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Fusion Energy
This division promotes the development and timely introduction of fusion energy as a sustainable energy source with favorable economic, environmental, and safety attributes. The division cooperates with other organizations on common issues of multidisciplinary fusion science and technology, conducts professional meetings, and disseminates technical information in support of these goals. Members focus on the assessment and resolution of critical developmental issues for practical fusion energy applications.
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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
Smarter waste strategies: Helping deliver on the promise of advanced nuclear
At COP28, held in Dubai in 2023, a clear consensus emerged: Nuclear energy must be a cornerstone of the global clean energy transition. With electricity demand projected to soar as we decarbonize not just power but also industry, transport, and heat, the case for new nuclear is compelling. More than 20 countries committed to tripling global nuclear capacity by 2050. In the United States alone, the Department of Energy forecasts that the country’s current nuclear capacity could more than triple, adding 200 GW of new nuclear to the existing 95 GW by mid-century.
Tatsuhiko Uda, Kenji Okuno, Yuji Naruse
Fusion Science and Technology | Volume 21 | Number 2 | March 1992 | Pages 436-441
Safety; Measurement and Accountability; Operation and Maintenance; Application | doi.org/10.13182/FST92-A29784
Articles are hosted by Taylor and Francis Online.
To study application of laser Raman spectroscopy for fusion fuel gas analysis by an in situ method, methane (CH4) and tritium (T2) mixed gases were measured. In the mixed gases, hydrogen isotope exchange reactions were induced by beta decay, and various isotopic hydrogens and methanes were produced. Spectral peaks of v1 and v3 bands were detected individually for CH4 and four tritiated methanes. The v1 bands between 1700–1900 cm−1 were selected as suitable ones for quantitative analysis. After mixing T2 and CH4 gases, while large amounts of tritiated methanes were produced as time lapsed, the equilibrium state was not reached by the time 1000 h had passed. It was presumed that the isotope exchange reactions were very slow compared to mixed gases of just hydrogen isotopes.
