Published January 15, 2007 | Version v1
Journal article

The evaluation of the pyrochemistry for the treatment of Gen IV nuclear fuels - Inert matrix chlorination studies in the gas phase or molten chloride salts

  • 1. Commissariat a l'Energie Atomique, DEN/VRH/DRCP/SCPS/LPP, Bat 399, CEA Marcoule, BP 17171, 30207 Bagnols/Ceze cedex (France)

Description

The structure of the fuels for the future Gen IV nuclear reactors will be totally different from those of PWR, especially for the GFR concept including a closed cycle. In these reactors, fissile materials (carbides or nitrides of actinides) should be surrounded by an inert matrix. In order to build a reprocessing process scheme, the behavior of the potential inert matrices (silicon carbide, titanium nitride, and zirconium carbide and nitride) was studied by hydro- and pyrometallurgy. This paper deals with the chlorination results at high temperature by pyrometallurgy. For the first time, the reactivity of the matrix towards chlorine gas was assessed in the gas phase. TiN, ZrN and ZrC are very reactive from 400 deg. C whereas it is necessary to be over 900 deg. C for SiC to be as fast. In molten chloride melts, the bubbling of chlorine gas is less efficient than in gas phase but it is possible to attack the matrices. Electrochemical methods were also used to dissolve the refractory materials, leading to promising results with TiN, ZrN and ZrC. The massive SiC samples used were not conductive enough to be studied and in this case specific SiC-coated carbon electrodes were used. The key point of these studies was to find a method to separate the matrix compounds from the fissile material in order to link the head to the core of the process (electrochemical separation or liquid-liquid reductive extraction in the case of a pyrochemical reprocessing)

Additional details

Identifiers

DOI
10.1016/j.jnucmat.2006.08.014;
PII
S0022-3115(06)00457-0;

Publishing Information

Journal Title
Journal of Nuclear Materials
Journal Volume
360
Journal Issue
1
Journal Page Range
p. 58-63
ISSN
0022-3115
CODEN
JNUMAM

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.