首页> 外文期刊>International Journal of Quantum Chemistry >Synthesis of new molybdenum-tungsten, vanadium-tungsten and vanadium-molybdenum-tungsten oxynitrides from freeze-dried precursors
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Synthesis of new molybdenum-tungsten, vanadium-tungsten and vanadium-molybdenum-tungsten oxynitrides from freeze-dried precursors

机译:由冻干前体合成新的钼钨,钒钨和钒钼钨氧氮化物

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Interstitial molybdenum-tungsten, vanadium-tungsten and vanadium-molybdenum-tungsten oxynitrides in the solid solution series Mo1-zWz(OxNy) and V1-zWz(OxNy) (z = 0, 0.2, 0.4, 0.5, 0.6, 0.8, 1), and V1-u-zMouWz(OxNy) (u, z = 0.2, 0.33, 0.4, 0.6; u + z < 1), have been obtained by ammonolysis of precursors resulting from the freeze-drying of aqueous solutions of the metal salts (NH4VO3, (NH4)(6)Mo(7)O(24)(.)4H(2)O and (NH4)(6)W(12)O(39)(.)18H(2)O). A study of the influence of the preparative variables on the outcomes of this procedure is presented. Compounds in the Mo1-zWz(OxNy) series are prepared as single phases by ammonolysis of the respective freeze-dried precursors (during 2h) at different temperatures between 973 and 1023 K, optimised for each composition, followed by slow cooling of the samples (except for the Mo-only containing phase, in which fast cooling has been used). Compounds in the V1-zWz(OxNy) and V1-u-zMouWz(OxNy) series are prepared as single phases by ammonolysis (during 2h) of crystalline precursors (as resulting from thermal treatment in air at 873 K, during 12 It, of the freeze-dried precursors) at 1073 K, followed by slow cooling of the samples. All the compounds in these series have the rock-salt crystal structure, in which the metal atoms are in an fee arrangement, with non-metal atoms occupying octahedral interstitial positions. The materials have been characterized by X-ray powder diffraction, elemental analysis, scanning electron microscopy and magnetic measurements. (C) 2004 Elsevier Inc. All rights reserved.
机译:固溶体Mo1-zWz(OxNy)和V1-zWz(OxNy)系列中的间隙钼-钨,钒-钨和钒-钼-钨氧氮化物(z = 0、0.2、0.4、0.5、0.6、0.8、1)通过对金属盐水溶液进行冷冻干燥而生成的前驱物进行氨解,得到V1-u-zMouWz(OxNy)(u,z = 0.2,0.33,0.4,0.6; u + z <1) (NH4VO3,(NH4)(6)Mo(7)O(24)(。)4H(2)O和(NH4)(6)W(12)O(39)(。)18H(2)O)。提出了对准备变量对该程序结果影响的研究。 Mo1-zWz(OxNy)系列化合物可通过在973和1023 K之间的不同温度下氨解相应的冻干前体(2小时内)制备为单相,针对每种组成进行优化,然后缓慢冷却样品(除了仅含Mo的相(已使用快速冷却)。 V1-zWz(OxNy)和V1-u-zMouWz(OxNy)系列化合物通过结晶前体的氨解作用(在2小时内)制备为单相(这是由于在873 K下于12 K的空气中于空气中进行热处理而制得的) (冷冻干燥的前体)在1073 K下进行,然后缓慢冷却样品。这些系列中的所有化合物均具有盐岩晶体结构,其中金属原子成规排列,非金属原子占据八面体间隙位置。该材料已通过X射线粉末衍射,元素分析,扫描电子显微镜和磁测量进行了表征。 (C)2004 Elsevier Inc.保留所有权利。

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