BRPI0609812B1 - Composição exibindo alta pega a quente e estrutura de película multicamada - Google Patents
Composição exibindo alta pega a quente e estrutura de película multicamada Download PDFInfo
- Publication number
- BRPI0609812B1 BRPI0609812B1 BRPI0609812-6A BRPI0609812A BRPI0609812B1 BR PI0609812 B1 BRPI0609812 B1 BR PI0609812B1 BR PI0609812 A BRPI0609812 A BR PI0609812A BR PI0609812 B1 BRPI0609812 B1 BR PI0609812B1
- Authority
- BR
- Brazil
- Prior art keywords
- ethylene
- polymer
- percent
- interpolymer
- petition
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
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| US71798205P | 2005-09-16 | 2005-09-16 | |
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| PCT/US2006/009854 WO2006102152A2 (en) | 2005-03-17 | 2006-03-15 | Compositions of ethylene/alpha-olefin multi-block interpolymer for blown films with high hot tack |
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| JP5227163B2 (ja) * | 2005-03-17 | 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−オレフィン共重合体での熱可塑性物質の耐衝撃性改良 |
| US8153243B2 (en) * | 2005-12-09 | 2012-04-10 | Dow Global Technologies Llc | Interpolymers suitable for multilayer films |
| CN103788276B (zh) | 2005-12-09 | 2017-10-17 | 陶氏环球技术有限责任公司 | 乙烯/α‑烯烃组合物中控制分子量分布的方法 |
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| JP5357169B2 (ja) | 2007-10-22 | 2013-12-04 | ダウ グローバル テクノロジーズ エルエルシー | 物品を成形するためのポリマー組成物及び方法 |
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| CN105001584A (zh) * | 2008-01-30 | 2015-10-28 | 陶氏环球技术有限责任公司 | 乙烯/α-烯烃嵌段互聚物 |
| US8642144B2 (en) | 2008-05-28 | 2014-02-04 | Bemis Company, Inc. | Innerliner with nylon skin layer |
| CN102239213A (zh) * | 2008-10-03 | 2011-11-09 | 陶氏环球技术有限责任公司 | 具有乙烯/α-烯烃互聚物的聚合物共混物 |
| TWI438264B (zh) * | 2009-11-02 | 2014-05-21 | Hosokawa Yoko Kk | 具有氧吸收功能的塑膠質薄膜及輸液袋 |
| US9388254B2 (en) * | 2010-12-21 | 2016-07-12 | Dow Global Technologies Llc | Olefin-based polymers and dispersion polymerizations |
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| DE202011110797U1 (de) | 2011-06-16 | 2016-08-10 | Flexopack S.A. | Abfallverpackungssystem und Folie |
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| BR112014014853A8 (pt) * | 2011-12-19 | 2017-06-13 | Dow Global Technologies Llc | composição e artigo |
| US9604430B2 (en) | 2012-02-08 | 2017-03-28 | Flexopack S.A. | Thin film for waste packing cassettes |
| ITMI20120522A1 (it) * | 2012-03-30 | 2013-10-01 | Getters Spa | Composizione sigillante |
| US8875350B2 (en) * | 2012-06-29 | 2014-11-04 | The Wooster Brush Company | Extension pole with reversible tip assembly |
| KR102133068B1 (ko) * | 2012-10-09 | 2020-07-10 | 다우 글로벌 테크놀로지스 엘엘씨 | 실란트 조성물 |
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| ES2818802T3 (es) * | 2015-06-30 | 2021-04-14 | Dow Global Technologies Llc | Estructuras de multicapa y artículos que comprenden las mismas |
| US10071837B2 (en) * | 2015-09-30 | 2018-09-11 | Dow Global Technologies Llc | Fitment with valve and ethylene/a-olefin multi-block copolymer |
| TW201713575A (zh) * | 2015-09-30 | 2017-04-16 | 陶氏全球科技有限責任公司 | 具有乙烯/α-烯烴多嵌段共聚物的配件 |
| KR102555307B1 (ko) * | 2017-12-12 | 2023-07-17 | 닛폰포리에치렌가부시키가이샤 | 적층용 폴리에틸렌 수지 조성물, 적층체 및 적층체의 제조 방법 |
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|---|---|---|---|---|
| US3456044A (en) | 1965-03-12 | 1969-07-15 | Heinz Erich Pahlke | Biaxial orientation |
| CA849081A (en) | 1967-03-02 | 1970-08-11 | Du Pont Of Canada Limited | PRODUCTION OF ETHYLENE/.alpha.-OLEFIN COPOLYMERS OF IMPROVED PHYSICAL PROPERTIES |
| US4339507A (en) | 1980-11-26 | 1982-07-13 | Union Carbide Corporation | Linear low density ethylene hydrocarbon copolymer containing composition for extrusion coating |
| US4352849A (en) | 1981-03-26 | 1982-10-05 | W. R. Grace & Co. | Coextruded, heat-shrinkable, multi-layer, polyolefin packaging film |
| JPS6088016A (ja) * | 1983-10-21 | 1985-05-17 | Mitsui Petrochem Ind Ltd | エチレン共重合体 |
| US5059481A (en) | 1985-06-17 | 1991-10-22 | Viskase Corporation | Biaxially stretched, heat shrinkable VLDPE film |
| US4865902A (en) | 1986-01-17 | 1989-09-12 | E. I. Du Pont De Nemours And Company | Multilayered polyolefin high shrinkage, low-shrink force shrink film |
| CA1324749C (en) | 1987-04-10 | 1993-11-30 | Vincent Wayne Herran | Flexible stretch/shrink film |
| US4963419A (en) | 1987-05-13 | 1990-10-16 | Viskase Corporation | Multilayer film having improved heat sealing characteristics |
| US4837084A (en) | 1987-07-02 | 1989-06-06 | W. R. Grace & Co.-Conn. | Thermoplastic multi-layer packaging film and bags made therefrom |
| US4820557A (en) | 1987-09-17 | 1989-04-11 | W. R. Grace & Co.-Conn. | Thermoplastic packaging film of low I10 /I2 |
| US4952451A (en) | 1988-11-17 | 1990-08-28 | W. R. Grace & Co.-Conn. | Stretch/shrink film with improved oxygen transmission |
| US5272236A (en) | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
| US5847053A (en) | 1991-10-15 | 1998-12-08 | The Dow Chemical Company | Ethylene polymer film made from ethylene polymer blends |
| DE69317862T2 (de) | 1992-12-03 | 1998-09-17 | Mitsubishi Chem Corp | Harzzusammensetzung für Laminate |
| ES2149262T3 (es) | 1993-01-29 | 2000-11-01 | Dow Chemical Co | Interpolimerizaciones de etileno. |
| US6380341B1 (en) * | 1998-01-09 | 2002-04-30 | The Board Of Trustees Of Leland Stanford Jr. University | Ethylene copolymers with narrow composition distribution and high melting temperatures, and methods of production thereof |
| DE19949235A1 (de) * | 1998-10-16 | 2000-05-11 | Chisso Corp | Propylen/Ethylen/alpha-Olefin-Terpolymere und Verfahren zu ihrer Herstellung |
| US6262174B1 (en) | 1999-06-17 | 2001-07-17 | The Dow Chemical Company | Polymer compositions which exhibit high hot tack |
| JP3404368B2 (ja) * | 1999-11-04 | 2003-05-06 | 日東電工株式会社 | 粘着テープ |
| MY131000A (en) * | 2001-03-16 | 2007-07-31 | Dow Global Technologies Inc | High melt strength polymers and method of making same |
| EP1444276A1 (en) * | 2001-11-06 | 2004-08-11 | Dow Global Technologies, Inc. | Isotactic propylene copolymers, their preparation and use |
| GB0201796D0 (en) | 2002-01-26 | 2002-03-13 | Rolls Royce Plc | A fuel cell module |
| JP4879882B2 (ja) * | 2004-03-17 | 2012-02-22 | ダウ グローバル テクノロジーズ エルエルシー | より高次のオレフィ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 |
| 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 |
| KR101277095B1 (ko) * | 2004-03-17 | 2013-06-20 | 다우 글로벌 테크놀로지스 엘엘씨 | 셔틀링제를 포함하는, 에틸렌 공중합체 형성용 촉매 조성물 |
-
2006
- 2006-03-15 ES ES06738857.9T patent/ES2673179T3/es active Active
- 2006-03-15 EP EP06738857.9A patent/EP1858946B1/en active Active
- 2006-03-15 MX MX2007011341A patent/MX2007011341A/es active IP Right Grant
- 2006-03-15 AR ARP060101016A patent/AR056640A1/es unknown
- 2006-03-15 CN CN2006800083703A patent/CN101305026B/zh active Active
- 2006-03-15 AU AU2006227350A patent/AU2006227350B2/en not_active Expired - Fee Related
- 2006-03-15 BR BRPI0609812-6A patent/BRPI0609812B1/pt active IP Right Grant
- 2006-03-15 JP JP2008502123A patent/JP5231988B2/ja active Active
- 2006-03-15 CA CA002601287A patent/CA2601287A1/en not_active Abandoned
- 2006-03-15 TW TW095108733A patent/TW200643044A/zh unknown
- 2006-03-15 WO PCT/US2006/009854 patent/WO2006102152A2/en not_active Ceased
- 2006-03-15 RU RU2007134421/04A patent/RU2007134421A/ru not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CA2601287A1 (en) | 2006-09-28 |
| WO2006102152A8 (en) | 2007-11-01 |
| CN101305026A (zh) | 2008-11-12 |
| TW200643044A (en) | 2006-12-16 |
| BRPI0609812A2 (pt) | 2010-04-27 |
| AU2006227350A1 (en) | 2006-09-28 |
| WO2006102152A3 (en) | 2007-08-16 |
| RU2007134421A (ru) | 2009-03-20 |
| ES2673179T3 (es) | 2018-06-20 |
| CN101305026B (zh) | 2011-08-10 |
| AU2006227350B2 (en) | 2011-11-03 |
| AR056640A1 (es) | 2007-10-17 |
| EP1858946A2 (en) | 2007-11-28 |
| EP1858946B1 (en) | 2018-04-25 |
| MX2007011341A (es) | 2007-10-03 |
| JP2008540699A (ja) | 2008-11-20 |
| JP5231988B2 (ja) | 2013-07-10 |
| WO2006102152A2 (en) | 2006-09-28 |
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