JP6894641B2 - 顔料組成物 - Google Patents
顔料組成物 Download PDFInfo
- Publication number
- JP6894641B2 JP6894641B2 JP2018224012A JP2018224012A JP6894641B2 JP 6894641 B2 JP6894641 B2 JP 6894641B2 JP 2018224012 A JP2018224012 A JP 2018224012A JP 2018224012 A JP2018224012 A JP 2018224012A JP 6894641 B2 JP6894641 B2 JP 6894641B2
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- anisidine
- group
- coupler
- acid
- 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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- 239000000049 pigment Substances 0.000 title claims description 164
- 239000000203 mixture Substances 0.000 title claims description 69
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 claims description 75
- 125000001931 aliphatic group Chemical group 0.000 claims description 36
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 14
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 7
- KSCKTBJJRVPGKM-UHFFFAOYSA-N octan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-] KSCKTBJJRVPGKM-UHFFFAOYSA-N 0.000 claims description 7
- ZRNCNTSXSYXHOW-UHFFFAOYSA-N butyl decanoate Chemical compound CCCCCCCCCC(=O)OCCCC ZRNCNTSXSYXHOW-UHFFFAOYSA-N 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims 1
- 239000000243 solution Substances 0.000 description 24
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 20
- 238000005859 coupling reaction Methods 0.000 description 19
- 239000000976 ink Substances 0.000 description 18
- -1 triazine compound Chemical class 0.000 description 13
- 150000004982 aromatic amines Chemical class 0.000 description 12
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 12
- 230000002378 acidificating effect Effects 0.000 description 11
- 239000002270 dispersing agent Substances 0.000 description 11
- 239000011164 primary particle Substances 0.000 description 11
- 239000002253 acid Substances 0.000 description 10
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- 238000005259 measurement Methods 0.000 description 10
- 230000033228 biological regulation Effects 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000654 additive Substances 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
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- 125000001424 substituent group Chemical group 0.000 description 7
- 238000011282 treatment Methods 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
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- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- 238000004220 aggregation Methods 0.000 description 4
- 125000005233 alkylalcohol group Chemical group 0.000 description 4
- 239000000987 azo dye Substances 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000012954 diazonium Substances 0.000 description 4
- 150000001989 diazonium salts Chemical class 0.000 description 4
- 239000003480 eluent Substances 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000000542 sulfonic acid group Chemical group 0.000 description 4
- GVBHRNIWBGTNQA-UHFFFAOYSA-N 2-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC=C1N GVBHRNIWBGTNQA-UHFFFAOYSA-N 0.000 description 3
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
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- 230000036541 health Effects 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000012860 organic pigment Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- 239000001052 yellow pigment Substances 0.000 description 3
- MXLMTQWGSQIYOW-UHFFFAOYSA-N 3-methyl-2-butanol Chemical compound CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 206010007269 Carcinogenicity Diseases 0.000 description 2
- 0 Cc(cc(Cc(cc1C)cc(C)c1NC(NC(N*)N1)NC1Cl)cc1C)c1N Chemical compound Cc(cc(Cc(cc1C)cc(C)c1NC(NC(N*)N1)NC1Cl)cc1C)c1N 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- GLLRIXZGBQOFLM-UHFFFAOYSA-N Xanthorin Natural products C1=C(C)C=C2C(=O)C3=C(O)C(OC)=CC(O)=C3C(=O)C2=C1O GLLRIXZGBQOFLM-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 231100000260 carcinogenicity Toxicity 0.000 description 2
- 230000007670 carcinogenicity Effects 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- KEMQGTRYUADPNZ-UHFFFAOYSA-N heptadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)=O KEMQGTRYUADPNZ-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-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
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
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- 239000012528 membrane Substances 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- KYYRTDXOHQYZPO-UHFFFAOYSA-N n-(2-methoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC=CC=C1NC(=O)CC(C)=O KYYRTDXOHQYZPO-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 2
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 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
- 229920006395 saturated elastomer Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000011163 secondary particle Substances 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000012086 standard solution Substances 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
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- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- UITKHKNFVCYWNG-UHFFFAOYSA-N 4-(3,4-dicarboxybenzoyl)phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 UITKHKNFVCYWNG-UHFFFAOYSA-N 0.000 description 1
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- 230000009477 glass transition Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- XEUHNWODXVYLFD-UHFFFAOYSA-N heptanedioic acid Chemical compound OC(=O)CCCCCC(O)=O.OC(=O)CCCCCC(O)=O XEUHNWODXVYLFD-UHFFFAOYSA-N 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- KYYWBEYKBLQSFW-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCC(O)=O KYYWBEYKBLQSFW-UHFFFAOYSA-N 0.000 description 1
- YVSCCMNRWFOKDU-UHFFFAOYSA-N hexanedioic acid Chemical compound OC(=O)CCCCC(O)=O.OC(=O)CCCCC(O)=O YVSCCMNRWFOKDU-UHFFFAOYSA-N 0.000 description 1
- ZILMEHNWSRQIEH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O.CCCCCC(O)=O ZILMEHNWSRQIEH-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- OLAPPGSPBNVTRF-UHFFFAOYSA-N naphthalene-1,4,5,8-tetracarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=C(C(O)=O)C2=C1C(O)=O OLAPPGSPBNVTRF-UHFFFAOYSA-N 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- RQFLGKYCYMMRMC-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O RQFLGKYCYMMRMC-UHFFFAOYSA-N 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- NIFHFRBCEUSGEE-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O.OC(=O)C(O)=O NIFHFRBCEUSGEE-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 125000005582 pentacene group Chemical group 0.000 description 1
- YKEKYBOBVREARV-UHFFFAOYSA-N pentanedioic acid Chemical compound OC(=O)CCCC(O)=O.OC(=O)CCCC(O)=O YKEKYBOBVREARV-UHFFFAOYSA-N 0.000 description 1
- HUPQYPMULVBQDL-UHFFFAOYSA-N pentanoic acid Chemical compound CCCCC(O)=O.CCCCC(O)=O HUPQYPMULVBQDL-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- HJSRRUNWOFLQRG-UHFFFAOYSA-N propanedioic acid Chemical compound OC(=O)CC(O)=O.OC(=O)CC(O)=O HJSRRUNWOFLQRG-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 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 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- ZTUXEFFFLOVXQE-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCC(O)=O ZTUXEFFFLOVXQE-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
- C09B29/33—Aceto- or benzoylacetylarylides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0096—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds from other diazotized amino heterocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0041—Blends of pigments; Mixtured crystals; Solid solutions mixtures containing one azo dye
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
- C09B29/33—Aceto- or benzoylacetylarylides
- C09B29/335—Aceto- or benzoylacetylarylides free of acid groups
- C09B29/337—Carbocyclic arylides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B41/00—Special methods of performing the coupling reaction
- C09B41/001—Special methods of performing the coupling reaction characterised by the coupling medium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B51/00—Nitro or nitroso dyes
-
- 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
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/322—Pigment inks
-
- 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
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/328—Inkjet printing inks characterised by colouring agents characterised by dyes
-
- 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
- C09D17/003—Pigment pastes, e.g. for mixing in paints containing an organic pigment
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/09—Colouring agents for toner particles
- G03G9/0906—Organic dyes
- G03G9/091—Azo dyes
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/09—Colouring agents for toner particles
- G03G9/0906—Organic dyes
- G03G9/0914—Acridine; Azine; Oxazine; Thiazine-;(Xanthene-) dyes
Description
全量フラスコに駒込ピペットを用いて100mg程度になるようにo−アニシジンを滴下し、精秤する。アセトニトリルで50mlにメスアップする。これを10倍、100倍、1000倍、4000倍に希釈し、それぞれPTEE製0.45μmメンブレンフィルターを用いて濾過し、2mlスクリューバイアル瓶に移し入れたものを、標準試料とする。
試料1.0gをPP製バイアル瓶に秤量し、これにアセトニトリル50mlを全量ピペットで加え、振盪機にて250rpmで30分間振盪する。5000rpmの遠心分離器に30分間かけて不溶物を沈降させ、上澄み液を0.45μmのメンブレンフィルターを用いて濾過したものを2mlバイアル瓶に移し入れて測定試料とする。
機器:Waters社製alliance e2695 Separations Module
カラム:ZORBAX Extend C18
温度:40℃
移動相:溶離液1 30mM 酢酸アンモニウム水溶液(pH5.40〜5.60)
溶離液2 メタノール
グラジエント送液条件 時間(分)溶離液1(体積%)溶離液2(体積%)
0 90 10
5 90 10
20 0 100
30 0 100
流 速:0.3mL/分
注入量:5μL
検 出:PDA 232nm
載の式(I−1)で示される化合物、アセト−o−アニシダイド等が挙げられる。したがって、式(a)で示される化合物をo−アニシジンの除去剤として使用することで、得られる顔料組成物は、前述のような他の不純物の含量も低減されている。
で示される基が挙げられる。
前述のHPLCによる測定方法により測定した。
水100部に塩化シアヌル7.3部と塩化シアヌルの1個のClと反応する量のスルファニル酸(商品名:ASAスルファニル酸、スガイ化学工業製)6.8部を加えて20℃で1時間反応させた。次に、この反応物の1個のClと反応する量の4,4’−メチレンジ−2,6−キシリジン(商品名:KAYABOND C−200S、日本化薬製)10部を加えて70℃で1時間反応させた。得られた反応物を濾過、残渣を水洗した後、80℃の恒温槽に1晩静置して乾燥させて、前記式(12)で示されるトリアジン化合物17.0部を得た。
ベースである2−メトキシ−4−ニトロ−アニリン(商品名:Kako Red B Base conc、昭和化工製)50部を、水400部と35%塩酸79部との混合液中に加えて撹拌した後、この液が0〜5℃になるまで冷却し、さらに亜硝酸ソーダ21.5部を加えて定法によりジアゾ化し、ジアゾニウム塩を含むジアゾ化液を調製した。
また、カップラーである2−メトキシ−アセトアセトアニライド(商品名:アセト酢酸O−アニシダイト、三星化学工業製)66部を、水300部と30%苛性ソーダ水溶液48部との混合液中に加えて溶解させた。そして、この溶解液を、水900部に酢酸ソーダ30部を添加して得られる水溶液に加えた後、水150部と80%酢酸28部との混合液を更に加えて、カップラーを析出させた。次いで、この析出液に、製造例1で得られたトリアジン化合物3部を添加して懸濁液(カップラー液)を調製した。
このカップラー液に前記ジアゾ化液を25℃において撹拌しながら120分間かけて徐々に添加して、ジアゾニウム塩をカップラーとカップリング反応をさせた。この時のベース(A)に対するカップラー(B)の過剰率((B−A)/A×100)は、0.8%とした。カップリング反応後、O−アニシジン除去剤としてマレイン酸ジブチル(DBM)(大八化学工業製、製品名DBM)を顔料100部に対して10部(10対顔料%)となるように添加し、90℃で30分間加熱した。
この液を常温で放置後、定法により濾過し、水洗し、乾燥させた後、サンプルミルにより粉砕して、式(12)で示されるトリアジン化合物とアゾ系黄色顔料C.I.ピグメントイエロー74を含む顔料組成物118部を得た。得られた顔料組成物のo−アニシジンの含有量を前述のように測定した。
o−アニシジン除去剤の種類を表1のものに変更した以外は実施例1と同様にして、顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
カップラーの過剰量が4.8%となるようにカップラー液を調製し、除去剤の添加量を顔料100部に対して5部(5対顔料%)とした以外は、実施例1と同様にして顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
o−アニシジン除去剤の添加量を顔料100部に対して10部(10対顔料%)とした以外は、実施例5と同様にして顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
実施例5と同様にして、ジアゾ化液及びカップラー液を調製してカップリング反応を行った後、90℃で30分間加熱した。この液を常温になるまで放置した後にマレイン酸ジブチルを添加し、1時間撹拌した。その後、定法により濾過し、水洗し、乾燥させた後、サンプルミルにより粉砕して、式(12)で示されるトリアジン化合物とアゾ系黄色顔料C.I.ピグメントイエロー74を含む顔料組成物118部を得た。得られた顔料組成物のo−アニシジンの含有量を前述のように測定した。
カップラーの過剰量が1.6%となるようにカップラー液を調製した以外は、実施例5と同様にして顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
o−アニシジン除去剤の添加量を顔料100部に対して10部(10対顔料%)とした以外は、実施例8と同様にして顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
カップラーの過剰量が0.8%となるようにカップラー液を調製した以外は、実施例5と同様にして顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
o−アニシジン除去剤を用いなかった以外は実施例5と同様にして顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
o−アニシジン除去剤を用いなかった以外は実施例8と同様にして顔料組成物を調製し、顔料組成物中のo−アニシジンの含有量を測定した。
<トナー用途の評価>
実施例1〜4及び比較例1、2の顔料組成物を用いて、各顔料組成物について、カラートナーを以下の手順でそれぞれ作製した。まず、結着樹脂としての線状ポリエステル樹脂(ビスフェノールAのエチレンオキサイド付加物−テレフタル酸縮合生成物、軟化点:107℃、ガラス転移点:63℃)60重量部をニーダーに投入し、110〜112℃で加熱溶融した中に、各実施例1〜4及び比較例1、2の顔料組成物40重量部を少しずつ投入し、常法により顔料分40重量%のマスターバッチをそれぞれ作製した。
次に、この各マスターバッチ10重量部をテトラヒドロフラン溶剤90重量部に溶解し、顔料分4重量%の黄色顔料分散液を調整した。この各顔料分散液を、0.15mmバーコーターで透明フィルムに展色し、試料とした。各試料をオーバーヘッドプロジェクター(OHP)にセットし、その透過色を目視により判定し、下記の基準で評価した。
◎ : 非常に鮮明な黄色に発現し、カラートナー用着色剤として使用できる。
○ : 鮮明な黄色に発現し、カラートナー用着色剤として使用できる。
△ : 若干赤味黄色となり、色に陰りはあるが、実用上問題なし。
× : 淡褐色〜 濃褐色に発現し、カラートナー用着色剤として使えない。
実施例1〜4及び比較例1、2の顔料組成物を用いて、インクジェットインクを以下の手順で作製した。まず、実施例1〜4及び比較例1、2の各顔料組成物7.5重量部、分散剤(ジョンクリル61J、BASF社製)4重量部、イソプロピルアルコール5重量部、脱イオン水13.5重量部、ガラスビーズ(直径2.5〜3.5mm)を140mLガラス容器に入れ、ペイントコンディショナーにて60分間分散させた。次いで、分散剤(ジョンクリル7001、BASF社製)20重量部をさらに添加し、同様にして5分間分散させた後ガラスビーズを除去し、各インクジェットインクを調製した。このインクを、バーコーターを用いてウェット膜厚が0.15μmとなるようにポリプロピレンフィルムに展色し、乾燥した。得られた各薄膜について、目視により透明性を確認し、下記の基準で評価した。
◎ :非常に優れている。
○ :優れている。
× :劣っている(不透明)。
Claims (3)
- o−アニシジンの除去剤として添加される式(a)で示される化合物が、マレイン酸ジブチル、セバシン酸ジエチル、フタル酸ジブチル、デカン酸ブチルから選択される少なくとも一種である請求項1記載の顔料組成物の製造方法。
- o−アニシジンの除去剤の存在下で、加熱する工程を含む、請求項1又は2に記載の顔料組成物の製造方法。
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EP (1) | EP3492527A1 (ja) |
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GB602886A (en) * | 1945-07-19 | 1948-06-04 | Geigy Co Ltd | Improvements in and relating to pigment emulsions, the manufacture thereof and the dyeing of fabrics therewith |
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JPS63245501A (ja) | 1987-03-31 | 1988-10-12 | Toshiba Corp | 制御装置 |
JPH01189732A (ja) | 1988-01-25 | 1989-07-28 | Fujitsu Ltd | タスク起動制御方法 |
JP2594086B2 (ja) | 1988-01-30 | 1997-03-26 | 東芝ケミカル株式会社 | 多層積板の内層基準穴の穴あけ方法 |
JP3232931B2 (ja) | 1995-02-03 | 2001-11-26 | 東洋インキ製造株式会社 | 低アミン含有率のジスアゾ顔料の製造方法およびそれにより得られるジスアゾ顔料 |
JPH08295810A (ja) | 1995-04-26 | 1996-11-12 | Toyo Ink Mfg Co Ltd | カラーフィルタ用顔料および着色組成物 |
JP3581243B2 (ja) | 1996-12-20 | 2004-10-27 | セイコーエプソン株式会社 | 顔料塊状体及びその製造方法、顔料水系分散液、並びに水系インク組成物 |
JPH10288862A (ja) * | 1997-04-14 | 1998-10-27 | Toyo Ink Mfg Co Ltd | 静電荷像現像用イエロートナー |
JPH10288863A (ja) * | 1997-04-14 | 1998-10-27 | Toyo Ink Mfg Co Ltd | 静電荷像現像用イエロートナー |
GB9910251D0 (en) | 1999-05-05 | 1999-06-30 | Ciba Geigy Ag | Process for the preparation of pigment compositions |
JP3940547B2 (ja) | 2000-06-14 | 2007-07-04 | Jsr株式会社 | カラーフィルタ |
JP2003240938A (ja) | 2002-02-22 | 2003-08-27 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
JP4311611B2 (ja) | 2002-07-12 | 2009-08-12 | 大日精化工業株式会社 | 顔料分散剤およびこれを含んだ顔料組成物 |
JP4398753B2 (ja) | 2004-02-23 | 2010-01-13 | 東洋インキ製造株式会社 | カラーフィルタ用着色組成物およびカラーフィルタ |
DE102004019560A1 (de) * | 2004-04-22 | 2005-11-10 | Clariant Gmbh | Hochreine Naphthol AS-Pigmente |
JP4668801B2 (ja) | 2005-02-22 | 2011-04-13 | 大日精化工業株式会社 | 顔料分散剤およびその使用 |
JP5393946B2 (ja) * | 2006-09-11 | 2014-01-22 | 御国色素株式会社 | C.i.ピグメントイエロー74を含有するインク組成物 |
CN101918497B (zh) | 2007-12-26 | 2014-05-28 | 东洋油墨制造股份有限公司 | 红色滤色器用颜料组合物、该颜料组合物的制造方法、使用该颜料组合物的着色组合物和滤色器 |
JP5299151B2 (ja) * | 2009-07-31 | 2013-09-25 | 山陽色素株式会社 | 微細顔料組成物およびその製造方法 |
JP5942377B2 (ja) | 2011-10-07 | 2016-06-29 | 山陽色素株式会社 | 顔料およびその製造方法 |
JP6326314B2 (ja) | 2014-07-23 | 2018-05-16 | 花王株式会社 | インク組成物 |
JP6294926B2 (ja) | 2015-10-13 | 2018-03-14 | 花王株式会社 | 顔料組成物の製造方法 |
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- 2018-11-30 CN CN201811459237.0A patent/CN109971211B/zh active Active
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US20190264030A1 (en) | 2019-08-29 |
US11549018B2 (en) | 2023-01-10 |
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EP3492527A1 (en) | 2019-06-05 |
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