Search Results (51)

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

The increasing threat of terrorism involving Radiological Dispersal Devices (RDDs) necessitates comprehensive evaluation and preparedness strategies, especially in densely populated public areas. This study aims to assess the potential consequences of RDD detonation, focusing on the effective doses received by individuals and the ground deposition of radioactive materials in a hypothetical urban environment. Utilizing the HotSpot code, simulations were performed to model the dispersion patterns of ¹³⁷Cs and ²⁴¹Am under varying meteorological conditions, mirroring the complexities of real-world scenarios as outlined in recent literature. The results demonstrate that ¹³⁷Cs dispersal produces a wider contamination footprint, with effective doses exceeding the public exposure limit of 1 mSv at distances up to 1 km, necessitating broad protective actions. In contrast, ²⁴¹Am generates higher localized contamination, with deposition levels surpassing cleanup thresholds near the release point, creating long-term remediation challenges. Dose estimates for first responders highlight the importance of adhering to operational dose limits, with scenarios approaching 100 mSv under urgent rescue conditions. Overall, the findings underscore the need for rapid dose assessment, early shelter-in-place orders, and targeted decontamination to reduce population exposure. These insights provide actionable guidance for emergency planners and first responders, enhancing preparedness protocols for RDD incidents in major urban centers. Full article

Many studies have examined the ability of polymer-based gels or hydrogels to serve various purposes, particularly as absorbents. Several studies have reported that polyvinyl alcohol (PVA), with specific compositions and additives, is an absorbent and a decontamination material usable for heavy metals and radioactive substances. PVA has a high cost and is slowly degradable under anaerobic conditions. This study investigated the potential of natural materials, namely cassava starch, which is an environmentally friendly, non-toxic, and readily available gel-forming polymer that, notably, is inexpensive in Indonesia. The FTIR analysis showed a bond and polymer formation between cassava starch and glycerol. The cassava starch–glycerol–water mixture was applied to media such as glass, aluminum plates, and ceramics contaminated with heavy-metal stable ions which correspond to a radionuclide. The media, stored at room temperature for 24 h, becomes a film. According to the SEM and XRF results, the gel becomes a film that binds and absorbs metals when dried. The SEM results showed the presence of metals corresponding with the sources of contamination, and the XRF results showed that the quantity of metals absorbed was large. The cassava starch gel absorption results indicated the formation of an amorphous compound, as indicated by the XRF results. Based on all the analyses, the cassava starch–glycerol gel has enormous potential. It is almost equivalent to a PVA gel as an absorbent material and heavy-metal decontamination material, when used for radioactive decontamination on the material’s surface. Full article

Decommissioning of nuclear facilities can be performed in stages. One of the stages and processes in decontamination is the decontamination process before dismantling or facility area recovery activities. Decontamination can be performed using various methods, primarily physical and chemical. One chemical method involves using a gel made of polymers for decontamination. In this study, a gel consisting of a mixture of 15 g polyvinyl alcohol (PVA), 15 mL of glycerol, and 2 g Na-EDTA was dissolved in 100 mL. The three materials were dissolved in hot conditions until they dissolved, and a gel was formed. The formed gel was applied to the material contaminated by Co-60 with a radioactivity of 81 µCi, as much as 5 µL. The decontamination radioactive efficiency test results range from 53% to 98%, with the highest decontamination efficiency observed on glass media. This study also showed that higher EDTA concentrations can increase the ability of the PVA-glycerol gel to absorb and bind Co. This study also found that decontamination efficiency was influenced by the type of contaminated material and the concentration of EDTA. It can be concluded that gels with a composition of PVA, glycerol, and EDTA can reduce the level of contamination on the surface of materials made of glass, ceramics, and metal plates. Full article

Biosorption is an impurity-free application developed from the use of nuclear technology for peaceful purposes in everyday life and can be used to treat wastewater streams contaminated with various radionuclides. In this study, a laboratory decontamination experimental approach was developed to apply commercial chitosan as a biosorbent applied for removing radiocesium (Cs-137) and/or radiocobalt (Co-60) from spiked aqueous media. The factors assumed to affect the biosorption of both radionuclides included contact time, pH, and initial radioactivity content. In addition, the biosorbent dose and temperature of the process were studied. Both the biosorption capacity and the biosorption efficiency of the treatment process were calculated. According to FT-IR analysis, it can be assumed that the chitosan amine group (-NH₂) is almost accountable for the biosorption of both radionuclides from waste solution simulates. Based on the data obtained, commercial chitosan can be considered an economical and efficient biosorbent for handling low- and medium-level radioactive wastewater streams containing cesium and/or cobalt radionuclides. The acquired data showed that 144 h is an adequate time to remove more than 94% of radiocobalt and about 93% of radiocesium, from a separate solution for each, at pH ~6.5 and using 0.5 g of commercial chitosan. Full article

Patient decontamination is the act of removing or neutralising hazardous substances from an affected individual. To ensure adequate emergency preparedness, regulations require hospitals to train personnel in decontamination procedures regularly. To supplement in-person training, a virtual reality (VR) system is being developed for the training of hospital staff members in the mass decontamination of hazardous and toxic materials (HAZMAT) and/or radioactively contaminated casualties. As a demonstration of the concept, a primary VR prototype is designed to help users familiarize themselves with a chemical scanner tool, intended for examining victims for residual chemical hazards. This initial prototype showcases the benefits of using VR to create training simulations, complementing existing decontamination training methods in a secure and cost-effective manner. The proposed approach features a modularized user-centric design, a novel scanning simulation, and a high-realism virtual environment and workflow to enhance training effectiveness. A pilot user study and assessment suggest that new users were able to achieve a significant level of competency with VR, compared to users who underwent traditional training. Full article

Nuclear power components contain radioactivity on their surfaces after long-term service, which can be harmful to personnel and the environment during maintenance, dismantling, and decommissioning. In this experiment, laser decontamination technology is utilized to remove radioactivity from their surfaces. In order to meet the actual needs, a laser decontamination process without spot overlapping has been studied. Under the same equipment conditions, the decontamination efficiency of the non-spot overlapping process is 10 times higher than that of the spot overlapping process. Alloy 690 is used as the test substrate, and non-radioactive specimens are prepared by simulating primary-circuit hydrochemical conditions. The surface morphology, elemental composition, and phase composition of the specimens before and after laser decontamination are investigated with SEM and XRD using the single-pulse experiment and power single-factor experiment methods, and the laser decontamination effect was evaluated. The results show that the decontamination efficiency reached 10.8 m²/h under the conditions of a pulse width of 500 ns, a laser repetition frequency of 40 kHz, a scanning speed of 15,000 mm/s, and a line spacing of 0.2 mm, according to which the removal effect was achieved when the laser power was 160 W and the oxygen content on the surface was 6.29%; additionally, there were no oxide phases in the XRD spectra after decontamination. Therefore, the laser cleaning process without spot overlap can provide reference for future practical operations to achieve efficient removal of radioactivity from nuclear power components. Full article

The binding of actinide ions (Am(III) and U(VI)) in aqueous solutions by hybrid silica–hyperbranched poly(ethylene imine) nanoparticles (NPs) and xerogels (XGs) has been studied by means of batch experiments at different pH values (4, 7, and 9) under ambient atmospheric conditions. Both materials present relatively high removal efficiency at pH 4 and pH 7 (>70%) for Am(III) and U(VI). The lower removal efficiency for the nanoparticles is basically associated with the compact structure of the nanoparticles and the lower permeability and access to active amine groups compared to xerogels, and the negative charge of the radionuclide species is formed under alkaline conditions (e.g., UO₂(CO₃)₃⁴⁻ and Am(CO₃)₂⁻). Generally, the adsorption process is relatively slow due to the very low radionuclide concentrations used in the study and is basically governed by the actinide diffusion from the aqueous phase to the solid surface. On the other hand, adsorption is favored with increasing temperature, assuming that the reaction is endothermic and entropy-driven, which is associated with increasing randomness at the solid–liquid interphase upon actinide adsorption. To the best of our knowledge, this is the first study on hybrid silica–hyperbranched poly(ethylene imine) nanoparticle and xerogel materials used as adsorbents for americium and uranium at ultra-trace levels. Compared to other adsorbent materials used for binding americium and uranium ions, both materials show far higher binding efficiency. Xerogels could remove both actinides even from seawater by almost 90%, whereas nanoparticles could remove uranium by 80% and americium by 70%. The above, along with their simple derivatization to increase the selectivity towards a specific radionuclide and their easy processing to be included in separation technologies, could make these materials attractive candidates for the treatment of radionuclide/actinide-contaminated water. Full article

Compared with high-pressure water and reagent washing decontamination, foam decontamination has a promising application due to its ability to significantly reduce the volume of radioactive waste liquids and effectively decontaminate the inner surface of the pipes, the interior of the large cavities, and the vertical walls. However, the foam is less stable, leading to a low decontamination rate. Currently, three main types of stabilizers with different stabilizing mechanisms, namely nanoparticles, polymers, and cosurfactants, are used to improve foam stability and thus increase the decontamination rate. Nanosilica (NS), xanthan gum (XG), and n-tetradecanol (TD) were used as typical representatives of nanoparticles, polymers, and cosurfactants, respectively, to improve the stability of the foam detergent with pH < 2 and chelating agents. The differences in the effects of these three types of stabilizers on foam properties were investigated. Although NS, XG, and TD all increase the half-life of the foam from 7.2 min to about 40 min, the concentration of TD is much lower than that of NS and XG in the foaming solution, and TD foaming solution has the highest foaming ratio. Moreover, TD can markedly lower the surface tension, resulting in a significant reduction of the wetting contact angle on the surfaces of glass, ceramic tile, stainless steel, and paint, while NS and XG cannot signally change the surface tension and have no obvious effect on the wetting contact angle. At low shear rates, TD can increase the apparent viscosity of foam by two orders of magnitude, and the wall-hanging time of the foam on the vertical wall is more than 30 min. In contrast, NS and XG cause a limited increase in the apparent viscosity of the foam, and the wall-hanging times are both less than 5 min. In addition, TD foaming solution has excellent storage stability, and the storage time has no obvious effect on the performance of the foam. And after only three days of storage, NS undergoes severe agglomeration and precipitation in the foaming solution, resulting in a complete loss of the stabilizing effect. After 90 days of storage, the half-life of XG foam decreases by 26%. For simulated radioactive uranium contamination on both horizontal and vertical surfaces, TD can significantly improve the decontamination rate, especially for vertical surfaces, where TD can increase the single decontamination rate by more than 50%. Full article

Kori Unit 1, which was permanently shut down on 18 June 2017, is planned to undergo full-system decontamination prior to major decommissioning activities. One of the advantages of performing FSD is the downgrading of the classification level of radioactive waste. From this perspective, the impact on the steam generator (SG) tubes, which account for a considerable portion of the total surface area during FSD operation, was examined. Initially, the CRUDTRAN code was used to predict the radioactivity inventory of the Kori Unit 1 SG tubes, which turned out to be approximately 21% more conservative than the measured value. To estimate the radioactivity in the tubes after FSD, decontamination factor values from overseas cases in the SG tubes section were selected and applied. Then, the regulations for radioactive waste in Korea were reviewed, and the specific activity was calculated by predicting the mass of the SG tubes. As a conclusion, it was confirmed that the SG tubes will be classified as low-level radioactive waste, whether FSD is performed or not. Furthermore, it was observed that even if a high efficiency of FSD is achieved, if stored, it would take more than 50 years for clearance. Full article

Microbial life can thrive in the most inhospitable places, such as nuclear facilities with high levels of ionizing radiation. Using direct meta-analyses, we have previously highlighted the presence of bacteria belonging to twenty-five different genera in the highly radioactive water of the cooling pool of an operating nuclear reactor core. In the present study, we further characterize this specific environment by isolating and identifying some of these microorganisms and assessing their radiotolerance and their ability to decontaminate uranium. This metal is one of the major radioactive contaminants of anthropogenic origin in the environment due to the nuclear and mining industries and agricultural practices. The microorganisms isolated when sampling was performed during the reactor operation consisted mainly of Actinobacteria and Firmicutes, whereas Proteobacteria were dominant when sampling was performed during the reactor shutdown. We investigated their tolerance to gamma radiation under different conditions. Most of the bacterial strains studied were able to survive 200 Gy irradiation. Some were even able to withstand 1 kGy, with four of them showing more than 10% survival at this dose. We also assessed their uranium uptake capacity. Seven strains were able to remove almost all the uranium from a 5 µM solution. Four strains displayed high efficiency in decontaminating a 50 µM uranium solution, demonstrating promising potential for use in bioremediation processes in environments contaminated by radionuclides. Full article

The paper deals with checking the possibility of using fly ash (FA) as a sorbent in the batch adsorption method of removing radionuclides from aqueous solutions. An adsorption-membrane filtration (AMF) hybrid process with a polyether sulfone ultrafiltration membrane with a pore size of 0.22 μm was also tested as an alternative to the commonly used column-mode technology. In the AMF method, metal ions are bound by the water-insoluble species prior to the membrane filtration of the purified water. Thanks to the easy separation of the metal-loaded sorbent, it is possible to improve water purification parameters using compact installations and reduce operating costs. This work evaluated the influence of such parameters on cationic radionuclide removal efficiency (EM): initial pH and composition of the solution, contact time of the phases, and the FA doses. A method for removing radionuclides, ordinarily present in an anionic form (e.g., TcO₄⁻), from water, has also been presented. The results show, that both batch adsorption of radionuclides and adsorption-membrane filtration (AMF) using the FA as an adsorbent can be effectively used for water purification and in the form of a solid directed to long-term storage. Full article

The present work describes the results of the removal of cesium by sorbents of various classes from highly mineralized alkaline solutions simulating the clarified phase of storage tanks with high-level radioactive waste (HLW) of the Mayak Production Association. Within the scope of the performed works, inorganic sorbents of the Clevasol^® and Fersal brands, as well as resorcinol-formaldehyde ion-exchange resins (RFRs: RFR-i, RFR-Ca, and Axionit RCs), were used. The sorbents’ characteristics under both static and dynamic conditions are presented. The Fersal sorbent has demonstrated the best sorption characteristics in the series of sorbents under study. The disadvantage of inorganic sorbents is the loss of mechanical strength upon cesium desorption, which complicates their repeated use. It has been demonstrated that RFRs, despite their lower selectivity towards cesium and adsorption capacity, can be used many times in repeated sorption-desorption cycles. The latter makes RFRs more technologically attractive in terms of the total volume of decontaminated HLW. However, RFRs tend to be oxidized during storage, which results in the formation of carboxyl groups and a decrease in sorption characteristics—this must be further taken into account in the real processes of liquid radioactive waste (LRW) management. Full article

The article presents the distribution coefficient (K_d) values of ¹³⁷Cs and ⁹⁰Sr tracer radionuclides in solutions of sodium and calcium salts for a wide range of commercially available inorganic sorbents: natural and synthetic aluminosilicates, manganese, titanium and zirconium oxyhydrates, titanium and zirconium phosphates, titanosilicates of alkali metals, and ferrocyanides of transition metals. The results were obtained using a standard technique developed by the authors for evaluating the efficiency of various sorption materials towards cesium and strontium radionuclides. It was shown that bentonite clays and natural and synthetic zeolites are the best for decontaminating low-salt natural water from cesium radionuclides, and ferrocyanide sorbents are the choice for decontaminating high-salt-bearing solutions. The manganese (III, IV) oxyhydrate-based MDM sorbent is the most effective for removing strontium from natural water; for seawater, the barium silicate-based SRM-Sr sorbent is the first-in-class. Results of the study provide a possibility of making a reasonable choice of sorbents for the most effective treatment of natural water and technogenic aqueous waste contaminated with cesium and strontium radionuclides. Full article

The removal of radionuclide/radioactivity from laboratory and environmental water samples under ambient conditions was investigated via batch-type experiments using polyurea-crosslinked calcium alginate (X-alginate) aerogels. Water samples were contaminated with traces of U-232 and Am-241. The removal efficiency of the material depends strongly on the solution pH; it is above 80% for both radionuclides in acidic solutions (pH 4), while it decreases at about 40% for Am-241 and 25% for U-232 in alkaline solutions (pH 9). This is directly associated with the presence of the radionuclide species in each case; the cationic species UO₂²⁺ and Am³⁺ prevail at pH 4, and the anionic species UO₂(CO₃)₃^4– and Am(CO₃)₂⁻ prevail at pH 9. Adsorption on X-alginate aerogels is realized by coordination of cationic species on carboxylate groups (replacing Ca²⁺) or other functional groups, i.e., –NH and/or –OH. In environmental water samples, i.e., ground water, wastewater and seawater, which are alkaline (pH around 8), the removal efficiency for Am-241 is significantly higher (45–60%) compared to that for U-232 (25–30%). The distribution coefficients (K_d) obtained for the sorption of Am-241 and U-232 by X-alginate aerogels are around 10⁵ L/kg, even in environmental water samples, indicating a strong sorption affinity of the aerogel material for the radionuclides. The latter, along with their stability in aqueous environments, make X-alginate aerogels attractive candidates for the treatment of radioactive contaminated waters. To the best of our knowledge, this is the first study on the removal of americium from waters using aerogels and the first investigation of adsorption efficiency of an aerogel material at the sub-picomolar concentration range. Full article