JPS62502899A - カチオン性電着塗料用水希釈性結合剤及びその製法 - Google Patents

カチオン性電着塗料用水希釈性結合剤及びその製法

Info

Publication number: JPS62502899A
Authority: JP; Japan
Prior art keywords: acid; alkylene; component; compounds; mixture
Prior art date: 1985-05-24
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.): Granted

Application number

JP61503035A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0137432B2 (2

Inventor

ドツベルシユタイン，アーノルト

ガイスト，ミヒヤエル

オツト，ギユンター

シエーン，ゲオルク

Original Assignee

ベ−　ア−　エス　エフ　ラツケ　ウント　フアルベン　アクチエンゲゼルシヤフト

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

1985-05-24

Filing date

1986-05-17

Publication date

1987-11-19

1986-05-17 Application filed by ベ−　ア−　エス　エフ　ラツケ　ウント　フアルベン　アクチエンゲゼルシヤフト filed Critical ベ−　ア−　エス　エフ　ラツケ　ウント　フアルベン　アクチエンゲゼルシヤフト

1987-11-19 Publication of JPS62502899A publication Critical patent/JPS62502899A/ja

1989-08-07 Publication of JPH0137432B2 publication Critical patent/JPH0137432B2/ja

Status Granted legal-status Critical Current

Links

239000011230 binding agent Substances 0.000 title claims description 30
238000004519 manufacturing process Methods 0.000 title claims description 19
125000002091 cationic group Chemical group 0.000 title claims description 18
238000004070 electrodeposition Methods 0.000 title claims description 11
239000003973 paint Substances 0.000 title claims description 8
150000001875 compounds Chemical class 0.000 claims description 72
239000002253 acid Substances 0.000 claims description 71
239000000203 mixture Substances 0.000 claims description 62
238000006243 chemical reaction Methods 0.000 claims description 58
XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 40
-1 -O-alkyl Chemical group 0.000 claims description 39
239000004593 Epoxy Substances 0.000 claims description 31
125000000217 alkyl group Chemical group 0.000 claims description 25
229920005989 resin Polymers 0.000 claims description 25
239000011347 resin Substances 0.000 claims description 25
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 23
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
238000000034 method Methods 0.000 claims description 20
229910000073 phosphorus hydride Inorganic materials 0.000 claims description 20
235000013824 polyphenols Nutrition 0.000 claims description 19
150000003839 salts Chemical class 0.000 claims description 19
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 17
239000003431 cross linking reagent Substances 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 14
150000008442 polyphenolic compounds Chemical class 0.000 claims description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
229920000768 polyamine Polymers 0.000 claims description 11
229920000728 polyester Polymers 0.000 claims description 11
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
150000003335 secondary amines Chemical class 0.000 claims description 10
238000000576 coating method Methods 0.000 claims description 9
238000004132 cross linking Methods 0.000 claims description 9
239000000126 substance Substances 0.000 claims description 8
150000003512 tertiary amines Chemical class 0.000 claims description 8
239000003054 catalyst Substances 0.000 claims description 7
239000007795 chemical reaction product Substances 0.000 claims description 7
229920000642 polymer Polymers 0.000 claims description 7
239000005077 polysulfide Substances 0.000 claims description 7
229920001021 polysulfide Polymers 0.000 claims description 7
150000008117 polysulfides Polymers 0.000 claims description 7
150000003141 primary amines Chemical class 0.000 claims description 7
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 7
229910052717 sulfur Inorganic materials 0.000 claims description 7
125000003396 thiol group Chemical group [H]S* 0.000 claims description 7
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 6
239000000654 additive Substances 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 6
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
230000005588 protonation Effects 0.000 claims description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
125000005496 phosphonium group Chemical group 0.000 claims description 5
239000011593 sulfur Chemical class 0.000 claims description 5
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
239000011248 coating agent Substances 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
229920000515 polycarbonate Polymers 0.000 claims description 4
239000004417 polycarbonate Substances 0.000 claims description 4
229920000570 polyether Polymers 0.000 claims description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
239000004952 Polyamide Substances 0.000 claims description 3
239000004721 Polyphenylene oxide Substances 0.000 claims description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
229920002647 polyamide Polymers 0.000 claims description 3
239000004814 polyurethane Substances 0.000 claims description 3
229920002635 polyurethane Polymers 0.000 claims description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims 9
229910052799 carbon Inorganic materials 0.000 claims 3
XXUXXCZCUGIGPP-ACAGNQJTSA-N 2-Hydroxy-3,5-dinitro-N-[(1Z)-(5-nitrofuran-2-yl)methylidene]benzene-1-carbohydrazonic acid Chemical class C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1C(=O)N\N=C/C1=CC=C([N+]([O-])=O)O1 XXUXXCZCUGIGPP-ACAGNQJTSA-N 0.000 claims 2
LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 claims 2
125000000732 arylene group Chemical group 0.000 claims 2
125000004429 atom Chemical group 0.000 claims 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
229910052760 oxygen Inorganic materials 0.000 claims 2
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
150000001721 carbon Chemical group 0.000 claims 1
150000002927 oxygen compounds Chemical class 0.000 claims 1
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 26
239000000049 pigment Substances 0.000 description 19
125000003700 epoxy group Chemical group 0.000 description 16
150000001412 amines Chemical class 0.000 description 15
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 14
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical class [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 14
229920000647 polyepoxide Polymers 0.000 description 14
229920005862 polyol Polymers 0.000 description 14
239000003822 epoxy resin Substances 0.000 description 13
229920001228 polyisocyanate Polymers 0.000 description 13
239000005056 polyisocyanate Substances 0.000 description 13
125000002887 hydroxy group Chemical group [H]O* 0.000 description 12
150000007513 acids Chemical class 0.000 description 11
NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 11
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 10
150000003077 polyols Chemical class 0.000 description 10
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 8
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
125000001931 aliphatic group Chemical group 0.000 description 6
229910000147 aluminium phosphate Inorganic materials 0.000 description 6
150000002009 diols Chemical class 0.000 description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
235000011007 phosphoric acid Nutrition 0.000 description 6
239000002904 solvent Substances 0.000 description 6
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
229960000583 acetic acid Drugs 0.000 description 5
150000008064 anhydrides Chemical class 0.000 description 5
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
239000004615 ingredient Substances 0.000 description 5
239000012948 isocyanate Substances 0.000 description 5
229920005906 polyester polyol Polymers 0.000 description 5
239000000047 product Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
235000011054 acetic acid Nutrition 0.000 description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
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 4
239000003795 chemical substances by application Substances 0.000 description 4
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
238000000227 grinding Methods 0.000 description 4
150000002513 isocyanates Chemical class 0.000 description 4
239000004310 lactic acid Substances 0.000 description 4
235000014655 lactic acid Nutrition 0.000 description 4
125000000466 oxiranyl group Chemical class 0.000 description 4
239000007787 solid Substances 0.000 description 4
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 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical group OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 description 3
150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
239000002981 blocking agent Substances 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
239000008367 deionised water Substances 0.000 description 3
229910021641 deionized water Inorganic materials 0.000 description 3
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
125000005442 diisocyanate group Chemical group 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000003925 fat Substances 0.000 description 3
235000019197 fats Nutrition 0.000 description 3
235000019253 formic acid Nutrition 0.000 description 3
238000009472 formulation Methods 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
238000002156 mixing Methods 0.000 description 3
238000012986 modification Methods 0.000 description 3
230000004048 modification Effects 0.000 description 3
150000003003 phosphines Chemical class 0.000 description 3
238000001556 precipitation Methods 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 2
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
229920000877 Melamine resin Polymers 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
QCOGKXLOEWLIDC-UHFFFAOYSA-N N-methylbutylamine Chemical compound CCCCNC QCOGKXLOEWLIDC-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
239000007983 Tris buffer Substances 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
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 2
239000001361 adipic acid Substances 0.000 description 2
235000011037 adipic acid Nutrition 0.000 description 2
125000002723 alicyclic group Chemical group 0.000 description 2
150000001346 alkyl aryl ethers Chemical class 0.000 description 2
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
239000002518 antifoaming agent Substances 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
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
239000004327 boric acid Substances 0.000 description 2
235000010338 boric acid Nutrition 0.000 description 2
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
239000006229 carbon black Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
238000000151 deposition Methods 0.000 description 2
230000008021 deposition Effects 0.000 description 2
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical compound CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 description 2
239000000539 dimer Substances 0.000 description 2
HASCQPSFPAKVEK-UHFFFAOYSA-N dimethyl(phenyl)phosphine Chemical compound CP(C)C1=CC=CC=C1 HASCQPSFPAKVEK-UHFFFAOYSA-N 0.000 description 2
238000010494 dissociation reaction Methods 0.000 description 2
230000005593 dissociations Effects 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
150000004658 ketimines Chemical group 0.000 description 2
239000004922 lacquer Substances 0.000 description 2
150000002596 lactones Chemical class 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000002245 particle Substances 0.000 description 2
NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 0.000 description 2
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920001281 polyalkylene Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000001294 propane Substances 0.000 description 2
235000019260 propionic acid Nutrition 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
238000005809 transesterification reaction Methods 0.000 description 2
RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 2
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
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DKZBBWMURDFHNE-UHFFFAOYSA-N trans-coniferylaldehyde Natural products COC1=CC(C=CC=O)=CC=C1O DKZBBWMURDFHNE-UHFFFAOYSA-N 0.000 description 1
TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
KCTAHLRCZMOTKM-UHFFFAOYSA-N tripropylphosphane Chemical compound CCCP(CCC)CCC KCTAHLRCZMOTKM-UHFFFAOYSA-N 0.000 description 1
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000012463 white pigment Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
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 1
229910000165 zinc phosphate Inorganic materials 0.000 description 1
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 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
- C09D5/4434—Polyepoxides characterised by the nature of the epoxy binder
- 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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- 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
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/901—Electrodepositable compositions

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Molecular Biology (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Epoxy Resins (AREA)
Paints Or Removers (AREA)

JP61503035A 1985-05-24 1986-05-17 カチオン性電着塗料用水希釈性結合剤及びその製法 Granted JPS62502899A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19853518770 DE3518770A1 (de)	1985-05-24	1985-05-24	Wasserverduennbare bindemittel fuer kationische elektrotauchlacke und verfahren zu ihrer herstellung
DE3518770.0		1985-05-24

Publications (2)

Publication Number	Publication Date
JPS62502899A true JPS62502899A (ja)	1987-11-19
JPH0137432B2 JPH0137432B2 (2)	1989-08-07

Family

ID=6271594

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61503035A Granted JPS62502899A (ja)	1985-05-24	1986-05-17	カチオン性電着塗料用水希釈性結合剤及びその製法

Country Status (8)

Country	Link
US (2)	US4780524A (2)
EP (1)	EP0241476B1 (2)
JP (1)	JPS62502899A (2)
BR (1)	BR8607119A (2)
CA (1)	CA1258740A (2)
DE (2)	DE3518770A1 (2)
ES (1)	ES8704191A1 (2)
WO (1)	WO1986007083A1 (2)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH021858A (ja) *	1988-06-13	1990-01-08	Kansai Paint Co Ltd	光重合性組成物
JPH04120122A (ja) *	1990-09-10	1992-04-21	Hitachi Chem Co Ltd	高分子量エポキシ樹脂の製造方法
JPH04122713A (ja) *	1990-09-12	1992-04-23	Hitachi Chem Co Ltd	高分子量エポキシ樹脂の製造方法
JP2001220540A (ja) *	1999-11-30	2001-08-14	Nippon Paint Co Ltd	カチオン電着塗料用顔料分散樹脂の製造方法

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* Cited by examiner, † Cited by third party
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DE3518732A1 (de) *	1985-05-24	1986-11-27	BASF Lacke + Farben AG, 4400 Münster	Wasserverduennbare bindemittel fuer kationische elektrotauchlacke und verfahren zu ihrer herstellung
US4715898A (en) *	1986-06-30	1987-12-29	Ppg Industries, Inc.	Sulfonium resins useful as pigment grinding vehicles in cationic electrodeposition
US5171765A (en) *	1987-03-27	1992-12-15	North Dakota State University	Water dispersible polymers for coatings based on polymers containing mesogenic groups
US5235006A (en) *	1987-03-27	1993-08-10	North Dakota State University	Mesogens and polymers with mesogens
AU611925B2 (en)	1987-07-29	1991-06-27	Basf Lacke & Farben Aktiengesellschaft	Aqueous electro-dipcoat baths containing cathodically depositable synthetic resins and process for coating electrically conductive substrates
DE3801787A1 (de) *	1988-01-22	1989-07-27	Basf Lacke & Farben	Verfahren zur beschichtung elektrisch leitfaehiger substrate, nach diesem verfahren beschichtete substrate und waessrige elektrotauchlackbaeder
DE3801786A1 (de) *	1988-01-22	1989-07-27	Basf Lacke & Farben	Verfahren zur beschichtung elektrisch leitfaehiger substrate, nach diesem verfahren beschichtete substrate und waessrige elektrotauchlackbaeder
CA1336523C (en) *	1988-04-04	1995-08-01	Hideo Nakamura	Polyol resin and process for preparing the same
ZA891937B (en) *	1988-04-04	1990-11-28	Ppg Industries Inc	Pigment grinding vehicles containing quaternary ammonium and ternary sulfonium groups
US5268435A (en) *	1988-04-04	1993-12-07	Mitsui Petrochemical Industries, Ltd.	Epoxy resin reacted with primary amine active hydrogen compound and esterifying agent to yield polyol resin
DE3825464A1 (de) *	1988-07-27	1990-02-01	Basf Lacke & Farben	Wasserdispergierbare bindemittel fuer kationische elektrotauchlacke, verfahren zu ihrer herstellung sowie verfahren zur beschichtung elektrisch leitfaehiger substrate
DE3825562A1 (de) *	1988-07-28	1990-02-01	Basf Lacke & Farben	Durch protonieren mit saeure wasserverduennbare bindemittel fuer die elektrotauchlackierung zur herstellung dickschichtiger ueberzuege
US4920162A (en) *	1988-12-22	1990-04-24	Clark Peter D	Electrocoating composition of a polyamine self-condensed epoxy adduct and coatings produced thereby
DE3902441A1 (de) *	1989-01-27	1990-08-16	Basf Lacke & Farben	Hitzehaertbares ueberzugsmittel fuer die kathodische elektrotauchlackierung
US5108575A (en) *	1990-02-23	1992-04-28	E. I. Du Pont De Nemours And Company	Polyamine enamine containing cationic resin
US5464913A (en) *	1990-03-15	1995-11-07	Kansai Paint Co., Ltd.	Cycloaliphatic epoxy and primary hydroxyl groups-containing cationic resin
US5095051A (en) *	1990-08-06	1992-03-10	E. I. Du Pont De Nemours And Company	Amide diol extended cathodic electrodeposition resins
US5089100A (en) *	1990-08-06	1992-02-18	E. I. Du Pont De Nemours And Company	Method of incorporating polyamine into a cationic resin
DE4133853A1 (de) *	1991-10-12	1993-04-15	Basf Lacke & Farben	Kunstharze
US5464924A (en) *	1994-01-07	1995-11-07	The Dow Chemical Company	Flexible poly(amino ethers) for barrier packaging
DE19541230A1 (de)	1995-11-06	1997-05-07	Basf Lacke & Farben	Elektrisch abscheidbares Überzugsmittel
DE19547786A1 (de)	1995-12-20	1997-06-26	Basf Lacke & Farben	Aufbau von modifizierten Epoxidharzen für die kathodische Elektrotauchlackierung mit Katalysator-Desaktivierung und Diolmodifizierung
US6037405A (en) *	1995-12-25	2000-03-14	Sakata Inx Corp.	Pigment dispersion and offset printing ink composition using the same
JP3396585B2 (ja) *	1995-12-25	2003-04-14	サカタインクス株式会社	顔料分散物及びそれを用いたオフセット印刷用インキ組成物
DE19618379A1 (de)	1996-05-08	1997-11-13	Basf Lacke & Farben	Mit Copolymeren des Vinylacetats modifizierte in Wasser dispergierbare Epoxidharze
DE19650157A1 (de) *	1996-12-04	1998-06-10	Basf Coatings Ag	Verfahren zur Beschichtung von Substraten, vorzugsweise aus Metall
DE19804291A1 (de) *	1998-02-04	1999-10-28	Basf Coatings Ag	Kathodisch abscheidbare, Schwefel enthaltende Elektrotauchlacke
DE19816626C2 (de)	1998-04-15	2002-07-18	Basf Coatings Ag	Mittel zum Blockieren von Polyisocyanaten, hiermit blockierte Polyisocyanate und Beschichtungsmittel, welche diese blockierten Polyisocyanate enthalten
US6423774B1 (en) *	2000-03-21	2002-07-23	Ppg Industries Ohio, Inc.	Cationic aliphatic polyester resins and their electrodeposition
US6902766B1 (en) *	2000-07-27	2005-06-07	Lord Corporation	Two-part aqueous metal protection treatment
DE102005012056A1 (de)	2005-03-16	2006-09-28	Basf Coatings Ag	Mehrschichtlackierungen, Verfahren zu ihrer Herstellung und deren Verwendung im Automobilbau
DE102005023728A1 (de)	2005-05-23	2006-11-30	Basf Coatings Ag	Lackschichtbildendes Korrosionsschutzmittel und Verfahren zu dessen stromfreier Applikation
DE102006053291A1 (de)	2006-11-13	2008-05-15	Basf Coatings Ag	Lackschichtbildendes Korrosionsschutzmittel mit guter Haftung und Verfahren zu dessen stromfreier Applikation
DE102007012406A1 (de)	2007-03-15	2008-09-18	Basf Coatings Ag	Verfahren zur Korrosionsschutzausrüstung metallischer Substrate
DE102008061329A1 (de)	2008-12-11	2010-06-17	Basf Coatings Ag	Verwendung von 1,3-substituierten Imidazoliumsalzen zur katalytischen Deblockierung blockierter Isocyanate
DE102009007632A1 (de)	2009-02-05	2010-08-12	Basf Coatings Ag	Beschichtungsmittel für korrosionsstabile Lackierungen
DE102010012047A1 (de)	2010-03-19	2011-09-22	Basf Coatings Gmbh	Verfahren zur Beschichtung eines Metall- oder Kunststoffsubstrats, daraus erhältliche Beschichtung und beschichtetes Substrat
MX374622B (es)	2012-12-03	2025-03-06	Basf Coatings Gmbh	Pintura de varias capas que induce efecto y/o color y método para su producción, y su uso.
EP3004257B1 (de)	2013-05-28	2018-10-24	BASF Coatings GmbH	Verfahren zur tauchlack-beschichtung elektrisch leitfähiger substrate unter nachbehandlung der tauchlack-beschichtung mit einer wässrigen sol-gel- zusammensetzung vor deren aushärtung
JP6293893B2 (ja)	2013-08-12	2018-03-14	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ＢＡＳＦＣｏａｔｉｎｇｓＧｍｂＨ	ゾル−ゲル組成物を含む、導電性基材のためのディップ−コーティング組成物
JP6375385B2 (ja)	2013-11-18	2018-08-15	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ＢＡＳＦＣｏａｔｉｎｇｓＧｍｂＨ	溶解と非溶解両方のビスマスを含む導電性基材のための水性ディップコーティング組成物
MX2016006412A (es)	2013-11-18	2016-12-09	Basf Coatings Gmbh	Composicion acuosa de recubrimiento por inmersion que comprende bismuto disuelto, para sustratos conductores de electricidad.
WO2015070929A1 (de)	2013-11-18	2015-05-21	Basf Coatings Gmbh	Zweistufiges verfahren zur tauchlack-beschichtung elektrisch leitfähiger substrate unter verwendung einer bi(iii)-haltigen zusammensetzung
HUE036975T2 (hu)	2013-11-19	2018-08-28	Henkel Ag & Co Kgaa	Vizes bevonó készítmény alumíniumoxidot tartalmazó elektromos vezetõ szubsztrátumnak egy elektrolitikus mártólakkal történõ bevonására
JP6285045B2 (ja)	2013-11-19	2018-02-28	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ＢＡＳＦＣｏａｔｉｎｇｓＧｍｂＨ	酸化マグネシウムを含む導電性基材のための水性ディップコーティング組成物
MX2016007453A (es)	2013-12-10	2016-12-09	Basf Coatings Gmbh	Composicion acuosa para recubrimiento por inmersion para sustratos que son conductores electricos, que comprende bismuto y un compuesto que contiene fosforo, bloqueado con aminas.
JP7357610B2 (ja)	2017-10-09	2023-10-06	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	少なくとも１種のトリアジン化合物を含む電気塗装材料
WO2020212074A1 (de)	2019-04-15	2020-10-22	Basf Coatings Gmbh	Wässrige beschichtungszusammensetzung zur tauchlack-beschichtung elektrisch leitfähiger substrate enthaltend bismut sowie lithium
US12460311B2 (en)	2019-12-19	2025-11-04	Basf Coatings Gmbh	Lamp black pigment containing electrodeposition coating material compositions
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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
WO2023117962A1 (en)	2021-12-21	2023-06-29	Basf Se	Chemical product passport
WO2023237284A1 (en)	2022-06-09	2023-12-14	Basf Coatings Gmbh	Electrodeposition coating material compositions comprising alkoxylated polyethyleneimines
EP4587521A1 (en)	2022-09-15	2025-07-23	BASF Coatings GmbH	Electrodeposition coating material compositions comprising composite particles containing metal-containing catalyst
CN119894996A (zh)	2022-09-15	2025-04-25	巴斯夫涂料有限公司	包含颜料浆料和含有含金属催化剂的复合颗粒的电沉积涂覆材料组合物
WO2026052296A1 (en)	2024-09-05	2026-03-12	Basf Coatings Gmbh	Serial cathodic electrodeposition coating process
WO2026052294A1 (en)	2024-09-05	2026-03-12	Basf Coatings Gmbh	Electrodeposition coating material with improved uv-stability
WO2026052295A1 (en)	2024-09-05	2026-03-12	Basf Coatings Gmbh	Electrodeposition coating material having good uv stability

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US4246089A (en) *	1979-11-30	1981-01-20	E. I. Du Pont De Nemours And Company	Graft copolymer useful in electrodeposition
DE3108073C2 (de) *	1981-03-04	1983-10-06	Basf Farben + Fasern Ag, 2000 Hamburg	Wasserdispergierbare Bindemittel für kationische Elektrotauchlacke
DE3300583A1 (de) *	1983-01-10	1984-07-12	Basf Farben + Fasern Ag, 2000 Hamburg	Wasserdispergierbare bindemittel fuer kationische elektrotauchlacke und verfahren zu ihrer herstellung
GB8315230D0 (en) *	1983-06-03	1983-07-06	Shell Int Research	Polyglycidyl ethers
DE3475524D1 (en) *	1983-06-03	1989-01-12	Shell Int Research	Novel polyglycidyl ethers, their preparation and their use as thermosetting coating compositions
DE3331903A1 (de) *	1983-09-03	1985-03-21	Basf Farben + Fasern Ag, 2000 Hamburg	Wasserdispergierbare bindemittel fuer kationische elektrotauchlacke und verfahren zu ihrer herstellung
DE3331904A1 (de) *	1983-09-03	1985-03-21	Basf Farben + Fasern Ag, 2000 Hamburg	Wasserdispergierbare bindemittel fuer kationische elektrotauchlacke und verfahren zu ihrer herstellung
US4686248A (en) *	1984-02-28	1987-08-11	Shell Oil Company	Preparation of binders for coatings, thermosetting coating compositions and their use

1985
- 1985-05-24 DE DE19853518770 patent/DE3518770A1/de not_active Withdrawn
1986
- 1986-05-17 WO PCT/EP1986/000303 patent/WO1986007083A1/de not_active Ceased
- 1986-05-17 JP JP61503035A patent/JPS62502899A/ja active Granted
- 1986-05-17 DE DE8686903341T patent/DE3673640D1/de not_active Expired - Lifetime
- 1986-05-17 BR BR8607119A patent/BR8607119A/pt not_active IP Right Cessation
- 1986-05-17 EP EP86903341A patent/EP0241476B1/de not_active Expired - Lifetime
- 1986-05-17 US US07/009,956 patent/US4780524A/en not_active Expired - Lifetime
- 1986-05-23 ES ES555300A patent/ES8704191A1/es not_active Expired
- 1986-05-23 CA CA000509886A patent/CA1258740A/en not_active Expired
1988
- 1988-07-14 US US07/202,144 patent/US4830722A/en not_active Expired - Lifetime

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH021858A (ja) *	1988-06-13	1990-01-08	Kansai Paint Co Ltd	光重合性組成物
JPH04120122A (ja) *	1990-09-10	1992-04-21	Hitachi Chem Co Ltd	高分子量エポキシ樹脂の製造方法
JPH04122713A (ja) *	1990-09-12	1992-04-23	Hitachi Chem Co Ltd	高分子量エポキシ樹脂の製造方法
JP2001220540A (ja) *	1999-11-30	2001-08-14	Nippon Paint Co Ltd	カチオン電着塗料用顔料分散樹脂の製造方法

Also Published As

Publication number	Publication date
DE3673640D1 (de)	1990-09-27
DE3518770A1 (de)	1986-11-27
CA1258740A (en)	1989-08-22
US4830722A (en)	1989-05-16
EP0241476B1 (de)	1990-08-22
US4780524A (en)	1988-10-25
ES555300A0 (es)	1987-03-16
BR8607119A (pt)	1988-02-09
EP0241476A1 (de)	1987-10-21
WO1986007083A1 (fr)	1986-12-04
ES8704191A1 (es)	1987-03-16
JPH0137432B2 (2)	1989-08-07

Legal Events

Date	Code	Title	Description
2004-08-03	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2005-08-02	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2006-05-17	EXPY	Cancellation because of completion of term

Publication	Publication Date	Title
JPS62502899A (ja)	1987-11-19	カチオン性電着塗料用水希釈性結合剤及びその製法
US4824927A (en)	1989-04-25	Products of diepoxide polyaddition with monofunctional initiators, which contain pendant epoxy groups in the backbone of the polymer
JP4149003B2 (ja)	2008-09-10	陽イオン電着塗料用の水性結合剤分散液
US4260720A (en)	1981-04-07	Novel mercapto chain extended products and their use in cationic electrodeposition
JP3293836B2 (ja)	2002-06-17	電着可能コーティング組成物およびカチオン性電着方法におけるこれらの使用
TWI434905B (zh)	2014-04-21	包含環胍之可電沈積塗料組合物
US5670441A (en)	1997-09-23	Bismuth catalysts useful for curing of cataphoretic deposition coating materials
US5385962A (en)	1995-01-31	Photodegradation-resistant electrodepositable primer compositions containing hindering aminoether light stabilizers
AU674236B2 (en)	1996-12-12	Photodegradation-resistant electrodepositable primer compositions
US5187198A (en)	1993-02-16	Resin composition for cationically electrodepositable paint containing as crosslinking agents the reaction products of hydroxy functional alicyclic epoxy compounds and polyisocyanates
JPH0647611B2 (ja)	1994-06-22	カチオン高度エポキシ樹脂の製造方法
JPH038390B2 (2)	1991-02-05
US4661541A (en)	1987-04-28	Alcohol-modified polyepoxides, their preparation and their use in curable mixtures
CN101583678B (zh)	2013-07-17	用于颜料分散体的阳离子树脂和包含它的可电沉积漆组合物
JPS6399277A (ja)	1988-04-30	エポキシ樹脂ブレンド
JPH01501069A (ja)	1989-04-13	陽イオン性エポキシ樹脂をベースとする組成物の被覆方法
US4566963A (en)	1986-01-28	Water-dispersible binders based on modified epoxide/amine adducts, and their preparation and use
EP0107098A1 (en)	1984-05-02	Novel pigment grinding vehicle
US4292155A (en)	1981-09-29	Cationic electrodeposition employing novel mercapto chain extended products
CA2075651C (en)	1999-01-26	Photodegradation-resistant electrodepositable primer compositions
DE3735603A1 (de)	1989-05-03	Waessrige elektrotauchlacke und verfahren zur beschichtung elektrisch leitfaehiger substrate
JPH0689105B2 (ja)	1994-11-09	陽イオン性電着塗料用の水に分散可能な結合剤、その製法並びに導電性基板の被覆法
KR20040073699A (ko)	2004-08-21	양이온 마이크로겔, 이의 제조방법 및 이를 포함하는 전착도료조성물
HK1142354B (en)	2015-07-31	Electrodepositable coating composition containing a cyclic guanidine
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JPS62502899A - カチオン性電着塗料用水希釈性結合剤及びその製法 - Google Patents

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