KR20010032662A - 비-극성 열가소성 탄성중합체 및 극성 열가소성 중합체의상용화된 배합물 - Google Patents
비-극성 열가소성 탄성중합체 및 극성 열가소성 중합체의상용화된 배합물 Download PDFInfo
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- KR20010032662A KR20010032662A KR1020007005943A KR20007005943A KR20010032662A KR 20010032662 A KR20010032662 A KR 20010032662A KR 1020007005943 A KR1020007005943 A KR 1020007005943A KR 20007005943 A KR20007005943 A KR 20007005943A KR 20010032662 A KR20010032662 A KR 20010032662A
- Authority
- KR
- South Korea
- Prior art keywords
- styrene
- copolymers
- copolymer
- rubber
- polymer
- 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.)
- Ceased
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Classifications
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- 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
- C08L23/10—Homopolymers or copolymers of propene
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- C08L53/025—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes modified
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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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
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/08—Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L23/16—Ethene-propene or ethene-propene-diene copolymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08L23/28—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or halogen-containing compounds
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- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
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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
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/16—Homopolymers or copolymers or vinylidene fluoride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/08—Polyurethanes from polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP97121288.1 | 1997-12-04 | ||
| EP97121288A EP0921153A1 (en) | 1997-12-04 | 1997-12-04 | Compatibilized blends of non-polar thermoplastic elastomers and polar thermoplastic elastomers |
| PCT/EP1998/007818 WO1999029777A1 (en) | 1997-12-04 | 1998-12-02 | Compatibilized blends of non-polar thermoplastic elastomers and polar thermoplastic polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20010032662A true KR20010032662A (ko) | 2001-04-25 |
Family
ID=8227735
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020007005943A Ceased KR20010032662A (ko) | 1997-12-04 | 1998-12-02 | 비-극성 열가소성 탄성중합체 및 극성 열가소성 중합체의상용화된 배합물 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6414081B1 (enExample) |
| EP (1) | EP0921153A1 (enExample) |
| JP (1) | JP2001525477A (enExample) |
| KR (1) | KR20010032662A (enExample) |
| CN (1) | CN1168772C (enExample) |
| AU (1) | AU743572B2 (enExample) |
| BR (1) | BR9815162A (enExample) |
| CA (1) | CA2312159A1 (enExample) |
| IL (1) | IL136508A0 (enExample) |
| MY (1) | MY117152A (enExample) |
| TW (1) | TW473505B (enExample) |
| WO (1) | WO1999029777A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009131904A3 (en) * | 2008-04-22 | 2010-03-04 | Polyone Corporation | Thermoplastic elastomers exhibiting superior barrier properties |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19845235C2 (de) * | 1998-10-02 | 2002-05-16 | Ticona Gmbh | Verbundkörper aus Polyacetal und Styrol-Olefin-Elastomeren und Verfahren zu dessen Herstellung |
| US6379791B1 (en) | 2000-02-08 | 2002-04-30 | 3M Innovative Properties Company | Compatibilized pressure-sensitive adhesives |
| US6448353B1 (en) | 2000-02-08 | 2002-09-10 | 3M Innovative Properties Company | Continuous process for the production of controlled architecture materials |
| CA2434805A1 (en) * | 2001-01-16 | 2002-07-25 | Arnco Corporation | Flame retardant shaped articles |
| RU2003136761A (ru) * | 2001-06-07 | 2005-05-27 | Эксонмобил Кемикэл Пейтентс Инк. (Us) | Галоидированные сополимеры на изобутиленовой основе, обладающие повышенной вязкостью, и их термопластичные композиции |
| FR2829141B1 (fr) * | 2001-09-03 | 2006-12-15 | Nexans | Procede de fabrication d'un corps cylindrique et cable comportant un corps obtenu par ce procede |
| US6930150B2 (en) * | 2002-08-29 | 2005-08-16 | Taylor Made Golf Company, Inc. | Method for making polymer mixtures and compositions thereof |
| EP1426411A1 (en) * | 2002-12-06 | 2004-06-09 | KRATON Polymers Research B.V. | Styrenic block copolymer compositions to be used for the manufacture of transparent, gel free films |
| WO2005007384A1 (en) * | 2003-07-03 | 2005-01-27 | Ticona, Llc | Method of making coextruded polyacetal articles with a shaped profile and a melt-bonded thermoplastic elastomer layer, and such an article |
| DE10361230A1 (de) * | 2003-12-24 | 2005-07-28 | Ticona Gmbh | Verbundkörper, Verfahren zu dessen Herstellung und dessen Verwendung |
| US7034097B2 (en) * | 2004-01-13 | 2006-04-25 | Lexmark International, Inc. | Polyurethane elastomers with combination of curatives |
| US7347808B2 (en) * | 2004-01-13 | 2008-03-25 | Lexmark International, Inc. | Polyurethane rolls and methods of manufacturing |
| US7166358B2 (en) * | 2004-01-13 | 2007-01-23 | Lexmark International, Inc. | Polyurethane rolls with graft polyacrylate curatives |
| US7151154B2 (en) * | 2004-01-13 | 2006-12-19 | Lexmark International, Inc. | Graft polymer curatives and polyurethanes formed therefrom |
| US7094836B2 (en) * | 2004-03-04 | 2006-08-22 | Teknor Apex Company | Compatibilizers for fluoropolymers and polyolefins; blends thereof |
| DE102004047200B4 (de) * | 2004-09-29 | 2010-06-02 | Ticona Gmbh | Verbundkörper aus Polyacetal und thermoplastischem Vulkanisat-Elastomer |
| US7909194B2 (en) * | 2005-07-01 | 2011-03-22 | Exxonmobil Chemical Patents Inc. | Thermoplastic vulcanizates and sealing devices made therewith |
| US20070044906A1 (en) * | 2005-08-31 | 2007-03-01 | Freudenberg-Nok General Partnership | Multilayer polymeric composites having a layer of dispersed fluoroelastomer in thermoplastic |
| US20070045967A1 (en) * | 2005-08-31 | 2007-03-01 | Freudenberg-Nok General Partnership | Assemblies sealed with multilayer composite torsion seals having a layer of dispersed fluoroelastomer in thermoplastic |
| US20070048476A1 (en) * | 2005-08-31 | 2007-03-01 | Freudenberg-Nok General Partnership | Assemblies sealed with multilayer composite compression seals having a layer of dispersed fluoroelastomer in thermoplastic |
| JP5225845B2 (ja) * | 2005-09-12 | 2013-07-03 | 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−オレフィン組成物から調製された自動車部品 |
| US20080081874A1 (en) * | 2006-09-29 | 2008-04-03 | Kim Balfour | Poly(arylene ether) composition, method, and article |
| US20080081879A1 (en) * | 2006-09-29 | 2008-04-03 | Kim Balfour | Crosslinked block copolymer composition and method |
| US20080113138A1 (en) * | 2006-11-13 | 2008-05-15 | William Eugene Pecak | Poly(arylene ether)/polyolefin composition, method, and article |
| US7718721B2 (en) | 2006-11-13 | 2010-05-18 | Sabic Innovative Plastics Ip B.V. | Poly(arylene ether)/polyolefin composition, method, and article |
| KR20080043424A (ko) * | 2006-11-14 | 2008-05-19 | 삼성전자주식회사 | 대전방지제 조성물 및 이를 이용한 반송용 롤러 제조방법 |
| WO2008080081A2 (en) | 2006-12-21 | 2008-07-03 | Dow Global Technologies Inc. | Functionalized olefin polymers, compositions and articles prepared thereform, and methods for making the same |
| BRPI0719496B1 (pt) * | 2006-12-21 | 2019-05-14 | Dow Global Technologies Inc. | Processo para formar uma composição |
| FR2918380B1 (fr) * | 2007-07-02 | 2009-09-04 | Arkema France | Melanges et compositions elastomeres thermoplastiques a proprietes ameliorees, procede de fabrication des compositions et applications |
| FR2918382B1 (fr) * | 2007-07-02 | 2009-12-25 | Arkema France | Melange de copolymeres greffes a blocs polyamide et d'elastomeres formules avec un systeme de reticulation, procede de fabrication des compositions correspondantes et leurs utilisations |
| WO2009013559A1 (en) * | 2007-07-23 | 2009-01-29 | Cellectis | Meganuclease variants cleaving a dna target sequence from the human hemoglobin beta gene and uses thereof |
| US8653191B2 (en) * | 2007-07-27 | 2014-02-18 | Dow Global Technologies Llc | Polyolefin compositions and articles prepared therefrom, and methods for making the same |
| EP2178980A4 (en) * | 2007-08-10 | 2012-01-18 | Bayer Materialscience Llc | THERMOPLASTIC POLYURETHANE COPOLYMER MOLDING COMPOSITIONS |
| US9334395B2 (en) | 2009-12-11 | 2016-05-10 | Dow Global Technologies Llc | Thermoplastic polymer blends comprising dynamically crosslinked polyurethane in an olefin polymer matrix |
| CN101983990B (zh) * | 2010-03-29 | 2012-07-18 | 金发科技股份有限公司 | 一种热塑性弹性体及其制备方法 |
| CN102464854B (zh) * | 2010-11-11 | 2014-04-02 | 中国石油天然气股份有限公司 | 一种低温增韧abs及其制备方法 |
| CN102181169A (zh) * | 2011-04-21 | 2011-09-14 | 深圳市塑源实业有限公司 | 一种用于pbt粘合包胶的tpe合金材料的制备方法 |
| SI2581411T1 (sl) * | 2011-10-11 | 2015-01-30 | Pts-Plastic Technologie Service | Sestavek umetne snovi in postopek za njegovo izdelavo |
| US8552105B2 (en) * | 2012-03-08 | 2013-10-08 | Sabic Innovative Plastics Ip B.V. | Compatibilized composition, method for the formation thereof, and article comprising same |
| CN103572604B (zh) * | 2012-07-20 | 2016-01-27 | 广东德美精细化工股份有限公司 | 一种防水防油剂及其制备方法和应用 |
| KR101897132B1 (ko) * | 2013-05-07 | 2018-09-12 | 제이더블유케미타운 주식회사 | 넌피브이시계 의료용 수액세트의 제조 방법 |
| CN103435962B (zh) * | 2013-08-07 | 2015-08-19 | 四川大学 | 一种用于聚甲醛/聚四氟乙烯体系的增容剂及其制备方法 |
| CN103509455B (zh) * | 2013-09-18 | 2016-06-01 | 江门市蓬江区盈通塑胶制品有限公司 | 一种橡胶弹性胶带用两亲性界面剂 |
| EP3071646A1 (en) * | 2013-11-22 | 2016-09-28 | Trinseo Europe GmbH | Polycarbonate containing compositions |
| CN103804887A (zh) * | 2014-02-27 | 2014-05-21 | 苏州市涵信塑业有限公司 | 一种改良性ppo塑料 |
| ES2645887T3 (es) | 2015-02-12 | 2017-12-11 | Dynasol Elastómeros S.A. | Composición de copolímero segmentado con propiedades mejoradas |
| KR102388821B1 (ko) | 2015-06-18 | 2022-04-21 | 다우 글로벌 테크놀로지스 엘엘씨 | 열전도성 엘라스토머 복합물 |
| CN107043531A (zh) * | 2017-03-14 | 2017-08-15 | 浙江环龙新材料科技有限公司 | 一种具有良好透湿率的tpu薄膜及其制造方法和用途 |
| CN107216594A (zh) * | 2017-06-18 | 2017-09-29 | 泉州盈创新材料技术开发有限公司 | 一种耐磨导热电缆用热塑性弹性体及其制备方法 |
| CN111303617B (zh) * | 2018-12-12 | 2022-03-11 | 万华化学集团股份有限公司 | 用于塑胶跑道的低密度热塑性聚氨酯弹性体颗粒及其制品 |
| CN111909504B (zh) * | 2020-07-17 | 2022-04-01 | 北京浦江兄弟科技有限公司 | 一种隐形车衣用聚氨酯阻燃薄膜及其制备方法和用途 |
| EP4363499A1 (en) * | 2021-06-30 | 2024-05-08 | Avient Corporation | Thermoplastic elastomer articles comprising polar elastomer and rubber |
| CN119391143B (zh) * | 2024-11-18 | 2025-06-10 | 金发科技股份有限公司 | 一种tpee复合材料及其制备方法与应用 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3312756A (en) * | 1959-03-23 | 1967-04-04 | Monsanto Co | Blends of vinyl chloride polymer and hydrocarbon elastomer containing graft copolymer as compatibilizer |
| JPH0618929B2 (ja) * | 1984-03-28 | 1994-03-16 | チッソ株式会社 | ガラス繊維強化ポリプロピレン組成物 |
| US4883837A (en) * | 1988-06-24 | 1989-11-28 | The Dow Chemical Company | Compatible blends of polyolefins with thermoplastic polyurethanes |
| EP0641828A1 (en) * | 1993-09-08 | 1995-03-08 | Bayer Corporation | A thermoplastic composition containing polyurethane and polypropylene |
| JPH07157651A (ja) * | 1993-12-08 | 1995-06-20 | Sumitomo Chem Co Ltd | 熱可塑性樹脂組成物 |
| EP0753027B1 (en) * | 1994-03-29 | 1997-10-01 | Advanced Elastomer Systems, L.P. | Thermoplastic elastomers having improved surface properties |
| JP2706759B2 (ja) * | 1995-02-02 | 1998-01-28 | 三洋化成工業株式会社 | 制振塗料組成物 |
| US5623019A (en) * | 1995-07-13 | 1997-04-22 | Bayer Corporation | Compatibilized thermoplastic molding composition |
| US6300418B1 (en) * | 1997-05-02 | 2001-10-09 | Dsm N.V. | Thermoplastic elastomer composition adapted for adhesion to polar materials |
| DE69714410T2 (de) * | 1997-05-16 | 2003-04-03 | Advanced Elastomer Systems, L.P. | Verfahren zum Hochfrekwenzschweissen von nichtpolaren thermoplastischen Elastomeren |
-
1997
- 1997-12-04 EP EP97121288A patent/EP0921153A1/en not_active Withdrawn
-
1998
- 1998-10-28 TW TW087117895A patent/TW473505B/zh not_active IP Right Cessation
- 1998-11-30 MY MYPI98005420A patent/MY117152A/en unknown
- 1998-12-02 JP JP2000524359A patent/JP2001525477A/ja active Pending
- 1998-12-02 WO PCT/EP1998/007818 patent/WO1999029777A1/en not_active Ceased
- 1998-12-02 AU AU16725/99A patent/AU743572B2/en not_active Ceased
- 1998-12-02 US US09/555,036 patent/US6414081B1/en not_active Expired - Fee Related
- 1998-12-02 IL IL13650898A patent/IL136508A0/xx unknown
- 1998-12-02 KR KR1020007005943A patent/KR20010032662A/ko not_active Ceased
- 1998-12-02 CA CA002312159A patent/CA2312159A1/en not_active Abandoned
- 1998-12-02 BR BR9815162-2A patent/BR9815162A/pt not_active Application Discontinuation
- 1998-12-02 CN CNB988117967A patent/CN1168772C/zh not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009131904A3 (en) * | 2008-04-22 | 2010-03-04 | Polyone Corporation | Thermoplastic elastomers exhibiting superior barrier properties |
Also Published As
| Publication number | Publication date |
|---|---|
| BR9815162A (pt) | 2000-10-03 |
| JP2001525477A (ja) | 2001-12-11 |
| AU1672599A (en) | 1999-06-28 |
| CA2312159A1 (en) | 1999-06-17 |
| IL136508A0 (en) | 2001-06-14 |
| CN1168772C (zh) | 2004-09-29 |
| TW473505B (en) | 2002-01-21 |
| WO1999029777A1 (en) | 1999-06-17 |
| MY117152A (en) | 2004-05-31 |
| CN1280595A (zh) | 2001-01-17 |
| AU743572B2 (en) | 2002-01-31 |
| US6414081B1 (en) | 2002-07-02 |
| EP0921153A1 (en) | 1999-06-09 |
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