Catalyst composition for polymerization of olefins

US10059656B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10059656-B2
Application numberUS-201415104822-A
CountryUS
Kind codeB2
Filing dateDec 19, 2014
Priority dateDec 20, 2013
Publication dateAug 28, 2018
Grant dateAug 28, 2018

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  5. First independent claim

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Abstract

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A catalyst composition including the compound of Formula I as an internal electron donor, wherein: R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are independently selected from a group consisting of hydrogen, straight, branched and cyclic alkyl and aromatic substituted and unsubstituted hydrocarbyl having 1 to 20 carbon atoms; R 7 is selected from a group consisting of straight, branched and cyclic alkyl and aromatic substituted and unsubstituted hydrocarbyl having 1 to 20 carbon atoms; and R 8 is selected from a group consisting of aromatic substituted and unsubstituted hydrocarbyl having 6 to 20 carbon atoms. Also disclosed is a process for preparing said polymerization catalyst composition; a polymerization catalyst system comprising said catalyst composition, a co-catalyst and optionally an external electron donor; a polyolefin obtainable by the process; and use of the compound of Formula I as in internal electron donor in catalysts for polymerization of olefins.

First claim

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The invention claimed is: 1. A catalyst composition for the polymerization of olefins, which catalyst composition comprises the compound represented by Formula I as an internal electron donor, wherein: R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are the same or different and are independently selected from the group consisting of hydrogen, straight, branched and cyclic alkyl and aromatic substituted and unsubstituted hydrocarbyl having 1 to 20 carbon atoms; R 7 is selected from the group consisting of straight, branched and cyclic alkyl and aromatic substituted and unsubstituted hydrocarbyl having 1 to 20 carbon atoms; and R 8 is selected from the group consisting of aromatic substituted and unsubstituted hydrocarbyl having 6 to 20 carbon atoms; N is nitrogen atom; O is oxygen atom; and C is carbon atom. 2. The catalyst composition according to claim 1 , wherein R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are independently selected from the group consisting of hydrogen, C 1 -C 10 straight and branched alkyl; C 3 -C 10 cycloalkyl; C 6 -C 10 aryl; and C 7 -C 10 alkaryl and aralkyl groups. 3. The catalyst composition according to claim 1 , wherein R 1 and R 2 are each a hydrogen atom and R 3 , R 4 , R 5 and R 6 are independently selected from the group consisting of C 1 -C 10 straight and branched alkyl; C 3 -C 10 cycloalkyl; C 6 -C 10 aryl; and C 7 -C 10 alkaryl and aralkyl groups. 4. The catalyst composition according to claim 1 , wherein when one of R 3 and R 4 and one of R 5 and R 6 has at least one carbon atom, then the other one of R 3 and R 4 and of R 5 and R 6 is each a hydrogen atom. 5. The catalyst composition according to claim 1 , wherein R 7 is selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, t-butyl, phenyl, benzyl, substituted benzyl and halophenyl groups. 6. The catalyst composition according to claim 1 , wherein R 8 is selected from the group consisting of C 6 -C 10 aryl; and C 7 -C 10 alkaryl and aralkyl groups. 7. The catalyst composition according claim 1 , wherein the internal electron donor is selected from the group consisting of 4-[benzoyl(methyl)amino]pentan-2-yl benzoate; 2,2,6,6-tetramethyl-5-(methylamino)heptan-3-ol dibenzoate; 4-[benzoyl (ethyl)amino]pentan-2-yl benzoate and 4-(methylamino)pentan-2-yl bis (4-methoxy)benzoate). 8. A process for preparing the catalyst composition according to claim 1 , comprising contacting a magnesium-containing support with a halogen-containing titanium compound and an internal electron donor according to Formula I. 9. The process according to claim 8 , which comprises: i) contacting a compound R 9 z MgX 2-z wherein R 9 is aromatic, aliphatic or cyclo-aliphatic group containing 1 to 20 carbon atoms, X is a halide, and z is in a range of larger than 0 and smaller than 2, with an alkoxy- or aryloxy-containing silane compound to give a first intermediate reaction product, which is a compound Mg(OR 1 ) x X 2-x in a solid form, wherein x is in a range of larger than 0 and smaller than 2; ii) contacting the compound Mg(OR 1 ) x X 2-x in a solid form with at least one activating compound selected from the group consisting of electron donors and compounds of formula M(OR 10 ) v-w (OR 11 ) w , wherein M is Ti, Zr, Hf, Al or Si and M(OR 10 ) v-w (R 11 ) w , wherein M is Si, each R 10 and R 11 , independently, represent an alkyl, alkenyl or aryl group, v is the valency of M, v being either 3 or 4 and w is smaller than v to give a second intermediate reaction product; and iii) contacting the second intermediate reaction product with a halogen-containing Ti-compound, an internal electron donor represented by Formula I, wherein: R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are the same or different and are independently selected from the group consisting of hydrogen, straight, branched and cyclic alkyl and aromatic substituted and unsubstituted hydrocarbyl having 1 to 20 carbon atoms; R 7 is selected from the group consisting of straight, branched and cyclic alkyl and aromatic substituted and unsubstituted hydrocarbyl having 1 to 20 carbon atoms; and R 8 is selected from the group consisting of aromatic substituted and unsubstituted hydrocarbyl having 6 to 20 carbon atoms; N is nitrogen atom; O is oxygen atom; and C is carbon atom. 10. A catalyst composition obtained by the process according to claim 8 . 11. A polymerization catalyst system comprising the catalyst composition according to claim 1 , a co-catalyst and optionally an external electron donor. 12. A process of making a polyolefin, comprising contacting an olefin with the catalyst system according to claim 11 . 13. The catalyst composition according to claim 3 , wherein R 3 , R 4 , R 5 and R 6 are independently selected from C 1 -C 10 straight and branched alkyl and phenyl. 14. The catalyst composition according to claim 6 , wherein R 8 is selected from the group consisting of substituted or unsubstituted phenyl, benzyl, naphthyl, ortho-tolyl, para-tolyl or anisol groups. 15. The process according to claim 9 , wherein the first intermediate reaction product is contacted with an alcohol and a titanium tetraalkoxide in step ii). 16. A polymerization catalyst system comprising the catalyst composition according to claim 7 , a co-catalyst and optionally an external electron donor. 17. The catalyst composition according to claim 10 , wherein R 1 and R 2 are each a hydrogen atom; R 3 , R 4 , R 5 and R 6 are selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, t-butyl, or phenyl groups; R 7 is selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, t-butyl, phenyl, benzyl, substituted benzyl and halophenyl groups; and R 8 is phenyl. 18. A polymerization catalyst system comprising the catalyst composition according to claim 17 , a co-catalyst and optionally an external electron donor.

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Inventors

Classifications

  • Additive used together with the catalyst, excluding compounds containing Al or B · CPC title

  • C08F4/651Primary

    Pretreating with non-metals or metal-free compounds · CPC title

  • Promoter-type Additives · CPC title

  • C07C233/69Primary

    of an acyclic saturated carbon skeleton · CPC title

  • Isotactic · CPC title

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What does patent US10059656B2 cover?
A catalyst composition including the compound of Formula I as an internal electron donor, wherein: R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are independently selected from a group consisting of hydrogen, straight, branched and cyclic alkyl and aromatic substituted and unsubstituted hydroca…
Who is the assignee on this patent?
Saudi Basic Ind Corp, Sabic Global Technologies Bv
What technology area does this patent fall under?
Primary CPC classification C08F4/651. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 28 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).