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Moreau, M.; Daughney, C. |
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Defining natural baselines for rates of change in New Zealand’s groundwater quality: Dealing with incomplete or disparate datasets, accounting for impacted sites, and merging into state of the-environment reporting |
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Journal Article |
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Year |
2021 |
Publication |
Science of The Total Environment |
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755 |
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143292 |
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Baseline, Groundwater quality, Machine-learning, Monitoring, New Zealand, Trends |
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To effectively manage sustainably groundwater bodies, it is essential to establish what the naturally occurring ranges of chemical concentrations in groundwaters are and how they change over time. We defined baseline trends for New Zealand groundwaters using: 1) pattern recognition techniques to deal with inconsistent monitoring suites between the national (110 sites) and the denser regional network (\textgreater1000 sites), and 2) multivariate statistics to identify and remove impacted sites from the enhanced dataset. Rates of changes were calculated for 13 parameters between January 2005 and December 2014 at more than 1000 groundwater quality monitoring sites. The resulting dataset included 262 complete cases (CC), which was enhanced using Machine-Learning (ML) techniques to a total of 607 sites. Hierarchical cluster analysis was used to identify trend clusters that were consistent between the CC, ML-enhanced datasets and a 2006 study based on solely on the national network. The largest cluster (WR) consisted of low magnitude changes across all parameters and was attributed to water-rock interaction processes. The second largest cluster (I) exhibited fast changes particularly for parameters linked to human-induced impact. The third largest cluster (D) comprised decreases of all parameters and was associated with dilution processes. Trend clusters were further refined using groundwater quality state information, enabling the identification of impacted sites outside of Cluster I in the ML-enhanced and CC datasets. Corresponding trend baselines were subsequently derived at unimpacted sites using univariate quantile distribution (5th and 95th percentile thresholds). Finally, we developed classifications combining baselines (state and trend) and natural variability to enhance state of the environment reporting. This allowed the new identification of deteriorating trends at sites where groundwater quality state is not yet affected in addition to trend reversals. These classifications can be adapted to incorporate new knowledge or align with surface water quality reporting. |
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0048-9697 |
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THL @ christoph.kuells @ moreau_defining_2021 |
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164 |
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Kharazi, P.; khazaeli, E.A.; Heshmatpour, A. |
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Delineation of suitable sites for groundwater dams in the semi-arid environment in the northeast of Iran using GIS-based decision-making method |
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Journal Article |
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Year |
2021 |
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Groundwater for Sustainable Development |
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15 |
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100657 |
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Subsurface dam, Hybrid decision-making method, Geographic information system, Analytical hierarchy process, EDAS, TOPSIS1 |
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Competing commercial demands on water resources need to be balanced as the world’s population rises. Generally, groundwater is raised by subsurface dams. In this paper, the geographic information system (GIS) software and a decision-making method were applied. As the first step, the limitations that affect the establishment of the subsurface dam were identified using eliminating criteria by the Boolean logic. Regarding the second step, the most appropriate axis was determined for subsurface dam construction in each of the limits. The analytical hierarchy process (AHP) was applied according to the evaluation criteria in this study. The aim of using AHP was to weigh and prioritize the criteria of the groundwater dam for recognizing appropriate sites. Among various places and regarding the subsurface dam construction, AHP was conducted using a hierarchy process for finding the most suitable sites in the third stage of the decision-making method. Finally, among the ten appropriate sites, cross comparison was drawn by using Decision Expert (DEX), Evaluation based on Distance from Average Solution (EDAS), and Technique for Order of Preference by Similarity to Ideal Solution (TOPSIS). Compared together (as a process of decision-making), DEX, TOPSIS, and EDAS methods assisted in ranking the most appropriate sites in the final step of subsurface dam pre-selection. A and C axes obtained scores between 1 and 2, among 10 axes according to the numerically ranked locations. Regarding the water shortage issue and better management of the underground water at certain levels, the findings of this study could be useful for the residents of Kajbid-Balaqly Watershed in the dry season. Further, water managers can use the above-mentioned methods for their decisions regarding the proper subsurface dam establishment. |
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2352-801x |
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THL @ christoph.kuells @ Kharazi2021100657 |
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250 |
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Zaeri, A.; Mohammadi, Z.; Rezanezhad, F. |
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Determining the source and mechanism of river salinity: An integrated regional study |
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Journal Article |
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Year |
2023 |
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Journal of Hydrology: Regional Studies |
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47 |
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101411 |
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River salinity, Salinization mechanism, Isotope, Halite brine, River sinuosity |
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Study region Zohreh River Basin, Southwest Iran Study focus The salinity of Zohreh River sharply increases in three salinity zones (SZs) along the river named SZ1, SZ2 (the focus of this study), and SZ3. Determining the salinity sources and salinization mechanism using an integrated approach including geological, hydrochemical, isotopic, geophysical, river sinuosity and hydrocarbon analysis are the main objectives of this study. The study focuses on the combination of evidence of regional-scale (i.e., river sinuosity and seismic data) and small-scale (i.e., drilling core analysis). New hydrologic insights for the region Among several known sources of river salinity, it was found that the water quality of the Zohreh River is mainly threatened by the salt-bearing Gachsaran Formation and oil-field brine. It is concluded that halite brine and oil-field brine simultaneously cause the salinization in SZ2, and their contributions were delineated to be 95% and 5%, respectively. The lack of reliable geological evidence to support halite dissolution in surficial layers by circulating waters suggests the possibility of a deep source of halite brine in SZ2. The results revealed that deep halite brine of the salt layers of Gachsaran Formation is mainly responsible for the salinization of SZ2. The mechanism of deep brine penetration to the river through the hidden fault failures detected by the combination of river sinuosity analysis and geophysical data for the first time. |
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2214-5818 |
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THL @ christoph.kuells @ Zaeri2023101411 |
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251 |
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Romeo, N.; Mabry, J.; Hillegonds, D.; Kainz, G.; Jaklitsch, M.; Matsumoto, T. |
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Developments of a field gas extraction device and krypton purification system for groundwater radio-krypton dating at the IAEA |
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Journal Article |
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2022 |
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Applied Radiation and Isotopes |
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189 |
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110450 |
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The long-lived radio-krypton isotope 81Kr (t1/2 = 2.29 × 105 yr) is an ideal tracer for old groundwater age dating in the range of 105–106 years which goes beyond the reach of radio-carbon (14C) age dating. Analytical breakthrough made over the last two decades in Atom Trap Trace Analysis (ATTA) has enabled the use of this isotope with extremely low abundance (81Kr/Kr = 6 × 10−13) to be used as a practical dating tool for very old groundwater. The International Atomic Energy Agency aims to provide this new isotope tool for better groundwater resource management of Member States and developed a field sampling device to collect dissolved gas samples from groundwater and a system to separate and purify trace amounts of krypton from the gas samples for the ATTA analysis. The design, setup and performances of our sampling and purification systems are described here. Our system can produce a high purity aliquot of about 5 μL of krypton from 5 L of air sample (recovery yield of >90%). The samples made by our system were confirmed to be acceptable for the ATTA analysis. |
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0969-8043 |
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THL @ christoph.kuells @ Romeo2022110450 |
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214 |
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Severi, A.; Masoudian, M.; Kordi, E.; Roettcher, K. |
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Discharge coefficient of combined-free over-under flow on a cylindrical weir-gate |
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2015 |
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ISH Journal of Hydraulic Engineering |
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21 |
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1 |
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42-52 |
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Taylor & Francis |
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THL @ christoph.kuells @ doi:10.1080/09715010.2014.939503 |
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88 |
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Pontér, S.; Rodushkin, I.; Engström, E.; Rodushkina, K.; Paulukat, C.; Peinerud, E.; Widerlund, A. |
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Early diagenesis of anthropogenic uranium in lakes receiving deep groundwater from the Kiruna mine, northern Sweden |
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Journal Article |
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Year |
2021 |
Publication |
Science of The Total Environment |
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793 |
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148441 |
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Isotope ratios, Mine water, Sediments, Uranium |
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The uranium (U) concentrations and isotopic composition of waters and sediment cores were used to investigate the transport and accumulation of U in a water system (tailings pond, two lakes, and the Kalix River) receiving mine waters from the Kiruna mine. Concentrations of dissolved U decrease two orders of magnitude between the inflow of mine waters and in the Kalix River, while the concentration of the element bound to particulate matter increases, most likely due to sorption on iron‑manganese hydroxides and organic matter. The vertical distribution of U in the water column differs between two polluted lakes with a potential indication of dissolved U supply from sediment’s pore waters at anoxic conditions. Since the beginning of exposure in the 1950s, U concentrations in lake sediments have increased \textgreater20-fold, reaching concentrations above 50 μg g-1. The distribution of anthropogenic U between the lakes does not follow the distribution of other mine water contaminants, with a higher relative proportion of U accumulating in the sediments of the second lake. Concentrations of redox-sensitive elements in the sediment core as well as Fe isotopic composition were used to re-construct past redox-conditions potentially controlling early diagenesis of U in surface sediments. Two analytical techniques (ICP-SFMS and MC-ICP-MS) were used for the determination of U isotopic composition, providing an extra dimension in the understanding of processes in the system. The (234 U)/(238 U) activity ratio (AR) is rather uniform in the tailings pond but varies considerably in water and lake sediments providing a potential tracer for U transport from the Kiruna mine through the water system, and U immobilization in sediments. The U mass balance in the Rakkurijoki system as well as the amount of anthropogenic U accumulated in lake sediments were evaluated, indicating the immobilization in the two lakes of 170 kg and 285 kg U, respectively. |
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0048-9697 |
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THL @ christoph.kuells @ ponter_early_2021 |
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154 |
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Lapworth, D.J.; Brauns, B.; Chattopadhyay, S.; Gooddy, D.C.; Loveless, S.E.; MacDonald, A.M.; McKenzie, A.A.; Muddu, S.; Nara, S.N.V. |
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Elevated uranium in drinking water sources in basement aquifers of southern India |
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Journal Article |
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Year |
2021 |
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Applied Geochemistry |
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133 |
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105092 |
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Anthropogenic, Drinking waters, Geogenic, India, Speciation, Uranium |
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Groundwater resources in the crystalline basement complex of India are crucial for supplying drinking water in both rural and urban settings. Groundwater depletion is recognised as a challenge across parts of India due to over-abstraction, but groundwater quality constraints are perhaps even more widespread and often overlooked at the local scale. Uranium contamination in basement aquifers has been reported in many parts of India, locally exceeding WHO drinking water guideline values of 30 μg/L and posing a potential health risk. In this study 130 water samples were collected across three crystalline basement catchments to assess hydrochemical, geological and anthropogenic controls on uranium mobility and occurrence in drinking water sources. Groundwaters with uranium concentrations exceeding 30 μg/L were found in all three study catchments (30% of samples overall), with concentrations up to 589 μg/L detected. There appears to be a geological control on the occurrence of uranium in groundwater with the granitic gneiss of the Halli and Bengaluru study areas having higher mean uranium concentrations (51 and 68 μg/L respectively) compared to the sheared gneiss of the Berambadi catchment (6.4 μg/L). Uranium – nitrate relationships indicate that fertiliser sources are not a major control on uranium occurrence in these case studies which include two catchments with a long legacy of intense agricultural land use. Geochemical modelling confirmed uranium speciation was dominated by uranyl carbonate species, particularly ternary complexes with calcium, consistent with uranium mobility being affected by redox controls and the presence of carbonates. Urban leakage in Bengaluru led to low pH and low bicarbonate groundwater hydrochemistry, reducing uranium mobility and altering uranium speciation. Since the majority of inhabitants in Karnataka depend on groundwater abstraction from basement aquifers for drinking water and domestic use, exposure to elevated uranium is a public health concern. Improved monitoring, understanding and treatment of high uranium drinking water sources in this region is essential to safeguard public health. |
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0883-2927 |
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THL @ christoph.kuells @ lapworth_elevated_2021 |
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147 |
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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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Shayakhmetov, N.M.; Alibayeva, K.A.; Kaltayev, A.; Panfilov, I. |
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Enhancing uranium in-situ leaching efficiency through the well reverse technique: A study of the effects of reversal time on production efficiency and cost |
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Journal Article |
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2023 |
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Hydrometallurgy |
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219 |
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106086 |
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Economic evaluation, Hydrodynamic enhancement of mineral production, In-situ leaching, Mineral recovery, Optimal reversal time, Well reversing technique |
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In this study, the application of the Well Reversal Technique (WRT) and the impact of reversal time on the efficiency of uranium mining via In-Situ Leaching (ISL) were investigated. A prevalent issue in ISL mineral extraction is the formation of stagnant zones caused by limited access of the lixiviant, which leads to increased operating expenditures. The WRT, which involves altering the function of some wells from injection to production or vice versa, is a potential solution to this problem. The efficiency of WRT is heavily dependent on the well pattern and reversal time. Two commonly used well patterns in ISL are the 9-spot (row arrangement) and 7-spot (hexagonal arrangement). The objective of this study was to determine the optimal reversal time for a 9-spot well pattern through mathematical modeling of hydrodynamic and physico-chemical processes and subsequent economic assessment. A mathematical model of uranium extraction processes was developed using the principles of mass conservation, Darcy’s, and mass action laws. The results obtained for a 9-spot well pattern without reversal, with two reversal options, and a 7-spot scheme were analyzed comparatively. The 7-spot scheme without reversal was found to be the most effective of the options examined. The application of WRT on a 9-spot well pattern allows to enhance production efficiency to a level comparable to that of a 7-spot well pattern. Additionally, the effect of reversal time on recovery was studied based on two well reversal options. The results from calculation revealed that the optimal scenario was when the well reversal is conducted immediately after the time point at which the average concentration of the pregnant solution in the production wells reaches its peak value. The overall efficiency of WRT application was determined through economic calculations of capital (CAPEX) and operating (OPEX) expenditures. Based on economic calculations, it was determined that the utilization of WRT results in a 3–18% increase in mineral production efficiency for a 9-point scheme, depending on the chosen reversal method. |
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0304-386x |
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THL @ christoph.kuells @ shayakhmetov_enhancing_2023 |
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203 |
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Etschmann, B.; Liu, W.; Li, K.; Dai, S.; Reith, F.; Falconer, D.; Kerr, G.; Paterson, D.; Howard, D.; Kappen, P.; Wykes, J.; Brugger, J. |
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Enrichment of germanium and associated arsenic and tungsten in coal and roll-front uranium deposits |
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Journal Article |
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2017 |
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Chemical Geology |
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463 |
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29-49 |
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Arsenic, Coal, EXAFS and XANES, germanium, Hydrothermal fluids, Metallogenesis, Speciation, Tungsten |
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Abstract |
Most of the World’s germanium (Ge) is mined from Ge-rich lignite, where it is commonly associated with elevated arsenic (As), tungsten (W) and beryllium (Be) contents. Over the past decade, new evidence showing that World-class Ge deposits result from the interaction of hydrothermal fluids with organic matter in coal seams has emerged. Yet, the chemical state of Ge and associated metals in lignite remains poorly understood. We used Mega-pixel Synchrotron X-ray Fluorescence (MSXRF), X-ray Absorption Near Edge Structure (XANES) and Extended X-ray Absorption Fine Structure (EXAFS) to characterize the oxidation states and chemical bonding environment of Ge, As, and W in two world-class Mesozoic Ge-in-lignite deposits (Lincang, Yunnan, southwestern China; Wulantuga, Inner Mongolia, northeastern China); in lignite-bearing uranium (U) ores from the Beverley deposit (South Australia) hosted in Eocene sandstones; and in lignite and preserved wood in late Oligocene-Miocene fluviatile sediments (Gore, Southland, New Zealand). The aim was to improve our understanding of the enrichment mechanism of Ge in lignite and better evaluate the environmental mobility of Ge and some of the associated metals (specifically As and W) in lignite ores. In all samples, chemical maps show that Ge is distributed homogeneously (down to 2μm) within the organic matter. XANES and EXAFS data show that Ge exists in the tetravalent oxidation state and in a distorted octahedral coordination with O, consistent with complexing of Ge by organic ligands. In some pyrite-bearing samples, a minor fraction of Ge is also present as Ge(IV) in association with pyrite. In contrast, As displays a more complex speciation pattern, sometimes even in a single sample, including As(III), As(V), and As(−I/+II) in solid solution in sulfides. Arsenic in sulfides occurs in anionic and cationic forms, i.e., it shows both the common substitution for S22− and the substitution for Fe recently discovered in some hydrothermal pyrites. Tungsten was present as W(VI) in distorted octahedral (3+3) coordination. The EXAFS data confirm the absence or minor contribution of individual W-rich minerals such as scheelite or ferberite to W mass balance in the studied samples. These data show that Ge, W, and probably some As are scavenged via formation of insoluble, oxygen-bridged metal organic complexes in lignite. Destruction of the organic ligands responsible for fixing Ge and W (As) in these lignites is required for liberating the metals, e.g. from waste materials. Geochemical modelling suggests that Ge, W, Be and As all can be extracted from granitic rocks by dilute, low temperature hydrothermal fluids. Germanium is transported mainly as the tetrahedral Ge(OH)4(aq) complex, but fixed as an octahedral oxy-bridged organic complex. The same situation is valid for W, which is transported at the tetrahedral tungstate ion, but most likely scavenged via formation of a 6-coordinated metal-organic species. The Ge-Be-W±As association in Ge-rich coals reflects the source of the metals as well as related scavenging mechanisms. |
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0009-2541 |
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THL @ christoph.kuells @ etschmann_enrichment_2017 |
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183 |
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