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Hydrocracking commencement method

A technology of hydrocracking and nitride, which is applied in hydroprocessing process, chemical instruments and methods, petroleum industry, etc., can solve the problems of catalyst activity influence, inert gas passivation effect poor, hazards, etc. Process, improve catalyst activity, simple process

Active Publication Date: 2019-05-21
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Passivators such as anhydrous liquid ammonia injected outside the device can make the start-up process smooth and safe, but it needs to be transported by a pressure pump, which not only increases the one-time investment of the device, but also wastes the floor area. Equipment that is intermittently opened often breaks down and affects the progress of the start-up. At the same time, the danger of anhydrous liquid ammonia has been described above, and its controllability is self-evident; if the cracking catalyst is not passivated outside the device If the catalyst is not injected, the stability and safety of the start-up process will inevitably be reduced, and the vulcanization process will also be shortened or terminated, which will have a great impact on the activity of the catalyst, which may affect the long-term stable operation of the catalyst.
[0008] Both CN101492613A and CN101492607A disclose the start-up method of the hydrocracking process, which has certain safety and convenience, but still belongs to the method of forced injection of ammonia outside the device to inject a certain passivating agent into the reaction system to inhibit the activity of the cracking agent. There are bound to be disadvantages of injecting ammonia in the above-mentioned prior art, which will bring certain hidden dangers and harm
However, there are still other liquid components that are additionally introduced, and the control control is difficult to achieve, and the start-up process takes a long time
[0012] CN102284299A and CN1602999A relate to a method of hydrogenation catalyst presulfurization outside the hydrogenation reactor-activation in the hydrogenation reactor, which completes the deactivation process of the sulfidation agent of the catalyst under specific working conditions outside the reactor, but the introduced The gas contains catalyst "poisons" and is relatively simple, which cannot completely complete the passivation process of the catalyst. In addition, it is difficult to ensure the adsorption and excess of the passivation gas during the transportation and vulcanization process. insufficient
[0013] CN102921441A has introduced a kind of preparation method of tungsten phosphide catalyst, it passes nitrogen flow to passivate the catalyst in the preparation process, although the effect of passivation can be played to a certain extent, but the passivation effect of inert gas is very poor , cannot be applied to the hydrocracking process
[0014] CN104593051A and CN104593050A disclose a method for starting a vulcanized hydrogenation catalyst. The oil film generated by the added chemical substance is used to passivate the exothermic process of the vulcanized catalyst, although it can completely solve the heat control problem of the concentrated release of sulfur during the vulcanization process , but it cannot be applied in the field of hydrocracking, the oil film formed by it will react or decompose during hydrocracking, and cannot play the role of passivation
Although the process of preparing the presulfurized catalyst outside the device is convenient and feasible, and the energy consumption is reduced, the passivation process still has a certain inhibitory effect on the heat release of the presulfurized catalyst outside the device, so it cannot be applied in the field of hydrocracking
[0016] CN104342200A discloses a method for selective hydrogenation of reformed oil, the core of which is to use some "poisons" to passivate the active metals in the catalyst. Although the effect is remarkable, it is not suitable for the hydrocracking process. For molecular sieves passivation process
[0017] The literature "Research on the Presulfidation and Passivation Process of Hydrogenation Catalysts" introduces the reaction mechanism of the passivation process of presulfided hydrogenation catalysts in detail. In the hydrogenation process with cracking reaction, it is different from the passivation mechanism of our conventional hydrocracking catalyst, so it cannot be applied to the hydrocracking process

Method used

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Experimental program
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Effect test

Embodiment 1

[0037] Firstly, low nitrogen start-up oil, hydrogen and vulcanizing agent are introduced into the hydrocracking unit, and then the hydrocracking catalyst is subjected to constant temperature vulcanization under the condition of 220°C. 4% of the theoretical dosage, after the hydrogen sulfide content in the circulating hydrogen reaches 4000ppm, reduce the adding rate of the sulfurizing agent to 1% of the theoretical dosage of the sulfurizing agent per hour and increase the bed temperature of the hydrocracking catalyst to 320°C, the time used is 15h, When the bed temperature of the hydrocracking catalyst reaches 320°C, increase the adding rate of the vulcanizing agent to 3% of the theoretical amount of the vulcanizing agent per hour, continue constant temperature vulcanization for 3 hours, then raise the temperature to 385°C and feed the raw material oil for reaction, wherein the The hydrocracking catalyst contains 2% nitrogen element, 6% nickel oxide, 23% tungsten oxide and 10% Y...

Embodiment 2

[0039] Firstly, low nitrogen start-up oil, hydrogen and vulcanizing agent are introduced into the hydrocracking unit, and then the hydrocracking catalyst is vulcanized at a constant temperature at 230°C. 5% of the theoretical dosage, after the hydrogen sulfide content in the circulating hydrogen reaches 5000ppm, reduce the adding rate of the sulfurizing agent to 1.5% of the theoretical dosage of the sulfurizing agent per hour and increase the bed temperature of the hydrocracking catalyst to 325°C, and the time used is 13h. When the bed temperature of the hydrocracking catalyst reaches 325°C, increase the addition rate of the vulcanizing agent to 4% of the theoretical amount of vulcanizing agent per hour, continue the constant temperature vulcanization for 2 hours, then raise the temperature to 385°C and feed the raw material oil for reaction, wherein the The hydrocracking catalyst contains 2% nitrogen element, 6% nickel oxide, 23% tungsten oxide and 10% Y-type molecular sieve b...

Embodiment 3

[0041] Firstly, low-nitrogen start-up oil, hydrogen and vulcanizing agent are introduced into the hydrocracking unit, and then the hydrocracking catalyst is subjected to constant temperature vulcanization under the condition of 240°C. 3% of the theoretical amount, after the hydrogen sulfide content in the circulating hydrogen reaches 3000ppm, reduce the addition rate of the sulfide agent to 0.8% of the theoretical amount of the sulfide agent per hour and increase the bed temperature of the hydrocracking catalyst to 330°C, and the time used is 10h. When the bed temperature of the hydrocracking catalyst reaches 330°C, increase the addition rate of the vulcanizing agent to 3% of the theoretical amount of vulcanizing agent per hour, continue constant temperature vulcanization for 4 hours, then raise the temperature to 380°C and feed the raw material oil for reaction, wherein the The hydrocracking catalyst contains 1.8% nitrogen element, 6% nickel oxide, 23% tungsten oxide, and 10% ...

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Abstract

The invention discloses a hydrocracking commencement method which comprises the following steps: firstly, introducing low-nitrogen commencement oil, hydrogen and a vulcanizing agent into a hydrocracking device, carrying out constant-temperature vulcanization on a hydrocracking catalyst at 220-260 DEG C, when the content of hydrogen sulfide in circulated hydrogen is up to 3000-5000ppm, reducing theaddition velocity of the vulcanizing agent, and increasing the temperature of a hydrocracking catalyst bed layer, when the temperature of the hydrocracking catalyst bed layer is up to 310-330 DEG C,increasing the addition velocity of the vulcanizing agent, continuously carrying out constant-temperature vulcanization, increasing the temperature to 380-390 DEG C, and introducing raw material oil to carry out a reaction, wherein the hydrocracking catalyst has 0.3-4% by weight of a nitrogen element, and the nitrogen element is derived from low-molecule-weight nitride and strong alkali cyclic nitride. The method is short in time for commencement, raw material switching and stable production state start, the consumption of a passivant in the commencement process and potential danger in the ammonia injection process can be avoided, and not only is energy consumption reduced, but also environment pollution and human body damage caused by the passivant can be reduced.

Description

technical field [0001] The invention relates to a hydrocracking start-up method, in particular to a hydrocracking start-up process method without external injection of a passivating agent. Background technique [0002] The hydrocracking process is under the action of hydrogen, high temperature, high pressure and catalysts to hydrodesulfurize, hydrodenitrogenate, polycyclic aromatic hydrocarbons, hydrosaturation and ring-opening cracking of heavy distillate oils (VGO, CGO, DAO). The process of conversion into target products such as light oil and middle distillates. The hydrocracking catalysts currently produced in domestic industry are basically oxidative. New catalysts or regenerated catalysts produced in industry contain active metal components (Mo, Ni, Co, W) in the oxidation state (MoO 3 , NiO, CoO, WO 3 ) exists in the form of The practice of basic research and industrial application shows that most of the active metal components of hydrogenation catalysts have high...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C10G65/12B01J31/02
Inventor 王仲义崔哲彭冲孙士可吴子明刘昶
Owner CHINA PETROLEUM & CHEM CORP
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