The results of investigations of the interaction of U-Zr-B-C-O melts with steel, which are performed as part of the OECD Masca international program, are presented. It is found that, as a result of the interaction, boron and carbon become concentrated predominately in the metallic phase of the melt.
As the initial mass ratio m Fe /m melt increases, the effect of the addition of B 4 C on the melt-iron interaction decreases because the metallic phase is diluted with iron. It is concluded on the basis of a comparison of the results of the STFM-B Nos. 3, 7 experiments with the STFM-Fe Nos. 3, 7 experiments performed previously without the participation of boron carbide that the effect of boron carbide on the interaction of the oxide melt with iron decreases as the degree of oxidation of zirconium increases.In order to develop measures that would guarantee control of safety even for low-probability severe accidents with core meltdown, it is necessary to understand the thermohydraulic and physicochemical phenomenon and processes occurring in the melt pool. The multi-component nature of the melt and the inadequacy of the database and computational methods make it necessary, first and foremost, to perform experiments with prototypical components of a light-water reactor, including uranium, zirconium, steel components of in-reactor structures and fission-product simulators, as well as other materials present in power reactors, for example, the materials of control rods and consumable absorbers, for example, B 4 C.The main sources of B 4 C in melt are absorbing rods of the control and protection system, which are made with partial use of boron carbide. The total mass of B 4 C in VVER-1000 is about 260 kg, which corresponds to 0.25 mass % of the core mass. It has been shown in previous work [1], in investigation of carbon on the behavior of suboxidized melt of the type C-32, that as a result of melting and subsequent solidification it stratifies into two layers with carbon concentration >0.2 mass% in the initial layer. The nature of the stratification is probably associated with the special features of Zr(O)-UO 2 phase diagrams [2,3], the fact that carbon is not appreciably soluble in the oxides UO 2 and ZrO 2 and their solid solutions, as well as the high affinity of zirconium to carbon. It is known that zirconium has a high affinity to other interstitial elements (B, N), which, in particular, can be seen in a comparison of the melting temperature of the corresponding stoichiometric com-