PL192282B1 - Sposób wytwarzania mikrokomórkowych lub niekomórkowych, odpornych na światło, elastomerycznych, giętkich lub półgiętkich wyprasek poliuretanowych - Google Patents
Sposób wytwarzania mikrokomórkowych lub niekomórkowych, odpornych na światło, elastomerycznych, giętkich lub półgiętkich wyprasek poliuretanowychInfo
- Publication number
- PL192282B1 PL192282B1 PL332552A PL33255297A PL192282B1 PL 192282 B1 PL192282 B1 PL 192282B1 PL 332552 A PL332552 A PL 332552A PL 33255297 A PL33255297 A PL 33255297A PL 192282 B1 PL192282 B1 PL 192282B1
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- PL
- Poland
- Prior art keywords
- weight
- catalyst
- component
- primary
- group
- Prior art date
Links
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Classifications
-
- 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/161—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
- C08G18/163—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22 covered by C08G18/18 and C08G18/22
-
- 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
-
- 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
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0008—Foam properties flexible
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0016—Foam properties semi-rigid
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0041—Foam properties having specified density
- C08G2110/0066—≥ 150kg/m3
-
- 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
- C08G2120/00—Compositions for reaction injection moulding processes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Artificial Filaments (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Materials For Medical Uses (AREA)
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96202738 | 1996-10-01 | ||
| PCT/BE1997/000112 WO1998014492A1 (en) | 1996-10-01 | 1997-10-01 | Light-stable elastomeric polyurethane mouldings and process for the production thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL332552A1 PL332552A1 (en) | 1999-09-13 |
| PL192282B1 true PL192282B1 (pl) | 2006-09-29 |
Family
ID=8224452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL332552A PL192282B1 (pl) | 1996-10-01 | 1997-10-01 | Sposób wytwarzania mikrokomórkowych lub niekomórkowych, odpornych na światło, elastomerycznych, giętkich lub półgiętkich wyprasek poliuretanowych |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US6242555B1 (enEXAMPLES) |
| EP (1) | EP0929586B1 (enEXAMPLES) |
| JP (1) | JP3911030B2 (enEXAMPLES) |
| KR (1) | KR100551978B1 (enEXAMPLES) |
| AT (1) | ATE200683T1 (enEXAMPLES) |
| AU (1) | AU4446697A (enEXAMPLES) |
| BR (1) | BR9712182A (enEXAMPLES) |
| CA (1) | CA2266623C (enEXAMPLES) |
| CZ (1) | CZ299115B6 (enEXAMPLES) |
| DE (1) | DE69704626T2 (enEXAMPLES) |
| DK (1) | DK0929586T3 (enEXAMPLES) |
| ES (1) | ES2157600T3 (enEXAMPLES) |
| HU (1) | HU223496B1 (enEXAMPLES) |
| ID (1) | ID21506A (enEXAMPLES) |
| IN (1) | IN1997CH00157A (enEXAMPLES) |
| MX (1) | MX216281B (enEXAMPLES) |
| PL (1) | PL192282B1 (enEXAMPLES) |
| PT (1) | PT929586E (enEXAMPLES) |
| RU (1) | RU2201940C2 (enEXAMPLES) |
| SK (1) | SK285340B6 (enEXAMPLES) |
| WO (1) | WO1998014492A1 (enEXAMPLES) |
| ZA (1) | ZA978803B (enEXAMPLES) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0995568A1 (en) * | 1998-10-21 | 2000-04-26 | Recticel | Method for manufacturing a multilayered moulded synthetic part and thus obtained part |
| JP4320846B2 (ja) * | 1999-06-10 | 2009-08-26 | 旭硝子株式会社 | 光硬化性組成物 |
| JP4540079B2 (ja) * | 2000-04-28 | 2010-09-08 | Ｊｓｒ株式会社 | 光ファイバ用硬化性樹脂組成物およびその硬化物 |
| EP1177949A1 (en) | 2000-08-01 | 2002-02-06 | Recticel | Method for manufacturing a trim part for the interior of an automobile vehicle or at least a skin therefor |
| DE10142296C1 (de) | 2001-08-29 | 2003-02-13 | Bayer Ag | Polyurethanelastomere, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US6919486B2 (en) * | 2001-12-21 | 2005-07-19 | Basf Corporation | Polyetherols produced using aluminium phosphonate catalysts |
| US20030213189A1 (en) * | 2002-05-16 | 2003-11-20 | Goldman Arthur S. | Thermoplastic polymer extrusion bending |
| RU2315780C2 (ru) * | 2002-06-21 | 2008-01-27 | Ректисел | Микроячеистый или неячеистый светоустойчивый полиуретановый материал и способ его приготовления |
| US6825238B2 (en) * | 2003-01-29 | 2004-11-30 | Air Products And Chemicals, Inc. | Low acid organometallic catalyst for the production of flexible, semi-flexible and rigid polyurethane foams |
| RU2314982C2 (ru) | 2003-04-18 | 2008-01-20 | Майекс Юса Кфт | Разливочная крышка |
| ES2450166T3 (es) * | 2003-07-14 | 2014-03-24 | Vencorex Us, Inc. | Estabilidad del color mejorada de isocianatos |
| US7296388B2 (en) | 2003-08-12 | 2007-11-20 | Valentz Arthur J | Skylight having a molded plastic frame |
| EP1510322A1 (en) | 2003-08-27 | 2005-03-02 | Recticel | Method for manufacturing a composite trim part for the interior of an automotive vehicle |
| US20050143478A1 (en) * | 2003-12-24 | 2005-06-30 | Kao Corporation | Catalyst for preparing polyurethane |
| DE102004009740A1 (de) * | 2004-02-25 | 2005-09-15 | Basf Ag | Zinn- und Übergangsmetallfreie Polyurethanschaumstoffe |
| US7021498B2 (en) | 2004-04-06 | 2006-04-04 | Advanced Controls And Engineering | Urethane spray gun assembly |
| RU2376321C2 (ru) * | 2004-05-12 | 2009-12-20 | Фритц Науэр Аг. | Гибкий пенополиуретан |
| US7268170B2 (en) * | 2004-10-13 | 2007-09-11 | Bayer Materialscience Llc | Foam modifier, foams prepared from this novel foam modifier and a process for the preparation of these foams |
| EP1657267A1 (en) * | 2004-11-10 | 2006-05-17 | INSA (Institut National des Sciences Appliqées) | Two-part polyisocyanate/polyol composition and its use for making casted products, in particular ophthalmic lenses |
| US8188208B2 (en) * | 2005-01-13 | 2012-05-29 | Bayer Materialscience Llc | Solid polyurethane elastomers which exhibit reduced dimensional shrinkage |
| US20060160977A1 (en) * | 2005-01-14 | 2006-07-20 | Jung-Shun Ou | Prescription for preparation of non-yellowing polyurethane foam |
| MX2007009228A (es) * | 2005-02-04 | 2007-08-21 | Procter & Gamble | Estructura absorbente con material absorbente de agua mejorado. |
| US20060225776A1 (en) * | 2005-04-08 | 2006-10-12 | Portable Pipe Hangers, Inc. | Skylight solar panel assembly |
| PL1757446T3 (pl) | 2005-08-23 | 2011-10-31 | Recticel Automobilsysteme Gmbh | Płytowy laminat i powłoka do wytwarzania takiego laminatu |
| US20070142601A1 (en) * | 2005-12-15 | 2007-06-21 | Bayer Materialscience Llc | RIM elastomers based on isocyanurates of isophorone diisocyanate and prepolymers thereof |
| US20070142610A1 (en) * | 2005-12-15 | 2007-06-21 | Harasin Stephen J | Polyurethane elastomers comprising allophanate modified isocyanates |
| US7772353B2 (en) * | 2005-12-15 | 2010-08-10 | Bayer Materialscience Llc | Fast curing aliphatic RIM elastomers |
| US20070142607A1 (en) * | 2005-12-15 | 2007-06-21 | Bayer Materialscience Llc | Weather resistant polyurethane elastomer |
| US20070185302A1 (en) * | 2006-02-08 | 2007-08-09 | Bayer Materialscience Llc | Polyurethane elastomers comprising allophanate modified isocyanates |
| DE102006016617B4 (de) * | 2006-04-06 | 2008-02-28 | Carl Freudenberg Kg | Polyurethanformteil, Verfahren zu dessen Herstellung und dessen Verwendung |
| RU2565080C2 (ru) * | 2006-05-30 | 2015-10-20 | Ректисел Аутомобилзюстем Гмбх | Способ изготовления гибкой эластомерной полиуретановой кожи |
| EP2032621B1 (en) * | 2006-06-14 | 2019-08-14 | Huntsman International LLC | Cross-linkable thermoplastic polyurethanes |
| WO2008025561A1 (en) * | 2006-08-31 | 2008-03-06 | Pilkington Italia S.P.A. | Method for encapsulating the edge of a glass sheet |
| DE102007005960A1 (de) * | 2007-02-07 | 2008-08-14 | Bayer Materialscience Ag | Ruß-gefüllte Polyurethane mit hoher Dielektrizitätskonstante und Durchschlagsfestigkeit |
| JP5368716B2 (ja) * | 2007-03-01 | 2013-12-18 | 花王株式会社 | ポリウレタン成形品の製造方法 |
| EP2009039A1 (en) | 2007-06-27 | 2008-12-31 | Universiteit Gent | Functionalised polyurethanes |
| CN101778877B (zh) * | 2007-07-23 | 2013-01-02 | 陶氏环球技术公司 | 在使用温度范围内g-模量基本一致的两部分聚氨酯可固化组合物 |
| AU2008293531B2 (en) * | 2007-08-27 | 2013-06-06 | Dow Global Technologies Inc. | Catalysis of natural oil based flexible polyurethane foams with bismuth compounds |
| JP5154187B2 (ja) * | 2007-10-03 | 2013-02-27 | アイカ工業株式会社 | 上水道用表面ウレタン樹脂組成物 |
| WO2009051104A1 (ja) | 2007-10-15 | 2009-04-23 | Mitsui Chemicals Polyurethanes, Inc. | 粒子状ポリウレタン樹脂組成物およびその成形品 |
| US8722752B2 (en) | 2007-10-15 | 2014-05-13 | Mitsui Chemicals, Inc. | Polyurethane resin |
| JP5386366B2 (ja) * | 2007-11-28 | 2014-01-15 | 三井化学株式会社 | 反応射出成形用ポリウレタン樹脂組成物および成形品 |
| DE102008008391A1 (de) * | 2008-02-09 | 2009-08-13 | Bayer Materialscience Ag | Geschäumte, lichtechte Polyurethanformteile |
| CN101412798B (zh) | 2008-11-21 | 2011-08-10 | 优洁（亚洲）有限公司 | 软质聚氨酯低回弹泡沫及其制备方法 |
| DE102009005712A1 (de) | 2009-01-22 | 2010-07-29 | Bayer Materialscience Ag | Polyurethanvergussmassen |
| JP5267207B2 (ja) * | 2009-02-25 | 2013-08-21 | 宇部興産株式会社 | フェノール性水酸基含有ポリウレタン |
| JP2010214298A (ja) | 2009-03-17 | 2010-09-30 | Japan Gore Tex Inc | 透湿性隔膜材料 |
| EP2269794A1 (en) | 2009-07-02 | 2011-01-05 | RECTICEL Automobilsysteme GmbH | Method of making an elastomeric skin and skin obtained by that method |
| CN101768251B (zh) * | 2009-12-31 | 2012-08-08 | 南京汇科高分子材料有限公司 | 用于汽车玻璃包边的聚氨酯弹性体及其制备方法 |
| EP2365012A1 (en) * | 2010-03-05 | 2011-09-14 | RECTICEL Automobilsysteme GmbH | Method for producing a skin layer of a flexible, elastomeric, thermoset, phase-separated polyurethane material |
| CN103189407A (zh) * | 2010-08-12 | 2013-07-03 | 拜耳知识产权有限责任公司 | 耐光性聚氨酯及其用途 |
| CN103314043B (zh) | 2010-09-07 | 2015-07-08 | 拜耳知识产权有限责任公司 | 发泡耐光聚氨酯成型件 |
| EP2522684A1 (en) | 2011-05-12 | 2012-11-14 | Recticel | Method for functionalising a thermoset isocyanate-based polymeric solid material. |
| KR101319684B1 (ko) | 2011-06-07 | 2013-10-17 | 금호미쓰이화학 주식회사 | 내열성 변성 이소시아네이트 조성물 및 이를 포함하는 내열성을 갖는 파이프 단열용 폴리우레탄 발포체 조성물 및 그 발포방법 |
| EP2679380A1 (en) | 2012-06-28 | 2014-01-01 | RECTICEL Automobilsysteme GmbH | Method for manufacturing a flexible skin having at least one insert adhered thereto. |
| ITMI20131026A1 (it) * | 2013-06-20 | 2014-12-20 | Dow Global Technologies Llc | Processo per la produzione di un espanso poliuretanico che utilizza un catalizzatore tetraalchilstannossi |
| EP2799201B1 (en) | 2013-04-30 | 2015-11-18 | Webasto SE | Method and mould for producing a panel assembly |
| DE102013022173B4 (de) | 2013-12-23 | 2017-03-30 | Gt Elektrotechnische Produkte Gmbh | Polyurethan-Elastomere auf der Basis von Polyetheralkoholgemischen und trimerisierten Diisocyanaten |
| EP2923812A1 (en) | 2014-03-25 | 2015-09-30 | Johan Ria Hugo Van Dyck | Method and mould for producing a panel assembly |
| EP3009248A1 (en) | 2014-10-13 | 2016-04-20 | RECTICEL Automobilsysteme GmbH | Method for producing an elastomeric skin having a grained surface |
| TWI713479B (zh) * | 2014-12-15 | 2020-12-21 | 美商陶氏全球科技責任有限公司 | 黏著劑組合物 |
| DE102015218869B4 (de) | 2015-09-30 | 2017-10-26 | Lisa Dräxlmaier GmbH | Verfahren und Vorrichtung zur Herstellung eines Zuschnitts einer Sprühhaut |
| PT3559070T (pt) | 2017-04-28 | 2020-08-20 | Recticel Automobilsysteme Gmbh | Películas de poliuretano compósito elastomérico |
| US10717714B2 (en) * | 2017-07-07 | 2020-07-21 | Chitec Technology Co., Ltd. | Reactive ultraviolet absorber and application thereof |
| US11046850B2 (en) | 2017-09-27 | 2021-06-29 | Evonik Operations Gmbh | Mixed metal catalyst compositions and methods for making polyurethane foam |
| US20210388150A1 (en) | 2018-11-19 | 2021-12-16 | Covestro Intellectual Property Gmbh & Co. Kg | A process for producing a polyurethane elastomer |
| CN111196871A (zh) * | 2018-11-19 | 2020-05-26 | 科思创德国股份有限公司 | 一种制备聚氨酯弹性体的方法 |
| CN110183843B (zh) * | 2019-05-16 | 2021-12-14 | 美瑞新材料股份有限公司 | 一种耐黄变的热塑性聚氨酯发泡材料及其制备方法 |
| WO2021130104A1 (en) * | 2019-12-24 | 2021-07-01 | Covestro Deutschland Ag | Flexible foam |
| EP3883806B1 (en) | 2020-01-16 | 2022-03-30 | Ascorium GmbH | Skin for a vehicle interior trim part comprising a light source |
| EP4090510B1 (en) | 2020-01-16 | 2024-12-11 | Ascorium GmbH | Skin for a vehicle interior trim part containing an operating element |
| ES2989620T3 (es) * | 2020-02-10 | 2024-11-27 | Indresmat Bv | Uso de isocianato alifático como supresor de humos tóxicos en espumas de poliuretano |
| JP7469611B2 (ja) * | 2020-02-27 | 2024-04-17 | 東ソー株式会社 | ウレタンプレポリマー組成物 |
| JP7413927B2 (ja) * | 2020-05-26 | 2024-01-16 | 東ソー株式会社 | ウレタンプレポリマー組成物 |
| US20240218591A1 (en) * | 2021-04-13 | 2024-07-04 | Basf Se | Non-solvent pu system, an artificial leather comprising the same and a process for producing the artificial leather |
| JP7629572B2 (ja) * | 2021-07-13 | 2025-02-13 | アクゾ ノーベル コーティングス インターナショナル ビー ヴィ | 一液型湿気硬化性接着剤組成物 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3931381A (en) * | 1970-09-04 | 1976-01-06 | The General Tire & Rubber Company | Mold release method for polyurethane integral-skin foam |
| LU81024A1 (fr) | 1979-03-09 | 1980-09-24 | Prb Sa | Procede pour la preparation de polyurethanne a peau integrale et polyurethanne obtenu |
| DE2914134A1 (de) | 1979-04-07 | 1980-10-23 | Bayer Ag | Verfahren zur herstellung von polyurethan-schaumstoffen |
| US4452924A (en) * | 1983-05-05 | 1984-06-05 | Mobay Chemical Corporation | Flexible polyurethane foams having improved load bearing characteristics |
| SU1275018A1 (ru) * | 1985-03-15 | 1986-12-07 | Казанский Ордена Трудового Красного Знамени Химико-Технологический Институт Им.С.М.Кирова | Способ получени эластичных пенополиуретанов |
| DE3866247D1 (de) | 1987-01-14 | 1992-01-02 | Bayer Ag | Verfahren zur herstellung von polyurethan-formteilen. |
| US5656677A (en) * | 1989-01-20 | 1997-08-12 | Recticel | Method for preparing and applying a sprayable, light stable polyurethane |
| US5100997A (en) * | 1990-05-29 | 1992-03-31 | Olin Corporation | Preparation of elastomers using high molecular weight polyols or polyamines, said polyols prepared using a double metal cyanide complex catalyst |
| US5502147A (en) * | 1993-12-21 | 1996-03-26 | Bayer Corporation | Aliphatic rim elastomers |
| CA2174305C (en) * | 1995-06-07 | 2007-07-03 | Ronald A. Cageao | Method of producing gaskets from polyurethane/urea compositions and gaskets produced therefrom |
-
1997
- 1997-09-30 IN IN157CH1997 patent/IN1997CH00157A/en unknown
- 1997-10-01 RU RU99108990/04A patent/RU2201940C2/ru not_active IP Right Cessation
- 1997-10-01 US US09/068,516 patent/US6242555B1/en not_active Expired - Lifetime
- 1997-10-01 AU AU44466/97A patent/AU4446697A/en not_active Abandoned
- 1997-10-01 ES ES97942719T patent/ES2157600T3/es not_active Expired - Lifetime
- 1997-10-01 MX MX9903192A patent/MX216281B/es not_active IP Right Cessation
- 1997-10-01 BR BR9712182-7A patent/BR9712182A/pt not_active IP Right Cessation
- 1997-10-01 JP JP51606098A patent/JP3911030B2/ja not_active Expired - Lifetime
- 1997-10-01 EP EP97942719A patent/EP0929586B1/en not_active Expired - Lifetime
- 1997-10-01 ID IDW990286A patent/ID21506A/id unknown
- 1997-10-01 CA CA002266623A patent/CA2266623C/en not_active Expired - Fee Related
- 1997-10-01 AT AT97942719T patent/ATE200683T1/de active
- 1997-10-01 CZ CZ0109299A patent/CZ299115B6/cs not_active IP Right Cessation
- 1997-10-01 HU HU0000054A patent/HU223496B1/hu not_active IP Right Cessation
- 1997-10-01 PT PT97942719T patent/PT929586E/pt unknown
- 1997-10-01 DE DE69704626T patent/DE69704626T2/de not_active Expired - Lifetime
- 1997-10-01 DK DK97942719T patent/DK0929586T3/da active
- 1997-10-01 PL PL332552A patent/PL192282B1/pl not_active IP Right Cessation
- 1997-10-01 KR KR1019997002826A patent/KR100551978B1/ko not_active Expired - Lifetime
- 1997-10-01 WO PCT/BE1997/000112 patent/WO1998014492A1/en active IP Right Grant
- 1997-10-01 ZA ZA9708803A patent/ZA978803B/xx unknown
- 1997-10-01 SK SK400-99A patent/SK285340B6/sk not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ATE200683T1 (de) | 2001-05-15 |
| KR20000048830A (ko) | 2000-07-25 |
| PL332552A1 (en) | 1999-09-13 |
| HU223496B1 (hu) | 2004-08-30 |
| DE69704626D1 (de) | 2001-05-23 |
| AU4446697A (en) | 1998-04-24 |
| US6242555B1 (en) | 2001-06-05 |
| KR100551978B1 (ko) | 2006-02-20 |
| JP2001501241A (ja) | 2001-01-30 |
| SK285340B6 (sk) | 2006-11-03 |
| MX216281B (es) | 2003-09-09 |
| ES2157600T3 (es) | 2001-08-16 |
| ID21506A (id) | 1999-06-17 |
| ZA978803B (en) | 1998-04-17 |
| CA2266623C (en) | 2009-12-15 |
| EP0929586A1 (en) | 1999-07-21 |
| RU2201940C2 (ru) | 2003-04-10 |
| CA2266623A1 (en) | 1998-04-09 |
| BR9712182A (pt) | 1999-08-31 |
| JP3911030B2 (ja) | 2007-05-09 |
| CZ109299A3 (cs) | 1999-09-15 |
| PT929586E (pt) | 2001-09-28 |
| HUP0000054A3 (en) | 2000-09-28 |
| EP0929586B1 (en) | 2001-04-18 |
| IN1997CH00157A (enEXAMPLES) | 2006-06-09 |
| DE69704626T2 (de) | 2001-11-08 |
| CZ299115B6 (cs) | 2008-04-23 |
| MX9903192A (es) | 1999-08-31 |
| HUP0000054A2 (hu) | 2000-05-28 |
| WO1998014492A1 (en) | 1998-04-09 |
| SK40099A3 (en) | 2000-07-11 |
| DK0929586T3 (da) | 2001-08-13 |
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| LAPS | Decisions on the lapse of the protection rights |
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