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Marine biofouling is one of the most significant challenges hindering practical uranium extraction from seawater. Single atoms have been widely used in catalytic applications because of their remarkable redox property, implying that the single atom is highly capable of catalyzing the generation of reactive oxygen species (ROS) and acts as an anti‐biofouling substance for controlling biofouling. In this study, the Co single atom loaded polyacrylamidoxime (PAO) material, PAO‐Co, is fabricated based on the binding ability of the amidoxime group to uranyl and cobalt ions. Nitrogen and oxygen atoms from the amidoxime group stabilize the Co single atom. The fabricated PAO‐Co exhibits a broad range of antimicrobial activity against diverse marine microorganisms by producing ROS, with an inhibition rate up to 93.4%. The present study is the first to apply the single atom for controlling biofouling. The adsorbent achieves an ultrahigh uranium adsorption capacity of 9.7 mg g−1 in biofouling‐containing natural seawater, which decreased only by 11% compared with that in biofouling‐removed natural seawater. These findings indicate that applying single atoms would be a promising strategy for designing biofouling‐resistant adsorbents for uranium extraction from seawater. [ABSTRACT FROM AUTHOR]

By chemical cross‐linking the amidoxime group onto dual‐surfaces of natural ore materials, namely halloysite nanotubes (HNTs), an efficient adsorbent, AO‐HNTs, is developed. AO‐HNTs show high uranium adsorption capacity of 456.24 mg g−1 in 32 ppm uranium‐spiked simulated seawater. In natural seawater, AO‐HNTs reach the high uranium extraction capacity of 9.01 mg g−1 after 30 days' field test. The dual‐surface amidoximated hollow nanotubular AO‐HNTs exhibit more coordination active sites for uranium adsorption, which is attributed to the high and fast uranium adsorption capacity. Because of the stable natural ore structure, AO‐HNTs also show long service life. Benefiting from the low cost of HNTs, the cost for uranium extraction from seawater is close to the uranium price in the spot uranium market, suggesting that AO‐HNTs could be used for economical extraction of uranium from the oceans. [ABSTRACT FROM AUTHOR]

Highlights from the article: Uranium Extraction: A Marine-Inspired Hybrid Sponge for Highly Efficient Uranium Extraction from Seawater (Adv. Funct. Keywords: alginate; amidoxime; marine sponges; melamine sponge; uranium extraction Alginate, marine sponges, amidoxime, uranium extraction, melamine sponge.

Marine sponges are used as biomonitors of heavy metals contamination in coastal environment as they process large amounts of water and have a high capacity for accumulating heavy metals. Here, inspired by the unique physical and physiological features of marine sponges, a surface engineered synthetic sponge for the highly efficient harvesting of uranium from natural seawater is developed. An ultrathin poly(imide dioxime) (PIDO)/alginate (Alg) interpenetrating polymer network hydrogel layer is uniformly wrapped around the skeleton of a melamine sponge (MS) substrate through a simple dipping–drying–crosslinking process, providing the hybrid MS@PIDO/Alg sponge with excellent uranium adsorption performance and sufficient mechanical strength to withstand the harsh conditions of practical applications. The maximum adsorption capacity reaches 910.98 mg‐U g‐gel‐1 for the PIDO/Alg hydrogel layer and 291.51 mg‐U g‐sponge‐1 for the whole hybrid MS@PIDO/Alg sponge in uranium‐spiked natural seawater. The adsorption capacity measured after 56 d of exposure in 5 tons of natural seawater is evaluated to be 5.84 mg‐U g‐gel‐1 (1.87 mg‐U g‐sponge‐1). This novel approach shows great promise for the mass production of high‐performance sponge adsorbent for uranium recovery from natural seawater and nuclear waste. [ABSTRACT FROM AUTHOR]

Highly efficient recovery of uranium from seawater is of great concern because of the growing demand for nuclear energy. The use of amidoxime‐based polymeric fiber adsorbents is considered to be a promising approach because of their relatively high specificity and affinity to uranyl. The surface area, hydrophility, and surface charge of the adsorbent are reported to be critical factors that influence uranium recovery efficiency. Here, a porous amidoxime‐based nanofiber adsorbent (SMON–PAO) that exhibits the highest uranium recovery capacity among the existing fiber adsorbents both in 8 ppm uranium spiked seawater (1089.36 ± 64.31 mg‐U per g‐Ads) and in natural seawater (9.59 ± 0.64 mg‐U per g‐Ads) is prepared by blow spinning. These nanofibers are obtained by compositing polyacrylamidoxime with montmorillonite and exhibit the increased surface area and more exposed functional amidoxime moieties for uranyl adsorption. The residual montmorillonite enhances the hydrophility and reduces the negative surface charge, thereby increasing the contact of the adsorbent with seawater and reducing the charge repulsion between negative amidoxime group and negative uranyl species ([UO2(CO3)3]4−). The finding of this study indicates that rational design of uranium recovery adsorbents by comprehensive utilizing the key factors that influence uranium recovery performance is a promising approach for developing economically feasible uranium recovery materials. A porous amidoxime‐based nanofiber adsorbent (SMON–PAO) is rationally designed to achieve high uranium recovery capacity from seawater and fabricated by blow spinning. This finding indicates that design of uranium recovery adsorbents by comprehensively utilizing the factors that influence uranium recovery performance, which are surface area, hydrophility, and surface charge, is a promising approach for developing economically feasible uranium recovery adsorbents. [ABSTRACT FROM AUTHOR]

In article number 1802607, Ning Wang, Xiaolin Wang, Hui Wu and co‐workers present a new strategy based on pre‐amidoximation and blow spinning technique for industry scale production of fully amidoximated poly(imide dioxime) nanofiber adsorbent with significantly enhanced capacity and practicability for uranium extraction from natural seawater. The outstanding performance is attributed to the full coverage of chelating sites, excellent hydrophilicity, 3D porous architecture and good mechanical properties. [ABSTRACT FROM AUTHOR]

The oceans contain hundreds of times more uranium than terrestrial ores. Fiber‐based adsorption is considered to be the most promising method to realize the industrialization of uranium extraction from seawater. In this work, a pre‐amidoximation with a blow spinning strategy is developed for mass production of poly(imide dioxime) nanofiber (PIDO NF) adsorbents with many chelating sites, excellent hydrophilicity, 3D porous architecture, and good mechanical properties. The structural evidences from 13C NMR spectra confirm that the main functional group responsible for the uranyl binding is not "amidoxime" but cyclic "imidedioxime." The uranium adsorption capacity of the PIDO NF adsorbent reaches 951 mg‐U per g‐Ads in uranium (8 ppm) spiked natural seawater. An average adsorption capacity of 8.7 mg‐U per g‐Ads is obtained after 56 d of exposure in natural seawater via a flow‐through column system. Moreover, up to 98.5% of the adsorbed uranium can be rapidly eluted out and the adsorbent can be regenerated and reused for over eight cycles of adsorption–desorption. This new blow spun PIDO nanofabric shows great potential as a new generation adsorbent for uranium extraction from seawater. Over hundreds of times more uranium exists in the oceans than exists in terrestrial ores. A novel strategy based on preamidoximation with blow spinning is developed for industrial scale production of fully amidoximated nanofiber adsorbents with significantly enhanced capacity and practicability for application in uranium extraction from natural seawater. [ABSTRACT FROM AUTHOR]

[Display omitted] • Magnetic-single-molecular material is used for uranium adsorption for the first time. • Fully exposure of functional group guarantees high uranium adsorption capacity. • The magnetism of the adsorbent endows it with high recyclability and reusability. • High adsorption capacity of 84.31 mg/g is achieved in simulated nuclear wastewater. • Highest uranium adsorption speed is achieved in simulated nuclear wastewater. Highly efficient treatment of uranium contamination is of great importance for the sustainable development of the environment. The recovery of uranium by adsorbents is a feasible strategy for treating uranium contamination. However, due to insufficient exposure of the contact interfaces, currently available adsorbents usually take extremely long time for uranium adsorption. Herein, a magnetic-single-molecular amidoxime adsorbent M−AO−Fc is fabricated for highly efficient recovery of uranium from nuclear wastewater by endowing the amidoximated cyanoferrocene with magnetism. The adsorbent M−AO−Fc shows a maximum uranium adsorption capacity of 510.60 mg/g in uranium solution. In an acidic simulated nuclear wastewater containing a large number of interfering ions, M−AO−Fc also shows a high uranium adsorption capacity of 84.31 mg/g within a short equilibrium time of 60 min. The full dispersion of M−AO−Fc and full exposure of functional groups are the critical reasons for the excellent uranium adsorption performance. Attributing to the magnetism of M−AO−Fc, this adsorbent can be efficiently recovered by magnetic recovery and shows high reusability. This study proves that the magnetic-single-molecule would be a promising adsorbent for uranium recovery and opens up a new direction for designing a uranium adsorbent. [ABSTRACT FROM AUTHOR]

• A new double-network hydrogel is explored for uranium recovery from seawater. • U-adsorption capacity of the hydrogel is greatly enhanced by added nanoclay. • Mechanical property of the hydrogel is largely improved by th double-network. • Used materials are lowcost and the hydrogel owns good U-adsorption reusability. Massive uranium recovery from seawater is a key project to provide the long-time consumption of global nuclear power, while it is still greatly difficult to achieve high-efficient adsorbents with high mechanical property. In this work, a new nanoclay-poly(amidoxime) (NC-PAO) high-strength double-network (DN) composite hydrogel adsorbent with high-efficient and fast uranium extraction capacity has been explored. The uranium adsorbing performance can be significantly enhanced by the small content of added super-hydrophilic NC (Laponite RDS sheets), because of the largely improved hydrophilicity of the hydrogel. Compared with the blank PAO DN hydrogel without nanoclay, the uranium adsorbing capacity of this NC-PAO DN hydrogel can largely increase 73.4% from 4.97 mg/g to 8.62 mg/g, after in seawater only 25 days. The uranium adsorption rate of this hydrogel from natural seawater, can reached 0.345 mg/(g∙day), which is excellent among existing uranium adsorbents. Furthermore, this hydrogel has high mechanical performance with 2.42 MPa of tensile strength and 16.13 MPa of compressive strength, which can be used in seawater for relatively longer time than traditional low-strength single-network hydrogel, owing to its double network (DN) structure (the weakly crosslinked gelatin soft network and the strongly crosslinked cellulose nanofiber (CNF) hard network). This NC-PAO DN hydrogel adsorbent will be an excellent candidate for fast uranium recovery from seawater in largescale. Most importantly, this work will inspire the development of new hydrogel-based adsorbents and even other type of adsorbents for high-efficient uranium extraction, through compositing various low-cost and super-hydrophilic nanomaterials to significantly improve the hydrophilicity of the adsorbent and designing double-network structure to largely enhance the mechanical property. [ABSTRACT FROM AUTHOR]