Process for transitioning between incompatible catalysts

US2018186906A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2018186906-A1
Application numberUS-201515538013-A
CountryUS
Kind codeA1
Filing dateDec 22, 2015
Priority dateDec 22, 2014
Publication dateJul 5, 2018
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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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 from a first catalyst feeding system into a reactor; (b) introducing a catalyst killer to at least partially deactivate the first catalyst in the reactor (c) introducing into the reactor a second catalyst from a second catalyst feeding system separate from the first catalyst feeding system.

First claim

Opening claim text (preview).

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 from a first catalyst feeding system into a reactor; (b) introducing a catalyst killer to at least partially deactivate the first catalyst in the reactor (c) introducing into the reactor a second catalyst from a second catalyst feeding system separate from the first catalyst feeding system. 2 . The process according to claim 1 , wherein the first catalyst is a Ziegler-Natta catalyst and the second catalyst is a metallocene catalyst. 3 . 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. 4 . The process according to claim 3 , wherein the compound (1) is tri-isobutylaluminum and the compound (2) is cyclohexylamine. 5 . The process according to claim 3 , 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′-dimethyl silyl-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. 6 . The process according to claim 1 , wherein the catalyst killer comprises cyclohexylamine. 7 . The process according to claim 1 , further comprising the following steps (b2), (b3) and (b4) after step (b) and before step (c): (b2) introducing an organometallic compound into the reactor to react with the catalyst killer, (b3) introducing a gas composition into the reactor for the second polymerization reaction and (b4) 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, 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. 9 . (canceled) 10 . (canceled) 11 . (canceled) 12 . (canceled) 13 . (canceled) 14 . The process according to claim 7 , wherein the compound (1) is tri-isobutylaluminum and the compound (2) is cyclohexylamine, octadecylamine, 2-ethylhexylamine, ethylhexylamine, bis(4-aminocyclohexyl)methane, hexamethylenediamine, 1,3-benzenedimethanamine, 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane and 6-amino-1,3-dimethyluracil or a mixture thereof. 15 . The process according to claim 1 , wherein the polymerization is conducted in a fluidized bed reactor. 16 . 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. 17 . 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. 18 . The process according to claim 1 , wherein a reversible catalyst killer is introduced to render the first catalyst inactive. 19 . The process according to claim 3 , 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. 20 . The process according to claim 18 , wherein the reversible catalyst killer is CO. 21 . The process according to claim 19 , wherein the compound (1) is tri-isobutylaluminum and the compound (2) is cyclohexylamine; and 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)benze

Assignees

Inventors

Classifications

  • C08F10/00Primary

    Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond · CPC title

  • using short-stopping agents · CPC title

  • Copolymers of ethene with alpha-alkenes, e.g. EP rubbers · CPC title

  • Titanium, zirconium, hafnium or compounds thereof · CPC title

  • Amines; Quaternary ammonium compounds · CPC title

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What does patent US2018186906A1 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 C08F10/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jul 05 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).