Catalytic cracking aid, preparation method and application thereof, and hydrocarbon oil catalytic cracking method
A technology of catalytic cracking additives and adhesives, applied in catalytic cracking, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of low propylene selectivity and limited propylene growth rate, and achieve simple operation, easy control of conditions, The effect of simple process
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[0023] According to the present invention, the binder can be selected with reference to the prior art, but according to a preferred embodiment, the binder includes the first binder and the second binder, that is, the preparation of the auxiliary agent The binder includes the first binder and the second binder; wherein, the first binder is at least one of kaolin, alumina, silicon oxide and diatomaceous earth, and the second binder is The mixture is acidic silica sol and / or acidic aluminum sol, and the mass ratio of the first binder to the second binder is 1:(0.5-2.0). In the present invention, the binder in the catalytic cracking additive is described in terms of its source, in order to better explain the present invention. It should be understood that the sol exists in the form of oxides in the catalytic cracking aid.
[0024] According to the present invention, the modifying agent can cover and neutralize the acid centers on the surface of the catalytic cracking aid, and at ...
Embodiment 1
[0067] 1) Preparation of one-dimensional through-channel mesoporous silica material
[0068] Add 20g of P123 and 30g of N,N-dimethylformamide into 600g of 1M hydrochloric acid, stir at 40°C until P123 is completely dissolved, then add 40g of methyl orthosilicate to the above solution dropwise, and stir at 40°C After 15 hours, the solution was transferred to a polytetrafluoroethylene-lined reactor and crystallized at 60°C for 24 hours. After the hydrothermal reaction, the solid product was separated from the mother liquor by filtration, washed with deionized water until neutral, and dried in air at 110° C. for 5 hours to obtain the raw powder of mesoporous silica material. Mix 20g of mesoporous silica material raw powder with 200g of tetrahydrofuran, reflux extraction at 70°C for 24h, then filter, wash, and vacuum dry at 60°C for 5h to obtain a one-dimensional through-channel mesoporous silica material. The pore structure parameters of the mesoporous silica material: the pore ...
Embodiment 2
[0074] 1) Preparation of one-dimensional through-channel mesoporous silica material
[0075] Add 20g of P123 and 60g of N,N-dimethylformamide into 1000g of 1M hydrochloric acid, stir at 25°C until P123 is completely dissolved, then add 60g of methyl orthosilicate to the above solution dropwise, and stir at 25°C After 30 hours, the solution was transferred to a polytetrafluoroethylene-lined reactor and crystallized at 50°C for 40 hours. After the hydrothermal reaction, the solid product was separated from the mother liquor by filtration, washed with deionized water until neutral, and dried in air at 70°C for 10 hours to obtain the raw powder of mesoporous silica material. Mix 20g of mesoporous silica material raw powder with 200mL of acidified methanol (the volume ratio of methanol to concentrated hydrochloric acid is 20:1), reflux extraction at 90°C for 12h, then filter, wash, and vacuum-dry at 60°C for 5h to obtain a Mesoporous silica materials with straight-through channels...
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Abstract
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