Conversion of supramolecular organic framework to uranyl-organic coordination complex: a new “matrix-free” strategy for highly efficient capture of uranium

Abstract

Herein, an innovative “matrix-free” strategy has been proposed for highly efficient uranium capture via uranyl-induced disassembly and reassembly of the two functional building blocks of the as-prepared hydrogen-bonded supramolecular organic framework (HSOF), which is composed of N-donor-containing melamine and O-donor-containing trimesic acid self-assembled through hydrogen bonding. The batch experimental results demonstrated that HSOF possesses excellent extraction capacity (qm = 444 mg g−1), >99% removal efficiency in the range of tested U(vi) concentration (20-130 ppm) with a considerably large KUd value of 1.3 × 107 mL g−1 at 130 ppm, and very fast extraction rate (<10 min) for UO22+. Especially, the uranium selectivity (SU = qe-U/qe-tol) of HSOF stays above 80% over the pH range tested in a uranium-containing solution with 11 competing cations, and distinctively, reaches the so far unreported 99% with a great capacity of 309 mg g−1 at pH 2.5. It is worth noting that a clear morphology transformation of HSOF nanowires to nanosheets of the uranyl-organic coordination complex (UOCC) after extraction has been observed only in the presence of uranyl ions. Moreover, according to experimental characterization and DFT studies, a possible mechanism for the efficient capture of uranium is proposed: the stronger coordination interaction among uranyl, TMA and MA could replace the weaker hydrogen-bond interaction originally linking the two building blocks in HSOF in the extraction process.