Thermodynamic properties of alloys In—Tb system

Abstract

The method of isoportic calorimetry investigated the thermochemical properties of the melt In—Tb system in the range of compositions 0 < xIn < 0,4 at 1625 ± 1 K. The obtained data were extrapolated on a non-investigated concentration interval, given that when xTb = 1 integral and partial to Tb enthalpia mixing is zero. It was established that the first partial for Terbium and the minimum enthalpy of mixing is –145 ± 7 and –40,1 ± 0,2 kJ/mol respectively. Comparison of ΔHmin, the melt of five previously investigated In—Ln systems from the serial number Ln (zLn), together with the data obtained in this papper, showed that they are described by one trend line. For ΔHmin In—Eu (Yb) melts (Yb) are very slight deviations from the trend line. But for dimensional factor, these deviations from the trend line are more significant. Enthalpia of the formation of some In—Ln intermetallides are known, with most of them relate to the LnIn3 compound. But there is no full reconciliation between these data. The results of the most modern work exhibit less dependence on the serial number of lanthanides and are more exothermic for heavy lanthanides, compared with other data. Comparing thermochemical properties of double Sn (Sb) —REM melt systems. It has been established that the energy of the interaction between the data p-elements and REM increases in such a sequence: In-REM → Sn—REM → Sb—REM. This is due to the fact that the stibium is the best acceptor of electrons. Keywords: thermochemical properties, melts, compounds, In, Tb.