JP2006509868A5 - - Google Patents
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- Publication number
- JP2006509868A5 JP2006509868A5 JP2004559862A JP2004559862A JP2006509868A5 JP 2006509868 A5 JP2006509868 A5 JP 2006509868A5 JP 2004559862 A JP2004559862 A JP 2004559862A JP 2004559862 A JP2004559862 A JP 2004559862A JP 2006509868 A5 JP2006509868 A5 JP 2006509868A5
- Authority
- JP
- Japan
- Prior art keywords
- ethylene
- compound
- supported catalyst
- activator
- pamphlet
- 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
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 8
- 239000012190 activator Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 6
- 150000001450 anions Chemical class 0.000 description 5
- 150000001768 cations Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 3
- -1 cationic ion compound Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 150000003623 transition metal compounds Chemical class 0.000 description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- QLNAVQRIWDRPHA-UHFFFAOYSA-N iminophosphane Chemical class P=N QLNAVQRIWDRPHA-UHFFFAOYSA-N 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 239000007848 Bronsted acid Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- SRKKQWSERFMTOX-UHFFFAOYSA-N cyclopentane;titanium Chemical group [Ti].[CH]1C=CC=C1 SRKKQWSERFMTOX-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- APRJFNLVTJWEPP-UHFFFAOYSA-M n,n-diethylcarbamate Chemical compound CCN(CC)C([O-])=O APRJFNLVTJWEPP-UHFFFAOYSA-M 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02358031 | 2002-12-17 | ||
| EP02358031.9 | 2002-12-17 | ||
| PCT/GB2003/005206 WO2004055061A1 (en) | 2002-12-17 | 2003-12-03 | Supported olefin polymerization catalyst |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006509868A JP2006509868A (ja) | 2006-03-23 |
| JP2006509868A5 true JP2006509868A5 (enExample) | 2013-08-29 |
| JP5362168B2 JP5362168B2 (ja) | 2013-12-11 |
Family
ID=32524110
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004559862A Expired - Fee Related JP5362168B2 (ja) | 2002-12-17 | 2003-12-03 | 担持オレフィン重合触媒 |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US20060247397A1 (enExample) |
| EP (1) | EP1578811B1 (enExample) |
| JP (1) | JP5362168B2 (enExample) |
| KR (1) | KR101118495B1 (enExample) |
| CN (1) | CN100355793C (enExample) |
| AT (1) | ATE360037T1 (enExample) |
| AU (1) | AU2003288399A1 (enExample) |
| DE (1) | DE60313362T2 (enExample) |
| ES (1) | ES2285220T3 (enExample) |
| MY (1) | MY136117A (enExample) |
| TW (1) | TWI357907B (enExample) |
| WO (1) | WO2004055061A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7041617B2 (en) | 2004-01-09 | 2006-05-09 | Chevron Phillips Chemical Company, L.P. | Catalyst compositions and polyolefins for extrusion coating applications |
| US6982306B2 (en) | 2003-11-26 | 2006-01-03 | Chevron Phillips Chemical Company, L.P. | Stannoxy-substituted metallocene catalysts for olefin and acetylene polymerization |
| US7119153B2 (en) | 2004-01-21 | 2006-10-10 | Jensen Michael D | Dual metallocene catalyst for producing film resins with good machine direction (MD) elmendorf tear strength |
| US7094857B2 (en) | 2004-03-10 | 2006-08-22 | Chevron Phillips Chemical Company, L.P. | Ethylene polymers and copolymers with high optical opacity |
| EP1693388A1 (en) * | 2005-02-21 | 2006-08-23 | Innovene Europe Limited | Polymerisation catalysts |
| EP1834983A1 (en) * | 2006-03-14 | 2007-09-19 | Ineos Europe Limited | Polymer films |
| WO2011017092A1 (en) | 2009-07-28 | 2011-02-10 | Univation Technologies, Llc | Polymerization process using a supported constrained geometry catalyst |
| CN106632751B (zh) * | 2015-10-29 | 2019-12-24 | 中国石油化工股份有限公司 | 一种催化剂的制备方法和制得的催化剂及其应用 |
| CA3159350A1 (en) | 2019-10-28 | 2021-05-06 | China Petroleum & Chemical Corporation | Biphenol metal complex, preparation method therefor and use thereof |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5006500A (en) * | 1988-10-27 | 1991-04-09 | Exxon Chemical Patents Inc. | Olefin polymerization catalyst from trialkylaluminum mixture, silica gel and a metallocene |
| NZ235032A (en) * | 1989-08-31 | 1993-04-28 | Dow Chemical Co | Constrained geometry complexes of titanium, zirconium or hafnium comprising a substituted cyclopentadiene ligand; use as olefin polymerisation catalyst component |
| JP2807571B2 (ja) * | 1990-04-18 | 1998-10-08 | 三井化学株式会社 | オレフィン重合用固体触媒およびオレフィンの重合方法 |
| JP2812566B2 (ja) * | 1990-08-08 | 1998-10-22 | 三井化学株式会社 | オレフィン重合体の製造方法 |
| JP3197314B2 (ja) * | 1992-02-24 | 2001-08-13 | 三井化学株式会社 | 分子量分布の広いポリオレフィンの製造方法 |
| DE69312306T2 (de) * | 1992-10-02 | 1997-11-13 | Dow Chemical Co | Aufträger homogener komplexkatalysator für olefinpolymerisation |
| JPH06345808A (ja) * | 1993-06-14 | 1994-12-20 | Mitsui Toatsu Chem Inc | オレフィン重合用固体触媒成分の製造方法およびこれを用いたポリオレフィンの製造方法 |
| IT1273701B (it) * | 1994-07-29 | 1997-07-09 | Enichem Elastomers | Derivati metallorganici del grupo iiia e procedimento per la loro preparazione |
| US5527929A (en) * | 1994-08-02 | 1996-06-18 | The Dow Chemical Company | Zwitterionic biscyclopentadienyl complexes |
| JPH09309926A (ja) * | 1996-05-17 | 1997-12-02 | Dow Chem Co:The | エチレン共重合体の製造方法 |
| IL129929A0 (en) * | 1996-12-17 | 2000-02-29 | Du Pont | Polymerization of ethylene with specific iron or cobalt complexes novel pyridinebis (imines) and novel complexes of pyridinebis(imines) with iron and cobalt |
| ATE218147T1 (de) * | 1997-09-05 | 2002-06-15 | Bp Chem Int Ltd | Polymerisationskatalysatoren |
| WO1999028353A1 (en) * | 1997-12-01 | 1999-06-10 | Asahi Kasei Kogyo Kabushiki Kaisha | Olefin polymerization catalyst and method for polymerizing an olefin using the catalyst |
| AU743376B2 (en) * | 1998-06-12 | 2002-01-24 | Univation Technologies Llc | Olefin polymerization process using activated lewis acid-base complexes |
| ATE355308T1 (de) * | 1998-07-16 | 2006-03-15 | Univation Tech Llc | Lewis-säure cokatalysatoren auf aluminium-basis für die olefinpolymerisation |
| WO2000015672A1 (en) * | 1998-09-16 | 2000-03-23 | The Dow Chemical Company | Functionalized catalyst supports and supported catalyst systems |
| BE1012568A3 (fr) * | 1999-03-24 | 2000-12-05 | Solvay | Procede pour la polymerisation des alphaolefines. |
| JP2001302716A (ja) * | 2000-04-25 | 2001-10-31 | Asahi Kasei Corp | オレフィン重合体の製造方法 |
| US6908972B2 (en) * | 2002-04-16 | 2005-06-21 | Equistar Chemicals, Lp | Method for making polyolefins |
-
2003
- 2003-12-03 AT AT03780316T patent/ATE360037T1/de active
- 2003-12-03 WO PCT/GB2003/005206 patent/WO2004055061A1/en not_active Ceased
- 2003-12-03 CN CNB200380109629XA patent/CN100355793C/zh not_active Expired - Fee Related
- 2003-12-03 US US10/539,573 patent/US20060247397A1/en not_active Abandoned
- 2003-12-03 AU AU2003288399A patent/AU2003288399A1/en not_active Abandoned
- 2003-12-03 EP EP03780316A patent/EP1578811B1/en not_active Expired - Lifetime
- 2003-12-03 KR KR1020057011111A patent/KR101118495B1/ko not_active Expired - Fee Related
- 2003-12-03 JP JP2004559862A patent/JP5362168B2/ja not_active Expired - Fee Related
- 2003-12-03 DE DE60313362T patent/DE60313362T2/de not_active Expired - Lifetime
- 2003-12-03 ES ES03780316T patent/ES2285220T3/es not_active Expired - Lifetime
- 2003-12-04 TW TW092134241A patent/TWI357907B/zh not_active IP Right Cessation
- 2003-12-15 MY MYPI20034805A patent/MY136117A/en unknown
-
2008
- 2008-07-02 US US12/216,323 patent/US7811956B2/en not_active Expired - Fee Related
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