ABSTRACT
The efficient segregation of radioactive nuclides from low-level radioactive liquid waste (LLRW) is paramount for nuclear emergency protocols and waste minimization. Here, we synthesized Na3FePO4CO3 (NFPC) via a one-pot hydrothermal method and applied it for the first time to the selective separation of Sr2+ from simulated LLRW. Static adsorption experimental results indicated that the distribution coefficient Kd remained above 5000 mL·g-1, even when the concentration of interfering ions was more than 40 times that of Sr2+. Furthermore, the removal efficiency of Sr2+ showed no significant change within the pH range of 4 to 9. The adsorption of Sr2+ fitted the pseudo-second-order kinetic model and the Langmuir isotherm model, with an equilibrium time of 36 min and a maximum adsorption capacity of 99.6 mg·g-1. Notably, the adsorption capacity was observed to increment marginally with an elevation in temperature. Characterization analyses and density functional theory (DFT) calculations elucidated the adsorption mechanism, demonstrating that Sr2+ initially engaged in an ion exchange reaction with Na+. Subsequently, Sr2+ coordinated with four oxygen atoms on the NFPC (100) facet, establishing a robust Sr-O bond via orbital hybridization.
ABSTRACT
As a competitive radioactive wastewater treatment technology, electrodialysis (ED) has the advantages of low operating pressure and high cycles of concentration. In order to analyze the migration performance of radionuclides during the treatment of radioactive wastewater by ED, a radionuclide migration model was constructed based on the mass conservation law and Faraday's law with the typical radionuclide cesium as the research object. Experiments were carried out for the treatment of simulated radioactive wastewater in a small-scale ED system, and the average migration rate of radionuclides under different operating conditions was predicted by the model. The results showed that the experimental values of concentration and average migration rate of Cs(I) were significantly correlated with the calculated values of the model, in which the relative error of the average migration rate was 4.54%. The variation characteristics of Cs(I) concentration in diluted solution under different current and volume ratio conditions can be predicted by the model. The average variation rate of Cs(I) concentration decreases significantly with the increase of current and volume ratio.