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Materials Science & Technology
The objectives of MSTD are: promote the advancement of materials science in Nuclear Science Technology; support the multidisciplines which constitute it; encourage research by providing a forum for the presentation, exchange, and documentation of relevant information; promote the interaction and communication among its members; and recognize and reward its members for significant contributions to the field of materials science in nuclear technology.
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ANS Student Conference 2025
April 3–5, 2025
Albuquerque, NM|The University of New Mexico
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The Standards Committee is responsible for the development and maintenance of voluntary consensus standards that address the design, analysis, and operation of components, systems, and facilities related to the application of nuclear science and technology. Find out What’s New, check out the Standards Store, or Get Involved today!
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Latest News
First astatine-labeled compound shipped in the U.S.
The Department of Energy’s National Isotope Development Center (NIDC) on March 31 announced the successful long-distance shipment in the United States of a biologically active compound labeled with the medical radioisotope astatine-211 (At-211). Because previous shipments have included only the “bare” isotope, the NIDC has described the development as “unleashing medical innovation.”
Hirokazu Hayashi, Mitsuo Akabori, Kazuo Minato
Nuclear Technology | Volume 162 | Number 2 | May 2008 | Pages 129-134
Technical Paper | First International Pyroprocessing Research Conference | doi.org/10.13182/NT08-A3939
Articles are hosted by Taylor and Francis Online.
The electrode reactions of americium at a liquid cadmium electrode were investigated by cyclic voltammetry of AmCl3-(LiCl-KCl)eut. at both 723 and 773 K in comparison with those at a molybdenum electrode. The redox peaks assigned to Am(III)/Am(0) (in Cd) were observed with the liquid Cd electrode, while the redox reactions of Am(III)/Am(II) and Am(II)/Am(0) were observed with the Mo electrode. The formal standard potential of Am(III)/Am(0) obtained with the liquid Cd electrode is more positive than those calculated for the Mo electrode at both 723 and 773 K. The potential shifts were attributed to the lowering of the activity of Am by the formation of the intermetallic compound at the interface between Cd and the molten salt. The Gibbs free energies of formation of the Am-Cd intermetallic compound, which could be AmCd6, are estimated to be -119 and -113 kJ/mol at 723 and 773 K, respectively.
