WO2022132860A1 - Procédé de production d'alpha-oléfines - Google Patents

Procédé de production d'alpha-oléfines Download PDF

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Publication number
WO2022132860A1
WO2022132860A1 PCT/US2021/063446 US2021063446W WO2022132860A1 WO 2022132860 A1 WO2022132860 A1 WO 2022132860A1 US 2021063446 W US2021063446 W US 2021063446W WO 2022132860 A1 WO2022132860 A1 WO 2022132860A1
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reaction
reaction temperature
temperature
catalyst
oligomerization
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PCT/US2021/063446
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English (en)
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Glenn Charles Komplin
Heejae HUH
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Shell Oil Company
Shell Internationale Research Maatschappij Bv
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/001—Controlling catalytic processes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0006—Controlling or regulating processes
    • B01J19/002—Avoiding undesirable reactions or side-effects, e.g. avoiding explosions, or improving the yield by suppressing side-reactions
    • B01J19/0026—Avoiding carbon deposits
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08—Catalytic processes
    • C07C2/26—Catalytic processes with hydrides or organic compounds
    • C07C2/32—Catalytic processes with hydrides or organic compounds as complexes, e.g. acetyl-acetonates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08—Catalytic processes
    • C07C2/26—Catalytic processes with hydrides or organic compounds
    • C07C2/32—Catalytic processes with hydrides or organic compounds as complexes, e.g. acetyl-acetonates
    • C07C2/34—Metal-hydrocarbon complexes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008—Controlling the process
    • B01J2208/00654—Controlling the process by measures relating to the particulate material
    • B01J2208/00707—Fouling
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049—Controlling or regulating processes
    • B01J2219/00245—Avoiding undesirable reactions or side-effects
    • B01J2219/00247—Fouling of the reactor or the process equipment
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/582—Recycling of unreacted starting or intermediate materials

Definitions

  • the invention relates to a process for producing alpha-olefins by oligomerizing an ethylene feed.
  • Linear alpha olefins are a valuable comonomer for linear low-density polyethylene and high-density polyethylene.
  • Such olefins are also valuable as a chemical intermediate in the production of plasticizer alcohols, fatty acids, detergent alcohols, polyalphaolefins, oil field drilling fluids, lubricant oil additives, linear alkylbenzenes, alkenylsuccinic anhydrides, alkyldimethylamines, dialkylmethylamines, alpha-olefin sulfonates, internal olefin sulfonates, chlorinated olefins, linear mercaptans, aluminum alkyls, alkyldiphenylether disulfonates, and other chemicals.
  • US 6,683,187 describes a bis(arylimino)pyridine ligand, catalyst precursors and catalyst systems derived from this ligand for ethylene oligomerization to form linear alpha olefins.
  • the patent teaches the production of linear alpha olefins with a Schulz-Flory oligomerization product distribution. In such a process, a wide range of oligomers are produced, and the fraction of each olefin can be determined by calculation on the basis of the K-factor.
  • the K-factor is the molar ratio of (C n +2)/C n , where n is the number of carbons in the linear alpha olefin product.
  • the invention provides a process for producing alpha-olefins comprising contacting an ethylene feed with an oligomerization catalyst system, the catalyst system comprising a metal-ligand complex and a co-catalyst, in an oligomerization reaction zone under oligomerization reaction conditions, the reaction conditions comprising a first reaction temperature of at least 70 °C, to produce a product stream comprising alpha-olefins and higher molecular weight oligomers and optionally polyethylene wherein after a first time period, the presence of higher molecular weight oligomers and optionally polyethylene reduces the flow rate through the reaction zone, fouls the reactor surface and/or reduces heat transfer and after that first time period, increasing the temperature of the reaction zone to a second reaction temperature that is at least 5 °C greater than the first reaction temperature for a second time period.
  • the invention further provides a process for producing alpha-olefins comprising: a) contacting an ethylene feed with an oligomerization catalyst system, the catalyst system comprising a metal-ligand complex and a co-catalyst, in an oligomerization reaction zone under oligomerization reaction conditions, the reaction conditions comprising a first reaction temperature of at least 70 °C for a first time period; b) increasing the temperature of the reaction zone to a second reaction temperature that is at least 5 °C greater than the first reaction temperature for a second time period; c) reducing the temperature of the reaction zone to a third reaction temperature that is at least 5 °C less than the second reaction temperature; and d) increasing the temperature of the reaction zone to a fourth reaction temperature that is at least 5 °C greater than the third reaction temperature.
  • Figure 1 depicts the reaction temperature and circulation flow of Example 1
  • Figure 2 depicts the reaction temperature and circulation flow of Example 2
  • Figure 3 depicts the pilot plant configuration used in the Examples
  • the process comprises converting an olefin feed into a higher oligomer product stream by contacting the feed with an oligomerization catalyst system and a co-catalyst in an oligomerization reaction zone under oligomerization conditions.
  • an ethylene feed may be contacted with an iron-ligand complex and modified methyl aluminoxane under oligomerization conditions to produce a product slate of alpha olefins having a specific k-factor.
  • the olefin feed to the process comprises ethylene.
  • the feed may also comprise olefins having from 3 to 8 carbon atoms.
  • the ethylene may be pretreated to remove impurities, especially impurities that impact the reaction, product quality or damage the catalyst.
  • the ethylene may be dried to remove water.
  • the ethylene may be treated to reduce the oxygen content of the ethylene. Any pretreatment method known to one of ordinary skill in the art can be used to pretreat the feed. Oligomerization Catalyst
  • the oligomerization catalyst system may comprise one or more oligomerization catalysts as described further herein.
  • the oligomerization catalyst is a metal-ligand complex that is effective for catalyzing an oligomerization process.
  • the ligand may comprise a bis(arylimino)pyridine compound, a bis(alkylimino)pyridine compound or a mixed aryl-alkyl iminopyridine compound.
  • the ligand comprises a pyridine bis(imine) group.
  • the ligand may be a bis(arylimino)pyridine compound having the structure of Formula I.
  • R 1 , R 2 and R 3 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano or an inert functional group.
  • R 4 and R 5 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano or an inert functional group.
  • R 6 and R 7 are each independently an aryl group as shown in Formula II. The two aryl groups ( R 6 and R 7 ) on one ligand may be the same or different.
  • R 8 , R 9 , R 10 , R 11 , R 12 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano, an inert functional group, fluorine, or chlorine. Any two of R 1 - R 3 , and R 9 - R 11 vicinal to one another taken together may form a ring. R 12 may be taken together with R 11 , R 4 or R 5 to form a ring. R 2 and R 4 or R 3 and R 5 may be taken together to form a ring.
  • a hydrocarbyl group is a group containing only carbon and hydrogen.
  • the number of carbon atoms in this group is preferably in the range of from 1 to 30.
  • An optionally substituted hydrocarbyl is a hydrocarbyl group that optionally contains one or more “inert” heteroatom-containing functional groups.
  • Inert means that the functional groups do not interfere to any substantial degree with the oligomerization process. Examples of these inert groups include fluoride, chloride, iodide, stannanes, ethers, hydroxides, alkoxides and amines with adequate steric shielding.
  • the optionally substituted hydrocarbyl group may include primary, secondary and tertiary carbon atoms groups.
  • Primary carbon atom groups are a -CH 2 -R group wherein R may be hydrogen, an optionally substituted hydrocarbyl or an inert functional group.
  • Examples of primary carbon atom groups include -CH 3 , -C 2 H 5 , -CH 2 CI, -CH 2 OCH 3 , -CH 2 N(C 2 H 5 ) 2 , and -CH 2 Ph.
  • Secondary carbon atom groups are a -CH-R 2 or -CH (R)(R') group wherein R and R' may be optionally substituted hydrocarbyl or an inert functional group.
  • Tertiary carbon atom groups are a -C-(R)(R')(R") group wherein R, R', and R" may be optionally substituted hydrocarbyl or an inert functional group.
  • Examples of tertiary carbon atom groups include -C(CH 3 ) 3 , -CCI 3 , - C ⁇ CPh, 1-Adamantyl, and -C(CH 3 ) 2 (OCH 3 )
  • An inert functional group is a group other than optionally substituted hydrocarbyl that is inert under the oligomerization conditions. Inert has the same meaning as provided above.
  • Examples of inert functional groups include halide, ethers, and amines, in particular tertiary amines.
  • R 1 -R 5 , R 8 - R 12 and R 13 -R 17 may be selected to enhance other properties of the ligand, for example, solubility in non-polar solvents.
  • R 8 - R 12 and R 13 -R 17 may be selected to enhance other properties of the ligand, for example, solubility in non-polar solvents.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 11 and R 14 -R 16 are hydrogen; and R 8 , R 12 , R 13 and R 17 are fluorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 , R 10 , R 12 , R 14 and R 16 are hydrogen; R 13 , R 15 and R 17 are methyl and R 9 and R 11 are tert-butyl.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 8 , R 12 , R 14 and R 16 , are hydrogen; R 13 , R 15 and R 17 are methyl; R 9 and R 11 are phenyl and R 10 is an alkoxy.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 , R 10 , R 11 and R 14 - R 16 are hydrogen; R 9 and R 12 are methyl; and R 13 and R 17 are fluorine.
  • a ligand of Formula III wherein R 1 -R 3 , R 9 -R 11 and R 14 -R 16 are hydrogen; R 4 and R 5 are phenyl and R 8 , R 12 , R 13 and R 17 are fluorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 - R 9 , R 11 -R 12 , R 13 - R 14 and R 16 -Ru are hydrogen; and R 10 and R 15 are fluorine.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 8 , R 10 , R 12 , R 13 , R 15 and R 17 are hydrogen; and R 9 , R 11 , R 14 and R 16 are fluorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 ,R 11 -R 12 , R 14 and R 16 -R 17 are hydrogen; and R 8 , R 10 , R 13 and R 15 are fluorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 -R 9 ,R 11 -R 12 , R 14 and R 16 are hydrogen; R 10 is tert-butyl; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 12 , R 14 and R 16 are hydrogen; R 8 is fluorine; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 12 , R 13 , R 15 and R 17 are hydrogen; R 8 is tert-butyl; and R 14 and R 16 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 12 , R 13 -R 14 and R 16 -R 17 are hydrogen; and R 8 and R 15 are tert-butyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 -R 10 , R 13 -R 14 andR 16 -R 17 are hydrogen; R 15 is tert-butyl; and R 11 and R 12 are taken together to form an aryl group.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 -R 12 , R 14 -R 17 are hydrogen; and R 8 and R 13 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 -R 9 .
  • R 11 - R 12 , R 14 and R 16 are hydrogen;
  • R 10 is fluorine;
  • R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 , R 10 , R 12 , R 14 and R 16 are hydrogen; R 9 and R 11 are fluorine; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , RS-R 9 .R 11 -R 12 , R 14 and R 16 are hydrogen; R 10 is an alkoxy; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , RS-R 9 .R 11 -R 12 , R 14 and R 16 are hydrogen; R 10 is a silyl ether; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 , R 10 , R 12 , R 14 -R 16 are hydrogen; R 9 and R 11 are methyl; and R 13 and R 17 are ethyl.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 -R 12 , and R 14 -R 17 are hydrogen; and R 8 and R 13 are ethyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 11 and R 14 -R 16 are hydrogen; and R 8 , R 12 , R 13 and R 17 are chlorine.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 , R 11 , R 14 and R 16 are hydrogen; and R 8 , R 10 , R 12 , R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 - R 10 , R 12 , R 14 -R 15 and R 17 are hydrogen; and R 8 , R 11 , R 13 and R 16 are methyl.
  • a ligand of Formula III is provided wherein R 1 -R 17 are hydrogen.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 8 , R 10 , R 12 , R 13 , R 15 and R 17 are hydrogen; and R 9 , R 11 , R 14 and R 16 are tert-butyl.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 8 -R 12 , R 14 and R 16 are hydrogen; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 , R 11 -R 12 , R 14 and R 16 are hydrogen; R 8 and R 10 are fluorine; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 , R 11 -R 12 , R 14 and R 16 -R 17 are hydrogen; and R 8 , R 10 , R 13 and R 15 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 11 and R 14 -R 16 are hydrogen; R 8 and R 12 are chlorine; and R 13 and R 17 are fluorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 , R 10 , R 12 , R 14 and R 16 are hydrogen; and R 9 , R 11 , R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 11 and R 13 -R 14 and R 16 -R 17 are hydrogen; R 8 and R 12 are chlorine; and R 15 is tert-butyl.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 -R 11 and R 13 -R 17 are hydrogen; and R 8 and R 12 are chlorine.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 -R 12 , and R 14 -R 17 are hydrogen; and R 8 and R 13 are chlorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 ,R 11 -R 12 , R 14 andR 16 -R 17 are hydrogen; and R 8 , R 10 , R 13 and R 15 are chlorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 , R 11 -R 12 , and R 14 , and R 16 -R 17 are hydrogen; R 10 and R 15 are methyl; and R 8 and R 13 are chlorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 11 and R 13 -R 14 and R 16 -R 17 are hydrogen; R 15 is fluorine; and R 8 and R 12 are chlorine.
  • a ligand of Formula III wherein R 1 -R 5 , R 8 -R 9 , R 11 -R 12 , R 14 - R 15 and R 17 are hydrogen; R 10 is tert-butyl; and R 13 and R 16 are methyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 11 , R 14 and R 16 are hydrogen; R 8 and R 12 are fluorine; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III is provided wherein R 1 -R 5 , R 9 -R 10 , R 12 , R 14 -R 15 and R 17 are hydrogen; R 8 and R 13 are methyl; and R 11 and R 16 are isopropyl.
  • a ligand of Formula III wherein R 1 -R 5 , R 9 -R 12 and R 14 -R 10 are hydrogen; R 8 is ethyl; and R 13 and R 17 are fluorine.
  • a ligand of Formula III wherein R 2 -R 5 , R 9 -R 10 , R 12 , R 14 -R 15 and R 17 are hydrogen; R 1 is methoxy; and R 8 , R 11 , R 13 and R 16 , are methyl.
  • a ligand of Formula III wherein R 2 -R 5 , R 8 -R 12 , R 14 and R 10 are hydrogen; R 1 is methoxy; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 2 -R 5 , R 9 -R 12 , and R 14 -R 17 are hydrogen; R 1 is methoxy; and R 8 and R 13 are ethyl.
  • a ligand of Formula III wherein R 2 -R 5 , R 9 , R 11 -R 12 , R 14 and R 16 -R 17 are hydrogen; R 1 is tert-butyl; and R 8 , R 10 , R 13 and R 15 are methyl.
  • a ligand of Formula III wherein R 2 -R 5 , R 8 -R 12 , R 14 and R 16 are hydrogen; R 1 is tert-butyl; and R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 2 -R 5 , R 9 , R 11 , R 14 and R 10 are hydrogen; R 1 is methoxy; and R 8 , R 10 , R 12 , R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 2 -R 5 , R 9 , R 11 , R 14 and R 10 are hydrogen; R 1 is alkoxy; and R 8 , R 10 , R 12 , R 13 , R 15 and R 17 are methyl.
  • a ligand of Formula III wherein R 2 -R 5 , R 9 , R 11 , R 14 and R 10 are hydrogen; R 1 is tert-butyl; and Rs, R 10 , R 12 , R 13 , R 15 and R 17 are methyl.
  • the ligand may be a compound having the structure of Formula I, wherein one of R 6 and R 7 is aryl as shown in Formula II and one of R 6 and R 7 is pyridyl as shown in Formula IV.
  • R 6 and R 7 may be pyrrolyl.
  • R 1 , R 2 and R 3 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano or an inert functional group.
  • R 4 and R 5 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano or an inert functional group.
  • R 8 -R 12 and R 18 -R 21 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano, an inert functional group, fluorine, or chlorine. Any two of R 1 -R 3 , and R 9 -R 11 vicinal to one another taken together may form a ring.
  • R 12 may be taken together with R 11 , R 4 or R 5 to form a ring.
  • R 2 and R 4 or R 3 and R 5 may be taken together to form a ring.
  • a ligand of Formula V is provided wherein R 1 -R 5 , R 9 , R 11 and R 18 -R 21 are hydrogen; and R 8 , R 10 , and R 12 are methyl.
  • a ligand of Formula V is provided wherein R 1 -R 5 , R 9 -R 11 and R 18 -R 21 are hydrogen; and R 8 and R 12 are ethyl.
  • the ligand may be a compound having the structure of Formula I, wherein one of R 6 and R 7 is aryl as shown in Formula II and one of R 6 , and R 7 is cyclohexyl as shown in Formula VI.
  • R 6 and R 7 may be cyclohexyl.
  • R 1 , R 2 and R 3 ate each independently hydtogen, optionally substituted hydtocatbyl, hydtoxo, cyano or an inert functional group.
  • R 4 and R 5 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano or an inert functional group.
  • R 8 -R 12 and R 22 -R 26 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano, an inert functional group, fluorine, or chlorine. Any two of R 1 -R 3 , and R 9 -R 11 vicinal to one another taken together may form a ring.
  • R 12 may be taken together with R 11 , R 4 or R 5 to form a ring.
  • R 2 and R 4 or R 3 and R 5 may be taken together to form a ring.
  • a ligand of Formula VII is provided wherein R 1 -R 5 , R 9 , R 11 and R 22 -R 26 are hydrogen; and R 8 , R 10 , and R 12 are methyl.
  • R 6 and R 7 may be adamantyl or another cycloalkane.
  • the ligand may be a compound having the structure of Formula I, wherein one of R 6 and R 7 is aryl as shown in Formula II and one of R 6 and R 7 is ferrocenyl as shown in Formula VIII. In another embodiment, R 6 and R 7 may be ferrocenyl.
  • R 1 , R 2 and R 3 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano or an inert functional group.
  • R 4 and R 5 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano or an inert functional group.
  • R 8 -R 12 and R 27 -R 35 are each independently hydrogen, optionally substituted hydrocarbyl, hydroxo, cyano, an inert functional group, fluorine, or chlorine. Any two of R 1 -R 3 , and R 9 -R 11 vicinal to one another taken together may form a ring.
  • R 12 may be taken together with R 11 , R 4 or R 5 to form a ring.
  • R 2 and R 4 or R 3 and R 5 may be taken together to form a ring.
  • a ligand of Formula IX is provided wherein R 1 -R 5 , R 9 , R 11 and R 27 -R 35 are hydrogen; and R 8 , R 10 , and R 12 are methyl.
  • a ligand of Formula IX is provided wherein R 1 -R 5 , R 9 -R 11 , and R 27 -R 35 are hydrogen; and R 8 and R 12 are ethyl.
  • the ligand may be a bis(alkylamino)pyridine.
  • the alkyl group may have from 1 to 50 carbon atoms.
  • the alkyl group may be a primary, secondary, or tertiary alkyl group.
  • the alkyl group may be selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, isobutyl, and tert-butyl.
  • the alkyl group may be selected from any n-alkyl or structural isomer of an n-alkyl having 5 or more carbon atoms, e.g., n-pentyl; 2-methyl-butyl; and 2,2-dimethylpropyl.
  • the ligand may be an alkyl-alkyl iminopyridine, where the two alkyl groups are different. Any of the alkyl groups described above as being suitable for a bis(alkylamino)pyridine are also suitable for this alkyl-alkyl iminopyridine.
  • the ligand may be an aryl alkyl iminopyridine.
  • the aryl group may be of a similar nature to any of the aryl groups described with respect to the bis(arylimino)pyridine compound and the alkyl group may be of a similar nature to any of the alkyl groups described with respect to the bis(alkylamino)pyridine compound.
  • any structure that combines features of any two or more of these ligands can be a suitable ligand for this process.
  • the oligomerization catalyst system may comprise a combination of one or more of any of the described oligomerizations catalysts.
  • the ligand feedstock may contain between 0 and 10 wt.% bisimine pyridine impurity, preferably 0-1 wt.% bisimine pyridine impurity, most preferably 0-0.1 wt.% bisimine pyridine impurity. This impurity is believed to cause the formation of polymers in the reactor, so it is preferable to limit the amount of this impurity that is present in the catalyst system.
  • the bisimine pyridine impurity is a ligand of Formula II in which three of R 8 , R 12 , R 13 , and R 17 are each independently optionally substituted hydrocarbyl.
  • the bisimine pyridine impurity is a ligand of Formula II in which all four of R 8 , R 12 , R 13 , and R 17 are each independently optionally substituted hydrocarbyl.
  • the metal may be a transition metal, and the metal is preferably present as a compound having the formula MX n , where M is the metal, X is a monoanion and n represents the number of monoanions (and the oxidation state of the metal).
  • the metal can comprise any Group 4-10 transition metal.
  • the metal can be selected from the group consisting of titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, manganese, iron, cobalt, nickel, palladium, platinum, ruthenium and rhodium.
  • the metal is cobalt or iron.
  • the metal is iron.
  • the metal of the metal compound can have any positive formal oxidation state of from 2 to 6 and is preferably 2 or 3.
  • the monoanion may comprise a halide, a carboxylate, a ⁇ -diketonate, a hydrocarboxide, an optionally substituted hydrocarbyl, an amide or a hydride.
  • the hydrocarboxide may be an alkoxide, an aryloxide or an aralkoxide.
  • the halide may be fluorine, chlorine, bromine or iodine.
  • the carboxylate may be any C 1 to C 20 carboxylate.
  • the carboxylate may be acetate, a propionate, a butyrate, a pentanoate, a hexanoate, a heptanoate, an octanoate, a nonanoate, a decanoate, an undecanoate, or a dodecanoate.
  • the carboxylate may be 2-ethylhexanoate or trifluoroacetate.
  • the ⁇ -dikctonatc may be any C 1 to C 20 ⁇ -diketonate.
  • the p-diketonatc may be acetylacetonate, hexafluoroacetylacetonate, or benzoylacetonate.
  • the hydrocarboxide may be any C 1 to C 20 hydrocarboxide.
  • the hydrocarboxide may be a C 1 to C 20 alkoxide, or a C 6 to C 20 aryloxide.
  • the alkoxide may be methoxide, ethoxide, a propoxide (e.g., iso-propoxide) or a butoxide (e.g., tert-butoxide).
  • the aryloxide may be phenoxide
  • the number of monoanions equals the formal oxidation state of the metal atom.
  • metal compounds include iron acetylacetonate, iron chloride, and iron bis (2-ethylhexanoate).
  • a co-catalyst is used in the oligomerization reaction.
  • the co-catalyst may be a compound that is capable of transferring an optionally substituted hydrocarbyl or hydride group to the metal atom of the catalyst and is also capable of abstracting an X- group from the metal atom M.
  • the co-catalyst may also be capable of serving as an electron transfer reagent or providing sterically hindered counterions for an active catalyst.
  • the co-catalyst may comprise two compounds, for example one compound that is capable of transferring an optionally substituted hydrocarbyl or hydride group to metal atom M and another compound that is capable of abstracting an X- group from metal atom M.
  • Suitable compounds for transferring an optionally substituted hydrocarbyl or hydride group to metal atom M include organoaluminum compounds, alkyl lithium compounds, Grignards, alkyl tin and alkyl zinc compounds.
  • Suitable compounds for abstracting an X- group from metal atom M include strong neutral Lewis acids such as SbF 5 , BF 3 and Ar 3 B wherein Ar is a strong electron-withdrawing aryl group such as C 6 F 5 or 3,5-(CF 3 ) 2 C 6 H 3 .
  • a neutral Lewis acid donor molecule is a compound which may suitably act as a Lewis base, such as ethers, amines, sulfides and organic nitrites.
  • the co-catalyst is preferably an organoaluminum compound which may comprise an alkylaluminum compound, an aluminoxane or a combination thereof.
  • the alkylaluminum compound may be trialkylaluminum, an alkylaluminum halide, an alkylaluminum alkoxide or a combination thereof.
  • the alkyl group of the alkylaluminum compound may be any C 1 to C 20 alkyl group.
  • the alkyl group may be methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl or octyl.
  • the alkyl group may be an iso-alkyl group.
  • the trialkylaluminum compound may comprise trimethylaluminum (TMA), triethylaluminum (TEA), tripropylaluminum, tributylaluminum, tripentylaluminum, trihexylaluminum, triheptylaluminum, trioctylaluminum or mixtures thereof.
  • the trialkylaluminum compound may comprise tri-n-propylaluminum (TNPA), tri-n-butylaluminum (TNBA), tri-iso- butylaluminum (TIBA), tri-n-hexylaluminum, tri-n-octylaluminum (TNOA).
  • the halide group of the alkylaluminum halide may be chloride, bromide or iodide.
  • the alkylaluminum halide may be diethylaluminum chloride, diethylaluminum bromide, ethylaluminum dichloride, ethylaluminum sesquichloride or mixtures thereof.
  • the alkoxide group of the alkylaluminum alkoxide may be any C 1 to C 20 alkoxy group.
  • the alkoxy group may be methoxy, ethoxy, propoxy, butoxy, pentoxy, hexoxy, heptoxy or octoxy.
  • the alkylaluminum alkoxide may be diethylaluminum ethoxide.
  • the aluminoxane compound may be methylaluminoxane (MAO), ethylaluminoxane, modified methylaluminoxane (MMAO), n-propylaluminoxane, iso-propyl-aluminoxane, n- butylaluminoxane, sec-butylaluminoxane, iso-butylaluminoxane, t-butylaluminoxane, 1-pentyl- aluminoxane, 2-pentyl-aluminoxane, 3-pentyl-aluminoxane, iso-pentyl-aluminoxane, neopentylaluminoxane, or mixtures thereof.
  • MAO methylaluminoxane
  • MMAO modified methylaluminoxane
  • n-propylaluminoxane iso-propyl-aluminoxane
  • the preferred co-catalyst is modified methylaluminoxane.
  • the synthesis of modified methylaluminoxane may be carried out in the presence of other trialkylaluminum compounds in addition to trimethylaluminum.
  • the products incorporate both methyl and alkyl groups from the added trialkylaluminum and are referred to as modified methyl aluminoxanes, MMAO.
  • the MMAO may be more soluble in nonpolar reaction media, more stable to storage, have enhanced performance as a cocatalyst, or any combination of these.
  • the performance of the resulting MMAO may be superior to either of the trialkylaluminum starting materials or to simple mixtures of the two starting materials.
  • the added trialkylaluminum may be triethylaluminum, triisobutylaluminum or triisooctylaluminum.
  • the co-catalyst is MMAO, wherein preferably about 25% of the methyl groups are replaced with iso-butyl groups.
  • the co-catalyst may be formed in situ in the reactor by providing the appropriate precursors into the reactor.
  • the solvent(s) may be used to dissolve or suspend the catalyst or the co-catalyst and/ or keep the ethylene dissolved.
  • the solvent may be any solvent that can modify the solubility of any of these components or of reaction products. Suitable solvents include hydrocarbons, for example, alkanes, alkenes, cycloalkanes, and aromatics. Different solvents may be used in the process, for example, one solvent can be used for the catalyst and another for the co-catalyst. It is preferred for the solvent to have a boiling point that is not substantially similar to the boiling point of any of the alpha olefin products as this will make the product separation step more difficult.
  • Aromatic solvents can be any solvent that contains an aromatic hydrocarbon, preferably having a carbon number of 6 to 20. These solvents may include pure aromatics, or mixtures of pure aromatics, isomers as well as heavier solvents, for example C 9 and C 10 solvents. Suitable aromatic solvents include benzene, toluene, xylene (including ortho-xylene, meta-xylene, para-xylene and mixtures thereof) and ethylbenzene.
  • Alkane solvents may be any solvent that contains an alkyl hydrocarbon. These solvents may include straight chain alkanes and branched or iso-alkanes having from 3 to 20 carbon atoms and mixtures of these alkanes. The alkanes may be cycloalkanes.
  • Suitable solvents include propane, isobutane, n-butane, butane (n-butane or a mixture of linear and branched C 4 acyclic alkanes), pentane (n-pentane or a mixture of linear and branched acyclic alkanes), hexane (n-hexane or a mixture of linear and branched C 6 acyclic alkanes), heptane (n-heptane or a mixture of linear and branched C 7 acyclic alkanes), octane (n-octane or a mixture of linear and branched C 8 acyclic alkanes) and isooctane.
  • Suitable solvents also include cyclohexane and methylcyclohexane.
  • the solvent comprises C 6 , C 7 and C 8 alkanes, that may include linear, branched and iso-alkanes.
  • the catalyst system may be formed by mixing together the ligand, the metal, the co-catalyst and optional additional compounds in a solvent.
  • the feed may be present in this step.
  • the catalyst system may be prepared by contacting the metal or metal compound with the ligand to form a catalyst precursor mixture and then contacting the catalyst precursor mixture with the co-catalyst in the reactor to form the catalyst system.
  • the catalyst system may be prepared outside of the reactor vessel and fed into the reactor vessel. In other embodiments, the catalyst system may be formed in the reactor vessel by passing each of the components of the catalyst system separately into the reactor. In other embodiments, one or more catalyst precursors may be formed by combining at least two components outside of the reactor and then passing the one or more catalyst precursors into the reactor to form the catalyst system.
  • the oligomerization reaction is a reaction that converts the olefin feed in the presence of an oligomerization catalyst and a co-catalyst into a higher oligomer product stream.
  • Typical oligomerization reactions may be conducted over a range of temperatures of from -100 °C to 300 °C.
  • the oligomerization reaction conditions of the present invention comprise a reaction temperature of at least 70 °C.
  • the reaction temperature is preferably at least 90 °C.
  • the oligomerization reaction described herein also produces higher olefins (having a carbon number of greater than 40) and possibly some polyethylene by a side reaction. These higher olefins and polyethylene can foul the physical surfaces in the reactor and the oligomerization system.
  • the presence of higher molecular weight oligomers and optionally polyethylene may reduce the flow rate through the reaction zone, foul the reactor surface and/ or reduce the heat transfer.
  • the reaction temperature may be increased to a second reaction temperature that is at least 5 °C greater than the first reaction temperature for a second time period.
  • the higher reaction temperature results in higher molecular weight oligomers and optionally polyethylene being removed from the reactor. This results in an increase in the flow rate through the reaction zone, a reduction in reactor surface fouling and/ or an increase in heat transfer in the system.
  • the second reaction temperature may be at least 10 °C greater than the first reaction temperature or at least 15 °C greater than the first reaction temperature.
  • the first reaction temperature is at least 70 °C, preferably at least 90 °C, more preferably at least 110 °C.
  • the second reaction temperature is at least 118 °C, and preferably at least 121 °C.
  • the first reaction temperature may be in the range of from 70 to 120 °C, preferably from 90 to 120 °C, and more preferably from 110 to 120 °C.
  • the first reaction temperature may be in the range of from 70 to 117 °C, preferably from 90 to 117 °C, more preferably from 110 to 117 °C.
  • the second reaction temperature may be in the range of from 118 to 200 °C, preferably from 118 to 150, and more preferably from 118 to 127 °C.
  • the second reaction temperature may be in the range of from 121 to 200 °C, preferably from 121 to 150 °C, and more preferably from 121 to 127 °C.
  • the process may be conducted by: a) contacting an ethylene feed with an oligomerization catalyst system, the catalyst system comprising a metal-ligand complex and a cocatalyst, in an oligomerization reaction zone under oligomerization reaction conditions, the reaction conditions comprising a first reaction temperature of at least 70 °C for a first time period; b) increasing the temperature of the reaction zone to a second reaction temperature that is at least 5 °C greater than the first reaction temperature for a second time period; c) reducing the temperature of the reaction zone to a third reaction temperature that is at least 5 °C less than the second reaction temperature; and d) increasing the temperature of the reaction zone to a fourth reaction temperature that is at least 5 °C greater than the third reaction temperature.
  • the second and fourth reaction temperatures may be at least 10 °C greater than the first and/ or third reaction temperatures or at least 15 °C greater than the first and/ or third reaction temperatures.
  • the process may be operated by periodically lowering the temperature and then after a further time period raising the temperature. At lower temperatures, the catalyst is more active, but fouling also tends to be a larger issue at lower temperatures.
  • the process can be operated at a lower temperature to maximize catalyst activity, and when the process exhibits fouling, reduced flow rates or a decreased heat transfer, the reaction temperature can be increased to reverse those effects. Once the reactor exhibits improved flow rates, reduced fouling and/ or increased heat transfer, the temperature can be reduced to again maximize catalyst activity.
  • the first and third reaction temperatures are in the range of from 70 to 120 °C and the second and fourth reaction temperatures are in the range of from 121 to 150 °C.
  • the steps described above as steps c) and d) are repeated a plurality of times (and possibly throughout the duration of operation of the reactor. When steps c) and d) are repeated, the reaction temperature during the repeated step c) is in the range of from 70 to 120 °C and the reaction temperature during the repeated step d) is in the range of from 121 to 150 °C
  • the catalyst and/ or co-catalyst feed into the reactor may be stopped during the time periods where the temperature is increased to a higher temperature.
  • the catalyst and co-catalyst may be fed during the first and third time periods, and then the catalyst and co-catalyst feed may be stopped during the second and fourth time periods.
  • the reactor would have to be regularly shut down to clean out the higher olefins and polyethylene, resulting in significant shutdown time.
  • the oligomerization reaction may be conducted at a pressure of from 0.01 to 15 MPa and more preferably from 1 to 10 MPa.
  • the optimum conditions of temperature and pressure used for a specific catalyst system, to maximize the yield of oligomer, and to minimize the impact of competing reactions, for example dimerization and polymerization can be determined by one of ordinary skill in the art.
  • the temperature and pressure are selected to yield a product slate with a K-factor in the range of from 0.40 to 0.90, preferably in the range of from 0.45 to 0.80, more preferably in the range of from 0.5 to 0.7.
  • the oligomerization reaction can be carried out in the liquid phase or mixed gas-liquid phase, depending on the volatility of the feed and product olefins at the reaction conditions.
  • the oligomerization reaction may be carried out in a conventional fashion. It may be carried out in a stirred tank reactor, wherein solvent, olefin and catalyst or catalyst precursors are added continuously to a stirred tank and solvent, product, catalyst, and unused reactant are removed from the stirred tank with the product separated and the unused reactant recycled back to the stirred tank.
  • the oligomerization reaction may be carried out in a batch reactor, wherein the catalyst precursors and reactant olefin are charged to an autoclave or other vessel and after being reacted for an appropriate time, product is separated from the reaction mixture by conventional means, for example, distillation.
  • the oligomerization reaction may be carried out in a gas lift reactor.
  • This type of reactor has two vertical sections (a riser section and a downcomer section) and a gas separator at the top.
  • the gas feed (ethylene) is injected at the bottom of the riser section to drive circulation around the loop (up the riser section and down the downcomer section).
  • This type of reactor may be especially sensitive to the formation of fouling and web-like polymers and the formation of those polymers in the reactor system can reduce the circulation flow significantly.
  • the oligomerization reaction may be carried out in a pump loop reactor.
  • This type of reactor has two vertical sections, and it uses a pump to drive circulation around the loop.
  • a pump loop reactor can be operated at a higher circulation rate than a gas lift reactor.
  • the oligomerization reaction may be carried out in a once-through reactor.
  • This type of reactor feeds the catalyst, co-catalyst, solvent and ethylene to the inlet of the reactor and/ or along the reactor length and the product is collected at the reactor outlet.
  • This type of reactor is a plug flow reactor.
  • the higher oligomers produced in the oligomerization reaction contains catalyst from the reaction step. To stop further reactions that can produce byproducts and other undesired components, it is important to deactivate the catalyst downstream from the reactor.
  • the catalyst is deactivated by addition of an acidic species having a pK a (aq) of less than 25. The deactivated catalyst can then be removed by water washing in a liquid/liquid extractor.
  • the resulting alpha-olefins have a chain length of from 4 to 100 carbon atoms, preferably 4 to 30 carbon atoms and most preferably 4 to 20 carbon atoms.
  • the alpha-olefins are even- numbered alpha-olefins.
  • the product olefins can be recovered by distillation or other separation techniques depending on the intended use of the products.
  • the solvents) used in the reaction preferably have a boiling point that is different from the boiling point of any of the alpha-olefin products to make the separation easier.
  • the distillation steps comprise columns for separating ethylene and the main linear alpha olefin products, for example, butene, hexene, and octene.
  • the products produced by the process may be used in a number of applications.
  • the olefins produced by this process may have improved qualities as compared to olefins produced by other processes.
  • the butene, hexene and/ or octene produced may be used as a comonomer in making polyethylene.
  • the octene produced may be used to produce plasticizer alcohols.
  • the decene produced may be used to produce polyalphaolefins.
  • the dodecene and/ or tetradecene produced may be used to produce alkylbenzene and/ or detergent alcohols.
  • the hexadecene and/ or octadecene produced may be used to produce alkenyl succinates and/or oilfield chemicals.
  • the C20+ products may be used to produce lubricant additives and/ or waxes.
  • a portion of any unreacted ethylene that is removed from the reactor with the products may be recycled to the reactor.
  • This ethylene may be recovered in the distillation steps used to separate the products.
  • the ethylene may be combined with the fresh ethylene feed or it may be fed separately to the reactor.
  • a portion of any solvent used in the reaction may be recycled to the reactor.
  • the solvent may be recovered in the distillation steps used to separate the products. Examples
  • Figure 3 depicts the ethylene oligomerization reactor that was operated with continuous feed as a gas-lift loop reactor to produce alpha olefins (AO).
  • the reactor volume was 9.5 L and the typical circulation velocity is from 0.6 to 1.1 m/ sec.
  • Circulation for the gas Eft reactor is provided by injecting ethylene at the bottom of the riser 110.
  • the gas holdup in the riser creates a differential head pressure between the riser 110 and the downcomer 120 that drives Equid circulation down the downcomer and up the riser.
  • the riser and downcomer each are coaxial pipes with an outer heat exchanger shell for heat removal from the exothermic oEgomerization reaction.
  • the heat transfer fluid in the exchangers is water and each exchanger has an internal temperature indicator probe at the inlet and outlet as well as a mass flow controller to quantify the heat of reaction.
  • Reactor temperature is controlled by a jacketed water heating system to preheat the reactor for startup or remove heat of reaction from the oEgomerization reaction.
  • the temperature of the gas Eft reactor can be controlled from 60 to 99° C.
  • the heating system is also able to operate in a melt out mode at a temperature of 121 to 154° C.
  • Ethylene feed is pretreated in a carbon bed, a molecular sieve bed, and then an oxygen removal bed (not shown) and then compressed to about 345 kPa above the reactor operating pressure and fed to the reactor through a control valve.
  • the ethylene is suppEed on pressure demand to maintain the reactor operating pressure from 2.8 MPa to 6.2 MPa.
  • a regulated 0-18 kg/hr fresh ethylene feed 200 provides ethylene to the reaction zone by feeding at the reactor bottom through an injection nozzle 130.
  • the ethylene recycle compressor 140 circulates ethylene for the gas Eft and operates between 0.45 and 18 kg/hr.
  • Solvent feed is provided at a flow rate of 4.5 to 11.3 kg/hr. Solvent is fed through a diaphragm pump and then through two control valves before mixing with the catalyst feed solutions and entering the reactor. The solvent flow is divided between the two catalyst feed streams using the control valves.
  • the reactor can use separate feed lines for ligand, iron, and MMAO catalyst solutions fed to the reactor zone.
  • the ligand and iron are precomplexed and added as a single feed stream 210.
  • the MMAO is added through line 220.
  • Each catalyst stream is fed through an ISCO pump that is supplied by a catalyst supply feed vessel.
  • the ISCO pump outlet operates at reactor pressure and the feed rate range for the pump is from 0.001 to 100 ml/min.
  • MMAO and ligand/iron catalyst feeds are each blended with part of the total solvent recycle feed before entering the reactor.
  • the reactor top has an overhead separator 160 that allows for liquid to overflow into a heat traced pipe to control level.
  • a downstream valve controls the level in the overflow pipe and this downstream product flow 170 is distilled to separate AO products from the solvent which is recycled back to the reactor.
  • the liquid reactor outlet and downstream lines are heat traced with steam to maintain a temperature of 127° C to 160° C.
  • Example 1 The gas phase that exits the top of the overhead separator goes through a cooler and then a gas/liquid separator to remove liquid upstream of the recycle compressor 140. This gas phase is recycled back to the reactor bottom via recycle line 180 and the liquid feeds forward to distillation.
  • Example 1 The gas phase that exits the top of the overhead separator goes through a cooler and then a gas/liquid separator to remove liquid upstream of the recycle compressor 140. This gas phase is recycled back to the reactor bottom via recycle line 180 and the liquid feeds forward to distillation.

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Abstract

L'invention concerne un procédé de production d'alpha-oléfines comprenant la mise en contact d'une charge d'éthylène avec un système de catalyseur d'oligomérisation, le système de catalyseur comprenant un complexe métal-ligand et un co-catalyseur, dans une zone de réaction d'oligomérisation dans des conditions de réaction d'oligomérisation, les conditions de réaction comprenant une première température de réaction d'au moins 70 °C, pour produire un flux de produit comprenant des alpha-oléfines et des oligomères de poids moléculaire plus élevé et éventuellement du polyéthylène, après un premier laps de temps, la présence d'oligomères de poids moléculaire plus élevé et éventuellement de polyéthylène réduit le débit à travers la zone de réaction, l'encrassement de la surface du réacteur et/ou réduit le transfert de chaleur et après ce premier laps de temps, augmente la température de la zone de réaction jusqu'à une seconde température de réaction qui est supérieure d'au moins 5 °C à la première température de réaction pendant un second laps de temps.
PCT/US2021/063446 2020-12-15 2021-12-15 Procédé de production d'alpha-oléfines WO2022132860A1 (fr)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6683187B2 (en) 2000-06-30 2004-01-27 Shell Oil Company Ligands and catalyst systems thereof for ethylene oligomerization to linear alpha olefins
WO2010036446A1 (fr) * 2008-09-24 2010-04-01 Univation Technologies, Llc Procédés de nettoyage de la plaque distributrice dans un système de réacteur à lit fluidisé
WO2017163158A1 (fr) * 2016-03-21 2017-09-28 Sabic Global Technologies B.V. Procédé de traitement de flux de produit d'oligomérisation
US9856184B2 (en) * 2015-03-03 2018-01-02 Evonik Degussa Gmbh Regeneration of a heterogeneous catalyst in ethene oligomerization

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6683187B2 (en) 2000-06-30 2004-01-27 Shell Oil Company Ligands and catalyst systems thereof for ethylene oligomerization to linear alpha olefins
WO2010036446A1 (fr) * 2008-09-24 2010-04-01 Univation Technologies, Llc Procédés de nettoyage de la plaque distributrice dans un système de réacteur à lit fluidisé
US9856184B2 (en) * 2015-03-03 2018-01-02 Evonik Degussa Gmbh Regeneration of a heterogeneous catalyst in ethene oligomerization
WO2017163158A1 (fr) * 2016-03-21 2017-09-28 Sabic Global Technologies B.V. Procédé de traitement de flux de produit d'oligomérisation

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Title
SPAMER R WALSH H HARTMAN A ED - DARL KUHN: "Tetramerisation Process Technology Review", IP.COM, IP.COM INC., WEST HENRIETTA, NY, US, 13 July 2004 (2004-07-13), XP013020830, ISSN: 1533-0001 *

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