Experiments on the Capture of Li, H, and D by Lithium Collectors at Different Surface Temperatures at the T-11M Tokamak


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Abstract

Prototypes of lithium emitters and collectors designed on the basis of capillary-porous systems (CPS) are being tried-out at the T-11M tokamak within the concept of continuous lithium circulation, previously proposed for stationary fusion neutron sources (FNSs). One of the goals of the T-11M tokamak research program are to implement the closure of the lithium circulation circuit and to develop the technology of recuperation (extraction and removal from the tokamak chamber) of hydrogen isotopes by using special lithium CPS-based collectors in order to prevent hydrogen isotope accumulation on the inner surface of the discharge chamber. In order to determine the optimal temperature regime for the future FNS operation, the effect of the temperature of the collector surface on its ability to capture lithium and hydrogen isotopes was studied. It is ascertained that the efficiency of capturing lithium and hydrogen isotopes by metal (12Cr18Ni10Ti) collectors in the operating regimes of the T-11M tokamak depends on the temperature of their collecting surfaces; namely, it remains almost constant in the temperature range from–196 to 50°С and then gradually decreases as the temperature rises to 300–400°С. In this case, the amount of the collected lithium is reduced by no more than sixfold, whereas the amount of collected hydrogen isotopes decreases by more than two orders of magnitude. Thus, the wall of a tokamak reactor chamber, which will be heated to 400°С but still coated with residual lithium (or its chemical compounds), will serve as a “mirror” for the incident hydrogen isotopes. It is found that the liquid lithium surface of the CPS-based collector can efficiently capture hydrogen isotopes falling onto it. As the lithium CPS-based collector is heated from 100 to 240°С, the amount of captured deuterium is reduced only twofold. This means that, in a steady-state mode, if, e.g., an MHD pump is used to transport liquid lithium from the collector back to the emitter, then, together with lithium, the captured hydrogen isotopes can also be transported into the recuperation zone.

About the authors

M. Yu. Zharkov

Krasnaya Zvezda State Enterprise

Email: shcherbak@triniti.ru
Russian Federation, Moscow, 115230

A. N. Shcherbak

Troitsk Institute for Innovation and Fusion Research

Author for correspondence.
Email: shcherbak@triniti.ru
Russian Federation, Troitsk, Moscow, 108840

S. V. Mirnov

Troitsk Institute for Innovation and Fusion Research

Email: shcherbak@triniti.ru
Russian Federation, Troitsk, Moscow, 108840

A. S. Dzhurik

Troitsk Institute for Innovation and Fusion Research

Email: shcherbak@triniti.ru
Russian Federation, Troitsk, Moscow, 108840

V. B. Lazarev

Troitsk Institute for Innovation and Fusion Research

Email: shcherbak@triniti.ru
Russian Federation, Troitsk, Moscow, 108840

Ya. A. Vasina

Troitsk Institute for Innovation and Fusion Research

Email: shcherbak@triniti.ru
Russian Federation, Troitsk, Moscow, 108840

V. G. Otroshchenko

Troitsk Institute for Innovation and Fusion Research

Email: shcherbak@triniti.ru
Russian Federation, Troitsk, Moscow, 108840

I. E. Lyublinski

Krasnaya Zvezda State Enterprise

Email: shcherbak@triniti.ru
Russian Federation, Moscow, 115230

A. V. Vertkov

Krasnaya Zvezda State Enterprise

Email: shcherbak@triniti.ru
Russian Federation, Moscow, 115230


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