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11.
Mobility of Al, Co, Cr, Cu, Fe, Mn, Ni and V in sulphide-bearing fine-grained sediments exposed to atmospheric O2: an experimental study 总被引:1,自引:0,他引:1
Mats Åström 《Environmental Geology》1998,36(3-4):219-226
The major aim was to increase our knowledge on the behaviour of Al, Co, Cr, Cu, Fe, Mn, Ni and V in sulphide-bearing fine-grained
sediments exposed to atmospheric oxygen. Samples of this type of sediment collected in a previous investigation at eight sites
in western Finland were digested in HClO4-HNO3-HCl-HF at 200 °C and in HCl:HNO3:H2O at 95 °C (aqua regia), and subjected to extractions with ammonium acetate and hydrogen peroxide. Metals and S in the leachates
were determined with ICP-AES. The results of the chemical analyses are compared with previously reported experimental data.
The concentrations of Al and Fe in the sulphide-bearing fine-grained sediments are about 7% and 5%, respectively. Of the trace
metals studied, Mn is most abundant followed in decreasing order by V>Cr>Ni>Cu>Co. On oxidation of the sediments, high proportions
of Co, Mn and Ni, intermediate proportions of Cu but low proportions of Fe, Al, Cr and V are released. The extent of the release
of a metal on oxidation is controlled either by (1) the level to which the pH of the sediments drops on oxidation (Al, Cu,
Cr, V), (2) the amount of the metal associated with easily reduced phases (metal sulphides) in the sediments (Ni, Co) or (3)
the sum of the amount associated with reduced phases and adsorbed on soil compounds (Mn). No control of the release of Fe
on oxidation of the sediments was identified. Based on the results of the study it is argued that artificial drainage and
the subsequent oxidation of sulphide-bearing sediments will result in extensive leaching of Co, Mn and Ni, moderate leaching
of Cu and limited leaching of Cr and V into drainages. The major elements, Fe and Al, have the potential to be mobilised and
leached in large amounts, though the proportions mobilised/leached will remain low. It is suggested that the identification
of sulphide-bearing sediments with a high potential of metal release should be based on determination of metals in easily
mobilised reduced compounds (dissolved e.g. in H2O2) and of the level to which the pH of the sediments drops on oxidation.
Received: 16 October 1997 · Accepted: 9 March 1998 相似文献
12.
Linda J. Alakangas Frédéric A. Mathurin Mikko Faarinen Bill Wallin Mats E. Åström 《Aquatic Geochemistry》2014,20(4):405-418
Several countries are preparing to dispose of radioactive nuclear waste deep underground in crystalline rock. This type of bedrock is commonly extensively fractured and consequently carries groundwater that serves as a medium for transporting metals and radionuclides. A group of metals of particular interest in this context is the rare earth elements (REEs), because they are analogues of actinides contained within radioactive waste and are tracers of hydrological pathways and geochemical processes. Concentrations of REEs are commonly low in these groundwaters, leading to values below detection limits of standard monitoring methods, particularly for the heavy REEs. We present a new technical set-up for monitoring REEs (and other trace metals) in groundwater in fractured crystalline rock. The technique consists of passing the fracture groundwater, commonly under high pressure and containing reduced chemical species, through a device that maintains the physicochemical character of the groundwater. Within the device, diffusive gradient in thin-film (DGT) discs are installed in triplicate. With this set-up, we studied REEs in groundwater in fractures at depths of approximately ?144, ?280, and ?450 m in granitoids in the Äspö Hard Rock Laboratory in southern Sweden. The entire REE suite was detected (concentrations down to 0.1 ng L?1) and was differently fractionated among the groundwaters. The shallowest groundwater, composed of dilute modern Baltic Sea water, was enriched in the heavy REEs, whereas the deeper groundwaters, dominated by old saline water, were depleted in the heavy REEs. Deployment periods varying from 1 to 4 weeks delivered similar REE concentrations, indicating stability and reproducibility of the experimental set-up. The study finds that 1 week of deployment may be enough. However, if the overall setting and construction allow for longer deployment times, 2–3 weeks will be optimal in terms of reaching reliable REE concentrations well above the detection limit while maintaining the performance of the DGT samplers. 相似文献
13.
Nils Perttu Kamhaeng Wattanasen Khamphouth Phommasone Sten-Åke Elming 《Journal of Applied Geophysics》2011,73(3):207-220
The aim of this study is to define and characterize water bearing geological formation and to test the possibility of using geophysical techniques to determine the hydrogeological parameters in three areas in the Vientiane basin, Laos. The investigated areas are part of the Khorat Plateau where halite is naturally occurring at depths as shallow as 50 m in the Thangon Formation. Magnetic Resonance Sounding (MRS) has been used in combination with Vertical Electrical Sounding (VES) in different geological environments. In total, 46 sites have been investigated and the MRS and VES recognized the stratigraphic unit N2Q1–3, consisting of alluvial unconsolidated sediments, as the main water bearing unit. The aquifer thickness varies usually between 10 and 40 m and the depth to the main aquifer range from 5 to 15 m. The free water content is here up to 30%, and the decay times vary between 100 and 400 ms, suggesting a mean pore size equivalent to fine sand to gravel. The resistivity is highly variable, but usually around 10–1500 Ω-m, except for some sites in areas 1 and 2, where the aquifer is of low resistivity, probably related to salt water. Hydraulic and storage-related parameters such as transmissivity, hydraulic column, have been estimated from the MRS. The MRS together with VES has been shown to be a useful and important tool for identifying and distinguishing freshwater from possible salt-affected water as well as the salt-related clay layer of the Thangon Formation. This clay layer is characterized by very low free water content and a resistivity lower than 5 Ω-m and can be found in all 3 areas at depths from 15 to 50 m. 相似文献
14.
This paper discusses a geostatistical approach to model a groundwater aquifer in 3-D. The study aims at utilizing geostatistics as a tool for characterizing zones of better-water quality in a brackish-saline aquifer. In particular, the geostatistical model was constructed to characterize the aquifer’s salinity, represented by total dissolved solids (TDS), using logs of porosity and resistivity. Quality-checked estimated TDS vertical profiles were employed to construct and model horizontal and vertical semivariograms. Parameters of semivariogram models were used to develop both the kriging plan and the generated model. Results of this modeling process are shown in the form of horizontal salinity distribution maps. The aquifer was sliced into 20 layers, each 20 m thick, to represent its overall thickness. Salinity layers maps reflect vertical stratification of TDS concentrations in the aquifer and show that water quality deteriorates with depth and toward the northern part of the aquifer. Relatively better-quality water (TDS ≤10,000 mg/l) can be found at depths between 100 and 250 m below the aquifer’s top in both eastern and southeastern parts. Water in the same interval to the western and southwestern parts reflects the presence of higher TDS concentration. From a planning point of view, it is more feasible to target the eastern part of the aquifer for pumping and desalination purposes. In addition, the generated model could be utilized as an initial condition for flow simulation. 相似文献
15.
If we are to limit global warming to 2 °C, all sectors in all countries must reduce their emissions of GHGs to zero not later than 2060–2080. Zero-emission options have been less explored and are less developed in the energy-intensive basic materials industries than in other sectors. Current climate policies have not yet motivated major efforts to decarbonize this sector, and it has been largely protected from climate policy due to the perceived risks of carbon leakage and a focus on short-term reduction targets to 2020. We argue that the future global climate policy regime must develop along three interlinked and strategic lines to facilitate a deep decarbonization of energy-intensive industries. First, the principle of common but differentiated responsibility must be reinterpreted to allow for a dialogue on fairness and the right to development in relation to industry. Second, a greater focus on the development, deployment and transfer of technology in this sector is called for. Third, the potential conflicts between current free trade regimes and motivated industrial policies for deep decarbonization must be resolved. One way forward is to revisit the idea of sectoral approaches with a broader scope, including not only emission reductions, but recognizing the full complexity of low-carbon transitions in energy-intensive industries. A new approach could engage industrial stakeholders, support technology research, development and demonstration and facilitate deployment through reducing the risk for investors. The Paris Agreement allows the idea of sectoral approaches to be revisited in the interests of reaching our common climate goals.Policy relevanceDeep decarbonization of energy-intensive industries will be necessary to meet the 2 °C target. This requires major innovation efforts over a long period. Energy-intensive industries face unique challenges from both innovation and technical perspectives due to the large scale of facilities, the character of their global markets and the potentially high mitigation costs. This article addresses these challenges and discusses ways in which the global climate policy framework should be developed after the Paris Agreement to better support transformative change in the energy-intensive industries. 相似文献
16.
Luísa D.V.Carvalho Tiago Jalowitzki Ricardo Scholz Guilherme O.Gonalves Marcelo Peres Rocha Rogério Silvestre Pereir Cristiano Lana Marco Paulo de Castro Gláucia Queiroga Reinhardt A.Fuck 《地学前缘(英文版)》2022,(1):182-203
We present major and trace element compositions of mineral concentrates comprising garnet xenocrysts,ilmenite,phlogopite,spinel,zircon,and uncommon minerals (ti... 相似文献
17.
Alessandro Sandrin sa Edfelt Tod E. Waight Robert Berggren Sten-ke Elming 《Journal of Geochemical Exploration》2009,103(2-3):80-96
The Tjårrojåkka Fe–Cu-prospect in northern Sweden is considered an example of a Fe-oxide Cu–Au (IOCG) deposit and is hosted in metamorphosed Paleoproterozoic volcanic and intrusive rocks. Rock samples from 24 outcrops were collected for petrophysical analysis (magnetic susceptibility, remanent magnetization, variation of magnetic susceptibility with temperature, Curie temperature and density). The major Cu-prospect in the area has been studied by magnetic and electron microprobe analyses of four selected rock samples. The samples are from an exploration well that intersects the main Cu-mineralized body.The magnetic analyses show that magnetite is the dominant magnetic mineral, while hematite and other Fe-minerals are present in minor amounts. The electron microprobe observations confirm the presence of magnetite and further indicate that hematite is an alteration product of magnetite. Moreover, microprobe observations indicate that Fe-sulfides are present in negligible amounts in the samples from the Tjårrojåkka area. The strong spatial relationship of Cu-minerals (e.g., chalcopyrite) and the oxidation of magnetite to hematite suggest that the presence of rocks with low magnetic susceptibility in areas dominated by high susceptibility rocks may be a signal of related Cu-prospects. 相似文献
18.
Deep massive sulphide exploration using 2D and 3D geoelectrical and induced polarization data in Skellefte mining district,northern Sweden
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Saman Tavakoli Tobias E. Bauer Thorkild M. Rasmussen Pär Weihed Sten‐Åke Elming 《Geophysical Prospecting》2016,64(6):1602-1619
Geoelectrical and induced polarization data from measurements along three profiles and from one 3D survey are acquired and processed in the central Skellefte District, northern Sweden. The data were collected during two field campaigns in 2009 and 2010 in order to delineate the structures related to volcanogenic massive sulphide deposits and to model lithological contacts down to a maximum depth of 1.5 km. The 2009 data were inverted previously, and their joint interpretation with potential field data indicated several anomalous zones. The 2010 data not only provide additional information from greater depths compared with the 2009 data but also cover a larger surface area. Several high‐chargeability low‐resistivity zones, interpreted as possible massive sulphide mineralization and associated hydrothermal alteration, are revealed. The 3D survey data provide a detailed high‐resolution image of the top ~450 m of the upper crust around the Maurliden East, North, and Central deposits. Several anomalies are interpreted as new potential prospects in the Maurliden area, which are mainly concentrated in the central conductive zone. In addition, the contact relationship between the major geological units, e.g., the contact between the Skellefte Group and the Jörn Intrusive Complex, is better understood with the help of 2010 deep‐resistivity/chargeability data. The bottommost part of the Vargfors basin is imaged using the 2010 geoelectrical and induced polarization data down to ~1‐km depth. 相似文献
19.
Lead has been exploited by man over thousands of years for a variety of metallurgical, medicinal, and industrial purposes. The cumulative output of Pb from mining is estimated to be 260 million metric tonnes and 85% of this has occurred over the last two centuries. Global annual production of Pb from mining was about 3 million tonnes at the turn of the millenium. Terrestrial ecosystems all over Norway have been contaminated moderately to strongly by Pb and other trace elements from atmospheric deposition. With the aim of developing a method for mapping the accumulated content of anthropogenic Pb and how deep in the soil profile the atmospherically deposited Pb has penetrated, the concentration of Pb and the 206Pb/207Pb ratio has been studied in podzolic forest soils at four locations with different lithology, i.e. age and type of bedrock, in the Oslo area. The concentrations of Pb in the soil profiles are 6.6–38.1 mg/kg (median 10.3). The 206Pb/207Pb ratio ranges between 1.168 and 1.314 (median 1.267) over the entire profile. In the upper 5 cm the range is 1.168–1.191, similar to ratios determined in recent atmospheric deposition. Applying three different methods, the amount of anthropogenically deposited Pb is estimated at 1–6 t/km2. 相似文献
20.
Åke Nordlund 《Solar physics》1985,100(1-2):209-235
The hydrodynamics of solar convection is reviewed. In particular, a discussion is given of convection on the scale of granulation; i.e., the energy carrying convection patterns in the solar surface layers, and its penetration into the stable layers of the solar photosphere. Convection on global and intermediate scales, and interaction with rotation and magnetic fields is discussed briefly. 相似文献