH of 2.0. The capacity of chromium adsorption under equilibrium conditions increased with the decrease in particle sizes. The equilibrium was achieved for chromium ion after 30?min. Experimental results showed that low-cost biosorbents are effective for the removal of pollutants from aqueous solution. The pseudo-second-order kinetic model gave a better fit of the experimental data as compared to the pseudo-first-order kinetic model. Experimental data showed a good fit with the Freundlich isotherm model. Changes in the thermodynamic parameters, including Gibbs free energy (??Go), enthalpy (??Ho), and entropy (??So), indicated that the biosorption of hexavalent chromium onto almond shell, activated sawdust, and activated carbon was feasible, spontaneous, and endothermic in the temperature range 28?C50?°C.  相似文献   

16.
In this study, the removal of free cyanide from aqueous solutions by activated carbon was investigated. Effects of metal impregnation (Cu and Ag), aeration, and concentrations of adsorbent and cyanide on the rate and extent of the removal of cyanide were studied. The results have shown that the capacity of activated carbon for the removal of cyanide can be significantly improved (up to 6.3-fold) via impregnation of activated carbon with metals such as copper and silver. Silver-impregnated activated carbon was found to be the most effective at the reduction of cyanide level in solution. This appeared to be coupled with its comparatively high metal content after impregnation process where silver (5.07%) could be more readily loaded on activated carbon than copper (0.43%). Kinetics and equilibrium data for cyanide removal by plain and metal-impregnated activated carbons were determined to be consistent with the pseudo second-order kinetics and the Langmuir adsorption isotherms, respectively. Aeration (0.27 l/min) was found to exert a profound effect on the process leading to a 5.5–49.1% enhancement in the performances of plain and metal-impregnated activated carbons. This enhancement could be attributed to the increase in the availability of active sites on activated carbon for adsorption and the catalytic oxidising activity of activated carbon in the presence of oxygen. Practical limiting capacity of plain, copper- and silver-impregnated activated carbons for the removal of cyanide were experimentally determined to be 19.7, 22.4 and 29.6 mg/g, respectively.  相似文献   

17.
《Applied Geochemistry》2003,18(9):1297-1312
The concentrations of As in surface- and up to 90 °C ground waters in a tholeiite flood basalt area in N-Iceland lie in the range <0.03–10 μg/kg. With few exceptions surface waters contain <0.5 μg/kg As whereas ground waters generally contain >0.5 μg/kg As. The As content of ground waters increases on the whole with rising temperature. Arsenic is highly mobile in the basalt-water environment of the study area. An insignificant fraction of the As dissolved from the rock is taken up into secondary minerals. Arsenic is less mobile than B but considerably more mobile than Na which has the highest mobility among the major aqueous components. A significant fraction of the As in the basalt occurs in an easily soluble form. The As hosted in the primary minerals is expected to be concentrated in the titano-magnetite. This mineral is stable in contact with both surface- and ground waters and does not, therefore, supply As to the water, explaining the difference in mobility between As and B. Aqueous As concentrations are a reflection of water/rock ratios, i.e. how much rock a given quantity of water has dissolved. This ratio increases with increasing temperature and increasing residence time of the water in contact with the rock. The distribution of As species has been calculated on the assumption of equilibrium at the redox potential retrieved from measurement of aqueous Fe(II) and Fe(III) concentrations. These calculations indicate that pentavalent As is stable in surface waters and in ground waters with an in situ pH of <10 and would occur mostly as H2AsO4− and HAsO4−2. In higher pH ground waters the concentrations of the arsenite species H2AsO3− is significant at equilibrium, up to 65% of the total dissolved As.  相似文献   

18.
The kinetics of the formation and precipitation of nanocolloidal silica from geologically relevant aqueous solutions is investigated. Changes in monomeric (SiO2(mono)), nanocolloidal (SiO2(nano)) and precipitated silica (SiO2(ppt)) concentrations in aqueous solutions from pH 3 to 7, ionic strengths (IS) of 0.01 and 0.24 molal, and initial SiO2 concentrations of 20.8, 12.5 and 4.2 mmolal (reported in [Icopini, G.A., Brantley, S.L., Heaney, P.J., 2005. Kinetics of silica oligomerization and nanocolloid formation as a function of pH and ionic strength at 25 °C. Geochim. Cosmochim. Acta69(2), 293-303.]) were fit using two kinetic models. The first model, termed the concentration model, is taken from Icopini et al. (2005) and assumes that the rate of change of SiO2(mono) as a function of time has a fourth-order dependence on the concentration of SiO2(mono) in solution. The second model, termed the supersaturation model, incorporates the equilibrium concentration of amorphous silica and predicts that polymerization will be a function of the degree of silica supersaturation in solution with respect to amorphous silica. While both models generally predicted similar rate constants for a given set of experimental conditions, the supersaturation model described the long-term equilibrium behavior of the SiO2(mono) fraction more accurately, resulting in significantly better fits of the monomeric data. No difference was seen between the model fits of the nanocolloidal silica fraction. At lower pH values (3-4), a metastable equilibrium was observed between SiO2(mono) and SiO2(nano). This equilibrium SiO2(mono) concentration was found to be 6 mmolal, or three times the reported solubility of bulk amorphous silica under the experimental conditions studied and corresponds to the predicted solubility of amorphous silica colloids approximately 3 nm in diameter. Atomic force microscopy was used to determine the average size of the primary nanocolloidal particles to be ∼3 nm, which is in direct agreement with the solubility calculations. Larger aggregates of the primary nanocolloids were also observed to range in size from 30 to 40 nm. This work provides the first kinetic models describing the formation and evolution of nanocolloidal silica in environmentally relevant aqueous solutions. Results indicate that nanocolloidal silica is an important species at low pH and neutral pH at low ionic strengths and may play a more important role in geochemical cycles in natural aqueous systems than previously considered.  相似文献   

19.
The flotation response of gersdorffite has been determined in a series of batch flotation tests in which a sulphide sample containing about 76% gersdorffite was floated from mixtures with quartz.Using xanthate as collector, the arsenide floated strongly at pH 9, irrespective of whether lime, sodium hydroxide or sodium carbonate was used as pH modifier. When the pH was raised further to 10 or more using lime, the flotability decreased sharply.Changing the pulp potential at pH 9 also strongly affected the flotation response. Above about − 230 mV SHE, the mineral floated strongly, but below this potential it was essentially non-flotable. As far as it was tested (up to + 400 mV SHE), no upper limiting potential was found.Adding cyanide to the grinding mill brought about only a weak depressant effect on subsequent gersdorffite flotation at both pH 9 and 10. However, adding the same amount of cyanide to the flotation cell produced a strong depressant effect at the same pH values. At both pH 9 and pH 10, a threshold cyanide addition existed below which gersdorffite floated strongly, and above which it did not. For the conditions used in this study, this addition equates to about 100 g/t at pH 9 and about 80 g/t at pH 10. A hypothesis for the depression effect is presented which is consistent with both the available flotation data and a series of diagnostic analyses of grinding and flotation pulps completed during the test work.  相似文献   

20.
采用不排水有效应力法,利用Geo-slope软件,对金堆城栗西沟尾矿坝进行了地震响应的综合分析与液化计算。结果显示: a .栗西沟尾矿坝在静态条件下是稳定的; b .在7度地震条件下,尾矿坝的加速度反应较小,其放大倍数为2.204; c .栗西沟尾矿坝内动剪应力和动孔压绝大部分是随着地震历时的增加而逐渐增大; d .坝内孔压比都较小,抗液化安全系数较大,但局部液化区的存在,仍可能影响到整个坝体的安全性,应在液化区采取加固措施。   相似文献   

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