Abstract

Searching for new efficient, selective, and stable, adsorbents for 90Srgenerated in the nuclear fuel cycle remains important. In the last year, 18 crown 6ether and its derivatives have been intensively studied as highly efficient ion-exchangers for removal of 90Sr. However, one of the main problems for further application of these expensive macrocyclic ligands is loss in solid-liquid media due to their solubility. To overcome this problem, in this work, we have developed a new organic – inorganic layer α-ZrP composite by intercalation of 4-amino-benzo-18 crown 6. This new α-ZrP composite (AM-ZrP) not only inherits the advantages of 4-amino-benzo-18 crown 6 and α-ZrP, exhibiting excellent stability under acid and radioactive conditions, but also efficiently decreases the loss of valuable4-amino-benzo-18 crown 6 in the adsorption process. Furthermore, the preparation process for AM-ZrP is simple and it can be easily produced on a large-scale. Remarkably, having a pore size matching4-amino-benzo-18 crown 6, AM-ZrP shows high selectivity for capturing Sr2+ from complicated mixed solutions. The maximum adsorption capacity for Sr2+ onto AM-ZrP is 320.16 mg·g−1, which is about five times that of neat α-ZrP. Itsurpasses most other inorganic adsorbents, which can be attributed to the much higher number of adsorption sites and the wide interlayer spacing of α-ZrP after interactionwith4-amino-benzo-18 crown 6. Our present work not only poses a new way to promote crown ether compounds and α-ZrP materials, furthering their application in nuclear wastewater disposal, but also develops a new way of thinking about the design and preparation of new adsorbents for removal of difficult-to-capture ions from nuclear wastewater.

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