Process for transitioning between incompatible catalysts

US9944727B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9944727-B2
Application numberUS-201515537997-A
CountryUS
Kind codeB2
Filing dateDec 22, 2015
Priority dateDec 22, 2014
Publication dateApr 17, 2018
Grant dateApr 17, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The invention relates to a process for transitioning from a first continuous polymerization reaction in a gas phase reactor conducted in the presence of a first catalyst to a second polymerization reaction conducted in the presence of a second catalyst in the gas phase reactor wherein the first and second catalysts are incompatible, the process comprising: (a) discontinuing the introduction of the first catalyst into the gas phase reactor; (b) introducing an effective amount of cyclohexylamine into the reactor to at least partially deactivate the first catalyst; (c) introducing an organometallic compound into the reactor and reacting the organometallic compound with cyclohexylamine; (d) introducing a gas composition into the reactor for the second polymerization reaction and (e) introducing the second catalyst into the reactor.

First claim

Opening claim text (preview).

The invention claimed is: 1. A process for transitioning from a first continuous polymerization reaction in a gas phase reactor conducted in the presence of a first catalyst to a second polymerization reaction conducted in the presence of a second catalyst in the gas phase reactor wherein the first and second catalysts are incompatible, the process comprising: (a) discontinuing the introduction of the first catalyst into the gas phase reactor; (b) introducing an effective amount of cyclohexylamine into the reactor to at least partially deactivate the first catalyst; (c) introducing an organometallic compound into the reactor and reacting the organometallic compound with cyclohexylamine; (d) introducing a gas composition into the reactor for the second polymerization reaction and (e) introducing the second catalyst into the reactor. 2. The process according to claim 1 , wherein the organometallic compound is a trialkylaluminum compound. 3. The process according to claim 1 , further comprising the step (d2) after step (d) and before step (e), wherein step (d2) comprises introducing a reaction product of an aluminum compound of general formula (1) and an amine compound of general formula (2) wherein R 1 is hydrogen or a branched or straight, substituted or unsubstituted hydrocarbon group having 1-30 carbon atoms, R 2 and R 3 are the same or different and selected from branched or straight, substituted or unsubstituted hydrocarbon groups having 1-30 carbon atoms and R 4 is hydrogen or a functional group with at least one active hydrogen R 5 is hydrogen or a branched, straight or cyclic, substituted or unsubstituted hydrocarbon group having 1-30 carbon atoms, R 6 is a branched, straight or cyclic, substituted or unsubstituted hydrocarbon group having 1-30 carbon atoms is introduced into the reactor. 4. The process according to claim 3 , wherein the compound (1) is tri-isobutylaluminum and the compound (2) is cyclohexylamine or octadecylamine or cyclohexylamine, octadecylamine, 2-ethylhexylamine, ethylhexylamine, bis(4-amino cyclohexyl)methane, hexamethylenediamine, 1,3-benzenedimethanamine, 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane, 6-amino-1,3-dimethyluracil or a mixture thereof. 5. The process according to claim 1 , wherein the first catalyst is a Ziegler-Natta catalyst and the second catalyst is a metallocene catalyst. 6. The process according to claim 1 , wherein the second catalyst is a metallocene catalyst composition comprising a support containing a metallocene catalyst, a catalyst activator and an optional modifier. 7. The process according to claim 6 , wherein the modifier is a reaction product of compound (1) being tri-isobutylaluminum and compound (2) being cyclohexylamine. 8. The process according to claim 6 , wherein the metallocene catalyst is selected from the group consisting of: [ortho-bis(4-phenyl-2-indenyl)-benzene]zirconiumdichloride, [ortho-bis(5-phenyl-2-indenyl)-benzene]zirconiumdichloride, [ortho-bis(2-indenyl)benzene]zirconiumdichloride, [ortho-bis(2-indenyl)benzene]hafniumdichloride, [ortho-bis(1-methyl-2-indenyl)-benzene]zirconiumdichloride, [2.2′-(1.2-phenyldiyl)-1.1′-dimethylsilyl-bis(indene)]zirconiumdichloride, [2,2′-(1,2-phenyldiyl)-1, 1′-diphenylsilyl-bis(indene)]zirconiumdichloride, [2,2′-(1.2-phenyldiyl)-1.1′-(1.2-ethanediyl)-bis(indene)]zirconiumdichloride, [2.2′-bis(2-indenyl)biphenyl]zirconiumdichloride and [2,2′-bis(2-indenyl)biphenyl]hafniumdichloride. 9. The process according to claim 1 , wherein the first catalyst is introduced from a first catalyst feeding system and the second catalyst is introduced from a second catalyst feeding system separate from the first catalyst feeding system. 10. The process according to claim 1 , wherein the polymerization is conducted in a fluidized bed reactor. 11. The process according to claim 1 , wherein the first continuous polymerization reaction is operated in a condensed mode in which 5-17.4 wt % of the gas composition entering the gas phase reactor is liquid or a supercondensed mode in which more than 17.4 wt % of the gas composition entering the gas phase reactor is liquid. 12. The process according to claim 1 , wherein the gas phase reactor is a multi-zone reactor operable in condensed mode, which multi-zone reactor comprises a first zone, a second zone, a third zone, a fourth zone and a distribution plate, wherein the first zone is separated from the second zone by the distribution plate, wherein the multi-zone reactor is extended in the vertical direction, wherein the second zone of the multi-zone reactor is located above the first zone and wherein the third zone of the multi-zone reactor is located above the second zone, and wherein the fourth zone of the multi-zone reactor is located above the third zone, wherein the second zone contains an inner wall, wherein at least part of the inner wall of the second zone is either in the form of a gradually increasing inner diameter or a continuously opening cone, wherein the diameter or the opening increases in the vertical direction towards the top of the multi-zone reactor, wherein the third zone contains an inner wall, wherein at least part of the inner wall of the third zone is either in the form of a gradually increasing inner diameter or a continuously opening cone, wherein the diameter or the opening increases in the vertical direction towards the top of the multi-zone reactor, and wherein the largest diameter of the inner wall of the third zone is larger than the largest diameter of the inner wall of the second zone. 13. The process according to claim 1 , wherein a reversible catalyst killer is introduced to render the first catalyst inactive. 14. The process according to claim 1 , wherein the organometallic compound is triethylaluminum, trimethylaluminum, tri-isobutylaluminum, or tri-n-hexylaluminum. 15. The process according to claim 1 , wherein the organometallic compound is tri-isobutylaluminum. 16. The process according to claim 6 , wherein the optional modifier is present and is [A] a reaction product of an aluminum compound of general formula (1) and an amine compound of general formula (2) wherein R 1 is hydrogen or a branched or straight, substituted or unsubstituted hydrocarbon group having 1-30 carbon atoms, R 2 and R 3 are the same or different and are selected from branched or straight, substituted or unsubstituted hydrocarbon groups having 1-30 carbon atoms, R 4 is hydrogen or a functional group with at least one active hydrogen, R 5 is hydrogen or a branched, straight or cyclic, substituted or unsubstituted hydrocarbon group having 1-30 carbon atoms, and R 6 is a branched, straight or cyclic, substituted or unsubstituted hydrocarbon group having 1-30 carbon atoms, or [B] an amine compound of general formula (3) where R 7 is hydrogen or a linear or branched alkyl group of from 1 to 50 carbon atoms, R 8 is a hydroxy group of a (CH 2 ) X radical and x is an integer from 1 to 50. 17. The process according to claim 7 , wherein

Assignees

Inventors

Classifications

  • C08F2/34Primary

    Polymerisation in gaseous state · CPC title

  • according to "fluidised-bed" technique (B01J8/20 takes precedence) · CPC title

  • Feeding · CPC title

  • C08F10/02Primary

    Ethene · CPC title

  • Feeding of the particles in the reactor; Evacuation of the particles out of the reactor · CPC title

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What does patent US9944727B2 cover?
The invention relates to a process for transitioning from a first continuous polymerization reaction in a gas phase reactor conducted in the presence of a first catalyst to a second polymerization reaction conducted in the presence of a second catalyst in the gas phase reactor wherein the first and second catalysts are incompatible, the process comprising: (a) discontinuing the introduction of …
Who is the assignee on this patent?
Sabic Global Technologies Bv
What technology area does this patent fall under?
Primary CPC classification C08F2/34. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).