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Nuclear Energy Conference & Expo (NECX)
September 8–11, 2025
Atlanta, GA|Atlanta Marriott Marquis
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Hash Hashemian: Visionary leadership
As Dr. Hashem M. “Hash” Hashemian prepares to step into his term as President of the American Nuclear Society, he is clear that he wants to make the most of this unique moment.
A groundswell in public approval of nuclear is finding a home in growing governmental support that is backed by a tailwind of technological innovation. “Now is a good time to be in nuclear,” Hashemian said, as he explained the criticality of this moment and what he hoped to accomplish as president.
J. Bourges, C. Madic, G. Koehly, T. H. Nguyen, D. Baltes, C. Landesman, A. Simon
Nuclear Technology | Volume 113 | Number 2 | February 1996 | Pages 204-220
Technical Paper | Radioisotopes and Isotope | doi.org/10.13182/NT96-A35189
Articles are hosted by Taylor and Francis Online.
In 1985, the Commissariat à I’Energie Atomique (CEA), France, decided to set up an industrial unit at the Saclay Nuclear Research Center to produce fission 99Mo and to supply this isotope to the ORIS Company, France, for medical applications. The CEA’s role in this project was to develop a brand-new process for 99Mo production and to assume responsibility for the design and construction of the industrial plant. Production was based on 74 TBq (2 kCi) of 99Mo per week, under particularly severe constraints to protect the environment and the workers. The production unit, run in a semiautomatic mode, was built at Saclay in 1987 and cold tested from 1987 to 1989. The unit was never upgraded to active experiments because of the sudden drop in the price of 99Mo on the world market, which made the French project uneconomic. The focus here is mainly on the research conducted at the time to define and to validate the entire fission molybdenum chemical process. The process flowchart incorporates two original features. First, in the head-end of the process, the irradiated targets are dissolved in a sulfuric acid medium, entailing the maintenance of radioiodine and radiotellurium, for safety reasons, in the form of I‾(AgI) and Te(0), respectively, allowing their easy removal as solids from the dissolution liquors and their subsequent storage for radioactive decay. Second, in the core of the process, the molybdenum is purified by extraction with tri-n-butylacetohydroxamic acid, an extractant with exceptional affinity and selectivity for Mo(VI). The 99Mo(VI) extraction cycles employ the extraction chromatographic mode.