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In order to protect environment and save uranium resources, it was necessary to find a highly efficient adsorbent for uranium recovery from wastewater. In this work, we used a freeze-drying-calcination method to synthesize HAP aerogel to effectively remove uranium. Compared with commercially available nano-hydroxyapatite, HAP aerogel presented better adsorption performance. This was because the as-prepared HAP aerogel presented continuous porous structure, which could provide more active sites for the adsorption to uranium. The uranium removal efficiency of HAP aerogel arrived 99.4% within 10 min and the maximum adsorption capacity was up to 2087.6 mg g−1 at pH = 4.0 and 298 K. In addition, the immobilization of uranium on HAP aerogel was chemisorption, which was probably due to adsorption, dissolution-precipitation and ions exchange. These results indicated that the as-prepared HAP aerogel could be widely used as a high efficiency and potential adsorbent for the treatment of uranium-containing wastewater in the future.

In this work, three kinds of biochars (PMBC-H2O, PMBC-PP and PMBC-HP) with excellent adsorption performance were obtained by carbonizing pig manure pre-treated with different agents. These biochars had the ordered mesoporous structures and possessed abundant active functional groups on their surface. The adsorption behaviors of the biochars towards UVI under various conditions were evaluated by batch experiment. The results showed that KMnO4 and H2O2 could enormously improve the adsorption performance of PMBC to UVI. After KMnO4 and H2O2 pretreatment, the maximum adsorption capacities of PMBC-PP (979.3 mg/g) and PMBC-HP (661.7 mg/g) were about 2.6 and 1.8 times higher than that of PMBC-H2O (369.9 mg/g), respectively, which was much higher than previously reported biochar-based materials. Obviously, KMnO4 pretreatment leaded to a higher enhancement than that of H2O2. The removal mechanism of UVI on PMBC-PP was discussed in-depth. The interaction between UVI species and PMBC-PP was mainly ascribed to the abundant active sites on the surface of PMBC-PP. In a word, conversion of pig manure pre-treated with KMnO4 into biochar not only demonstrates that PMBC-PP has great potential in the treatment of actual uranium-containing wastewater, but also provides a method for the rational utilization of pig manure to reduce the pollution.

The reduction of U(VI) to U(IV) in wastewater by semiconductor photocatalysis has become a new highly efficient and low-cost method for U(VI) removal. However, due to the weak absorption of visible light led by wide band gap and low carrier utilization rate resulted from the severe electron-holes recombination, the photoreduction performance of U(VI) is limited. Herein, the Ti vacancies and doped Fe atoms were simultaneously introduced into TiO

How to efficiently treat radioactive uranium-containing nuclear wastewater is one of the significant challenges to ensure the safety of nuclear technology and to avoid environmental pollution. Here we firstly prepare the metal-free 2D/2D C

Biochar has attracted increasing attention in water pollution control, attributed to its various merits, e.g., tunable physico-chemical properties. The oxygenated functional groups (OFGs) on biochar are key active sites for removing pollutants from water through interfacial adsorption/redox reaction. However, there is still a lack of comprehensive knowledge and perspective on tuning OFGs on biochar for enhanced performance in water pollution control. Here, this review highlighted the mechanisms of biochar OFGs in water pollution control, analyzed the strategies and mechanisms for tuning OFGs on biochar, and investigated the performances of biochars with tuned OFGs in removing inorganic/organic pollutants via adsorption/redox reactions. Specifically, strategies for tuning OFGs on biochar are far more than the well-recognized ex-situ oxidation of pristine biochar. These strategies include in-situ low temperature preservation of hydroxyl and carboxyl, in-/ex-situ oxidation of biochar, and in-/ex-situ grafting of carboxyl on biochar via cycloaddition/acylation reaction. The resultant biochars showed enhanced performances in adsorption (mainly mediated by hydroxyl, carboxyl and ketone through surface complexation, H-bonding, and electrostatic attraction) and redox reaction (mainly mediated by redox-active hydroxyl and ketone). Finally, this review presented future directions on developing biochar with specially tuned surface OFGs as a sustainable high-performance adsorbent/carbocatalyst for water pollution control.

Photocatalytic reduction of soluble hexavalent uranium (U(VI)) is a novel and efficient avenue to enriching U(VI), where the free U(VI) is firstly bound on the surface of photocatalysts and then reduced to insoluble tetravalent uranium (U(IV)) by photoelectrons. Therefore, constructing the efficient U(VI) binding sites on photocatalysts is an efficient strategy to boost catalytic activity toward U(VI) photoreduction. Herein, we successfully constructed an efficient catalyst for U(VI) photoreduction by depositing Ag nanoparticles on Ti3C2Tx MXene with abundant U(VI) binding sites (Ag/Ti3C2Tx-O). Impressively, the U(VI) extracting mass over Ag/Ti3C2Tx-O under light reached up to 1257.6 mg/g in 120 min, which was almost 11 times as high as that without light. Further mechanistic studies indicated that the U(VI) binding sites on Ti3C2Tx MXene in Ag/Ti3C2Tx-O were beneficial to the reduction of U(VI) by significantly decreasing its reduction potential. More importantly, hot electrons generated by Ag nanoparticles were transferred into the binding sites to easily reduce the bound U(VI), resulting in the remarkable performance of Ag/Ti3C2Tx-O during U(VI) enrichment.

The reduction of U(VI) to U(IV) in wastewater by semiconductor photocatalysis has become a new highly efficient and low-cost method for U(VI) removal. However, due to the weak absorption of visible light led by wide band gap and low carrier utilization rate resulted from the severe electron-holes recombination, the photoreduction performance of U(VI) is limited. Herein, the Ti vacancies and doped Fe atoms were simultaneously introduced into TiO2 nanosheet (labeled as 4%Fe-Ti1−xO2) as a highly active and stable catalysis for U(VI) photoreduction. Without adding any hole sacrifice agent, 4%Fe-Ti1−xO2 nanosheets achieved 99.7% removal efficiency for U(VI) within 120 min. And the 92.1% removal efficiency of U(VI) via 4%Fe-Ti1−xO2 nanosheets was still maintained after 5 cycles. Moreover, 4%Fe-Ti1−xO2 exhibited dramatic removal rate, 81.6% U(VI) in the solution was removed in 10 min. Further study on the mechanism showed that simultaneously introducing the Ti vacancies and doped Fe atoms in 4%Fe-Ti1−xO2 nanosheets improved the visible light utilization and decreased the recombination of photogenerated electron-hole pairs, contributing to the highly efficiency removal of U(VI).

How to efficiently treat radioactive uranium-containing nuclear wastewater is one of the significant challenges to ensure the safety of nuclear technology and to avoid environmental pollution. Here we firstly prepare the metal-free 2D/2D C3N5/GO nanosheets, and customize a type-II heterojunction based on the band bending theory to achieve enhanced uranium extraction capacity via synergistic adsorption photoreduction engineering. The structure of C3N5 is explained by electron energy loss spectroscopy and synchrotron-based near-edge X-ray absorption fine structure. And C3N5 with larger π-conjugated structure expands the light response range to 747 nm, which is about 1.67 times that of C3N4. Further, we also use density functional theory to prove the existence of alternating energy levels so that photogenerated electrons could be continuously injected into the surface of GO to ensure the effective separation of electron-hole pairs and increase the material activity. The results show that the removal ratio of uranium by 2D/2D C3N5/GO heterojunction is achieved as high as 96.1% even at a low uranium concentration of 10 ppm, and reached 93.4% after exposure to gamma-ray. This work will lay a foundation for customizing the energy band structure of nonmetal-based 2D/2D nanohybrids and enriching uranium-containing wastewater through adsorption photoreduction engineering in the future.

As an effective way to obtain solar energy and separate the soluble contaminants from water, solar-driven interfacial evaporation is used in desalination, wastewater treatment, electricity generation, and domestic water heating system. Herein, we demonstrate a monolithic sponge with three-dimensional porous structure as the solar-energy evaporator, which is composed of hydrophilic polymer (Konjac Glucomannan, KGM) and solar absorbent (reduced graphene oxide, rGO). Under one sun irradiation, the sponge achieves a rapid evaporation rate (1.60 kg m−2 h−1) and high interfacial water evaporation efficiency (92 %) due to its good absorption, photothermal, thermal insulation, and fast water transport properties. Meanwhile, the concentrations of radioactive elements (strontium, cesium, and uranium) in wastewater dropped from grams to micrograms after purification, even under radiation and acidic conditions. Additionally, the durability and repeatability of the sponge also have been verified. The results showed that solar-driven interfacial evaporation can effectively treat radioactive wastewater and enrich various radionuclides in a more energy-saving manner.

The presence of organics in radioactive wastewater decreased the extraction efficiency in traditional adsorption treatment of nuclide. Herein, we developed g-C