CN100395312C - Method for catalytic cracking petroleum hydrocarbons - Google Patents
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- CN100395312C CN100395312C CNB2005100730912A CN200510073091A CN100395312C CN 100395312 C CN100395312 C CN 100395312C CN B2005100730912 A CNB2005100730912 A CN B2005100730912A CN 200510073091 A CN200510073091 A CN 200510073091A CN 100395312 C CN100395312 C CN 100395312C
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Abstract
The present invention relates to a catalytic cracking method of petroleum hydrocarbons, which comprises: the preheated petroleum hydrocarbons are conveyed into a cracking reactor comprising two reaction zones, the preheated petroleum hydrocarbons contact a hot cracking catalyst and react with the hot cracking catalyst orderly in a first reaction zone and a second reaction zone in the presence of water vapor, the temperature of the first reaction zone is from 495 to 550DEG C, and the reaction time is from 0.5 to 2.0 seconds; the temperature of the second reaction zone is from 460 to 495DEG C, and the reaction time is from 2 to 30 seconds. The cracking catalyst comprises 25 to 50 wt% of zinc and rare earth modified Y-type zeolite, 20 to 50 wt% of clay and 20 to 50 wt% of inorganic oxide; the content of the zinc in the zinc and rare earth modified Y-type zeolite, which is measured by ZnO, is from 0.5 to 10 wt%, and the content of the rare earth, which is measured by RE2O3, is from 0.5 to 5.8 wt%. The method can be used for effectively reducing the content of olefins in gasoline components and greatly improve the yield of light oil in cracked products.
Description
Technical field
The present invention is a kind of catalyst cracking method of petroleum hydrocarbon, specifically, is a kind of two reaction zones that have, and can effectively reduce the method for catalytic cracking petroleum hydrocarbons of gasoline product olefin(e) centent.
Background technology
Along with the increasingly stringent of environmental protection requirement, gasoline products develops into reformulated gasoline from white gasoline.In the standard of reformulated gasoline, require the vapour pressure and the benzene content of restriction gasoline on the one hand, on the other hand, also will progressively limit the content of olefin component.China carries out new gasoline standard in beginning on January 1st, 2003 in the whole nation, require the olefin(e) centent in the gasoline component to be lower than 35 volume %, also will further limit the content of olefin component in the gasoline from now on.
Catalytic cracking is to produce one of major technique of motor spirit component, and its gasoline yield reaches as high as more than the 50 quality %, and catalytically cracked gasoline is the main blend component of motor spirit.In China, catalytically cracked gasoline accounts for more than 80% of motor spirit blend component.Since the 1980s, the unleaded catalytic cracking technology that forces of motor spirit develops to the direction of producing stop bracket gasoline.For this reason, wide variation have taken place in the processing condition of catalytic cracking and catalyst type.At process aspect, mainly be to improve temperature of reaction, shorten the reaction times, improve the reaction severity, suppressed cracking reaction, improve the contact efficiency of riser tube bottom oil gas and catalyzer; Aspect catalyzer, developed USY type zeolite in conjunction with the catalyzer of inert base or active matrix and the composite catalyst of dissimilar zeolites.
Applied catalysis cracking technology is produced white gasoline, has higher octane value for guaranteeing gasoline component, adopts the content that increases alkene in the gasoline component to increase gasoline octane rating mostly.Olefin(e) centent is 35～65 quality % in the gasoline component of Sheng Chaning in this way, and this and reformulated gasoline differ greatly to the requirement of olefin(e) centent.Therefore, using the high performance cracking catalyst that reduces content of olefin in gasoline in the catalytic cracking process process, is one of both economical approach that directly reduces catalytically cracked gasoline product olefin(e) centent.
Industrial application data (the NPRA Annual Mtg. that U.S. Grace Davison company reports in american petroleum NPRA (NPRA) in 1998 annual meeting, 1998, AM-98-11) show, guaranteeing under the condition that product distributes that the new catalyst of its development can make alkene reduction by 5～10 volume % in the crackate.Akzo Noble Catalysts company has reported olefine lowering catalyst in American Chemical Society (ACS) in 1999 annual meeting, under the condition that guarantees product distribution and gasoline octane rating, can reduce gasoline olefin 8 volume % (ACS PREPRINTS, 43 (3) 1999,515).
CN1100849C discloses a kind of cracking catalyst that reduces catalytic cracking gasoline olefine content and while boosting of octane rating and preparation method thereof.This catalyzer is the y-type zeolite by 1～54 quality %, the ZSM-5 zeolite of 1～20 quality %, and the binding agent of the carrier of 35～60 quality % and 10～25 quality % is formed, and described y-type zeolite is REY, REHY, USY or REUSY.Described ZSM-5 zeolite is by two or more the element modified modified zeolite that makes in zinc, gallium or the rare earth, and described carrier is the kaolin of mishmetal modification and the aluminum-spinel mixture of zinc modification.Contained modified ZSM-5 zeolite is more in this catalyzer, makes to contain more gas in the crackate, and yield of light oil significantly reduces.
CN1142019C discloses a kind of phosphorus-containing catalyst that can reduce olefin(e) centent in the catalytically cracked gasoline cut.This catalyzer is the y-type zeolite by 10～60 quality %, or the mixture of y-type zeolite and MFI structural zeolite or β zeolite, the clay of 0～75 quality %, two kinds of aluminum oxide from pseudo-boehmite and aluminium colloidal sol of 10～40 quality %, contain with P in the described catalyzer
2O
5Count the phosphorus of 0.1～7.0 quality %.Its used y-type zeolite is selected from HY, REHY, USY or REUSY.This Preparation of catalysts method adopts the catalyzer of spray shaping is all used the P contained compound solution-treated, and is dry then.This catalyzer can be reduced to the product olefin content in gasoline 20～26 quality %, but active on the low side, and yield of light oil still remains further to be improved in the product.
EP0461851A2 discloses that a kind of what have anti-Ni and V poisoning performance is the cracking catalyst of active ingredient with the modified Y zeolite.Modified metal element in the described Y zeolite of this catalyzer is selected from Zn, Cu, Co, Ga, Ge, In, Sn, Sb or Fe, but the effect of this catalyzer reduction gasoline product olefin(e) centent is limited.
USP3 discloses a kind of Y zeolite by rare earth and Zn exchange modification in 835,030, the content of this zeolite middle-weight rare earths up to 6～13 heavy % (with RE
2O
3Note).This patent points out that the cracking catalyst that adopts this kind zeolite to make has good thermostability and hydrothermal stability, if content of rare earth is lower than 6 heavy %, then hydrothermal stability reduces, if content of rare earth surpasses 13 heavy %, then thermostability descends.Zeolite with high rare-earth content like this will cause catalyzer to show relatively poor coke selectivity.
Except that form to improve improving from catalyzer the gasoline isoparaffin content, CN1076751C discloses and has a kind ofly produced the method that is rich in isoparaffin gasoline by the improvement catalytic cracking process.This method is divided into two reaction zones with the catalytic cracking reaction of routine, first reaction zone carries out the reaction based on a cracking reaction, control reaction temperature is 530～620 ℃, reaction times is 0.5～2.0 second, second reaction zone diameter increases, the flow velocity of catalyzer and oil gas reduces, temperature of reaction is lower, residence time of material is longer, its temperature of reaction is 460～530 ℃, and the reaction times is 2～30 seconds, thereby can suppress the secondary cracking reaction, increase alkylated reaction and hydrogen transfer reactions, improve the content of isoparaffin in the gasoline composition.The riser reactor that uses in the described method can be the equal diameter riser tube, etc. one of linear speed riser tube, fluidized-bed or reducing riser tube, also can be the compound reactor that constitutes by diameter riser tube-fluidized-bed.CN1078094C has at length introduced structure and its result of use of reducing riser reactor.Catalyzer uses conventional cracking catalyst in this method, and lightweight oil component in the crackate (liquefied gas+gasoline+solar oil) still remains to be improved.
Summary of the invention
The purpose of this invention is to provide a kind of method for catalytic cracking petroleum hydrocarbons, this method can effectively reduce catalytic cracking gasoline olefine content and can improve yield of light oil by a relatively large margin.
Method for catalytic cracking petroleum hydrocarbons provided by the invention, comprise the petroleum hydrocarbon after the preheating is sent in the cracking case that comprises two reaction zones, in the presence of water vapor, successively with a kind of cracking catalyst of heat in first reaction zone and the second reaction zone contact reacts, the temperature of first reaction zone is 495～550 ℃, and the reaction times is 0.5～2.0 second; The temperature of second reaction zone is 460～495 ℃, reaction times is 2～30 seconds, described cracking catalyst comprises zinc and rare earth modified y-type zeolite, the clay of 20～50 quality % and the inorganic oxide of 20～50 quality % of 25～50 quality %, and the zinc content in described zinc and the rare earth modified y-type zeolite is counted 0.5～10 quality %, content of rare earth with RE with ZnO
2O
3Count 0.5～5.8 quality %.
It is active ingredient that the inventive method adopts with zinc and an amount of rare earth modified y-type zeolite, and suitably allocate active ingredient in the catalyzer, clay and make cracking catalyst as the proportioning of the inorganic oxide of binding agent, the catalyst cracking method that is rich in isoparaffin with production is used, make the heavy oil cracking ability of catalytic cracking improve, yield of light oil improves in the product, and olefin(e) centent descends in the gasoline component.
Description of drawings
Fig. 1 is the structural representation of the used reducing riser reactor of the inventive method.
Embodiment
Activity of such catalysts component provided by the invention is zinc and an amount of rare earth modified Y zeolite, and matrix is clay and inorganic oxide, by each components contents of allotment catalyzer, makes its performance improve.This kind catalyzer is applied in the catalyst cracking method with two reaction zones, the productive rate of lightweight oil in the crackate, particularly gasoline is further increased, the olefin(e) centent in the gasoline component further reduces.
Preferred 26～45 quality % of described catalyzer medium clay soil content, preferred 20～40 quality % of inorganic oxide content.Zinc content in the catalyzer in zinc and the rare earth modified y-type zeolite is preferably 0.5～5.0 quality %, content of rare earth with RE in ZnO
2O
3Meter is preferably 2.0～5.0 quality %.
Also further contain 0.5～3.0 quality % in the described catalyzer, the MFI type zeolite of preferred 0.5～1.5 quality %.The described preferred ZSM-5 of MFI type zeolite or contain the ZSM-5 of modifying element, described modifying element is selected from Zn, Mn, Ti, Zr, Cr, Ni, Cu, Fe, Co, P.Described phosphorous ZSM-5, the preparation method who contains the ZSM-5 of rare earth ZSM-5 or phosphorous and rare earth see CN1020269C, CN1059133C, CN1027632C, CN1049406C.The silicon oxide of ZSM-5 zeolite and the mol ratio of aluminum oxide are 10～500, preferred 20～120.
The preferred mishmetal of rare earth in the described modified Y zeolite.The kind of mishmetal is not limit, and the major metal component that it contains is lanthanum and/or cerium, is selected from the metal constituent element of lanthanide series metal simultaneously with other one to multiple kind.
Y-type zeolite in the described modified Y zeolite can be Hydrogen or ammonium type, also can be the Hydrogen or the ammonium type Y zeolite of phosphorus modification, the ultrastable Y that described y-type zeolite is preferably handled through super stabilizing.
Described clay is selected from kaolin, sepiolite, attapulgite, montmorillonite or tires out and take off stone, and described inorganic oxide is aluminum oxide, silicon-dioxide or the mixture of the two.
Zinc of the present invention and rare earth modified y-type zeolite should adopt the ion-exchange techniques preparation.Can earlier the NaY zeolite be made the HY zeolite in the preparation process, introduce zinc and rare earth element respectively by ion-exchange again, perhaps introduce zinc and rare earth simultaneously; Also can be earlier the NaY zeolite be carried out ion-exchange with the mixing solutions of rare earth compound and ammonium salt and prepare REHY, and then by ion-exchange introducing zinc, or earlier the NaY zeolite is carried out ion-exchange with the mixing solutions of zinc compound and ammonium salt and prepare ZnHY, again by ion-exchange introducing rare earth element.
Described modified zeolite of Y-type is preferably zinc and rare earth modified overstable gamma zeolite.The method for making of modification overstable gamma zeolite and the method for making of modified zeolite of Y-type are similar, can prepare Hydrogen USY earlier, introduce zinc and rare earth element more respectively, or introduce this two kinds of elements simultaneously; Also can prepare REUSY earlier, introduce zinc again, or prepare ZnUSY earlier, introduce rare earth element again.
In the above-mentioned modified Y zeolite preparation process, the zinc compound of introducing the zinc element use is any water-soluble zinc compound, preferred zinc chloride.The compound that contains rare earth of introducing the rare earth element use is any water-solubility rare-earth compound, the muriate of preferred mishmetal.Preparation h-type zeolite used ammonium salt is selected from one or more among ammonium chloride, ammonium sulfate ammonium nitrate, Secondary ammonium phosphate, primary ammonium phosphate, ammonium phosphate, ammonium phosphite, dihydrogen phosphite ammonium, ammonium acetate, ammonium formiate, Neutral ammonium fluoride or the ammonium silicofluoride.
In described Y zeolite, a kind of element of every introducing can carry out one or repeatedly ion-exchange, and content of rare earth in zeolite or zinc content reach till the catalyst modification Y zeolite desired content of the present invention.The temperature of carrying out ion-exchange is 35～105 ℃, and preferred 50～95 ℃, be 0.2～10 hour suitable swap time, preferred 0.5～2 hour.The gained zeolite all needs roasting after each ion-exchange, and maturing temperature is 350～850 ℃, and preferred 450～650 ℃, suitable roasting time is 0.5～10 hour, preferred 1～3 hour.
Catalyzer of the present invention can adopt the method preparation of any routine.Generally clay can be made slurries earlier, add the colloidal sol contain inorganic oxide again and make matrix slurries, add spray shaping behind the abundant mixing of modified zeolite again with viscosity.Solid need be used ammonium salt and/or ammonia soln thorough washing after the moulding, with further reduction sodium content.Washing back solid drying promptly gets catalyzer.When inorganic oxide in the catalyzer is silicon oxide, in clay slurry, add silicon sol, perhaps add water glass, make it change into silicon sol with sulfuric acid acidation again, promptly make the matrix slurries.When inorganic oxide is aluminum oxide, in clay slurry, adds aluminium colloidal sol, or add acidification pseudo-boehmite, or add acidification pseudo-boehmite simultaneously and aluminium colloidal sol can make the matrix slurries.
When inorganic oxide in the catalyzer is aluminum oxide, preferably adopt following method to prepare catalyzer:
(1) clay is pulled an oar with deionized water, add pseudo-boehmite again and continue making beating, add an amount of concentrated hydrochloric acid afterwards, wearing out 0.5～4 hour in the back that stirs, obtains the slurries that solid content is 15～35 quality %.
(2) zinc and rare earth modified y-type zeolite are mixed with the slurries that solid content is 20～40 quality %, add (1) with an amount of aluminium colloidal sol and go on foot in the slurries that make, mix the back spray drying forming.
Above-mentioned preparation method (1) is in the step, and the beating time of preparation clay slurry is 0.5～3 hour, and the time that adds pseudo-boehmite continuation making beating is 0.5～2 hour.The add-on of concentrated hydrochloric acid is 0.05～0.25 times of pseudo-boehmite.(2) aluminium colloidal sol that the step adds is 0.2～1: 1 with the mass ratio of (1) pseudo-boehmite that the step adds.
Catalyzer behind the described spray shaping also needs with the ammonium salt solution washing, further to remove contained sodium ion.PH value to 2.5～4.0 that need add the dilute hydrochloric acid regulator solution during washing, wash temperature are 45～90 ℃, preferred 15～60 minutes of time.After the washing solids drying is promptly made catalyzer.
Clay in the described method for preparing catalyst is selected from kaolin, sepiolite, attapulgite, montmorillonite or the tired stone that takes off.
Cracking method of the present invention is that a kind of hydrocarbon feed of controlling is in two reaction zones in differential responses temperature and reaction times, the method for carrying out cracking reaction in the presence of catalyzer provided by the invention.The temperature of first reaction zone is higher, and residence time of material is short, mainly carries out a cracking reaction; The temperature of second reaction zone is low, and residence time of material is longer, mainly is that a crackate carries out alkylated reaction and hydrogen transfer reactions, and suppresses the secondary cracking reaction.
The reactor that above-mentioned cracking method uses be selected from the equal diameter riser reactor, etc. linear speed riser reactor, fluidized-bed or reducing riser reactor.
The aspect ratio of described cracking case first reaction zone and second reaction zone is 10～40: 90～60.
Described reducing riser reactor comprises vertically co-axial each other successively from bottom to up pre lift zone, first reaction zone, second radially big than first reaction zone reaction zone, radially little than second reaction zone outlet area, and the end of outlet area links to each other with settling vessel by level pipe.
The outlet area of described reducing riser reactor: second reaction zone: first reaction zone: the diameter ratio of pre lift zone is 0.8～1.4: 1.5～6.0: 1.0～1.2: 1, and aspect ratio is 1～20: 30～60: 10～30: 5～20.
The similar of first reaction zone is in the equal diameter riser reactor of routine, and its diameter can be identical with the diameter of pre lift zone, and also comparable pre lift zone is big slightly; The diameter of second reaction zone is big than first reaction zone, height proportion maximum in each section of reactor to slow down the flow velocity of oil gas and catalyzer, increases the reaction times, reducing this district's method of temperature can inject the cold shock agent from the joint portion of itself and first reaction zone, or in this district heat collector is set; The similar of outlet area is in the top exit part of conventional equal diameter riser reactor; Described first and second reaction zone, the joint portion of second reaction zone and outlet area is truncated cone-shaped.The detailed structure of reducing riser reactor is referring to CN1078094C.
Describe the inventive method in detail below in conjunction with Fig. 1.Among Fig. 1, pre-lifting steam enters the pre lift zone 2 of reducing riser reactor through pipeline 1, the regenerated catalyst of heat enters pre lift zone 2 through regenerator sloped tube 3, promoted steam in advance with crude oil that enters by pipeline 4 and atomizing steam and be promoted to first reaction zone 5, under defined terms, carried out cracking reaction.Reactant flow with enter second reaction zone 7 after cold shock agent from pipeline 6 mixes, under defined terms, carry out secondary reaction, reacted logistics enters outlet area 8, this reaction zone improves the linear speed of logistics, make reacted logistics enter settling vessel, reaction product isolated and solid catalyst in the gas solid separation system fast through level pipe 9.Reaction product after the separation is gone the cut separation system, and catalyzer enters the reactor cycles utilization by regenerator sloped tube 3 again through coke burning regeneration.
Petroleum hydrocarbon described in the inventive method is the cracking reaction raw material, is selected from crude oil or boiling range and is 220～560 ℃ distillate, comprises time processing cut and secondary processing distillate, as the time processing distillate of decompressed wax oil, residual oil or blending coking distillate.
Below by example in detail the present invention, but the present invention is not limited to this.
The ZnO of zeolite described in the example, RE
2O
3And Na
2O content is by x-ray fluorescence spectrometry; Lattice constant and relative crystallinity by X-ray diffraction method (XRD) adopt the RIPP145-90 standard method (see " petrochemical complex analytical procedure (RIPP test method) ", volumes such as Yang Cuiding, Science Press, nineteen ninety version) measure.
Example 1
Prepare zinc of the present invention and rare earth modified Y zeolite.
With 60 kilograms of decationized Y sieve water, 3 kilograms of (NH
4)
2SO
4(Qilu Petrochemical company catalyst plant is produced, Na with 3 kilograms of (butt) NaY zeolites
2O content 14 quality %, lattice constant 2.473 nanometers) add in the stirring tank, 90 ℃ were carried out ion-exchange 0.5 hour.Filter, solids is through washing, and roasting is 2 hours under 600 ℃, 100% water vapor, makes the HUSY zeolite.In the HUSY zeolite, add 60 kilograms of decationized Y sieve water reslurries, add 2 liters of chlorination mishmetals and ZnCl again
2Mixing solutions, wherein zinc content with ZnO count 60 the gram, content of rare earth is with RE
2O
3Count 150 grams, 90 ℃ were carried out ion-exchange 0.5 hour.Filter, the gained solid product is through washing, and roasting is 2 hours in 600 ℃ of air, makes modified zeolite a, and its chemical constitution and main physico-chemical property see Table 1.
Example 2
Prepare zinc of the present invention and rare earth modified Y zeolite.
With 60 kilograms of decationized Y sieve water, 3 kilograms of (NH
4)
2SO
4, 3 kilograms of example 1 described NaY zeolites and 2 liters of content of rare earth are with RE
2O
3Count the chlorination mixed rare earth solutions of 100 grams, add in the stirring tank, carried out ion-exchange 0.5 hour under 90 ℃.Filter, the gained solid product is through washing, and roasting is 2 hours under 600 ℃, 100% water vapor, makes the REUSY zeolite.To pull an oar with 60 kilograms of decationized Y sieve water in the gained REUSY zeolite, add 2 liters of zinc content are counted 60 grams with ZnO ZnCl again
2Solution carried out ion-exchange 0.5 hour under 90 ℃.Filter, solids is through washing, and roasting is 2 hours in 600 ℃ of air, makes modified zeolite b, and its chemical constitution and main physical and chemical performance see Table 1.
Example 3
Prepare zinc of the present invention and rare earth modified Y zeolite.
With 60 kilograms of decationized Y sieve water, 3 kilograms of (NH
4)
2SO
4, 3 kilograms of example 1 described NaY zeolites, 2 liters of zinc content count the ZnCl of 100 grams with ZnO
2Solution adds in the stirring tank, and 90 ℃ were carried out ion-exchange 0.5 hour.Filter, solids is through washing, and roasting is 2 hours under 600 ℃, 100% water vapor, makes the ZnUSY zeolite.Gained ZnUSY zeolite is pulled an oar with 60 kilograms of decationized Y sieve water, add 2 liters of content of rare earth again with RE
2O
3Count the chlorination mixed rare earth solution of 150 grams, 90 ℃ were carried out ion-exchange 0.5 hour, filtered, and solids is through washing, and roasting is 2 hours in 600 ℃ of air, makes modified zeolite c, and its chemical constitution and main physical and chemical performance see Table 1.
Example 4
Prepare catalyzer of the present invention.
Get 3.6 kilograms of (butt) kaolin (kaolin company in Suzhou produces, solid content 78 quality %), add 15 kilograms of decationized Y sieve water making beating 90 minutes, add 1.2 kilograms of (butt) pseudo-boehmites and continue making beating 45 minutes.Add 0.22 liter of hydrochloric acid that concentration is 36 quality %, stir, be warming up to 60 ℃ and wore out 1 hour.To contain 2.8 kilograms of (butt) modified zeolite a, solid contents is the zeolite slurry of 30 quality %, 1.86 kg aluminium colloidal sol (produce by the Qilu Petrochemical catalyst plant, solid content 21.5 quality %) join in the said mixture, after making beating mixes, spray drying forming.Get moulding after product 1 kilogram (butt) and add 10 kilograms in decationized Y sieve water and 30 gram ammonium chlorides, regulate slurry pH value to 3.0 with the hydrochloric acid of 2 quality %, 20 minutes after-filtration of 60 ℃ of following agitator treatings, 120 ℃ of dryings make catalyst A, and its composition sees Table 2.
Example 5
Method by example 4 prepares catalyst B, and different is to replace modified zeolite a with modified zeolite b, and the composition of the catalyst B that makes sees Table 2.
Example 6
Method by example 4 prepares catalyzer C, and different is to replace modified zeolite a with modified zeolite c, and the composition of the catalyzer C that makes sees Table 2.
Example 7
Method by example 4 prepares catalyzer D, and the dosage of different is modified zeolite a is 2.4 kilograms (butts), and the dosage of pseudo-boehmite is 1.6 kilograms (butts), and the composition of the catalyzer D that makes sees Table 2.
Example 8
Method by example 4 prepares catalyzer E, the dosage of different is modified zeolite a is 3.2 kilograms (butts), and kaolinic dosage is 2.4 kilograms, and the dosage of pseudo-boehmite is 1.6 kilograms (butts), the dosage of aluminium colloidal sol is 2.98 kilograms, and the composition of the catalyzer E that makes sees Table 2.
Example 9
Method by example 4 prepares catalyzer F, and (the Qilu Petrochemical catalyst plant is produced, SiO to add the modified zeolite c that contains 2.8 kilograms (butts) and the ZSM-5 zeolites of 80 grams in the slurries that different is after aging
2/ AL
2O
335), solid content is the zeolite slurry of 30 quality %, and the composition of the catalyzer F that makes sees Table 2.
Comparative Examples 1
Method by example 4 prepares comparative catalyst M, and different is that the zeolite that adds is REUSY, RE among the REUSY
2O
3Content is 4.5 quality %, the solid of the method for pressing CN1142019C afterwards again after with shaping and drying, at 60 ℃ is respectively 3～4 water, ammoniacal liquor and decationized Y sieve water washing with the pH of 20 times of solid masses, after the filtration, with the filter cake phosphorus content is that the phosphoric acid solution of 0.7 quality % was handled 1 hour, 120 ℃ of dryings made catalyzer M in 2 hours, wherein contained the kaolin of REUSY, the 44 quality % of 35 quality %, the aluminum oxide of 20 quality %, the P of 1.0 quality %
2O
5
Comparative Examples 2
Method by example 4 prepares comparative catalyst N, and different is that the zeolite that adds is REUSY, RE among the REUSY
2O
3Content is 3.5 quality %.Contain the kaolin of REUSY, the 45 quality % of 35 quality %, the aluminum oxide of 20 quality % in the catalyst n.
Example 10～17
Following example is estimated catalyzer of the present invention and comparative catalyst's reactivity worth in the reactor with two reaction zones.
With catalyzer of the present invention and comparative catalyst in the fluidized-bed aging equipment under 800 ℃, 100% water vapor condition aging 10 hours, on micro-reactor, estimate earlier, the control reaction is that 500 ℃, raw material charging mass space velocity are 10 hours during evaluation
-1, catalyzer and raw materials quality ratio be 5, water injection rate is 10 quality %.
With the method that the catalyzer after aging is pressed CN1076751C again, the reactivity worth of evaluate catalysts on reducing riser tube reaction unit.15 meters of the pre lift zones of used reducing riser reactor, first reaction zone, second reaction zone, outlet area height overall, the pre lift zone diameter is 0.25 meter, and is high 1.5 meters; 0.25 meter of first reaction zone diameter is high 4 meters; 1 meter of second reaction zone diameter is high 6.5 meters; 0.25 meter of outlet area diameter, high 3 meters, each is distinguished reaction conditions and sees Table 4.
Estimate raw materials used oil nature and see Table 3, evaluation result sees Table 4.
As shown in Table 4, catalyzer of the present invention has higher lightweight oil productive rate than the comparative catalyst, and particularly gasoline yield is higher, and olefin(e) centent wherein is lower, and octane value still can remain on higher level.
Table 1
Table 2
Table 3
Claims (16)
1. method for catalytic cracking petroleum hydrocarbons, comprise the petroleum hydrocarbon after the preheating is sent in the cracking case that comprises two reaction zones, in the presence of water vapor, successively with a kind of cracking catalyst of heat in first reaction zone and the second reaction zone contact reacts, the temperature of first reaction zone is 495～550 ℃, and the reaction times is 0.5～2.0 second; The temperature of second reaction zone is 460～495 ℃, reaction times is 2～30 seconds, described cracking catalyst comprises zinc and rare earth modified y-type zeolite, the clay of 20～50 quality % and the inorganic oxide of 20～50 quality % of 25～50 quality %, described inorganic oxide is aluminum oxide, silicon-dioxide or the mixture of the two, and the zinc content in zinc and the rare earth modified y-type zeolite is counted 0.5～10 quality %, content of rare earth with RE with ZnO
2O
3Count 0.5～5.8 quality %.
2. in accordance with the method for claim 1, it is characterized in that the zinc content in described zinc and the rare earth modified y-type zeolite counts 0.5～5.0 quality %, content of rare earth with RE with ZnO
2O
3Count 2.0～5.0 quality %.
3. according to claim 1 or 2 described catalyzer, it is characterized in that catalyzer medium clay soil content is 26～45 quality %, inorganic oxide content is 20～40 quality %.
4. in accordance with the method for claim 1, it is characterized in that also further containing in the described catalyzer MFI type zeolite of 0.5～3.0 quality %.
5. in accordance with the method for claim 4, it is characterized in that described MFI type zeolite is selected from ZSM-5.
6. in accordance with the method for claim 5, it is characterized in that described ZSM-5 is selected from phosphorous ZSM-5, contains the ZSM-5 of rare earth ZSM-5 or phosphorous and rare earth.
7. in accordance with the method for claim 1, it is characterized in that described rare earth is a mishmetal.
8. in accordance with the method for claim 1, it is characterized in that described y-type zeolite is an overstable gamma zeolite.
9. in accordance with the method for claim 1, it is characterized in that described y-type zeolite is Hydrogen or ammonium type.
10. in accordance with the method for claim 1, it is characterized in that described y-type zeolite is the Hydrogen or the ammonium type Y zeolite of phosphorus modification.
11. in accordance with the method for claim 1, it is characterized in that described clay is selected from kaolin, sepiolite, attapulgite, montmorillonite or the tired stone that takes off.
12. in accordance with the method for claim 1, it is characterized in that described cracking case be selected from the equal diameter riser reactor, etc. linear speed riser reactor, fluidized-bed or reducing riser reactor.
13., it is characterized in that the aspect ratio of described cracking case first reaction zone and second reaction zone is 10～40: 90～60 according to claim 1 or 12 described methods.
14. in accordance with the method for claim 12, it is characterized in that described reducing riser reactor comprises vertically co-axial each other successively from bottom to up pre lift zone, first reaction zone, second radially big than first reaction zone reaction zone, radially little than second reaction zone outlet area, the end of outlet area links to each other with settling vessel by level pipe.
15. in accordance with the method for claim 14, the outlet area that it is characterized in that described reducing riser reactor: second reaction zone: first reaction zone: the diameter ratio of pre lift zone is 0.8～1.4: 1.5～6.0: 1.0～1.2: 1, and aspect ratio is 1～20: 30～60: 10～30: 5～20.
16. in accordance with the method for claim 1, it is characterized in that it is 220～560 ℃ distillate that described petroleum hydrocarbon is selected from crude oil or boiling range.
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| CN102344828B (en) * | 2010-08-05 | 2014-05-28 | 中国石油化工股份有限公司 | Processing method of inferior residual oil |
| CN102839014A (en) * | 2011-06-23 | 2012-12-26 | 中国石油天然气集团公司 | Reactor and method for reinforcing heavy oil conversion and reducing gasoline olefin |
| CN102974386B (en) * | 2012-11-27 | 2015-08-19 | 山东迅达化工集团有限公司 | Catalytic cracking catalyst and preparation method thereof |
| CN110841697B (en) * | 2018-08-20 | 2021-06-01 | 中国石油化工股份有限公司 | Modified Y-type molecular sieve and preparation method thereof |
| CN110841694B (en) * | 2018-08-20 | 2021-06-01 | 中国石油化工股份有限公司 | Catalytic cracking catalyst for processing hydrogenated LCO and preparation method thereof |
| CN110841696B (en) * | 2018-08-20 | 2021-04-06 | 中国石油化工股份有限公司 | Catalytic cracking catalyst for processing hydrogenated LCO and preparation method thereof |
| CN110841691B (en) * | 2018-08-20 | 2021-06-01 | 中国石油化工股份有限公司 | Catalytic cracking catalyst for processing hydrogenated LCO and preparation method thereof |
| CN110841690B (en) * | 2018-08-20 | 2021-06-01 | 中国石油化工股份有限公司 | Modified Y-type molecular sieve and preparation method thereof |
| CN110841695B (en) * | 2018-08-20 | 2021-06-01 | 中国石油化工股份有限公司 | Modified Y-type molecular sieve and preparation method thereof |
| CN110841692B (en) * | 2018-08-20 | 2021-04-06 | 中国石油化工股份有限公司 | Catalytic cracking catalyst for processing hydrogenated LCO and preparation method thereof |
| CN110841693B (en) * | 2018-08-20 | 2021-04-06 | 中国石油化工股份有限公司 | Modified Y-type molecular sieve and preparation method thereof |
| CN109135824B (en) * | 2018-09-20 | 2020-11-03 | 中宁县鑫杞航农业发展有限公司 | Petroleum catalytic cracking process optimization method |
| CN113385223A (en) * | 2021-07-19 | 2021-09-14 | 郑州中科新兴产业技术研究院 | Catalyst for directly catalytically cracking crude oil to increase yield of low-carbon olefin and preparation method thereof |
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| JP2000210567A (en) * | 1999-01-26 | 2000-08-02 | Sanyo Sekiyu Kagaku Kk | Catalyst for reforming gasoline and usage thereof |
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| JP2000210567A (en) * | 1999-01-26 | 2000-08-02 | Sanyo Sekiyu Kagaku Kk | Catalyst for reforming gasoline and usage thereof |
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