Niobium–oxygen interaction in mixed ligand melts

L.P. Polyakova , T.V. Stogova , E.G. Polyakov , A.V. Arakcheeva , V.V. Grinevich
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引用次数: 7

Abstract

The niobium–oxygen interaction in chloride–fluoride melts has been studied by methods of linear sweep voltammetry, X-ray diffraction, IR-spectroscopy and optic crystallography. The chemical reactions and their products in NaCl–KCl–K2NbF7; NaCl–KCl–K3NbOF6 and NaCl–KCl–K3NbO2F4 melts have been studied. Moreover, a comparative study of the Na2O and Nb2O5 dissolution in NaCl–KCl–K2NbF7 melt in the molar ratio range O/Nb from 0 to 2.5 was carried out. The crucial role of the relative excess K2NbF7 fluorine in reactions of ligand substitution in the coordination shell of niobium is shown. When the fluorine concentration in the melt is limited by its content in complex niobium fluoride, only mono oxohalide complexes are identified in the liquid phase. The addition of “free” fluoride ions results in the formation of a wide range of oxohalide complexes up to niobates depending on the O/Nb ratio.

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混合配体熔体中铌氧相互作用
用线性扫描伏安法、x射线衍射、红外光谱和光学晶体学等方法研究了氟氯化物熔体中铌氧相互作用。NaCl-KCl-K2NbF7中的化学反应及其产物研究了NaCl-KCl-K3NbOF6和NaCl-KCl-K3NbO2F4熔体。并对NaCl-KCl-K2NbF7熔体在O/Nb摩尔比0 ~ 2.5范围内Na2O和Nb2O5的溶解进行了比较研究。揭示了相对过量的K2NbF7氟在铌配位壳的配体取代反应中的关键作用。当熔体中的氟浓度受其在络合氟化铌中的含量限制时,液相中只鉴定出单氧卤化物络合物。“自由”氟离子的加入导致形成范围广泛的氧卤化物配合物,直至铌酸盐,这取决于O/Nb比。
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