DE102007061856A1 - Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität - Google Patents
Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität Download PDFInfo
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- DE102007061856A1 DE102007061856A1 DE102007061856A DE102007061856A DE102007061856A1 DE 102007061856 A1 DE102007061856 A1 DE 102007061856A1 DE 102007061856 A DE102007061856 A DE 102007061856A DE 102007061856 A DE102007061856 A DE 102007061856A DE 102007061856 A1 DE102007061856 A1 DE 102007061856A1
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- KCAMXZBMXVIIQN-UHFFFAOYSA-N octan-3-yl 2-methylprop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C(C)=C KCAMXZBMXVIIQN-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000013074 reference sample Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 238000002444 silanisation Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical class O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- UZIAQVMNAXPCJQ-UHFFFAOYSA-N triethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)COC(=O)C(C)=C UZIAQVMNAXPCJQ-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical group CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- UOKUUKOEIMCYAI-UHFFFAOYSA-N trimethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)COC(=O)C(C)=C UOKUUKOEIMCYAI-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- 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
- C08G18/778—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur silicon
-
- 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
- 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
- C08G18/8083—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/809—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Polyurethanes Or Polyureas (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007061856A DE102007061856A1 (de) | 2007-12-19 | 2007-12-19 | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| JP2010538459A JP5523337B2 (ja) | 2007-12-19 | 2008-12-18 | 高い耐引掻性と高い耐候性とを有する被覆剤 |
| EP08862534.8A EP2225301B1 (de) | 2007-12-19 | 2008-12-18 | Beschichtungsmittel mit hoher kratzbeständigkeit und witterungsstabilität |
| PCT/EP2008/010809 WO2009077181A1 (de) | 2007-12-19 | 2008-12-18 | Beschichtungsmittel mit hoher kratzbeständigkeit und witterungsstabilität |
| CN200880121759.8A CN101952339B (zh) | 2007-12-19 | 2008-12-18 | 具有高耐刮擦性和耐候性的涂层剂 |
| KR1020167005688A KR20160030338A (ko) | 2007-12-19 | 2008-12-18 | 높은 내스크래치성 및 높은 내후성을 갖는 코팅제 |
| US12/808,973 US8679589B2 (en) | 2007-12-19 | 2008-12-18 | Coating agent having high scratch resistance and high weathering resistance |
| KR1020107015730A KR101634736B1 (ko) | 2007-12-19 | 2008-12-18 | 높은 내스크래치성 및 높은 내후성을 갖는 코팅제 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007061856A DE102007061856A1 (de) | 2007-12-19 | 2007-12-19 | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102007061856A1 true DE102007061856A1 (de) | 2009-06-25 |
Family
ID=40548723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102007061856A Ceased DE102007061856A1 (de) | 2007-12-19 | 2007-12-19 | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8679589B2 (https=) |
| EP (1) | EP2225301B1 (https=) |
| JP (1) | JP5523337B2 (https=) |
| KR (2) | KR20160030338A (https=) |
| CN (1) | CN101952339B (https=) |
| DE (1) | DE102007061856A1 (https=) |
| WO (1) | WO2009077181A1 (https=) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2196016B (en) | 1986-08-29 | 1991-05-15 | Humphreys & Glasgow Ltd | Clean electric power generation process |
| JP5637687B2 (ja) * | 2006-12-19 | 2014-12-10 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | 高い引掻耐性及び耐候性を有する被覆剤 |
| DE102007061855A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102007061854A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102008030304A1 (de) | 2008-06-25 | 2009-12-31 | Basf Coatings Ag | Verwendung teilsilanisierter Verbindungen auf Polyisocyanatbasis als Vernetzungsmittel in Beschichtungszusammensetzungen und Beschichtungszusammensetzung enthaltend die Verbindungen |
| DE102010015675A1 (de) * | 2010-04-21 | 2011-10-27 | Basf Coatings Gmbh | Beschichtungsmittel mit verbesserter Ablaufneigung |
| US8133964B2 (en) * | 2010-06-29 | 2012-03-13 | Science Applications International Corporation | Single-component coating having alkoxysilane-terminated N-substituted urea resins |
| EP2465886A1 (de) * | 2010-12-16 | 2012-06-20 | Bayer MaterialScience AG | Polyisocyanat-Polyadditionsprodukte, ein Verfahren zu ihrer Herstellung und ihre Verwendung |
| KR101962493B1 (ko) | 2011-06-09 | 2019-03-26 | 바스프 코팅스 게엠베하 | 높은 내스크래치성 및 우수한 연마성을 나타내는 코팅제 조성물, 이로부터 제조된 코팅, 및 이의 용도 |
| US9371469B2 (en) | 2011-06-09 | 2016-06-21 | Basf Coatings Gmbh | Coating agent compositions, coatings made therefrom and exhibiting high scratch resistance and good polishability, and use thereof |
| US9909029B2 (en) | 2011-06-09 | 2018-03-06 | Basf Coatings Gmbh | Coating material compositions, coatings made therefrom and exhibiting high scratch resistance and good polishability, and use thereof |
| EP2877512B1 (de) | 2012-07-25 | 2017-08-09 | BASF Coatings GmbH | Polyurethan-beschichtungsmittelzusammensetzung und ihre verwendung, mehrstufige beschichtungsverfahren |
| WO2014016019A1 (de) | 2012-07-25 | 2014-01-30 | Basf Coatings Gmbh | Polyurethan-beschichtungsmittelzusammensetzung, mehrstufige beschichtungsverfahren |
| KR102182771B1 (ko) * | 2012-12-03 | 2020-11-25 | 바스프 코팅스 게엠베하 | 높은 내스크래치성 및 양호한 연마성 및 양호한 광학 특성을 가지는 코팅 재료 조성물 및 이로부터 제조된 코팅, 및 이의 용도 |
| EP2925459B1 (de) * | 2012-12-03 | 2016-08-31 | BASF Coatings GmbH | Effekt- und/oder farbgebende mehrschichtlackierung und verfahren zu ihrer herstellung sowie ihre verwendung |
| EP2896639A1 (de) | 2014-01-15 | 2015-07-22 | BASF Coatings GmbH | Beschichtete metallisierte Oberflächen |
| JP6619008B2 (ja) | 2014-12-08 | 2019-12-11 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | コーティング材料組成物、およびそれらから生成されるコーティング、ならびにその使用方法 |
| RU2670274C1 (ru) | 2014-12-08 | 2018-10-22 | БАСФ Коатингс ГмбХ | Неводные композиции покрывающего материала, покрытия, получаемые из них и имеющие улучшенную адгезию и стойкость к царапанию, а также их применение |
| CN104672968A (zh) * | 2015-02-06 | 2015-06-03 | 孙慧霞 | 一种耐磨耐刮擦美术涂料的制备方法 |
| US10590229B2 (en) | 2015-05-21 | 2020-03-17 | Covestro Deutschland Ag | Polyurethane coating compositions |
| EP3307833A1 (de) | 2015-06-15 | 2018-04-18 | BASF Coatings GmbH | Verfahren zur beschichtung von radfelgen sowie die hierbei erhaltenen schmutzabweisenden und bremsstraubresistenten beschichtungen |
| CN107771200A (zh) | 2015-06-15 | 2018-03-06 | 巴斯夫涂料有限公司 | 涂覆轮辋的方法及以此得到的防污和防制动粉尘的涂层 |
| ES2785680T3 (es) | 2016-05-24 | 2020-10-07 | Basf Coatings Gmbh | Agentes de recubrimiento y recubrimientos producidos a partir de ello con resistencias a la suciedad y propiedades de (auto)limpieza mejoradas así como su uso |
| US11028287B2 (en) * | 2017-03-03 | 2021-06-08 | The Government Of The United States Of America, As Represented By The Secretary Of The Navy | Moisture-curable omniphobic coatings |
| US11499075B2 (en) | 2017-09-29 | 2022-11-15 | Ddp Specialty Electronics Materials Us, Llc | Isocyanate functional adhesive which bonds primerless to silanated acrylic polyol based coatings |
| MX2023010768A (es) | 2021-03-19 | 2023-11-29 | Basf Coatings Gmbh | Sistemas de recubrimiento multicapa obtenidos a partir de composiciones del recubrimiento de base que contienen copolimeros en bloque. |
| CA3211760A1 (en) | 2021-03-19 | 2022-09-22 | Basf Coatings Gmbh | Multilayer coating systems obtained from block copolymer containing topcoat compositions |
| CN117062849A (zh) | 2021-03-26 | 2023-11-14 | 巴斯夫涂料有限公司 | 用于提供无白化或白化减少的透明涂层的透明涂料组合物 |
| MX2024002501A (es) | 2021-08-30 | 2024-03-15 | Basf Coatings Gmbh | Recubrimiento multicapa blanco sedoso. |
| KR20250022150A (ko) | 2022-06-09 | 2025-02-14 | 바스프 코팅스 게엠베하 | 탁월한 외관을 갖는 저온 경화성 다층 코팅 시스템 |
| KR20250022788A (ko) | 2022-06-09 | 2025-02-17 | 바스프 코팅스 게엠베하 | 탁월한 내수성을 달성하기 위한 프라이머 코팅 시스템 및 조성물 |
| WO2024074642A1 (en) | 2022-10-07 | 2024-04-11 | Basf Coatings Gmbh | Multilayer coating systems obtained from block copolymer containing basecoat compositions |
| EP4353786A1 (en) | 2022-10-13 | 2024-04-17 | BASF Coatings GmbH | Sustainably producible pigments and dyes for automotive coatings |
| WO2026027456A1 (en) | 2024-07-29 | 2026-02-05 | Basf Coatings Gmbh | Scratch resistant coatings with good appearance and plastic compatibility |
| WO2026077939A1 (en) | 2024-10-08 | 2026-04-16 | Basf Coatings Gmbh | Clearcoat compositions for providing clearcoats with stable gloss across varying dry layer thicknesses |
Citations (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0008127A1 (de) | 1978-08-12 | 1980-02-20 | Saarbergwerke Aktiengesellschaft | Verfahren zum Verfestigen von Kohle und/oder Gestein im Bergbau |
| US4598131A (en) | 1984-12-19 | 1986-07-01 | Ppg Industries, Inc. | Catalysts for curable coating vehicle based upon aminoalkyloxy silanes and organic isocyanates |
| US4710542A (en) | 1986-05-16 | 1987-12-01 | American Cyanamid Company | Alkylcarbamylmethylated amino-triazine crosslinking agents and curable compositions containing the same |
| EP0249201A2 (en) | 1986-06-10 | 1987-12-16 | Union Carbide Corporation | High solids sag resistant cycloaliphatic epoxy coatings containing low molecular weight high Tg organic polymeric sag resisting additives |
| EP0276501A2 (en) | 1987-01-24 | 1988-08-03 | Akzo Nobel N.V. | Thickening compositions and thickened aqueous acid solutions |
| US5225248A (en) | 1991-05-13 | 1993-07-06 | E. I. Du Pont De Nemours And Company | Method of curing a topcoat |
| EP0571073A2 (en) | 1992-05-19 | 1993-11-24 | Imperial Chemical Industries Plc | Silane functional oligomer |
| WO1994022968A1 (de) | 1993-03-31 | 1994-10-13 | Basf Lacke + Farben Ag | Nichtwässriger thixotropierter lack und verfahren zur herstellung mehrschichtiger überzüge damit |
| EP0626888A1 (de) | 1992-02-15 | 1994-12-07 | Basf Lacke & Farben | Verfahren zur herstellung einer zweischichtigen lackierung und für dieses verfahren geeignete nicht-wässrige lacke. |
| EP0692007A1 (de) | 1993-03-31 | 1996-01-17 | BASF Lacke + Farben AG | Verfahren zur herstellung einer zweischichtigen decklackierung auf einer substratoberfläche |
| WO1997012945A1 (en) | 1995-10-06 | 1997-04-10 | Cabot Corporation | Aqueous thixotropes for waterborne systems |
| EP0994117A1 (en) | 1998-10-14 | 2000-04-19 | Bayer Aktiengesellschaft | Silane-modified polyurethane resins, a process for their preparation and their use as moisture-curable resins |
| WO2001009260A1 (en) | 1999-07-30 | 2001-02-08 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
| WO2001098393A1 (en) | 2000-06-22 | 2001-12-27 | Basf Corporation | Coating compositions having improved adhesion to aluminum substrates |
| EP1273640A2 (de) | 2001-07-06 | 2003-01-08 | Degussa AG | Nichtwässriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel |
| DE69625241T2 (de) * | 1995-03-08 | 2003-09-11 | E.I. Du Pont De Nemours And Co., Wilmington | Reaktive organosiliciumverbindungen |
| WO2004014991A1 (en) * | 2002-08-07 | 2004-02-19 | E.I. Du Pont De Nemours And Company | One-pack primer sealer compositions for smc automotive body panels |
| DE102004050746A1 (de) * | 2004-10-19 | 2006-04-20 | Basf Coatings Ag | Hochkratzfeste und hochelastische Beschichtungsmittel auf Basis von Alkoxysilan-funktionellen Komponenten |
| WO2006042585A1 (de) | 2004-10-19 | 2006-04-27 | Basf Coatings Ag | Beschichtungsmittel enthaltend addukte mit alkoxysilanfunktionalität |
| US20060217472A1 (en) | 2005-03-11 | 2006-09-28 | Staunton Thomas J | Scratch resistant curable coating composition |
| WO2006131314A1 (de) | 2005-06-07 | 2006-12-14 | Construction Research & Technology Gmbh | Silan-modifizierte harnstoff-derivate, verfahren zu ihrer herstellung und deren verwendung als rheologiehilfsmittel |
| WO2007003857A2 (fr) | 2005-06-30 | 2007-01-11 | Prismaflex International | Panneau de communication retroeclaire |
| DE102005045228A1 (de) | 2005-09-22 | 2007-04-05 | Basf Coatings Ag | Verwendung von Phosphonsäurediestern und Diphosphonsäurediestern sowie silangruppenhaltige, härtbare Gemische, enthaltend Phosphonsäurediester und Diphosphonsäurediester |
Family Cites Families (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3168483A (en) * | 1961-01-17 | 1965-02-02 | Air Prod & Chem | Diazabicyclooctane-alkylene oxide catalyst compositions |
| US3707521A (en) * | 1970-03-05 | 1972-12-26 | Essex Chemical Corp | Polyurethane sealant-primer system isocyanate-reactive surface primer composition for polyurethane sealants |
| US3718614A (en) * | 1971-02-23 | 1973-02-27 | American Cyanamid Co | Polymeric viscosity control additives for silica thixotropic compositions |
| US3959403A (en) * | 1975-03-31 | 1976-05-25 | General Electric Company | Process for making silarylenesilanediol, silarylenesiloxanediol and silarylenesiloxane-polydiorganosiloxane block copolymers |
| JPS5536216A (en) * | 1978-09-05 | 1980-03-13 | Mitsubishi Gas Chem Co Inc | Curing of organoalkoxysilane compound |
| US4479990A (en) * | 1982-07-30 | 1984-10-30 | Westinghouse Electric Co. | Arc and track resistant articles utilizing photosensitive sag resistant cycloaliphatic epoxy resin coating compositions |
| US4499151A (en) * | 1983-03-29 | 1985-02-12 | Ppg Industries, Inc. | Color plus clear coating method utilizing addition interpolymers containing alkoxy silane and/or acyloxy silane groups |
| US4499150A (en) * | 1983-03-29 | 1985-02-12 | Ppg Industries, Inc. | Color plus clear coating method utilizing addition interpolymers containing alkoxy silane and/or acyloxy silane groups |
| EP0158893A1 (en) * | 1984-03-29 | 1985-10-23 | Union Carbide Corporation | Silane containing isocyanate prepolymers |
| JPS6475578A (en) * | 1987-09-18 | 1989-03-22 | Showa Highpolymer | One-pack curing type coating having excellent preservation stability |
| US5250605A (en) * | 1990-12-17 | 1993-10-05 | E. I. Du Pont De Nemours And Company | Coating compositions comprising an organosilane polymer and reactive dispersed polymers |
| CA2098616C (en) * | 1990-12-17 | 2002-01-29 | Isidor Hazan | Coatings comprising an organosilane solution polymer and a crosslink functional dispersed polymer |
| DE4132430A1 (de) | 1991-09-28 | 1993-04-01 | Basf Lacke & Farben | Waessrige lacke und verfahren zur herstellung von automobildecklackierungen |
| JP3086737B2 (ja) * | 1992-01-17 | 2000-09-11 | 鐘淵化学工業株式会社 | 塗料用硬化性組成物 |
| EP0554684B1 (en) | 1992-01-17 | 1996-01-03 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition for paint |
| JP3144872B2 (ja) * | 1992-02-27 | 2001-03-12 | 鐘淵化学工業株式会社 | 硬化性組成物 |
| US5238993A (en) * | 1992-10-02 | 1993-08-24 | The Dow Chemical Company | Primer composition for improving the bonding of urethane adhesives to acid resistant paints |
| JP3482569B2 (ja) | 1994-06-14 | 2003-12-22 | 鐘淵化学工業株式会社 | 塗料用樹脂組成物、及び耐汚染性に優れた塗膜の形成方法 |
| DE19624972C2 (de) * | 1996-06-22 | 1998-06-04 | Herberts Gmbh | Wäßrige Dispersion von silanfunktionellen Polyurethanharzen, deren Herstellung und Verwendung |
| US5747590A (en) * | 1996-12-04 | 1998-05-05 | E. I. Du Pont De Nemours And Company | Acrylic-melamine-functionalized oligomer coating composition |
| US5691439A (en) * | 1996-12-16 | 1997-11-25 | Bayer Corporation | Low surface energy polyisocyanates and their use in one- or two-component coating compositions |
| DE19715427A1 (de) * | 1997-04-14 | 1998-10-15 | Bayer Ag | Wäßrige 2-Komponenten Bindemittel und deren Verwendung |
| JPH10306251A (ja) | 1997-05-07 | 1998-11-17 | Kanegafuchi Chem Ind Co Ltd | 塗料用硬化性組成物およびそれを塗布してなる塗装物 |
| SE510128C2 (sv) | 1997-06-26 | 1999-04-19 | Perstorp Ab | Förfarande för framställning av dendritisk polyol |
| JPH11116847A (ja) | 1997-10-09 | 1999-04-27 | Kanegafuchi Chem Ind Co Ltd | 上塗り塗料組成物およびその塗膜の形成方法 |
| US5952445A (en) | 1998-04-09 | 1999-09-14 | Bayer Corporation | Water dispersible compounds containing alkoxysilane groups |
| US5985463A (en) * | 1998-06-24 | 1999-11-16 | E.I. Du Pont De Nemours And Company | Coating containing hydroxy containing acrylosilane polymer to improve mar and acid etch resistance |
| CN1165561C (zh) * | 1999-03-17 | 2004-09-08 | 纳幕尔杜邦公司 | 高固含量耐酸蚀的透明涂料组合物 |
| DE10048615A1 (de) * | 2000-09-30 | 2002-04-11 | Degussa | Nichtwäßriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel |
| EP1197506B1 (en) | 2000-10-13 | 2006-01-25 | Tosoh Corporation | Catalyst for production of a two component polyurethane sealant |
| US6379807B1 (en) * | 2000-11-07 | 2002-04-30 | E. I. Du Pont De Nemours And Company | Coating composition having improved acid etch resistance |
| DE10103027A1 (de) * | 2001-01-24 | 2002-07-25 | Bayer Ag | Zweikomponenten-Polyurethan-Bindemittel als Haftvermittler |
| JP4334188B2 (ja) * | 2001-11-08 | 2009-09-30 | 株式会社カネカ | 上塗り塗料用硬化性樹脂組成物およびそれを塗布してなる塗装物。 |
| AT412090B (de) | 2002-01-29 | 2004-09-27 | Surface Specialties Austria | Hydroxyfunktionelle polyester |
| DE10219508A1 (de) | 2002-04-30 | 2003-11-13 | Basf Ag | Verfahren zur Herstellung hochfunktioneller, hyperverzweigter Polyester |
| US7056976B2 (en) * | 2002-08-06 | 2006-06-06 | Huntsman International Llc | Pultrusion systems and process |
| DE10352907A1 (de) | 2002-11-15 | 2004-08-05 | Henkel Kgaa | Silylgruppen enthaltende Präpolymere, deren Herstellung und Verwendung in Montageschäumen |
| DE10323206A1 (de) | 2003-05-22 | 2004-12-09 | Consortium für elektrochemische Industrie GmbH | Schäumbare Mischungen |
| EP1496114A1 (de) | 2003-07-07 | 2005-01-12 | Margraf, Stefan, Dr.med. | Verfahren zur Inaktivierung von Mikroorganismen |
| EP1502927A1 (de) | 2003-07-31 | 2005-02-02 | Sika Technology AG | Isocyanatfreie Primerzusammensetzung für Glas und Glaskeramiken |
| DE10344448A1 (de) | 2003-09-25 | 2005-04-28 | Henkel Kgaa | Bindemittel mit Barriere-Eigenschaft |
| US20050208312A1 (en) | 2004-03-17 | 2005-09-22 | Isidor Hazan | One-pack primer surfacer composition for SMC automotive body panels |
| US20050238899A1 (en) * | 2004-04-27 | 2005-10-27 | Isao Nagata | High solids clearcoat compositions containing silane functional compounds |
| DE102004026904A1 (de) | 2004-06-01 | 2005-12-22 | Basf Ag | Hochfunktionelle, hoch- oder hyperverzweigte Polyester sowie deren Herstellung und Verwendung |
| US7871669B2 (en) * | 2004-08-30 | 2011-01-18 | E.I. Du Pont De Nemours And Company | Method for achieving a durable two-tone finish on a vehicle |
| DE102004050748A1 (de) | 2004-10-19 | 2006-04-20 | Basf Coatings Aktiengesellschaft | Hochkratzfeste und hochelastische Beschichtungsmittel auf Basis von Alkoxysilanen |
| DE102005003299A1 (de) | 2005-01-24 | 2006-07-27 | Goldschmidt Gmbh | Nanopartikel für die Herstellung von Polyurethanschaum |
| FR2886284B1 (fr) | 2005-05-30 | 2007-06-29 | Commissariat Energie Atomique | Procede de realisation de nanostructures |
| WO2007016234A2 (en) | 2005-07-29 | 2007-02-08 | E. I. Du Pont De Nemours And Company | Method for producing damage resistant multi-layer coatings on an automotive body or part thereof |
| US7858190B2 (en) * | 2005-09-15 | 2010-12-28 | Basf Coatings Gmbh | Thermosetting coating compositions with multiple cure mechanisms |
| DE102006024823A1 (de) | 2006-05-29 | 2007-12-06 | Basf Coatings Ag | Verwendung von härtbaren Gemischen, enthaltend silangruppenhaltige Verbindungen sowie Phosphonsäurediester oder Diphosphonsäurediester, als Haftvermittler |
| US20080075871A1 (en) * | 2006-09-21 | 2008-03-27 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| JP5637687B2 (ja) | 2006-12-19 | 2014-12-10 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | 高い引掻耐性及び耐候性を有する被覆剤 |
| DE102007013242A1 (de) | 2007-03-15 | 2008-09-18 | Basf Coatings Ag | Hochkratzfeste Beschichtung mit guter Witterungs- und Rissbeständigkeit |
| DE102007026722A1 (de) | 2007-06-06 | 2008-12-11 | Basf Coatings Japan Ltd., Yokohama | Klarlackzusammensetzungen enthaltend hyperverzweigte, dendritische hydroxyfunktionelle Polyester |
| DE102007061854A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102007061855A1 (de) * | 2007-12-19 | 2009-06-25 | Basf Coatings Ag | Beschichtungsmittel mit hoher Kratzbeständigkeit und Witterungsstabilität |
| DE102008030304A1 (de) * | 2008-06-25 | 2009-12-31 | Basf Coatings Ag | Verwendung teilsilanisierter Verbindungen auf Polyisocyanatbasis als Vernetzungsmittel in Beschichtungszusammensetzungen und Beschichtungszusammensetzung enthaltend die Verbindungen |
| DE102008060454A1 (de) | 2008-12-05 | 2010-06-10 | Basf Coatings Ag | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzbeständigkeit und Witterungsstabilität sowie guten optischen Eigenschaften |
| DE102009024103A1 (de) * | 2009-06-06 | 2010-12-09 | Basf Coatings Gmbh | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzfestigkeit und hoher Kocherstabilität |
| DE102009030481A1 (de) * | 2009-06-24 | 2011-01-05 | Basf Coatings Gmbh | Beschichtungsmittel und daraus hergestellte Beschichtungen mit hoher Kratzfestigkeit bei gleichzeitig guten Ergebnissen in der Prüfung der Erichsentiefung und guten Steinschlagschutzeigenschaften |
-
2007
- 2007-12-19 DE DE102007061856A patent/DE102007061856A1/de not_active Ceased
-
2008
- 2008-12-18 WO PCT/EP2008/010809 patent/WO2009077181A1/de not_active Ceased
- 2008-12-18 JP JP2010538459A patent/JP5523337B2/ja active Active
- 2008-12-18 EP EP08862534.8A patent/EP2225301B1/de active Active
- 2008-12-18 US US12/808,973 patent/US8679589B2/en active Active
- 2008-12-18 KR KR1020167005688A patent/KR20160030338A/ko not_active Withdrawn
- 2008-12-18 KR KR1020107015730A patent/KR101634736B1/ko active Active
- 2008-12-18 CN CN200880121759.8A patent/CN101952339B/zh active Active
Patent Citations (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0008127A1 (de) | 1978-08-12 | 1980-02-20 | Saarbergwerke Aktiengesellschaft | Verfahren zum Verfestigen von Kohle und/oder Gestein im Bergbau |
| US4598131A (en) | 1984-12-19 | 1986-07-01 | Ppg Industries, Inc. | Catalysts for curable coating vehicle based upon aminoalkyloxy silanes and organic isocyanates |
| EP0245700B1 (en) | 1986-05-16 | 1994-08-24 | Cytec Technology Corp. | Alkylcarbamylmethylated aminotriazine crosslinking agents and curable compositions containing the same |
| US4710542A (en) | 1986-05-16 | 1987-12-01 | American Cyanamid Company | Alkylcarbamylmethylated amino-triazine crosslinking agents and curable compositions containing the same |
| EP0249201A2 (en) | 1986-06-10 | 1987-12-16 | Union Carbide Corporation | High solids sag resistant cycloaliphatic epoxy coatings containing low molecular weight high Tg organic polymeric sag resisting additives |
| EP0276501A2 (en) | 1987-01-24 | 1988-08-03 | Akzo Nobel N.V. | Thickening compositions and thickened aqueous acid solutions |
| US5225248A (en) | 1991-05-13 | 1993-07-06 | E. I. Du Pont De Nemours And Company | Method of curing a topcoat |
| EP0626888A1 (de) | 1992-02-15 | 1994-12-07 | Basf Lacke & Farben | Verfahren zur herstellung einer zweischichtigen lackierung und für dieses verfahren geeignete nicht-wässrige lacke. |
| EP0571073A2 (en) | 1992-05-19 | 1993-11-24 | Imperial Chemical Industries Plc | Silane functional oligomer |
| WO1994022968A1 (de) | 1993-03-31 | 1994-10-13 | Basf Lacke + Farben Ag | Nichtwässriger thixotropierter lack und verfahren zur herstellung mehrschichtiger überzüge damit |
| EP0692007A1 (de) | 1993-03-31 | 1996-01-17 | BASF Lacke + Farben AG | Verfahren zur herstellung einer zweischichtigen decklackierung auf einer substratoberfläche |
| DE69625241T2 (de) * | 1995-03-08 | 2003-09-11 | E.I. Du Pont De Nemours And Co., Wilmington | Reaktive organosiliciumverbindungen |
| WO1997012945A1 (en) | 1995-10-06 | 1997-04-10 | Cabot Corporation | Aqueous thixotropes for waterborne systems |
| EP0994117A1 (en) | 1998-10-14 | 2000-04-19 | Bayer Aktiengesellschaft | Silane-modified polyurethane resins, a process for their preparation and their use as moisture-curable resins |
| WO2001009260A1 (en) | 1999-07-30 | 2001-02-08 | Ppg Industries Ohio, Inc. | Coating compositions having improved scratch resistance, coated substrates and methods related thereto |
| WO2001098393A1 (en) | 2000-06-22 | 2001-12-27 | Basf Corporation | Coating compositions having improved adhesion to aluminum substrates |
| EP1273640A2 (de) | 2001-07-06 | 2003-01-08 | Degussa AG | Nichtwässriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel |
| WO2004014991A1 (en) * | 2002-08-07 | 2004-02-19 | E.I. Du Pont De Nemours And Company | One-pack primer sealer compositions for smc automotive body panels |
| DE102004050746A1 (de) * | 2004-10-19 | 2006-04-20 | Basf Coatings Ag | Hochkratzfeste und hochelastische Beschichtungsmittel auf Basis von Alkoxysilan-funktionellen Komponenten |
| WO2006042585A1 (de) | 2004-10-19 | 2006-04-27 | Basf Coatings Ag | Beschichtungsmittel enthaltend addukte mit alkoxysilanfunktionalität |
| US20060217472A1 (en) | 2005-03-11 | 2006-09-28 | Staunton Thomas J | Scratch resistant curable coating composition |
| WO2006131314A1 (de) | 2005-06-07 | 2006-12-14 | Construction Research & Technology Gmbh | Silan-modifizierte harnstoff-derivate, verfahren zu ihrer herstellung und deren verwendung als rheologiehilfsmittel |
| WO2007003857A2 (fr) | 2005-06-30 | 2007-01-11 | Prismaflex International | Panneau de communication retroeclaire |
| DE102005045228A1 (de) | 2005-09-22 | 2007-04-05 | Basf Coatings Ag | Verwendung von Phosphonsäurediestern und Diphosphonsäurediestern sowie silangruppenhaltige, härtbare Gemische, enthaltend Phosphonsäurediester und Diphosphonsäurediester |
Non-Patent Citations (6)
| Title |
|---|
| Artikel von B. Singh und Mitarbeiter "Carbamylmethylated Melamines, Novel Crosslinkers for the Coatings Industry" in Advanced Organic Coatings Science and Technology Series, 1991, Band 13, Seiten 193 bis 207 |
| DIN 53240-2 |
| DIN EN ISO 11341 |
| DIN EN ISO 2114 |
| DIN EN ISO 4892-2 |
| R�mpp Lexikon �Lacke und Druckfarben� Georg Thieme Verlag, Stuttgart, 1998, Seiten 250 bis 252 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20100095016A (ko) | 2010-08-27 |
| KR101634736B1 (ko) | 2016-06-30 |
| JP2011506708A (ja) | 2011-03-03 |
| CN101952339A (zh) | 2011-01-19 |
| US8679589B2 (en) | 2014-03-25 |
| EP2225301A1 (de) | 2010-09-08 |
| WO2009077181A1 (de) | 2009-06-25 |
| KR20160030338A (ko) | 2016-03-16 |
| US20110027489A1 (en) | 2011-02-03 |
| EP2225301B1 (de) | 2015-03-18 |
| CN101952339B (zh) | 2013-09-25 |
| JP5523337B2 (ja) | 2014-06-18 |
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| 8181 | Inventor (new situation) |
Inventor name: KLEIN, GUENTER, DR., 48165 MUENSTER, DE Inventor name: NIEMEIER, MANUELA, 48317 DRENSTEINFURT, DE Inventor name: HESENER, SIMONE, 48165 MUENSTER, DE Inventor name: HILGE, OLIVER, 48317 DRENSTEINFURT, DE Inventor name: STUEBBE, WILFRIED, 48268 GREVEN, DE Inventor name: POPPE, ANDREAS, DR., SHANGHAI, CN Inventor name: FELDMANN, BJOERN, 48165 MUENSTER, DE Inventor name: HOLTSCHULTE, SABINE, 59387 ASCHEBERG, DE Inventor name: GROENEWOLT, MATTHIJS, DR., 48147 MUENSTER, DE |
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Owner name: BASF COATINGS GMBH, 48165 MUENSTER, DE |
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