Residual oil hydrotreating method
A technology for hydrogenation and treatment of residual oil, which is applied in the treatment of hydrocarbon oil, petroleum industry, refined hydrocarbon oil, etc. It can solve the problems that the performance of carbon removal needs to be further improved, achieve good catalyst stability, speed up the rate, and promote fracture Effect
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[0083] Example 1
[0084] Weigh 1000.0 g of alumina dry rubber powder, add 20.0 g of citric acid, and 15.0 g of succulent powder. After mixing evenly, add 800.0 g of an aqueous solution containing 2.0% nitric acid by mass, and after rolling for 15.0 minutes, use clover with a diameter of 3.0 mm. Orifice plate extrusion. After drying at 120 °C for 4.0 h, it was calcined at 800 °C for 4.0 h. The calcined carrier is designated as S-1.
[0085] Weigh 64.3 g of ammonium heptamolybdate tetrahydrate, 5.0 g of 85% phosphoric acid, and 200 g of deionized water, heat at 80 °C for 2.0 h, and the obtained solution is recorded as QP-1.
[0086] 18.0 g of 25wt% acetaldehyde aqueous solution was added to QP-1, heated at 75 °C for 2.0 h, and the resulting liquid was recorded as QL-1.
[0087] 76.0 g of nickel citrate was added to QL-1, and after fully stirring for 20 min, 3.0 g of dodecyl alcohol polyoxyethylene ether-11 was added, and after fully stirring for 20 min, the obtained colloid ...
Example Embodiment
[0089] Example 2
[0090] The preparation method of carrier S-1 is the same as that in Example 1.
[0091] Weigh 56.5 g of ammonium tetramolybdate dihydrate, 4.6 g of ammonium dihydrogen phosphate, and 200 g of deionized water, heat at 80 °C for 2.0 h, and the obtained solution is recorded as QP-2.
[0092] 18.0 g of fructose was added to QP-2, heated at 75ºC for 2.0 h, and the resulting liquid was recorded as QL-2.
[0093] 35.0 g of nickel acetate was added to QL-2, and after fully stirring for 20 min, 3.0 g of nonylphenol polyoxyethylene ether-10, after fully stirring for 20 min, the obtained colloid was recorded as QJ-2.
[0094] S-1 was impregnated with QJ-2, air-dried for 12.0 h, and dried at 140 ºC for 4 h. The obtained catalyst was denoted as CA-2.
Example Embodiment
[0095] Example 3
[0096] The preparation method of carrier S-1 is the same as that in Example 1.
[0097] Take 43.5 g of molybdenum trioxide, 4.6 g of ammonium dihydrogen phosphate, and 200 g of ionized water, heat at 80 °C for 2.0 h, and the obtained solution is recorded as QP-3.
[0098] Add 16.0 g MoS to QP-3 2 , heated at 85 °C for 3.0 h, and the liquid obtained after filtration was recorded as QL-3.
[0099] 35.0 g of nickel acetate was added to QL-3, and after fully stirring for 20 min, 3.0 g of dodecylphenol polyoxyethylene ether-10 was added, and after fully stirring for 20 min, the obtained colloid was recorded as QJ-3.
[0100] S-1 was impregnated with QJ-3, air-dried for 12.0 h, and dried at 140 °C for 4 h. The obtained catalyst was denoted as CA-3.
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