JP2007533824A - ヘテロ相コポリマ−及びメタロセン触媒系並びにこのメタロセン触媒系を用いる該ヘテロ相コポリマ−の製造法 - Google Patents
ヘテロ相コポリマ−及びメタロセン触媒系並びにこのメタロセン触媒系を用いる該ヘテロ相コポリマ−の製造法 Download PDFInfo
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- JP2007533824A JP2007533824A JP2007509494A JP2007509494A JP2007533824A JP 2007533824 A JP2007533824 A JP 2007533824A JP 2007509494 A JP2007509494 A JP 2007509494A JP 2007509494 A JP2007509494 A JP 2007509494A JP 2007533824 A JP2007533824 A JP 2007533824A
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- catalyst system
- metallocene catalyst
- polymer
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- 239000010457 zeolite Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 description 1
- QMBQEXOLIRBNPN-UHFFFAOYSA-L zirconocene dichloride Chemical compound [Cl-].[Cl-].[Zr+4].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 QMBQEXOLIRBNPN-UHFFFAOYSA-L 0.000 description 1
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- 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
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- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
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- C08F10/06—Propene
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- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/06—Catalyst characterized by its size
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- 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
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- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
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- 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
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
- C08F4/65922—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not
- C08F4/65927—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not two cyclopentadienyl rings being mutually bridged
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- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/02—Heterophasic composition
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/16—Ethene-propene or ethene-propene-diene copolymers
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| PCT/US2005/011605 WO2005104940A2 (en) | 2004-04-20 | 2005-04-07 | Heterophasic copolymer and metallocene catalyst system |
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| JP2020521024A (ja) * | 2017-05-19 | 2020-07-16 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 触媒系およびその使用のための重合方法 |
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| US8003739B2 (en) | 2007-10-17 | 2011-08-23 | Fina Technology, Inc. | Multi-component catalyst systems and polymerization processes for forming in-situ heterophasic copolymers and/or varying the xylene solubles content of polyolefins |
| EP1988122A1 (en) * | 2007-05-04 | 2008-11-05 | Total Petrochemicals Research Feluy | Blend for use in automobile application |
| US20080287619A1 (en) * | 2007-05-18 | 2008-11-20 | William Gauthier | Supported metallocene catalysts |
| EP2075284B1 (en) * | 2007-12-17 | 2013-05-29 | Borealis Technology OY | Heterophasic polypropylene with high flowability and excellent low temperature impact properties |
| EP2141200A1 (en) * | 2008-07-03 | 2010-01-06 | Total Petrochemicals Research Feluy | Heterophasic propylene copolymer with improved properties for injection molding applications |
| EP2275476A1 (en) * | 2009-06-09 | 2011-01-19 | Borealis AG | Automotive material with excellent flow, high stiffness, excellent ductility and low CLTE |
| EP2426171A1 (en) | 2010-08-30 | 2012-03-07 | Borealis AG | Heterophasic polypropylene with high flowability and enhanced mechanical properties |
| US10570219B2 (en) * | 2015-06-05 | 2020-02-25 | Exxonmobil Chemical Patents Inc. | Production of heterophasic polymers in gas or slurry phase |
| JP6396523B2 (ja) * | 2017-02-17 | 2018-09-26 | 旭化成株式会社 | ポリエチレン系重合体及びその製造方法 |
| WO2020009336A1 (ko) * | 2018-07-03 | 2020-01-09 | 엘에스전선 주식회사 | 전력 케이블 |
| KR102103087B1 (ko) * | 2018-07-03 | 2020-04-21 | 엘에스전선 주식회사 | 전력 케이블 |
| WO2025157819A1 (en) * | 2024-01-22 | 2025-07-31 | Sabic Global Technologies B.V. | Catalyst system for multi-stage olefin polymerisation |
Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05287035A (ja) * | 1992-04-07 | 1993-11-02 | Tokuyama Soda Co Ltd | プロピレン系ブロック共重合体 |
| JPH07224128A (ja) * | 1994-02-10 | 1995-08-22 | Tosoh Corp | プロピレンブロック共重合体の製造方法 |
| JPH07286022A (ja) * | 1994-04-18 | 1995-10-31 | Mitsui Petrochem Ind Ltd | プロピレン系ブロック共重合体 |
| JP2000239462A (ja) * | 1998-08-25 | 2000-09-05 | Tokuyama Corp | プロピレン系樹脂組成物、その製造方法および用途 |
| JP2001310921A (ja) * | 2000-04-26 | 2001-11-06 | Chisso Corp | プロピレン/オレフィン・ブロック共重合体 |
| JP2002030128A (ja) * | 2000-07-19 | 2002-01-31 | Grand Polymer Co Ltd | プロピレン系ブロック共重合体粒子およびその製造方法 |
| JP2002105119A (ja) * | 2000-09-29 | 2002-04-10 | Sumitomo Chem Co Ltd | 立体規則性α−オレフィン重合用触媒および立体規則性α−オレフィン重合体の製造方法 |
| JP2002275342A (ja) * | 2001-03-15 | 2002-09-25 | Mitsui Chemicals Inc | ポリオレフィン樹脂組成物 |
| JP2003055464A (ja) * | 2001-07-26 | 2003-02-26 | Fina Technol Inc | ポリプロピレンコポリマーおよびポリプロピレンコポリマーの製造方法 |
| JP2004002259A (ja) * | 2001-08-06 | 2004-01-08 | Chisso Corp | メタロセン化合物、それを含む触媒を用いたオレフィン重合体の製造方法、および、該製造方法により製造されたオレフィン重合体 |
| JP2004359877A (ja) * | 2003-06-06 | 2004-12-24 | Mitsui Chemicals Inc | プロピレン系樹脂組成物 |
Family Cites Families (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1209255B (it) * | 1980-08-13 | 1989-07-16 | Montedison Spa | Catalizzatori per la polimerizzazione di olefine. |
| DE3127133A1 (de) * | 1981-07-09 | 1983-01-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von polyolefinen und deren copolymerisaten |
| US5324800A (en) * | 1983-06-06 | 1994-06-28 | Exxon Chemical Patents Inc. | Process and catalyst for polyolefin density and molecular weight control |
| US4937299A (en) * | 1983-06-06 | 1990-06-26 | Exxon Research & Engineering Company | Process and catalyst for producing reactor blend polyolefins |
| US4530914A (en) * | 1983-06-06 | 1985-07-23 | Exxon Research & Engineering Co. | Process and catalyst for producing polyethylene having a broad molecular weight distribution |
| DE3508887A1 (de) * | 1985-03-13 | 1986-09-25 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von optisch aktiven polyolefinen |
| US4808561A (en) * | 1985-06-21 | 1989-02-28 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
| US4665208A (en) * | 1985-07-11 | 1987-05-12 | Exxon Chemical Patents Inc. | Process for the preparation of alumoxanes |
| JPH0780933B2 (ja) * | 1986-11-20 | 1995-08-30 | 三井石油化学工業株式会社 | オレフインの重合方法 |
| US5198401A (en) * | 1987-01-30 | 1993-03-30 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| PL276385A1 (en) * | 1987-01-30 | 1989-07-24 | Exxon Chemical Patents Inc | Method for polymerization of olefines,diolefins and acetylene unsaturated compounds |
| US5384299A (en) * | 1987-01-30 | 1995-01-24 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| JPH0742301B2 (ja) * | 1987-02-14 | 1995-05-10 | 三井石油化学工業株式会社 | 微粒子状アルミノオキサン、その製法およびその用途 |
| US4769910A (en) * | 1987-03-30 | 1988-09-13 | Northern Telecom Limited | Cutting tool for cylindrical articles |
| JP2538588B2 (ja) * | 1987-04-03 | 1996-09-25 | 三井石油化学工業株式会社 | オレフイン重合用固体触媒の製法 |
| US4794096A (en) * | 1987-04-03 | 1988-12-27 | Fina Technology, Inc. | Hafnium metallocene catalyst for the polymerization of olefins |
| US5206199A (en) * | 1987-04-20 | 1993-04-27 | Mitsui Petrochemical Industries, Ltd. | Catalyst for polymerizing an olefin and process for polymerizing an olefin |
| US4975403A (en) * | 1987-09-11 | 1990-12-04 | Fina Technology, Inc. | Catalyst systems for producing polyolefins having a broad molecular weight distribution |
| US4931417A (en) * | 1987-11-09 | 1990-06-05 | Chisso Corporation | Transition-metal compound having a bis-substituted-cyclopentadienyl ligand of bridged structure |
| US5120867A (en) * | 1988-03-21 | 1992-06-09 | Welborn Jr Howard C | Silicon-bridged transition metal compounds |
| US5017714A (en) * | 1988-03-21 | 1991-05-21 | Exxon Chemical Patents Inc. | Silicon-bridged transition metal compounds |
| US4871705A (en) * | 1988-06-16 | 1989-10-03 | Exxon Chemical Patents Inc. | Process for production of a high molecular weight ethylene a-olefin elastomer with a metallocene alumoxane catalyst |
| US5091352A (en) * | 1988-09-14 | 1992-02-25 | Mitsui Petrochemical Industries, Ltd. | Olefin polymerization catalyst component, olefin polymerization catalyst and process for the polymerization of olefins |
| US4908463A (en) * | 1988-12-05 | 1990-03-13 | Ethyl Corporation | Aluminoxane process |
| US5103031A (en) * | 1989-02-21 | 1992-04-07 | Ethyl Corporation | Falling film aluminoxane process |
| DE3907964A1 (de) * | 1989-03-11 | 1990-09-13 | Hoechst Ag | Verfahren zur herstellung eines syndiotaktischen polyolefins |
| US4968827A (en) * | 1989-06-06 | 1990-11-06 | Ethyl Corporation | Alkylaluminoxane process |
| US4924018A (en) * | 1989-06-26 | 1990-05-08 | Ethyl Corporation | Alkylaluminoxane process |
| JPH0735503B2 (ja) * | 1989-07-27 | 1995-04-19 | サンスター技研株式会社 | 湿気硬化性熱溶融型接着剤 |
| IT1231769B (it) * | 1989-08-02 | 1991-12-21 | Himont Inc | Procedimento per la stabilizzazione di poliolefine e prodotti da esso ottenuti. |
| US5026798A (en) * | 1989-09-13 | 1991-06-25 | Exxon Chemical Patents Inc. | Process for producing crystalline poly-α-olefins with a monocyclopentadienyl transition metal catalyst system |
| US5057475A (en) * | 1989-09-13 | 1991-10-15 | Exxon Chemical Patents Inc. | Mono-Cp heteroatom containing group IVB transition metal complexes with MAO: supported catalyst for olefin polymerization |
| US5239022A (en) * | 1990-11-12 | 1993-08-24 | Hoechst Aktiengesellschaft | Process for the preparation of a syndiotactic polyolefin |
| ES2090209T3 (es) * | 1990-11-12 | 1996-10-16 | Hoechst Ag | Metalocenos con ligandos basados en derivados de indenilo sustituidos en posicion 2, procedimiento para su preparacion y su empleo como catalizadores. |
| US5243001A (en) * | 1990-11-12 | 1993-09-07 | Hoechst Aktiengesellschaft | Process for the preparation of a high molecular weight olefin polymer |
| EP0485823B1 (de) * | 1990-11-12 | 1995-03-08 | Hoechst Aktiengesellschaft | 2-Substituierte Bisindenylmetallocene, Verfahren zu ihrer Herstellung und ihre Verwendung als Katalysatoren bei der Olefinpolymerisation |
| US5436305A (en) * | 1991-05-09 | 1995-07-25 | Phillips Petroleum Company | Organometallic fluorenyl compounds, preparation, and use |
| DE4120009A1 (de) * | 1991-06-18 | 1992-12-24 | Basf Ag | Loesliche katalysatorsysteme zur herstellung von polyalk-1-enen mit hohen molmassen |
| US5235081A (en) * | 1992-03-18 | 1993-08-10 | Ethyl Corporation | Method of removing gel forming materials from methylaluminoxanes |
| US5308815A (en) * | 1991-07-26 | 1994-05-03 | Ethyl Corporation | Heterogeneous methylaluminoxane catalyst system |
| TW300901B (enExample) * | 1991-08-26 | 1997-03-21 | Hoechst Ag | |
| US5416228A (en) * | 1991-10-07 | 1995-05-16 | Fina Technology, Inc. | Process and catalyst for producing isotactic polyolefins |
| ATE286918T1 (de) * | 1991-10-15 | 2005-01-15 | Basell Polyolefine Gmbh | Verfahren zur herstellung eines olefinpolymers unter verwendung von metallocenen mit speziell substituierten indenylliganden |
| TW318184B (enExample) * | 1991-11-30 | 1997-10-21 | Hoechst Ag | |
| US5329032A (en) * | 1992-03-18 | 1994-07-12 | Akzo Chemicals Inc. | Polymethylaluminoxane of enhanced solution stability |
| US5243752A (en) * | 1992-03-20 | 1993-09-14 | Delco Electronics Corporation | Process of manufacturing an instrumentation apparatus with curable internal magnets |
| US5350723A (en) * | 1992-05-15 | 1994-09-27 | The Dow Chemical Company | Process for preparation of monocyclopentadienyl metal complex compounds and method of use |
| DE69224184T2 (de) * | 1992-06-13 | 1999-06-02 | Targor GmbH, 55116 Mainz | Verfahren zur Herstellung von verbrückten, chiralen Metallocenkatalysatoren des Types Bisindenyl |
| EP0584609B1 (de) * | 1992-08-15 | 1999-03-10 | TARGOR GmbH | Verfahren zur Herstellung von Polyolefinen |
| US5248801A (en) * | 1992-08-27 | 1993-09-28 | Ethyl Corporation | Preparation of methylaluminoxanes |
| JP3307704B2 (ja) * | 1993-02-19 | 2002-07-24 | 三菱化学株式会社 | α‐オレフィン重合体の製造法 |
| DE4344688A1 (de) * | 1993-12-27 | 1995-06-29 | Hoechst Ag | Metallocenverbindung |
| DE4344689A1 (de) * | 1993-12-27 | 1995-06-29 | Hoechst Ag | Metallocenverbindung |
| BR9508119A (pt) * | 1994-06-24 | 1997-08-12 | Exxon Chemical Patents Inc | Sistemas de catalisador de polimerização produção e uso dos mesmos |
| US6143686A (en) * | 1994-08-03 | 2000-11-07 | Exxon Chemical Patents, Inc. | Supported ionic catalyst compositions |
| US5643847A (en) * | 1994-08-03 | 1997-07-01 | Exxon Chemical Patents Inc. | Supported ionic catalyst composition |
| US6140432A (en) * | 1995-07-13 | 2000-10-31 | Exxon Chemical Patents Inc. | Polymerization catalyst systems, their production and use |
| US6124230A (en) * | 1995-07-13 | 2000-09-26 | Exxon Chemical Patents, Inc. | Polymerization catalyst systems, their production and use |
| IT1275573B (it) * | 1995-07-20 | 1997-08-07 | Spherilene Spa | Processo ed apparecchiatura per la pomimerizzazione in fase gas delle alfa-olefine |
| US5723402A (en) * | 1996-05-30 | 1998-03-03 | Pq Corporation | Silicas with specific contents of cations as supports for olefin polymerization catalysts |
| HU223533B1 (hu) * | 1996-06-17 | 2004-08-30 | Exxonmobil Chemical Patents Inc. | Vegyes átmenetifém katalizátor-rendszer olefinek polimerizálására |
| ES2196241T3 (es) * | 1996-11-26 | 2003-12-16 | Basell North America Inc | Una composicion de poliolefina para la fabricacion de hojas con extrusiones con retencion mejorada de granulacion. |
| EP0881236A1 (en) * | 1997-05-26 | 1998-12-02 | Fina Research S.A. | Metallocene catalyst component for use in producing isotactic polyolefins |
| US6228795B1 (en) * | 1997-06-05 | 2001-05-08 | Exxon Chemical Patents, Inc. | Polymeric supported catalysts |
| EP0986586B1 (en) * | 1997-06-05 | 2008-06-18 | ExxonMobil Chemical Patents Inc. | Polymeric supported catalysts for olefin polymerization |
| DE69925853T2 (de) * | 1998-06-16 | 2006-05-18 | Borealis Technology Oy | Olefin polymerizations verfahren |
| US6492465B1 (en) * | 2000-02-08 | 2002-12-10 | Exxonmobil Chemical Patents, Inc. | Propylene impact copolymers |
| US6777367B2 (en) * | 2001-02-13 | 2004-08-17 | Fina Technology, Inc. | Method for the preparation of metallocene catalysts |
| US6777366B2 (en) * | 2001-02-13 | 2004-08-17 | Fina Technology, Inc. | Method for the preparation of metallocene catalysts |
| US7019157B2 (en) * | 2001-08-06 | 2006-03-28 | Chisso Corporation | Metallocene compounds, production process for olefin polymers using catalysts containing them and olefin polymers produced by the production process |
| US20030236365A1 (en) * | 2002-06-24 | 2003-12-25 | Fina Technology, Inc. | Polyolefin production with a high performance support for a metallocene catalyst system |
-
2004
- 2004-04-20 US US10/827,959 patent/US20050234198A1/en not_active Abandoned
-
2005
- 2005-04-07 JP JP2007509494A patent/JP2007533824A/ja active Pending
- 2005-04-07 CA CA002553496A patent/CA2553496A1/en not_active Abandoned
- 2005-04-07 EP EP05732650A patent/EP1737909A4/en not_active Withdrawn
- 2005-04-07 KR KR1020067015334A patent/KR20070004604A/ko not_active Withdrawn
- 2005-04-07 CN CN2005800115432A patent/CN1972994B/zh not_active Expired - Fee Related
- 2005-04-07 WO PCT/US2005/011605 patent/WO2005104940A2/en not_active Ceased
- 2005-04-11 TW TW094111377A patent/TW200604230A/zh unknown
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05287035A (ja) * | 1992-04-07 | 1993-11-02 | Tokuyama Soda Co Ltd | プロピレン系ブロック共重合体 |
| JPH07224128A (ja) * | 1994-02-10 | 1995-08-22 | Tosoh Corp | プロピレンブロック共重合体の製造方法 |
| JPH07286022A (ja) * | 1994-04-18 | 1995-10-31 | Mitsui Petrochem Ind Ltd | プロピレン系ブロック共重合体 |
| JP2000239462A (ja) * | 1998-08-25 | 2000-09-05 | Tokuyama Corp | プロピレン系樹脂組成物、その製造方法および用途 |
| JP2001310921A (ja) * | 2000-04-26 | 2001-11-06 | Chisso Corp | プロピレン/オレフィン・ブロック共重合体 |
| JP2002030128A (ja) * | 2000-07-19 | 2002-01-31 | Grand Polymer Co Ltd | プロピレン系ブロック共重合体粒子およびその製造方法 |
| JP2002105119A (ja) * | 2000-09-29 | 2002-04-10 | Sumitomo Chem Co Ltd | 立体規則性α−オレフィン重合用触媒および立体規則性α−オレフィン重合体の製造方法 |
| JP2002275342A (ja) * | 2001-03-15 | 2002-09-25 | Mitsui Chemicals Inc | ポリオレフィン樹脂組成物 |
| JP2003055464A (ja) * | 2001-07-26 | 2003-02-26 | Fina Technol Inc | ポリプロピレンコポリマーおよびポリプロピレンコポリマーの製造方法 |
| JP2004002259A (ja) * | 2001-08-06 | 2004-01-08 | Chisso Corp | メタロセン化合物、それを含む触媒を用いたオレフィン重合体の製造方法、および、該製造方法により製造されたオレフィン重合体 |
| JP2004359877A (ja) * | 2003-06-06 | 2004-12-24 | Mitsui Chemicals Inc | プロピレン系樹脂組成物 |
Non-Patent Citations (1)
| Title |
|---|
| JPN6013005435; エドワード・P・ムーア・Jr/編集者: ポリプロピレンハンドブック 初版第2刷, 20010720, 第115頁, 株式会社 工業調査会/発行所 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020521024A (ja) * | 2017-05-19 | 2020-07-16 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 触媒系およびその使用のための重合方法 |
| JP7025453B2 (ja) | 2017-05-19 | 2022-02-24 | エクソンモービル ケミカル パテンツ インコーポレイテッド | 触媒系およびその使用のための重合方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005104940A3 (en) | 2006-11-09 |
| WO2005104940A2 (en) | 2005-11-10 |
| CN1972994B (zh) | 2013-01-16 |
| CA2553496A1 (en) | 2005-11-10 |
| EP1737909A2 (en) | 2007-01-03 |
| TW200604230A (en) | 2006-02-01 |
| KR20070004604A (ko) | 2007-01-09 |
| CN1972994A (zh) | 2007-05-30 |
| EP1737909A4 (en) | 2008-07-23 |
| US20050234198A1 (en) | 2005-10-20 |
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