Catalyst system for polymerization of an olefin
US-2016311946-A1 · Oct 27, 2016 · US
US10059656B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10059656-B2 |
| Application number | US-201415104822-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 19, 2014 |
| Priority date | Dec 20, 2013 |
| Publication date | Aug 28, 2018 |
| Grant date | Aug 28, 2018 |
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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.
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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.
Additive used together with the catalyst, excluding compounds containing Al or B · CPC title
Pretreating with non-metals or metal-free compounds · CPC title
Promoter-type Additives · CPC title
of an acyclic saturated carbon skeleton · CPC title
Isotactic · CPC title
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