Uranium Deposits Research Articles

Evaluation of uranium migration during the maturation of hydrocarbon source rocks.

The source of uranium is an important research topic related to the exploration of sandstone-type uranium deposits, and potential uranium sources in deep basins are often overlooked. Black organic-rich shale is a common uranium-bearing rock in deep sedimentary basins. However, relatively few studies have investigated the migration of uranium during hydrocarbon generation in and release from uranium-rich shale. In this study, the uranium-rich shale in the Chang 7 member of the Yanchang Formation of the Upper Triassic in the Ordos Basin was selected to investigate the migration of uranium and other trace elements during the thermal maturation of uranium-rich shale via a semiopen pyrolysis simulation system. The gas and liquid products as well as the solid residue were thoroughly analysed by means of multiple instruments. The results showed that uranium significantly migrated before hydrocarbon generation (Ro < 0.61%), with a leaching rate between 12.1% and 18.8%. The leaching rate of uranium during the hydrocarbon generation stage (0.63% < Ro < 1.35%) was relatively low, ranging from 0 to 7.2%. Cu, Pb, Zn, Mo, and other trace elements also migrated considerably during the early stage of thermal evolution, with leaching rates ranging from 2.9 ~ 11.6%. The yield of low-molecular-weight organic acids (LOAs) was the highest in the early stage of thermal maturity, and the LOA yield exhibited a good correlation with the leaching rates of Cu, Pb, Zn, Co, Mo, etc. The generation of LOAs from source rocks was conducive to the leaching and migration of trace elements. Moreover, according to a statistical analysis of published geochemical data, the total organic carbon (TOC) content, uranium content, and U/TOC ratio in shale decreased significantly with increasing burial depth, indicating that uranium migrated significantly upon kerogen hydrocarbon generation during thermal evolution. Therefore, uranium-rich shale is an important deep uranium source in sedimentary basins.

The role of hydrothermal alteration in uranium mineralization at the Xiaoshan uranium deposit, South China

Hydrothermal alteration can be utilized to constrain element migrations during mineralization, as it records the effects of fluid-rock interactions. Previous studies have suggested that uranium in deposits primarily originates from uranium-bearing granites; however, limited knowledge exists regarding the leaching mechamisms of this element and rare earth elements (REEs) from these rocks. In recent years, the Xiaoshan Deposit, a newly discovered medium-sized uranium deposit, has been discovered in the central part of the Lujing uranium ore field, South China. In this study, we examine this deposit to investigate hydrothermal alterations and their impact on elemental mass change. The deposit exhibits seven types of alteration including K-feldspar, albite, illite, sericite, muscovite, quartz and chlorite alteration. These alterations follow a certain sequence, starting from chlorite alteration, followed by widespread K-feldspar alteration, then to albite alteration, accompanied by muscovite alteration, and finally illite, sericite and quartz alteration. The main uranium mineralization stage was coeval with the late acid siliceous hydrothermal fluid, illite and sericite alteration. The pre-ore alkaline alteration (K-feldspar alteration) resulted in the leaching and extraction of uranium, leading to the precipitation of a significant amount of apatite in mineral interstices and initial uranium enrichment (ΔCi (U) = 16.52 ppm). This process facilitated material preparation for subsequent acidic alterations and localized ore enrichment. The original dense rock structure was disrupted, creating fractures/cavities that served as conduits for uranium mineralization. Moreover, under alkaline metasomatism, uranium and REEs was extensively leached out of uranium-bearing accessory minerals such as the apatite. According to apatite compositional variations and alteration geochemistry, these variations reveal the process of uranium dissolution, migration, and precipitation enrichment into ore bodies. Uranium was completely released during alkaline metasomatism, causing a sharp decline in U content from 53.1 ppm to 0.96 ppm. The formation of alkaline alteration fluids facilitates the extraction of uranium from the surrounding rocks (the Indosinian granite).

In situ U–Pb dating of dolomite: Reliable ages for sandstone-hosted uranium deposits in the southern Songliao Basin, NE China

In situ U–Pb dating of dolomite: Reliable ages for sandstone-hosted uranium deposits in the southern Songliao Basin, NE China

Assessment of contamination levels, potential ecological and human health risks due to trace elements pollution in the vicinity of the Lolodorf uranium deposit, Southern Cameroon.

The current study assessed the contamination levels and associated ecological and health risks due to hazardous trace elements in soils from Awanda and Mvengue, located in the vicinity of the Lolodorf uranium deposit in Southern Cameroon. Qualitative and quantitative analyses of the soil samples were performed using energy-dispersive X-ray spectrometry. The results indicated that the mean concentrations of metallic and trace elements in soil samples increased in the following order: U < As < Th < Pb < Cu < Ni < Zn < Cr < Mn < Fe < Al. The average concentrations of U, As, Th, Pb, Cu, Ni, Zn, Cr, Mn, Fe, and Al ranged between 0.9-3, 2.9-3.8, 9.2-15, 13.1-20.3, 11.5-42.5, 31.1-60.7, 42.9-91.6, 94.50-170.9, 100.45-500.57, 4874.8-88340 and 226147.5-324240.0mg/kg, respectively. The contamination levels of trace elements were assessed and the human health risk of chemical elements was determined. The investigated elements' average contamination factors (CF) results showed the highest mean CF recorded for Al followed by Cr, Th, Pb, Zn, Cu, Ni, Fe, U, Mn, and As. Furthermore, the findings showed that 90% of soil samples can be classified as considerably contaminated with Al, 100%, and 60% as moderately contaminated with Cr and Th, respectively. The Geo-accumulation indices of Mn, Cr, Th, U, Ni, Zn, Cu, As, and Pb were lower than 1, suggesting low contamination levels for these elements. The ecological factors and risk indices indicated a low ecological risk in the investigated area. In terms of human health risk, ingestion was identified as the primary pathway for both carcinogenic and non-carcinogenic risks, with children found to be more exposed to both risks than adults. Al, Cr, and Fe were found to be the main contributors to non-carcinogenic health risks, while Cr and Ni were the main contributors to carcinogenic health risks.

Petrological, mineralogical, carbonate C-O and sulfide S isotope study of the Bayinqinggeli sandstone-hosted uranium deposit in the northern Ordos Basin

Many sandstone-hosted uranium deposits have been discovered in the northern Ordos Basin, including the Bayinqinggeli deposit, exhibiting tremendous potential for uranium exploration and prospecting. This region is characterized by complex fluid activities, yet unknowns or controversies still exist regarding the source and properties of the fluids and their influence on uranium mineralization. In this study, we employed optical and scanning electron microscopy (SEM), X-ray diffraction (XRD), micro X-ray fluorescence (μ-XRF), C-O isotope of calcite, and in situ S isotope of pyrite, to investigate the genesis and evolution of the Bayinqinggeli deposit. Pyrite and calcite are closely associated with uranium minerals, and all exhibit distinct characteristics in rocks of varying grades. In high-grade mineralized rocks, ore-related pyrite, characterized by euhedral and colloidal forms, mainly predated uranium mineralization, evidenced by the extensive coffinite replacement. The mostly negative δ34S values with a broad range (−24.6 ‰ to 23.9 ‰; mean = −4.2 ‰) point to microbial sulfate reduction under restricted conditions. In low-grade and barren rocks, pyrite unrelated to mineralization, mainly as large granular or colloidal cement, shows generally positive δ34S values with a wide range (−49.5 ‰ to 67.4 ‰; mean = 15.3 ‰). This suggests the involvement of both biological and abiological processes during different stages, with the latter possibly associated with deep-sourced fluids. Considering the heterogeneous isotope compositions of sulfur in pyrite and carbon in calcite (δ13C ranging from −21.4 ‰ to −4.9 ‰), it can be deduced that the deposit was strongly affected by two types of fluids: (1) surface oxidizing fluids and (2) deep reducing fluids. The mineralizing fluids were derived from oxidizing surface water, which dissolved uranium ions, carbonates, and sulfates from weathered source rocks and during infiltration through the sandstone, resulting in the formation of abundant uranium minerals and associated pyrite and calcite. The presence of low δ13C calcite further corroborates the influence of deep hydrocarbon-bearing fluids, which played a protective role in post-ore stage preservation, corresponding to the widespread green alteration in the Lower Zhiluo formation. Overall, the development of sandstone-hosted uranium deposits is a continuous and progressive process, with early-formed mineralization being transformed by late-stage fluid events. Calcite has a significant impact on the formation, development, and extraction uranium ore in the deposit, protecting the paleo-orebodies against remobilization and remigration. A significant portion of uranium ore is preserved by calcite cementation. Therefore, the careful management of carbonates during in situ leaching is essential for the effective extraction of uranium from the host sandstone.

Spatial Distribution of Water Quality Parameters in a Mineralized Region of Rajasthan

Water quality parameters, anionic concentrations and uranium levels were measured in groundwater samples collected from Rohil, Sikar District, Rajasthan as a part of radiological baseline survey. This region hosts disseminated uranium deposits. The uranium concentration in water samples showed a mean value of 107 ± 141 μg/L and more than 40% samples crossed the AERB limit. The mean conductivity and TDS of samples were 2221 ± 1513 μS/cm and 1583 ± 1085 ppm, respectively. The mean value of fluoride, chloride, nitrate and sulphate were 2.4 ± 1.4 ppm, 414 ± 466 ppm, 33.70 ± 37.2 ppm and 140 ±133 ppm, respectively. Measured parameters in many samples were above the respective limits set by BIS, AERB and WHO. No particular trend was observed for any of the parameters with increasing distance from the proposed site and no correlation was evident in the measured parameters.

Geochemical modeling of U-Ni-Co-As transport and deposition in acidic basinal brines: Implications for unconformity-related U-(Ni-Co-As) mineralization in the Athabasca Basin (Canada)

The unconformity-related uranium (URU) deposits, which are best developed in the Proterozoic Athabasca Basin (Canada), can be divided into the monometallic (U) and polymetallic (U-Ni-Co-As) subtypes. Different models have been proposed to explain the formation of the two subtypes of URU deposits. The conventional “diagenetic-hydrothermal” model suggests that both subtypes formed from oxidizing, acidic basinal brines in a unified mineralization system, whereas a newly proposed model suggests that the polymetallic deposits formed from monometallic U deposits superimposed by Ni-Co-As mineralization. While the second model has been the subject of ongoing debates, there are also unanswered questions in the diagenetic-hydrothermal model; in particular, it remains unclear what geological factors controlled the formation of one subtype or another in a unified mineralization system. This paper aims to address this question with geochemical modeling of hydrothermal U-Ni-Co-As transport and deposition using the Geochemist's Workbench (GWB) software. The conditions for U-Ni-Co-As transport were examined with thermodynamic modeling. The results indicate that highly oxidizing (log fO2(g) > −25), acidic (pH = 3.5) brines can transport large amounts (>100 ppm) of U together with Ni-Co-As, whereas moderately oxidizing (−40 < log fO2(g) < −25), less acidic (3.5 < pH < 6) brines can transport only minor amounts (<1 ppm) of U while still capable of carrying large amounts (>100 ppm) of Ni-Co-As, and very reducing (log fO2(g) < −40) brines with pH from 3.5 to 6 can dissolve only minor amounts (<1 ppm) of U and Ni-Co-As. The mechanisms of U-Ni-Co-As deposition were examined with reaction path modeling involving fluid-rock interaction and fluid-fluid mixing. The results indicate that as a U-Ni-Co-As-bearing, acidic, oxidizing brine progressively reacts with basement rocks or mixes with a reducing fluid, U precipitates before Ni-Co-As in relation to pH increase and fO2(g) decrease. In the case of fluid mixing, while U precipitation can be caused by any of the reducing agents (CH4(aq), H2(aq), H2S(aq), and Fe2+(aq)) in the reducing fluids examined, Ni-Co-As deposition requires the participation of CH4(aq) or H2(aq). Based on the modeling results, it is inferred that U and Ni-Co-As were not transported by the same fluid, otherwise all the URU deposits would be polymetallic. The U was most likely derived from the basin rather than from the basement, because as oxidizing basinal brines infiltrate and interact with basement rocks, their ability to dissolve and transport U quickly diminishes due to fO2(g) decrease and pH increase. In contrast, as these basinal brines infiltrate the upper part of the basement, which is moderately oxidizing, they retain the ability to dissolve and transport significant amounts of Ni-Co-As, enabling the scavenging of these metals from the basement. While all URU mineralization requires U-bearing basinal brines and reducing agents, the formation of polymetallic (U-Ni-Co-As) deposits depends on the availability of Ni-Co-As-rich lithologies in the upper part of the basement, together with an ample supply of robust reducing agents, such as CH4 and H2 that were derived from the deeper part of the basement. Therefore, although the possibility that polymetallic U-Ni-Co-As deposits formed from Ni-Co-As mineralization superimposing on monometallic U deposits cannot be ruled out, the results of this study demonstrate that both polymetallic and monometallic URU deposits can be formed in a unified diagenetic-hydrothermal mineralization system in the Athabasca Basin.

Characterization of groundwater and cores in the decommissioned acid in-situ leach uranium mining area: Enlightenment for uranium contaminated groundwater remediation

Acid In-situ Leach (AISL) is predominant technique for uranium mining in sandstone-type deposits in China. However, its impact on the biogeochemical conditions of sandstone uranium deposits remains poorly understood. In this study, we performed detailed physicochemical analyses of groundwater, as well as mineralogical, chemical and biogeochemical analyses of cores collected from the decommissioned AISL uranium mining area in the Yili Basin, northwestern China. After AISL uranium mining, U(IV) minerals and pyrite were oxidized and dissolved. The groundwater in the AISL-mined uranium deposit (AISLMUD) became highly acidic and oxidizing after mining ceased. Pyrite, which significantly influences the migration, transformation and immobilization of uranium, was minimal in all cores. Kaolinite, chlorite, quartz, K-feldspar, albite and muscovite exhibited poor adsorption capacity of U(VI) under strong acid conditions. The AISLMUD demonstrated limited capacity to retain U(VI) under highly acid conditions. Furthermore, high-throughput sequencing analysis revealed a substantial reduction in both microbial diversity and abundance in the cores. Microorganisms associated with U(VI) reduction were detected in the cores, with the exception of sulfate reduction bacteria. However, the results of microbial incubation showed that U(VI) reduction-related bacteria could not be in-situ activated by the addition of electron donors under the environmental stresses induced by prolonged acid in-situ leaching. These findings cast doubt on the feasibility of remediating uranium-contaminated groundwater with a pH below 3 through in-situ activation of U(VI) reduction-related bacteria. This research holds significant implications for evaluating the suitability of existing methods and developing new approaches for the restoration of AISLMUD.

Mineralogical and radiological studies on some Paleozoic yellow ochre deposits in Southwestern Sinai, Egypt

Yellow ochre is the basic material used in the manufacture of yellow oxide (a commercial product). Yellow ochre samples were taken from three different formations in southwestern Sinai: Abu Hamata, Um Bogma, and Abu Zarab. Yellow ochre occasionally exists in Abu Hamata Formation particularly in El Ferah area, associated with Fe–Mn ore in Wadi El Sahu (Um Bogma Formation) and in Himayer area (Abu Zarab Formation). The XRD analysis of the raw material reveals that they are mainly composed of goethite, which is associated with quartz and kaolinite in El Ferah area, hematite, kaolinite and quartz in Himayer area, and kaolinite, gypsum and quartz in Wadi El Sahu. The commercial product is mainly composed of goethite, quartz, and calcite. The heavy mineral investigation shows that some yellow ochre samples contain zircon and rare earth sulfate which may be responsible for the radioactivity of ochre due to their thorium and uranium content. The average values of specific radio-activities of most radionuclides in the samples of Himayer area I and II, and El Sahu I are higher than the respective world averages, while their activities are lower in El Ferah and El Sahu II. Th/U and Ra/U ratios exhibit vigorous changes in physico-chemical conditions during uranium leaching and deposition. Most of the radiological parameters in the ferruginous sediment and commercial product samples from El Ferah, El Sahu II, and Himayer II are lower than the recommended international values but higher than those from Himayer I and El Sahu I samples. The plotted hierarchical cluster analysis (HCA) exhibits that the main contributors for the hazards of these sediments and their commercial product are 238U, 232Th and 226Ra in Himayer I &II, commercial products, and El Ferah area, 232Th and 226Ra in El Sahu II , 232Th, 40K and 226Ra in El Sahu I.

Unraveling the metallogenic mechanisms of uranium-rich ore bodies: Insights from Xinqiaoxi’s pitchblende geochronology and pyrite geochemistry

Granite-related uranium deposits are essential for the global uranium supply, with the uranium-rich ore bodies within these deposits being crucial to their value. However, the sources of uranium, fluid characteristics, and metallogenic mechanisms within these uranium-rich ore bodies remain unclear. In this study, we analyzed pitchblende and pyrite from the Xinqiaoxi uranium deposit to determine uranium age and clarify the mineralization of uranium-rich ore bodies. The pitchblende samples provided a U-Pb age of 58.5 ± 3 Ma (MSWD = 3.4), closely aligns with the mineralization ages in other uranium deposits within the Xiazhuang uranium ore-field. This consistency suggests a significant uranium mineralization event in South China during this period. The vein-like and concentric structure of the pitchblende, coupled with its enrichment in U, Sr, As, W, and Mo but depletion in Th, Pb, and REEs, indicates a strong association with hydrothermal activity. Moreover, its REE pattern closely resembles that of the host rock (Xiazhuang and Maofeng granites), suggesting the latter as a crucial uranium source. Pyrite and pitchblende are coeval, yet pyrite was formed slightly earlier than pitchblende. Pyrite exhibits depletion in Co and Ni but enrichment in As, along with high Co/Ni ratios ranging from 1.68 to 12.2, indicative of a medium- to low temperature hydrothermal genesis. Furthermore, the positive cerium (Ce) anomaly observed in pyrite may indicate elevated oxygen fugacity in the fluids during precipitation. The δ34S values of pyrite (−10.42 ‰ to −15.26 ‰, averaging −13.44 ‰) are consistent with those of the host rock (Xiazhuang and Maofeng granites), indicating a primary sulfur source from the host rock. Additionally, pyrite may serve as a reductant, facilitating the formation of uranium ore. Our proposed genetic model suggests that CO2-rich oxidizing fluids facilitate uranium leaching from host rocks, resulting in the formation of a uranium-enriched fluid that migrates along faults, where U6+ undergoes reduction to U4+ within secondary fracture zones, facilitated by reductants such as pyrite.

Occurrence and enrichment mechanism of uranium in the Yankong phosphorite-type uranium deposit, Northern Guizhou

Occurrence and enrichment mechanism of uranium in the Yankong phosphorite-type uranium deposit, Northern Guizhou

Framboidal pyrite in Dongsheng sandstone-hosted uranium deposit, northern Ordos Basin: Implications for fluid evolution and uranium mineralization

Occurrence characteristics, internal morphology patterns, size variations and trace elements contents for framboidal pyrite in the sandstone of middle Jurassic Zhiluo Formation hosting U deposit in the northern Ordos Basin collectively demonstrate three types of framboids: (i) Py1 is the synsedimentary origin, characterized by the close association with clay minerals, equal-sized microcrystals with globular or octahedral shape, the diameter of framboids and microcrystals ranging from 2.1 to 9.3 µm (mean = 5.9 µm) and from 0.1 to 1.4 µm (mean = 0.5 µm), respectively, and relatively low trace element contents (mean = 0.83 wt% of Co, Ni, As, Mo in total); (ii) Py2 is the early diagenetic origin, characterized by equal-sized pyritohedral microcrystals while other substance also occurs within the framboid, or non-uniform size and morphology of microcrystals with the diameter of framboids and microcrystals ranging from 7.3 to 26.3 µm (mean = 11.8 µm) and from 0.3 to 1.9 µm (mean = 0.8 µm), respectively, and similar trace element compositions with Py1; and (iii) Py3 is the U ore-stage origin, characterized by equal-sized cubic microcrystals in the loosely packed pattern with U-bearing minerals filling between microcrystals, the diameter of framboids and microcrystals ranging from 7.6 to 27.4 µm (mean = 15.9 µm) and from 0.7 to 3.2 µm (mean = 1.5 µm), respectively, and the highest trace element contents (mean = 1.07 wt% of Co, Ni, As, Mo and Se in total). During mineralization, Py1 and Py2 are dissolved by the interlayer oxidation fluid, providing S source and trace elements for the precipitation of Py3 with larger diameter. Its strong reducing ability, large specific surface area and abundant internal porosity facilitate the fixation of U in the interstices of Py3 through reduction or adsorption. Negative sulfur isotope compositions suggest biogenic redox processes for U mineralization. The formation and transformation relationship of different stages of framboidal pyrite indicates the complex evolution process of synsedimentary, early diagenetic and U ore-forming fluids.

3D Geological Modeling and Metallogenic Prediction of Kamust Sandstone-Type Uranium Deposit in the Eastern Junggar Basin, NW China

Sandstone-type uranium deposits hold significant value and promise within China’s uranium resource portfolio, with the majority of these deposits found at the junctions of basins and mountains within Mesozoic and Cenozoic basins. The Kamust uranium mining area, located in the eastern part of the Junggar Basin, represents a significant recent discovery. Prior research on this deposit has been confined to two-dimensional analyses, which pose limitations for a comprehensive understanding of the deposit’s three-dimensional characteristics. To address the issue of uranium resource reserve expansion, this study employs 3D geological modeling and visualization techniques, guided by uranium deposit models and mineral prediction methods. First, a 3D model database of the Kamust uranium deposit was constructed, comprising drill holes, uranium ore bodies, ore-controlling structures, interlayer oxidation zones, and provenance areas. This model enables a transparent and visual representation of the spatial distribution of favorable mineralization horizons, structures, stratigraphy, and other predictive elements in the mining area. Second, based on the three-dimensional geological model, a mineral prediction model was established by summarizing the regional mineralization mechanisms, ore-controlling factors, and exploration indicators. Combined with big-data technology, this approach facilitated the quantitative analysis and extraction of ore-controlling factors, providing data support for the three-dimensional quantitative prediction of deep mineralization in the Kamust uranium deposit. Finally, using three-dimensional weights of evidence and three-dimensional information-quantity methods, comprehensive information analysis and quantitative prediction of deep mineralization were conducted. One prospective area was quantitatively delineated, located east of the Kalasay monocline, which has been well-validated in geological understanding. The research indicates that the area east of the Kalasay monocline in the Kamust mining district has significant exploration potential.

Comprehensive Study on Hydrogeological Conditions and Suitability Evaluation of In Situ Leaching for Sandstone-Hosted Uranium Deposit in Erlian Basin

As a strategic mineral and energy resource, the enrichment and metallogenic mechanism of sandstone-hosted uranium deposits are highly dependent on hydrogeological conditions. However, the relationship between sandstone uranium mineralization and hydrogeological conditions has not received sufficient attention yet. The pumping test, hydrogeological parameters and hydrochemical characteristics were employed to analyze the change characteristics of hydrogeological conditions and evaluate the suitability of in situ leaching (ISL). The results showed that the study area in the Inner Mongolia Autonomous Region could be divided into two groundwater subsystems, namely Quanzha-Engeriyin and Luhai-Zhendai. The latter with relatively high water richness is confined and a main ore-bearing aquifer, which consists of four orebodies. The well discharge (Q) and hydraulic conductivity (K) of Orebody II ranged from 98.40 to 867.36 m3/d and 0.25 to 5.64 m/d, respectively, indicating the aquifer is suitable for the migration, enrichment and mineralization of uranium due to relatively high permeability and fast flow rate. The water storage of Orebodies III-IV gradually deteriorated from east to west in a stepped pattern. And the highest values of Q and K in Orebodies III-IV decreased from 1200 m3/d to 120 m3/d and 1.75 m/d to 0.035 m/d, respectively, suggesting these were conducive to a reduction in and accumulation of uranium under poor hydrodynamic conditions. Additionally, the study area would be defined as three grades, including favorable, relatively favorable and unfavorable areas of ISL according to a comprehensive evaluation. This study provided a scientific basis for evaluating the possibility of in situ leaching for sandstone-hosted uranium deposit.

Uranium isotopes and several heavy elements in selected waters in Quang Nam-Da Nang provinces, Central Vietnam

238U and 234U concentrations, 238U/234U ratios and Na, Ca, Mg, K, Al, As, Cd concentrations were measured in selected surface waters (streams, rivers and lakes), ground waters (dug wells) and underground waters (drill wells and thermal waters) in Quang Nam and Da Nang provinces, Central Vietnam. The mineralization was < 500 mg L−1 and Al, As, Cd contents were a few tenths of µg L−1. 234U and 238U activities were between 0.47–27.6 mBq L−1 and 0.6–15.0 mBq L−1 respectively, these values are lower than WHO recommended limits. Uranium contents trended as Urivers < Ustreams < Ulakes < Udig wells < Uthermal water < Udrill wells. The 234U/238U ratio ranged from 0.69 to 2.31 with 1.26 on average. For groundwaters, the ratio scattered around one. Effects of Nong Son uranium deposit located in Quang Nam region were not observed.

Study on precipitation and plugging mechanism in CO2 + O2 in-situ leaching of uranium in Nalinggou uranium deposit

Study on precipitation and plugging mechanism in CO2 + O2 in-situ leaching of uranium in Nalinggou uranium deposit

Quantifying element mass transfer in the Jiling Na-metasomatic hydrothermal uranium deposit, Northwest China

The Na-metasomatic hydrothermal uranium deposits are relatively widespread, low in grade (less than 1 % U3O8) but high in tonnage. Although it has been considered that this type of deposit was formed due to hydrothermal alteration unrelated to magmatic activity, the detailed evolution of fluids and ore-forming process are still not well understood. Through element-mass-balance calculation and geochemical mapping of regional rocks, we investigated the Jiling uranium deposit in northwestern China and evaluated the composition and source of fluids and element-transfer behavior through Na-metasomatism and uranium mineralization. The findings show that, in the early Na-metasomatism stage, the Na-, HFSE- and REE-rich late-magmatic hydrothermal fluids caused Na-metasomatism of wall rocks, enriching Na2O (>53 %) while removing K2O (<-78 %), depleting SiO2 (30 % in granite and 3 % in diorite), and massively mass-transferring Fe, Ti, P and some incompatible elements. With increased rock permeability and the formation of partial Fe2+-bearing minerals, the Na-metasomatic alteration produced reducing agents and migration channels for ore-forming fluids, as well as the creation of ∼ 15 vol% porosity in the altered granite for metallogenic space. In the late uranium mineralization stage, CO2-rich fluids extracted uranium and HREEs, converted Fe2+ to Fe3+, and subsequently precipitated uranium to form pitchblende with apatite, calcite and chlorite. Thus, the Na-metasomatic alteration caused by late-magmatic hydrothermal fluids is critical for the production of large Na-metasomatic hydrothermal uranium deposits. Our new geochemical mapping reveals that the mass-concentration changes of Na, K and Si are more credible to defining Na-metasomatic alteration, while Fe, Ti, P, ∑(Zr-Hf-Nb-Ta) and ∑LREE/∑HREE vary strikingly during the uranium mineralization process.

The genesis of intersection-type uranium deposits in south China: Insights from zircon and pitchblende U-Pb geochronology and pyrite sulfur isotopes of the Egongtang uranium deposit, southern Jiangxi

Intersection-type uranium deposits refer to the uranium deposits that are located at the intersection of mafic dykes and silicified faults and are an important type of granite-related uranium deposits in South China. However, the genesis of these deposits still remain poorly understood. The Egongtang uranium deposit is a typical intersection-type uranium deposit in the Huangsha uranium ore district (southern Jiangxi) that bears a number of NWW-trending mafic dykes, thus providing an excellent opportunity to study the genesis of intersection-type uranium deposits. In this study, the mineralization age and genesis of this deposit were constrained using in situ zircon and pitchblende U-Pb geochronology, whole-rock geochemistry, and pyrite sulfur isotope data. The zircon U-Pb dating constrains the crystallization ages of 240.4 ± 1.3 Ma and 160.7 ± 1.6 Ma for granites in the Huangsha ore district. The samples (including altered and unaltered) of the granites are characterized by variable whole-rock U contents of 5.8–14.1 ppm and Th/U ratios of 2.4–7.7, which favor the crystallization of uraninite in the granites and suggest U leaching from the granites during alteration. In situ U-Pb dating on pitchblende from the Egongtang uranium deposit yielded a lower intercept age of 89.8 ± 1.1 Ma, indicating that the uranium mineralization took place at the Late Cretaceous. Pyrite associated with pitchblende has δ34S values ranging from 1.6‰ to 3.8‰, suggesting a magmatic source. This study indicates that granites in this area might have represented the source of uranium for the Egongtang deposit, and that the uranium mineralization was probably related to the Late Cretaceous crustal extension in South China.

К истории открытия и изучения феномена Окло

The paper dwells on the brief history of the discovery and studies of the Oklo uranium deposit, a natural nuclear reactor, is considered. It was shown by French specialists in 1972. The discovery was made by studying the isotope ratio 235U§238U in ore. Several years earlier, such research was carried out at the All-Union Scientific Research Institute of Mineral Raw Materials (VIMS). Unfortunately, the application for the discovery of domestic scientists was rejected.

Classification of Logging Data Using Machine Learning Algorithms

A log data analysis plays an important role in the uranium mining process. Automating this analysis using machine learning methods improves the results and reduces the influence of the human factor. In particular, the identification of reservoir oxidation zones (ROZs) using machine learning allows a more accurate determination of ore reserves, and correct lithological classification allows the optimization of the mining process. However, training and tuning machine learning models requires labeled datasets, which are hardly available for uranium deposits. In addition, in problems of interpreting logging data using machine learning, data preprocessing is of great importance, in other words, a transformation of the original dataset that allows improving the classification or prediction result. This paper describes a uranium well log (UWL) dataset generated with the employment of floating data windows and designed to solve the problems of identifying ROZ and lithological classification (LC) on sandstone-type uranium deposits. Comparative results of the ways of solving these problems using classical machine learning methods and ensembles of machine learning algorithms are presented. It has been shown that an increase in the size of the floating data window can improve the quality of ROZ classification by 7–9% and LC by 6–12%. As a result, the best-quality indicators for solving these problems were obtained, f1_score_macro = 0.744 (ROZ) and accuracy = 0.694 (LC), using the light gradient boosting machine and extreme gradient boosting, respectively.