Search Results (30)

Sunflower (Helianthus annuus) can potentially be used for uranium (U) phytoremediation. However, the influence of arbuscular mycorrhizal fungi (AMF) on key rhizosphere processes and plant U uptake remains insufficiently researched. We hypothesized that AMF inoculation could enhance sunflower tolerance to U stress by improving plant physiological performance and modifying rhizosphere properties. To test this hypothesis, this study examined the effects of AMF (Funneliformis mosseae, Glomus etunicatum, and their co-inoculation) on sunflowers under U stress, encompassing plant growth and physiological traits, rhizosphere properties, enzyme activities in the rhizosphere soil, uranium speciation in the rhizosphere soil, and the accumulation and distribution of uranium within the plant. Results showed that AMF successfully colonized the roots, enhancing plant growth, biomass, and gas exchange, while improving photosynthetic efficiency and reducing non-photochemical quenching. In the rhizosphere, AMF elevated soil respiration, organic matter, dissolved organic carbon, and microbial biomass carbon; improved phosphatases, urease, catalase, and sucrase activities; also reshaped U speciation, increasing exchangeable and carbonate-bound fractions while decreasing those bound to organic matter, Fe/Mn oxides, and residual phases. Moreover, AMF reduced U concentration in leaves and stems, promoted U retention in belowground tissues, and significantly lowered the U translocation factor. These findings demonstrate that AMF inoculation improves sunflower tolerance to U stress by enhancing physiological performance, modifying rhizosphere properties, and immobilizing U in roots, supporting its potential use in phytoremediation strategies for U-contaminated environments. Full article

In this study, chicken bone biochar (CBC) was prepared from waste chicken bones via oxygen-limited pyrolysis. A magnetic component (Fe₃O₄) was introduced, and the composite was embedded in a sodium alginate (SA) gel network, successfully constructing magnetic chicken bone biochar/sodium alginate composite gel beads (M-CBC/SA). The experimental results showed that under the conditions of pH = 4.5, 25 °C, and an adsorbent dosage of 0.5 g/L, the removal efficiency of M-CBC/SA toward 50 mg/L U(VI) reached 91.67%, corresponding to an adsorption capacity of 91.67 mg/g. The adsorption process followed the pseudo-second-order kinetic model and the Langmuir isotherm model, with a theoretical maximum adsorption capacity of 322.58 mg/g, indicating that the adsorption was dominated by monolayer chemisorption. The material exhibited excellent magnetic separability and good anti-interference ability against coexisting ions such as K⁺, Na⁺, Cl⁻, and SO₄²⁻, and its adsorption behavior was only weakly affected by ionic strength. Characterization by XRD, FTIR, XPS, SEM-EDS and other techniques revealed that the immobilization mechanism of U(VI) involved the synergistic effects of dissolution–precipitation (the formation of a new autunite phase), surface complexation (involving hydroxyl and phosphate groups), ion exchange (exchange with Ca²⁺), and electrostatic attraction. Using waste chicken bones as the raw material, this composite achieves both efficient uranium immobilization and convenient magnetic separation, fully embodying the environmental concept of “treating waste with waste”, and shows promising application prospects in the treatment of uranium-containing wastewater. Full article

The Mianhuakeng deposit, located within the Zhuguangshan batholith in the Nanling area, is currently recognized as the largest granite-related uranium deposit in China. A portion of the uranium ore bodies is spatially associated with NE-trending mafic veins within the granite. In this study, the field investigation, zircon U-Pb dating, S and Pb isotope analysis, and whole-rock geochemical analysis were conducted on these mafic veins to explore their crystallization age, petrogenesis, tectonic setting, and relationships with uranium mineralization. The weighted mean result of zircon U-Pb is 189 ± 3 Ma, suggesting that the mafic dyke was crystallized during the Early Jurassic. The whole-rock geochemistry and isotopes exhibit characteristics of intraplate basalts, suggesting that the mafic dykes originate from an enriched mantle source consisting of garnet–spinel lherzolite, with an estimated partial melting of 1%–5%. Mafic magmas underwent low-degree contamination from the lower crust during upwelling, induced by the extension of the lithosphere during the Early Jurassic. The analyses of pyrite sulfur isotopes in mafic samples vary between −2.9‰ and 1.8‰, significantly different from that of pyrite (−14.4‰ to −7.8‰) formed during the uranium mineralization. Furthermore, the ages of the pitchblende of 127–54 Ma are much younger than the crystallization ages of mafic dykes, indicating that the mafic magmas did not contribute to the uranium mineralization of Mianhuakeng deposit during magmatism. However, the abundant reducing minerals (e.g., pyrite, hornblende, and Fe²⁺-bearing minerals) in the mafic dykes can act as a redox barrier, reducing mobile U⁶⁺ to immobile U⁴⁺ during fluid–rock interaction, thereby facilitating uranium precipitation from the hydrothermal ore-forming fluids. The secondary fractures created by the intrusion of mafic magma probably provided favorable pathways for the movement of hydrothermal fluids. Full article

Thorium has emerged as a promising alternative to uranium in nuclear energy systems due to its higher natural abundance, favorable conversion to fissile ²³³U, and reduced generation of long-lived transuranic waste. This review provides a comprehensive overview of advanced techniques for thorium recovery from primary ores and secondary resources. The main mineralogical carriers—including monazite, thorianite, thorite, and cheralite as well as industrial by-products such as rare-earth processing tailings—are critically examined with respect to their occurrence and processing potential. Physical enrichment methods (gravity, magnetic, and electrostatic separation) and hydrometallurgical approaches (acidic and alkaline leaching) are analyzed in detail, highlighting their efficiencies, limitations, and environmental implications. Particular emphasis is placed on modern separation strategies such as solvent extraction with organophosphorus reagents, diglycolamides, and ionic liquids, as well as extraction chromatography, nanocomposite sorbents, ion-imprinted polymers, and electrosorption on carbon-based electrodes. These techniques demonstrate significant progress in enhancing selectivity, reducing reagent consumption, and enabling recovery from low-grade and secondary feedstocks. Environmental and radiological aspects, including waste minimization, immobilization, and regulatory frameworks, are discussed as integral components of sustainable thorium management. Finally, perspectives on hybrid technologies, digital process optimization, and economic feasibility are outlined, underscoring the need for interdisciplinary approaches that combine chemistry, materials science, and environmental engineering. Collectively, the analysis highlights the transition from conventional practices to integrated, scalable, and environmentally responsible technologies for thorium recovery. Full article

Given the pressing demand for efficient uranium (U(VI)) enrichment and its elimination from wastewater to curtail the risks of radioactive contamination inherent in nuclear energy applications, it is crucial to design materials with high removal efficiency and straightforward separation processes. In the current study, we incorporated konjac gum (KGM) into MgAl-double oxide (MgAl-LDO) and synthesized an innovative, economical, and environmentally friendly LDO-KGM material by using the freeze-drying-calcination (FDC) method, which provided a solution for U(VI) concentration from aqueous solutions. The nanoflower structures LDO-KGM with abundant pore structure and high specific surface area exhibited an optimal U(VI) adsorptive capacity (3019.56 mg·g⁻¹) at pH = 6.0 and 293 K, which was 2.3 times greater than that of MgAl-LDO (1296.39 mg·g⁻¹). LDO-KGM also showed great adaptability for the immobilization of U(VI) over a broad pH range (4.0 to 9.0) and coexisting ions. U(VI) adsorption onto LDO-KGM adhered to the pseudo-second-order kinetic model (R² ≥ 0.99) and the Langmuir isotherm model (R² ≥ 0.99). The analysis of thermodynamic parameters derived from isotherms at varying temperatures revealed that U(VI) adsorption onto LDO-KGM was an endothermic and spontaneous process. The mechanism underlying U(VI) adsorption by LDO-KGM was mainly complexation, carbonate co-precipitation, and electrostatic adsorption. Furthermore, the adsorption efficiency of LDO-KGM for U(VI) could still retain more than 84.5% after five cycles. The findings indicate that the synthesized LDO-KGM exhibits potential as an exceptionally potent adsorbent for the purification of wastewater contaminated with U(VI). Full article

Understanding the fate of contaminants in heterogeneous aquifer systems is crucial to explain their transport behavior. Although it has been proven that heterogeneity has a significant control over the quantification of these processes, the extent of this impact is yet to be studied. The unique contribution of this work lies in the assessment of field-scale physical and chemical heterogeneity in modeling reactive transport processes in the subsurface. The main objective of this study is to investigate the impact of physical and chemical heterogeneity in understanding biogeochemical processes of contaminants in the subsurface environment, coupled with advective and dispersive transport in situ with mixing limitations. This study is particularly focused on an example of uranium, where especially coupled bioreduction and reoxidation processes in the presence of Fe (III) hydroxides are considered. For this purpose, 2D numerical biogeochemical reactive transport models are developed to simulate the fate and transport of uranium in a heterogeneously distributed subsurface. Results have shown that neglecting spatial heterogeneity might lead to an overestimation of uranium bioreduction, where physical heterogeneity has been observed to have a greater impact than chemical heterogeneity in the absence of adsorption reactions. On the other hand, when adsorption of uranium is included, the significance of chemical heterogeneity is more pronounced. Thus, when potential adsorption of contaminants is ignored or if chemical heterogeneity is ignored in the presence of adsorption reactions, the contaminant concentrations might be underestimated. The underestimation is more pronounced in low hydraulic conductivity zones due to the mixing limitations for soluble compounds, whereas for immobile phase interactions, high hydraulic conductivity regions became significant. The impact of U(IV) reoxidation process is also more pronounced in the presence of chemical heterogeneity and particularly enhanced in the zones with the highest mixing. The findings of this study can shed light on identifying the conditions that necessitate the accurate characterizations of physical and chemical heterogeneity in predicting contaminant transport with mixing limitations subject to competing biogeochemical reactions in the natural subsurface. Full article

Once the uranium tailings dam collapses, it will cause great harm to the surrounding ecological environment and people’s safety. This study experimentally investigates microbial grouting reinforcement of uranium tailings to advance microbial reinforcement technology and facilitate its large-scale engineering applications. The study simulated original environmental conditions and used tap water to prepare the culture medium and cement without sterilization or pH adjustment. The response surface method was employed to optimize parameters affecting the immobilization of uranium tailings, and the results were verified. The mechanical strength of the immobilized uranium tailings was determined through unconfined compression tests, while their microstructures were analyzed using X-ray diffraction, scanning electron microscopy and computed tomography. The findings indicate that the response surface method optimizes test parameters accurately, with the concentration of the cementation solution and the grouting amount being two main factors influencing the compressive strength of the solidified uranium tailings. Without pH adjustment, sterilization, or slurry modification using tap water, the bacteria−cementation ratio was set at 1, the concentration of the cementation solution was 1.3 mol/L, and the grouting volume was 70 mL. Notably, the strength of the uranium tailings increased 27-fold after seven rounds of grouting compared to the water-only group, and 6-fold compared to the cementation solution-only group. This study contributes to reducing the complexity associated with the application of microbial grouting technology in soil stabilization and provides valuable references for other engineering practices. Full article

The most promising material for uranium extraction from saltwater is generally acknowledged to be fibrous adsorbents. An irradiation-modified anti-biofouling ultra-high-molecular-weight polyethylene (UHMWPE-g-PGAO) fibrous adsorbent with a hyperbranched structure was synthesized. It exhibited adsorption capacities of 314.8 mg-U/g-Ads in aqueous solution and 4.04 mg-U/g-Ads in simulated seawater over a 28-day period. The ultra-high-molecular-weight polyethylene (UHMWPE) fiber was functionalized by covalently linking hyperbranched polyethyleneimine (h-PEI) to facilitate the migration of uranyl ions within the fibers. Additionally, amidoxime and quaternary ammonium groups were immobilized on the fiber surface to enhance uranium affinity and provide defense against marine organisms. This three-dimensional design of amidoxime and h-PEI-modified UHMWPE fiber retained more than 91.0% of its maximum adsorption capacity after undergoing five adsorption-desorption cycles. The UHMWPE-g-PGAO adsorbent exhibits significant antibacterial activity against Escherichia coli and Staphylococcus aureus, achieving an inactivation efficiency of over 99.9%. It is proved to be an innovative fiber adsorbent for uranium extraction from seawater for its biofouling resistance, robustness, and reusability. Full article

This study presents findings regarding the kinetics of ferrous iron oxidation in solution mediated by Acidithiobacillus ferrooxidans bacteria within a continuous-flow bioreactor employing diverse types of immobilizers. The objective is to augment the rate of ferrous iron oxidation in solutions utilizing an immobilizer for Acidithiobacillus ferrooxidans strains. Immobilization represents a promising avenue for enhancing the efficiency of Fe²⁺ oxidation via acidophilic ferrooxidizing bacteria, leading to a several-fold increase in oxidation rate. A comparative analysis was conducted to evaluate the efficacy of different types of immobilizer in facilitating iron oxidation within a continuous-flow bioreactor, including the application of wood chips coated with Fe(OH)₃. The results indicate that wood chips coated with iron hydroxide serve as effective type of immobilizer, facilitating the robust attachment of Acidithiobacillus ferrooxidans via electrostatic interactions between negatively charged bacteria and positively charged surfaces. Experimental investigations were conducted using novel immobilization matrices in pilot-scale tests simulating the underground borehole leaching (UBL) of uranium. The bioactivation of leaching solutions enhances the efficiency and environmental compatibility of UBL compared to conventional chemical oxidation methods. The relationships between redox potential and ferric iron content in bioactivated solutions during the UBL of uranium were delineated. The significance of this study lies in its elucidating the pivotal role of Fe²⁺ oxidation in uranium extraction processes, particularly in the context of UBL. By employing bioactivation mediated by Acidithiobacillus ferrooxidans, the study demonstrates not only enhanced uranium extraction efficiency, but also markedly improved environmental sustainability compared to traditional chemical oxidation methods. The findings reveal crucial correlations between redox potential and ferric iron concentration in bioactivated solutions. Full article

Uranium (U) and nickel (Ni) released 50 years ago have been immobilized in the Tims Branch wetlands located on the Savannah River Site in the United States. Sediments were collected from seven locations to identify the factors responsible for this attenuation. Ni and U contents in the solids were significantly correlated, suggesting that depositional as opposed to chemical processes contributed to their spatial distribution. Based on sequential extractions, 63 ± 16% of the U was partitioned into the organic fraction, whereas Ni was distributed between several sediment fractions. An inverse pH-organic matter (OM) correlation and positive correlations of OM with total U and organic-bound U/Ni suggest that increased OM preservation and binding to the mineral surfaces were likely responsible for Ni- and especially U-sediment retention (Tims Branch pH = 4.84 ± 0.68). EXAFS analysis indicated the predominance of U(VI) coordinated with clay minerals (~65%), together with ~35% coordinated to either OM (in areas with elevated OM levels) or iron oxides. The desorption-K_d coefficients of U (3972 ± 1370 L/kg) and Ni (30 ± 8 L/kg) indicate that dissolved Ni poses a greater long-term risk than dissolved U for migrating downstream. This study suggests that a delicate balance of geochemical properties controls whether wetlands behave as sinks or sources of contaminants. Full article

Among the many radiochemical problems, the search for new materials and technologies for the immobilization of radioactive waste remains relevant, and the range continues to change and expand. The possibility of immobilizing the spent chloride electrolyte after the pyrochemical processing of the mixed uranium-plutonium spent nuclear fuel of the new fast reactor BREST-OD-300 on lead coolant into glass-composite phosphate materials synthesized at temperatures of 650–750 °C was studied. The structure of the obtained samples was studied using XRD and SEM/EDS methods. It has been shown that the spent electrolyte simulator components create stable mixed pyrophosphate phases in the glass composite structure. The materials were found to have high hydrolytic stability. This indicates the promise of using phosphate glass composites as materials for the reliable immobilization of the spent electrolyte. Full article

The long-term operation of uranium sludge storages causes serious problems: it contaminates the neighboring aquifers with dangerous substances (uranium, nitrate, ammonium, and sulfate). To purify the aquifers can be costly and time-consuming; therefore, it is important to use the potential of in situ conditions, e.g., the aboriginal microflora and its ability to biologically remediate water reservoirs. In this work, we study the geological, geochemical, and microbiological characteristics of groundwater contaminated by uranium sludge storages resulting from the production cycles of four Russian chemical plants. All of the sites under consideration were extremely contaminated with nitrate (up to 15 g/L); in each case, we used denitrifying bacteria as a dominant group of microorganisms for purification. Our laboratory studies showed that microbial stimulation of water samples by milk whey promotes O₂ and nitrate removal; this, in turn, started the cycle of anaerobic processes of authigenic precipitation caused by the reduction of iron and sulfate in the system. Thus, a mineral geochemical barrier preventing uranium immobilization formed. As a result, the uranium of the liquid phase decreased about 92–98% after 3–6 months (decomposition time depends on the nitrate concentration in the groundwater probe). The resulting amorphous biogenic phases contain sulfur, iron, phosphorus, and uranium. Full article

The complex contamination of groundwater near radioactive waste repositories by nitrates and actinides is a common problem for many nuclear fuel cycle facilities. One of the effective methods to remove nitrates and reduce actinide migration activity is bioremediation through the activation of native microbial communities by soluble electron donors and carbon sources. This work evaluated the effectiveness of using simple and complex electron donors to remove nitrate in the microbial community in an aquifer near the B2 storage of the Siberian Chemical Combine (Seversk, Siberia). The addition of sugar and milk whey led to the maximum efficiency of nitrate-ion removal and a decrease in the redox potential of the system, creating optimal conditions for the immobilization of actinide. Special attention was paid to the behavior of uranium, plutonium, neptunium, and americium under conditions simulating groundwater when sugar, acetate, and milk whey were added and when microbial metabolic products were formed. Neither microbial metabolites nor organic solutions were found to have a significant effect on the leaching of neptunium. At the same time, for plutonium, a decrease in yield was observed when rocks were treated with organic solutions were compared to groundwater treatment without them. Plutonium leaching is significantly affected by rock composition. In rocks with a low clay fraction content, its yield can reach 40%. At the same time, microbial metabolites can increase americium (Am) desorption from rocks with a low clay fraction content. Additionally, particle size analysis was performed using a step-by-step filtration approach, aiming to evaluate the risks that are associated with colloidal phase formation. It was shown that microbiological stimulation resulted in particle enlargement, substantially diminishing the presence of actinides in the form of dissolved or sub-50 nm nanoparticles. This outcome significantly reduced the potential for colloidal and pseudocolloidal transfer, thereby lowering associated risks. Full article

The contamination of groundwater by uranium, nitrate, ammonium, and sulfate near uranium sludge storage sites due to the degradation of engineering safety barriers is an urgent problem during their long-term operation. The purification of such multicomponent contaminants is a complex task and one of the promising methods for this purpose is in situ bioremediation using the metabolic potential of aborigenic microflora. The work focused on the geochemical, geological, and microbiological parameters of groundwater with multi-component contamination near the uranium sludge storage sites of four chemical plants. In conditions of extreme nitrate contamination (up to 15 g/L), denitrifying bacteria were found to be the dominant group of microorganisms. In conditions of nitrate–ammonium contamination, bacteria responsible for the Anammox process were found. In laboratory, optimal conditions were selected to stimulate microflora to promote nitrate removal. For this purpose, sources of carbon (acetate, whey) were added to the water samples in concentrations necessary for the complete removal of nitrate by microbial denitrification. The experiment was carried out at ambient temperature in hermetically sealed vials. Uranyl nitrate was added to the samples at a concentration of 5 mg/L for uranium. It was found that nitrate removal contributes to the cycle of anaerobic processes of authigenic sedimentation because of sulfate and iron reduction processes, which provide the formation of a mineral geochemical barrier for uranium immobilization. As a result of the experiment, after 3–6 months, depending on the concentration of nitrate in the groundwater sample, the uranium content in the liquid phase decreased by 92–98%. Full article

The agricultural soils of West Limerick, Ireland, contain very localised, extremely high natural Se concentrations that reach levels that are very toxic to grazing livestock. The Carboniferous shales that formed in anoxic deep-water marine environments are the source of the selenium, which, along with the other redox-sensitive elements of molybdenum, uranium, arsenic and vanadium, were mobilised and reprecipitated in post-glacial anoxic marshes. The result has been a history of selenosis and molybdenosis in livestock in this important dairy province. Soils collected at 10–20 cm from five different agricultural sites were analysed, and all yielded concentrations greatly in excess of the safe Se limits of 3–10 mg kg⁻¹; the highest value recorded was 1265.8 mg kg⁻¹ Se. The highest recorded value for Mo in these soils was 1627.5 mg kg⁻¹, and for U, 658.8 mg kg⁻¹. There was a positive correlation between Se, Mo U and organic matter in the soils. Analysis of non-accumulator pasture grasses (Lolium perenne (perennial ryegrass), Festuca arundinacea (tall fescue), Dactylis glomerata (cocksfoot) and Phleum pretense (timothy grass)) revealed the shoot/leaf to contain up to 78.05 mg kg⁻¹ Se while Trifolium repens (white clover) leaves contained 296.15 mg kg⁻¹ Se. An in situ growing experiment using the Se accumulator species Brassica oleracea revealed 971.2 mg kg⁻¹ Se in the leaves of premier kale, which also contained 1000.4 mg kg⁻¹ Mo. Translocation factors (TFs) were generally higher for Mo than Se across all plant species. Combined X-ray absorption near edge spectroscopy (XANES) with micro-X-ray fluorescence (μ-XRF) showed the Se was present in the soil predominantly as the reduced immobile phase, elemental Se (Se⁰), but also as bioavailable organoselenium species, mainly selenomethionine (SeMet). SeMet was also the main species identified within both the Se non-accumulator and Se accumulator plants. The Se soil–plant system in West Limerick is dominated by SeMet, and uptake into the cattle pasture results in selenosis in the grazing dairy herds. The hyperaccumulating Brassica oleracea species could be used to extract both the Se and Mo to reduce the toxicity of the blighted fields. Full article