Mineral spirit platreating catalyzer and preparation method thereof
A hydrofining and catalyst technology, applied in the direction of catalyst activation/preparation, chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problem of incomplete reduction of active metals, affecting catalyst performance, and production processes Complicated problems, to achieve the effect of improving anti-sintering stability, ensuring anti-sintering performance, and simple process
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Embodiment 1
[0034]Take 750g of nickel nitrate and add it to 630g of deionized water, stir to dissolve, filter and replenish water to obtain 1000ml of nickel nitrate aqueous solution A, the nickel content in the solution is 18.9g / 100ml as NiO.
Embodiment 2
[0036] Take 150g of sodium carbonate and add it to 700g of deionized water, stir to dissolve, filter and rehydrate to obtain 1000ml of sodium carbonate solution, then take 450g of nickel nitrate and add it to 500g of deionized water, stir to dissolve, filter and rehydrate to obtain 1000ml of nickel nitrate aqueous solution. Take 500ml of the above-mentioned sodium carbonate solution, then slowly add the above-mentioned nickel nitrate solution into the sodium carbonate solution for neutralization, control the pH value of the end point to 7.0-7.5, and neutralize the temperature at 70°C, then dry at 110°C for 4 hours and roast at 400°C for 4 hours. to nickel oxide. The nickel oxide used in the following examples all adopts this example to make.
Embodiment 3
[0038] Take 3g of concentrated nitric acid, 3g of citric acid, and 70g of deionized water to make a solution. Get macroporous aluminum hydroxide dry powder (meaning that the pore volume is greater than 0.8ml g -1 72g of aluminum hydroxide dry powder), 38g of SB powder, 15g of nickel oxide, and 3g of scallop powder are fully mixed, then kneaded with the prepared solution to form a plastic paste, extruded, dried at 110°C for 3h, and roasted at 450°C for 3h Make a carrier.
[0039] Take 100g of the above-mentioned carrier, saturate impregnate it with solution A at 20°C for 3h, dry at 110°C for 3h, and calcinate at 450°C for 3h to prepare Catalyst E 1 . Its main physicochemical properties are listed in Table 1.
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