The separation of 213Bi from its parent radionuclide 225Ac via radionuclide generators has proven to be a challenge due to the limited performance of the current sorbents. This study evaluated the separation performance of La3+ (as a surrogate for 225Ac) and Bi3+ using bis(2-ethylhexyl)phosphate monofunctionalized activated carbon (HDEHP/AC). The potential applications of phosphate groups as active sites and the carbon structure as a sorbent support were confirmed and validated. Various factors, including pH values, salt concentration, halide ions, contact time, solid-to-liquid ratio, initial La3+/Bi3+ concentration, and gamma irradiation were examined through batch sorption experiments in both single and binary systems. HDEHP/AC had a high sorption capacity for La3+ via electrostatic attraction, with the sorption data fitting well to the pseudo-second-order kinetic equation and Langmuir model. The sorption performance of La3+ on HDEHP/AC was minimally affected as the NaCl/NaI concentrations increased at pH = 2, whereas the sorption capacity for Bi3+ decreased significantly. Additionally, selective desorption of La3+ and Bi3+ was achieved using HNO3 and NaI solutions, respectively. These results backed up by a conceptual separation process point toward a potential use of these materials in a direct/inverse 225Ac/213Bi radionuclide generator. Further optimization of the material and separation process will be required to bring this class of promising materials into an actual generator for medical applications.
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