CN108559010A - A kind of process units of F- T synthesis olefinic polymerization production polyalphaolefin - Google Patents

A kind of process units of F- T synthesis olefinic polymerization production polyalphaolefin Download PDF

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CN108559010A
CN108559010A CN201810304521.4A CN201810304521A CN108559010A CN 108559010 A CN108559010 A CN 108559010A CN 201810304521 A CN201810304521 A CN 201810304521A CN 108559010 A CN108559010 A CN 108559010A
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polyalphaolefin
carbon
rectifying column
alkene
synthesis
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CN108559010B (en
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刘辰
孟永建
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He Run Technology Co Ltd
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He Run Technology Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/04Reduction, e.g. hydrogenation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/04Purification; Separation; Use of additives by distillation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F110/00Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F110/14Monomers containing five or more carbon atoms
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Abstract

A kind of process units of F- T synthesis olefinic polymerization production polyalphaolefin, is related to a kind of polyalphaolefin process units, ten Alkyl distillation tower of carbon(4), ten alkene rectifying column of carbon(5), polymer reactor(6), hydrogenation reactor(10), oligomer rectifying column(12), molecular sieve treater(15), catalyst recycling can(17)With polyalphaolefin rectifying column(20)Between by suitably combining connection;The present invention removes water F- T synthesis alkene using molecular sieve treater, ten Alkyl distillation tower of carbon, ten alkene rectifying column of carbon purify F- T synthesis alkene to obtain ten alkene of carbon, catalyst boron trifluoride, which is added, makes ten alkene of carbon be converted into polyalphaolefin, hydrogenation catalyst, which is added, makes hydrogen and polyalphaolefin reaction be converted into saturation polyalphaolefin, oligomer is detached by oligomer rectifying column, three kinds of different polyalphaolefins of viscosity are obtained by polyalphaolefin rectifying column.

Description

A kind of process units of F- T synthesis olefinic polymerization production polyalphaolefin
【Technical field】
The present invention relates to a kind of polyalphaolefin process units, and polyalphaolefin is produced more particularly, to a kind of F- T synthesis olefinic polymerization Process units.
【Background technology】
F- T synthesis alkene is that coal is made by indirect liquefaction, is produced with n-alkane, alhpa olefin liquid coal liquifaction as main component Product.The main component of F- T synthesis alkene be 60% light dydrocarbon to the alhpa olefin of carbon 16,30%-35% light dydrocarbon to 16 positive structure of carbon Alkane, a small amount of isoparaffin, cycloalkane and isomeric olefine, impurity grade for minor amount of water.With the development of coal liquifaction technology, I The production capacity of state's F- T synthesis alkene just improves year by year, has preferable warp using the alkene as the raw material for preparing polyalphaolefin Ji property.
Polyalphaolefin(PAO)It is the base oil of fully synthetic lubricating oil, is widely used in high-end lubricating area, is by carbon ten Linear alpha olefin(The 1- last of the ten Heavenly stems is dilute)It is prepared by polymerization and hydrogenation technique;General import alhpa olefin is by ethylene oligomerization method in the world It prepares, higher price.China not yet grasps ethylene oligomerization technology, mainly by wax destructive distillation method produce alhpa olefin, positive structure content compared with Low, product quality is poor.
【Invention content】
In order to overcome the shortcomings of in background technology, the present invention discloses a kind of production of F- T synthesis olefinic polymerization production polyalphaolefin Device, the present invention remove water F- T synthesis alkene using molecular sieve treater, ten Alkyl distillation tower of carbon, ten alkene rectifying column pair of carbon F- T synthesis alkene is purified to obtain ten alkene of carbon, and catalyst boron trifluoride, which is added, makes ten alkene of carbon be converted into polyalphaolefin, adds Entering hydrogenation catalyst makes hydrogen and polyalphaolefin reaction be converted into saturation polyalphaolefin, is divided oligomer by oligomer rectifying column From obtaining three kinds of different polyalphaolefins of viscosity by polyalphaolefin rectifying column.
In order to realize that the goal of the invention, the present invention adopt the following technical scheme that:
A kind of process units of F- T synthesis olefinic polymerization production polyalphaolefin, including ten Alkyl distillation tower of carbon, ten alkene rectifying of carbon Tower, polymer reactor, hydrogenation reactor, oligomer rectifying column, molecular sieve treater, catalyst recycling can and polyalphaolefin rectifying Tower, F- T synthesis alkene import are located at the top of molecular sieve treater, and the outlet that molecular sieve treater bottom is equipped with passes through pipeline The entrance being equipped in the middle part of ten Alkyl distillation tower of connection carbon, ten alkane of carbon and more light fraction outlet are located at the top of ten Alkyl distillation tower of carbon End, the outlet that ten Alkyl distillation tower bottom of carbon is equipped with pass through the entrance being equipped in the middle part of ten alkene rectifying column of piping connection carbon, carbon ten One alkane and more recombination sub-export are located at the bottom of ten alkene rectifying column of carbon, and the outlet being equipped at the top of ten alkene rectifying column of carbon passes through The entrance being equipped in the middle part of piping connection polymer reactor, catalyst boron trifluoride entrance are located at the top of polymer reactor, polymerize The outlet that reactor bottom is equipped with passes through the entrance being equipped in the middle part of piping connection catalyst recycling can, the outlet of catalyst boron trifluoride Positioned at the top of catalyst recycling can, the outlet that catalyst recycling pot bottom is equipped at the top of piping connection hydrogenation reactor by setting Some entrances, the outlet that hydrogenation reactor bottom is equipped with pass through the entrance being equipped in the middle part of piping connection oligomer rectifying column, hydrogen Entrance is located at the bottom of hydrogenation reactor, and positioned at the top of oligomer rectifying column, oligomer rectifier bottoms are set for oligomer outlet Some exports the entrance being equipped with by piping connection polyalphaolefin rectifying column middle and lower part, and the outlet of polyalphaolefin four is located at polyalphaolefin essence The top of tower is evaporated, the outlet of polyalphaolefin ten is located at polyalphaolefin essence positioned at the middle part of polyalphaolefin rectifying column, the outlet of polyalphaolefin 20 Evaporate the bottom of tower.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, in ten alkane of molecular sieve treater and carbon The pipeline between ten alkene rectifying column of pipeline, ten Alkyl distillation tower of carbon and carbon, ten alkene rectifying column of carbon between rectifying column and poly- Close pipeline, catalyst recycling can and the hydrogenation reaction between pipeline, polymer reactor and the catalyst recycling can between reactor Pipeline, oligomer rectifying column and polyalphaolefin rectifying column between pipeline, hydrogenation reactor between device and oligomer rectifying column it Between pipeline on be respectively equipped with delivery pump.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, in the pipeline of F- T synthesis alkene import It is equipped with regulating valve, vacuum pump is equipped on the pipeline of catalyst boron trifluoride outlet.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, molecular sieve treater is 3A or 4A molecules Sieve.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, ten Alkyl distillation tower of carbon, carbon ten alkene essence It is respectively regular stainless steel helices tower or ligulate float valve plate column, effective plate number 60-80 to evaporate tower and polyalphaolefin rectifying column.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, polymer reactor are that turbine fan leaf type stirs Mix kettle.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, catalyst recycling can is regular stainless steel Pressurized tank.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, hydrogenation reactor are solid for stainless steel autoclave Hydrogenation catalyst is filled at fixed bed reactor, middle part, and catalyst is platinum base hydrogenation catalyst.
The process units of the F- T synthesis olefinic polymerization production polyalphaolefin, oligomer rectifying column is regular stainless steel Packed tower or ligulate float valve plate column, effective plate number 45-60.
By adopting the above-described technical solution, the present invention has the advantages that:
The process units of F- T synthesis olefinic polymerization production polyalphaolefin of the present invention, the present invention use molecular sieve treater F- T synthesis alkene is removed water, ten Alkyl distillation tower of carbon, ten alkene rectifying column of carbon are purified to obtain carbon to F- T synthesis alkene Ten alkene, catalyst boron trifluoride, which is added, makes ten alkene of carbon be converted into polyalphaolefin, and hydrogenation catalyst, which is added, makes hydrogen and poly- α alkene Hydrocarbon reaction is converted into saturation polyalphaolefin, detaches oligomer by oligomer rectifying column, three are obtained by polyalphaolefin rectifying column The different polyalphaolefin of kind viscosity;The advantageous effect that the present invention has reasonable design, technique unique, energy-saving, environmentally protective.
【Description of the drawings】
Fig. 1 is the structural diagram of the present invention.
In figure:1, F- T synthesis alkene import;2, regulating valve;3, ten alkane of carbon and more light fraction outlet;4, ten alkane of carbon Rectifying column;5, ten alkene rectifying column of carbon;6, polymer reactor;7, catalyst boron trifluoride entrance;8, catalyst boron trifluoride goes out Mouthful;9, vacuum pump;10, hydrogenation reactor;11, oligomer exports;12, oligomer rectifying column;13, polyalphaolefin four exports;14、 Polyalphaolefin ten exports;15, molecular sieve treater;16, carbon hendecane hydrocarbon and sub-export is more recombinated;17, catalyst recycling can;18、 Hydrogen inlet;19, delivery pump;20, polyalphaolefin rectifying column;21, polyalphaolefin 20 exports.
【Specific implementation mode】
The present invention can be explained in more detail by the following examples, the invention is not limited in the following examples, open The purpose of the present invention is intended to all changes and improvements in the protection scope of the invention;
The process units of F- T synthesis olefinic polymerization production polyalphaolefin in conjunction with described in attached drawing 1, including ten Alkyl distillation tower 4 of carbon, Ten alkene rectifying column 5 of carbon, polymer reactor 6, hydrogenation reactor 10, oligomer rectifying column 12, molecular sieve treater 15, catalyst Recycling can 17 and polyalphaolefin rectifying column 20, F- T synthesis alkene import 1 are located at the top of molecular sieve treater 15, molecular sieve essence The entrance that the outlet that 15 bottom of device processed is equipped with is equipped with by the middle part of ten Alkyl distillation tower of piping connection carbon 4, ten alkane of carbon and lighter Group sub-export 3 is located at the top of ten Alkyl distillation tower 4 of carbon, and the outlet that ten Alkyl distillation tower of carbon, 4 bottom is equipped with passes through piping connection The entrance that ten alkene rectifying column of carbon, 5 middle part is equipped with, carbon hendecane hydrocarbon and more recombination sub-export 16 are located at ten alkene rectifying column 5 of carbon Bottom, the entrance that the outlet that ten alkene rectifying column of carbon, 5 top is equipped with is equipped with by 6 middle part of piping connection polymer reactor, catalysis Agent boron trifluoride entrance 7 is located at the top of polymer reactor 6, and the outlet that 6 bottom of polymer reactor is equipped with is urged by piping connection The entrance that 17 middle part of agent recycling can is equipped with, catalyst boron trifluoride outlet 8 are located at the top of catalyst recycling can 17, catalyst The entrance that the outlet that 17 bottom of recycling can is equipped with is equipped with by 10 top of piping connection hydrogenation reactor, 10 bottom of hydrogenation reactor The entrance that the outlet being equipped with is equipped with by 12 middle part of piping connection oligomer rectifying column, hydrogen inlet 18 are located at hydrogenation reactor 10 Bottom, oligomer outlet 11 be located at oligomer rectifying column 12 tops, the outlet that 12 bottom of oligomer rectifying column is equipped with passes through The entrance that 20 middle and lower part of piping connection polyalphaolefin rectifying column is equipped with, the outlet of polyalphaolefin four 13 are located at polyalphaolefin rectifying column 20 Top, the outlet of polyalphaolefin ten 14 are located at the middle part of polyalphaolefin rectifying column 20, and the outlet of polyalphaolefin 20 21 is located at polyalphaolefin essence Evaporate the bottom of tower 20, molecular sieve treater 15 is 3A or 4A molecular sieves, ten Alkyl distillation tower 4 of carbon, ten alkene rectifying column 5 of carbon and poly- Alhpa olefin rectifying column 20 is respectively regular stainless steel helices tower or ligulate float valve plate column, effective plate number 60-80, polymerisation Device 6 is turbine fan leaf type stirred tank, and catalyst recycling can 17 is regular stainless steel pressure tank, and hydrogenation reactor 10 is stainless steel kettle Formula fixed bed reactors, middle part fill hydrogenation catalyst, catalyst be platinum base hydrogenation catalyst, oligomer rectifying column 12 be it is regular not Stainless steel helices tower or ligulate float valve plate column, effective plate number 45-60, in ten Alkyl distillation tower 4 of molecular sieve treater 15 and carbon Between ten alkene rectifying column 5 of pipeline, ten Alkyl distillation tower 4 of carbon and carbon between pipeline, ten alkene rectifying column 5 of carbon and polymerization it is anti- It answers the pipeline between pipeline, polymer reactor 6 and the catalyst recycling can 17 between device 6, catalyst recycling can 17 and adds hydrogen anti- Answer pipeline, oligomer rectifying column 12 and the poly- α alkene between pipeline, hydrogenation reactor 10 and the oligomer rectifying column 12 between device 10 It is respectively equipped with delivery pump 19 on pipeline between hydrocarbon rectifying column 20, regulating valve is equipped on the pipeline of F- T synthesis alkene import 1 2, it is equipped with vacuum pump 9 on the pipeline of catalyst boron trifluoride outlet 8.
The process units for implementing F- T synthesis olefinic polymerization production polyalphaolefin of the present invention, in use, F- T synthesis Alkene enters molecular sieve treater 15 from F- T synthesis alkene import 1, by the moisture in F- T synthesis alkene under 25 DEG C, normal pressure Content is down to 10ppm or less;
F- T synthesis alkene comes out from 15 bottom of molecular sieve treater, will be most of after entering from ten Alkyl distillation tower of carbon, 4 middle part Ten alkane of carbon and more light fraction outlet 3 is separated that ten alkane of carbon and more light component are equipped with from tower top, it is 99.5% to obtain purity Above ten alkene of carbon and more heavy constituent make ten alkane of carbon and more light component content be less than 0.5%;
Ten alkene of carbon and more heavy constituent that purity is 99.5% or more come out from ten Alkyl distillation tower of carbon, 4 bottom, from carbon ten alkene essence It evaporates and separates carbon hendecane hydrocarbon that most of carbon hendecane hydrocarbon and more heavy constituent are equipped with from bottom of tower and more recombination after the middle part of tower 5 enters Mouth 16 is separated, and is obtained ten alkene of carbon that purity is 99% or more, is made ten alkane of carbon and more light component content less than 0.5%, carbon Hendecane hydrocarbon and more heavy constituent content are less than 0.5%;
Ten alkene of carbon that purity is 99% or more comes out from ten alkene rectifying column of carbon, 5 top, enters from the middle part of polymer reactor 6 Afterwards, boron trifluoride is added in the catalyst boron trifluoride entrance 7 being equipped with from the top of polymer reactor 6,50 DEG C, 0.2Mpa, stirring Under conditions of 200 revs/min of rotating speed, catalyst boron trifluoride is catalyzed ten alkene of carbon, and ten alkene of carbon is made to react, warp 5 hours are spent, ten olefin conversion of carbon is not less than 98%, and it is low to obtain polyalphaolefin, a small amount of polyalphaolefin that product is 95% or more purity The mixture of polymers, a small amount of ten alkene of unreacted carbon and the micro boron trifluoride for being dissolved in liquid phase;
The polyalphaolefin of 95% or more purity, a small amount of polyalphaolefin oligomer, a small amount of ten alkene of unreacted carbon and micro it is dissolved in liquid phase The mixture of boron trifluoride come out from 6 bottom of polymer reactor, after entering from 17 middle part of catalyst recycling can, open setting and exist The vacuum pump 9 that the catalyst boron trifluoride outlet 8 at 17 top of catalyst recycling can is equipped with, pressure inside the tank are -0.2Mpa, temperature It 50 DEG C, by the boron triflouride gas being blended on a small quantity in polyalphaolefin by 8 separation and recovery of catalyst boron trifluoride outlet, is produced Product are the polyalphaolefin, a small amount of polyalphaolefin oligomer, ten alkene mixture of a small amount of unreacted carbon of 95% or more purity, borontrifluoride Boron content is less than 10ppm;
The polyalphaolefin of 95% or more purity, a small amount of polyalphaolefin oligomer, a small amount of ten alkene mixture of unreacted carbon are from catalyst 17 bottom of recycling can comes out, and after entering from 10 top of hydrogenation reactor, the hydrogen that hydrogen is equipped with from 10 bottom of hydrogenation reactor enters Mouth 18 enters, and hydrogen and polyalphaolefin, polyalphaolefin oligomer, ten alkene mixture of unreacted carbon are reacted, and reaction stops Time is 2 hours, is continually fed into hydrogen, keeps pressure 5.0Mpa, and 300 DEG C of temperature, hydrogen is all consumed after reaction, reaction production Object is saturation polyalphaolefin, a small amount of saturation polyalphaolefin oligomer and ten alkane of a small amount of carbon;
Saturation polyalphaolefin, a small amount of saturation polyalphaolefin oligomer and ten alkane of a small amount of carbon come out from 10 bottom of hydrogenation reactor, from It after 12 middle part of oligomer rectifying column enters, is detached at 200 DEG C of temperature, normal pressure, by saturation polyalphaolefin oligomer and carbon ten The oligomer outlet 11 that alkane is equipped with from 12 top of oligomer rectifying column is separated, and it is saturation polyalphaolefin, impurity to obtain product Content is negligible;
Saturation polyalphaolefin comes out from 12 bottom of oligomer rectifying column, after entering from 20 middle and lower part of polyalphaolefin rectifying column, according to evaporating The polyalphaolefin that content is 30%-40% is isolated in Cheng Butong, the outlet of polyalphaolefin four 13 being equipped with from 20 top of polyalphaolefin rectifying column Four, the outlet of polyalphaolefin ten 14 being equipped with from the middle part of polyalphaolefin rectifying column 20 isolate polyalphaolefin ten that content is 45%-55%, Isolate the polyalphaolefin 20 that content is 10%-20% in the outlet of polyalphaolefin 20 21 being equipped with from 20 bottom of polyalphaolefin rectifying column.
Part not in the detailed description of the invention is the prior art.

Claims (9)

1. a kind of process units of F- T synthesis olefinic polymerization production polyalphaolefin, including ten Alkyl distillation tower of carbon(4), ten alkene of carbon Hydrocarbon rectifying column(5), polymer reactor(6), hydrogenation reactor(10), oligomer rectifying column(12), molecular sieve treater(15), urge Agent recycling can(17)With polyalphaolefin rectifying column(20), it is characterized in that:F- T synthesis alkene import(1)It is refined positioned at molecular sieve Device(15)Top, molecular sieve treater(15)The outlet that bottom is equipped with passes through ten Alkyl distillation tower of piping connection carbon(4)Middle part The entrance being equipped with, ten alkane of carbon and more light fraction outlet(3)Positioned at ten Alkyl distillation tower of carbon(4)Top, ten Alkyl distillation of carbon Tower(4)The outlet that bottom is equipped with passes through ten alkene rectifying column of piping connection carbon(5)The entrance that middle part is equipped with, carbon hendecane hydrocarbon and more Recombinate sub-export(16)Positioned at ten alkene rectifying column of carbon(5)Bottom, ten alkene rectifying column of carbon(5)The outlet that top is equipped with passes through Piping connection polymer reactor(6)The entrance that middle part is equipped with, catalyst boron trifluoride entrance(7)Positioned at polymer reactor(6)'s Top, polymer reactor(6)The outlet that bottom is equipped with passes through piping connection catalyst recycling can(17)The entrance that middle part is equipped with, is urged Agent boron trifluoride exports(8)Positioned at catalyst recycling can(17)Top, catalyst recycling can(17)The outlet that bottom is equipped with Pass through piping connection hydrogenation reactor(10)The entrance that top is equipped with, hydrogenation reactor(10)The outlet that bottom is equipped with passes through pipeline Connect oligomer rectifying column(12)The entrance that middle part is equipped with, hydrogen inlet(18)Positioned at hydrogenation reactor(10)Bottom, it is oligomeric Object exports(11)Positioned at oligomer rectifying column(12)Top, oligomer rectifying column(12)The outlet that bottom is equipped with is connected by pipeline Connect polyalphaolefin rectifying column(20)The entrance that middle and lower part is equipped with, polyalphaolefin four export(13)Positioned at polyalphaolefin rectifying column(20)'s Top, polyalphaolefin ten export(14)Positioned at polyalphaolefin rectifying column(20)Middle part, polyalphaolefin 20 export(21)Positioned at poly- α Alkene rectifying column(20)Bottom.
2. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:Dividing Son sieve treater(15)With ten Alkyl distillation tower of carbon(4)Between pipeline, ten Alkyl distillation tower of carbon(4)With ten alkene rectifying column of carbon (5)Between pipeline, ten alkene rectifying column of carbon(5)And polymer reactor(6)Between pipeline, polymer reactor(6)And catalysis Agent recycling can(17)Between pipeline, catalyst recycling can(17)And hydrogenation reactor(10)Between pipeline, hydrogenation reactor (10)With oligomer rectifying column(12)Between pipeline, oligomer rectifying column(12)With polyalphaolefin rectifying column(20)Between pipe Road is respectively equipped with delivery pump(19).
3. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:Taking Support synthesis alkene import(1)Pipeline be equipped with regulating valve(2), exported in catalyst boron trifluoride(8)Pipeline be equipped with it is true Sky pump(9).
4. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:Molecule Sieve treater(15)For 3A or 4A molecular sieves.
5. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:Carbon ten Alkyl distillation tower(4), ten alkene rectifying column of carbon(5)With polyalphaolefin rectifying column(20)Respectively regular stainless steel helices tower or tongue Shape float valve plate column, effective plate number 60-80.
6. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:Polymerization Reactor(6)For turbine fan leaf type stirred tank.
7. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:Catalysis Agent recycling can(17)For regular stainless steel pressure tank.
8. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:Add hydrogen Reactor(10)For stainless steel autoclave fixed bed reactors, hydrogenation catalyst is filled at middle part, and catalyst is platinum base hydrogenation catalyst.
9. the process units of F- T synthesis olefinic polymerization production polyalphaolefin according to claim 1, it is characterized in that:It is oligomeric Object rectifying column(12)For regular stainless steel helices tower or ligulate float valve plate column, effective plate number 45-60.
CN201810304521.4A 2018-04-08 2018-04-08 Production device for producing poly alpha olefin by Fischer-Tropsch synthesis olefin polymerization Active CN108559010B (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111875725A (en) * 2020-06-17 2020-11-03 南京延长反应技术研究院有限公司 Micro-interface enhanced reaction system and method for preparing polyethylene by slurry method
CN111892673A (en) * 2020-06-17 2020-11-06 南京延长反应技术研究院有限公司 Micro-interface enhanced reaction system and method for preparing polypropylene
CN111909293A (en) * 2020-06-17 2020-11-10 南京延长反应技术研究院有限公司 Micro-interface enhanced reaction system and method for preparing poly-alpha-olefin
RU2815103C1 (en) * 2020-06-17 2024-03-11 Наньцзин Яньчан Реэкшн Текнолоджи Рисерч Институт Ко. Лтд SYSTEM FOR CARRYING OUT REACTION OF PRODUCING POLY α-OLEFIN

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102008007081A1 (en) * 2008-01-31 2009-08-06 Evonik Oxeno Gmbh Producing n-butene-oligomers and 1-butene from mixture-I made of hydrocarbons having four carbon atoms, comprises e.g. optionally washing the mixture to produce a mixture-II and removing 1,3-butadiene from mixture-I to produce a mixture-III
CN104003833A (en) * 2014-05-30 2014-08-27 神华集团有限责任公司 System for preparing low-carbon olefin by coal-based methanol
CN104370678A (en) * 2014-11-15 2015-02-25 太原理工大学 Comprehensive utilization method of olefin in Fischer-Tropsch-synthesized light distillate
CN104592426A (en) * 2014-12-24 2015-05-06 浙江大学 Method and device for polymerization of olefins
CN105062555A (en) * 2015-07-23 2015-11-18 中国科学院上海高等研究院 Method for synthesizing metallocene poly-alpha-olefin from alpha-olefin-prepared-from-coal as raw material
CN105647575A (en) * 2016-02-18 2016-06-08 惠生工程(中国)有限公司 Natural gasoline upgrading and utilizing technology

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102008007081A1 (en) * 2008-01-31 2009-08-06 Evonik Oxeno Gmbh Producing n-butene-oligomers and 1-butene from mixture-I made of hydrocarbons having four carbon atoms, comprises e.g. optionally washing the mixture to produce a mixture-II and removing 1,3-butadiene from mixture-I to produce a mixture-III
CN104003833A (en) * 2014-05-30 2014-08-27 神华集团有限责任公司 System for preparing low-carbon olefin by coal-based methanol
CN104370678A (en) * 2014-11-15 2015-02-25 太原理工大学 Comprehensive utilization method of olefin in Fischer-Tropsch-synthesized light distillate
CN104592426A (en) * 2014-12-24 2015-05-06 浙江大学 Method and device for polymerization of olefins
CN105062555A (en) * 2015-07-23 2015-11-18 中国科学院上海高等研究院 Method for synthesizing metallocene poly-alpha-olefin from alpha-olefin-prepared-from-coal as raw material
CN105647575A (en) * 2016-02-18 2016-06-08 惠生工程(中国)有限公司 Natural gasoline upgrading and utilizing technology

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
宋彩霞等: "煤制乙烯及乙烯聚合生产现状" *

Cited By (5)

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CN111875725A (en) * 2020-06-17 2020-11-03 南京延长反应技术研究院有限公司 Micro-interface enhanced reaction system and method for preparing polyethylene by slurry method
CN111892673A (en) * 2020-06-17 2020-11-06 南京延长反应技术研究院有限公司 Micro-interface enhanced reaction system and method for preparing polypropylene
CN111909293A (en) * 2020-06-17 2020-11-10 南京延长反应技术研究院有限公司 Micro-interface enhanced reaction system and method for preparing poly-alpha-olefin
CN111909293B (en) * 2020-06-17 2023-02-03 南京延长反应技术研究院有限公司 Micro-interface enhanced reaction system and method for preparing poly-alpha-olefin
RU2815103C1 (en) * 2020-06-17 2024-03-11 Наньцзин Яньчан Реэкшн Текнолоджи Рисерч Институт Ко. Лтд SYSTEM FOR CARRYING OUT REACTION OF PRODUCING POLY α-OLEFIN

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