CN1530423A - Descending naphtholite catalytic cracking method - Google Patents
Descending naphtholite catalytic cracking method Download PDFInfo
- Publication number
- CN1530423A CN1530423A CNA031195571A CN03119557A CN1530423A CN 1530423 A CN1530423 A CN 1530423A CN A031195571 A CNA031195571 A CN A031195571A CN 03119557 A CN03119557 A CN 03119557A CN 1530423 A CN1530423 A CN 1530423A
- Authority
- CN
- China
- Prior art keywords
- descending
- reactor
- reaction tubes
- cylinder body
- outer cylinder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
A down-flow catalytic cracking process for hydrocarbon oil includes such steps as spraying the raw hydrocarbon oil in an reactor by nozzle, atomizing in atomizing chamber, contacting with catalyst, reacting in reaction pipe, quick separating of oil mixture, introducing the oil gas to the followed separation system, and stripping and regenerating the used catalyst for cyclic use. It can increase the conversion power of heavy oil and improve the distribution of products.
Description
Technical field
The invention belongs to the catalysis conversion method of petroleum hydrocarbon under the situation that does not have hydrogen, more particularly, is a kind of hydrocarbon oil catalytic cracking method of downstriker.
Background technology
Along with expanding economy, countries in the world are that the demand of the low-carbon alkene of raw material will constantly increase to vehicle fuel with the oil.Because petroleum resources are limited, the deep processing of development heavy oil, the supply that increases light-end products and low-carbon alkene will be the significant development strategy of 21 century oil refining industry.Catalytically cracked material wide adaptability, depth of conversion are big, when heavy feed stock is converted into automobile-used fuel such as vapour, diesel oil, contain more low-carbon alkene in the liquefied gas of generation, are that mink cell focus is carried out the most important technology of secondary processing.The catalytic cracking unit scale is big, facility investment is less relatively, is the pillar of all refinery's economic benefits in the world.The product that improves catalytic cracking unit distributes and product selectivity, for the economic benefit and the market competitiveness that improve oil refining enterprise crucial meaning is arranged all, is the target that all refineries lay siege to.
Because the value of petroleum chemicals is far above refined oil product, oil-refining chemical is integrated to be the important channel of improving utilization of resources, increasing the oil refining enterprise economic benefit, also is the development trend of current international petroleum processing industry.Because the demand of propylene increases sharply,, all pay attention to both at home and abroad in recent years by the FCC apparatus propylene enhancing in order to satisfy the demand in market.
On promoting the tubular type catalyst cracker by adopting high temperature, the reaction conditions of high agent-oil ratio and the productive rate that appropriate catalyst can increase low-carbon alkene in the product.In the riser reactor, hydrocarbon oil crude material sprays in the dense-phase catalyst bed of riser tube bottom by nozzle, is difficult to all atomize fully and vaporization in time.In order to make conversion that whole raw materials obtain enough degree of depth, must there be the long reaction times to generate more low-carbon alkene.Simultaneously, because catalyzer contrary gravity direction in riser tube flows, exist more serious back-mixing.Under such reaction environment, raw material has also generated a large amount of dry gas and coke when generating more low-carbon alkene, and the result causes the yield of high value added product to reduce.
In the down pipe reactor, oil gas and catalyzer flow along gravity direction, are approximately plug flow, and back-mixing seldom.The back-mixing degree of catalyzer reduces reduces its surperficial carbon distribution, thereby helps improving its catalytic activity and to the selectivity of high value added product.Since the eighties, external famous oil company is as Exxon, Mobil, UOP, Stone ﹠amp; Webster etc. have successively developed down-flow reactor separately, are used for improving the product selectivity of catalytic cracking or catalytic cracking reaction, and have applied for a series of patent.
USP4514285 discloses a kind of down pipe and dilute phase riser regenerated catalytic-cracking reaction system.After catalyzer is regenerated by dilute phase riser, in the regeneration degassing vessel, remove flue gas, improve density of catalyst, after forming dense-phase bed, enter descending reaction tubes by the catalyst distribution plate, stock oil distributes endless tube by hydrocarbon oil feed, radially sprays into descending reaction tubes through multitube, contact with the catalyzer in the free-falling process, and in descending reaction tubes, carry out cracking reaction.Catalyst concentration was lower when this down pipe reactor initially contacted with catalyzer owing to raw material hydrocarbon, and finish contacts, blended efficient is not ideal enough, and feed stock conversion is lower.
USP5296131, CN1205028A disclose a kind of down pipe reactor.In this reactor, regenerated catalyst flows out a formation annular " curtain " by the spool and the circumferential weld between the valve seat of conical-plug valve, stock oil by the nozzle radial spray of circumferentially evenly arranging under the conical surface to catalyzer " curtain ", contact with the catalyzer cross-flow, enter in the down-flow reactor then and react.Although this down-flow reactor has been strengthened the mixing of catalyzer and stock oil by the cross-flow contact, but, hydrocarbon oil crude material contacts because being still after nozzle ejection with catalyzer in the freely falling body process, catalyst concentration is still very low, and the quantity in the active centre that is provided is very limited.Therefore, the heavy oil conversion performance of this reactor is not good enough yet.
USP4985136, USP5462652 have disclosed a kind of ultrashort contact catalysis cracking method, i.e. MSCC.In the method, catalyzer flows downward with the form of curtain, and petroleum hydrocarbon vertically sprays in this catalyzer curtain, after reaction product and levels of catalysts are passed reaction zone, and finish mixture sharp separation; Catalyzer behind the part stripping directly enters the catalyst mix device without regeneration, with the catalyst mix after the holomorphosis, with the rising agent oil ratio.Though this method has improved the initial contact segment catalyst concentration of agent oil a little by the way that adds high agent-oil ratio, but, therefore also exist the agent oil problem that contact efficiency is not high, the heavy oil conversion degree of depth is not enough because catalyzer can not reach heavy oil and fully transform needed concentration in the freely falling body process.
USP5997726 has disclosed a kind of catalyst cracker of downstriker.Regenerated catalyst removes the regenerated flue gas of being carried secretly through degassing vessel, makes that catalyst density is improved in the degassing vessel; Above-mentioned catalyzer enters in the down-flow reactor by the plug valve of a control regenerated catalyst flow.In the finish exposure chamber that catalyzer falls into the bottom from the spool and the annulus between the valve seat of plug valve.Stock oil is sprayed onto in the agent oil exposure chamber by the hydrocarbon ils nozzle and is on the catalyzer of curtain shape freely falling body, enters down pipe reactor internal reaction together with catalyzer then.Though regenerated catalyst density after the degassing of holder gas tank can be improved in this reactor, but it still is free falling body state when initially contacting with stock oil, can't reach the needed concentration of hydrocarbon oil conversion, so the contact efficiency of finish is still not high enough, the changing effect of hydrocarbon ils is also not ideal enough.
Number of research projects is also being done by domestic units such as Qinghua university aspect the exploitation of down-flow reactor, and has applied for several patents of invention.
CN1265937A discloses a kind of at the telescopic reactor that promotes inner concentric tube installation down pipe.In this reactor, there are two kinds of schemes the position that hydrocarbon oil crude material sprays into beds, first kind of scheme is that hydrocarbon oil crude material is sprayed into ring catalyst lifting zone between riser tube and the down pipe by nozzle, in this annular region, contact to react and rise to the down pipe inlet simultaneously with catalyzer, flow into down pipe again, parallel flowing downward reacted simultaneously in down pipe; Second kind of scheme is that hydrocarbon oil crude material is directly sprayed in the down pipe, contacts with catalyzer in the freely falling body process.Thereby though the efficient that first kind of scheme can the catalyst concentration rising agent oil contact of the initial zone of action of rising agent oil, but the heavy hydrocarbon oil raw material is sprayed in the annular chuck district between riser tube and the down pipe by nozzle, hydrocarbon ils can be ejected on the outside wall surface of down pipe in the chuck inevitably, thereby cause heavy oil serious coking on the wall of chuck, influence the normal operation of device; And contact with catalyzer and stream on the catalyzer that is ejected in the freely falling body process owing to hydrocarbon oil crude material remains in second kind of scheme, because catalyst concn is low, the efficient that agent oil contacts is not high, the ability of heavy oil conversion also just can not be desirable.
CN1275434 discloses a kind of catalyst inlet device that is suitable for the gas-solid cocurrent flow descending bed reactor.This apparatus features is its shell and the coaxial installation of descending-bed reactor main body, and the top of shell is gas-solid biphase turbulent flow mixing zone, and carrier gas inlet is arranged on the following side wall of outer shell of down pipe reactor inlet.Carrier gas mixes the gas-solid two-phase turbulent flow mixing zone that the catalyzer of the pre-lifting zone of ring catalyst between shell and the down pipe is blown into cover top portion, enters in the down pipe reactor again and reacts.Hydrocarbon oil crude material contacts with the catalyzer of the unrestrained state of dilute phase in nozzle sprays into down pipe.Though this catalyst inlet device can make the catalyst distribution in the down pipe more even, but can't improve the catalyst concn in the down pipe, thereby still having the low problem of finish contact efficiency, the transformation efficiency of hydrocarbon oil crude material on the down-flow reactor that adopts this entrance structure is on the low side.
CN1371960A discloses a kind of gas-solid cocurrent flow descending and up coupled catalytic cracking reaction technology and reaction unit, the up reaction process in first descending back has been adopted in this invention, and by be provided with or be not provided with two kinds of structure formations of gas-solid quick disconnector in descending conversion zone exit, improve the yield of gasoline and liquefied gas, reduce the growing amount of dry gas and coke; Or carrying out selectivity hydrogen transference and isomerization reaction, the content of isomeric hydrocarbon and aromatic hydrocarbon reduces olefin(e) centent in the raising gasoline.The descending conversion zone of this invention is because hydrocarbon oil crude material directly sprays into dilute phase bed in the down pipe, and the result causes the initial contact efficiency of finish low, the heavy oil conversion performance deficiency.If in the down pipe outlet gas-solid quick disconnector is set, then must contains more heavy oil in the product; If in the down pipe outlet gas-solid quick disconnector is not set, product that then descending reaction generates and unconverted hydrocarbon oil crude material will enter up conversion zone together and continue reaction, and the result will cause the portioned product overcracking, and the productive rate of dry gas and coke is risen.
In sum, existing down-flow reactor exists to some extent all that the finish contact efficiency is low, heavy oil conversion performance is not enough or catalyzer back-mixing and the serious problem of equipment coking tendency, up to now, can properly settle the good down-flow reactor of the problems referred to above and reactivity worth does not appear in the newspapers as yet.
Through research and experiment repeatedly, we recognize: the major cause that the down-flow reactor heavy oil conversion performance is low is that the initial zone of action of finish density of catalyst is low, generally only is 10kg/m
2S can not provide abundant active centre for hydrocarbon oil crude material carries out cracking reaction.In Desending catalytic cracking reactor, if the density of heavy petroleum hydrocarbon and the formed finish mixture of catalyzer can be controlled at 150～500kg/m in the stage that hydrocarbon oil crude material and regenerated catalyst initially contact
2Scope in, and control oil gas and catalyzer well in initial contact segment back-mixing degree, just can obtain comparatively ideal heavy oil conversion performance and better products selectivity.
Summary of the invention
The object of the present invention is to provide a kind of downstriker catalytic conversion method of hydrocarbon oil, with the atomizing effect that improves hydrocarbon oil crude material, improve the contact efficiency of hydrocarbon oil crude material and catalyzer and the back-mixing of oil gas and catalyzer and the cracking level of raw material be controlled in the suitable scope, thereby when improving heavy oil conversion performance, increase the productive rate of low-carbon alkene in the product, reduce dry gas and coke in the product.
Downstriker catalytic conversion method of hydrocarbon oil provided by the invention is as follows: hydrocarbon oil crude material injects this reactor through the vertically disposed feed nozzle in down-flow reactor top, the formed hydrocarbon oil crude material that is atomizing state contacts, reacts with catalyzer after passing the atomizing raw materials chamber, the finish mixture separates rapidly behind descending reaction tubes, reaction oil gas is sent into subsequent separation system, and reacted catalyzer recycles after stripping, regeneration.
Compared with prior art, method provided by the present invention and downstriker reactor for catalytic conversion of hydrocarbon oil thereof mainly have the advantage of following several respects:
1, down-flow reactor of the present invention provides enough spaces for the abundant atomizing of petroleum hydrocarbon, i.e. the atomizing raw materials chamber.In the present invention, the hydrocarbon oil crude material nozzle placement has sufficiently long distance above down pipe and apart from the down pipe ingress, raw material sprays after could contact with catalyzer after a period of time through nozzle, therefore, raw material has obtained abundant atomizing at this section in the period, for follow-up reaction process has been created favourable condition.
2, by evidence, to compare with the FCC method of routine, downstriker method provided by the invention not only has splendid atomizing raw materials effect, and has good macromole cracking ability, and heavy oil conversion performance is improved significantly.
3, the packing area that is provided with in the pre-lifting zone of down-flow reactor catalyzer of the present invention, the bed of pre-lifting zone is separated into a lot of little spaces, in these little spaces, can not generate big bubble, so just avoided the violent back-mixing of catalyzer that causes in pre-lifting zone bed face fragmentation because of air pocket, thereby improved the activity of such catalysts and the light-end products selectivity that contact with raw material, suppressed the generation of coke.Simultaneously, because the reserve of filler rear catalyst is set in the pre-lifting zone to be reduced, the residence time of catalyzer in pre-lifting zone also shortens thereupon, avoided catalyzer to contact with pre-lifting medium (being generally water vapor) for a long time under hot environment and caused active the reduction.
4, down-flow reactor of the present invention can be arranged a plurality of regenerated catalyst symmetrically, thereby can avoid catalyzer in pre-lifting zone generation bias current, and the catalyst activity that pre-lifting zone bed face is contacted with raw material is more even.Because these transfer limes can a shared regenerated catalyst flowrate control valve, thereby reactor of the present invention adopts a plurality of regenerator transfer limes can not increase the difficulty of the flow control of regenerated catalyst.
5, downstriker catalytic conversion method of hydrocarbon oil provided by the invention not only has very strong heavy oil conversion performance, and can suppress the liquefied gas and the light-end products overcracking that generate after the heavy oil conversion, thereby can reduce the productive rate of low value-added products such as heavy oil, dry gas and coke, improve the yield of high value added products such as low-carbon alkene, gasoline, diesel oil.
Description of drawings
Fig. 1 is the structural representation of down-flow reactor of the present invention.
Fig. 2 is the principle flow chart of method provided by the present invention.
Embodiment
At first, be described with reference to the accompanying drawings the structure of down-flow reactor of the present invention.
Described downstriker reactor for catalytic conversion of hydrocarbon oil comprises with lower member: raw material nozzles 1, top cover 3, reactor outer cylinder body 4, catalyst transport 6, promote dielectric distribution device 9, descending reaction tubes 8, reactor base plate 10 in advance; Wherein, the vertically coaxial setting of raw material nozzles 1, top cover 3, descending reaction tubes 8 and reactor outer cylinder body 4; The outer cylinder body upper edge is connected with the top cover lower edge is along the circumferential direction airtight; Base plate is connected with the outer wall of the lower edge of outer cylinder body, descending reaction tubes is airtight; Descending reaction tubes epimere is positioned at reactor outer cylinder body inside, and its hypomere stretches out through base plate; Catalyst transport 6 is fixedlyed connected with outer cylinder body, and is connected with the pre-lifting zone of ring catalyst that outer cylinder body and descending reaction tubes are constituted; Pre-lifting dielectric distribution device 9 is arranged on the bottom of the pre-lifting zone of catalyzer.
The present invention does not have specific requirement for the shape of reactor head, and it both can be the truncated cone-shaped with trapezoid cross section as shown in Figure 1, can be the top cover of sphere, elliposoidal or torispherical head form yet.Formed space is the atomizing raw materials chamber between top cover and the outer cylinder body upper edge.
A preferred design of reactor of the present invention is near the outlet of the top of atomizing raw materials chamber raw material nozzles anti-scorch steam distributor 2 to be set, to prevent that raw material is in the coking of spray chamber inwall.
As shown in Figure 1, the vertically coaxial setting of raw material nozzles 1, anti-scorch steam distributor 2, top cover 3, descending reaction tubes 8 and reactor outer cylinder body 4.Wherein, raw material nozzles 1, anti-scorch steam distributor 2, top cover 3 and reactor outer cylinder body 4 are vertically coaxial settings from top to bottom; And descending reaction tubes 8 and reactor outer cylinder body 4 are vertically coaxial settings.Descending reaction tubes epimere is positioned at reactor outer cylinder body inside, and its hypomere stretches out through base plate 10.The outer cylinder body upper edge is connected with the top cover lower edge is along the circumferential direction airtight, and base plate is connected with the outer wall of the lower edge of outer cylinder body, descending reaction tubes is airtight.Catalyst transport 6 is fixedlyed connected with outer cylinder body, and is connected with the pre-lifting zone of ring catalyst that outer cylinder body and descending reaction tubes are constituted.Pre-lifting dielectric distribution device 9 is arranged on the bottom of the pre-lifting zone of catalyzer.
A distinguishing feature of this reactor is that the position and the atomizing type of the catalytically cracked material nozzle of its raw material nozzles and routine has bigger difference.The raw material nozzles 1 of this reactor be arranged in descending reaction tubes directly over, the vertical range H0=0.5～5D of it and down pipe ingress, preferred H0=0.8～4D, D is the internal diameter of descending reaction tubes.The internal diameter of descending reaction tubes can be determined according to device raw material treatment capacity, be advisable built in 3～30m/s with gas superficial gas speed control in the down pipe.
The preferred design of another of reactor of the present invention is to be provided with packing area 5 on the pre-lifting zone of annular catalyzer top.The present invention is not strict with the height of packing area and the filler that is adopted, and structured packing or non-structured packing can be used, and preferably use regular shape filler; The height H 2 of packing area can be 0.1～2 times of down pipe internal diameter, preferred 0.2～1.5 times, and most preferably 0.3～1 times.The material of making filler should be able to be high temperature resistant and wear-resisting, and for example the high-temperature alloy steel of corundum coating etc. is with on pottery, surface.For preventing that filler from being poured down pipe by catalyzer or falling into pre-lifting zone bottom, the upper surface of packing area and lower surface preferably perforated panel are set or grid fixes filler.The material of making perforated panel or grid equally preferably can be high temperature resistant and wear-resisting.Packing area upper surface to the vertical range of down pipe upper surface can be 0.2～3 times of down pipe internal diameter, preferred 0.3～2.5 times, and most preferably 0.5～2 times.
The outer cylinder body of this reactor can adopt isodiametric cylinder, also can adopt the cylindrical shell of reducing.For example, top shown in Figure 1 is that cylindrical, bottom is the outer cylinder body of taper, the cone angle gamma of its tapered section 7 can be 0～30 °, and its lower end diameter D1 can be 1.5～3 times of descending tube inner diameter, and its upper end diameter D2 can be 1.5～5 times of descending tube inner diameter; And the height H 1 of top cylindrical tube can be 0.5～5 times of descending tube inner diameter.The vertical height of reactor outer cylinder body is 2～12 times of descending tube inner diameter, preferred 2.5～10 times, and most preferably 3～8 times.
Carry the transfer lime 6 of regenerated catalyst can adopt single tube to the pre-lifting zone of this reactor, but preferably regenerated catalyst is divided into two-way symmetrically or multichannel is transported to the pre-lifting zone (as shown in Figure 1) of reactor, thereby makes the velocity distribution of catalyzer on the annular cross section of pre-lifting zone more even in the guiding valve back of a total transfer lime.Regenerated catalyst 6 radially or is tangentially fixedlyed connected with outer cylinder body along outer cylinder body 4, the angle β of its medullary ray and vertical line can be 15～60 °, and the intersection point of this medullary ray and outer cylinder body 4 can be 0.5～3 times of descending tube inner diameter to the distance H 3 of base plate; The cross-sectional area sum of the cross-sectional area of regenerated catalyst or a plurality of transfer limes can be 0.4～1.5 times of down pipe cross-sectional area.
The down pipe total length of this reactor can be chosen arbitrarily in the scope of 3 to 50 times of down pipe internal diameters according to the requirement in reaction times, and preferred 4～40 times, most preferably 5～30 times.Down pipe is positioned at the height H=2～12D of the pre-lifting zone of catalyzer inside, preferred H=2.5～10D, most preferably H=3～8D.
The pre-lifting dielectric distribution device 9 of this reactor is arranged in the bottom of pre-lifting zone as shown in the figure, and the present invention is not strict with the structural shape of this sparger, and this area pre-lifting dielectric distribution device commonly used all can use, for example distribution rings, distribution pipe etc.
Hydrocarbon oil catalytic cracking method provided by the invention can be used for the different purpose product of fecund, for example, and gas alkene, liquefied gas, gasoline and diesel oil etc. such as ethene, propylene.
Method provided by the present invention does not have special requirement to the catalyzer that is adopted, and any catalyzer in catalytic cracking field that is applicable to all can be used for the present invention.For example, the active ingredient of catalyst system therefor can be selected from: contain or do not contain Y type, HY type or USY type zeolite, β zeolite, the ZSM-5 zeolite of rare earth or in other supersiliceous zeolite with five-membered ring structure one or more.
Main operational condition of the present invention is as follows: reactor provided by the present invention does not also have particular requirement to the processing condition that adopted, and for example, can adopt following processing condition: 450～700 ℃ of down pipe reactor outlet temperature, preferred 480～650 ℃; Agent-oil ratio 3～40, preferred 5～35; Finish duration of contact is 0.1～3 second in the descending reaction tubes, preferred 0.2～2 second; Stock oil atomizing steam amount accounts for 3～30 heavy % of total feed, preferred 4～25 heavy %; The anti-scorch steam injection rate in atomizing raw materials chamber accounts for 0～30 heavy % of total feed, preferred 3～25 heavy %; Pre-2～30 heavy % that medium (water vapour or dry gas) accounts for total feed, preferred 3～25% of promoting.Reaction pressure (absolute pressure) 0.05～0.3MPa, preferred 0.07～0.2MPa.
The present invention has no particular limits stock oil character, any hydrocarbon feed of catalytic cracking process that is applicable to all can adopt, for example, can be to be selected from: the mixture of one or more in long residuum, vacuum residuum, decompressed wax oil, deasphalted oil, wax tailings, hydrogenation tail oil, gasoline fraction, the diesel oil distillate.
Further specify method provided by the invention below in conjunction with accompanying drawing 1 and accompanying drawing 2.
As depicted in figs. 1 and 2, the pyritous regenerated catalyst enters a plurality of regenerated catalyst 6 of or symmetric arrangement from regenerator bottoms standpipe 11 by flowrate control valve 12, flows into the pre-lifting zone 18 of catalyzer of descending reactor under the promotion of pressure reduction.The pre-medium (water vapor or dry gas) that promotes feeds pre-lifting zone bottom by sparger 9.Regulate the pre-flow that promotes gas, make catalyzer form dense-phase bed, and the density of bed is controlled at 100～500kg/m in pre-lifting zone
3Fuel oil preheating to 50～350 ℃ are by nozzle 1 ejection, in the stock oil spray chamber fully after the atomizing, contacts with catalyzer and vaporization generation catalytic cracking reaction rapidly.It is indoor that anti-scorch steam sprays into atomizing raw materials by gas distributor 2.Oil gas, atomized water steam, anti-scorch water vapor, promote medium and catalyzer in advance and enter together in the down pipe reactor 8.Reaction pressure in the down pipe reactor (gauge pressure) is controlled at 0.05～0.3Kpa, the ratio (abbreviation agent-oil ratio) of the inlet amount of the flow of unit time inner catalyst and hydrocarbon oil crude material is controlled at 3～40 in the reactor, and the temperature in down pipe exit is controlled at 450～700 ℃.Oil gas is after carrying out 0.1～3 second catalytic cracking reaction in descending tubular reactor under the above-mentioned processing condition, arriving the down pipe outlet flows in the gas-solid Quick Separation System 13, separate rapidly with catalyzer, in order to avoid the catalytic cracking product because of contacting with catalyst excess cracking reaction took place.Isolated catalyzer is accepted stripping in the stripper 14 of settling vessel bottom, wherein entrained oil gas stripping comes out, enter in the catalyst regeneration system 17 through reclaimable catalyst line of pipes 15 and flowrate control valve 16, Returning reactor recycles behind the coke burning regeneration.Process isolated oil gas of gas solid separation system and stripping medium enter the fractionation and the absorbing-stabilizing system (not drawing among the figure) at rear portion together by pipeline, fractionate out product streams such as dry gas, liquefied gas, gasoline, light cycle oil, heavy cycle oil and slurry oil.
3 following embodiment will give further instruction to downstriker reactor for catalytic conversion of hydrocarbon oil of the present invention and that adopted, but not thereby limiting the invention.
Comparative Examples 1-3
Comparative Examples 1-3 is a resulting test-results on the Desending catalytic cracking reactor middle-scale device of routine.
The treatment capacity of the middle-scale device that Comparative Examples 1-3 adopted is 0.24t/d.Testing sequence is as follows: stock oil is after the process furnace preheating, inject down-flow reactor by the high-efficient atomizing nozzle, contact with high temperature catalyst and react from revivifier, reacted oil gas separates rapidly with catalyzer, oil gas is sent into subsequent separation system through transfer line and is carried out product separation, the long-pending catalyzer that coke is arranged is sent into the revivifier coke burning regeneration after the reaction behind the water vapor stripping, and the catalyzer after the regeneration is delivered to reactor cycles and used.Various products are measured, analyze.
The used three kinds of raw material oil propertiess of 3 Comparative Examples are referring to table 1.Comparative Examples 1,2,3 catalyst system therefors are respectively to be MLC-500, CRP-1 and CEP catalyzer by the industrial trade names of Sinopec Qilu Petrochemical branch office catalyst plant, and its character sees Table 2.3 main operational conditions of Comparative Examples, product distribute and main products character sees Table 3, table 4 and table 5.
Present embodiment explanation: adopt method provided by the present invention and down-flow reactor thereof resulting test-results under conventional catalytic cracking reaction condition.
Inside diameter D=the 20mm of used down pipe reactor among this embodiment; The outer cylinder body of the pre-lifting zone of catalyzer is straight tube, and its diameter D1=2D highly is 6D; The down pipe upper surface is to the height difference H=6D of base plate 10; The upper surface height difference H 0=2D of the outlet of nozzle 1 and down pipe 8.Catalyst transport pipeline 6 is the inclined tube of a diameter d=0.8D, and this transfer lime is fixedlyed connected with outer cylinder body along the line direction of cutting sth. askew of outer cylinder body 4, and vertical angle β=30 of its medullary ray ° and outer cylinder body intersection point are to the height difference H 3=2D of outer cylinder body bottom.Be provided with the regular shape filler that stupalith is made, the height H 2=1D of packing area in the pre-lifting zone.The atomizing raw materials water vapor accounts for 6 heavy % of hydrocarbon oil feed, and anti-scorch water vapor accounts for 5 heavy % of hydrocarbon oil feed, promotes the 4 heavy % that water vapor accounts for hydrocarbon oil feed in advance.
The raw materials used oil of embodiment, catalyzer and testing sequence are all identical with Comparative Examples 1, and main operational condition, product distribute and main products character sees Table 3.
As can be seen from Table 3, compare with Comparative Examples, heavy oil content has reduced percentage point more than 10 in the product of embodiment, the lighter hydrocarbons productive rate has improved nearly 9 percentage points, though the productive rate of dry gas and coke rises to some extent, but this causes because of there being more heavy oil to obtain transforming, if calculate by relative productive rate (dry gas yied/heavy oil conversion rate or coke yield/heavy oil conversion rate), dry gas yied of the present invention and liquefied gas yield are all low than Comparative Examples.As seen adopt method provided by the invention and down-flow reactor thereof to transform the heavy hydrocarbon oil raw material, can obviously improve the transformation efficiency of heavy oil and increase the yield of lighter hydrocarbons.
Present embodiment explanation: the test-results that adopts method provided by the present invention and down-flow reactor thereof under harsh reaction conditions, to obtain.
Among this embodiment the structure of used down-flow reactor as shown in Figure 1, the diameter D=20mm of down pipe reactor; The lower end diameter D1=2.5D of the lower taper cylindrical shell 7 of the pre-lifting zone of catalyzer, upper end diameter D2=3.5D, it highly is 3D; The height H 1=2D of top straight barrel 4; The down pipe ingress is to the height difference H=5D of the bottom of outer cylinder body 7; The ingress height difference H 0=1.5D of the outlet of nozzle 1 and down pipe 8.Catalyst transport pipeline 6 is the inclined tube of the diameter d=0.7D of two symmetric arrangement, and vertical angle β=30 of its medullary ray ° and outer cylinder body intersection point are to the difference of altitude h3=2D of outer cylinder body bottom.Be provided with the regular shape filler that stupalith is made, the height H 2=1D of packing area in the pre-lifting zone.The atomizing raw materials water vapor accounts for 15 heavy % of hydrocarbon oil feed, promotes the 15 heavy % that water vapor accounts for hydrocarbon oil feed in advance.
The raw materials used oil of embodiment, catalyzer and testing sequence are all identical with Comparative Examples 2, and main operational condition, product distribute and main products character sees Table 4.
As can be seen from Table 4, compare with Comparative Examples, heavy oil content has reduced percentage point more than 8 in the product of embodiment, and the lighter hydrocarbons productive rate has improved nearly 8 percentage points, and the productive rate of dry gas and coke has only increased less than 0.5 percentage point.The productive rate of propylene has improved percentage point more than 3 in the product.As seen adopt method provided by the invention and down-flow reactor thereof to transform hydrocarbon oil crude material, can obviously improve the yield of lighter hydrocarbons and increase the productive rate of propylene.
Present embodiment explanation: the test-results that adopts method provided by the present invention and down-flow reactor thereof under the reaction conditions of high severity, to obtain.
Among this embodiment the structure of used down-flow reactor as shown in Figure 1, the diameter D=20mm of down pipe reactor; The lower end diameter D1=2.5D of the lower taper cylindrical shell 7 of the pre-lifting zone of catalyzer, upper end diameter D2=4D, it highly is 4D; The height H 1=2D of top straight barrel 4; The down pipe ingress is to the height difference H=6D of the bottom of outer cylinder body 7; The ingress height difference H 0=iD of the outlet of nozzle 1 and down pipe 8.Catalyst transport pipeline 6 is the inclined tube of the diameter d=0.7D of three symmetric arrangement, and its medullary ray vertical angle β=30 ° and outer cylinder body intersection point are to the difference of altitude h3=2D of outer cylinder body bottom.The atomizing raw materials water vapor accounts for 15 heavy % of hydrocarbon oil feed, and anti-scorch steam injection rate is 20 heavy % of hydrocarbon oil feed, promotes the 25 heavy % that water vapor accounts for hydrocarbon oil feed in advance.
The raw materials used oil of embodiment, catalyzer and testing sequence are all identical with Comparative Examples 3, and main operational condition, product distribute and main products character sees Table 5.
As can be seen from Table 5, compare with Comparative Examples, heavy oil content has reduced percentage point more than 6 in the product of embodiment, and ethylene yield has improved nearly 3 percentage points, and productivity of propylene has improved nearly 2.5 percentage points, and the productive rate of coke does not rise basically.As seen adopt method provided by the invention and down-flow reactor thereof to transform hydrocarbon oil crude material, can obviously improve the transformation efficiency of heavy oil and increase the productive rate of low-carbon alkene.
Table 1
| Raw material type | ????A | ????B | ????C |
| Density (20 ℃)/gcm -3 | ????0.9005 | ????0.8648 | ????0.9012 |
| Carbon residue/% | ????6.9 | ????1.29 | ????4.8 |
| Elementary composition/% | |||
| C | ????86.00 | ????85.65 | ????86.53 |
| H | ????12.59 | ????13.56 | ????12.84 |
| Metal content, ppm | |||
| Ni | ????6.3 | ????0.48 | ????6.3 |
| V | ????3.4 | ????＜0.01 | ????0.05 |
| Boiling range/℃ | |||
| Initial boiling point | ????279 | ????274 | ????284 |
| 10％ | ????363 | ????365 | ????388 |
| 30％ | ????425 | ????407 | ????429 |
| 50％ | ????484 | ????465 | ????492 |
Table 2
| Physical properties | ????MLC-500 | ????CRP-1 | ????CEP |
| Specific surface area m 2g | ????298 | ????160 | ????152 |
| Pore volume, ml/g | ????0.40 | ????0.26 | ????0.24 |
| Tap density, g/cm 3 | ????0.69 | ????0.86 | ????0.91 |
| Size composition, heavy % | |||
| 0～40μm | ????17.4 | ????26.0 | ????16.6 |
| 40～80μm | ????44.1 | ????60.8 | ????42 |
| ＞80μm | ????38.5 | ????13.2 | ????41.4 |
| Micro-activity, 800 ℃, 4hr | ????74 | ????63 | ????70 |
Table 3
| Project | Comparative Examples 1 | Embodiment 1 |
| Raw material type | ????A | ????A |
| Catalyzer | ????MLC-500 | ????MLC-500 |
| Main operational condition: | ||
| Temperature of reaction, ℃ | ????500 | ????500 |
| Reaction pressure (table), kPa | ????100 | ????100 |
| Raw material preheating temperature, ℃ | ????220 | ????220 |
| The regenerator temperature, ℃ | ????712 | ????715 |
| Agent-oil ratio | ????10.2 | ????10.5 |
| Reaction times, s | ????0.5 | ????0.5 |
| Product distributes, heavy % | ||
| Dry gas | ????2.37 | ????2.53 |
| Liquefied gas | ????10.25 | ????12.79 |
| Gasoline | ????28.53 | ????31.20 |
| Diesel oil | ????33.75 | ????37.62 |
| Heavy oil | ????15.34 | ????5.16 |
| Coke | ????9.13 | ????9.92 |
| Loss | ????0.63 | ????0.78 |
| Amount to | ????100.00 | ????100.00 |
| The heavy oil conversion rate, heavy % | ????84.66 | ????94.84 |
| Total lighter hydrocarbons liquid is received, heavy % | ????72.53 | ????81.61 |
| Dry gas yied/heavy oil conversion rate | ????0.0280 | ????0.0267 |
| Coke yield/heavy oil conversion rate | ????0.1078 | ????0.1046 |
| Main products character: | ||
| Gasoline density, g/cm 3 | ????0.71 | ????0.71 |
| Gasoline RON | ????90 | ????91 |
| ??MON | ????77 | ????78 |
| Diesel oil density, g/cm 3 | ????0.86 | ????0.90 |
| Condensation point of diesel oil, ℃ | ????0 | ????-12 |
Table 4
| Project | Comparative Examples 2 | Embodiment 2 |
| Raw material type | ????B | ????B |
| Catalyzer | ????CRP-1 | ????CRP-1 |
| Main operational condition: | ||
| Temperature of reaction, ℃ | ????560 | ????560 |
| Reaction pressure (table), kPa | ????100 | ????100 |
| Raw material preheating temperature, ℃ | ????260 | ????260 |
| The regenerator temperature, ℃ | ????710 | ????690 |
| Agent-oil ratio | ????18.6 | ????18.1 |
| Reaction times, s | ????0.6 | ????0.6 |
| Product distributes, heavy % | ||
| Dry gas | ????6.77 | ????7.16 |
| Liquefied gas | ????43.13 | ????48.70 |
| Gasoline | ????22.31 | ????23.65 |
| Diesel oil | ????11.25 | ????12.33 |
| Heavy oil | ????9.70 | ????1.02 |
| Coke | ????6.11 | ????6.43 |
| Loss | ????0.73 | ????0.71 |
| Amount to | ????100 | ????100 |
| Wherein the light olefin productive rate weighs % | ||
| Ethene | ????3.28 | ????3.45 |
| Propylene | ????20.67 | ????24.15 |
| Main products character: | ||
| Gasoline density, g/cm 3 | ????0.75 | ????0.75 |
| Gasoline RON | ????96 | ????95 |
| ??MON | ????82 | ????81 |
| Diesel oil density, g/cm 3 | ????0.88 | ????0.93 |
| Condensation point of diesel oil, ℃ | ????-8 | ????-17 |
Table 5
| Project | Comparative Examples 3 | Embodiment 3 |
| Raw material type | ????C | ????C |
| Catalyzer | ????CEP | ????CEP |
| Main operational condition: | ||
| Temperature of reaction, ℃ | ????650 | ????650 |
| Reaction pressure (table), kPa | ????100 | ????100 |
| Raw material preheating temperature, ℃ | ????320 | ????320 |
| The regenerator temperature, ℃ | ????745 | ????742 |
| Agent-oil ratio | ????23.2 | ????22.4 |
| Reaction times, s | ????0.8 | ????0.8 |
| Product distributes, heavy % | ||
| H 2～C 2 | ????28.76 | ????33.25 |
| C 3～C 4 | ????29.17 | ????32.61 |
| C + 5Cracking naphtha | ????18.24 | ????16.53 |
| Cracking light oil | ????7.13 | ????6.87 |
| Heavy oil | ????6.64 | ????0.53 |
| Coke | ????9.25 | ????9.36 |
| Loss | ????0.81 | ????0.85 |
| Amount to | ????100 | ????100 |
| Wherein the light olefin productive rate weighs % | ||
| Ethene | ????15.73 | ????18.57 |
| Propylene | ????18.43 | ????20.85 |
| Main products character: | ||
| Gasoline density, g/cm 3 | ????0.81 | ????0.82 |
| Gasoline RON | ????97 | ????99 |
| MON | ????84 | ????85 |
| Diesel oil density, g/cm 3 | ????0.90 | ????0.97 |
| Condensation point of diesel oil, ℃ | ????-12 | ????-23 |
Claims (19)
1, a kind of downstriker catalytic conversion method of hydrocarbon oil, it is characterized in that hydrocarbon oil crude material injects this reactor through the vertically disposed feed nozzle in down-flow reactor top, the formed hydrocarbon oil crude material that is atomizing state contacts, reacts with catalyzer after passing the atomizing raw materials chamber, the finish mixture separates rapidly behind descending reaction tubes, reaction oil gas is sent into subsequent separation system, and reacted catalyzer recycles after stripping, regeneration.
2, according to the method for claim 1, it is characterized in that described down-flow reactor comprises with lower member: raw material nozzles (1), top cover (3), reactor outer cylinder body (4), catalyst transport (6), promote dielectric distribution device (9), descending reaction tubes (8), reactor base plate (10) in advance; Wherein, the vertically coaxial setting of raw material nozzles, top cover, descending reaction tubes and reactor outer cylinder body; The outer cylinder body upper edge is connected with the top cover lower edge is along the circumferential direction airtight; Base plate is connected with the outer wall of the lower edge of outer cylinder body, descending reaction tubes is airtight; Descending reaction tubes epimere is positioned at reactor outer cylinder body inside, and its hypomere stretches out through base plate; Catalyst transport is fixedlyed connected with outer cylinder body, and is connected with the pre-lifting zone of ring catalyst that outer cylinder body and descending reaction tubes are constituted; Pre-lifting dielectric distribution device is arranged on the bottom of the pre-lifting zone of catalyzer.
3,, it is characterized in that described top cover (3) top is provided with anti-scorch steam distributor (2), and raw material nozzles, anti-scorch steam distributor, top cover and reactor outer cylinder body are vertically coaxial settings from top to bottom according to the method for claim 2.
4, according to the method for claim 2, it is characterized in that the exit of described raw material nozzles (1) and the vertical range H0=0.5～5D between the descending reaction tubes upper surface, D is the internal diameter of descending reaction tubes.
5,, it is characterized in that the pre-lifting zone of described catalyzer top is provided with packing area (5) according to the method for claim 2.
6,, it is characterized in that the upper surface of described packing area and lower surface are provided with perforated panel or grid according to the method for claim 5.
7, according to the method for claim 2, it is characterized in that described reactor outer cylinder body (4) can be isodiametric cylinder, also can be the cylindrical shell of reducing.
8, according to the method for claim 2, the vertical height that it is characterized in that described reactor outer cylinder body is 2～12 times of descending tube inner diameter.
9, according to the method for claim 8, the vertical height that it is characterized in that described reactor outer cylinder body is 2.5～10 times of descending tube inner diameter.
10, according to the method for claim 2, it is characterized in that described catalyst transport (6) can be single transfer lime, also can be two or many symmetrically arranged transfer limes.
11, according to the method for claim 2 or 10, it is characterized in that the described catalyst transport (6) and the angle of vertical direction are 15～60 °, this pipe radially or is tangentially fixedlyed connected with outer cylinder body along outer cylinder body (4).
12, according to the method for claim 2, the length that it is characterized in that described descending reaction tubes (8) is 3～50 times of descending tube inner diameter.
13, according to the method for claim 12, the length that it is characterized in that described descending reaction tubes (8) is 4～40 times of descending tube inner diameter.
14,, it is characterized in that height that described descending reaction tubes (8) is positioned at the pre-lifting zone of catalyzer inside is 2～12 times of descending tube inner diameter according to the method for claim 2.
15,, it is characterized in that height that described descending reaction tubes (8) is positioned at the pre-lifting zone of catalyzer inside is 2.5～10 times of descending tube inner diameter according to the method for claim 14.
16,, it is characterized in that the described catalyzer that contacts with the hydrocarbon oil crude material that passes the atomizing raw materials chamber is from the pre-lifting zone of ring catalyst according to the method for claim 1.
17, according to the method for claim 1, it is characterized in that the reaction conditions of described hydrocarbon oil crude material is: 0.1～3 second duration of contact of finish in the agent-oil ratio 3～40 in 450～700 ℃ of the down pipe reactor outlet temperature, descending reaction tubes, the descending reaction tubes.
18,, it is characterized in that in the agent-oil ratio 5～35 in 480～650 ℃ of the described down pipe reactor outlet temperature, descending reaction tubes, the descending reaction tubes 0.2～2 second duration of contact of finish according to the method for claim 17.
19,, it is characterized in that in the agent-oil ratio 6～30 in 500～650 ℃ of the described down pipe reactor outlet temperature, descending reaction tubes, the descending reaction tubes 0.3～1 second duration of contact of finish according to the method for claim 18.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 03119557 CN1224663C (en) | 2003-03-11 | 2003-03-11 | Descending naphtholite catalytic cracking method |
| PCT/CN2003/000294 WO2003090918A1 (en) | 2002-04-26 | 2003-04-23 | Downflow catalytic cracking reactor and use thereof |
| AU2003236150A AU2003236150A1 (en) | 2002-04-26 | 2003-04-23 | Downflow catalytic cracking reactor and use thereof |
| GB0424083A GB2403434B (en) | 2002-04-26 | 2003-04-23 | A downflow catalytic cracking reactor and its application |
| BRPI0309560-6B1A BR0309560B1 (en) | 2002-04-26 | 2003-04-23 | catalytic downflow cracking reactor and its application |
| KR1020047017146A KR100939503B1 (en) | 2002-04-26 | 2003-04-23 | Downflow catalytic cracking reactor and use thereof |
| JP2003587536A JP4456876B2 (en) | 2002-04-26 | 2003-04-23 | Downflow catalytic cracking reactor and its application |
| US10/421,785 US7153478B2 (en) | 2002-04-26 | 2003-04-24 | Downflow catalytic cracking reactor and its application |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 03119557 CN1224663C (en) | 2003-03-11 | 2003-03-11 | Descending naphtholite catalytic cracking method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1530423A true CN1530423A (en) | 2004-09-22 |
| CN1224663C CN1224663C (en) | 2005-10-26 |
Family
ID=34285162
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 03119557 Expired - Lifetime CN1224663C (en) | 2002-04-26 | 2003-03-11 | Descending naphtholite catalytic cracking method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1224663C (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102559239A (en) * | 2010-12-30 | 2012-07-11 | 中国石油天然气集团公司 | Cut-over ultrashort contact rotational flow reactor |
| CN102079984B (en) * | 2009-11-26 | 2013-06-05 | 中国石油化工股份有限公司 | Fractionating column feed method for improving distillate yield |
| CN110540860A (en) * | 2018-05-28 | 2019-12-06 | 中国石油化工股份有限公司 | Process and system for catalytic cracking by adopting double descending pipes |
| CN112705127A (en) * | 2019-10-24 | 2021-04-27 | 中国石油化工股份有限公司 | Reactor and method for producing low-carbon olefin |
-
2003
- 2003-03-11 CN CN 03119557 patent/CN1224663C/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102079984B (en) * | 2009-11-26 | 2013-06-05 | 中国石油化工股份有限公司 | Fractionating column feed method for improving distillate yield |
| CN102559239A (en) * | 2010-12-30 | 2012-07-11 | 中国石油天然气集团公司 | Cut-over ultrashort contact rotational flow reactor |
| CN110540860A (en) * | 2018-05-28 | 2019-12-06 | 中国石油化工股份有限公司 | Process and system for catalytic cracking by adopting double descending pipes |
| CN110540860B (en) * | 2018-05-28 | 2021-08-06 | 中国石油化工股份有限公司 | Process and system for catalytic cracking by adopting double descending pipes |
| CN112705127A (en) * | 2019-10-24 | 2021-04-27 | 中国石油化工股份有限公司 | Reactor and method for producing low-carbon olefin |
| CN112705127B (en) * | 2019-10-24 | 2022-11-01 | 中国石油化工股份有限公司 | Reactor and method for producing low-carbon olefin |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1224663C (en) | 2005-10-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1078094C (en) | Lift pipe reactor for fluidized catalytic conversion | |
| CN102286294B (en) | Method for producing propylene and light arenes by catalytic conversion of hydrocarbons | |
| CN101045881A (en) | Catalytic converter | |
| CN1912065A (en) | Catalytic conversion method for preducing more propylene | |
| CN101210191B (en) | Descending reactor and riser reactor serially connected catalytic cracking method | |
| CN102086402B (en) | Catalytic cracking method and device capable of increasing propylene yield and improving properties of gasoline | |
| CN102533311B (en) | Axial-flow ultrashort contact cyclone reactor | |
| CN102250641B (en) | Method and apparatus for preparing ethylene and propylene with maximized yield | |
| CN1224663C (en) | Descending naphtholite catalytic cracking method | |
| CN1912059A (en) | Catalytic conversion method for producing more propylene | |
| CN103788993A (en) | Catalytic cracking unit | |
| CN1272405C (en) | Descending catalytic cracking reactor | |
| CN102399579A (en) | Catalytic cracking method | |
| CN102559239A (en) | Cut-over ultrashort contact rotational flow reactor | |
| CN1224662C (en) | Descending naphtholite catalytic cracking reactor | |
| CN1657150A (en) | Riser reactor for hydrocarbon fluidized catalytic conversion | |
| CN1179018C (en) | Catalytic conversion process of heavy petroleum hydrocarbon for increasing output of ethylene and propylene | |
| CN103788992A (en) | Catalytic cracking method | |
| CN109385302B (en) | Catalytic conversion method for increasing yield of gasoline and low-carbon olefin | |
| CN1279270A (en) | Catalytic transform process for preparing diesel oil and liquified gas with higher outputs | |
| CN109666503B (en) | Descending reactor and catalytic conversion method | |
| CN201962247U (en) | Catalytic cracking device | |
| CN1142249C (en) | Contact method for catalytic cracking of oil | |
| CN2791050Y (en) | Fluidized catalytic-cracking lift pipe reactor | |
| CN1191324C (en) | Desending catalytic cracking reactor and its application |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CX01 | Expiry of patent term |
Granted publication date: 20051026 |
|
| CX01 | Expiry of patent term |