KR101399699B1 - 관능화된 에틸렌/α-올레핀 혼성중합체 조성물 - Google Patents
관능화된 에틸렌/α-올레핀 혼성중합체 조성물 Download PDFInfo
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- KR101399699B1 KR101399699B1 KR1020077021234A KR20077021234A KR101399699B1 KR 101399699 B1 KR101399699 B1 KR 101399699B1 KR 1020077021234 A KR1020077021234 A KR 1020077021234A KR 20077021234 A KR20077021234 A KR 20077021234A KR 101399699 B1 KR101399699 B1 KR 101399699B1
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Images
Classifications
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- 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
- 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
- C08F297/086—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 the block polymer contains at least three blocks
-
- 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
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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
- C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
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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
- C08F295/00—Macromolecular compounds obtained by polymerisation using successively different catalyst types without deactivating the intermediate polymer
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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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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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
- C08L23/08—Copolymers of ethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- 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
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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
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/01—Additive used together with the catalyst, excluding compounds containing Al or B
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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
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/21—Rubbery or elastomeric properties
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- Chemical Kinetics & Catalysis (AREA)
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- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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| USPCT/US2005/008917 | 2005-03-17 | ||
| PCT/US2005/008917 WO2005090427A2 (en) | 2004-03-17 | 2005-03-17 | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
| US71818405P | 2005-09-16 | 2005-09-16 | |
| US60/718,184 | 2005-09-16 | ||
| PCT/US2006/009591 WO2006102016A2 (en) | 2005-03-17 | 2006-03-15 | FUNCTIONALIZED ETHYLENE/α-OLEFIN INTERPOLYMER COMPOSITIONS |
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| KR20080006541A KR20080006541A (ko) | 2008-01-16 |
| KR101399699B1 true KR101399699B1 (ko) | 2014-05-27 |
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Cited By (1)
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| KR20210024596A (ko) * | 2018-06-29 | 2021-03-05 | 다우 글로벌 테크놀로지스 엘엘씨 | 폼 비드 및 소결된 폼 구조물 |
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| US7786216B2 (en) * | 2005-03-17 | 2010-08-31 | Dow Global Technologies Inc. | Oil based blends of interpolymers of ethylene/α-olefins |
| CN103304751B (zh) | 2006-12-21 | 2016-04-06 | 陶氏环球技术有限责任公司 | 官能化烯烃聚合物、由其制备的组合物和制品及它们的制备方法 |
| MX345234B (es) | 2009-07-24 | 2017-01-04 | Bostik Inc | Adhesivo termocontraíble basado en copolímeros de bloque de olefina. |
| BR112012001942B1 (pt) * | 2009-07-29 | 2019-10-22 | Dow Global Technologies Llc | agente de permuta de cadeia multifuncional, processo para preparar um agente de permuta de cadeia multifuncional, processo para preparar uma composição multifuncional, composição multifuncional, processo para preparar um agente de permuta de cadeia multifuncional contendo poli-radical poliolefina, poliolefina telequélica, processo para preparar uma poliolefina com funcionalidade terminal e separador de bateria |
| JP5814241B2 (ja) * | 2009-09-18 | 2015-11-17 | ダウ グローバル テクノロジーズ エルエルシー | スラッシュ成形方法用の粉末状熱可塑性ポリオレフィンエラストマー組成物 |
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| JP5711713B2 (ja) * | 2012-10-01 | 2015-05-07 | 住友電気工業株式会社 | 多層熱回復物品 |
| IN2015DN03074A (enExample) | 2012-10-09 | 2015-10-02 | Avery Dennison Corp | |
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| EP3090003B1 (en) * | 2013-12-30 | 2023-02-15 | Dow Global Technologies LLC | Method to produce functionalized, low viscosity ethylene-based polymers |
| US10081212B2 (en) | 2014-07-03 | 2018-09-25 | Bostik, Inc. | Cohesively failing, non-staining hot melt adhesives |
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| WO2019125742A1 (en) * | 2017-12-22 | 2019-06-27 | Rohm And Haas Company | Method of making graft copolymer |
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| KR102259442B1 (ko) * | 2018-11-30 | 2021-06-01 | 롯데케미칼 주식회사 | 자동차 시트 쿠션용 발포체 조성물, 자동차 시트 쿠션용 발포체 및 이의 제조 방법 |
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| US11787939B2 (en) | 2019-10-24 | 2023-10-17 | Inv Nylon Polymers Americas, Llc | Polyamide compositions and articles made therefrom |
| EP3988614B1 (en) * | 2020-04-16 | 2025-08-13 | LG Chem, Ltd. | Composition for encapsulant film comprising ethylene/alpha-olefin copolymer and encapsulant film comprising the same |
| EP3988588B1 (en) * | 2020-04-16 | 2025-08-13 | LG Chem, Ltd. | Ethylene/alpha-olefin copolymer having excellent electrical insulation |
| JP7371228B2 (ja) | 2020-04-16 | 2023-10-30 | エルジー・ケム・リミテッド | 電気絶縁性に優れたエチレン/α-オレフィン共重合体 |
| JP7258411B2 (ja) | 2020-04-16 | 2023-04-17 | エルジー・ケム・リミテッド | エチレン/α-オレフィン共重合体を含む封止材フィルム用組成物およびそれを含む封止材フィルム |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4762890A (en) * | 1986-09-05 | 1988-08-09 | The Dow Chemical Company | Method of grafting maleic anhydride to polymers |
| US4927888A (en) * | 1986-09-05 | 1990-05-22 | The Dow Chemical Company | Maleic anhydride graft copolymers having low yellowness index and films containing the same |
| US4950541A (en) * | 1984-08-15 | 1990-08-21 | The Dow Chemical Company | Maleic anhydride grafts of olefin polymers |
| JP2004204057A (ja) * | 2002-12-25 | 2004-07-22 | Mitsui Chemicals Inc | プロピレン系樹脂組成物 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5643862B2 (enExample) * | 1973-07-27 | 1981-10-15 | ||
| JPS60228552A (ja) * | 1984-04-27 | 1985-11-13 | Ube Ind Ltd | ガラス繊維強化ポリプロピレン組成物 |
| CA1318734C (en) * | 1987-11-20 | 1993-06-01 | Mitsuyuki Okada | Modified polyolefin resin |
| EP0467178B1 (de) * | 1990-07-16 | 1996-10-09 | BASF Aktiengesellschaft | Gepfropfte und vernetzte Propylencopolymerisate |
| DE69419497T2 (de) * | 1993-11-12 | 1999-12-23 | Kanegafuchi Kagaku Kogyo K.K., Osaka | Polyolefinharzmischung |
| JP2000239405A (ja) * | 1999-02-18 | 2000-09-05 | Nippon Polyolefin Kk | エチレン(共)重合体の配向フィルムおよびその製造方法 |
| JP4178404B2 (ja) * | 2001-06-29 | 2008-11-12 | 東洋化成工業株式会社 | バインダー樹脂溶液組成物、塗料、インキ、接着剤およびプライマー |
| US6887943B2 (en) * | 2001-11-01 | 2005-05-03 | Mitsubishi Chemical Corporation | Modified propylene polymer, composition containing the same and use thereof |
| JP2004018812A (ja) * | 2002-06-20 | 2004-01-22 | Japan Polychem Corp | エチレン系重合体からなる中空成形体 |
| JP2004204058A (ja) * | 2002-12-25 | 2004-07-22 | Mitsui Chemicals Inc | オレフィン系ブロック共重合体 |
| US6759474B1 (en) * | 2003-03-03 | 2004-07-06 | Ferro Corporation | Glass reinforced nylon blend with improved knitline strength |
| EP2357203B1 (en) * | 2004-03-17 | 2017-05-24 | Dow Global Technologies LLC | Catalyst composition comprising shuttling agent for higher olefin multi-block copolymer formation |
| AU2005224258B2 (en) * | 2004-03-17 | 2010-09-02 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for ethylene copolymer formation |
| 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 |
| BRPI0508210B1 (pt) * | 2004-03-19 | 2016-04-05 | Dow Global Technologies Inc | fibra , artigo e tela não tecida extensível |
| JP2007084806A (ja) * | 2005-08-22 | 2007-04-05 | Mitsui Chemicals Inc | プロピレン系樹脂組成物 |
-
2006
- 2006-03-15 EP EP06748414.7A patent/EP1858937B1/en active Active
- 2006-03-15 AR ARP060100999A patent/AR055043A1/es unknown
- 2006-03-15 BR BRPI0609829-0A patent/BRPI0609829B1/pt active IP Right Grant
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- 2006-03-15 AU AU2006227475A patent/AU2006227475A1/en not_active Abandoned
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- 2006-03-15 JP JP2008502067A patent/JP5231986B2/ja active Active
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-
2012
- 2012-08-31 JP JP2012190893A patent/JP5860367B2/ja active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4950541A (en) * | 1984-08-15 | 1990-08-21 | The Dow Chemical Company | Maleic anhydride grafts of olefin polymers |
| US4762890A (en) * | 1986-09-05 | 1988-08-09 | The Dow Chemical Company | Method of grafting maleic anhydride to polymers |
| US4927888A (en) * | 1986-09-05 | 1990-05-22 | The Dow Chemical Company | Maleic anhydride graft copolymers having low yellowness index and films containing the same |
| JP2004204057A (ja) * | 2002-12-25 | 2004-07-22 | Mitsui Chemicals Inc | プロピレン系樹脂組成物 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20210024596A (ko) * | 2018-06-29 | 2021-03-05 | 다우 글로벌 테크놀로지스 엘엘씨 | 폼 비드 및 소결된 폼 구조물 |
| KR102601945B1 (ko) * | 2018-06-29 | 2023-11-16 | 다우 글로벌 테크놀로지스 엘엘씨 | 폼 비드 및 소결된 폼 구조물 |
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|---|---|
| EP1858937A2 (en) | 2007-11-28 |
| EP1858937B1 (en) | 2019-09-25 |
| WO2006102016A2 (en) | 2006-09-28 |
| SG160417A1 (en) | 2010-04-29 |
| BRPI0609829A2 (pt) | 2010-04-27 |
| JP5860367B2 (ja) | 2016-02-16 |
| WO2006102016A3 (en) | 2007-08-16 |
| RU2007134419A (ru) | 2009-01-20 |
| CA2601344A1 (en) | 2006-09-28 |
| BRPI0609829B1 (pt) | 2017-08-01 |
| AR055043A1 (es) | 2007-08-01 |
| TW200700441A (en) | 2007-01-01 |
| AU2006227475A1 (en) | 2006-09-28 |
| JP5231986B2 (ja) | 2013-07-10 |
| MX2007011313A (es) | 2007-10-08 |
| KR20080006541A (ko) | 2008-01-16 |
| JP2012251165A (ja) | 2012-12-20 |
| JP2008533285A (ja) | 2008-08-21 |
| TWI388576B (zh) | 2013-03-11 |
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