Molten salt synthesis of MXene-derived hierarchical titanate for effective strontium removal.

The removal and recovery of radioactive Sr(II) from wastewater and seawater has been of great concern due to the negative environmental impacts of nuclear energy development and the potential risk of nuclear accidents. Herein, a facile molten salt synthesis strategy was developed to systematically investigated the reaction of different types of MXenes with nitrates. Among the products, K+ intercalated hierarchical titanate nanostructures (K-HTNs) obtained from the direct chemical transformation of multilayered Ti3C2Tx exhibited unique layered structures, good physicochemical properties, and outstanding adsorption performance for Sr(II). The maximum adsorption capacity of Sr(II) by K-HTNs reached 204 mg·g-1 at ambient temperature, and the good regeneration and reusability of the titanate was also demonstrated. K-HTNs showed preferential selectivity for Sr(II) in different environmental media containing competing ions, and the removal efficiency of Sr(II) in real seawater was as high as 93.3 %. The removal mechanism was elaborated to be the exchange of Sr2+ with K+/H+ in the interlayers of K-HTNs, and the adsorbed Sr(II) had a strong interaction with Ti-O- termination on the titanate surface. Benefiting from the merits of rapid and scalable synthesis and excellent adsorption performance, MXene-derived K-HTNs have broad application prospects for the purification of 90Sr-contaminated wastewater and seawater.

Adsorption of Zn(II) from aqueous solution and separation of zinc isotopes by displacement chromatography using chelating adsorbent.

The removal of zinc ions (Zn(II)) in water and the separation of zinc isotopes were fully investigated in this study. Imidodiacetic acid (IDA) type adsorbent (named PSGI) based on polystyrene spheres (PS) was synthesized by simultaneous irradiation grafting. By adsorption method, the removal of Zn(II) from water by the chelating adsorbent was studied in batch experiments. Under optimized condition, PSGI showed the removal efficiency of more than 98 % for Zn(II) and the adsorption capacity of 70.1 mg/g. Langmuir isothermal and pseudo-second-order kinetic model fitted the experimental results better, indicating that the adsorption is dominated by chemical adsorption. The spent adsorbent (PSGI-Zn) was used for further zinc isotope separation by displacement chromatography using EDTA-NH4 solution as eluent. Due to the mass effect of isotopes, 70Zn was found to preferentially fractionated into the front-end effluents with the highest front enrichment values of 70Zn/64Zn. By extending the migration distance to 20 m, we obtained the best isotope enrichment with the front maximum enrichment values as 1.0949, 1.0739 and separation coefficient values as 1.977 × 10-3, 8.33 × 10-3 corresponding to the isotope pairs 66Zn/64Zn, 68Zn/64Zn.

Facile synthesis and properties of a cation exchange membrane with bifunctional groups prepared by pre-irradiation graft copolymerization.

A new type of a cation exchange membrane named ETFE-g-poly(AA-co-SSS) with bifunctional groups was synthesized by a one-step method. Its preparation by an electron beam-induced pre-irradiation grafting method and the effects of reaction temperature, monomer concentration, pH value of the grafting solution, storage time and temperature of the irradiated poly(ethylene-alt-tetrafluoroethylene) (ETFE) films on the grafting yield were studied. A total concentration of 2 mol L-1 of monomers was found to be beneficial for acrylic acid (AA) and sodium styrene sulfonate (SSS) co-grafting onto the ETFE films. Infrared spectroscopic analysis of the grafted membrane confirmed the existence of sulfonate and carboxylic acid groups. The contact angle of the grafted membrane decreased from 94.3 to 46.7° with the increase in grafting yield. The higher the grafting yield, the faster the response and recovery rate with respect to humidity. AFM images showed that the diameter of the grafted chains on the surface of ETFE membranes was about 30 nm. The voltage of the grafted membrane was stable after 100 cycles of charge-discharge; thus, the prepared membranes have great potentials to be used as separators in secondary batteries.

Effect of electron beam irradiation on the degradation of monochlorophenols in aqueous solution.

Electron beam was successfully used for the degradation of 2-chlorophenol (2-CP) and 4-chlorophenol (4-CP) in aqueous solutions in this research. The effect of radiation dose on substrate degradation and dechlorination of solutions with concentration of 50 mg/L was investigated. The effect of initial concentration, pH and presence of oxygen was also investigated. The concentration of 2-CP and 4-CP remaining in solution after irradiation were measured by HPLC. The results showed that increased radiation dose led to increased degradation of the chlorophenols and increased Cl- yield. Deaeration was also found to significantly increase the rate of degradation of chlorophenols in water while degradation and dechlorination under alkaline condition was lower than at low to neutral pH.