Method for preparing supported metallocene catalyst and method for preparing polyolefin using the same

Patent metadata

Field	Value
Publication number	US-9637566-B2
Application number	US-201414222127-A
Country	US
Kind code	B2
Filing date	Mar 21, 2014
Priority date	Mar 8, 2010
Publication date	May 2, 2017
Grant date	May 2, 2017

Abstract

The present invention relates to a method for preparing a supported metallocene catalyst, and a method for preparing polyolefin using the same, in which the supported metallocene catalyst prepared from the simple process according to the method for preparing the supported metallocene catalyst of the present invention can apply to the polymerization of the polyolefin that is polymerized at low pressure or high pressure; the molecular weight distribution of polyolefin prepared can be easily controlled; and there are effects such that its catalyst activity is significantly higher than that of the existed supported metallocene catalyst, and the molecular weight distribution can be easily controlled.

First claim

The invention claimed is:

1. A method for preparing a supported metallocene catalyst, comprising:
i) preparing a support supported with metallocene compounds 1 and 2 by reacting metallocene compounds 1 and 2 with a support;
ii) preparing a support supported with the metallocene compounds 1 and 2, and a co-catalyst 1 by reacting the support supported with the metallocene compounds 1 and 2 with the co-catalyst 1;
iii) preparing a catalyst precursor that is sequentially supported with the metallocene compounds 1 and 2, the co-catalyst 1 and further metallocene compounds in the support by reacting the metallocene compounds 1 and 2 with the support supported with the metallocene compounds 1 and 2 and the co-catalyst 1; and
iv) preparing a metallocene catalyst by reacting the catalyst precursor and a co-catalyst 2,
wherein the supported amount of the co-catalyst 2 is 0.2 to 10 mole, based on 1 mole of the transition metal that is supported in the metallocene compound, by the boron contained in the co-catalyst 2, and
wherein the metallocene compound 1 is [A-O—(CH 2 ) a —C 5 H 4 ] 2 ZrCl 2 , in which a is an integer of 4-8, and A is one selected from the group consisting of methoxymethyl, t-bytixymethyl, tetrahydropyranyl, tetrahydrofuranyl, 1-ethyoxyethyl, 1-methyl-1-methoxyethyl and t-butyl,
wherein the metallocene compound 2 is [(A′-D-(CH 2 ) a )](CH 3 )X(C 5 Me 4 )(NCMe 3 )TiCl 2 , in which a is an integer of 4-8, X is methylene, ethylene or silicon, D is oxygen or nitrogen atom, and A′ is one selected from the group consisting of alkyl, alkenyl, aryl, alkylaryl, arylalkyl, alkylsilyl, arylsilyl of carbon number 1-20, hydrogen, methoxymethyl, t-butoxymethyl, tetrahydropranyl, tetrahydrofuranyl, 1-ethoxyethyl, and 1-methyl-1-metoxyethyl and t-butyl,
wherein the co-catalyst 2 is a borate compound represented by Formula 8;
T + [BQ 4 ] −   [Formula 8]

wherein T + is a polyatomic ion having a valency of +1; B is boron in an oxidation state of +3 form; and Q is independently selected from the group consisting of hydride, dialkylamido, alk oxide, aryloxide, hydrocarbyl, halocarbyl, and halo-substituted-hydrocarbyl radical, respectively, the above Q has below 20 carbons.

2. The method for preparing the supported metallocene catalyst according to claim 1 , wherein the support is dried at 200 to 800° C.

3. The method for preparing the supported metallocene catalyst according to claim 1 , wherein the support is one selected from the group consisting of silica, silica-alumina, and silica-magnesia.

4. The method for preparing the supported metallocene catalyst according to claim 1 , wherein the co-catalyst 1 is the compound represented by Formula 7:
—[Al(R 3 )—O] n —  [Formula 7]

wherein,
R 3 is the same or different halogen radical, hydrocarbyl radical of carbon number 1 to 20 or hydrocarbyl radical of carbon number 1 to 20 substituted with halogen to each other, and n is an integer of above 2.

5. The method for preparing the supported metallocene catalyst according to claim 4 , wherein the compound represented by Formula 7 is one selected from the group consisting of methylaluminoxane (MAO), ethylaluminoxane, isobutylaluminoxane, and butylaluminoxane.

6. The method for preparing the supported metallocene catalyst according to claim 1 , wherein the co-catalyst 2 is one or more selected from the group consisting of trimethylammonium tetraphenylborate, methyloctadecylammonium tetraphenylborate, triethylammonium tetraphenylborate, tripropylammonium tetraphenylborate, tri(n-butyl)ammonium tetraphenylborate, methyltetradecyclooctadecylammonium tetraphenylborate, N,N-dimethylanilinium tetraphenylborate, N,N-diethylanilinium tetraphenylborate, N,N-dimethyl(2,4,6-trimethylanilinium)tetraphenylborate, trimethylammonium tetrakis(pentafluorophenyl)borate, methylditetradecylammonium tetrakis(pentafluorophenyl)borate, triethylammonium tetrakis(pentafluorophenyl)borate, tripropylammonium tetrakis (pentafluorophenyl)borate, tri(n-butyl)ammonium tetrakis(pentafluorophenyl)borate, tri(sec-butyl)ammonium tetrakis(pentafluorophenyl)borate, N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate, N,N-diethylanilinium tetrakis(pentafluorophenyl)borate, N,N-dimethyl(2,4,6-trimethylanilinium)tetrakis(pentafluorophenyl)borate, trimethylammonium tetrakis(2,3,4,6-tetrafluorophenyl)borate, triethylammonium tetrakis(2,3,4,6-tetrafluorophenyl)borate, tripropylammonium tetrakis(2,3,4,6-tetrafluorophenyl)borate, tri(n-butyl)ammonium tetrakis(2,3,4,6-tetrafluorophenyl)borate, dimethyl(t-butyl)ammonium tetrakis(2,3,4,6-tetrafluorophenyl)borate, N,N-dimethylanilinium tetrakis(2,3,4,6-tetrafluorophenyl)borate, N,N-diethylanilinium tetrakis(2,3,4,6-tetrafluorophenyl)borate, N,N-dimethyl-(2,4,6-trimethylanilinium)tetrakis-(2,3,4,6-tetrafluorophenyl)borate, dioctadecylammonium tetrakis(pentafluorophenyl)borate, ditetradecylammonium tetrakis(pentafluorophenyl)borate, dicyclohexylammonium tetrakis(pentafluorophenyl)borate, triphenylphosphonium tetrakis(pentafluorophenyl)borate, methyloctadecylphosphonium tetrakis(pentafluorophenyl)borate, tri(2,6-dimethylphenyl)phosphonium tetrakis(pentafluorophenyl)borate, methyldi(octadecyl)ammonium tetrakis(pentafluorophenyl)borate, and methyldi(tetradecyl)-ammonium tetrakis(pentafluorophenyl)borate.

7. A method for preparing a polyolefin, wherein an olefin-based monomer is polymerized under the presence of the supported metallocene catalyst prepared according to the method of claim 1 .

8. The method for preparing the polyolefin according to claim 7 , wherein the polymerization is performed in a slurry process or a gas-phase process.

9. The method for preparing the polyolefin according to claim 7 , wherein the supported metallocene catalyst is injected to the olefin-based monomer, in which the supported metallocene catalyst is a type of slurry that is prepared by diluting in aliphatic hydrocarbon solvent of carbon number 5 to 12, aromatic hydrocarbon solvent, or hydrocarbon solvent substituted with Chlorine atom when it is injected.

Assignees

• Lg Chemical Ltd

Inventors

• Kwon Hyuck-Ju
• Hwang San-Ak
• Lee Dong-Gil
• Park Churl-Young

Classifications

• C08F110/02

  Ethene · CPC title

• C08F4/65912

  in combination with an organoaluminium compound · CPC title

• C08F10/00 Primary

  Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond · CPC title

• C08F4/65904

  in combination with another component of C08F4/64 · CPC title

• C08F4/65922 Primary

  containing at least two cyclopentadienyl rings, fused or not · CPC title