CA2516516A1 - Propylene polymerization process - Google Patents
Propylene polymerization process Download PDFInfo
- Publication number
- CA2516516A1 CA2516516A1 CA002516516A CA2516516A CA2516516A1 CA 2516516 A1 CA2516516 A1 CA 2516516A1 CA 002516516 A CA002516516 A CA 002516516A CA 2516516 A CA2516516 A CA 2516516A CA 2516516 A1 CA2516516 A1 CA 2516516A1
- Authority
- CA
- Canada
- Prior art keywords
- group
- transition metal
- propylene
- radicals
- complex
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/04—Monomers containing three or four carbon atoms
- C08F10/06—Propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—Propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65916—Component covered by group C08F4/64 containing a transition metal-carbon bond supported on a carrier, e.g. silica, MgCl2, polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/943—Polymerization with metallocene catalysts
Abstract
A process for polymerizing propylene is disclosed. The propylene is polymerized with a catalyst system which comprises an activator and a [1,2-b]indenoindolyl Group 4-6 transition metal complex having open architecture. The process has high catalyst activity and gives high molecular weight elastomeric polypropylene.
Claims (13)
1. ~A process which comprises polymerizing propylene in the presence of a catalyst system which comprises an activator and a [1,2-b]indenoindolyl Group 4-6 transition metal complex having open architecture.
2. ~The process of claim 1 wherein the complex is a Group 4 transition metal complex.
3. ~The process of claim 1 wherein the activator is selected from the group consisting of alumoxanes, alkylaluminum compounds, organoboranes, ionic borates, ionic aluminates, aluminoboronates and mixtures thereof.
4. ~The process of claim 1 wherein propylene is copolymerized with at least one olefin.
5. ~The process of claim 4 wherein the olefin is selected from the group consisting of ethylene, propylene, 1-hexene and 1-octene.
6. ~The process of claim 1 wherein the [1,2-b]indenoindolyl Group 4-6 transition metal complex has the structure:
in which R1 is selected from the group consisting of C1-C30 hydrocarbyl, C1-C6 halocarbyl, C1-C30 halohydrocarbyl and trialkylsilyl; each R2 is independently selected from the group consisting of R1, H, F, Cl, Br and C1-C6 alkoxy; G is a divalent radical selected from the group consisting of hydrocarbyl and heteroatom containing alkylene radicals, diorgano silyl radicals, diorgano germanium radicals and diorgano the radicals; L is a ligand that is covalently bonded to G and M; M is a Group 4 to 6 transition metal; each X is independently selected from the group consisting of halide, alkoxy, siloxy, alkylamino, and C1-C30 hydrocarbyl and n satisfies the valence of M
.
in which R1 is selected from the group consisting of C1-C30 hydrocarbyl, C1-C6 halocarbyl, C1-C30 halohydrocarbyl and trialkylsilyl; each R2 is independently selected from the group consisting of R1, H, F, Cl, Br and C1-C6 alkoxy; G is a divalent radical selected from the group consisting of hydrocarbyl and heteroatom containing alkylene radicals, diorgano silyl radicals, diorgano germanium radicals and diorgano the radicals; L is a ligand that is covalently bonded to G and M; M is a Group 4 to 6 transition metal; each X is independently selected from the group consisting of halide, alkoxy, siloxy, alkylamino, and C1-C30 hydrocarbyl and n satisfies the valence of M
.
7. ~The process of claim 6 wherein M is a Group 4 transition metal, L
is alhylamido and G is dialkylsilyl.
is alhylamido and G is dialkylsilyl.
8. The process of claim 7 wherein M is Ti or Zr, L is t-butylamido, G is dimethylsilyl and X is halide or alkyl.
9. The process of claim 1 wherein the polymerization is performed at a temperature within the range of about 20°C to about 90°C.
10. The process of claim 1 wherein the complex is supported on silica.
11. A slurry polymerization process of claim 1.
12. A gas-phase polymerization process of claim 1.
13. A solution polymerization process of claim 1.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/379,752 | 2003-03-05 | ||
US10/379,752 US6693155B1 (en) | 2003-03-05 | 2003-03-05 | Propylene polymerization process |
PCT/US2004/003072 WO2004078802A1 (en) | 2003-03-05 | 2004-02-04 | Propylene polymerization process |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2516516A1 true CA2516516A1 (en) | 2004-09-16 |
CA2516516C CA2516516C (en) | 2010-08-03 |
Family
ID=31188312
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2516516A Expired - Fee Related CA2516516C (en) | 2003-03-05 | 2004-02-04 | Propylene polymerization process |
Country Status (11)
Country | Link |
---|---|
US (1) | US6693155B1 (en) |
EP (1) | EP1599513B1 (en) |
JP (1) | JP2006519297A (en) |
KR (1) | KR20050115888A (en) |
CN (1) | CN100387626C (en) |
AT (1) | ATE363495T1 (en) |
CA (1) | CA2516516C (en) |
DE (1) | DE602004006724T2 (en) |
ES (1) | ES2286605T3 (en) |
MX (1) | MXPA05009470A (en) |
WO (1) | WO2004078802A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6818713B1 (en) * | 2003-08-11 | 2004-11-16 | Equistar Chemicals, Lp | Process for making polyethylene |
US6939930B2 (en) * | 2003-09-09 | 2005-09-06 | Equistar Chemicals, Lp | Hydrosilane additives for increased polyolefin molecular weight |
US7196147B2 (en) * | 2005-07-01 | 2007-03-27 | Equistar Chemicals, Lp | Olefin polymerization process with improved operability and polymer properties |
US7230056B2 (en) * | 2005-07-01 | 2007-06-12 | Equistar Chemicals, Lp | Catalyst preparation method |
KR20080064801A (en) * | 2005-08-04 | 2008-07-09 | 더 리젠츠 오브 더 유니버시티 오브 콜로라도, 어 바디 코포레이트 | Catalysts for radical polymerization |
US7423098B2 (en) * | 2006-01-17 | 2008-09-09 | Equistar Chemicals, Lp | Polyethylene process |
WO2019022569A1 (en) | 2017-07-27 | 2019-01-31 | 주식회사 엘지화학 | Novel transition metal compound and method for preparing same |
CN112920227B (en) * | 2021-02-18 | 2022-09-23 | 山东京博石油化工有限公司 | Indenoindole structure-containing metallocene compound, preparation method and application thereof, and preparation method of alpha-olefin |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5153157A (en) | 1987-01-30 | 1992-10-06 | Exxon Chemical Patents Inc. | Catalyst system of enhanced productivity |
US5198401A (en) | 1987-01-30 | 1993-03-30 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
US5241025A (en) | 1987-01-30 | 1993-08-31 | Exxon Chemical Patents Inc. | Catalyst system of enhanced productivity |
US5064802A (en) | 1989-09-14 | 1991-11-12 | The Dow Chemical Company | Metal complex compounds |
US5449650A (en) | 1992-12-08 | 1995-09-12 | Mitsubishi Petrochemical Company Limited | Catalyst components for polymerization of olefins and use thereof |
US5414180A (en) | 1993-07-14 | 1995-05-09 | Phillips Petroleum Company | Organo-aluminoxy product and use |
US5495035A (en) | 1994-06-01 | 1996-02-27 | University Of Iowa Research Foundation | Synthesis of ANSA-metallocene catalysts |
US5539124A (en) * | 1994-12-19 | 1996-07-23 | Occidental Chemical Corporation | Polymerization catalysts based on transition metal complexes with ligands containing pyrrolyl ring |
WO1998018842A1 (en) * | 1996-10-31 | 1998-05-07 | Mobil Oil Corporation | Lldpe copolymers |
ID22914A (en) | 1997-11-12 | 1999-12-16 | Montell Technology Company Bv | METALOSEN AND CATALYST FOR OLEFIN POLYMERIZATION |
CN1222531A (en) * | 1997-12-23 | 1999-07-14 | 蒙岱尔北美股份有限公司 | Catalyst for polymerization of alpha-olefins containing substituted amino silane compounds |
CN1243763C (en) * | 1998-01-14 | 2006-03-01 | 蒙特尔技术有限公司 | Method for preparing metallocene compounds |
US6211311B1 (en) | 1999-05-25 | 2001-04-03 | Equistar Chemicals, L.P. | Supported olefin polymerization catalysts |
US6232260B1 (en) | 1999-10-14 | 2001-05-15 | Equistar Chemicals, L.P. | Single-site catalysts for olefin polymerization |
ES2239665T3 (en) | 2000-01-18 | 2005-10-01 | Basell Polyolefine Gmbh | PROCEDURE TO PRODUCE AA PROPYLENE BASED POLYMERS, SUBSTANTIALLY AMORPHES. |
US6559251B1 (en) | 2002-08-02 | 2003-05-06 | Equistar Chemicals, Lp | Process for making low-density polyolefins |
-
2003
- 2003-03-05 US US10/379,752 patent/US6693155B1/en not_active Expired - Fee Related
-
2004
- 2004-02-04 EP EP04708126A patent/EP1599513B1/en not_active Expired - Lifetime
- 2004-02-04 KR KR1020057016370A patent/KR20050115888A/en not_active Application Discontinuation
- 2004-02-04 CN CNB2004800060238A patent/CN100387626C/en not_active Expired - Fee Related
- 2004-02-04 ES ES04708126T patent/ES2286605T3/en not_active Expired - Lifetime
- 2004-02-04 MX MXPA05009470A patent/MXPA05009470A/en unknown
- 2004-02-04 JP JP2006508653A patent/JP2006519297A/en not_active Withdrawn
- 2004-02-04 DE DE602004006724T patent/DE602004006724T2/en not_active Expired - Lifetime
- 2004-02-04 CA CA2516516A patent/CA2516516C/en not_active Expired - Fee Related
- 2004-02-04 AT AT04708126T patent/ATE363495T1/en not_active IP Right Cessation
- 2004-02-04 WO PCT/US2004/003072 patent/WO2004078802A1/en active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
WO2004078802A1 (en) | 2004-09-16 |
US6693155B1 (en) | 2004-02-17 |
CA2516516C (en) | 2010-08-03 |
MXPA05009470A (en) | 2005-11-23 |
JP2006519297A (en) | 2006-08-24 |
CN100387626C (en) | 2008-05-14 |
ES2286605T3 (en) | 2007-12-01 |
EP1599513A1 (en) | 2005-11-30 |
DE602004006724T2 (en) | 2008-02-14 |
KR20050115888A (en) | 2005-12-08 |
ATE363495T1 (en) | 2007-06-15 |
CN1756776A (en) | 2006-04-05 |
DE602004006724D1 (en) | 2007-07-12 |
EP1599513B1 (en) | 2007-05-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed | ||
MKLA | Lapsed |
Effective date: 20120206 |