The Functionalized N-Rich Covalent Organic Framework for Palladium Removal from Nuclear Wastewater

Abstract

Efficiently adsorbing Pd(II) from acidic radioactive waste liquid is crucial for ensuring the safety of the radioactive waste vitrification process and significantly alleviating the scarcity of precious metals. However, the stability and selectivity of most current adsorbents are limited, hindering their practical application under acidic conditions. To address these limitations, a covalent organic framework (DHTP-TPB COF) was prepared with a high nitrogen content, leveraging the high affinity of its soft ligand N with palladium to achieve high selectivity. This work demonstrated that DHTP-TPB COF exhibits rapid adsorption kinetics, with equilibrium achieved within 10 min. The framework also boasts a high adsorption capacity of 142.8 mg/g and impressive reusability in 1.0 M nitric acid. Moreover, the DHTP-TPB COF displays excellent selectivity for Pd(II), even in the presence of 13 interfering ions. By combining FT-IR, XPS spectroscopy, and DFT theoretical calculations, the dense N sites in the framework have a strong affinity for Pd(II), resulting in exceptional adsorption performance that was confirmed. The findings of this study highlight the potential of COFs with robust linkers and customized functional groups to effectively and selectively capture Pd(II) under harsh environmental conditions of high-level liquid waste.