Dual Ion-Imprinted Mesoporous Silica for Selective Adsorption of U(VI) and Cs(I) through Multiple Interactions

Separation of uranium and cesium from low-level radioactive effluents (LLRE) is of great significance for sustainable development of the nuclear industry and for the environment. However, high salinity and massive coexisting ions of LLRE are giant challenges for the separation. To address the challenges, we report a strategy for efficient and simultaneous separation of uranium and cesium from a high-salt environment by dual ion-imprinted mesoporous silica based on multiple interactions. The as-prepared adsorbents can reach equilibrium for uranium and cesium within 1 h with a maximum capacity of 221.7 mg U g(-1) and 34.5 mg Cs g(-1). The sorption mechanism demonstrates that the highly active phenolic hydroxyl groups of imprinted cavities can extract uranium and cesium effectively through multiple interactions, including coulomb attraction, redox, ion exchange, and complexation. The synergism of multiple interactions and imprinted cavity endows the sorbent with good selectivity for uranium and cesium over other cations and with excellent salt tolerance. This work demonstrates a new strategy of selective extraction of nuclides by multifunction adsorbent through multiple interactions.