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Antares achieves zero-power criticality at INL
Leveraging more than $140 million in private capital fundraising, over 322,000 square feet of operational manufacturing space, and multifaceted partnerships with the Departments of Energy and Defense, reactor start-up Antares has become the first company involved in the Reactor Pilot Program to achieve zero-power fueled criticality—a full month ahead of the July 4 deadline set by President Trump’s Executive Order 14301.
This milestone, announced yesterday, was achieved with the company’s Mark-0: a sodium heat-pipe-cooled, TRISO-fueled microreactor. The Mark-0 is a forerunner to the company’s flagship design, which it calls the R1. For Antares, this development represents a key validation of its reactor physics, control systems, and supply chain.
Satoshi Fukada, Makoto Ueda, Kazutaka Izumi
Fusion Science and Technology | Volume 64 | Number 3 | September 2013 | Pages 538-542
Fusion Technologies: Heating and Fueling | Proceedings of the Twentieth Topical Meeting on the Technology of Fusion Energy (TOFE-2012) (Part 2) Nashville, Tennessee, August 27-31, 2012 | doi.org/10.13182/FST13-A19149
Articles are hosted by Taylor and Francis Online.
Multi-component adsorption isotherm is determined experimentally when He, H2 (or D2) and CH4 are adsorbed on activated carbon (AC) plated on a cryopanel cooled at cryogenic temperature and desorbed at room one. It is correlated to the Langmuir-Freundlich-type one. The equilibrium isotherms for their respective single-component adsorption processes are correlated in terms of the Langmuir-Freundlich-type ones, and the isotherm when the three components of He, H2 and CH4 are adsorbed at the same time is correlated in terms of a naturally-extended multi-component one without any changes in the original constants included in the single-component one. Rates of the isotopic exchange reaction of D atom between CH4 and D2 on AC between 10 K and room temperature are also determined. After eliminating the effects of natural isotope of 13C included in CH3D, CH2D2, CHD3, CD4 on mass-spectrometric measurements, it was found that the isotopic exchange rate of CH4 + D2 = CH3D +HD and so on was found to be so late that any detectable effect was not observed.