JP2023523494A - 触媒および触媒組成物の調製プロセス - Google Patents
触媒および触媒組成物の調製プロセス Download PDFInfo
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- JP2023523494A JP2023523494A JP2022544670A JP2022544670A JP2023523494A JP 2023523494 A JP2023523494 A JP 2023523494A JP 2022544670 A JP2022544670 A JP 2022544670A JP 2022544670 A JP2022544670 A JP 2022544670A JP 2023523494 A JP2023523494 A JP 2023523494A
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- Prior art keywords
- clay
- smectite
- heteroadduct
- slurry
- colloidal
- Prior art date
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- 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
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- 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
- C08F110/02—Ethene
-
- 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
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Polymerization Catalysts (AREA)
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Family Cites Families (96)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB489769A (en) | 1937-01-25 | 1938-08-03 | Ig Farbenindustrie Ag | Improvements in the manufacture and production of water-soluble basic aluminium compounds |
US3248179A (en) | 1962-02-26 | 1966-04-26 | Phillips Petroleum Co | Method and apparatus for the production of solid polymers of olefins |
US3242099A (en) | 1964-03-27 | 1966-03-22 | Union Carbide Corp | Olefin polymerization catalysts |
US4003712A (en) | 1970-07-29 | 1977-01-18 | Union Carbide Corporation | Fluidized bed reactor |
US3709853A (en) | 1971-04-29 | 1973-01-09 | Union Carbide Corp | Polymerization of ethylene using supported bis-(cyclopentadienyl)chromium(ii)catalysts |
US3962135A (en) | 1973-12-26 | 1976-06-08 | Filtrol Corporation | Shaped catalyst support |
US4011382A (en) | 1975-03-10 | 1977-03-08 | Union Carbide Corporation | Preparation of low and medium density ethylene polymer in fluid bed reactor |
US4176090A (en) | 1975-11-18 | 1979-11-27 | W. R. Grace & Co. | Pillared interlayered clay materials useful as catalysts and sorbents |
US4302566A (en) | 1978-03-31 | 1981-11-24 | Union Carbide Corporation | Preparation of ethylene copolymers in fluid bed reactor |
US4248739A (en) | 1979-09-04 | 1981-02-03 | W. R. Grace & Co. | Stabilized pillared interlayered clays |
US4737280A (en) | 1980-09-17 | 1988-04-12 | Phillips Petroleum Company | Separation of solid polymers and liquid diluent |
US4367163A (en) | 1981-04-15 | 1983-01-04 | Research Corporation | Silica-clay complexes |
US4424341A (en) | 1981-09-21 | 1984-01-03 | Phillips Petroleum Company | Separation of solid polymers and liquid diluent |
US4501885A (en) | 1981-10-14 | 1985-02-26 | Phillips Petroleum Company | Diluent and inert gas recovery from a polymerization process |
US4543399A (en) | 1982-03-24 | 1985-09-24 | Union Carbide Corporation | Fluidized bed reaction systems |
US4588790A (en) | 1982-03-24 | 1986-05-13 | Union Carbide Corporation | Method for fluidized bed polymerization |
US4613484A (en) | 1984-11-30 | 1986-09-23 | Phillips Petroleum Company | Loop reactor settling leg system for separation of solid polymers and liquid diluent |
US4637992A (en) | 1984-12-17 | 1987-01-20 | Shell Oil Company | Intercalated clay compositions |
US4808561A (en) | 1985-06-21 | 1989-02-28 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
US5202295A (en) | 1987-03-05 | 1993-04-13 | Uop | Intercalated clay having large interlayer spacing |
US5059568A (en) | 1987-03-05 | 1991-10-22 | Uop | Intercalated clay having large interlayer spacing |
US4939217A (en) | 1987-04-03 | 1990-07-03 | Phillips Petroleum Company | Process for producing polyolefins and polyolefin catalysts |
US4794096A (en) | 1987-04-03 | 1988-12-27 | Fina Technology, Inc. | Hafnium metallocene catalyst for the polymerization of olefins |
FR2618786B1 (fr) | 1987-07-31 | 1989-12-01 | Bp Chimie Sa | Procede de polymerisation d'olefines en phase gazeuse dans un reacteur a lit fluidise |
FR2634212B1 (fr) | 1988-07-15 | 1991-04-19 | Bp Chimie Sa | Appareillage et procede de polymerisation d'olefines en phase gazeuse dans un reacteur a lit fluidise |
US5705478A (en) | 1989-02-21 | 1998-01-06 | Washington University | Covalently linked β subunits of the glycoprotein hormones as antagonists |
US5575979A (en) | 1991-03-04 | 1996-11-19 | Phillips Petroleum Company | Process and apparatus for separating diluents from solid polymers utilizing a two-stage flash and a cyclone separator |
US5191132A (en) | 1991-05-09 | 1993-03-02 | Phillips Petroleum Company | Cyclopentadiene type compounds and method for making |
US5436305A (en) | 1991-05-09 | 1995-07-25 | Phillips Petroleum Company | Organometallic fluorenyl compounds, preparation, and use |
US5571880A (en) | 1991-05-09 | 1996-11-05 | Phillips Petroleum Company | Organometallic fluorenyl compounds and use thereof in an alpha-olefin polymerization process |
US5631335A (en) | 1991-05-09 | 1997-05-20 | Phillips Petroleum Company | Process of polymerizing olefins using diphenylsilyl or dimethyl tin bridged 1-methyl fluorenyl metallocenes |
US5347026A (en) | 1993-06-11 | 1994-09-13 | Phillips Petroleum Company | Fluorene compounds and methods for making |
US5401817A (en) | 1991-05-09 | 1995-03-28 | Phillips Petroleum Company | Olefin polymerization using silyl-bridged metallocenes |
US5466766A (en) | 1991-05-09 | 1995-11-14 | Phillips Petroleum Company | Metallocenes and processes therefor and therewith |
US5399636A (en) | 1993-06-11 | 1995-03-21 | Phillips Petroleum Company | Metallocenes and processes therefor and therewith |
US5210352A (en) | 1991-05-09 | 1993-05-11 | Phillips Petroleum Company | Fluorene compounds |
US5451649A (en) | 1991-05-09 | 1995-09-19 | Phillips Petroleum Company | Organometallic fluorenyl compounds, preparation, and use |
US5668230A (en) | 1991-07-23 | 1997-09-16 | Phillips Petroleum Company | Olefin polymerization |
US5594078A (en) | 1991-07-23 | 1997-01-14 | Phillips Petroleum Company | Process for producing broad molecular weight polyolefin |
JPH05170429A (ja) | 1991-12-18 | 1993-07-09 | Mitsubishi Materials Corp | 粘土架橋多孔体及びその製造方法 |
US5352749A (en) | 1992-03-19 | 1994-10-04 | Exxon Chemical Patents, Inc. | Process for polymerizing monomers in fluidized beds |
US5436304A (en) | 1992-03-19 | 1995-07-25 | Exxon Chemical Patents Inc. | Process for polymerizing monomers in fluidized beds |
US5317036A (en) | 1992-10-16 | 1994-05-31 | Union Carbide Chemicals & Plastics Technology Corporation | Gas phase polymerization reactions utilizing soluble unsupported catalysts |
US5462999A (en) | 1993-04-26 | 1995-10-31 | Exxon Chemical Patents Inc. | Process for polymerizing monomers in fluidized beds |
CA2161419C (en) | 1993-04-26 | 1999-05-04 | Marc Louis Dechellis | Process for polymerizing monomers in fluidized beds |
ZA943399B (en) | 1993-05-20 | 1995-11-17 | Bp Chem Int Ltd | Polymerisation process |
US5414049A (en) | 1993-06-01 | 1995-05-09 | Howmedica Inc. | Non-oxidizing polymeric medical implant |
AU673752B2 (en) | 1993-06-07 | 1996-11-21 | Colloidal Dynamics Pty. Ltd. | Particle size and charge measurement in multi-component colloids |
US5354721A (en) | 1993-06-22 | 1994-10-11 | Phillips Petroleum Company | Organo-aluminoxy product and use |
US5804678A (en) | 1993-07-13 | 1998-09-08 | Mitsui Petrochemical Industries, Ltd. | Process for gas phase polymerization of olefin |
US5576259A (en) | 1993-10-14 | 1996-11-19 | Tosoh Corporation | Process for producing α-olefin polymer |
EP0649992B1 (de) | 1993-10-23 | 1997-07-30 | WABCO GmbH | Betätigungseinrichtung für eine Scheibenbremse |
US5496781A (en) | 1994-05-16 | 1996-03-05 | Phillips Petroleum Company | Metallocene catalyst systems, preparation, and use |
EP0683180B1 (de) | 1994-05-18 | 2002-03-06 | Mitsubishi Chemical Corporation | Katalysator zur Polymerisation eines Olefins und Verfahren zum Polymerisieren des Olefins |
US5498581A (en) | 1994-06-01 | 1996-03-12 | Phillips Petroleum Company | Method for making and using a supported metallocene catalyst system |
US5541272A (en) | 1994-06-03 | 1996-07-30 | Phillips Petroleum Company | High activity ethylene selective metallocenes |
US5420320A (en) | 1994-06-08 | 1995-05-30 | Phillips Petroleum Company | Method for preparing cyclopentadienyl-type ligands and metallocene compounds |
US5563284A (en) | 1994-09-09 | 1996-10-08 | Phillips Petroleum Company | Cyclopentadienyl-type ligands, metallocenes, catalyst systems, preparation, and use |
US6140432A (en) | 1995-07-13 | 2000-10-31 | Exxon Chemical Patents Inc. | Polymerization catalyst systems, their production and use |
US5534057A (en) * | 1995-01-13 | 1996-07-09 | J. M. Huber Corporation | Process for treating kaolin clays for pitch control and the treated clays |
DE69611554T2 (de) | 1995-02-20 | 2001-07-05 | Tosoh Corp | Katalysator für die Polymerisation von Olefinen und Verfahren zur Herstellung von Olefinpolymerisaten |
US5616661A (en) | 1995-03-31 | 1997-04-01 | Union Carbide Chemicals & Plastics Technology Corporation | Process for controlling particle growth during production of sticky polymers |
US5631203A (en) | 1995-05-04 | 1997-05-20 | Phillips Petroleum Company | Metallocene compounds and preparation thereof containing terminal alkynes |
US5654454A (en) | 1995-05-30 | 1997-08-05 | Phillips Petroleum Company | Metallocene preparation and use |
US5677375A (en) | 1995-07-21 | 1997-10-14 | Union Carbide Chemicals & Plastics Technology Corporation | Process for producing an in situ polyethylene blend |
US5753577A (en) | 1996-02-23 | 1998-05-19 | Tosoh Corporation | Olefin polymerization catalyst based on organometallic complexes and process for production of polyolefins using the catalyst |
US5665818A (en) | 1996-03-05 | 1997-09-09 | Union Carbide Chemicals & Plastics Technology Corporation | High activity staged reactor process |
EP0889912B1 (de) | 1996-03-27 | 2000-07-12 | The Dow Chemical Company | Hochlösliches aktivierungsmittel für olefinpolymerisationskatalysator |
US5627242A (en) | 1996-03-28 | 1997-05-06 | Union Carbide Chemicals & Plastics Technology Corporation | Process for controlling gas phase fluidized bed polymerization reactor |
US5705579A (en) | 1996-07-17 | 1998-01-06 | Phillips Petroleum Company | Olefin polymerization |
US6107230A (en) | 1998-05-18 | 2000-08-22 | Phillips Petroleum Company | Compositions that can produce polymers |
US6369174B1 (en) | 1999-09-09 | 2002-04-09 | Univation Technologies, Llc | Catalyst modifier and its use in the polymerization of olefin(s) |
US6346584B1 (en) | 1999-09-09 | 2002-02-12 | Univation Technologies, Llc | Catalyst modifiers and their use in the polymerization of olefins(s) |
US6271325B1 (en) | 1999-05-17 | 2001-08-07 | Univation Technologies, Llc | Method of polymerization |
US6355594B1 (en) | 1999-09-27 | 2002-03-12 | Phillips Petroleum Company | Organometal catalyst compositions |
US6395666B1 (en) | 1999-09-29 | 2002-05-28 | Phillips Petroleum Company | Organometal catalyst compositions |
US6559090B1 (en) | 1999-11-01 | 2003-05-06 | W. R. Grace & Co.-Conn. | Metallocene and constrained geometry catalyst systems employing agglomerated metal oxide/clay support-activator and method of their preparation |
EP1242179B1 (de) | 1999-12-16 | 2013-05-15 | Chevron Phillips Chemical Company LP | Organo-metall-verbundkatalysator |
US6281306B1 (en) | 1999-12-16 | 2001-08-28 | Univation Technologies, Llc | Method of polymerization |
US6632894B1 (en) | 1999-12-30 | 2003-10-14 | Phillips Petroleum Company | Organometal catalyst compositions |
DE60129075T2 (de) | 2000-05-29 | 2008-03-06 | Japan Polychem Corp. | Olefinpolymerisationskatalysator, Verfahren zur Olefinpolymerisation damit |
ATE421542T1 (de) | 2000-09-13 | 2009-02-15 | Japan Polychem Corp | Katalysatorkomponente für die olefinpolymerisation |
US6713573B2 (en) | 2000-11-30 | 2004-03-30 | Univation Technologies, Llc | Catalyst modifiers and their use in the polymerization of olefin(s) |
US6943224B2 (en) | 2001-04-30 | 2005-09-13 | W. R. Grace & Co.-Conn. | Process for preparing supported transition metal catalyst systems and catalyst systems prepared thereby |
US7220695B2 (en) | 2004-01-07 | 2007-05-22 | Exxonmobil Chemical Patents Inc. | Supported activator |
PL1888653T3 (pl) | 2005-06-07 | 2016-08-31 | Saudi Basic Ind Corp | Sposób polimeryzacji olefin |
KR101509826B1 (ko) | 2006-12-07 | 2015-04-07 | 더블유.알. 그레이스 앤드 캄파니-콘. | 개선된 바텀 전환율을 갖는 접촉 분해 촉매 조성물 |
US7884163B2 (en) | 2008-03-20 | 2011-02-08 | Chevron Phillips Chemical Company Lp | Silica-coated alumina activator-supports for metallocene catalyst compositions |
US8440772B2 (en) | 2011-04-28 | 2013-05-14 | Chevron Phillips Chemical Company Lp | Methods for terminating olefin polymerizations |
HUE034931T2 (en) | 2011-08-05 | 2018-03-28 | Total Res & Technology Feluy | Catalysts for the production of ultra high molecular weight polyethylene (UHMWPE) |
CA2777461C (en) | 2012-05-17 | 2019-01-15 | Nova Chemicals Corporation | Improved ligand synthesis |
US9616412B2 (en) | 2012-11-23 | 2017-04-11 | Council Of Scientific & Industrial Research | Mixed metal oxidic nano sheets coated monolithic catalysts useful for the decomposition of toxic N2O and a process for the preparation thereof |
EP3061774B1 (de) | 2013-10-25 | 2018-04-18 | Japan Polypropylene Corporation | Katalysatorkomponente zur olefinpolymerisation, katalysator zur olefinpolymerisation und verfahren zur herstellung eines olefin(co)polymers damit |
RU2736492C2 (ru) | 2015-05-11 | 2020-11-17 | У.Р. Грейс Энд Ко.-Конн. | Способ производства модифицированной глины, металлоценового катализатора полимеризации на подложке, производимого катализатора и их применение |
CN107864635B (zh) | 2015-05-11 | 2021-06-25 | 格雷斯公司 | 制备改性粘土的方法、所制备的改性粘土及其用途 |
US11059918B2 (en) | 2016-05-27 | 2021-07-13 | Exxonmobil Chemical Patents Inc. | Metallocene catalyst compositions and polymerization process therewith |
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2020
- 2020-01-27 WO PCT/US2020/015217 patent/WO2021154204A1/en unknown
- 2020-01-27 CN CN202080094571.XA patent/CN115023446A/zh active Pending
- 2020-01-27 JP JP2022544670A patent/JP2023523494A/ja active Pending
- 2020-01-27 EP EP20712074.2A patent/EP4097153A1/de active Pending
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WO2021154204A1 (en) | 2021-08-05 |
EP4097153A1 (de) | 2022-12-07 |
CN115023446A (zh) | 2022-09-06 |
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