Composite multi-metal oxide catalyst and preparation method thereof
A composite metal and catalyst technology, applied in the field of manufacturing the composite oxide catalyst, can solve the problems of fragility, decrease in catalyst strength, increase in pressure drop in a reaction tube, and the like
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Embodiment 1
[0112] 1. Catalyst Preparation
[0113] Add 450ml of water into the beaker and heat it to 65°C, add 148.64g of ammonium molybdate, 0.81g of potassium nitrate, and 1.89g of antimony trioxide, stir and dissolve to obtain solution A, and keep the temperature of solution A at 70°C. Then add 130ml of water to another beaker and heat it to 60°C, then add 56.90g of ferric nitrate, 104.98g of cobalt nitrate, 51.19g of nickel nitrate, 1.47g of cerium nitrate, and 1.07g of calcium acetate, stir and mix thoroughly, then add 3ml of nitric acid, Then slowly add 49.02g of bismuth nitrate, fully stir and dissolve to obtain solution B, and keep the temperature of solution B at 60°C. Prepare 30ml of ammonia water. Under vigorous stirring at 70°C, drop (B) solution into (A) solution, and add ammonia water to maintain the pH value of the slurry, and continue stirring until the mixture is uniform after adding. Pour the slurry into a disk, and dry it in an oven at 200° C. for 20 hours. The dried...
Embodiment 2
[0120] 1. Preparation of Catalyst
[0121] Add 450ml of water into the beaker and heat it to 65°C, add 148.64g of ammonium molybdate and 0.81g of potassium nitrate, stir and dissolve to obtain solution A, and keep the temperature of solution A at 70°C. Then add 130ml of water to another beaker and heat it to 60°C, then add 56.90g of iron nitrate, 104.98g of cobalt nitrate, and 51.19g of nickel nitrate in sequence, stir and mix thoroughly, then add 3ml of nitric acid, and then slowly add 49.02g of bismuth nitrate, Thoroughly stir to dissolve to obtain solution B, and keep the temperature of solution B at 60°C. Prepare 30ml of ammonia water. Under vigorous stirring at 70°C, drop (B) solution into (A) solution, and at the same time add ammonia water to maintain the pH value of the slurry, and continue stirring until the mixture is uniform after the addition. The slurry liquid was poured into a disk, and dried in an oven at 150° C. for 20 hours, and the dried product was pulveri...
Embodiment 3
[0135] 1. Preparation of Catalyst
[0136] The preparation method of the catalyst active precursor is the same as in Example 1. Get active phase precursor powder 200g, carry out pre-calcination under the air condition of leading 300ml / min, pre-calcination procedure is with embodiment 1, the catalyst precursor powder 100g after cooling down mixes with 10g hydroxypropyl cellulose, molding, roasting obtains catalyst.
[0137] The lateral compressive strength and wear resistance of the catalyst were measured, and the results are listed in the following table.
[0138] 2. Catalytic reaction
[0139] The catalyst prepared above was used for the partial oxidation of propylene to produce acrolein. The reaction conditions for the selective oxidation of propylene are: absolute pressure 0.1MPa, the volume space velocity of olefin relative to the catalyst is 120h -1 (STP), O 2 The molar ratio to propylene is 1.6, and the molar ratio of water vapor to propylene is 1.5.
[0140] Deter...
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