JPS6253025B2 - - Google Patents

Info

Publication number: JPS6253025B2
Authority: JP; Japan
Prior art keywords: paint; coating; monomer; heated; film
Prior art date: 1982-01-29
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

JP1173782A

Other languages

English (en)

Japanese (ja)

Other versions

JPS58129067A (ja

Inventor

Yoshiaki Nakamura

Hideaki Imura

Norihisa Iijima

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

Toagosei Co Ltd

Original Assignee

Toagosei Co Ltd

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

1982-01-29

Filing date

1982-01-29

Publication date

1987-11-09

1982-01-29 Application filed by Toagosei Co Ltd filed Critical Toagosei Co Ltd

1982-01-29 Priority to JP1173782A priority Critical patent/JPS58129067A/ja

1983-08-01 Publication of JPS58129067A publication Critical patent/JPS58129067A/ja

1987-11-09 Publication of JPS6253025B2 publication Critical patent/JPS6253025B2/ja

Status Granted legal-status Critical Current

Links

239000003973 paint Substances 0.000 claims description 44
239000000178 monomer Substances 0.000 claims description 37
229920000642 polymer Polymers 0.000 claims description 24
239000000203 mixture Substances 0.000 claims description 23
229920001577 copolymer Polymers 0.000 claims description 22
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 20
229920005989 resin Polymers 0.000 claims description 13
239000011347 resin Substances 0.000 claims description 13
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 9
238000004132 cross linking Methods 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 4
238000000576 coating method Methods 0.000 description 33
239000000243 solution Substances 0.000 description 29
239000011248 coating agent Substances 0.000 description 26
238000006116 polymerization reaction Methods 0.000 description 16
238000006243 chemical reaction Methods 0.000 description 13
238000000034 method Methods 0.000 description 13
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 12
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
239000006185 dispersion Substances 0.000 description 12
239000007787 solid Substances 0.000 description 12
239000002904 solvent Substances 0.000 description 11
OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 10
239000010419 fine particle Substances 0.000 description 10
239000002245 particle Substances 0.000 description 10
239000000049 pigment Substances 0.000 description 9
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 7
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 6
239000004925 Acrylic resin Substances 0.000 description 6
229920000178 Acrylic resin Polymers 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
238000003756 stirring Methods 0.000 description 6
238000007334 copolymerization reaction Methods 0.000 description 5
229920006037 cross link polymer Polymers 0.000 description 5
238000007598 dipping method Methods 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000009503 electrostatic coating Methods 0.000 description 4
229920000515 polycarbonate Polymers 0.000 description 4
239000004417 polycarbonate Substances 0.000 description 4
238000005507 spraying Methods 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
239000004677 Nylon Substances 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
239000000470 constituent Substances 0.000 description 3
230000008030 elimination Effects 0.000 description 3
238000003379 elimination reaction Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229920001778 nylon Polymers 0.000 description 3
-1 polyethylene Polymers 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
239000003505 polymerization initiator Substances 0.000 description 3
230000000171 quenching effect Effects 0.000 description 3
229920005992 thermoplastic resin Polymers 0.000 description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-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
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000001476 alcoholic effect Effects 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000003093 cationic surfactant Substances 0.000 description 2
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
230000007423 decrease Effects 0.000 description 2
238000004070 electrodeposition Methods 0.000 description 2
230000005484 gravity Effects 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
230000007774 longterm Effects 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
238000004062 sedimentation Methods 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
239000000126 substance Substances 0.000 description 2
229920001187 thermosetting polymer Polymers 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
SCNZQDHXZKQTMA-UHFFFAOYSA-N 2-hydroxyethyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CC(=C)C(=O)OCCO SCNZQDHXZKQTMA-UHFFFAOYSA-N 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
102100026735 Coagulation factor VIII Human genes 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 1
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
238000007605 air drying Methods 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
230000002421 anti-septic effect Effects 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
239000007809 chemical reaction catalyst Substances 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000011362 coarse particle Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000003618 dip coating Methods 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
238000001879 gelation Methods 0.000 description 1
238000004898 kneading Methods 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000012046 mixed solvent Substances 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
238000010422 painting Methods 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000010791 quenching Methods 0.000 description 1
229920013730 reactive polymer Polymers 0.000 description 1
239000004576 sand Substances 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000007592 spray painting technique Methods 0.000 description 1
239000010959 steel Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000012463 white pigment Substances 0.000 description 1
239000008096 xylene 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

Landscapes

Paints Or Removers (AREA)

JP1173782A 1982-01-29 1982-01-29 艶消塗料組成物 Granted JPS58129067A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP1173782A JPS58129067A (ja)	1982-01-29	1982-01-29	艶消塗料組成物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1173782A JPS58129067A (ja)	1982-01-29	1982-01-29	艶消塗料組成物

Publications (2)

Publication Number	Publication Date
JPS58129067A JPS58129067A (ja)	1983-08-01
JPS6253025B2 true JPS6253025B2 (fr)	1987-11-09

Family

ID=11786338

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1173782A Granted JPS58129067A (ja)	1982-01-29	1982-01-29	艶消塗料組成物

Country Status (1)

Country	Link
JP (1)	JPS58129067A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0539321U (ja) *	1991-11-08	1993-05-28	寛了劔持	携帯用身回品

1982
- 1982-01-29 JP JP1173782A patent/JPS58129067A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0539321U (ja) *	1991-11-08	1993-05-28	寛了劔持	携帯用身回品

Also Published As

Publication number	Publication date
JPS58129067A (ja)	1983-08-01

Publication	Publication Date	Title
JPS5824464B2 (ja)	1983-05-21	カルボキシアクリルジユウゴウタイオユウスルフンタイコ−テイングソセイブツ
JPS5825388B2 (ja)	1983-05-27	マツタンニカルボキシルキオモツカキヨウザイオフクムフンタイトソウソセイブツ
JPS5825389B2 (ja)	1983-05-27	粉体塗装組成物
JPS6162510A (ja)	1986-03-31	非造膜性樹脂エマルジヨンの製法及びその粉末化法
JP2637955B2 (ja)	1997-08-06	水性被覆用組成物
CA1295891C (fr)	1992-02-18	Methode de peinturage
US4540740A (en)	1985-09-10	Cross-linked polymeric microgel prepared from polymerizing epoxy-containing monomer in the presence of an acid
JPH0753913A (ja)	1995-02-28	水性塗料組成物
JPS6363756A (ja)	1988-03-22	分散型塗料樹脂組成物
US4611026A (en)	1986-09-09	Emulsion and dispersion comprising cross-linked polymeric microgel prepared from polymerizing epoxy-containing monomer in the presence of an acid
US3300428A (en)	1967-01-24	Hammer finish from aqueous composition containing non-leafing aluminum particles
JPS59147058A (ja)	1984-08-23	彩石プラスタ−用の濃化結合剤
JPS6253025B2 (fr)	1987-11-09
JP2873151B2 (ja)	1999-03-24	水性プライマー組成物
JPS6166710A (ja)	1986-04-05	非造膜性ビニル系樹脂エマルジヨンの製造法及びその粉末化法
JPS5934743B2 (ja)	1984-08-24	アルミニウムおよびアルミニウム合金の艶消し塗装方法
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JP2018080297A (ja)	2018-05-24	水性塗料組成物
JPS63137902A (ja)	1988-06-09	部分架橋コポリマ−粒子の水性分散液
JPS5833900B2 (ja)	1983-07-22	水分散型熱硬化性被覆組成物
JP3468583B2 (ja)	2003-11-17	アニオン性水分散型樹脂組成物及びその製造方法
CN103589262A (zh)	2014-02-19	基材标记系统
JPH062790B2 (ja)	1994-01-12	非水分散型樹脂組成物の製造方法
US5093428A (en)	1992-03-03	Anionic matte electrodeposition coating composition and process for the formation of matte film

JPS6253025B2 - - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=11786338

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Also Published As

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