KR101628792B1 - 에틸렌/α-올레핀 혼성중합체를 갖는 중합체 블렌드 - Google Patents
에틸렌/α-올레핀 혼성중합체를 갖는 중합체 블렌드 Download PDFInfo
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- KR101628792B1 KR101628792B1 KR1020117010046A KR20117010046A KR101628792B1 KR 101628792 B1 KR101628792 B1 KR 101628792B1 KR 1020117010046 A KR1020117010046 A KR 1020117010046A KR 20117010046 A KR20117010046 A KR 20117010046A KR 101628792 B1 KR101628792 B1 KR 101628792B1
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- Prior art keywords
- ethylene
- olefin
- block
- polymer
- interpolymer
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- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
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- 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
- C08F295/00—Macromolecular compounds obtained by polymerisation using successively different catalyst types without deactivating the intermediate polymer
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- 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
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- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
- C08F297/083—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
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- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms
- C08L23/0815—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms with aliphatic 1-olefins containing 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
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
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| US10263508P | 2008-10-03 | 2008-10-03 | |
| US61/102,635 | 2008-10-03 |
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Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8273826B2 (en) * | 2006-03-15 | 2012-09-25 | Dow Global Technologies Llc | Impact modification of thermoplastics with ethylene/α-olefin interpolymers |
| US7858706B2 (en) * | 2004-03-17 | 2010-12-28 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
| US8293859B2 (en) * | 2008-01-30 | 2012-10-23 | Dow Global Technologies, Llc | Butene/α-olefin block interpolymers |
| WO2009097535A1 (en) * | 2008-01-30 | 2009-08-06 | Dow Global Technologies Inc. | BUTENE/α-OLEFIN BLOCK INTERPOL YMERS |
| TW201122045A (en) * | 2009-07-17 | 2011-07-01 | Mitsubishi Plastics Inc | Solar cell sealing material and solar cell module made by using the same |
| CN102770487B (zh) * | 2009-10-02 | 2014-10-01 | 陶氏环球技术有限责任公司 | 热塑性硫化材料应用中的嵌段复合材料 |
| BR112012031998B1 (pt) | 2010-06-18 | 2020-10-27 | Dow Global Technologies Llc | composição e artigo de fio ou cabo |
| JP5792294B2 (ja) | 2010-06-21 | 2015-10-07 | ダウ グローバル テクノロジーズ エルエルシー | 相溶化剤としての結晶性ブロック複合体 |
| IT1400743B1 (it) * | 2010-06-30 | 2013-07-02 | Dow Global Technologies Inc | Composizioni polimeriche |
| US9062146B2 (en) | 2011-01-20 | 2015-06-23 | Lg Chem, Ltd. | Olefin block copolymer |
| KR101170491B1 (ko) | 2011-01-20 | 2012-08-01 | 주식회사 엘지화학 | 올레핀 블록 공중합체 및 시트상 성형체 |
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| EP4143260A1 (en) * | 2020-04-29 | 2023-03-08 | Dow Global Technologies LLC | Compositions containing high melt index ethylene/alpha-olefin multi-block interpolymers |
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| CN115651302B (zh) * | 2022-11-03 | 2024-04-05 | 日丰企业(天津)有限公司 | Eva软管及其制备方法和应用 |
| US12398248B2 (en) * | 2023-02-03 | 2025-08-26 | National Industrialization Company (Tasnee) | Pressure pipes with improved barrier properties to CO2 |
| WO2025059983A1 (zh) * | 2023-09-21 | 2025-03-27 | 无锡金通高纤股份有限公司 | 连续动态热交联聚烯烃弹性纤维及其制造方法 |
| WO2025207892A1 (en) | 2024-03-28 | 2025-10-02 | Dow Global Technologies Llc | Olefin-based polymer compositions with good impact performance, stiffness and light transmittance |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006101966A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies, Inc. | ETHYLENE/α-OLEFINS BLOCK INTERPOLYMERS |
| WO2008030953A1 (en) | 2006-09-06 | 2008-03-13 | Dow Global Technologies Inc. | Polymer blends from interpolymer of ethylene/alpha olefin with improved compatibility |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0574040B1 (en) | 1987-07-08 | 1998-02-04 | Sumitomo Chemical Company Limited | Olefinic thermoplastic elastomer composition |
| US5272236A (en) | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
| US6797779B1 (en) | 2003-03-28 | 2004-09-28 | The Goodyear Tire & Rubber Company | Thermoplastic composition |
| AU2005224257B2 (en) | 2004-03-17 | 2010-08-19 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for higher olefin multi-block copolymer formation |
| SG151310A1 (en) | 2004-03-17 | 2009-04-30 | Dow Global Technologies Inc | Catalyst composition comprising shuttling agent for ethylene copolymer formation |
| US7622529B2 (en) | 2004-03-17 | 2009-11-24 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/alpha-olefin with improved compatibility |
| US7863379B2 (en) | 2004-03-17 | 2011-01-04 | Dow Global Technologies Inc. | Impact modification of thermoplastics with ethylene/alpha-olefin interpolymers |
| US7858706B2 (en) | 2004-03-17 | 2010-12-28 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
| AR055046A1 (es) * | 2005-03-17 | 2007-08-01 | Dow Global Technologies Inc | Mezcla de polimeros a partir de interpolimeros de etileno / alfa-oleofinas y articulos moldeados flexibles efectuados a partir de los mismos |
| US7737215B2 (en) * | 2005-03-17 | 2010-06-15 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| TW200643044A (en) * | 2005-03-17 | 2006-12-16 | Dow Global Technologies Inc | Compositions of ethylene/α-olefin multi-block interpolymer for blown films with high hot tack |
| CN103172961B (zh) * | 2005-03-17 | 2016-08-17 | 陶氏环球技术有限责任公司 | 利用乙烯/α-烯烃共聚体对热塑性塑料的抗冲改性 |
| EP1861441B1 (en) * | 2005-03-17 | 2017-05-31 | Dow Global Technologies LLC | Interpolymers of ethylene/alpha-olefins blends and profiles and gaskets made therefrom |
| ATE507251T1 (de) * | 2005-03-17 | 2011-05-15 | Dow Global Technologies Llc | Zusammensetzungen aus einem ethylen/alpha-olefin- multiblock-interpolymer für elastische folien und laminate |
| SG160420A1 (en) * | 2005-03-17 | 2010-04-29 | Dow Global Technologies Inc | Rheology modification of interpolymers of ethylene/alpha-olefins and articles made therefrom |
| RU2408622C2 (ru) * | 2005-03-17 | 2011-01-10 | Дау Глобал Текнолоджиз Инк. | ПОЛИМЕРНЫЕ СМЕСИ ИЗ ИНТЕРПОЛИМЕРОВ ЭТИЛЕН/α-ОЛЕФИН С УЛУЧШЕННОЙ СОВМЕСТИМОСТЬЮ |
| US7695812B2 (en) * | 2005-09-16 | 2010-04-13 | Dow Global Technologies, Inc. | Fibers made from copolymers of ethylene/α-olefins |
| CA2644907A1 (en) * | 2006-03-15 | 2007-09-20 | Dow Global Technologies Inc. | Propylene/alpha-olefins block interpolymers |
| CN101983214A (zh) * | 2008-01-30 | 2011-03-02 | 陶氏环球技术公司 | 乙烯/α-烯烃嵌段互聚物 |
| WO2009097565A1 (en) * | 2008-01-30 | 2009-08-06 | Dow Global Technologies Inc. | ETHYLENE/α-OLEFIN BLOCK INTERPOLYMERS |
-
2009
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006101966A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies, Inc. | ETHYLENE/α-OLEFINS BLOCK INTERPOLYMERS |
| WO2008030953A1 (en) | 2006-09-06 | 2008-03-13 | Dow Global Technologies Inc. | Polymer blends from interpolymer of ethylene/alpha olefin with improved compatibility |
Also Published As
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| JP6317055B2 (ja) | 2018-05-09 |
| WO2010039628A3 (en) | 2010-06-17 |
| JP2012504684A (ja) | 2012-02-23 |
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| US20100113698A1 (en) | 2010-05-06 |
| JP2018066024A (ja) | 2018-04-26 |
| EP2344583A2 (en) | 2011-07-20 |
| BRPI0913808B1 (pt) | 2020-05-05 |
| US8921491B2 (en) | 2014-12-30 |
| TW201022355A (en) | 2010-06-16 |
| WO2010039628A2 (en) | 2010-04-08 |
| EP2344583B1 (en) | 2019-06-05 |
| KR20110066961A (ko) | 2011-06-17 |
| CN102239213A (zh) | 2011-11-09 |
| CN105778272A (zh) | 2016-07-20 |
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