Efficient Removal of [UO₂]²⁺, Cs⁺, and Sr²⁺ Ions by Radiation-Resistant Gallium Thioantimonates

Unconventional ion exchangers can achieve efficient removal of [UO₂]²⁺, Cs⁺, and Sr²⁺ ions from complex aqueous solutions and are of great interest for environmental remediation. We report two new gallium thioantimonates, [Me₂NH₂]₂[Ga₂Sb₂S₇]·H₂O (FJSM-GAS-1) and [Et₂NH₂]₂[Ga₂Sb₂S₇]·H₂O (FJSM-GAS-2), which present excellent ion exchange properties for [UO₂]²⁺, Cs⁺, and Sr²⁺ ions. They exhibit high ion exchange capacities for [UO₂]²⁺, Cs⁺, and Sr²⁺ ions (q_m ^U = 196 mg/g, q_m ^Cs = 164 mg/g, and q_m ^Sr = 80 mg/g for FJSM-GAS-1, q_m ^U = 144 mg/g for FJSM-GAS-2) and short equilibrium times for [UO₂]²⁺ ion exchange (5 min for FJSM-GAS-1 and 15 min for FJSM-GAS-2, respectively). Both compounds display active ion exchange with [UO₂]²⁺ in the pH range of 2.9-10.5. Moreover, the sulfide compounds could maintain high distribution coefficients K_d ^U even in the presence of excess Na⁺, Ca²⁺, and HCO₃ ^-. The distribution coefficient K_d ^U of 6.06 × 10⁶ mL/g exhibited by FJSM-GAS-1 is the highest among the reported U adsorbents. The [UO₂]²⁺-laden products can be recycled by conveniently eluting the uranium with a low-cost method. These advantages combined with facile synthesis, as well as β and Î radiation resistance, make FJSM-GAS-1 and FJSM-GAS-2 promising for selective separations in nuclear waste remediation.