NZ517033A - Cathodic electrocoating compositions including an additive comprising the reaction product of a polyoxy alkylene amide, a glycidoxy alkyl alkoxy silane and either a glycidyl ester of a carboxylic acid or an alkyl glycidyl ether - Google Patents
Cathodic electrocoating compositions including an additive comprising the reaction product of a polyoxy alkylene amide, a glycidoxy alkyl alkoxy silane and either a glycidyl ester of a carboxylic acid or an alkyl glycidyl etherInfo
- Publication number
- NZ517033A NZ517033A NZ517033A NZ51703300A NZ517033A NZ 517033 A NZ517033 A NZ 517033A NZ 517033 A NZ517033 A NZ 517033A NZ 51703300 A NZ51703300 A NZ 51703300A NZ 517033 A NZ517033 A NZ 517033A
- Authority
- NZ
- New Zealand
- Prior art keywords
- glycidyl
- bath
- amine
- additive
- glycidoxy
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 52
- -1 polyoxy Polymers 0.000 title claims abstract description 50
- 238000004070 electrodeposition Methods 0.000 title claims abstract description 47
- 239000000654 additive Substances 0.000 title claims abstract description 31
- 230000000996 additive effect Effects 0.000 title claims abstract description 29
- 239000007795 chemical reaction product Substances 0.000 title claims abstract description 14
- 125000005417 glycidoxyalkyl group Chemical group 0.000 title claims abstract description 14
- 229910000077 silane Inorganic materials 0.000 title claims abstract description 11
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 title claims abstract description 10
- 150000001732 carboxylic acid derivatives Chemical class 0.000 title abstract 2
- 239000011230 binding agent Substances 0.000 claims abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 11
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 10
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 10
- 238000000576 coating method Methods 0.000 claims abstract description 9
- 125000005372 silanol group Chemical group 0.000 claims abstract description 8
- 239000002253 acid Substances 0.000 claims abstract description 7
- 239000008365 aqueous carrier Substances 0.000 claims abstract description 3
- 239000000049 pigment Substances 0.000 claims description 22
- 150000001412 amines Chemical class 0.000 claims description 18
- 239000000839 emulsion Substances 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 11
- 150000002148 esters Chemical class 0.000 claims description 10
- 150000001735 carboxylic acids Chemical class 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 6
- 150000004985 diamines Chemical class 0.000 claims description 6
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- QQWAKSKPSOFJFF-UHFFFAOYSA-N oxiran-2-ylmethyl 2,2-dimethyloctanoate Chemical compound CCCCCCC(C)(C)C(=O)OCC1CO1 QQWAKSKPSOFJFF-UHFFFAOYSA-N 0.000 claims description 4
- 229920001451 polypropylene glycol Polymers 0.000 claims description 4
- 230000003746 surface roughness Effects 0.000 claims description 4
- BBBUAWSVILPJLL-UHFFFAOYSA-N 2-(2-ethylhexoxymethyl)oxirane Chemical compound CCCCC(CC)COCC1CO1 BBBUAWSVILPJLL-UHFFFAOYSA-N 0.000 claims description 3
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 claims description 3
- VMSIYTPWZLSMOH-UHFFFAOYSA-N 2-(dodecoxymethyl)oxirane Chemical compound CCCCCCCCCCCCOCC1CO1 VMSIYTPWZLSMOH-UHFFFAOYSA-N 0.000 claims description 3
- YPIFGDQKSSMYHQ-UHFFFAOYSA-N 7,7-dimethyloctanoic acid Chemical compound CC(C)(C)CCCCCC(O)=O YPIFGDQKSSMYHQ-UHFFFAOYSA-N 0.000 claims description 3
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 claims description 3
- 230000007797 corrosion Effects 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 230000003472 neutralizing effect Effects 0.000 claims description 2
- 230000007547 defect Effects 0.000 claims 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims 5
- 239000002184 metal Substances 0.000 claims 2
- 101100295091 Arabidopsis thaliana NUDT14 gene Proteins 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000007921 spray Substances 0.000 claims 1
- 239000010959 steel Substances 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 abstract description 2
- 229920005989 resin Polymers 0.000 description 16
- 239000011347 resin Substances 0.000 description 16
- 239000011541 reaction mixture Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 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
- 238000000227 grinding Methods 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 8
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 5
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 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
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 150000007522 mineralic acids Chemical class 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 3
- 239000002981 blocking agent Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 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 3
- 239000000080 wetting agent Substances 0.000 description 3
- 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
- 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
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001298 alcohols 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
- 239000008199 coating composition Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 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
- 239000000047 product Substances 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
- 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 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
- 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
- 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
- 241000220317 Rosa Species 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-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
- 235000011054 acetic acid Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229940072282 cardura Drugs 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
- 239000000470 constituent 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
- 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
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 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
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 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
- 235000005985 organic acids Nutrition 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
- 229920000642 polymer Polymers 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 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
- 239000000126 substance Substances 0.000 description 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-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
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0836—Compounds with one or more Si-OH or Si-O-metal linkage
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Paints Or Removers (AREA)
- Conductive Materials (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/401,697 US6207731B1 (en) | 1999-09-23 | 1999-09-23 | Cathode electrocoating compositions having improved appearance, improved edge coverage and reduced craters |
| PCT/US2000/025859 WO2001021718A1 (en) | 1999-09-23 | 2000-09-21 | Cathodic electrocoating compositions having improved appearance, improved edge coverage and reduced craters |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ517033A true NZ517033A (en) | 2004-01-30 |
Family
ID=23588837
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ517033A NZ517033A (en) | 1999-09-23 | 2000-09-21 | Cathodic electrocoating compositions including an additive comprising the reaction product of a polyoxy alkylene amide, a glycidoxy alkyl alkoxy silane and either a glycidyl ester of a carboxylic acid or an alkyl glycidyl ether |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US6207731B1 (enExample) |
| EP (1) | EP1226217B1 (enExample) |
| JP (1) | JP4722358B2 (enExample) |
| KR (1) | KR100713732B1 (enExample) |
| CN (1) | CN1374991A (enExample) |
| AT (1) | ATE286948T1 (enExample) |
| AU (1) | AU777593B2 (enExample) |
| BR (1) | BR0014618B1 (enExample) |
| CA (1) | CA2380628C (enExample) |
| DE (1) | DE60017441T2 (enExample) |
| ES (1) | ES2234667T3 (enExample) |
| IL (1) | IL147973A0 (enExample) |
| MX (1) | MXPA02003086A (enExample) |
| NZ (1) | NZ517033A (enExample) |
| WO (1) | WO2001021718A1 (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| US6846400B2 (en) * | 2002-01-10 | 2005-01-25 | E. I. Du Pont De Nemours And Company | Cathodic electrodeposition coating agents |
| CN100383174C (zh) * | 2003-04-10 | 2008-04-23 | 关西涂料株式会社 | 聚加成物和含有该聚加成物的阳离子电淀积涂料 |
| WO2004090055A1 (ja) * | 2003-04-10 | 2004-10-21 | Kansai Paint Co., Ltd. | 重付加体及び該重付加体を含有するカチオン電着塗料 |
| US20060024511A1 (en) * | 2004-07-29 | 2006-02-02 | Joseph Elmer | Electro-coat adhesion layer with a siloxane top coat |
| 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 |
| JP2010521552A (ja) * | 2007-03-13 | 2010-06-24 | ビー・エイ・エス・エフ、コーポレーション | シランを含有する膜形成材料、架橋剤、およびコーティング組成物と、コーティング組成物およびコーティングされた基板を製造するための方法 |
| US7772333B2 (en) * | 2007-03-13 | 2010-08-10 | Basf Coatings Gmbh | Film-forming material containing resin with -Si(OR)3 and crosslinkable groups |
| DE102008000360A1 (de) | 2008-02-21 | 2009-08-27 | Evonik Goldschmidt Gmbh | Neue Alkoxysilylgruppen tragende Polyetheralkohole durch Alkoxylierung epoxidfunktioneller Alkoxysilane an Doppelmetallcyanid (DMC)-Katalysatoren, sowie Verfahren zu deren Herstellung |
| DE102009028636A1 (de) * | 2009-08-19 | 2011-02-24 | Evonik Goldschmidt Gmbh | Neuartige Urethangruppen enthaltende silylierte Präpolymere und Verfahren zu deren Herstellung |
| DE102009028640A1 (de) | 2009-08-19 | 2011-02-24 | Evonik Goldschmidt Gmbh | Härtbare Masse enthaltend Urethangruppen aufweisende silylierte Polymere und deren Verwendung in Dicht- und Klebstoffen, Binde- und/oder Oberflächenmodifizierungsmitteln |
| US8491770B2 (en) | 2010-12-10 | 2013-07-23 | Axalta Coating Systems IP Co. LLC | Cathodic electrocoating compositions |
| US9133350B2 (en) | 2011-01-11 | 2015-09-15 | Axalta Coating Systems Ip Co., Llc | Anticrater agent for electrocoat composition |
| EP3033396B1 (de) * | 2013-08-12 | 2017-11-29 | BASF Coatings GmbH | Beschichtungszusammensetzung zur tauchlack-beschichtung elektrisch leitfähiger substrate enthaltend eine sol-gel-zusammensetzung |
| US20150337074A1 (en) * | 2014-05-23 | 2015-11-26 | Axalta Coating Systems Ip Co., Llc | Coating compositions for coil coating, methods for making such coating compositions and coil coating methods |
| WO2016069545A1 (en) * | 2014-10-31 | 2016-05-06 | Valspar Sourcing, Inc. | High edge cathodic epoxy electrocoat composition |
| EP3256533B1 (en) | 2015-02-10 | 2024-04-24 | Swimc Llc | Novel electrodeposition system |
| BR112018013275A2 (pt) | 2015-12-31 | 2018-12-11 | Henkel Ag & Co Kgaa | revestimentos de autodeposição de baixo cozimento |
| CN106318114A (zh) * | 2016-08-19 | 2017-01-11 | 浩力森涂料（上海）有限公司 | 阳离子电沉积涂料 |
| DE102017100961A1 (de) * | 2017-01-19 | 2018-07-19 | GEDIA Gebrüder Dingerkus GmbH | Verfahren zur Vorbereitung von Metallblech für eine Beschichtung |
| US11186734B2 (en) * | 2019-05-31 | 2021-11-30 | Axalta Coating Systems Ip Co., Llc | Epoxy resin emulsions for electrocoating |
| US11976210B2 (en) | 2019-10-11 | 2024-05-07 | Axalta Coating Systems Ip Co., Llc | Edge protection for electrocoat |
| US12398289B2 (en) | 2019-12-30 | 2025-08-26 | Axalta Coating Systems Ip Co., Llc | Electrocoat composition |
| JP7447286B2 (ja) * | 2020-01-24 | 2024-03-11 | 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 | シラン含有架橋剤を含む水性電着コーティング材料 |
| US20210269667A1 (en) | 2020-02-27 | 2021-09-02 | Axalta Coating Systems Ip Co., Llc | Electrocoating composition |
| US20210371679A1 (en) | 2020-05-28 | 2021-12-02 | Axalta Coating Systems Ip Co., Llc | Electrocoating composition |
| US20210371678A1 (en) | 2020-05-28 | 2021-12-02 | Axalta Coating Systems Ip Co., Llc | Electrocoating composition |
| CA3181256A1 (en) | 2020-06-03 | 2021-12-09 | Sukhwan Soontravanich | Non-caustic cleaning methods and uses |
| WO2021247834A1 (en) | 2020-06-03 | 2021-12-09 | Ecolab Usa Inc. | Antifouling compounds used for microbial fouling control |
| US11932795B2 (en) | 2020-06-03 | 2024-03-19 | Ecolab Usa Inc. | Aromatic amine epoxide adducts for corrosion inhibition |
| KR102889295B1 (ko) | 2020-07-22 | 2025-11-21 | 주식회사 케이씨씨 | 전착도료 조성물 |
| EP4095202A1 (en) | 2021-05-28 | 2022-11-30 | Axalta Coating Systems GmbH | Electrocoating composition |
| EP4095201A1 (en) | 2021-05-28 | 2022-11-30 | Axalta Coating Systems GmbH | Cathodic electrocoating composition having reduced volatile organic compounds |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3560515D1 (en) * | 1985-02-27 | 1987-10-01 | Corona Peintures | Polyoxyalkylenepolyamine reaction products and their use in cationic electrodeposition |
| JPH06287267A (ja) * | 1993-04-07 | 1994-10-11 | Kansai Paint Co Ltd | カチオン電着性微粒子及びそれを含む電着塗料組成物 |
| JPH06287484A (ja) * | 1993-04-01 | 1994-10-11 | Kansai Paint Co Ltd | カチオン電着塗料 |
| JP3287643B2 (ja) * | 1993-04-07 | 2002-06-04 | 関西ペイント株式会社 | カチオン電着塗料組成物及びその調製方法 |
| US5356960A (en) * | 1993-08-11 | 1994-10-18 | E. I. Du Pont De Nemours And Company | Cathodic electrocoating compositions containing an anticrater agent |
| US5723519A (en) | 1997-02-25 | 1998-03-03 | E. I. Du Pont De Nemours And Company | Cathodic electrocoating compositions containing an anticrater agent |
-
1999
- 1999-09-23 US US09/401,697 patent/US6207731B1/en not_active Expired - Lifetime
-
2000
- 2000-09-21 CN CN00812983A patent/CN1374991A/zh active Pending
- 2000-09-21 AU AU75983/00A patent/AU777593B2/en not_active Ceased
- 2000-09-21 NZ NZ517033A patent/NZ517033A/en unknown
- 2000-09-21 WO PCT/US2000/025859 patent/WO2001021718A1/en not_active Ceased
- 2000-09-21 JP JP2001525282A patent/JP4722358B2/ja not_active Expired - Fee Related
- 2000-09-21 BR BRPI0014618-8A patent/BR0014618B1/pt not_active IP Right Cessation
- 2000-09-21 IL IL14797300A patent/IL147973A0/xx unknown
- 2000-09-21 MX MXPA02003086A patent/MXPA02003086A/es active IP Right Grant
- 2000-09-21 AT AT00965237T patent/ATE286948T1/de not_active IP Right Cessation
- 2000-09-21 EP EP00965237A patent/EP1226217B1/en not_active Expired - Lifetime
- 2000-09-21 ES ES00965237T patent/ES2234667T3/es not_active Expired - Lifetime
- 2000-09-21 CA CA002380628A patent/CA2380628C/en not_active Expired - Fee Related
- 2000-09-21 DE DE60017441T patent/DE60017441T2/de not_active Expired - Lifetime
- 2000-09-21 KR KR1020027003770A patent/KR100713732B1/ko not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CA2380628A1 (en) | 2001-03-29 |
| CN1374991A (zh) | 2002-10-16 |
| EP1226217B1 (en) | 2005-01-12 |
| WO2001021718A1 (en) | 2001-03-29 |
| ES2234667T3 (es) | 2005-07-01 |
| JP2003510399A (ja) | 2003-03-18 |
| JP4722358B2 (ja) | 2011-07-13 |
| CA2380628C (en) | 2009-05-19 |
| AU7598300A (en) | 2001-04-24 |
| IL147973A0 (en) | 2002-09-12 |
| BR0014618B1 (pt) | 2009-05-05 |
| BR0014618A (pt) | 2002-06-18 |
| ATE286948T1 (de) | 2005-01-15 |
| DE60017441D1 (de) | 2005-02-17 |
| KR100713732B1 (ko) | 2007-05-02 |
| MXPA02003086A (es) | 2002-10-31 |
| KR20020031198A (ko) | 2002-04-26 |
| EP1226217A1 (en) | 2002-07-31 |
| AU777593B2 (en) | 2004-10-21 |
| US6207731B1 (en) | 2001-03-27 |
| DE60017441T2 (de) | 2005-12-22 |
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| PSEA | Patent sealed | ||
| RENW | Renewal (renewal fees accepted) |