JP2000080328A - 水性分散液から物理乾燥性塗膜を作製するための方法 - Google Patents
水性分散液から物理乾燥性塗膜を作製するための方法Info
- Publication number
- JP2000080328A JP2000080328A JP22988699A JP22988699A JP2000080328A JP 2000080328 A JP2000080328 A JP 2000080328A JP 22988699 A JP22988699 A JP 22988699A JP 22988699 A JP22988699 A JP 22988699A JP 2000080328 A JP2000080328 A JP 2000080328A
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- Pending
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/006—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers provided for in C08G18/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- 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
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/631—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers onto polyesters and/or polycarbonates
-
- 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
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
- C08G18/8077—Oximes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- 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]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Compounds Of Unknown Constitution (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1998137062 DE19837062A1 (de) | 1998-08-17 | 1998-08-17 | Wäßrige Beschichtungsmittel, dessen Herstellung und Verwendung für Einbrennlacke |
| DE1998137063 DE19837063A1 (de) | 1998-08-17 | 1998-08-17 | Verwendung einer wäßrigen Bindemittelkombination zur Herstellung von physikalisch trocknenden Überzügen |
| DE19837062.8 | 1998-08-17 | ||
| DE19837063.6 | 1998-08-17 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000080328A true JP2000080328A (ja) | 2000-03-21 |
| JP2000080328A5 JP2000080328A5 (https=) | 2006-09-21 |
Family
ID=26048177
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22988699A Pending JP2000080328A (ja) | 1998-08-17 | 1999-08-16 | 水性分散液から物理乾燥性塗膜を作製するための方法 |
| JP22988399A Expired - Fee Related JP4579359B2 (ja) | 1998-08-17 | 1999-08-16 | 水性塗料組成物、その製造及び焼付ラッカーにおける使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22988399A Expired - Fee Related JP4579359B2 (ja) | 1998-08-17 | 1999-08-16 | 水性塗料組成物、その製造及び焼付ラッカーにおける使用 |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US6139918A (https=) |
| EP (2) | EP0980880B1 (https=) |
| JP (2) | JP2000080328A (https=) |
| KR (2) | KR100672869B1 (https=) |
| AT (2) | ATE282651T1 (https=) |
| AU (2) | AU743019B2 (https=) |
| BR (2) | BR9903717A (https=) |
| CA (2) | CA2280108A1 (https=) |
| DE (2) | DE59911076D1 (https=) |
| ES (2) | ES2234190T3 (https=) |
| PL (1) | PL190131B1 (https=) |
| PT (2) | PT980881E (https=) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2000063482A (ja) * | 1998-08-17 | 2000-02-29 | Bayer Ag | 水性塗料組成物、その製造及び焼付ラッカ―における使用 |
| JP2005068404A (ja) * | 2003-06-26 | 2005-03-17 | Bayer Materialscience Ag | エポキシ官能性粉末ラッカー結合剤用のカルボキシ官能性架橋剤 |
| JP2008514804A (ja) * | 2004-09-30 | 2008-05-08 | ザ シャーウィン−ウィリアムズ カンパニー | 低温焼成低ｖｏｃの導電性下塗剤 |
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| US6780908B1 (en) * | 2000-06-21 | 2004-08-24 | E. I. Du Pont De Nemours And Company | Coating composition |
| DE10047289A1 (de) * | 2000-09-25 | 2002-04-11 | Bayer Ag | Niedertemperatur-trocknende wässrige Beschichtungen |
| US7371965B2 (en) * | 2002-05-09 | 2008-05-13 | Finisar Corporation | Modular cage with heat sink for use with pluggable module |
| US6881786B2 (en) * | 2002-05-20 | 2005-04-19 | Ppg Industries Ohio, Inc. | One-component, waterborne film-forming composition |
| US6884845B2 (en) * | 2002-05-20 | 2005-04-26 | Ppg Industries Ohio, Inc. | Low temperature curable, two-component, waterborne film-forming composition |
| DE102004003894A1 (de) * | 2004-01-27 | 2005-08-11 | Bayer Materialscience Ag | Lösemittelarme, OH-funktionelle Dispersionen II |
| WO2005121209A1 (ja) * | 2004-06-11 | 2005-12-22 | Kansai Paint Co., Ltd. | ポリエステル樹脂及び熱硬化性水性塗料組成物 |
| DE102004054500A1 (de) * | 2004-11-11 | 2006-05-18 | Bayer Materialscience Ag | Polyester-Polyacrylat-Dispersionen mit Reaktivverdünner auf Basis von hydroxyfunktionellen Estern |
| DE102004054499A1 (de) * | 2004-11-11 | 2006-05-18 | Bayer Materialscience Ag | Polyester-Polyacrylat-Dispersionen mit Reaktivverdünnern auf Basis von lactongruppenhaltigen Verbindungen |
| CN101265389B (zh) * | 2007-03-15 | 2010-10-06 | 上海天地涂料有限公司 | 一种车辆漆及所使用的聚酯树脂的制备方法 |
| US20110021694A1 (en) * | 2009-07-23 | 2011-01-27 | E.I. Du Pont De Nemours And Company | Polyesterurethane for coating compositions |
| US10035872B2 (en) | 2010-04-01 | 2018-07-31 | Ppg Industries Ohio, Inc. | Branched polyester-urethane resins and coatings comprising the same |
| CN105111902A (zh) * | 2015-10-09 | 2015-12-02 | 广东顺德漆强化工科技有限公司 | 一种不含蜡的钢琴清面漆及制备方法 |
| WO2017106152A2 (en) * | 2015-12-14 | 2017-06-22 | Ppg Industries Ohio, Inc. | Branched polyester-urethane resins and coatings comprising the same |
| CN107057540A (zh) * | 2017-01-11 | 2017-08-18 | 成都展辰涂料有限公司 | 一种三聚氰胺板用免打磨不饱和聚酯涂料及其制备方法 |
| KR101773003B1 (ko) * | 2017-04-10 | 2017-09-12 | 김광원 | 기재필름을 포함하지 않는 디스플레이 보호필름 |
| CN107868204B (zh) * | 2017-11-30 | 2020-06-26 | 上海大学 | 阴离子型水性聚氨酯树脂、其制备方法及其应用 |
| WO2021094242A1 (en) * | 2019-11-15 | 2021-05-20 | Basf Coatings | A low voc resin composition, its obtained resin and a coating composition comprising the same |
| CN112646459A (zh) * | 2020-12-17 | 2021-04-13 | 广东花王涂料有限公司 | 一种木器色漆组合物及木器色漆涂料 |
| EP4279522A1 (de) | 2022-05-17 | 2023-11-22 | Covestro Deutschland AG | In wasser dispergierbare polyisocyanate mit aldehydblockierung und daraus erhältliche wässrige zusammensetzungen |
| WO2024243374A1 (en) * | 2023-05-24 | 2024-11-28 | Ppg Industries Ohio, Inc. | A coating composition |
| EP4720151A1 (en) * | 2023-05-24 | 2026-04-08 | PPG Industries Ohio Inc. | A coating composition |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1084203A (https=) * | 1960-06-27 | |||
| CA1154013A (en) | 1979-09-01 | 1983-09-20 | Alberto Bargiotti | Antitumor glycosides, their preparation, use and compositions thereof |
| DE3805629C1 (https=) * | 1988-02-24 | 1989-05-18 | Herberts Gmbh, 5600 Wuppertal, De | |
| DE3813866A1 (de) | 1988-04-23 | 1989-11-02 | Basf Lacke & Farben | Wasserverduennbare einbrennlacke und ihre verwendung als fuellermaterial und steinschlagzwischengrund sowie verfahren zur lackierung von automobilkarosserien |
| DE3918510A1 (de) | 1989-06-07 | 1990-12-13 | Basf Lacke & Farben | Verfahren zur herstellung von steinschlagbestaendigen beschichtungen |
| DE4000748A1 (de) | 1990-01-12 | 1991-07-18 | Hoechst Ag | Waessrige ueberzugsmasse, deren herstellung und verwendung |
| JP3094109B2 (ja) * | 1990-08-22 | 2000-10-03 | 関西ペイント株式会社 | 水性塗料及びそれを用いる塗装法 |
| DE4237957A1 (en) * | 1991-11-15 | 1993-05-19 | Herberts Gmbh | Stone impact-resistant coating materials - contain specified unsatd. polyester, polyunsaturated reactive diluent, heat-activated radical initiator and opt. fillers, pigments, solvent etc. |
| DE4137896A1 (de) * | 1991-11-18 | 1993-05-19 | Bayer Ag | Waessrige bindemittelkombination und ihre verwendung |
| ES2115780T3 (es) | 1993-01-13 | 1998-07-01 | Herberts & Co Gmbh | Composicion de revestimiento termoendurecible, exenta de emulsionante, su preparacion y utilizacion. |
| DE4427227A1 (de) | 1994-08-01 | 1996-02-08 | Bayer Ag | Wäßrige Bindemittelkombination und ihre Verwendung |
| DE19525375A1 (de) * | 1995-07-12 | 1997-01-16 | Herberts Gmbh | Überzugsmittel, deren Verwendung und Verfahren zur Herstellung von Mehrschichtüberzügen |
| DE19617086A1 (de) * | 1996-04-29 | 1997-10-30 | Bayer Ag | Verfahren zur Herstellung wäßriger Beschichtungsmittel für Einbrennlackierungen |
| ES2234190T3 (es) * | 1998-08-17 | 2005-06-16 | Bayer Materialscience Ag | Agente de recubrimiento acuoso, su fabricacion y uso para pinturas de secado al horno. |
-
1999
- 1999-08-04 ES ES99115062T patent/ES2234190T3/es not_active Expired - Lifetime
- 1999-08-04 PT PT99115062T patent/PT980881E/pt unknown
- 1999-08-04 DE DE59911076T patent/DE59911076D1/de not_active Expired - Fee Related
- 1999-08-04 EP EP19990115061 patent/EP0980880B1/de not_active Expired - Lifetime
- 1999-08-04 ES ES99115061T patent/ES2234189T3/es not_active Expired - Lifetime
- 1999-08-04 EP EP19990115062 patent/EP0980881B1/de not_active Expired - Lifetime
- 1999-08-04 PT PT99115061T patent/PT980880E/pt unknown
- 1999-08-04 AT AT99115061T patent/ATE282651T1/de not_active IP Right Cessation
- 1999-08-04 AT AT99115062T patent/ATE282652T1/de not_active IP Right Cessation
- 1999-08-04 DE DE59911077T patent/DE59911077D1/de not_active Expired - Lifetime
- 1999-08-05 US US09/368,709 patent/US6139918A/en not_active Expired - Fee Related
- 1999-08-11 US US09/371,822 patent/US6380342B2/en not_active Expired - Lifetime
- 1999-08-12 CA CA 2280108 patent/CA2280108A1/en not_active Abandoned
- 1999-08-12 CA CA 2280109 patent/CA2280109C/en not_active Expired - Fee Related
- 1999-08-13 PL PL99334913A patent/PL190131B1/pl not_active IP Right Cessation
- 1999-08-16 JP JP22988699A patent/JP2000080328A/ja active Pending
- 1999-08-16 KR KR1019990033569A patent/KR100672869B1/ko not_active Expired - Fee Related
- 1999-08-16 JP JP22988399A patent/JP4579359B2/ja not_active Expired - Fee Related
- 1999-08-16 KR KR1019990033570A patent/KR100672868B1/ko not_active Expired - Fee Related
- 1999-08-17 BR BR9903717A patent/BR9903717A/pt not_active IP Right Cessation
- 1999-08-17 BR BR9903723A patent/BR9903723A/pt not_active Application Discontinuation
- 1999-08-17 AU AU44530/99A patent/AU743019B2/en not_active Ceased
- 1999-08-17 AU AU44528/99A patent/AU755832B2/en not_active Ceased
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000063482A (ja) * | 1998-08-17 | 2000-02-29 | Bayer Ag | 水性塗料組成物、その製造及び焼付ラッカ―における使用 |
| JP2005068404A (ja) * | 2003-06-26 | 2005-03-17 | Bayer Materialscience Ag | エポキシ官能性粉末ラッカー結合剤用のカルボキシ官能性架橋剤 |
| JP2008514804A (ja) * | 2004-09-30 | 2008-05-08 | ザ シャーウィン−ウィリアムズ カンパニー | 低温焼成低ｖｏｃの導電性下塗剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| PT980881E (pt) | 2005-03-31 |
| BR9903723A (pt) | 2000-09-12 |
| KR20000017316A (ko) | 2000-03-25 |
| AU4452899A (en) | 2000-03-09 |
| EP0980881B1 (de) | 2004-11-17 |
| US20020002237A1 (en) | 2002-01-03 |
| EP0980880A1 (de) | 2000-02-23 |
| CA2280109C (en) | 2007-07-24 |
| ES2234189T3 (es) | 2005-06-16 |
| US6380342B2 (en) | 2002-04-30 |
| DE59911077D1 (de) | 2004-12-23 |
| KR100672868B1 (ko) | 2007-01-24 |
| ATE282652T1 (de) | 2004-12-15 |
| CA2280108A1 (en) | 2000-02-17 |
| EP0980880B1 (de) | 2004-11-17 |
| AU755832B2 (en) | 2002-12-19 |
| JP2000063482A (ja) | 2000-02-29 |
| JP4579359B2 (ja) | 2010-11-10 |
| AU743019B2 (en) | 2002-01-17 |
| ATE282651T1 (de) | 2004-12-15 |
| DE59911076D1 (de) | 2004-12-23 |
| EP0980881A1 (de) | 2000-02-23 |
| ES2234190T3 (es) | 2005-06-16 |
| PT980880E (pt) | 2005-03-31 |
| BR9903717A (pt) | 2000-09-12 |
| US6139918A (en) | 2000-10-31 |
| KR100672869B1 (ko) | 2007-01-24 |
| PL190131B1 (pl) | 2005-11-30 |
| KR20000017315A (ko) | 2000-03-25 |
| CA2280109A1 (en) | 2000-02-17 |
| AU4453099A (en) | 2000-03-09 |
| PL334913A1 (en) | 2000-02-28 |
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