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A closer look at the initial NLIC selections—Part 2
In January, the Department of Energy announced its new Nuclear Lifecycle Innovation Campus (NLIC) program, inviting states via a request for information to express their interest in hosting a facility supporting work from the front to the back end of the nuclear fuel cycle.
By April, 26 states had expressed interest in hosting such a facility. At the end of July, the DOE signed memorandums of understanding with five states—Idaho, Louisiana, Oklahoma, Tennessee, and Utah—to more closely explore the possibilities of state-federal partnerships. These MOUs are not firm commitments from either the federal or state governments. Time will tell which—if any—of the five states develop projects through the program. In the meantime, today, we are taking a close look at what Utah, Idaho, Tennessee can offer in terms of a preexisting nuclear sector that could support new fuel cycle developments.
Shameem Hasan, Tushar K. Ghosh
Nuclear Technology | Volume 181 | Number 2 | February 2013 | Pages 371-379
Technical Paper | Miscellaneous | doi.org/10.13182/NT13-A15791
Articles are hosted by Taylor and Francis Online.
Uranium oxide (U3O8) nanoparticles were synthesized and coated in situ with porous, mesostructured silica using a modified sol-gel method for use as a catalyst. The catalytic property of coated U3O8 nanoparticles was evaluated by exposing them to an aqueous solution of benzene at 500 mg/l at room temperature. The presence of benzene was not detected by an ultraviolet (UV)-visible (UV-vis) spectrometer after 6 weeks of exposure to coated uranium oxide nanoparticles, indicating the particles' potential as a catalyst. Based on the results of the benzene destruction, it may be suggested that the coated U3O8 nanoparticle-based catalyst has the potential to destroy hydrocarbons, aromatics, and various toxic substances such as perchlorates and 1,4-dioxane from groundwater. However, further experiments are necessary to explore the full potential of the catalyst. Pluronic-123, n-butanol, and 2-propanol were used as surfactant, cosurfactant, and continuous phase, respectively, for the synthesis of the U3O8 nanoparticles, which were formed through nucleation, growth, and subsequent aggregation in the solution phase. The nanoparticles were coated in situ using an aqueous solution of tetraethyl orthosilicate. The coated particles were characterized using transmission electron microscopy, diffuse reflectance infrared Fourier transform spectroscopy, nitrogen physisorption, X-ray diffraction, and diffuse reflectance UV-vis spectroscopy. These measurements revealed that U3O8 particles ranging from 4- to 10-nm were distributed exclusively inside the silica matrix.