CN109111563B - Pigment dispersion resin for primer-topcoat cathode electrophoretic coating and preparation method thereof - Google Patents
Pigment dispersion resin for primer-topcoat cathode electrophoretic coating and preparation method thereof Download PDFInfo
- Publication number
- CN109111563B CN109111563B CN201810797749.1A CN201810797749A CN109111563B CN 109111563 B CN109111563 B CN 109111563B CN 201810797749 A CN201810797749 A CN 201810797749A CN 109111563 B CN109111563 B CN 109111563B
- Authority
- CN
- China
- Prior art keywords
- primer
- acid
- resin
- epoxy resin
- diisocyanate
- 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.)
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- 229920005989 resin Polymers 0.000 title claims abstract description 40
- 239000011347 resin Substances 0.000 title claims abstract description 40
- 238000000576 coating method Methods 0.000 title claims abstract description 38
- 239000011248 coating agent Substances 0.000 title claims abstract description 36
- 239000000049 pigment Substances 0.000 title claims abstract description 28
- 239000006185 dispersion Substances 0.000 title claims abstract description 27
- 238000002360 preparation method Methods 0.000 title claims description 11
- 239000003822 epoxy resin Substances 0.000 claims abstract description 28
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 28
- 239000003973 paint Substances 0.000 claims abstract description 26
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 9
- 238000005956 quaternization reaction Methods 0.000 claims abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000012948 isocyanate Substances 0.000 claims description 13
- 150000002513 isocyanates Chemical class 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000004970 Chain extender Substances 0.000 claims description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 8
- 239000005056 polyisocyanate Substances 0.000 claims description 8
- 229920001228 polyisocyanate Polymers 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 6
- 238000010992 reflux Methods 0.000 claims description 6
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- -1 dimercaptoalcohol Chemical class 0.000 claims description 5
- 125000003700 epoxy group Chemical group 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 5
- 239000004593 Epoxy Substances 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 claims description 4
- 238000004070 electrodeposition Methods 0.000 claims description 4
- 239000004310 lactic acid Substances 0.000 claims description 4
- 235000014655 lactic acid Nutrition 0.000 claims description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 4
- 150000003335 secondary amines Chemical class 0.000 claims description 4
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 3
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 claims description 2
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 claims description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims description 2
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 claims description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 2
- UPGSWASWQBLSKZ-UHFFFAOYSA-N 2-hexoxyethanol Chemical compound CCCCCCOCCO UPGSWASWQBLSKZ-UHFFFAOYSA-N 0.000 claims description 2
- ALRHLSYJTWAHJZ-UHFFFAOYSA-N 3-hydroxypropionic acid Chemical compound OCCC(O)=O ALRHLSYJTWAHJZ-UHFFFAOYSA-N 0.000 claims 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 claims description 2
- YSWBFLWKAIRHEI-UHFFFAOYSA-N 4,5-dimethyl-1h-imidazole Chemical compound CC=1N=CNC=1C YSWBFLWKAIRHEI-UHFFFAOYSA-N 0.000 claims description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 2
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 claims description 2
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 claims description 2
- OAOABCKPVCUNKO-UHFFFAOYSA-N 8-methyl Nonanoic acid Chemical compound CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- 235000011054 acetic acid Nutrition 0.000 claims description 2
- 150000001334 alicyclic compounds Chemical class 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims description 2
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 2
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 2
- 125000005442 diisocyanate group Chemical group 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 235000019253 formic acid Nutrition 0.000 claims description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 2
- 150000004658 ketimines Chemical class 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- OZCWUNHGNVXCCO-UHFFFAOYSA-N oxiran-2-ylmethyl hydrogen carbonate Chemical group OC(=O)OCC1CO1 OZCWUNHGNVXCCO-UHFFFAOYSA-N 0.000 claims description 2
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims description 2
- 229920005906 polyester polyol Polymers 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 229920006389 polyphenyl polymer Polymers 0.000 claims description 2
- 238000007142 ring opening reaction Methods 0.000 claims description 2
- CMSYDJVRTHCWFP-UHFFFAOYSA-N triphenylphosphane;hydrobromide Chemical compound Br.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 CMSYDJVRTHCWFP-UHFFFAOYSA-N 0.000 claims description 2
- LRWZZZWJMFNZIK-UHFFFAOYSA-N 2-chloro-3-methyloxirane Chemical compound CC1OC1Cl LRWZZZWJMFNZIK-UHFFFAOYSA-N 0.000 claims 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 claims 1
- 239000004842 bisphenol F epoxy resin Substances 0.000 claims 1
- 238000005260 corrosion Methods 0.000 abstract description 12
- 230000007797 corrosion Effects 0.000 abstract description 12
- 238000009736 wetting Methods 0.000 abstract description 3
- 239000000945 filler Substances 0.000 abstract description 2
- 239000007787 solid Substances 0.000 description 14
- 239000000839 emulsion Substances 0.000 description 7
- 239000008367 deionised water Substances 0.000 description 6
- 229910021641 deionized water Inorganic materials 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 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
- 238000002156 mixing Methods 0.000 description 5
- 238000004321 preservation Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 229940049676 bismuth hydroxide Drugs 0.000 description 3
- TZSXPYWRDWEXHG-UHFFFAOYSA-K bismuth;trihydroxide Chemical compound [OH-].[OH-].[OH-].[Bi+3] TZSXPYWRDWEXHG-UHFFFAOYSA-K 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- LQRUPWUPINJLMU-UHFFFAOYSA-N dioctyl(oxo)tin Chemical compound CCCCCCCC[Sn](=O)CCCCCCCC LQRUPWUPINJLMU-UHFFFAOYSA-N 0.000 description 3
- 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 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- JOLVYUIAMRUBRK-UHFFFAOYSA-N 11',12',14',15'-Tetradehydro(Z,Z-)-3-(8-Pentadecenyl)phenol Natural products OC1=CC=CC(CCCCCCCC=CCC=CCC=C)=C1 JOLVYUIAMRUBRK-UHFFFAOYSA-N 0.000 description 2
- YLKVIMNNMLKUGJ-UHFFFAOYSA-N 3-Delta8-pentadecenylphenol Natural products CCCCCCC=CCCCCCCCC1=CC=CC(O)=C1 YLKVIMNNMLKUGJ-UHFFFAOYSA-N 0.000 description 2
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 2
- JOLVYUIAMRUBRK-UTOQUPLUSA-N Cardanol Chemical compound OC1=CC=CC(CCCCCCC\C=C/C\C=C/CC=C)=C1 JOLVYUIAMRUBRK-UTOQUPLUSA-N 0.000 description 2
- FAYVLNWNMNHXGA-UHFFFAOYSA-N Cardanoldiene Natural products CCCC=CCC=CCCCCCCCC1=CC=CC(O)=C1 FAYVLNWNMNHXGA-UHFFFAOYSA-N 0.000 description 2
- 241001262617 Japonica Species 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- PTFIPECGHSYQNR-UHFFFAOYSA-N cardanol Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1 PTFIPECGHSYQNR-UHFFFAOYSA-N 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- 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 description 2
- 229910000165 zinc phosphate Inorganic materials 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000005586 carbonic acid group Chemical group 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 230000005662 electromechanics Effects 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000010998 test method Methods 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1477—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing nitrogen
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/62—Alcohols or phenols
-
- 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
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C09D17/004—Pigment pastes, e.g. for mixing in paints containing an inorganic pigment
- C09D17/007—Metal oxide
-
- 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
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C09D17/004—Pigment pastes, e.g. for mixing in paints containing an inorganic pigment
- C09D17/007—Metal oxide
- C09D17/008—Titanium dioxide
-
- 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
- C09D5/08—Anti-corrosive paints
- C09D5/082—Anti-corrosive paints characterised by the anti-corrosive pigment
- C09D5/084—Inorganic compounds
-
- 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
- C09D5/4488—Cathodic paints
- C09D5/4492—Cathodic paints containing special additives, e.g. grinding agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Paints Or Removers (AREA)
Abstract
The invention discloses a pigment dispersion resin for a primer-topcoat cathode electrophoretic coating, which comprises a quaternization reagent and a modified epoxy resin. The pigment dispersion resin has good pigment and filler wetting dispersibility, corrosion resistance, weather resistance and flexibility, so that a paint film has good corrosion resistance and weather resistance, meanwhile, the fullness and color stability of the paint film can be remarkably improved, and the requirements of hardware such as bicycles, household appliances, decorative articles and the like on the paint film can be met.
Description
Technical Field
The invention relates to the technical field of electrophoretic paint, in particular to pigment dispersion resin for primer-topcoat cathode electrophoretic paint and a preparation method thereof.
Background
The electrophoretic coating is a novel coating with low pollution, energy conservation, resource conservation, protection and corrosion resistance, has the characteristics of smooth coating, good water resistance and chemical resistance and the like, is easy to realize the mechanization and automation of the coating industry, is suitable for coating workpieces with edges, corners and holes, and is widely applied to coating hardware such as automobiles, automatic vehicles, electromechanics, household appliances and the like. Most of the anticorrosive electrophoretic coatings on the market only have excellent anticorrosive performance, but often have poor weather resistance, and the electrophoretic coating needs to be coated for the second time if the electrophoretic coating has excellent anticorrosive performance and weather resistance, so that the coating process and cost are greatly increased.
Disclosure of Invention
The present invention is directed to a pigment dispersion resin for primer-topcoat cathode electrophoretic paint and a method for preparing the same, which solves one or more of the above-mentioned problems of the prior art.
The pigment dispersion resin for the primer-topcoat cathode electrophoretic coating comprises a quaternization reagent and a modified epoxy resin.
In some embodiments, the method of preparing the quaternizing agent comprises the steps of:
reacting tertiary carbonic acid glycidyl ester with secondary amine at 50-150 ℃, adding organic acid aqueous solution after epoxy groups are completely disappeared, and reacting at 70-80 ℃ to prepare the quaternization reagent.
In some embodiments, glycidyl versatate is formed by reacting versatic acid with epichlorohydrin, and has a highly branched monomer with more than ten carbon atoms, and has the following chemical structure:
wherein: r1+ R2 is 7C atoms.
In some embodiments, the secondary amine is one or more of methylethanolamine, N-ethylethanolamine, ketimine; the organic acid is one or more of formic acid, acetic acid, lactic acid, hydroxy propionic acid and isooctanoic acid.
In some embodiments, a method of preparing a modified epoxy resin comprises the steps of:
carrying out ring-opening chain extension reaction at 130-190 ℃ under the action of a catalyst by using basic epoxy resin and a chain extender, adding an isocyanate prepolymer after the theoretical epoxy equivalent is reached, carrying out grafting reaction at 130-140 ℃, and finally adding ethylene glycol butyl ether to prepare modified epoxy resin;
the basic epoxy resin is an aromatic or alicyclic compound containing 2 epoxy groups on each molecular structure, and the epoxy equivalent of the epoxy resin is between 100-600 g/mol;
the chain extender is acid, alcohol or phenol with two or more active hydrogen, and the molecular weight of the chain extender is between 50 and 4000;
the catalyst is at least one of triethanolamine, triethylamine, diethanolamine, diethylamine, triphenylphosphine bromide, dimethylbenzylamine, imidazole, dimethylimidazole and 2-ethyl-4-methylimidazole;
the isocyanate prepolymer is prepared by reacting polyisocyanate with a compound containing active hydrogen.
In some embodiments, the epoxy resin is at least one of a bisphenol a type epoxy resin, a bisphenol S type epoxy resin, a bisphenol F type epoxy resin.
In some embodiments, the chain extender is at least one of dicarboxylic acids, polyether polyols, polyester polyols, dimercaptoalcohols, bisphenols.
In some embodiments, a method of preparing an isocyanate prepolymer includes the steps of:
slowly dripping a compound containing active hydrogen into a polyisocyanate compound for reaction, keeping the temperature of 70-110 ℃ after dripping is finished, and reacting for 1-5 h, wherein the molar ratio of isocyanate groups to the compound containing active hydrogen in the isocyanate prepolymer is 1: 0.45-1: 0.65;
the polyisocyanate comprises at least one of aliphatic diisocyanate, alicyclic diisocyanate and aromatic diisocyanate;
the active hydrogen-containing compound is at least one of alcohol, alcohol ether, phenol and carboxylic acid containing 1-20 carbon atoms.
In some embodiments, the polyisocyanate is at least one of toluene diisocyanate, diphenylmethane diisocyanate, polymethylene polyphenyl diisocyanate, hexamethylene diisocyanate, xylylene diisocyanate, isophorone diisocyanate, trimethylhexamethylene diisocyanate;
the compound containing active hydrogen is at least one of methanol, ethanol, isopropanol, phenol, ethylene glycol monobutyl ether, ethylene glycol ethyl ether, ethylene glycol hexyl ether, diethylene glycol monobutyl ether and diethylene glycol ethyl ether.
The preparation method of the pigment dispersion resin for the primer-topcoat cathode electrophoretic coating comprises the following steps of:
and (2) sequentially adding modified epoxy resin, a quaternization reagent and primary pure water into a reaction bottle provided with a thermometer, a stirrer and a reflux condenser pipe, stirring, heating the reaction system to 90 ℃, carrying out heat preservation reaction for 6 hours, measuring the acid value of the resin, adding secondary pure water when the acid value of the resin is less than 1, cooling to 65 ℃, carrying out heat preservation reaction for 1 hour, and finally preparing the quaternary ammonium salt type pigment dispersion resin with the solid content of 40%.
The beneficial effects are that:
the pigment dispersion resin suitable for the bottom-surface-combined cathode electrophoretic coating has good pigment and filler wetting dispersibility, corrosion resistance, weather resistance and flexibility, so that a paint film has good corrosion resistance and weather resistance, the fullness and color stability of the paint film can be obviously improved, and the requirements of hardware such as bicycles, household appliances, decorative articles and the like on the paint film can be met.
Detailed Description
The present invention will be described in further detail below with reference to embodiments.
Example 1:
the first step is as follows: preparation of quaternizing agent
In a reaction bottle provided with a thermometer, a stirrer and a reflux condenser tube, the glycidyl versatate and the methylethanolamine with the formula amount are sequentially added, the stirring is started, the temperature of a reaction system is raised to 130 ℃ to react for 1h, after epoxy groups are completely disappeared, the temperature is lowered to 70 ℃, 50% of lactic acid aqueous solution is added, the temperature is raised to 80 ℃ to react for 2h, the MEQA and MEQB values are tested, and finally the quaternization reagent with the solid content of 80% is prepared.
Specific amounts of addition are shown in table 1:
components | Dosage (g) |
Tertiary carboxylic acid glycidyl ester | 480 |
Methylethanolamine | 180 |
50% lactic acid (aqueous solution) | 453.6 |
Total amount of | 1113.6 |
Table 1: the amount of the quaternary amination reagent raw material
The second step is that: preparation of isocyanate prepolymer
Toluene diisocyanate and methyl isobutyl ketone with the formula amount are sequentially added into a reaction bottle provided with a thermometer, a stirrer and a reflux condenser. Stirring in a nitrogen atmosphere to raise the temperature of a reaction system to 45-50 ℃, slowly dropwise adding isooctyl alcohol into the reaction system of toluene diisocyanate and methyl isobutyl ketone, wherein the temperature of the reaction system is between 50 and 55 ℃ when dropwise adding is finished within about 4-5h, after all dropwise adding are finished, raising the temperature to 75 ℃ for heat preservation reaction for 1h, measuring the content of isocyanate groups, and obtaining the isocyanate prepolymer with the solid content of 94 percent when the NCO value is 120-125 mg/g.
Specific amounts of addition are shown in table 2:
components | Dosage (g) |
Toluene diisocyanate (NCO = 480) | 382.72 |
Methyl isobutyl ketone | 44 |
Isooctyl alcohol | 322.77 |
Total amount of | 749.49 |
Table 2: the dosage of the isocyanate prepolymer raw material
The third step: preparation of modified epoxy resin
Sequentially adding epoxy resin, bisphenol A, cardanol and methyl isobutyl ketone in formula amount into a reaction bottle provided with a thermometer, a stirrer and a reflux condenser, after the addition is finished, stirring, heating the reaction system to 100 ℃, adding a dimethylbenzylamine catalyst, after the addition is finished, heating to 180-.
Specific amounts of addition are shown in table 3:
components | Dosage (g) |
Basic epoxy resin (EEW = 180-190) | 2180 |
Bisphenol A | 600 |
Cardanol | 156.2 |
Methyl isobutyl ketone | 100 |
Dimethylbenzylamine | 3 |
Isocyanate prepolymer | 700 |
Ethylene glycol monobutyl ether | 189.4 |
Total up to | 3928.6 |
Isocyanate prepolymer: NCO value 120-
Table 3: the amount of the modified epoxy resin raw material
The fourth step: preparation of pigment dispersing resin:
and (3) sequentially adding the modified epoxy resin prepared in the third step, the quaternization reagent prepared in the first step and pure water in formula amount into a reaction bottle provided with a thermometer, a stirrer and a reflux condenser pipe, stirring, heating the reaction system to 90 ℃, carrying out heat preservation reaction for 6 hours, measuring the acid value of the resin, adding the pure water for the second time when the acid value of the resin is less than 1, cooling to 65 ℃, carrying out heat preservation reaction for 1 hour, and finally preparing the quaternary ammonium salt type pigment dispersion resin with the solid content of 40%. Specific amounts of addition are shown in table 4:
components | Dosage (g) |
Modified epoxy resin | 1522.3 |
Quaternizing agents | 499.8 |
First time pure water | 400 |
Second time pure water | 2002.67 |
Total up to | 4424.77 |
Table 4: the amount of the pigment dispersion resin raw material
Preparing cathode electrophoretic paint color paste:
red paste A: as comparative examples, conventional pigment-dispersing resins were used
830g of the conventional pigment dispersion resin with the solid content of 40%, 1450g of titanium oxide, 700g of kaolin, 30g of iron oxide red, 100g of dioctyltin oxide, 100g of bismuth hydroxide and 200g of deionized water are added, and after uniform mixing, grinding is carried out for 15 hours by a ball mill, so as to obtain color slurry with the solid content of 50%.
And (3) red paste B: pigment Dispersion resin prepared in example 1 was used
830g of the pigment dispersion resin having a solid content of 40% prepared in example 1, 1450g of titanium oxide, 700g of kaolin, 30g of red iron oxide, 100g of dioctyltin oxide, 100g of bismuth hydroxide and 200g of deionized water were added, and after mixing uniformly, the mixture was ground with a ball mill for 15 hours to obtain a color paste having a solid content of 50%.
And (3) red paste C: as comparative examples, conventional pigment dispersing resins plus UV absorbers were used
830g of the conventional pigment dispersion resin with the solid content of 40%, 50g of an ultraviolet absorber, 1400g of titanium oxide, 700g of kaolin, 30g of iron oxide red, 100g of dioctyltin oxide, 100g of bismuth hydroxide and 200g of deionized water are added, and after uniform mixing, the mixture is ground by a ball mill for 15 hours to obtain color slurry with the solid content of 50%.
The above red pastes A, B and C were used to prepare cationic electrodeposition paints, respectively:
mixing 1000g of bottom-in-one cathode electrophoretic coating emulsion (HR-4000 type emulsion), 500g of red paste A and 2500g of deionized water to prepare a bottom-in-one cathode electrophoretic coating A with the solid content of 15 percent;
mixing 1000g of bottom-in-one cathode electrophoretic coating emulsion (HR-4000 type emulsion), 500g of red paste B and 2500g of deionized water to prepare a bottom-in-one cathode electrophoretic coating B with the solid content of 15 percent;
1000g of primer-topcoat cathode electrophoretic paint emulsion (HR-4000 type emulsion), 500g of red paste C and 2500g of deionized water are mixed to prepare the primer-topcoat cathode electrophoretic paint C with the solid content of 15%.
Among them, HR-4000 type emulsion was purchased from Haolison paint (Shanghai) Co., Ltd.
Test methods and criteria:
high-temperature stability of color paste
And sealing 500g of color paste in a special test bottle, placing the special test bottle into a 50 ℃ oven for high-temperature stability test, and respectively testing for 10 days to investigate whether the color paste is precipitated or not and to examine the fineness change.
●: after standing for 10 days, the color paste has no hard precipitate and no coarse particles;
very good: after standing for 10 days, the color paste has no hard precipitate, and the fineness is reverse to the thickness but still in a qualified range;
and (delta): after standing for 10 days, the color paste has no hard precipitate, and the fineness is too coarse and unqualified;
□: after standing for 10 days, the color paste has precipitate, and the fineness is too coarse and unqualified.
Second, corrosion resistance
A cold-rolled sheet (0.8 mm. about.150 mm. about.70 mm) was subjected to chemical conversion treatment (trade name, zinc phosphate treatment agent, manufactured by JAPONICA JASMIC INC.) as a to-be-coated member, which was coated with the cationic electrodeposition coating composition obtained in the examples, and the coated film was baked at 165 ℃ for 20min, with the film thickness controlled to 18 to 22 μm, and the number of blisters on the cut portion and the width of the developed portion were evaluated in accordance with the national NSS test 700h salt spray test.
●: no more than 2.0mm from the cut part, no bubble near the cut part,
very good: the side from the cutting part is not more than 2.0mm, 1-2 bubbles are formed near the cutting part,
and (delta): more than 2.0mm but less than 3.0mm from the cut part, 1-2 blisters near the cut part,
□: the size of the bubble is larger than 2.0mm but smaller than 3.0mm from the cutting part, and 2-5 bubbles are formed near the cutting part.
Third, weather resistance
Cold-rolled sheet (0.8 mm. about.150 mm. about.70 mm) was subjected to chemical conversion treatment (trade name, zinc phosphate treatment agent, manufactured by JAPONICA JASMIC INC.) and used as a part to be coated, which was coated with the cationic electrodeposition coating composition obtained in the examples, and the coated paint film was baked at 165 ℃ for 20min, the film thickness was controlled to 18 to 22 μm, and the color difference value of the paint film was evaluated according to QUV A test of national standard for 500 h.
●: color difference value less than 2
Very good: the color difference value is greater than 2 and less than 4
And (delta): the color difference value is more than 4 and less than 6
□: the color difference value is more than 6
The stability, corrosion resistance and weatherability of the primer-topcoat cathodic electrocoat A, B, C are tested in Table 5.
Primer-topcoat cathode electrophoretic coating A | Primer-topcoat cathode electrophoretic coating B | Primer-topcoat cathode electrophoretic coating C | |
Film thickness (um) | 20 | 21 | 21 |
Stability of color paste | ◎ | ● | △ |
Corrosion resistance | ● | ● | ● |
Weather resistance | △ | ● | ● |
Table 5: experimental data
As can be seen from the above table, the primer-topcoat cathode electrophoretic coating B has better stability than the primer-topcoat cathode electrophoretic coating a, the corrosion resistance of the primer-topcoat cathode electrophoretic coating B is equivalent to that of the primer-topcoat cathode electrophoretic coating a, and the weather resistance of the primer-topcoat cathode electrophoretic coating B is better than that of the primer-topcoat cathode electrophoretic coating a; compared with the primer-topcoat cathode electrophoretic coating C, the primer-topcoat cathode electrophoretic coating B has stability obviously superior to that of the primer-topcoat cathode electrophoretic coating C, the corrosion resistance of the primer-topcoat cathode electrophoretic coating B is equivalent to that of the primer-topcoat cathode electrophoretic coating C, and the weather resistance of the primer-topcoat cathode electrophoretic coating B is equivalent to that of the primer-topcoat cathode electrophoretic coating C.
Therefore, after the pigment dispersion resin with the solid content of 40 percent prepared in the example 1 is added, the color paste stability and the weather resistance of the primer-topcoat cathode electrophoretic paint B are obviously improved compared with those of the primer-topcoat cathode electrophoretic paint A using the conventional dispersion resin; the cathode electrophoretic coating C is combined on the bottom surface, and after the ultraviolet absorber is added, the weather resistance can be improved, but the stability of the color paste is greatly reduced.
The pigment dispersing resin in the embodiment provided by the invention has good wetting and dispersing performance on inorganic pigment and filler, the contained tertiary carbonic acid group provides excellent weather resistance, acid-base resistance and water resistance of the resin, and the contained modified epoxy resin provides excellent corrosion resistance of the resin. The color paste prepared by the resin can provide good corrosion resistance and weather resistance of a paint film, and can obviously improve the fullness and color stability of the paint film.
The above description is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various changes and modifications can be made without departing from the inventive concept of the present invention, and these should be considered as within the scope of the present invention.
Claims (7)
1. The pigment dispersion resin for the primer-topcoat cathode electrophoretic coating is characterized by comprising a quaternizing agent and a modified epoxy resin;
wherein: the preparation method of the modified epoxy resin comprises the following steps: carrying out ring-opening chain extension reaction at 130-190 ℃ under the action of a catalyst by using basic epoxy resin and a chain extender, adding an isocyanate prepolymer after the theoretical epoxy equivalent is reached, carrying out grafting reaction at 130-140 ℃, and finally adding ethylene glycol butyl ether to prepare modified epoxy resin;
the preparation method of the quaternizing agent comprises the following steps:
reacting tertiary carbonic acid glycidyl ester with secondary amine at 50-150 ℃, adding organic acid aqueous solution after epoxy groups completely disappear, and reacting at 70-80 ℃ to prepare a quaternization reagent;
the glycidyl versatate is generated by reacting versatic acid with epoxy chloropropane, contains more than ten highly branched monomers with carbon atoms, and has the following chemical structure:
wherein: r1+ R2 is 7C atoms;
the preparation method of the pigment dispersion resin comprises the following steps: adding modified epoxy resin, a quaternization reagent and pure water into a reaction bottle provided with a thermometer, a stirrer and a reflux condenser, after the addition is finished, starting the stirrer to heat the reaction bottle to 90 ℃, preserving heat, reacting for 6 hours, measuring the acid value of the resin, adding the pure water again when the acid value of the resin is less than 1, cooling to 65 ℃, preserving heat, reacting for 1 hour, and finally preparing the pigment dispersion resin.
2. The pigment dispersion resin for a primer-topcoat cathode electrophoretic paint according to claim 1, wherein the secondary amine is one or more of methylethanolamine, N-ethylethanolamine, ketimine; the organic acid is one or more of formic acid, acetic acid, lactic acid, hydroxy propionic acid and isooctanoic acid.
3. The pigment-dispersion resin for primer-topcoat cathode electrodeposition paint according to claim 1,
the basic epoxy resin is an aromatic or alicyclic compound containing 2 epoxy groups on each molecular structure, and the epoxy equivalent of the epoxy resin is between 100 and 600 g/mol;
the chain extender is acid, alcohol or phenol with two or more active hydrogen, and the molecular weight of the chain extender is between 50 and 4000;
the catalyst is at least one of triethanolamine, triethylamine, diethanolamine, diethylamine, triphenylphosphine bromide, dimethylbenzylamine, imidazole, dimethylimidazole and 2-ethyl-4-methylimidazole;
the isocyanate prepolymer is prepared by reacting polyisocyanate with a compound containing active hydrogen.
4. The pigment dispersion resin for primer-topcoat cathode electrophoretic paint according to claim 3, wherein the epoxy resin is at least one of bisphenol A epoxy resin, bisphenol S epoxy resin, and bisphenol F epoxy resin.
5. The pigment dispersion resin for a primer-topcoat cathode electrophoretic paint according to claim 3, wherein the chain extender is at least one of dicarboxylic acid, polyether polyol, polyester polyol, dimercaptoalcohol, and bisphenol compounds.
6. The pigment-dispersion resin for primer-topcoat cathode electrophoretic paint according to claim 3, wherein the isocyanate prepolymer is prepared by a method comprising the following steps:
slowly dripping a compound containing active hydrogen into a polyisocyanate compound for reaction, keeping the temperature of 70-110 ℃ after dripping is finished, and reacting for 1-5 h, wherein the molar ratio of isocyanate groups to the compound containing active hydrogen in the isocyanate prepolymer is 1: 0.45-1: 0.65;
the polyisocyanate comprises at least one of aliphatic diisocyanate, alicyclic diisocyanate and aromatic diisocyanate;
the compound containing active hydrogen is at least one of alcohol, alcohol ether, phenol and carboxylic acid containing 1-20 carbon atoms.
7. The pigment-dispersion resin for primer-topcoat cathode electrophoretic paint according to claim 6, wherein the polyisocyanate is at least one of toluene diisocyanate, diphenylmethane diisocyanate, polymethylene polyphenyl diisocyanate, hexamethylene diisocyanate, xylylene diisocyanate, isophorone diisocyanate, and trimethylhexamethylene diisocyanate;
the compound containing active hydrogen is at least one of methanol, ethanol, isopropanol, phenol, ethylene glycol monobutyl ether, ethylene glycol ethyl ether, ethylene glycol hexyl ether, diethylene glycol monobutyl ether and diethylene glycol ethyl ether.
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CN111269619B (en) * | 2020-03-16 | 2022-05-27 | 立邦涂料(中国)有限公司 | Cathode electrophoretic paint color paste and preparation method thereof |
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