CN105566029A - Method for reducing ethene device energy consumption - Google Patents
Method for reducing ethene device energy consumption Download PDFInfo
- Publication number
- CN105566029A CN105566029A CN201410542718.3A CN201410542718A CN105566029A CN 105566029 A CN105566029 A CN 105566029A CN 201410542718 A CN201410542718 A CN 201410542718A CN 105566029 A CN105566029 A CN 105566029A
- Authority
- CN
- China
- Prior art keywords
- oil
- tower
- quenching
- quenching oil
- energy consumption
- 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
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
The invention discloses a method for reducing ethene device energy consumption. The method comprises cooling pyrolysis gas from an outlet of a pyrolysis furnace through a quench cooler, feeding the cooled pyrolysis gas into an oil washing tower, carrying out substance separation, discharging quenching oil from the bottom of the oil washing tower, feeding a part of the quenching oil into the quench cooler, returning a part of the quenching oil back to the oil washing tower, feeding a part of the quenching oil into an extraction tower, carrying out solvent-based extraction, returning the material at the top of the extraction tower back to the oil washing tower and discharging an asphalt phase at the bottom of the extraction tower, wherein the solvent used in the extraction tower is pyrolysis gas from an outlet of an ethene device compressor.
Description
Technical field
The present invention relates to ethylene production field, furtherly, relate to a kind of method reducing ethylene unit energy consumption.
Background technology
At present, main ethylene unit adopts steam heat cracking technology to produce the basic organic chemical raw materials such as ethene, propylene, divinyl, aromatic hydrocarbons in the world.The raw materials such as lighter hydrocarbons, petroleum naphtha, hydrogenation tail oil and a certain proportion of dilution steam generation are blended in industrial pyrolysis furnace and scission reaction occur under hot conditions, and split product goes out the industrial chemicals such as ethene, propylene, divinyl through operation final production such as over-quenching, compression, separation.
Quenching system is the throat of ethylene unit, it is made up of equipment such as quencher, oil scrubber, water wash columns, carry the task of separating and cracking distillate (gasoline, diesel oil, oil fuel) component and recovery process water, simultaneously or in cracking process, reclaim the key equipment of heat.The splitting gas that the outlet of industrial pyrolysis furnace waste heat boiler comes is sent into bottom oil scrubber at quencher after quenching oil spraying cooling, after reflux cooling, light constituent in split product, from oil scrubber Base top contact, enters water wash column and continues to be cooled to about 40 DEG C, enter follow-up compression separation system.
Most of dilution steam generation required for cracking process all derives from the UTILIZATION OF VESIDUAL HEAT IN of device internal quench oil, and minority insufficient section is supplemented by pipe network steam.Oil scrubber bottom temperature is higher, steam generation more, and it is better that device by utilizing waste heat utilizes, and outer benefit steam consumption is fewer.Therefore the height of oil scrubber bottom temperature directly determines the size of waste heat recovery volume, and the energy consumption height of operation quality on ethylene unit of quenching system has important impact, thus also affects the production cost of device.
Ethylene unit quenching system is regarded as an entirety, inflow be split product, outflow be splitting gas and cracking distillate; Quenching oil, process water etc. are all at system internal recycle.Therefore ethylene unit quenching system runs well and will ensure two balances, heat balance, material balance.The heat that namely heat balance brings quenching system into by splitting gas will utilize by there is the heat exchange modes such as dilution steam generation.Material balance is relative complex then, because split product, after entering quenching system, the reactions such as polymerization can occur, changes, and quenching system needs the split product after change to discharge, and stablizes to keep component in quenching system.
Ethylene quenching system now practical problems is aborning exactly that oil scrubber bottom temperature is low, and quenching oil viscosity is high.Quenching oil bottom temperature is low, and dilution steam generation temperature difference of heat exchanger is little, dilution steam generation generating capacity wretched insufficiency, therefore needs a large amount of steam to fill into system; Quenching oil viscosity is high, and the power consumption of quenching oil circulation pump is high, causes ethylene unit energy consumption to remain high, also can cause parking by blocking pipeline when viscosity is too high.
The reason of ethylene quenching system problem is caused to be exactly that the bituminous matter generated in quenching oil cannot be discharged in time.In order to the splitting gas cooling produced to pyrolyzer, in quenching system, quenching oil circulates between quencher and oil wash tower reactor, it is per hour that its internal circulating load often reaches a few kiloton, and the extraction of cracking distillate only has tens tphs, quenching oil is detained for a long time in system, produce a large amount of bituminous matter, viscosity significantly raises.And in order to control quenching oil viscosity, the speed that oil wash bottom temperature generates to reduce bituminous matter can only be reduced.Reduce oil scrubber still temperature when pyrolyzer load is identical, quenching oil internal circulating load can be increased, to such an extent as to the time that quenching oil is detained in system is longer, turn increase the amount that bituminous matter produces.So oil wash bottom temperature can only be maintained about 180 DEG C in actual production, the bituminous matter generated in guarantee quenching oil and the bituminous matter of discharge balance each other, and maintain quenching oil stable viscosity.Oil scrubber tower reactor design temperature 210 DEG C that Here it is, can actual motion less than the basic reason of 190 DEG C.
At present, on full scale plant, employing adds modified thinning oil, adds viscosity depressant and use visbreaking tower three kinds of methods, to reduce oil scrubber bottom temperature for cost, can only control quenching oil viscosity reluctantly, cause ethylene unit energy consumption to remain high.
First method adds modified thinning oil (Pyrolysis gas oil PGO) to reduce viscosity, and by a large amount of Pyrolysis gas oil PGO blending in quenching oil, its side effect is very large.First, the internal circulating load of Pyrolysis gas oil PGO in oil scrubber can be increased, strengthen the gas phase load in the middle part of oil scrubber tower reactor to tower, correspondingly reduce the processing power of oil scrubber; Secondly, containing a large amount of components such as vinylbenzene, naphthalene, indenes in Pyrolysis gas oil PGO, when they are along with quenching oil circulation time, polymkeric substance can be produced by polymerization reaction take place, and on the column plate accumulating in oil scrubber or filler, affect heat transfer and the mass transfer effect of column plate and filler, make tower pressure reduction increase, the processing power of tower declines; Again, due to the increase of Pyrolysis gas oil PGO internal circulating load, can component containing part diesel oil in the pyrolysis gasoline of tower top and the Pyrolysis fuel oil PFO of tower reactor extraction, have influence on the quality of pyrolysis gasoline and oil fuel, the operation of follow-up quenching water column time serious, can be made to worsen; Finally, because the amount of quenching oil is very large, therefore in order to reduce chilling oil viscosity, usual needs mix a large amount of Pyrolysis gas oil PGOs for a long time.Adopt in this way, cannot reduce bituminous matter growing amount, quenching oil viscosity generally can only control at 1000 ~ 2000mm
2/ s (50 DEG C), oil scrubber bottom temperature is without significantly improving.
Viscosity depressant is that research department and ethene patent business worked out the chemical agent of various applicable reduction quenching oil viscosity both at home and abroad in recent years, suppresses the activity of polyreaction free radical to realize visbreaking target by adding chemical assistant.CN101062880A proposes a kind of quench oil viscosity reductant be made up of stopper, dispersion agent and metal passivator, has the effect suppressing polymerization, prevent gathering and passivating metallic surfaces.Although add viscosity depressant to reduce bitum formation speed to a certain extent, quenching system is discharged without any help to bituminous matter, fundamentally cannot solve the problem that quenching oil viscosity is high and oil scrubber bottom temperature is low.In actual use, viscosity depressant is seldom used alone, and is all using visbreaking tower technology while, using viscosity depressant as supplementary means.
Visbreaking tower technology be the quenching oil will exported from quenching oil circulation pump, under the control of temperature control valve (TCV), with Control for Pyrolysis Furnace Area come ethane cracking gas contact in nozzle mixer, the light constituent in quenching oil is vaporized, and enters visbreaking tower with splitting gas.The light constituent of vaporizing in ethane cracking gas and quenching oil enters oil scrubber tower reactor from visbreaking tower tower top, and the heavy liquid phase component of not vaporizing enters visbreaking tower tower reactor, outputs to tank field as byproduct (Pyrolysis fuel oil PFO).Like this, fractionate out from quenching oil selectively containing more bitum heavier feeds and light material is stayed in systems in which, the light component concentration in quench oil circulated is increased, thus reducing quenching oil viscosity.But in fact, the light constituent below this temperature, at 250-290 DEG C, can only be returned oil scrubber, have a large amount of low viscous component in the oil fuel of discharge by visbreaking tower tower top temperature, the efficiency of discharging pitch is low.Meanwhile, because quenching oil will contact with the ethane stove splitting gas of about 500 DEG C, at high temperature stop and add quenching oil studies on asphaltene growing amount, negative impact is caused to quenching oil viscosity.In actual motion, oil scrubber bottom temperature can only be limited in about 180 DEG C, just can control quenching oil viscosity.
Prior art is owing to cannot effectively discharge the bituminous matter generated in quenching oil, and the temperature that can only reduce oil scrubber tower reactor, to control quenching oil viscosity, considerably increases ethylene unit energy consumption.Especially, cracking stock progressively lighting in recent years, because the Pyrolysis fuel oil PFO produced is little, namely under identical internal circulating load, output is less, and that is quenching oil residence time in system is longer, and the bituminous matter of generation is more, that can discharge is less, makes prior art substantially lose effect.Therefore, be badly in need of a kind of technology of exploitation, reduce quenching oil viscosity, improve quenching oil column bottom temperature, reduce ethylene unit comprehensive energy consumption.
Summary of the invention
For solving problems of the prior art, the invention provides a kind of method reducing ethylene unit energy consumption.Chilling oil viscosity is reduced by solvent extraction, by improving oil scrubber bottom temperature to improve quenching oil temperature, and then increase dilution steam generation output, with the splitting gas of compressor outlet for solvent, reduce solvent consumption and compression power consumption, reduce the comprehensive energy consumption of ethylene unit.
The object of this invention is to provide a kind of above-mentioned method reducing ethylene unit energy consumption, it is characterized in that, the splitting gas that pyrolyzer outlet comes sends into oil scrubber after quencher cooling, carries out separating substances, at the bottom of oil scrubber tower, draw quenching oil, part quenching oil is sent to quencher; Part quenching oil returns oil scrubber; Part quenching oil enters extraction tower and carries out solvent extraction, and extraction tower tower top material returns oil scrubber, and extraction tower materials at bottom of tower pitch is drawn mutually, the splitting gas that the solvent that wherein extraction tower uses exports for ethylene device compressor.
Oil scrubber bottom temperature of the present invention brings up to 190-250 DEG C, preferably brings up to 195-235 DEG C.
During extraction tower solvent extraction, the weight ratio of solvent and quenching oil is 0.01-20, is preferably 0.5-5; Extraction tower pressure is 0.5MPa-10MPa, and the temperature of extraction tower is 0 DEG C-250 DEG C.
Described quenching oil is the oil distillate of oil scrubber tower reactor in ethylene unit quenching system, and its typical composition is polycyclic aromatic hydrocarbons, colloid, bituminous matter.Described ethylene unit primarily of industrial pyrolysis furnace and chilling, compression, the System's composition such as to be separated, quenching system mainly comprises quencher, oil scrubber, water wash column.
Method of the present invention specifically can by the following technical solutions:
The Pintsch process gas that pyrolyzer 1 exports (contains from H
2to compositions such as Pyrolysis fuel oil PFOs, also comprise dilution steam generation), after waste heat boiler reclaims heat and be cooled, enter quencher 2, directly contact with quenching oil, cool.Cooled splitting gas enters oil scrubber 3 together with quenching oil, carries out gas-oil separation.The splitting gas that oil scrubber tower top is drawn enters after water wash column 4 is separated with water, is separated into various hydrocarbon products through compression system 5 and separation system 6.The quench oil circulated that oil scrubber tower reactor is drawn, enters Dilution steam generator 11, produces dilution steam generation.Improve quench oil circulated temperature by improving ethylene unit quenching system oil scrubber 3 bottom temperature mode, thus improve the generating capacity of dilution steam generation.
Be divided into three tunnels after quench oil circulated is cooled, pyrolyzer quencher 2 is removed on a road; One tunnel returns oil scrubber again through process water preheater 12, after topping-up pump 10 of leading up to pressurization, enters the quenching oil opening for feed of extraction tower 7.
Drawing one decomposition under high pressure gas from ethylene unit compression system is solvent, enter the solvent feed mouth of extraction tower 7, solvent and quenching oil implement extracting in extraction tower 7, the extract oil (mixture of solvent and quenching oil light constituent) obtained is drawn from the extract oil outlet at extraction tower top, and the heeltap green grass or young crops of taking out obtained is drawn from the asphalt outlet bottom extraction tower.
Extract oil, after reducing valve 8 reduces pressure, through interchanger 9 raised temperature, returns oil scrubber 3, reduces overall quenching oil viscosity.
The present invention increases dilution steam generation steam exhaling amount by improving oil scrubber bottom temperature, quenching oil viscosity is reduced by solvent extraction diasphaltene, and by with ethylene unit compression system decomposition under high pressure gas out for solvent, reduce compression power consumption, improve ethylene unit heat recovery efficiency, reduce the energy consumption of ethylene unit.
Accompanying drawing explanation
Fig. 1 system schematic of the present invention
Description of reference numerals:
1 pyrolyzer, 2 quenchers, 3 oil scrubbers, 4 water wash columns, 5 compression systeies, 6 separation systems, 7 extraction towers, 8 reducing valve, 9 preheaters, 10 topping-up pumps, 11 Dilution steam generators, 12 preheaters.
Embodiment
Below in conjunction with embodiment, further illustrate the present invention.
Embodiment:
200kt/a produced per year by certain ethylene unit, and year runs 8000h, ethylene yield 25t/h.The Pintsch process gas of pyrolyzer outlet (contains from H
2to compositions such as Pyrolysis fuel oil PFOs, also comprise dilution steam generation), after waste heat boiler reclaims heat and be cooled, total amount is 147t/h, enters quencher, directly contacts, cools with quenching oil.Cooled splitting gas enters oil scrubber together with quenching oil, carries out gas-oil separation, bottom temperature 200 DEG C, and tower reactor draws quench oil circulated, enters Dilution steam generator, and produce dilution steam generation 41t/h, quench oil circulated total amount is 1200t/h.Three tunnels are divided into after quenching oil is cooled, pyrolyzer quencher is removed on one tunnel, one tunnel returns oil scrubber again through process water preheater, the quenching oil of one road 6t/h enters extraction tower quenching oil opening for feed, drawing one 6t/h splitting gas from compression system is solvent, by solvent extraction in extraction tower, bottom extraction tower, remove the heavy constituent 1.5t/h based on pitch.The extract oil step-down that extracting tower top obtains returns oil scrubber after heating up, and reducing quenching oil viscosity is 58.Ethylene unit energy consumption is 545GJ/h.
Comparative example
200kt produced per year by certain ethylene unit, year runs 8000h, ethylene yield 25t/h, and quenching system charging total amount is 147t/h, the quench oil circulated of drawing at the bottom of oil scrubber produces dilution steam generation by Dilution steam generator, then goes pyrolyzer quencher to return oil scrubber to after splitting gas cooling.Quenching oil viscosity 2000mm
2/ s, consume tempering oil 4t/h, oil scrubber bottom temperature is 178 DEG C, and generate dilution steam generation and only have 12t/h, ethylene unit energy consumption is 643GJ/h.
Claims (4)
1. reduce a method for ethylene unit energy consumption, it is characterized in that, the splitting gas that pyrolyzer outlet comes sends into oil scrubber after quencher cooling, carries out separating substances, and at the bottom of oil scrubber tower, draw quenching oil, part quenching oil is sent to quencher; Part quenching oil returns oil scrubber; Part quenching oil enters extraction tower and carries out solvent extraction, and extraction tower tower top material returns oil scrubber, and extraction tower materials at bottom of tower pitch is drawn mutually, the splitting gas that the solvent that wherein extraction tower uses exports for ethylene device compressor.
2. the method reducing ethylene unit energy consumption as claimed in claim 1, it is characterized in that, oil scrubber bottom temperature is 190-250 DEG C, preferred 195-235 DEG C.
3. the method reducing ethylene unit energy consumption as claimed in claim 1, it is characterized in that, the weight ratio of the solvent and quenching oil that enter extraction tower is 0.01-20, preferred 0.5-5.
4. the method reducing ethylene unit energy consumption as claimed in claim 1, it is characterized in that, the pressure of described extraction tower is 0.5MPa-10MPa, and tower top temperature is 0 DEG C-250 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410542718.3A CN105566029B (en) | 2014-10-14 | 2014-10-14 | A kind of method for reducing ethylene unit energy consumption |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410542718.3A CN105566029B (en) | 2014-10-14 | 2014-10-14 | A kind of method for reducing ethylene unit energy consumption |
Publications (2)
Publication Number | Publication Date |
---|---|
CN105566029A true CN105566029A (en) | 2016-05-11 |
CN105566029B CN105566029B (en) | 2017-09-29 |
Family
ID=55876745
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201410542718.3A Active CN105566029B (en) | 2014-10-14 | 2014-10-14 | A kind of method for reducing ethylene unit energy consumption |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105566029B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111320525A (en) * | 2020-03-02 | 2020-06-23 | 大连理工大学 | Non-low temperature separation process for ethylene-rich catalytic cracking gas |
CN114432844A (en) * | 2020-11-04 | 2022-05-06 | 中国石油化工股份有限公司 | Method and system for purifying pyrolysis gas |
WO2022166740A1 (en) * | 2021-02-02 | 2022-08-11 | 中国石油化工股份有限公司 | Cracked gas heat recovery apparatus and cracked gas heat recovery method |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103055260A (en) * | 2012-12-19 | 2013-04-24 | 范克锋 | Traditional Chinese medicine composition for treating ulcerative colitis and preparation method thereof |
CN103305258A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | Method for reducing viscosity of quenching oil of ethylene unit |
CN103305260A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | System and method for reducing viscosity of quenching oil of ethylene unit |
CN103305257A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | Method for reducing viscosity of quenching oil of ethylene unit |
CN103305259A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | Method for reducing viscosity of quenching oil of ethylene unit |
-
2014
- 2014-10-14 CN CN201410542718.3A patent/CN105566029B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103305258A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | Method for reducing viscosity of quenching oil of ethylene unit |
CN103305260A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | System and method for reducing viscosity of quenching oil of ethylene unit |
CN103305257A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | Method for reducing viscosity of quenching oil of ethylene unit |
CN103305259A (en) * | 2012-03-16 | 2013-09-18 | 中国石油化工股份有限公司 | Method for reducing viscosity of quenching oil of ethylene unit |
CN103055260A (en) * | 2012-12-19 | 2013-04-24 | 范克锋 | Traditional Chinese medicine composition for treating ulcerative colitis and preparation method thereof |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111320525A (en) * | 2020-03-02 | 2020-06-23 | 大连理工大学 | Non-low temperature separation process for ethylene-rich catalytic cracking gas |
CN114432844A (en) * | 2020-11-04 | 2022-05-06 | 中国石油化工股份有限公司 | Method and system for purifying pyrolysis gas |
CN114432844B (en) * | 2020-11-04 | 2023-05-12 | 中国石油化工股份有限公司 | Method and system for purifying pyrolysis gas |
WO2022166740A1 (en) * | 2021-02-02 | 2022-08-11 | 中国石油化工股份有限公司 | Cracked gas heat recovery apparatus and cracked gas heat recovery method |
Also Published As
Publication number | Publication date |
---|---|
CN105566029B (en) | 2017-09-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103305259B (en) | A kind of method reducing ethylene unit quenching oil viscosity | |
CN103305257B (en) | Method for reducing viscosity of quenching oil of ethylene unit | |
CN103305260B (en) | A kind of system and method reducing ethylene unit quenching oil viscosity | |
CN105154134B (en) | Method for preparing catalytic thermal cracking raw materials from full-fraction shale oil | |
CN103305258B (en) | Method for reducing viscosity of quenching oil of ethylene unit | |
CN105566029A (en) | Method for reducing ethene device energy consumption | |
CN102309863A (en) | Reduced pressure distillation method and device | |
CN105567290A (en) | Method for reducing ethene device energy consumption | |
CN105567292A (en) | Method for reducing ethene device energy consumption | |
CN105713647B (en) | A kind of utilization coal tar maximization prepares the method and device of carbolic oil and diesel oil | |
CN105567294A (en) | Method for reducing energy consumption of ethylene device | |
CN104449807B (en) | A kind of quenching oil extracting visbreaking system | |
CN103497782B (en) | Method of producing low-sulfur low freezing point diesel by full-range shale oil | |
CN105567295A (en) | Method for reducing energy consumption of ethylene device | |
CN105567291A (en) | Method for reducing ethene device energy consumption | |
CN101962565A (en) | Quench oil viscosity reducing process for two quench oil systems | |
CN101948698A (en) | Novel energy-saving device for condensing and recovering oil shale in retorting oil gas and method | |
CN105567296A (en) | Method for reducing energy consumption of ethylene device | |
CN104449820A (en) | System for reducing ethylene unit quenching oil viscosity and method for improving solvent recovery rate | |
CN105505436A (en) | Method for reducing energy consumption of ethylene device | |
CN105567293A (en) | Method for reducing ethene device energy consumption | |
CN104449827A (en) | System and method for reducing ethylene unit quenching oil viscosity | |
CN104449825B (en) | A kind of method reducing ethylene unit quenching oil viscosity and improve solvent recovering rate | |
CN104449826A (en) | Method for reducing ethylene unit quenching oil viscosity | |
CN104449808A (en) | System and method for reducing ethylene unit quenching oil viscosity |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |