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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Embodiment 1
[0084] Add 16.0 g MoS to QP-3 2 , heated at 85 °C for 3.0 h, and the liquid obtained after filtration was designated as QL-3.
[0085] Add 35.0 g of nickel acetate to QL-3, stir well for 20 min, then add 3.0 g of dodecylphenol ethoxylate-10, stir well for 20 min, and the colloid obtained is designated as QJ-3.
[0086] S-1 was impregnated with QJ-3, air-dried for 12.0 h, and dried at 140 °C for 4 hours. The obtained catalyst was designated as CA-3.
[0087] Example 4
[0088] Take 43.5 g of molybdenum trioxide, 4.6 g of ammonium dihydrogen phosphate, and 200 g of ionized water, heat at 80 ºC for 2.0 h, and the resulting solution is designated as QP-4.
Embodiment 2
[0090] Add 35.0 g of nickel acetate to QL-4, stir well for 20 min, then add 3.0 g of dodecylphenol ethoxylate-10, stir well for 20 min, and the colloid obtained is designated as QJ-4.
[0091] S-1 was impregnated with QJ-4, air-dried for 12.0 h, and dried at 140 °C for 4 hours. The obtained catalyst was designated as CA-4.
[0092] Example 5
Weigh 1000.0g of alumina dry rubber powder, add 10.0g of citric acid and 10.0g of safflower powder, mix well, add 800.0g of aqueous solution containing 1.0% nitric acid mass fraction, roll for 15.0 min, and use a clover with a diameter of 2.0mm Orifice extruded strips. After drying at 120 °C for 4.0 h, it was calcined at 600 °C for 4.0 h. The calcined carrier is denoted as S-2.
[0093] Weigh 74.2 g of ammonium heptamolybdate tetrahydrate, 7.5 g of 85% mass fraction of phosphoric acid, 200 g of deionized water, and heat at 80 °C for 2.0 h. The resulting solution is designated as QP-5.
[0094] Add 24.0 g of 25wt% acetaldehyde aqueous ...
Embodiment 3
[0096] S-2 was impregnated with QJ-5, air-dried for 12.0 h, and dried at 140 °C for 4 hours. The obtained catalyst was designated as CN-1.
[0097] Example 6
The preparation method of carrier S-2 is the same as that in Example 5.
[0098] Weigh 59.7 g of ammonium tetramolybdate dihydrate, 6.0 g of ammonium dihydrogen phosphate, and 200 g of deionized water, heat at 80 ºC for 2.0 h, and record the obtained solution as QP-6.
[0099] Add 24.0 g fructose to QP-6, heat at 80 °C for 2.0 h, and the obtained liquid is designated as QL-6.
[0100] Add 40.0 g of nickel acetate and 10.0 g of amine triacetic acid to QL-6, stir thoroughly for 20 min, add 4.0 g of nonylphenol polyoxyethylene ether-8, and stir thoroughly for 20 min, the obtained colloid is designated as QJ- 6.
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