DE69802266T2 - Antikratermittel enthaltende, kathodisch abscheidbare elektrotauchzusammensetzungen - Google Patents
Antikratermittel enthaltende, kathodisch abscheidbare elektrotauchzusammensetzungenInfo
- Publication number
- DE69802266T2 DE69802266T2 DE69802266T DE69802266T DE69802266T2 DE 69802266 T2 DE69802266 T2 DE 69802266T2 DE 69802266 T DE69802266 T DE 69802266T DE 69802266 T DE69802266 T DE 69802266T DE 69802266 T2 DE69802266 T2 DE 69802266T2
- Authority
- DE
- Germany
- Prior art keywords
- agent
- composition
- gamma
- cratering
- average molecular
- Prior art date
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 44
- 238000006748 scratching Methods 0.000 title 1
- 238000004070 electrodeposition Methods 0.000 claims description 50
- 239000003795 chemical substances by application Substances 0.000 claims description 48
- 239000011230 binding agent Substances 0.000 claims description 23
- 238000000576 coating method Methods 0.000 claims description 21
- 239000000049 pigment Substances 0.000 claims description 21
- 239000011248 coating agent Substances 0.000 claims description 17
- 239000000839 emulsion Substances 0.000 claims description 14
- 239000003431 cross linking reagent Substances 0.000 claims description 11
- 239000008199 coating composition Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 238000005227 gel permeation chromatography Methods 0.000 claims description 8
- 239000005056 polyisocyanate Substances 0.000 claims description 8
- 229920001228 polyisocyanate Polymers 0.000 claims description 8
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 239000004793 Polystyrene Substances 0.000 claims description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 239000008365 aqueous carrier Substances 0.000 claims description 2
- 230000003472 neutralizing effect Effects 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 229910000077 silane Inorganic materials 0.000 claims 1
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 239000000243 solution Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 10
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 239000003973 paint Substances 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 5
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 5
- -1 amine compound Chemical class 0.000 description 5
- 239000012948 isocyanate Substances 0.000 description 5
- 239000004310 lactic acid Substances 0.000 description 5
- 235000014655 lactic acid Nutrition 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 230000000415 inactivating effect Effects 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- 101100295091 Arabidopsis thaliana NUDT14 gene Proteins 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 238000004581 coalescence Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 125000005372 silanol group Chemical group 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- CJTNLEQLKKYLFO-UHFFFAOYSA-N 1-butoxyethanol Chemical compound CCCCOC(C)O CJTNLEQLKKYLFO-UHFFFAOYSA-N 0.000 description 1
- LXOFYPKXCSULTL-UHFFFAOYSA-N 2,4,7,9-tetramethyldec-5-yne-4,7-diol Chemical compound CC(C)CC(C)(O)C#CC(C)(O)CC(C)C LXOFYPKXCSULTL-UHFFFAOYSA-N 0.000 description 1
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 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
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- PZZYQPZGQPZBDN-UHFFFAOYSA-N aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229960002887 deanol Drugs 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
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 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
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000008096 xylene Substances 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- 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
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5096—Polyethers having heteroatoms other than oxygen containing silicon
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4419—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications with polymers obtained otherwise than by polymerisation reactions only involving carbon-to-carbon unsaturated bonds
- C09D5/443—Polyepoxides
- C09D5/4434—Polyepoxides characterised by the nature of the epoxy binder
- C09D5/4438—Binder based on epoxy/amine adducts, i.e. reaction products of polyepoxides with compounds containing amino groups only
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4419—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications with polymers obtained otherwise than by polymerisation reactions only involving carbon-to-carbon unsaturated bonds
- C09D5/443—Polyepoxides
- C09D5/4457—Polyepoxides containing special additives, e.g. pigments, polymeric particles
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Polyethers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/806,868 US5723519A (en) | 1997-02-25 | 1997-02-25 | Cathodic electrocoating compositions containing an anticrater agent |
| PCT/US1998/003134 WO1998037155A1 (en) | 1997-02-25 | 1998-02-18 | Cathodic electrocoating compositions containing an anticrater agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69802266D1 DE69802266D1 (de) | 2001-12-06 |
| DE69802266T2 true DE69802266T2 (de) | 2002-07-25 |
Family
ID=25195012
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69802266T Expired - Lifetime DE69802266T2 (de) | 1997-02-25 | 1998-02-18 | Antikratermittel enthaltende, kathodisch abscheidbare elektrotauchzusammensetzungen |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US5723519A (https=) |
| EP (1) | EP0963417B1 (https=) |
| JP (1) | JP2001512520A (https=) |
| KR (1) | KR100510229B1 (https=) |
| CN (1) | CN1156543C (https=) |
| AU (1) | AU739053B2 (https=) |
| BR (1) | BR9807378A (https=) |
| CA (1) | CA2279872A1 (https=) |
| DE (1) | DE69802266T2 (https=) |
| WO (1) | WO1998037155A1 (https=) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6207731B1 (en) | 1999-09-23 | 2001-03-27 | E. I. Du Pont De Nemours And Company | Cathode electrocoating compositions having improved appearance, improved edge coverage and reduced craters |
| US20040238362A1 (en) * | 1999-12-15 | 2004-12-02 | December Timothy S. | Cured multilayer coating providing improved edge corrosion to a substrate and a method of making same |
| US20020056641A1 (en) * | 1999-12-15 | 2002-05-16 | December Timothy S. | Cured multilayer coating providing improved edge corrosion resistance to a substrate and a method of making same |
| JP3849872B2 (ja) * | 2000-09-27 | 2006-11-22 | チッソ株式会社 | アミノ基含有シラノール化合物水溶液、その用途、およびその製造方法 |
| KR100833942B1 (ko) * | 2002-07-11 | 2008-05-30 | 삼성테크윈 주식회사 | 리이드 프레임과 그것을 구비한 반도체 팩키지 및, 리이드프레임 제조 방법 |
| WO2004022619A1 (en) * | 2002-09-09 | 2004-03-18 | Reactamine Technology, Llc | Silicone modified polyurea |
| US7348392B2 (en) * | 2002-09-09 | 2008-03-25 | Reactamine Technology, Llc | Silicone modified acrylics and epoxies |
| US20070270240A1 (en) * | 2002-09-09 | 2007-11-22 | Reactamine Technology, Llc | Pure polyurea and method for making same |
| US20060131543A1 (en) * | 2003-04-10 | 2006-06-22 | Hideki Iijima | Polyaddition product and cationic electrodeposition coating comprising said polyaddition product |
| US7264705B2 (en) * | 2004-10-18 | 2007-09-04 | E. I. Dupont De Nemours And Company | Cathodic electrocoating compositions containing an anti-crater agent |
| US7264706B2 (en) * | 2004-10-18 | 2007-09-04 | E. I. Du Pont De Nemours And Company | Cathodic electrocoating compositions containing an anti-crater agent |
| JP4892208B2 (ja) * | 2005-07-26 | 2012-03-07 | トヨタ自動車株式会社 | 塗膜形成方法及び塗装物品 |
| DE102005041951A1 (de) * | 2005-09-03 | 2007-03-08 | Bayer Materialscience Ag | Wässrige 2K-PUR Systeme enthaltend hydroxy-funktionelle Polydimethylsiloxane |
| US9133350B2 (en) | 2011-01-11 | 2015-09-15 | Axalta Coating Systems Ip Co., Llc | Anticrater agent for electrocoat composition |
| US12460311B2 (en) * | 2019-12-19 | 2025-11-04 | Basf Coatings Gmbh | Lamp black pigment containing electrodeposition coating material compositions |
| CN116234883A (zh) * | 2020-12-15 | 2023-06-06 | 巴斯夫涂料有限公司 | 包含烷氧基化聚乙烯亚胺的电沉积涂料组合物 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3252825A (en) * | 1959-09-14 | 1966-05-24 | Owens Corning Fiberglass Corp | Process of coating glass fibers with hydrolyzed condensation product of amino silane and copolymerizable monomer |
| US3922253A (en) * | 1971-10-28 | 1975-11-25 | Ppg Industries Inc | Self-crosslinking cationic electrodepositable compositions |
| US3947339A (en) * | 1971-12-01 | 1976-03-30 | Ppg Industries, Inc. | Method of electrodepositing primary amine group-containing cationic resins |
| US3949140A (en) * | 1974-05-06 | 1976-04-06 | Owens-Corning Fiberglas Corporation | Organo silicon derivatives coated on glass fibers |
| US4017438A (en) * | 1974-12-16 | 1977-04-12 | Ppg Industries, Inc. | Ketimine-blocked primary amine group-containing cationic electrodepositable resins |
| BE857754A (fr) * | 1976-08-18 | 1978-02-13 | Celanese Polymer Special Co | Composition de resine pour revetements, notamment par electrodeposition cathodique |
| US4423166A (en) * | 1981-07-20 | 1983-12-27 | Ppg Industries, Inc. | Ungelled polyepoxide-polyoxyalkylenepolyamine resins, aqueous dispersions thereof, and their use in cationic electrodeposition |
| US4468307A (en) * | 1981-09-14 | 1984-08-28 | Ppg Industries, Inc. | Method of cationic electrodeposition |
| US4419467A (en) * | 1981-09-14 | 1983-12-06 | Ppg Industries, Inc. | Process for the preparation of cationic resins, aqueous, dispersions, thereof, and electrodeposition using the aqueous dispersions |
| KR900008464B1 (ko) * | 1986-05-30 | 1990-11-22 | 도시바 실리콘 가부시끼가이샤 | 폴리에테르의 제조방법 및 폴리에테르를 이용한 실온 경화성 조성물 |
| DE3777618D1 (de) * | 1986-12-23 | 1992-04-23 | Kansai Paint Co Ltd | Elektroabscheidungsverfahren und waesserige harz-lackzusammensetzung. |
| JPH07116390B2 (ja) * | 1987-02-28 | 1995-12-13 | 関西ペイント株式会社 | 電着塗装方法 |
| US5162060A (en) * | 1989-12-14 | 1992-11-10 | Rohm And Haas Company | Polymer-modified cements with improved chemical resistance |
| US5017632A (en) * | 1989-12-14 | 1991-05-21 | Rohm And Haas Company | Water-based composites with superior cure in thick films, and chemical and shock resistance |
| US4988778A (en) * | 1990-01-18 | 1991-01-29 | Ppg Industries, Inc. | Polyamine-functional silane resin |
| US5096556A (en) * | 1990-06-25 | 1992-03-17 | Ppg Industries, Inc. | Cationic microgels and their use in electrodeposition |
| US5380781A (en) * | 1992-07-27 | 1995-01-10 | Kansai Paint Co., Ltd. | Cationically electrodepositable fine particles derived from alkoxysilane-modified epoxy resins and cationic electrodeposition paint composition comprising the same |
| US5356960A (en) * | 1993-08-11 | 1994-10-18 | E. I. Du Pont De Nemours And Company | Cathodic electrocoating compositions containing an anticrater agent |
-
1997
- 1997-02-25 US US08/806,868 patent/US5723519A/en not_active Expired - Fee Related
- 1997-10-22 US US08/956,223 patent/US5883276A/en not_active Expired - Fee Related
-
1998
- 1998-02-18 BR BR9807378-8A patent/BR9807378A/pt not_active IP Right Cessation
- 1998-02-18 JP JP53683598A patent/JP2001512520A/ja not_active Withdrawn
- 1998-02-18 DE DE69802266T patent/DE69802266T2/de not_active Expired - Lifetime
- 1998-02-18 KR KR10-1999-7007684A patent/KR100510229B1/ko not_active Expired - Fee Related
- 1998-02-18 WO PCT/US1998/003134 patent/WO1998037155A1/en not_active Ceased
- 1998-02-18 CA CA002279872A patent/CA2279872A1/en not_active Abandoned
- 1998-02-18 AU AU61738/98A patent/AU739053B2/en not_active Ceased
- 1998-02-18 EP EP98906541A patent/EP0963417B1/en not_active Expired - Lifetime
- 1998-02-18 CN CNB988027488A patent/CN1156543C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR100510229B1 (ko) | 2005-08-26 |
| EP0963417A1 (en) | 1999-12-15 |
| KR20000075621A (ko) | 2000-12-26 |
| CN1156543C (zh) | 2004-07-07 |
| AU739053B2 (en) | 2001-10-04 |
| CN1248280A (zh) | 2000-03-22 |
| US5723519A (en) | 1998-03-03 |
| EP0963417B1 (en) | 2001-10-31 |
| JP2001512520A (ja) | 2001-08-21 |
| AU6173898A (en) | 1998-09-09 |
| WO1998037155A1 (en) | 1998-08-27 |
| US5883276A (en) | 1999-03-16 |
| BR9807378A (pt) | 2000-03-14 |
| DE69802266D1 (de) | 2001-12-06 |
| CA2279872A1 (en) | 1998-08-27 |
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| 8364 | No opposition during term of opposition |