Search Results (92)

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

Nuclear energy has become a promising substitute for traditional fossil fuels (e.g., coal, oil, and natural gas) by reason of its ultra-high energy density, firm power generation, and near-zero carbon emissions. However, the shortage of uranium resources is threatening the sustainable development of nuclear power, and meanwhile the nuclear fuel front-end cycle inevitably causes radioactive uranium-bearing wastewater discharge, resulting in severe environmental pollution. Nowadays, the extraction and enrichment of uranium in seawater and uranium-containing wastewater offer a prospective avenue to secure the long-term viability of nuclear power with environmental conservation. Among numerous strategies, photocatalytic extraction of soluble hexavalent uranyl (U(VI)) over graphitic carbon nitride (g-C₃N₄), a conjugated polymer semiconductor, is increasingly attracting widespread attention due to its high solar energy utilization, environmental friendliness, high selectivity, good stability, and low cost. A comprehensive overview that pinpoints research directions for novice researchers is urgently required. Herein, the development progress of g-C₃N₄-mediated photocatalytic U(VI) extraction is briefly introduced. Subsequently, the possible mechanisms are discussed with the assistance of advanced characterization techniques, and the influential factors for catalytic efficiency are also discussed. Moreover, multiple applications of g-C₃N₄-based catalysts on photocatalytic U(VI) reduction and extraction are elaborated, especially for modularization approaches on a large scale. At length, the future challenges and prospects in photocatalytic uranium extraction from water bodies are proposed. This review aims to offer fundamental insights into designing and exploring novel g-C₃N₄-based photocatalysts for soluble U(VI) enrichment in water bodies, especially opening up new avenues for the future development of sustainable uranium extraction technologies in practice. Full article

The article presents a comprehensive comparative performance evaluation and validation of composite adsorbents based on the Se-derivative of 4-amino-N′-hydroxy-1,2,5-oxadiazole-3-carboximidamide for U (VI) recovery from complex multicomponent aqueous media. Our results indicate the composite materials to be comparable to, and in some cases to surpass, existing adsorbents in recovery efficiency. Under static sorption conditions for trace U (VI) from real multicomponent solutions (tap, river, and sea water), the sorption efficiency reached 80–98%, while the distribution coefficients ranged from 10⁴ to 10⁶ cm³ g⁻¹. The sorption-selectivity properties of the materials were evaluated in the presence of competing ions (EDTA and oxalate ions), which possess a high chelating capacity and a strong tendency to form complexes with uranium. The dependence of sorption efficiency on the concentration of these ions and the solution pH was investigated. The possibility of reusing the materials over multiple sorption-desorption cycles was assessed. An optimal regenerating eluent agent was identified (NaHCO₃/NH₄NO₃), providing a desorption efficiency of >95% without degrading the material’s sorption properties over repeated cycles. Using a combination of physicochemical methods, including sorption techniques, the mechanism of uranium sorption and its dependence on the material structure were determined. The efficiency of uranium recovery from multicomponent natural waters was also investigated under dynamic conditions over repeated sorption-desorption cycles. The results demonstrate through comparative analysis that the developed composites exhibit a high sorption capacity and possess a high practical potential for the concentration and recovery of uranium from high-salinity solutions with complex composition. Full article

The exploit of an efficient method for uranium (U) extraction is crucial for the development of nuclear energy. In this study, an aminated lignin-based microsphere (AL-PEI/GMS) was synthesized and used as an adsorbent for the recovery of hexavalent uranium (U(VI)) from salt-lake brine. The effects of adsorbent dosage, initial solution pH value, interfering ions, adsorption time, and temperature on the U(VI) adsorption performance of AL-PEI/GMSs were systematically investigated. The results show that when the adsorbent dosage was 2 g/L, the temperature was 45 °C, and the pH was 8, the adsorption capacity of AL-PEI/GMS for U(VI) could reach 256.4 mg/g. In addition, after five cycles, a high U(VI) adsorption efficiency of over 90% could still be achieved. Furthermore, through a fixed-bed system, AL-PEI/GMS could rapidly adsorb U(VI) from actual salt-lake brine. Therefore, the prepared AL-PEI/GMS is a competitive alternative material compared with other adsorbents in terms of efficiently recovering U(VI) from actual salt-lake brine. Full article

Organophosphonates have manifold applications in the chemical industry, of which one of the most commonly used is 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTC). It is widely used as a cement additive and may pose a potential risk of complexing radionuclides such as uranium in nuclear waste repositories. PBTC, in its fully deprotonated form, has four negatively charged groups, one phosphonate and three carboxylate groups, which makes it a superior ligand for metal ion complexation. In this study, for the first time, its complexation behavior towards hexavalent uranium, U(VI), in the pH range from 2 to 11, has been investigated using various spectroscopic methods. The structure-sensitive methods NMR, IR, and Raman spectroscopy were used to characterize the complex structure. The interpretation of the results was supported by density functional calculations. Over almost the entire pH range studied, U(VI) and PBTC form a chelate complex via the phosphonate and the geminal carboxylate group, highlighting the strong chelating ability of the ligand. UV-Vis spectroscopy combined with factor analysis was applied to determine the distribution of differently protonated chelate species and their stability constants. Time-resolved laser-induced luminescence spectroscopy (TRLFS) was additionally used as a complementary method. Full article

In this study, a novel adsorbent, UiO-66-H₃IMDC, was successfully prepared by functionalizing UiO-66 with imidazole-4,5-dicarboxylic acid (H3IMDC). The effective functionalization of H₃IMDC on UiO-66 was confirmed by powder X-ray diffraction (PXRD) and Fourier transform infrared spectroscopy (FT-IR). The relationships between the adsorption of U(VI) on UiO-66-H₃IMDC and the contact time, the pH of the solution, as well as the initial concentration of U(VI) were investigated. Additionally, the selective adsorption of U(VI) by UiO-66-H₃IMDC and its cyclic regeneration performance were also studied. The results demonstrate that the UiO-66-H₃IMDC adsorbent exhibits excellent adsorption performance for uranium in aqueous solutions. Full article

N,O-donor hybrid heterocyclic extractants have great potential for separation of actinides from lanthanides in spent nuclear fuel reprocessing processes. We demonstrate that this type of reagents can be used for primary concentration of actinides contained in eudialyte, a promising mineral containing a heavy group of lanthanides. With respect to lanthanide ions, the efficiency of their extraction decreases in the series L3 >> L1 > L2, and the extraction of actinides decreases in the series L1 ≈ L3 >> L2. For the extractant L2 based on 2,2′-bipyridine-6,6′-dicarboxylic acid diamide, the efficiency of lanthanide purification from U, Th exceeds 50. The structure and stereochemical features of the ligands do not have a significant effect on the composition of the formed complexes. The solvation numbers are close to 1 for all range f-elements studied, except for thorium, which indicates the predominant formation of complexes with the composition ratio of 1:1. The solvation numbers 1.4–1.5 are observed for thorium(IV), and the established values indicate the formation of a mixture of complexes with the composition ratios of 1:1 and 2:1. Full article

With the continuous expansion of urban areas, the treatment of urban sewage is facing significant challenges. Tens of thousands of tons of municipal sludge (MS) are produced annually, which not only occupies substantial land resources but also poses potential environmental threats, thereby complicating wastewater treatment processes. Proper management of MS has thus become a critical issue requiring urgent attention. Meanwhile, water pollution continues to worsen, endangering both ecological systems and human health. MS contains a variety of organic compounds with active functional groups capable of forming strong coordination interactions with various waterborne pollutants. Building on this foundation, we successfully develop a multifunctional adsorbent using MS as the raw material through biomineralization. The synthesized adsorbent shows outstanding performance, exhibiting high adsorption capacity for fluoride (F⁻) and hexavalent uranium (U(VI)) in high-fluorine uranium-containing wastewater, effectively reducing the concentrations of these harmful substances. Additionally, the adsorbent shows strong affinity for the cationic dye methylene blue, making it highly suitable for the treatment of wastewater from the printing and dyeing industries. Notably, the adsorbent also possesses antibacterial properties, demonstrating significant bactericidal activity against Gram-negative E. coli in wastewater. The multifunctional adsorbent not only offers a novel solution to enhancing water quality and safety, but also represents a promising strategy for sustainable wastewater treatment. Full article

Bacillus subtilis exhibits a great affinity to soluble U(VI) through non-reducing biomineralization. The pH value, temperature, initial uranium concentration, bacterial concentration, and adsorption time are recognized as the five environmental sensitive factors that can regulate the degree of non-reductive biomineralization. Most of the current studies have focused on the regulatory mechanisms of these factors on uranium non-reductive mineralization. However, there are still few reports on the importance of these factors in influencing non-reductive mineralization, as well as on how to regulate these factors to increase the efficiency of non-reductive mineralization and enhance the enrichment of Bacillus subtilis on uranium. In this work, a deep learning neural network model was constructed to effectively predict the effects of changes in these five environmental sensitivity factors on the non-reducing mineralization of Bacillus subtilis to uranium. Accuracy (99.6%) and R² (up to 0.89) confirm a high degree of agreement between the predicted output and the observed values. Sensitivity analysis shows that in this model, pH value is the most important influencing factor. However, under different pH values, temperature, initial uranium concentration, adsorption time, and bacterial concentration have different effects. When the pH value is lower than 6, the most important factor is temperature, and once the pH value is greater than 6, the initial concentration is the most important factor. The results are expected to provide a theoretical basis for regulating the enrichment degree of U(VI) by Bacillus subtilis, achieving the maximum long-term stable fixation of U(VI), and understanding the environmental chemical behavior of uranium under different conditions. Full article

Some of the largest Mexican uranium (U) deposits are located in Chihuahua. The most important is in Sierra Peña Blanca, northwest of the capital, which was explored and partially exploited in the 1980s. After the closure of activities, the mining projects were left exposed to weathering. To characterize the spread of U minerals towards the neighboring Laguna del Cuervo, sediment samples were collected in the main streams of the drainage pattern of the largest deposits. The U mineral fragments from the fine sand portion were extracted using fluorescence light at 365 nm. The morphology and elemental composition of these particles were analyzed by focused ion beam microscopy (FIB) and scanning transmission electron microscopy (STEM). The particle density in samples close to the U sources was quantified using gamma spectrometry. The highest density was 2500 part./g, and the lowest was 124 part./g. X-ray absorption spectroscopy (XAS) allowed us to establish via XANES the speciation of U in the U particles, confirming the U(VI) oxidation state, while the exploitation of the EXAFS spectrum put in evidence of the presence of uranophane. Finally, the Fe, Sr, and U distributions in the particle and its matrix were obtained via X-ray fluorescence microtomography (XRF-µCT). It was concluded that the particle is composed of uranophane, imbricated with quartz and other oxides. 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

A genetic linkage between U–Cu–Mo mineralization with feldspar and chlorite minerals and the discrimination of different mineralization events in the hydrothermal and metasomatic system in the Rohil polymetallic uranium deposit in India is presented on the basis of textural relationships and mineral chemistry. Field and EPMA studies reveal that the chlorite formed in two possible modes, viz. (a) replacement of ferromagnesian minerals of the host rock and (b) precipitated directly from hydrothermal solutions. Chlorites follow a distinctive composition from Al-saturated to Al-undersaturated and, in most cases, from Mg- to Fe-rich species as alteration progressed. The chlorites show a wide range of Fe content (1.86–5.06 apfu), high Mg content (3.96–6.28 apfu), and Si contents (5.99–6.90 apfu) with an Fe/(Fe + Mg) ratio (0.23–0.56), leading to their classification as Diabantite/Pycnochlorite. Empirical and thermodynamic geothermometers have been used to determine the temperature of chlorite formation based on chemical composition, which revealed a large variation in temperatures from 130 °C to 260 °C. The feldspar geothermometry reveals a temperature range of 158 to 236 °C, which is in congruence with that of chlorites. Geothermometry by two different methods provides the range of temperature that prevailed in the study area during and succeeding the crystallization of uraninite and associated ore minerals. Mineral chemistry vis-à-vis geothermometry of feldspars and chlorite can provide impetus to geochemical evolution in the North Delhi Fold Belt (NDFB) and similar geological setups in metasomatite-type uranium deposits. Full article

With the rapid development of nuclear energy, the contamination of environmental water systems by uranium has become a significant threat to human health. To efficiently remove uranium from these systems, three types of silica-based polyamine resins—SiPMA-DETA (SiPMA: silica/poly methyl acrylate; DETA: diethylenetriamine), SiPMA-TETA (TETA: triethylenetetramine), and SiPMA-TEPA (TEPA: tetraethylenepentamine)—were successfully prepared, characterized, and evaluated in batch experiments. Characterization results showed that the silica-based polyamine resins were successfully prepared, and they exhibited a uniform shape and high specific surface area. SiPMA-DETA, SiPMA-TETA, and SiPMA-TEPA had nitrogen contents of 4.08%, 3.72%, and 4.26%, respectively. Batch experiments indicated that these adsorbents could efficiently remove uranium from aqueous solutions with a pH of 5–9. The adsorption kinetics of U(VI) were consistent with the pseudo-second-order model, indicating that the adsorption process was chemisorption and that adsorption equilibrium was achieved within 10 min. SiPMA-TEPA, with the longest polyamine chain, exhibited the highest adsorption capacity (>198.95 mg/g), while SiPMA-DETA, with the shortest polyamine chain, demonstrated the highest U(VI) adsorption efficiency (83%) with 100 mM Na₂SO₄. SiPMA-TEPA still removed over 90% of U(VI) from river water and tap water. The spectral analysis revealed that the N-containing functional groups on the ligand were bound to anionic uranium–carbonate species and possibly contributed to the adsorption efficiency. In general, this work presents three effective adsorbents for removing uranium from environmental water systems and thus significantly contributes to the field of environmental protection. Full article

Recent years have seen increasing interest in uranyl(VI) photocatalysis. In this study, uranyl complexes were successfully synthesized from ligands L1–L6 and UO₂(NO₃)₂·6H₂O under reflux conditions, yielding products 1–6 with yields ranging from 30% to 50%. The complexes were thoroughly characterized using NMR spectroscopy, single-crystal X-ray diffraction, and elemental analysis. The results indicate that complexes 1–5 possess a pentagonal bipyramidal geometry, whereas complex 6 exhibits an octahedral structure. The photocatalytic properties of these novel complexes for sp³ C-H bond functionalization were explored. The results demonstrate that complex 4 functions as an efficient photocatalyst for converting C-H bonds to C-C bonds via hydrogen atom transfer under blue light irradiation. Full article

Mn-substituted FeOOH with different Mn/(Mn + Fe) molar ratios are synthesized, and characterized using FESEM, XRD, FTIR, ICP-OES, BET, Zeta potential, TG-DSC, XPS, and VSM. The results show that the actual doping amounts of Mn are 0%, 3.05%, 6.13%, 9.04%, 12.70%, and 15.14%, respectively. The substitution of Mn promotes the transformation of goethite from FeOOH to MnFe₂O₄, resulting in a saturation magnetization intensity of up to 14.90 emu/g for G-Mn15%, laying a theoretical foundation for magnetic recovery. The specific surface area of Mn-substituted FeOOH increases from 57.15 m²/g to 315.26 m²/g with an increasing Mn substitution amount. Combined with the abundant oxygen-containing functional groups such as -OH, Fe-O, and Mn-O on the surface, sufficient active sites are provided for the efficient adsorption of U(VI). The TG-DSC analysis results indicate that the substitution of Mn improves the thermal stability of goethite. In addition, XPS analysis results indicate that the substitution of Mn leads to the conversion of Fe³⁺ to Fe²⁺ in goethite, and the conversion of Mn²⁺ to Mn³⁺ replaces Fe³⁺ in the structure of goethite. Fe-O and Mn-O coordinate participate in the adsorption and reduction process of U(VI). The batch experiment results show that the substitution of Mn promotes the adsorption performance of goethite for U(VI). When T = 303 K, pH = 4.0, m/V = 0.5 g/L, and I = 0.01 mol/L NaCl, the maximum adsorption capacity of G-Mn15% for U(VI) is 79.24 mg/g, indicating the potential value of Mn substitution for goethite in the treatment of uranium-containing wastewater. Full article