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Sökning: LAR1:ltu > (2000-2009) > Öhlander Björn

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1.
  • Alakangas, Lena, et al. (författare)
  • Changes of groundwater quality in sulphide-bearing mine-tailings as a result of remediation at Kristineberg, northern Sweden
  • 2007
  • Ingår i: Mining and the Environment International Conference. - : Centre for Environmental Monitoring, Laurentian University. - 9780886670726
  • Konferensbidrag (refereegranskat)abstract
    • At the Kristineberg mine in northern Sweden, sulphide-rich tailings left open for 50 years were remediated in 1996 by applying double dry cover on one part of an impoundment, and raised groundwater level combined with simple till cover on the other part. Groundwater pipes installed in the impoundment were sampled from 1998 during a period of 6 years. The results showed that the groundwater quality varied considerably in the impoundment, even under the same type of cover. Secondarily retained Fe, S, Mg, Mn and Z were remobilised when the groundwater was raised. In the part with raised groundwater level, the average concentration of Fe ranged from 2700 to 9000mg/l in 1998, and the range for S was 2200 to 7000mg/l. During 2003 the average concentrations had decreased and ranged between 150 and 900 mg/l for Fe and between 130 and 900 mg/l for S. The improvement of the water quality was caused by inflow of less contaminated groundwater and decreasing sulphide oxidation rate. The redox potential generally decreased and pH increased. The concentrations of Cd, Cu and Pb in groundwater decreased rather rapidly all over the impoundment after remediation. In areas with relatively high pH and low redox potential, Al, Cd, Co, Cr, Cu, Fe, Ni, Pb and Zn were almost depleted.
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3.
  • Alakangas, Lena, et al. (författare)
  • Formation and composition of cemented layers in low-sulphide mine tailings, Laver, northern Sweden
  • 2006
  • Ingår i: Environmental Geology. - : Springer Science and Business Media LLC. - 0943-0105 .- 1432-0495. ; 50:6, s. 809-819
  • Tidskriftsartikel (refereegranskat)abstract
    • Cemented layers (hardpans) are common in carbonate or sulphide-rich mine tailings and where pyrrhotite is the predominating Fe-sulphide. Laver, northern Sweden, is an abandoned Cu-mine where the tailings have low pyrrhotite content, almost no pyrite and no carbonates. Two cemented layers at different locations in the Laver tailings impoundment were investigated, with the aim to determine their effects on metal mobility. The cementing agents were mainly jarosite and Fe-oxyhydroxides in the layer formed where the tailings have a barren surface, whereas only Fe-oxyhydroxides were identified below grass-covered tailings surface. Arsenic was enriched in both layers which also exhibit high concentrations of Mo, V, Hg and Pb compared to unoxidised tailings. Sequential extraction indicates that these metals and As were mainly retained with crystalline Fe-oxides, and therefore potentially will be remobilised if the oxic conditions become more reducing, for instance as a result of remediation of the tailings impoundment.
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4.
  • Alakangas, Lena, et al. (författare)
  • Pilot-scale studies of different covers on unoxidised sulphide-rich tailings in northern Sweden : the geochemistry of leachate waters
  • 2006
  • Ingår i: Mine Water and the Environment. - : Springer Science and Business Media LLC. - 1025-9112 .- 1616-1068. ; 25:3, s. 171-183
  • Tidskriftsartikel (refereegranskat)abstract
    • Leachate water quality from covered and uncovered unoxidised sulphide-rich tailings in six pilot-scale (5x5x3 m3) test cells was monitored during 2004 and 2005. The covers consisted of a layer of clayey till, sewage sludge, apatite or Trisoplast (a commercial mixture of tailings, bentonite, and a polymer). All layers were protected by an unspecified till except in one reference cell, where the tailings were left open. All leachate waters showed near-neutral pH as a result of neutralization by calcite in the tailings and by Ca(OH)2 added prior to deposition. Average dissolved sulphur concentrations in the leachates were ≈ 600 mg L-1, except in the cell with sewage sludge (300 mg L-1). The source of sulphur was mainly pyrite oxidation, but residual sulphur probably remained from the enrichment process. The near-neutral pH favoured precipitation of metal-(oxy)hydroxides with subsequent removal of trace elements such as Cd, Cu and Pb (< 15 μg L-1) from the solutions. High concentrations of Co, Mn, Ni, and Zn were found in leachates from the apatite, Trisoplast, and uncovered tailings cells. High As concentrations were found in the leachates in the sewage sludge and clayey till cells. The lowest metal concentrations, redox potential, and highest pH were found in the sewage sludge cell. Decreased elemental metal concentrations during 2004 suggest improved performance over time.
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6.
  • Alakangas, Lena, et al. (författare)
  • The effect of vegetation on mine tailings
  • 2003
  • Ingår i: Program with Abstracts : Joint Annual Meeting. - : Geological Association of Canada; Mineralogical Association of Canada.
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
    • One of the major aims with passive remediation of sulfide-bearing mine tailings is to minimize or exclude oxygen diffusion through the tailings and decrease the oxidation of sulfides. A vegetation cover could potentially decrease the oxygen flux by oxygen consumption during decay of organic matter. The abandoned Cu mine at Laver in northern Sweden has not been remediated except for establishment of vegetation, and this offers the opportunity to investigate the effect of a vegetation cover on tailings.Whole-year sampling of surface drainage water from the tailings impoundment was performed during 1993 and 2001. The release of metals was only 5-10 % of the estimated weathering rate in the tailings during 1993 because of secondary retainment within the tailings. Results from 2001 show decreasing concentrations of several elements and increasing pH, indicating decreasing oxidation rate.Pore-gas measurement in two vertical profiles shows that vegetation on the tailings has no effect as a barrier for oxygen diffusion in comparison with barren parts.Cemented layers, which have formed at various depths in the tailings, have decreased the flux of oxygen to deeper parts; this could be an explanation of the decreased oxidation rate. The different cemented layers in the tailings differ in chemical composition and physical characteristics. There are two major types, both of which both contain iron oxides and carbon. The origin of the carbon is possibly the vegetation cover. None of the cemented layers acts as a trap for heavy metals, but As is enriched.The effect of vegetation as a oxygen barrier is negligible, but vegetation could act as a source for organic matter that could increase aggregation of iron oxides and clay minerals, thereby enhancing the formation of cemented layers or increasing metal-organic complexes which decrease the mobility of metals.
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8.
  • Axelsson, Mikael D., et al. (författare)
  • High spatial resolution analysis of ferromanganese concretions by LA-ICP-MS
  • 2002
  • Ingår i: Geochemical Transactions. - : Springer Science and Business Media LLC. - 1467-4866. ; 3:5, s. 40-47
  • Tidskriftsartikel (refereegranskat)abstract
    • A procedure was developed for the determination of element distributions in cross-sections of ferromanganese concretions using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The effects of carrier flow rates, rf forward power, ablation energy, ablation spot size, repetition rate and number of shots per point on analyte intensity were studied. It is shown that different carrier gas flow rates are required in order to obtain maximum sensitivities for different groups of elements, thus complicating the optimisation of ICP parameters. On the contrary, LA parameters have very similar effects on almost all elements studied, thus providing a common optimum parameter set for the entire mass range. However, for selected LA parameters, the use of compromise conditions was necessary in order to compensate for relatively slow data acquisition by ICP-MS and maintain high spatial resolution without sacrificing the multielemental capabilities of the technique. Possible variations in ablation efficiency were corrected for mathematically using the sum of Fe and Mn intensities. Quantification by external calibration against matrix-matched standards was successfully used for more than 50 elements. These standards, in the form of pressed pellets (no binder), were prepared in-house using
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9.
  • Axelsson, Mikael D., et al. (författare)
  • Multielemental analysis of Mn–Fe nodules by ICP-MS: optimisation of analytical method
  • 2002
  • Ingår i: The Analyst. - 0003-2654 .- 1364-5528. ; 127:1, s. 76-82
  • Tidskriftsartikel (refereegranskat)abstract
    • Two acid digestion procedures (microwave-assisted and room temperature) were developed for the quantitative analysis of ferromanganese nodules by inductively coupled plasma double focusing sector field mass spectrometry (ICP-SFMS). Different compositions of the acid mixture, dilution factors and corrections for spectral interferences were tested. A combination of nitric, hydrochloric and hydrofluoric acids is necessary for complete sample digestion, with lowest acid to sample ratios (v/m) of 15 and 1.5. respectively, for the last two acids. Sample dilution factors higher than 2 X 104 should be used in order to decrease matrix effects and provide robust long-term instrumental operation. In spite of high dilution. method detection limits in the sub-mug g(-1) range were obtained for 54 out of 71 elements tested. due to the high detection capability of ICP-SFMS, as well as the special care taken to ensure the purity of reagents, to clean the instrument sample introduction system and to minimise sample handling. Owing to the presence of unresolved (at the resolution available) spectral interferences, accurate determination of Au, Hg, Os, Pd, Re and Rh is impossible without matrix separation. The accuracy of the entire analytical method was tested by the analysis of two nodule reference materials. The results generated agreed to within +/-2% for about 10, within +/-10% for more than 40 and within +/-20% for about 50 of 53 elements for which certified, recommended or literature values are available. A precision better than 3%, expressed as the between-digestion relative standard deviation (n=4). was obtained for the majority of elements, except in cases limited by low analyte concentrations
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10.
  • Carlsson, Erik, et al. (författare)
  • Geochemistry of the infiltrating water in the vadose zone of a remediated tailings impoundment, Kristineberg, northern Sweden
  • 2003
  • Ingår i: Applied Geochemistry. - 0883-2927 .- 1872-9134. ; 18:5, s. 659-674
  • Tidskriftsartikel (refereegranskat)abstract
    • At the remediated tailings Impoundment 1 at Kristineberg, Northern Sweden, installations of tension lysimeters were performed in the protective cover (10, 50, and 100 cm), in the oxidised tailings (150 cm), in the unoxidised secondarily enriched tailings (200 cm) and in the unoxidised tailings (260 cm). The lysimeters in the till protective cover contained relatively low concentrations of most elements. After infiltration through the sealing layer, consisting of 0.3 m compacted clayey till, pH decreased and conductivity, together with the concentrations of several major and trace elements, increased significantly. In the lysimeters installed in the tailings at depths of 150 and 200 cm average pH decreased to 3.4 at 150 cm and 3.2 at 200 and average conductivity increased to 2.9 mS/cm. Elements such as Al, Cd, Co, Fe, Mn, Mo, Ni,Pb, S, Si and Zn had the highest concentrations in the lysimeter at 200 cm depth. Examples of concentration averages for this lysimeter are Cd 600 μg/L, Fe 1500 mg/L, Mn 11 mg/L, Ni 1.06 μg/L, S 1800 mg/L, and Zn 190 mg/L. Between the depths of 200 and 260 cm the concentration of most elements decreased. The increase between the lysimeters at the depths of 150 and 200 cm can be explained by remobilization of secondarily retained oxidation products as well as from the continued oxidation. The decrease between the second and the third lysimeters is interpreted as co-precipitation with different Fe oxyhydroxides as well as adsorption onto secondarily formed minerals and primary mineral surfaces. Calculations of saturation indices indicate that several different hydroxides might precipitate at this level. This retainment takes place mainly due to the increase in pH. The pH increases from 3.2 up to 4-4.4 in this depth interval. Between the deepest lysimeter and the groundwater table, the element concentrations probably decrease even further. pH increases to 5-6.5 in the groundwater. Most of the pre-remediation oxidation products that are secondarily retained above or below the oxidation front and are released by the small amount of infiltrating water together with the present oxidation products are retained again during continued transport downwards. If the depth to the groundwater table is large enough, most of the metals released by the infiltrating water and the diffusing O2 do not reach the groundwater.
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