GADOLINIUM(III) COMPLEX OXIDE COMPOUNDS OF OBTAINED FROM MOLYBDATE-PHOSPHATE MOLTEN SALT

K. Terebilenko, Valeriia Zozuliia, I. Tokmenko, M. Slobodyanik
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Abstract

The peculiarities of K2Gd(PO4)(MoO4) single crystal growth from combined phosphate-molybdate melts have been investigated. The formation regions of GdPO4,  KGd(MoO4)2 and their cocrystallization fields with the mixed anionic compound potassium – gadolinium have been established. IR spect­roscopy showed that in all compounds molybdenum and phosphorus are in a tetrahedral environment, and the phase composition was confirmed by X-ray powder. Crystallization of the target compound K2Gd(PO4)(MoO4) is observed in the pseudobinary section K2Mo2O7-KPO3 orthiorombic system, space group Ibca, Z = 8, а = 19,694(4) Å, b = 12,260(3) Å, c = 6,961(3) Å. Double phosphate K3Gd(PO4)2 crystallizes in the form of colorless prismatic crystals from the melts with the initial ratio K/P = 1.7–3.3, which practically corresponds to the section K2MoO4 – K4P2O7. Phosphate GdPO4 crystallizes in the form of colorless prismatic crystals up to 0.1 mm in size at the maximum KPO3 content in the melt, which corresponds to K/P ratio = 0.20–0.50 and K/(Mo+P) = 0.25–0.33. Crystal-chemical criteria for the formation of mixed-anion-type layered frameworks, island structures, and three-dimensional frameworks based on mixed phosphate-molybdate systems and rare earth elements are proposed. The key factor in the formation of complex oxide compounds of rare earth elements from combined molybdate-phosphate melts is the ratio of K/Mo in the initial solution - melt: 1) at  K/Mo = 0.5–1.1, LnPO4 orthophosphates are formed, which are characterized by a 3D framework on the basis of LnO7/LnO8poly­hedra condensed into a three-dimensional framework; at K/Mo = 1.2–1.5, mixed anionic compounds of the composition K2Ln(PO4)(MoO4) (Ln – Gd- Tb) with a layered structure are formed, where LnО8 forms zigzag chains; 3) at K/Mo = 1.6–3.0, double orthophosphates of the composition K3Ln(PO4)2 with an island structure are formed.
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从钼酸盐-磷酸盐熔盐中得到的钆(iii)络合氧化物
研究了磷酸盐-钼酸盐复合熔体中K2Gd(PO4)(MoO4)单晶生长的特点。建立了GdPO4、KGd(MoO4)2与混合阴离子化合物钾-钆的形成区及其共结晶场。红外光谱分析表明,所有化合物中钼、磷均处于四面体环境,并通过x射线粉末证实了物相组成。靶化合物K2Gd(PO4)(MoO4)在K2Mo2O7-KPO3正配体系的赝二元截面中观察到结晶,空间群为Ibca, Z = 8, Z = 19694 (4) Å, b = 12260 (3) Å, c = 6961 (3) Å。双磷酸盐K3Gd(PO4)2在熔体中以无色棱柱晶的形式结晶,初始比K/P = 1.7 ~ 3.3,与截面K2MoO4 - K4P2O7基本一致。磷酸盐GdPO4在熔体中KPO3含量最大时结晶为大小为0.1 mm的无色棱柱状晶体,对应的K/P比值为0.20 ~ 0.50,K/(Mo+P) = 0.25 ~ 0.33。提出了基于混合磷酸盐-钼酸盐体系和稀土元素的混合阴离子型层状框架、岛状结构和三维框架形成的晶体化学标准。钼磷酸盐复合熔体中形成稀土元素复合氧化物的关键因素是初始溶液熔体中K/Mo的比值:1)在K/Mo = 0.5 ~ 1.1时,形成正磷酸盐LnPO4,其特征是LnO7/ lno8多面体凝聚成三维框架;在K/Mo = 1.2 ~ 1.5时,形成了具有层状结构的K2Ln(PO4)(MoO4) (Ln - Gd- Tb)混合阴离子化合物,其中LnО8形成之字形链;3)在K/Mo = 1.6 ~ 3.0时,形成具有岛状结构的K3Ln(PO4)2二元正磷酸盐。
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