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DOE announces Genesis Mission request for applications
Ian Buck, Nvidia’s vice president of hyperscale and HPC computing (left), and Darío Gil, DOE Under Secretary for Science and Genesis Mission lead, at the Nvidia GPU Technology Conference. (Photo: Nvidia)
Department of Energy Under Secretary for Science and Genesis Mission lead Darío Gil participated in a session at the Nvidia GPU Technology Conference on March 17 that coincided with the announcement of the DOE’s $293 million Genesis Mission request for applications, which invites interdisciplinary teams to submit ideas for projects addressing over 20 of Genesis’s stated national challenges, several of which focus on accelerating nuclear research and nuclear energy output.
“We seek breakthrough ideas and novel collaborations leveraging the scientific prowess of our national laboratories, the private sector, universities, and science philanthropies,” said Gil.
Thomas H. Handley
Nuclear Science and Engineering | Volume 16 | Number 4 | August 1963 | Pages 440-447
Technical Paper | doi.org/10.13182/NSE63-A26556
Articles are hosted by Taylor and Francis Online.
The solvent-extraction properties of the sulfur analogs, both neutral and acid, of those organophosphorus compounds that have been used so extensively in solvent extraction have been investigated. These sulfur analogs have one or more oxygen atoms replaced by sulfur atoms. The neutral esters, trialkyl phosphorothioates, selectively extract Ag+ and Hg+2 from a nitric acid medium. In general, the acid esters, dialkyl phosphorothioic and -dithioic acids, extract from mineral acid solutions those metal ions that form insoluble sulfides. Dialkyl phosphorothioic acids appear to be more selective extractants than are the corresponding dithioic acids. The effects of various organic solvents, of concentration of mineral acid, and of concentration of dialkyl phosphorothioic and -dithioic acids were studied. The relative order of extraction and the limits of extraction were determined. The nature of the zinc di-n-butyl phosphorothioate and -dithioate complexes as they exist in the aqueous and organic phases were investigated.