Hydrocracking catalyst and preparation method thereof
A hydrocracking and catalyst technology, applied in catalyst activation/preparation, physical/chemical process catalyst, organic compound/hydride/coordination complex catalyst, etc. The probability of secondary cracking reaction increases, etc., to achieve the effects of improved C5+ selectivity, high thermal stability, and structure determination.
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Embodiment 1
[0017] Embodiment 1: first make 200ml concentration be 0.03mol L ~1 cesium carbonate solution, 180ml concentration is 1mol L ~1 The concentration of nickel nitrate solution and 120ml is 3mol·L ~1 citric acid solution to prepare a mixed solution, then add 36g of phosphotungstic acid, stir at 70°C until gelatinized, and dry at 120°C for 18min. Dry the dried solid in a muffle furnace at 6°C min ~1 The speed is increased to 350 ° C, and the temperature is kept for 4 hours to prepare Ni and CsH 2 PW 12 o 40 Catalyst with a molar ratio of 15.
[0018] Put the catalyst into the reaction tube, feed hydrogen, and the volume space velocity is 1500h ~1 , the pressure of the reaction system is gradually increased to 2.0MPa. After checking that there is no air leakage, the temperature of the reaction system is raised to 300°C, and the heating rate is 2°C·min ~1 , kept for 1h, at a stable hydrogen volumetric space velocity of 1500h ~1 Down cut into n-decane, its mass space velocity ...
Embodiment 2
[0019] Embodiment 2: the mixed solution is changed from 210ml concentration to 0.03mol L ~1 Cesium carbonate solution, 150ml concentration is 1mol L ~ 1 The concentration of nickel nitrate solution and 100ml is 3mol·L ~1 prepared from a citric acid solution. Add 38g phosphotungstic acid then, all the other are with embodiment 1, Ni and CsH in the gained catalyst 2 PW 12 o 40 The molar ratio was 12.
[0020] The evaluation of the catalyst is the same as in Example 1, and the results of the conversion rate and the selectivity of cracked products are shown in Table 1.
Embodiment 3
[0021] Embodiment 3: 170ml concentration is 0.03mol L ~1 cesium carbonate solution, 250ml concentration is 1mol L ~1 The concentration of nickel nitrate solution and 170ml is 3mol·L ~1 citric acid solution to prepare a mixed solution, then add 31g of phosphotungstic acid, stir at 70°C until gelling, and dry at 150°C for 12min. Dry the dried solid in a muffle furnace at 6°C min ~1 The speed is raised to 300°C, and the temperature is kept constant for 6h to prepare Ni and CsH 2 PW 12 o 40 Catalyst with a molar ratio of 24.
[0022] The evaluation of the catalyst is the same as in Example 1, and the results of the conversion rate and the selectivity of cracked products are shown in Table 1.
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