Nano grade transition metal oxidation catalyst and its preparing method and use
A technology for oxidizing catalysts and transition metals, applied in metal/metal oxide/metal hydroxide catalysts, catalyst activation/preparation, physical/chemical process catalysts, etc., can solve high reaction pressure, high operating costs, high reaction temperature, etc. problem, to achieve the effect of long reaction life and low price
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Embodiment 1
[0041]SiO involved in the catalyst of the present invention 2 -Al 2 o 3 -TiO 2 - Preparation of rare earth oxide nanocomposite powder. 4000g of solid aluminum sulfate is added to 3.25L of distilled water while heating and stirring to dissolve completely into aluminum sulfate solution (a), and 500gH 2 TiO 3 (Metatitanic acid) was added into 900ml of concentrated sulfuric acid and fully reacted titanium sulfate solution (b), and 185g of solid cerium nitrate or lanthanum nitrate was added into 2L of water and fully dissolved to obtain cerium nitrate solution or lanthanum nitrate solution (c). Add an appropriate amount of deionized water to the ammonia water and dilute it into 10% dilute ammonia water (d), add 4.8L industrial primary modulus 3.0 concentrated water glass to 8L water to obtain dilute water glass solution (e), 10% isobutanol (or methanol or Ethanol) 500ml (f), take a 20-liter stainless steel reaction tank with heating control system and double-layer paddle stirr...
Embodiment 2
[0043] Add 95 grams of neodymium nitrate and 90 grams of niobium nitrate to 2 L of water, respectively, and fully dissolve to form a mixed solution (c). Other steps and process conditions are all with embodiment 1.
[0044] 2. Preparation of catalyst
Embodiment 3
[0046] It is carrier A and catalyst KA involved in the catalyst of the present invention. Weigh 150g of the nanocomposite powder obtained in Example 1, add about 111ml of 5% dilute nitric acid and knead for 20min, roll it into a wet block, mechanically shape it into a ring, dry and activate it to obtain carrier A, and then use 300ml of V 2 o 5 Wt% 3-8% ammonium metavanadate immersion solution is excessively impregnated 120g carrier A for 4-6 hours, dried and activated, and then 300ml containing MnO 2 wt% 8-17% Mn(NO 3 ) 2 The solution is excessively impregnated with 120g carrier A for 4 to 6 hours, and after being dried and activated to obtain the catalyst KA of the present invention, the total amount of transition metal Mn-V supported on the catalyst is about 20% in terms of oxides.
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