“…Unfortunately, for Cd 0.9 Zn 0.1 Te 17d and Cd 0.85 Zn 0.15 Te 17d strict calculation of dX S is impossible because the quantitative contribution of the ideal solution model approximation into dX S is unknown. Nevertheless, an attempt was made to assess this contribution by repeating the whole set of calculations with CdTe and ZnTe activities in Cd 1Àx Zn x Te 17d taken from the mass spectrometric experiment [15,16] rather from the ideal solution approximation. It turned out that the compositions of the solid obtained in these two models were the same to within 10 À5 -10 À6 at%, which is 1 to 2 orders of magnitude less than dX S resulting from the experimental errors for CdTe [7,8].…”