Please use this identifier to cite or link to this item:
|Title:||Selective sorption of actinides by titania nanoparticles covalently functionalized with simple organic ligands|
|Publisher:||American Chemical Society|
|Citation:||Veliscek-Carolan, J., Jolliffe, K. A., & Hanley, T. L. (2013). Selective sorption of actinides by titania nanoparticles covalently functionalized with simple organic ligands. ACS Applied Materials & Interfaces, 5(22), 11984-11994. doi:10.1021/am403727x|
|Abstract:||Although current and proposed reprocessing of used nuclear fuel is performed predominantly by solvent extraction processes, solid phase sorbent materials have many advantages including the ability to avoid production of large volumes of organic waste. Therefore, three titania nanoparticle based sorbent materials have been developed, functionalized with organic ligands designed to impart selectivity for elements relevant to important separations at the back end of the nuclear fuel cycle. A novel, simplified method of covalent functionalization to the titania surface has been utilized, and the resulting materials have been shown to be hydrolytically stable at pH 2. The sorption behavior of these organofunctionalized titania materials was investigated over a wide pH range with a selection of elements including fission products and actinides. Titania nanoparticles functionalized with an amine or phosphate moiety were able to demonstrate exclusive extraction of uranium under optimized conditions. Titania nanoparticles functionalized with a picolinamide moiety exhibited superior minor actinide sorption properties, in terms of both efficiency and selectivity, to solvent extraction processes using similar organic moieties. As such, organo-functionalized titania materials as solid phase sorbents show promise as a future alternative to solvent extraction processes for nuclear separations. © 2013, American Chemical Society.|
|Gov't Doc #:||6210|
|Appears in Collections:||Journal Articles|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.