CA1234441A - Peinture d'appret acrylique a usage multiples - Google Patents

Peinture d'appret acrylique a usage multiples

Info

Publication number: CA1234441A
Authority: CA; Canada
Prior art keywords: weight; binder; composition; coating composition; pigment
Prior art date: 1982-05-21
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA000428353A

Other languages

English (en)

Inventor

Paul P. Bruylants

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

EIDP Inc

Original Assignee

EI Du Pont de Nemours and Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1982-05-21

Filing date

1983-05-17

Publication date

1988-03-22

1983-05-17 Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co

1988-03-22 Application granted granted Critical

1988-03-22 Publication of CA1234441A publication Critical patent/CA1234441A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 48
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title abstract description 12
239000000049 pigment Substances 0.000 claims abstract description 25
239000011230 binding agent Substances 0.000 claims abstract description 21
229920000058 polyacrylate Polymers 0.000 claims abstract description 20
239000008199 coating composition Substances 0.000 claims abstract description 15
230000007797 corrosion Effects 0.000 claims abstract description 11
238000005260 corrosion Methods 0.000 claims abstract description 11
229920001228 polyisocyanate Polymers 0.000 claims abstract description 11
239000005056 polyisocyanate Substances 0.000 claims abstract description 11
229910052751 metal Inorganic materials 0.000 claims abstract description 8
239000002184 metal Substances 0.000 claims abstract description 8
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 7
230000002401 inhibitory effect Effects 0.000 claims abstract description 7
LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 claims abstract description 7
229910000165 zinc phosphate Inorganic materials 0.000 claims abstract description 7
125000004185 ester group Chemical group 0.000 claims abstract description 3
239000007787 solid Substances 0.000 claims description 13
125000004432 carbon atom Chemical group C* 0.000 claims description 12
-1 glycidyl ester Chemical class 0.000 claims description 11
229920000642 polymer Polymers 0.000 claims description 11
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical group OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 5
239000003054 catalyst Substances 0.000 claims description 4
BWLBGMIXKSTLSX-UHFFFAOYSA-N 2-hydroxyisobutyric acid Chemical compound CC(C)(O)C(O)=O BWLBGMIXKSTLSX-UHFFFAOYSA-N 0.000 claims description 3
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 3
239000012975 dibutyltin dilaurate Substances 0.000 claims description 3
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 2
239000007809 chemical reaction catalyst Substances 0.000 claims description 2
239000007788 liquid Substances 0.000 claims description 2
229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
239000012974 tin catalyst Substances 0.000 claims description 2
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 claims 2
BIOOACNPATUQFW-UHFFFAOYSA-N calcium;dioxido(dioxo)molybdenum Chemical compound [Ca+2].[O-][Mo]([O-])(=O)=O BIOOACNPATUQFW-UHFFFAOYSA-N 0.000 claims 1
125000005609 naphthenate group Chemical group 0.000 claims 1
125000000962 organic group Chemical group 0.000 claims 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
XAEWLETZEZXLHR-UHFFFAOYSA-N zinc;dioxido(dioxo)molybdenum Chemical compound [Zn+2].[O-][Mo]([O-])(=O)=O XAEWLETZEZXLHR-UHFFFAOYSA-N 0.000 claims 1
239000000758 substrate Substances 0.000 abstract description 18
229920000180 alkyd Polymers 0.000 abstract description 12
210000003298 dental enamel Anatomy 0.000 abstract description 12
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract description 6
239000011152 fibreglass Substances 0.000 abstract description 3
229920005989 resin Polymers 0.000 abstract description 3
239000011347 resin Substances 0.000 abstract description 3
239000005057 Hexamethylene diisocyanate Substances 0.000 abstract description 2
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 abstract description 2
239000004033 plastic Substances 0.000 abstract description 2
229920003023 plastic Polymers 0.000 abstract description 2
229920000178 Acrylic resin Polymers 0.000 abstract 1
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 abstract 1
238000007796 conventional method Methods 0.000 abstract 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 abstract 1
125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
238000002156 mixing Methods 0.000 description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
239000007921 spray Substances 0.000 description 9
238000000576 coating method Methods 0.000 description 8
239000011248 coating agent Substances 0.000 description 7
239000000470 constituent Substances 0.000 description 7
239000006185 dispersion Substances 0.000 description 7
239000012190 activator Substances 0.000 description 6
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
229910000831 Steel Inorganic materials 0.000 description 5
150000002430 hydrocarbons Chemical class 0.000 description 5
239000012948 isocyanate Substances 0.000 description 5
150000002513 isocyanates Chemical class 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000010959 steel Substances 0.000 description 5
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
239000004215 Carbon black (E152) Substances 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 4
239000003638 chemical reducing agent Substances 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
229910052725 zinc Inorganic materials 0.000 description 4
239000011701 zinc Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000004793 Polystyrene Substances 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
230000007547 defect Effects 0.000 description 3
150000002367 halogens Chemical group 0.000 description 3
239000001034 iron oxide pigment Substances 0.000 description 3
239000003973 paint Substances 0.000 description 3
229920002223 polystyrene Polymers 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000002981 blocking agent Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
229940031098 ethanolamine Drugs 0.000 description 2
238000005227 gel permeation chromatography Methods 0.000 description 2
238000000227 grinding Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
WTFXARWRTYJXII-UHFFFAOYSA-N iron(2+);iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+2].[Fe+3].[Fe+3] WTFXARWRTYJXII-UHFFFAOYSA-N 0.000 description 2
SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
238000000034 method Methods 0.000 description 2
239000011707 mineral Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
235000015096 spirit Nutrition 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000004408 titanium dioxide Substances 0.000 description 2
229910000859 α-Fe Inorganic materials 0.000 description 2
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
239000004923 Acrylic lacquer Substances 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241001315286 Damon Species 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
159000000032 aromatic acids Chemical class 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
229940072282 cardura Drugs 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
RUZYUOTYCVRMRZ-UHFFFAOYSA-N doxazosin Chemical compound C1OC2=CC=CC=C2OC1C(=O)N(CC1)CCN1C1=NC(N)=C(C=C(C(OC)=C2)OC)C2=N1 RUZYUOTYCVRMRZ-UHFFFAOYSA-N 0.000 description 1
238000011049 filling Methods 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
238000003801 milling Methods 0.000 description 1
WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000037452 priming Effects 0.000 description 1
239000002990 reinforced plastic Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
238000005507 spraying Methods 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
239000000126 substance Substances 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
238000003466 welding Methods 0.000 description 1
229910052726 zirconium Inorganic materials 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
- C08G18/70—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
- C08G18/7806—Nitrogen containing -N-C=0 groups
- C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
- C08G18/7831—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing biuret groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
- C08G18/6241—Polymers of esters containing hydroxy groups of alpha-beta ethylenically unsaturated carboxylic acids with epoxy compounds other than alkylene oxides and hydroxyglycidyl compounds

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)

CA000428353A 1982-05-21 1983-05-17 Peinture d'appret acrylique a usage multiples Expired CA1234441A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US38077082A	1982-05-21	1982-05-21
US380,770		1995-01-30

Publications (1)

Publication Number	Publication Date
CA1234441A true CA1234441A (fr)	1988-03-22

Family

ID=23502373

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000428353A Expired CA1234441A (fr)	1982-05-21	1983-05-17	Peinture d'appret acrylique a usage multiples

Country Status (2)

Country	Link
BE (1)	BE896806A (fr)
CA (1)	CA1234441A (fr)

1983
- 1983-05-17 CA CA000428353A patent/CA1234441A/fr not_active Expired
- 1983-05-20 BE BE0/210820A patent/BE896806A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
BE896806A (fr)	1983-11-21

Legal Events

Date	Code	Title	Description
2005-03-22	MKEX	Expiry

Publication	Publication Date	Title
US3558564A (en)	1971-01-26	Thermosetting coating composition of an organic polyisocyanate and a polymer having pendant hydroxyl containing ester groups
CA2442545C (fr)	2008-07-22	Matieres d'enduction fonctionnelles aqueuses et procede integre de production de peintures multicouches produisant une couleur et / ou un effet
EP0212457B2 (fr)	1994-10-12	Revêtements colorés et transparents dont la couche transparente contient des polyépoxides et des agents durcisseurs polyacides
JPH09509434A (ja)	1997-09-22	改良されたインターコート付着性を有するカラー‐クリアー複合コーティング
US4131571A (en)	1978-12-26	Polyurethane metallic enamel
CA2184839A1 (fr)	1995-10-12	Compositions de revetement aqueuses au poli ameliore
WO2001098393A1 (fr)	2001-12-27	Compositions de revetement pourvues d'une adherence amelioree a des substrats d'aluminum
JP7589383B2 (ja)	2024-11-25	水性塗料組成物および塗装物品の製造方法
CA1146687A (fr)	1983-05-17	Email de revetement a base de polyurethane a forte teneur en matieres solides
US4215023A (en)	1980-07-29	Urethane enamel coating composition
US4321169A (en)	1982-03-23	Water based alkyd resin coating composition containing a polyisocyanate crosslinking agent
JP2002518566A (ja)	2002-06-25	耐擦傷性および耐酸腐食性を改善するためのヒドロキシ含有アクリロシランポリマーを含むコーティング
CN100551549C (zh)	2009-10-21	着色和/或美饰多层漆体系的制备
CA2191110C (fr)	2008-03-25	Procede de formation de films multicouches de peinture, composition de revetement de base et procede d'application de peinture
US20050038204A1 (en)	2005-02-17	Increased pot-life urethane coatings
CA1062834A (fr)	1979-09-18	Revetement thermodurcissable constitue d'un polyisocyanate organique, d'un polymere a groupes esters et a groupes hydroxyles libres et d'un agent modifiant les proprietes rheologiques
JP2801561B2 (ja)	1998-09-21	熱硬化性被覆組成物
CA1162694A (fr)	1984-02-21	Enduit a base de polyurethane aliphatique
AU651200B2 (en)	1994-07-14	Process for primimg plastic substrates, coating compositions for this purpose, and the use thereof
US5977245A (en)	1999-11-02	Automotive undercoat coating compositions containing reactive urea/urethane compounds
CA1234441A (fr)	1988-03-22	Peinture d'appret acrylique a usage multiples
JP2853121B2 (ja)	1999-02-03	塗料用樹脂組成物
JPH10128234A (ja)	1998-05-19	熱硬化性被覆組成物
JP2000189887A (ja)	2000-07-11	自動車車体の複層塗膜形成方法及び自動車車体
US3829397A (en)	1974-08-13	Acrylic coating composition for refinishing flexible substrates