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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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2024 ANS Annual Conference
June 16–19, 2024
Las Vegas, NV|Mandalay Bay Resort and Casino
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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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Nicholas Tsoulfanidis—ANS member since 1969
As an undergraduate I studied physics at the University of Athens. I entered the university in 1955 after successfully passing a national exam (came up fourth in a field of about 700 candidates). Upon graduation and finishing my mandatory two-year military service, the plan was to teach physics either in a public high school or as a tutor for a private for-profit institution, preparing high school students for the national exam.
B. W. N. Fitzpatrick, J. W. Davis, A. A. Haasz
Fusion Science and Technology | Volume 73 | Number 4 | May 2018 | Pages 552-558
Technical Note | doi.org/10.1080/15361055.2017.1404346
Articles are hosted by Taylor and Francis Online.
If both carbon and tungsten were to be part of the plasma-facing armor in a future fusion reactor, it is inevitable that carbon co-deposits containing tungsten impurities will form. This work examines the effectiveness of thermo-oxidation in removing hydrogen from W-containing carbon co-deposits. Amorphous deuterated hydrocarbon (a-C:D) films were created with a CD4/Ar direct-current glow discharge and doped with W sputtered from a W mesh in front of the specimen. The W concentration in the specimens ranged from 0 to 35 at. % W/(W + C). The films were oxidized at 350°C, in 2 Torr pure O2 for time increments totaling 8 h. The D content of the films was measured before and at various stages of the oxidation exposure using laser thermal desorption spectroscopy. Essentially all deuterium was removed from films containing very little or no W doping [<0.1% W/(W + C)]. For films with more W [few percent W/(W + C)], oxidation was less effective at removing D. For two specimens with 2.4% and 35% W/(W + C), oxidation was completely ineffective at removing D.