AU2001274057B2 - Pressure-sensitive adhesives exhibiting an improved shear strength at elevated temperatures - Google Patents
Pressure-sensitive adhesives exhibiting an improved shear strength at elevated temperatures Download PDFInfo
- Publication number
- AU2001274057B2 AU2001274057B2 AU2001274057A AU2001274057A AU2001274057B2 AU 2001274057 B2 AU2001274057 B2 AU 2001274057B2 AU 2001274057 A AU2001274057 A AU 2001274057A AU 2001274057 A AU2001274057 A AU 2001274057A AU 2001274057 B2 AU2001274057 B2 AU 2001274057B2
- Authority
- AU
- Australia
- Prior art keywords
- pressure
- temperature
- sensitive adhesive
- adhesive layer
- isocyanate
- 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
Links
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Classifications
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- C—CHEMISTRY; METALLURGY
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- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/625—Polymers of alpha-beta ethylenically unsaturated carboxylic acids; hydrolyzed polymers of esters of these acids
- C08G18/6254—Polymers of alpha-beta ethylenically unsaturated carboxylic acids and of esters of these acids containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/703—Isocyanates or isothiocyanates transformed in a latent form by physical means
- C08G18/705—Dispersions of isocyanates or isothiocyanates in a liquid medium
- C08G18/706—Dispersions of isocyanates or isothiocyanates in a liquid medium the liquid medium being water
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2170/00—Compositions for adhesives
- C08G2170/40—Compositions for pressure-sensitive adhesives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2170/00—Compositions for adhesives
- C08G2170/80—Compositions for aqueous adhesives
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31547—Of polyisocyanurate
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
- Polyurethanes Or Polyureas (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00810518.1 | 2000-06-15 | ||
| EP20000810518 EP1164154A1 (de) | 2000-06-15 | 2000-06-15 | Haftklebstoffe mit verbesserter Scherfestigkeit bei erhöhten Temperaturen |
| PCT/EP2001/005777 WO2001096439A1 (de) | 2000-06-15 | 2001-05-21 | Haftklebstoffe mit verbesserter scherfestigkeit bei erhöhten temperaturen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2001274057A1 AU2001274057A1 (en) | 2002-03-14 |
| AU2001274057B2 true AU2001274057B2 (en) | 2006-03-09 |
Family
ID=8174754
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2001274057A Ceased AU2001274057B2 (en) | 2000-06-15 | 2001-05-21 | Pressure-sensitive adhesives exhibiting an improved shear strength at elevated temperatures |
| AU7405701A Pending AU7405701A (en) | 2000-06-15 | 2001-05-21 | Pressure-sensitive adhesives exhibiting an improved shear strength at elevated temperatures |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU7405701A Pending AU7405701A (en) | 2000-06-15 | 2001-05-21 | Pressure-sensitive adhesives exhibiting an improved shear strength at elevated temperatures |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7316828B2 (enExample) |
| EP (2) | EP1164154A1 (enExample) |
| JP (2) | JP5081362B2 (enExample) |
| KR (1) | KR100787717B1 (enExample) |
| AT (1) | ATE388178T1 (enExample) |
| AU (2) | AU2001274057B2 (enExample) |
| BR (1) | BR0111573B1 (enExample) |
| CA (1) | CA2412099C (enExample) |
| DE (1) | DE50113702D1 (enExample) |
| ES (1) | ES2301550T3 (enExample) |
| PL (1) | PL359218A1 (enExample) |
| PT (1) | PT1297046E (enExample) |
| WO (1) | WO2001096439A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10210082A1 (de) * | 2002-03-08 | 2003-09-25 | Henkel Kgaa | Verfahren zum Verbinden von transparenten Kunststoffsubstraten |
| US20050087290A1 (en) * | 2002-03-08 | 2005-04-28 | Julius Herold | Method for joining transparent plastic substrates |
| DE10210477A1 (de) * | 2002-03-11 | 2003-10-02 | Henkel Kgaa | Verfahren zum Herstellen von flächigen Formteilen |
| PL1711147T3 (pl) * | 2004-01-27 | 2011-06-30 | Coloplast As | Produkt absorbujący ze strefami o różnych właściwościach powierzchni |
| DE102004026118A1 (de) * | 2004-05-28 | 2005-12-15 | Bayer Materialscience Ag | Klebstoffe |
| DE102004044086A1 (de) | 2004-09-09 | 2006-03-16 | Tesa Ag | Thermisch vernetzte Acrylat-Hotmelts |
| US7415807B2 (en) * | 2005-08-05 | 2008-08-26 | Owens Corning Intellectual Capital Llc | Structured adhesive system |
| DE102006058527A1 (de) * | 2006-12-12 | 2008-06-19 | Bayer Materialscience Ag | Klebstoffe |
| EP2283097B1 (en) * | 2008-06-03 | 2019-10-30 | Dow Global Technologies LLC | Pressure sensitive adhesive compositions and method of making the same |
| KR20110077403A (ko) * | 2009-12-30 | 2011-07-07 | 삼성전기주식회사 | 기판 제조용 캐리어 부재 및 이를 이용한 기판의 제조방법 |
| US20110183148A1 (en) * | 2010-01-27 | 2011-07-28 | Gm Global Technology Operations, Inc. | Reversible adhesive bonding system |
| EP2423247A1 (de) * | 2010-08-30 | 2012-02-29 | Rhein Chemie Rheinau GmbH | Neuartige wässrige Resorcin-Formaldehyd-Latex-Dispersionen, ein Verfahren zu deren Herstellung und deren Verwendung |
| JP6288935B2 (ja) * | 2013-04-18 | 2018-03-07 | 株式会社ディスコ | シート |
| JP6426738B2 (ja) | 2013-07-30 | 2018-11-21 | エイチ．ビー．フラー カンパニー | ポリウレタン接着フィルム |
| US9481814B2 (en) | 2014-02-26 | 2016-11-01 | H.B. Fuller Company | Tacky, heat curable multi-layer adhesive films |
| KR101754757B1 (ko) | 2014-06-27 | 2017-07-20 | 주식회사 닥터미즈 | 체지방 분해 기능성 직물의 제조 방법 |
| JP2017531056A (ja) * | 2014-08-12 | 2017-10-19 | エイチ．ビー．フラー カンパニー | 熱硬化性接着フィルム |
| US10703843B2 (en) | 2014-12-08 | 2020-07-07 | University Of Virginia Patent Foundation | Compositions and methods for bonding glues, adhesives, and coatings to surfaces |
| TWI696677B (zh) | 2014-12-15 | 2020-06-21 | 美商Ｈ Ｂ 富勒公司 | 具有強化對金屬表面之黏著性的反應性膜黏著劑 |
| KR20160001587A (ko) | 2014-12-17 | 2016-01-06 | 김민성 | 체지방 분해 기능성 직물 및 그 제조 방법 |
| EP3034576B1 (en) | 2014-12-18 | 2019-06-26 | 3M Innovative Properties Company | Pressure sensitive adhesive for outdoor applications |
| EP3124515A1 (de) * | 2015-07-28 | 2017-02-01 | Evonik Degussa GmbH | Reaktive nicht wässrige dispersionen für lacke, kleb- und dichtstoffe |
| FR3063080B1 (fr) * | 2017-02-23 | 2021-04-30 | Bostik Sa | Composition comprenant un polyester et film adhesif activable a basse temperature |
| WO2020035573A1 (en) * | 2018-08-15 | 2020-02-20 | Covestro Deutschland Ag | An adhesive and application thereof |
| CN111154067A (zh) * | 2020-01-21 | 2020-05-15 | 江苏景宏新材料科技有限公司 | 一种低粘度高剥离强度uv固化复合胶及其制备方法 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU1257100A (en) * | 1998-12-21 | 2000-07-12 | Thomas P. Abend | Aqueous dispersions or solutions having a long shelf life and containing isocyanate-reactive polymers and surface-deactivating solid polyisocyanates, method forproducing same and method for producing a layer |
| US6348548B1 (en) * | 1997-12-11 | 2002-02-19 | Bayer Ag | Method for producing and using storage-stable, latent-reactive layers or powders of surface-deactivated, solid polyisocyanates and dispersion polymers with functional groups |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS512742A (enExample) * | 1974-06-28 | 1976-01-10 | Dainippon Ink & Chemicals | |
| JPS6038368B2 (ja) * | 1981-09-12 | 1985-08-31 | 日東電工株式会社 | 貼付剤の製造方法 |
| DE3378319D1 (en) * | 1982-07-31 | 1988-12-01 | Basf Lacke & Farben | Thermosetting mixtures of polyisocyanates and polyoles having an extended storage life, process for their preparation, and their use |
| DE3325735A1 (de) * | 1983-07-16 | 1985-01-24 | Basf Ag, 6700 Ludwigshafen | Bei raumtemperatur fluessige, lagerstabile, waermeaktivierbare stoffgemische aus polyolen und/oder polyaminen und polyisocyanaten fuer polyurethan-haftkleber |
| US5371133A (en) * | 1990-09-12 | 1994-12-06 | National Starch And Chemical Investment Holding Corporation | Process for preparing urethane/acrylic-or-vinyl latexes |
| JPH06108031A (ja) * | 1992-09-28 | 1994-04-19 | Nippon Synthetic Chem Ind Co Ltd:The | 偏光板用粘着剤組成物 |
| JP2622804B2 (ja) * | 1992-11-11 | 1997-06-25 | 日本製紙株式会社 | 水性樹脂組成物 |
| JPH07331197A (ja) * | 1994-06-09 | 1995-12-19 | Sekisui Chem Co Ltd | ゴム系粘着テープの製造方法 |
| JPH07331219A (ja) * | 1994-06-15 | 1995-12-19 | Sekisui Chem Co Ltd | 粘着剤組成物 |
| JP3221285B2 (ja) * | 1995-06-05 | 2001-10-22 | 株式会社神戸製鋼所 | 感熱接着性樹脂塗装金属板およびその製造方法 |
| JP3065923B2 (ja) * | 1995-12-11 | 2000-07-17 | 三洋化成工業株式会社 | 一液型アクリル系感圧接着剤組成物 |
| DE19743014A1 (de) * | 1997-09-29 | 1999-04-01 | Basf Ag | Verfahren zur Vernetzung von strahlungsvernetzbaren Haftklebstoffschichten |
-
2000
- 2000-06-15 EP EP20000810518 patent/EP1164154A1/de not_active Withdrawn
-
2001
- 2001-05-21 EP EP01940509A patent/EP1297046B1/de not_active Expired - Lifetime
- 2001-05-21 WO PCT/EP2001/005777 patent/WO2001096439A1/de not_active Ceased
- 2001-05-21 BR BR0111573A patent/BR0111573B1/pt not_active IP Right Cessation
- 2001-05-21 KR KR1020027017111A patent/KR100787717B1/ko not_active Expired - Fee Related
- 2001-05-21 AU AU2001274057A patent/AU2001274057B2/en not_active Ceased
- 2001-05-21 AT AT01940509T patent/ATE388178T1/de not_active IP Right Cessation
- 2001-05-21 DE DE50113702T patent/DE50113702D1/de not_active Expired - Lifetime
- 2001-05-21 ES ES01940509T patent/ES2301550T3/es not_active Expired - Lifetime
- 2001-05-21 PT PT01940509T patent/PT1297046E/pt unknown
- 2001-05-21 PL PL01359218A patent/PL359218A1/xx not_active Application Discontinuation
- 2001-05-21 US US10/297,823 patent/US7316828B2/en not_active Expired - Lifetime
- 2001-05-21 CA CA 2412099 patent/CA2412099C/en not_active Expired - Lifetime
- 2001-05-21 AU AU7405701A patent/AU7405701A/xx active Pending
- 2001-05-21 JP JP2002510571A patent/JP5081362B2/ja not_active Expired - Lifetime
-
2012
- 2012-07-05 JP JP2012150990A patent/JP5462913B2/ja not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6348548B1 (en) * | 1997-12-11 | 2002-02-19 | Bayer Ag | Method for producing and using storage-stable, latent-reactive layers or powders of surface-deactivated, solid polyisocyanates and dispersion polymers with functional groups |
| AU1257100A (en) * | 1998-12-21 | 2000-07-12 | Thomas P. Abend | Aqueous dispersions or solutions having a long shelf life and containing isocyanate-reactive polymers and surface-deactivating solid polyisocyanates, method forproducing same and method for producing a layer |
Also Published As
| Publication number | Publication date |
|---|---|
| US7316828B2 (en) | 2008-01-08 |
| EP1164154A8 (de) | 2002-04-03 |
| JP2004503631A (ja) | 2004-02-05 |
| PT1297046E (pt) | 2008-05-19 |
| JP5462913B2 (ja) | 2014-04-02 |
| JP2012229429A (ja) | 2012-11-22 |
| BR0111573A (pt) | 2003-03-25 |
| JP5081362B2 (ja) | 2012-11-28 |
| AU7405701A (en) | 2001-12-24 |
| CA2412099A1 (en) | 2002-12-09 |
| US20030157337A1 (en) | 2003-08-21 |
| BR0111573B1 (pt) | 2011-06-14 |
| EP1164154A1 (de) | 2001-12-19 |
| PL359218A1 (en) | 2004-08-23 |
| CA2412099C (en) | 2011-03-22 |
| EP1297046A1 (de) | 2003-04-02 |
| ES2301550T3 (es) | 2008-07-01 |
| DE50113702D1 (de) | 2008-04-17 |
| WO2001096439A1 (de) | 2001-12-20 |
| ATE388178T1 (de) | 2008-03-15 |
| EP1297046B1 (de) | 2008-03-05 |
| KR100787717B1 (ko) | 2007-12-21 |
| KR20030022147A (ko) | 2003-03-15 |
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