Abstract

The development of novel porous materials as adsorbents for highly effective separation of thorium from ore or nuclear wastewater co-existing with uranium and rare earth elements is one of the most desirable methods but remains challenging. In this work, we prepare a N,O-functionalized two-dimensional covalent organic framework (2D COF), namely TAPT-DHTA, with a permanent porous structure and plenty of nitrogen and oxygen adsorption sites throughout the skeletons, which displays an ultrahigh Th(IV) saturated adsorption capacity of 1394 mg g−1 (at pH = 4.0), higher than all adsorbents reported so far. Moreover, the TAPT-DHTA COF has a large distribution coefficient (Kd) of up to 5.2 × 104 mL g−1, implying its extremely strong affinity for Th(IV) due to the collaborative coordination interactions between N/O atoms and Th(IV) as well as their specific binding mechanism. The distinguished adsorption behavior of the TAPT-DHTA COF affords an important platform for highly selective separation of Th(IV) from uranium and rare earth elements, thereby shedding some light on the design of novel adsorbents for thorium separation in the thorium fuel cycle.

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