Antimicrobial polymer-based zeolite imidazolate framework composite membranes for uranium extraction from wastewater and seawater.

Extraction uranium (VI) (U(VI)) from wastewater and seawater is highly important for environmental protection and life safety, but it remains a great challenge. In this work, the growth of the zeolitic imidazolate framework-8 (ZIF-8) nanoparticles on the tannic acid (TA)-3-aminopropyltriethoxysilane (APTES) modified PVDF (TAP) membrane was designed to obtain an excellent U(VI) adsorbent. The zeolite imidazolate framework composite membrane (TAPP-ZIF-60) was prepared through polyethyleneimine (PEI) bridging strategy and temperature regulation strategy in solvothermal method. The coordination bond between PEI and ZIF-8 and the covalent bond between PEI and TAP are essential in forming stable composite membrane. TAPP-ZIF with different properties was synthesized through a temperature regulation process and the TAPP-ZIF prepared at 60 °C has the uniform morphology and good performance. The adsorption capacity of TAPP-ZIF-60 is 153.68 mg/g (C0 = 95.01 mg/L and pH = 8.0) and water permeability is 5459 L m-2 h-1 bar-1. After ten adsorption-desorption cycles, it is proved that TAPP-ZIF-60 has good repeatability and stability. In addition, the TAPP-ZIF-60 composites membrane has a good inhibitory effect on Staphylococcus aureus and Escherichia coli. X-ray photoelectron spectroscopy (XPS) and density functional theory (DFT) analysis reveal that the coordination between TAPP-ZIF-60 and uranyl ions is the primary factor contributing to the high adsorption capacity.

Ti3C2Tx/Cd0.8Zn0.2S composites constructed of Schottky heterojunction for efficient photocatalytic reduction of U(VI).

Photocatalysis has emerged as a extremely promising green technology for the treatment of uranium-containing wastewater. This study focuses on the fabrication of Ti3C2Tx/Cd0.8Zn0.2S composites with Schottky junctions through the in-situ growth of Cd0.8Zn0.2S on Ti3C2Tx nanosheets, enabling efficient photoreduction of U(VI) without the requirement of sacrificial agents. The results demonstrate that the Ti3C2Tx/Cd0.8Zn0.2S composites achieve remarkable 99.48 % U(VI) reduction efficiency within 60 min in a 100 ppm uranium solution. Furthermore, the removal rate remains above 90 % after five cycles. The formation of Schottky heterojunctions by Ti3C2Tx and Cd0.8Zn0.2S leads to the generation of an internal electric field that significantly promotes the rapid separation and transfer of photogenerated carriers, thereby enhancing the photocatalytic reduction efficiency of Ti3C2Tx/Cd0.8Zn0.2S-3:100 (TC/CZS-3:100). A considerable amount of electrons accumulate on Ti3C2Tx via the Schottky barrier, effectively facilitating the reduction of U(VI) to U(IV). As a co-catalyst, Ti3C2Tx enhances the photocatalytic performance and stability of Cd0.8Zn0.2S. Moreover, the practical application in the waste liquid of rare earth tailings reveals that the removal rate can be as high as 91.24 %. This research is of significant value in the development of effective photocatalysts for the elimination of uranium from wastewater.

The Electron-Density Distribution of UCl4 and Its Topology from X-ray Diffraction.

The chemistry of $5f$ electrons in actinide complexes and materials is still poorly understood and represents a serious challenge and opportunity for experiment and theory. The study of the electron density distribution of the ground state of such systems through X-ray diffraction represents a unique opportunity to quantitatively investigate different chemical bonding interactions at once, but was considered ``almost impossible'' on heavy-atom systems, until very recently. Here, we present a combined experimental and theoretical investigation of the electron density distribution in UCl$_4$ crystals and comparison with the previously reported spin density distribution from polarized neutron diffraction. All approaches provide a consistent picture in terms of electron and spin density distribution, and chemical bond characterization. More importantly, the synergy between experiments and quantum-mechanical calculations allows to highlight the remarkable sensitivity of X-ray diffraction to $5f$ electrons in materials.

Radiological risk and impact on soil microbial diversity of radionuclides in agricultural topsoils downstream of a decommissioned hydrometallurgical uranium plant.

Containing only low levels of U-bearing minerals, U ores often have to undergo hydrometallurgical processing for the separation of other minerals. Hydrometallurgical operations, even after being shut down, could pose radiological risk to the ecosystem and human health due to the radionuclide contamination of surrounding environmental media. This study investigated the contamination of radionuclides in the agricultural topsoils downstream of a decommissioned hydrometallurgical U plant in southern China, and assessed the corresponding radiological risk and evaluated its impact on soil microbial communities. The values of geoaccumulation index and potential ecological risk index indicate that all soil samples were significantly contaminated with U and 226Ra, with their concentrations being 4.4-28.7 times and 4.4-114.8 times higher than the corresponding regional background values, respectively. The mean outdoor annual effective dose (OAED) in the sampling plot next to the drainage ditch downstream of the decommissioned plant was up to 3.9 and 8.2 times higher than the Chinese annual effective dose limit and global average, respectively, which is indicative of unacceptable radiological risk for the local farm workers. Soil microbial composition was obviously impacted by the soil physicochemical properties and radionuclides. Specifically, Cladophialophora, which belongs to the fungal genus, exhibited significantly positive correlations with the contents of total Cd, total U, organic U, residual U, and total K, while Methanosarcina, which belongs to the archaeal genus, exhibited significantly positive correlations with the contents of 226Ra and residual U. Soil pH and total N content were significantly correlated with the abundance of several bacterial genera and the dominant archaeal genus (i.e., Candidatus Nitrocosmicus). These findings demonstrate the existence of potentially significant radiological risk associated with the radionuclides released from historical hydrometallurgical processing of U ores to the surrounding environment, and the need for proper site management and remediation.

New insights into uranium biomineralization mediated by Pseudomonas sp. WG2-6 in the presence of organic phosphorus: Promoting effect of extracellular polymeric substance and formation of U-P nanominerals.

Microbial biomineralization significantly affects the uranium (U) behavior in the environment. However, the mechanism of microbial biomineralization of U is still not fully understood. In this study, a dominant bacterium (Pseudomonas sp. WG2-6) was isolated from U tail mining area. Abiotic precipitation tests demonstrated that U biomineralization was entirely attributed to the mediation of Pseudomonas sp. WG2-6 when the concentration ratio of exogenous ß-glycerophosphate (SGP) to U was 10:1. Pseudomonas sp. WG2-6 exhibited strong immobilization ability towards U (97.59 %) according to batch experiments, and acylamide, carbonyls, and phosphate groups were the main functional groups that interacted with U. Besides, U mainly existed in the form of amorphous U-P complexes after biomineralization by Pseudomonas WG2-6, which could be converted into crystalline nano-minerals H2(UO2)2(PO4)2·8H2O in the presence of SGP. In particular, the formation and structural composition changes of extracellular polymeric substance (EPS) as well as the decrease in U4f binding energy were observed during the U biomineralization process of Pseudomonas sp. WG2-6 in the presence of SGP, indicating that EPS provided the nucleation site for the formation of stable biomineralized products. This work provides new insight into the mechanism of U microbial biomineralization and a theoretical basis for the remediation of U contaminated environments through microbial biomineralization.

Uranium Repartitioning during Microbial Driven Reductive Transformation of U(VI)-Sorbed Schwertmannite and Jarosite.

This study exposes U(VI)-sorbed schwertmannite and jarosite to biotic reductive incubations under field-relevant conditions and examines the changes in aqueous and solid-phase speciation of U, Fe, and S as well as associated microbial communities over 180 days. The chemical, X-ray absorption spectroscopy, X-ray diffraction, and microscopic data demonstrated that the U(VI)-sorbed schwertmannite underwent a rapid reductive dissolution and solid-phase transformation to goethite, during which the surface-sorbed U(VI) was partly reduced and mostly repartitioned to monomeric U(VI)/U(IV) complexes by carboxyl and phosphoryl ligands on biomass or organic substances. Furthermore, the microbial data suggest that these processes were likely driven by the consecutive developments of fermentative and sulfate- and iron- reducing microbial communities. In contrast, the U(VI)-sorbed jarosite only stimulated the growth of some fermentative communities and underwent very limited reductive dissolution and thus, remaining in its initial state with no detectable mineralogical transformation and solid-phase U reduction/repartitioning. Accordingly, these two biotic incubations did not induce increased risk of U reliberation to the aqueous phase. These findings have important implications for understanding the interactions of schwertmannite/jarosite with microbial communities and colinked behavior and fate of U following the establishment of reducing conditions in various acidic and U-rich settings.

Measurement of radioactivity and hazard index of Gonadal dose in selected Cement samples in Iraq.

Given the importance of cement as a basic material in construction, this study was undertaken to evaluate the level of radioactivity in a selected group of cement samples most used in construction to determine whether they are safe for human health. In this investigative study, nine samples of cement, both domestic and imported, that are often used in construction projects in Iraq were gathered. A NaI (Tl) gamma-ray spectrometer (3"x3") was used to measure the radioactivity in the samples. The average specific activity levels in the tested cement samples were 11.373±0.522, 5.795 ± 0.230, and 179.123±2.207 Bq/Kg, respectively. Also calculated was the average of the radium, which was equivalent to 33.449±1.022 Bq/kg. As for the risk indicators, the internal risk coefficient was 0.121±0.004 and external risk coefficient was 0.090 ±0.002. While studying the radiation doses, the values of effective annual internal dose was 0.080 mSv/y, external dose rates were 0.020 mSv/y, absorbed dose ratio was 16.321±0.476 nGy/h, and gamma index was 0.253±0.007. In the end, and depending on what was studied from various variables, with an average of 115.59 Sv/y, the annual gonadal equivalent dose risk (AGED) was calculated. The world average values were used to compare all the results. Finally, it was discovered that the radiation parameter levels of none of the samples had a detrimental effect on human health.

Constructing Ce-OH groups on CeO2 for enhancing removal and recovery of uranium from wastewater and seawater.

Efficient recovery of uranium from wastewater and seawater provides an important guarantee for the sustainable growth of nuclear energy. Herein, we skillfully use the alkali etching method to construct CeO2 hollow spheres rich in Ce-OH groups for the removal and recovery of uranium from water matrixes. It is found that the CeO2 exhibits fast adsorption kinetics (equilibrium time within 10 min) and moderate adsorption capacity (143.1 mg/g), and the removal efficiency of low concentration uranium (0.1 g/L and 1 g/L) reaches 100% within 1 min of adsorption. Moreover, the adsorption of uranium by CeO2 is almost unaffected by common anions and cations in the environment, even if the concentration of anions is 1000 times that of uranium. More importantly, the CeO2 can enrich uranium concentration in seawater by 167.9 times and the recovery rate reaches 83.9%. Mechanistic studies reveal that the adsorption of uranium by CeO2 is mainly attributed to the rich Ce-OH groups on the surface of CeO2, resulting in the rapid adsorption of U(VI) and mainly forms a single-bridge model. The findings of this study provide a green and efficient path for the removal and recovery of uranium from wastewater and seawater.

Microbial production of methyl-uranium via the Wood-Ljungdahl pathway.

The misuse of uranium is a major threat to human health and the environment. In microbial ecosystems, microbes deploy various strategies to cope with uranium-induced stress. However, the exact ecological strategies and mechanisms underlying uranium tolerance in microbes remain unclear. Therefore, this study aimed to investigate the survival strategies and tolerance mechanisms of microbial communities in uranium-contaminated soil and groundwater. Microbial co-occurrence networks and molecular biology techniques were used to analyze the properties of microbes in groundwater and soil samples from various depths of uranium-contaminated areas in Northwest China. Uranium pollution altered microbial ecological strategies. Uranium stress facilitated the formation of microbial community structures, leading to symbiosis. Furthermore, microbes primarily resisted uranium hazards by producing polysaccharides and phosphate groups that chelate uranium, releasing phosphate substances that precipitate uranium, and reducing U(VI) through sulfate- and iron-reducing processes. The relative abundance of metal-methylation genes in soil microorganisms positively correlated with uranium concentration, indicating that soil microorganisms can produce methyl uranium via the Wood-Ljungdahl pathway. Furthermore, soil and groundwater microorganisms demonstrated different responses to uranium stress. This study provides new insights into microbial responses to uranium stress and novel approaches for the bioremediation of uranium-contaminated sites.

Precise Electrocatalysis on Fe-Porphyrin Conjugated Networks Achieves Energy-Efficient Extraction of Uranium.

Electrochemical extraction has the potential to enhance uranium (U) extraction capacity and rates, but thus far, high selectivity and energy efficiency have not been achieved through the design of electrode materials. Herein, a precise electrocatalysis strategy is developed using a Ferrum (Fe) porphyrin-phenanthroline conjugated network (Fe@PDACN) for energy-efficient uranium extraction. The phenanthroline provides specific binding sites for selective enrichment of U(VI) at active sites (Kd = 2.79 × 105 mL g-1 in multi-ion solution). The Fe(II) sites have strong trap-redox activity for U(VI) and act as dynamic electron donors to rapidly mediate electrocatalytic U(VI) extraction through the redox reaction of Fe(0/II)/Fe(III). Moreover, the Fe-porphyrin blocks support sustained electron donation for U(VI) electrocatalysis by pre-storing electrons. These features enable selective uranium capture and a high electroextraction capacity of 24 646.3 mg g-1 from simulated nuclear wastewater in 280 h at a low voltage of -1.5 V. An ultra-high Faraday efficiency of 90.1% is achieved, and the energy cost is 3.22 × 10-2 $ kg-1 U, significantly lower than the previously reported materials. This work provides a highly efficient strategy for uranium extraction from water.

Uranium removal from contaminated groundwater using goethite-loaded composite microporous membrane.

In this study, we have coupled adsorption and membrane separation for the removal of uranium from contaminated groundwater in environmentally relevant conditions at low energy requirements. This study mainly focuses on elucidating uranium, U(VI), adsorption mechanisms using surface complexation modeling approach in a novel goethite-loaded composite microfiltration membrane (GLM). This experiment involved immobilizing goethite nanorods in a microporous (0.22 µm pore size) poly (vinylidene fluoride) (PVDF) membrane. The effect of varying goethite loading and hydraulic residence time on U(VI) removal was investigated at field-relevant pH (i.e. pH 8.5). U(VI) adsorption (i.e. 4.95 µg·mg-1) was optimum at a goethite loading 1.20 mg·cm-2. The effect of varying hydraulic residence time had no impact on U(VI) removal which was also confirmed via performing batch adsorption kinetic experiments. GLM membrane loaded at 1.2 mg·cm-2 could treat 275 L of U(VI) contaminated water having 200 µg of U L-1 below WHO drinking water limit (i.e. 30 µg of U L-1) with 1 m2 of membrane surface area with a adsorption capacity of 6.12 µg·mg-1. Varying the pH of aqueous solution, containing U(VI) from pH 4.0 to pH 10.0, showed a significant impact on uranium uptake ranging from 0.7 µg·mg-1 to 2.63 µg·mg-1 by the composite membrane. The adsorption mechanism of uranium onto goethite was explained via the formation of bidentate surface complexes using the Surface Complexation Model (SCM). The results of batch pH edge experiments and SCM have been compared with pH experiments performed using GLM. The results of SCM predicted the batch pH edge experiment within a RMSE of 0.055. The trend of U(VI) removal in membrane experiments was observed to be similar to that of batch pH edge experiments and was well predicted SCM model. Our results showed that the novel goethite-loaded membrane has the potential for the effective removal of uranium with a lower specific energy consumption.

Sonochemical synthesis of guar gum - Zirconium phosphate composite for efficient capture of uranium from water.

The increasing presence of uranium as a radionuclide contaminant in water is a threat to human health and the environment. Sonication-assisted crosslinking of guar gum, a biopolymer, is carried out with zirconium phosphate to form an adsorbent (GG@ZrP) for the removal of uranium from water. The surface characteristics, functionalities, and thermal stability of the composite were established using various analytical and spectral tools. Langmuir, Freundlich, and Sips models were used to evaluate the batch adsorption parameters. The adsorbent exhibited an excellent Langmuir adsorption capacity of 500 mg g-1 towards adsorption of uranium at pH 6. The adsorption was endothermic (ΔH, 22.63 kJ mol-1) and followed pseudo-second order kinetics. The synergistic influence of hydroxyl-rich guar gum and phosphate moieties resulted in efficient binding of uranium. With a high selectivity towards interfering cations and anions and applicability over a good range of pH, this adsorbent is a promising candidate for uranium remediation from water.

Prediction of Biochar Adsorption of Uranium in Wastewater and Inversion of Key Influencing Parameters Based on Ensemble Learning.

With the rapid development of industrialization, the problem of heavy metal wastewater treatment has become increasingly serious, posing a serious threat to the environment and human health. Biochar shows great potential for application in the field of wastewater treatment; however, biochars prepared from different biomass sources and experimental conditions have different physicochemical properties, resulting in differences in their adsorption capacity for uranium, which limits their wide application in wastewater treatment. Therefore, there is an urgent need to deeply explore and optimize the key parameter settings of biochar to significantly improve its adsorption capacity. This paper combines the nonlinear mapping capability of SCN and the ensemble learning advantage of the Adaboost algorithm based on existing experimental data on wastewater treatment. The accuracy of the model is evaluated by metrics such as coefficient of determination (R2) and error rate. It was found that the Adaboost-SCN model showed significant advantages in terms of prediction accuracy, precision, model stability and generalization ability compared to the SCN model alone. In order to further improve the performance of the model, this paper combined Adaboost-SCN with maximum information coefficient (MIC), random forest (RF) and energy valley optimizer (EVO) feature selection methods to construct three models, namely, MIC-Adaboost-SCN, RF-Adaboost-SCN and EVO-Adaboost-SCN. The results show that the prediction model with added feature selection is significantly better than the Adaboost-SCN model without feature selection in each evaluation index, and EVO has the most significant effect on feature selection. Finally, the correlation between biochar adsorption properties and production parameters was discussed through the inversion study of key parameters, and optimal parameter intervals were proposed to improve the adsorption properties. Providing strong support for the wide application of biochar in the field of wastewater treatment helps to solve the urgent environmental problem of heavy metal wastewater treatment.

Uranium and Radium in Groundwater and Incidence of Colorectal Cancer in Georgia Counties, USA: An Ecologic Study.

Colorectal cancer (CRC) is the third most commonly occurring cancer in the United States, with higher incidence rates among Black populations. Groundwater concentrations of natural radionuclides uranium and radium have seldom been investigated in relation to CRC despite their known carcinogenicity. We investigate spatial patterns of CRC by race, and in relation to groundwater concentrations of uranium and radium, testing the hypothesis that uranium and radium in groundwater might differentially contribute to incident CRC in Black and White populations in counties of Georgia, USA. Black populations showed a higher incidence of CRC than White populations; the median incident rate difference was 9.23 cases per 100,000 (95% CI: 2.14, 19.40). Spatial cluster analysis showed high incidence clusters of CRC in similar regions for Black and White populations. Linear regression indicated there are, on average, 1-2 additional cases of colorectal cancer in counties with higher levels of radium in their groundwater, irrespective of race. Uranium was not associated with CRC. This ecologic study suggests that radium in groundwater may be linked with increased incidence of CRC, although it did not explain higher CRC incidence rates in Black populations. Further studies are needed to verify this association given the inherent limitations in the ecologic study design and the crude exposure assessment.

Efficient Uranium Removal from Aqueous Solutions Using Silica-Based Adsorbents Functionalized with Various Polyamines.

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.

Uranium (VI) reduction by an iron-reducing Desulfitobacterium species as single cells and in artificial multispecies bio-aggregates.

Microbial U(VI) reduction plays a major role in new bioremediation strategies for radionuclide-contaminated environments and can potentially affect the safe disposal of high-level radioactive waste in a deep geological repository. Desulfitobacterium sp. G1-2, isolated from a bentonite sample, was used to investigate its potential to reduce U(VI) in different background electrolytes: bicarbonate buffer, where a uranyl(VI)­carbonate complex predominates, and synthetic Opalinus Clay pore water, where a uranyl(VI)-lactate complex occurs, as confirmed by time-resolved laser-induced fluorescence spectroscopic measurements. While Desulfitobacterium sp. G1-2 rapidly removed almost all U from the supernatants in bicarbonate buffer, only a low amount of U was removed in Opalinus Clay pore water. UV/Vis measurements suggest a speciation-dependent reduction by the microorganism. Scanning transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy revealed the formation of two different U-containing nanoparticles inside the cells. In a subsequent step, artificial multispecies bio-aggregates were formed using derivatized polyelectrolytes with cells of Desulfitobacterium sp. G1-2 and Cobetia marina DSM 50416 to assess their potential for U(VI) reduction under aerobic and anaerobic conditions. These findings provide new perspectives on microbial U(VI) reduction and contribute to the development of a safety concept for high-level radioactive waste repositories, as well as to new bioremediation strategies.

In vitro analysis of urinary uranium of cancerous patients in Dhi_Qar governorate, southern Iraq.

BACKGROUND: The simple and effective technique of fission track etch has been applied to determine trace concentration of uranium in human urine samples taken from two groups of male and female participants: cancer patients and healthy subjects are living in Dhi-Qar governorate, southern of Iraq. This governorate was the center of industrialization and the prior military activities especially during the Gulf wars in 1991 and 2003, and the abandoned weaponry is still present in these regions. The induced fission track registration was done using the CR-39 track detector. Patients with cancer were statistically significantly distinguished by significantly higher concentrations of uranium as compared with members of a control group, the mean value of uranium concentration for the cancer patients was 3.67 ± 0.16 µg/L, with the maximum recorded uranium concentration was 5.33 ± 0.25 µg/L (male, 75 years old, has prostate cancer) and the minimum concentration was 2.04 ± 0.07 µg/L (female, 7 years old, has leukemia cancer). While the mean value of uranium concentration for the healthy group was 2.80 ± 0.14 µg/L, with the maximum uranium concentration was 4.19 ± 0.23 µg/L (male, 73 years old) and the minimum concentration was 1.28 ± 0.07 µg/L (male, 7 years old). The results also showed a variation in uranium concentration according to gender, smoking status, and age. A gender comparison employed in the study showed that men had higher concentrations of uranium in them than female subjects and this may dawn from the difference in hormonal makeup of the body. While the smoking habit, it was found that persons who smokers, contained higher levels of uranium than those who does not smokers, demonstrating that smoking is the main route for uranium absorption. The finding indicated a significant of uranium excretion with age, which matches the predictions of theICRP (International Commission on Radiological Protection) uranium model. Based on these findings, it remains necessary for increasing targeted public health interventions, strictly monitoring the environment, and utilizing campaigns to avoid uranium exposure along with related complications in high-risk patient populations.

Soybean Extract Ameliorates Lung Injury induced by Uranium Inhalation: An integrated strategy of network pharmacology, metabolomics, and transcriptomics.

AIM: This study aimed to evaluate the protective effect of soybean extract (SE) against uranium-induced lung injury in rats. MATERIALS AND METHODS: A rat lung injury model was established through nebulized inhalation of uranyl nitrate. Pretreatment with SE or sterile water (control group) by gavage for seven days before uranium exposure and until the experiment endpoints. The levels of uranium in lung tissues were detected by ICP-MS. Paraffin embedding-based hematoxylin & eosin staining and Masson's staining for the lung tissue were performed to observe the histopathological imaging features. A public database was utilized to analyze the network pharmacological association between SE and lung injury. The expression levels of proteins indicating fibrosis were measured by enzyme-linked immunosorbent assay. RNA-seq transcriptomic and LC-MS/MS targeted metabolomics were conducted in lung tissues. RESULTS: Uranium levels in the lung tissues were lower in SE-pretreated rats than in the uranium-treated group. Inflammatory cell infiltration and the deposition of extracellular matrix were attenuated, and the levels of alpha-smooth muscle actin, transforming growth factor beta1, and hydroxyproline decreased in SE-pretreated rats compared to the uranium-treated group. Active ingredients of SE were related to inflammation, oxidative stress, and drug metabolism. A total of 67 differentially expressed genes and 39 differential metabolites were identified in the SE-pretreated group compared to the uranium-treated group, focusing on the drug metabolism-cytochrome P450, glutathione metabolism, IL-17 signaling pathway, complement, and coagulation cascades. CONCLUSIONS: These findings suggest that SE may ameliorate uranium-induced pulmonary inflammation and fibrosis by regulating glutathione metabolism, chronic inflammation, and immune regulation.

Identification and Quantification of Multiphase U(VI) Speciation on Gibbsite with pH Using TRLFS and PARAFAC of Excitation Emission Matrices.

The significant abundance of uranium in radioactive waste inventories worldwide necessitates a thorough understanding of its behavior. In this work, the speciation of uranyl(VI), (UO22+) in a gibbsite system under ambient conditions has been determined as a function of pH by deconvolution and analysis of luminescence spectroscopic data. Uniquely, a combined experimental and statistical approach utilizing time-resolved luminescence spectroscopy and parallel factor analysis (PARAFAC) of excitation emission matrices has been successfully utilized to identify four separate luminescent U(VI) species in the uranyl-gibbsite system for the first time. The speciation of all luminescent U(VI) species in an environmentally relevant system over a pH range of 6-11 is discerned through the analysis of emission fingerprints at low temperature (20 K). Comparison of the deconvoluted luminescence spectra with mineral standards and geochemical models of the system allows the assignment of the luminescent chemical species as metaschoepite, Na-compreignacite, surface adsorbed ≡AlO2-UO2(OH) and ≡AlO2-UO2(CO3)24- complexes, with assignments supported by fitting of extended X-ray absorption fine structure data. The combined spectroscopic techniques in this study show that assignment and quantification of uranyl(VI) species in a sorption system over a large pH range can be accurately achieved using PARAFAC to deconvolute a three way emission spectroscopic data set.

In-situ assembly of polyoxometalate-based metal-organic framework for high-efficiency recovery of uranium.

Extracting uranium from water is crucial for environmental protection and the sustainable nuclear power industry. However, high-efficiency extraction and mild desorption condition still poses significant challenges. Herein, a polyoxometalate-based metal-organic framework (POMOF) for high-performance uranium extraction is prepared by in situ confined encapsulating H3[PW12O40] (PW12) into MIL-101(Cr). The highly dispersed PW12 enables adsorption sites to be sufficiently exposed, supports the pore structure of MIL-101(Cr), while being protected by spatial confinement. Furthermore, its abundant oxygen groups form high-affinity coordination with uranium and provide the pH-dependent conformation switch to achieve selective adsorption and instantaneous structural transformation. The assembly of structure and function makes POMOF exhibit substantial synergistic stability and adsorption capacity. Consequently, the constructed MIL-101(Cr)@PW12 exhibits excellent uranium adsorption ability of 461.88 mg/g, as well as superior selectivity towards a wide variety of metal ions. Remarkably, instantaneous desorption can be achieved in 2 s under mild desorption conditions of 0.005 mol/L HCl, and the adsorption capacity remained at 94.30 % after 8 adsorption cycles. POMOF demonstrates the vast potential for uranium capture from water and offers new insight into designing structure and functional synergistic materials for the selective adsorption and instantaneous desorption of uranium.