Polypropylene And Method For Preparing The Same
US-2020140583-A1 · May 7, 2020 · US
US12358938B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12358938-B2 |
| Application number | US-202017264593-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 10, 2020 |
| Priority date | Jun 13, 2019 |
| Publication date | Jul 15, 2025 |
| Grant date | Jul 15, 2025 |
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Provided are a novel transition metal compound of the following Chemical Formula 1 that exhibits excellent catalytic activity, allows formation of a macromonomer which is a polymer in which a double bond is formed at the end of a chain, and improves a melt strength characteristic when used in polymerizing polypropylene, and a method of preparing a polypropylene using the same.wherein A, M, R1 to R10, X1 and X2, Y1 and Y2 and m are described herein.
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The invention claimed is: 1. A transition metal compound represented by Chemical Formula 1: in Chemical Formula 1, A is an element of Group 14; M is a transition metal of Group 4, R 1 to R 5 are each independently linear C 1-6 alkyl, R 6 is C 6-20 aryl unsubstituted or substituted with linear or branched C 1-8 alkyl, R 7 to R 9 are each independently hydrogen, or two adjacent groups of R 7 to R 9 combine with each other to form a cyclopentyl group, R 10 is each independently hydrogen, one of X 1 or X 2 is S, and the other is a single bond, Y 1 and Y 2 are each independently halogen, and m is an integer of 4. 2. The transition metal compound of claim 1 , wherein A is silicon and M is zirconium. 3. The transition metal compound of claim 1 , wherein all of R 1 to R 5 are methyl. 4. The transition metal compound of claim 1 , wherein R 6 is phenyl or naphthyl, each of which is unsubstituted or substituted with branched C 3-6 alkyl. 5. The transition metal compound of claim 1 , wherein R 6 is phenyl, 4-t-butylphenyl, 3,5-di-t-butylphenyl, or naphthyl. 6. The transition metal compound of claim 1 , wherein the transition metal compound is selected from the group consisting of compounds of the following structures: 7. A catalyst composition comprising the transition metal compound of claim 1 . 8. The catalyst composition of claim 7 , further comprising at least one selected from a carrier, a cocatalyst, or an antistatic agent. 9. The catalyst composition of claim 8 , wherein the carrier comprises silica. 10. The catalyst composition of claim 8 , wherein the cocatalyst comprises one or more of compounds represented by the following Chemical Formulae 4 to 6: —[Al(R 11 )—O] m — [Chemical Formula 4] in Chemical Formula 4, R 11 is the same as or different from each other, and is each independently halogen; C 1-20 hydrocarbon; or C 1-20 hydrocarbon substituted with halogen; and m is an integer of 2 or more; J(R 12 ) 3 [Chemical Formula 5] in Chemical Formula 5, R 12 is the same as or different from each other, and is each independently halogen; C 1-20 hydrocarbon; or C 1-20 hydrocarbon substituted with halogen; and J is aluminum or boron; and [E-H] + [ZQ 4 ] − or [E] + [ZQ 4 ] − [Chemical Formula 6] in Chemical Formula 6, E is a neutral or cationic Lewis base; H is a hydrogen atom; Z is an element of Group 13; and Q is the same as or different from each other, and is each independently a C 6-20 aryl group or a C 1-20 alkyl group in which one or more hydrogen atoms are unsubstituted or substituted with halogen, C 1-20 hydrocarbon, alkoxy, or phenoxy. 11. The catalyst composition of claim 8 , wherein the cocatalyst is alkylaluminoxane. 12. A method of preparing a homopolypropylene, which comprises polymerizing propylene monomers by adding hydrogen in the presence of the catalyst composition of claim 7 . 13. The method of claim 12 , wherein the hydrogen is added in an amount of 50 ppm to 2000 ppm, based on a total weight of the propylene monomers. 14. The method of claim 12 , wherein the homopolypropylene has a ratio of vinyl end groups (:CH═CH 2 ) of 70% or more, as calculated according to Equation 1, and a ratio of vinylidene end groups (:C═CH 2 ) of 10% or less, as calculated according to Equation 2, Ratio of vinyl end groups (%)=[( Mn/ 42)×2×([ Vi]/ 1000)]×100 [Equation 1] Ratio of vinylidene end groups (%)=[( Mn/ 42)×2×([ Vd]/ 1000)]×100 [Equation 2] in Equations 1 and 2, Mn is a value of a number average molecular weight (g/mol) of homopolypropylene, [Vi] is a number of the vinyl end groups per 1000 carbon atoms, and [Vd] is a number of the vinylidene end groups per 1000 carbon atoms.
Propene · CPC title
of silicon, germanium, tin, lead, titanium, zirconium or hafnium · CPC title
Organic complexes · CPC title
containing silicium · CPC title
containing sulfur · CPC title
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