JP2011523968A - ポリプロピレンおよびオレフィンインターポリマーの反応処理された高耐熱性組成物 - Google Patents
ポリプロピレンおよびオレフィンインターポリマーの反応処理された高耐熱性組成物 Download PDFInfo
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- JP2011523968A JP2011523968A JP2011512525A JP2011512525A JP2011523968A JP 2011523968 A JP2011523968 A JP 2011523968A JP 2011512525 A JP2011512525 A JP 2011512525A JP 2011512525 A JP2011512525 A JP 2011512525A JP 2011523968 A JP2011523968 A JP 2011523968A
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- olefin
- polymer
- olefin interpolymer
- propylene
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- 150000001336 alkenes Chemical class 0.000 title claims abstract description 53
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- 238000000034 method Methods 0.000 claims abstract description 39
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- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 13
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- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 5
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- LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- C08L23/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
- C08J3/246—Intercrosslinking of at least two polymers
-
- 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
-
- 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
- C08L53/00—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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—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
- C08L53/005—Modified block copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
Landscapes
- 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)
- Organic Insulating Materials (AREA)
- Inorganic Insulating Materials (AREA)
- Insulated Conductors (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
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| US5935608P | 2008-06-06 | 2008-06-06 | |
| US61/059,356 | 2008-06-06 | ||
| PCT/US2009/044805 WO2009148842A1 (en) | 2008-06-06 | 2009-05-21 | Reactively processed, high heat resistant composition of polypropylene and an olefinic interpolymer |
Publications (2)
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| JP2011523968A true JP2011523968A (ja) | 2011-08-25 |
| JP2011523968A5 JP2011523968A5 (enExample) | 2012-06-28 |
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| JP2011512525A Pending JP2011523968A (ja) | 2008-06-06 | 2009-05-21 | ポリプロピレンおよびオレフィンインターポリマーの反応処理された高耐熱性組成物 |
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| Country | Link |
|---|---|
| US (1) | US20110147639A1 (enExample) |
| EP (1) | EP2288644A1 (enExample) |
| JP (1) | JP2011523968A (enExample) |
| CN (1) | CN102083894A (enExample) |
| TW (1) | TW201011064A (enExample) |
| WO (1) | WO2009148842A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015522925A (ja) * | 2012-06-27 | 2015-08-06 | ダウ グローバル テクノロジーズ エルエルシー | 被覆導体用ポリマーコーティング |
| JP2017500379A (ja) * | 2013-11-07 | 2017-01-05 | アクゾ ノーベル ケミカルズ インターナショナル ベスローテン フエンノートシャップAkzo Nobel Chemicals International B.V. | エチレンベースのポリマー及びコポリマーを改質するための方法 |
| JP2022546466A (ja) * | 2019-08-30 | 2022-11-04 | ダウ グローバル テクノロジーズ エルエルシー | 改善された電気的特性を有するポリオレフィン組成物 |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8829090B2 (en) | 2010-11-24 | 2014-09-09 | Dow Global Technologies Llc | Composition comprising propylene-alpha-olefin copolymer, olefin block copolymer and DPO-BSA molecular melt |
| JP6003023B2 (ja) * | 2011-08-19 | 2016-10-05 | 日立金属株式会社 | 電線・ケーブルおよび組成物 |
| 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 |
| CN108350176A (zh) * | 2015-06-15 | 2018-07-31 | 布拉斯科美国有限公司 | 长链支化聚合物及制备方法 |
| US11555473B2 (en) | 2018-05-29 | 2023-01-17 | Kontak LLC | Dual bladder fuel tank |
| US11638331B2 (en) | 2018-05-29 | 2023-04-25 | Kontak LLC | Multi-frequency controllers for inductive heating and associated systems and methods |
| CA3103587A1 (en) | 2018-06-15 | 2019-12-19 | Borealis Ag | Flame retardant polyolefin composition |
| KR102884944B1 (ko) * | 2019-06-28 | 2025-11-12 | 다우 글로벌 테크놀로지스 엘엘씨 | 커플링된 소비 후 재순환 폴리프로필렌 및 이를 제공하는 공정 |
Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1002A (en) * | 1838-11-09 | Joseph evens | ||
| GB1470464A (en) * | 1975-01-10 | 1977-04-14 | Moore Co S | Electrically insulated conductor |
| JPH06290637A (ja) * | 1993-03-30 | 1994-10-18 | Hitachi Cable Ltd | 難燃性電気絶縁組成物,及びそれを用いた絶縁電線 |
| JPH09512301A (ja) * | 1994-04-20 | 1997-12-09 | ザ・ダウ・ケミカル・カンパニー | シラン架橋性の実質的に線状であるエチレンポリマー類およびそれらの使用 |
| JP2002212378A (ja) * | 2001-01-19 | 2002-07-31 | Sumitomo Wiring Syst Ltd | 樹脂組成物、その製法およびそれにより被覆された電線 |
| US6465547B1 (en) * | 2001-04-19 | 2002-10-15 | Shawcor Ltd. | Crosslinked compositions containing silane-modified polypropylene blends |
| JP2003507849A (ja) * | 1999-08-12 | 2003-02-25 | ザ ダウ ケミカル カンパニー | 高分子部材を有する電子装置 |
| JP2003160704A (ja) * | 2001-08-29 | 2003-06-06 | Riken Technos Corp | 難燃性樹脂組成物およびこれを用いた配線材 |
| JP2005325280A (ja) * | 2004-05-17 | 2005-11-24 | Tmg Kk | 難燃性樹脂組成物 |
| JP2006241182A (ja) * | 2005-02-28 | 2006-09-14 | Furukawa Electric Co Ltd:The | 絶縁樹脂組成物および絶縁電線 |
| JP2007070602A (ja) * | 2005-08-10 | 2007-03-22 | Hitachi Cable Ltd | 非ハロゲン難燃性熱可塑性エラストマー組成物及びその製造方法並びにこれを用いた電線・ケーブル |
| JP2008266389A (ja) * | 2007-04-17 | 2008-11-06 | Nitto Denko Corp | 難燃性ポリオレフィン系樹脂組成物及び該組成物よりなる粘着テープ基材、並びに、粘着テープ |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE794718Q (fr) * | 1968-12-20 | 1973-05-16 | Dow Corning Ltd | Procede de reticulation d'olefines |
| US4018852A (en) * | 1974-11-27 | 1977-04-19 | Union Carbide Corporation | Composition with triallyl compounds and process for avoiding scorching of ethylene polymer composition |
| US4857600A (en) * | 1988-05-23 | 1989-08-15 | Union Carbide Corporation | Process for grafting diacid anhydrides |
| US5064802A (en) * | 1989-09-14 | 1991-11-12 | The Dow Chemical Company | Metal complex compounds |
| US5272236A (en) * | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
| US5278272A (en) * | 1991-10-15 | 1994-01-11 | The Dow Chemical Company | Elastic substantialy linear olefin polymers |
| US5783638A (en) * | 1991-10-15 | 1998-07-21 | The Dow Chemical Company | Elastic substantially linear ethylene polymers |
| US5346961A (en) * | 1993-04-07 | 1994-09-13 | Union Carbide Chemicals & Plastics Technology Corporation | Process for crosslinking |
| US5575965A (en) * | 1995-05-19 | 1996-11-19 | Union Carbide Chemicals & Plastics Technology Corporation | Process for extrusion |
| US6828022B2 (en) * | 2000-02-21 | 2004-12-07 | Cables Pirelli | Fire-resistant and water-resistant halogen-free low-voltage cables |
| TWI327995B (en) * | 2003-04-11 | 2010-08-01 | Vinnolit Gmbh & Co Kg | Vorrichtung und verfahren zur herstellung von vinylchlorid durch thermische spaltung von 1,2-dichlorethan |
| US7355089B2 (en) * | 2004-03-17 | 2008-04-08 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| US7608668B2 (en) * | 2004-03-17 | 2009-10-27 | Dow Global Technologies Inc. | Ethylene/α-olefins block interpolymers |
| US7514517B2 (en) * | 2004-03-17 | 2009-04-07 | Dow Global Technologies Inc. | Anti-blocking compositions comprising interpolymers of ethylene/α-olefins |
| US8816006B2 (en) * | 2004-03-17 | 2014-08-26 | Dow Global Technologies Llc | Compositions of ethylene/α-olefin multi-block interpolymer suitable for films |
| US7671131B2 (en) * | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Interpolymers of ethylene/α-olefins blends and profiles and gaskets made therefrom |
| US7795321B2 (en) * | 2004-03-17 | 2010-09-14 | Dow Global Technologies Inc. | Rheology modification of interpolymers of ethylene/α-olefins and articles made therefrom |
| US7579408B2 (en) * | 2004-03-17 | 2009-08-25 | Dow Global Technologies Inc. | Thermoplastic vulcanizate comprising interpolymers of ethylene/α-olefins |
| US7582716B2 (en) * | 2004-03-17 | 2009-09-01 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for blown films with high hot tack |
| US7504347B2 (en) * | 2004-03-17 | 2009-03-17 | Dow Global Technologies Inc. | Fibers made from copolymers of propylene/α-olefins |
| US7671106B2 (en) * | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Cap liners, closures and gaskets from multi-block polymers |
| US7687442B2 (en) * | 2004-03-17 | 2010-03-30 | Dow Global Technologies Inc. | Low molecular weight ethylene/α-olefin interpolymer as base lubricant oils |
| US7622529B2 (en) * | 2004-03-17 | 2009-11-24 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/alpha-olefin with improved compatibility |
| US7741397B2 (en) * | 2004-03-17 | 2010-06-22 | Dow Global Technologies, Inc. | Filled polymer compositions made from interpolymers of ethylene/α-olefins and uses thereof |
| US7897689B2 (en) * | 2004-03-17 | 2011-03-01 | Dow Global Technologies Inc. | Functionalized ethylene/α-olefin interpolymer compositions |
| US7524911B2 (en) * | 2004-03-17 | 2009-04-28 | Dow Global Technologies Inc. | Adhesive and marking compositions made from interpolymers of ethylene/α-olefins |
| US7666918B2 (en) * | 2004-03-17 | 2010-02-23 | Dow Global Technologies, Inc. | Foams made from interpolymers of ethylene/α-olefins |
| US7662881B2 (en) * | 2004-03-17 | 2010-02-16 | Dow Global Technologies Inc. | Viscosity index improver for lubricant compositions |
| US7803728B2 (en) * | 2004-03-17 | 2010-09-28 | Dow Global Technologies Inc. | Fibers made from copolymers of ethylene/α-olefins |
-
2009
- 2009-05-21 JP JP2011512525A patent/JP2011523968A/ja active Pending
- 2009-05-21 CN CN2009801210875A patent/CN102083894A/zh active Pending
- 2009-05-21 WO PCT/US2009/044805 patent/WO2009148842A1/en not_active Ceased
- 2009-05-21 US US12/996,030 patent/US20110147639A1/en not_active Abandoned
- 2009-05-21 EP EP09759003A patent/EP2288644A1/en not_active Withdrawn
- 2009-05-26 TW TW098117449A patent/TW201011064A/zh unknown
Patent Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1002A (en) * | 1838-11-09 | Joseph evens | ||
| GB1470464A (en) * | 1975-01-10 | 1977-04-14 | Moore Co S | Electrically insulated conductor |
| JPH06290637A (ja) * | 1993-03-30 | 1994-10-18 | Hitachi Cable Ltd | 難燃性電気絶縁組成物,及びそれを用いた絶縁電線 |
| JPH09512301A (ja) * | 1994-04-20 | 1997-12-09 | ザ・ダウ・ケミカル・カンパニー | シラン架橋性の実質的に線状であるエチレンポリマー類およびそれらの使用 |
| JP2003507849A (ja) * | 1999-08-12 | 2003-02-25 | ザ ダウ ケミカル カンパニー | 高分子部材を有する電子装置 |
| JP2003507848A (ja) * | 1999-08-12 | 2003-02-25 | ザ ダウ ケミカル カンパニー | 高分子部材を有する電子装置 |
| JP2002212378A (ja) * | 2001-01-19 | 2002-07-31 | Sumitomo Wiring Syst Ltd | 樹脂組成物、その製法およびそれにより被覆された電線 |
| US6465547B1 (en) * | 2001-04-19 | 2002-10-15 | Shawcor Ltd. | Crosslinked compositions containing silane-modified polypropylene blends |
| JP2003160704A (ja) * | 2001-08-29 | 2003-06-06 | Riken Technos Corp | 難燃性樹脂組成物およびこれを用いた配線材 |
| JP2005325280A (ja) * | 2004-05-17 | 2005-11-24 | Tmg Kk | 難燃性樹脂組成物 |
| JP2006241182A (ja) * | 2005-02-28 | 2006-09-14 | Furukawa Electric Co Ltd:The | 絶縁樹脂組成物および絶縁電線 |
| JP2007070602A (ja) * | 2005-08-10 | 2007-03-22 | Hitachi Cable Ltd | 非ハロゲン難燃性熱可塑性エラストマー組成物及びその製造方法並びにこれを用いた電線・ケーブル |
| JP2008266389A (ja) * | 2007-04-17 | 2008-11-06 | Nitto Denko Corp | 難燃性ポリオレフィン系樹脂組成物及び該組成物よりなる粘着テープ基材、並びに、粘着テープ |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015522925A (ja) * | 2012-06-27 | 2015-08-06 | ダウ グローバル テクノロジーズ エルエルシー | 被覆導体用ポリマーコーティング |
| JP2017500379A (ja) * | 2013-11-07 | 2017-01-05 | アクゾ ノーベル ケミカルズ インターナショナル ベスローテン フエンノートシャップAkzo Nobel Chemicals International B.V. | エチレンベースのポリマー及びコポリマーを改質するための方法 |
| JP2022546466A (ja) * | 2019-08-30 | 2022-11-04 | ダウ グローバル テクノロジーズ エルエルシー | 改善された電気的特性を有するポリオレフィン組成物 |
| JP7608441B2 (ja) | 2019-08-30 | 2025-01-06 | ダウ グローバル テクノロジーズ エルエルシー | 改善された電気的特性を有するポリオレフィン組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| TW201011064A (en) | 2010-03-16 |
| WO2009148842A1 (en) | 2009-12-10 |
| EP2288644A1 (en) | 2011-03-02 |
| US20110147639A1 (en) | 2011-06-23 |
| CN102083894A (zh) | 2011-06-01 |
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