Radioactive Metal Research Articles

Synthesis and Preclinical Evaluation of a Novel FAPI-04 Dimer for Cancer Theranostics.

Overexpression of fibroblast activation protein (FAP) in cancer-associated fibroblasts in a wide variety of tumors enables a highly selective targeting strategy using FAP inhibitors (FAPIs). Quinoline-based FAPIs labeled with radionuclides have been widely developed for tumor-targeted nuclear medicine imaging. However, the short retention time of FAPIs at the tumor site limits their application in radionuclide therapy. In this study, a novel FAPI-04 dimer was synthesized and labeled with radionuclides to prolong the retention time in tumors for imaging and therapy. To prepare the FAPI-04 dimer complex, DOTA-Suc-Lys-(FAPI-04)2, we used Fmoc-Lys(Boc)-OH as the linker to conjugate two FAPI-04 structures by an amide reaction. The resulting product was further modified by DOTA groups to allow for conjugation with radioactive metals. Both [68Ga]Ga-(FAPI-04)2 and [177Lu]Lu-(FAPI-04)2 showed a radiochemical purity of >99% and remained stable in vitro. In vivo, micro-PET images of SKOV3, A431, and H1299 xenografts revealed that the tumor uptake of [68Ga]Ga-(FAPI-04)2 was about twice that of [68Ga]Ga-FAPI-04 and that the accumulation of [68Ga]Ga-(FAPI-04)2 at the tumor site did not significantly decrease even 3h after injection. The tumor-abdomen ratio of [68Ga]Ga-(FAPI-04)2 images was significantly higher than that of [18F]F-FDG images. For radionuclide therapy, [177Lu]Lu-(FAPI-04)2 effectively retarded tumor growth and displayed good tolerance. In conclusion, the DOTA-Suc-Lys-(FAPI-04)2 design enhanced its uptake in FAP-expressing tumors, improved its retention time at the tumor site, and produced high-contrast imaging in xenografts after radionuclide labeling. Furthermore, it showed a noticeable antitumor effect. DOTA-Suc-Lys-(FAPI-04)2 provides a new approach for applying FAPI derivatives in tumor theranostics.

Oxygen-containing functional groups enhance uranium adsorption by aged polystyrene microplastics: Experimental and theoretical perspectives

Although oxygen-containing functional groups generated during unavoidable aging play a key role in improving the adsorption performance of heavy metals by microplastics (MPs), little is known about the contribution of such groups to the interactions between highly toxic radioactive heavy metals and aged MPs. Here, we used a combination of batch experiments and density functional theory calculations to examine the effects and mechanisms of aging and the produced oxygen-containing functional groups, i.e., C═O, –OH, phenolic hydroxyl (–OHm), and –COOH, on the adsorption behavior of representative radionuclide uranium (U) on polystyrene (PS) MPs. The kinetic experimental results showed that the amount of U adsorption by the aged PS MPs was significantly higher than that of virgin PS MPs (P < 0.05). Binding-energy and thermodynamic data indicated that the affinity of PS MPs to a typical U species, i.e., uranyl, followed the order of PS═O–OHm > PS═O > PS–COOH > PS–OH > PS–OHm > virgin PS. Characterization and surface potential analyses demonstrated that the electronegative oxygen atoms in oxygen-containing functional groups in the aged PS MPs increased along with the aging time, and could serve as potential sites for electrostatic interactions with uranyl. Intramolecular interaction calculations confirmed that hydrogen bonding by oxygen-containing functional groups could strengthen the interactions between uranyl and aged PS MPs via electrostatic and polarization effects. Our findings provide an in-depth understanding of the role of aging in U adsorption by MPs, which is critical for assessing the fate of coexisting radionuclides and MPs in the environment, and their associated risks.

Probing Unexpected Reactivity in Radiometal Chemistry: Indium-111-Mediated Hydrolysis of Hybrid Cyclen-Hydroxypyridinone Ligands

Chelators based on hydroxypyridinones have utility in incorporating radioactive metal ions into diagnostic and therapeutic agents used in nuclear medicine. Over the course of our hydroxypyridinone studies, we have prepared two novel chelators, consisting of a cyclen (1,4,7,10-tetraazacyclododecane) ring bearing two pendant hydroxypyridinone groups, appended via methylene acetamide motifs at either the 1,4-positions (L1) or 1,7-positions (L2) of the cyclen ring. In radiolabeling reactions of L1 or L2 with the γ-emitting radioisotope, [111In]In3+, we have observed radiometal-mediated hydrolysis of a single amide group of either L1 or L2. The reaction of either [111In]In3+ or [natIn]In3+ with either L1 or L2, in aqueous alkaline solutions at 80 °C, initially results in formation of [In(L1)]+ or [In(L2)]+, respectively. Over time, each of these species undergoes In3+-mediated hydrolysis of a single amide group to yield species in which In3+ remains coordinated to the resultant chelator, which consists of a cyclen ring bearing a single hydroxypyridinone group and a single carboxylate group. The reactivity toward hydrolysis is higher for the L1 complex compared to that for the L2 complex. Density functional theory calculations corroborate these experimental findings and importantly indicate that the activation energy required for the hydrolysis of L1 is significantly lower than that required for L2. This is the first reported example of a chelator undergoing radiometal-mediated hydrolysis to form a radiometalated complex. It is possible that metal-mediated amide bond cleavage is a source of instability in other radiotracers, particularly those in which radiometal complexation occurs in aqueous, basic solutions at high temperatures. This study highlights the importance of appropriate characterization of radiolabeled products.

Elevated uranium concentration and low activity ratio (234U/238U) in the Œuf river as the result of groundwater–surface water interaction (Essonne river valley, South of Paris Basin, France)

Uranium (U) is a naturally occurring radioactive heavy metal widely distributed on Earth. Noticeable elevated U concentration and low activity ratio (AR) were occasionally detected in headwater stream of the Essonne river (Seine Basin, France), the namely Œuf river. This paper aims at providing new insight on geogenic U features in headwater streams and examines the role of river-groundwater interaction. The Œuf river was sampled four times in 2020 to investigate the influence of heterogeneous geology and hydrological seasonality. The dissolved fraction of water samples was analyzed for a variety of chemical parameters (anion, major, minor and trace element concentrations, isotopes 234U and 238U). The Œuf river was shown to exhibit elevated U concentration up to 19.3 μg L−1 (exceeding by 100-fold the value of 0.19 μg L−1 known for riverine average) and low AR down to 0.41 (almost the third of the value expected in surface water, i.e., 1.17). The Œuf river got enriched in U when receiving groundwater from Beauce Limestone Aquifer System. High U concentration (above 15 μg L−1) was found in association with low AR (below 0.5) in the stream water when flowing in the outcrop zone of one BLAS unit. Taking advantage of changes in the stream flow conditions and the geochemical contrast between surface and ground waters, mixing volumes were calculated. This study first examined the potential of using U isotopes in combination with selenium as hydrogeochemical tracers of the river-groundwater continuum. In HWS, the aquifer discharge was shown to supply 12 to 59 % of the river water. This study demonstrates the key role played by the river-groundwater interaction on river water chemistry in small streams draining catchment with various geology setting. It also supports the use of combining redox sensitive trace elements to track the river-groundwater continuum.

Application of Hydrogen-Bonded Organic Frameworks in Environmental Remediation: Recent Advances and Future Trends

The hydrogen-bonded organic frameworks (HOFs) are a class of porous materials with crystalline frame structures, which are self-assembled from organic structures by hydrogen bonding in non-covalent bonds π-π packing and van der Waals force interaction. HOFs are widely used in environmental remediation due to their high specific surface area, ordered pore structure, pore modifiability, and post-synthesis adjustability of various physical and chemical forms. This work summarizes some rules for constructing stable HOFs and the synthesis of HOF-based materials (synthesis of HOFs, metallized HOFs, and HOF-derived materials). In addition, the applications of HOF-based materials in the field of environmental remediation are introduced, including adsorption and separation (NH3, CO2/CH4 and CO2/N2, C2H2/C2He and CeH6, C2H2/CO2, Xe/Kr, etc.), heavy metal and radioactive metal adsorption, organic dye and pesticide adsorption, energy conversion (producing H2 and CO2 reduced to CO), organic dye degradation and pollutant sensing (metal ion, aniline, antibiotic, explosive steam, etc.). Finally, the current challenges and further studies of HOFs (such as functional modification, molecular simulation, application extension as remediation of contaminated soil, and cost assessment) are discussed. It is hoped that this work will help develop widespread applications for HOFs in removing a variety of pollutants from the environment.

Phytoremediation of Heavy Metals from Irrigation Water, Faisalabad, Pakistan

A technique called phytoremediation makes use of a plant’s root system to draw contaminants, primarily heavy metals (zn, cr, and ni), from the surrounding rhizosphere. These are the end result of human actions such the use of pesticides, waste byproducts, cosmetics, and pharmaceuticals. This analysis focuses on soil contamination removal since prolonged exposure to heavy metals can cause respiratory illnesses, cardiovascular disorders, cancer of the liver, lungs, and kidneys, among other problems. In order to immobilise metals and change their harmful states into less toxic states, plants use a process called phytoremediation and tactics like phyto(rhizo) stabilisation. Chromium 6 is changed into chromium 3 through phytostabalization, a process in which plants are utilised to change a pollutant’s more hazardous form into a less hazardous volatile form that may be transported. Macrophytes, such as Arbidopsis thaliana and Cgara canescens, have been found to use phytofiltration and phytovolatization to remove radioactive and heavy metals. Indian mustard (Brassica juncea) and sun flower (Helianthus annus) are suitable plants for rhizofilteration, which is essential to prevent environmental and health problems. A heavy metal that is widely present in soil is cadmium. Cd can be removed physically in a number of ways, with membrane filtration and adsorption being the most often utilised techniques for doing so. Chemical (in which the addition of barium acetate caused coagulation) and biological (which uses microorganisms such bacteria, yeast species, fungal aspergillus, and green algea chlorel for the Bioremediation of Cd.) approaches are also employed for the removal of cadmium. In essence, phytoremediation uses the already-existing power of plant systems. This approach is more economical and environmentally benign than conventional approaches for cleaning up contaminated soil and ground water. Since drinking water contaminated with heavy metals is thought to be the primary cause of death in Pakistan, getting rid of these pollutants is our top priority.

Removal and isolation of radioactive cobalt using DNA aptamers

Abstract Electricity generation using nuclear power has various advantages, such as carbon reduction, but the treatment of nuclear waste is emerging as a big issue in many countries. The development of technology that can selectively remove radionuclides from liquid radioactive waste is one of the ways to reduce nuclear waste. Here, we assessed a new way of removing radioactive cobalt from a liquid using an aptamer. Aptamers specifically binding cobalt ions were selected through systematic evolution of ligands by exponential enrichment (SELEX). Their binding strength and stability of their complexes with cobalt were analyzed through surface plasmon resonance assay and 2D program Mfold, respectively. The optimal aptamer/bead conjugate conditions for binding cobalt were established using an FA-C1 aptamer with the strongest binding to cobalt. Under these conditions, more than 80% of radioactive cobalt was removed, and more than 99.95% of removed cobalt was recovered. These results proved that radioactive cobalt removal using this aptamer can effectively reduce liquid radioactive waste. This means that the aptamer/bead complex can be utilized to remove various radioactive metal ions.

Flowthrough of 239PU and 55FE during RNA extraction

Analysis of gene expression has become an important tool in understanding low-dose effect mechanisms of ionizing radiation at the cellular level. Metal binding to nucleic acids needs to be considered when interpreting these results, as some radioactive metals, particularly actinides, may produce free radicals and cause oxidative stress damage via chemical means at rates much higher than free radical formation related to their radiological properties. Bacteria exposed in situ to low dose rates of plutonium-239 (239Pu) and iron-55 (55Fe) were previously analysed for gene expression. The work herein was motivated by an interest in more precisely identifying the distribution of radionuclides in these bacteria as well as the practical need to ensure appropriate transport and handling of the associated ribonucleic acid (RNA) extractions. RNA extractions were performed on bacteria growth media with and without bacteria cells (i.e. with and without RNA) at several different concentrations of 239Pu and 55Fe to inform the level of specificity of the extraction membrane as well as provide insight into internal (uptake) vs external (sorption) accumulation of these radionuclides in bacteria cells. Results of the study suggest that 239Pu and 55Fe detected in RNA extraction samples during long term cell studies is the result of binding to RNA prior to the time of extraction, as opposed to flow through or binding after cell lysis, and it highlights the practical importance of nucleic acid sample characterization to radiation protection more generally.

Modification in Applying Appendix D of 40 CFR Part 61 to Heated Solid Radionuclide Materials With High Melting and Boiling Points.

Appendix D of Title 40 Part 61 of the US Code of Federal Regulations (CFR) provides a procedure that US Department of Energy (US DOE) facility owners and operators can use to estimate radionuclide emissions to the atmosphere for dose calculations instead of measuring emissions for minor sources under the 40 CFR Part 61, Subpart H, National Emission Standards for Emissions of Radionuclides Other Than Radon From Department of Energy Facilities, regulation. The procedure assumes that any radioactive material heated above 100 °C is completely vaporized and emitted to the atmosphere. In 1991, the US DOE Oak Ridge Reservation (ORR) requested approval to use different release fractions (RFs) for uranium because of its high melting and boiling points. In response to the request, the US Environmental Protection Agency (US EPA) Region IV approved the use of modified RFs for elemental uranium provided no reaction had taken place to alter its chemical form. In 2015, the ORR requested approval to use different RFs for tungsten, again because of its high melting and boiling points. EPA Region IV approved the use of modified RFs for heated radioactive tungsten metal. In accordance with the two precedents set for heating uranium and radioactive tungsten metals, in 2016, the ORR requested approval to use modified RFs in a similar fashion for other radioactive solid metals and compounds with melting and boiling points above 500 °C that might be heated above 100 °C in future research projects and experiments. EPA Region IV again granted approval to use modified RFs for the list of compounds. This note discusses the proposed modified RFs and their development.

Flumequine-mediated fluorescent zeolitic imidazolate framework functionalized by Eu3+ for sensitive and selective detection of UO22+, Ni2+ and Cu2+ in nuclear wastewater

Currently, antibiotics and heavy metal contaminants have posed a great threat for ecological security and human health. Herein, the lanthanide functionalized ZIF (named ZIF-90-PABA-Eu) is constructed by coordinating with Eu3+ via p-aminobenzoic acid intermediate. Due to the excellent fluorescence properties, the novel fluorescent probe can selectively monitor flumequine based on “turn on” mode. Furthermore, the obtained new material (named ZIF-90-PABA-Eu-Flu) can be used as “turn off” sensor for selective detection of both radioactive and nonradioactive heavy metal ions (UO22+, Ni2+ and Cu2+) which are the main component of nuclear industrial wastewater. ZIF-90-PABA-Eu-Flu shows ultra-short fluorescence response time (3 s) and ultra-low limit of detection (9.0 × 10−3, 1.3 × 10−2 and 6.1 × 10−4 ppm) for three metal ions, which may be attributed to its good affinity with UO22+, Ni2+ and Cu2+. Moreover, principal component analysis (PCA) is applied to distinguish the three metal ions. Additionally, the possible sensing mechanism is investigated by the UV–vis spectra, luminescence lifetimes and theoretical calculation analysis. Based on these results, ZIF-90-PABA-Eu possesses promising potential in practical application and provides insight for the design of novel probes to continuously monitor flumequine, radioactive and nonradioactive heavy metal ions.

In Vivo Preclinical Assessment of the VEGF Targeting Potential of the Newly Synthesized [52Mn]Mn-DOTAGA-Bevacizumab Using Experimental Cervix Carcinoma Mouse Model.

Among humanized monoclonal antibodies, bevacizumab specifically binds to vascular endothelial growth factor A (VEGF-A). VEGF-A is an overexpressed biomarker in cervix carcinoma and is involved in the development and maintenance of tumor-associated neo-angiogenesis. The non-invasive positron emission tomography using radiolabeled target-specific antibodies (immuno-PET) provides the longitudinal and quantitative assessment of tumor target expression. Due to antibodies having a long-circulating time, radioactive metal ions (e.g., 52Mn) with longer half-lives are the best candidates for isotope conjugation. The aim of our preclinical study was to assess the biodistribution and tumor-targeting potential of 52Mn-labeled DOTAGA-bevacizumab. The VEGF-A targeting potential of the new immuno-PET ligand was assessed by using the VEGF-A expressing KB-3-1 (human cervix carcinoma) tumor-bearing CB17 SCID mouse model and in vivo PET/MRI imaging. Due to the high and specific accumulation found in the subcutaneously located experimental cervix carcinoma tumors, [52Mn]Mn-DOTAGA-bevacizumab is a promising PET probe for the detection of VEGF-A positive gynecological tumors, for patient selection, and monitoring the efficacy of therapies targeting angiogenesis.

Elaboration of geopolymer package derived from uncalcined phosphate sludge and its solidification performance on nuclear grade resins loaded with 134Cs.

Nuclear-grade Spent Organic Resin (SOR) contains high concentrations of radioactive nuclides and metal contaminants, while phosphate sludge contains high amount of fine clayey particles and CO32-, both posing a major threat to the biosphere. In this study, a novel geopolymer package (GP) was proposed to directly solidify SOR loaded with 134Cs by incorporating uncalcined phosphate sludge (UPS) as feedstocks, activated by NaOH/KOH. The results showed that alkali-mixed reagents-activated GP is more advantageous in terms of chemical stability and mechanical properties than NaOH-activated GP, recording compressive strength values greater than the waste acceptance criteria and OPC. The 28-day compressive strength of solidified packages can exceed 31 MPa at the highest amount of 42 wt% UPS. The addition of NaF powder into the solidified packages generates more hybrid type gels, which are more conducive to partial dissolution and bonding UPS particles, thereby producing stable and stronger GP. Leaching results of solidified GP in presence of up to 13 wt% SORs showed that only 0.15 % of total 134Cs was leached, even under aggressive solutions. Solidification mechanism revealed that activation of UPS-MK blend forms N,K-A-S-H, (N,K,C)-A-S-H/C-S-H gels coexisting with unreacted particles, thereby solidify/stabilize metal contaminants and Cs+ by a synergetic immobilization action of hydration products via substitution and encapsulation. This study provides a promising paradigm for effective solidification of nuclear-grade resins and synergetic harmless treatment of industrial/phosphate mine solid wastes.

Non-targeted metabolomics and 16s rDNA reveal the impact of uranium stress on rhizosphere and non-rhizosphere soil of ryegrass

As a radioactive heavy metal element with a long half-life, uranium causes environmental pollution when it enters the surrounding soil. This study analyzed the changes about soil enzyme activity, non-targeted metabolomics, microbial community structure and function microbial community structure and function to assess the differences in the effects of uranium stress on rhizosphere and non-rhizosphere soil. Results showed that uranium stress significantly inhibited the activities of urease and sucrase in rhizosphere and non-rhizosphere, which had less effect on rhizosphere. Compare to the non-rhizosphere soil, the uranium stress induced the production of gibberellin A1, to promoted several metabolic pathways, such as nitrogen and PTS (Phosphotransferase system) metabolic in rhizosphere soil. The species and abundance of Aspergillus, Acidobacter, and Synechococcus in both rhizosphere and non-rhizosphere soil were decreased by uranium stress. However, the microorganisms in rhizosphere soil were less inhibited according to the soil metabolism and microbial network map analysis. Furthermore, the Chujaibacter in rhizosphere soil under uranium stress was found significantly positively correlated with lipid and organic oxygen compounds. Overall, the results indicated that ryegrass roots significantly alleviated the effects of uranium stress on soil microbial activity and population abundances, thus playing a protective role. The study also provided a theoretical basis for in-depth understanding of the biological effects, prevention and control mechanisms of uranium-contaminated soil.

One-Pot Environmentally Friendly Synthesis of Nanomaterials Based on Phytate-Coated Fe3O4 Nanoparticles for Efficient Removal of the Radioactive Metal Ions 90Sr, 90Y and (UO2)2+ from Water.

We report the fast (three minutes) synthesis of green nanoparticles based on nanoparticles coated with the natural organic receptor phytate for the recognition and capture of 90Sr, 90Y, and (UO2)2+. The new material shows excellent retention for (UO2)2+, 97%; these values were 73% and 100% for 90Sr and 90Y, respectively. Recovery of the three radioactive metal ions occurs through a non-competitive process. The new hybrid material is harmless, easy to prepare, and immobilizes these radioactive contaminants in water with great efficiency.

Cellular transport of uranium and its cytotoxicity effects on CHO-k1 cells

Uranium is a radioactive heavy metal and a significant public health concern; however, its associated underlying toxicological mechanisms remain largely unknown. In this work, the uptake and efflux processes of uranium in CHO-k1 cells were studied and the cytotoxicity effects were explored. It was found that both the uptake and efflux processes took place rapidly and half of the internalized uranium was expelled within 8 h. The uranium exposure caused a decrease of cell viability and adhesion ability in a dose-dependent manner and blocked the cell cycle at the G1 stage. In addition, gene expression analysis revealed relative changes in the transcription of metabolism related genes. Further studies revealed that the cytotoxicity of uranium could be alleviated by exposing cells to a lower temperature or by the addition of amantadine-HCl, an endocytosis inhibitor. Interestingly, after uranium exposure, needle-like precipitates were observed in both intracellular and extracellular regions. These findings collectively suggest that the cellular transport of uranium is a rapid process that disturbs cell metabolism and induces cytotoxicity, and this impact could be reduced by slowing down endocytic processes.

Amino-functionalized 3D crosslinked Ti3C2Tx nanosheets for highly efficient UO22+ and ReO4− immobilization simultaneously from aqueous solutions

Construction of the multifunctional Ti3C2Tx for efficient extraction of radioactive metal cations and anions from radioactive waste simultaneously remained challenging. Decorating Ti3C2Tx into multifunctional materials with controllable and desired properties was an efficient strategy for eliminating UO22+ and ReO4−. In this work, a novel amino-functionalized 3D crosslinked Ti3C2Tx nanosheets (N-CTC) were designed by covalent bonding crosslinking method, followed by a facile hard template to prevent the delamination Ti3C2Tx nanosheets from stacking. Introducing amino functional groups and adjusting surface charge of N-CTC considerably enhances the removal of simultaneously UO22+ and ReO4− from aqueous solutions. Impressively, N-CTC exhibited the exceptional trapping capacities toward UO22+ (550.71 mg/g) and ReO4− (105.01 mg/g), which were significantly superior than that of the pristine Ti3C2Tx nanosheets. More importantly, N-CTC also possessed fast rapidly and recyclable UO22+/ReO4− extraction in different artificial water samples. The elimination mechanism was clearly visualized by spectral analysis, uncovering UO22+ removal was abided by chelation effect, whereas the ReO4− adsorption was determined by both inner-sphere complexation and electrostatic interaction. The present results illustrate an effective strategy to design functionalized 3D crosslinked Ti3C2Tx nanosheets with effectively extraction of radioactive metal cations and anions from wastewater.

Mining industry of the Far Eastern Federal District: Structure, macroeconomic performance and growth prospects

The Far Eastern Federal District holds more than 6000 mineral deposit, including both proven and provisionally geologically appraised minefields. The deposits contain almost all minerals entered in the Mineral Resources Balance Sheet of Russia, including strategic minerals. The region possesses ferrous, nonferrous, rare and radioactive metals; nonmetallic, coal, peat, etc. In this connection, the growth prospects of the mining industry of Russia&rsquo;s Far East are assessed. Metallic mineral production in the Far Eastern District, including export, is insufficient to eliminate or reduce dependence of the local economic agents on the governmental grants. Reproduction of solid mineral resources dramatically lagged behind the needs because of the long deficiency of advanced planning and adequate geological exploration. The processing industry infrastructure is either underdeveloped or absent at all. In view of the size of the District and its remoteness from the industrial centers of Russia, the international market trends and the District&rsquo;s economic self-sufficiency with the own mineral resources, it is critical in the long view to identify new strategies of mineral mining. The export-aimed concept should be denied in favor of the self-contained development of the backbone industries using the own feedstock. The proven ferrous and nonferrous metal reserves, their structure and spatial location allow creating the fundamental mineral processing centers, first of all, metallurgical (ferrous metals and copper).

Metal chelating and anti-radical activity of Salvia officinalis in the ameliorative effects against uranium toxicity

Uranium is a highly radioactive heavy metal that is toxic to living things. In this study, physiological, cytogenetic, biochemical and anatomical toxicity caused by uranium and the protective role of sage (Salvia officinalis L.) leaf extract against this toxicity were investigated with the help of Allium test. Germination percentage, root length, weight gain, mitotic index (MI), micronucleus (MN) formation, chromosomal aberrations (CAs), superoxide dismutase (SOD) and catalase (CAT) enzyme activities, malondialdehyde (MDA) levels and changes in root meristem cells were used as indicators of toxicity. In the experimental stage, a total of six groups, one of which was the control, were formed. Group I was treated with tap water, while group II and III were treated only with sage (190 mg/L and 380 mg/L). Groups IV, V and VI were germinated with uranyl acetate dihydrate (0.1 mg/mL), uranyl acetate dihydrate + 190 mg/L sage and uranyl acetate dihydrate + 380 mg/L sage, respectively. Allium cepa L. bulbs of each group were germinated for 72 h, and at the end of the period, routine preparation techniques were applied and physiological, cytogenetic, biochemical and anatomical analyzes were performed. As a result, uranium application caused a significant decrease (p < 0.05) in all physiological parameters and MI values. MN, CAs numbers, SOD and CAT enzyme activities and MDA levels increased significantly (p < 0.05) with uranium application. Uranium promoted CAs in the root tip cells in the form of fragment, vagrant chromosome, sticky chromosome, bridge and unequal distribution of chromatin. In addition, it caused anatomical damages such as epidermis cell damage, cortex cell damage and flattened cell nucleus in root tip meristem cells. Sage application together with uranium caused significant (p < 0.05) increases in physiological parameters and MI values and significant decreases in MN, CAs, SOD and CAT activities and MDA levels. In addition, the application of sage resulted in improvement in the severity of anatomical damages induced by uranium. It was determined that the protective role of sage observed for all parameters investigated was even more pronounced at dose of 380 mg/L. The protective role of sage against uranium toxicity is related to its antioxidant activity, and sage has 82.8% metal chelating and 72.9% DPPH removal activity. As a result, uranyl acetate exhibited versatile toxicity in A. cepa, caused cytotoxicity by decreasing the MI rate, and genotoxicity by increasing the frequencies of MN and CAs. And also, Sage acted as a toxicity-reducing agent by displaying a dose-dependent protective role against the toxic effects induced by uranyl acetate.

Adsorptive sequestration of noxious uranium (VI) from water resources: A comprehensive review

Groundwater is usually utilized as a drinking water asset everywhere. Therefore, groundwater defilement by poisonous radioactive metals such as uranium (VI) is a major concern due to the increase in nuclear power plants as well as their by-products which are released into the watercourses. Waste Uranium (VI) can be regarded as a by-product of the enrichment method used to produce atomic energy, and the hazard associated with this is due to the uranium radioactivity causing toxicity. To manage these confronts, there are so many techniques that have been introduced but among those adsorptions is recognized as a straightforward, successful, and monetary innovation, which has gotten major interest nowadays, despite specific drawbacks regarding operational as well as functional applications. This review summarizes the various adsorbents such as Bio-adsorbent/green materials, metal oxide-based adsorbent, polymer based adsorbent, graphene oxide based adsorbent, and magnetic nanomaterials and discuss their synthesis methods. Furthermore, this paper emphasis on adsorption process by various adsorbents or modified forms under different physicochemical conditions. In addition to this adsorption mechanism of uranium (VI) onto different adsorbent is studied in this article. Finally, from the literature reviewed conclusion have been drawn and also proposed few future research suggestions.

Preparation and high temperature properties of Nb/Y2O3 coating on the pure Nb substrate by laser cladding

In nuclear industry, the refractory metal of niobium (Nb) is an important candidate as the crucible substrate material for melting radioactive metals, such as uranium (U). However, since Nb readily reacts with molten metals at high temperatures, a protective coating is required. In this work, Nb/Y2O3 coatings were prepared on the pure Nb substrates by laser cladding with a dip coating technique. Phase microstructure, composition, thermal cycle durability, and corrosion resistance of the coating were investigated. The results show that dense Nb/Y2O3 coatings with a Ra value of 0.94 and an average bond strength of 73.1 MPa were obtained. The Y2O3 layer with thermochemical stability, located on the upper layer, was the main body of the coating. Also, few defects, such as microcracks, were observed in the coating. The Nb/Y2O3 coating reached 14 thermal cycles over a constant temperature of 1400 °C. The molten cerium (Ce) was selected for simulating corrosive environment. After corrosion for 4 h, the Nb substrate was severely damaged, and a corrosion reaction layer with a thickness of 18 ± 4 μm was formed between the Nb substrate and Ce. No corrosion layer was observed on the surface of Nb/Y2O3 coatings, indicating that the Y2O3 layer resulted in a considerable improvement in the corrosion resistance. During corrosion for 8 h, the accumulated thermal stress resulted in the crack propagation. Furthermore, the melt preferentially diffused towards the interior of the coating along the microcracks (as percolation channels) on the surface due to the capillary effect, aggravating the propagation of the crack tips. In addition, the melt performed poor wettability on the coating surface.