One-step synthesis of phospho-rich, silica-enhanced chitosan aerogel for the efficient adsorption of uranium(VI).

In this study, an amorphous silica reinforced, phosphoric-crosslinked chitosan foam (P-CTS@SixOy) was prepared. The introduction of amorphous silica not only increased the affinity of the adsorbent for uranium, but also improved the stability of the material. The number of active sites of P-CTS@SixOy was increased by the introduction of phosphate groups. The material exhibited excellent uranium adsorption performance with the removal capacity and efficiency of 850.5 mg g-1 and 98.1 %, respectively. After regenerations, the morphology of P-CTS@SixOy still maintained, and the uranium adsorption efficiency remained above 90 %, manifesting the excellent cycle performance of P-CTS@SixOy. In the dynamic adsorption experiment, P-CTS@SixOy successfully concentrated the volume of uranium-containing solution, and exhibited excellent uranium adsorption performance. The analysis of kinetics, isotherms, and thermodynamics manifested that the uranium adsorption behavior of P-CTS@SixOy was a spontaneous, endothermic, monolayer chemical adsorption process. X-ray photoelectron spectroscopy, Scanning Electron Microscope, and Fourier Transform Infrared Spectrometer were used to characterized the P-CTS@SixOy before and after adsorption, which demonstrated that the main interaction mechanism between uranium and P-CTS@SixOy was the complexation. These studies indicated the huge application prospect of P-CTS@SixOy in the treatment of large-scale uranium-containing wastewater.

Integration of high visible-light-driven ternary dual Z-scheme AgVO3-InVO4/g-C3N4 heterojunction nanocomposite for enhanced uranium(VI) photoreduction separation.

With deepening application of nuclear power technology, the problem of water ecological environment pollution caused by uranium (U(VI)) is becoming increasingly serious. Photoreduction separation of U(VI) on photocatalysts is considered as an effective strategy to solve uranium pollution. In this work, a novel ternary dual Z-scheme AgVO3-InVO4/g-C3N4 heterojunction (Z-AIGH) nanocomposite with high surface area (73.45 m2 g-1, Z-AIGH2) was designed. The batch adsorption experiment in dark environment showed that Z-AIGH2 nanocomposite had an excellent U(VI) adsorption performance. As for photocatalytic experiments, Z-AIGH2 exhibited a rapid photocatalytic response for separating U(VI) without any organic sacrifice agents. The U(VI) separation rate on Z-AIGH2 nanocomposite was over 98.7% after only 20.0 min visible light irradiation (T = 298 K, CU(Ⅵ) = 10.0 mg L-1, m/V = 0.1 g L-1 and pH = 7.0). Z-AIGH2 nanocomposite also showed good selectivity and cycle stability. The U(VI) removal rate of Z-AIGH2 nanocomposite after fifth cycles was about 96.1% (T = 298 K, CU(Ⅵ) = 10.0 mg L-1, m/V = 0.1 g L-1 and pH = 7.0). High photocatalytic activity of Z-AIGH2 for U(VI) was attributed to the construction of ternary dual Z-scheme heterojunction structure and ant nest-like hole structure. Based on above results, Z-AIGH2 nanocomposite had great potential for water environment renovation.