Polyethylene compositions and closures for bottles
US-9221966-B2 · Dec 29, 2015 · US
US10570221B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10570221-B2 |
| Application number | US-201615764758-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 22, 2016 |
| Priority date | Dec 23, 2015 |
| Publication date | Feb 25, 2020 |
| Grant date | Feb 25, 2020 |
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The present invention provides a metallocene supported catalyst that can prepare a polyolefin having excellent transparency even when processed into a film, as well as excellent processibility and mechanical properties, with high catalytic activity, and a method for preparing a polyolefin using the same.
Opening claim text (preview).
The invention claimed is: 1. A metallocene supported catalyst comprising: one or more kinds of metallocene compounds, two or more kinds of cocatalyst compounds, and a carrier, wherein the cocatalyst compounds include a first cocatalyst compound represented by the following Chemical Formula 1 and diethyl zinc as a second cocatalyst compound, and the diethyl zinc is included in the content of 0.1 to 3 mmol/g, based on the weight (g) of the carrier, and at least a part of the diethyl zinc is supported on the first cocatalyst compound: —[Al(R a )—O] n — [Chemical Formula 1] wherein, in Chemical Formula 1, each R a is identical to or different from each other, and are independently a halogen, a C1-20 hydrocarbon, or a C1-20 hydrocarbon substituted with a halogen; and n is an integer of 2 or more. 2. The metallocene supported catalyst according to claim 1 , wherein the compound represented by Chemical Formula 1 is methylaluminoxane, ethylaluminoxane, isobutylaluminoxane or butylaluminoxane. 3. The metallocene supported catalyst according to claim 1 , wherein the metallocene compound is represented by the following Chemical Formulae 2 to 5: (Cp 5 R b ) n (Cp 6 R c )M 1 Z 1 3-n [Chemical Formula 2] wherein, in Chemical Formula 2, M 1 is Group 4 transition metal; Cp 5 and Cp 6 are identical to or different from each other, and are independently one selected from the group consisting of cyclopentadienyl, indenyl, 4,5,6,7-tetrahydro-1-indenyl, and fluorenyl radicals, which are substituted with a C1-20 hydrocarbon; R b and R c are identical to or different from each other, and are independently hydrogen, a C1-20 alkyl, a C1-10 alkoxy, a C2-20 alkoxyalkyl, a C6-20 aryl, a C6-10 aryloxy, a C2-20 alkenyl, a C7-40 alkylaryl, a C7-40 arylalkyl, a C8-40 arylalkenyl, or a C2-10 alkynyl; Z 1 is a halogen atom, a C1-20 alkyl, a C2-10 alkenyl, a C7-40 alkylaryl, a C7-40 arylalkyl, a C6-20 aryl, a substituted or unsubstituted C1-20 alkylidene, a substituted or unsubstituted amino group, a C2-20 alkylalkoxy, or a C7-40 arylalkoxy; and n is 1 or 0, (Cp 7 R d ) m B 1 (Cp 8 R e )M 2 Z 2 3-m [Chemical Formula 3] wherein, in Chemical Formula 3, M 2 is Group 4 transition metal; Cp 7 and Cp 8 are identical to or different from each other, and are independently one selected from the group consisting of cyclopentadienyl, indenyl, 4,5,6,7-tetrahydro-1-indenyl, and fluorenyl radicals, which are substituted with a C1-20 hydrocarbon; R d and R e are identical to or different from each other, and are independently hydrogen, a C1-20 alkyl, a C1-10 alkoxy, a C2-20 alkoxyalkyl, a C6-20 aryl, a C6-10 aryloxy, a C2-20 alkenyl, a C7-40 alkylaryl, a C7-40 arylalkyl, a C8-40 arylalkenyl, or a C2-10 alkynyl; Z 2 is a halogen atom, a C1-20 alkyl, a C2-10 alkenyl, a C7-40 alkylaryl, a C7-40 arylalkyl, a C6-20 aryl, a substituted or unsubstituted C1-20 alkylidene, a substituted or unsubstituted amino group, a C2-20 alkylalkoxy, or a C7-40 arylalkoxy; B 1 is one or more selected from carbon, germanium, silicon, phosphorous, or nitrogen atom-containing radicals or a combination thereof, which crosslinks a Cp 7 R d ring with a Cp 8 R e ring, or crosslinks one Cp 8 R e ring to M 2 ; and m is 1 or 0, (Cp 9 R f )B 2 (J)M 3 Z 3 2 [Chemical Formula 4] wherein, in Chemical Formula 4, M 3 is Group 4 transition metal; Cp 9 is one selected from the group consisting of cyclopentadienyl, indenyl, 4,5,6,7-tetrahydro-1-indenyl, and fluorenyl radicals, which are substituted with a C1-20 hydrocarbon; R f is hydrogen, a C1-20 alkyl, a C1-10 alkoxy, a C2-20 alkoxyalkyl, a C6-20 aryl, a C6-10 aryloxy, a C2-20 alkenyl, a C7-40 alkylaryl, a C7-40 arylalkyl, a C8-40 arylalkenyl, or a C2-10 alkynyl; Z 3 is a halogen atom, a C1-20 alkyl, a C2-10 alkenyl, a C7-40 alkylaryl, a C7-40 arylalkyl, a C6-20 aryl, a substituted or unsubstituted C1-20 alkylidene, a substituted or unsubstituted amino group, a C1-20 alkylalkoxy, or a C7-40 arylalkoxy; B 2 is one or more selected from carbon, germanium, silicon, phosphorous, or nitrogen atom-containing radicals or a combination thereof, which crosslinks a Cp 9 R f ring with J; and J is one selected from the group consisting of NR g , O, PR g , and S, and R g is a C1-20 alkyl, aryl, substituted alkyl, or substituted aryl, wherein, in Chemical Formula 5, A is hydrogen, a halogen, a C1-20 alkyl, a C2-20 alkenyl, a C6-20 aryl, a C7-20 alkylaryl, a C7-20 arylalkyl, a C1-20 alkoxy, a C2-20 alkoxyalkyl, a C3-20 heterocycloalkyl, or a C5-20 heteroaryl; D is —O—, —S—, —N(R)—, or —Si(R)(R′)—, wherein R and R′ are identical to or different from each other, and are independently hydrogen, a halogen, a C1-20 alkyl, a C2-20 alkenyl, or a C6-20 aryl; L is a C1-10 linear or branched alkylene group; B is carbon, silicon, or germanium; Q is hydrogen, a halogen, a C1-20 alkyl, a C2-20 alkenyl, a C6-20 aryl, a C7-20 alkylaryl, or a C7-20 arylalkyl; M is a Group 4 transition metal; X 1 and X 2 are identical to or different from each other, and are independently a halogen, a C1-20 alkyl, a C2-20 alkenyl, a C6-20 aryl, a nitro, an amido, a C1-20 alkylsilyl, a C1-20 alkoxy, or a C1-20 sulfonate group; and C 1 and C 2 are identical to or different from each other, and are independently represented by one of the following Chemical Formula 6a, Chemical Formula 6b, or Chemical Formula 6c, provided that both C 1 and C 2 are not Chemical Formula 6c: wherein, in Chemical Formulas 6a, 6b, and 6c, R1 to R17 and R1′ to R9′ are identical to or different from each other, and are independently hydrogen, a halogen, a C1-20 alkyl, a C2-20 alkenyl, a C1-20 alkylsilyl, a C1-20 silylalkyl, a C1-20 alkoxysilyl, a C1-20 alkoxy, a C6-20 aryl, a C7-20 alkylaryl, or a C7-20 arylalkyl group, and two or more neighboring groups of the R10 to R17 are linked to form a substituted or unsubstituted aliphatic or aromatic ring. 4. The metallocene supported catalyst according to claim 1 , wherein the cocatalyst compounds include, at least one compound represented by a compound of Chemical Formula 7 or a compound of Chemical Formula 8: J(R 23 ) 3 [Chemical Formula 7] wherein, in Chemical Formula 7, each R23 is identical to or different from each other, and are is independently a halogen, a C1-20 hydrocarbon, or a C1-20 hydrocarbon substituted with a halogen; and J is aluminum or boron, [E-H] + [ZA′ 4 ] − or [E] + [ZA′ 4 ] − [Chemical Formula 8] wherein, in Chemical Formula 8, E is a neutral or cationic Lewis acid; H is a hydrogen atom; Z is a Group 13 atom; and each A is identical to or different from each other, and is independently a C6-20 aryl or a C1-20 alkyl group, in which at least one hydrogen atom is unsubstituted or substituted with a halogen, a C1-20 hydrocarbon, an alkoxy or a phenoxy group. 5. The metallocene supported catalyst according to claim 1 , wherein the carrier is silica, silica-alumina or silica-magnesia. 6. A method for preparing a metallocene supported catalyst comprising: supporting two or more kinds of cocatalyst compounds including a first cocatalyst compound and a second cocatalyst compound on a carrier, and then supporting one or more kinds of metallocene compounds, wherein the first cocatalyst compound is a compound represented by the following Chemical Formula 1 and the second cocatalyst compound is diethyl zinc, and the diethyl zinc is supported in the content of 0.1 to 3 mmol/g based on the weight (g) of the carrier, after the firs
containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring · CPC title
Monomers containing three or four carbon atoms · CPC title
Aza-Cp ligands, i.e. [CnN(5-n)Rn]- in which n is 0-4 and R is H or hydrocarbyl, or analogous condensed ring systems · CPC title
Polymerisation in gaseous state · CPC title
in combination with an organoaluminium compound · CPC title
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