The environmental geochemistry of trace elements and naturally radionuclides in a coal gangue brick-making plant.

PubMed

Zhou, Chuncai; Liu, Guijian; Cheng, Siwei; Fang, Ting; Lam, Paul K S

2014-08-28

An investigation focused on the transformation and distribution behaviors of trace elements and natural radionuclides around a coal gangue brick plant was conducted. Simultaneous sampling of coal gangue, brick, fly ash and flue gas were implemented. Soil, soybean and earthworm samples around the brick plant were also collected for comprehensive ecological assessment. During the firing process, trace elements were released and redistributed in the brick, fly ash and the flue gas. Elements can be divided into two groups according to their releasing characteristics, high volatile elements (release ratio higher than 30%) are represented by Cd, Cu, Hg, Pb, Se and Sn, which emitted mainly in flue gas that would travel and deposit at the northeast and southwest direction around the brick plant. Cadmium, Ni and Pb are bio-accumulated in the soybean grown on the study area, which indicates potential health impacts in case of human consumption. The high activity of natural radionuclides in the atmosphere around the plant as well as in the made-up bricks will increase the health risk of respiratory system.

The Environmental Geochemistry of Trace Elements and Naturally Radionuclides in a Coal Gangue Brick-Making Plant

PubMed Central

Zhou, Chuncai; Liu, Guijian; Cheng, Siwei; Fang, Ting; Lam, Paul K. S.

2014-01-01

An investigation focused on the transformation and distribution behaviors of trace elements and natural radionuclides around a coal gangue brick plant was conducted. Simultaneous sampling of coal gangue, brick, fly ash and flue gas were implemented. Soil, soybean and earthworm samples around the brick plant were also collected for comprehensive ecological assessment. During the firing process, trace elements were released and redistributed in the brick, fly ash and the flue gas. Elements can be divided into two groups according to their releasing characteristics, high volatile elements (release ratio higher than 30%) are represented by Cd, Cu, Hg, Pb, Se and Sn, which emitted mainly in flue gas that would travel and deposit at the northeast and southwest direction around the brick plant. Cadmium, Ni and Pb are bio-accumulated in the soybean grown on the study area, which indicates potential health impacts in case of human consumption. The high activity of natural radionuclides in the atmosphere around the plant as well as in the made-up bricks will increase the health risk of respiratory system. PMID:25164252

Potential ecological risk assessment and prediction of soil heavy-metal pollution around coal gangue dump

NASA Astrophysics Data System (ADS)

Jiang, X.; Lu, W. X.; Zhao, H. Q.; Yang, Q. C.; Yang, Z. P.

2014-06-01

The aim of the present study is to evaluate the potential ecological risk and trend of soil heavy-metal pollution around a coal gangue dump in Jilin Province (Northeast China). The concentrations of Cd, Pb, Cu, Cr and Zn were monitored by inductively coupled plasma mass spectrometry (ICP-MS). The potential ecological risk index method developed by Hakanson (1980) was employed to assess the potential risk of heavy-metal pollution. The potential ecological risk in the order of ER(Cd) > ER(Pb) > ER(Cu) > ER(Cr) > ER(Zn) have been obtained, which showed that Cd was the most important factor leading to risk. Based on the Cd pollution history, the cumulative acceleration and cumulative rate of Cd were estimated, then the fixed number of years exceeding the standard prediction model was established, which was used to predict the pollution trend of Cd under the accelerated accumulation mode and the uniform mode. Pearson correlation analysis and correspondence analysis are employed to identify the sources of heavy metals and the relationship between sampling points and variables. These findings provided some useful insights for making appropriate management strategies to prevent or decrease heavy-metal pollution around a coal gangue dump in the Yangcaogou coal mine and other similar areas elsewhere.

Potential ecological risk assessment and prediction of soil heavy metal pollution around coal gangue dump

NASA Astrophysics Data System (ADS)

Jiang, X.; Lu, W. X.; Yang, Q. C.; Yang, Z. P.

2014-03-01

Aim of the present study is to evaluate the potential ecological risk and predict the trend of soil heavy metal pollution around a~coal gangue dump in Jilin Province (Northeast China). The concentrations of Cd, Pb, Cu, Cr and Zn were monitored by inductively coupled plasma mass spectrometry (ICP-MS). The potential ecological risk index method developed by Hakanson (1980) was employed to assess the potential risk of heavy metal pollution. The potential ecological risk in an order of E(Cd) > E(Pb) > E(Cu) > E(Cr) > E(Zn) have been obtained, which showed that Cd was the most important factor led to risk. Based on the Cd pollution history, the cumulative acceleration and cumulative rate of Cd were estimated, and the fixed number of years exceeding standard prediction model was established, which was used to predict the pollution trend of Cd under the accelerated accumulation mode and the uniform mode. Pearson correlation analysis and correspondence analysis are employed to identify the sources of heavy metal, and the relationship between sampling points and variables. These findings provide some useful insights for making appropriate management strategies to prevent and decrease heavy metal pollution around coal gangue dump in Yangcaogou coal mine and other similar areas elsewhere.

Integrated Utilization of Sewage Sludge and Coal Gangue for Cement Clinker Products: Promoting Tricalcium Silicate Formation and Trace Elements Immobilization

PubMed Central

Yang, Zhenzhou; Zhang, Yingyi; Liu, Lili; Seetharaman, Seshadri; Wang, Xidong; Zhang, Zuotai

2016-01-01

The present study firstly proposed a method of integrated utilization of sewage sludge (SS) and coal gangue (CG), two waste products, for cement clinker products with the aim of heat recovery and environment protection. The results demonstrated that the incremental amounts of SS and CG addition was favorable for the formation of tricalcium silicate (C3S) during the calcinations, but excess amount of SS addition could cause the impediment effect on C3S formation. Furthermore, it was also observed that the C3S polymorphs showed the transition from rhombohedral to monoclinic structure as SS addition was increased to 15 wt %. During the calcinations, most of trace elements could be immobilized especially Zn and cannot be easily leached out. Given the encouraging results in the present study, the co-process of sewage sludge and coal gangue in the cement kiln can be expected with a higher quality of cement products and minimum pollution to the environment. PMID:28773400

Modification of waste coal gangue and its application in the removal of Mn(2+) from aqueous solution.

PubMed

Qiu, Ruifang; Cheng, Fangqin

We developed a new calcination method to convert coal gangue (CG), a common waste generated from coal production process, into a modified form, which could be used as an adsorbent to remove Mn(2+) from aqueous solution. Sodium tetraborate (Na2B4O7·10H2O) was added into the CG calcination process as an additive, and the concentrations of Na2B4O7·10H2O were optimized along with the calcination temperature to obtain the best adsorbent capacity of modified coal gangue (MCG). We applied multiple analytical methods such as scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy and Brunauer-Emmett-Teller analysis to characterize the MCG. The results showed it had a smaller particle size and a larger specific surface area and pore volume after modification. It also indicated that the phase of CG transformed from kaolinite to metakaolinite after calcination. Moreover, a new substance was generated with two new peaks at 1,632 cm(-1) and 799 cm(-1). The Mn(2+) absorption capacity of MCG was evaluated using a series of experiments with different adsorbent doses, pH values and initial Mn(2+) concentrations during the adsorption process. We found that Mn(2+) adsorbent capacity of MCG increased by more than seven-fold compared to that of CG. The Langmuir isotherm model and the pseudo-second-order kinetic model provided the best fit to the adsorption processes.

Environmental investigation on co-combustion of sewage sludge and coal gangue: SO2, NOx and trace elements emissions.

PubMed

Yang, Zhenzhou; Zhang, Yingyi; Liu, Lili; Wang, Xidong; Zhang, Zuotai

2016-04-01

To promote the utilization of waste material as alternative fuel, the mono- and co-combustion characteristics of sewage sludge (SS) and coal gangue (CG) were systematically investigated, with emphasis on environmental influences. The emission of SO2, NOx as well as the trace elements during combustion of SS and CG were studied with regard to the effects of their chemistries, structures and interactions. Results showed that co-combustion can be beneficial for ignition performance. A synergic effect on both desulfurization and denitrification can be expected at ca. 800°C. Further, an enhanced retention of trace elements during co-combustion was also observed, especially for Pb and Zn. On the basis of the results, it can be expected that, with proper operation, co-combustion of SS and CG can be a promising method for the disposal of these two wastes. Copyright © 2015 Elsevier Ltd. All rights reserved.

Environment-oriented low-cost porous mullite ceramic membrane supports fabricated from coal gangue and bauxite.

PubMed

Lü, Qikai; Dong, Xinfa; Zhu, Zhiwen; Dong, Yingchao

2014-05-30

Porous mullite ceramic supports for filtration membrane were successfully fabricated via recycling of coal gangue and bauxite at sintering temperatures from 1100 to 1500°C with corn starch as pore-forming agent. The dynamic sintering behaviors, phase evolution, shrinkage, porosity and pore size, gas permeation flux, microstructure and mechanical property were systematically studied. A unique volume-expansion stage was observed at increased temperatures from 1276 to 1481°C caused by a mullitization-crystal-growth process. During this stage, open porosity increases and pore size distributions broaden, which result in a maximum of nitrogen gas flux at 1400°C. The X-ray diffraction results reveal that secondary mullitization took place from 1100°C and the major phase is mullite with a content of ∼84.7wt.% at 1400°C. SEM images show that the as-fabricated mullite supports have a porous microstructure composed of sintered glassy particles embedded with inter-locked mullite crystals, which grew gradually with increasing temperature from rod-like into blocky-like morphologies. To obtain mullite membrane supports with sufficient porosity and acceptable mechanical strength, the relationship between porosity and mechanical strength was investigated, which was fitted using a parabolic equation. Copyright © 2014 Elsevier B.V. All rights reserved.

Purification of trona ores by conditioning with an oil-in-water emulsion

DOEpatents

Miller, J. D.; Wang, Xuming; Li, Minhua

2009-04-14

The present invention is a trona concentrate and a process for floating gangue material from trona ore that comprises forming an emulsion, conditioning the trona ore at a high solids content in a saturated trona suspension, and then floating and removing the gangue material. The process for separating trona from gangue materials in trona ore can include emulsifying an oil in an aqueous solution to form an oil-in-water emulsion. A saturated trona suspension having a high solids content can also be formed having trona of a desired particle size. The undissolved trona in the saturated suspension can be conditioned by mixing the saturated suspension and the oil-in-water emulsion to form a conditioning solid suspension of trona and gangue material. A gas can be injected through the conditioning solid suspension to float the gangue material. Thus, the floated gangue material can be readily separated from the trona to form a purified trona concentrate without requirements of additional heat or other expensive processing steps.

Variations in organic carbon, aggregation, and enzyme activities of gangue-fly ash-reconstructed soils with sludge and arbuscular mycorrhizal fungi during 6-year reclamation.

PubMed

Yin, Ningning; Zhang, Zhen; Wang, Liping; Qian, Kuimei

2016-09-01

Mining activities can cause drastic disturbances in soil properties, which adversely affect the nutrient cycling and soil environment. As a result, many efforts have been made to explore suitable reclamation strategies that can be applied to accelerate ecology restoration. In this study, we reconstructed mine soils with fly ash, gangue, sludge, planted ryegrass, and inoculated arbuscular mycorrhizal fungi (AMF) in Pangzhuang mine of Xuzhou during 2009 to 2015. The soil aggregation process, enzyme activities (i.e., invertase, urease and acid phosphatase activities), soil organic carbon (SOC) as well as other soil nutrients such as nitrogen, phosphorus, and potassium contents of the reconstructed mine soils were monitored during 6-year reclamation. The integrated application of sludge and AMF led to a promising reclamation performance of mining areas, in which soil aggregate stability, enzyme activities, SOC, and ryegrass biomass were effectively enhanced. The micro-aggregates (< 0.25 mm) decreased with the increase of macro-aggregates (> 0.25 mm) during the reclamation, indicating that macro-aggregates were gradually formed from micro-aggregates during the pedogenesis of reconstructed mine soils. The correlation analysis shows that SOC contents in aggregate fraction of 0.25∼0.5 mm were correlated with aggregate distribution and enzyme activities. Enzyme activities, however, were not significantly correlated with aggregate distribution. The outcomes from the present study could enrich our understanding on soil property changes in pedogenesis process of reconstructed mine soils, and meanwhile, the employment of sludge combined with AMF is suggested to be an effective alternative for the mine soil reclamation.

Lead distribution in Permo-Carboniferous coal from the North China Plate, China.

PubMed

Kunli, Luo; Jidong, Lu; Lianwu, Chen

2005-02-01

The content and distribution of the lead in coal, gangue and the sulfur ball and the pyritic gangue of the Permo-Carboniferous in the North China Plate have been systematically studied (nearly 300 samples) in this paper. The Permo-Carboniferous coals in the North China Plate account for nearly 44.45% of total Chinese coal resources, and most of the steam coals in China come from the Permo-Carboniferous coals in the North China Plate. The result shows that lead content in the coal varied from 1.45 to 63.60 mg kg(-1), averaging 23.95 mg kg(-1); the lead content of the sulfur ball and the pyritic gangue in the coal seam ranges from 70.26-1060 mg kg(-1), with an average of 271.28 mg kg(-1); the lead content of the gangue is from 29.5 to 77.81 mg kg(-1), averaging at 40.77 mg kg(-1). The lead in the coal seam is mainly concentrated in the pyrite, such as sulfur ball, pyritic gangue or pyrite, and is the least concentrated in the organic of coal. The content of the lead has a direct ratio with the ash and the pyretic sulfur. Coal washing can reduce the content of the pyretic sulfur and the lead.

Preparation and Characteristics of Porous Ceramics by a foaming Technology at Low Temperature

NASA Astrophysics Data System (ADS)

Zhang, H. Q.; Wang, S. P.; Wen, J.; Wu, N.; Xu, S. H.

2017-12-01

Recycling and converting coal gangue and red mud into porous ceramics with good performance is a feasible disposal route. In this present work, porous foam ceramics was prepared using coal gangue and red mud as main raw materials at low sintering temperature, The amount of coal gangue and red mud were up to 70 wt%. To regulate the forming and sintering performance of the product, quartz sands and clay material were added to the formula. The green body was formed by a foaming technology using aluminum powders as foaming agents at room temperature. After foamed, the specimens were dried at 60-80 °C, and then calcined at 1060°C. Effects of concentration of NaOH and amount of aluminum powders on the phase, mechanical properties and microstructure were investigated here. Such study is expected to provide a new utilization route of the coal gangue and red mud, and brings both intensive environmental and economic benefits.

Distribution and assessment of Pb in the supergene environment of the Huainan Coal Mining Area, Anhui, China.

PubMed

Fang, Ting; Liu, Guijian; Zhou, Chuncai; Yuan, Zijiao; Lam, Paul Kwan Sing

2014-08-01

Coal mining area is highly subject to lead (Pb) pollution from coal mining activities. Several decades of coal mining and processing practices in dozens of coal mines in the Huainan Coal Mining Area (HCMA) have led to the accumulation of massive amounts of coal gangue, which piled in dumps. In order to investigate the impacts of coal gangue dumps on Pb level in the supergene media of the HCMA, a systematic sampling campaign comprising coal gangue, soil, wheat, and earthworm samples was conducted. The average Pb content in the coal mining area soil is 24 mg/kg, which is slightly higher than the associated coal gangues (23 mg/kg) and markedly higher than reference region soil (12.6 mg/kg). Soil in the HCMA present a slight to moderate Pb contamination, which might be related to the weathering and leaching of coal gangue dumps. Lateral distribution of Pb in HCMA soil differed among individual coal mines. The soil profile distribution of Pb depends on both natural and anthropogenic contributions. Average Pb content is higher in roots than in stems, leaves, and wheat husks, while the Pb level in seeds exceeded the maximum Pb allowance for foods (Maximum Levels of Contaminants in Foods of China, GB 2762-2012). Earthworms in the selected area are significantly enriched in Pb, suggesting higher bio-available Pb level in soil in the HCMA.

Ore genesis constraints on the Idaho Cobalt Belt from fluid inclusion gas, noble gas isotope, and ion ratio analyses

USGS Publications Warehouse

Hofstra, Albert H.; Landis, Gary P.

2012-01-01

The Idaho cobalt belt is a 60-km-long alignment of deposits composed of cobaltite, Co pyrite, chalcopyrite, and gold with anomalous Nb, Y, Be, and rare-earth elements (REEs) in a quartz-biotite-tourmaline gangue hosted in Mesoproterozoic metasedimentary rocks of the Lemhi Group. It is the largest cobalt resource in the United States with historic production from the Blackbird Mine. All of the deposits were deformed and metamorphosed to upper greenschist-lower amphibolite grade in the Cretaceous. They occur near a 1377 Ma anorogenic bimodal plutonic complex. The enhanced solubility of Fe, Co, Cu, and Au as chloride complexes together with gangue biotite rich in Fe and Cl and gangue quartz containing hypersaline inclusions allows that hot saline fluids were involved. The isotopes of B in gangue tourmaline are suggestive of a marine source, whereas those of Pb in ore suggest a U ± Th-enriched source. The ore and gangue minerals in this belt may have trapped components in fluid inclusions that are distinct from those in post-ore minerals and metamorphic minerals. Such components can potentially be identified and distinguished by their relative abundances in contrasting samples. Therefore, we obtained samples of Co and Cu sulfides, gangue quartz, biotite, and tourmaline and post-ore quartz veins as well as Cretaceous metamorphic garnet and determined the gas, noble gas isotope, and ion ratios of fluid inclusion extracts by mass spectrometry and ion chromatography. The most abundant gases present in extracts from each sample type are biased toward the gas-rich population of inclusions trapped during maximum burial and metamorphism. All have CO2/CH4 and N2/Ar ratios of evolved crustal fluids, and many yield a range of H2-CH4-CO2-H2S equilibration temperatures consistent with the metamorphic grade. Cretaceous garnet and post-ore minerals have high RH and RS values suggestive of reduced sulfidic conditions. Most extracts have anomalous 4He produced by decay of U and Th and

The action of macrosounds on graphite ore and derived products

NASA Technical Reports Server (NTRS)

Bradeteanu, C.; Dragan, O.

1974-01-01

A suspension of graphite ore, floated graphite, and the gangue left over from flotation were subjected to the action of macrosounds under determinant conditions. The following was found: (1) The graphite ore undergoes an efficient settling action. (2) The floated graphite is strongly crushed down to the dimensions of colloidal graphite. (3) The gangue left over from flotation can be further processed to recuperate graphite from its nuclei.

Supporting technology of roadside in gob-side entry in 110 longwall mining method

NASA Astrophysics Data System (ADS)

He, Manchao; Guo, Pengfei; Chen, Shangyuan; Gao, Yubing; Wang, Yajun

2017-05-01

To get better results of shaping roadside in 110 longwall mining method, the roadside support can be reasonably choose and designed through theoretical analysis, engineering test and other methods. The roadway support need to be designed based on the mining height and influence of mining pressure, and it is necessary to consider the "limited deformation" but also "given deformation". Because of the small mining high and short time under mining pressure effect in thin coal seam, roadside support can meet the requirements of block rock from gob using I-steel, but I-steel can't satisfy the deformation of roadway roof and easily lead to I-steel flexural buckling. In that condition we should use the U-steel that can compatible deformation with subsidence of roadway roof and enough torque in overlapping part between tow U-steel should be given when the U-steel is used to support gangue from gob and the U steel assembling two cards can coordinal deformation in dynamic pressure area keeping constant resistance with the deformation of roadway roof and can get a good effect. Through field test, due to the great impact force of the gangue from gob, single props and I-steel and U-steel are easily knocked down when the mining height is more than 4m. For large mining height, gangue blocking hydraulic support is designed and developed which can guarantee the stability and integrity of the roadway roof in the dynamic pressure area and can prevent the impact of gangue from gob. So it has better effect of forming roadway side using gangue from gob. According to above classification, the field experiments were carried out and obtained satisfactory results.

Geometallurgy of ironsand from the Waikato North Head deposit, New Zealand

USGS Publications Warehouse

Mauk, Jeffrey L.; Cocker, Helen A; Rogers, Harold; Ogiliev, Jamie; Padya, Alex B

2016-01-01

The Waikato North Head deposit produces a magnetic mineral concentrate from Quaternary sands that formed in a coastal setting in the North Island of New Zealand. Detailed examination of the magnetic mineral fraction of the different stratigraphic horizons mined at Waikato North Head shows that the youngest units yield concentrates with significant concentrations of gangue minerals that are included as composite grains, inclusions in titanomagnetite, and as gangue grains with titanomagnetite inclusions. The most abundant gangue minerals in the magnetic fractions of all mined units are pyroxene and amphibole; feldspar, quartz, and biotite are less abundant. The magnetic minerals, which are predominantly titanomagnetite, are used as feed for the Iron Plant in New Zealand Steel’s Glenbrook Steel Mill. From time to time, excessive accretion formation impacts the operation of the rotary reduction kilns of the Iron Plant. Olivine group minerals are the most common silicate phase in these accretions, and we hypothesise that the silicon and magnesium in these minerals are derived from the gangue minerals that are included in the magnetic mineral concentrate from the ironsands. Although various remediation processes are possible, the simplest and most cost effective would appear to be ensuring adequate blending of material from different stratigraphic units, particularly when the youngest strata are being mined in the deposit.

Polycyclic aromatic hydrocarbons (PAHs) in multimedia environment of Heshan coal district, Guangxi: distribution, source diagnosis and health risk assessment.

PubMed

Huang, Huan-Fang; Xing, Xin-Li; Zhang, Ze-Zhou; Qi, Shi-Hua; Yang, Dan; Yuen, Dave A; Sandy, Edward H; Zhou, Ai-Guo; Li, Xiao-Qian

2016-10-01

Mining activities are among the major culprits of the wide occurrences of soil and water pollution by PAHs in coal district, which have resulted in ecological fragilities and health risk for local residents. Sixteen PAHs in multimedia environment from the Heshan coal district of Guangxi, South China, were measured, aiming to investigate the contamination level, distribution and possible sources and to estimate the potential health risks of PAHs. The average concentrations of 16 PAHs in the coal, coal gangue, soil, surface water and groundwater were 5114.56, 4551.10, 1280.12 ng g(-1), 426.98 and 381.20 ng L(-1), respectively. Additionally, higher soil and water PAH concentrations were detected in the vicinities of coal or coal gangue dump. Composition analysis, isomeric ratio, Pearson correlation analysis and principal component analysis were performed to diagnose the potential sources of PAHs in different environmental matrices, suggesting the dominant inputs of PAHs from coal/coal combustion and coal gangue in the soil and water. Soil and water guidelines and the incremental lifetime risk (ICLR) were used to assess the health risk, showing that soil and water were heavily contaminated by PAHs, and mean ICLRcoal/coal-gangue and mean ICLRsoil were both significantly higher than the acceptable levels (1 × 10(-4)), posing high potential carcinogenic risk to residents, especially coal workers. This study highlights the environmental pollution problems and public health concerns of coal mining, particularly the potential occupational health hazards of coal miners exposed in Heshan.

Surface chemistry and flotation behavior of monazite, apatite, ilmenite, quartz, rutile, and zircon using octanohydroxamic acid collector

NASA Astrophysics Data System (ADS)

Nduwa Mushidi, Josue

Global increase in rare earth demand and consumption has led to further understanding their beneficiation and recovery. Monazite is the second most important rare earth mineral that can be further exploited. In this study, the surface chemistry of monazite in terms of zeta potential, adsorption density, and flotation response by microflotation using octanohydroxamic acid is determined. Apatite, ilmenite, quartz, rutile, and zircon are minerals that frequently occur with monazite among other minerals. Hence they were chosen as gangue minerals in this study. The Iso Electric Point (IEP) of monazite, apatite, ilmenite, quartz, rutile, and zircon are 5.3, 8.7, 3.8, 3.4, 6.3, and 5.1 respectively. The thermodynamic parameters of adsorption were also evaluated. Ilmenite, rutile and zircon have high driving forces for adsorption with DeltaGads. = 20.48, 22.10, and 22.4 kJ/mol respectively. The free energy of adsorption is 14.87 kJ/mol for monazite. Adsorption density testing shows that octanohydroxamic acid adsorbs on negatively charged surfaces of monazite and its gangue minerals which indicates chemisorption. This observation was further confirmed by microflotation experiments. Increasing the temperature to 80°C raises the adsorption and flotability of monazite and gangue minerals. This does not allow for effective separation. Sodium silicate appeared to be most effective to depress associated gangue minerals. Finally, the fundamentals learned were applied to the flotation of monazite ore from Mt. Weld. However, these results showed no selectivity due to the presence of goethite as fine particles and due to a low degree of liberation of monazite in the ore sample.

The composition of fluid inclusions in ore and gangue minerals from the Silesian-Cracow Mississippi Valley-type Zn-Pb deposits Poland: Genetic and environmental implications

USGS Publications Warehouse

Viets, J.G.; Hofstra, A.H.; Emsbo, P.; Kozlowski, A.

1996-01-01

The composition of fluids extracted from ore and gangue sulfide minerals that span most of the paragenesis of the Silesian-Cracow district was determined using a newly developed ion chromatographic (IC) technique. Ionic species determined were Na+, NH+4, Ca2+, Mg2+, K+, Rb+, Sr2+, Ba2+, Cl-, Br-, F-, I-, PO3-4, CO2-3, HS-, S2O2-3, SO2-4, NO-3, and acetate. Mineral samples included six from the Pomorzany mine and one from the Trzebionka mine which are hosted in the Triassic Muschelkalk Formation, and two samples of drill core from mineralized Upper Devonian strata. Nine paragenetically identifiable sulfide minerals occur throughout the Silesian-Cracow district. These include from earliest to latest: early iron sulfides, granular sphalerite, early galena, light-banded sphalerite, galena, dark-banded sphalerite, iron sulfides, late dark-banded sphalerite with late galena, and late iron sulfides. Seven of the minerals were sampled for fluid inclusion analysis in this study. Only the early iron sulfides and the last galena stage were not sampled. Although the number of analyses are limited to nine samples and two replicates and there is uncertainty about the characteristics of the fluid inclusions analyzed, the data show clear temporal trends in the composition of the fluids that deposited these minerals. Fluid inclusions in minerals deposited later in the paragenesis have significantly more K+, Br-, NH+4, and acetate but less Sr2+ than those deposited earlier in the paragenesis. The later minerals are also characterized by isotopically lighter sulfur and significantly more Tl and As in the solid minerals. The change in ore-fluid chemistry is interpreted to reflect a major change in the hydrologic regime of the district. Apparently, the migrational paths of ore fluids from the Upper Silesian basin changed during ore deposition and the fluids which deposited early minerals reacted with aquifers with very different geochemical characteristics than those that deposited

Study of talcum charging status in parallel plate electrostatic separator based on particle trajectory analysis

NASA Astrophysics Data System (ADS)

Yunxiao, CAO; Zhiqiang, WANG; Jinjun, WANG; Guofeng, LI

2018-05-01

Electrostatic separation has been extensively used in mineral processing, and has the potential to separate gangue minerals from raw talcum ore. As for electrostatic separation, the particle charging status is one of important influence factors. To describe the talcum particle charging status in a parallel plate electrostatic separator accurately, this paper proposes a modern images processing method. Based on the actual trajectories obtained from sequence images of particle movement and the analysis of physical forces applied on a charged particle, a numerical model is built, which could calculate the charge-to-mass ratios represented as the charging status of particle and simulate the particle trajectories. The simulated trajectories agree well with the experimental results obtained by images processing. In addition, chemical composition analysis is employed to reveal the relationship between ferrum gangue mineral content and charge-to-mass ratios. Research results show that the proposed method is effective for describing the particle charging status in electrostatic separation.

Appraisement of environment remote sensing method in mining area

NASA Astrophysics Data System (ADS)

Yang, Fengjie; Zhen, Han; Jiang, Tao; Lei, Liqing; Gong, Cailan

1998-08-01

Coal mining is attached great importance by society as a key profession of environmental pollution. The monitor and protection of coal-mine environment is a developing profession in China. The sulfur dioxide, carbon dioxide, carbon monoxide and other waste gases, which are put out by the spontaneous combustion or weathering of gangue are an important pollution resource of atmosphere. The stack of gangue held down many farmlands. Smoke, coal dust and powder coal ash pollute the environment of mining area and surroundings though the affection of monsoon. The pH value of water which coal mine drained off is low, and the drinking, farming and animal husbandry water where it flowed are affected. The surface subsidence which mining caused is a typical destruction of ground environment. The people pay attention to remote sensing as a method of rapidly, cheaply regional environment investigation. The paper tires making an appraisement of mining area environment monitor by many kind methods of remote sensing from the characteristic of mining area environment.

PROCESS FOR THE CONCENTRATION OF ORES CONTAINING GOLD AND URANIUM

DOEpatents

Gaudin, A.M.; Dasher, J.

1958-06-10

ABS>A process is described for concentrating certain low grade uranium and gold bearing ores, in which the gangue is mainly quartz. The production of the concentrate is accomplished by subjecting the crushed ore to a froth floatation process using a fatty acid as a collector in conjunction with a potassium amyl xanthate collector. Pine oil is used as the frothing agent.

Feasibility Studies for Production of Pellet Grade Concentrate from Sub Grade Iron Ore Using Multi Gravity Separator

NASA Astrophysics Data System (ADS)

Rao, Gottumukkala Venkateswara; Markandeya, R.; Kumar, Rajan

2018-04-01

An attempt has been made to utilise Sub Grade Iron Ore by producing pellet grade concentrate from Deposit 5, Bacheli Complex, Bailadila, Chhattisgarh, India. The `as received' Run of Mine (ROM) sample assayed 40.80% Fe, 40.90% SiO2. Mineralogical studies indicated that the main ore mineral is Hematite and lone gangue mineral is Quartz. Mineral liberation studies indicated that, the ore mineral Hematite and gangue mineral Quartz are getting liberated below 100 microns. The stage crushed and ground sample was subjected to concentration by using a Multi Gravity Separator (MGS). Rougher Multi Gravity Separation (MGS) experimental results were optimised to recover highest possible iron values. A concentrate of 55.80% Fe with a yield of 61.73% by weight with a recovery of 84.42% Iron values was obtained in rougher MGS concentrate. Further experiments were carried out with rougher MGS concentrate to produce a concentrate suitable for commercial grade pellet concentrate. It was proved that a concentrate assaying 66.67% Fe, 3.12% SiO2 with an yield of 45.08% by weight and with a recovery of 73.67% iron values in the concentrate.

Occurrence and mobility of toxic elements in coals from endemic fluorosis areas in the Three Gorges Region, SW China.

PubMed

Xiong, Yan; Xiao, Tangfu; Liu, Yizhang; Zhu, Jianming; Ning, Zengping; Xiao, Qingxiang

2017-10-01

Fluorine (F) is a topic of great interest in coal-combustion related endemic fluorosis areas. However, little extent research exists regarding the environmental geochemistry of toxic elements that are enriched in coals and coal wastes in traditional endemic fluorosis areas, particularly focusing on their occurrences and mobilities during the weathering-leaching processes of coals and coal wastes in the surface environment. This paper addressed the issue of toxic elements in coals and coal wastes in the Three Gorges Region, Southwest (SW) China, where endemic fluorosis has historically prevailed, and investigated the distribution, occurrence, mobility features, and associated potential health risks. For this purpose, a modified experiment combined with long-term humidity cell test and column leaching trial was applied to elucidate the mobility of toxic elements in coals and coal wastes. In addition, sequential chemical extraction (SCE) was used to ascertain the modes of occurrence of toxic elements. The results demonstrated that the contents of toxic elements in the study area followed the order: stone coals > gangues > coal balls > coals. Furthermore, modes of occurrence of toxic elements were obviously different in coals and coal wastes. For example, cadmium (Cd) was mainly associated with monosulfide fraction in coals, molybdenum (Mo) and arsenic (As) were mainly associated with carbonate and silicate in coal gangues and stone coals, chromium (Cr) mainly existed in silicate and insoluble matter in coal gangues and coal balls, thallium (Tl) mainly occurred in organic matter in stone coals and sulfide in coals, and the occurrence of antimony (Sb) varied with different kinds of samples. Moreover, a large amount of toxic elements released to the leachates during the weathering and leaching process, which might pollute the environment and threaten human health. Based on the geo-accumulation index (I geo ), single factor index (P i ) and Nemerow index (P N ), soils i n

Textural and structural evidence for a predeformation hydrothermal origin of the Tungsten Queen Deposit, Hamme District, North Carolina

USGS Publications Warehouse

Foose, M.P.; Slack, J.F.; Casadevall, T.

1980-01-01

The Hamme tungsten district is composed of a series of steeply dipping quartz-wolframite veins in the Piedmont of North Carolina. Veins are concentrated near the border of the lower Paleozoic Vance County pluton, along its western contact with green-schist-facies metapelites and metavolcanic rocks of the Carolina slate belt. One of these quartz veins, the Snead-Walker, hosts the Tungsten Queen deposit. The vein is 0 to 10 m thick and trends N 35 degrees E for approximately 3,500 m through slate belt rocks and the granitic pluton. The deposit has been worked to a depth of nearly 520 m and contains eight en echelon ore lodes that plunge 42 degrees to 65 degrees between S 10 degrees E and S 10 degrees W. Ore lodes commonly are encased in thin lenses of quartz-sericite greisen. The principal ore mineral is huebnerite and is accompanied by scattered occurrences of pyrite, sphalerite, galena, chalcopyrite, and tetrahedrite. The gangue is predominantly quartz with minor amounts of fluorite, sericite, and carbonate.Studies of minor structures and mineral textures indicate that both the wall rock and the ore and gangue minerals within the vein have been deformed by at least two events. The first event produced relatively gentle, open, and shallow-plunging folds; later, an intense episode of right-lateral shearing developed steeply plunging, tight folds and numerous northeast-trending shears. This latter deformation also developed a prominent alignment of ore and gangue minerals oblique to the vein walls and may have formed the en echelon distribution of ore lodes.In relatively undeformed parts of the vein, clusters of euhedral huebnerite crystals are oriented perpendicular to vein layering. Some prismatic crystals have terminations with cappings of sulfides and in polished thin section show concentric growth zones. These features are similar to textures found in unmetamorphosed tungsten-bearing hydrothermal vein deposits such as those at Pasto Bueno, Peru; Carrock Fell

The Balmat-Edwards zinc-lead deposits-synsedimentary ore from Mississippi valley-type fluids.

USGS Publications Warehouse

Whelan, J.F.; Rye, R.O.; Delorraine, W.

1984-01-01

The Balmat-Edwards Zn-Pb district in New York is in Mid-Proterozoic Grenville marbles. Tabular to podiform, generally conformable massive sphalerite-galena orebodies occur at various horizons in the approx 1 km-thick marbles. Metamorphism obscured or obliterated most primary characteristics, whose reconstruction is attempted through detailed S, C, and O isotope studies of the Fowler orebody, and trace element and S isotope studies of sphalerite concentrates and composite ore samples from 22 orebodies. Sulphur isotope data reflect equilibration at near peak metamorphism with some indication of re-equilibration during retrograde metamorphism. The carbon and oxygen isotope composition of gangue carbonates suggests derivation from the host marbles. The oxygen isotope composition of gangue quartz is compatible with a chert origin or metamorphism-equilibration with other minerals. Sulphur and lead isotopes and sulphide mineralogy suggests that the ore fluids were evolved basin brines, chemically like those responsible for Mississippi Valley-type deposits. The large stratigraphic span (> 600 m) of the Balmat orebodies may be due to basin dewatering of million-year intervals. Stratigraphically increasing 34S values of evaporite-anhydrite are postulated to record hydrothermal events and to imply bacterial sulphate reduction on an unusually large scale. Such a stratigraphic increase may be a general exploration guide where sediment-hosted exhalative deposits or Mississippi Valley-type deposits occur.-G.J.N.

Raman Spectroscopic Characterisation of Australian Banded Iron Formation and Iron Ore

NASA Astrophysics Data System (ADS)

Wells, M. A.; Ramanaidou, E. R.

2012-04-01

In Australia and world-wide over the past 5-10 years, declining reserves of premium, high-grade (>64% Fe), low-P bearing iron ore, have seen iron ore producers increase their utilisation of lower Fe-grade, higher P/Al/Si ore. In Australia, the channel iron deposits (CID), bedded iron deposits (BID) and, more recently, BIF-derived magnetite iron deposits (MID) have seen increased usage driven mainly by the increased demand from Chinese steel mills (Ramanaidou and Wells, 2011). Efficient exploitation and processing of these lower-grade iron ores requires a detailed understanding of their iron oxide and gangue mineralogy and geochemistry. The common Fe-bearing minerals (e.g., hematite, magnetite, goethite and kenomagnetite) in these deposits, as well as gangue minerals such as quartz and carbonates, are all strongly Raman active (e.g., de Faria et al., 1997). Their distinct Raman spectra enable them to be easily detected and mapped in situ in either unprepared material or samples prepared as polished blocks. In this paper, using representative examples of Australian CID ore, martite-goethite bedded iron deposit (BID) ore and banded iron formation (BIF) examined as polished blocks, we present a range of Raman spectra of the key iron ore minerals, and discuss how Raman spectroscopy can be applied to characterising iron ore mineralogy. Raman imaging micrographs, obtained using a StreamLine Plus Raman imaging system, clearly identified the main Fe-oxide and gangue components in the CID, BID and BIF samples when compared to optical micrographs. Raman analysis enabled the unequivocal identification of diamond in the CID ore as a contaminant from the polishing paste used to prepare the sample, and confirmed the presence of hematite in the BID ore in the form of martite, which can be morphologically similar to magnetite and, thus, difficult to otherwise distinguish. Image analysis of Raman mineral maps could be used to quantify mineral abundance based on the number of 'pixels

Column bioleaching of low-grade mining ore containing high level of smithsonite, talc, sphaerocobaltite and azurite.

PubMed

Ilyas, Sadia; Chi, Ruan; Bhatti, H N; Bhatti, I A; Ghauri, M A

2012-03-01

Present work describes the bioleaching potential of metals from low-grade mining ore containing smithsonite, sphaerocobaltite, azurite and talc as main gangue minerals with adapted consortium of Sulfobacillus thermosulfidooxidans strain-RDB and Thermoplasma acidophilum. Bioleaching potential improved markedly by added energy source, acid preleaching and adaptation of microbial consortium with mixed metal ions. During whole leaching period including acid preleaching stage of 960 h and bioleaching stage of 212 days about 76% Co, 70% Zn, 84% Cu, 72% Ni and 63% Fe leached out.

Modèle de formation du gisement d'argent d'Imiter (Anti-Atlas oriental, Maroc). Nouveaux apports de l'analyse structurale et minéralogique

NASA Astrophysics Data System (ADS)

Tuduri, Johann; Chauvet, Alain; Ennaciri, Aomar; Barbanson, Luc

2006-03-01

Based on a combined geometrical and mineralogical analysis, a three-stage model of formation of the mineralized veins of the giant Imiter silver deposit (Anti-Atlas, Morocco) is herein proposed. A first episode is characterized by the development of quartz, pink dolomite and Ag-rich minerals veins formed during a dextral transpressive event. The second episode is associated with a normal left-lateral motion that re-opens previous structures, filled by pink dolomite gangue. Alteration stages contribute to a local Ag enrichment. To cite this article: J. Tuduri et al., C. R. Geoscience 338 (2005).

Mineralogy and fluid inclusions study of carbonate-hosted Mississippi valley-type Ain Allega Pb-Zn-Sr-Ba ore deposit, Northern Tunisia

NASA Astrophysics Data System (ADS)

Abidi, R.; Slim-Shimi, N.; Somarin, A.; Henchiri, M.

2010-05-01

The Ain Allega Pb-Zn-Sr-Ba ore deposit is located in the flysch zone on the Eastern edge of the Triassic diapir of Jebel Hamra. It is part of the extrusive Triassic evaporate formation along the Ghardimaou-Cape Serrat faults. The ore body consists of argilic-dolomite breccias surrounded by argilo-gypsum Triassic formation, which forms the hanging wall of the deposit, and rimmed by the Paleocene marls. The ore minerals show a cap-rock type mineralization with different styles particularly impregnation in dolomite, cement of breccias, replacement ore and open space filling in the dissolution cavities and fractures. Ore minerals include sphalerite, galena, marcasite and pyrite. Principal gangue minerals are composed of barite, celestite, calcite, dolomite and quartz. The ore minerals are hosted by the Triassic carbonate rocks which show hydrothermal alteration, dissolution and brecciation. X-ray - crystallographic study of barite-celestite mineral series shows that pure barite and celestite are the abundant species, whereas strontianiferous barite (85-96.5% BaSO 4) and barian-celestite (95% SrSO 4) are minor. Primary and secondary mono-phase (liquid only) fluid inclusions are common in celestite. Microthermometric analyses in two-phases (liquid and vapour) fluid inclusions suggest that gangue and ore minerals were precipitated by a low-temperature (180 °C) saline (16.37 wt.% NaCl equivalent) solution originated possibly from a basinal brine with some input from magmatic or metamorphic fluid. Based on geology, mineralogy, texture and fluid characteristics, the Ain Allega deposit is classified as a carbonate-hosted Mississippi valley-type deposit.

An investigation into heterogeneity in a single vein-type uranium ore deposit: Implications for nuclear forensics.

PubMed

Keatley, A C; Scott, T B; Davis, S; Jones, C P; Turner, P

2015-12-01

Minor element composition and rare earth element (REE) concentrations in nuclear materials are important as they are used within the field of nuclear forensics as an indicator of sample origin. However recent studies into uranium ores and uranium ore concentrates (UOCs) have shown significant elemental and isotopic heterogeneity from a single mine site such that some sites have shown higher variation within the mine site than that seen between multiple sites. The elemental composition of both uranium and gangue minerals within ore samples taken along a single mineral vein in South West England have been measured and reported here. The analysis of the samples was undertaken to determine the extent of the localised variation in key elements. Energy Dispersive X-ray spectroscopy (EDS) was used to analyse the gangue mineralogy and measure major element composition. Minor element composition and rare earth element (REE) concentrations were measured by Electron Probe Microanalysis (EPMA). The results confirm that a number of key elements, REE concentrations and patterns used for origin location do show significant variation within mine. Furthermore significant variation is also visible on a meter scale. In addition three separate uranium phases were identified within the vein which indicates multiple uranium mineralisation events. In light of these localised elemental variations it is recommended that representative sampling for an area is undertaken prior to establishing the REE pattern that may be used to identify the originating mine for an unknown ore sample and prior to investigating impact of ore processing on any arising REE patterns. Copyright © 2015 Elsevier Ltd. All rights reserved.

Mineral and whole-rock compositions of seawater-dominated hydrothermal alteration at the Arctic volcanogenic massive sulfide prospect, Alaska

USGS Publications Warehouse

Schmidt, J.M.

1988-01-01

The Arctic volcanogenic massive sulfide prospect, located in the Ambler mineral district of northwestern Alaska, includes three types of hydrothermally altered rocks overlying, underlying, and interlayered with semimassive sulfide mineralization. Hydrothermal alteration of wall rocks and deposition of sulfide and gangue minerals were contemporaneous with Late Devonian of Early Mississippian basalt-rhyolite volcanism. Alteration developed asymmetrically around a linear fissure, suggesting fracture control of ore fluids rather than a point source. Microprobe analyses of phyllosilicates from the Arctic area indicate two discrete mineral populations. These differences in mineral chemistry are the result of differences in protolith composition caused by hydrothermal alteration-metasomatism. -from Author

PHYSICAL BENEFICATION OF LOW-GRADE URANIUM ORES

DOE Office of Scientific and Technical Information (OSTI.GOV)

Butler, J.N.

1958-07-30

Investigations are presented of methods for the physi cal beneficiation of low-grade and other uranium ores. The investlgations which have been in progress since September 1952 cover work done on a variety of natural ores, as well as a certain amount of basic research on mixtures of synthetic or high-grade natural uranium minerais with various gangues. Methods of beneficlation investigated include flotation, wet and dry attroftioning, magnetic separation. electresiatie separation, and misceilaneous minor methods. A rapid, routine method oicolorimeiric determlnation of uranium was also developed in order to facilitaie analyzing of low-grade materials for uranium. This proeedure is presenied inmore » condensed form. (auth)« less

Atmospheric emission of mercury due to combustion of steam coal and domestic coal in China

NASA Astrophysics Data System (ADS)

Wang, Shaobin; Luo, Kunli

2017-08-01

To study the mercury emission due to the combustion of steam coal and domestic coal in China, we analyzed the mercury contents of coal, fly ash, bottom ash and sluicing water in thermal power plants, steam boilers as well as domestic coal-stoves, in Shaanxi, Shanxi, Shandong and Yunnan Provinces. This study conduct an estimate of the Hg emission rates from steam coal and domestic coal combustion based on the method of mass distribution ratio of fly ash and bottom ash. The results show that the Hg emission rate of coal combustion in thermal power plants is about 50.21% (electrostatic precipitators + wet flue gas desulfurization), and that in heating boilers is about 67.23%, and 92.28% in industrial boilers without flue gas desulphurisation equipment. Furthermore, Hg emission rate is 83.61% due to domestic coal combustion in coal-stoves. The Hg emission amount into the atmosphere from power and heat generation, industrial boilers, domestic coal-stoves and spontaneous combustion of coal gangue is roughly estimated to be 133 ± 4, 100 ± 17, 11 ± 0.1 and 47 ± 26 tons in China in 2014, respectively, and the total Hg emission amount from this paper is estimated at 292 tons. The trends of Hg emission in China from 1991 to 2014 show an accelerating growth after 2002. The proportion of mercury emission due to thermal power, heating generation and industrial energy utilization continuously increased. The atmospheric emission of mercury due to combustion of steam coal, domestic coal and coal gangue accounts nearly 50% in total anthropogenic Hg emissions in China, indicating one of the largest sources of Hg emission in China which should draw more public and scientific attention in the future.

Mineralized aplite—pegmatite at Jabal Sa'id, Hijaz region, Kingdom of Saudi Arabia

NASA Astrophysics Data System (ADS)

Hackett, Damien

The Jabal Sa'id aplite—pegmatite, located at 23°49'03″N, 40°56'30″E, is part of the Jabal Hadb ash Sharar granite complex and resulted from emplacement of a residual volatile-rich fraction of alkali granite magma dominantly above a chilled carapace. Mineralization is layered, with four peak grades in layers 20-25 m wide, one of which may represent a mineral resource with greater potential than the aplite—pegmatite as a whole. The grades of all elements, except Zr, increase towards the upper part of the body. Chemical composition is extremely variable. Major-oxide data confirm previously determined geochemical characteristics and genetic relationships that suggested this body is an apogranite. However, the abundant new data also show that differences between the aplite—pegmatite and cognate alkali microgranite are not as great as previously reported, except for Na 2O which is extremely depleted in the apogranite. REE data support suggested genetic relationships and indicate that feldspar fractionation was important during crystallization. They also show that the content of HREE is comparatively constant throughout the aplite—pegmatite, and that variations in total REE content are caused by variations in the content of LREE. Bastnaesite and synchysite-(Y) are the principal rare-earth-element minerals, and are accompanied by monazite and synchesite; pyrochlore and thorite are also important ore minerals. Other elements concentrated in the aplite—pegmatite, such as Ta, Sn and U, occur only in solid solution in these minerals. The grain size of the ore minerals is commonly in the range 0.02-0.2 mm, and the grain size of gangue minerals, quartz, microcline and lesser amounts of aegirine and arfvedsonite, is typically in the range 1.0-4.0 mm. The ore minerals occur typically along gangue mineral boundaries. Zoning within the body permits calculation of high- and low-grade reserves which correspond to the upper and lower part of the apogranite.

Microbial Variants from Iron Ore Slimes: Mineral Specificity and pH Tolerance.

PubMed

Abhilash; Ghosh, A; Pandey, B D; Sarkar, S

2015-12-01

This paper describes the isolation of the native bacterial strains from the iron ore mines slime pond and its extremophilic characteristics. The two microbial isolates designated as CNIOS-1 and CNIOS-2 were grown in selective silicate broth at pH 7.0 and the organisms were tested for their selective adhesion on silicate and alumina minerals. The silicate bacteria with their exopolymers are very potent to grow over aluminosilicates. It was established that CNIOS-1 grew preferentially in the presence of silicate mineral compared to CNIOS-2 which grew in the presence of alumina. The organisms were tested for growth at various pH and trials were carried to define their efficacy for eventual applications to remove gangue minerals of silica and alumina from the raw material.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Aydin, M.E.; Yildirim, I.; Dogan, M.Z.

The Istanbul Region coals are characterized by high moisture contents (avg. 35%), high volatile matter values (avg. 45%), and more importantly high levels of sulfur in the range of 1 to 5%. These lignitic coals generally have relatively low ash (10%), and higher levels of calorific values over 5,000 Kcal/kg. The Multi-Gravity Separator (MGS), a new fine size gravity separation equipment, was tested to evaluate its potential for the desulfurization of these low-rank coals. Systematic tests conducted on two different samples of minus 1 mm size indicate that despite the finely distributed nature of coal and relatively small difference betweenmore » coal and its associated gangue minerals, the degree of pyritic sulfur removal is 65.7% and 85.9% for the respective coals.« less

Geology of the epithermal Ag-Au Huevos Verdes vein system and San José district, Deseado massif, Patagonia, Argentina

NASA Astrophysics Data System (ADS)

Dietrich, Andreas; Gutierrez, Ronald; Nelson, Eric P.; Layer, Paul W.

2012-03-01

The San José district is located in the northwest part of the Deseado massif and hosts a number of epithermal Ag-Au quartz veins of intermediate sulfidation style, including the Huevos Verdes vein system. Veins are hosted by andesitic rocks of the Bajo Pobre Formation and locally by rhyodacitic pyroclastic rocks of the Chon Aike Formation. New 40Ar/39Ar constraints on the age of host rocks and mineralization define Late Jurassic ages of 151.3 ± 0.7 Ma to 144.7 ± 0.1 Ma for volcanic rocks of the Bajo Pobre Formation and of 147.6 ± 1.1 Ma for the Chon Aike Formation. Illite ages of the Huevos Verdes vein system of 140.8 ± 0.2 and 140.5 ± 0.3 Ma are 4 m.y. younger than the volcanic host rock unit. These age dates are among the youngest reported for Jurassic volcanism in the Deseado massif and correlate well with the regional context of magmatic and hydrothermal activity. The Huevos Verdes vein system has a strike length of 2,000 m, with several ore shoots along strike. The vein consists of a pre-ore stage and three main ore stages. Early barren quartz and chalcedony are followed by a mottled quartz stage of coarse saccharoidal quartz with irregular streaks and discontinuous bands of sulfide-rich material. The banded quartz-sulfide stage consists of sulfide-rich bands alternating with bands of quartz and bands of chlorite ± illite. Late-stage sulfide-rich veinlets are associated with kaolinite gangue. Ore minerals are argentite and electrum, together with pyrite, sphalerite, galena, chalcopyrite, minor bornite, covellite, and ruby silver. Wall rock alteration is characterized by narrow (< 3 m) halos of illite and illite/smectite next to veins, grading outward into propylitic alteration. Gangue minerals are dominantly massive quartz intergrown with minor to accessory adularia. Epidote, illite, illite/smectite, and, preferentially at deeper levels, Fe-chlorite gangue indicate near-neutral pH hydrothermal fluids at temperatures of >220°C. Kaolinite occurring with

Implementation of Paste Backfill Mining Technology in Chinese Coal Mines

PubMed Central

Chang, Qingliang; Zhou, Huaqiang; Bai, Jianbiao

2014-01-01

Implementation of clean mining technology at coal mines is crucial to protect the environment and maintain balance among energy resources, consumption, and ecology. After reviewing present coal clean mining technology, we introduce the technology principles and technological process of paste backfill mining in coal mines and discuss the components and features of backfill materials, the constitution of the backfill system, and the backfill process. Specific implementation of this technology and its application are analyzed for paste backfill mining in Daizhuang Coal Mine; a practical implementation shows that paste backfill mining can improve the safety and excavation rate of coal mining, which can effectively resolve surface subsidence problems caused by underground mining activities, by utilizing solid waste such as coal gangues as a resource. Therefore, paste backfill mining is an effective clean coal mining technology, which has widespread application. PMID:25258737

Direct Reduction of Iron Ore

NASA Astrophysics Data System (ADS)

Small, M.

1981-04-01

In the search for a pure, available iron source, steelmakers are focusing their attention on Directly Reduced Iron (DRI). This material is produced by the reaction of a low gangue iron ore with a hydrocarbonaceous substance. Commercially, DRI is generated in four different reactors: shaft (moving-bed), rotary kiln, fluidized bed, and retort (fixed-bed). Annual worldwide production capacity approaches 33 million metric tons. Detailed assessments have been made of the uses of DRI, especially as a substitute for scrap in electric furnace (EF) steelmaking. DRI is generally of a quality superior to current grades of scrap, with steels produced more efficiently in the EF and containing lower levels of impurities. However, present economics favor EF steel production with scrap. But this situation could change within this decade because of a developing scarcity of good quality scrap.

Implementation of paste backfill mining technology in Chinese coal mines.

PubMed

Chang, Qingliang; Chen, Jianhang; Zhou, Huaqiang; Bai, Jianbiao

2014-01-01

Implementation of clean mining technology at coal mines is crucial to protect the environment and maintain balance among energy resources, consumption, and ecology. After reviewing present coal clean mining technology, we introduce the technology principles and technological process of paste backfill mining in coal mines and discuss the components and features of backfill materials, the constitution of the backfill system, and the backfill process. Specific implementation of this technology and its application are analyzed for paste backfill mining in Daizhuang Coal Mine; a practical implementation shows that paste backfill mining can improve the safety and excavation rate of coal mining, which can effectively resolve surface subsidence problems caused by underground mining activities, by utilizing solid waste such as coal gangues as a resource. Therefore, paste backfill mining is an effective clean coal mining technology, which has widespread application.

EPITHERMAL GOLD-SILVER MINERALIZATION RELATED TO VOLCANIC SUBSIDENCE IN THE CUSTER GRABEN, CUSTER COUNTY, IDAHO.

USGS Publications Warehouse

Johnson, Kathleen M.; McIntyre, David H.

1984-01-01

The Custer graben is a 13 by 32 km northeast-trending volcano-tectonic graben in the Challis volcanic field of central Idaho. Andesites, rhyolites, and associated pyroclastic rocks host vein and disseminated gold-silver deposits that are localized along discrete northeast- and northwest-trending fracture zones. Ore minerals in vein deposits are electrum, native gold and silver, chalcopyrite, and various sulfosalts in a gangue of pyrite and fine-grained quartz. At the Sunbeam Mine, near the center of the graben, vein and disseminated gold-silver mineralization occurred in hydrothermally altered rhyolite and pyroclastic rocks. The host rock has been pervasively silicified, and the feldspars altered to clay minerals. Analyses of surface and drill-core samples show that altered rocks are variably enriched in gold, silver, molybdenum, arsenic, zirconium, and selenium. Intense silicification is shown by SiO//2 values at high as 93%.

Petro-mineralogical Studies of the Paleoproterozoic Phosphorites in the Sonrai basin, Lalitpur District, Uttar Pradesh, India

DOE Office of Scientific and Technical Information (OSTI.GOV)

Dar, Shamim A., E-mail: sjshamim@gmail.com; Khan, K. F.; Khan, Saif A.

2015-09-15

The Paleoproterozoic phosphorites constitute an economically significant component of the Sonrai basin of Lalitpur district. These are associated with ferruginous shale, ironstone, limestone and quartz breccia. Petro-mineralogical studies of samples of the phosphorites, using X-ray diffractometry and scanning electron microscopy, reveal that the collophane (carbonate-fluorapatite) is the dominant phosphate mineral. Calcite, dolomite, quartz, mica and haematite are the dominant gangue constituents. The phosphate minerals occur as oolites mutually replaced by carbonate and silica. The presence of iron oxides has been found in most of the thin sections. There is meagre evidence of organic matter in the form of filaments ofmore » microbial phosphate laminae in the samples of phosphorite. The mineral assemblages, their texture and various forms in these phosphorites may be due to some environmental vicissitudes followed by replacement processes and biogenic activities.« less

Tourmaline in Appalachian - Caledonian massive sulphide deposits and its exploration significance.

USGS Publications Warehouse

Slack, J.F.

1982-01-01

Tourmaline is a common gangue mineral in several types of stratabound mineral deposits, including some massive base-metal sulphide ores of the Appalachian - Caledonian orogen. It is most abundant (sometimes forming massive foliated tourmalinite) in sediment-hosted deposits, such as those at the Elizabeth Cu mine and the Ore Knob Cu mine (North Carolina, USA). Trace amounts of tourmaline occur associated with volcanic-hosted deposits in the Piedmont and New England and also in the Trondheim district. Tourmaline associated with the massive sulphide deposits are Mg- rich dravites with major- and trace-element compositions significantly different from schorl. It is suggested that the necessary B was produced by submarine exhalative processes as a part of the same hydrothermal system that deposited the ores. An abundance of dravite in non-evaporitic terrains is believed to indicate proximity to former subaqueous fumarolic centres.-R.A.H.

Extraction of uranium from tailings by sulfuric acid leaching with oxidants

NASA Astrophysics Data System (ADS)

Huang, Jing; Li, Mi; Zhang, Xiaowen; Huang, Chunmei; Wu, Xiaoyan

2017-06-01

Recovery of uranium have been performed by leaching uranium-containing tailings in sulfuric acid system with the assistance of HF, HClO4, H2O2 and MnO2. The effect of reagent dosage, sulfuric acid concentration, Liquid/solid ratio, reaction temperature and particle size on the leaching of uranium were investigated. The results show that addiction of HF, HClO4, H2O2 and MnO2 significantly increased the extraction of uranium under 1M sulphuric acid condition and under the optimum reaction conditions a dissolution fraction of 85% by HClO4, 90% by HF, 95% by H2O2 can be reached respectively. The variation of technological mineralogy properites of tailings during leaching process show that the assistants can break gangue effectively. These observations suggest that optimum oxidants could potentially influence the extraction of uranium from tailings even under dilute acid condition.

Lunar mineral feedstocks from rocks and soils: X-ray digital imaging in resource evaluation

NASA Technical Reports Server (NTRS)

Chambers, John G.; Patchen, Allan; Taylor, Lawrence A.; Higgins, Stefan J.; Mckay, David S.

1994-01-01

The rocks and soils of the Moon provide raw materials essential to the successful establishment of a lunar base. Efficient exploitation of these resources requires accurate characterization of mineral abundances, sizes/shapes, and association of 'ore' and 'gangue' phases, as well as the technology to generate high-yield/high-grade feedstocks. Only recently have x-ray mapping and digital imaging techniques been applied to lunar resource evaluation. The topics covered include inherent differences between lunar basalts and soils and quantitative comparison of rock-derived and soil-derived ilmenite concentrates. It is concluded that x-ray digital-imaging characterization of lunar raw materials provides a quantitative comparison that is unattainable by traditional petrographic techniques. These data are necessary for accurately determining mineral distributions of soil and crushed rock material. Application of these techniques will provide an important link to choosing the best raw material for mineral beneficiation.

Approaches for controlling air pollutants and their environmental impacts generated from coal-based electricity generation in China.

PubMed

Xu, Changqing; Hong, Jinglan; Ren, Yixin; Wang, Qingsong; Yuan, Xueliang

2015-08-01

This study aims at qualifying air pollutants and environmental impacts generated from coal-based power plants and providing useful information for decision makers on the management of coal-based power plants in China. Results showed that approximately 9.03, 54.95, 62.08, and 12.12% of the national carbon dioxide, sulfur dioxide, nitrogen oxides, and particulate matter emissions, respectively, in 2011were generated from coal-based electricity generation. The air pollutants were mainly generated from east China because of the well-developed economy and energy-intensive industries in the region. Coal-washing technology can simply and significantly reduce the environmental burden because of the relativity low content of coal gangue and sulfur in washed coal. Optimizing the efficiency of raw materials and energy consumption is additional key factor to reduce the potential environmental impacts. In addition, improving the efficiency of air pollutants (e.g., dust, mercury, sulfur dioxide, nitrogen oxides) control system and implementing the strict requirements on air pollutants for power plants are important ways for reducing the potential environmental impacts of coal-based electricity generation in China.

Benefaction studies on the Hasan Celebi magnetite deposit, Turkey

USGS Publications Warehouse

Pressler, Jean W.; Akar, Ali

1972-01-01

Bench-scale and semicontinuous tests were performed on surface, trench, and diamond drill core samples from the Hasan Celebi low-grade magnetite deposit to determine the optimum benefication procedures utilizing wet magnetic separation techniques. Composite core samples typically contain about 27 percent recoverable magnetite and require crushing and grinding through 1 mm in size to insure satisfactory separation of the gangue from the magnetite. Regrinding and cleaning the magnetite concentrate to 80 percent minus 150-mesh is necessary to obtain an optimum of 66 percent iron. Semicontinuous pilot-plant testing with the wet magnetic drum using the recycled middling technique indicates that as much as 83 percent of the acid-soluble iron can be recovered into a concentrate containing 66 percent iron, with minimum deleterious elements. This represents 27 weight percent of the original ore. Further tests will continue when the Maden Tetkik ve Arama Enstitusu (MTA) receives 24 tons of bulk sample from an exploratory drift and cross-cut now being driven through a section of the major reserve area.

New insights into the extraction of invisible gold in a low-grade high-sulfur Carlin-type gold concentrate by bio-pretreatment

NASA Astrophysics Data System (ADS)

Qiu, Xiao-bin; Wen, Jian-kang; Huang, Song-tao; Yang, Hong-ying; Liu, Mei-lin; Wu, Biao

2017-10-01

To extract gold from a low-grade (13.43 g/t) and high-sulfur (39.94wt% sulfide sulfur) Carlin-type gold concentrate from the Nibao deposit, Guizhou, a bio-pretreatment followed by carbon-in-pulp (CIP) cyanide leaching process was used. Various methods were used to detect the low-grade gold in the concentrate; however, only time-of-flight secondary-ion mass spectrometry (TOF-SIMS) was successful. With bio-pretreatment, the gold recovery rate increased by approximately 70.16% compared with that obtained by direct cyanide leaching of the concentrate. Various attempts were made to increase the final gold recovery rate. However, approximately 20wt% of the gold was non-extractable. To determine the nature of this non-extractable gold, mineralogy liberation analysis (MLA), formation of secondary product during the bio-pretreatment, and the preg-robbing capacity of the carbonaceous matter in the ore were investigated. The results indicated that at least four factors affected the gold recovery rate: gold occurrence, tight junctions of gold-bearing pyrite with gangue minerals, jarosite coating of the ore, and the carbonaceous matter content.

Bismuth selenides from St. Andreasberg, Germany: an oxidised five-element style of mineralisation and its relation to post-Variscan vein-type deposits of central Europe

NASA Astrophysics Data System (ADS)

Cabral, Alexandre Raphael; Ließmann, Wilfried; Jian, Wei; Lehmann, Bernd

2017-10-01

Carbonate veinlets at Roter Bär, a former underground mine in the polymetallic St. Andreasberg vein district of the Harz Mountains, Germany, host selenide minerals that are characterised as Bi-Ag-bearing clausthalite (PbSe), tiemannite (HgSe), guanajuatite (Bi2Se3) and a number of selenides of Bi, Zn, Cu, Ag and Pd. An unnamed Bi-Pb-Ag selenide species with some Hg and Cu, ideally Bi4Pb3Ag2Se10, is reported here. Specular hematite is disseminated within the clausthalite, at the marginal zones of which other selenide minerals are located. The occurrence of bohdanowiczite (AgBiSe2) and umangite (Cu3Se2) constrains the formation temperature to ≤120 °C, and the selenide-hematite assemblage (plus barite in the carbonate gangue) identifies highly oxidised conditions. Selenide assemblages of Pb, Bi, Ag, with and without Co and Ni, occur in many parts of the Variscan basement of central Europe (Harz, Erzgebirge, Schwarzwald and Bohemian Massif) and represent a high-oxidation variety of five-element (Ag-As-Bi-Co-Ni) veins.

Co-treatment of spent cathode carbon in caustic and acid leaching process under ultrasonic assisted for preparation of SiC.

PubMed

Yuan, Jie; Xiao, Jin; Li, Fachuang; Wang, Bingjie; Yao, Zhen; Yu, Bailie; Zhang, Liuyun

2018-03-01

Spent cathode carbon (SCC) from aluminum electrolysis has been treated in ultrasonic-assisted caustic leaching and acid leaching process, and purified SCC used as carbon source to synthesize silicon carbide (SiC) was investigated. Chemical and mineralogical properties have been characterized by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM), and thermogravimetry and differential scanning calorimetry (TGA-DSC). Various experimental factors temperature, time, liquid-solid ratio, ultrasonic power, and initial concentration of alkali or acid affecting on SCC leaching result were studied. After co-treatment with ultrasonic-assisted caustic leaching and acid leaching, carbon content of leaching residue was 97.53%. SiC power was synthesized by carbothermal reduction at 1600 °C, as a result of yield of 76.43%, and specific surface area of 4378 cm 2 /g. This is the first report of using purified SCC and gangue to prepare SiC. The two industrial wastes have been used newly as secondary sources. Furthermore, ultrasonic showed significant effect in SCC leaching process. Copyright © 2017 Elsevier B.V. All rights reserved.

Mineralogy, textures, and relative age relationships of massive sulfide ore in the West Shasta district, California ( USA).

USGS Publications Warehouse

Howe, S.S.

1985-01-01

The Devonian massive sulfide orebodies of the West Shasta district in N California are composed primarily of pyrite, with lesser amounts of other sulfide and gangue minerals. Examination of polished thin sections of more than 100 samples from the Mammoth, Shasta King, Early Bird, Balaklala, Keystone, and Iron Mountain mines suggests that mineralization may be divided into 6 paragenetic stages, the last 5 each separated by an episode of deformation: 1) precipitation of fine-grained, locally colloform and framboidal pyrite and sphalerite; 2) deposition of fine-grained arsenopyrite and coarse-grained pyrite; 3) penetration and local replacement of sulfide minerals of stages 1 and 2 along growth zones and fractures by chalcopyrite, sphalerite, galena, tennantite, pyrrhotite, bornite, and idaite; 4) recrystallization and remobilization of existing minerals; 5) deposition of quartz, white mica, chlorite, and calcite; and 6) formation of bornite, digenite, chalcocite, and covellite during supergene enrichment of several orebodies at the Iron Mountain mine. Mineralogic and textural evidence do not support a second major episode of massive sulfide mineralization during the Permian. -from Author

[Study on the determination of trace gallium in molybdenum-coated pyrolytic graphite tube by electrothermal absorption spectrometry].

PubMed

Huang, Yu-an; Zhou, Fang-qin; Long, Si-hua; Yang, Liu

2004-02-01

The effects on gallium atomization in the pyrolytic graphite tube imposed by different matrix modifiers and different coatings were discussed detailedly in this paper. In the presence of matrix modifier of Ni(NO3)2 the matrix interference was eliminated efficiently. The pyrolytic graphite tubes were coated differently with lanthanum, zirconium, and molybdenum to avoid producing gallium carbide. Results showed that the tube with molybdenum coating was the best. On this basis, the mechanism of gallium atomization in the molybdenum-coated pyrolytic graphite tube using Ni(NO3)2 as a matrix modifier was studied furthermore; in addition, the parameters of the operation were optimized. As a result, a new method improved in many aspects was developed to detect trace gallium in complicated sample of gangue. The outcomes of practical applications indicated that the method could satisfy the requests of analysis and that the manipulations were simple to achieve. The characteristic content, the detection limit, and the adding recoveries were 2.12 x 10(-11) g, 1.4 x 10(-10) g and 97.4%-102.7% respectively, and the relative standard deviation was less than or equal to 3.6% (n = 11).

Application of Laser Scanning for Creating Geological Documentation

NASA Astrophysics Data System (ADS)

Buczek, Michał; Paszek, Martyna; Szafarczyk, Anna

2018-03-01

A geological documentation is based on the analyses obtained from boreholes, geological exposures, and geophysical methods. It consists of text and graphic documents, containing drilling sections, vertical crosssections through the deposit and various types of maps. The surveying methods (such as LIDAR) can be applied in measurements of exposed rock layers, presented in appendices to the geological documentation. The laser scanning allows obtaining a complete profile of exposed surfaces in a short time and with a millimeter accuracy. The possibility of verifying the existing geological cross-section with laser scanning was tested on the example of the AGH experimental mine. The test field is built of different lithological rocks. Scans were taken from a single station, under favorable measuring conditions. The analysis of the signal intensity allowed to divide point cloud into separate geological layers. The results were compared with the geological profiles of the measured object. The same approach was applied to the data from the Vietnamese hard coal open pit mine Coc Sau. The thickness of exposed coal bed deposits and gangue layers were determined from the obtained data (point cloud) in combination with the photographs. The results were compared with the geological cross-section.

Discriminating fluid source regions in orogenic gold deposits using B-isotopes

NASA Astrophysics Data System (ADS)

Lambert-Smith, James S.; Rocholl, Alexander; Treloar, Peter J.; Lawrence, David M.

2016-12-01

The genesis of orogenic gold deposits is commonly linked to hydrothermal ore fluids derived from metamorphic devolatilization reactions. However, there is considerable debate as to the ultimate source of these fluids and the metals they transport. Tourmaline is a common gangue mineral in orogenic gold deposits. It is stable over a very wide P-T range, demonstrates limited volume diffusion of major and trace elements and is the main host of B in most rock types. We have used texturally resolved B-isotope analysis by secondary ion mass spectrometry (SIMS) to identify multiple fluid sources within a single orogenic gold ore district. The Loulo Mining District in Mali, West Africa hosts several large orogenic gold ore bodies with complex fluid chemistry, associated with widespread pre-ore Na- and multi-stage B-metasomatism. The Gara deposit, as well as several smaller satellites, formed through partial mixing between a dilute aqueous-carbonic fluid and a hypersaline brine. Hydrothermal tourmaline occurs as a pre-ore phase in the matrix of tourmalinite units, which host mineralization in several ore bodies. Clasts of these tourmalinites occur in mineralized breccias. Disseminated hydrothermal and vein hosted tourmaline occur in textural sites which suggest growth during and after ore formation. Tourmalines show a large range in δ11B values from -3.5 to 19.8‰, which record a change in fluid source between paragenetic stages of tourmaline growth. Pre-mineralization tourmaline crystals show heavy δ11B values (8-19.8‰) and high X-site occupancy (Na ± Ca; 0.69-1 apfu) suggesting a marine evaporite source for hydrothermal fluids. Syn-mineralization and replacement phases show lighter δ11B values (-3.5 to 15.1‰) and lower X-site occupancy (0.62-0.88 apfu), suggesting a subsequent influx of more dilute fluids derived from devolatilization of marine carbonates and clastic metasediments. The large, overlapping range in isotopic compositions and a skew toward the

Mineralogical variation of skarn ore from the Tellerhäuser deposit, Pöhla, Germany

NASA Astrophysics Data System (ADS)

Simons, Bethany; Andersen, Jens Christian; Rollinson, Gavyn; Armstrong, Robin; Dolgopolova, Alla; Seltmann, Reimar; Stanley, Chris; Roscher, Marco

2017-04-01

The polymetallic Zn-Fe-Sn-Cu-In skarns at Pöhla Tellerhäuser in the western Erzgebirge represent some of the largest unexploited occurrences of Sn and In in Europe. The skarns developed in schists and gneisses at the margin of the Schwarzenberg Gneiss cupola and the Eibenstock granites. The flat-lying skarn layers display extreme mineralogical variability with alternating units of pyroxene, sphalerite, magnetite, amphibole and calc-silicate skarns with hanging wall schist and feeder stockwork. The polymetallic skarn ores represent a complex challenge for mineral processing, with fine-grained, locked target minerals and partitioning of target metals into silicates (e.g. Sn in malayaite). Optical microscopy, QEMSCAN® and electron-probe microanalysis have been used to determine the mineralogical variability of the skarn types with the aim to determine the deportment of the target metals to guide mineral processing test work. The composition of the skarns is extremely variable reflecting the complex mineralogy and indicating substantial variability associated with replacement reactions through the protolith(s). Cassiterite (SnO2) is the dominant Sn-bearing mineral in all the skarn types. However, the skarns also carry malayaite (CaSnO[SiO4], up to 0.03 vol%), which locally dominates over cassiterite. Cassiterite is intergrown with Fe-amphibole, grossular garnet, fluorite and magnetite. The cassiterite is unaltered, but some grains have rare iron oxide rims and inclusions. Malayaite shows a similar association to cassiterite and is intergrown as clusters of grains with silicate gangue, particularly Fe amphibole and grossular garnet and remains unaltered with no inclusions. Zinc is exclusively hosted in sphalerite and varies from 0.02 wt.% in the hanging wall schist to 36.5 wt.% in the sphalerite skarn. The high Zn values are accompanied by high values of Cd (locally in excess of 1000 ppm) and In (up to 180 ppm). Sphalerite grains are locally up to 4 mm, subhedral

Evolution of the Bucium Rodu and Frasin magmatic-hydrothermal system, Metaliferi Mountains, Romania

NASA Astrophysics Data System (ADS)

Iatan, Elena Luisa; Berbeleac, Ion; Visan, Madalina; Minut, Adrian; Nadasan, Laurentiu

2013-04-01

The Miocene Bucium Rodu and Frasin maar-diatreme structures and related Au-Ag epithermal low sulfidation with passing to mesothermal mineralizations are located in the Bucium-Rosia Montana-Baia de Aries metallogenetic district, within so called the "Golden Quatrilaterum", in the northeastern part of the Metaliferi Mountains. These structures are situated at about 5 km southeast from Rosia Montana, the largest European Au-Ag deposit. The total reserves for Bucium Rodu-Frasin are estimated at 43.3 Mt with average contents of 1.3 g/t Au and 3 g/t Ag. The Miocene geological evolution of Bucium Rodu and Frasin magmatic-hydrothermal system took place in closely relationships with tectonic, magmatic and metallogenetic activity from Bucium-Rosia Montana-Baia de Aries district in general, and adjacent areas, in special. The hydrothermal alteration is pervasive; adularia followed by phyllic, carbonatization and silicification alterations, usually show a close relationship with the mineralizations. Propylitic alteration occurs dominantly towards the depth; argillic alteration shows a local character. The mineralization occurs in veins, breccias, stockworks and disseminations and is hosted within two volcanic structures emplaced into a sequence of Cretaceous sediments in closely genetically relations with the Miocene phreatomagmatic fracturing and brecciation events. Within Rodu maar-diatreme structure the mineralizations follow especially the contact between the diatreme and Cretaceous flysch. The vein sets with low, moderately and near vertical dippings, cover 400x400m with N-S trend. The most important mineralization style is represented by veins, accompanied by hydrothermal breccias and disseminations. The veins spatial distribution relives as "en echelon" tension veins. They carry gold, minor base metal sulphides (pyrite, chalcopyrite, sphalerite, galena, tetrahedrite, arsenopyrite). Gangue is represented by carbonates (calcite, dolomite, ankerite, siderite, rhodochrosite

Study on environment detection and appraisement of mining area with RS

NASA Astrophysics Data System (ADS)

Yang, Fengjie; Hou, Peng; Zhou, Guangzhu; Li, Qingting; Wang, Jie; Cheng, Jianguang

2006-12-01

In this paper, the big coal mining area Yanzhou is selected as the typical research area. According to the special dynamic change characteristic of the environment in the mining area, the environmental dynamic changes are timely monitored with the remote sensing detection technology. Environmental special factors, such as vegetation, water, air, land-over, are extracted by the professional remote sensing image processing software, then the spatial information is managed and analyzed in the geographical information system (GIS) software. As the result, the dynamic monitor and query for change information is achieved, and the special environmental factor dynamic change maps are protracted. On the base of the data coming from the remote sensing image, GIS and the traditional environment monitoring, the environmental quality is appraised with the method of indistinct matrix analysis, the multi-index and the analytical hierarchy process. At last, those provide the credible science foundation for the local environment appraised and the sustained development. In addition, this paper apply the hyper spectrum graphs by the FieldSpec Pro spectroradiometer, together with the analytical data from environmental chemical, to study the growth of vegetation which were seed in the land-over consisting of gangue, which is a new method to study the impact to vegetation that are growing in the soil.

New influence factor inducing difficulty in selective flotation separation of Cu-Zn mixed sulfide minerals

NASA Astrophysics Data System (ADS)

Deng, Jiu-shuai; Mao, Ying-bo; Wen, Shu-ming; Liu, Jian; Xian, Yong-jun; Feng, Qi-cheng

2015-02-01

Selective flotation separation of Cu-Zn mixed sulfides has been proven to be difficult. Thus far, researchers have found no satisfactory way to separate Cu-Zn mixed sulfides by selective flotation, mainly because of the complex surface and interface interaction mechanisms in the flotation solution. Undesired activation occurs between copper ions and the sphalerite surfaces. In addition to recycled water and mineral dissolution, ancient fluids in the minerals are observed to be a new source of metal ions. In this study, significant amounts of ancient fluids were found to exist in Cu-Zn sulfide and gangue minerals, mostly as gas-liquid fluid inclusions. The concentration of copper ions released from the ancient fluids reached 1.02 × 10-6 mol/L, whereas, in the cases of sphalerite and quartz, this concentration was 0.62 × 10-6 mol/L and 0.44 × 10-6 mol/L, respectively. As a result, the ancient fluid is a significant source of copper ions compared to mineral dissolution under the same experimental conditions, which promotes the unwanted activation of sphalerite. Therefore, the ancient fluid is considered to be a new factor that affects the selective flotation separation of Cu-Zn mixed sulfide ores.

Characteristics of the Roof Behaviors and Mine Pressure Manifestations During the Mining of Steep Coal Seam

NASA Astrophysics Data System (ADS)

Hong-Sheng, Tu; Shi-Hao, Tu; Cun, Zhang; Lei, Zhang; Xiao-Gang, Zhang

2017-12-01

A steep seam similar simulation system was developed based on the geological conditions of a steep coal seam in the Xintie Coal Mine. Basing on similar simulation, together with theoretical analysis and field measurement, an in-depth study was conducted to characterize the fracture and stability of the roof of steep working face and calculate the width of the region backfilled with gangue in the goaf. The results showed that, as mining progressed, the immediate roof of the steep face fell upon the goaf and backfilled its lower part due to gravity. As a result, the roof in the lower part had higher stability than the roof in the upper part of the working face. The deformation and fracture of main roof mainly occurred in the upper part of the working face; the fractured main roof then formed a "voussoir beam" structure in the strata's dip direction, which was subjected to the slip- and deformation-induced instability. The stability analysis indicated that, when the dip angle increased, the rock masses had greater capacity to withstand slip-induced instability but smaller capacity to withstand deformation-induced instability. Finally, the field measurement of the forces exerted on the hydraulic supports proved the characteristics of the roof's behaviors during the mining of a steep seam.

Fe and Mn removal from mining drainage using goaf filling materials obtained from coal mining process.

PubMed

Zhang, Liping; Chen, Aolei; Qu, Hongbin; Xu, Shouqiang; Zhang, Xue; He, Xuwen

2015-01-01

Coal gangue, sandy soil and clay (mass ratio 45:4:1) as goaf filling materials acquired from coal mining processes were applied to remove Fe and Mn effectively from mining drainage. The results of an adsorption kinetic study showed that the Fe adsorption equation was y=21.454y+8.4712, R2=0.9924 and the Mn adsorption equation was y=7.5409x+0.905, R2=0.9957. Meanwhile, the goaf filling materials had low desorption capacity (Fe 6.765 μg/g, Mn 1.52 μg/g) and desorption ratio (Fe 8.98%, Mn 11.04%). Experiments demonstrated that Fe and Mn from mining drainage could be removed stably at a flow rate of 1.2 L/min, Fe inlet concentration of less than 40 mg/L, Mn inlet concentration of less than 2 mg/L and neutral or alkaline conditions. During a procedure of continuous experiments, the effluent quality could meet the requirement of the 'Code for Engineering Design of Sewage Regeneration-GB503352-2002'. A real-application project using goaf filling materials to treat mining drainage in Shendong coal mine showed that the average cost per ton of mining drainage was about 0.55 RMB, which could bring about considerable economic benefit for coal mining enterprises.

Ba'id al Jimalah tungsten prospect, Najd region, Kingdom of Saudi Arabia

NASA Astrophysics Data System (ADS)

Lofts, P. G.

The Ba'id al Jimalah tungsten prospect is located in the NE of the Arabian Shield, at 25°09'N, 42°41'E. Mineralization is associated with a late-Proterozoic, porphyritic microgranite emplaced in folded, fine-grained clastic rocks of the Murdama group, within an aureole of biotite-rich hornfels. The microgranite forms a 30 m-thick sill and numerous smaller sills and dikes cropping out along two low, sub-parallel ridges and several small hills in an area 700 m square. The form of the intrusion at depth is uncertain. It is slightly to intensely sericitized, in places greisenized, and is enriched in Li, F and Rb. Wolframite occurs with minor cassiterite, scheelite and sulfides in quartz veins cutting both microgranite and hornfelsed wall-rock. The veins have a dominant trend of 110-115°, and are thicker and more numerous in the microgranite. Gangue minerals include plagioclase and potassium feldspar, muscovite, sericite, fluorite and minor siderite. A major Najd fault trending 130-135° probably controlled magma emplacement and subsequent hydrothermal and pneumatolytic activity. A percussion drilling program, restricted to the outcrop of the sill on the north ridge, has outlined 800,000 tonnes grading 0.10% WO 3 and 0.01% Sn.

Are modern geothermal waters in northwest Nevada forming epithermal gold deposits?

USGS Publications Warehouse

Breit, George N.; Hunt, Andrew G.; Wolf, Ruth E.; Koenig, Alan E.; Fifarek, Richard; Coolbaugh, Mark F.

2010-01-01

Hydrothermal systems currently are active near some gold deposits in northwestern Nevada. Possible links of these modern systems to gold mineralization were evaluated by chemically and isotopically analyzing water samples from the Brady, Dixie Valley, Humboldt House, San Emidio-Empire, Soda Lake, and Wabuska geothermal areas. In addition, quartz veins from Humboldt House and the adjacent Florida Canyon Mine were analyzed to compare ore and gangue phases with those predicted to form from proximal hydrothermal fluids.Nearly all water samples are alkali-chloride-type. Total dissolved solids range from 800 to 3900 mg/L, and pH varies from 5.6 to 7.8. Geochemical modeling with SOLVEQ, WATCH, and CHILLER predict the precipitation of silica in all systems during cooling. Anhydrite, calcite, barite, pyrite, base-metal sulfides, and alumino-silicates are variably saturated at calculated reservoir temperatures and also precipitate during boiling/cooling of some fluids. Measured dissolved gold concentrations are low (<0.2μg/L), but are generally consistent with contents predicted by equilibrium of sampled solutions with elemental gold at reservoir temperatures.  Although the modern geothermal waters can precipitate ore minerals, the low gold and other ore metal concentrations require very large fluid volumes to form a deposit of economic interest.

Metal mobilization under alkaline conditions in ash-covered tailings.

PubMed

Lu, Jinmei; Alakangas, Lena; Wanhainen, Christina

2014-06-15

The aim of this study was to determine element mobilization and accumulation in mill tailings under alkaline conditions. The tailings were covered with 50 cm of fly ash, and above a sludge layer. The tailings were geochemically and mineralogically investigated. Sulfides, such as pyrrhotite, sphalerite and galena along with gangue minerals such as dolomite, calcite, micas, chlorite, epidote, Mn-pyroxene and rhodonite were identified in the unoxidized tailings. The dissolution of the fly ash layer resulted in a high pH (close to 12) in the underlying tailings. This, together with the presence of organic matter, increased the weathering of the tailings and mobilization of elements in the uppermost 47 cm of the tailings. All primary minerals were depleted, except quartz and feldspar which were covered by blurry secondary carbonates. Sulfide-associated elements such as Cd, Fe, Pb, S and Zn and silicate-associated elements such as Fe, Mg and Mn were released from the depletion zone and accumulated deeper down in the tailings where the pH decreased to circum-neutral. Sequential extraction suggests that Cd, Cu, Fe, Pb, S and Zn were retained deeper down in the tailings and were mainly associated with the sulfide phase. Calcium, Cr, K and Ni released from the ash layer were accumulated in the uppermost depletion zone of the tailings. Copyright © 2014 Elsevier Ltd. All rights reserved.

A risk assessment for exposure to grunerite asbestos (amosite) in an iron ore mine

PubMed Central

Nolan, R. P.; Langer, A. M.; Wilson, Richard

1999-01-01

The potential for health risks to humans exposed to the asbestos minerals continues to be a public health concern. Although the production and use of the commercial amphibole asbestos minerals—grunerite (amosite) and riebeckite (crocidolite)—have been almost completely eliminated from world commerce, special opportunities for potentially significant exposures remain. Commercially viable deposits of grunerite asbestos are very rare, but it can occur as a gangue mineral in a limited part of a mine otherwise thought asbestos-free. This report describes such a situation, in which a very localized seam of grunerite asbestos was identified in an iron ore mine. The geological occurrence of the seam in the ore body is described, as well as the mineralogical character of the grunerite asbestos. The most relevant epidemiological studies of workers exposed to grunerite asbestos are used to gauge the hazards associated with the inhalation of this fibrous mineral. Both analytical transmission electron microscopy and phase-contrast optical microscopy were used to quantify the fibers present in the air during mining in the area with outcroppings of grunerite asbestos. Analytical transmission electron microscopy and continuous-scan x-ray diffraction were used to determine the type of asbestos fiber present. Knowing the level of the miner’s exposures, we carried out a risk assessment by using a model developed for the Environmental Protection Agency. PMID:10097051

Microbial Beneficiation of Salem Iron Ore Using Penicillium purpurogenum

NASA Astrophysics Data System (ADS)

Mishra, M.; Pradhan, M.; Sukla, L. B.; Mishra, B. K.

2011-02-01

High alumina and silica content in the iron ore affects coke rate, reducibility, and productivity in a blast furnace. Iron ore is being beneficiated all around the world to meet the quality requirement of iron and steel industries. Choosing a beneficiation treatment depends on the nature of the gangue present and its association with the ore structure. The advanced physicochemical methods used for the beneficiation of iron ore are generally unfriendly to the environment. Biobeneficiation is considered to be ecofriendly, promising, and revolutionary solutions to these problems. A characterization study of Salem iron ore indicates that the major iron-bearing minerals are hematite, magnetite, and goethite. Samples on average contains (pct) Fe2O3-84.40, Fe (total)-59.02, Al2O3-7.18, and SiO2-7.53. Penicillium purpurogenum (MTCC 7356) was used for the experiment . It removed 35.22 pct alumina and 39.41 pct silica in 30 days in a shake flask at 10 pct pulp density, 308 K (35 °C), and 150 rpm. In a bioreactor experiment at 2 kg scale using the same organism, it removed 23.33 pct alumina and 30.54 pct silica in 30 days at 300 rpm agitation and 2 to 3 l/min aeration. Alumina and silica dissolution follow the shrinking core model for both shake flask and bioreactor experiments.

The role of intrusions in the formation of Irish-type mineralisation

NASA Astrophysics Data System (ADS)

McCusker, Jim; Reed, Christopher

2013-08-01

The Stonepark Prospect is located in County Limerick, south-central Ireland. Multiple zones of Zn-Pb mineralisation have been identified at Stonepark and these are approximately 5 km west of the Pallas Green Prospect. At Stonepark, the sulphide bodies are hosted within the Waulsortian Limestone and closely resemble other Irish-type deposits. The mineralisation is composed of pyrite-marcasite, sphalerite and galena with gangue Fe-dolomite and calcite cements. A key difference at Stonepark is the presence of Chadian-aged volcanic rocks (Knockroe Volcanics) that intrude into and overlie the Waulsortian Limestone. Subsequent hydrothermal brecciation of the Waulsortian Limestone and Knockroe intrusions resulted in the formation of tabular polymict breccia bodies containing mixed carbonate and clasts of intrusive rocks. These have then been overprinted by massive sulphide mineralisation. Further syn-mineralisation brecciation has overprinted the earlier breccias. Drilling has demonstrated a spatial relationship between the volume of intrusive rocks (dykes and polymict breccias) and Zn-Pb mineralisation. This association suggests that the intrusive rocks provided a mechanism for the introduction of the mineralising fluids into the breccia bodies. This is significant as to date no large controlling fault has been identified, as is seen at other Irish-type deposits. Further work is required to understand the alteration process of the intrusive rocks and how this may relate to the mineralising process.

The Technological Mineralogical Research of Molybdenum in Skarn-type Ore of Huangshaping Polymetallic Mining Area, Hunan, China

NASA Astrophysics Data System (ADS)

Liu, W. H.; Pan, J. Y.

2017-10-01

Huangshaping is one of the most important polymetallic deposits in the south of Hunan Province. Through field investigation, chemical analysis, observation under the optical microscope, energy spectrum analysis of the SEM and X-ray diffraction, the author made a technological mineralogical research of molybdenum on skarn-type ore, and the result shows that the ore containing molybdenum is mainly on the contact of the granite porphyry and the impure limestone in the lower carboniferous Shidengzi group. Besides molybdenum, the ore minerals contain scheelite, native bismuth, bismuthinite, magnetite and so on; and the gangue minerals are mainly andradite, fluorite and wollastonite. Part of the molybdenum exists in the scheelite in form of isomorphism, and there is an obvious negative correlation between MoO3 and WO3. The molybdenite granularity is mainly located in the 0.04~ 0.08mm area, which accounts for 29.5% of the total and is the finely disseminated ore. For samples of 70%, 90%, and 100% with the particle size of more than 200 meshes, the maximum recovery of the molybdenite are 75.15%, 86.45% and 91.25% respectively. So there will be a better use of molybdenum if we properly improve the grinded particle size of the comprehensive samples. As part of the molybdenum is distributed in the scheelite lattice, the actual recovery rate in this area may decline compared with the ideal value.

Source identification of uranium-containing materials at mine legacy sites in Portugal.

PubMed

Keatley, A C; Martin, P G; Hallam, K R; Payton, O D; Awbery, R; Carvalho, F P; Oliveira, J M; Silva, L; Malta, M; Scott, T B

2018-03-01

Whilst prior nuclear forensic studies have focused on identifying signatures to distinguish between different uranium deposit types, this paper focuses on providing a scientific basis for source identification of materials from different uranium mine sites within a single region, which can then be potentially used within nuclear forensics. A number of different tools, including gamma spectrometry, alpha spectrometry, mineralogy and major and minor elemental analysis, have been utilised to determine the provenance of uranium mineral samples collected at eight mine sites, located within three different uranium provinces, in Portugal. A radiation survey was initially conducted by foot and/or unmanned aerial vehicle at each site to assist sample collection. The results from each mine site were then compared to determine if individual mine sites could be distinguished based on characteristic elemental and isotopic signatures. Gamma and alpha spectrometry were used to differentiate between samples from different sites and also give an indication of past milling and mining activities. Ore samples from the different mine sites were found to be very similar in terms of gangue and uranium mineralogy. However, rarer minerals or specific impurity elements, such as calcium and copper, did permit some separation of the sites examined. In addition, classification rates using linear discriminant analysis were comparable to those in the literature. Crown Copyright © 2018. Published by Elsevier Ltd. All rights reserved.

Occurrence of silver minerals in a silver-rich pocket in the massive sulfide zinc-lead ores in the Edwards mine, New York

DOE Office of Scientific and Technical Information (OSTI.GOV)

Serviss, C.R.; Grout, C.M.; Hagni, R.D.

1985-01-01

Ore microscopic examination of uncommon silver-rich ores from the Edwards mine has detected three silver minerals, native silver, freibergite, and argentite, that were previously unreported in the literature from the Balmat-Edwards district. The zinc-lead ore deposits of the Balmat-Edwards District in northern New York are composed of very coarse-grained massive sulfides, principally sphalerite, galena, and pyrite. The typical ores contain small amounts of silver in solid solution galena. Galena concentrates produced from those ores have contained an average of 15 ounces of silver per ton of 60% lead concentrates. In contrast to the typical ore a silver-rich pocket, that measuredmore » three feet by three feet on the vertical mine face and was the subject of this study, contained nearly 1% silver in a zinc ore. Ore microscopic study shows that this ore is especially characterized by abundant, relatively fine-grained chalcopyrite with anhedral pyrite inclusions. Fine-grained sphalerite, native silver, argentite, freibergite and arsenopyrite occur in association with the chalcopyrite and as fracture-fillings in gangue minerals. Geochemically anomalous amounts of tin, barium, chromium, and nickel also are present in the silver-rich pocket. The silver-rich pocket may mark the locus of an early feeder vent or alternatively it may record a hydrothermal event that was superimposed upon the event responsible for the metamorphic ore textures.« less

Base and precious metal occurrences along the San Andreas Fault, Point Delgada, California

USGS Publications Warehouse

McLaughlin, Robert J.; Sorg, D.H.; Ohlin, H.N.; Heropoulos, Chris

1979-01-01

Previously unrecognized veins containing lead, zinc, and copper sulfide minerals at Point Delgada, Calif., are associated with late Mesozoic(?) and Tertiary volcanic and sedimentary rocks of the Franciscan assemblage. Sulfide minerals include pyrite, sphalerite, galena, and minor chalcopyrite, and galena-rich samples contain substantial amounts of silver. These minerals occur in a quartz-carbonate gangue along northeast-trending faults and fractures that exhibit (left?) lateral and vertical slip. The sense of fault movement and the northeasterly strike are consistent with predicted conjugate fault sets of the present San Andreas fault system. The sulfide mineralization is younger than the Franciscan rocks of Point Delgada and King Range, and it may have accompanied or postdated the inception of San Andreas faulting. Mineralization largely preceded uplift, the formation of a marine terrace, and the emplacement of landslide-related debris-flow breccias that overlie the mineralized rocks and truncate the sulfide veins. These field relations indicate that the sulfide mineralization and inception of San Andreas faulting were clearly more recent than the early Miocene and that the mineralization could be younger than about 1.2 m.y. The sulfide veins at Point Delgada may be of economic significance. However, prior to any exploitation of the occurrence, economic and environmental conflicts of interest involving private land ownership, the Shelter Cove home development, and proximity of the coast must be resolved.

Geology and geochemistry of the Reocín zinc-lead deposit, Basque-Cantabrian Basin, Northern Spain

USGS Publications Warehouse

Velasco, Francisco; Herrero, Jose Miguel; Yusta, Inaki; Alonso, Jose Antonio; Seebold, Ignacio; Leach, David

2003-01-01

The Reoci??n Zn-Pb deposit, 30 km southwest of Santander, Spain, occurs within Lower Cretaceous dolomitized Urgonian limestones on the southern flank of the Santillana syncline. The Reoci??n deposit is one of the largest known strata-bound, carbonate-hosted, zinc-lead deposits in Europe. The total metal endowment of the deposit, including past production and remaining reserves, is 62 Mt of ore grading 8.7 percent Zn and 1.0 percent Pb. The epigenetic mineralization consists of sphalerite and galena, with lesser marcasite and trace pyrite with dolomite as gangue. Microprobe analyses of different generations of dolomite revealed nonstoichiometric compositions with various amounts of iron (up to 14 mol % of FeCO3). Replacement of host dolomite, open-space filling of fractures, and cementation of breccias derived from dissolution collapse are the principal types of ore occurrence. Detailed cross-section mapping indicates a stratigraphic and structural control on the deposit. A stratiform morphology is present in the western part of the orebody (Capa Sur), whereas mineralization in the eastern part is highly discordant but strata bound (Barrendera). Stratigraphic studies demonstrate that synsedimentary tectonic activity, related to the rifting of the North Atlantic (Bay of Biscay), was responsible for variation in sedimentation, presence of unconformities (including paleokarsts), local platform emergence and dolomitization along the N60 fault trend. In the Reoci??n area, two stages of dolomitization are recognized. The first stage is a pervasive dolomitization of the limestone country rocks that was controlled by faulting and locally affected the upper part of the Aptian and the complete Albian sequence. The second dolomitization event occurred after erosion and was controlled by karstic cavities. This later dolomitization was accompanied by ore deposition and, locally, filling of dolomite sands and clastic sediments in karstic cavities. The circulation of hydrothermal

DOE Office of Scientific and Technical Information (OSTI.GOV)

Carnahan, T.G.; Kazonich, G.; Raddatz, A.E.

The U.S. Bureau of Mines conducted a bench-scale study to delineate the important parameters in a three-step process to produce commercial-quality tungsten carbide (WC) directly from tungsten minerals. In the process, tungsten concentrates of wolframite or wolframite and scheelite are decomposed at 1,050{sup 0}C in a molten mixture of NcCl and Na{sub 2}SiO{sub 3} that forms two immiscible phases. Tungsten, as sodium tungstate, reports to the halide phase and is separated from the gangue constituents, which report to the silicate phase. After decanting to separate the two phases, natural gas is sparged into the molten halide phase a 1,070{sup 0}C.more » Submicrometer crystals of WC are initially produced. These crystals grow into thin triangular-shaped plates up to 100 {mu}m on a side or into popcorn-shaped conglomerates. Sparged WC was examined for its suitability for use in sintered carbide products. In physical evaluations, sparged WC ground to an average particle size of 1.52 {mu}m and compacted with 10 pct Co binder into standard 6-by 22-mm test bars had a density of 14.35 and a Rockwell A hardness of 89.6. This compared favorably with 14.39 and 89.7 respectively, for test bars made from a standard commercial 1.52-{mu}m WC powder. Test bars made from Bureau of Mines WC had no C'' porosity or eta phase.« less

Mineral sulphide-lime reactions and effect of CaO/C mole ratio during carbothermic reduction of complex mineral sulphides

NASA Astrophysics Data System (ADS)

Hara, Yotamu Stephen Rainford

2014-01-01

Mineral sulphide (MS)-lime (CaO) ion exchange reactions (MS + CaO = MO + CaS) and the effect of CaO/C mole ratio during carbothermic reduction (MS + CaO + C = M + CaS + CO(g)) were investigated for complex froth flotation mineral sulphide concentrates. Phases in the partially and fully reacted samples were characterised by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The primary phases during mineral sulphide-lime ion exchange reactions are Fe3O4, CaSO4 Cu2S, and CaS. A complex liquid phase of Ca2CuFeO3S forms during mineral sulphide-lime exchange reactions above 1173 K. The formation mechanisms of Ca2CuFeO3S liquid phase are determined by characterising the partially reacted samples. The reduction rate and extent of mineral sulphides in the presence of CaO and C increase with the increase in CaO/C ratio. The metallic phases are surrounded by the CaS rich phase at CaO/C > 1, but the metallic phases and CaS are found as separate phases at CaO/C < 1. Experimental results show that the stoichiometric ratio of carbon should be slightly higher than that of CaO. The reactions between CaO and gangue minerals (SiO2 and Al2O3) are only observed at CaO/C > 1 and the reacted samples are excessively sintered.

Chemical and colloidal aspects of collectorless flotation behavior of sulfide and non-sulfide minerals.

PubMed

Aghazadeh, Sajjad; Mousavinezhad, Seyed Kamal; Gharabaghi, Mahdi

2015-11-01

Flotation has been widely used for separation of valuable minerals from gangues based on their surface characterizations and differences in hydrophobicity on mineral surfaces. As hydrophobicity of minerals widely differs from each other, their separation by flotation will become easier. Collectors are chemical materials which are supposed to make selectively valuable minerals hydrophobic. In addition, there are some minerals which based on their surface and structural features are intrinsically hydrophobic. However, their hydrophobicities are not strong enough to be floatable in the flotation cell without collectors such as sulfide minerals, coal, stibnite, and so forth. To float these minerals in a flotation cell, their hydrophobicity should be increased in specific conditions. Various parameters including pH, Eh, size distribution, mill types, mineral types, ore characterization, and type of reaction in flotation cells affect the hydrophobicity of minerals. Surface analysis results show that when sulfide minerals experience specific flotation conditions, the reactions on the surface of these minerals increase the amount of sulfur on the surface. These phenomenons improve the hydrophobicity of these minerals due to strong hydrophobic feature of sulfurs. Collectorless flotation reduces chemical material consumption amount, increases flotation selectivity (grade increases), and affects the equipment quantities; however, it can also have negative effects. Some minerals with poor surface floatability can be increased by adding some ions to the flotation system. Depressing undesirable minerals in flotation is another application of collectorless flotation.

Effects of Sodium Citrate on the Ammonium Sulfate Recycled Leaching of Low-Grade Zinc Oxide Ores

NASA Astrophysics Data System (ADS)

Yang, Kun; Li, Shi-wei; Zhang, Li-bo; Peng, Jin-hui; Ma, Ai-yuan; Wang, Bao-bao

2016-03-01

The effects of sodium citrate on ammonium sulfate recycled leaching of low-grade zinc oxide ores were studied. By applying various kinds of detection and analysis techniques such as chemical composition analysis, chemical phase method, scanning electron microscopy and energy dispersive spectrum (SEM/EDS), X-ray diffraction (XRD) and Fourier-transforming infrared spectrum (FT-IR), zinc raw ore, its leaching slag and the functional mechanism of sodium citrate were investigated. Based on a comprehensive analysis, it can be concluded that in contrast to hemimorphite (Zn4Si2O7(OH)2 · H2O), amorphous smithsonite (ZnCO3) and zinc silicate (Zn2SiO4) prove to be refractory phases under ammonium sulfate leaching, while sodium citrate has a better chelating action with the refractory phases, resulting in a higher zinc leaching rate. Under conditions of [NH3]/[NH3]T molar ratio being 0.5, [NH3]T being 7.5 mol/L, [Na3C6H5O7] being 0.2 mol/L, S/L ratio being 1:5, temperature being 303 K, holding time being 1 h in each of the two stages, and stirring rate being 300 rpm, the leaching rate of zinc reached 93.4%. In this article, sulfate ammonium recycled technology also reveals its unique advantage in processing low-grade zinc oxide ores accompanied by high silicon and high alkaline gangue.

Reactivities of some thiol collectors and their interactions with Ag (+1) ion by molecular modeling

NASA Astrophysics Data System (ADS)

Yekeler, Hulya; Yekeler, Meftuni

2004-09-01

The most commonly used collectors for sulfide minerals in the mining industry are the thiol collectors for the recovery of these minerals from their associated gangues by froth flotation. For this reason, a great deal of attention has been paid to understand the attachment mechanism of thiol collectors to metal sulfide surfaces. The density functional theory (DFT) calculations at the B3LYP/3-21G* and B3LYP/6-31++G** levels were employed to propose the flotation responses of these thiol collectors, namely, diethyl dithiocarbamate, ethyl dithiocarbamate, ethyl dithiocarbonate, ethyl trithiocarbonate and ethyl dithiophosphate ions, and to study the interaction energies of these collectors with Ag (+1) ion in connection to acanthite (Ag 2S) mineral. The calculated interaction energies, Δ E, were interpreted in terms of the highest occupied molecular orbital (HOMO) energies of the isolated collector ions. The results show that the HOMOs are strongly localized to the sulfur atoms and the HOMO energies can be used as a reactivity descriptor for the flotation ability of the thiol collectors. Using the HOMO and Δ E energies, the reactivity order of the collectors is found to be (C 2H 5) 2NCS 2- > C 2H 5NHCS 2- > C 2H 5OCS 2- > C 2H 5SCS 2- > (C 2H 5O)(OH)PS 2-. The theoretically obtained results are in good agreement with the experimental data reported.

Earth Observations taken by the Expedition 15 Crew

NASA Image and Video Library

2007-09-20

ISS015-E-29867 (20 Sept. 2007) --- Bingham Canyon Mine, Utah is featured in this image photographed by an Expedition 15 crewmember on the International Space Station. The Bingham Canyon Mine (center) located approximately 32 kilometers to the southeast of Salt Lake City, UT is one of the largest open-pit mines in the world, measuring over 4 kilometers wide and 1,200 meters deep. The mine exploits a porphyry copper, a type of geological structure formed by crystal-rich magma moving upwards through pre-existing rock layers. As the magma cools and crystallizes (forming an igneous rock with large crystals in a fine-grained matrix, known as a porphyry), hot fluids circulate through the magma and surrounding rocks via fractures. This process of hydrothermal alteration typically forms copper-bearing and other minerals in spatial patterns that a geologist recognizes as a potential porphyry copper deposit. Parallel benches (stepped terraces), visible along the western pit face (center left), range from 16 to 25 meters high - these provide access for equipment to work the rock face, as well as maintaining stability of the sloping pit walls. A dark, larger roadway is also visible directly below the benches. Brown to gray, flat topped hills of gangue (waste rock) surround the pit, and are thrown into sharp relief by shadows and the oblique viewing angle of this image. Leachate reservoirs associated with ore processing are visible to the south of the city of Bingham Canyon, UT (right).

Geostatistical and GIS analysis of the spatial variability of alluvial gold content in Ngoura-Colomines area, Eastern Cameroon: Implications for the exploration of primary gold deposit

NASA Astrophysics Data System (ADS)

Takodjou Wambo, Jonas Didero; Ganno, Sylvestre; Djonthu Lahe, Yannick Sthopira; Kouankap Nono, Gus Djibril; Fossi, Donald Hermann; Tchouatcha, Milan Stafford; Nzenti, Jean Paul

2018-06-01

Linear and nonlinear geostatistic is commonly used in ore grade estimation and seldom used in Geographical Information System (GIS) technology. In this study, we suggest an approach based on geostatistic linear ordinary kriging (OK) and Geographical Information System (GIS) techniques to investigate the spatial distribution of alluvial gold content, mineralized and gangue layers thicknesses from 73 pits at the Ngoura-Colomines area with the aim to determine controlling factors for the spatial distribution of mineralization and delineate the most prospective area for primary gold mineralization. Gold content varies between 0.1 and 4.6 g/m3 and has been broadly grouped into three statistical classes. These classes have been spatially subdivided into nine zones using ordinary kriging model based on physical and topographical characteristics. Both mineralized and barren layer thicknesses show randomly spatial distribution, and there is no correlation between these parameters and the gold content. This approach has shown that the Ngoura-Colomines area is located in a large shear zone compatible with the Riedel fault system composed of P and P‧ fractures oriented NE-SW and NNE-SSW respectively; E-W trending R fractures and R‧ fractures with NW-SE trends that could have contributed significantly to the establishment of this gold mineralization. The combined OK model and GIS analysis have led to the delineation of Colomines, Tissongo, Madubal and Boutou villages as the most prospective areas for the exploration of primary gold deposit in the study area.

Trace and minor element variations and sulfur isotopes in crystalline and colloform ZnS: Incorporation mechanisms and implications for their genesis

USGS Publications Warehouse

Pfaff, Katharina; Koenig, Alan; Wenzel, Thomas; Ridley, Ian; Hildebrandt, Ludwig H.; Leach, David L.; Markl, Gregor

2011-01-01

Various models have been proposed to explain the formation mechanism of colloform sphalerite, but the origin is still under debate. In order to decipher influences on trace element incorporation and sulfur isotope composition, crystalline and colloform sphalerite from the carbonate-hosted Mississippi-Valley Type (MVT) deposit near Wiesloch, SW Germany, were investigated and compared to sphalerite samples from 52 hydrothermal vein-type deposits in the Schwarzwald ore district, SW Germany to study the influence of different host rocks, formation mechanisms and fluid origin on trace element incorporation. Trace and minor element incorporation in sphalerite shows some correlation to their host rock and/or origin of fluid, gangue, paragenetic minerals and precipitation mechanisms (e.g., diagenetic processes, fluid cooling or fluid mixing). Furthermore, crystalline sphalerite is generally enriched in elements like Cd, Cu, Sb and Ag compared to colloform sphalerite that mainly incorporates elements like As, Pb and Tl. In addition, sulfur isotopes are characterized by positive values for crystalline and strongly negative values for colloform sphalerite. The combination of trace element contents, typical minerals associated with colloform sphalerite from Wiesloch, sulfur isotopes and thermodynamic considerations helped to evaluate the involvement of sulfate-reducing bacteria in water-filled karst cavities. Sulfate-reducing bacteria cause a sulfide-rich environment that leads in case of a metal-rich fluid supply to a sudden oversaturation of the fluid with respect to galena, sphalerite and pyrite. This, however, exactly coincides with the observed crystallization sequence of samples involving colloform sphalerite from the Wiesloch MVT deposit.

The genesis of the newly discovered giant Wuben magmatic Fe-Ti oxide deposit in the Emeishan Large Igneous Province: a product of the late-stage redistribution and sorting of crystal slurries

NASA Astrophysics Data System (ADS)

Bai, Zhong-Jie; Zhong, Hong; Zhu, Wei-Guang; Hu, Wen-Jun; Chen, Cai-Jie

2018-04-01

A giant Fe-Ti oxide deposit hosted by the Wuben mafic intrusion has recently been discovered in the Pan-Xi area of the Emeishan Large Igneous Province (ELIP). The evolved compositions of the gangue minerals within the Fe-Ti oxide ores indicate that they formed during later stages of magma differentiation than those within the neighboring Panzhihua intrusion or other ore-bearing intrusions in this area. The rocks from the Wuben intrusion and MZb of the Panzhihua intrusion contain compositionally similar silicate minerals and have similar titanomagnetite/ilmenite ratios, suggesting that the former is related to and probably connected to the latter by subsurface magmatic conduits. This indicates that unconsolidated minerals that formed in the MZb flowed as crystal slurries into the Wuben magma chamber during the later stages of evolution of the parental magma. The later secondary enrichment of Fe-Ti oxides by mechanical redistribution and the sorting of crystals as a result of density and size differences generated the Wuben massive Fe-Ti oxide bodies. The ilmenite was commonly saturated in the magma at late stage of differentiation in the ELIP, thereby the associated deposit contains much higher contents of ilmenite. This indicates that future exploration for Fe-Ti oxide mineralization in the ELIP should not merely focus on the lower parts of large layered intrusions but should also include nearby relatively small intrusions or even the upper parts of large intrusions, especially as ilmenite-enriched Fe-Ti oxide deposits may have greater economic value than ilmenite-poor deposits.

The Krásná Hora, Milešov, and Příčovy Sb-Au ore deposits, Bohemian Massif: mineralogy, fluid inclusions, and stable isotope constraints on the deposit formation

NASA Astrophysics Data System (ADS)

Němec, Matěj; Zachariáš, Jiří

2018-02-01

The Krásná Hora-Milešov and Příčovy districts (Czech Republic) are the unique examples of Sb-Au subtype orogenic gold deposits in the Bohemian Massif. They are represented by quartz-stibnite veins and massive stibnite lenses grading into low-grade, disseminated ores in altered host rocks. Gold postdates the stibnite and is often replaced by aurostibite. The ore zones are hosted by hydrothermally altered dikes of lamprophyres (Krásná Hora-Milešov) or are associated with local strike-slip faults (Příčovy). Formation of Sb-Au deposits probably occurred shortly after the main gold-bearing event (348-338 Ma; Au-only deposits) in the central part of the Bohemian Massif. Fluid inclusion analyses suggest that stibnite precipitated at 250 to 130 °C and gold at 200 to 130 °C from low-salinity aqueous fluids. The main quartz gangue hosting the ore precipitated from the same type of fluid at about 300 °C. Early quartz-arsenopyrite veins are not associated with the Sb-Au deposition and formed from low-salinity, aqueous-carbonic fluid at higher pressure and temperature ( 250 MPa, 400 °C). The estimated oxygen isotope composition of the ore-bearing fluid (4 ± 1‰ SMOW; based on post-ore calcite) suggests its metamorphic or mixed magmatic-metamorphic origin and excludes the involvement of meteoric water. Rapid cooling of warm hydrothermal fluids reacting with "cold" host rock was probably the most important factor in the formation of both stibnite and gold.

Feasibility study on the use of soil washing to remediate the As-Hg contamination at an ancient mining and metallurgy area.

PubMed

Sierra, C; Menéndez-Aguado, J M; Afif, E; Carrero, M; Gallego, J R

2011-11-30

Soils in abandoned mining sites generally present high concentrations of trace elements, such as As and Hg. Here we assessed the feasibility of washing procedures to physically separate these toxic elements from soils affected by a considerable amount of mining and metallurgical waste ("La Soterraña", Asturias, NW Spain). After exhaustive soil sampling and subsequent particle-size separation via wet sieving, chemical and mineralogical analysis revealed that the finer fractions held very high concentrations of As (up to 32,500 ppm) and Hg (up to 1600 ppm). These elements were both associated mainly with Fe/Mn oxides and hydroxides. Textural and geochemical data were correlated with the geological substrate by means of a multivariate statistical analysis. In addition, the Hg liberation size (below 200 μm) was determined to be main factor conditioning the selection of suitable soil washing strategies. These studies were finally complemented with a specific-gravity study performed with a C800 Mozley separator together with a grindability test, both novel approaches in soil washing feasibility studies. The results highlighted the difficulties in treating "La Soterraña" soils. These difficulties are attributed to the presence of contaminants embedded in the soil and spoil heap aggregates, caused by the meteorization of gangue and ore minerals. As a result of these two characteristics, high concentrations of the contaminants accumulate in all grain-size fractions. Therefore, the soil washing approach proposed here includes the grinding of particles above 125 μm. Copyright © 2011 Elsevier B.V. All rights reserved.

Wetting Behavior of Calcium Ferrite Slags on Cristobalite Substrates

NASA Astrophysics Data System (ADS)

Yang, Mingrui; Lv, Xuewei; Wei, Ruirui; Xu, Jian; Bai, Chenguang

2018-03-01

Calcium ferrite (CF) is a significant intermediate adhesive phase in high-basicity sinters. The wettability between calcium ferrite (CF) and gangue plays an important role in the assimilation process. The wettability of CF-based slags, in which a constant amount (2 mass pct.) of Al2O3, MgO, SiO2, and TiO2 was added, on solid SiO2 (cristobalite) substrates at 1523 K (1250 °C) was investigated. The interfacial microstructure and spreading mechanisms were discussed for each sample. All the tested slag samples exhibited good wettability on the SiO2 substrate. The initial apparent contact angles were in the range of 20 to 50 deg, while the final apparent contact angles were 5 deg. The wetting process could be divided into three stages on the basis of the change in diameter, namely the "linear spreading" stage, "spreading rate reduction" stage, and "wetting equilibrium" stage. It was found that the CF-SiO2 wetting system exhibits dissolutive wetting and the dissolution of SiO2 into slag influences its spreading process. The spreading rate increases with a decrease in the ratio of viscosity to interfacial tension, which is a result of the addition of Al2O3, MgO, SiO2, and TiO2. After cooling, a deep corrosion pit was formed in the substrate and a diffusion layer was generated in front of the residual slag zone; further, some SiO2 and Fe2O3 solid solutions precipitated in the slag.

Geochemistry of rare earth elements within waste rocks from the Montviel carbonatite deposit, Québec, Canada.

PubMed

Edahbi, Mohamed; Plante, Benoît; Benzaazoua, Mostafa; Pelletier, Mia

2018-04-01

Several rare earth element (REE) mine projects around the world are currently at the feasibility stage. Unfortunately, few studies have evaluated the contamination potential of REE and their effects on the environment. In this project, the waste rocks from the carbonatites within the Montviel proterozoic alkaline intrusion (near Lebel-sur-Quévillon, Quebec, Canada) are assessed in this research. The mineralization is mainly constituted by light REE (LREE) fluorocarbonates (qaqarssukite-Ce, kukharenkoite-Ce), LREE carbonates (burbankite, Sr-Ba-Ca-REE, barytocalcite, strontianite, Ba-REE-carbonates), and phosphates (apatite, monazite). The gangue minerals are biotites, chlorite, albite, ankerite, siderite, and calcite. The SEM-EDS analyses show that (i) the majority of REE are associated with the fine fraction (< 106 μm), (ii) REE are mainly associated with carbonates, (iii) all analyzed minerals preferably contain LREE (La, Ce, Pr, Nd, Sm, Eu), (iv) the sum of LREE in each analyzed mineral varies between ~ 3 and 10 wt%, (v) the heavy REE (HREE) identified are Gd and Yb at < 0.4 wt%, and (vi) three groups of carbonate minerals were observed containing variable concentrations of Ca, Na, and F. Furthermore, the mineralogical composition of REE-bearing minerals, REE mobility, and REE speciation was investigated. The leachability and geochemical behavior of these REE-bearing mine wastes were tested using normalized kinetic testing (humidity cells). Leachate results displayed higher LREE concentrations, with decreasing shale-normalized patterns. Thermodynamical equilibrium calculations suggest that the precipitation of secondary REE minerals may control the REE mobility.

On the origin of the Neoproterozoic Peresopolis graphite deposit, Paraguay Belt, Brazil

NASA Astrophysics Data System (ADS)

Manoel, Talitta Nunes; Dexheimer Leite, Jayme Alfredo

2018-07-01

The Peresopolis graphite deposit is located northeast of Brasilândia Town in Mato Grosso State (Brazil). It consists of an 1800 m long, 200 m wide low-crystallinity graphite-bearing tabular layer that trends ENE and dips 65°ESE. The deposit is hosted in carbonaceous phyllites, which along with basal metadiamictites and upper metarenites make up the upper unit (Coxipó Formation) of the Cuiabá Group in the late Cryogenian to Cambrian Paraguay Belt (ca. 650-500Ma). The carbonaceous phyllites show a mineral assemblage consisting mostly of graphite-quartz-muscovite-albite and pyrite and dolomite to a lesser extent; alteration minerals include tosudite and kaolinite. XRD analysis confirmed the gangue material and defined the graphite as low-order crystallinity. Carbon isotope data for graphite ore returned a light and very restricted range of δ13Corg between -29 and -28‰ suggesting organic matter as the source of carbon. One hundred and sixty measurements of Raman graphite spectrum returned a well-fit between full width at half maximum parameter (FWHM) which allowed its use as a geothermometer. Resulting temperatures are in the range between 285 and 300 °C ± 30 °C, indicating low-to very-low metamorphic conditions for transformation of organic matter into amorphous graphite. The deposition of the organic matter should have taken place in an outer slope of a glaciomarine system and its transformation into the ore occurred because of deformation and low-grade metamorphism related to the development of the Neoproterozoic Brasiliano/Pan-African Orogeny (850-500Ma).

Metallogenic and tectonic significance of oxygen isotope data and whole-rock potassium-argon ages of the Nikolai Greenstone, McCarthy Quadrangle, Alaska

USGS Publications Warehouse

Silberman, M.L.; MacKevett, E.M.; Connor, C.L.; Matthews, Alan

1980-01-01

The Middle and (or) Late Triassic Nikolai Greenstone, part of the allochthonous terrane of Wrangellia, is typically altered and locally metamorphosed to prehnite-pumpellyite facies with chlorite and epidote as the most common secondary minerals. Intrinsic copper content averages 155 ppm, and two types of concentrations of copper in the Nikolai are common: (1) native copper fillings of amygdules and rubble zones typically near flow tops, and (2) veins and thin replacement zones that contain native copper and copper-iron sulfides in quartz-epidote or calcite gangue in faults and fractures. Oxygen isotope data from quartz and epidote from three copperbearing veins yield calculated ore fluid temperatures of approximately 200°C and 6180 of approximately +1 per mil in agreement with a metamorphicsegregation origin of these deposits, as suggested by Sinclair (1977). Seven K-Ar ages of chloritized greenstone, including those adjacent to veins fall on an initial argon diagram with a zero intercept and a slope which yields an isochron age of 112 + 11 m.y. The ages define a Cretaceous thermalmetamorphic episode which is responsible for alteration and mineralization. The episode is younger than a major Jurassic progeny, accompanied by granitic intrusion, in the area, and appears to be unaffected by minor granitic intrusion in the middle to late Tertiary. We believe the Cretaceous event is related to accretion of Wrangellia to its present relative position in North America. This age of accretion agrees with stratigraphic and structural evidence cited by other workers. 

Wetting Behavior of Calcium Ferrite Slags on Cristobalite Substrates

NASA Astrophysics Data System (ADS)

Yang, Mingrui; Lv, Xuewei; Wei, Ruirui; Xu, Jian; Bai, Chenguang

2018-06-01

Calcium ferrite (CF) is a significant intermediate adhesive phase in high-basicity sinters. The wettability between calcium ferrite (CF) and gangue plays an important role in the assimilation process. The wettability of CF-based slags, in which a constant amount (2 mass pct.) of Al2O3, MgO, SiO2, and TiO2 was added, on solid SiO2 (cristobalite) substrates at 1523 K (1250 °C) was investigated. The interfacial microstructure and spreading mechanisms were discussed for each sample. All the tested slag samples exhibited good wettability on the SiO2 substrate. The initial apparent contact angles were in the range of 20 to 50 deg, while the final apparent contact angles were 5 deg. The wetting process could be divided into three stages on the basis of the change in diameter, namely the "linear spreading" stage, "spreading rate reduction" stage, and "wetting equilibrium" stage. It was found that the CF-SiO2 wetting system exhibits dissolutive wetting and the dissolution of SiO2 into slag influences its spreading process. The spreading rate increases with a decrease in the ratio of viscosity to interfacial tension, which is a result of the addition of Al2O3, MgO, SiO2, and TiO2. After cooling, a deep corrosion pit was formed in the substrate and a diffusion layer was generated in front of the residual slag zone; further, some SiO2 and Fe2O3 solid solutions precipitated in the slag.

Regenerable cement sorbent for recycle fluidized-bed combustion systems. Final report

DOE Office of Scientific and Technical Information (OSTI.GOV)

Yoo, H.J.; Steinberg, M.

1985-04-01

Agglomerated cement sorbent pellets (ACS) were investigated as a regenerable sorbent for the purpose of removing SO/sub 2/ in a circulating fluidized-bed combustion (CFBC) system. The systems concept is to use an intermediate size sorbent pellet so that fine flyash can be separated from the sorbent at the top end of the CFBC and the coarse gangue can be separated from the sorbent remaining in the bottom end. In this study, basic experimental data were obtained on the sulfur capture capacity and regenerability of the ACS pellets as a function of the concentration of flyash mixed with the pellets andmore » as a function of temperature. Thermogravimetric Analysis (TGA) was used for this purpose. A 40 mm bench-scale fluidized-bed unit operated with a simulated combustion gas mixture was used to determine the attrition resistance of the pellets. The results indicate that 30-100 mesh ACS pellets at 958/sup 0/C (1756/sup 0/F) maintain a 55-60% sulfation capacity mixed with coal flyash concentration up to 75% by weight. The sorbent pellets were 100% regenerable and did not lose reactivity in repeated cyclical sulfation and regeneration tests. At higher temperatures up to 1158/sup 0/C (2116/sup 0/F) reactivity towards SO/sub 2/ declines due to sintering of the flyash on the surface of the ACS pellets. Tests showed good attrition resistance with only 1% loss per cycle in cyclical operation. These initial basic results indicate that ACS pellets are potentially useful as a recoverable and regenerable high capacity SO/sub 2/ sorbent in a circulating fluidized-bed combustion system. 5 refs., 7 figs., 8 tabs.« less

Heavy metals contamination and their risk assessment around the abandoned base metals and Au-Ag mines in Korea

NASA Astrophysics Data System (ADS)

Chon, Hyo-Taek

2017-04-01

Heavy metals contamination in the areas of abandoned Au-Ag and base metal mines in Korea was investigated in order to assess the level of metal pollution, and to draw general summaries about the fate of toxic heavy metals in different environments. Efforts have been made to compare the level of heavy metals, chemical forms, and plant uptake of heavy metals in each mine site. In the base-metals mine areas, significant levels of Cd, Cu, Pb and Zn were found in mine dump soils developed over mine waste materials and tailings. Leafy vegetables tend to accumulate heavy metals(in particular, Cd and Zn) higher than other crop plants, and high metal concentrations in rice crops may affect the local residents' health. In the Au-Ag mining areas, arsenic would be the most characteristic contaminant in the nearby environment. Arsenic and heavy metals were found to be mainly associated with sulfide gangue minerals, and the mobility of these metals would be enhanced by the effect of continuing weathering and oxidation. According to the sequential extraction of metals in soils, most heavy metals were identified as non-residual chemical forms, and those are very susceptible to the change of ambient conditions of a nearby environment. The concept of pollution index(PI) of soils gives important information on the extent and degree of multi-element contamination, and can be applied to the evaluation of mine soils before their agricultural use and remediation. The risk assessment process comprising exposure assessment, dose-response assessment, and risk characterization was discussed, and the results of non-cancer risk of As, Cd, and Zn, and those of cancer risk of As were suggested.

Gold-bearing skarns

USGS Publications Warehouse

Theodore, Ted G.; Orris, Greta J.; Hammerstrom, Jane M.; Bliss, James D.

1991-01-01

In recent years, a significant proportion of the mining industry's interest has been centered on discovery of gold deposits; this includes discovery of additional deposits where gold occurs in skarn, such as at Fortitude, Nevada, and at Red Dome, Australia. Under the classification of Au-bearing skarns, we have modeled these and similar gold-rich deposits that have a gold grade of at least 1 g/t and exhibit distinctive skarn mineralogy. Two subtypes, Au-skarns and byproduct Au-skarns, can be recognized on the basis of gold, silver, and base-metal grades, although many other geological factors apparently are still undistinguishable largely because of a lack of detailed studies of the Au-skarns. Median grades and tonnage for 40 Au-skarn deposits are 8.6 g/t Au, 5.0 g/t Ag, and 213,000 t. Median grades and tonnage for 50 byproduct and Au-skarn deposits are 3.7 g/t Au, 37 g/t Ag, and 330,000 t. Gold-bearing skarns are generally calcic exoskarns associated with intense retrograde hydrosilicate alteration. These skarns may contain economic amounts of numerous other commodities (Cu, Fe, Pb, Zn, As, Bi, W, Sb, Co, Cd, and S) as well as gold and silver. Most Au-bearing skarns are found in Paleozoic and Cenozoic orogenic-belt and island-arc settings and are associated with felsic to intermediate intrusive rocks of Paleozoic to Tertiary age. Native gold, electru, pyrite, pyrrhotite, chalcopyrite, arsenopyrite, sphalerite, galena, bismuth minerals, and magnetite or hematite are the most common opaque minerals. Gangue minerals typically include garnet (andradite-grossular), pyroxene (diopside-hedenbergite), wollastonite, chlorite, epidote, quartz, actinolite-tremolite, and (or) calcite.

A review of the surface features and properties, surfactant adsorption and floatability of four key minerals of diasporic bauxite resources.

PubMed

Zhang, Ningning; Nguyen, Anh V; Zhou, Changchun

2018-04-01

Diasporic bauxite represents one of the major aluminum resources. Its upgrading for further processing involves a separation of diaspore (the valuable mineral) from aluminosilicates (the gangue minerals) such as kaolinite, illite, and pyrophyllite. Flotation is one of the most effective ways to realize the upgrading. Since flotation is a physicochemical process based on the difference in the surface hydrophobicity of different components, determining the adsorption characteristics of various flotation surfactants on the mineral surfaces is critical. The surfactant adsorption properties of the minerals, in turn, are controlled by the surface chemistry of the minerals, while the latter is related to the mineral crystal structures. In this paper, we first discuss the crystal structures of the four key minerals of diaspore, kaolinite, illite, and pyrophyllite as well as the broken bonds on their exposed surfaces after grinding. Next, we summarize the surface chemistry properties such as surface wettability and surface electrical properties of the four minerals, and the differences in these properties are explained from the perspective of mineral crystal structures. Then we review the adsorption mechanism and adsorption characteristics of surfactants such as collectors (cationic, anionic, and mixed surfactants), depressants (inorganic and organic), dispersants, and flocculants on these mineral surfaces. The separation of diaspore and aluminosilicates by direct flotation and reverse flotation are reviewed, and the collecting properties of different types of collectors are compared. Furthermore, the abnormal behavior of the cationic flotation of kaolinite is also explained in this section. This review provides a strong theoretical support for the optimization of the upgrading of diaspore bauxite ore by flotation and the early industrialization of the reverse flotation process. Copyright © 2018 Elsevier B.V. All rights reserved.

A review of zinc oxide mineral beneficiation using flotation method.

PubMed

Ejtemaei, Majid; Gharabaghi, Mahdi; Irannajad, Mehdi

2014-04-01

In recent years, extraction of zinc from low-grade mining tailings of oxidized zinc has been a matter of discussion. This is a material which can be processed by flotation and acid-leaching methods. Owing to the similarities in the physicochemical and surface chemistry of the constituent minerals, separation of zinc oxide minerals from their gangues by flotation is an extremely complex process. It appears that selective leaching is a promising method for the beneficiation of this type of ore. However, with the high consumption of leaching acid, the treatment of low-grade oxidized zinc ores by hydrometallurgical methods is expensive and complex. Hence, it is best to pre-concentrate low-grade oxidized zinc by flotation and then to employ hydrometallurgical methods. This paper presents a critical review on the zinc oxide mineral flotation technique. In this paper, the various flotation methods of zinc oxide minerals which have been proposed in the literature have been detailed with the aim of identifying the important factors involved in the flotation process. The various aspects of recovery of zinc from these minerals are also dealt with here. The literature indicates that the collector type, sulfidizing agent, pH regulator, depressants and dispersants types, temperature, solid pulp concentration, and desliming are important parameters in the process. The range and optimum values of these parameters, as also the adsorption mechanism, together with the resultant flotation of the zinc oxide minerals reported in the literature are summarized and highlighted in the paper. This review presents a comprehensive scientific guide to the effectiveness of flotation strategy. Copyright © 2013 Elsevier B.V. All rights reserved.

PRIMARY MINERALIZATION OF URANIUM-BEARING "SILICEOUS REEF" VEINS IN THE BOULDER BATHOLITH, MONTANA. PART I. THE HOST ROCKS

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wright, H.D.; Bieler, B.H.

1960-01-01

Between 1952 and 1956 a study was made of some of the uranium-bearing hydrothermal veins in the northern part of the Boulder batholith, Montana. Three mines, the W. Wilson, G. Washington, and Free Enterprise, were investigated in detail. The veins are characterized by a microcrystalline quartz gangue containing sparsely scattered, very fine-grained sulfide minerals and uraninite. Above the present water table, secondary uranium minerals are abundant locally. Throughout the area the veins --called "siliceous reefs"--strike east to northeast, are of steep dip, and vary in thickness from a fraction of an inch to several feet. The country rock is granodioritemore » containing, in order of abundance, plagioclase (An/sub 30/ to An/sub 36/), quartz, orthoclase, biotite, and hornblende, with apatite, zircon, and sphene. Small bodies of aplite, pegmatite, and alaskite occur along some veins. The granodiorite adjacent to the veins is rather strongly altered. The alteration is similar throughout all of the deposits studied, in barren and orebearing portions alike. The essential minerals show a characteristic sequence of alteration, in the order hornblende, andesine, biotite, orthoclase, and quartz. Successive zones of alteration are characterized, from the vein outward, by maximum development of sericite (muscovite polytype 1M, in part), kaolinite, and montmorillonite. Other alteration products are quartz, pyrite, calcite, leucoxene, and chlorite. The alteration resulted in an increase in silica and ferric iron, a decrease in alumina, total iron, ferrous iron, lime, soda, and magnesia, and little change in potash, titania, phosphorus, carbon dioxide, and sulfur. Consideration of the stability fields of the sheet structure silicate minerals indicates little basis for interpretation of the temperatures prevailing during mineralization. (auth)« less

Thermal and chemical variations of the Nigerian Benue trough lead-zinc-barite-fluorite deposits

NASA Astrophysics Data System (ADS)

Ogundipe, Ibukun Emmanuel

2017-08-01

The Benue trough is an intra-continental rift initiated in the Cretaceous during the opening of the South Atlantic Ocean. Lead-zinc-barite-fluorite mineralization occurs along the 600 km axis of the trough in three discrete sub-basins which coincide with the lower, middle and upper mineral districts of the Benue Valley. Lithologically these sub-basins are dominated by black carbonaceous shale in the Lower Benue, platform carbonates in the Middle Benue and sandstones in the Upper Benue. Micro-thermometric analysis of fluid inclusions in sphalerite, fluorite, barite and quartz have shown that each mineral district has its own unique thermal and chemical imprint. For example, the temperature can be bracketed between 109 °C and 160 °C for lower Benue, 89 °C-144 °C for the Middle Benue and 176 °C-254 °C for the Upper Benue. Chemical differentiation also exists between each mineral district with the Lower Benue having 22 wt % equivalent NaCl while the Middle and Upper Benue have 18 and 16 wt % equivalent NaCl respectively. This study shows that inter-district thermal and chemical variations exist between the ore-stage sulfide and post-sulfide gangue minerals of the entire Benue Valley. Similarly, intra-district thermal and chemical variations have also been observed among all the paragenetic minerals of each district. The thermal variations may be as a result of variations in the geothermal gradient accompanying continental rifting from one district to the other. The variations in the chemistry between the Lower Benue and the Upper Benue paragenic minerals may be as a result of the distinct lithological differences across the Benue Trough.

Precious metal-bearing epithermal deposits in western Patagonia (NE Lago Fontana region), Argentina

NASA Astrophysics Data System (ADS)

Lanfranchini, Mabel Elena; Etcheverry, Ricardo Oscar; de Barrio, Raúl Ernesto; Recio Hernández, Clemente

2013-04-01

Precious metal-bearing quartz veins occur at the northeastern sector of the Lago Fontana region in southwestern Argentina, within the context of the Andean continental magmatic arc environment. The deposits and their associated alteration zones are spatially related to a Cretaceous calc-alkaline magmatism represented by silicic dikes and hypabyssal intrusions, and hosted by a Late Jurassic to Cretaceous volcano-sedimentary sequence. The veins and related veinlets crop out discontinuously, in general terms in a NW-SE belt. The primary vein mineral assemblage is composed mostly of pyrite ± galena ± chalcopyrite > hematite ± arsenopyrite in silica gangue minerals. Chemical analyses of grab samples from selected quartz veins show as much as 5.7 ppm Au and 224 ppm Ag, as well as elevated Pb, Cu, and Zn. Hydrothermal fluids caused an innermost silicification and adularia-sericite alteration assemblage, and an external propylitic halo. Sulfur isotope values measured for sulfides (δSS from -1.90 to +1.56‰), and oxygen and hydrogen isotopes measured on quartz crystals and extracted primary fluid inclusion waters (δOO = -2.85 to +5.40‰; δDO = -106.0 to -103.4‰) indicate that mineralization probably formed from magmatic fluids, which were mixed with meteoric waters. Also, fluid inclusion data from quartz veins point out that these fluids had low salinity (1.7-4.2 wt% NaCl equiv.), and temperatures of homogenization between 180 and 325 °C. Mineralogical, petrographic and geochemical features for mineralized surface exposures indicate a typical adularia-sericite, low sulfidation epithermal system in the Lago Fontana area that represents a promising target for further exploration programs.

Evidence for Late-Paleozoic brine migration in Cambrian carbonate rocks of the central and southern Appalachians: Implications for Mississippi Valley-type sulfide mineralization

USGS Publications Warehouse

Hearn, P.P.; Sutter, J.F.; Belkin, H.E.

1987-01-01

Many Lower Paleozoic limestones and dolostones in the Valley and Ridge province of the central and southern Appalachians contain 10 to 25 weight percent authigenic potassium feldspar. This was considered to be a product of early diagenesis, however, 40Ar 39Ar analyses of overgrowths on detrital K-feldspar in Cambrian carbonate rocks from Pennsylvania, Maryland, Virginia, and Tennessee yield Late Carboniferous-Early Permian ages (278-322 Ma). Simple mass balance calculations suggest that the feldspar could not have formed isochemically, but required the flux of multiple pore volumes of fluid through the rocks, reflecting regional fluid migration events during the Late-Paleozoic Alleghanian orogeny. Microthermometric measurements of fluid inclusions in overgrowths on detrital K-feldspar and quartz grains from unmineralized rocks throughout the study area indicate homogenization temperatures from 100?? to 200??C and freezing point depressions of -14?? to -18.5??C (18-21 wt.% NaCl equiv). The apparent similarity of these fluids to fluid inclusions in ore and gangue minerals of nearby Mississippi Valley-type (MVT) deposits suggests that the regional occurrences of authigenic K-feldspar and MVT mineralization may be genetically related. This hypothesis is supported by the discovery of authigenic K-feldspar intergrown with sphalerite in several mines of the Mascot-Jefferson City District, E. Tennessee. Regional potassic alteration in unmineralized carbonate rocks and localized occurrences of MVT mineralization are both explainable by a gravity-driven flow model, in which deep brines migrate towards the basin margin under a hydraulic gradient established during the Alleghanian orogeny. The authigenic K-feldspar may reflect the loss of K during disequilibrium cooling of the ascending brines. MVT deposits are probably localized manifestations of the same migrating fluids, occurring where the necessary physical and chemical traps are present. ?? 1987.

The genesis of Mo-Cu deposits and mafic igneous rocks in the Senj area, Alborz magmatic belt, Iran

NASA Astrophysics Data System (ADS)

Nabatian, Ghasem; Li, Xian-Hua; Wan, Bo; Honarmand, Maryam

2017-11-01

The geochemical and isotopic investigations were provided on the Upper Eocene Senj mafic intrusion and Mo-Cu mineralization to better understand the tectono-magmatic evolution and metallogeny of the central part of the Alborz magmatic belt. The Senj mafic intrusion is composed of gabbro to monzodiorite and monzonite in lithology, and intruded as a sill into volcano-sedimentary rocks of the Eocene Karaj Formation. The Karaj Formation consists of volcano-sedimentary rocks, such as altered crystalline to shaly tuffs. The Senj intrusion (39.7 ± 0.4 Ma) shows LILE and LREE enrichment and negative anomaly of Nb, Ta and Ti, the geochemical signatures similar to those from subduction-related mafic magmas. The Hf-O zircon analyses yield ɛHf(t) values of + 4.1 to + 11.1 and δ18O values of + 4.8 to + 6.2‰. The zircon isotopic signatures together with shoshonitic affinity in the Senj mafic samples suggest partial melting of an enriched lithospheric mantle that had already been metasomatized by slab-derived melts and fluids. The Mo-Cu mineralization mainly occurs as veins and veinlets in the volcano-sedimentary rocks of the Karaj Formation and is dominated by molybdenite with minor amounts of chalcopyrite, bornite, pyrite and tetrahedrite-tennantite. The associated gangue minerals are tremolite, actinolite, quartz, calcite, chlorite and epidote. The Senj Mo-Cu deposit formed in volcano-sedimentary rocks following the emplacement of the Late Eocene Senj sill. The source of molybdenite in the Senj deposit is dominantly from crustal materials as it is revealed by Re contents in the molybdenite minerals (0.5 to 0.7 ppm). In fact, the molybdenite occurrence may be a remobilization process related to the emplacement of the Senj mafic magma.

Uranium deposits of the northern part of the Boulder Batholith, Montana

USGS Publications Warehouse

Becraft, George E.

1955-01-01

Uranium minerals and radioactivity anomalies occur in many silver-lead veins and chalcedony veins and vein zones in the Boulder batholith of southwestern Montanao Pitchblende has been identified in a few silver-lead veins. These veins occupy shear zones along which there is no evidence of large-scale lateral displacement. The wall rock adjacent to the veins is intensely silicified and sencitized quartz monzonite and granodiortte. The veins have yielded substantial quantities of lead, silver, zinc, and gold. The silver-lead veins consist principal1y of galena, spha1erite, tetrahedrite, cha1copyrite and pyrite in a gangue of light to dark gray quartz, altered rock, gouge, and subordinate chalcedony and carbonate minerals. No anomalous radioactivity nor uranium minerals have been found in similar veins in pre-batholithic rocks of the area. Chalcedony veins and vein zones, some of which are ttraniferous, are distinctly different from the silver-lead veins and, with a single except1on, are known only in the batholith. The chalcedony vein zones consist of one or more discontinuous stringers or veins of cha1cedony and microcrystalline quartz in silicified and sericitized quartz monzonite and granodiorite, and in less strongly altered alaskite. On1y small amounts of silver ore have been produced from these chalcedony veins and vein zones. All of the veins are ear1y Tertiary in age, but the silver-lead veins probably are older than the chalcedony veins. Uranium is closely associated with chalcedory and microcrystalline quartz in both types of veins. This association suggests that all of the uranium in the area is of the same age. If so, some of the silver-lead veins must have been reopened during the period of chalcedony vein formation.

Fluid evolution and ore genesis of the Dalingshang deposit, Dahutang W-Cu ore field, northern Jiangxi Province, South China

NASA Astrophysics Data System (ADS)

Peng, Ning-Jun; Jiang, Shao-Yong; Xiong, Suo-Fei; Pi, Dao-Hui

2018-02-01

The Dalingshang W-Cu deposit is located in the North section of the Dahutang ore field, northern Jiangxi Province, South China. Vein- and breccia-style tungsten-copper mineralization is genetically associated with Mesozoic S-type granitic rocks. Infrared and conventional microthermometric studies of both gangue and ore minerals show that the homogenization temperatures for primary fluid inclusions in wolframite ( 340 °C) are similar to those in scheelite ( 330 °C), but about 40 °C higher than those of apatite ( 300 °C) and generally 70 °C higher than those in coexisting quartz ( 270 °C). Laser Raman analysis identifies CH4 and N2 without CO2 in fluid inclusions in scheelite and coexisting quartz, while fluid inclusions in quartz of the sulfide stage have variable CO2 content. The ore-forming fluids overall are characterized by high- to medium-temperature, low-salinity, CH4, N2, and/or CO2-bearing aqueous fluids. Chalcopyrite, muscovite, and sphalerite are the most abundant solids recognized in fluid inclusions from different ores. The H-O-S-Pb isotope compositions favor a dominantly magmatic origin for ores and fluids, while some depleted δ34S values (- 14.4 to - 0.9‰) of sulfides from the sulfide stage are most likely produced by an increase of oxygen fugacity, possibly caused by inflow of oxidized meteoric waters. The microthermometric data also indicate that a simple cooling process formed early scheelite and wolframite. However, increasing involvement of meteoric waters and fluid mixing may trigger a successive deposition of base metal sulfides. Fluid-rock interaction was critical for scheelite mineralization as indicated by in-situ LA-ICP-MS analysis of trace elements in scheelite.

The uranium-bearing nickel-cobalt-native silver deposits in the Black Hawk district, Grant County, New Mexico

USGS Publications Warehouse

Gillerman, Elliot; Whitebread, Donald H.

1953-01-01

The Black Hawk (Bullard Peak) district, Grant County, N. Mex., is 21 miles by road west of Silver City. From 1881 to 1893 more than $1,000,000.00 of high-grade silver ore is reported to have been shipped from the district. Since 1893 there has been no mining in the district except during a short period in 1917 when the Black Hawk mine was rehabilitated. Pre-Cambrian quartz diorite gneiss, which contains inclusions of quartzite, schist, monzonite, and quartz monzonite, is the most widespread rock in the district. The quartz diorite gneiss is intruded by many pre-Cambrian and younger rocks, including diorite granite, diabase, monzonite porphyry and andesite and is overlain by the Upper Cretaceous Beartooth quartzite. The monzonite porphyry, probably of late Cretaceous or early Tertiary age, forms a small stock along the northwestern edge of the district and numerous dikes and irregular masses throughout the district. The ore deposits are in fissure veins that contain silver, cobalt, and uranium. The ore minerals, which include native silver, niccolite, millerite, skutterudite, nickel skutterudite, bismuthinite, pitchblende, and sphalerite, are in a carbonate gangue in narrow, persistent veins, most of which trend northeasterly. Pitchblende has been identified in the Black Hawk and the Alhabra deposits and unidentified radioactive minerals were found at five other localities. The deposits that contain the radioactive minerals constitude a belt 600 to 1,500 feet wide that trends about N. 45° E., and is approximately parallel to the southeastern boundary of the monzonite porphyry stock. All the major ore deposits are in the quartz diorite gneiss in close proximity to the monzonite porphyry. The ore deposits are similar to the deposits at Great Bear Lake, Canada, and Joachimstahl, Czechoslovakia.

Geochemical hosts of solubilized radionuclides in uranium mill tailings

USGS Publications Warehouse

Landa, E.R.; Bush, C.A.

1990-01-01

The solubilization and subsequent resorption of radionuclides by ore components or by reaction products during the milling of uranium ores may have both economic and environmental consequences. Particle-size redistribution of radium during milling has been demonstrated by previous investigators; however, the identification of sorbing components in the tailings has received little experimental attention. In this study, uranium-bearing sandstone ore was milled, on a laboratory scale, with sulfuric acid. At regular intervals, filtrate from this suspension was placed in contact with mixtures of quartz sand and various potential sorbents which occur as gangue in uranium ores; the potential sorbents included clay minerals, iron and aluminum oxides, feldspar, fluorspar, barite, jarosite, coal, and volcanic glass. After equilibration, the quartz sand-sorbent mixtures were separated from the filtrate and radioassayed by gamma-spectrometry to determine the quantities of 238U, 230Th, 226Ra, and 210Pb sorbed, and the radon emanation coefficients. Sorption of 238U was low in all cases, with maximal sorptions of 1-2% by the bentonite- and coal-bearing samples. 230Th sorption also was generally less than 1%; maximal sorption here was observed in the fluorspar-bearing sample and appears to be associated with the formation of gypsum during milling. 226Ra and 210 Pb generally showed higher sorption than the other nuclides - more than 60% of the 26Ra solubilized from the ore was sorbed on the barite-bearing sample. The mechanism (s) for this sorption by a wide variety of substrates is not yet understood. Radon emanation coefficients of the samples ranged from about 5 to 30%, with the coal-bearing samples clearly demonstrating an emanating power higher than any of the other materials. ?? 1990.

Gold ores related to shear zones, West Santa Comba-Fervenza Area (Galicia, NW Spain): A mineralogical study

NASA Astrophysics Data System (ADS)

Castroviejo, R.

1990-12-01

Recent research has discovered high-grade Au ores in NNE-SSW trending shear zones in metamorphic proterozoic and palaeozoic terranes, some 40 km NW of Santiago de Compostela (NW Spain). The orebodies are bound to late-stage Hercynian structures, mainly due to brittle deformation, which are superimposed on earlier ductile shear zones, cutting through various catazonal lithologies, including ortho- and paragneisses, amphibolites, eclogites, and granites. Ore mineralogy, alteration, and ore textures define a frame whose main features are common to all prospects in the area. Main minerals are arsenopyrite and pyrite — accompanied by quartz, adularia, sericite, ± (tourmaline, chlorite, carbonates, graphite), as main gangue minerals -with subordinate amounts of boulangerite, bismuthinite, kobellite, jamesonite, chalcopyrite, marcasite, galena, sphalerite, rutile, titanite, scheelite, beryl, fluorite, and minor native gold, electrum, native bismuth, fahlore, pyrrhotite, mackinawite, etc., defining a meso-catathermal paragenesis. Detailed microscopic study allows the author to propose a general descriptive scheme of textural classification for this type of ore. Most of the ores fill open spaces or veins, seal cracks or cement breccias; disseminated ores with replacement features related to alteration (mainly silicification, sericitization, and adularization) are also observed. Intensive and repeated cataclasis is a common feature of many ores, suggesting successive events of brittle deformation, hydrothermal flow, and ore precipitation. Gold may be transported and accumulated in any of these events, but tends to be concentrated in later ones. The origin of the gold ores is explained in terms of hydrothermal discharge, associated with mainly brittle deformation and possibly related to granitic magmas, in the global tectonic frame of crustal evolution of West Galicia. The mineralogical and textural study suggests some criteria which will be of practical value for

Geology and mineral deposits of the Minnie Moore and Bullion mineralized areas, Blaine County, Idaho

USGS Publications Warehouse

Link, Paul Karl; Worl, Ronald G.

2001-01-01

In the early 1880?s the discovery of rich ores in the Minnie Moore and Bullion mineralized areas sparked a rush to settle and develop the Wood River valley. Silver and lead discoveries in these areas spurred the boom in mining after completion of the Oregon Short Line Railroad to Hailey in 1883. In both areas the ore comprises galena, sphalerite, and tetrahedrite in a gangue of siderite, calcite, or quartz. Minor goldbearing quartz veins are also present. The ore is in fissure and replacement veins along fracture systems that formed in Late Cretaceous time, after intrusion of nearby granodiorite or quartz diorite stocks. The ore formed under mesothermal conditions and heat was supplied by the nearby plutons. In the Minnie Moore area, the mineralized veins are cut by low-angle normal faults that are of probable Eocene age. In the Minnie Moore mineralized area, the host rock is the middle part of the Devonian Milligen Formation, (the informal Lucky Coin limestone and Triumph argillite), which is the same stratigraphic level as the host ore in the rich Triumph mine northeast of Hailey. In the Bullion mineralized area, the ore is hosted by the lower member of the Middle Pennsylvanian to Lower Permian Dollarhide Formation. Rich ore was mined in several tunnels that reached the Mayflower vein, a northwest-striking mineralized shear zone. The deposits are thought to be mainly mesothermal veins that formed in association with Cretaceous magmatism. The syngenetic stratiform model of ore formation has often been applied to these deposits, however, no evidence of syngenetic mineralization was found in this study. Faulting has displaced most of the major orebodies and thus has made mining these deposits a challenge.

Reburning Characteristics of Residual Carbon in Fly Ash from CFB Boilers

NASA Astrophysics Data System (ADS)

Zhang, S. H.; Luo, H. H.; Chen, H. P.; Yang, H. P.; Wang, X. H.

The content of residual carbon in fly ash of CFB boilers is a litter high especially when low-grade coal, such as lean coal, anthracite coal, gangue, etc. is in service, which greatly influences the efficiency of boilers and fly ash further disposal. Reburn of fly ash through collection, recirculation in CFB furnace or external combustor is a possibly effective strategy to decrease the carbon content, mainly depending on the residual carbon reactivity. In this work, the combustion properties of residual carbon in fly ash and corresponding original coal from large commercial CFB boilers (Kaifeng (440t/h), and Fenyi (410t/h), all in china) are comparably investigated through experiments. The residual carbon involved was firstly extracted and enriched from fly ash by means of floating elutriation to mitigate the influence of ash and minerals on the combustion behavior of residual carbon. Then, the combustion characteristic of two residual carbons and the original coal particles was analyzed with thermogravimetric analyzer (TGA, STA409C from Nestch, Germany). It was observed that the ignition temperature of the residual carbon is much higher than that of original coal sample, and the combustion reactivity of residual carbon is not only dependent on the original coal property, but also the operating conditions. The influence of oxygen content and heating rate was also studied in TGA. The O2 concentration is set as 20%, 30%, 40% and 70% respectively in O2/N2 gas mixture with the flow rate of 100ml/min. It was found that higher oxygen content is favor for decreasing ignition temperature, accelerating the combustion rate of residual carbon. And about 40% of oxygen concentration is experimentally suggested as an optimal value when oxygen-enriched combustion is put into practice for decreasing residual carbon content of fly ash in CFB boilers.

Preliminary report on the geology and deposits of monazite, thorite and niobium-bearing rutile of the Mineral Hill district, Lemhi County, Idaho

USGS Publications Warehouse

Kaiser, Edward Peck

1956-01-01

Deposits of minerals containing niobium (columbium), thorium, and rare earths occur in the Mineral Hill district, 30 miles northwest of Salmon, Lemhi County, Idaho. Monazite, thorite, allanite, and niobium-bearing rutile form deposits in metamorphic limestone layers less than 8 feet thick. The known deposits are small, irregular, and typically located in or near small folds. Minor faults are common. Monazite generally is coarsely crystalline and contains less than one percent thorium. Rutile forms massive lumps up to 3 inches across; it contains between 5 and 10 percent niobium. Rutile occurs in the northwestern half of the district, thorite in the central and southeastern parts. Monazite occurs in all deposits. Allanite is locally abundant and contains several percent thorium. Magnetite and ilmenite are also locally abundant. A major thrust fault trending northwest across the map-area separates moderately folded quartzite and phyllitic rocks of Belt age, on the northeast, from more intensely metamorphosed and folded rocks on the southwest. The more metamorphosed rocks include amphibolite, porphyroblastic feldspar gneiss, quartzite, and limestone, all probably of sedimentary origin, and probably also of Belt (late Precambrian) age. The only rocks of definite igneous origin are rhyolite dikes of probable Tertiary age. The more metamorphosed rocks were formed by metasomatic metamorphism acting on clastic sediments, probably of Belt age, although they may be older than Belt. Metamorphism doubtless was part of the episode of emplacement of the Idaho batholith, but the history of that episode is not well understood. The rare-element deposits show no evidence of fracture-controlled hydrothermal introduction, such as special fracture systems, veining, and gangue material. They may, however, be of hydrothermal type. More likely they are metamorphic segregations or secretions, deposited in favorable stratigraphic and structural positions during regional metamorphism.

Ore deposits and epithermal evidences associated with intra-magmatic faults at Aïn El Araâr-Oued Belif ring structure (NW of Tunisia)

NASA Astrophysics Data System (ADS)

Aissa, Wiem Ben; Aissa, Lassaâd Ben; Amara, Abdesslem Ben Haj; Tlig, Said; Alouani, Rabah

2017-03-01

Hydrothermal ore deposits at Aïn El Araâr-Oued Belif location are classified as epithermal deposits type. The ore bodies are hosted by upper Turonian (8-9 M.y) volcanic rhyodacitic complex. Polymetallic sulfide orebodies are mainly concentrated within intra-magmatic faults. Petrographic, XRD, and TEM-STEM investigations revealed that ore minerals are essentially, arsenopyrite, pyrite, chalcopyrite, pyrrhotite, hematite, goethite and magnetite with Au, Ag and Pt trace metals. Gangue minerals are mainly adularia, quartz, sericite, alunite, tridymite, chlorite, phlogopite and smectite. Epithermal alteration is well zoned with four successive characteristic zones: (1) zone of quartz-adularia-sericite and rare alunite; (2) zone of kaolinite and plagioclase albitization; (3) intermediate zone of illite-sericite; (4) sapropelic alteration type zone of chlorite-smectite and rare illite. This can be interpreted as a telescoping of two different acidity epithermal phases; low sulfidation (adularia-sericite) and high sulfidation (quartz-alunite), separated in time or due to a gradual increase of fluids acidity and oxicity within the same mineralization phase. Brecciated macroscopic facies with fragments hosting quartz-adularia-sericite minerals (low-sulfidation phase) without alunite, support the last hypothesis. Geodynamic context and mineral alteration patterns are closely similar to those of Maria Josefa gold mine at SE of Spain which exhibit a volcanic-hosted epithermal ore deposit in a similar vein system, within rhyolitic ignimbrites, altered to an argillic assemblage (illite-sericite abundant and subordinate kaolinite) that grades outwards into propylitic alteration (Sanger-von Oepen et al. (1990)). Mineralogical and lithologic study undertaken in the volcanic host rock at Aïn El Araâr-Oued Belif reveals a typical epithermal low-sulfidation and high-sulfidation ore deposits with dominance of low-sulfidation. Host rocks in these systems range from silicic to

New insights into the oleate flotation response of feldspar particles of different sizes: Anisotropic adsorption model.

PubMed

Xu, Longhua; Tian, Jia; Wu, Houqin; Deng, Wei; Yang, Yaohui; Sun, Wei; Gao, Zhiyong; Hu, Yuehua

2017-11-01

The anisotropic adsorption of sodium oleate (NaOL) on feldspar surfaces was investigated to elucidate the different flotation properties of feldspar particles of four different size ranges. Microflotation experiments showed that the feldspar flotation recovery of particles with sizes spanning different ranges decreased in the order 0-19>19-38>45-75>38-45μm. Zeta potential and FTIR measurements showed that NaOL was chemically adsorbed on the Al sites of the feldspar surface. The anisotropic surface energies and broken bond densities estimated by density functional theory calculations showed that, although feldspar mostly exposed (010) and (001) surfaces, only the (001) surfaces contained the Al sites needed for NaOL adsorption. The interaction energies calculated by molecular dynamics simulations confirmed the more favorable NaOL adsorption on (001) than (010) surfaces, which may represent the main cause for the anisotropic NaOL adsorption on feldspar particles of different sizes. SEM measurements showed that the main exposed surfaces on coarse and fine feldspar particles were the side (010) and basal (001) ones, respectively. A higher fraction of Al-rich (001) surfaces is exposed on fine feldspar particles, resulting in better floatability compared with coarse particles. XPS and adsorption measurements confirmed that the Al content on the feldspar surface varied with the particle size, explaining the different NaOL flotation of feldspar particles of different sizes. Therefore, the present results suggest that coarsely ground ore should be used for the separation of feldspar gangue minerals. Further improvements in the flotation separation of feldspar from associated valuable minerals can be achieved through selective comminution or grinding processes favoring the exposure of (010) surfaces. Copyright © 2017 Elsevier Inc. All rights reserved.

Noble gas data from Goldfield and Tonopah epithermal Au-Ag deposits, ancestral Cascades Arc, USA: Evidence for a primitive mantle volatile source

USGS Publications Warehouse

Manning, Andrew H.; Hofstra, Albert H.

2017-01-01

The He, Ne, and Ar isotopic composition of fluid inclusions in ore and gangue minerals were analyzed to determine the source of volatiles in the high-grade Goldfield and Tonopah epithermal Au-Ag deposits in southwestern Nevada, USA. Ar and Ne are mainly atmospheric, whereas He has only a minor atmospheric component. Corrected 3He/4He ratios (with atmospheric He removed) range widely from 0.05 to 35.8 times the air 3He/4He ratio (RA), with a median of 1.43 RA. Forty-one percent of measured 3He/4He ratios are ≥4 RA, corresponding to ≥50% mantle He assuming a mantle ratio of 8 RA. These results suggest that mafic magmas were part of the magmatic-hydrothermal system underlying Goldfield and Tonopah, and that associated mantle-sourced volatiles may have played a role in ore formation. The three highest corrected 3He/4He ratios of 17.0, 23.7, and 35.8 RAindicate a primitive mantle He source and are the highest yet reported for any epithermal-porphyry system and for the Cascades arc region. Compiled 3He/4He measurements from epithermal-porphyry systems in subduction-related magmatic arcs around the world (n = 209) display a statistically significant correlation between 3He/4He and Au-Ag grade. The correlation suggests that conditions which promote higher fluid inclusion 3He/4He ratios (abundance of mantle volatiles and focused upward volatile transport) have some relation to conditions that promote higher Au-Ag grades (focused flow of metal-bearing fluids and efficient chemical traps). Results of this and previous investigations of He isotopes in epithermal-porphyry systems are consistent with the hypothesis posed in recent studies that mafic magmas serve an important function in the formation of these deposits.

Heavy metal migration in soils and rocks at historical smelting sites.

PubMed

Maskall, J; Whitehead, K; Thornton, I

1995-09-01

The vertical migration of metals through soils and rocks was investigated at five historical lead smelting sites ranging in age between 220 and 1900 years. Core samples were taken through metal-contaminated soils and the underlying strata. Concentration profiles of lead and zinc are presented from which values for the distances and rates of migration have been derived. Slag-rich soil horizons contain highly elevated metal concentrations and some contamination of underlying strata has occurred at all sites. However, the amounts of lead and zinc that have migrated from soils and been retained at greater depths are comparatively low. This low metal mobility in contaminated soils is partly attributed to the elevation of soil pH by the presence of calcium and carbonate originating from slag wastes and perhaps gangue minerals. Distances and rates of vertical migration were higher at those sites with soils underlain by sandstone than at those with soils underlain by clay. For sites with the same parent material, metal mobility appears to be increased at lower soil pH. The mean migration rates for lead and zinc reach maxima of 0.75 and 0.46 cm yr(-1) respectively in sandstone at Bole A where the elements have moved mean distances of 4.3 and 2.6 m respectively. There is some evidence that metal transport in the sandstone underlying Bole A and Cupola B occurs preferentially along rock fractures. The migration of lead and zinc is attenuated by subsurface clays leading to relatively low mean migration rates which range from 0.03 to 0.31 cm yr(-1) with many values typical of migration solely by diffusion. However, enhanced metal migration in clays at Cupola A suggest a preferential transport mechanism possibly in cracks or biopores.

Mass change calculations of hydrothermal alterations within the volcanogenic metasediments hosted Cu-Pb (-Zn) mineralization at Halilar area, NW Turkey

NASA Astrophysics Data System (ADS)

Kiran Yildirim, Demet; Abdelnasser, Amr; Doner, Zeynep; Kumral, Mustafa

2016-04-01

The Halilar Cu-Pb (-Zn) mineralization that is formed in the volcanogenic metasediments of Bagcagiz Formation at Balikesir province, NW Turkey, represents locally vein-type deposit as well as restricted to fault gouge zone directed NE-SW along with the lower boundary of Bagcagiz Formation and Duztarla granitic intrusion in the study area. Furthermore, This granite is traversed by numerous mineralized sheeted vein systems, which locally transgress into the surrounding metasediments. Therefore, this mineralization closely associated with intense hydrothermal alteration within brecciation, and quartz stockwork veining. The ore mineral assemblage includes chalcopyrite, galena, and some sphalerite with covellite and goethite formed during three phases of mineralization (pre-ore, main ore, and supergene) within an abundant gangue of quartz and calcite. The geologic and field relationships, petrographic and mineralogical studies reveal two alteration zones occurred with the Cu-Pb (-Zn) mineralization along the contact between the Bagcagiz Formation and Duztarla granite; pervasive phyllic alteration (quartz, sericite, and pyrite), and selective propylitic alteration (albite, calcite, epidote, sericite and/or chlorite). This work, by using the mass balance calculations, reports the mass/volume changes (gain and loss) of the chemical components of the hydrothermal alteration zones associated with Halilar Cu-Pb (-Zn) mineralization at Balikesir area (Turkey). It revealed that the phyllic alteration has enrichments of Si, Fe, K, Ba, and LOI with depletion of Mg, Ca, and Na reflect sericitization of alkali feldspar and destruction of ferromagnesian minerals. This zone has high Cu and Pb with Zn contents represents the main mineralized zone. On the other hand, the propylitic zone is characterized by addition of Ca, Na, K, Ti, P, and Ba with LOI and Cu (lower content) referring to the replacement of plagioclase and ferromagnesian minerals by albite, calcite, epidote, and sericite

Mineral types of hydrothermal alteration zones in the Dukat ore field and their relationships to leucogranite and epithermal gold-silver ore, northeastern Russia

NASA Astrophysics Data System (ADS)

Filimonova, L. G.; Trubkin, N. V.; Chugaev, A. V.

2014-05-01

The paper considers the localization of potassic and propylitic hydrothermal alteration zones in the domal volcanic-plutonic structure controlling the position of the Dukat ore field with the eponymous unique epithermal Au-Ag deposit. Comprehensive mineralogical and geochemical data on rocks and minerals in hydrothermal alteration zones and associated intrusions have shown that quartz-jarosite-sericite, quartz-pyrite-sericite, and quartz-adularia-chlorite alterations were formed with the participation of fluid flows related to a fingerlike projection of a high-K leucogranite porphyry intrusion with large phenocrysts. These hydrothermal alterations developed in the rifted graben under conditions of divergent plate boundaries, whereas quartz-clinozoisite-calcite, epidote-chlorite, and garnet-calcite-chlorite alterations were linked to K-Na leucogranite intrusive bodies and developed under conditions of convergent plate boundaries reactivated as a result of formation of the marginal Okhotsk-Chukotka volcanic belt. Phase separation and coagulation of specific portions of ascending fluids resulted in the formation and stabilization of small-sized particles of native silver and other ore components, which enabled involvement in flows of secondary geothermal solutions and ore-forming fluids. The Sr, Nd, and Pb isotopic compositions of rocks and minerals from the hydrothermal alteration zones, associated intrusions, and economic orebodies at the Dukat deposit indicate that their components have been derived from the juvenile continental crust, which was altered in pre-Cretaceous periods of endogenic activity. The components of gangue minerals of potassic and propylitic hydrothertmal alterations and associated intrusions have been taken from deep sources differing in 87Sr/86Sr and 143Nd/144Nd at similar U/Pb and Th/Pb ratios. Chalcophile lead in products of hydrothermal activity and melanocratic inclusions in leucogranite has been taken from regions with elevated U/Pb and

Separation of Iron Phase and P-Bearing Slag Phase from Gaseous-Reduced, High-Phosphorous Oolitic Iron Ore at 1473 K (1200 °C) by Super Gravity

NASA Astrophysics Data System (ADS)

Gao, Jintao; Zhong, Yiwei; Guo, Lei; Guo, Zhancheng

2016-04-01

In situ observation on the morphology evolution and phosphorous migration of gaseous-reduced, high-phosphorous oolitic iron ore during the melting process was carried out with a high-temperature confocal scanning laser microscope. The results showed that 1473 K (1200 °C) was a critical temperature at which the gangue minerals started to form into the slag phase while the iron grains remained in a solid state; in addition, the phosphorus remained in the slag phase. Since the separation of iron grains and P-bearing slag was not achieved at the low temperature under the conventional conditions, separate experiments of the iron phase and the P-bearing slag phase from gaseous-reduced, high-phosphorous oolitic iron ore at 1473 K (1200 °C) by super gravity were carried out in this study. Based on the iron-slag separation by super gravity, phosphorus was removed effectively from the iron phase at the temperature below the melting point of iron. Iron grains moved along the super-gravity direction, joined, and concentrated as the iron phase on the filter, whereas the slag phase containing apatite crystals broke through the barriers of the iron grains and went through the filter. Consequently, increasing the gravity coefficient was definitely beneficial for the separation of the P-bearing slag phase from the iron phase. With the gravity coefficient of G = 1200, the mass fractions of separated slag and iron phases were close to their respective theoretical values, and the mass fraction of MFe in the separated iron phase was up to 98.09 wt pct and that of P was decreased to 0.083 wt pct. The recovery of MFe in the iron phase and that of P in the slag phase were up to 99.19 and 95.83 pct, respectively.

Geology and mineral deposits of the St. Regis-Superior area, Mineral County, Montana

USGS Publications Warehouse

Campbell, Arthur B.

1960-01-01

County, has been traced to the east edge of the St. Regis- Superior area, thus extending the mapped length of the fault to about 100 miles. Evidence indicates that this major fault has diminished in intensity in this area and that most of the stress has been relieved along the Boyd Mountain fault that apparently splits from the Osburn fault a few miles west of St. Regis. Stratigraphic and structural evidence indicates a strike-slip right-lateral movement of about 3 miles along the Osburn fault. Horizontal stratigraphic separation along the Boyd Mountain fault indicates a right-lateral movement of about 13 miles.Low-grade regional metamorphism of the sedimentary rocks in the area has caused the recrystallization of quartz grains and the formation of sericite. Argillite and quartzite have been converted to phyllite and foliated quartzite by dynamic metamorphism in a large area north of the central part of the Osburn fault. Some of the shear zones contain a large amount of introduced carbonate minerals. From 1901 through 1953 this area has produced 8,086,827 pounds of zinc, 7,932,958 pounds of lead, 2,053,715 pounds of copper, 584,168 fine ounces of silver, and 588 fine ounces of gold. The lead, sine, and silver have come chiefly from veins in highly foliated rocks near the Osburn fault zone. The attitudes of these veins are controlled in large part by the cleavage. The principal ore minerals are galena, sphalerite, tetrahedrite, and boulangerite, and the gangue minerals are quartz, carbonate minerals, and barite. Most of the copper has come from the Amador vein where chalcopyrite and bornite are the principal ore minerals, and the gangue minerals are pyrite, quartz, and carbonate minerals. The Amador vein occurs in a belt of copper deposits that extends westward into the Coeur d'Alene district. These copper deposits may be genetically associated with diorite dikes and sills lying within the same belt. Fluorspar has been found in three closely spaced prospects along a

Genesis of the Bangbule Pb-Zn-Cu polymetallic deposit in Tibet, western China: Evidence from zircon U-Pb geochronology and S-Pb isotopes

NASA Astrophysics Data System (ADS)

Kan, Tian; Zheng, Youye; Gao, Shunbao

2016-04-01

The Banbule Pb-Zn-Cu skarn deposit is located in the Longger-Gongbujiangda volcanic magma arc in the Gangdese-Nyainqentanglha Plate. It is the only lead-zinc polymetallic deposit discovered in the westernmost Nyainqentanglha metallogenic belt. The measured and indicated resources include 0.9 Mt of Pb+Zn (4.77% Pb and 4.74% Zn, respectively), 6499 t of Cu, and 178 t of Ag (18.75g/t Ag). The orebodies mainly occur as lenses, veins and irregular shapes in the contact zone between the quartz-porphyry and limestone of the Upper Permian Xiala Formation, or in the boundaries between limestone and sandstone. Pb-Zn-Cu mineralization in the Banbule deposit is closely associated with skarns. The ore minerals are dominated by galena, sphalerite, chalcopyrite, bornite, and magnetite, with subordinate pyrite, malachite, and azurite. The gangue minerals are mainly garnet, actinolite, diopside, quartz, and calcite. The ore-related quartz-porphyry displays LA-ICP-MS zircon U-Pb age of 77.31±0.74 Ma. The δ34S values of sulfides define a narrow range of -0.8 to 4.7‰ indicating a magmatic source for the ore-forming materials. Lead isotopic systematics yield 206Pb/204Pb of 18.698 to 18.752, 207Pb/204Pb of 15.696 to 15.760, and 208Pb/204Pb of 39.097 to 39.320. The data points are constrained around the growth curves of upper crust and orogenic belt according to the tectonic discrimination diagrams. The calculated Δβ - Δγ values plot within the magmatic field according to the discrimination diagram of Zhu et al. (1995). The S-Pb isotopic data suggest that Bangbule is a typical skarn deposit, and the Pb-Zn-Cu mineralization is genetically related to the quartz-porphyry in the mining district. The discovery of the Bangbule deposit indicates that there is metallogenic potential in the westernmost Nyainqentanglha belt, which is of great importance for the exploration work in this area.

A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry

DOE Office of Scientific and Technical Information (OSTI.GOV)

Goverapet Srinivasan, Sriram; Shivaramaiah, Radha; Kent, Paul R. C.

Bastnäsite, a fluoro-carbonate mineral, is the single largest mineral source of light rare earth elements (REE), La, Ce and Nd. Enhancing the efficiency of separation of the mineral from gangue through froth flotation is the first step towards meeting an ever increasing demand for REE. To design and evaluate collector molecules that selectively bind to bastnäsite, a fundamental understanding of the structure and surface properties of bastnäsite is essential. In our earlier work (J Phys Chem C, 2016, 120, 16767), we carried out an extensive study of the structure, surface stability and water adsorption energies of La-bastnäsite. Here in thismore » work, we make a comparative study of the surface properties of Ce-bastnäsite, La-bastnäsite, and calcite using a combination of density functional theory (DFT) and water adsorption calorimetry. Spin polarized DFT+U calculations show that the exchange interaction between the electrons in Ce 4f orbitals is negligible and that these orbitals do not participate in bonding with the oxygen atom of the adsorbed water molecule. In agreement with calorimetry, DFT calculations predict larger surface energies and stronger water adsorption energies on Ce-bastnäsite than on La-bastnäsite. The order of stabilities for stoichiometric surfaces is as follows: [100] > [101] > [102] > [0001] > [112] > [104] and the most favorable adsorption sites for water molecules are the same as for La-bastnäsite. In agreement with water adsorption calorimetry, at low coverage water molecules are strongly stabilized via coordination to the surface Ce3+ ions, whereas at higher coverage they are adsorbed less strongly via hydrogen bonding interaction with the surface anions. Lastly, due to similar water adsorption energies on bastnäsite [101] and calcite [104] surfaces, the design of collector molecules that selectively bind to bastnäsite over calcite must exploit the structural differences in the predominantly exposed facets of these minerals.« less

A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry

DOE PAGES

Goverapet Srinivasan, Sriram; Shivaramaiah, Radha; Kent, Paul R. C.; ...

2017-02-24

Bastnäsite, a fluoro-carbonate mineral, is the single largest mineral source of light rare earth elements (REE), La, Ce and Nd. Enhancing the efficiency of separation of the mineral from gangue through froth flotation is the first step towards meeting an ever increasing demand for REE. To design and evaluate collector molecules that selectively bind to bastnäsite, a fundamental understanding of the structure and surface properties of bastnäsite is essential. In our earlier work (J Phys Chem C, 2016, 120, 16767), we carried out an extensive study of the structure, surface stability and water adsorption energies of La-bastnäsite. Here in thismore » work, we make a comparative study of the surface properties of Ce-bastnäsite, La-bastnäsite, and calcite using a combination of density functional theory (DFT) and water adsorption calorimetry. Spin polarized DFT+U calculations show that the exchange interaction between the electrons in Ce 4f orbitals is negligible and that these orbitals do not participate in bonding with the oxygen atom of the adsorbed water molecule. In agreement with calorimetry, DFT calculations predict larger surface energies and stronger water adsorption energies on Ce-bastnäsite than on La-bastnäsite. The order of stabilities for stoichiometric surfaces is as follows: [100] > [101] > [102] > [0001] > [112] > [104] and the most favorable adsorption sites for water molecules are the same as for La-bastnäsite. In agreement with water adsorption calorimetry, at low coverage water molecules are strongly stabilized via coordination to the surface Ce3+ ions, whereas at higher coverage they are adsorbed less strongly via hydrogen bonding interaction with the surface anions. Lastly, due to similar water adsorption energies on bastnäsite [101] and calcite [104] surfaces, the design of collector molecules that selectively bind to bastnäsite over calcite must exploit the structural differences in the predominantly exposed facets of these minerals.« less

Classification of Broken Hill-Type Pb-Zn-Ag Deposits: A Refinement

NASA Astrophysics Data System (ADS)

Spry, P. G.; Teale, G. S.; Steadman, J. A.

2009-05-01

Broken Hill Hill-type Pb-Zn-Ag (BHT) deposits constitute some of the largest ore deposits in the world. The Broken Hill deposit is the largest accumulation of Pb, Zn, and Ag on Earth and the Cannington deposit is currently the largest silver deposit. Characteristic features of BHT deposits include: 1. high Pb+Zn+Ag values with Pb > Zn; 2. Metamorphism to amphibolite-granulite facies; 3. Paleo-to Mesoprotoerozoic clastic metasedimentary host rocks; 4. Sulfides that are spatially associated with bimodal (felsic and mafic) volcanic rocks, and stratabound gahnite- and garnet-bearing rocks and iron formations, 5. Stacked orebodies with characteristic Pb:Zn:Ag ratios and skarn-like Fe-Mn-Ca-F gangue assemblages, and the presence of Cu, Au, Bi, As, and Sb; and 6. Sulfur-poor assemblages. Broken Hill (Australia) has a prominent footwall feeder zone whereas other BHT deposits have less obvious alteration zones (footwall garnet spotting and stratabound alteration haloes). Deposits previously regarded in the literature as BHT deposits are Broken Hill, Cannington, Oonagalabie, Menninie Dam, and Pegmont (Australia), Broken Hill, Swartberg, Big Syncline, and Gamsberg (South Africa), Zinkgruvan (Sweden), Sullivan, Cottonbelt, and Foster River (Canada), and Boquira (Brazil). Of these deposits, only the Broken Hill (Australia, South Africa), Pinnacles, Cannington, Pegmont, and Swartberg deposits are BHT deposits. Another BHT deposit includes the Green Parrot deposit, Jervois Ranges (Northern Territory). The Foster River, Gamsberg, and Sullivan deposits are considered to be "SEDEX deposits with BHT affinities", and the Oonagalabie, Green Mountain (Colorado), and Zinkgruvan are "VMS deposits with BHT affinities". In the Broken Hill area (Australia), Corruga-type Pb-Zn-Ag deposits occur in calc-silicate rocks and possess some BHT characteristics; the Big Syncline, Cottonbelt, Menninie Dam, and Saxberget deposits are Corruga-type deposits. SEDEX deposits with BHT affinities, VMS

Agricolaite, a new mineral of uranium from Jáchymov, Czech Republic

NASA Astrophysics Data System (ADS)

Skála, Roman; Ondruš, Petr; Veselovský, František; Císařová, Ivana; Hloušek, Jan

2011-11-01

The new mineral agricolaite, a potassium uranyl carbonate with ideal formula K4(UO2)(CO3)3, occurs in vugs of ankerite gangue in gneisses in the abandoned Giftkiesstollen adit at Jáchymov, Czech Republic. The name is after Georgius Agricola (1494-1555), German scholar and scientist. Agricolaite occurs as isolated equant irregular translucent grains to 0.3 mm with yellow color, pale yellow streak, and vitreous luster. It is brittle with uneven fracture and displays neither cleavage nor parting. Agricolaite is non-fluorescent. Mohs hardness is ~4. It is associated with aragonite, brochantite, posnjakite, malachite, rutherfordine, and "pseudo-voglite". Experimental density is higher than 3.3 g.cm-3, Dcalc is 3.531 g. cm-3. The mineral is monoclinic, space group C2/ c, with a 10.2380(2), b 9.1930(2), c 12.2110(3) Å, β 95.108(2)°, V 1144.71(4) Å3, Z = 4. The strongest lines in the powder X-ray diffraction pattern are d( I)( hkl): 6.061(55)(002), 5.087(57)(200), 3.740(100)(202), 3.393(43)(113), 2.281(52)(402). Average composition based on ten electron microprobe analyses corresponds to (in wt.%) UO3 48.53, K2O 31.49, CO2(calc) 22.04 which gives the empirical formula K3.98(UO2)1.01(CO3)3.00. The crystal structure was solved from single-crystal X-ray diffraction data and refined to R 1 = 0.0184 on the basis of the 1,308 unique reflections with F o > 4 σF o. The structure of agricolaite is identical to that of synthetic K4(UO2)(CO3)3 and consists of separate UO2(CO3)3 groups organized into layers parallel to (100) and two crystallographically non-equivalent sites occupied by K+ cations. Both the mineral and its name were approved by the IMA-CNMNC.

Source of boron in the Palokas gold deposit, northern Finland: evidence from boron isotopes and major element composition of tourmaline

NASA Astrophysics Data System (ADS)

Ranta, Jukka-Pekka; Hanski, Eero; Cook, Nick; Lahaye, Yann

2017-06-01

The recently discovered Palokas gold deposit is part of the larger Rompas-Rajapalot gold-mineralized system located in the Paleoproterozoic Peräpohja Belt, northern Finland. Tourmaline is an important gangue mineral in the Palokas gold mineralization. It occurs as tourmalinite veins and as tourmaline crystals in sulfide-rich metasomatized gold-bearing rocks. In order to understand the origin of tourmaline in the gold-mineralized rocks, we have investigated the major element chemistry and boron isotope composition of tourmaline from three areas: (1) the Palokas gold mineralization, (2) a pegmatitic tourmaline granite, and (3) the evaporitic Petäjäskoski Formation. Based on textural evidence, tourmaline in gold mineralization is divided into two different types. Type 1 is located within the host rock and is cut by rock-forming anthophyllite crystals. Type 2 occurs in late veins and/or breccia zones consisting of approximately 80% tourmaline and 20% sulfides, commonly adjacent to quartz veins. All the studied tourmaline samples belong to the alkali-group tourmaline and can be classified as dravite and schorl. The δ11B values of the three localities lie in the same range, from 0 to -4‰. Tourmaline from the Au mineralization and from the Petäjäskoski Formation has similar compositional trends. Mg is the major substituent for Al; inferred low Fe3+/Fe2+ ratios and Na values (<0.8 atoms per formula unit (apfu)) of all tourmaline samples suggest that they precipitated from reduced, low-salinity fluids. Based on the similar chemical and boron isotope composition and the Re-Os age of molybdenite related to the tourmaline-sulfide-quartz veins, we propose that the tourmaline-forming process is a result of a single magmatic-hydrothermal event related to the extensive granite magmatism at around 1.79-1.77 Ga. Tourmaline was crystallized throughout the hydrothermal process, which resulted in the paragenetic variation between type 1 and type 2. The close association of

Geologic setting, genesis and transformation of sulfide deposits in the northern part of Khetri copper belt, Rajasthan, India — an outline

NASA Astrophysics Data System (ADS)

Sarkar, S. C.; Dasgupta, Somnath

1980-07-01

The present study is confined to the northern part of the Khetri copper belt that extends for about 100 km in northern Rajasthan. Mineralization is more or less strata-bound and is confined to the garnetiferous chlorite schist and banded amphibolite quartzite, occurring towards the middle of the Proterozoic Delhi Supergroup. Preserved sedimentary features and re-estimation of the composition of the pre-metamorphic rocks suggest that the latter were deposited in shallow marine environment characterized by tidal activity. Cordierite-orthoamphibole-cummingtonite rock occurring in the neighbourhood of the ores is discussed, and is suggested to be isochemically metamorphosed sediment. The rocks together with the ores were deformed in two phases and metamorphosed in two progressive and one retrogressive events of metamorphism. Study of the host rocks suggests that the maximum temperature and pressure attained during metamorphism are respectively 550 600°C and < 5.5 kb. Principal ore minerals in Madan Kudan are chalcopyrite, pyrrhotite, pyrite and locally magnetite. In Kolihan these are chalcophyrite, pyrrhotite and cubanite. Subordinate phases are sphalerite, ilmenite, arsenopyrite, mackinawite, molybdenite, cobaltite and pentlandite. The last two are very rare. Gangue minerals comprise quartz, chlorite, garnet, amphiboles, biotite, scapolite, plagioclase and graphite. The ores are metamorphosed at temperatures > 491°C. Sulfide assemblages are explained in terms of fS 2 during metamorphism. Co-folding of the ore zone with the host rocks, confinement of the ores to the carbonaceous pelites or semi-pelitic rocks, strata-bound and locally even stratiform nature of the orebodies, lack of finite ‘wall rock alteration’, metamorphism of the ores in the thermal range similar to that for the host rocks, absence of spatial and temporal relationship with the granitic rocks of the region led the authors to conclude that the entire mineralization was originally sedimentary

Flash Flood Type Identification within Catchments in Beijing Mountainous Area

NASA Astrophysics Data System (ADS)

Nan, W.

2017-12-01

coal gangues. The pure water flood process catchments were mainly distributed in the transitional mountain front.

Micron to Mine: Synchrotron Science for Mineral Exploration, Production, and Remediation

NASA Astrophysics Data System (ADS)

Banerjee, N.; Van Loon, L.; Flynn, T.

2017-12-01

Synchrotron science for mineral exploration, production, and remediation studies is a powerful tool that provides industry with relevant micron to macro geochemical information. Synchrotron micro X-ray fluorescence (SR-µXRF) offers a direct, high-resolution, rapid, and cost-effective chemical analysis while preserving the context of the sample by mapping ore minerals with ppm detection limits. Speciation of trace and deleterious elements can then be probed using X-ray absorption near-edge structure (XANES) spectroscopy. Large-scale (tens of cm) µXRF mapping and XANES analysis of samples collected at various mine locations have been undertaken to address questions regarding mineralization history to develop novel trace element exploration vectors. This information provides integral insights into trace element associations with ore minerals, local redox conditions responsible for mineralization, and mineralizing mechanisms. Gold is commonly intimately associated with sulfide mineralization (e.g., pyrite, arsenopyrite, etc.) and is present both as inclusions and filling fractures in sulfide grains. Gold may also occur as nanoparticles and/or in the sulfide mineral crystal lattice, known as "invisible gold". Understanding the nature and distribution of invisible gold in ore is integral to processing efficiency. The high flux and energy of a synchrotron light source allows for the detection of invisible gold by µXRF, and can probe its nature (metallic Au0 vs. lattice bound Au1+) using XANES spectroscopy. The long-term containment and management of arsenic is necessary to protect the health of both humans and the environment. Understanding the relationship of arsenic mineralization to gold deposits can lead to more sophisticated planning for mineral processing and the eventual storage of gangue materials. µXANES spectroscopy is an excellent tool for determining arsenic speciation within the context of the sample. Mineral phases such as arsenopyrite, scorodite, and

Distribution and speciation of metals in soils of the former mining district of Touiref (Northwest Tunisia)

NASA Astrophysics Data System (ADS)

Othmani, M. A.; Soussi, F.; Ferreira da Silva, E.; Moussi, A.; Oueslati, W.; Jebali, R.

2012-04-01

The former mining district of Touiref (1901-1958), located North-West of Tunisia, and where the activities have stopped 50 years ago, gave rise to large volumes of mine (extraction, flotation) tailings containing sulphides (galena, sphalerite, jordanite, pyrite, marcasite) associated with a carbonate gangue. Analysis of a hundred samples of soil has been used to develop isoconcentration maps of Pb, Zn, Cd and As across the study area, beyond the local geochemical background (LGB). The drawing of these maps has allowed the delineation of the contaminated areas using Geographic Information Systems (GIS). In addition, the soils of the study area were characterized in terms physico-chemical (pH and Corg), grain size, mineralogical and chemical means. Their neutral to slightly alkaline pH is (7.91 to 8.81), and their clay (32 and 57%)-silt (26 and 42%) texture, are characteristic of soils developed on carbonate bedrocks. The percentages in organic carbon (Corg) are between 0.71 and 5.6%. From a mineralogical point of view, mainly Pb-Fe sulphides associated with their alteration products have been observed within these soils. The levels of Pb, Zn, Cd and As, may go up 0.99%, 1.99%, 140 ppm and 409 ppm, respectively. These high concentrations were recorded around the extraction, processing and storage sites on the one hand and through the flood zones and the prevailing wind direction (NW-SSE) on the other. These soils have also been subjected to sequential extraction tests in order to characterize the metal-bearing phases and assess the mobility and bioavailability of heavy metals. The results have shown that Pb is mainly associated with the acid-soluble fraction (carbonates) and to a lesser extent with the Fe-(oxy)hydroxides, whereas Zn and Cd are mainly associated with Fe-(oxy)hydroxides and to a lesser degree with sulphides. Metals associated with these phases can be easily mobilized in response to physico-chemical changes and become phytoaccessible.

Paragenetic and minor- and trace-element studies of Mississippi Valley-type ore deposits of the Silesian-Cracow district, Poland

USGS Publications Warehouse

Viets, J.G.; Leach, D.L.; Lichte, F.E.; Hopkins, R.T.; Gent, C.A.; Powell, J.W.

1996-01-01

Paragenetic and minor- and trace-element studies were conducted on samples of epigenetic ore and gangue minerals collected from mines and drill core in the Silesian-Cracow (S-C) district of southern Poland. Four discrete mineral suites representing four mineralizing stages can be identified throughout the district. The earliest epigenetic minerals deposited during stage 1 consist of a late dolomite cement together with minor pyrite and marcasite. Stage 2 was the first ore-forming stage and included repetitive deposition of sphalerite and galena in a variety of morphologies. Stage 3 abruptly followed the first ore stage and deposited marcasite and pyrite with variable amounts of late sphalerite and galena. In the samples studied, minerals deposited during stage 3 are predominately marcasite-pyrite with minor sphalerite and galena in the Pomorzany and Olkusz mines, whereas, at the Trzebionka mine, stage 3 mineralization deposited mostly galena and sphalerite with little marcasite or pyrite. Stage 4 minerals include contains barite, followed by calcite, with very minor pyrite and a rare, late granular sphalerite. Compared to other major Mississippi Valley-type (MVT) districts of the world, the Silesian-Cracow district contains sphalerite with the second largest range in Ag concentrations and the largest range in Fe and Cd concentrations of any district. Unlike in other districts, very wide ranges in minor- and trace-element concentrations are also observed in paragenetically equivalent samples collected throughout the district. This wide range indicates that the minor- and trace-element content of the ore-forming environment was highly variable, both spatially and temporally, and suggests that the hydrologic system that the ore fluids traversed from their basinal source was very complex. Throughout the district, a significant increase in Tl, Ge, and As concentrations is accompanied by a lightening of sulfur isotopes between stage 2 and stage 3 minerals. This change

Mineral exploration, Mahd adh Dhahab District, Kingdom of Saudi Arabia

USGS Publications Warehouse

Worl, Ronald G.

1978-01-01

Mahd adh Dhahab is the largest of numerous ancient gold mines scattered through the Precambrian shield of Saudi Arabia and the only one with recent production. During the period 1939-54, 765,768 fine ounces of gold and 1,002,029 ounces of silver were produced from the mines by the Saudi Arabian Mining Syndicate. Ore minerals at Mahd adh Dhahab include free gold and silver, tellurides, sphalerite, and chalcopyrite in and associated with a system of north-trending quartz veins and quartz veinlet stockworks. Pyrite is a common sulfide gangue mineral. Country rocks are a north dipping sequence of pyroclastic and transported pyroclastic rocks of the Hulayfah Group that are locally highly silicified and potassium-feldspathized. The prime target for this exploration program was a north-trending zone of quartz veins and breccias, faults, alteration, and metalization approximately 400 m wide and 1000 m long. The ancient and recent mine workings are located in the northern part of this zone. Although the quartz veins and alteration cut all lithologies, the major metalization is confined to the intersection of veins and agglomerate. Ten holes were diamond drilled to explore geochemical, geological, and geophysical targets in the area. A significant new zone of metalization was discovered 700 m south of the ancient and recent mine workings and within the same major zone of quartz veins, alteration, and faults. Metalization in this southern mineralized zone is at the intersection of the quartz veins and a distinctive and highly altered agglomerate. The total zone of vein and agglomerate intercept is potentially metalized and comprises a block of ground 40 m thick and 400 m wide along the strike of the agglomerate and projected downdip 250 m. Tonnage of this block is 17.2 million tons. The explored zone, approximately 25 percent of the potentially metalized rock, has a potential resource of 1.1 million tons containing 27 g/t gold and 73 g/t silver.

Co-Cu-Au deposits in metasedimentary rocks-A preliminary report

USGS Publications Warehouse

Slack, J.F.; Causey, J.D.; Eppinger, R.G.; Gray, J.E.; Johnson, C.A.; Lund, K.I.; Schulz, K.J.

2010-01-01

A compilation of data on global Co-Cu-Au deposits in metasedimentary rocks refines previous descriptive models for their occurrence and provides important information for mineral resource assessments and exploration programs. This compilation forms the basis for a new classification of such deposits, which is speculative at this early stage of research. As defined herein, the Co-Cu-Au deposits contain 0.1 percent or more by weight of Co in ore or mineralized rock, comprising disseminated to semi-massive Co-bearing sulfide minerals with associated Fe- and Cu-bearing sulfides, and local gold, concentrated predominantly within rift-related, siliciclastic metasedimentary rocks of Proterozoic age. Some deposits have appreciable Ag ? Bi ? W ? Ni ? Y ? rare earth elements ? U. Deposit geometry includes stratabound and stratiform layers, lenses, and veins, and (or) discordant veins and breccias. The geometry of most deposits is controlled by stratigraphic layering, folds, axial-plane cleavage, shear zones, breccias, or faults. Ore minerals are mainly cobaltite, skutterudite, glaucodot, and chalcopyrite, with minor gold, arsenopyrite, pyrite, pyrrhotite, bismuthinite, and bismuth; some deposits have appreciable tetrahedrite, uraninite, monazite, allanite, xenotime, apatite, scheelite, or molybdenite. Magnetite can be abundant in breccias, veins, or stratabound lenses within ore or surrounding country rocks. Common gangue minerals include quartz, biotite, muscovite, K-feldspar, albite, chlorite, and scapolite; many deposits contain minor to major amounts of tourmaline. Altered wall rocks generally have abundant biotite or albite. Mesoproterozoic metasedimentary successions constitute the predominant geologic setting. Felsic and (or) mafic plutons are spatially associated with many deposits and at some localities may be contemporaneous with, and involved in, ore formation. Geoenvironmental data for the Blackbird mining district in central Idaho indicate that weathering of

Geophysical exploration of historical mine dumps for the estimation of valuable residuals

NASA Astrophysics Data System (ADS)

Martin, Tina; Knieß, Rudolf; Noell, Ursula; Hupfer, Sarah; Kuhn, Kerstin; Günther, Thomas

2015-04-01

Within the project ROBEHA, funded by the German Federal Ministry of Education and Research (033R105) the economic potential of different abandoned dump sites for mine waste in the Harz Mountains was investigated. Two different mining dumps were geophysically and mineralogically analysed in order to characterize the mine dump structure and to estimate the volume of the potential recycling material. The geophysical methods comprised geoelectrics, radar, and spectral induced polarization (SIP). One about 100-year old mining dump containing residues from density separated Ag- and Sb-rich Pb (Zn)-gangue ores was investigated in detail. Like most small-scale mining waste disposal sites this investigated dump is very heterogeneously structured. Therefore, 27 geoelectrical profiles, more than 50 radar profiles, and several SIP profiles were measured and analysed. The results from the radar measurements, registered with the GSSI system and a shielded 200 MHz antenna, show the near surface boundary layer (down to 3-4 m beneath surface) of the waste residuals. These results can be used as pre-information for the inversion process of the geoelectrical data. The geoelectrical results reveal the mineral residues as layers with higher resistivities (> 300 Ohm*m) than the surrounding material. The SIP method found low phase signals (< 0.5°) for the residues. To estimate the volume of the potentially reusable material we analysed each geoelectrical profile and interpolated between the single profiles using the BERT algorithm. Taking into account the wooded areas of the mine dump and other parameters we get a first estimate for the volume of the residues but the economical viability and the environmental impact of the reworking of the dump still needs to be evaluated in detail. The results of the second mine dump, an abandoned Cu and Zn-rich slag heap, show that the slag residues are characterized by higher resistivities and higher phases. A localization of the slag residues which

A comparative study of surface energies and water adsorption on Ce-bastnäsite, La-bastnäsite, and calcite via density functional theory and water adsorption calorimetry.

PubMed

Goverapet Srinivasan, Sriram; Shivaramaiah, Radha; Kent, Paul R C; Stack, Andrew G; Riman, Richard; Anderko, Andre; Navrotsky, Alexandra; Bryantsev, Vyacheslav S

2017-03-15

Bastnäsite, a fluoro-carbonate mineral, is the single largest mineral source of light rare earth elements (REE), La, Ce and Nd. Enhancing the efficiency of separation of the mineral from gangue through froth flotation is the first step towards meeting an ever increasing demand for REE. To design and evaluate collector molecules that selectively bind to bastnäsite, a fundamental understanding of the structure and surface properties of bastnäsite is essential. In our earlier work (J. Phys. Chem. C, 2016, 120, 16767), we carried out an extensive study of the structure, surface stability and water adsorption energies of La-bastnäsite. In this work, we make a comparative study of the surface properties of Ce-bastnäsite, La-bastnäsite, and calcite using a combination of density functional theory (DFT) and water adsorption calorimetry. Spin polarized DFT+U calculations show that the exchange interaction between the electrons in Ce 4f orbitals is negligible and that these orbitals do not participate in bonding with the oxygen atom of the adsorbed water molecule. In agreement with calorimetry, DFT calculations predict larger surface energies and stronger water adsorption energies on Ce-bastnäsite than on La-bastnäsite. The order of stabilities for stoichiometric surfaces is as follows: [101[combining macron]0] > [101[combining macron]1] > [101[combining macron]2] > [0001] > [112[combining macron]2] > [101[combining macron]4] and the most favorable adsorption sites for water molecules are the same as for La-bastnäsite. In agreement with water adsorption calorimetry, at low coverage water molecules are strongly stabilized via coordination to the surface Ce 3+ ions, whereas at higher coverage they are adsorbed less strongly via hydrogen bonding interaction with the surface anions. Due to similar water adsorption energies on bastnäsite [101[combining macron]1] and calcite [101[combining macron]4] surfaces, the design of collector molecules that selectively bind to

Permo Triassic unconformity-related Au-Pd mineralisation, South Devon, UK: new insights and the European perspective

NASA Astrophysics Data System (ADS)

Shepherd, Tom J.; Bouch, Jon E.; Gunn, Andrew G.; McKervey, John A.; Naden, Jonathan; Scrivener, Richard C.; Styles, Michael T.; Large, Duncan E.

2005-07-01

An integrated mineralogical-geochemical study of unconformity-related Au-Pd occurrences within and around the Permo Triassic basins of southwest England, UK, has confirmed the importance of low temperature (86±13°C), hydrothermal carbonate veins as hosts for the mineralisation. Fluid inclusion data for the carbonate gangue, supported by stable isotope (13C and 18O) and radiogenic (87Sr/86Sr) data, have identified three principal fluids: (1) a reducing calcic brine [>25 wt% salinity, <0.5 NaCl/(NaCl+CaCl2)] originating in the sub-unconformity basement and an expression of advanced mineral fluid interaction; (2) an oxidising sodic brine [~16 wt% salinity, >0.9 NaCl/(NaCl+CaCl2)] originating in the post-unconformity red beds under evaporitic conditions, and (3) an oxygenated, low salinity groundwater (<3 wt% salinity). The sodic brine is reasoned to be the parent metalliferous fluid and to have acquired its enrichment in Au and Pd by the leaching of immature sediments and intra-rift volcanic rocks within the local Permo Triassic basins. Metal precipitation is linked to the destabilisation of Au and Pd chloride complexes by either mixing with calcic brines, dilution by groundwaters or interaction with reduced lithologies. This explains the diversity of mineralised settings below and above the unconformity and their affinity with red bed brines. The paucity of sulphide minerals, the development of selenides (as ore minerals and as mineral inclusion in gold grains), the presence of rhodochrosite and manganoan calcites (up to 2.5 wt% Mn in calcite) and the co-precipitation of hematite and manganese oxides are consistent with the overall high oxidation state of the ore fluids. A genetic model is proposed linking Permo Triassic red beds, the mixing of oxidising and reducing brines, and the development of unconformity-related precious metal mineralisation. Comparison with other European Permo Triassic basins reveals striking similarities in geological setting, mineralogy

Age and origin of base and precious metal veins of the Coeur d'Alene mining district, Idaho

USGS Publications Warehouse

Fleck, R.J.; Criss, R.E.; Eaton, G.F.; Cleland, R.W.; Wavra, C.S.; Bond, W.D.

2002-01-01

Ore-bearing quartz-carbonate veins of the Coeur d'Alene mining district yield 87Sr/86Sr ratios of 0.74 to >1.60 for low Rb/Sr, carbonate gangue minerals, similar to current ranges measured in Middle Proterozoic, high Rb/Sr rocks of the Belt Supergroup. Stable isotope and fluid inclusion studies establish a genetic relationship between vein formation and metamorphic-hydrothermal systems of the region. These extraordinary 87Sr/86Sr ratios require accumulation of radiogenic 87Sr in a high Rb/Sr system over an extended period prior to incorporation of Sr into the hydrothermal veins. Evaluation of the age and composition of potential sources of highly radiogenic Sr indicates that the ore-bearing veins of the Coeur d'Alene district formed during the Cretaceous from components scavenged from rocks of the Belt Supergroup, the primary host rocks of the district. Proterozoic Pb isotope ratios observed in galena from many Coeur d'Alene veins were established when Pb separated from uranium during deposition or diagenesis of the Belt Supergroup at 1400 to 1500 Ma, possibly as disseminated syngenetic deposits. K-Ar and Rb-Sr apparent ages and ??18O values of Belt Supergroup rocks decrease from the Coeur d'Alene district toward the Idaho and Kaniksu batholiths, approximately normal to the trends of metamorphic isograds, fold axes, foliation, and the major reverse faults of the district. Isoclinal folding, thrust faulting, high-temperature metamorphism, granitic plutonism, and regional-scale metamorphic-hydrothermal activity is documented in the region between 140 and 45 Ma, representing the only such combination of events in the Coeur d'Alene region subsequent to about 1300 Ma. The Sr and oxygen results and geologic evidence favor formation of the ore-bearing carbonate veins by fluids related to a complex metamorphic-hydrothermal system during the Cretaceous. Pb with Proterozoic isotopic compositions was probably mobilized and incorporated like other metals into the hydrothermal

A geochemical study of the Sweet Home Mine, Colorado Mineral Belt, USA: hydrothermal fluid evolution above a hypothesized granite cupola

NASA Astrophysics Data System (ADS)

Lüders, Volker; Romer, Rolf L.; Gilg, H. Albert; Bodnar, Robert J.; Pettke, Thomas; Misantoni, Dean

2009-05-01

Deposition of quartz-molybdenite-pyrite-topaz-muscovite-fluorite and subsequent hübnerite and sulfide-fluorite-rhodochrosite mineralization at the Sweet Home Mine occurred coeval with the final stage of magmatic activity and ore formation at the nearby world-class Climax molybdenum deposit about 26 to 25 m.y. ago. The mineralization occurred at depths of about 3,000 m and is related to at least two major fluid systems: (1) one dominated by magmatic fluids, and (2) another dominated by meteoric water. The sulfur isotopic composition of pyrite, strontium isotopes and REY distribution in fluorite suggest that the early-stage quartz-molybdenite-pyrite-topaz-muscovite-fluorite mineral assemblage was deposited from magmatic fluids under a fluctuating pressure regime at temperatures of about 400°C as indicated by CO2-bearing, moderately saline (7.5-12.5 wt.% NaCl equiv.) fluid inclusions. LA-ICPMS analyses of fluid inclusions in quartz demonstrate that fluids from the Sweet Home Mine are enriched in incompatible elements but have considerably lower metal contents than those reported from porphyry-Cu-Au-Mo or Climax-type deposits. The ore-forming fluid exsolved from a highly differentiated magma possibly related to the deep-seated Alma Batholith or distal porphyry stock(s). Sulfide mineralization, marking the periphery of Climax-type porphyry systems, with fluorite and rhodochrosite as gangue minerals was deposited under a hydrostatic pressure regime from low-salinity ± CO2-bearing fluids with low metal content at temperatures below 400°C. The sulfide mineralization is characterized by mostly negative δ34S values for sphalerite, galena, chalcopyrite, and tetrahedrite, highly variable δ18O values for rhodochrosite, and low REE contents in fluorite. The Pb isotopic composition of galena as well as the highly variable 87Sr/86Sr ratios of fluorite, rhodochrosite, and apatite indicates that at least part of the Pb and Sr originated from a much more radiogenic source than

Origin of ore-forming fluids of the Haigou gold deposit in the eastern Central Asian Orogenic belt, NE China: Constraints from H-O-He-Ar isotopes

NASA Astrophysics Data System (ADS)

Zeng, Qingdong; He, Huaiyu; Zhu, Rixiang; Zhang, Song; Wang, Yongbin; Su, Fei

2017-08-01

The Haigou lode deposit contains 40 t of gold at an average grade of 3.5 g/t, and is one of the largest deposits in the Jiapigou gold belt located along the eastern segment of the northern margin of the North China Craton. The deposit comprises 15 gold-bearing quartz veins hosted in a Carboniferous monzonite-monzogranite stock. Cretaceous dikes consisting of diorite, diabase, and granodiorite porphyries are well developed in the deposit. The diorite porphyry dikes (130.4 ± 6.3 Ma) occur together with gold-bearing quartz veins in NNE- and NE-striking faults. Gold-bearing quartz veins crosscut the diorite porphyry dikes, and the veins are in turn crosscut by E-W-striking 124.6 ± 2.2 Ma granodiorite porphyry dikes. The mineralization mainly occurs as auriferous quartz veins with minor amounts of sulfide minerals, including pyrite, galena, chalcopyrite, and molybdenite. Gold occurs as either native gold or calaverite. Common gangue minerals in the deposit include quartz, sericite, and calcite. The deposit is characterized by various types of hydrothermal alteration, including silicification, sericitization, chloritization, potassic alteration, and carbonatization. Three stages of hydrothermal activity have been recognized in the deposit: (1) a barren quartz stage; (2) a polymetallic sulfide (gold) stage; (3) a calcite stage. Fluid inclusions in hydrothermal pyrites have 3He/4He ratios of 0.3 to 3.3 Ra and 40Ar/36Ar ratios of 351 to 1353, indicating mixing of fluids of mantle and crustal origin. Hydrothermal quartz yielded δ18O values of -1.3‰ to +7.2‰ and δD values of fluid inclusions in the quartz vary between -80‰ and -104‰. These stable isotope data also suggest mixing of magmatic and meteoric fluids. Noble gas and stable isotopic data suggest that the ore fluids have a predominant mantle source with a significant crustal component. Based on the spatial association of gold-bearing quartz veins with early Cretaceous intrusions, and the H-O-He-Ar isotopic

Lithium and Beryllium By-product Recovery from the Round Top Mountain, Texas, Peraluminous Rhyolite Heavy Rare Earth Deposit

NASA Astrophysics Data System (ADS)

Pingitore, N. E., Jr.; Clague, J. W.; Gorski, D.

2016-12-01

The technology metals Li and Be combine low mass and unique properties. Li batteries are critical in applications at scales from micro-electronics to automotive and grid storage. Low mass Be structural components are essential in aerospace/defense applications and in non-sparking BeCu alloy oilfield tools. Most Li is sourced from desert salarsin the "Lithium Triangle" of Argentina—Bolivia—Chile. In contrast, Materion Corp mines >80% of global Be at Spor Mountain, UT. The massive peraluminous rhyolite heavy rare earth deposit at Round Top Mountain, TX is also enriched in Li, 500 ppm, and Be, 50 ppm. 2016 prices of 7000/tonne Li2CO3 (19% Li) and 1000/kg Be metal suggest favorable economics to extract Li and Be as by-products of HREE mining. Li and some Be are hosted in annite biotite that comprises up to 5% of the rhyolite. Texas Mineral Resources Corp proposes to heap leach crushed rhyolite with dilute H2SO4to release the yttrofluorite-hosted HREEs. At bench scale the annite biotite dissolves, but not quartz and feldspars (>90% of the rock). A series of 40 high-yield laboratory tests at various acid strength, particle size, and exposure time released up to 350 ppm (70%) of the Li and 14 ppm (30%) of the Be. For a 20,000 tonne/day operation, these recoveries correspond to daily production of >3 tonnes Li and 250 kg Be. Higher Li and Be recoveries also increased yields of gangue elements, Fe & Al, into solution. This complicates subsequent separation of Li, Be, and HREEs from the pregnant leach solution. Recovery of target HREEs did not increase beyond 200 ppm Li and 8 ppm Be recovery. Greater Li and Be recoveries increased acid consumption. Thus the "sweet spot" economics for heap leach is likely under conditions of acid strength, grain size, and exposure time that do not maximize by-product Li and Be recoveries. Evolving market prices for the full target element suite and additional costs to recover and purify the Li and Be must also be considered.

Positive feedback between strain localization and fluid flow at the ductile-brittle transition leading to Pb-Zn-Fe-Cu-Ag ore deposits in Lavrion (Greece)

NASA Astrophysics Data System (ADS)

Scheffer, Christophe; Tarantola, Alexandre; Vanderhaeghe, Olivier

2016-04-01

At the crustal scale, the ductile-brittle transition (DBT) might correspond to a physical barrier that separates a deep reservoir of metamorphic and magmatic fluids from a shallow reservoir of surficial fluids. Rock rheology, and thus the location of the DBT, is mainly governed by lithology, temperature and the presence/absence of fluids. Accordingly, the position of the DBT potentially evolves during orogenic evolution owing to thermal evolution and fluid circulation. In turn rocks are transferred across it during burial and exhumation. These processes induce connections between fluid reservoirs which might play a role on ore deposition. In this contribution, we discuss the impact of lithological heterogeneities on deformation, fluid flow and ore deposition based on the example of the Lavrion low-angle top-to-the-SSW detachment accommodating gravitational collapse of the Hellenides orogenic belt in Greece. The Lavrion peninsula, localized along the western boundary of the Attic-Cycladic Metamorphic Core Complex, is characterized by Pb-Zn-Fe-Cu-Ag ore mineralization mainly concentrated along a lithological contact (marble/schists) below and within a detachment shear zone. The mylonitic marble below the detachment shear zone is composed of white layers of pure marble alternating with blue layers containing impurities (SiO2, Al2O3, organic matter…). Development of the mylonitic fabric in competent impure blue marble is associated with its preferred dolomitization related to focused fluid infiltration. This mylonitic marble is cross-cut by several cataclastic horizons preferentially developed within the more competent impure blue marble and newly-crystallized dolomitic horizon. These cataclasites are invaded by fluorite and calcite gangue minerals showing locally Mn, Pb, Zn, Fe oxides and/or hydroxides, sphalerite, Ag-galena, Ag-sulfur and native Ag. Oxygen and carbon stable isotopes performed on marble sections point out decarbonation with magmatic contribution and

Chemical composition and evolution of tourmaline-supergroup minerals from the Sb hydrothermal veins in Rožňava area, Western Carpathians, Slovakia

NASA Astrophysics Data System (ADS)

Bačík, Peter; Dikej, Jakub; Fridrichová, Jana; Miglierini, Marcel; Števko, Martin

2017-09-01

Tourmaline-supergroup minerals are common gangue minerals in Sb-hydrothermal veins on Betliar - Straková, Čučma - Gabriela and Rožňava - Peter-Pavol vein deposits in the Rožňava area, Slovakia. Tourmaline-supergroup minerals form relatively large prismatic to radial aggregates of parallel black to greyish-black crystals. Tourmaline-supergroup minerals from Betliar - Straková and Rožňava - Peter-Pavol are almost homogeneous with intermediate schorl-dravite composition. Čučma - Gabriela tourmaline have distinct zoning with massive core of the schorlitic-to-feruvitic shifting to schorlitic-to-dravitic composition, and dravitic to magnesio-foititic rim. The tourmaline composition is influenced by two main substitutions, namely Ca(Mg,Fe)Na-1Al-1 and X □AlNa-1(Mg,Fe)-1. Betliar - Straková and Rožňava - Peter-Pavol tourmaline-supergroup minerals exhibit only small extents of the X □AlNa-1(Mg,Fe)-1 substitution. This substitution shifts the composition to magnesio-foitite in Čučma - Gabriela tourmaline. The decrease of Al in the core of Čučma - Gabriela tourmaline crystals is caused by extensive Ca(Mg,Fe)Na-1Al-1 substitution. The unit-cell dimensions of all investigated tourmaline-supergroup minerals indicate an octahedral disorder with the Z (Fe3++Mg) proportion calculated from empirical equations varying between 0.85 and 0.87 apfu (atoms per formula unit). Based on Mössbauer spectra, the Z Fe3+ content varied between 0.25 apfu in Betliar - Straková tourmaline and 0.45 apfu in Čučma - Gabriela sample. Based on Fe/(Fe + Mg) ratio, Betliar - Straková tourmaline is slightly enriched in Fe compared to Rožňava - Peter-Pavol, suggesting the impact of the host-rock composition; first are grown in Fe-richer acidic metarhyolitic rocks, latter in metapelites. In Čučma - Gabriela, the variations in Fe/(Fe + Mg) are very likely reflecting the change in fluid composition. Magnesio-foitite is the product of second-stage crystallization forming rims and

Manganese and ferromanganese ores from different tectonic settings in the NW Himalayas, Pakistan

NASA Astrophysics Data System (ADS)

Tahir Shah, Mohammad; Moon, Charles J.

2007-02-01

In Pakistan manganese and ferromanganese ores have been reported from the Hazara area of North West Frontier Province, Waziristan agencies in the Federally Administered Tribal Areas and the Lasbela-Khuzdar regions of Baluchistan. This study is focused on comparison of mineralogy and geochemistry of the continental ferromanganese ores of Hazara and the ophiolitic manganese ores of the Waziristan area of Pakistan. In the Hazara area, ferromanganese ores occur at Kakul, Galdanian and Chura Gali, near Abbottabad, within the Hazira Formation of the Kalachitta-Margala thrust belt of the NW Himalayas of the Indo-Pakistan Plate. The Cambrian Hazira Formation is composed of reddish-brown ferruginous siltstone, with variable amounts of clay, shale, ferromanganese ores, phosphorite and barite. In Waziristan, manganese ores occur at Shuidar, Mohammad Khel and Saidgi, within the Waziristan ophiolite complex, on the western margin of the Indo-Pakistan Plate in NW Pakistan. These banded and massive ores are hosted by metachert and overlie metavolcanics. The ferromanganese ores of the Hazara area contain variable amount of bixbyite, partridgeite, hollandite, pyrolusite and braunite. Bixbyite and partridgeite are the dominant Mn-bearing phases. Hematite dominates in Fe-rich ores. Gangue minerals are iron-rich clay, alumino-phosphate minerals, apatite, barite and glauconite are present in variable amounts, in both Fe-rich and Mn-rich varieties. The texture of the ore phases indicates greenschist facies metamorphism. The Waziristan ores are composed of braunite, with minor pyrolusite and hollandite. Hematite occurs as an additional minor phase in the Fe-rich ores of the Shuidar area. The only silicate phase in these ores is cryptocrystalline quartz. The chemical composition of the ferromanganese ores in Hazara suggests that the Mn-Fe was contributed by both hydrogenous and hydrothermal sources, while the manganese ores of Waziristan originated only from a hydrothermal source. It is

238U, and its decay products, in grasses from an abandoned uranium mine

NASA Astrophysics Data System (ADS)

Childs, Edgar; Maskall, John; Millward, Geoffrey

2016-04-01

Bioaccumulation of radioactive contaminants by plants is of concern particularly where the sward is an essential part of the diet of ruminants. The abandoned South Terras uranium mine, south west England, had primary deposits of uraninite (UO2) and pitchblende (U3O8), which contained up to 30% uranium. When the mine was active uranium and radium were extracted but following closure it was abandoned without remediation. Waste rock and gangue, consisting of inefficiently processed minerals, were spread around the site, including a field where ruminants are grazed. Here we report the activity concentrations of 238U, 235U 214,210Pb, and the concentrations of selected metals in the soils, roots and leaves of grasses taken from the contaminated field. Soil samples were collected at the surface, and at 30 cm depth, using an auger along a 10-point transect in the field from the foot of a waste heap. Whole, individual grass plants were removed with a spade, ensuring that their roots were intact. The soils and roots and grass leaves were freeze-dried. Activity concentrations of the radionuclides were determined by gamma spectroscopy, following 30 days incubation for development of secular equilibrium. Dried soils, roots and grasses were also digested in aqua regia and the concentrations of elements determined by ICP techniques. Maximum activity concentrations of 238U, 235U, 214Pb and 210Pb surface soils were 63,300, 4,510, 23,300 and 49,400 Bq kg-1, respectively. The mean 238U:235U ratio was 11.8 ± 1.8, an order of magnitude lower than the natural value of 138, indicating disequilibrium within the decay chain due to mineral processing. Radionuclides in the roots had 5 times lower concentration and only grass leaves in the vicinity of the waste heap had measureable values. The mean soil to root transfer factor for 238U was 36%, the mean root to leaf was 3% and overall only 0.7% of 238U was transferred from the soil to the leaves. The roots contained 0.8% iron, possibly as

Geological controls on refractory ore in an orogenic gold deposit, Macraes mine, New Zealand

NASA Astrophysics Data System (ADS)

Petrie, B. S.; Craw, D.; Ryan, C. G.

2005-07-01

sulphides. This black, sheared ore releases gold readily, but the gold is then adsorbed on to gangue minerals (preg-robbed) and net cyanidation recovery can be less than 50%. Hence, low gold recovery during cyanidation results from (1) poor liberation of gold encapsulated in microcrystalline quartz and unfractured sulphide grains, and (2) preg-robbing of liberated gold during cyanidation. Introduction of pressure-oxidation of ore prior to cynidation has mitigated these issues.

Geology of the Ralston Buttes district, Jefferson County, Colorado: a preliminary report

USGS Publications Warehouse

Sheridan, Douglas M.; Maxwell, Charles H.; Albee, Arden L.; Van Horn, Richard

1956-01-01

The Ralston Buttes district in Jefferson County is one of the most significant new uranium districts located east of the Continental Divide in Colorado. The district is east of the Colorado Front Range mineral belt, along the east front of the range. From November 1953 through October 1956, about 10,000 tons of uranium ore, much of which was high-grade pitchblende-bearing vein material, was shipped from the district. The ore occurs in deposits that range in size from bodies containing less than 50 tons to ore shoots containing over 1,000 tons. The only other mining activity in the area has been a sporadic production of beryl, feldspar, and scrap mica from Precambrian pegmatites, and quarrying of dimension stone, limestone, and clay from sedimentary rocks. Most of the Ralston Buttes district consists of complexly folded Precambrian metamorphic and igneous rocks - gneiss, schist, quartzite, amphibolite, and granodiorite. Paleozoic and Mesozoic sedimentary rocks crop out in the northeastern part of the district. These rocks are cut by northwesterly-trending fault systems of Laramide age and by small bodies of intrusive rocks that are Tertiary in age. The typical uranium deposits in the district are hydrothermal veins occupying openings in Laramide fault breccias or related fractures that cut the Precambrian rocks. Pitchblende and lesser amounts of secondary uranium minerals are associated with sparse base-mental sulfides in a gangue of carbonate minerals, potash feldspar, and, more rarely, quartz. Less common types of deposits consist of pitchblende and secondary uranium minerals that occupy fractures cutting pegmatites and quartz veins. The uranium deposits are concentrated in two areas, the Ralston Creek area and the Golden Gate Canyon area. The deposits in the Ralston Creek area are located along the Rogers fault system, and the deposits in the Golden Gate Canyon area are along the Hurricane Hill fault system. Two geologic factors were important to the localization

Use of structural geology in exploration for and mining of sedimentary rock-hosted Au deposits

USGS Publications Warehouse

Peters, Stephen G.

2001-01-01

Structural geology is an important component in regional-, district- and orebody-scale exploration and development of sedimentary rock-hosted Au deposits.Identification of timing of important structural events in an ore district allows analysis and classification of fluid conduits and construction of genetic models for ore formation.The most practical uses of structural geology deal with measurement and definition of various elements that comprise orebodies, which can then be directly applied to ore-reserve estimation,ground control,grade control, safety issues,and mine planning.District- and regional-scale structural studies are directly applicable to long-term strategic planning,economic analysis,and land ownership. Orebodies in sedimentary rock-hosted Au deposits are discrete, hypogene, epigenetic masses usually hosted in a fault zone,breccia mass, or lithologic bed or unit. These attributes allow structural geology to be directly applied to the mining and exploration of sedimentary rock-hosted Au deposits. Internal constituents in orebodies reflect unique episodes relating to ore formation.The main internal constituents in orebodies are ore minerals, gangue, and alteration minerals that usually are mixed with one another in complex patterns, the relations among which may be used to interpret the processes of orebody formation and control.Controls of orebody location and shape usually are due to structural dilatant zones caused by changes in attitude, splays, lithologic contacts,and intersections of the host conduit or unit.In addition,conceptual parameters such as district fabric,predictable distances, and stacking also are used to understand the geometry of orebodies.Controls in ore districts and location and geometry of orebodies in ore districts can be predicted to various degrees by using a number of qualitative concepts such as internal and external orebody plunges,district plunge, district stacking, conduit classification, geochemical, geobarometric and

Geology of the Eymir iron mine, Edremit, Turkey

USGS Publications Warehouse

Jacobson, Herbert Samuel; Turet, Erdogan

1972-01-01

The Eymir mine near Edremit on Turkey's Aegean coast (long 27?30'E.,1at 39?36'N.) was investigated as part of the Maden Tetkik ve Arama Enstitutsu (MTA)-U. S. Geological Survey (USGS) mineral exploration and training project, for the purpose of increasing the known mineral reserves. Geologic mapping of the mine area indicates that hematite is restricted to argillized, silicified, and pyritized dacite and possibly andesite. Hematite is present as massive replacements, impregnations, disseminations, and fracture fillings. Most of the upper part of the iron deposit consists of a breccia composed mostly of silicifiled dacite fragments in a hematite matrix. The iron deposit was apparently formed in three steps: 1. Argillation, silicification, and pyritization of the andesitic lava and dacite units as a result of a regional intrusion. 2. Intrusion of the Dere Oren dacite stock, with associated faulting, fracturing, and breccia formation at the surface. 3. Deposition of hematite by oxidation of pyrite, and transfer of iron via fractures and faults by hydrothermal or meteoric fluids. The Eymir iron deposit is a blanketlike deposit on the crest of the Sivritepe-Eymir ridge. It is 1300 meters long, 80 to 450 meters wide, and has an average thickness of 18.6 meters. Drill holes in the deposit show the iron content to range from 32.0 to 57.6 percent, and to average 46.5 percent. Most of the gangue is silica, and an arsenic impurity averaging 0.39 percent is present. Most of the deposit cannot be utilized as iron ore because of low iron content, high silica content, and high arsenic content. Ore-dressing tests have shown that it is feasible to concentrate the low-grade material, producing a concentrate having increased iron content and reduced silica content. Tests have shown also that the arsenic content of the ore can be reduced substantially by sintering. Further tests and economic feasibility studies are necessary to determine whether an economic marketable iron ore can be

The Robinson and Weatherly uraniferous pyrobitumen deposits near Placerville, San Miguel County, Colorado

USGS Publications Warehouse

Wilmarth, V.R.; Vickers, R.C.

1953-01-01

Uranium deposits that contain uraniferous pyrobitumen of possible hydrothermal origin occur at the Weatherly and Robinson properties near Placerville, San Miguel County, Colo. These deposits were mined for copper, silver, and gold more than 50 years ago and were developed for uranium in 1950. The Robinson property, half a mile east of Placerville, consists of the White Spar, New Discovery Lode, and Barbara Jo claims. The rocks in this area are nearly horizontal sandstones, shales, limestones, and conglomerates of the Cutler formation of Permian age and the Dolores formation of Triassic and Jurassic (?) age. These rocks have been faulted extensively and intruded by a Tertiary (?) andesite porphyry dike. Uranium-bearing pyrobitumen associated with tennantite, tetrahedrite, galena, sphalerite, chalcopyrite, bornite, azurite, malachite, calcite, barite, and quartz occurs in a lenticular body as much as 40 feet long and 6 feet wide along a northwest-trending, steeply dipping normal fault. The uranium content of eleven samples from the uranium deposit ranges from 0.001 to 0.045 percent uranium and averages about 0.02 percent uranium. The Weatherly property, about a mile northwest of Placerville, consists of the Black King claims nos. 1, 4, and 5. The rocks in this area include the complexly faulted Cutler formation of Permian age and the Dolores formation of Triassic and Jurassic (?) age. Uranium-bearing pyrobitumen arid uranophane occur, along a northwest-trending, steeply dipping normal fault and in the sedimentary rocks on the hanging wall of the fault. Lens-shaped deposits in the fault zone are as much as 6 feet long and 2 feet wide and contain as much as 9 percent uranium; whereas channel samples across the fault zone contain from 0.001 to 0.014 percent uranium. Tetrahedrite, chalcopyrite, galena, sphalerite, fuchsite, malachite, azurite, erythrite, bornite, and molybdite in a gangue of pyrite, calcite, barite, and quartz are associated with the uraniferous material

Orogenic-type copper-gold-arsenic-(bismuth) mineralization at Flatschach (Eastern Alps), Austria

NASA Astrophysics Data System (ADS)

Raith, Johann G.; Leitner, Thomas; Paar, Werner H.

2015-10-01

Structurally controlled Cu-Au mineralization in the historic Flatschach mining district (Styria, Austria) occurs in a NE-SW to NNE-WSW oriented vein system as multiple steep-dipping calcite-(dolomite)-quartz veins in amphibolite facies metamorphic rocks (banded gneisses/amphibolites, orthogneisses, metagranitoids) of the poly-metamorphosed Austroalpine Silvretta-Seckau nappe. Vein formation postdated ductile deformation events and Eoalpine (Late Cretaceous) peak metamorphism but predated Early to Middle Miocene sediment deposition in the Fohnsdorf pull-apart basin; coal-bearing sediments cover the metamorphic basement plus the mineralized veins at the northern edge of the basin. Three gold-bearing ore stages consist of a stage 1 primary hydrothermal (mesothermal?) ore assemblage dominated by chalcopyrite, pyrite and arsenopyrite. Associated minor minerals include alloclasite, enargite, bornite, sphalerite, galena, bismuth and matildite. Gold in this stage is spatially associated with chalcopyrite occurring as inclusions, along re-healed micro-fractures or along grain boundaries of chalcopyrite with pyrite or arsenopyrite. Sericite-carbonate alteration is developed around the veins. Stage 2 ore minerals formed by the replacement of stage 1 sulfides and include digenite, anilite, "blue-remaining covellite" (spionkopite, yarrowite), bismuth, and the rare copper arsenides domeykite and koutekite. Gold in stage 2 is angular to rounded in shape and occurs primarily in the carbonate (calcite, Fe-dolomite) gangue and less commonly together with digenite, domeykite/koutekite and bismuth. Stage 3 is a strongly oxidized assemblage that includes hematite, cuprite, and various secondary Cu- and Fe-hydroxides and -carbonates. It formed during supergene weathering. Stage 1 and 2 gold consists mostly of electrum (gold fineness 640-860; mean = 725; n = 46), and rare near pure gold (fineness 930-940; n = 6). Gold in stage 3 is Ag-rich electrum (fineness 350-490, n = 12), and has a

Late Pleistocene Activity and deformation features of the North Margin Fault of West Qinling Mountains, northeastern Tibet

NASA Astrophysics Data System (ADS)

Chen, P.; Lin, A.; Yan, B.

2017-12-01

Abstract: A precise constraints of slip rates of active faults within and around Tibetan Plateau will provide us a definite and explicit knowledge of continental dynamics and present-day tectonic evolution. The major strike-slip faults in the northern and northeastern Tibetan Plateau, including the Altyn Tagh fault and Kunlun fault play a vital role in dissipating and transferring the strain energy. The WNW-trending North Margin Fault of West Qinling Mountains (hereafter name NMFWQM, the target of this study) developed along the topographic boundary between Longzhong basin and the Qinling mountains. Intensive Historic records show that large earthquakes repeatedly in the area around the NMFWQM, including the AD 143 M 7.0 Gangu West earthquake; AD 734 M≥7.0 Tianshui earthquake; AD 1654 M 8.0 Tianshui South earthquake and the most recent 2013 Mw6.0 Zhangxian earthquake. In this study, we investigated the structural features and activity of the NMFWQM including the nature of the fault, slip rate, and paleoseismicity by interpretation of high-resolution remote sensing images and field investigation. Based on the interpretations of high resolution satellite images, field investigations and 14C dating ages, we conclude the following conclusions: 1) The drainage systems have been systematical deflected or offset sinistrally along the fault trace; 2) The amounts of displacement (D) show a positive linear correlation with the upstream length (L) from the deflected point of offset river channels as DaL (a: a certain coefficient); 3) The alluvial fans and terrace risers formed in the last interglacial period are systematically offset by 16.4m to 93.9 m, indicating an accumulation of horizontal displacements as that observed in the offset drainages; 4) A horizontal slip rate is estimated to be 2.5-3.1 mm/yr with an average of 2.8 mm/yr. Comparing with the well-know strike-slip active faults developed in the northern Tibetan Plateau, such as the Altyn Tagh fault and Kunlun

Arkachan: A new gold-bismuth-siderite-sulfide type of deposits in the West Verkhoyansky tin district, Yakutia

NASA Astrophysics Data System (ADS)

Gamyanin, G. N.; Vikent'eva, O. V.; Prokof'ev, V. Yu.; Bortnikov, N. S.

2015-11-01

The formation sequence of orebodies, chemical composition of gangue and ore minerals, fluid inclusions, REE patterns, 40Ar/39Ar isotopic age, and relationships of stable isotopes (C, O, S) in minerals of the Arkachan gold-bismuth-siderite-sulfide deposit have been studied. The deposit has been localized in the Kuranakh Anticlinorium of the Verkhoyansky Fold-Nappe Belt at the intersection of the near-meridional Kygyltas and the NE-trending North Tirekhtyakh faults. The orebodies are extended (>2 km) and steeply dipping zones of veins and veinlets are hosted in Carbonaceous and Permian sandstones and siltstones deformed in anticlines and cut through by dikes pertaining to diorite-granodiorite-granite association. The deposit was formed during hydrothermal-metamorphic, productive main gold, silver-polymetallic, and silver-antimony stages. The orebodies are largely composed of quartz and siderite; arsenopyrite, pyrite, and pyrrhotite are widespread; bismuthinite, chalcopyrite, sphalerite, galena, and bismuth sulfosalts (gustavite, cosalite, matildite) are less abundant. The REE patterns of carbonates and quartz are characterized by a negative Eu anomaly. Three types of fluid inclusions (FI) in quartz and carbonates are distinguished: (I) liquid H2O + CO2 ± CH4 + NaCl, (II) gaseous CO2 ± CH4, and (III) aqueous salt solutions. The homogenization temperature and salinity of FI I vary from 385 to 280°C and 18.8 to 26.2 wt % NaCl equiv, respectively, whereas in FI III these parameters vary from 261 to 324°C and 3.7 to 9.5 wt % NaCl equiv. The pressure is estimated at 1830 to 1060 bar. The δ18O of quartz II associated with siderite I, native gold, and sulfosalts changes from +13.6 to 16.3‰(SMOW); δ18O and δ13C of siderite I related to gold-ore stage vary from +13.6 to +17.7‰ (SMOW) and from-6.0 to-3.0 (PDB). A wide range of δ34S from-5.7 to 16.0‰ (CDT) has been obtained for sulfides. The isotopic 40Ar/39Ar age of muscovite is 101.9 ± 1.4 Ma. The isotopic

Hydrothermal oxidation in the Biwabik Iron Formation, MN, USA

NASA Astrophysics Data System (ADS)

Losh, Steven; Rague, Ryan

2018-02-01

Precambrian iron formations throughout the world, notably in Australia, Brazil, and South Africa, show evidence of hypogene (≥ 110 °C, mostly > 250 °C) oxidation, alteration, and silica dissolution as a result of tectonic or magmatic activity. Although hydrothermal oxidation has been proposed for the prototype Lake Superior-type iron formation, the Biwabik Iron Formation in Minnesota (USA), it has not been documented there. By examining oxidized and unoxidized Biwabik Iron Formation in three mines, including material from high-angle faults that are associated with oxidation, we document an early hypogene oxidation event ( 175 °C) involving medium-salinity aqueous fluids (8.4 ± 4.9 wt% NaCl equiv) that infiltrated iron formation along high-angle faults. At the Hibbing Taconite Mine, hydrothermal fluids oxidized iron carbonates and silicates near faults, producing goethite ± quartz. In contrast with much of the oxidized iron ores on the Mesabi Range, silica was not removed but rather recrystallized during this event, perhaps lying in a rock-dominated system at low cumulative fluid flux. During the hydrothermal oxidation event in the Hibbing Taconite deposit, quartz-filled microfractures and irregular inclusions commonly formed in coarse variably oxidized magnetite, currently the ore mineral: these inclusions degrade the ore by introducing excess silica in magnetic concentrate. Hydrothermal oxidation at Hibbing Taconite Mine is overprinted by later, relatively minor supergene oxidation both along faults and near the surface, which locally dissolved quartz. At the Fayal Reserve Mine, widespread silicate and carbonate gangue dissolution and iron oxidation was followed by precipitation of pyrite, Mn-siderite, apatite, and other minerals in void spaces, which prevented post-oxidation compaction and significant volume loss in the sampled rocks. Although definitive temperature data for this assemblage are needed, the weight of evidence indicates that this

Tourmalines from the siderite-quartz-sulphide hydrothermal veins, Gemeric unit, western Carpathians, Slovakia: crystal chemistry and evolution

NASA Astrophysics Data System (ADS)

Bačík, P.; Uher, P.; Dikej, J.; Puškelová, Ľ.

2018-02-01

Tourmaline is an important gangue mineral in a large number of Cretaceous siderite-quartz-sulphide hydrothermal veins in the Gemeric Unit, Slovak Ore Mountains, Slovakia, such as Dobšiná, Vlachovo, Rožňavské Bystré, Hnilčík, Rakovnica, Novoveská Huta, Gretla, Rudňany, and Bindt. In this study we combine by electron microprobe analysis, powder X-ray diffraction, Mössbauer and optical emission spectroscopy to determine the range of tourmaline compositions in the deposits and constrain the mechanisms of its precipitation. Selected samples from the mentioned deposits belong mostly to the alkali group, schorl to dravite series, rarely dominant X-site vacant foititic tourmaline (Vlachovo and Bindt) and oxy-dravite compositions (Hnilčík) were detected. Rim zones of some schorlitic tourmalines show high concentrations of Ti (up to 2.35 wt.% TiO2, 0.30 apfu; Rožňavské Bystré). The chemical composition is mostly controlled by alkali-deficient X □AlNa-1(Mg,Fe2+)-1 and proton-deficient AlO(Mg,Fe2+)-1(OH)-1 substitutions. Titanium is incorporated into the structure by Y Ti Y (Mg,Fe) Y Al-2, Y Ti Z Mg Y Al-1 Z Al-1, Y TiO( Y AlOH), and X Ca Y Ti Z MgO2 X □-1 Y,Z Al-2(OH)-2 substitutions. Along trace elements, Sr and V attain concentrations of 80-450 and 70-320 ppm, respectively. The unit-cell parameter a varies between 15.960 and 15.985 Å; variations in c are larger, between 7.177 and 7.236 Å indicating the presence of Fe3+ and Mg2+ at Z site. Mössbauer spectroscopy has shown variable Fe3+ proportions (0.17 -0.55 apfu) in all samples. The gathered dataset suggests some qualitative considerations on the mechanisms controlling tourmaline compositions at the regional scale. The highest Fe3+ concentrations occur in samples from Rudňany and Gretla in the external part of Gemeric unit, suggesting higher oxidation during longer transport of fluids. We propose that the determined XFe in the samples are correlated with the compositions of the host rocks, as

Preliminary Report on the White Canyon Area, San Juan County, Utah

USGS Publications Warehouse

Benson, William Edward Barnes; Trites, A.F.; Beroni, E.P.; Feeger, J.A.

1952-01-01

chrysocolla. The principal gangue minerals are quartz, clay minerals, chlorite, oxides of iron and manganese, alunite, calcite, gypsum, pyrite, allophane, gibbsite, opal, and chalcedony. The origin of the copper-uranium ores has not been determined, but the association of many deposits with fractures, the mineralogic assemblage, and a lead-uranium age determination of 50 to 60 million years for the pitchblende in the Happy Jack mine favor the hypothesis that the ores are of hydrothermal origin and were deposited in early Tertiary time. Criteria believed to be the most useful in prospecting for new deposits are (1) visible uranium minerals; (2) visible copper minerals; (3) alunite; (4) hydrocarbons; and (5) bleaching of the underlying Moenkopi formation.

Genesis of Middle Miocene Yellowstone hotspot-related bonanza epithermal Au-Ag deposits, Northern Great Basin, USA

NASA Astrophysics Data System (ADS)

Saunders, J. A.; Unger, D. L.; Kamenov, G. D.; Fayek, M.; Hames, W. E.; Utterback, W. C.

2008-09-01

Epithermal deposits with bonanza Au-Ag veins in the northern Great Basin (NGB) are spatially and temporally associated with Middle Miocene bimodal volcanism that was related to a mantle plume that has now migrated to the Yellowstone National Park area. The Au-Ag deposits formed between 16.5 and 14 Ma, but exhibit different mineralogical compositions, the latter due to the nature of the country rocks hosting the deposits. Where host rocks were primarily of meta-sedimentary or granitic origin, adularia-rich gold mineralization formed. Where glassy rhyolitic country rocks host veins, colloidal silica textures and precious metal-colloid aggregation textures resulted. Where basalts are the country rocks, clay-rich mineralization (with silica minerals, adularia, and carbonate) developed. Oxygen isotope data from quartz (originally amorphous silica and gels) from super-high-grade banded ores from the Sleeper deposit show that ore-forming solutions had δ 18O values up to 10‰ heavier than mid-Miocene meteoric water. The geochemical signature of the ores (including their Se-rich nature) is interpreted here to reflect a mantle source for the “epithermal suite” elements (Au, Ag, Se, Te, As, Sb, Hg) and that signature is preserved to shallow crustal levels because of the similar volatility and aqueous geochemical behavior of the “epithermal suite” elements. A mantle source for the gold in the deposits is further supported by the Pb isotopic signature of the gold ores. Apparently the host rocks control the mineralization style and gangue mineralogy of ores. However, all deposits are considered to have derived precious metals and metalloids from mafic magmas related to the initial emergence of the Yellowstone hotspot. Basalt-derived volatiles and metal(loid)s are inferred to have been absorbed by meteoric-water-dominated geothermal systems heated by shallow rhyolitic magma chambers. Episodic discharge of volatiles and metal(loid)s from deep basaltic magmas mixed with

Late-stage anhydrite-gypsum-siderite-dolomite-calcite assemblages record the transition from a deep to a shallow hydrothermal system in the Schwarzwald mining district, SW Germany

NASA Astrophysics Data System (ADS)

Burisch, Mathias; Walter, Benjamin F.; Gerdes, Axel; Lanz, Maximilian; Markl, Gregor

2018-02-01

The majority of hydrothermal vein systems of economic interest occur at relatively shallow crustal levels, although many of them formed at significantly greater depths. Their present position is a consequence of uplift and erosion. Although, many aspects of their formation are well constrained, the temporal chemical evolution of such systems during uplift and erosion is still poorly understood. These vein minerals comprise calcite, dolomite-ankerite, siderite-magnesite, anhydrite and gypsum forming the last gangue assemblages in Jurassic and Tertiary sulphide-fluorite-quartz-barite veins of the Schwarzwald mining district, SW Germany. Mineral textures of samples from nine localities reveal that in these sequences, mineral precipitation follows a recurring pattern: early calcite is followed by anhydrite or gypsum, siderite and/or dolomite. This succession may repeat up to three times. In-situ (LA-ICP-MS) U-Pb age dating of 15 carbonates from three subsequent generations of the late-stage vein assemblage yield robust ages between 20 and 0.6 Ma. Each mineral sequence forms in a distinctive period of about 2-5 Ma. These ages clearly relate these late-stage mineral phases to the youngest geological episode of the Schwarzwald, which is associated with the Cenozoic Rhine Graben rifting and basement uplift. Based on thermodynamic modelling, the formation of the observed mineral assemblages required an deeply sourced Mg-, Fe- and SO4-rich fluid (b), which was episodically mixed with a shallow crustal HCO3-rich fluid (a). As a consequence of fluid mixing, concentrations of Mg, Fe and SO4 temporarily increased and initiated the formation of the observed sulphate-carbonate mineral sequences. This discontinuous large-scale vertical fluid mixing was presumably directly related to episodes of active tectonics associated with the Cenozoic strike-slip regime of the Upper Rhine Graben. Analogously, episodic fluid mixing is a major key in the formation of older (Jurassic to early

U-Pb isotope systematics and age of uranium mineralization, Midnite mine, Washington.

USGS Publications Warehouse

Ludwig, K. R.; Nash, J.T.; Naeser, C.W.

1981-01-01

and marcasite). Also, long-term continuous leakage of radioactive daughters of 238 U (probably 222 Rn) has occurred on scales of from approximately 100 mu m approximately 10 cm. The isotopic composition of unsupported radiogenic Pb in pyrite-marcasite seems to depend on the mineralogical microenvironment of the grains, so that the radiogenic Pb in pyrite-marcasite intimately intermixed with pitchblende-coffinite tends to be deficient in 206 Pb, and the radiogenic Pb in pyrite-marcasite in gangue tends to have excess 206 Pb. These systematics probably reflect differences between the average distances of Pb and 222 Rn diffusion since the formation of the ores.

Gold deposits of the northern margin of the North China craton: Multiple late Paleozoic-Mesozoic mineralizing events

USGS Publications Warehouse

Hart, C.J.R.; Goldfarb, R.J.; Qiu, Yumin; Snee, L.; Miller, L.D.; Miller, M.L.

2002-01-01

The northern margin of the North China craton is well-endowed with lode gold deposits hosting a resource of approximately 900 tonnes (t) of gold. The ???1,500-km-long region is characterized by east-trending blocks of metamorphosed Archean and Proterozoic strata that were episodically uplifted during Variscan, Indosinian, and Yanshanian deformational and magmatic events. At least 12 gold deposits from the Daqinshan, Yan-Liao (includes the Zhangjiakou, Yanshan, and Chifeng gold districts), and Changbaishan gold provinces contain resources of 20-100 t Au each. Most deposits are hosted in uplifted blocks of Precambrian metamorphic rocks, although felsic Paleozoic and Mesozoic plutons are typically proximal and host ???30% of the deposits. The lodes are characterized by sulfide-poor quartz veins in brittle structures with low base metal values and high Au:Ag ratios. Although phyllic alteration is most common, intensive alkali feldspar metasomatism characterizes the Wulashan, Dongping, and Zhongshangou deposits, but is apparently coeval with Variscan alkalic magmatism only at Wulashan. Stepwise 40Ar-39Ar geochronology on 16 samples from gangue and alteration phases, combined with unpublished SHRIMP U-Pb dates on associated granitoids, suggest that gold mineralizing events occured during Variscan, Indosinian, and Yanshanian orogenies at circa 350, 250, 200, 180, 150, and 129 Ma. However, widespread Permo-Triassic (???250 Ma) and Early Jurassic (???180 Ma) thermal events caused variable resetting of most of the white mica and K-feldspar argon spectra, as well as previously reported K-Ar determinations. Compiled and new stable isotope and fluid inclusion data show that most ??18O values for ore-stage veins range from 8 to 14???, indicating a fluid in equilibrium with the Precambrian metamorphic basement rocks; ??D values from fluid inclysions range widely from -64 to -154???, which is indicative of a local meteoric component in some veins; and highly variable ??34S data

Geochemistry of the Patricia Zn-Pb-Ag Deposit (paguanta, NE Chile)

NASA Astrophysics Data System (ADS)

Chinchilla Benavides, D.; Merinero Palomares, R.; Piña García, R.; Ortega Menor, L.; Lunar Hernández, R.

2013-12-01

The Patricia Zn-Pb-Ag ore deposit is located within the Paguanta mining project, situated at the northern end of the Andean Oligocene Porphyry Copper Belt of Chile. The sulfide mineralization occurs as W-E oriented veins hosted in volcanic rocks, mainly andesite (pyroclastic, ash and lavas), of Upper Cretaceous to Middle Tertiary age. The ore mineralogy (obtained by EMPA analyses) comprises in order of abundance, pyrite, sphalerite (5.5 - 10.89 wt % Fe, 9.8-19 % molar FeS and 0.52 wt % Cd), galena, arsenopyrite, chalcopyrite and Ag-bearing sulfosalts. The veins show a zoned and banded internal structure with pyrite at the edges and sphalerite in the center. The Ag occurs mostly as Ag-Cu-Sb sulfosalts, in order of abundance: series freibergite - argentotennantite -polybasite and stephanite. Other minor Ag phases such as argentite, pyrargirite and diaphorite were also identified. These Ag phases are typically associated with the base-metal sulfides. Freibergite occurs filling voids within sphalerite, chalcopyrite and at the contact between sphalerite and galena. Polybasite, stephanite, pyrargirite and argentite are mostly in close association with freibergite. In the case of diaphorite, it commonly occurs filling voids between galena crystals or as inclusions within galena. Some minor Ag-bearing sulfosalts are also identified between pyrite crystals. The alteration minerals are dominated by chlorite, illite and kaolinite. The gangue minerals consist of quartz and carbonates identified by XRD as kutnahorite. We obtained linear correlation statistically significant only for Ag, As Au, Cd, Cu, Pb, Sb and Zn and therefore we generated an enhanced scatter plot matrix of these elements. Bulk rock analyses (ICP/MS and XRF) of drill cores show that Ag is strongly and positively correlated with Pb and As, moderately with Cd, Sb, Au and Zn and weakly with Cu, while Au is moderately and positively correlated with Ag, As, Cd, Sb and Zn and weakly with Cu and Pb. These results

Ecological response of benthic foraminifera to the acid drainage from mine areas. An example from the Gromolo torrent mouth (Eastern Ligurian Sea, Italy)

NASA Astrophysics Data System (ADS)

Bergamin, Luisa; Capello, Marco; Carbone, Cristina; Magno, Maria Celia; Consani, Sirio; Cutroneo, Laura; Ferraro, Luciana; Pierfranceschi, Giancarlo; Romano, Elena

2016-04-01

Benthic foraminiferal assemblages react in short time to natural and anthropogenic environmental changes and, for this, they are considered as reliable indicators of environmental quality. An interesting application of these indicators is the study of their response to environmental changes in coastal marine areas, affected by dismissed mines and dump areas. The Libiola Fe-Cu sulphide mine was intensively exploited in 19th and 20th centuries, and the activity ended in 1962. The sulphide mineral assemblages consist of pyrite and chalcopyrite, with minor sphalerite and pyrrhotite, in a gangue of quartz and chlorite. The sulphide ore occurs within the Jurassic ophiolites of the Northern Apennines which were subjected to metamorphic and tectonic processes during the subsequent Apennine orogenesis. Waters circulating in the Libiola mine area, and discharging in the adjacent streams and creeks, are strongly polluted due to the diffuse occurrence of Acid Mine Drainage processes. The Gromolo torrent collects these acidic waters enriched of heavy metals which flow into Ligurian Sea. The study area is characterised by a shelf with a gentle slope, mainly constituted by sediment supplied by Entella torrent. The general circulation has trend from East to West and the coastal drift is generally eastwards. A total of 15 marine sediment samples (upper 2 cm) were collected by means of Van Veen grab in the coastal zone close to the Gromolo mouth and analyzed for living (rose Bengal stained) and dead benthic foraminifera, together with grain size, metals and trace elements, and metal fractioning. Quantitative foraminiferal parameters, like as abundance, species diversity, heterogeneity and assemblage composition, were determined and evaluated for environmental purpose. Additionally, possible increase above the natural background level of deformed specimens was considered as indicative of metal contamination. The grain-size analyses highlighted mainly sandy sediments, characterized by

Fluid inclusion, rare earth element geochemistry, and isotopic characteristics of the eastern ore zone of the Baiyangping polymetallic Ore district, northwestern Yunnan Province, China

NASA Astrophysics Data System (ADS)

Feng, Caixia; Bi, Xianwu; Liu, Shen; Hu, Ruizhong

2014-05-01

The Baiyangping Cu-Ag polymetallic ore district is located in the northern part of the Lanping-Simao foreland fold belt, which lies between the Jinshajiang-Ailaoshan and Lancangjiang faults in western Yunnan Province, China. The source of ore-forming fluids and materials within the eastern ore zone were investigated using fluid inclusion, rare earth element (REE), and isotopic (C, O, and S) analyses undertaken on sulfides, gangue minerals, wall rocks, and ores formed during the hydrothermal stage of mineralization. These analyses indicate: (1) The presence of five types of fluid inclusion, which contain various combinations of liquid (l) and vapor (v) phases at room temperature: (a) H2O (l), (b) H2O (l) + H2O (v), (c) H2O (v), (d) CmHn (v), and (e) H2O (l) + CO2 (l), sometimes with CO2 (v). These inclusions have salinities of 1.4-19.9 wt.% NaCl equivalents, with two modes at approximately 5-10 and 16-21 wt.% NaCl equivalent, and homogenization temperatures between 101 °C and 295 °C. Five components were identified in fluid inclusions using Raman microspectrometry: H2O, dolomite, calcite, CH4, and N2. (2) Calcite, dolomitized limestone, and dolomite contain total REE concentrations of 3.10-38.93 ppm, whereas wall rocks and ores contain REE concentrations of 1.21-196 ppm. Dolomitized limestone, dolomite, wall rock, and ore samples have similar chondrite-normalized REE patterns, with ores in the Huachangshan, Xiaquwu, and Dongzhiyan ore blocks having large negative δCe and δEu anomalies, which may be indicative of a change in redox conditions during fluid ascent, migration, and/or cooling. (3) δ34S values for sphalerite, galena, pyrite, and tetrahedrite sulfide samples range from -7.3‰ to 2.1‰, a wide range that indicates multiple sulfur sources. The basin contains numerous sources of S, and deriving S from a mixture of these sources could have yielded these near-zero values, either by mixing of S from different sources, or by changes in the geological

Geology of the Copper King Mine area, Prairie Divide, Larimer County, Colorado (Part 1)

USGS Publications Warehouse

Sims, Paul Kibler; Phair, George

1952-01-01

. The pitchblende in the deposit forms a steeply plunging ore shoot that has a horizontal length of more than 50 feet and a vertical height of about 85 feet. The thickness of the ore shoot averages about 2 feet, but it ranges from a feather edge to about 4 feet. The hard pitch-blende is intimately intergrown with siderite; other gangue minerals include pyrite, quartz, and finely comminuted fragments of the wall rocks. The vein was repeatedly reopened during mineral deposition as shown by several stages of brecciation and recommended by the vein matter. The pitchblende deposit probably formed at intermediate temperatures and depths and, according to the Pb/U ratio, is about 60 million years old--an early Tertiary age.

Beneficiation and agglomeration of manganese ore fines (an area so important and yet so ignored)

NASA Astrophysics Data System (ADS)

Sane, R.

2018-01-01

. Sinters have already been proved to bring enormous technical benefits in smelting operation. However small mine owners find it practically impossible to set up a small beneficiation and/or sintering unit at mine site. Recent advances in dry or pneumatic separation which depends on density difference between valuable mineral and gangue/waste rock, are proving to be advantageous & effective because of its small capacity. Capacity is 5 T/hr or 10 T/hr. When applied to low grade high silica Iron ores Iron content has been found to be enhanced by 8 to 10 % from 48% to 58 %, with overall wt. recovery of 60 to 70 %. Recently this technique was applied to low grade siliceous Mn ore with very encouraging results. Mn content has been found to be enhanced from 25 +/- 2 % to 37 +/- 2 % and with 50 to 65% wt. recovery. Size of feed is restricted to (i) 6 to 25 mm and (ii) 2 to 6 mm. Due to Modular design it is possible to put up units from 50 TPD to 800 TPD capacity.

Paleozoic magmatism and porphyry Cu-mineralization in an evolving tectonic setting in the North Qilian Orogenic Belt, NW China

NASA Astrophysics Data System (ADS)

Qiu, Kun-Feng; Deng, Jun; Taylor, Ryan D.; Song, Kai-Rui; Song, Yao-Hui; Li, Quan-Zhong; Goldfarb, Richard J.

2016-05-01

The NWW-striking North Qilian Orogenic Belt records the Paleozoic accretion-collision processes in NW China, and hosts Paleozoic Cu-Pb-Zn mineralization that was temporally and spatially related to the closure of the Paleo Qilian-Qinling Ocean. The Wangdian Cu deposit is located in the eastern part of the North Qilian Orogenic Belt, NW China. Copper mineralization is spatially associated with an altered early Paleozoic porphyritic granodiorite, which intruded tonalites and volcaniclastic rocks. Alteration zones surrounding the mineralization progress outward from a potassic to a feldspar-destructive phyllic assemblage. Mineralization consists mainly of quartz-sulfide stockworks and disseminated sulfides, with ore minerals chalcopyrite, pyrite, molybdenite, and minor galena and sphalerite. Gangue minerals include quartz, orthoclase, biotite, sericite, and K-feldspar. Zircon LA-ICPMS U-Pb dating of the ore-bearing porphyritic granodiorite yielded a mean 206Pb/238U age of 444.6 ± 7.8 Ma, with a group of inherited zircons yielding a mean U-Pb age of 485 ± 12 Ma, consistent with the emplacement age (485.3 ± 6.2 Ma) of the barren precursor tonalite. Rhenium and osmium analyses of molybdenite grains returned model ages of 442.9 ± 6.8 Ma and 443.3 ± 6.2 Ma, indicating mineralization was coeval with the emplacement of the host porphyritic granodiorite. Rhenium concentrations in molybdenite (208.9-213.2 ppm) suggest a mantle Re source. The tonalities are medium-K calc-alkaline. They are characterized by enrichment of light rare-earth elements (LREEs) and large-ion lithophile elements (LILEs), depletion of heavy rare-earth elements (HREEs) and high-field-strength elements (HFSEs), and minor negative Eu anomalies. They have εHf(t) values in the range of +3.6 to +11.1, with two-stage Hf model ages of 0.67-1.13 Ga, suggesting that the ca. 485 Ma barren tonalites were products of arc magmatism incorporating melts from the mantle wedge and the lithosphere. In contrast, the

Geochemical Modeling of Zinc Silicate Ore Formation from Sedimentary Hydrothermal Fluids

NASA Astrophysics Data System (ADS)

Appold, M. S.

2008-12-01

Sediment-hosted zinc deposits dominated by willemite (Zn2SiO4) instead of sphalerite (ZnS) are known from several prominent occurrences worldwide, including Vazante, Brazil, the Aroona Trend, Australia, Kabwe, Zambia, Berg Aukas, Namibia, and Abu Samar, Sudan. Although willemite-dominant zinc deposits appear to be much less common and are on average smaller than sphalerite-dominant zinc deposits, they nonetheless represent major enrichments of zinc in the Earth's crust, reaching sizes on the order of 1's to 10's of millions of tons and grades commonly between 20 and 40%. Sediment-hosted willemite- and sphalerite-dominant deposits share many similarities including their predominantly carbonate host rocks, gangue mineralogy, presumed derivation from sedimentary basinal brines, and spatial proximity. However, the conditions and processes that led to one style of mineralization versus the other have only recently begun to be investigated. The current study presents solubility, reaction path, and reactive transport modeling results that attempt to define more clearly the conditions that favor willemite ore formation in sedimentary basins, with a focus on the Vazante deposit. Solubility calculations for willemite and sphalerite as a function of temperature, pH, salinity, and oxidation potential were carried out using a simple 3 molal NaCl solution saturated with respect to quartz. The results show that (1) willemite solubility is relatively insensitive to changes in temperature and oxidation potential whereas sphalerite solubility decreases sharply with decreasing temperature and oxidation potential, (2) willemite solubility decreases more strongly than sphalerite with increasing pH, (3) willemite and sphalerite have a similar strong decrease in solubility with decreasing salinity. The results support a previously proposed genetic model for a willemite-dominant, sphalerite-subordinate ore body like Vazante in which a hot, acidic, metal-rich ore fluid mixed with a cooler

The mangazeya Ag-Pb-Zn vein deposit hosted in sedimentary rocks, Sakha-Yakutia, Russia: Mineral assemblages, fluid inclusions, stable isotopes (C, O, S), and origin

NASA Astrophysics Data System (ADS)

Anikina, E. Yu.; Bortnikov, N. S.; Klubnikin, G. K.; Gamyanin, G. N.; Prokof'ev, V. Yu.

2016-05-01

The succession of mineral assemblages, chemistry of gangue and ore minerals, fluid inclusions, and stable isotopes (C, O, S) in minerals have been studied in the Mangazeya silver-base-metal deposit hosted in terrigenous rocks of the Verkhoyansk Fold-Thrust Belt. The deposit is localized in the junction zone of the Kuranakh Anticlinorium and the Sartanga Synclinorium at the steep eastern limb of the Endybal Anticline. The deposit is situated at the intersection of the regional Nyuektame and North Tirekhtyakh faults. Igneous rocks are represented by the Endybal massif of granodiorite porphyry 97.8 ± 0.9 Ma in age and dikes varying in composition. One preore and three types of ore mineralization separated in space are distinguished: quartz-pyrite-arsenopyrite (I), quartz-carbonate-sulfide (II), and silver-base-metal (III). Quartz and carbonate (siderite) are predominant in ore veins. Ore minerals are represented by arsenopyrite, pyrite, sphalerite, galena, fahlore, and less frequent sulfosalts. Three types of fluid inclusions in quartz differ in phase compositions: two- or three-phase aqueous-carbon dioxide (FI I), carbon dioxide gas (FI II), and two-phase (FI III) containing liquid and a gas bubble. The homogenization temperature and salinity fall within the ranges of 367-217°C and 13.8-2.6 wt % NaCl equiv in FI I; 336-126°C and 15.4-0.8 wt % NaCl equiv in FI III. Carbon dioxide in FI II was homogenized in gas at +30.2 to +15.3°C and at +27.2 to 29.0°C in liquid. The δ34S values for minerals of type I range from-1.8 to +4.7‰ (V-CDT); of type II, from-7.4 to +6.6‰; and of type III, from-5.6 to +7.1‰. δ13C and δ18O vary from-7.0 to-6.7‰ (V-PDB) and from +16.6 to +17.1 (V-SMOW) in siderite-I; from-9.1 to-6.9‰ (V-PDB) and from +14.6 to +18.9 (V-SMOW) in siderite-II; from-5.4 to-3.1‰ (V-PDB) and from +14.6 to +19.5 (V-SMOW) in ankerite; and from-4.2 to-2.9‰ (V-PDB) and from +13.5 to +16.8 (V-SMOW) in calcite. The data on mineral assemblages, fluid

Geological Assessment of Cores from the Great Bay National Wildlife Refuge, New Hampshire

USGS Publications Warehouse

Foley, Nora K.; Ayuso, Robert A.; Ayotte, Joseph D.; Montgomery, Denise L.; Robinson, Gilpin R.

2007-01-01

buffer to reduce acidity, forced precipitation of iron-oxyhydroxide minerals and the removal of trace elements, including arsenic and lead, from ground waters in the refuge. Zinc may have remained in solution to a greater extent because of complexing with carbonate and its solubility in near-neutral ground and surface waters. The regional link between anomalously high arsenic contents in ground water and a bedrock source as established by Ayotte and others (1999, 2003) and Montgomery and others (2003) was confirmed by the presence of some arsenic-bearing minerals in rocks of the Kittery and Eliot Formations. The relatively low amounts of arsenic and metals in wells in the Great Bay National Wildlife Refuge as reported by Ayotte and others (U.S. Geological Survey Water Resources Data, 2005) were likely controlled by local geochemical environments in partially filled fractures, fissures, and permeable zones within the bedrock formations. Carbonate and silicate gangue minerals that line fractures, fissures, and permeable zones likely limited the movement of arsenic from bedrock to ground water. Sources other than the two geologic formations might have been required to account for anomalously high arsenic contents measured in private bedrock aquifer wells of Rockingham County.

Relantionships between gold mineralization and granite - Discussion with the support of a pluridisciplinary study of the Passa Tres gold deposit (South Brazil)

NASA Astrophysics Data System (ADS)

Dressel, Bárbara; Chauvet, Alain; Trzaskos, Barbara; Biondi, Joao Carlos; Bruguier, Olivier; Monie, Patrick; Villanova, Sandro; Bazille, Jose

2016-04-01

The Passa Três Granite, located at East of the Paraná State is elongated following a NNE-SSW direction. This sienogranite is emplaced within metapelites of the meso to neoproterozoic Açungui Group, between the Morro Agudo and Lancinha transcurrent faults, comprising the N040°E trending Lancinha Transcurrent Fault System. Gold mineralization within the Passa Três Granite is constituted by huge quartz veins with sulfides, variable quantities of fluorite and carbonates, forming orebodies with different internal textures, including massive, banded, sheared and brecciated. Structural data indicate the existence of two major fault systems, one N-S and the other E-W, with dips of 15-45°W and 20-75°S, respectively. Both NS and EW systems are interpreted to be contemporaneous and conjugate. Normal motions are everywhere suspected and main mineralized veins are located at opening sites at these fault systems, such as pull-aparts. The structural model suggests that the normal motion can be initiated by shearing along a "guide" level, in which sulfides and clay minerals are concentrated. This configuration can be observed at several scales, such as field, hand samples and thin section. Mineralized veins mainly contain, in addition to the quartz of the gangue, sulphides (pyrite, chalcopyrite, galena, molybdenite), fluorite, chlorite, muscovite, sericite, and carbonate. The presence of sericite, kaolinite and chlorite indicate the occurrence of, at least, propylitic and phyllic-type alterations, both in core of the granite and best-expressed at the rim of quartz-rich orebodies. Gold occurs as native grains in core of the quartz veins, within fractures that affect pyrite and frequently exhibiting normal motions consistent with the one observed at larger scale and systematically associated with chalcopyrite and galena. Quartz veins are sometimes bordered by aplitic dike. Additionally, some of the veins can exhibit a very thin margin of adularia minerals that seems to

A new approach to evaluate natural zeolite ability to sorb lead (Pb) from aqueous solutions

NASA Astrophysics Data System (ADS)

Drosos, Evangelos I. P.; Karapanagioti, Hrissi K.

2013-04-01

Lead (Pb) is a hazardous pollutant commonly found in aquatic ecosystems. Among several methods available, the addition of sorbent amendments to soils or sediments is attractive, since its application is relatively simple, while it can also be cost effective when a low cost and re-usable sorbent is used; e.g. natural zeolites. Zeolites are crystalline aluminosilicates with a three-dimensional structure composed of a set of cavities occupied by large ions and water molecules. Zeolites can accommodate a wide variety of cations, such as Na+, K+, Ca2+, Mg2+, which are rather loosely held and can readily be exchanged for others in an aqueous solution. Natural zeolites are capable of removing cations, such as lead, from aqueous solutions by ion exchange. There is a wide variation in the cation exchange capacity (CEC) of natural zeolites because of the different nature of various zeolites cage structures, natural structural defects, adsorbed ions, and their associated gangue minerals. Naturally occurring zeolites are rarely pure and are contaminated to varying degrees by other minerals, such as clays and feldspars, metals, quartz, or other zeolites as well. These impurities affect the CEC even for samples originated from the same region but from a different source. CEC of the material increases with decreasing impurity content. Potentially exchangeable ions in such impurities do not necessarily participate in ion exchange mechanism, while, in some cases, impurities may additionally block the access to active sites. For zeoliferous rocks having the same percentage of a zeolitic phase, the CEC increases with decreasing Si/Al ratio, as the more Si ions are substituted by Al ions, the more negative the valence of the matrix becomes. Sodium seems to be the most effective exchangeable ion for lead. On the contrary, it is unlikely that the potassium content of the zeolite would be substituted. A pretreatment with high concentration solutions of Na, such as 2 M NaCl, can

Paleozoic magmatism and porphyry Cu-mineralization in an evolving tectonic setting in the North Qilian Orogenic Belt, NW China

USGS Publications Warehouse

Qiu, Kun-Feng; Deng, Jun; Taylor, Ryan D.; Song, Kai-Rui; Song, Yao-Hui; Li, Quan-Zhong; Goldfarb, Richard J.

2016-01-01

The NWW-striking North Qilian Orogenic Belt records the Paleozoic accretion–collision processes in NW China, and hosts Paleozoic Cu–Pb–Zn mineralization that was temporally and spatially related to the closure of the Paleo Qilian-Qinling Ocean. The Wangdian Cu deposit is located in the eastern part of the North Qilian Orogenic Belt, NW China. Copper mineralization is spatially associated with an altered early Paleozoic porphyritic granodiorite, which intruded tonalites and volcaniclastic rocks. Alteration zones surrounding the mineralization progress outward from a potassic to a feldspar-destructive phyllic assemblage. Mineralization consists mainly of quartz-sulfide stockworks and disseminated sulfides, with ore minerals chalcopyrite, pyrite, molybdenite, and minor galena and sphalerite. Gangue minerals include quartz, orthoclase, biotite, sericite, and K-feldspar. Zircon LA-ICPMS U–Pb dating of the ore-bearing porphyritic granodiorite yielded a mean 206Pb/238U age of 444.6 ± 7.8 Ma, with a group of inherited zircons yielding a mean U–Pb age of 485 ± 12 Ma, consistent with the emplacement age (485.3 ± 6.2 Ma) of the barren precursor tonalite. Rhenium and osmium analyses of molybdenite grains returned model ages of 442.9 ± 6.8 Ma and 443.3 ± 6.2 Ma, indicating mineralization was coeval with the emplacement of the host porphyritic granodiorite. Rhenium concentrations in molybdenite (208.9–213.2 ppm) suggest a mantle Re source. The tonalities are medium-K calc-alkaline. They are characterized by enrichment of light rare-earth elements (LREEs) and large-ion lithophile elements (LILEs), depletion of heavy rare-earth elements (HREEs) and high-field-strength elements (HFSEs), and minor negative Eu anomalies. They have εHf(t) values in the range of +3.6 to +11.1, with two-stage Hf model ages of 0.67–1.13 Ga, suggesting that the ca. 485 Ma barren tonalites were products of arc magmatism incorporating melts from the mantle wedge and

Metalliferous deposits of the greater Helena mining region, Montana

USGS Publications Warehouse

Pardee, Joseph Thomas; Schrader, F.C.

1933-01-01

out to the neighboring wide intermontane valleys. The area is underlain mostly by shale, sandstone, and limestone of the upper part of the Belt series. Beds of Paleozoic and Mesozoic age occur south of the Belt area and extend from Helena west and northwest. The igneous rocks of the area include diorite and gabbro sills and dikes of probable Cretaceous age, extrusive andesite that is probably Oligocene or Miocene, and stocks of quartz monzonite, granodiorite, and quartz diorite, probably of Oligocene or Miocene age. The ore deposits of the northern districts are chiefly lodes that are valuable for gold and silver but contain some lead and copper. In the Ophir district bodies of gold and silver ore occur mainly in limestone near a body of quartz monzonite. In the Scratchgravel Hills and Grass Valley districts veins of gold quartz and veins containing lead-silver ore occur in quartz monzonite and in the adjoining metamorphic rocks. In the Austin district lodes containing gold; silver, lead, and copper are found in limestone near intrusive quartz monzonite. An unusual mineral in one of these lodes is corkite, a hydrous sulphate of lead containing arsenic. A small stock of quartz diorite in the Marysville district has invaded and domed Belt rocks. Marginal and radial fractures formed during the cooling and contraction of the igneous body became the receptacles of gold and silver veins, one of which, the Drumlummon, has produced $16,000,000. The veins filled open fractures and are characterized by a gangue of platy calcite and quartz. Lodes in Towsley Gulch in the western part of the district contain lead in addition to gold. In the Gould district a small stock of the granodiorite has invaded the Belt rocks and caused the deposition of veins similar to those near Marysville. In the Heddleston district lodes valuable for gold, silver, lead, and copper occur in Belt sedimentary rocks and diorite, some of them associated with porphyry dikes. In the Wolf Creek district veins

The Genesis of Precious and Base Metal Mineralization at the Miguel Auza Deposit, Zacatecas, Mexico

NASA Astrophysics Data System (ADS)

Findley, A. A.; Olivo, G. R.; Godin, L.

2009-05-01

The Miguel Auza mine located in Zacatecas State, Mexico, is a vein-type polymetallic epithermal deposit hosted in deformed argillite, siltstone and, greywacke of the Cretaceous Caracol Formation. Silver-rich base metal veins (0.2 m to >1.5 m wide) are spatially associated with the NE-striking, steeply SE- dipping (70-80°) Miguel Auza fault over a strike length of 1.6 km and a depth of 460 m. A 2 km2 monzonitic stock located in the proximity of the mineralized zones, has previously been interpreted as the source of the mineralizing fluids. Four distinct structural stages are correlated with hydrothermal mineral deposition: (I) The Pre-ore stage is characterized by normal faulting, fracturing of host rock, and rotation of bedding planes. This stage consists of quartz, illite, chlorite, +/- pyrite alteration of sedimentary wall rocks. (II) The Pyrite-vein stage is associated with reverse-sense reactivation of early normal faults, dilation of bedding planes/fractures, and deposition of generally barren calcite + pyrite veinlets. (III) The Main-ore stage is related to the development of reverse-fault- hosted massive sulphide veins. During this stage three phases of mineral deposition are recorded: early pyrite and arsenopyrite, intermediate chalcopyrite, pyrite, arsenopyrite, and base metals, and late base metals and Ag-bearing minerals. Associated gangue minerals during the main ore stage are quartz, muscovite, calcite and chlorite. (IV) The Post-ore stage involves late NW-SE striking block faulting, brecciation and calcite veining. Later supergene oxidation of veins led to deposition of Fe-oxides and hydroxides, commonly filling fractures or replacing early-formed sulphide assemblages. The various vein types display classic epithermal textures including open space filling, banding, comb quartz and brecciation. The Ag-bearing minerals comprise pyrargyrite [Ag3(Sb,As)S3], argentotennantite [(Cu,Ag)10(Zn,Fe)2(Sn,As)4S13], polybasite-pearceite [(Ag,Cu)16(Sb,As)2S11], and

Hydrothermal Evolution of the Giant Cenozoic Kadjaran porphyry Cu-Mo deposit, Tethyan metallogenic belt, Armenia, Lesser Caucasus: mineral paragenetic, cathodoluminescence and fluid inclusion constraints

NASA Astrophysics Data System (ADS)

Hovakimyan, Samvel; Moritz, Robert; Tayan, Rodrik; Rezeau, Hervé

2016-04-01

stockwork. One of them is the east-west-oriented 6th vein zone in the northern part of the deposit, which contains quartz-molybdenite veins and late quartz-galena-sphalerite veins. This is interpreted as a telescoping between porphyry and epithermal environments. It is supported by microscopic studies of mineral paragenesis, which reveal the presence of enargite and tennantite-tetrahedrite, luzonite, sphalerite, and galena, generally in a gangue of quartz, followed by a late carbonate and gypsum stage. On-going fluid inclusion studies are being carried out on quartz samples from the different mineralization stages. Five types of fluid inclusions were distinguished according to their nature, bubble size, and daughter mineral content: vapor-rich, aqueous-carbonic, brine, polyphase brine and liquid-rich inclusions. Cathodoluminescence images from the porphyry veins reveal four generations of quartz. Molybdenite and chalcopyrite are associated with two different dark luminescent quartz generations, which contain typical brine, aqueous-carbonic and vapour-rich H2O fluid inclusions, with some of them coexisting locally as boiling assemblages. Epithermal veins are mainly characterized by liquid-rich H2O fluid inclusions. Microthermometric studies of fluid inclusions reveal a major difference in homogenisation temperatures between the early quartz-molybdenite- chalcopyrite stage (Thtotal between 3600 and 4250C) and the late quartz-galena-sphalerite vein stage (Thtotal 300-2700C), which is attributed to the transition from a porphyry to an epithermal environment in the Kadjaran deposit.

Fluid Inclusion characteristics of syn-late orogenic Co-Ni-Cu-Au deposits in the Siegerland District of the Rhenish Massif, Germany

NASA Astrophysics Data System (ADS)

Wohlgemuth, Christoph; Hellmann, André; Meyer, Franz Michael

2013-04-01

The Siegerland District is located in the fold-and-thrust-belt of the Rhenish Massif and hosts various syn- late orogenic vein-hosted hydrothermal mineralization types. Peak-metamorphism and deformation occurred at 312-316 ± 10 Ma (Ahrendt et al., 1978) at pT-conditions of 280 - 320 °C and 0.7 - 1.4 kbar (Hein, 1993). The district is known for synorogenic siderite-quartz mineralization formed during peak-metamorphic conditions. At least 4 syn-late orogenic mineralization types are distinguished: Co-Ni-Cu-Au, Pb-Zn-Cu, Sb-Au and hematite-digenite-bornite mineralization (Hellmann et al., 2012b). Co-Ni-Cu-Au mineralization of the Siegerland District belongs to the recently defined class of metasediment hosted synorogenic Co-Cu-Au deposits (i.e. Slack et al, 2010). Ore minerals are Fe-Co-Ni sulpharsenides, bearing invisible gold, chalcopyrite, and minor As-bearing pyrite. The gangue is quartz. The alteration mineralogy comprises chlorite, illite-muscovite and quartz. The epigenetic quartz veins are closely related to the formation of reverse faults (Hellmann et al., 2011a). Microthermometric studies of fluid inclusions concerning the relationship between mineralization and microstructures have not been done so far for this deposit-class and this will be addressed here. Fluid inclusions are investigated in hydrothermally formed vein-quartz, selected from Co-Ni-Cu-Au mineralization bearing veins showing only minor overprints by later mineralization types. Two quartz generations are distinguished: subhedral quartz-I showing growth zonation and fine grained, recrystallized- and newly formed quartz-II grains forming irregular masses and fracture fillings in quartz-I. Co-Ni-Fe sulpharsenides and chalcopyrite are closely intergrown with quartz-II, implying their contemperaneous formation. However, fluid inclusions in quartz-II are often small, therefore fluid inclusions in quartz-I have been mostly investigated. In total, 180 inclusions from 4 different deposits have been

Preliminary report on the White Canyon area, San Juan county, Utah

USGS Publications Warehouse

Benson, William E.; Trites, Albert F.; Beroni, Ernest P.; Feeger, John A.

1952-01-01

. All uranium ore produced has been from the lower part of the Shinarump conglomerate, where it commonly occurs with copper as disseminations and fracture coatings in sandstone. Uranium and copper minerals also occur in low-grade disseminated deposits in the lower Chinle and in the Moenkopi formation and in veins cutting these formations. Although some uranium deposits occur in Chinarump channels and scours, copper and uranium minerals along fractures suggest that channel control may be secondary. Logs and clay balls apparently have exerted some chemical influences for deposition. The uranium occurs as the oxide in some deposits, and as secondary hydrous sulfates, phosphates, oxides, and silicates in these and several other deposits. Charcoal, iron and manganese oxides, and veinlets of hydrocarbon are abnormally radioactive in most of the deposits. Base-metal sulfides are commonly found inside the oxidized zone. Secondary copper minerals include the hydrous sulfates and carbonate. Gangue minerals include quarts, clay minerals, and manganese oxides, dickite (?), calcite, gypsum, pyrite, and chalcedony (?). Principal wall-rock alteration appears to have been silicification, clay alteration, and bleaching. Most of the shipped ore has contained more than 0.3 percent uranium. The ore also contains copper, commonly in grades lower than 1.0 percent. Criteria believed to be most useful for prospecting for concealed uranium deposits are (1) visible uranium minerals; (2) sulfide minerals; (3) secondary copper minerals; (4) dickite (?); (5) hydrocarbons; and (6) bleaching and alteration of the Moenkopi formation.

Strata-bound Fe-Co-Cu-Au-Bi-Y-REE deposits of the Idaho Cobalt Belt: Multistage hydrothermal mineralization in a magmatic-related iron oxide copper-gold system

USGS Publications Warehouse

Slack, John F.

2012-01-01

Mineralogical and geochemical studies of strata-bound Fe-Co-Cu-Au-Bi-Y-rare-earth element (REE) deposits of the Idaho cobalt belt in east-central Idaho provide evidence of multistage epigenetic mineralization by magmatic-hydrothermal processes in an iron oxide copper-gold (IOCG) system. Deposits of the Idaho cobalt belt comprise three types: (1) strata-bound sulfide lenses in the Blackbird district, which are cobaltite and, less commonly, chalcopyrite rich with locally abundant gold, native bismuth, bismuthinite, xenotime, allanite, monazite, and the Be-rich silicate gadolinite-(Y), with sparse uraninite, stannite, and Bi tellurides, in a gangue of quartz, chlorite, biotite, muscovite, garnet, tourmaline, chloritoid, and/or siderite, with locally abundant fluorapatite or magnetite; (2) discordant tourmalinized breccias in the Blackbird district that in places have concentrations of cobaltite, chalcopyrite, gold, and xenotime; and (3) strata-bound magnetite-rich lenses in the Iron Creek area, which contain cobaltiferous pyrite and locally sparse chalcopyrite or xenotime. Most sulfide-rich deposits in the Blackbird district are enclosed by strata-bound lenses composed mainly of Cl-rich Fe biotite; some deposits have quartz-rich envelopes.Whole-rock analyses of 48 Co- and/or Cu-rich samples show high concentrations of Au (up to 26.8 ppm), Bi (up to 9.16 wt %), Y (up to 0.83 wt %), ∑REEs (up to 2.56 wt %), Ni (up to 6,780 ppm), and Be (up to 1,180 ppm), with locally elevated U (up to 124 ppm) and Sn (up to 133 ppm); Zn and Pb contents are uniformly low (≤821 and ≤61 ppm, respectively). Varimax factor analysis of bulk compositions of these samples reveals geochemically distinct element groupings that reflect statistical associations of monazite, allanite, and xenotime; biotite and gold; detrital minerals; chalcopyrite and sparse stannite; quartz; and cobaltite with sparse selenides and tellurides. Significantly, Cu is statistically separate from Co and As

Geology of the Alaska-Juneau lode system, Alaska

USGS Publications Warehouse

Twenhofel, William Stephens

1952-01-01

inches to 3 feet wide and extending along their strike and dip for several tens to hundreds of feet. In addition to quartz, the only other vein gangue mineral is ankerite. It occurs in small amounts along the borders of the quartz veins. Metallic vein minerals, in addition to native gold, are, in order of decreasing abundance, pyrrhotite, galena, sphalerite, and arsenopyrite. In the aggregate the metallic minerals comprise only 1 to 2 percent of the total amount of vein material. The wall rock, particularly the meta-gabbro, was profoundly altered by the vein-forming processes. The principal effects on the meta-gabbro were the addition of large amounts of soda, potash, titanium, carbon dioxide, and phosphorous, and the removal of considerable quantities of iron, magnesia, lime, and combined water. Silica also may have been decreased. The mineralogical changes involved in the alteration were the development of biotite and ankerite at the expense of original hornblende and feldspar, resulting in a brown-colored biotite- and ankerite-rich rock. The slates are relatively unaffected by the vein-forming processes. Because of their small size, relatively low grade, and discontinuity, no attempt has been made to mine any individual vein. The prevailing practice has been to mine large blocks of ground by a system of modified block-caving, followed by hand sorting to remove the barren country rock from the gold-bearing quartz prior to milling.

A study of contaminated soils near Crucea-Botus, ana uranium mine (East Carpathians, Romania): metal distribution and partitioning of natural actinides with implications for vegetation uptake

NASA Astrophysics Data System (ADS)

Petrescu, L.; Bilal, E.

2012-04-01

Between 1962 and 2009, National Company of Uranium - CNU, the former Romanian Rare Metals Mining Company, mined over 1,200,000 tones of pitchblende ore in the East Carpathians (Crucea-Botušana area, Bistrita Mountains). The exploration and mining facilities include 32 adits, situated between 780 and 1040 m above sea level. Radioactive waste resulted from mining are disposed next to the mining facilities. Mine dumps (32) cover an area of 364,000 square meters and consist of waste rock (rocks with sub-economic mineralization) and gangue minerals. Older dumps (18) have been already naturally reclaimed by forest vegetation, which played an important role in stabilizing the waste dump cover and in slowing down the uranium migration processes. The soils samples have been collected from different mine dumps in the Crucea-Botušana uranium deposit, mainly from 1, 4, 5, 6, 8, 9, 1/30 and 950 mine waste galleries. Soil samples were collected from the upper part and slope at each mine dump, from the vegetation root zones. Total uranium concentration in soils collected from Crucea-Botušana site ranged from 6.10 to 680.70 ppm, with a mean of 52.48 ppm (dry wt.). Total thorium varies between 7.70 and 115.30 ppm (dry wt.). This indicates that the adsorption of the radioactive elements by the soils is high and variable, influenced by the ore dump - sample relationship. The sequential extraction has emphasized the fact that the uranium is associated with all the mineral fractions present in the soil samples. A great percentage of U can be found in the carbonate (21.77%), organic (15.04%) and oxides fractions (15.88%) - in accordance with the high absorbed/adsorbed properties of this element. The percentage of uranium detected in the exchangeable fraction is rather small - 2.16%. It is also to be expected that the uranium should be irreversible adsorbed by the organic matter and by the clay minerals due to its ionic radius and to its positive charge. The fact that 21.77% of the

Mesozoic Magmatism and Base-Metal Mineralization in the Fortymile Mining District, Eastern Alaska - Initial Results of Petrographic, Geochemical, and Isotopic Studies in the Mount Veta Area

USGS Publications Warehouse

Dusel-Bacon, Cynthia; Slack, John F.; Aleinikoff, John N.; Mortensen, James K.

2009-01-01

We present here the initial results of a petrographic, geochemical, and isotopic study of Mesozoic intrusive rocks and spatially associated Zn-Pb-Ag-Cu-Au prospects in the Fortymile mining district in the southern Eagle quadrangle, Alaska. Analyzed samples include mineralized and unmineralized drill core from 2006 and 2007 exploration by Full Metal Minerals, USA, Inc., at the Little Whiteman (LWM) and Fish prospects, and other mineralized and plutonic samples collected within the mining district is part of the USGS study. Three new ion microprobe U-Pb zircon ages are: 210 +- 3 Ma for quartz diorite from LWM, 187 +- 3 Ma for quartz monzonite from Fish, and 70.5 +- 1.1 Ma for altered rhyolite porphyry from Fish. We also present 11 published and unpublished Mesozoic thermal ionization mass spectrometric U-Pb zircon and titanite ages and whole-rock geochemical data for the Mesozoic plutonic rocks. Late Triassic and Early Jurassic plutons generally have intermediate compositions and are slightly foliated, consistent with synkinematic intrusion. Several Early Jurassic plutons contain magmatic epidote, indicating emplacement of the host plutons at mesozonal crustal depths of greater than 15 km. Trace-element geochemical data indicate an arc origin for the granitoids, with an increase in the crustal component with time. Preliminary study of drill core from the LWM Zn-Pb-Cu-Ag prospect supports a carbonate-replacement model of mineralization. LWM massive sulfides consist of sphalerite, galena, and minor pyrite and chalcopyrite, in a gangue of calcite and lesser quartz; silver resides in Sb-As-Ag sulfosalts and pyrargyrite, and probably in submicroscopic inclusions within galena. Whole-rock analyses of LWM drill cores also show elevated In, an important metal in high-technology products. Hypogene mineralized rocks at Fish, below the secondary Zn-rich zone, are associated with a carbonate host and also may be of replacement origin, or alternatively, may be a magnetite

Chromite deposits of the north-central Zambales Range, Luzon, Philippines

USGS Publications Warehouse

Rossman, D.L.

1970-01-01

of ores, association of chromite with dunite as gangue and as halos, and the transecting nature of the layering, foliation, and lineation in relation to chromite, are similar in all deposits regardless of composition of the chromite mineral itself. Textures in chromite ores, and structural relationships between chromite deposits and country rocks, show that layering and related foliation and lineation were formed or modified by flowage. Gabbro is believed to form the upper part of the Complex in general. Geophysical methods have been rather unsuccessful in finding chromite in the Zambales Complex. Gravity surveys, in order to be successful, must correct for all features influencing gravity except for the chromite itself. Too often the uncertainties in position of rock units and in knowledge of rock densities or position of hidden geologic features (dikes, zones of alteration) preclude the possibility of making adequate corrections. Magnetic surveys have failed to reveal any magnetic patterns attributable to the presence of chromite. Exploration for chromite should be guided by the knowledge that chromite occurs only in certain geologic environments. Thus because nearly all known chromite deposits in the Zambales Complex lie in peridotite near the gabbro contact, search for chromite should be concentrated there. Likewise it is evident from structural evidence presented here that there is little relation between layering and distribution of either major rock units or chromite deposits. Thus one is not justified in using the layered structure to predict either the position or attitude of major rock unit contacts, or presence or position of chromite deposits. In such a productive complex it is geologically certain that unknown deposits still remain undiscovered. The most promising areas for exploration are near known groups of large deposits like Acoje and Chromite Reservation No. 1. Underground drilling has been very successful in finding buried tabular

Sedimentary carbonate-hosted giant Bayan Obo REE-Fe-Nb ore deposit of Inner Mongolia, China; a cornerstone example for giant polymetallic ore deposits of hydrothermal origin

USGS Publications Warehouse

Chao, E.C.T.; Back, J.M.; Minkin, J.A.; Tatsumoto, M.; Junwen, Wang; Conrad, J.E.; McKee, E.H.; Zonglin, Hou; Qingrun, Meng; Shengguang, Huang

1997-01-01

Detailed, integrative field and laboratory studies of the textures, structures, chemical characteristics, and isotopically determined ages and signatures of mineralization of the Bayan Obo deposit provided evidence for the origin and characteristics favorable for its formation and parameters necessary for defining giant polymetallic deposits of hydrothermal origin. Bayan Obo is an epigenetic, metasomatic, hydrothermal rare earth element (REE)-Fe-Nb ore deposit that is hosted in the metasedimentary H8 dolostone marble of the Middle Proterozoic Bayan Obo Group. The metasedimentary sequence was deposited on the northern continental slope of the North China craton. The mine area is about 100 km south of the suture marking Caledonian subduction of the Mongolian oceanic plate from the north beneath the North China craton. The mineralogy of the deposit is very complex, consisting of more than 120 different minerals, some of which are epigenetic minerals introduced by hydrothermal solutions, and some of which are primary and secondary metamorphic minerals. The major REE minerals are monazite and bastnaesite, whereas magnetite and hematite are the dominant Fe-ore minerals, and columbite is the most abundant Nb mineral. Dolomite, alkali amphibole, fluorite, barite, aegirine augite, apatite, phlogopite, albite, and microcline are the most widespread gangue minerals. Three general types of ores occur at Bayan Obo: disseminated, banded, and massive ores. Broad zoning of these ore types occurs in the Main and East Orebodies. Disseminated ores are in the outermost zone, banded ores are in the intermediate zone, and massive ores are in the cores of the orebodies. On the basis of field relations, host rocks, textures, structures, and mineral assemblages, many varieties of these three types of ores have been recognized and mapped. Isotopic dating of monazite, bastnaesite, aeschynite, and metamorphic and metasomatic alkali amphiboles associated with the deposit provides constraints

Geology and description of thorium and rare-earth deposits in the southern Bear Lodge Mountains, northeastern Wyoming

USGS Publications Warehouse

Staatz, M.H.

1983-01-01

areas that total 1.69 km 2 . These deposits could be mined by open pit. The Bear Lodge disseminated deposits have one of the largest resources of both total rare earths and thorium in the United States, and although the grade of both commodities is lower than some other deposits, their large size and relative cheapness of mining make them an important future resource. Vein deposits in the Bear Lodge Mountains include all tabular bodies at least 5 cm thick. Twenty-six veins were noted in this area. These veins are thin and short; the longest vein was traced for only 137 m. Minerals vary greatly in the amount present. Gangue minerals are commonly potassium feldspar, quartz, or cristobalite intermixed with varying amounts of limonite, hematite, and various manganese oxides. Rare earths and thorium occur in the minerals monazite, brockite, and bastnaesite. Thorium content of 35 samples ranged from 0.01 to 1.2 percent, and the total rare-earth content of 21 samples from 0.23 to 9.8 percent. Indicated reserves were calculated to a depth of one-third the exposed length of the vein. Inferred reserves lie in a block surrounding indicated reserves. Indicated reserves of all veins are only 50 t of Th0 2 and 1,360 t of total rare-earth oxides; inferred reserves are 250 t of Th0 2 and 6,810 t of total rare-earth oxides. The Bear Lodge dome, which underlies the greater part of this area, is formed by multiple intrusive bodies of Tertiary age that dome up the surrounding sedimentary rocks. In the southern part of the core, the younger intrusive bodies surround and partly replace a granite of Precambrian age. This granite is approximately 2.6 b.y. old. The sedimentary rocks around the core are (from oldest to youngest): Deadwood Formation of Late Cambrian and Early Ordovician age, Whitewood Limestone of Late Ordovician age, Pahasapa Limestone of Early Mississippian age, Minnelusa Sandstone of Pennsylvanian and Early Permian age, Opeche Formation of Permian age, Minnek

A salt diapir-related Mississippi Valley-type deposit: the Bou Jaber Pb-Zn-Ba-F deposit, Tunisia: fluid inclusion and isotope study

NASA Astrophysics Data System (ADS)

Bouhlel, Salah; Leach, David L.; Johnson, Craig A.; Marsh, Erin; Salmi-Laouar, Sihem; Banks, David A.

2016-08-01

evaporation of seawater to halite saturation and requires a dilution of more than two times by meteoric water. The higher K/Na values in fluid inclusions from barite suggest that the brines interacted with K-rich rocks in the basement or siliciclastic sediments in the basin. Carbonate gangue minerals (ankerite and calcite) have δ13C and δ18O values that are close to the carbonate host rock and indicate fluid equilibrium between carbonate host rocks and hydrothermal brines. The δ34S values for sphalerite and galena fall within a narrow range (1 to 10 ‰) with a bulk value of 7.5 ‰, indicating a homogeneous source of sulfur. The δ34S values of barite are also relatively homogeneous (22 ‰), with 6 ‰ higher than the δ34S of local and regional Triassic evaporites (15 ‰). The latter are believed to be the source of sulfate. Temperature of deposition together with sulfur isotope data indicate that the reduced sulfur in sulfides was derived through thermochemical sulfate reduction of Triassic sulfate via hydrocarbons produced probably from Late Cretaceous source rocks. The 87Sr/86Sr ratio in the Bou Jaber barite (0.709821 to 0.711408) together with the lead isotope values of Bou Jaber galena (206Pb/204Pb = 18.699 to 18.737; 207Pb/204Pb = 15.635 to 15.708 and 208Pb/204Pb = 38.321 to 38.947) show that metals were extracted from homogeneous crustal source(s). The tectonic setting of the Bou Jaber ore deposit, the carbonate nature of the host rocks, the epigenetic style of the mineralization and the mineral associations, together with sulfur and oxygen isotope data and fluid inclusion data show that the Bou Jaber lead-zinc mineralization has the major characteristics of a salt diapir-related Mississippi Valley-type (MVT) deposit with superimposed events of fluorite and of barite deposition. Field relations are consistent with mineral deposition during the Eocene-Miocene Alpine orogeny from multiple hydrothermal events: (1) Zn-Pb sulfides formed by mixing of two fluids: one

Fluid-inclusion data on samples from Creede, Colorado, in relation to mineral paragenesis

USGS Publications Warehouse

Woods, T.L.; Roedder, Edwin; Bethke, P.M.

1982-01-01

Published and unpublished data on 2575 fluid inclusions in ore and gangue minerals from the Creede, Colorado, Ag-Pb-Zn-Cu vein deposit collected in our laboratories from 1959 to 1981 have shown that the average salinity (wt. % NaCl equivalent, hereinafter termed wt.% eq.) and homogenization temperature (Th), and the ranges of these two parameters for fluid inclusions in sphalerite, quartz, fluorite, and rhodochrosite, respectively, are 8.1 (4.6 - 13.4), 239?C (195-274?C); 6.1 (1.1-10.0), 260?C (190->400?C); 10.7 (6.1-11.1), 217?C (213-229?C) and 260?C (247-268?C) (bimodal distribution of Th); and 9.9 (9.3 - 10.6), 214?C (185-249?C). Inclusions have been measured in minerals from four of the five stages of mineralization previously recognized at Creede. The few inclusions of fluids depositing rhodochrosite (A-stage, earliest in the paragenesis) yield Th and salinity values more similar to those of the low-temperature (average Th 217?C) fluids forming some of the much later fluorite (C-stage) than to any of the other fluids. Th measurements on A-stage quartz range from 192?C to 263?C and average 237?C. The early, fine-grained, B-stage sphalerites yielded Th of 214 to 241?C and salinities of 6.1 to 10.2 wt. % eq. D-stage sphalerite (late in the paragenesis) has been studied in detail (growth-zone by growth-zone) for several localities along the OH vein and reveals a generally positive correlation among Th, salinity and iron content of the host sphalerite. The deposition of D-stage sphalerite was characterized by repeated cycling through different regions of salinity/Th space, as Th and salinity generally decreased with time. Seventeen salinity-Th measurements were made on D-stage sphalerite from one locality on the Bulldog Mountain vein system, which, like the OH vein, is one of four major ore-producing vein systems at Creede. These data suggest a lower Th for a given salinity fluid from sphalerite on the Bulldog Mountain vein than on the OH vein. The very high values

New geologic, fluid inclusion and stable isotope studies on the controversial Igarapé Bahia Cu-Au deposit, Carajás Province, Brazil

NASA Astrophysics Data System (ADS)

Dreher, Ana M.; Xavier, Roberto P.; Taylor, Bruce E.; Martini, Sérgio L.

2008-02-01

The Igarapé Bahia Cu-Au deposit in the Carajás Province, Brazil, is hosted by steeply dipping metavolcano-sedimentary rocks of the Igarapé Bahia Group. This group consists of a low greenschist grade unit of the Archean (˜2,750 Ma) Itacaiúnas Supergroup, in which other important Cu-Au and iron ore deposits of the Carajás region are also hosted. The orebody at Igarapé Bahia is a fragmental rock unit situated between chloritized basalt, with associated hyaloclastite, banded iron formation (BIF), and chert in the footwall and mainly coarse- to fine-grained turbidites in the hanging wall. The fragmental rock unit is a nearly concordant, 2 km long and 30-250 m thick orebody made up of heterolithic, usually matrix-supported rocks composed mainly of coarse basalt, BIF, and chert clasts derived from the footwall unit. Mineralization is confined to the fine-grained matrix and comprises disseminated to massive chalcopyrite accompanied by magnetite, gold, U- and light rare earth element (LREE)-minerals, and minor other sulfides like bornite, molybdenite, cobaltite, digenite, and pyrite. Gangue minerals include siderite, chlorite, amphibole, tourmaline, quartz, stilpnomelane, epidote, and apatite. A less important mineralization style at Igarapé Bahia is represented by late quartz-chalcopyrite-calcite veins that crosscut all rocks in the deposit area. Fluid inclusions trapped in a quartz cavity in the ore unit indicate that saline aqueous fluids (5 to 45 wt% NaCl + CaCl2 equiv), together with carbonic (CO2 ± CH4) and low-salinity aqueous carbonic (6 wt% NaCl equiv) fluids, were involved in the mineralization process. Carbonates from the fragmental layer have δ13C values from -6.7 to -13.4 per mil that indicate their origin from organic and possibly also from magmatic carbon. The δ34S values for chalcopyrite range from -1.1 to 5.6 per mil with an outlier at -10.8 per mil, implying that most sulfur is magmatic or leached from magmatic rocks, whereas a limited

The "chessboard" classification scheme of mineral deposits: Mineralogy and geology from aluminum to zirconium

NASA Astrophysics Data System (ADS)

Dill, Harald G.

2010-06-01

Economic geology is a mixtum compositum of all geoscientific disciplines focused on one goal, finding new mineral depsosits and enhancing their exploitation. The keystones of this mixtum compositum are geology and mineralogy whose studies are centered around the emplacement of the ore body and the development of its minerals and rocks. In the present study, mineralogy and geology act as x- and y-coordinates of a classification chart of mineral resources called the "chessboard" (or "spreadsheet") classification scheme. Magmatic and sedimentary lithologies together with tectonic structures (1 -D/pipes, 2 -D/veins) are plotted along the x-axis in the header of the spreadsheet diagram representing the columns in this chart diagram. 63 commodity groups, encompassing minerals and elements are plotted along the y-axis, forming the lines of the spreadsheet. These commodities are subjected to a tripartite subdivision into ore minerals, industrial minerals/rocks and gemstones/ornamental stones. Further information on the various types of mineral deposits, as to the major ore and gangue minerals, the current models and the mode of formation or when and in which geodynamic setting these deposits mainly formed throughout the geological past may be obtained from the text by simply using the code of each deposit in the chart. This code can be created by combining the commodity (lines) shown by numbers plus lower caps with the host rocks or structure (columns) given by capital letters. Each commodity has a small preface on the mineralogy and chemistry and ends up with an outlook into its final use and the supply situation of the raw material on a global basis, which may be updated by the user through a direct link to databases available on the internet. In this case the study has been linked to the commodity database of the US Geological Survey. The internal subdivision of each commodity section corresponds to the common host rock lithologies (magmatic, sedimentary, and

Mineral-deposit model for lithium-cesium-tantalum pegmatites

USGS Publications Warehouse

Bradley, Dwight C.; McCauley, Andrew D.; Stillings, Lisa L.

2017-06-20

Lithium-cesium-tantalum (LCT) pegmatites comprise a compositionally defined subset of granitic pegmatites. The major minerals are quartz, potassium feldspar, albite, and muscovite; typical accessory minerals include biotite, garnet, tourmaline, and apatite. The principal lithium ore minerals are spodumene, petalite, and lepidolite; cesium mostly comes from pollucite; and tantalum mostly comes from columbite-tantalite. Tin ore as cassiterite and beryllium ore as beryl also occur in LCT pegmatites, as do a number of gemstones and high-value museum specimens of rare minerals. Individual crystals in LCT pegmatites can be enormous: the largest spodumene was 14 meters long, the largest beryl was 18 meters long, and the largest potassium feldspar was 49 meters long.Lithium-cesium-tantalum pegmatites account for about one-fourth of the world’s lithium production, most of the tantalum production, and all of the cesium production. Giant deposits include Tanco in Canada, Greenbushes in Australia, and Bikita in Zimbabwe. The largest lithium pegmatite in the United States, at King’s Mountain, North Carolina, is no longer being mined although large reserves of lithium remain. Depending on size and attitude of the pegmatite, a variety of mining techniques are used, including artisanal surface mining, open-pit surface mining, small underground workings, and large underground operations using room-and-pillar design. In favorable circumstances, what would otherwise be gangue minerals (quartz, potassium feldspar, albite, and muscovite) can be mined along with lithium and (or) tantalum as coproducts.Most LCT pegmatites are hosted in metamorphosed supracrustal rocks in the upper greenschist to lower amphibolite facies. Lithium-cesium-tantalum pegmatite intrusions generally are emplaced late during orogeny, with emplacement being controlled by pre-existing structures. Typically, they crop out near evolved, peraluminous granites and leucogranites from which they are inferred to be

Geology of the southern Elkhorn Mountains, Jefferson and Broadwater Counties, Montana

USGS Publications Warehouse

Klepper, M.R.; Weeks, R.A.; Ruppel, E.T.

1957-01-01

remnant of a northward-plunging anticline, the major part of which was engulfed by the batholith. The folded rocks are cut by many faults of small to moderate displacement and by two faults of large displacement. Most of the faults were probably formed by the same forces that produced the folds. The origin of the two major faults, however, is uncertain, and may be related to igneous activity. The batholith crosscuts the folded structure and is in turn cut by small faults. Some parts of the area were elevated along steep normal faults in late Tertiary time. The southern part of the Elkhorn Mountains has been mountainous at least since early Oligocene time, and probably began to take form during the Cretaceous. As a consequence of long continued erosion, the modern topography reflects the structure and lithologic character of the underlying rocks except in a few areas blanketed by poorly consolidated Tertiary rocks and in the higher mountains where glaciation has been prominent. Silver, lead, zinc, and gold have been produced, either singly or, more typically, as a combination of metals from a number of types of ore deposits. Replacement deposits in carbonate rocks are the most common type, but veins, contact metamorphic deposits, and pipelike bodies of breccia cemented by ore and gangue minerals also are present. The Elkhorn mining district has the largest number of mines and the greatest variety of types of deposits. In the Tizer Basin several narrow goldbearing veins cut andesitic volcanic rocks, and in the southern part of the area sporadic small veins and replacement deposits occur in carbonate rocks. The mines and prospects of the area are described, and some suggestions for future prospecting are outlined. The application of geochemical prospecting techniques may prove of value, judging from the results of reconnaissance soil sampling in the vicinity of the Elkhorn mine.

Geology and ore deposits of the Pioche district, Nevada

USGS Publications Warehouse

Westgate, L.G.; Knopf, Adolph

1932-01-01

attention occur at the intersections of steep fissures with the limestone members of the Pioche shale. In recent years the " bedded " ore of the Combined Metals mine has been of main interest. The ore is essentially a.n intimate intergrowth of pyrite, sphalerite, and galena. Although above water level, the ore is unoxidized. It extends on both sides of the mineralizing fissure as far as 100 feet. At the Prince mine ore beds were formed at seven successively higher horizons in the Pioche shale and the overlying Lyndon and Highland Peak limestones. The ore " beds " above water level in the Prince mine are thoroughly oxidized and consist of manganese-iron oxides low in silver, lead, and zinc. About 800,000 tons of ore carrying 2.5 to 3 ounces of silver to the ton, 3 per cent of lead, 35 per cent of iron, and 15 per cent of manganese has been shipped. The Prince mine was in 1915-1918 the premier producer of lead in Nevada. The ore " bed " that occurs here below water level consists of sphalerite, galena, and pyrite in a gangue of manganosiderite and minor quartz. This is the only locality in the district in which the primary source of the abundant oxidized manganese minerals (wad, pyrolusite, and braunite) has so far been found. Some of the stratiform ore bodies the ore beds, as they are locally called were formed adjacent to exceedingly insignificant-looking fissures; and this dependence on inconspicuous mineralizing fissures is beyond doubt one of the most impressive features in the geology of the district. It opens the possibility that there may be many other bedded deposits which, like the Combined Metals ore bed, do not crop out. To find these ore bodies will be difficult, but their discovery will be aided primarily by applying skillfully a knowledge of the geologic column and by determining the faulting that has disturbed or changed the normal sequence of the strata.