JP4852715B2 - インクジェット用インク組成物 - Google Patents
インクジェット用インク組成物 Download PDFInfo
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- JP4852715B2 JP4852715B2 JP2001256482A JP2001256482A JP4852715B2 JP 4852715 B2 JP4852715 B2 JP 4852715B2 JP 2001256482 A JP2001256482 A JP 2001256482A JP 2001256482 A JP2001256482 A JP 2001256482A JP 4852715 B2 JP4852715 B2 JP 4852715B2
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- formula
- ink composition
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- weight
- pigment
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 85
- -1 alkali metal salt Chemical class 0.000 claims description 68
- 239000000049 pigment Substances 0.000 claims description 66
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- 239000000126 substance Substances 0.000 claims description 25
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 24
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
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- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 13
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- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 claims description 8
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- 150000003839 salts Chemical class 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 235000010443 alginic acid Nutrition 0.000 description 3
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- 229910021529 ammonia Inorganic materials 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
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- 235000014113 dietary fatty acids Nutrition 0.000 description 3
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- 238000002156 mixing Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
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- LXOFYPKXCSULTL-UHFFFAOYSA-N 2,4,7,9-tetramethyldec-5-yne-4,7-diol Chemical compound CC(C)CC(C)(O)C#CC(C)(O)CC(C)C LXOFYPKXCSULTL-UHFFFAOYSA-N 0.000 description 2
- JQXYBDVZAUEPDL-UHFFFAOYSA-N 2-methylidene-5-phenylpent-4-enoic acid Chemical compound OC(=O)C(=C)CC=CC1=CC=CC=C1 JQXYBDVZAUEPDL-UHFFFAOYSA-N 0.000 description 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
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- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 2
- UXHQLGLGLZKHTC-CUNXSJBXSA-N 4-[(3s,3ar)-3-cyclopentyl-7-(4-hydroxypiperidine-1-carbonyl)-3,3a,4,5-tetrahydropyrazolo[3,4-f]quinolin-2-yl]-2-chlorobenzonitrile Chemical compound C1CC(O)CCN1C(=O)C1=CC=C(C=2[C@@H]([C@H](C3CCCC3)N(N=2)C=2C=C(Cl)C(C#N)=CC=2)CC2)C2=N1 UXHQLGLGLZKHTC-CUNXSJBXSA-N 0.000 description 2
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- 238000010521 absorption reaction Methods 0.000 description 2
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- 125000005907 alkyl ester group Chemical group 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000003139 biocide Substances 0.000 description 2
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- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 2
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- CYKDLUMZOVATFT-UHFFFAOYSA-N ethenyl acetate;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=O)OC=C CYKDLUMZOVATFT-UHFFFAOYSA-N 0.000 description 2
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| JP4525012B2 (ja) * | 2003-07-31 | 2010-08-18 | Ｄｉｃ株式会社 | インクジェットインク記録用着色混練物、及びその製造法 |
| JP4452912B2 (ja) * | 2003-07-31 | 2010-04-21 | Ｄｉｃ株式会社 | インクジェットインク用水性顔料分散液、インクジェットインク用水性インク組成物及びその製造方法 |
| JP4600724B2 (ja) * | 2004-01-20 | 2010-12-15 | Ｄｉｃ株式会社 | インクジェット記録用水性顔料分散液、インクジェット記録用インク組成物およびその製造方法 |
| WO2006004006A1 (ja) | 2004-07-01 | 2006-01-12 | General Company Limited | インクジェットインクとそれを用いる印刷方法 |
| JP2014094495A (ja) * | 2012-11-09 | 2014-05-22 | Seiko Epson Corp | インクジェット記録方法 |
| EP3645496A1 (de) * | 2017-06-26 | 2020-05-06 | Basf Se | Alkoxylierung von hydroxysäuren |
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| JP3191881B2 (ja) * | 1991-11-27 | 2001-07-23 | 大日本インキ化学工業株式会社 | 水性インク |
| JP3689444B2 (ja) * | 1993-12-20 | 2005-08-31 | キヤノン株式会社 | 液体組成物、インクセット及びこれを用いた画像形成方法と装置 |
| JP3507934B2 (ja) * | 1996-08-08 | 2004-03-15 | 株式会社リコー | 記録用インク及びこれを用いた記録方法 |
| JPH10226763A (ja) * | 1997-02-13 | 1998-08-25 | Ricoh Co Ltd | 記録用インクおよび記録方法 |
| JP3785630B2 (ja) * | 1997-08-25 | 2006-06-14 | セイコーエプソン株式会社 | インクジェット用インク組成物、その製造方法、及びそのインク組成物を用いるインクジェット記録方法 |
| JPH11131003A (ja) * | 1997-10-29 | 1999-05-18 | Ricoh Co Ltd | 記録用インクおよび記録方法 |
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