Heat Transfer During Evaporation of Cesium From Graphite Surface in an Argon Environment

Bespala, E. V.; Novoselov, Ivan; Ushakov, Ivan

doi:10.1051/matecconf/20167201011

Cited by 7 publications

(1 citation statement)

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“…Results of experimental studies of processing the surface of irradiated graphite taken from PUGR and RBMK reactor stacks in the environment consisting of argon and oxygen concentration of which was lower than stoichiometric quantity were presented earlier (Pavliuk et al 2017, Kashcheev et al 2017, Bespala et al 2016. Intensive extraction of 14 C from the near subsurface layer occurred without significant loss of mass of the sample at temperature equal to ~ 850°C.…”

Section: Discussionmentioning

confidence: 91%

About chemical form and binding energy of 14C in irradiated graphite of uranium-graphite nuclear reactors

Bespala¹,

Pavliuk²,

Zagumennov³

et al. 2018

NUCET

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Issues associated with handling irradiated graphite of uranium-graphite nuclear reactors are examined. It is demonstrated that selection of approaches, methods and means for handling irradiated graphite are determined by the form of occurrence and binding energy of long-lived 14C radionuclide with graphite crystalline lattice. The purpose of the present study is the determination of possible chemical compounds in which 14C can be found and assessment of fastness of its binding in the structure of irradiated graphite. Indigent and foreign experience of handling graphite radioactive wastes was analyzed, calculations and measurements were performed. Information was provided on the channels of accumulation of 14C in the structure of reactor graphite and it was demonstrated that the largest quantities of the radionuclide in question are generated according to the reaction 14N(n, p)14C. Here, most part of radioactive carbon is generated on 14N nuclei found in the form of impurities in non-irradiated graphite and in the composition of gas used for purging nuclear reactor in the process of operation. 14C radionuclide generated according to 14N(n, p)14C nuclear reaction is localized in the near subsurface graphite layer (in the near subsurface layer of pores) at the depth of not more than 50 nm. Analysis was performed of possible chemical compounds which may incorporate radioactive carbon. It was established that the form of occurrence is determined by the operational properties of specific graphite element in the reactor core. 14C binding energy in the structure of irradiated graphite was evaluated and depth of its penetration in the structure was calculated. It was established that selective extraction of this radionuclide is possible only under elevated temperatures in weakly oxidizing environment which is explained by the binding energy reaching up to 800 kJ/mole in the process of chemical sorption of 14C on the surface of graphite and depth of its occurrence equal to ~ 70 nm in the course of ion implantation. It was demonstrated that radioactive carbon generated according to 13C(n, γ)14C nuclear reaction is uniformly distributed among graphite elements and possesses binding energy ~477 kJ/mole. Its selective extraction is possible only under the condition of destruction of graphite crystalline lattice and organization of the process of isotopic separation. The obtained results allow recommending the most efficient methods of handling irradiated graphite during decommissioning uranium-graphite reactors.

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Section: Discussionmentioning

confidence: 91%