CN101466742A - 担载的抗静电聚合催化剂 - Google Patents
担载的抗静电聚合催化剂 Download PDFInfo
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- CN101466742A CN101466742A CN200780020135.2A CN200780020135A CN101466742A CN 101466742 A CN101466742 A CN 101466742A CN 200780020135 A CN200780020135 A CN 200780020135A CN 101466742 A CN101466742 A CN 101466742A
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- catalyzer
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- compound
- metal oxide
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- 239000002685 polymerization catalyst Substances 0.000 title abstract description 6
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 50
- 230000003068 static effect Effects 0.000 claims abstract description 33
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- 150000004706 metal oxides Chemical class 0.000 claims abstract description 21
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- 238000000034 method Methods 0.000 claims description 40
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- 239000002904 solvent Substances 0.000 claims description 15
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- 229910052796 boron Inorganic materials 0.000 claims description 13
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- SCWWDULYYDFWQV-UHFFFAOYSA-N (2-hydroxyphenoxy)boronic acid Chemical compound OB(O)OC1=CC=CC=C1O SCWWDULYYDFWQV-UHFFFAOYSA-N 0.000 description 4
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 4
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Classifications
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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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- 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
-
- 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
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/02—Anti-static agent incorporated into the catalyst
-
- 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+
-
- 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
- C08F4/65916—Component covered by group C08F4/64 containing a transition metal-carbon bond supported on a carrier, e.g. silica, MgCl2, polymer
-
- 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
- C08F4/6592—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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/901—Monomer polymerized in vapor state in presence of transition metal containing catalyst
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/943—Polymerization with metallocene catalysts
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- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Polymerisation Methods In General (AREA)
Abstract
Description
催化剂 | STADISTM浓度(ppm) | 加入方法 | 活性1(gPE/mmol Ti-[C2 =]-hr) | 生产率2(gPE/g) | 平均生产率 |
1 | 400 | 依次 | 39759 | 484.6 | |
1 | 400 | 依次 | 36591 | 446.0 | 498.0 |
1 | 400 | 依次 | 46228 | 563.5 | |
2 | 10000 | 依次 | 29141 | 368.0 | |
2 | 10000 | 依次 | 36038 | 455.1 | 428.5 |
2 | 10000 | 依次 | 36624 | 462.5 | |
3 | 19600 | 依次 | 31549 | 382.7 | |
3 | 19600 | 依次 | 37663 | 456.9 | 407.5 |
3 | 19600 | 依次 | 31576 | 383.0 | |
4 | 400 | 同时 | 32557 | 413.0 | |
4 | 400 | 同时 | 36938 | 468.6 | 417.3 |
4 | 400 | 同时 | 29191 | 370.2 | |
5 | 10000 | 同时 | 39957 | 480.0 | |
5 | 10000 | 同时 | 38564 | 463.3 | 481.8 |
5 | 10000 | 同时 | 41791 | 502.0 | |
6 | 19600 | 同时 | 57721 | 712.0 | |
6 | 19600 | 同时 | 38309 | 472.5 | 507.1 |
6 | 19600 | 同时 | 27298 | 336.7 |
依次加入 | 负载 | 平均生产率 | 标准偏差 | 方差 | Nobs | 描述 |
1 | 400 | 498 | 60 | 3587 | 3 | |
2 | 10000 | 429 | 53 | 2762 | 3 | |
3 | 19600 | 408 | 43 | 1828 | 3 | |
同时加入 | 负载 | 平均生产率 | 标准偏差 | 方差 | Nobs | 描述 |
4 | 400 | 417 | 49 | 2434 | 3 | |
5 | 10000 | 482 | 19 | 377 | 3 | |
6 | 19600 | 507 | 190 | 36109 | 3 | |
双面t-试验 | 合并方差 | 计算值t | 95%置信度的统计t | DofF | 显著不同 | |
依次加入 | 1vs.2 | 3174 | 1.5108 | 2.776 | 4 | 无 |
1vs.3 | 2707 | 2.1302 | 2.776 | 4 | 无 | |
2vs.3 | 2295 | 0.5369 | 2.776 | 4 | 无 | |
同时 | 4vs.5 | 1406 | -2.1071 | 2.776 | 4 | 无 |
4vs.6 | 19271 | -0.7923 | 2.776 | 4 | 无 | |
4vs.6 | 18243 | -0.2294 | 2.776 | 4 | 无 | |
依次加入vs.同时加入 | 1vs.4 | 3011 | 1.8028 | 2.776 | 4 | 无 |
2vs.5 | 1569 | -1.6458 | 2.776 | 4 | 无 | |
3vs.6 | 18968 | -0.8851 | 2.776 | 4 | 无 |
Claims (10)
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GB0610668.6 | 2006-05-30 | ||
GBGB0610668.6A GB0610668D0 (en) | 2006-05-30 | 2006-05-30 | Supported antistatic polymerization catalysts |
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CN201310198576.9A Active CN103360519B (zh) | 2006-05-30 | 2007-05-02 | 担载的抗静电聚合催化剂 |
CN200780020135.2A Pending CN101466742A (zh) | 2006-05-30 | 2007-05-02 | 担载的抗静电聚合催化剂 |
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US (1) | US7476715B2 (zh) |
EP (1) | EP2021382B1 (zh) |
JP (1) | JP5562636B2 (zh) |
CN (2) | CN103360519B (zh) |
CA (1) | CA2587238C (zh) |
ES (1) | ES2598483T3 (zh) |
GB (1) | GB0610668D0 (zh) |
WO (1) | WO2007137396A1 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102471408A (zh) * | 2009-07-28 | 2012-05-23 | 尤尼威蒂恩技术有限责任公司 | 使用负载型受限几何构型催化剂的聚合方法 |
CN105452166A (zh) * | 2013-08-26 | 2016-03-30 | 巴塞尔聚烯烃意大利有限公司 | 用于提高烯烃聚合反应器的可操作性的方法 |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010080871A1 (en) | 2009-01-08 | 2010-07-15 | Univation Technologies, Llc | Additive for gas phase polymerization processes |
EP2440564A4 (en) * | 2009-06-11 | 2014-07-09 | Grace W R & Co | PROCESS FOR PRODUCING ALUMINOXANE AND CATALYSTS COMPRISING ALUMINOXANE THUS PREPARED |
CA2739969C (en) | 2011-05-11 | 2018-08-21 | Nova Chemicals Corporation | Improving reactor operability in a gas phase polymerization process |
CA2749835C (en) | 2011-08-23 | 2018-08-21 | Nova Chemicals Corporation | Feeding highly active phosphinimine catalysts to a gas phase reactor |
CA2760264C (en) | 2011-12-05 | 2018-08-21 | Nova Chemicals Corporation | Passivated supports for use with olefin polymerization catalysts |
US9115233B2 (en) | 2012-06-21 | 2015-08-25 | Nova Chemicals (International) S.A. | Ethylene copolymer compositions, film and polymerization processes |
CA2798855C (en) | 2012-06-21 | 2021-01-26 | Nova Chemicals Corporation | Ethylene copolymers having reverse comonomer incorporation |
CA2797620C (en) | 2012-12-03 | 2019-08-27 | Nova Chemicals Corporation | Controlling resin properties in a gas phase polymerization process |
CA2800056A1 (en) | 2012-12-24 | 2014-06-24 | Nova Chemicals Corporation | Polyethylene blend compositions |
CA2871463A1 (en) | 2014-11-19 | 2016-05-19 | Nova Chemicals Corporation | Passivated supports: catalyst, process and product |
CA2874344C (en) | 2014-12-15 | 2021-08-31 | Nova Chemicals Corporation | Spheroidal catalyst for olefin polymerization |
CA2891693C (en) | 2015-05-21 | 2022-01-11 | Nova Chemicals Corporation | Controlling the placement of comonomer in an ethylene copolymer |
CA2892552C (en) | 2015-05-26 | 2022-02-15 | Victoria Ker | Process for polymerization in a fluidized bed reactor |
CA2892882C (en) | 2015-05-27 | 2022-03-22 | Nova Chemicals Corporation | Ethylene/1-butene copolymers with enhanced resin processability |
KR101845625B1 (ko) * | 2016-09-27 | 2018-04-05 | 롯데케미칼 주식회사 | 폴리올레핀 제조방법 |
KR20200059350A (ko) | 2018-11-20 | 2020-05-29 | 롯데케미칼 주식회사 | 폴리에틸렌 중합용 촉매의 제조방법 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2660926B1 (fr) * | 1990-04-11 | 1992-07-31 | Bp Chemicals Snc | Prepolymere d'alpha-olefine contenant un metal de transition et procede de polymerisation d'alpha-olefine en phase gazeuse mettant en óoeuvre le prepolymere. |
US5194526A (en) * | 1992-07-30 | 1993-03-16 | Union Carbide Chemicals & Plastics Technology Corporation | Process for producing sticky polymers |
US5498581A (en) * | 1994-06-01 | 1996-03-12 | Phillips Petroleum Company | Method for making and using a supported metallocene catalyst system |
DE19615953A1 (de) * | 1996-04-22 | 1997-10-23 | Basf Ag | Verfahren zur Herstellung von Polymerisaten von Alk-1-enen in Gegenwart eines geträgerten Metallocenkatalysatorsystems und eines Antistatikums |
AU739861B2 (en) * | 1996-05-17 | 2001-10-25 | Ineos Sales (Uk) Limited | Polyolefin composition with molecular weight maximum occuring in that part of the composition that has the highest comonomer content |
GB9800245D0 (en) * | 1998-01-07 | 1998-03-04 | Bp Chem Int Ltd | Novel polymers |
US6245868B1 (en) * | 1998-05-29 | 2001-06-12 | Univation Technologies | Catalyst delivery method, a catalyst feeder and their use in a polymerization process |
PT1177225E (pt) * | 1999-05-05 | 2009-02-11 | Ineos Europe Ltd | Copolímeros de etileno e respectivos filmes |
ATE276279T1 (de) * | 1999-05-07 | 2004-10-15 | Bp Chem Int Ltd | Verfahren zur gasphasen (co-)polymerisation von olefinen in einem fliessbettreaktor |
GB9918668D0 (en) * | 1999-08-06 | 1999-10-13 | Bp Chem Int Ltd | Polymerisation catalysts |
CN1387540A (zh) * | 1999-09-09 | 2002-12-25 | 英国石油化学品有限公司 | 在流化床反应器上烯烃的连续气相(共)聚合的方法 |
GB0017547D0 (en) * | 2000-07-17 | 2000-09-06 | Bp Chem Int Ltd | Supported polymerisation catalysts |
AU7684901A (en) * | 2000-08-02 | 2002-02-13 | Univation Tech Llc | Method for producing highly productive supported ionic catalyst for gas phase polymerization |
US7244795B2 (en) * | 2003-12-08 | 2007-07-17 | Univation Technologies, Llc | Polymerization process using metallocene catalyst systems |
GB0425443D0 (en) * | 2004-11-18 | 2004-12-22 | Bp Chem Int Ltd | Supported polymerisation catalysts |
-
2006
- 2006-05-30 GB GBGB0610668.6A patent/GB0610668D0/en not_active Ceased
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- 2007-05-02 EP EP07719662.4A patent/EP2021382B1/en active Active
- 2007-05-02 JP JP2009512378A patent/JP5562636B2/ja active Active
- 2007-05-02 CN CN201310198576.9A patent/CN103360519B/zh active Active
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- 2007-05-02 CA CA2587238A patent/CA2587238C/en active Active
- 2007-05-02 CN CN200780020135.2A patent/CN101466742A/zh active Pending
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102471408A (zh) * | 2009-07-28 | 2012-05-23 | 尤尼威蒂恩技术有限责任公司 | 使用负载型受限几何构型催化剂的聚合方法 |
CN105452166A (zh) * | 2013-08-26 | 2016-03-30 | 巴塞尔聚烯烃意大利有限公司 | 用于提高烯烃聚合反应器的可操作性的方法 |
US9574026B2 (en) | 2013-08-26 | 2017-02-21 | Basell Poliolefine Italia S.R.L. | Method for improving the operability of an olefin polymerization reactor |
CN105452166B (zh) * | 2013-08-26 | 2018-03-30 | 巴塞尔聚烯烃意大利有限公司 | 用于提高烯烃聚合反应器的可操作性的方法 |
US10155888B2 (en) | 2013-08-26 | 2018-12-18 | Basell Poliolefine Italia S.R.L. | Method for improving the operability of an olefin polymerization reactor |
Also Published As
Publication number | Publication date |
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ES2598483T3 (es) | 2017-01-27 |
US20070282085A1 (en) | 2007-12-06 |
CA2587238A1 (en) | 2007-11-30 |
WO2007137396A1 (en) | 2007-12-06 |
JP5562636B2 (ja) | 2014-07-30 |
CN103360519A (zh) | 2013-10-23 |
CN103360519B (zh) | 2016-07-20 |
US7476715B2 (en) | 2009-01-13 |
CA2587238C (en) | 2015-11-24 |
JP2009538936A (ja) | 2009-11-12 |
GB0610668D0 (en) | 2006-07-12 |
EP2021382B1 (en) | 2016-08-17 |
EP2021382A4 (en) | 2014-01-01 |
EP2021382A1 (en) | 2009-02-11 |
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