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Conference Spotlight
Nuclear Energy Conference & Expo (NECX)
September 8–11, 2025
Atlanta, GA|Atlanta Marriott Marquis
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A new ANSI/ANS standard for liquid metal fire protection published
ANSI/ANS-54.8-2025, Liquid Metal Fire Protection in LMR Plants, received approval from the American National Standards Institute on September 2 and is now available for purchase.
The 2025 edition is a reinvigoration of the withdrawn ANS-54.8-1988 of the same title. The Advanced Reactor Codes and Standards Collaborative (ARCSC) identified the need for a current version of the standard via an industry survey.
Typical liquid metal reactor designs use liquid sodium as the coolant for both the primary and intermediate heat-transport systems. In addition, liquid sodium and NaK (a mixture of sodium and potassium that is liquid at room temperature) are often used in auxiliary heat-removal systems. Since these liquid metals can react readily with oxygen, water, and other compounds, special precautions must be taken in the design, construction, testing, and maintenance of the sodium/NaK systems to ensure that the potential for leakage is very small.
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.