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Content available remote Phase equilibria in the Er-Co-In system and crystal structure of Er8CoIn3 compound
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EN
Isothermal section of the Er-Co-In system at T = 870 K was constructed by means of X-ray powder diffraction, microstructure, and EDX-analyses. Twelve ternary compounds, namely ErCoIn5 (HoCoGa5-type), Er6Co17.92In14 (Lu6Co17.92In14-type), ErCo4In (MgCu4Sn-type), Er2CoIn8 (Ho2CoGa8-type), Er10Co9In20 (Ho10Ni9In20-type), Er3Co1.87In4 (Lu3Co1.87In4-type), ErCoIn, Er11Co4In9 (Nd11Pd4In9-type), Er11Co3In6, Er8CoIn3 (Pr8CoGa3-type), Er6Co2.19In0.81 (Ho6Co2Ga-type), and Er13.83Co2.88In3.10 (Lu14Co2In3-type) exist in the Er-Co-In system at this temperature. The crystal structure of the Er8CoIn3 compound was determined by means of X-ray powder method (Pr8CoGa3-type, P63mc space group, a = 1.02374(2) nm, c = 0.68759(2) nm). Almost none of the binary compounds dissolve the third component. The exception is the existence of the solid solution based on ErCo3 binary compound, which dissolves up to 8 at.% of In. [...]
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EN
Holmium, erbium and lutetium citrates can be synthesized by transforming freshly precipitated holmium, erbium and lutetium hydroxides in the citric acid solution under the hydrothermal conditions (above 100 ℃) after 3 days of reaction. In this paper in order to determine the synthesis conditions, the hydroxide and citrate stability areas of selected lanthanides were compared. The studies of the structure of the obtained holmium citrate, erbium and lutetium samples showed that these compounds crystallize in a monoclinic system. The crystallite sizes determined by the HalderWagner method were 67.8 ± 8.0nm, 103.7 ± 4.5nm and 68.1 ± 4.2nm, respectively for the holmium citrate, erbium citrate and lutetium citrate samples. The shifts of the hydroxyl and carboxyl groups of citric acid in the FTIR spectrum indicate the interactions of both groups with holmium, erbium and lutetium cations. Then the obtained samples were subjected to the analysis of composition, and their particle size distribution was determined.
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