Highly efficient and selective removal of 90Sr by the carboxylated COFs (Tp-DTA) from radionuclides-contaminated groundwater

In this study, a carboxyl-functionalized covalent organic framework (COF) rich in nitrogen (N) and oxygen (O) functional groups was prepared and characterized, which provided a new opportunity for the efficient and rapid treatment of radioactive contamination in nuclear wastewater. The synthesis of the COF (Tp-DTA) was constructed using 1,3,5-triformylphloroglucinol (TFP) and 2,5-diaminoterephthalic acid (DTA), providing a large specific surface area, mesoporous pore, and abundant coordination sites with high adsorption capacity and exceptional affinity for Sr2+. Batch adsorption experiments exhibited that Tp-DTA achieved a maximum adsorption capacity of 145.4 mg/g for Sr2+ in alkaline solutions, reaching adsorption equilibrium within 60 min. Tp-DTA exhibited rapid kinetics for 90Sr, with the amounts of 90Sr removed more than 95 % within 3 min. In the presence of coexisting ions (Na+, K+, Cs+, Mg2+, and Ca2+), Tp-DTA displayed excellent preferential selectivity for Sr2+ and high removal efficiency. Even in simulated groundwater containing multiple complex ions, Tp-DTA demonstrated a strong affinity for Sr2+ and showed practical applicability with a nearly 100 % removal efficiency for 90Sr. XPS and FTIR characterizations confirmed that the adsorption mechanism of Sr2+ involved chelation exchange between the carboxyl groups of Tp-DTA and Sr2+ in the solution. Furthermore, the desorption efficiency of HCl (>0.01 mol/L) can reach 95 % and five cyclic desorption-adsorption experiments demonstrated the reusability of Tp-DTA, endowing the carboxyl-functional COF with great potential in the treatment of 90Sr-contaminated radioactive wastewater and environmental remediation.