Selective adsorption of uranyl and potentially toxic metal ions at the core-shell MFeO-TiO (M=Mn, Fe, Zn, Co, or Ni) nanoparticles.

J Hazard Mater

Key Laboratory of Solid Waste Treatment and Resource Recycle, Ministry of Education, State Key Laboratory Cultivation Base for Nonmetal Composites and Functional Materials, South West University of Science and Technology, Mianyang, 621010, Sichuan, China.

Published: March 2019

Potentially toxic metal ions (X: Rb, Sr, Cr, Mn, Ni, Zn, Cd) usually coexist with uranyl (UO), which will have a great influence on the selective adsorption process. Here, the core-shell MFeO-TiO (M = Mn, Fe, Zn, Co, or Ni) nanoparticles were synthesized and assessed as new selective adsorbents. The results reveal that TiO(101) preferentially grows along the MFeO(311)/(111) orientation. The M ions as the mediators transfer the holes from MFeO to TiO, at the conduction bands. On the TiO(101) surfaces and TiO(101)-TiO(101) gaps, the paired active electrons mainly complex with water molecules as hydroxyl radicals to capture X ions, forming an ion layer to block UO from being adsorbed. Simultaneously, it should be noted that an interesting adsorption pathway was UO being horizontally and irreversibly adsorbed in the MFeO(311)/(111)-TiO(101) interface, and therein, the stable adsorption capacity was found to be 66.78 mg g in the MnFeO(311)/(111)-TiO(101) interface. Finally, a mechanism of hybrid orbitals between MnFeO-TiO and UO-X was proposed.

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Source
http://dx.doi.org/10.1016/j.jhazmat.2018.11.076DOI Listing

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