• Journal of the Mineralogical Society of Korea
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• v.15 no.1
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• pp.11-21
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• 2002

A mineralogical study was made in order to identify the relationship between uranium content in groundwater and rock chemistry using core rocks recovered from the drilling holes for wells in the Daebo Granite areas. Uraniferous minerals are of primary origin and occur as inclusions in accessory minerals such as zircon, monazite, and xenotime. Since the uraniferous minerals are very small to be 1 ~ 2 $\mu$m in size, it is difficult to distinguish their mineralogical species precisely. The frequent presence of dissolution cavities or dissolved textures in the accessory minerals suggests that uraniferous minerals dissolved partially and contributed to the groundwater chemistry. Because there is no clear relationship between host rocks and groundwater for uranium concentration, mineralogical characteristics of uraniferous minerals, together with aqueous geochemical conditions favorable for uranium dissolution, could play important roles in groundwaster chemistry.

• The Journal of Engineering Geology
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• v.23 no.4
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• pp.399-407
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• 2013

Some groundwater in Korea contains high U concentrations, especially where two-mica granite occurs in the Daejeon area. The elemental U in the two-mica granite is lower than that in normal granites elsewhere in the world, and U-minerals have yet to be reported in the two-mica granite in the Daejeon area. This study focuses on investigating the occurrence of U-minerals serving as the U source in groundwater. In situ gamma ray spectrometry and mineralogical analyses using EPMA were performed. U-count anomalies were identified in a granitic dyke and in hydrothermally altered granite. Uraniferous granitic dykes occur along the contact zone between the two-mica granite and mica-schist. The uraniferous parts within the two-mica granite are developed in the hydrothermally altered zone, which contains numerous quartz veinlets within a fracture zone. Hydrothermal alteration is dominated by potassic and prophylitic alteration. Uraninite is a common U-mineral in granitic dykes and hydrothermally altered granite. Coffinite and uranophane occur in the hydrothermally altered granite. All of these U-minerals are commonly accompanied by hydrothermal alteration minerals such as muscovite, chlorite, epidote, and calcite. It is concluded that granitic dyke and hydrothermally altered granite are the main source rocks of U in groundwater.

• Journal of the Mineralogical Society of Korea
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• v.23 no.2
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• pp.107-115
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• 2010

Removal and mineralization of dissolved uranium by bacteria in KURT (KAERI Underground Research Tunnel), Korea Atomic Energy Research Institute (KAERI) was investigated. Two different bacteria, IRB (iron-reducing bacteria) and SRB (sulfate-reducing bacteria) was used, and minerals formed by these bacteria were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Compared to uranyl ions, ferric ions were preferentially reduced by IRB, showing that there is no significant reduction and removal of uranium. However, uranium concentration considerably decreased by addition of Mn(II). Results show that a sulfide mineral such as mackinawite (FeS) is formed by SRB respiration through combination of Fe(II) and S without manganese sulfide formation. In the presence of Mn(II), however, uranium is removed effectively, suggesting that the sorption and incorporation of uranium could be affected by Mn(II) onto the sulide minerals.

• Journal of the Mineralogical Society of Korea
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• v.25 no.4
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• pp.263-270
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• 2012

Two kinds of uranium species, oxidized uranium(VI) and reduced uranium(IV), were prepared to be interacted with goethite and montmorillonite to identify sorption characteristic of uranium species, which are very sensitive to the redox-reaction. The reduced uranium was prepared by diluting a substantial uranium(IV) that was concomitantly produced during a sulfate reduction via a sulfate-reducing bacterium. The sorption amount of uranium(IV) by the minerals was relatively lower than that of uranium(VI) because the aqueous uranium(IV) had fine colloidal forms to cause its weak adsorption onto the mineral surfaces. We found that the uranium(IV) phase has a nano-colloid character by the transmission electron microscope, suggesting that the uranium species possibly migrating with the flow of groundwater in underground environments can be the colloidal uranium(IV) as well as the ionic uranium(VI).

• Economic and Environmental Geology
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• v.42 no.5
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• pp.471-477
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• 2009

An experimental removal of dissolved uranium (U) exsiting as uranyl ion (${UO_2}^{2+}$) was carried out using Shewanella p., iron-reducing bacterium. By the microbial reductive reaction, initial U concentration ($50{\mu}M$) was constantly decreased, and most U were removed from solution after 2 weeks. Major mechanism that U was removed from the solution was adsorption, precipitation and mineralization on the microbe surface. Under the transmission electron microscopy, the U adsorbed on the microbe was observed as being crystallized and eventually enlarged to several ${\mu}m$ sizes of minerals by combining with individual microbes and organic exudates. It seems that such U growth and mineralization on the microbial surface could affect the U behavior in a radioactive waste disposal site. Thus, the biogechemical reaction of metal-reducing bacteria observed in this experiment could give an affirmative measure that the microbial activity may retard U movement in subsurface environment.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.7 no.1
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• pp.33-38
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• 2009

An experiment for uranium sorption onto fresh and weathered biotites was performed. After centrifugation, concentrations of uranium in the supernatants were analyzed using ICP-MS, and biotite samples were investigated using XRD and SEM. With powdered biotites (<3 mm in size), we have conducted uranium sorption experiments about fresh and weathered biotites to obtain uranium sorption amounts in various pH conditions. The uranium sorption was not high at a low pH (e.g., pH 3), but increased with increasing pH. There were lower uranium sorption by the weathered biotites than by the fresh ones, and the difference was much larger at higher pH (e.g., pH 11). The lower sorption values of uranium by the weathered biotites may be caused by a change of mineral surfaces and a chemical behavior of surrounding dissolved elements. It seems that the uranium-mineral interaction has been diminished, especially, in the weathered biotite by a destruction and dissolution of preferential sorption sites on the mineral surfaces and by the colloidal formation from dissolved elements.

• Mineral and Industry
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• v.21 no.1
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• pp.73-77
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• 2008

• Mineral and Industry
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• v.22 no.2
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• pp.84-97
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• 2009

• Mineral and Industry
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• v.20 no.2
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• pp.66-75
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• 2007

• Proceedings of the Mineralogical Society of Korea Conference
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• 2001.06a
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• pp.41-44
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• 2001