Procatalyst composition made with a combination of internal electron donors
US-2019211118-A1 · Jul 11, 2019 · US
US11945896B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11945896-B2 |
| Application number | US-202017761451-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 10, 2020 |
| Priority date | Sep 18, 2019 |
| Publication date | Apr 2, 2024 |
| Grant date | Apr 2, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A Ziegler-Natta catalyst composition is disclosed. The catalyst composition includes an internal electron donor with improved polymerization kinetics, a long lifetime, improved stereoselectivity and/or improved hydrogen response.
Opening claim text (preview).
What is claimed: 1. A catalyst composition for stereoselective polymerization of propylene comprising: a combination of a magnesium moiety, a titanium moiety, and an internal electron donor, the internal electron donor comprising: wherein: R 1 and R 4 are each a hydrocarbyl group having from 1 to 20 carbon atoms; R 2 is hydrogen; R 3 is a substituted or unsubstituted hydrocarbyl group having from 5 to 15 carbon atoms, the hydrocarbyl group having a branched or linear structure or comprising a cycloalkyl group having from 7 to 15 carbon atoms; E 1 and E 2 are the same or different and selected from the group consisting of an alkyl having 1 to 20 carbon atoms, a substituted alkyl having 1 to 20 carbon atoms, an aryl having 6 to 20 carbon atoms, a substituted aryl having 6 to 20 carbon atoms, and an inert functional group having 1 to 20 carbon atoms and optionally containing heteroatoms; X 1 is NR 5 and X 2 is O, S, or NR 5 , or X 2 is NR 5 and X 1 is O, S, or NR 5 ; and R 5 is a hydrocarbyl group having 1 to 20 carbon atoms or is hydrogen. 2. The catalyst composition of claim 1 , wherein R 3 is a branched alkyl or alkenyl group. 3. The catalyst composition of claim 2 , wherein the branched alkyl or alkenyl group contains from 5 to 10 carbon atoms. 4. The catalyst composition of claim 1 , wherein R 3 is a 3-pentyl group, a 2-pentyl group, a cycloheptyl group, or a cyclooctyl group. 5. The catalyst composition of claim 1 , wherein R 1 and R 4 are the same. 6. The catalyst composition of claim 1 , wherein R 1 and R 4 are linear hydrocarbyl groups. 7. The catalyst composition of claim 1 , wherein R 1 and R 4 comprise a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or mixtures thereof. 8. The catalyst composition of claim 1 , wherein the magnesium moiety comprises a magnesium halide. 9. The catalyst composition of claim 1 , wherein E 1 and E 2 both comprise phenyl groups. 10. The catalyst composition of claim 1 , further comprising a cocatalyst, optionally an activity limiting agent and optionally a selectivity control agent. 11. The catalyst composition of claim 10 , wherein the cocatalyst comprises a hydrocarbon aluminum cocatalyst. 12. The catalyst composition of claim 10 , wherein the selectivity control agent is present and comprises an alkoxysilane. 13. The catalyst composition of claim 10 , wherein the selectivity control agent comprises dicyclopentyldimethoxysilane, di-tert-butyldimethoxysilane, methylcyclohexyldimethoxysilane, methylcyclohexyldiethoxysilane, ethylcyclohexyldimethoxysilane, diphenyldimethoxysilane, diisopropyldimethoxysilane, di-n-propyldimethoxysilane, diisobutyldimethoxysilane, diisobutyldiethoxysilane, isobutylisopropyldimethoxysilane, di-n-butyldimethoxysilane, cyclopentyltrimethoxysilane, isopropyltrimethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, ethyltriethoxysilane, tetramethoxysilane, tetraethoxysilane, diethylaminotriethoxysilane, cyclopentylpyrrolidinodimethoxysilane, bis(pyrrolidino)dimethoxysilane, bis(perhydroisoquinolino)dimethoxysilane, dimethyldimethoxysilane or mixtures thereof. 14. The catalyst composition of claim 1 , wherein the magnesium moiety comprises a spray crystallized magnesium halide compound comprising ethanol and magnesium chloride in a weight ratio of from about 1.5:1 to about 3.1:1. 15. A polymerization process comprising: polymerizing an olefin in the presence of a catalyst composition comprising the catalyst composition of claim 1 . 16. The polymerization process of claim 15 , wherein the olefin comprises propylene for forming a propylene homopolymer or comprises propylene and ethylene for forming a propylene and ethylene copolymer. 17. The polymerization process of claim 16 , wherein the process produces a heterophasic polymer. 18. The polymerization process of claim 17 , wherein the heterophasic polymer comprises a first polymer phase comprising a polypropylene homopolymer or a polypropylene random copolymer, the heterophasic polymer further comprising a second polymer phase combined with the first polymer phase, the second polymer phase comprising an elastomeric propylene ethylene copolymer. 19. The polymerization process of claim 18 , wherein the first polymer phase is formed in a first reactor and the second polymer phase is formed in a second reactor, the catalyst composition remaining active in both the first reactor and the second reactor. 20. An olefin polymer containing the catalyst composition of claim 1 . 21. The catalyst composition of claim 11 , wherein the hydrocarbon aluminum cocatalyst comprises triethylaluminum.
and metals of C08F4/64 or compounds thereof · CPC title
containing silicium · CPC title
Propene · CPC title
Benzoic acid esters · CPC title
Propene · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.