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Prusty, S.; Somu, P.; Sahoo, J.K.; Panda, D.; Sahoo, S.K.; Sahoo, S.K.; Lee, Y.R.; Jarin, T.; Sundar, L.S.; Rao, K.S. |
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Title |
Adsorptive sequestration of noxious uranium (VI) from water resources: A comprehensive review |
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Journal Article |
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Year |
2022 |
Publication |
Chemosphere |
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308 |
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136278 |
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Adsorbents, Adsorption, Techniques, Uranium, Wastewater |
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Groundwater is usually utilized as a drinking water asset everywhere. Therefore, groundwater defilement by poisonous radioactive metals such as uranium (VI) is a major concern due to the increase in nuclear power plants as well as their by-products which are released into the watercourses. Waste Uranium (VI) can be regarded as a by-product of the enrichment method used to produce atomic energy, and the hazard associated with this is due to the uranium radioactivity causing toxicity. To manage these confronts, there are so many techniques that have been introduced but among those adsorptions is recognized as a straightforward, successful, and monetary innovation, which has gotten major interest nowadays, despite specific drawbacks regarding operational as well as functional applications. This review summarizes the various adsorbents such as Bio-adsorbent/green materials, metal oxide-based adsorbent, polymer based adsorbent, graphene oxide based adsorbent, and magnetic nanomaterials and discuss their synthesis methods. Furthermore, this paper emphasis on adsorption process by various adsorbents or modified forms under different physicochemical conditions. In addition to this adsorption mechanism of uranium (VI) onto different adsorbent is studied in this article. Finally, from the literature reviewed conclusion have been drawn and also proposed few future research suggestions. |
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0045-6535 |
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THL @ christoph.kuells @ prusty_adsorptive_2022 |
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131 |
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Post, V.E.A.; Vassolo, S.I.; Tiberghien, C.; Baranyikwa, D.; Miburo, D. |
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Title |
Weathering and evaporation controls on dissolved uranium concentrations in groundwater – A case study from northern Burundi |
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Journal Article |
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Year |
2017 |
Publication |
Science of The Total Environment |
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607-608 |
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281-293 |
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Geochemical modelling, Hydrochemistry, Lake Tshohoha South, Public health, Radionuclides, Water supply |
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The potential use of groundwater for potable water supply can be severely compromised by natural contaminants such as uranium. The environmental mobility of uranium depends on a suite of factors including aquifer lithology, redox conditions, complexing agents, and hydrological processes. Uranium concentrations of up to 734μg/L are found in groundwater in northern Burundi, and the objective of the present study was to identify the causes for these elevated concentrations. Based on a comprehensive data set of groundwater chemistry, geology, and hydrological measurements, it was found that the highest dissolved uranium concentrations in groundwater occur near the shores of Lake Tshohoha South and other smaller lakes nearby. A model is proposed in which weathering and evapotranspiration during groundwater recharge, flow and discharge exert the dominant controls on the groundwater chemical composition. Results of PHREEQC simulations quantitatively confirm this conceptual model and show that uranium mobilization followed by evapo-concentration is the most likely explanation for the high dissolved uranium concentrations observed. The uranium source is the granitic sand, which was found to have a mean elemental uranium content of 14ppm, but the exact mobilization process could not be established. Uranium concentrations may further be controlled by adsorption, especially where calcium-uranyl‑carbonate complexes are present. Water and uranium mass balance calculations for Lake Tshohoha South are consistent with the inferred fluxes and show that high‑uranium groundwater represents only a minor fraction of the overall water input to the lake. These findings highlight that the evaporation effects that cause radionuclide concentrations to rise to harmful levels in groundwater discharge areas are not only confined to arid regions, and that this should be considered when selecting suitable locations for water supply wells. |
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0048-9697 |
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THL @ christoph.kuells @ post_weathering_2017 |
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132 |
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Petisco-Ferrero, S.; Idoeta, R.; Rozas, S.; Olondo, C.; Herranz, M. |
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Radiological environmental monitoring of groundwater around NPP: A proposal for its assessment |
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Journal Article |
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2023 |
Publication |
Heliyon |
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9 |
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9 |
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19470 |
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Detection limit, Nuclear power plant dismantling and decommissioning, Radiological environmental monitoring, Radionuclides in groundwater |
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Whether a nuclear installation has radiological impact and, in that case, its extension, are the questions behind any environmental analysis of the installation along its operational life. This analysis is based on the detailed establishment of the radiological background of the area. Accordingly, the dismantling and decommissioning process (D&D) of a nuclear power plant starts with a radiological monitoring plan, which includes the radiological characterization of the area and of its surroundings. At the completion of the D&D, unrestricted use for the site will be permitted strictly in accordance with results of the radiological survey within the limits established by the local authorities. Groundwater quality is typically included in any radiological analysis since, among other reasons, a significant part of it is highly likely to end up being extracted for domestic use and hence, human consumption. While there is no regulation containing maximum activity concentration or radionuclide guidance values for water that may be destined for uses other than public consumption, if groundwater is considered a “part” of the land, dose criteria for site release can be applied. Therefore, together with the guidance levels to be established for the different radionuclides expected in the groundwater, the detection limits to be employed when performing routine radio analytical characterization procedures in the laboratory should also be provided. In this paper, we first propose a relation of the potential radionuclides to be analyzed in groundwater, together with their detection limits to be achieved when the determinations are performed in a laboratory, and subsequently, we discuss the most suitable analytical methodologies and resources that would be necessary to undertake radiological characterization plans from a practical point of view. |
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2405-8440 |
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THL @ christoph.kuells @ petisco-ferrero_radiological_2023 |
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133 |
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Alexander, A.C.; Ndambuki, J.M. |
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Title |
Impact of mine closure on groundwater resource: Experience from Westrand Basin-South Africa |
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Journal Article |
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Year |
2023 |
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Physics and Chemistry of the Earth, Parts A/B/C |
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131 |
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103432 |
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Acid mine drainage, Groundwater quality, Mine closure, Spatio-temporal variation, Westrand Basin |
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The mining sector is at the edge of expanding to cater for natural resources that are much needed for technological development and manufacturing. Mushrooming of mines will consequently increase the number of mines closure. Moreover, mines closure have adverse impact on the environment at large and specifically on water resources. This study analyses historical groundwater quality parameters in mine intensive basin of Westrand Basin (WRB) to understand the status of groundwater quality in relation to mining activities and mine closure. Geographic information system (GIS) was used to map the spatio-temporal variation of groundwater quality in the basin and groundwater quality index (GQI) to evaluate its status. The coefficient of variation (CV) was applied to understand the stability of groundwater quality after the mine closure. Results indicated unstable and altered trend with increasing levels of acidity and salts concentration around the mines vicinity following the mine closure. The resultant maps indicated a significant deterioration of groundwater quality around the WRB with concentrations decreasing downstream. Obtained average GQI for the study period of 1996–2015 suggested a moderate groundwater quality at a range of GQI = 64–73. The CV indicated varying water quality at CV \textgreater 30% suggesting presence of source of contamination. Observed groundwater quality trends in Westrand basin suggested that mines closure present potential threat on groundwater quality and thus, a need for a robust mine closure plan and implementation. |
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1474-7065 |
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THL @ christoph.kuells @ alexander_impact_2023 |
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134 |
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Paradis, C.J.; Hoss, K.N.; Meurer, C.E.; Hatami, J.L.; Dangelmayr, M.A.; Tigar, A.D.; Johnson, R.H. |
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Elucidating mobilization mechanisms of uranium during recharge of river water to contaminated groundwater |
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Journal Article |
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2022 |
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Journal of Contaminant Hydrology |
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251 |
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104076 |
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Desorption, Dissolution, Groundwater, Surface water, Tracer, Uranium |
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The recharge of stream water below the baseflow water table can mobilize groundwater contaminants, particularly redox-sensitive and sorptive metals such as uranium. However, in-situ tracer experiments that simulate the recharge of stream water to uranium-contaminated groundwater are lacking, thus limiting the understanding of the potential mechanisms that control the mobility of uranium at the field scale. In this study, a field tracer test was conducted by injecting 100 gal (379 l) of oxic river water into a nearby suboxic and uranium-contaminated aquifer. The traced river water was monitored for 18 days in the single injection well and in the twelve surrounding observation wells. Mobilization of uranium from the solid to the aqueous phase was not observed during the tracer test despite its pre-test presence being confirmed on the aquifer sediments from lab-based acid leaching. However, strong evidence of oxidative immobilization of iron and manganese was observed during the tracer test and suggested that immobile uranium was likely in its oxidized state as U(VI) on the aquifer sediments; these observations ruled out oxidation of U(IV) to U(VI) as a potential mobilization mechanism. Therefore, desorption of U(VI) appeared to be the predominant potential mobilization mechanism, yet it was clearly not solely dependent on concentration as evident when considering that uranium-poor river water (\textless0.015 mg/L) was recharged to uranium-rich groundwater (≈1 mg/L). It was possible that uranium desorption was limited by the relatively higher pH and lower alkalinity of the river water as compared to the groundwater; both factors favor immobilization. However, it was likely that the immobile uranium was associated with a mineral phase, as opposed to a sorbed phase, thus desorption may not have been possible. The results of this field tracer study successfully ruled out two common mobilization mechanisms of uranium: (1) oxidative dissolution and (2) concentration-dependent desorption and ruled in the importance of advection, dispersion, and the mineral phase of uranium. |
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0169-7722 |
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THL @ christoph.kuells @ paradis_elucidating_2022 |
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135 |
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Orloff, K.G.; Mistry, K.; Charp, P.; Metcalf, S.; Marino, R.; Shelly, T.; Melaro, E.; Donohoe, A.M.; Jones, R.L. |
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Human exposure to uranium in groundwater |
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Journal Article |
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2004 |
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Environmental Research |
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94 |
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3 |
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319-326 |
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Groundwater, Human exposure, Uranium, Urine |
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High concentrations of uranium (mean=620μg/L) were detected in water samples collected from private wells in a residential community. Based on isotopic analyses, the source of the uranium contamination appeared to be from naturally occurring geological deposits. In homes where well water concentrations of uranium exceeded the drinking water standard, the residents were advised to use an alternate water source for potable purposes. Several months after the residents had stopped drinking the water, urine samples were collected and tested for uranium. Elevated concentrations of uranium (mean=0.40μg/g creatinine) were detected in urine samples, and 85 percent of the urine uranium concentrations exceeded the 95th percentile concentration of a national reference population. Urine uranium concentrations were positively correlated with water uranium concentrations, but not with the participants’ ages or how long they had been drinking the water. Six months later, a second urine sample was collected and tested for uranium. Urine uranium concentrations decreased in most (63 percent) of the people. In those people with the highest initial urine uranium concentrations, the urine levels decreased an average of 78 percent. However, urine uranium concentrations remained elevated (mean=0.27μg/g), and 87 percent of the urine uranium concentrations exceeded the 95th percentile concentration of the reference population. The results of this investigation demonstrated that after long-term ingestion of uranium in drinking water, elevated concentrations of uranium in urine could be detected up to 10 months after exposure had stopped. |
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0013-9351 |
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THL @ christoph.kuells @ orloff_human_2004 |
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136 |
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Gimeno, M.J.; Tullborg, E.-L.; Nilsson, A.-C.; Auqué, L.F.; Nilsson, L. |
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Hydrogeochemical characterisation of the groundwater in the crystalline basement of Forsmark, the selected area for the geological nuclear repositories in Sweden |
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Journal Article |
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2023 |
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Journal of Hydrology |
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624 |
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129818 |
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Crystalline bedrock, Deep geological repository, Glacial meltwater intrusion, Groundwater mixing, Hydrogeochemical model, Nuclear waste disposal |
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Numerous groundwater analyses from the crystalline bedrock in the Forsmark area have been performed between 2002 and 2019, together with thorough geological, geophysical, and hydrogeological studies, within the site investigations carried out by the Swedish Nuclear Fuel and Waste Management Company. The groundwater samples have been taken from boreholes down to ≈ 1000 m and the analysis include major- and trace-elements, stable and radiogenic isotopes, gases and microbes. The chemical and isotopic composition of these groundwaters evidences the presence of non-marine brackish to saline groundwaters with very long residence times (many hundreds of thousands of years) and a series of complex mixing events resulting from the recharge of different waters over time: glacial meltwaters, probably from different glaciations of which the latest culminated some 20,000 years ago, and marine waters from the Baltic starting some 7000 years ago. Later, meteoric water and present Baltic Sea water have recharged in different parts of the upper 100 m. These mixing events have also triggered chemical and microbial reactions that have conditioned some of the important groundwater parameters and, together with the structural complexity of the area, they have promoted a heterogeneous distribution of groundwater compositions in the bedrock. Due to these evident differences in chemistry, residence time and origin of the groundwater, several groundwater types were defined in order to facilitate the visualisation and communication. The differentiation (linked to the paleohydrological history of the area) was based on Cl concentration, Cl/Mg ratio (marine component), and δ18O value (glacial component). The work presented in this paper increases the understanding of the groundwater evolution in fractured and compartmentalised aquifers where mixing processes are the most important mechanisms. The model proposed to characterise the present groundwater system of the Forsmark area will also help to predict the future hydrogeochemical behaviour of the groundwater system after the construction of the repositories for the nuclear wastes. |
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0022-1694 |
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THL @ christoph.kuells @ gimeno_hydrogeochemical_2023 |
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137 |
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Jroundi, F.; Povedano-Priego, C.; Pinel-Cabello, M.; Descostes, M.; Grizard, P.; Purevsan, B.; Merroun, M.L. |
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Evidence of microbial activity in a uranium roll-front deposit: Unlocking their potential role as bioenhancers of the ore genesis |
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Journal Article |
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2023 |
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Science of The Total Environment |
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861 |
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160636 |
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ISR, Metatranscriptomes, Microbial metabolisms, Ore genesis, Roll-front deposit, Uranium |
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Uranium (U) roll-front deposits constitute a valuable source for an economical extraction by in situ recovery (ISR) mining. Such technology may induce changes in the subsurface microbiota, raising questions about the way their activities could build a functional ecosystem in such extreme environments (i.e.: oligotrophy and high SO4 concentration and salinity). Additionally, more information is needed to dissipate the doubts about the microbial role in the genesis of such U orebodies. A U roll-front deposit hosted in an aquifer driven system (in Zoovch Ovoo, Mongolia), intended for mining by acid ISR, was previously explored and showed to be governed by a complex bacterial diversity, linked to the redox zonation and the geochemical conditions. Here for the first time, transcriptional activities of microorganisms living in such U ore deposits are determined and their metabolic capabilities allocated in the three redox-inherited compartments, naturally defined by the roll-front system. Several genes encoding for crucial metabolic pathways demonstrated a strong biological role controlling the subsurface cycling of many elements including nitrate, sulfate, metals and radionuclides (e.g.: uranium), through oxidation-reduction reactions. Interestingly, the discovered transcriptional behaviour gives important insights into the good microbial adaptation to the geochemical conditions and their active contribution to the stabilization of the U ore deposits. Overall, evidences on the importance of these microbial metabolic activities in the aquifer system are discussed that may clarify the doubts on the microbial role in the genesis of low-temperature U roll-front deposits, along the Zoovch Ovoo mine. |
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0048-9697 |
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THL @ christoph.kuells @ jroundi_evidence_2023 |
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138 |
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Jaireth, S.; Roach, I.C.; Bastrakov, E.; Liu, S. |
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Basin-related uranium mineral systems in Australia: A review of critical features |
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Journal Article |
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2016 |
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Ore Geology Reviews |
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76 |
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360-394 |
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Australia’s uranium deposits, Calcrete-uranium, Sandstone-hosted uranium, Unconformity-related uranium |
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This paper reviews critical features of basin-related uranium mineral systems in Australia. These mineral systems include Proterozoic unconformity-related uranium systems formed predominantly from diagenetic fluids expelled from sandstones overlying the unconformity, sandstone-hosted uranium systems formed from the influx of oxidised groundwaters through sandstone aquifers, and calcrete uranium systems formed from oxidised groundwaters flowing through palaeochannel aquifers (sand and calcrete). The review uses the so-called ‘source-pathway-trap’ paradigm to summarise critical features of fertile mineral systems. However, the scheme is expanded to include information on the geological setting, age and relative timing of mineralisation, and preservation of mineral systems. The critical features are also summarised in three separate tables. These features can provide the basis to conduct mineral potential and prospectivity analysis in an area. Such analysis requires identification of mappable signatures of above-mentioned critical features in geological, geophysical and geochemical datasets. The review of fertile basin-related systems shows that these systems require the presence of at least four ingredients: a source of leachable uranium (and vanadium and potassium for calcrete-uranium deposits); suitable hydrological architecture enabling connection between the source and the sink (site of accumulation); physical and chemical sinks or traps; and a post-mineralisation setting favourable for preservation. The review also discusses factors that may control the efficiency of mineral systems, assuming that world-class deposits result from more efficient mineral systems. The review presents a brief discussion of factors which may have controlled the formation of large deposits in the Lake Frome region in South Australia, the Chu-Sarysu and Syrdarya Basins in Kazakhstan and calcrete uranium deposits in the Yilgarn region, Western Australia. |
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THL @ christoph.kuells @ jaireth_basin-related_2016 |
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139 |
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Silva, M.L. da; Bonotto, D.M. |
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Uranium isotopes in groundwater occurring at Amazonas State, Brazil |
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2015 |
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Applied Radiation and Isotopes |
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97 |
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24-33 |
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Amazon area, Dissolved uranium, Groundwater, Tube wells, U/U activity ratio |
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This paper reports the behavior of the dissolved U-isotopes 238U and 234U in groundwater providing from 15 cities in Amazonas State, Brazil. The isotope dilution technique accompanied by alpha spectrometry were utilized for acquiring the U content and 234U/238U activity ratio (AR) data, 0.01–1.4µgL−1 and 1.0–3.5, respectively. These results suggest that the water is circulating in a reducing environment and leaching strata containing minerals with low uranium concentration. A tendency to increasing ARs values following the groundwater flow direction is identified in Manaus city. The AR also increases according to the SW–NE directions: Uarini→Tefé; Manacapuru→Manaus; Presidente Figueiredo→São Sebastião do Uatumã; and Boa Vista do Ramos→Parintins. Such trends are possibly related to several factors, among them the increasing acid character of the waters. The waters analyzed are used for human consumption and the highest dissolved U content is much lower than the maximum established by the World Health Organization. Therefore, in view of this radiological parameter they can be used for drinking purposes. |
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THL @ christoph.kuells @ silva_uranium_2015 |
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140 |
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