An auxiliary agent for removing catalytic cracking regeneration flue gas pollutants and its preparation method
A technology for catalytic cracking and regenerating flue gas, applied in chemical instruments and methods, separation methods, air quality improvement, etc., can solve the problems of poor continuous activity of auxiliary technology, high investment cost, complicated operation, etc., and achieve hydrothermal stability. Good, long life, good effect of continuous activity
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[0031] The above-mentioned adjuvant for removing catalytic cracking regeneration flue gas pollutants and its preparation method include the following specific steps:
[0032] Add an appropriate amount of deionized water into the beaker, add the accurately weighed rare earth nitrate into it, stir, and raise the temperature to 50-70°C to completely dissolve the rare earth nitrate, add the weighed magnesium aluminum spinel, and stir for 0.5- After 1.5 hours, add the weighed ternary hydrotalcite and pseudo-boehmite sequentially, stir for 1.0-2.5 hours, finally add the binder, and stir for 4.0-10.0 hours to obtain a slurry. The slurry is spray-dried and molded, and the temperature of the spray-drying furnace is controlled at 320-460°C, the outlet temperature is 120-200°C, and the spray pressure is at 30-50 atmospheres. After spray-drying and forming, drying at 120-140°C for 4-10 hours, and roasting at 550-750°C for 3-12 hours to obtain the auxiliary agent carrier.
[0033] Weigh a...
Embodiment 1
[0037] Preparation of the first step multi-effect auxiliary agent carrier
[0038] Add 800gH in a 2-liter three-neck flask 2 O, heat up to 65°C, stir, and add 13.3g La (NO 3 ) 2 .6H 2 O, 44.4gCe(NO 3 ) 2 .6H 2 O, stirred for 0.4 hours to completely dissolve the nitrate; added 55.5g of magnesium-aluminum spinel with a magnesium-aluminum molar ratio of 2:1 (the ignition loss of the spinel was 28.0% by weight) and stirred for 0.8 hours; added 102.9g of zinc-magnesium-aluminum Ternary hydrotalcite (the ignition loss of zinc-magnesium-aluminum ternary hydrotalcite is 32.0% by weight), stirring for 1.0 hour; add 67g pseudo-boehmite (the ignition loss of pseudo-boehmite is 32.0% by weight), and stir for 2.0 hours; Finally add 200.0g aluminum sol (converted into Al 2 o 3 content is 18% by weight), and stirred for 6.0 hours. The slurry was obtained; the slurry was statically crystallized at room temperature for 24 hours, then spray-dried at a furnace temperature of 380°C, an o...
Embodiment 2
[0042] Weigh 50 g of the auxiliary agent carrier prepared in Example 1 and put it into a beaker, then weigh 6.67 g of an aqueous solution with a palladium content of 3000 μg / g in another beaker, add 13.33 g of deionized water, and then, under stirring, batch Add the palladium aqueous solution to the auxiliary carrier, let it stand for 14 hours after the addition, and dry at 120°C for 6 hours. The obtained sample was calcined at 580°C for 6 hours to obtain the auxiliary carrier A2, with an auxiliary noble metal content of 400 μg / g.
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