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In this study, a cesium ion imprinted polymer (Cs(I)-IIP) was prepared by free radical thermal polymerization using 18-crown-6-ether (18C6) as ligand, methacrylic acid (MAA) as functional monomer, and ethylene glycol dimethacrylate (EGDMA) as crosslinking agent, which can be used for adsorption and separation of cesium ions from low-concentration solutions. The adsorption kinetic and isotherm results showed that the adsorption of Cs + fitted to the pseudo-second-order kinetic model and Langmuir model, indicating that the adsorption of Cs + on Cs(I)-IIP was the monolayer chemical adsorption. The maximum adsorption capacity was 84.21 mg·g − 1 . The selective adsorption properties are performed in Cs + , Li + , Na + , and K + multicomponent systems. The results showed that the Cs(I)-IIP has a high selectivity in the presence of coexisting Li + , Na + , and K + , and the selectivity coefficients ( K’ ) of Cs(I)-IIP for Cs + /Li + , Cs + /Na + , Cs + /K + are 2.1, 1.56, and 1.33, respectively. The high adsorption capacity and selectivity are attributed to the introduction of imprinting technology to form specific Cs + recognition adsorption sites, and the 18C6 cavity was easier to recognize Cs + in the competitive adsorption process. Finally, the Cs(I)-IIP can be regenerated and reused for 10 times with the adsorption capacity only decreased by 8.1%, indicating that the polymer has good reuse performance.

In this study, polyacrylonitrile/polyaniline (PAN/PANI) blend nanofibers were prepared by the electrospinning method, and their performance was evaluated as an effective cesium ions adsorbent. The adsorption behavior of cesium ions onto the synthesized nanofibers was explored as a function of pH, contact time, temperature, and initial adsorbate concentration. The isotherm results revealed that the Freundlich model is the best-fit isotherm for cesium adsorption. The adsorption kinetics could be modeled by a pseudo-second-order kinetic model. The thermodynamic parameters imply that the sorption process is spontaneous and exothermic. The maximum uptake of Cesium ions by PAN/PANI nanofibers was 80 mg/g.

A new type of potentiometric sensor for cesium ions based on a crown ether (dibenzo-21-crown-7) is proposed; its analytical characteristics are presented: limit of detection, slope of electrode function, selectivity to a number of interfering ions, and the working pH range of solutions.

This study introduces a novel fluorescent light‐up electrospun membrane, integrating PbBr2, which serves as an exceptionally selective probe for the detection of cesium ions (Cs+). Leveraging the superior optical properties of CsPbBr3 perovskite nanocrystals (PNCs), the researchers employ electrospinning technology to fabricate a test strip, namely PbBr2@polyacrylonitrile (PbBr2@PAN) nanofiber membranes, capable of swiftly detecting Cs+ in water merely by observing changes in the nanocrystals' luminescence with the naked eye. By the introduction of NH4+‐modified montmorillonite (NH4+‐MMT), PbBr2‐MT@PAN nanofiber membranes is obtained. The selectivity and sensitivity to Cs+ can be further improved because NH4+‐MMT endows PbBr2‐MT@PAN nanofiber membranes with the hydrophilic property and selective adsorption toward Cs+ ions. The membrane's fabrication is simple, scalable, and cost‐effective, with high cesium selectivity and sensitivity down to 44 ppb. This innovation enables efficient, on‐site cesium monitoring critical for environmental safety and nuclear waste management. This study presents a novel PbBr2‐MMT@PAN electrospinning membrane for selective Cs+ detection, which can be attributed to the luminescent CsPbBr3 perovskite nanocrystals. The incorporation of NH4+‐MMT into the PbBr2‐MMT@PAN nanofiber membrane can further enhance its hydrophilicity and selective adsorption of Cs+ ions, enabling rapid detection of cesium ions with a detection limit of 44 ppb.

Selective screening followed by the sensing of cesium radionuclides from contaminated water is a challenging technical issue. In this study, the adsorption functionality of Prussian blue (PB) nanoparticles was utilized for the detection and efficient removal of cesium cations. An efficient PB nanoparticle-modified screen-printed electrode (SPE) in the three-electrode configuration was developed for the electrochemical sensing and removal of Cs+. PB nanoparticles inks were obtained using a facile two-step process that was previously described as suitable for dispensing over freshly prepared screen-printed electrodes. The PB nanoparticle-modified SPE induced a cesium adsorption-dependent chronoamperometric signal based on ion exchange as a function of cesium concentration. This ion exchange, which is reversible and rapid, is associated with electron transfer in the PB nanoparticle-modified SPE. Using this electrochemical adsorption system (EAS) based on chronoamperometry, the maximum adsorption capacity (Qmax) of Cs+ ions in the PB nanoparticle-modified SPE reached up to 325 ± 1 mg·g−1 in a 50 ± 0.5 μM Cs+ solution, with a distribution coefficient (Kd) of 580 ± 5 L·g−1 for Cs+ removal. The cesium concentration-dependent adsorption of PB nanoparticles was also demonstrated by fluorescence spectroscopy based on fluorescence quenching of PB nanoparticles as a function of cesium concentration using a standard fluorophore like fluorescein in a manner analogous to that previously reported for As(III).

In this paper, beads-shaped hybrid sorbents composed of pectin and Prussian blue were prepared. Various ratios of pectin and Prussian blue in hybrid sorbents were tested. Obtained sorbents had high and roughly constant sorption capacity in a broad pH range (4–10), in which also the swelling index and stability of sorbents were satisfactory. The preliminary sorption studies proved that almost 100% of cesium removal efficiency may be achieved by using the proper sorbent dose. The sorption capacity of the hybrid sorbent with a 1:1 ratio of pectin to Prussian blue equaled q = 36.5 ± 0.8 mg/g (dose 3 g/L, pH = 6, temp. = 22 ± 1 °C, t = 24 h). The obtained results showed that the prepared hybrid pectin-based sorbents are promising for cesium ions removal.

Selective separation of 137 Cs is significant for the sustainable development of nuclear energy and environmental protection, due to its strong radioactivity and long half-life. However, selective capture of 137 Cs + from radioactive liquid waste is challenging due to strong coulomb interactions between the adsorbents and high-valency metal ions. Herein, we propose a strategy to resolve this issue and achieve specific Cs + ion recognition and separation by modulating the stacking modes of layered perovskites. We demonstrate that among niobate-based perovskites, A LaNb 2 O 7 ( A  = Cs, H, K, and Li), HLaNb 2 O 7 shows an outstanding selectivity for Cs + even in the presence of a large amount of competing M n+ ions ( M n+  = K + , Ca 2+ , Mg 2+ , Sr 2+ , Eu 3+ , and Zr 4+ ) owing to its suitable void fraction and space shape, brought by the stacking mode of layers. The Cs + capture mechanism is directly elucidated at molecular level by single-crystal structural analyses and density functional theory calculations. This work not only provides key insights in the design and property optimization of perovskite-type materials for radiocesium separation, but also paves the way for the development of efficient inorganic materials for radionuclides remediation. Selective capture of radiocaesium is challenging due to strong coulomb interactions between adsorbents and high valent metal ions. Here, authors propose a strategy of modulating the stacking modes of layered perovskites to achieve specific Cs + recognition and separation.

Cesium is the major fission product of uranium, which widely exists in radioactive wastewater. Radiocesium has potential adverse effects on human health and ecological environment. Different methods such as chemical precipitation, coagulation/co-precipitation, solvent extraction, membrane process, chemical reduction, and adsorption have been used to remove radioactive cesium from aqueous solution. However, the development of innovative technologies capable of selectively removing radioactive cesium is still imperative yet challenging. This review focused on cesium removal using various separation technologies, including chemical precipitation, solvent extraction, membrane separation, and adsorption. The key restraints for cesium removal, as well as the recent progress of these methods have also been discussed. Particular attention has been paid to the adsorption methods, which has been highlighted by introducing the latest advances in inorganic adsorbents (such as metal hexacyanoferrates, clay minerals, carbon-based-adsorbents, and ammonium molybdophosphate), organic adsorbents (such as ion exchange resin, metal–organic frameworks and supramolecular/indicator grafting adsorbents), and biosorbents (such as agroforestry wastes and microbial biomass). Adsorption-based methods are high efficient in separation of cesium ions from aqueous streams, and adsorption of cesium ions has been investigated intensively and even used in practical applications, there is still considerable scope for improvement in terms of adsorption capacity and selectivity.

Formamidinium lead iodide perovskites are promising light-harvesting materials, yet stabilizing them under operating conditions without compromising optimal optoelectronic properties remains challenging. We report a multimodal host–guest complexation strategy to overcome this challenge using a crown ether, dibenzo-21-crown-7, which acts as a vehicle that assembles at the interface and delivers Cs + ions into the interior while modulating the material. This provides a local gradient of doping at the nanoscale that assists in photoinduced charge separation while passivating surface and bulk defects, stabilizing the perovskite phase through a synergistic effect of the host, guest, and host–guest complex. The resulting solar cells show power conversion efficiencies exceeding 24% and enhanced operational stability, maintaining over 95% of their performance without encapsulation for 500 h under continuous operation. Moreover, the host contributes to binding lead ions, reducing their environmental impact. This supramolecular strategy illustrates the broad implications of host–guest chemistry in photovoltaics. It remains a challenge to achieve a balance between performance and stability, as well as addressing the environmental impact of perovskite solar cells. Here, the authors propose a multimodal host-guest complexation strategy enabling these shortcomings to be addressed simultaneously.

● Removal of cesium from radioactive wastewater is still a challenging. ● Main approaches used for waste treatment in Fukushima Daiichi accident were reviewed. ● Kurion/SARRY system + desalination system and ALPS were briefly introduced. ● The removal of cesium by adsorption and membrane separation were summarized. Radiocesium is frequently present in radioactive wastewater, while its removal is still a challenge due to its small hydrated radius, high diffusion coefficient, and similar chemical behavior to other alkali metal elements with high background concentrations. This review summarized and analyzed the recent advances in the removal of Cs + from aqueous solutions, with a particular focus on adsorption and membrane separation methods. Various inorganic, organic, and biological adsorbents have undergone assessments to determine their efficacy in the removal of cesium ions. Additionally, membrane-based separation techniques, including reverse osmosis, forward osmosis, and membrane distillation, have also shown promise in effectively separating cesium ions from radioactive wastewater. Additionally, this review summarized the main approaches, including Kurion/SARRY system + desalination system and advanced liquid processing system, implemented after the Fukushima Daiichi nuclear power plant accident in Japan to remove radionuclides from contaminated water. Adsorption technology and membrane separation technology play a vital role in treatment of contaminated water.