CN100558756C - 催化组合物及其制备,以及在从烯键式不饱和单体制备聚合物中的应用 - Google Patents
催化组合物及其制备,以及在从烯键式不饱和单体制备聚合物中的应用 Download PDFInfo
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- CN100558756C CN100558756C CNB2006100848961A CN200610084896A CN100558756C CN 100558756 C CN100558756 C CN 100558756C CN B2006100848961 A CNB2006100848961 A CN B2006100848961A CN 200610084896 A CN200610084896 A CN 200610084896A CN 100558756 C CN100558756 C CN 100558756C
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- STRAHSCTRLRZNU-UHFFFAOYSA-N 4-(9h-carbazol-3-ylamino)phenol Chemical compound C1=CC(O)=CC=C1NC1=CC=C(NC=2C3=CC=CC=2)C3=C1 STRAHSCTRLRZNU-UHFFFAOYSA-N 0.000 description 1
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- DBDNZCBRIPTLJF-UHFFFAOYSA-N boron(1-) monohydride Chemical compound [BH-] DBDNZCBRIPTLJF-UHFFFAOYSA-N 0.000 description 1
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- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
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- 238000012685 gas phase polymerization Methods 0.000 description 1
- 125000000262 haloalkenyl group Chemical group 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
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- 125000005843 halogen group Chemical group 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
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- 239000003999 initiator Substances 0.000 description 1
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- 150000007517 lewis acids Chemical class 0.000 description 1
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- 239000011777 magnesium Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- OTUXRAAQAFDEQT-UHFFFAOYSA-N magnesium oxosilicon(2+) oxygen(2-) Chemical compound [O-2].[Mg+2].[Si+2]=O.[O-2] OTUXRAAQAFDEQT-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
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- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QATBRNFTOCXULG-UHFFFAOYSA-N n'-[2-(methylamino)ethyl]ethane-1,2-diamine Chemical compound CNCCNCCN QATBRNFTOCXULG-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
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- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical compound CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- UZUCNKUDGDAMJW-UHFFFAOYSA-N phenyl(trifluoromethyl)boron Chemical compound FC(F)(F)[B]C1=CC=CC=C1 UZUCNKUDGDAMJW-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
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- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
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- 229920000570 polyether Polymers 0.000 description 1
- 238000000710 polymer precipitation Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010107 reaction injection moulding Methods 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- 238000010572 single replacement reaction Methods 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- WWVNWQJKWKSDQM-UHFFFAOYSA-N triethylarsane Chemical compound CC[As](CC)CC WWVNWQJKWKSDQM-UHFFFAOYSA-N 0.000 description 1
- QQAHNNMLPUNNNJ-UHFFFAOYSA-N trifluoromethylphosphane Chemical compound FC(F)(F)P QQAHNNMLPUNNNJ-UHFFFAOYSA-N 0.000 description 1
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
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
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
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US7968487B2 (en) * | 2003-02-28 | 2011-06-28 | The Regents Of The University Of California | Single component, phosphine-free, initiators for ethylene homopolymerization and copolymerization with functionalized co-monomers |
JP5016512B2 (ja) | 2007-02-28 | 2012-09-05 | ローム アンド ハース カンパニー | 実質的に線状のコポリマーおよびその製造方法 |
JP5292059B2 (ja) * | 2007-10-30 | 2013-09-18 | 日本ポリプロ株式会社 | α−オレフィン・(メタ)アクリル酸エステル共重合体の製造方法ならびにα−オレフィン・(メタ)アクリル酸エステル共重合体 |
US8080681B2 (en) * | 2007-12-28 | 2011-12-20 | Chevron Phillips Chemical Company Lp | Nano-linked metallocene catalyst compositions and their polymer products |
US7863210B2 (en) | 2007-12-28 | 2011-01-04 | Chevron Phillips Chemical Company Lp | Nano-linked metallocene catalyst compositions and their polymer products |
US8012900B2 (en) * | 2007-12-28 | 2011-09-06 | Chevron Phillips Chemical Company, L.P. | Nano-linked metallocene catalyst compositions and their polymer products |
US8236907B2 (en) * | 2008-10-14 | 2012-08-07 | Northwestern University | Neutral bimetallic transition metal phenoxyiminato catalysts and related polymerization methods |
FR2937643B1 (fr) * | 2008-10-27 | 2011-10-14 | Arkema France | Nouveaux copolymeres a blocs d'olefines polaires et apolaires |
US10190030B2 (en) | 2009-04-24 | 2019-01-29 | Alger Alternative Energy, Llc | Treated geothermal brine compositions with reduced concentrations of silica, iron and lithium |
US9034294B1 (en) | 2009-04-24 | 2015-05-19 | Simbol, Inc. | Preparation of lithium carbonate from lithium chloride containing brines |
US8637428B1 (en) | 2009-12-18 | 2014-01-28 | Simbol Inc. | Lithium extraction composition and method of preparation thereof |
US8741256B1 (en) | 2009-04-24 | 2014-06-03 | Simbol Inc. | Preparation of lithium carbonate from lithium chloride containing brines |
US7919639B2 (en) | 2009-06-23 | 2011-04-05 | Chevron Phillips Chemical Company Lp | Nano-linked heteronuclear metallocene catalyst compositions and their polymer products |
WO2011025053A2 (en) | 2009-08-28 | 2011-03-03 | The University Of Tokyo | Production method of copolymer of allyl monomer containing polar group |
CN102127116B (zh) * | 2010-11-26 | 2013-11-20 | 吉林大学 | 钳型铬配合物及其制备方法和应用 |
US8809221B2 (en) | 2011-05-09 | 2014-08-19 | Reliance Industries Limited | Nitrogen containing external donor system for propylene polymerization |
US9296836B2 (en) | 2011-05-12 | 2016-03-29 | Dow Global Technologies Llc | Non-cyclopentadienyl-based chromium catalysts for olefin polymerization |
US9233996B2 (en) * | 2011-09-13 | 2016-01-12 | California Institute Of Technology | Multi-metallic organometallic complexes, and related polymers, compositions, methods and systems |
EP2738187B1 (en) * | 2012-11-29 | 2016-05-04 | Solvay SA | Process for the manufacture of vinyl chloride-containing copolymers |
KR101680776B1 (ko) | 2015-03-24 | 2016-12-12 | 고재덕 | 초절전 축열식 전열 온수관 |
KR101582665B1 (ko) | 2015-10-08 | 2016-01-06 | 고재덕 | 초절전 축열식 전열 온수관 및 이를 포함하는 온수관 시스템 |
JP7175741B2 (ja) * | 2017-12-25 | 2022-11-21 | 日本ポリエチレン株式会社 | 多元系極性基含有オレフィン共重合体 |
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CN113559928A (zh) * | 2021-07-30 | 2021-10-29 | 四川信乙化工有限公司 | 一种苯乙酸可循环合成催化剂 |
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DE1495160A1 (de) | 1964-02-28 | 1969-03-27 | Basf Ag | Verfahren zur Polymerisation olefinisch ungesaettigter Verbindungen und Verwendung von pi-Olefinkomplexen als Polymerisationsinitiatoren |
DE1292854B (de) | 1965-03-06 | 1969-04-17 | Hoechst Ag | Verfahren zur Herstellung von Homo- und Mischpolymerisaten von Mono- und Diolefinen |
US4906754A (en) | 1985-10-15 | 1990-03-06 | E. I. Du Pont De Nemours And Company | Nickel catalysts for copolymerization of ethylene |
US5131918A (en) * | 1990-12-13 | 1992-07-21 | Hoechst Celanese Corporation | Process for dyeing mixed anionic/cationic polyamide substrates with a specific type of vinyl sulfone dye |
DE19503119A1 (de) | 1995-02-01 | 1996-08-08 | Hoechst Ag | Verfahren zur Herstellung von aromatischen Olefinen unter Katalyse von Palladacyclen |
JPH1029994A (ja) * | 1996-07-15 | 1998-02-03 | Chichibu Onoda Cement Corp | ポルフィリン二量化化合物 |
US6174975B1 (en) | 1998-01-13 | 2001-01-16 | E.I. Du Pont De Nemours And Company | Polymerization of olefins |
US5929181A (en) * | 1997-06-09 | 1999-07-27 | The B.F.Goodrich Co. | Method for preparation of copolymers of ethylene/norbornene-type monomers with nickel catalysts |
US6511936B1 (en) | 1998-02-12 | 2003-01-28 | University Of Delaware | Catalyst compounds with β-diminate anionic ligands and processes for polymerizing olefins |
WO1999047474A1 (en) | 1998-03-18 | 1999-09-23 | Ciba Specialty Chemicals Holding Inc. | Coupling reactions with palladium catalysts |
US6410660B1 (en) * | 1998-03-27 | 2002-06-25 | E. I. Du Pont De Nemours And Company | Polymerization of olefins |
FR2784110B1 (fr) | 1998-10-06 | 2003-08-01 | Atochem Elf Sa | Procede de polymerisation des olefines en presence d'eau |
US6544919B1 (en) | 1999-10-06 | 2003-04-08 | Sri International | Multinuclear transition metal catalysts for preparation of multimodal polymer compositions |
FR2814169B1 (fr) | 2000-09-19 | 2005-07-08 | Atofina | Catalyseur pour la polymerisation des olefines |
US6919292B2 (en) | 2000-12-20 | 2005-07-19 | Tosoh Corporation | Transition metal compound, coordinative compound, catalyst for polymerization of olefin, and process for polymerization of olefin using the catalyst |
WO2003102038A1 (en) | 2002-06-04 | 2003-12-11 | Thales Technologies, Ag | Polymerization catalysts |
US6864210B2 (en) * | 2003-02-06 | 2005-03-08 | Equistar Chemicals, Lp | Bimetallic olefin polymerization catalysts containing indigoid ligands |
US7094898B2 (en) | 2003-05-29 | 2006-08-22 | University Of Ottawa | Ruthenium compounds, their production and use |
US7087687B2 (en) * | 2003-08-21 | 2006-08-08 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
US7172986B2 (en) | 2004-06-14 | 2007-02-06 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
US7199074B2 (en) | 2004-06-14 | 2007-04-03 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
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后过渡金属配合物催化乙烯齐聚与聚合的研究进展. 张闻等.化学进展,第17卷第2期. 2005 |
后过渡金属配合物催化乙烯齐聚与聚合的研究进展. 张闻等.化学进展,第17卷第2期. 2005 * |
新型双核中性镍催化剂的研制及催化性能研究. 崔永刚.浙江大学硕士学位沦文. 2005 |
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Publication number | Publication date |
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CA2547094A1 (en) | 2006-11-27 |
US20060270811A1 (en) | 2006-11-30 |
EP1728553A3 (en) | 2006-12-20 |
KR100882891B1 (ko) | 2009-02-10 |
KR20070118060A (ko) | 2007-12-13 |
TWI322035B (en) | 2010-03-21 |
US7435701B2 (en) | 2008-10-14 |
JP5173932B2 (ja) | 2013-04-03 |
CA2547094C (en) | 2011-08-02 |
KR20060122768A (ko) | 2006-11-30 |
JP2006328402A (ja) | 2006-12-07 |
JP2009203479A (ja) | 2009-09-10 |
JP4410774B2 (ja) | 2010-02-03 |
TW200700445A (en) | 2007-01-01 |
CN1891721A (zh) | 2007-01-10 |
EP1728553A2 (en) | 2006-12-06 |
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