CN102732305B - Naphtha hydrogenation method and decoking tank - Google Patents
Naphtha hydrogenation method and decoking tank Download PDFInfo
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- CN102732305B CN102732305B CN201110095287.7A CN201110095287A CN102732305B CN 102732305 B CN102732305 B CN 102732305B CN 201110095287 A CN201110095287 A CN 201110095287A CN 102732305 B CN102732305 B CN 102732305B
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Abstract
The invention discloses a naphtha hydrogenation method and a decoking tank. The naphtha hydrogenation method comprises the following steps of heating a mixture of a naphtha feedstock and hydrogen in a heating surface to a temperature required by hydrofining, then carrying out decoking by the decoking tank, and then feeding the decoked mixture into a fixed bed hydrogenation reactor. The decoking tank comprises a cylindrical body, an upper head, a lower head and a separation assembly. The separation assembly is a vertical filtration separation assembly and divides the decoking tank into two parts, wherein one part is an outflow channel of a filtered material and the other part is a coke deposition zone. Compared with the prior art, the naphtha hydrogenation method and the decoking tank can effectively and economically prolong a naphtha hydrogenation device running period.
Description
Technical field
The present invention relates to a kind of petroleum naphtha hydrogenation method and decoking tank, the decoking tank that specifically a kind of method of hydrotreating that extends Naphtha hydrofining unit running period and the method are used.
Background technology
Petroleum naphtha (being gasoline fraction) is important gasoline stocks and industrial chemicals, mainly for the production of the Fuel Petroleum of the various trades mark, catalytic reforming is produced aromatic hydrocarbons (or stop bracket gasoline blend component) raw material, steam cracking or catalytic pyrolysis are produced the industrial chemicals such as ethene, propylene, butylene, and for the production of the raw material of hydrogen etc.Petroleum naphtha generally derives from the virgin naphtha that petroleum distillation obtains, and the petroleum naphtha that secondary processing obtains, as coking naphtha, catalytic cracking petroleum naphtha, cracking naphtha etc.The various uses of various sources petroleum naphtha all needs the sulphur in raw material, nitrogen, rare hydrocarbon, metal impurities deep removal, and hydrogen addition technology is the optimum technology that removes various impurity in feed naphtha at present.Produce stop bracket gasoline as catalytic cracking naphtha selective hydrogenation, coking naphtha hydrogenation is produced steam crack material or hydrogen feedstock, and the pre-hydrogenation of virgin naphtha is produced catalytic reforming raw material etc.
In the various hydrogen addition technologies of petroleum naphtha, what generally use is fixed bed hydrogenation technology, be that fixed bed hydrogenation beds is set in hydrogenator, under hydrofining condition, feed naphtha and hydrogen enter reactor from top, carry out hydrofining by hydrogenation catalyst bed and remove the various impurity in raw material, the reaction product after refining is discharged reactor from reactor bottom, carries out obtaining hydrotreated naphtha product after follow-up separation.
In petroleum naphtha hydrogenation technology, the principal element of restriction hydrogenation unit long period steady running is the pressure drop rising speed of fixed bed hydrogenation reactor, in general, in the time that the pressure drop of hydrogenator reaches 0.3MPa, must shutdown process.
For example, concerning coking naphtha Hydrofining Technology, owing to containing the impurity such as diolefine, tiny coke powder in raw material, often affect the operational stability of device.Daqing petrochemical company 300kt/a Hydrogenation of Coker Gasoline device went into operation after half a year, occurred that continuously twice system pressure difference is too high, caused being forced to stop work (the rising analysis of causes of coking gasoline hydrogenation refining system pressure difference and countermeasure, " refining and chemical industry ", the 19th volume: 20).Also there is the reactor catalyst bed pressure drop too fast problem that rises when coker gasoline processing in Guangzhou Branch 300kt/a hydrogenation unit.This device once, within the time of a year and a half, caused stopping work defect elimination 5 times (analysis of causes and countermeasure that hydrofining reaction system pressure drop raises, " China and foreign countries' energy ", 2007, the 12 volumes) because reactive system bed pressure drop raises.Anqing branch office general 3～5 days needs of two I Hydrogenation of Coker Gasoline devices of oil refining clean strainer No. one time, hydrogenator will be stopped work in 1 year and be skimmed for 2～3 times, has a strong impact on normal operation (Coke Inhibitor for Coker Gasoline Hydrofining Unit, " petrochemical technology " of device, 2006,13(4): 5).All there is in various degree Similar Problems in domestic and international device of the same type, the increase of pressure difference between bed, make the inner member such as support bar and back up pad of catalyzer in bearing catalyst weight, the pressure outside necessary commitment, brings hidden trouble to the safety operation of device again.Therefore, it is the conspicuous contradiction that affects coking naphtha hydrogenation unit long-term operation that bed pressure drop rises too fast always, in the urgent need to working out effective means, solves coking problem.
Also often there is the similar problem of above-mentioned coking naphtha hydrogenation unit in catalytic cracking Naphtha hydrofining unit, virgin naphtha hydrogenation unit etc., be the hydrogenation unit running short period to occur the problem that reactor pressure falling-rising is high, can only the stop work partially catalyzed agent on purge reactor beds top, goes into operation after removable parts live catalyst again.
Naphtha hydrofining unit running is put into practice and is shown, the rising of hydrogenator pressure drop all comes from the bed coking of catalyzer top.Coking factor is very complicated, is converted into and is deposited on beds top after settling and causes mainly due to the polymerization of the unsaturated hydro carbons such as the diolefine in raw material and mechanical impurity that upstream device is brought into or impurity precursor.Diolefine in raw material is being easy to occur polymerization, particularly contain other impurity as oxygen, water, iron etc. in raw material time, is easier to polymerization coking.In the sample of coking, the content of general iron is also higher, may be to have formed naphthenic acid with organic hydrocarbon after stock oil dissolved oxygen, the iron of naphthenic acid corrosion device generates iron naphthenate, stably be dissolved in stock oil, iron naphthenate is easy to occur hydrogenolysis after mixed hydrogen, and react generation Iron sulfuret with hydrogen sulfide and be deposited on reactor top bed, the coking reaction that promotes coking parent, has accelerated the obstruction of beds.In addition, in some raw material, containing a small amount of tiny coke powder and tiny microorganism may be also one of reason of some feed naphthas coking in hydrogenator.Varied due to petroleum naphtha source, in the production of some feed naphtha, storage, transportation, introduce and cannot filter the impurity of removing by raw material, these impurity are oil-soluble sometimes, are the particulate suspending sometimes, cannot effectively remove by a kind of or simple several method.And the feed naphtha of hydrogenation unit source is fixing, often change, therefore, also certain device can not be fixed as to certain raw material of processing and use the fixing impurity method of falling.
The method that existing solution petroleum naphtha hydrogenation reactor step-down raises has following several:
1, carry out the management work of raw material, adopt the modes such as nitrogen protection, avoid raw material to contact with air, at utmost reduced the chance of unsaturated hydro carbons formation colloid in raw material.This is a kind of passive raw material guard method, if the raw material mechanical impurity of upstream input is more, diene content is very high, or carries a lot of coke powders secretly, and the party's rule is helpless.
2, mix artificial coal oil or diesel oil distillate, diluted the unsaturated hydro carbons such as the diolefine in raw material, reduced the severity of hydrogenation unit, make device operation more stable.But the method has been sacrificed the amount of finish of hydrogenation device for treatment feed naphtha, has in fact reduced the air speed to feed naphtha, also to increase follow-up tripping device burden (existing tripping device can not meet the demands), economy is poor.
3, between the entrance and exit of pretreatment reaction device, by-pass is set, when normal production, reaction mass enters process furnace after by pretreatment reaction device, in the time that pretreatment reaction device beds Pressure Drop raises, reaction mass enters process furnace through by-pass, until pretreatment reaction device, partly or entirely more after catalyst changeout, reaction mass switches to pretreatment reaction device again and enters process furnace.Although the method can not operation downtime of assurance device, in the not pretreated situation of raw material, can cause larger impact to main reactor temperature rise, make the more difficult control of operation.The replacing of pretreatment catalyst simultaneously also can cause financial loss.Pretreatment reaction device is the impurity adopting in protective material bed deposition raw material, holds impurity limited in one's ability, needs often to change the protective material in pretreatment reaction device.
CN1109495A discloses a kind of Rifining method for catalylic cracking gasoline by adding hydrogen, and described is by the pre-sulfide catalyst series connection of two different activities and variable grain diameter.Adopt the mode of different catalysts grating to there is certain effect for alleviating the coking of hydrogenation catalyst bed, but effect is not outstanding.US4,113,603 reports use the hydrofinishing process of two sections to process diolefine and the sulfide in pyrolysis gasoline, first paragraph uses the catalyzer of nickeliferous-tungsten to remove mercaptan, second segment uses precious metals palladium catalyst to remove diolefine, this technique is comparatively complicated, can not effectively play a role with the coking of other factor for etidine hydrocarbon.
Summary of the invention
For the deficiencies in the prior art, the invention provides the decoking tank that a kind of petroleum naphtha hydrogenation method and the method are used, can effectively guarantee the steady running of Naphtha hydrofining unit, extend the running period of Naphtha hydrofining unit.
Petroleum naphtha hydrogenation method of the present invention comprises the steps:
(1) mixture of feed naphtha and hydrogen is heated to the required temperature of hydrofining in process furnace;
(2) feed naphtha after heating and the mixture of hydrogen enter decoking tank;
(3) enter fixed bed hydrogenation reactor through feed naphtha and the hydrogen of decoking tank decoking, feed naphtha and hydrogen are by the Hydrobon catalyst bed of fixed bed hydrogenation reactor under hydrofining condition, and the petroleum naphtha after hydrofining separates and obtains hydrotreated naphtha with hydrogen discharge reactor.
Decoking tank wherein comprises cylindrical shell, upper cover, lower cover and separation assembly, cylindrical shell and upper cover, lower cover forms decoking tank shell jointly, upper cover top arranges material inlet, lower cover bottom arranges material discharging hole, separation assembly structure is the vertical filtering separation assembly that is arranged on inner barrel one side, vertical filtering separation assembly is made up of the incrustation agent of filling between two-layer screen cloth and two-layer screen cloth, the both sides of vertical filtering separation assembly and decoking tank cylinder inboard wall are sealedly and fixedly connected, the top of vertical filtering separation assembly arranges cover plate, vertical filtering separation assembly, the space that cover plate and decoking tank cylindrical shell form is for going out passage except defocused streams, on the above-mentioned decoking tank cylindrical shell that goes out passage except defocused streams, material outlet is set, except defocused material is discharged decoking tank from this material outlet.
In the inventive method, feed naphtha can be virgin naphtha, coking naphtha, catalytic cracking petroleum naphtha, cracking naphtha etc., can be also the mixture of two or more petroleum naphtha.It is 180～350 ℃ that the refining condition of petroleum naphtha hydrogenation is generally reactor inlet temperature, and reaction pressure is 0.5～12MPa, and when the liquid of feed naphtha, volume space velocity is 0.5～20h
-1, hydrogen to oil volume ratio is 50:1～1500:1(standard state), concrete reaction conditions can specifically be determined according to the specification of quality of product after the character of feed naphtha and hydrogenation.Hydrobon catalyst is generally take aluminum oxide as carrier, take one or more in W, Mo, Ni and Co as hydrogenation activity component, can also contain suitable auxiliary agent, and active ingredient is generally sulphided state in use, to improve the catalytic activity of catalyzer.
The decoking tank concrete structure that the inventive method is used comprises cylindrical shell, upper cover, lower cover and separation assembly, cylindrical shell and upper cover, lower cover forms decoking tank shell jointly, upper cover top arranges material inlet, lower cover bottom arranges material rinse mouth, separation assembly structure is the vertical filtering separation assembly that is arranged on inner barrel one side, vertical filtering separation assembly is made up of the incrustation agent of filling between two-layer screen cloth and two-layer screen cloth, the both sides of vertical filtering separation assembly and decoking tank cylinder inboard wall are sealedly and fixedly connected, the top of vertical filtering separation assembly arranges cover plate, vertical filtering separation assembly, the space that cover plate and decoking tank cylindrical shell form is for going out passage except defocused streams, on the above-mentioned decoking tank cylindrical shell that goes out passage except defocused streams, material outlet is set.
In decoking tank of the present invention, vertical filtering separation assembly is straight plate structure, can be also arc plate structure.Decoking tank is divided into two portions by vertical filtering separation assembly, and a part is material flow pass after filtering, a part of Wei Chenjiao district in addition, and after filtering, the ratio of the cross-sectional area in material flow pass Yu Chenjiao district is 1:9～5:5.The height of vertical filtering separation assembly is general contour with decoking tank cylindrical shell, can also can seal by opening bottom vertical filtering separation assembly.
In decoking tank of the present invention, cylindrical shell is preferably cylindrical tube.The incrustation agent of filling in the middle of vertical filtering separation assembly screen cloth is particle diameter 1.1～3mm, the preferably filler of 1.2 ~ 1.5mm, the material of filler can be aluminum oxide, silicon oxide, pottery etc., also can make spent hydroprocessing catalyst or useless hydrogenation catalyst, and the thickness of filler is generally 10～200mm.Vertical filtering separation assembly upper end height is suitable with decoking tank cylindrical shell height.Ash mouthful is let out in the bottom head setting of decoking tank, and cylindrical shell bottom, decoking Guan Chenjiao district arranges ash blowing mouth.Decoking tank upper cover material inlet below can arrange the inlet diffuser of dispersed material, and inlet diffuser can be conventional taper or plywood structure etc.
When work, feed naphtha through process furnace heating has at high temperature gasified as gas phase, the petroleum naphtha of gasification and hydrogen mixture are from the material inlet of decoking tank upper cover, enter decoking tank through inlet diffuser, vapor phase stream is through vertical filtering separation assembly, incrustation agent has suitable porosity, gas enters material flow pass after the filtration of separation assembly through incrustation agent, flows out decoking tank through material outlet.Solid impurity in gaseous phase materials is trapped, and is deposited on decoking Guan Chenjiao district.Along with the accumulation of solid impurity, vertical filter assemblies is mended gradually solid impurity and is flooded, decoking tank loses decoking effect, from system, excise this decoking tank, open and let out ash mouth and ash blowing mouth, to ash blowing mouth injecting compressed air or nitrogen, the solid coke powder in decoking tank tank to be removed, the decoking tank after excretion solid coke powder can recover to use.Also can between the entrance and exit of decoking tank, pressure recorder be set, judge whether to clear up decoking tank according to the pressure drop rising situation of decoking tank.
Show through research, in Naphtha hydrofining unit, although the reason that causes hydrogenator pressure drop to raise is fast that in hydrogenator, beds coking and fouling causes, but these dirty thing overwhelming majority are not to form after hydrogenation catalyst carries out hydrogenation reaction, but feed naphtha and hydrogen are heated to after high temperature at process furnace, along with feed naphtha transfers gas phase to from liquid phase, coking precursor is assembled and is transformed gradually owing to gasifying, finally become burnt shape solid matter, these burnt shape solid matters enter in hydrogenator under gaseous stream conveying effect, be deposited in beds, and then blocking catalyst bed causes hydrogenator pressure drop rising.Show by great many of experiments, petroleum naphtha and hydrogen are heated to the coking material forming in high-temperature gasification process, with heating before be diverse material, cannot address this problem by the filtration of raw material.Meanwhile, these coking materials are easy to deposition, in the deposition equipment of suitable structure, can effectively separate.Adopt decoking tank of the present invention, the gaseous stream of entrained solids impurity enters after decoking tank, because circulation area expands, gas flow rate reduces, solid impurity particle is because inertia effect drops down onto fast decoking pot bottom and deposits, and can not brought in the deposition agent of the vertical filtering separation assembly of decoking tank by gas phase major part, because now gas phase flow velocity is slower, gas phase separates with the fluidised form of solid impurity, therefore, separation assembly can not lose efficacy by fast blocking, only can constantly rise and bury vertical filtering separation assembly and partial failure with settling, the work-ing life of this decoking tank is very long.The present invention, by the mechanism of the above-mentioned petroleum naphtha hydrogenation process of research coking, arranges the incrustation decoking tank that structure is suitable, has designed rational petroleum naphtha hydrogenation technical process, can effectively solve hydrogenator short problem running period in petroleum naphtha hydrogenation technology.
That decoking tank of the present invention has is simple in structure, it is little to take up an area, no-rotary part, space utilization fully, the feature such as large, the less investment of solid impurity deposition, in petroleum naphtha hydrogenation technology after process furnace the solid impurity of material separate very suitable.
Accompanying drawing explanation
Fig. 1 is the decoking jar structure schematic diagram that the present invention uses;
Fig. 2 is Fig. 1 middle section A-A structural representation;
Fig. 3 is Fig. 1 middle section B-B structural representation.
Wherein: 1-material inlet, 2-inlet diffuser, 3-upper cover, 4-material outlet, the vertical filtering separation assembly of 5-, 6-cylindrical shell, 7-ash blowing mouth, 8-exit collector, 9-material discharging hole, 10-skirt, 11-lets out ash mouthful, 12-lower cover.
Embodiment
Further illustrate the technology contents of the inventive method and decoking tank below in conjunction with accompanying drawing, and further illustrate the technique effect of the inventive method by embodiment.
Decoking tank is as shown in Figure 1 set between the process furnace of petroleum naphtha hydrogenation processing method of the present invention in existing petroleum naphtha hydrogenation technique and hydrogenator, and other content does not need to change substantially.As shown in Figure 1, decoking tank forms body skin by upper cover 3, cylindrical shell 6 and lower cover 12, and upper cover 3 tops arrange material inlet 1, material inlet 1 bottom inlet porting scatterer 2, lower cover 12 bottoms arrange exit collector 8, and exit collector 8 communicates with material discharging hole 9.Vertical filtering separation assembly 5 is vertically set in decoking tank cylindrical shell 5, and vertical filtering separation assembly 5 is that the agent of the inner filling of two-layer screen cloth incrustation forms.Decoking tank lower cover bottom arranges lets out ash mouth 11, and decoking tank cylindrical shell 6 bottoms arrange ash blowing mouth 7.Whole decoking tank is fixed on working face by skirt 10.
Further illustrate the result of use of the inventive method and decoking tank below by embodiment.The decoking jar structure that embodiment uses is: the high and diameter ratio of cylindrical shell aspect ratio 5(), incrustation agent thickness in vertical filtering separation assembly is 50mm, incrustation agent is the alumina globule of 1.5mm, cylindrical shell is divided into two portions by vertical filtering separation assembly, and after filtering, the ratio of the cross-sectional area in material flow pass Yu Chenjiao district is 2:8.
Embodiment 1 and comparative example 1
Coking naphtha hydrofining technology.Coking naphtha mixes through process furnace and is heated to 230 ℃ with hydrogen, enters hydrogenator after entering decoking tank decoking.Hydrogenation catalyst FH-40A is the business Hydrobon catalyst of Sinopec Fushun Petrochemical Research Institute development and production.Feedstock property is in table 1, operational condition and the results are shown in Table 2.The difference of comparative example is not for arranging decoking tank.
Table 1 stock oil character.
| Raw material | Coking naphtha |
| Boiling range scope, ℃ | 36～192 |
| Sulphur, μ g/g | 4960 |
| Nitrogen, μ g/g | 126 |
| Bromine valency, gBr/ (100mL) | 48 |
Table 2 operational condition and product property.
| ? | Embodiment 1 | Comparative example 1 |
| Reaction hydrogen pressure, MPa | 4.0 | 4.0 |
| Hydrogen to oil volume ratio | 800:1 | 800:1 |
| Volume space velocity, h -1 | 2.0 | 2.0 |
| Reactor inlet temperature, ℃ | 230 | 230 |
| Hydrogenation catalyst | FH-40A | FH-40A |
| Reactor pressure decrease, MPa(30 days) | 0.10 | 0.12 |
| Reactor pressure decrease, MPa(60 days) | 0.10 | 0.20 |
| Reactor pressure decrease, MPa(90 days) | 0.10 | 0.28 |
| Reactor pressure decrease, MPa(100 days) | 0.10 | Stop work |
Can find out from above-mentioned contrast, the inventive method can solve the pressure drop rising problem of coking naphtha hydrogenation unit, can effectively extend the running period of hydrogenation unit.
Catalytic cracking heavy naphtha selective hydrogenation desulfurization process.Catalytic cracking petroleum naphtha adopts commodity AFS-12 catalyzer (University of Petroleum's production), at pressure 0.5MPa, 35 ℃～45 ℃ of temperature, volume space velocity 2.0h
-1, carry out deodorization under gas-oil ratio (air/gasoline) 4:1 condition.Deodorization product is through fractionation, and cut point is 70 ℃ and obtains catalytic cracking heavy naphtha, and catalytic cracking heavy naphtha mixes through process furnace and is heated to 250 ℃ with hydrogen, enters hydrogenator after entering decoking tank decoking.Hydrogenation catalyst FGH-11 is the business catalyst for selectively hydrodesulfurizing of Sinopec Fushun Petrochemical Research Institute development and production.Feedstock property is in table 3, operational condition and the results are shown in Table 4.The difference of comparative example is not for arranging decoking tank.
Table 3 catalytic cracking heavy naphtha main character.
| Raw material | The last running of catalytic cracking petroleum naphtha |
| Sulphur content, μ g/g | 900 |
| Olefin(e) centent, v% | 22 |
| Research octane number (RON), RON | 91.0 |
| Boiling range, ℃ (initial boiling point～final boiling point) | 58～179 |
Table 4 operational condition and result.
| ? | |
Comparative example 2 |
| Reaction hydrogen pressure, MPa | 1.6 | 1.6 |
| Hydrogen to oil volume ratio | 300:1 | 300:1 |
| Volume space velocity, h -1 | 2.0 | 2.0 |
| Reactor inlet temperature, ℃ | 250 | 250 |
| Hydrogenation catalyst | FGH-11 | FGH-11 |
| Reactor pressure decrease, MPa(5 days) | 0.09 | 0.15 |
| Reactor pressure decrease, MPa(10 days) | 0.09 | 0.20 |
| Reactor pressure decrease, MPa(20 days) | 0.09 | Stop work |
| Reactor pressure decrease, MPa(50 days) | 0.09 | ? |
Virgin naphtha is hydrogenated in advance catalytic reforming and supplies raw materials.Virgin naphtha mixes through process furnace and is heated to 300 ℃ with hydrogen, enters hydrogenator after entering decoking tank decoking.Hydrogenation catalyst FH-40C is the business Hydrobon catalyst of Sinopec Fushun Petrochemical Research Institute development and production.Feedstock property is in table 5, operational condition and the results are shown in Table 6.The difference of comparative example is not for arranging decoking tank.
Table 5 virgin naphtha main character.
| Raw material | Virgin naphtha |
| Source | Mix virgin naphtha |
| Density (20 ℃), g/cm 3 | 0.7348 |
| Sulphur content, μ g/g | 800 |
| Nitrogen content, μ g/g | 2.8 |
Table 6 operational condition and result.
| | Embodiment | 3 | Comparative example 3 |
| Reaction pressure, MPa | 1.6 | 1.6 | |
| Temperature of reaction, ℃ | 300 | 300 | |
| Volume space velocity, h -1 | 6.0 | 6.0 | |
| Hydrogen-oil ratio, Nm 3/m 3 | 100 | 100 | |
| Oil property | Treated oil | Treated oil | |
| Sulphur content, μ g/g | <0.5 | <0.5 | |
| Nitrogen content, μ g/g | <0.5 | <0.5 | |
| Hydrogenation catalyst | FH-40C | FH-40C | |
| Reactor pressure decrease, MPa(30 days) | 0.11 | 0.15 | |
| Reactor pressure decrease, MPa(60 days) | 0.11 | 0.20 | |
| Reactor pressure decrease, MPa(100 days) | 0.11 | 0.26 | |
| Reactor pressure decrease, MPa(120 days) | 0.11 | Stop work |
Can find out by embodiment, by using the decoking tank of suitable structure, the pressure drop of petroleum naphtha hydrogenation reactor is not risen substantially, can estimate, within catalyzer work-ing life, can not stop work because of problem of pressure drop.
Claims (9)
1. a petroleum naphtha hydrogenation method, is characterized in that comprising the steps:
(1) mixture of feed naphtha and hydrogen is heated to the required temperature of hydrofining in process furnace;
(2) feed naphtha after heating and the mixture of hydrogen enter decoking tank;
(3) enter fixed bed hydrogenation reactor through feed naphtha and the hydrogen of decoking tank decoking, feed naphtha and hydrogen are by the Hydrobon catalyst bed of fixed bed hydrogenation reactor under hydrofining condition, and the petroleum naphtha after hydrofining separates and obtains hydrotreated naphtha with hydrogen discharge reactor;
Decoking tank wherein comprises cylindrical shell, upper cover, lower cover and separation assembly, cylindrical shell and upper cover, lower cover forms decoking tank shell jointly, upper cover top arranges material inlet, lower cover bottom arranges material discharging hole, separation assembly structure is the vertical filtering separation assembly that is arranged on inner barrel one side, vertical filtering separation assembly is made up of the incrustation agent of filling between two-layer screen cloth and two-layer screen cloth, the both sides of vertical filtering separation assembly and decoking tank cylinder inboard wall are sealedly and fixedly connected, the top of vertical filtering separation assembly arranges cover plate, vertical filtering separation assembly, the space that cover plate and decoking tank cylindrical shell form is for going out passage except defocused streams, on the above-mentioned decoking tank cylindrical shell that goes out passage except defocused streams, material outlet is set, except defocused material is discharged decoking tank from this material outlet.
2. in accordance with the method for claim 1, it is characterized in that: feed naphtha is virgin naphtha, coking naphtha, catalytic cracking petroleum naphtha, cracking naphtha, or the mixture of two or more petroleum naphtha.
3. in accordance with the method for claim 1, it is characterized in that: the refining condition of petroleum naphtha hydrogenation is that reactor inlet temperature is 180～350 ℃, and reaction pressure is 0.5～12MPa, when the liquid of feed naphtha, volume space velocity is 0.5～20h
-1, hydrogen to oil volume ratio is 50:1～1500:1.
4. in accordance with the method for claim 1, it is characterized in that: in decoking tank, vertical filtering separation assembly is straight plate structure, or arc plate structure.
5. according to the method described in claim 1 or 4, it is characterized in that: decoking tank is divided into two portions by vertical filtering separation assembly, a part is material flow pass after filtering, a part of Wei Chenjiao district in addition, and after filtering, the ratio of the cross-sectional area in material flow pass Yu Chenjiao district is 1:9～5:5.
6. in accordance with the method for claim 1, it is characterized in that: the height of vertical filtering separation assembly and decoking tank cylindrical shell are contour vertical filtering separation assembly bottom opening or sealing.
7. it is characterized in that in accordance with the method for claim 1: the incrustation agent of filling in the middle of vertical filtering separation assembly screen cloth is the filler of particle diameter 1.1～3mm.
8. in accordance with the method for claim 7, it is characterized in that: the material of filler is aluminum oxide, silicon oxide, pottery, or make spent hydroprocessing catalyst or useless hydrogenation catalyst, the thickness of filler is 10～200mm.
9. in accordance with the method for claim 1, it is characterized in that: ash mouthful is let out in the bottom head setting of decoking tank, and cylindrical shell bottom, decoking Guan Chenjiao district arranges ash blowing mouth.
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2011
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| US4343693A (en) * | 1979-10-01 | 1982-08-10 | Phillips Petroleum Company | Method of removing contaminant from a feedstock stream |
| CN2414824Y (en) * | 2000-03-01 | 2001-01-17 | 华中理工大学 | Collision inertia separator |
| CN101376828A (en) * | 2007-08-27 | 2009-03-04 | 中国石油化工股份有限公司 | Hydrofinishing method for coker gasoline |
| CN101352634A (en) * | 2008-09-26 | 2009-01-28 | 隆鑫工业有限公司 | Air filter |
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