Method and system for producing low-carbon olefin from inferior oil
阅读说明：本技术 一种劣质油生产低碳烯烃的方法和系统 (Method and system for producing low-carbon olefin from inferior oil ) 是由 魏晓丽 龚剑洪 陈学峰 侯焕娣 申海平 张执刚 张策 梁家林 戴立顺 张久顺 侯 于 2019-03-04 设计创作，主要内容包括：一种劣质油生产低碳烯烃的方法,该方法包括：劣质油转化反应、萃取分离和加氢改质后,改质的劣质油进入催化裂解反应器的第一反应区和第二反应区,与再生后的催化剂接触进行催化裂解反应,反应油气和待生催化剂进入旋风分离器进行气固分离,分离出的反应油气引出装置,进一步分离得到乙烯、丙烯和其他产物；分离出的待生催化剂经汽提后进入催化剂再生器中烧焦再生,再生催化剂返回反应器中循环使用。本发明提供的方法和系统实现了劣质油高价值利用生产低碳烯烃。(A method for producing low-carbon olefin from poor-quality oil comprises the following steps: after the conversion reaction, extraction separation and hydro-upgrading of the inferior oil, the upgraded inferior oil enters a first reaction zone and a second reaction zone of a catalytic cracking reactor to contact with regenerated catalysts for catalytic cracking reaction, reaction oil gas and spent catalysts enter a cyclone separator for gas-solid separation, the separated reaction oil gas is led out of a device for further separation to obtain ethylene, propylene and other products; the separated spent catalyst enters a catalyst regenerator for coke burning regeneration after steam stripping, and the regenerated catalyst returns to the reactor for recycling. The method and the system provided by the invention realize the high-value utilization of the inferior oil to produce the low-carbon olefin.)
1. A method for producing low-carbon olefin from poor-quality oil comprises the following steps:
(1) the inferior oil enters a conversion reaction unit for conversion reaction, and the generated reaction product is separated to obtain heavy fraction with the boiling point of more than 350 ℃;
(2) sending the heavy fraction into an extraction separation unit for extraction separation to obtain modified oil and residues;
(3) sending the modified oil into a hydro-modification unit for hydro-modification to obtain hydro-modified oil;
(4) the preheated hydro-upgrading oil enters a first reaction zone of a catalytic cracking reactor, contacts with a regenerated catalyst to perform catalytic cracking reaction, flows upwards to enter a second reaction zone at the same time, continues to perform catalytic cracking reaction, reaction oil gas at the outlet of the reactor and a catalyst to be generated enter a cyclone separator to perform gas-solid separation, and the separated reaction oil gas is led out of a device and further separated to obtain a product containing low-carbon olefin; the separated spent catalyst enters a catalyst regenerator for coke burning regeneration after steam stripping, and the regenerated catalyst returns to the reactor for recycling.
2. The method of claim 1, wherein the low grade oil comprises at least one selected from the group consisting of low grade crude oil, heavy oil, deoiled bitumen, coal derived oil, shale oil, and petrochemical waste oil.
3. The process of claim 1, wherein the upgraded feedstock meets one or more criteria selected from the group consisting of an API degree of less than 27, a distillation range of greater than 350 ℃, an asphaltene content of greater than 2 wt%, and a heavy metal content of greater than 100 micrograms/gram, based on the total weight of nickel and vanadium.
4. The method of claim 1, wherein the conversion reactor of the conversion reaction unit is a fluidized bed reactor.
5. The method of claim 1, wherein the reforming catalyst of the reforming reaction unit comprises at least one selected from the group consisting of a group VB metal compound, a group VIB metal compound, and a group VIII metal compound.
6. According to claim 1The method, wherein the reaction conditions of the conversion reaction unit comprise: the temperature is 380-470 ℃, the hydrogen partial pressure is 10-25 MPa, and the volume space velocity of the inferior oil is 0.01-2 hours-1The volume ratio of the hydrogen to the poor-quality oil is 500-5000, and the amount of the conversion catalyst is 10-50000 micrograms/g based on the weight of the poor-quality oil and calculated by the metal in the conversion catalyst.
7. The method of claim 1, wherein the reaction conditions of the extraction unit comprise: the pressure is 3-12 MPa, the temperature is 55-300 ℃, and the extraction solvent is C3-C7The weight ratio of the hydrocarbon to the solvent to the heavy fraction is (1-7): 1.
8. The process of claim 1, said hydro-upgrading unit reaction conditions comprising: the hydrogen partial pressure is 5.0-20.0 MPa, the reaction temperature is 330--1The volume ratio of hydrogen to oil is 300-3000.
9. The process of claim 1, the catalyst used in the hydro-upgrading unit comprising a hydrofinishing catalyst and a hydrocracking catalyst, the hydrofinishing catalyst comprising a support and an active metal component selected from group VIB metals and/or group VIII non-noble metals; the hydrocracking catalyst comprises zeolite, alumina, at least one group VIII metal component and at least one group VIB metal component.
10. The process of claim 1, wherein the hydrocracking catalyst comprises, on a catalyst basis: 3-60 wt% of zeolite, 10-80 wt% of alumina, 1-15 wt% of nickel oxide and 5-40 wt% of tungsten oxide.
11. The method of claim 1, the reactor of the catalytic cracking unit comprising a first reaction zone and a second reaction zone, the first reaction zone being a riser reactor and the second reaction zone being a fluidized bed reactor.
12. The process of claim 1, the first reaction zone conditions comprising: the reaction temperature is 560-750 ℃, the reaction time is 1-10 seconds, and the agent-oil ratio is 1-50: 1; the second reaction zone conditions include: the reaction temperature is 550-700 ℃, and the space velocity is 0.5-20h-1。
13. The process of claim 1 wherein said catalyst in step (4) comprises: 1-60 wt% of zeolite, 5-99 wt% of inorganic oxide and 0-70 wt% of clay, wherein the zeolite is selected from medium-pore zeolite and optional large-pore zeolite, the medium-pore zeolite accounts for 50-100 wt% of the total weight of the zeolite, and the large-pore zeolite accounts for 0-50 wt% of the total weight of the zeolite.
14. The process of claim 13 wherein the medium pore zeolite comprises 70 to 100 weight percent of the total weight of the zeolite and the large pore zeolite comprises 0 to 30 weight percent of the total weight of the zeolite.
15. The method of claim 1, wherein said residue of step (2) is returned to step (1) for said conversion reaction; or, throwing the residue obtained in the step (2) outwards; or returning part of the residue obtained in the step (2) to the step (1) for the conversion reaction, and throwing the rest of the residue outwards.
16. The process as claimed in claim 1, wherein the conversion rate of the conversion reaction is 30-70 wt%, the conversion rate of the conversion reaction is (weight of components with distillation range above 524 ℃ in the poor oil-weight of components with distillation range above 524 ℃ in the conversion product)/weight of components with distillation range above 524 ℃ in the poor oil x 100 wt%; and/or the content of components with the distillation range between 350 ℃ and 524 ℃ in the heavy fraction is 20-60 wt%.
17. The system for producing the low-carbon olefin from the inferior oil comprises a conversion reaction unit, an extraction separation unit, a hydrogenation modification unit and a catalytic cracking unit, wherein the conversion reaction unit is connected with the extraction separation unit, the extraction separation unit is connected with the hydrogenation modification unit, and the hydrogenation modification unit is connected with the catalytic cracking unit.
Technical Field
The invention relates to a catalytic conversion method of hydrocarbon oil, in particular to a method for producing low-carbon olefin by carrying out catalytic cracking process on inferior oil after modification.
Background
Ethylene and propylene are important petrochemical industry base stocks. Currently, about 98% of the world's ethylene comes from tubular furnace steam cracking technology, with 46% naphtha and 34% ethane in the ethylene production feed. About 62% of the propylene comes from the co-production of ethylene by steam cracking. The steam cracking technology is perfected day by day, and is a process of consuming a large amount of energy, and is limited by the use of high-temperature materials, and the potential of further improvement is very small.
With the slow recovery of the world economy, the oil demand is slowly increased, and the supply and demand of the world oil market are basically kept loose. The international energy agency considers that, on the supply side, the crude oil production in non-european peck countries, represented by the united states, will continue to rise in the coming years, and the global crude oil demand will tend to tighten in 2022; on the demand side, the global crude oil demand will continuously rise in the next 5 years, and in 2019, 1 hundred million barrels per day will be broken through; the processing amount of unconventional oil and inferior heavy oil is increased year by year. Therefore, the method for producing chemical raw materials such as low-carbon olefin to the maximum extent by utilizing unconventional oil or poor-quality oil is the key and key point for broadening the source of the raw materials for producing the low-carbon olefin, adjusting the product structure, improving the quality and enhancing the effect of the low-carbon olefin in petrochemical enterprises.
Chinese patent CN200610066445.5 discloses a method for producing clean diesel oil and low-carbon olefin from residual oil and heavy distillate oil. The method comprises the steps that residual oil and optional catalytic cracking slurry oil enter a solvent deasphalting unit, the obtained deasphalted oil and optional heavy distillate oil enter a hydrogenation unit, hydrocracking reaction is carried out in the presence of hydrogen, and light and heavy naphtha fraction, diesel oil fraction and hydrogenation tail oil are obtained by separating products; the hydrogenated tail oil enters a catalytic cracking unit to carry out catalytic cracking reaction, and products are separated to obtain low-carbon olefin, gasoline fraction, diesel oil fraction and slurry oil; the diesel oil is recycled to the catalytic cracking unit and all or part of the oil slurry is returned to the solvent deasphalting unit. The method processes the mixture of vacuum residue and catalytic cracking slurry oil, and can obtain the yield of propylene of about 27.3 weight percent and the yield of ethylene of 10.6 weight percent.
WO2015084779a1 discloses a process for producing lower olefins, especially propylene, using a combination of solvent deasphalting and high severity catalytic cracking. The method comprises the following steps: mixing the vacuum residue oil and the solvent, and then performing solvent deasphalting treatment to obtain deasphalted oil and deoiled asphalt rich in the solvent; the deasphalted oil rich in solvent enters a heavy oil deep catalytic cracking device for deep cracking reaction after the solvent is separated, and a target product rich in low-carbon olefin, especially propylene is obtained. The method firstly carries out solvent deasphalting treatment on residual oil, and then realizes the high-efficiency conversion of deasphalted oil and the generation of low-carbon olefin through a combined process, but the deasphalted oil is not used and processed.
Chinese patent cn201510769091.x discloses a residual oil treatment method, comprising a solvent deasphalting device, a hydrogenation pretreatment reaction zone, a hydrotreating reaction zone and a catalytic cracking reaction zone; the process method comprises the following steps: the method comprises the steps of fractionating a residual oil raw material to obtain a light fraction and a heavy fraction, treating the heavy fraction in a solvent deasphalting device to obtain deasphalted oil and deoiled asphalt, mixing the light fraction, the deasphalted oil and hydrogen, sequentially passing through a hydrogenation pretreatment reaction zone and a hydrotreating reaction zone which are connected in series, carrying out gas-liquid separation on reaction effluent in the hydrotreating reaction zone, circulating a gas phase to the hydrogenation pretreatment reaction zone and/or the hydrotreating reaction zone, directly feeding a liquid phase into a catalytic cracking reaction zone to carry out catalytic cracking reaction, and separating the catalytic cracking reaction effluent to obtain dry gas, liquefied gas, a catalytic cracking gasoline fraction, a catalytic cracking diesel fraction, catalytic cracking heavy cycle oil and catalytic cracking slurry oil. The method of the invention can prolong the stable operation period of the device.
Chinese patent CN01119808.7 discloses a high-sulfur high-metal residual oil conversion method, wherein deasphalted oil obtained by extracting residual oil, slurry oil and solvent, and heavy cycle oil and optional solvent refined extract oil enter a hydrotreater together, react in the presence of hydrogen and a hydrogenation catalyst, and the product is separated to obtain gas, naphtha, hydrogenated diesel oil and hydrogenated tail oil, wherein the hydrogenated tail oil enters a catalytic cracking device, and is subjected to cracking reaction in the presence of a cracking catalyst, and the reaction product is separated, wherein the heavy cycle oil can be circulated to the hydrotreater, and the slurry oil is circulated to the solvent deasphalting device. The method reduces the investment and operation cost of a hydrotreater and improves the yield and quality of the light oil.
In order to obtain more low-carbon olefins from poor-quality oil, the prior art adopts a technical method combining solvent deasphalting and hydrotreating to provide a high-quality raw material for catalytic cracking, but the yield of deasphalted oil is low, the yield is limited from the economical point of the whole process, and in addition, the deasphalted oil is not well utilized, so that the utilization rate of the poor-quality oil in the prior art is low, and more residues are still generated. Therefore, there is a need to develop a green and efficient conversion technology for producing low-carbon olefins from inferior oil, so as to increase the utilization rate of inferior oil and to produce more ethylene, propylene and the like with high added values.
Disclosure of Invention
The invention aims to provide a method and a system for producing low-carbon olefin from low-quality oil.
In order to achieve the above object, the present invention provides a method for producing lower olefins from low quality oil, comprising:
(1) converting and separating the inferior oil serving as the upgrading raw material in a reactor of a conversion reaction unit under the condition of hydrogen to obtain heavy fraction with the distillation range of more than 350 ℃;
(2) extracting and separating the heavy fraction obtained in the step (1) in an extraction and separation unit by adopting a solvent to obtain modified oil and residue;
(3) returning the residue obtained in the step (2) to the step (1) for carrying out the conversion reaction; carrying out hydro-upgrading on the upgraded oil obtained in the step (2) to obtain hydro-upgraded oil;
(4) the hydrogenated modified oil obtained in the step (3) enters a first reaction zone and a second reaction zone of a catalytic cracking reactor, contacts with a regenerated catalyst to perform catalytic cracking reaction, reaction oil gas and a spent catalyst enter a cyclone separator to perform gas-solid separation, the separated reaction oil gas is led out of a device, and further separated to obtain a product containing low-carbon olefin; the separated spent catalyst enters a catalyst regenerator for coke burning regeneration after steam stripping, and the regenerated catalyst returns to the reactor for recycling.
The invention also provides a system for producing low-carbon olefins from the inferior oil, which comprises a conversion reaction unit, an extraction separation unit, a hydrogenation modification unit and a catalytic cracking unit, wherein the conversion reaction unit is connected with the extraction separation unit, the extraction separation unit is connected with the hydrogenation modification unit, and the hydrogenation modification unit is connected with the catalytic cracking unit.
Compared with the prior art, the method provided by the invention has the advantages that:
1. the method can process the inferior oil with high metal and high asphaltene content, realizes the efficient lightening of the asphaltene by introducing inferior pre-conversion reaction in the prior art, and greatly reduces the residue amount.
2. The distillation range and the composition of the raw materials for extraction and separation are optimized, the extraction and separation process is easy to operate, and the physical properties of the residues obtained in the extraction and separation process are improved, so that the subsequent division of labor is facilitated.
3. Can provide high-quality raw materials basically free of metal and asphaltene for catalytic cracking, and realize the maximum production of chemical raw materials.
Additional features and advantages of the invention will be set forth in the detailed description which follows. Additional features and advantages of the invention will be set forth in the detailed description which follows.
Drawings
The accompanying drawings, which are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and together with the description serve to explain the principles of the invention and not to limit the invention. In the drawings:
FIG. 1 is a schematic flow diagram of a process for producing lower olefins according to a preferred embodiment of the present invention.
Description of reference numerals:
1 catalytic cracking
4
7 gas collection chamber 8 spent inclined tube 9 spent slide valve
10
13
16
18
22
25
31
34
37
40 hydro-upgrading
Detailed Description
The following describes in detail specific embodiments of the present invention. It should be understood that the detailed description and specific examples, while indicating the present invention, are given by way of illustration and explanation only, not limitation.
The invention provides a method for producing low-carbon olefins, which comprises the following steps: the inferior oil as the upgrading raw material is converted and separated in a conversion reactor under the condition of hydrogen to obtain heavy fraction with the distillation range of more than 350 ℃; extracting and separating the obtained heavy fraction in an extraction separation unit by adopting an extraction solvent to obtain modified oil and residue; returning the obtained residue to the conversion reactor or/and throwing outwards, and carrying out hydro-upgrading on the obtained upgraded oil to obtain hydro-upgraded oil; the obtained hydrogenated modified oil enters a first reaction zone and a second reaction zone of a catalytic cracking reactor, contacts with a regenerated catalyst to carry out catalytic cracking reaction, reaction oil gas and a spent catalyst enter a cyclone separator to carry out gas-solid separation, and the separated reaction oil gas is led out of a device and further separated to obtain a product containing low-carbon olefin; the separated spent catalyst enters a catalyst regenerator for coke burning regeneration after steam stripping, and the regenerated catalyst returns to the reactor for recycling. The low-carbon olefin comprises ethylene, propylene and butylene.
In the method provided by the invention, the low-quality oil can comprise at least one selected from the group consisting of low-quality crude oil, heavy oil, deoiled asphalt, coal derived oil, shale oil and petrochemical waste oil; the low quality oil is preferably selected from one or more of an API value of less than 27, a boiling range of greater than 350 ℃ (preferably greater than 500 ℃, more preferably greater than 524 ℃), an asphaltene content of greater than 2 wt.% (preferably greater than 5 wt.%, more preferably greater than 10 wt.%, even more preferably greater than 15 wt.%), and a heavy metal content of greater than 100 micrograms/gram based on the total weight of nickel and vanadium.
The conversion rate of the conversion reaction is 30-70 wt%, the conversion rate of the conversion reaction is (the weight of the component with the distillation range of 524 ℃ or above in the inferior oil-the weight of the component with the distillation range of 524 ℃ or above in the conversion product)/the weight of the component with the distillation range of 524 ℃ or above in the inferior oil x 100 wt%; and/or the content of components with the distillation range between 350 ℃ and 524 ℃ in the heavy fraction is 20-60 wt%.
In the method provided by the invention, the reactor of the conversion reaction unit can be a fluidized bed reactor, and the fluidized bed reactor refers to a reactor in which reaction raw materials and a catalyst are reacted in a flowing state, and generally comprises a slurry bed reactor, a suspension bed reactor and a boiling bed reactor, and the slurry bed reactor is preferably used in the method. The conversion catalyst may contain at least one selected from group VB metal compounds, group VIB metal compounds and group VIII metal compounds, preferably at least one of Mo compounds, W compounds, Ni compounds, Co compounds, Fe compounds, V compounds and Cr compounds; the conditions of the conversion reaction may include: the temperature is 380-470 ℃, preferably 400-440 ℃, the hydrogen partial pressure is 10-25 MPa, preferably 13-20 MPa, and the volume space velocity of the modified raw material is 0.01-2 hours-1Preferably 0.1 to 1.0 hour-1The volume ratio of the hydrogen to the modifying raw material is 500-5000, preferably 800-2000, and the amount of the converting catalyst is 10-50000 micrograms/g, preferably 30-25000 micrograms/g based on the weight of the modifying raw material and calculated by the metal in the converting catalyst.
In the process provided by the present invention, the extraction unit can be carried out in any prior art extraction apparatus, such as an extraction column; wherein the extraction separation conditions include pressure of 3-12 MPa, preferably 3.5-10 MPa, temperature of 55-300 deg.C, preferably 70-220 deg.C, and extraction solvent selected from C3-C7A hydrocarbon, preferably C3-C5Alkane and C3-C5At least one of olefins, more preferably C3-C4Alkane and C3-C4The weight ratio of the extraction solvent to the heavy fraction obtained by the conversion reaction unit is (1-7):1, preferably (1.5-5): 1. Other conventional extraction methods can be adopted by the person skilled in the art for extraction, and the description of the invention is omitted.
In the process provided by the present invention, the hydro-upgrading unit may be carried out in any manner known in the art, and is not particularly limited, and may be any hydro-treating unit known in the artThe reaction is carried out in a reactor (such as a fixed bed reactor and a fluidized bed reactor), and the reasonable selection can be carried out by the person skilled in the art. For example, the hydro-upgrading treatment is carried out in the presence of a hydrogenation catalyst under conditions comprising: the hydrogen partial pressure is 5.0-20.0 MPa, the preferential pressure is 8-15 MPa, the reaction temperature is 330-450 ℃, the preferential pressure is 350-420 ℃, and the volume space velocity is 0.1-3 hours-1Preferably 0.3 to 1.5 hours-1The hydrogen-oil volume ratio is 300-3000, preferably 800-1500.
The catalyst used by the hydrogenation upgrading unit comprises a hydrofining catalyst and a hydrocracking catalyst, wherein the hydrofining catalyst comprises a carrier and an active metal component, and the active metal component is selected from VIB group metals and/or VIII group non-noble metals; the hydrocracking catalyst comprises zeolite, alumina, at least one group VIII metal component and at least one group VIB metal component. Preferably, the hydrocracking catalyst comprises 3 to 60 wt% of zeolite, 10 to 80 wt% of alumina, 1 to 15 wt% of nickel oxide and 5 to 40 wt% of tungsten oxide based on the dry weight of the hydrocracking catalyst, wherein the zeolite is a Y-type zeolite.
The filling volume ratio of the hydrofining catalyst to the hydrocracking catalyst is 1-5: 1, according to the flow direction of reaction materials, the hydrofining catalyst is filled at the upstream of the hydrocracking catalyst.
The hydrogenation catalyst may be any hydrogenation catalyst conventionally used for this purpose in the art, or may be produced by any production method conventionally known in the art, and the amount of the hydrogenation catalyst used in the step may be conventionally known in the art, and is not particularly limited. By way of specific example, the hydrogenation catalyst generally comprises a support and an active metal component. More specifically, examples of the active metal component include metals of group VIB and non-noble metals of group VIII of the periodic table, and particularly a combination of nickel and tungsten, a combination of nickel, tungsten and cobalt, a combination of nickel and molybdenum, or a combination of cobalt and molybdenum. These active metal components may be used singly or in combination in any ratio. Examples of the carrier include alumina, silica, and amorphous silica-alumina. These carriers may be used singly or in combination in any ratio. The respective contents of the carrier and the active metal component are not particularly limited in the present invention, and conventional knowledge in the art can be referred to.
In the method provided by the present invention, the reactor used in the catalytic cracking unit has two reaction zones in a series structure, the first reaction zone is a riser reactor, the second reaction zone is a fluidized bed reactor, and the reactor can be a conventional catalytic cracking riser reactor in series connection with a fluidized bed reactor known to those skilled in the art. The fluidized bed reactor is positioned at the downstream of the riser reactor and is connected with the outlet of the riser reactor, the riser reactor sequentially comprises a pre-lifting section and at least one reaction zone from bottom to top, and in order to ensure that the raw oil can be fully reacted, and the number of the reaction zones can be 2-8, preferably 2-3 according to the quality requirements of different target products.
In the present invention, both "upstream" and "downstream" of the reactor are based on the direction of flow of the reaction mass, and upstream of the riser reactor is the bottom or lower portion of the reactor.
In the method provided by the present invention, the reaction conditions in the first reaction zone of the catalytic cracking reactor may include: the reaction temperature is 560-750 ℃, preferably 580-730 ℃, and more preferably 600-700 ℃; the reaction time is 1-10 seconds, preferably 2-5 seconds; the agent-oil ratio is 1-50:1, preferably 5-30: 1. The reaction conditions of the second reaction zone may include: the reaction temperature is 550-730 ℃, and preferably 570-720 ℃; the space velocity is 0.5-20h-1Preferably 2-10h-1。
In the method provided by the invention, water vapor can be injected into the riser reactor. The water vapour is preferably injected in the form of atomised steam. The weight ratio of the injected steam to the light hydrocarbon oil feedstock may be in the range of from 0.01 to 1:1, preferably from 0.05 to 0.5: 1.
According to the catalytic cracking method of the present invention, the spent catalyst and the reaction oil gas are separated to obtain the spent catalyst and the reaction oil gas, then the obtained reaction oil gas is subjected to a subsequent separation system (such as a cyclone separator) to separate fractions such as dry gas, liquefied gas, pyrolysis gasoline and pyrolysis diesel, then the dry gas and the liquefied gas are further separated by a gas separation device to obtain ethylene, propylene, etc., and the method for separating ethylene, propylene, etc. from the reaction product is similar to the conventional technical method in the art, and the method of the present invention is not limited thereto, and is not described in detail herein.
According to the catalytic cracking method of the present invention, it is preferable that the method of the present invention further comprises: regenerating the spent catalyst; and preferably at least a part of the catalytic cracking catalyst is regenerated, and for example, the whole of the catalyst may be regenerated catalyst.
According to the catalytic cracking method of the present invention, it is preferable that the method of the present invention further comprises stripping (generally steam stripping) the regenerated catalyst obtained by regeneration to remove impurities such as gas.
According to the catalytic cracking method, in the regeneration process, oxygen-containing gas is generally introduced from the bottom of the regenerator, the oxygen-containing gas can be air, for example, after the air is introduced into the regenerator, the catalyst to be generated is contacted with oxygen for coke burning regeneration, the gas-solid separation is carried out on the upper part of the regenerator on the flue gas generated after the catalyst is burned and regenerated, and the flue gas enters a subsequent energy recovery system.
According to the catalytic cracking method, the regeneration operation conditions of the spent catalyst are as follows: the regeneration temperature is 550-750 ℃, preferably 600-730 ℃, and more preferably 650-700 ℃; the gas apparent linear velocity is 0.5-3 m/s, preferably 0.8-2.5 m/s, more preferably 1-2 m/s, and the average residence time of the spent catalyst is 0.6-3 min, preferably 0.8-2.5 min, more preferably 1-2 min.
According to the catalytic cracking process of the present invention, the catalytic cracking catalyst may be selected conventionally in the art, and for the purposes of the present invention, it is preferred that the catalytic cracking catalyst contains, based on the total weight of the catalyst: 1 to 60 wt% of zeolite, 5 to 99 wt% of inorganic oxide and 0 to 70 wt% of clay.
The catalytic cracking method of the present invention, wherein the zeolite is used as an active component, preferably the zeolite is selected from medium pore zeolite and/or large pore zeolite, and preferably the medium pore zeolite accounts for 50-100 wt% of the total weight of the zeolite, preferably the medium pore zeolite accounts for 70-100 wt% of the total weight of the zeolite, and the large pore zeolite accounts for 0-50 wt% of the total weight of the zeolite, preferably the large pore zeolite accounts for 0-30 wt% of the total weight of the zeolite.
In the invention, the average pore diameter of the medium pore zeolite is 0.5-0.6 nm, and the average pore diameter of the large pore zeolite is 0.7-1.0 nm. For example, the large pore zeolite may be selected from a mixture of one or more of the group of zeolites consisting of rare earth Y (rey), rare earth hydrogen Y (rehy), ultrastable Y obtained by different methods, high silicon Y.
The intermediate pore size zeolite may be selected from zeolites having the MFI structure, such as ZSM-series zeolites and/or ZRP zeolites, which may also be modified with non-metallic elements such as phosphorus and/or transition metal elements such as iron, cobalt, nickel, as described in more detail in connection with ZRP, see U.S. Pat. No. 5,232,675, and the ZSM-series zeolites may be selected from one or more mixtures of ZSM-5, ZSM-11, ZSM-12, ZSM-23, ZSM-35, ZSM-38, ZSM-48 and other zeolites of similar structure, as described in more detail in connection with ZSM-5, see U.S. Pat. No. 3,702,886.
In the present invention, the inorganic oxide is preferably selected from silicon dioxide (SiO) as a binder2) And/or aluminum oxide (Al)2O3)。
In the present invention, the clay is preferably selected from kaolin and/or halloysite as a matrix (i.e., carrier).
According to one embodiment of the present invention, when the process of the present invention is carried out in a conversion reaction unit, it is generally carried out as follows: the poor oil, hydrogen and the conversion catalyst enter a reactor of the conversion reaction unit for reaction, and the reaction product is separated into a gas product and a liquid product to finally obtain heavy fraction with the distillation range of more than 350 ℃.
According to one embodiment of the present invention, when carried out in the extractive separation unit of the process of the present invention, the heavy fraction having a distillation range of greater than 350 ℃ obtained from the conversion reaction unit is sent to the extractive separation unit for countercurrent contact with an extraction solvent for extractive separation to obtain an upgraded oil and a residue. The residue is returned to the conversion reactor for further conversion, and the modified oil is sent to a hydro-upgrading unit.
According to one embodiment of the invention, when the process of the invention is carried out in a hydro-upgrading unit, the upgraded oil from the extractive separation unit is reacted over a hydrotreating catalyst to obtain a hydrogenated upgraded oil which is sent to a catalytic cracking unit.
According to one embodiment of the invention, when the process of the invention is carried out in a catalytic cracking unit, it is generally carried out as follows: the catalytic cracking catalyst enters a pre-lifting section of a first reaction zone of a catalytic cracking reactor, flows upwards under the action of a pre-lifting medium, preheated hydro-upgrading oil and atomized steam are injected into the first reaction zone together, contact with a regenerated catalyst to perform catalytic cracking reaction and flow upwards at the same time, and enter a second reaction zone to continue reaction, the reacted material flow enters a cyclone separator through an outlet of the reactor, the separated reaction oil gas is led out of a device, and fractions such as ethylene, propylene, pyrolysis gasoline and the like are further separated; the separated spent catalyst enters a regenerator for coke burning regeneration, and the regenerated catalyst with recovered activity returns to the riser reactor for recycling.
The following detailed description of embodiments of the invention refers to the accompanying drawings. It should be understood that the detailed description and specific examples, while indicating the present invention, are given by way of illustration and explanation only, not limitation.
The attached figure is a flow schematic diagram of a method for producing ethylene and propylene from poor-quality oil provided by the invention.
The process flow and system of the method provided by the invention are described in detail below with reference to the accompanying drawings as follows:
the poor raw material is transferred to the
The pre-lifting medium enters a
The regenerated catalyst enters a
The following examples further illustrate the process but do not limit the invention.
- 上一篇：一种医用注射器针头装配设备
- 下一篇：一种由低品质油生产低碳烯烃的改质方法和系统