A kind of catalytic diesel reaction distillation method
A technology for catalyzing diesel oil and reactive distillation, which is applied in the petroleum industry, hydrocarbon oil treatment, hydrotreating process, etc., can solve the problems of fast catalyst deactivation, small heating space, short operation period, etc., and achieves high hydrogen utilization rate, The effect of improving the reaction speed and simplifying the process
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Embodiment 1
[0057] Weigh raw material NH 4 NaY type molecular sieve (80% ammonium exchange degree, 27.1% weight loss on ignition, SiO 2 / Al 2 o 3 The molar ratio is 5.3, the sodium oxide content is 4.0wt%) 2057.6 grams, add 9 liters of distilled water to make a slurry, and heat the slurry to 95 ° C under stirring conditions; add dropwise 495.0 grams of ammonium hexafluorosilicate to the above slurry The solution prepared with 3500 ml of distilled water was dripped in 2 hours, then continued to stir at 95°C for 2 hours, stopped stirring and allowed to stand for about 10 minutes, separated the precipitated fluoro(silicon)ammonium aluminate sodium crystals by decantation, And after washing with water and drying, the Y-type molecular sieve precursor A1 is obtained.
[0058] Weigh raw material NH 4 NaY type molecular sieve (ammonium exchange degree is 75%, burning weight loss is 26%, SiO 2 / Al 2 o 3 The molar ratio is 4.5, the sodium oxide content is 4.0wt%) 270 grams, add 1.2 liters of...
Embodiment 2
[0060] The present embodiment prepares hydrocracking catalyst C1, and concrete steps are as follows:
[0061] (1) The Y-type molecular sieve precursor A1 was subjected to hydrothermal treatment, and the hydrothermal treatment conditions were as follows: the temperature was 600° C., the water pressure was 0.1 MPa, and the treatment time was 1 hour to obtain the Y-type molecular sieve Y1.
[0062] (2) Take 30.6 grams of the Y-type molecular sieve Y1 obtained in step (1), made of 240 grams of small-pore alumina (pore volume 0.47mL / g, specific surface area 280m 2 / g), 0.2N dilute nitric acid solution 440mL peptized binder mixed, extruded and shaped, then dried at 110°C for 5 hours, and calcined at 600°C for 6 hours to obtain a catalyst carrier.
[0063] (3) The catalyst carrier obtained in step (2) was impregnated with an aqueous solution containing molybdenum and nickel, dried at 110°C for 5 hours, and calcined at 500°C for 5 hours to prepare the hydrocracking catalyst C1 of the pr...
Embodiment 3
[0065] This embodiment prepares hydrocracking catalyst C2, and concrete steps are as follows:
[0066] (1) Mix 68g of Y-type molecular sieve precursor A1 with a binder prepared by peptizing 160g of small-pore alumina and dilute nitric acid solution (same as in implementation 2), extrude and shape.
[0067] (2) Treat the molded product obtained in step (1) with ammonia-water vapor 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 The carrier contains Y-type molecular sieve Y2.
[0068] (3) The catalyst support obtained in step (2) is impregnated with an aqueous solution containing tungsten and nickel, dried at 110°C for 5 hours, and calcined at 500°C for 5 hours to prepare the hydrocracking catalyst C2 of the present invention.
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