JP6279323B2 - 耐引掻性のある補修用クリアコート - Google Patents
耐引掻性のある補修用クリアコート Download PDFInfo
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- JP6279323B2 JP6279323B2 JP2013535024A JP2013535024A JP6279323B2 JP 6279323 B2 JP6279323 B2 JP 6279323B2 JP 2013535024 A JP2013535024 A JP 2013535024A JP 2013535024 A JP2013535024 A JP 2013535024A JP 6279323 B2 JP6279323 B2 JP 6279323B2
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- Prior art keywords
- component
- repair
- coating composition
- fatty acid
- unsaturated fatty
- Prior art date
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 49
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- 229920005862 polyol Polymers 0.000 claims description 32
- 239000005056 polyisocyanate Substances 0.000 claims description 25
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- 239000012933 diacyl peroxide Substances 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical class OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Chemical class CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- 239000013500 performance material Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical class OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
- 229940103494 thiosalicylic acid Drugs 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 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
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
-
- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/36—Hydroxylated esters of higher fatty acids
-
- 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
- C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
- C08G18/6225—Polymers of esters of acrylic or methacrylic acid
- C08G18/6229—Polymers of hydroxy groups containing esters of acrylic or methacrylic acid with aliphatic polyalcohols
-
- 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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/6547—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen the low-molecular compounds being compounds of group C08G18/36 or hydroxylated esters of higher fatty acids of C08G18/38
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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
- 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)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Polyurethanes Or Polyureas (AREA)
Description
本発明は、自動車の補修用組成物、そのような組成物を作製及び使用するための方法、基材上への補修用塗料、並びに補修用塗料が付与された自動車両などの物品に関する。
自動車のトップコート仕上げ材料は、着色されたベースコート組成物の第一の層及びクリアコート組成物の第二の層の2層中にトップコートが塗布されている、ベースコート/クリアコートのトップコート、並びに一層の、着色され、光沢のあるトップコートである単段若しくはモノコートのトップコートを含んでいる。ベースコート/クリアコート塗料は、高水準の色の光沢及び深さがあることが望ましい。さらに、特殊な効果顔料、例えば、メタリック顔料及び真珠箔顔料などのフレーク顔料を有するベースコートは、ベースコート/クリアコート複合塗料における優れたゴニオ外観性(gonioapparent)効果を達し得る。
本発明者らは、クリアコート又は単段トップコートであってもよい、耐引掻性のある塗料のための組成物、該組成物から作られる塗料、並びに該塗料で塗装された物品を発明した。また、本発明者らは、該組成物を作製及び使用するための方法をも開示する。
以下の記載は、特定の本発明の実施形態の詳細を含んでいる。
2成分クリアコート補修用塗料組成物を、個別の第一成分及び個別の第二成分における以下の材料を混ぜ合わせることで作製した。
2成分クリアコート補修用塗料組成物を、個別の第一成分及び個別の第二成分における以下の材料を混ぜ合わせることで作製した。
成分1: 49質量%の不揮発性のクリアコート調合物を作製した。該クリアコート調合物は、9℃のTg、125mgのヒドロキシル価(KOH/gm.,)及び2700ダルトンの数平均分子量を有するスチレン化アクリル樹脂から構成されていた。該クリアコート調合物の残分は、エチレングリコールブチルエーテル、メチルアセテート、パラクロロベンゾトリフルオリド、エチル3−エトキシプロピオネート及びアセトンなどの溶剤、並びにUV吸収剤、シリコーンベースの流動剤、可塑剤及びスズベースの触媒などの当該技術分野において周知の添加剤であった。
成分#1: 実施例3の成分#1に対し、Polycin M−365(登録商標)(Vertellus Specialties Incorporated)を7:3の質量比で添加した。
Claims (12)
- (a)少なくとも2つのヒドロキシル基を有する不飽和脂肪酸エステルポリオール及び (b)120〜170のヒドロキシル価を有するアクリルポリマーを含む第一の成分;並びに
ポリイソシアネートを含む第二の成分
を含む、補修用多成分トップコート塗料組成物であって、
その際、前記組成物は、成分(a)及び(b)の全不揮発性物質の質量に対し、10質量%〜35質量%の成分(a)を含み、
前記アクリルポリマーは、スチレン化アクリル樹脂であり、かつ1100〜8200の数平均分子量を有し、
前記アクリルポリマー中、15質量%までヒドロキシル官能性モノマーが含まれており、
前記ポリイソシアネートは、ヘキサメチレンジイソシアネート及び/又はイソホロンジイソシアネートのイソシアヌレートであり、かつ、
前記第一の成分及び第二の成分の両方が、1以上の有機溶剤を含んでいる、前記補修用多成分トップコート塗料組成物。 - 前記不飽和脂肪酸エステルポリオールが、大豆油又はヒマシ油ベースのポリオールである、請求項1記載の補修用多成分トップコート塗料組成物。
- 前記不飽和脂肪酸エステルポリオールが、エステル化されたリシノール酸を含んでいる、請求項1又は2記載の補修用多成分トップコート塗料組成物。
- 前記不飽和脂肪酸エステルポリオールが、3又は4つのヒドロキシル基を有している、請求項1〜3のいずれか1項に記載の補修用多成分トップコート塗料組成物。
- 前記組成物は、成分(a)及び(b)の全不揮発性物質の質量に対し、20質量%〜35質量%の成分(a)を含んでいる、請求項1〜4のいずれか1項に記載の前記補修用多成分トップコート塗料組成物。
- 複数の着色された第一の成分を含む、請求項1〜5のいずれか1項に記載の前記補修用多成分トップコート塗料組成物。
- (I) (a)少なくとも2つのヒドロキシル基を有する不飽和脂肪酸エステルポリオール及び(b)120〜170のヒドロキシル価を有するアクリルポリマーを含む第一の成分;並びにポリイソシアネートを含む第二の成分を混ぜ合わせて、補修用塗料組成物の混合物を形成する工程であって、
その際、前記組成物は、成分(a)及び(b)の全不揮発性物質の質量に対し、10質量%〜35質量%の成分(a)を含み
前記アクリルポリマーは、スチレン化アクリル樹脂であり、かつ1100〜8200の数平均分子量を有し、
前記アクリルポリマー中、15質量%までヒドロキシル官能性モノマーが含まれており、
前記ポリイソシアネートは、ヘキサメチレンジイソシアネート及び/又はイソホロンジイソシアネートのイソシアヌレートであり、かつ、
前記第一の成分及び第二の成分の両方が、1以上の有機溶剤を含んでおり;
(II) 前記補修用塗料組成物の混合物を、基材の所望とする領域に塗布する工程;並びに
(III) 前記塗布した組成物の混合物を硬化させて、基材上に硬化した補修用塗料層を形成する工程
を含む、基材を補修する方法。 - 工程(I)において、更に1以上の還元剤を混ぜ合わせる、請求項7記載の基材を補修する方法。
- 工程(I)において、複数の第一の成分を混ぜ合わせる、請求項7又は8記載の基材を補修する方法。
- 工程(I)において、少なくとも1つの着色された第一の成分を混ぜ合わせる、請求項7〜9のいずれか1項に記載の基材を補修する方法。
- 前記不飽和脂肪酸エステルポリオールが、大豆油又はヒマシ油ベースのポリオールである、請求項7〜10のいずれか1項に記載の基材を補修する方法。
- 前記不飽和脂肪酸エステルポリオールが、3又は4つのヒドロキシル基を有している、請求項7〜11のいずれか1項に記載の基材を補修する方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US39496210P | 2010-10-20 | 2010-10-20 | |
US61/394,962 | 2010-10-20 | ||
PCT/US2011/056797 WO2012054547A1 (en) | 2010-10-20 | 2011-10-19 | Scratch-resistant refinish clearcoat |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2016152937A Division JP2016188387A (ja) | 2010-10-20 | 2016-08-03 | 耐引掻性のある補修用クリアコート |
Publications (2)
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JP2013544915A JP2013544915A (ja) | 2013-12-19 |
JP6279323B2 true JP6279323B2 (ja) | 2018-02-14 |
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EP (1) | EP2630177B1 (ja) |
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ES2545993T3 (es) * | 2010-10-20 | 2015-09-17 | Basf Coatings Gmbh | Revestimiento transparente de retoque resistente al rayado |
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EP3024867A1 (en) * | 2013-07-22 | 2016-06-01 | Basf Se | A coating system |
US9221985B2 (en) | 2013-12-09 | 2015-12-29 | Tbf Environmental Technology Inc. | Solvent compositions |
JP6305806B2 (ja) | 2014-03-28 | 2018-04-04 | 日本コントロールシステム株式会社 | 情報処理装置、情報処理方法、およびプログラム |
US9777180B2 (en) | 2015-02-03 | 2017-10-03 | Basf Coatings Gmbh | Method of forming a passivated pigment slurry for an aqueous topcoat coating composition |
CN108368220B (zh) | 2015-10-16 | 2021-05-25 | 汉高知识产权控股有限责任公司 | 由可再生源制成的反应性树脂 |
CN105348487B (zh) * | 2015-12-16 | 2018-03-20 | 江南大学 | 一种蓖麻油酸基uv固化水性树脂的制备方法 |
KR101776434B1 (ko) | 2015-12-16 | 2017-09-07 | 현대자동차주식회사 | 천연소재 필름의 복층 도막 형성방법 |
US10273371B2 (en) | 2016-07-25 | 2019-04-30 | Basf Coatings Gmbh | Method of forming a slurry of encapsulated pigment for an aqueous topcoat coating composition |
CN117178038A (zh) * | 2021-05-18 | 2023-12-05 | 关西涂料株式会社 | 高固体成分涂料组合物和多层涂膜形成方法 |
JP2024103209A (ja) * | 2023-01-20 | 2024-08-01 | 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 | 複層塗膜の形成方法、および複層塗膜の製造に用いられるクリヤ塗料 |
CN117402541B (zh) * | 2023-08-21 | 2024-10-11 | 巴斯夫涂料有限公司 | 双组分清漆组合物及其制备和用途 |
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-
2011
- 2011-10-19 ES ES11776992.7T patent/ES2545993T3/es active Active
- 2011-10-19 WO PCT/US2011/056797 patent/WO2012054547A1/en active Application Filing
- 2011-10-19 US US13/878,435 patent/US9309434B2/en active Active
- 2011-10-19 JP JP2013535024A patent/JP6279323B2/ja active Active
- 2011-10-19 EP EP11776992.7A patent/EP2630177B1/en active Active
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ES2545993T3 (es) | 2015-09-17 |
US9309434B2 (en) | 2016-04-12 |
JP2013544915A (ja) | 2013-12-19 |
US20130202893A1 (en) | 2013-08-08 |
EP2630177B1 (en) | 2015-08-12 |
EP2630177A1 (en) | 2013-08-28 |
WO2012054547A1 (en) | 2012-04-26 |
JP2016188387A (ja) | 2016-11-04 |
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