Preparation method of sulfurization type hydro-cracking catalyst

A hydrocracking and catalyst technology, applied in physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of delayed start-up time, high cost, low metal utilization rate, etc., so as to improve hydrogenation performance, The effect of improving performance and improving utilization efficiency

Active Publication Date: 2014-05-07
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Conventional catalyst vulcanization methods use "in-vessel" vulcanization or "in-situ" vulcanization, that is, the catalyst in the oxidized state is first loaded into the hydrogenation reactor, and then hydrogen and sulfurizing agent are introduced into the reactor during the process of continuous heating. Pre-sulfurization, this method brings the following problems: (1) special pre-sulfurization equipment should be set up on the hydrogenation unit; (2) the vulcanizing agent added during the vulcanization process and the water and hydrogen sulfide generated by the reaction can easily cause high pressure Corrosion of reactors and related equipment, resulting in equipment damage and potential safety hazards; (3) The vulcanization process is longer, delaying the start-up time
(4) The vulcanizing agent used is flammable and toxic, and pollutes the environment during the vulcanization process; (5...

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] The catalyst catA involved in the present invention.

[0032] Prepare 250 ml of ammonium heptamolybdate solution (a), 100ml of 10g molybdenum in the solution, 500ml of 10wt% ammonium sulfide solution (b), 40ml of nickel nitrate solution (c), 5g nickel / 100ml in the slurry, weigh 120g Amorphous silica-alumina dry rubber powder, 30gY molecular sieve powder (SiO 2 / Al 2 o 3 The molar ratio is 40, the unit cell constant is 2.432nm, the infrared acidity is 0.19mmol / g, and the specific surface area is 866m 2 / g, pore volume 0.52ml / g), was added to 1500g water to make a slurry (d), 10g polyethylene glycol ether was dissolved in 100mL water to form a solution (e), (a), (b) and (c) ) into the slurry (d) slowly, while introducing the solution (e), stirring evenly, controlling the system temperature at 65°C, reacting for 1 hour, filtering, washing, and drying the obtained material at 100°C for 6 hours under the protection of an inert gas to obtain Catalyst intermediate. Put th...

Embodiment 2

[0034] The catalyst catB involved in the present invention.

[0035] Prepare 400 ml of ammonium tetramolybdate solution (a), containing 5g molybdenum 100 / ml in the solution, prepare 300 ml of 15wt% ammonium sulfide solution (b), prepare 30 ml of nickel nitrate solution (c), contain 8 nickel / 100ml in the slurry, weigh Get 110g amorphous silica-alumina dry rubber powder, 28gβ molecular sieve powder (SiO 2 / A1 2 o 3 =28 (molecular ratio), unit cell constant is 1.198nm, relative crystallinity is 95%, infrared acidity is 0.19mmol / g, 0.174mol / g, specific surface area is 894 / g, pore volume is 0.54l / g), added to 1500g Make a slurry in water (d), dissolve 8g of polyoxyethylene amine in 100mL of water to form a solution (e), slowly add (a), (b) and (c) into the slurry (d), and introduce solution (e) at the same time , stir evenly, control the system temperature at 65°C, filter and wash after reacting for 1 hour, and dry the obtained material at 110°C for 5 hours under the protection ...

Embodiment 3

[0037] The catalyst catC involved in the present invention.

[0038] Prepare 250 ml of ammonium metatungstate solution (a), 100ml of 10g tungsten in the solution, 500ml of 10wt% ammonium sulfide solution (b), 40ml of nickel nitrate solution (c), 5g nickel / 100ml in the slurry, weigh 120g Amorphous silica-alumina dry rubber powder, 30gY molecular sieve powder (SiO 2 / Al 2 o 3 The molar ratio is 40, the unit cell constant is 2.432nm, the infrared acidity is 0.19mmol / g, and the specific surface area is 866m 2 / g, pore volume 0.52ml / g), was added to 1500g water to make slurry (d), 15g polyoxyethylene amide was dissolved in 100ml water to form solution (e), and (a), (b) and (c) Slowly add to the slurry (d), introduce the solution (e) at the same time, stir evenly, control the system temperature at 60°C, react for 1 hour, filter, wash, and dry the obtained material at 100°C for 6 hours under the protection of an inert gas to obtain a catalyst intermediate. Put the catalyst inter...

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PUM

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Abstract

The invention discloses a preparation method of a sulfurization type hydro-cracking catalyst. The preparation method comprises the following steps: selecting a hydro-cracking catalyst carrier component, wherein the carrier component at least comprises a molecular sieve and an amorphous acidic component; adding water into the carrier component powder, pulping so as to obtain slurry (d), then adding an ammonium molybdate and/or ammonium tungstate solution (a), an ammonium sulphide solution (b), and a nickel salt and/or cobalt solution (c) into the slurry (d) to carry out reactions, adding a surfactant at the same time, evenly stirring, filtering, washing, and drying the reaction product in the protection of inert gas, adding an adhesive, kneading, forming, and finally drying and burning in the protection of inert gas so as to obtain the sulfurization type hydro-cracking catalyst. The preparation method makes the active metal be evenly distributed on the carrier so as to generate more II type Ni(Co)Mo(W)S active phases with a higher activity; thus the catalyst has a high sulfurization degree and a high utilization rate of active metal, the hydrogenation activity of the catalyst matches the acidity more reasonably, so the hydrogenation activity and selectivity of the catalyst are both improved.

Description

technical field [0001] The invention relates to a preparation method of a sulfurized hydrocracking catalyst. Background technique [0002] In recent years, with the decrease of oil reserves, the rising international oil price, and the trend of heavy and inferior crude oil becoming more and more serious, the market demand for high-quality middle distillate products continues to increase. Therefore, it is particularly important to increase the production of middle distillates, increase the ratio of diesel to gasoline, and improve the contradiction between supply and demand. The key to solving this contradiction lies in the development of hydrocracking catalysts with high selectivity for middle distillates. Most of the metal active components of the current industrialized hydrocracking catalysts exist in the form of oxides, but in actual use, the active metal oxides on the catalyst need to be converted into sulfides. Therefore, the catalysts need to be sulfurized or Called pre...

Claims

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Application Information

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IPC IPC(8): B01J29/16B01J29/78C10G47/20
Inventor 孙晓艳樊宏飞王占宇
Owner CHINA PETROLEUM & CHEM CORP
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