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Browsing by Subject "Uranium"

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  • Suominen, Topi (2020)
    Naturally occurring radioactive material (NORM) is defined by the IAEA as “Radioactive material containing no significant amounts of radionuclides other than naturally occurring radionuclides”. In the EC directive 2013/58/Euratom several industry sectors are listed that are known to often deal with NORM, either in residues, wastes, by-products, or products, the mining industry is one of these. The risk posed by NORM is defined by exposure potential and concentration. In the wastes created by the mining industry these are tied to the management of wastes and concentration of radionuclides in the exploited mineral resource. Wastes created by the mining industry are often of environmental concern as they are in many cases piled on the mining site after closure. The tailings of a mine may contain pyrite, which when oxidized creates acid mine drainage. The acidic waters in such sites can enhance the mobility of radionuclides and other harmful elements. In this thesis two mine waste sites were selected for study, which were known to have had issues with natural radioactivity. These two sites were the old Zn, Pb, Cu mine of Vihanti and the Pb, REE mine of Korsnäs. The current state of these two sites was studied. Possible transport of radionuclides or other harmful elements and the dose to a member of the public on the sites was also studied. Soil, waste, sediment, and water samples were collected from both sites and analyzed. Solid samples were analyzed using gamma spectrometry and the radionuclides of interest were: 238U, 226Ra, 210Pb, 232Th, 228Th, 228Ra. Water samples were analyzed with ICP-MS and the elements measured with this method were: Al, Si, P, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Pb and U. In addition, some mine waste samples were studied further using XRF and SR-XRPD methods. The results of this thesis indicate that in Vihanti, the wastes have been adequately covered, reducing the external radiation dose to near background levels. The gamma spectrometry results showed no concerning activity concentrations in soil, sediment or waste samples. Two locations were found where the ICP-MS analyses yielded high concentrations of nearly all measured elements, the pH of these sites was low as well. Signs of acid mine drainage were found in these locations, but the effects seem to be localized and no evidence of large-scale transport of contaminants through waterways was found. In Korsnäs the wastes are split into two piles, one containing tailings, and the other enriched lanthanide that was never sold. The results indicate that the lanthanide pile has been adequately covered and the external radiation dose around the pile is near background levels. While the tailings have not been covered like the lanthanide pile has, the results showed that a member of the public is unlikely to receive a dose exceeding 0.1 mSv/a from spending time on the site. Activity concentrations exceeding 1 Bq/g were detected in samples collected from the lanthanide pile, with some evidence of uranium mobilization also seen. In addition, uranium concentrations in the waters of the old open pit mine were relatively high.
  • Matara-aho, Minja (2020)
    Uranium and thorium are naturally occurring radionuclides with trace concentrations found in seawater. The growing use of nuclear energy has increased the risk of non-negligible releases of radioactivity into the environment. Most of the radioactivity is derived from uranium, which is why it is essential to understand more about the speciation of uranium in seawater and evaluate its possible impact on living organisms. The significance of thorium speciation studies rises from the use of plutonium, a more toxic actinide used in nuclear activities. Thorium is chemically similar to plutonium but less toxic and with simpler solution chemistry, so it can be used as an analogue for plutonium speciation studies. In this thesis, the role of earth alkaline cations in the structure of uranyl carbonate complex was investigated. The Ca2UO2(CO3)3 complex was previously identified as the main uranyl species in seawater but the role of calcium cations in the structure was not yet established. We prepared artificial seawater free of Mg2+ and Ca2+ using Sr2+ as a spectroscopic probe, spiked it with uranium ([U]=5·10-5 M) and measured with EXAFS spectroscopy. Together with FTIR spectroscopy and DFT calculations, the formation of Sr2UO2(CO3)3 complex was identified. Bioaccumulation of uranium was studied in sea urchins in a marine-like environment exposing the sea urchins to uranium for at least 200 hours. The U concentration in the seawater was followed throughout the experiment and at the end of the experiment the sea urchins were sacrificed and measured with ICP-OES. Accumulation of uranium was found mostly in the entrails of the sea urchins and in the excrement. The measured U from the seawater settled to about 10 % of the added uranium suggesting that there might be an equilibrium between seawater, sea urchins and sand. Th stability in seawater was studied by using Xylenol Orange as a colored complexing agent and UV-vis spectroscopy to follow the change in thorium concentration in time. Results show that thorium is rather stable in seawater if it is examined with Teflon covered instruments to prevent the thorium adsorption onto surfaces.