Abstract

Polystyrene resins (PS) have been practical ion exchangers for radionuclides removal from water. However, nonspecific effects of ion exchange groups continue to be a major obstacle for emergency treatment with coexisting ions of high concentrations. The selectivity for Cs+ enables zirconium phosphate (ZrP) to be the most promising inorganic sorbent for radioactive cesium extraction, despite being difficult to synthesize and causing excessive pressure loss in fixed-bed reactors due to fine powder. Herein, through facile confined crystallization in host macropores, we prepared PS confined α-ZrP nanocrystalline (ZrP-PS). Size-screen sorption of layered α-ZrP and sulfonic acid group preconcentration of PS synergistically enable a considerably higher Cs+ affinity of ZrP-PS than PS, as confirmed by X-ray photoelectron spectroscopy (XPS) analysis. ZrP-PS demonstrated remarkable cesium sequestration performance in both batch and continuous experiments, with a high adsorption capacity of 269.58 mg/g, a rapid equilibrium within 80 min, and a continuous effluent volume of 2300 L/kg sorbents. Given the excellent selectivity for Cs+ and flexibility to separate from treated water, ZrP-PS holds great promise as purification packages for the emergency treatment of radioactively contaminated water.

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