Search Results (186)

Iron (Fe) chelators are used to treat iron-overloaded disorders, metal detoxification, radionuclides, and molecular imaging; however, they can cause side effects. In this study, we identified and characterized Coprogen B (CPGB), a hexadentate trihydroxamate siderophore secreted by the opportunistic dimorphic fungus Talaromyces marneffei and compared its properties with deferoxamine (DFO). Siderophore production was enriched from a ΔsreA strain and purified via Amberlite XAD2 and Sephadex LH20 chromatography, followed by reverse-phase HPLC. Active fractions were confirmed by Ultraviolet–Visible (UV–Vis) spectral fingerprints (≈230 nm) for hydroxamate, with a band at 430–450 nm upon Fe(III) complexation, as well as by chrome azurol A assay, Nuclear Magnetic Resonane (NMR) spectroscopy, High-Performance Liquid Chromatography–Mass Spectrometry (HPLC-MS), and Matrix-Assisted Laser Desorption/Ionization–Time-of-Flight Mass Spectrometry (MALDI-TOF-MS). CPGB exhibited strong molar absorptivity and rapid, concentration-dependent chelation of Fe(III), yielding a sustained binding profile that matched or exceeded that of DFO over time. In determining n-octanol/water partitioning for CPGB and DFO (230 nm) and their Fe(III) complexes, the partitioning (P) assay revealed that CPGB was moderately hydrophilic (P = 0.505 ± 0.063; cLogP = −0.299 ± 0.053), while DFO was strongly hydrophilic (P = 0.098 ± 0.005; cLogP = −1.010 ± 0.022). Fe(III) complexation reduced lipophilicity: CPGB–Fe partitioned ~30–35% into octanol, while DFO–Fe complex partitioned ~7–8%, remaining largely aqueous. Overall, this outcome potentially suggested improved clearance in vivo. These data nominate CPGB as a promising alternative to existing iron chelators. The siderophore exhibited greater lipophilicity, emphasizing better passive membrane permeability than DFO, while siderophore–Fe(III) binding indicated increased biases toward the aqueous phase. Future in vivo studies are warranted to confirm its pharmacokinetics, safety, and therapeutic efficacy. Full article

This study explores, for the first time, the bioaccumulation of americium-241 (²⁴¹Am) by Cupriavidus metallidurans and Ochrobactrum anthropi, two bacterial strains previously investigated mainly for their interactions with other heavy metals and radionuclides. To the best of our knowledge, no prior studies have reported the use of these microorganisms for ²⁴¹Am removal from aqueous solutions. The effects of initial ²⁴¹Am concentration and solution pH on removal performance were evaluated through batch experiments. Kinetic analyses were performed using pseudo-first-order (PFO) and pseudo-second-order (PSO) models, with the PSO model providing a better fit, suggesting chemisorption as the rate-limiting step in the process. Initial ²⁴¹Am concentrations ranged from 75 to 300 Bq mL⁻¹, and both bacterial strains demonstrated comparable maximum bioaccumulation capacities of approximately 1.5 × 10⁻⁸ mmol g⁻¹. However, O. anthropi exhibited superior resistance to ²⁴¹Am, maintaining colony growth at activity levels up to 1200 Bq mL⁻¹, compared to a threshold of 400 Bq mL⁻¹ for C. metallidurans. These findings highlight the robustness and efficiency of these bacterial strains—particularly O. anthropic—in removing ²⁴¹Am from liquid radioactive waste, offering promising implications for bioremediation technologies. Full article

The remediation of soils contaminated with heavy metals and radionuclides remains a significant environmental challenge. This study evaluated the phytoremediation potential of industrial hemp (Cannabis sativa L.) in soil collected from a historical evaporation dam, characterized by high levels of diverse metals, including Al, Cr, Fe, and radioactive elements (U, Th). Three treatments were applied: a control, a metal-spiked treatment (chelated with citric acid), and an NPK + spike treatment. A separate six-month greenhouse trial compared plants grown with and without NPK nutrients. Results demonstrated that the addition of a chelating agent significantly enhanced the bioavailability and subsequent uptake of key metals, including U, Se, and Pd. NPK fertilization combined with chelation resulted in the greatest plant biomass (≈4.5 g) and height (>18 cm), which correlated with higher total metal accumulation. Bioaccumulation factors (BAF > 1) were highest for B, Sr, Cd, and Bi, with values for Cd and U reaching 1.3 and 2.1, respectively. Foliar analysis revealed that leaves accumulated significantly higher metal concentrations than stems (e.g., Translocation Factor (TF) ~ 2.0 for Cd, Pb, and U), acting as the primary sink. This study concludes that hemp, particularly when assisted with chelating agents and adequate nutrition, is a highly effective candidate for the phytoremediation of multi-metal contaminated soils. The NPK + chelation strategy is the most promising for maximizing both biomass production and metal extraction efficiency. 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

Among the main man-made water pollutants that pose a danger to the environment are oil products, heavy metals, and radionuclides, as well as micro- and nanoplastics. To purify such waters, it is necessary to use advanced methods, with sorption being one of them. The aim of this work is to develop a nano-functionalized composite, comprising magnetically responsive, thermally expanded graphite (TEG) and the natural clay bentonite, and to assess its ability to purify man-made contaminated waters. Throughout the course of the research, the methods of scanning electron microscopy, optical microscopy, dynamic light scattering, radiometry, and atomic absorption spectrophotometry were used. The use of the TEG–bentonite composite for the purification of the model water, simulating radioactively contaminated nuclear power plant (NPP) effluent, reduced the content of organic substances by 10–15 times, and the degree of extraction of cesium, strontium, cobalt, and manganese was between 81.4% and 98.8%. The use of the TEG–bentonite composite for the purification of real radioactively contaminated water obtained from the object “Shelter” (“Ukryttya” in Ukrainian), in the Chernobyl Exclusion Zone, Ukraine, with high activity, containing organic substances, including micro- and nanoplastics, reduced the radioactivity by three orders of magnitude. The use of cesium-selective sorbents for additional purification of the filtrate allowed for further decontamination of radioactively contaminated water with an efficiency of 99.99%. Full article

Phosphogypsum (PG) is a byproduct of the wet phosphoric acid (WPA) production process. Since PG originates from phosphate rock (PR), it holds various concentrations of heavy metal and radionuclide, posing an environmental threat because of its large production and long-term accumulation. In addition to toxic heavy metals, PG may also be an alternative source of rare earth elements (REEs), since over 60% of REEs in PR transfer to PG during acid digestion. With the increasing demand of phosphoric acid (PA), global PG generation is approaching 300 million tons annually. Since 1994, an estimated 6.73 billion tons of PG has been produced worldwide, with approximately 58% (approx. 3.7 billion tons) ending up in stacks. Assuming a conservative REE content of 0.1%, these stacks may hold over 3.7 million tons of REEs. This review discusses phosphoric acid production processes and the transfer of REEs from PR to PG. In addition, it also discusses the current REEs world reserves, their presence in primary and secondary sources, and their uses. The review critically evaluates the research that has been conducted so far and the recent innovations in REE recovery from PG, and discusses the challenges associated with scalability and raw material variability. Full article

Terbium-161 (¹⁶¹Tb) is an emerging β⁻-emitting radionuclide of high interest for targeted radionuclide therapy. However, its reactor-based production presents significant challenges in the efficient separation of ¹⁶¹Tb from target ¹⁶⁰Gd and co-produced ¹⁶¹Dy. In this study, the separation of ¹⁶¹Tb by a solvent-impregnated resin P350@resin has been evaluated. A combination of static adsorption and dynamic column experiments was conducted to investigate the separation behavior of Gd³⁺, Tb³⁺, and Dy³⁺. Optimal separation performance was achieved at 0.4–0.6 mol/L HNO₃, using a column bed height of 20–28 cm and flow rates of 0.5–1.0 mL/min. A two-step elution protocol enabled near-baseline resolution between Tb and Gd, Dy within 3 h, ensuring high-purity and fast product recovery. Comprehensive characterization using SEM-EDS, FT-IR, and XPS confirmed that metal ion uptake occurs via coordination with phosphoryl groups on the resin. The P350@resin thus enables a simple and selective separation platform for the production of no-carrier-added ¹⁶¹Tb, with high potential for clinical radiopharmaceutical manufacturing. Full article

Some of nuclear power’s primary detractors are the unique environmental challenges and impacts of radioactive wastes generated during fuel cycle operations. Key benefits of spent fuel reprocessing (SFR) are reductions in primary high active waste (HAW) masses, volumes, and lengths of radiotoxicity at the expense of secondary waste generation and high capital and operational costs. By employing advanced waste management and resource recovery concepts in SFR beyond the existing standard PUREX process, such as minor actinide and fission product partitioning, these challenges could be mitigated, alongside further reductions in HAW volumes, masses, and duration of radiotoxicity. This work assesses various current and proposed SFR and fuel cycle options as base cases, with further options for fission product partitioning of the high heat radionuclides (HHRs), rare earths, and platinum group metals investigated. A focus on primary waste outputs and the additional energy that could be generated by the reprocessing of high-burnup PWR fuel from Gen III(+) reactors using a simple fuel cycle model is used; the effects of 5- and 10-year spent fuel cooling times before reprocessing are explored. We demonstrate that longer cooling times are preferable in all cases except where short-lived isotope recovery may be desired, and that the partitioning of high-heat fission products (Cs and Sr) could allow for the reclassification of traditional raffinates to intermediate level waste. Highly active waste volume reductions approaching 50% vs. PUREX raffinate could be achieved in single-target partitioning of the inactive and low-activity rare earth elements, and the need for geological disposal could potentially be mitigated completely if HHRs are separated and utilised. Full article

Between approximately 725 and 518 Ma, a suite of specialized felsic plutons and granitic stocks were emplaced across the Arabian Shield, many of which are now recognized as highly mineralized prospects enriched in rare earth elements (REEs), rare metals, and radioactive elements bearing mineralizations. The current investigation focused on the radiological and geochemical characterization of naturally occurring radionuclides, specifically ²³⁸U, ²²⁶Ra, ²³²Th, and ⁴⁰K, within three strategically selected granitic prospects, namely, J. Tawlah albite granite (TW), J. Hamra (HM), and J. Abu Al Dod alkali feldspar syenite and granites (AD). Concerning the radioactivity levels of the investigated granitic stocks, specifically the activity concentrations of ²³⁸U, ²²⁶Ra, ²³²Th, and ⁴⁰K, the measured average values demonstrate significant variability across the TW, HM, and AD stocks. The average ²³⁸U concentrations are 195 (SD = 38.7), 88.66 (SD = 25.6), and 214.3 (SD = 140.8) Bq/kg for TW, HM, and AD granitic stocks, respectively. Corresponding ²²⁶Ra levels are recorded at 172.4 (SD = 34.6), 75.62 (SD = 25.9), and 198.4 (SD = 139.5) Bq/kg. For ²³²Th, the concentrations are markedly elevated in TW at 5453.8 (SD = 2182.9) Bq/kg, compared to 77.16 (SD = 27.02) and 160.2 (SD = 103.8) Bq/kg in HM and AD granitic stocks, respectively. Meanwhile, ⁴⁰K levels are reported at 1670 (SD = 535.9), 2846.2 (SD = 249.9), and 3225 (SD = 222.3) Bq/kg for TW, HM, and AD granitic plutons, respectively. Notably, these values exceed the global average background levels, indicating an anomalous enrichment of the studied granitic occurrences. The mean radiological hazard indices for each granitic unit generally exceed global benchmarks, except for AEDE_out in the HM and AD stocks, which remain below international limits. The geochemical disparities observed are indicative of post-magmatic alteration processes, as substantiated by the interpretation of remote sensing datasets. In light of the significant radiological burden presented by these granitic stocks, it is essential to implement a rigorous precautionary framework for any future mining. These materials must be categorically excluded from uses that entail direct human exposure, especially in residential construction or infrastructure projects. Full article

Zirconium-89 (⁸⁹Zr) is a widely used radionuclide in immune-PET imaging due to its physical decay characteristics. Despite its importance, the production of ⁸⁹Zr radiopharmaceuticals remains largely manual, with limited cost-effective automation solutions available. To address this, we developed an automated system for the agile and reliable production of radiopharmaceuticals. The system performs transmutations, dissolution, and separation for a range of radioisotopes. Steps in the production of ⁸⁹Zr-oxalate are used as an exemplar to illustrate its use. Three-dimensional (3D) printing was exploited to design and manufacture a target holder able to include solid targets, in this case an ⁸⁹Y foil. Spot welding was used to attach ⁸⁹Y to a refractory tantalum (Ta) substrate. A commercially available CPU chiller was repurposed to efficiently cool the metal target. Furthermore, a commercial resin (ZR Resin) and compact peristaltic pumps were employed in a compact (10 × 10 × 10 cm³) chemical separation unit that operates automatically via computer-controlled software. Additionally, a standalone 3D-printed unit was designed with three automated functionalities: photolabelling, vortex mixing, and controlled heating. All components of the assembly, except for the target holder, are housed inside a commercially available hot cell, ensuring safe and efficient operation in a controlled environment. This paper details the design, construction, and modelling of the entire assembly, emphasising its innovative integration and operational efficiency for widespread radiopharmaceutical automation. Full article

For the first time, the deposition area of heavy metals and other trace elements (Al, Ba, Cd, Co, Cr, Cu, Fe, Mn, Ni, P, Pb, S, Sr, Sb, V, Zn, and Hg) on the territory surrounding a landfill of domestic (municipal) waste at the 9th km of the Vilyuisky tract of Yakutsk within a radius of 51 km was assessed using the method of moss biomonitors and ICP-OES as an analytical technique. Mosses were analyzed for radionuclide content (⁴⁰K, ¹³⁷Cs, ²¹² Pb, ²¹⁴Pb, ²¹²Bi, ²¹⁴Bi, ²⁰⁸Tl, ⁷Be, and ²²⁸Ac) in a number of selected samples by semiconductor gamma spectrometry. The results of the examination of moss samples by ICP-OES indicate the presence of large amounts of toxic Ba and metal debris (Al, Co, Cr, Fe, S, and Pb) at the landfill. In addition, it is shown that the investigated samples contain elements such as Cd, Co, Cr, Cu, Cu, Mn, Ni, Pb, Sr, V, Zn, and Hg. The method of gamma spectrometry revealed that the studied samples contain such radioactive elements as ¹³⁷Cs, daughter products of ²³⁸U and ²³²Th. Detection of the same heavy metals and radionuclides in the atmospheric air of the city and in the vegetation near the landfill may indicate that one of the sources of environmental pollution may be products of incineration of the landfill contents at the 9th km of the Vilyuisky tract. Full article

The decommissioning and dismantling of nuclear research reactors can lead to a large amount of low- and intermediate-level radioactive waste. For repositories, the materials must be kept confined and safety must be ensured for extended time spans. Waste is encapsulated in concrete, which leads to alkaline conditions with pH values of 12 and higher. This can be advantageous for some radionuclides due to their precipitation at high pH. For other materials, such as reactive metals, however, it can be disadvantageous because it might foster their corrosion. The Studsvik R2 research reactor contained an AlMg3.5 alloy with a composition close to that of commercial Al5154 for its core internals and the reactor tank. Aluminum corrosion is known to start rapidly due to the formation of an oxidation layer, which later functions as natural protection for the surface. The corrosion can lead to pressure build-up through the accompanied production of hydrogen gas. This can lead to cracks in the concrete, which can be pathways for radioactive nuclides to migrate and must therefore be prevented. In this study, unirradiated rod-shaped samples were cut from the same material as the original reactor tank manufacture. They were embedded in concrete with elevated water–cement ratios of 0.7 compared to regular commercial concrete (ca. 0.45) to ensure water availability throughout all of the experiments. The sample containers were stored in pressure vessels with attached high-definition pressure gauges to read the hydrogen-induced pressure build-up. A second set of samples were exposed in simplified artificial cement–water to study similarities in corrosion characteristics between concrete and cement–water. Additionally, the samples were exposed to concrete and cement–water in free-standing sample containers for deconstructive examinations. In concrete, the corrosion rates started extremely high, with values of more than 10,000 µm/y, and slowed down to less than 500 µm/y after 2000 h, which resulted in visible channels inside the concrete. In the cement–water, the samples showed similar behavior after early fluctuations, most likely caused by the surface coverage of hydrogen bubbles. These trends were further supported by mass loss evaluations. Full article

Radionuclides and heavy metals pose potential risks to marine ecosystems and human health. Daya Bay, the site of China’s first commercial nuclear power plant, has experienced significant anthropogenic impacts, yet the extent of radionuclide and heavy metal contamination remains unclear. Nineteen surface sediment samples were collected in January 2024 and analyzed for natural (²¹⁰Pb, ²²⁸Th, ²²⁶Ra, ²²⁸Ra, and ⁴⁰K) and anthropogenic (¹³⁷Cs) radionuclides, heavy metals (Cu, Pb, Zn, Cd, Cr, Mn, Hg, and As), grain size, and total organic carbon (TOC). The surface sediments of Daya Bay were predominantly fine-grained, with TOC levels ranging from 0.41% to 1.83%, influenced significantly by riverine input from the Dan’ao River. Natural radionuclides exhibited distinct spatial patterns: ²¹⁰Pb and ²²⁸Th activity levels were higher in fine-grained sediments, and correlated with TOC, indicating adsorption and sedimentation controls. In contrast, anthropogenic ¹³⁷Cs activity was low and showed no significant impact from the nuclear power plant. Notably, the absence in the samples of key anthropogenic radionuclides typically associated with nuclear power plant operations further confirmed the negligible impact of the power plant on local sediment contamination. The results indicated that the baseline levels of both natural and anthropogenic radionuclides and heavy metals were predominantly influenced by natural processes and local anthropogenic activities rather than the operation of the nuclear power plant. This study establishes critical baselines for radioactivity and heavy metals in Daya Bay, underscoring effective pollution control measures and the resilience of local ecosystems despite anthropogenic pressures. Full article

Since water contamination has become a serious concern, more effective environmental remediation methods are required. Chitosan (CHT)-based adsorbents have demonstrated high efficacy in removing pollutants due to their unique chemical and structural properties. However, their utilization remains limited by low environmental stability and the absence of effective adsorption sites. The functional moieties of CHT can be altered to improve its performance via graft modification and crosslinking. Compared to conventional hydrogel synthesis techniques, ionizing radiation-induced fabrication, using gamma or electron-beam irradiation, offers a promising platform for innovation across diverse fields. The prime focus of this review is on ionizing radiation developed CHT-based hydrogels to remove toxic heavy metals, dyes, organic contaminants, radionuclides, and humic substances. The fabrication strategy, adsorption mechanism, and factors affecting the adsorption capacity of CHT-based hydrogels are presented. This review aims to underscore the transformative potential of ionizing radiation-induced CHT hydrogels in environmental remediation by examining current research trends and identifying future prospects. Full article

The rapid expansion of shale gas development has revolutionized global energy markets, yet it has also introduced substantial environmental challenges, particularly concerning groundwater resources. This comprehensive review systematically examines the multifaceted impacts of shale gas extraction on groundwater, with a focus on contamination mechanisms, pollutant sources, and mitigation strategies. The study identifies key operational stages—exploration, drilling, hydraulic fracturing, and flowback—as potential sources of groundwater contamination. Inorganic pollutants, including heavy metals and radionuclides, as well as organic compounds such as hydrocarbons and chemical additives, are identified as primary contaminants. The review critically evaluates current wastewater treatment technologies, including reinjection, internal reuse, and advanced desalination methods, highlighting their efficacy and limitations. Additionally, the study proposes a refined environmental management framework that integrates wellbore integrity optimization, enhanced shale gas wastewater treatment, and stringent monitoring protocols. The adoption of clean fracturing technologies and renewable energy applications is recommended to minimize environmental footprints. By establishing comprehensive baseline data and robust pollution monitoring systems, this research provides a scientific foundation for sustainable shale gas development, ensuring the protection of groundwater resources. This review emphasizes the imperative of balancing energy security with environmental sustainability, offering actionable insights for policymakers, industry stakeholders, and environmental scientists. Full article