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Fusion energy: Progress, partnerships, and the path to deployment
Over the past decade, fusion energy has moved decisively from scientific aspiration toward a credible pathway to a new energy technology. Thanks to long-term federal support, we have significantly advanced our fundamental understanding of plasma physics—the behavior of the superheated gases at the heart of fusion devices. This knowledge will enable the creation and control of fusion fuel under conditions required for future power plants. Our progress is exemplified by breakthroughs at the National Ignition Facility and the Joint European Torus.
H. Katsui, A. Hasegawa, Y. Katoh, Y. Hatano, T. Tanaka, S. Nogami, T. Hinoki, T. Shikama
Fusion Science and Technology | Volume 60 | Number 1 | July 2011 | Pages 288-291
In-Vessel Components - FW, Blanket, Shield & VV | Proceedings of the Nineteenth Topical Meeting on the Technology of Fusion Energy (TOFE) (Part 1) | doi.org/10.13182/FST11-A12367
Articles are hosted by Taylor and Francis Online.
Compatibility of monolithic silicon carbide (SiC) with ternary lithium ceramics (Li1-xAlO2-y, Li2-xTiO3-y, Li2-xZrO3-y and Li4-xSiO4-y) under irradiation of neutrons at high temperatures was studied. Disk samples of SiC in contact with sintered ternary lithium ceramics were irradiated in High Flux Isotope Reactor (HFIR) at 800 °C to 5.9 displacements per atom (dpa). Chemical reactions of SiC as determined by appearance of the surface were relatively less significant for the systems of SiC/Li1-xAlO2-y and SiC/Li2-xTiO3-y, whereas some bonding likely due to chemical reaction between SiC and the lithium ceramics and broken samples were observed in the systems of SiC/Li2-xZrO3-y and SiC/Li4-xSiO4-y. The effect of lithium burnup due to the (n, ) nuclear reaction was also examined by using samples of lithium ceramics whose lithium ratio was hypo-stoichiometric in the fabrication process. More reaction products were observed on the surface of -SiC in contact with Li1-xAlO2-y having the lower lithium ratio (Li/Al). It was considered that the formation of LiAl5O8 phase due to lithium loss could deteriorate the compatibility of the SiC - Li1-xAlO2-y system.