The study aims to investigate uranium species in the sediments of the natural-technogenic system within a sludge storage facility in Russia.The relevance of this work is underscored by the need to assess the geochemic...The study aims to investigate uranium species in the sediments of the natural-technogenic system within a sludge storage facility in Russia.The relevance of this work is underscored by the need to assess the geochemical mobility of radionuclides,a critical factor for predicting their migration and environmental impact.The objective of the research was to determine the uranium species in both peat and sedimentary rock samples of the sludge storage facility and the adjacent area.Laboratory analyses included XRD,XRF analysis using synchrotron radiation,and scanning electron microscopy to study the composition and properties of minerals.The uranium species were further identified using a modified Tessier sequential extraction method.The results revealed that uranium predominantly occurs in a stable silicate-bound form(up to 80%)in sedimentary rocks,indicating minimal geochemical mobility.In contrast,in peat deposits,uranium is primarily associated with manganese and iron oxides(30–60%)as well as organic matter(5–40%),with the most mobile forms constituting less than 5%.The decrease in uranium concentration with distance from the facility was attributed to sorption onto organic matter and co-precipitation with mineral compounds,manganese and iron oxides,which serve as effective natural sorbents.The findings highlight the critical role of organic matter and metal oxides in limiting uranium migration,thus identifying them as key components in the formation of natural barriers for radionuclides.These results are crucial for assessing environmental risks associated with radioactive waste management and for developing strategies to minimize the ecological impact of sludge storages.展开更多
Rapid adsorption of radioactive substances is of great significance in emergency situations.A novel approach combining S-defect introduction and in situ phosphorization was employed to synthesize phosphorized WS_(2)(W...Rapid adsorption of radioactive substances is of great significance in emergency situations.A novel approach combining S-defect introduction and in situ phosphorization was employed to synthesize phosphorized WS_(2)(WS_(2)-PO_(4))for ultra-efficient uranium extraction.At an initial U(VI)concentration of 50 mg·L^(-1),the adsorption of U(VI)by WS_(2)-PO_(4) nanosheets exceeds77%within just 1 min,with high selectivity(SU=78.7%)and good adsorption capacity of 268.82 mg·g^(-1).The phosphate groups have grown on the S defects and taken part in U(VI)extraction through surface complexation,leading to fast,reusable,and highly selective uranium adsorption,showing great potential in emergency treatment of radioactive nuclear wastewater.展开更多
The discharge of effluents containing uranium(U)ions into aquatic ecosystems poses significant risks to both human health and marine organisms.This study investigated the biosorption of U(VI)ions from aqueous solution...The discharge of effluents containing uranium(U)ions into aquatic ecosystems poses significant risks to both human health and marine organisms.This study investigated the biosorption of U(VI)ions from aqueous solutions using corncob-sodium alginate(SA)-immobilized Trichoderma aureoviride hyphal pellets.Experimental parameters,including initial solution pH,initial concentration,temperature,and contact time,were systematically examined to understand their influence on the bioadsorption process.Results showed that the corncob-SA-immobilized T.aureoviride hyphal pellets exhibited maximum uranium biosorption capacity at an initial pH of 6.23 and a contact time of 12 h.The equilibrium data aligned with the Langmuir isotherm model,with a maximum biosorption capacity of 105.60 mg/g at 301 K.Moreover,biosorption kinetics followed the pseudo-second-order kinetic model.In terms of thermodynamic parameters,the changes in Gibbs-free energy(△G°)were determined to be-4.29 kJ/mol at 301 K,the changes in enthalpy(△H°)were 46.88 kJ/mol,and the changes in entropy(△S°)was 164.98 J/(mol·K).Notably,the adsorbed U(VI)could be efficiently desorbed using Na_(2)CO_(3),with a maximum readsorption efficiency of 53.6%.Scanning electron microscopic(SEM)analysis revealed U(VI)ion binding onto the hyphal pellet surface.This study underscores the efficacy of corncob-SA-immobilized T.aureoviride hyphal pellets as a cost-effective and environmentally favorable biosorbent material for removing U(VI)from aquatic ecosystems.展开更多
It has been shown that the age of minerals in which U±Th are a major(e.g.,uraninite,pitchblende and thorite)or minor(e.g.,monazite,xenotime)component can be calculated from the concentrations of U±Th and Pb ...It has been shown that the age of minerals in which U±Th are a major(e.g.,uraninite,pitchblende and thorite)or minor(e.g.,monazite,xenotime)component can be calculated from the concentrations of U±Th and Pb rather than their isotopes,and such ages are referred to as chemical ages.Although equations for calculating the chemical ages have been well established and various computation programs have been reported,there is a lack of software that can not only calculate the chemical ages of individual analytical points but also provide an evaluation of the errors of individual ages as well as the whole dataset.In this paper,we develop a software for calculating and assessing the chemical ages of uranium minerals(CAUM),an open-source Python-based program with a friendly Graphical User Interface(GUI).Electron probe microanalysis(EPMA)data of uranium minerals are first imported from Excel files and used to calculate the chemical ages and associated errors of individual analytical points.The age data are then visualized to aid evaluating if the dataset comprises one or multiple populations and whether or not there are meaningful correlations between the chemical ages and impurities.Actions can then be taken to evaluate the errors within individual populations and the significance of the correlations.The use of the software is demonstrated with examples from published data.展开更多
Fast development of nuclear power plants requires sustainable support of uranium for nuclear fuel.Uranium is the most critical radionuclide to prepare nuclear fuel.However,the extraction of low concentration of uraniu...Fast development of nuclear power plants requires sustainable support of uranium for nuclear fuel.Uranium is the most critical radionuclide to prepare nuclear fuel.However,the extraction of low concentration of uranium in uranium ore or complex systems needs highly efficient selective binding of uranium in the presence of other competing metal ions.The excellent oxidative capacity of excited*UO_(2)^(2+)active species makes uranyl-based materials high photocatalytic performance in phototransformation of organic chemicals into high valuable products under visible light irradiation.In this mini review,the selective preconcentration of uranium through photocatalytic and electrocatalytic strategies was mainly described.The application of uranyl-based materials in photocatalytic conversion and degradation of organic pollutants was summarized.This review reports the utilization of uranium from its first step(i.e.,extraction of uranium for nuclear fuel supply)to its last additional application(i.e.,uranyl-based materials as photocatalysts in transformation and conversion of organic pollutants for environmental pollution treatment)from the viewpoint of“turning uranium wastes into treasure,from waste recycling to reutilization.”In the end of this review,the challenges and perspectives of uranium separation and catalytic properties were described.展开更多
Prompt fission neutron uranium logging(PFNUL)is an advanced method for utilizing pulsed neutron bombardment of the ore layer and a fission reaction with uranium(^(235)U)to detect the transient neutrons produced by fis...Prompt fission neutron uranium logging(PFNUL)is an advanced method for utilizing pulsed neutron bombardment of the ore layer and a fission reaction with uranium(^(235)U)to detect the transient neutrons produced by fission and then directly measure and quantify uranium;however,the stability and lifetime performance of pulsed neutron sources are the key constraints to its rapid promotion.To address these problems,this study proposes a PFNUL technique for acquiring the time spectrum of dual-energy neutrons(epithermal and thermal neutrons)from the upper and lower detection structures and establishes a novel uranium quantification algorithm based on the ratio of epithermal and thermal neutron time windows(E/T)via a mathematical-physical modeling derivation.Through simulations on well-logging models with di erent uranium contents,the starting and stopping times of the time window(Δt)for uranium quantification in the dual-energy neutron time spectrum are determined to be 200 and 800μs,respectively.The minimum radius and height of the model wells are 60 and 120 cm,respectively,and the E/T values in the time window show an excellent linear relationship with the uranium content.The scale factor is K_(E/T)=1.92 and R^(2)=0.999,which verifies the validity of the E/T uranium quantification algorithm.In addition,experiments were carried out in the Nu series of uranium standard model wells,and the results showed that under di erent neutron source yields,the E/T-based uranium quantification method reduced the relative standard deviation of the scale factor of the uranium content from 33.41%to 1.09%,compared with a single epithermal neutron quantification method.These results prove that the E/T value uranium quantification method is una ected by the change in the neutron source yield,e ectively improves the accuracy and service life of the logging instrument,and has great scientific and popularization value.展开更多
The study of uranium isotopes plays a crucial role in advancing our knowledge of nuclear physics,particularly in the realm of isospin and exotic nuclei.This study focused on the ground-state properties of uranium isot...The study of uranium isotopes plays a crucial role in advancing our knowledge of nuclear physics,particularly in the realm of isospin and exotic nuclei.This study focused on the ground-state properties of uranium isotopes ranging from A=203 to A=305.The key physical quantities examined included binding energy,quadrupole deformation,isotopic displacement,single-particle energy levels,and nucleon density distributions.Recent experimental advancements in uranium isotope studies have emphasized the indispensable role of theoretical models in interpreting experimental data.Moreover,the industrial applications of uranium—especially in nuclear energy production and weapons development—underscore the importance and necessity of accurate theoretical insights.The framework of the finite-range droplet model(FRDM)was utilized for comparative analysis because its predictions closely align with the experimental results.Through an analysis of the single-particle energy levels and continuous-state occupancy,this study identified 207 U as the proton drip line nucleus.This research not only deepens our understanding of uranium isotopes but also provides a solid theoretical foundation to guide future experimental investigations.展开更多
Uranium extraction from seawater(UES)is crucial for reducing nuclear fuel supply pressure and promoting the comprehensive utilization of marine resources.The successful implementations of UES engineering critically re...Uranium extraction from seawater(UES)is crucial for reducing nuclear fuel supply pressure and promoting the comprehensive utilization of marine resources.The successful implementations of UES engineering critically rely on the highly efficient sorbent materials with exceptional performance in binding uranyl ions.Herein,a universal and facile“organic ion building blocks self-assembly”strategy is established to realize a first class of carboxyl functionalized ionic single crystals,named BPTC-BPY-R(R=1–6,the R corresponds to alkyl chain length modifier,e.g.,R=1 corresponds to iodomethane derivatives,R=2 corresponds to bromoethane derivatives,etc.),derived from rationally designed viologen-derivatives with different alkyl chain lengths and polycarboxylic acid.This strategy effectively exploits the organic ion building block properties to achieve U(VI)adsorption based on the synergistic effects of anions(ligand interaction)and cations(electrostatic interaction).Notably,attributed to the special crystal stacking mode and higher specific surface area,the resulting BPTC-BPY-3 not only achieves ultrahigh selectivity for U(VI)adsorption with a partition coefficient of 3.998×10^(6) mL/g,but also possesses an ultrafast U(VI)adsorption kinetics and an uptake capacity of 686.8 mg/g within 2 min.More importantly,it realizes a U(VI)uptake capacity of 7.41 mg/g from natural seawater in 20 days.The designed material with ultra-selectivity,high capacity,ultrafast kinetics,and good recyclability exhibits a great promise for efficient U(VI)extraction from seawater.展开更多
The Erlian Basin is one of the most important multi-energy basins in China.The Baiyanhua area of the Chuanjing depression in the western Erlian Basin has recently become a favorable area for new progress in sandstone-...The Erlian Basin is one of the most important multi-energy basins in China.The Baiyanhua area of the Chuanjing depression in the western Erlian Basin has recently become a favorable area for new progress in sandstone-type uranium prospecting.However,the Cretaceous source-to-sink evolution of the Chuanjing depression in the Erlian Basin is poorly known.This paper presents the systematic geochemical and zircon U-Pb studies on the Saihantala Formation and Erlian Formation in the Baiyanhua area.The data obtained are functionally important for revealing the provenance and tectonic setting of the source rocks.The results show that the upper part of the Saihantala Formation and the lower part of the Erlian Formation are mainly composed of felsic sedimentary rocks.The source rocks originated from a continental margin arc environment in terms of tectonic setting.The detrital zircons ages have the dominant populations at ca.250-270 Ma,with two subdominant age groups at ca.1400-1800 and 1900-2100 Ma,respectively.Combined with the tectono-sedimentary evolution of the Chuanjing depression,we conclude that:(1)the provenance of the Cretaceous strata was mostly sourced from the Baiyanhua uplift;(2)the water depth became shallow in the Southern Sangendalai sag during the middle period of Saihantala,further preventing the formation of coal beds;(3)the formation of Baiyanhua uplift might provide the beneficial tectonic condition for uranium mineralization in the upper Saihantala Formation in southern Sangendalai sag.This is significant for us to understand the space allocation of coal and uranium in Chuanjing depression and evaluate the uranium metallogenic prospects in southern Sangendalai sag.展开更多
Objective To explore the protective effects and underlying mechanisms of H_(2)S against lipid peroxidation-mediated carbonyl stress in the uranium-treated NRK-52E cells.Methods Cell viability was evaluated using CCK-8...Objective To explore the protective effects and underlying mechanisms of H_(2)S against lipid peroxidation-mediated carbonyl stress in the uranium-treated NRK-52E cells.Methods Cell viability was evaluated using CCK-8 assay. Apoptosis was measured using flow cytometry. Reagent kits were used to detect carbonyl stress markers malondialdehyde, 4-hydroxynonenal, thiobarbituric acid reactive substances, and protein carbonylation. Aldehyde-protein adduct formation and alcohol dehydrogenase, aldehyde dehydrogenase 2, aldo-keto reductase, nuclear factor E2-related factor 2(Nrf2), and cystathionine β-synthase(CBS) expression were determined using western blotting or real-time PCR. Sulforaphane(SFP) was used to activate Nrf2. RNA interference was used to inhibit CBS expression.Results GYY4137(an H_(2)S donor) pretreatment significantly reversed the uranium-induced increase in carbonyl stress markers and aldehyde-protein adducts. GYY4137 effectively restored the uraniumdecreased Nrf2 expression, nuclear translocation, and ratio of nuclear to cytoplasmic Nrf2, accompanied by a reversal of the uranium-decreased expression of CBS and aldehyde-metabolizing enzymes. The application of CBS siRNA efficiently abrogated the SFP-enhanced effects on the expression of CBS, Nrf2 activation, nuclear translocation, and ratio of nuclear to cytoplasmic Nrf2 and concomitantly reversed the SFP-enhanced effects of the uranium-induced mRNA expression of aldehyde-metabolizing enzymes.Simultaneously, CBS siRNA reversed the SFP-mediated alleviation of the uranium-induced increase in reactive aldehyde levels, apoptosis rates, and uranium-induced cell viability.Conclusion H_(2)S induces Nrf2 activation and nuclear translocation, which modulates the expression of aldehyde-metabolizing enzymes and the CBS/H_(2)S axis. Simultaneously, the Nrf2-controlled CBS/H_(2)S axis may at least partially promote Nrf2 activation and nuclear translocation. These events form a cycleregulating mode through which H_(2)S attenuates the carbonyl stress-mediated NRK-52E cytotoxicity triggered by uranium.展开更多
Urchin-like W_(18)O_(49),with a large specific surface area(113.738 m^(2)g^(-1))and abundant oxygen vacancies(OVs),was prepared using an active sites tuning and microstructure engineering method.This material was appl...Urchin-like W_(18)O_(49),with a large specific surface area(113.738 m^(2)g^(-1))and abundant oxygen vacancies(OVs),was prepared using an active sites tuning and microstructure engineering method.This material was applied for U(Ⅵ)adsorption for the first time,demonstrating a high adsorption capacity of 567.55 mg g^(-1),which exceeds that of most inorganic adsorbents.Characterization via active site masking experiments and theoretical calculations,etc.,indicated that the excellent adsorption performance toward U(Ⅵ)was due to strong complexation between UO_(2)^(2+)and W–O bond of W_(18)O_(49),facile oxygen vacancy adsorption,and interface electron transfer from W^(5+)to UO_(2)^(2+),which acted as a reducing agent,partially converting U(Ⅵ)to U(IV).Furthermore,W_(18)O_(49)exhibited practical applicability with a removal rate exceeding 82%after 5 cycles,a 92.79%removal rate for real uranium-containing wastewater,and a high uranium recovery rate of 75.96%.Additionally,the synergistic adsorption-photocatalytic effect significantly enhanced U(Ⅵ)extraction,reaching an extraction capacity of 988.0mg g^(-1).This work provides a promising strategy for developing highly efficient U(Ⅵ)WO_(3)-based adsorbents.展开更多
0 INTRODUCTION The Haidewula uranium deposit is located in the Haidewula volcanic basin,which hosts a suite of basic,intermediate to felsic volcanic and subvolcanic rocks,including basalt,trachyte,trachyandesite.Previ...0 INTRODUCTION The Haidewula uranium deposit is located in the Haidewula volcanic basin,which hosts a suite of basic,intermediate to felsic volcanic and subvolcanic rocks,including basalt,trachyte,trachyandesite.Previous geochronological studies of the intrusions within this volcanic basin suggest that they primarily formed during the Silurian and Triassic periods(Dai et al.,2025;Sun et al.,2024;Wang et al.,2024;Zhu et al.,2022;Lei et al.,2021).展开更多
基金supported by the Russian Science Foundation grant number 23-27-00362,https://rscf.ru/en/project/23-27-00362/.
文摘The study aims to investigate uranium species in the sediments of the natural-technogenic system within a sludge storage facility in Russia.The relevance of this work is underscored by the need to assess the geochemical mobility of radionuclides,a critical factor for predicting their migration and environmental impact.The objective of the research was to determine the uranium species in both peat and sedimentary rock samples of the sludge storage facility and the adjacent area.Laboratory analyses included XRD,XRF analysis using synchrotron radiation,and scanning electron microscopy to study the composition and properties of minerals.The uranium species were further identified using a modified Tessier sequential extraction method.The results revealed that uranium predominantly occurs in a stable silicate-bound form(up to 80%)in sedimentary rocks,indicating minimal geochemical mobility.In contrast,in peat deposits,uranium is primarily associated with manganese and iron oxides(30–60%)as well as organic matter(5–40%),with the most mobile forms constituting less than 5%.The decrease in uranium concentration with distance from the facility was attributed to sorption onto organic matter and co-precipitation with mineral compounds,manganese and iron oxides,which serve as effective natural sorbents.The findings highlight the critical role of organic matter and metal oxides in limiting uranium migration,thus identifying them as key components in the formation of natural barriers for radionuclides.These results are crucial for assessing environmental risks associated with radioactive waste management and for developing strategies to minimize the ecological impact of sludge storages.
基金supported by the National Key Laboratory of Uranium Resources Exploration-Mining and Nuclear Remote Sensing(No.2024QZ-KF-05)the National Natural Science Foundation of China(Nos.U24A20194,22366006)+2 种基金Key R&D Program of Jiangxi Province(No.20243BBG71020)Natural Science Foundation of Jiangxi province(Nos.20224BAB213027,20242BAB20109)the Academic and Technical Leaders Training Program of Jiangxi Province(Nos.20212BCJL23046,20212BCJL23047)。
文摘Rapid adsorption of radioactive substances is of great significance in emergency situations.A novel approach combining S-defect introduction and in situ phosphorization was employed to synthesize phosphorized WS_(2)(WS_(2)-PO_(4))for ultra-efficient uranium extraction.At an initial U(VI)concentration of 50 mg·L^(-1),the adsorption of U(VI)by WS_(2)-PO_(4) nanosheets exceeds77%within just 1 min,with high selectivity(SU=78.7%)and good adsorption capacity of 268.82 mg·g^(-1).The phosphate groups have grown on the S defects and taken part in U(VI)extraction through surface complexation,leading to fast,reusable,and highly selective uranium adsorption,showing great potential in emergency treatment of radioactive nuclear wastewater.
基金supported by the National Natural Science Foundation of China(Grant No.21968001).
文摘The discharge of effluents containing uranium(U)ions into aquatic ecosystems poses significant risks to both human health and marine organisms.This study investigated the biosorption of U(VI)ions from aqueous solutions using corncob-sodium alginate(SA)-immobilized Trichoderma aureoviride hyphal pellets.Experimental parameters,including initial solution pH,initial concentration,temperature,and contact time,were systematically examined to understand their influence on the bioadsorption process.Results showed that the corncob-SA-immobilized T.aureoviride hyphal pellets exhibited maximum uranium biosorption capacity at an initial pH of 6.23 and a contact time of 12 h.The equilibrium data aligned with the Langmuir isotherm model,with a maximum biosorption capacity of 105.60 mg/g at 301 K.Moreover,biosorption kinetics followed the pseudo-second-order kinetic model.In terms of thermodynamic parameters,the changes in Gibbs-free energy(△G°)were determined to be-4.29 kJ/mol at 301 K,the changes in enthalpy(△H°)were 46.88 kJ/mol,and the changes in entropy(△S°)was 164.98 J/(mol·K).Notably,the adsorbed U(VI)could be efficiently desorbed using Na_(2)CO_(3),with a maximum readsorption efficiency of 53.6%.Scanning electron microscopic(SEM)analysis revealed U(VI)ion binding onto the hyphal pellet surface.This study underscores the efficacy of corncob-SA-immobilized T.aureoviride hyphal pellets as a cost-effective and environmentally favorable biosorbent material for removing U(VI)from aquatic ecosystems.
基金supported by the Natural Science Foundation Program of China(42173072,41503037,U1967207)Postgraduate Innovative Cultivation Program(CDUT2023BJCX013)Uranium Resources Exploration and Exploitation Innovation Center&and Everest Scientific Research Program(CDUT).
文摘It has been shown that the age of minerals in which U±Th are a major(e.g.,uraninite,pitchblende and thorite)or minor(e.g.,monazite,xenotime)component can be calculated from the concentrations of U±Th and Pb rather than their isotopes,and such ages are referred to as chemical ages.Although equations for calculating the chemical ages have been well established and various computation programs have been reported,there is a lack of software that can not only calculate the chemical ages of individual analytical points but also provide an evaluation of the errors of individual ages as well as the whole dataset.In this paper,we develop a software for calculating and assessing the chemical ages of uranium minerals(CAUM),an open-source Python-based program with a friendly Graphical User Interface(GUI).Electron probe microanalysis(EPMA)data of uranium minerals are first imported from Excel files and used to calculate the chemical ages and associated errors of individual analytical points.The age data are then visualized to aid evaluating if the dataset comprises one or multiple populations and whether or not there are meaningful correlations between the chemical ages and impurities.Actions can then be taken to evaluate the errors within individual populations and the significance of the correlations.The use of the software is demonstrated with examples from published data.
基金support from the National Natural Science Foundation of China(Nos.U24B20195,U23A20105,U2341289,22341602,22327807)was acknowledged.
文摘Fast development of nuclear power plants requires sustainable support of uranium for nuclear fuel.Uranium is the most critical radionuclide to prepare nuclear fuel.However,the extraction of low concentration of uranium in uranium ore or complex systems needs highly efficient selective binding of uranium in the presence of other competing metal ions.The excellent oxidative capacity of excited*UO_(2)^(2+)active species makes uranyl-based materials high photocatalytic performance in phototransformation of organic chemicals into high valuable products under visible light irradiation.In this mini review,the selective preconcentration of uranium through photocatalytic and electrocatalytic strategies was mainly described.The application of uranyl-based materials in photocatalytic conversion and degradation of organic pollutants was summarized.This review reports the utilization of uranium from its first step(i.e.,extraction of uranium for nuclear fuel supply)to its last additional application(i.e.,uranyl-based materials as photocatalysts in transformation and conversion of organic pollutants for environmental pollution treatment)from the viewpoint of“turning uranium wastes into treasure,from waste recycling to reutilization.”In the end of this review,the challenges and perspectives of uranium separation and catalytic properties were described.
基金supported by the National Natural Science Foundation of China(No.42374226)Jiangxi Provincial Natural Science Foundation(Nos.20232BAB201043,gpyc20240073,and 20232BCJ23006)+2 种基金Nuclear Energy Development Project(20201192-01)Fundamental Science on Radioactive Geology and Exploration Technology Laboratory(2022RGET20)National Key Laboratory of Uranium Resource Exploration-Mining and Nuclear Remote Sensing(ECUT)(2024QZ-TD-09)。
文摘Prompt fission neutron uranium logging(PFNUL)is an advanced method for utilizing pulsed neutron bombardment of the ore layer and a fission reaction with uranium(^(235)U)to detect the transient neutrons produced by fission and then directly measure and quantify uranium;however,the stability and lifetime performance of pulsed neutron sources are the key constraints to its rapid promotion.To address these problems,this study proposes a PFNUL technique for acquiring the time spectrum of dual-energy neutrons(epithermal and thermal neutrons)from the upper and lower detection structures and establishes a novel uranium quantification algorithm based on the ratio of epithermal and thermal neutron time windows(E/T)via a mathematical-physical modeling derivation.Through simulations on well-logging models with di erent uranium contents,the starting and stopping times of the time window(Δt)for uranium quantification in the dual-energy neutron time spectrum are determined to be 200 and 800μs,respectively.The minimum radius and height of the model wells are 60 and 120 cm,respectively,and the E/T values in the time window show an excellent linear relationship with the uranium content.The scale factor is K_(E/T)=1.92 and R^(2)=0.999,which verifies the validity of the E/T uranium quantification algorithm.In addition,experiments were carried out in the Nu series of uranium standard model wells,and the results showed that under di erent neutron source yields,the E/T-based uranium quantification method reduced the relative standard deviation of the scale factor of the uranium content from 33.41%to 1.09%,compared with a single epithermal neutron quantification method.These results prove that the E/T value uranium quantification method is una ected by the change in the neutron source yield,e ectively improves the accuracy and service life of the logging instrument,and has great scientific and popularization value.
基金supported by the National Natural Science Foundation of China(Nos.12175170 and 11675066)。
文摘The study of uranium isotopes plays a crucial role in advancing our knowledge of nuclear physics,particularly in the realm of isospin and exotic nuclei.This study focused on the ground-state properties of uranium isotopes ranging from A=203 to A=305.The key physical quantities examined included binding energy,quadrupole deformation,isotopic displacement,single-particle energy levels,and nucleon density distributions.Recent experimental advancements in uranium isotope studies have emphasized the indispensable role of theoretical models in interpreting experimental data.Moreover,the industrial applications of uranium—especially in nuclear energy production and weapons development—underscore the importance and necessity of accurate theoretical insights.The framework of the finite-range droplet model(FRDM)was utilized for comparative analysis because its predictions closely align with the experimental results.Through an analysis of the single-particle energy levels and continuous-state occupancy,this study identified 207 U as the proton drip line nucleus.This research not only deepens our understanding of uranium isotopes but also provides a solid theoretical foundation to guide future experimental investigations.
基金supported by the National Natural Science Foundation of China(No.22374159)the Youth Innovation Promotion Association CAS(No.2021420).
文摘Uranium extraction from seawater(UES)is crucial for reducing nuclear fuel supply pressure and promoting the comprehensive utilization of marine resources.The successful implementations of UES engineering critically rely on the highly efficient sorbent materials with exceptional performance in binding uranyl ions.Herein,a universal and facile“organic ion building blocks self-assembly”strategy is established to realize a first class of carboxyl functionalized ionic single crystals,named BPTC-BPY-R(R=1–6,the R corresponds to alkyl chain length modifier,e.g.,R=1 corresponds to iodomethane derivatives,R=2 corresponds to bromoethane derivatives,etc.),derived from rationally designed viologen-derivatives with different alkyl chain lengths and polycarboxylic acid.This strategy effectively exploits the organic ion building block properties to achieve U(VI)adsorption based on the synergistic effects of anions(ligand interaction)and cations(electrostatic interaction).Notably,attributed to the special crystal stacking mode and higher specific surface area,the resulting BPTC-BPY-3 not only achieves ultrahigh selectivity for U(VI)adsorption with a partition coefficient of 3.998×10^(6) mL/g,but also possesses an ultrafast U(VI)adsorption kinetics and an uptake capacity of 686.8 mg/g within 2 min.More importantly,it realizes a U(VI)uptake capacity of 7.41 mg/g from natural seawater in 20 days.The designed material with ultra-selectivity,high capacity,ultrafast kinetics,and good recyclability exhibits a great promise for efficient U(VI)extraction from seawater.
基金funded by the project initiated by the China Geological Survey“Investigation of sandstone-type uranium deposits in the Ordos and Qaidam Basins”(No.DD20190119)the National Key Research and Development Project(No.2018YFC0604200)from the Ministry of Science and Technology of the International Geoscience Programme(No.IGCP675),which is a joint endeavor of UNESCO and IUGS。
文摘The Erlian Basin is one of the most important multi-energy basins in China.The Baiyanhua area of the Chuanjing depression in the western Erlian Basin has recently become a favorable area for new progress in sandstone-type uranium prospecting.However,the Cretaceous source-to-sink evolution of the Chuanjing depression in the Erlian Basin is poorly known.This paper presents the systematic geochemical and zircon U-Pb studies on the Saihantala Formation and Erlian Formation in the Baiyanhua area.The data obtained are functionally important for revealing the provenance and tectonic setting of the source rocks.The results show that the upper part of the Saihantala Formation and the lower part of the Erlian Formation are mainly composed of felsic sedimentary rocks.The source rocks originated from a continental margin arc environment in terms of tectonic setting.The detrital zircons ages have the dominant populations at ca.250-270 Ma,with two subdominant age groups at ca.1400-1800 and 1900-2100 Ma,respectively.Combined with the tectono-sedimentary evolution of the Chuanjing depression,we conclude that:(1)the provenance of the Cretaceous strata was mostly sourced from the Baiyanhua uplift;(2)the water depth became shallow in the Southern Sangendalai sag during the middle period of Saihantala,further preventing the formation of coal beds;(3)the formation of Baiyanhua uplift might provide the beneficial tectonic condition for uranium mineralization in the upper Saihantala Formation in southern Sangendalai sag.This is significant for us to understand the space allocation of coal and uranium in Chuanjing depression and evaluate the uranium metallogenic prospects in southern Sangendalai sag.
基金supported by the National Natural Science Foundation of China(No.82160627)the Natural Science Foundation of the Guangxi Autonomous Region(No.2020GXNFSAA297262)。
文摘Objective To explore the protective effects and underlying mechanisms of H_(2)S against lipid peroxidation-mediated carbonyl stress in the uranium-treated NRK-52E cells.Methods Cell viability was evaluated using CCK-8 assay. Apoptosis was measured using flow cytometry. Reagent kits were used to detect carbonyl stress markers malondialdehyde, 4-hydroxynonenal, thiobarbituric acid reactive substances, and protein carbonylation. Aldehyde-protein adduct formation and alcohol dehydrogenase, aldehyde dehydrogenase 2, aldo-keto reductase, nuclear factor E2-related factor 2(Nrf2), and cystathionine β-synthase(CBS) expression were determined using western blotting or real-time PCR. Sulforaphane(SFP) was used to activate Nrf2. RNA interference was used to inhibit CBS expression.Results GYY4137(an H_(2)S donor) pretreatment significantly reversed the uranium-induced increase in carbonyl stress markers and aldehyde-protein adducts. GYY4137 effectively restored the uraniumdecreased Nrf2 expression, nuclear translocation, and ratio of nuclear to cytoplasmic Nrf2, accompanied by a reversal of the uranium-decreased expression of CBS and aldehyde-metabolizing enzymes. The application of CBS siRNA efficiently abrogated the SFP-enhanced effects on the expression of CBS, Nrf2 activation, nuclear translocation, and ratio of nuclear to cytoplasmic Nrf2 and concomitantly reversed the SFP-enhanced effects of the uranium-induced mRNA expression of aldehyde-metabolizing enzymes.Simultaneously, CBS siRNA reversed the SFP-mediated alleviation of the uranium-induced increase in reactive aldehyde levels, apoptosis rates, and uranium-induced cell viability.Conclusion H_(2)S induces Nrf2 activation and nuclear translocation, which modulates the expression of aldehyde-metabolizing enzymes and the CBS/H_(2)S axis. Simultaneously, the Nrf2-controlled CBS/H_(2)S axis may at least partially promote Nrf2 activation and nuclear translocation. These events form a cycleregulating mode through which H_(2)S attenuates the carbonyl stress-mediated NRK-52E cytotoxicity triggered by uranium.
基金financially supported by the National Natural Science Foundation of China(Nos.22366004 and 42302293)the National Key Laboratory of Uranium Resources Exploration-Mining and Nuclear Remote Sensing Independent Project(No.2024QZ-TD-19)+2 种基金the Key R&D Plan of Jiangxi Province(No.20212BBG71011)China Uranium Corporation Limited-East China University of Technology State Key Laboratory of Nuclear Resources and Environment Joint Innovation Fund(No.2023NRE-LH-19)the Innovation Special Fund Project of Graduate Student in East China University of Technology(No.DHYC-202414)
文摘Urchin-like W_(18)O_(49),with a large specific surface area(113.738 m^(2)g^(-1))and abundant oxygen vacancies(OVs),was prepared using an active sites tuning and microstructure engineering method.This material was applied for U(Ⅵ)adsorption for the first time,demonstrating a high adsorption capacity of 567.55 mg g^(-1),which exceeds that of most inorganic adsorbents.Characterization via active site masking experiments and theoretical calculations,etc.,indicated that the excellent adsorption performance toward U(Ⅵ)was due to strong complexation between UO_(2)^(2+)and W–O bond of W_(18)O_(49),facile oxygen vacancy adsorption,and interface electron transfer from W^(5+)to UO_(2)^(2+),which acted as a reducing agent,partially converting U(Ⅵ)to U(IV).Furthermore,W_(18)O_(49)exhibited practical applicability with a removal rate exceeding 82%after 5 cycles,a 92.79%removal rate for real uranium-containing wastewater,and a high uranium recovery rate of 75.96%.Additionally,the synergistic adsorption-photocatalytic effect significantly enhanced U(Ⅵ)extraction,reaching an extraction capacity of 988.0mg g^(-1).This work provides a promising strategy for developing highly efficient U(Ⅵ)WO_(3)-based adsorbents.
基金financially supported by projects from the National Natural Science Foundation of China(No.42321001)the Qinghai Provincial Department of Science and Technology Key R&D Project(No.2025-SF-141)+1 种基金the Qinghai“Kunlun Talent”Program(Qing RC Talent Zi(2024)No.1)the Academician Zhao Pengda Innovation Center in Qinghai Geological Bureau of Nuclear Industry。
文摘0 INTRODUCTION The Haidewula uranium deposit is located in the Haidewula volcanic basin,which hosts a suite of basic,intermediate to felsic volcanic and subvolcanic rocks,including basalt,trachyte,trachyandesite.Previous geochronological studies of the intrusions within this volcanic basin suggest that they primarily formed during the Silurian and Triassic periods(Dai et al.,2025;Sun et al.,2024;Wang et al.,2024;Zhu et al.,2022;Lei et al.,2021).
