Abstract

Cryogenic distillation (CD) is a crucial process for separating and concentrating tritium in the tritium fuel cycle of fusion reactors. The equilibrator plays a vital role in decomposing HD, DT, and HT to improve the separation efficiency of hydrogen isotopes in CD. As the equilibrium reaction temperature decreases, a larger proportion of HD, HT, and DT decomposes into H2, D2, and T2, which enhances the performance of the equilibrator. While Pt/Al2O3 catalyst exhibits high activity at 303 K in the H2-D2 equilibrium reaction, it is almost inactive at 77 K. Non-thermal plasma (NTP) technology offers a promising and attractive alternative to conventional catalytic technology. In this study, H2-D2 equilibrium reaction was carried out without catalysts in a dielectric barrier discharge (DBD) reactor, achieving efficient conversion of HD even at 77 K. In the single-electrode DBD plasma reactor (S-P-Reactor), with an input power of 50 W, the conversion efficiency of HD was found to be 99.5% at 303 K, 99.5% at 273 K, and 99.2% at 77 K. To further optimize the energy efficiency of the S-P-Reactor, the reactor structure was enhanced, leading to the development of a multi-high-voltage DBD reactor (M-P-Reactor). The input power of the M-P-Reactor was reduced by approximately 10 W compared to the S-P-Reactor, while maintaining a conversion efficiency of over 95% for HD. The energy density of the reactor was calculated using the Q-V Lissajous graphic method, demonstrating that the M-P-Reactor exhibited superior energy conversion efficiency compared to the S-P-Reactor. Furthermore, the yield of HD was solely determined by the energy density and temperature. At a specific energy density, the yield of HD remained consistent for the same temperature. However, generating HD at lower temperatures required more energy due to the lower reactant activity. These results illustrate the potential application of NTP technology in improving hydrogen isotope separation performance in the cryogenic distillation process for fusion applications.

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