Abstract
The radioactive pollution caused by uranium containing wastewater generated during the nuclear fuel cycle seriously threatens human health and environmental safety. The electrosorption (or capacitive deionization, CDI) separation of U(VI) from wastewater has the advantages of high efficiency, low energy consumption, convenient operation, and no secondary pollution, making it a promising new separation technology. By combining double layer capacitive materials with pseudo capacitive materials, the specific capacitance and ion storage capacity of the composites can be significantly improved, thereby improving the electrosorption performance. This work used natural biomass as raw material to prepare hierarchical porous biocarbon through high-temperature pyrolysis and chemical activation, and then it was incorporated with hydrothermally synthesized α-MnO2 nanofibers to obtain novel composites (BC/α-MnO2) with high hybrid capacitance for U(VI) removal in CDI. The electrochemical characteristics of the composites and their electrosorption performances for U (VI) were respectively investigated in a three electrode system and a CDI device. The results suggested that BC/α-MnO2 exhibited an ideal capacitive behavior, and theoretical calculations indicated the synergistic effect of capacitive and diffusion control processes on ion storage. Among different BC/α-MnO2 electrodes, BC/α-MnO2-2 had the highest specific capacitance (130.48 F/g) and also the highest adsorption capacity for U (VI) (280.20 mg/g at 0.9 V and pH 4.0). The isotherms and kinetics of U (VI) electrosorption were consistent with the Langmuir and PFO models, respectively. The electrosorption mechanism was mainly related to the contribution of pseudocapacitance and EDL adsorption. Overall, BC/α-MnO2-2 exhibited ideal electrochemical properties and excellent electrsorption performance for U (VI) (high electrosorption capacity, fast kinetic rate, and good cycling stability), facile fabrication and environmentally friendly, and thus it has promising application in CDI treatment of radioactive wastewater.
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