RU2232766C2 - Связанные мостиками металлоцены, способ полимеризации - Google Patents
Связанные мостиками металлоцены, способ полимеризации Download PDFInfo
- Publication number
- RU2232766C2 RU2232766C2 RU2001113445/04A RU2001113445A RU2232766C2 RU 2232766 C2 RU2232766 C2 RU 2232766C2 RU 2001113445/04 A RU2001113445/04 A RU 2001113445/04A RU 2001113445 A RU2001113445 A RU 2001113445A RU 2232766 C2 RU2232766 C2 RU 2232766C2
- Authority
- RU
- Russia
- Prior art keywords
- cyclopentadienyl
- polymerization
- methylene
- substituted
- fluorenyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 70
- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 55
- 239000003446 ligand Substances 0.000 claims abstract description 60
- 125000003118 aryl group Chemical group 0.000 claims abstract description 29
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000005977 Ethylene Substances 0.000 claims abstract description 21
- 238000006243 chemical reaction Methods 0.000 claims abstract description 18
- 239000000178 monomer Substances 0.000 claims abstract description 16
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- 229920001038 ethylene copolymer Polymers 0.000 claims abstract description 7
- 125000002524 organometallic group Chemical group 0.000 claims abstract description 4
- -1 di (p-trimethylsilylphenyl) methylene (cyclopentadienyl) Chemical group 0.000 claims description 56
- 150000001875 compounds Chemical class 0.000 claims description 55
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 30
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims description 26
- 239000012190 activator Substances 0.000 claims description 21
- 150000001450 anions Chemical class 0.000 claims description 21
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 14
- 229910052735 hafnium Inorganic materials 0.000 claims description 12
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 11
- 125000004429 atom Chemical group 0.000 claims description 11
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 10
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 8
- 239000004711 α-olefin Substances 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000002091 cationic group Chemical group 0.000 claims description 6
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 6
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical group [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 238000010348 incorporation Methods 0.000 claims description 4
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 4
- 238000005804 alkylation reaction Methods 0.000 claims description 3
- 150000001993 dienes Chemical class 0.000 claims description 3
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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 claims description 2
- 230000029936 alkylation Effects 0.000 claims description 2
- 238000010924 continuous production Methods 0.000 claims description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims 2
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- VCHQGHCBFOFZJK-UHFFFAOYSA-N 1-cyclopenta-1,3-dien-1-ylcyclopenta-1,3-diene Chemical group C1C=CC=C1C1=CC=CC1 VCHQGHCBFOFZJK-UHFFFAOYSA-N 0.000 claims 1
- OJOWICOBYCXEKR-UHFFFAOYSA-N 5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=CC)CC1C=C2 OJOWICOBYCXEKR-UHFFFAOYSA-N 0.000 claims 1
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- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 1
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000005517 carbenium group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims 1
- 125000003367 polycyclic group Chemical group 0.000 claims 1
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
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- 229910052782 aluminium Inorganic materials 0.000 description 6
- 239000012683 anionic precursor Substances 0.000 description 6
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- 238000007429 general method Methods 0.000 description 6
- 239000012041 precatalyst Substances 0.000 description 6
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- 150000001721 carbon Chemical group 0.000 description 5
- 125000005842 heteroatom Chemical group 0.000 description 5
- 150000004678 hydrides Chemical class 0.000 description 5
- 239000012968 metallocene catalyst Substances 0.000 description 5
- 229910052752 metalloid Inorganic materials 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 5
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- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 3
- 0 C*c1c(C)c(*)c(*C)c(*)c1C Chemical compound C*c1c(C)c(*)c(*C)c(*)c1C 0.000 description 3
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- 150000001342 alkaline earth metals Chemical group 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
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- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 3
- 125000006659 (C1-C20) hydrocarbyl group Chemical group 0.000 description 2
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 2
- PZASAAIJIFDWSB-CKPDSHCKSA-N 8-[(1S)-1-[8-(trifluoromethyl)-7-[4-(trifluoromethyl)cyclohexyl]oxynaphthalen-2-yl]ethyl]-8-azabicyclo[3.2.1]octane-3-carboxylic acid Chemical compound FC(F)(F)C=1C2=CC([C@@H](N3C4CCC3CC(C4)C(O)=O)C)=CC=C2C=CC=1OC1CCC(C(F)(F)F)CC1 PZASAAIJIFDWSB-CKPDSHCKSA-N 0.000 description 2
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Images
Classifications
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- C07F17/00—Metallocenes
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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
- C08F2/00—Processes of polymerisation
- C08F2/04—Polymerisation in solution
- C08F2/06—Organic solvent
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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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- 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
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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
- 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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- 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
-
- 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
- C08F10/02—Ethene
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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
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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
- C08F2420/00—Metallocene catalysts
- C08F2420/10—Heteroatom-substituted bridge, i.e. Cp or analog where the bridge linking the two Cps or analogs is substituted by at least one group that contains a heteroatom
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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
- 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
- C08F4/65908—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
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- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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| US10532998P | 1998-10-23 | 1998-10-23 | |
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| US13106799P | 1999-04-26 | 1999-04-26 | |
| US60/131,067 | 1999-04-26 |
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| RU2001113445A RU2001113445A (ru) | 2003-05-20 |
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| RU2001113445/04A RU2232766C2 (ru) | 1998-10-23 | 1999-10-22 | Связанные мостиками металлоцены, способ полимеризации |
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| EP (1) | EP1196464B9 (https=) |
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| HK (1) | HK1041705A1 (https=) |
| MX (1) | MXPA01003978A (https=) |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2410388C2 (ru) * | 2005-03-18 | 2011-01-27 | Базелль Полиолефине Гмбх | Металлоценовые соединения |
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| ATE327241T1 (de) * | 1999-10-22 | 2006-06-15 | Exxonmobil Chem Patents Inc | Für polymerisationskatalysatoren geeignete carbenium-kationische komplexe |
| US6476164B1 (en) | 1999-10-22 | 2002-11-05 | Exxonmobil Chemical Patents Inc. | Carbenium cationic complexes suitable for polymerization catalysts |
| US6475946B1 (en) | 1999-10-22 | 2002-11-05 | Exxonmobil Chemical Patents Inc. | Olefin polymerization catalysis with aryl substituted carbenium cationic complexes |
| JP4610859B2 (ja) * | 2002-09-27 | 2011-01-12 | 三井化学株式会社 | オレフィン重合用の架橋メタロセン化合物およびそれを用いたオレフィンの重合方法 |
| EP2465879B1 (en) * | 2002-09-27 | 2019-04-24 | Mitsui Chemicals, Inc. | Bridged metallocene compound for olefin polymerization and method of polymerizing olefin using the same |
| ES2394304T3 (es) | 2002-10-15 | 2013-01-30 | Exxonmobil Chemical Patents, Inc. | Sistema de múltiples catalizadores para la polimerización de olefinas y polímeros producidos a partir de éstos |
| DE602004004222T2 (de) | 2003-08-11 | 2007-11-15 | Exxonmobil Chemical Patents Inc., Baytown | Polymere, bestehend aus Ethylen und gegebenenfalls copolimerisierbaren Estern,Filme aus diesen Polymeren und diese Filme verwendendes Strechfolienhaubenverpackungsverfahren |
| JP5255833B2 (ja) * | 2004-03-24 | 2013-08-07 | エクソンモービル・ケミカル・パテンツ・インク | エチレン・インターポリマーの製造方法、該方法により製造されたインターポリマー、組成物、および該インターポリマーを含む電気デバイス |
| KR20070061567A (ko) * | 2004-03-31 | 2007-06-13 | 미쓰이 가가쿠 가부시키가이샤 | 올레핀 중합체의 제조 방법 |
| EP1802699B1 (en) * | 2004-10-13 | 2011-07-27 | ExxonMobil Chemical Patents Inc. | Elastomeric reactor blend compositions |
| EP1734059A1 (en) * | 2005-06-13 | 2006-12-20 | Total Petrochemicals Research Feluy | Carbon-bridged cyclopentadienyl-fluorenyl ligands |
| SG169377A1 (en) * | 2006-03-02 | 2011-03-30 | Exxonmobil Chem Patents Inc | Process for producing propylene copolymers |
| CN101490094B (zh) * | 2006-05-17 | 2013-06-26 | 陶氏环球技术有限责任公司 | 高温聚乙烯溶液聚合法 |
| EP1903061A1 (en) * | 2006-09-25 | 2008-03-26 | Total Petrochemicals Research Feluy | Preparation of diphenyl-bridged substituted cyclopentadienyl-fluorenyl ligands |
| EP2083046A1 (en) | 2008-01-25 | 2009-07-29 | ExxonMobil Chemical Patents Inc. | Thermoplastic elastomer compositions |
| WO2009123609A1 (en) | 2008-03-31 | 2009-10-08 | Advanced Elastomer Systems, L.P. | Thermoplastic vulcanizates |
| FR2934599B1 (fr) * | 2008-07-29 | 2012-12-21 | Arkema France | Fabrication de polyethylene a partir de matieres renouvelables, polyethylene obtenu et utilisations |
| US8378042B2 (en) * | 2009-04-28 | 2013-02-19 | Exxonmobil Chemical Patents Inc. | Finishing process for amorphous polymers |
| KR101914794B1 (ko) | 2009-12-23 | 2018-11-02 | 인비스타 테크놀러지스 에스.에이 알.엘. | 폴리올레핀 탄성 섬유를 포함하는 직물 |
| KR101996322B1 (ko) | 2009-12-23 | 2019-07-05 | 인비스타 테크놀러지스 에스.에이 알.엘. | 점착 방지 첨가제를 함유하는 탄성 섬유 |
| KR101851409B1 (ko) | 2009-12-23 | 2018-05-31 | 인비스타 테크놀러지스 에스.에이 알.엘. | 폴리올레핀 탄성 섬유 |
| BR112012015382A2 (pt) | 2009-12-23 | 2016-03-15 | Invista Tech Sarl | artigo de estiramento e método para a produção |
| WO2011087731A1 (en) | 2010-01-14 | 2011-07-21 | Exxonmobil Chemical Patents Inc. | Processes and apparatus for continuous solution polymerization |
| WO2011087729A2 (en) | 2010-01-14 | 2011-07-21 | Exxonmobil Chemical Patents Inc. | Processes and apparatus for polymer finishing and packaging |
| CN102190749B (zh) * | 2010-03-05 | 2013-02-20 | 中国石油天然气股份有限公司 | 一种乙烯/α-烯烃共聚合的方法 |
| KR101791810B1 (ko) * | 2014-03-21 | 2017-10-30 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 에틸렌 프로필렌 공중합체의 제조 방법 |
| EP3201270B1 (en) | 2014-09-30 | 2018-10-24 | ExxonMobil Chemical Patents Inc. | Low ethylene amorphous propylene-ethylene-diene terpolymer compositions |
| EP3245253B1 (en) | 2015-01-14 | 2019-12-04 | ExxonMobil Chemical Patents Inc. | Polymer compositions and processes for their production |
| EP3274381B1 (en) * | 2015-04-20 | 2019-05-15 | ExxonMobil Chemical Patents Inc. | Catalyst composition comprising fluorided support and processes for use thereof |
| CN107636029B (zh) | 2015-04-20 | 2020-05-22 | 埃克森美孚化学专利公司 | 包含氟化载体的催化剂组合物及其使用方法 |
| JP2018522099A (ja) | 2015-06-15 | 2018-08-09 | エクソンモービル・ケミカル・パテンツ・インク | 連続溶液重合プロセス |
| CN108026190B (zh) | 2015-09-29 | 2019-11-15 | 埃克森美孚化学专利公司 | 使用螺旋换热器的聚合 |
| CN108602928B (zh) | 2016-02-12 | 2022-01-28 | 埃克森美孚化学专利公司 | 环烯烃共聚物及其制备方法 |
| CN109641989B (zh) | 2016-07-13 | 2022-05-03 | 埃克森美孚化学专利公司 | 双金属茂催化剂共聚物组合物 |
| CN109641990B (zh) | 2016-07-13 | 2022-08-19 | 埃克森美孚化学专利公司 | 双金属茂催化剂共聚物组合物 |
| JP6850862B2 (ja) | 2016-07-14 | 2021-03-31 | エクソンモービル・ケミカル・パテンツ・インク | 粘度調整剤として有用な、２元メタロセン触媒で重合されたバイモーダルのコポリマー組成物 |
| WO2018022263A1 (en) | 2016-07-29 | 2018-02-01 | Exxonmobil Chemical Patents Inc. | Polymerization processes using high molecular weight polyhydric quenching agents |
| KR102505086B1 (ko) | 2016-11-18 | 2023-02-28 | 보레알리스 아게 | 촉매 |
| US11530280B2 (en) | 2016-12-15 | 2022-12-20 | Borealis Ag | Catalyst system for producing polyethylene copolymers in a high temperature solution polymerization process |
| KR102534541B1 (ko) | 2016-12-15 | 2023-05-18 | 보레알리스 아게 | 고온 용액 중합 공정으로 폴리에틸렌 공중합체를 제조하기 위한 촉매 시스템 |
| EP3562831B1 (en) | 2016-12-29 | 2021-10-20 | Borealis AG | Catalysts |
| WO2018160300A1 (en) | 2017-02-28 | 2018-09-07 | Exxonmobil Chemical Patents Inc. | Thermoplastic vulcanizate prepared with oil-extended, bimodal metallocene-synthesized epdm |
| US10730978B2 (en) | 2017-04-10 | 2020-08-04 | Exxonmobil Chemical Patents Inc. | Linear ethylene cyclic olefin polymers |
| US11390704B2 (en) | 2017-06-14 | 2022-07-19 | Exxonmobil Chemical Patents Inc. | Ethylene copolymer blends for cross-linking applications |
| US10683376B2 (en) * | 2017-11-07 | 2020-06-16 | Nova Chemicals (International) S.A. | Manufacturing ethylene interpolymer products at higher production rate |
| US10995166B2 (en) | 2017-11-07 | 2021-05-04 | Nova Chemicals (International) S.A. | Ethylene interpolymer products and films |
| KR102455607B1 (ko) * | 2017-11-10 | 2022-10-14 | 한화솔루션 주식회사 | 올레핀 중합 촉매용 전이금속 화합물, 이를 포함하는 올레핀 중합 촉매 및 이를 이용하여 중합된 폴리올레핀 |
| US11008449B2 (en) | 2017-11-14 | 2021-05-18 | Exxonmobil Chemical Patents Inc. | Bimodal ethylene, alpha-olefin, and diene polymers using dual organometallic catalysts |
| US11142593B2 (en) | 2018-02-22 | 2021-10-12 | Exxonmobil Chemical Patents Inc. | Lecithin quenching agent |
| US10654949B2 (en) | 2018-02-22 | 2020-05-19 | Exxonmobil Chemical Patents Inc. | High molecular weight functionalized olefin copolymer quenching agent |
| US11046793B2 (en) | 2018-02-22 | 2021-06-29 | Exxonmobil Chemical Patents Inc. | Silica quenching agents for use in polymerization process |
| EP3768735B1 (en) | 2018-03-19 | 2021-12-29 | Borealis AG | Catalysts for olefin polymerization |
| CN112424241B (zh) | 2018-06-28 | 2023-06-06 | 博里利斯股份公司 | 催化剂 |
| JP7216184B2 (ja) | 2018-07-23 | 2023-01-31 | エクソンモービル・ケミカル・パテンツ・インク | バイモーダルゴム、熱可塑性加硫物の調製およびそれから作られた物品 |
| US11466149B2 (en) | 2018-07-23 | 2022-10-11 | Exxonmobil Chemical Patents Inc. | Preparation of bimodal rubber, thermoplastic vulcanizates, and articles made therefrom |
| WO2020060745A1 (en) | 2018-09-19 | 2020-03-26 | Exxonmobil Chemical Patents Inc. | Devolatilization processes |
| WO2020096732A1 (en) * | 2018-11-06 | 2020-05-14 | Dow Global Technologies Llc | Alkane-soluble non-metallocene precatalysts |
| US20200172715A1 (en) | 2018-11-30 | 2020-06-04 | Exxonmobil Chemical Patents Inc. | Blends of Cyclic Olefin Copolymers and Films Prepared Therefrom |
| WO2020167399A1 (en) | 2019-02-11 | 2020-08-20 | Exxonmobil Chemical Patents Inc. | Biphasic polymerization processes and ethylene-based polyolefins therefrom |
| EP3763745A1 (en) * | 2019-07-10 | 2021-01-13 | Borealis AG | High temperature solution process for the copolymerization of alpha-olefins |
| WO2021126443A2 (en) | 2019-12-17 | 2021-06-24 | Exxonmobil Chemical Patents Inc. | Solution polymerization process for making high-density polyethylene long-chain branching |
| EP4176005A1 (en) | 2020-07-02 | 2023-05-10 | Celanese International Corporation | Thermoplastic vulcanizate compositions containing metallocene multimodal copolymer rubber and processes for making same |
| US20230295354A1 (en) * | 2020-09-30 | 2023-09-21 | Borealis Ag | Ethylene copolymers with improved melting and glass transition temperature |
| EP4222211B1 (en) * | 2020-09-30 | 2026-04-22 | Borealis GmbH | Ethylene copolymers with improved melting and glass transition temperature |
| KR102691775B1 (ko) * | 2020-11-25 | 2024-08-06 | 한화솔루션 주식회사 | 전이금속 화합물, 이를 포함하는 촉매 및 이들의 제조방법 |
| WO2022260891A1 (en) | 2021-06-11 | 2022-12-15 | Exxonmobil Chemical Patents Inc. | Processes for making polypropylene random copolymers and products made therefrom |
| KR20240093897A (ko) | 2021-11-23 | 2024-06-24 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 중합체 형성을 위한 플랜트 및 방법 |
| CA3241034A1 (en) | 2021-12-17 | 2023-06-22 | Exxonmobil Chemical Patents Inc. | Processes for making propylene-based copolymers having broad cds and mwds |
| KR102831436B1 (ko) * | 2022-01-13 | 2025-07-09 | 한화솔루션 주식회사 | 올레핀계 중합체 및 그 제조방법 |
| KR102888044B1 (ko) * | 2022-01-13 | 2025-11-18 | 한화솔루션 주식회사 | 올레핀계 중합체 및 그 제조방법 |
| JP2025526711A (ja) | 2022-08-09 | 2025-08-15 | 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 | ジフェニルシラン架橋ｃ１対称触媒及びそれから製造するポリマー |
| WO2024073260A1 (en) | 2022-09-28 | 2024-04-04 | Exxonmobil Chemical Patents Inc. | Ethylene copolymers for photovoltaic cells |
| CN115572341B (zh) * | 2022-11-04 | 2024-04-23 | 大连万慷工业科技有限公司 | 一类功能化聚烯烃弹性体及其制备方法 |
| WO2025034262A1 (en) | 2023-08-07 | 2025-02-13 | ExxonMobil Technology and Engineering Company | Ethylene copolymer compositions and articles made thereof |
| WO2025136494A1 (en) | 2023-12-20 | 2025-06-26 | ExxonMobil Technology and Engineering Company | Ethylene copolymers for photovoltaic cells |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5324800A (en) | 1983-06-06 | 1994-06-28 | Exxon Chemical Patents Inc. | Process and catalyst for polyolefin density and molecular weight control |
| US5408017A (en) | 1987-01-30 | 1995-04-18 | Exxon Chemical Patents Inc. | High temperature polymerization process using ionic catalysts to produce polyolefins |
| US5155080A (en) | 1988-07-15 | 1992-10-13 | Fina Technology, Inc. | Process and catalyst for producing syndiotactic polyolefins |
| US4892851A (en) | 1988-07-15 | 1990-01-09 | Fina Technology, Inc. | Process and catalyst for producing syndiotactic polyolefins |
| DE3907964A1 (de) | 1989-03-11 | 1990-09-13 | Hoechst Ag | Verfahren zur herstellung eines syndiotaktischen polyolefins |
| DE3916553A1 (de) * | 1989-05-20 | 1990-11-22 | Hoechst Ag | Syndio- isoblockpolymer und verfahren zu seiner herstellung |
| US5171919A (en) | 1990-10-17 | 1992-12-15 | Idemitsu Kosan Co., Ltd. | Process for producing propylene based oligomers |
| DE69127811T3 (de) | 1990-11-30 | 2012-04-26 | Idemitsu Kosan Co., Ltd. | Verfahren zur herstellung von olefinpolymeren |
| JP3193066B2 (ja) | 1991-05-02 | 2001-07-30 | 三菱化学株式会社 | プロピレンランダム共重合体の製造法 |
| US5401817A (en) | 1991-05-09 | 1995-03-28 | Phillips Petroleum Company | Olefin polymerization using silyl-bridged metallocenes |
| US5710222A (en) | 1992-06-22 | 1998-01-20 | Fina Technology, Inc. | Method for controlling the melting points and molecular weights of syndiotactic polyolefins using metallocene catalyst systems |
| KR100292158B1 (ko) | 1992-08-04 | 2001-06-01 | 가지와라 야스시 | 올레핀중합용 촉매 및 올레핀의 중합방법 |
| KR100311244B1 (ko) | 1993-02-22 | 2001-12-15 | 가지와라 야스시 | 에틸렌/α-올레핀공중합체의제조방법 |
| US6313240B1 (en) | 1993-02-22 | 2001-11-06 | Tosoh Corporation | Process for producing ethylene/α-olefin copolymer |
| US5631202A (en) * | 1993-09-24 | 1997-05-20 | Montell Technology Company B.V. | Stereospecific metallocene catalysts with stereolocking α-CP substituents |
| JP3454827B2 (ja) * | 1993-09-30 | 2003-10-06 | 出光興産株式会社 | 遷移金属化合物，オレフィン重合触媒，該触媒を用いたオレフィン系重合体の製造方法 |
| JP3423378B2 (ja) | 1993-11-12 | 2003-07-07 | 三井化学株式会社 | 新規な遷移金属化合物および該遷移金属化合物からなるオレフィン重合用触媒成分、該オレフィン重合用触媒成分を含むオレフィン重合用触媒ならびにオレフィンの重合方法 |
| US5502017A (en) | 1994-03-10 | 1996-03-26 | Northwestern University | Metallocene catalyst containing bulky organic group |
| IT1273420B (it) * | 1994-04-06 | 1997-07-08 | Spherilene Srl | Composti metallocenici, procedimento per la preparazione e loro utilizzo in catalizzatori per la polimerizzazione delle olefine |
| EP0707016B1 (en) | 1994-10-13 | 1997-09-24 | Japan Polyolefins Co., Ltd. | Catalyst component for producing polyolefin, catalyst for producing polyolefin comprising the catalyst component, and process for producing polyolefin in the presence of the catalyst |
| JP3850048B2 (ja) | 1994-12-08 | 2006-11-29 | 東ソー株式会社 | 有機遷移金属化合物およびそれを用いたポリオレフィンの製造方法 |
| ATE233790T1 (de) | 1995-03-10 | 2003-03-15 | Dow Global Technologies Inc | Geträgerter katalysatorbestandteil, trägerkatalysator, herstellungsverfahren, polymerisationsverfahren, komplexverbindungen und ihre herstellung |
| AT403376B (de) * | 1995-07-03 | 1998-01-26 | Danubia Petrochem Polymere | Metallocene mit silylsubstituierten brücken und deren einsatz für die olefinpolymerisation |
| US5767208A (en) | 1995-10-20 | 1998-06-16 | Exxon Chemical Patents Inc. | High temperature olefin polymerization process |
| PT856518E (pt) * | 1997-02-01 | 2003-08-29 | Repsol Quimica Sa | Compostos de metaloceno e respectivos processo de sintese e utilizacao |
| JPH10292006A (ja) * | 1997-04-18 | 1998-11-04 | Mitsui Chem Inc | オレフィンの重合方法 |
| US6300433B1 (en) * | 1998-10-23 | 2001-10-09 | Exxonmobil Chemical Patents Inc. | Olefin copolymerization process with bridged hafnocenes |
| US6169051B1 (en) * | 1999-01-25 | 2001-01-02 | Chisso Corporation | Metallocene compounds, processes for the preparation thereof, catalyst components for olefin polymerization, and processes for the production of olefin polymers |
-
1999
- 1999-10-22 US US09/426,099 patent/US6528670B1/en not_active Expired - Lifetime
- 1999-10-22 KR KR1020017004930A patent/KR100568839B1/ko not_active Expired - Fee Related
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- 1999-10-22 AT AT99974265T patent/ATE284422T1/de not_active IP Right Cessation
- 1999-10-22 ES ES99974265T patent/ES2233109T3/es not_active Expired - Lifetime
- 1999-10-22 DE DE69922548T patent/DE69922548T2/de not_active Expired - Lifetime
- 1999-10-22 EP EP99974265A patent/EP1196464B9/en not_active Expired - Lifetime
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- 1999-10-22 JP JP2000578362A patent/JP4689829B2/ja not_active Expired - Lifetime
-
2002
- 2002-03-07 US US10/092,660 patent/US6506857B2/en not_active Expired - Lifetime
Non-Patent Citations (1)
| Title |
|---|
| SOGA, KAZUO et al. Synthesis of a dinuclear ansa-Zirconocene catalyst having a biphenyl bridge and application to ethene polymerization. J. Mol. Catal. А.Chem. (1998), 128(1-3), 273-278. * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2410388C2 (ru) * | 2005-03-18 | 2011-01-27 | Базелль Полиолефине Гмбх | Металлоценовые соединения |
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| CN1328580A (zh) | 2001-12-26 |
| DE69922548T2 (de) | 2006-01-05 |
| EP1196464B1 (en) | 2004-12-08 |
| US6528670B1 (en) | 2003-03-04 |
| KR100568839B1 (ko) | 2006-04-10 |
| CA2345628C (en) | 2010-02-16 |
| AU757241B2 (en) | 2003-02-06 |
| WO2000024793A8 (en) | 2001-10-11 |
| EP1196464A1 (en) | 2002-04-17 |
| MXPA01003978A (es) | 2003-06-06 |
| BR9914717A (pt) | 2001-07-10 |
| ES2233109T3 (es) | 2005-06-01 |
| JP4689829B2 (ja) | 2011-05-25 |
| CA2345628A1 (en) | 2000-05-04 |
| US6506857B2 (en) | 2003-01-14 |
| ATE284422T1 (de) | 2004-12-15 |
| HK1041705A1 (zh) | 2002-07-19 |
| WO2000024793A1 (en) | 2000-05-04 |
| AU1321200A (en) | 2000-05-15 |
| EP1196464B9 (en) | 2005-03-23 |
| CN1138796C (zh) | 2004-02-18 |
| US20020137959A1 (en) | 2002-09-26 |
| JP2002528463A (ja) | 2002-09-03 |
| KR20010099705A (ko) | 2001-11-09 |
| DE69922548D1 (de) | 2005-01-13 |
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