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Liquid-phase hydrogenation catalyst composition

A hydrogenation catalyst and liquid-phase hydrogenation technology, which is applied in the field of liquid-phase hydrogenation of oil products, can solve the problems such as the decrease of total processing capacity

Pending Publication Date: 2022-05-06
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This scheme avoids the cyclic enrichment of hydrogen sulfide by flashing its hydrogenation effluent, but the recycling of the material leads to a decrease in the total treatment capacity

Method used

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  • Liquid-phase hydrogenation catalyst composition
  • Liquid-phase hydrogenation catalyst composition

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Preparation of hydrogenation catalyst component D1 with desulfurization activity:

[0035] Take 1000 grams of macroporous aluminum hydroxide, add nitric acid and water to obtain HNO 3 Content is 2.2%, water content is the pasty mixture of 65%, extrude above-mentioned mixture on extruder, obtain the clover-shaped bar of diameter 1.5 millimeters, 100 ℃ of drying 2 hours, then obtain carrier at 600 ℃ of roasting 5 hours, take Ammonium heptamolybdate and nickel nitrate were prepared into an aqueous solution, and the above carrier was impregnated with equal volume for 30 minutes to obtain a wet strip with a molybdenum oxide content of 24% and a nickel oxide content of 4% (calculated on a dry basis after roasting), and dried at 100°C for 2 hours. Then calcined at 550° C. for 2 hours to obtain catalyst D1.

[0036] It was determined that the average pore diameter of the catalyst D1 was 9.5 nanometers, and the specific surface area was 268.9 square meters per gram.

Embodiment 2

[0038] Preparation of hydrogenation catalyst component D2 with desulfurization activity:

[0039] Take 1000 grams of macroporous amorphous silica-alumina, add nitric acid and water to obtain HNO 3 Content is 2.3%, and water content is 68% pasty mixture, extrude above-mentioned mixture on extruder, obtain the cylindrical bar of diameter 1.5 millimeters, dry 18 hours at 80 ℃, then obtain carrier at 500 ℃ roasting 9 hours, take Ammonium heptamolybdate and nickel nitrate were prepared into an aqueous solution, and the above carrier was impregnated with equal volume for 30 minutes to obtain a wet strip with a molybdenum oxide content of 27% and a nickel oxide content of 5% (calculated on a dry basis after roasting), and dried at 100°C for 2 hours. Then calcined at 500° C. for 9 hours to obtain catalyst D2.

[0040] It was determined that the average pore diameter of the catalyst D2 was 9.8 nanometers, and the specific surface area was 253.3 square meters per gram.

Embodiment 3

[0042] Preparation of hydrogenation catalyst component D3 with desulfurization activity:

[0043] Take 1000 grams of aluminum hydroxide containing 0.9% fluorine, add nitric acid and water to obtain HNO 3 Content is 1.3%, water content is 60% pasty mixture, extrude above-mentioned mixture on extruder, obtain the cylindrical bar of diameter 1.5mm, dry 6 hours at 140 ℃, then obtain carrier at 550 ℃ roasting 2 hours, take Ammonium heptamolybdate and cobalt nitrate were prepared into an aqueous solution, and the above carrier was impregnated with equal volume for 30 minutes to obtain a wet strip with a molybdenum oxide content of 16% and a cobalt oxide content of 3% (calculated on a dry basis after roasting), and dried at 100°C for 2 hours. Then calcined at 580° C. for 3 hours to obtain catalyst D3.

[0044] It was determined that the average pore diameter of the catalyst D3 was 10.7 nanometers, and the specific surface area was 277.5 square meters per gram.

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Abstract

The liquid-phase hydrogenation catalyst composition comprises at least one hydrogenation catalyst component with desulfurization activity and at least one sulfur adsorption catalyst component, the sulfur adsorption catalyst component comprises an adsorptive porous material and a hydrogenation active metal loaded on the adsorptive porous material, based on the total weight of the sulfur adsorption catalyst component, the mass percentage of the adsorptive porous material is more than 90%, and the mass percentage of the hydrogenation active metal based on oxide is less than 10%. The sulfur adsorption catalyst component is added into the hydrogenation catalyst, hydrogen sulfide can be adsorbed in the liquid-phase hydrogenation process, desorption of hydrogen sulfide on the sulfur adsorption catalyst component is promoted through flowing of a liquid material, and adsorption and desorption reach dynamic balance, so that aggregation of hydrogen sulfide in the material is achieved; the influence of hydrogen sulfide on hydrogenation reaction is reduced, and the reaction efficiency is improved.

Description

technical field [0001] The invention relates to the technical field of liquid-phase hydrogenation of oil products, in particular to a liquid-phase hydrogenation catalyst composition. Background technique [0002] Traditional diesel hydrodesulfurization adopts trickle bed technology to hydrogenate sulfur-containing and nitrogen-containing compounds in diesel raw materials in the state of gas-liquid-solid three-phase coexistence to produce clean fuels that meet national requirements. Liquid-phase diesel hydrogenation is a new technology that has emerged in recent years. It hydrogenates diesel raw materials containing impurities such as sulfur and nitrogen in a liquid-solid two-phase state. Compared with the trickle bed technology, the raw material of liquid-phase diesel hydrogenation is in continuous contact with the catalyst, in which the dissolved hydrogen and the compounds containing sulfur and nitrogen to be reacted have more advantages in terms of mass transfer. [0003]...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/06B01J23/745B01J23/755B01J23/883B01J23/888B01J27/043B01J27/049B01J27/051B01J35/10B01J37/02B01J37/20C10G45/08
CPCB01J27/043B01J27/049B01J27/0515B01J23/883B01J23/888B01J23/745B01J23/755B01J23/06B01J37/0201B01J37/20C10G45/08C10G2300/202C10G2300/70C10G2400/04B01J35/615B01J35/647
Inventor 杨成敏刘丽段为宇郭蓉周勇李扬姚运海郑步梅孙进
Owner CHINA PETROLEUM & CHEM CORP