A kind of two-component transition metal sulfide nanotube and its preparation method and application
A transition metal and sulfide technology, applied in the field of catalytic technology and petrochemical industry, can solve the problems of low hydrodesulfurization activity, and achieve the effects of high desulfurization rate, high desulfurization performance and high specific surface area.
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Embodiment 1
[0026] Preparation of two-component oxide precursors:
[0027] Weigh cobalt acetate (0.002mol in terms of cobalt atoms) and ammonium heptamolybdate (0.004mol in terms of molybdenum atoms) and dissolve them in 50ml water respectively, pour the ammonium molybdate aqueous solution into the cobalt acetate polar solution rapidly, and transfer to 80 ℃ in a constant temperature water bath, stirred and refluxed under normal pressure for 4 hours, and a light purple solid precipitated. Afterwards, the obtained product was filtered, washed with water, and dried at 110°C for 8 hours to obtain a rod-shaped Co-Mo hydrated oxide powder, as shown in the attached figure 1 shown.
[0028] Replace the above-mentioned ammonium heptamolybdate with ammonium metatungstate, dissolve cobalt acetate (0.002 mol in terms of cobalt atoms) and ammonium metatungstate (0.004 mol in terms of tungsten atoms) in 50 ml of water, and dissolve the ammonium metatungstate aqueous solution Quickly pour it into the ...
Embodiment 2
[0030] Weigh cobalt acetate (0.004mol in terms of cobalt atoms) and ammonium heptamolybdate (0.004mol in terms of molybdenum atoms) and dissolve them in 50ml water respectively, pour the ammonium molybdate aqueous solution into the cobalt acetate polar solution rapidly, and transfer to 80 ℃ in a constant temperature water bath, stirred and refluxed under normal pressure for 4 hours, and a light purple solid precipitated. Afterwards, the obtained product was filtered, washed with water, and dried at 110° C. for 8 hours to obtain a rod-shaped Co—Mo hydrated oxide powder.
Embodiment 3
[0032] Weigh cobalt acetate (0.008mol in terms of cobalt atoms) and ammonium heptamolybdate (0.004mol in terms of molybdenum atoms) and dissolve them in 50ml water respectively, pour the ammonium molybdate aqueous solution into the cobalt acetate polar solution rapidly, and transfer to 80 ℃ in a constant temperature water bath, stirred and refluxed under normal pressure for 4 hours, and a light purple solid precipitated. Afterwards, the obtained product was filtered, washed with water, and dried at 110° C. for 8 hours to obtain a rod-shaped Co—Mo hydrated oxide powder.
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