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 & Material Sciences (AREA)
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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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| TW (1) | TW201022355A (enExample) |
| WO (1) | WO2010039628A2 (enExample) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5133050B2 (ja) * | 2004-03-17 | 2013-01-30 | ダウ グローバル テクノロジーズ エルエルシー | エチレンマルチブロックコポリマーを形成するためのシャトリング剤を含む触媒組成物 |
| US8273826B2 (en) | 2006-03-15 | 2012-09-25 | Dow Global Technologies Llc | Impact modification of thermoplastics with ethylene/α-olefin interpolymers |
| US8362184B2 (en) * | 2008-01-30 | 2013-01-29 | Dow Global Technologies, Llc | Butene/α-olefin block interpolymers |
| CN102977295B (zh) * | 2008-01-30 | 2016-03-09 | 陶氏环球技术有限责任公司 | 丁烯/α-烯烃嵌段互聚物 |
| KR101097009B1 (ko) * | 2009-07-17 | 2011-12-20 | 미쓰비시 쥬시 가부시끼가이샤 | 태양 전지 봉지재 및 그것을 이용하여 제작된 태양 전지 모듈 |
| BR112012007275B1 (pt) | 2009-10-02 | 2021-08-10 | Dow Global Technologies Llc | Vulcanizado termoplástico e artigo |
| US9607728B2 (en) | 2010-06-18 | 2017-03-28 | Dow Global Technologies Llc | Electrically conductive, mesophase-separated olefin multiblock copolymer compositions |
| CN103180379B (zh) | 2010-06-21 | 2015-07-08 | 陶氏环球技术有限责任公司 | 用作增容剂的结晶嵌段复合材料 |
| IT1400743B1 (it) * | 2010-06-30 | 2013-07-02 | Dow Global Technologies Inc | Composizioni polimeriche |
| KR101170491B1 (ko) * | 2011-01-20 | 2012-08-01 | 주식회사 엘지화학 | 올레핀 블록 공중합체 및 시트상 성형체 |
| WO2012099443A2 (ko) * | 2011-01-20 | 2012-07-26 | 주식회사 엘지화학 | 올레핀 블록 공중합체 |
| US8476367B1 (en) | 2011-01-31 | 2013-07-02 | Spartech Corporation | Pelletized plastic compounds and method of manufacture |
| CN104220551A (zh) * | 2012-03-30 | 2014-12-17 | 陶氏环球技术有限责任公司 | 聚烯烃粘合剂组合物 |
| US9127113B2 (en) | 2012-05-16 | 2015-09-08 | Rohm And Haas Electronic Materials Llc | Polystyrene-polyacrylate block copolymers, methods of manufacture thereof and articles comprising the same |
| KR101445350B1 (ko) * | 2012-10-18 | 2014-09-29 | 금호석유화학 주식회사 | 내열성 고무의 제조방법 |
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| JP6469098B2 (ja) | 2013-10-18 | 2019-02-13 | ダウ グローバル テクノロジーズ エルエルシー | 光ファイバーケーブル構成要素 |
| US10138364B2 (en) * | 2014-01-28 | 2018-11-27 | Ineos Styrolution Group Gmbh | Thermoplastic molding compounds with optimized flowability-toughness ratio |
| JP6384145B2 (ja) * | 2014-06-24 | 2018-09-05 | Ｍｃｐｐイノベーション合同会社 | 熱可塑性エラストマー組成物、成形体、食品器具及び衛生器具 |
| KR20160087618A (ko) * | 2015-01-14 | 2016-07-22 | 한화토탈 주식회사 | 폴리프로필렌 수지 조성물 |
| TWI703041B (zh) * | 2015-03-17 | 2020-09-01 | 美商陶氏全球科技有限責任公司 | 用於將撓性配件密封至撓性膜之方法 |
| KR101831418B1 (ko) | 2015-04-13 | 2018-02-22 | 주식회사 엘지화학 | 가공성 및 표면 특성이 우수한 에틸렌/알파-올레핀 공중합체 |
| CN104804358B (zh) * | 2015-04-24 | 2018-03-30 | 茂泰(福建)鞋材有限公司 | 一种轻量耐老化热塑性鞋底及其制备方法 |
| KR101889598B1 (ko) | 2015-12-08 | 2018-08-17 | 주식회사 엘지화학 | 올레핀계 중합체 |
| EP3390475B1 (en) * | 2015-12-15 | 2025-05-21 | Dow Global Technologies LLC | Cross-linked foams made from interpolymers of ethylene/alpha-olefins |
| KR102524316B1 (ko) | 2016-05-31 | 2023-04-25 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌 풍부 중합체를 포함하는 열가소성 폴리올레핀 블렌드 |
| JP6903689B2 (ja) | 2016-05-31 | 2021-07-14 | ダウ グローバル テクノロジーズ エルエルシー | 改善された低温衝撃性能を有する熱可塑性ポリオレフィンブレンド |
| WO2017206043A1 (en) | 2016-05-31 | 2017-12-07 | Dow Global Technologies Llc | Thermoplastic polyolefin blends including block composites as compatibilizers |
| EP3665223B2 (en) | 2017-08-08 | 2024-12-25 | SABIC Global Technologies B.V. | Composition comprising heterophasic propylene copolymer |
| CN110809603B (zh) * | 2018-03-21 | 2022-05-03 | Lg化学株式会社 | 聚烯烃树脂组合物和使用其的拉伸膜 |
| JP7130301B2 (ja) * | 2018-05-04 | 2022-09-05 | エルジー・ケム・リミテッド | オレフィン系共重合体及びその製造方法 |
| WO2019212302A1 (ko) * | 2018-05-04 | 2019-11-07 | 주식회사 엘지화학 | 올레핀계 공중합체 및 이의 제조방법 |
| SE542754C2 (en) * | 2018-06-14 | 2020-07-07 | Tepe Munhygienprodukter Ab | Toothbrush handle, toothbrush and methods of manufacturing |
| BR112021014780A2 (pt) * | 2019-02-12 | 2021-10-26 | Dow Global Technologies Llc | Cabo |
| TWI860420B (zh) * | 2019-11-18 | 2024-11-01 | 美商陶氏全球科技有限責任公司 | 抗熱老化之可撓性聚烯烴調配物 |
| WO2021188361A1 (en) | 2020-03-20 | 2021-09-23 | Exxonmobil Chemical Patents Inc. | Linear alpha-olefin copolymers and impact copolymers thereof |
| EP4047051A4 (en) * | 2020-04-16 | 2023-01-18 | LG Chem, Ltd. | ENCAPSULATING FILM COMPOSITION COMPRISING ETHYLENE/ALPHA-OLEFIN COPOLYMER AND ENCAPSULATING FILM COMPRISING THE SAME |
| US11884801B2 (en) | 2020-04-16 | 2024-01-30 | Lg Chem, Ltd. | Composition for encapsulant film comprising ethylene/alpha-olefin copolymer and encapsulant film comprising the same |
| WO2021210748A1 (ko) * | 2020-04-16 | 2021-10-21 | 주식회사 엘지화학 | 전기 절연성이 우수한 에틸렌/알파-올레핀 공중합체 |
| KR102348518B1 (ko) * | 2020-04-16 | 2022-01-10 | 주식회사 엘지화학 | 전기 절연성이 우수한 에틸렌/알파-올레핀 공중합체 |
| JP7778085B2 (ja) * | 2020-04-29 | 2025-12-01 | ダウ グローバル テクノロジーズ エルエルシー | 高メルトインデックスのエチレン／アルファ－オレフィンマルチブロックインターポリマーを含有する組成物 |
| EP4341082A4 (en) * | 2021-05-18 | 2025-03-19 | Saint-Gobain Performance Plastics Corporation | A composite tube and method of making |
| WO2024045165A1 (en) * | 2022-09-02 | 2024-03-07 | Dow Global Technologies Llc | Ethylene/alpha-olefin multi-block interpolymer-based compositions with excellent bally flex resistance |
| KR20250076606A (ko) | 2022-09-30 | 2025-05-29 | 다우 글로벌 테크놀로지스 엘엘씨 | 충격 강도 및 광투과율이 우수한 폴리올레핀 조성물 |
| 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 |
|---|---|---|---|---|
| EP0298739B1 (en) * | 1987-07-08 | 1994-10-19 | 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 |
| JP5133050B2 (ja) | 2004-03-17 | 2013-01-30 | ダウ グローバル テクノロジーズ エルエルシー | エチレンマルチブロックコポリマーを形成するためのシャトリング剤を含む触媒組成物 |
| AU2005224258B2 (en) | 2004-03-17 | 2010-09-02 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for ethylene copolymer formation |
| US7863379B2 (en) * | 2004-03-17 | 2011-01-04 | Dow Global Technologies Inc. | Impact modification of thermoplastics with ethylene/alpha-olefin interpolymers |
| EP2357203B1 (en) | 2004-03-17 | 2017-05-24 | Dow Global Technologies LLC | Catalyst composition comprising shuttling agent for higher olefin multi-block 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 |
| 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 |
| EP1871817B1 (en) * | 2005-03-17 | 2016-12-28 | Dow Global Technologies LLC | IMPACT MODIFICATION OF THERMOPLASTICS WITH ETHYLENE/alpha-OLEFIN INTERPOLYMERS |
| BR122017015865B1 (pt) * | 2005-03-17 | 2019-10-01 | Dow Global Technologies Inc. | Mistura polimérica, perfil, gaxeta, espuma e artigo termoformado |
| AU2006227350B2 (en) * | 2005-03-17 | 2011-11-03 | Dow Global Technologies Llc | Compositions of ethylene/alpha-olefin multi-block interpolymer for blown films with high hot tack |
| CA2601330A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Compositions of ethylene/alpha-olefin multi-block interpolymer for elastic films and laminates |
| MX2007011312A (es) * | 2005-03-17 | 2007-10-08 | Dow Global Technologies Inc | Mezclas de interpolimeros de etileno/alfa-olefinas y perfiles y juntas hechas a partir de los mismos. |
| CA2601241A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Polymer blends from interpolymer of ethylene/alpha-olefin with improved compatibility |
| MX2007011331A (es) * | 2005-03-17 | 2007-10-02 | Dow Global Technologies Inc | Mezclas de polimeros a partir de interpolimeros de etileno/alfa-olefinas y articulos moldeados flexibles hechos a partir de los mismos. |
| US7695812B2 (en) | 2005-09-16 | 2010-04-13 | Dow Global Technologies, Inc. | Fibers made from copolymers of ethylene/α-olefins |
| TW200738759A (en) * | 2006-03-15 | 2007-10-16 | Dow Global Technologies Inc | Propylene/α-olefins block interpolymers |
| JP5781769B2 (ja) * | 2008-01-30 | 2015-09-24 | ダウ グローバル テクノロジーズ エルエルシー | エチレン／α−オレフィンブロックインターポリマー |
| EP2238186B1 (en) * | 2008-01-30 | 2018-11-28 | Dow Global Technologies LLC | Ethylene/alpha-olefin block interpolymers |
-
2009
- 2009-09-28 WO PCT/US2009/058539 patent/WO2010039628A2/en not_active Ceased
- 2009-09-28 EP EP09756596.4A patent/EP2344583B1/en active Active
- 2009-09-28 JP JP2011530124A patent/JP6317055B2/ja active Active
- 2009-09-28 CN CN2009801486391A patent/CN102239213A/zh active Pending
- 2009-09-28 US US12/568,021 patent/US8921491B2/en active Active
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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
| Publication number | Publication date |
|---|---|
| CN105778272A (zh) | 2016-07-20 |
| KR20110066961A (ko) | 2011-06-17 |
| WO2010039628A2 (en) | 2010-04-08 |
| EP2344583A2 (en) | 2011-07-20 |
| CN102239213A (zh) | 2011-11-09 |
| JP2012504684A (ja) | 2012-02-23 |
| US20100113698A1 (en) | 2010-05-06 |
| BRPI0913808B1 (pt) | 2020-05-05 |
| TW201022355A (en) | 2010-06-16 |
| BRPI0913808A2 (pt) | 2017-06-20 |
| US8921491B2 (en) | 2014-12-30 |
| JP6317055B2 (ja) | 2018-05-09 |
| JP2018066024A (ja) | 2018-04-26 |
| WO2010039628A3 (en) | 2010-06-17 |
| EP2344583B1 (en) | 2019-06-05 |
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