Hydrocracking method
A hydrocracking and hydrotreating technology, applied in hydrotreating process, petroleum industry, processing hydrocarbon oil, etc., can solve problems such as difficult to effectively treat, not economically reasonable, large hydrogen consumption, etc., to prevent The effect of excessive reduction of unit cell constant, increase of latent aromatics content, and increase of yield
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Embodiment 1
[0050] Weigh raw material NH 4 NaY type molecular sieve (ammonium exchange degree is 80%, weight loss on ignition is 27.1%, SiO 2 / Al 2 o 3 Molar ratio is 5.3, sodium oxide content is 4.0wt%) 2057.6 grams, add 9 liters of distilled water to make slurry, and under stirring condition, heat slurry and be warmed up to 95 ℃; Add dropwise by 495.0 grams of ammonium hexafluorosilicate The solution prepared with 3500 milliliters of distilled water was dripped in 2 hours, then continued to stir at 95° C. for 2 hours, stopped stirring and stood for about 10 minutes, and separated the precipitated sodium ammonium fluoride (silicon) aluminate crystals by decantation. And after washing with water and drying, the Y-type molecular sieve precursor A1 is obtained.
[0051] Weigh raw material NH 4 NaY type molecular sieve (ammonium exchange degree is 75%, weight loss on ignition is 26%, SiO 2 / Al 2 o 3 Molar ratio is 4.5, sodium oxide content is 4.0wt%) 270 grams, add 1.2 liters of disti...
Embodiment 2
[0053] The present embodiment prepares hydrocracking catalyst C1, and concrete steps are as follows:
[0054] (1) The Y-type molecular sieve precursor A1 is subjected to hydrothermal treatment, wherein the hydrothermal treatment conditions are as follows: the temperature is 600° C., the water pressure is 0.1 MPa, and the treatment time is 1 hour to obtain the Y-type molecular sieve Y1.
[0055] (2) Get the Y-type molecular sieve Y1 of 153.5 grams of step (1) gained, by 120 grams of small hole alumina (pore volume 0.47ml / g, specific surface area is 280m 2 / g), 0.2N dilute nitric acid solution 440ml peptized binder mixed, after extrusion, molding, then through 110 ℃ of drying 5 hours, 600 ℃ of roasting 6 hours obtain catalyst carrier,
[0056] (3) impregnating the catalyst carrier obtained in step (2) with an aqueous solution containing molybdenum and nickel, drying at 110°C for 5 hours, and calcining at 500°C for 5 hours to prepare the hydrocracking catalyst C1 of the present i...
Embodiment 3
[0058] This embodiment prepares hydrocracking catalyst C2, and concrete steps are as follows:
[0059] (1) 170g Y type molecular sieve precursor A1 is mixed with the binder (same as implementation 2) prepared by peptizing 80g small-pore alumina and dilute nitric acid solution, extruded, shaped,
[0060] (2) Use ammonia-water vapor to treat the molded product obtained in step (1) at high temperature, the treatment conditions are as follows: temperature 550°C, pressure 0.1MPa, ammonia partial pressure 0.01MPa, treatment time 1 hour, obtained Carrier, which contains Y-type molecular sieve Y2;
[0061](3) impregnating the catalyst carrier obtained in step (2) with an aqueous solution containing tungsten and nickel, drying at 110°C for 5 hours, and calcining at 500°C for 5 hours to prepare the hydrocracking catalyst C2 of the present invention.
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