Crystalline transition metal tungstate
A transition metal, tungstate technology, applied in metal/metal oxide/metal hydroxide catalysts, chemical/physical process, physical/chemical process catalysts, etc., can solve problems such as questions about the quality of material structure evaluation
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Embodiment 1
[0059] Ammonium metatungstate hydrate (17.68 g, 0.07 moles of W) and ammonium carbonate (24 g, 0.25 moles) were thoroughly mixed together in a sealed container at room temperature for 24 hours. Add nickel nitrate hexahydrate (29.1 g, 0.1 moles of Ni) and DI H 2 O (5 g), and the resulting mixture was continuously mixed at room temperature for 24 hours, then heat treated at 95° C. in an open vessel for 24 hours with intermittent mixing. After 24 hours, the materials were mixed into a fine powder and dried at 100 °C for an additional 24 hours. The resulting product was analyzed by X-ray powder diffraction, and the X-ray powder diffraction pattern is shown in the accompanying drawing.
Embodiment 2
[0061] Nickel nitrate hexahydrate (20 g, 0.069 mol), ammonium metatungstate hydrate (25.2 g, 0.1 mol of W), ammonium carbonate (24 g, 0.25 mol) and deionized (DI) water (5 g) were incubated at room temperature for 24 hours. Mix together thoroughly. The resulting mixture was transferred to a PTFE-lined stainless steel digestion vessel, followed by heat treatment at 105 °C for 72 hours. The product was then dried for a further 24 hours at 110°C. The resulting product was analyzed by X-ray powder diffraction, and the X-ray powder diffraction pattern is shown in the accompanying drawing.
Embodiment 3
[0063] Ammonium metatungstate hydrate (20.16 g, 0.08 moles of W) and ammonium carbonate (24 g, 0.5 moles of NH 3 ) were mixed well together for 24 hours in a PTFE-lined stainless steel digestion vessel. After that, nickel nitrate hexahydrate (29 g, 0.1 mole of Ni) and zinc nitrate hexahydrate (2.97 g, 0.01 mole of Zn) were added to the mixture. The resulting slurry was then heat treated at 90°C for 24 hours and then dried at 100°C for an additional 24 hours. The resulting product was analyzed by X-ray powder diffraction, and the X-ray powder diffraction pattern is shown in the accompanying drawing.
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