JP5223947B2

JP5223947B2 - 水性インク

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Publication number: JP5223947B2
Authority: JP; Japan
Prior art keywords: dispersion; water; pigment; ink; polymer
Prior art date: 2003-09-02
Legal status : Expired - Fee Related

Application number

JP2011114818A

Other languages

English (en)

Japanese (ja)

Other versions

JP2011236426A (ja

JP2011236426A5 (enExample

Inventor

英彦小松

正弘矢竹

和彦原

雅明板野

淳伊東

基城増田

Current Assignee

Seiko Epson Corp

Original Assignee

Seiko Epson Corp

Priority date

2003-09-02

Filing date

2011-05-23

Publication date

2013-06-26

2011-05-23 Application filed by Seiko Epson Corp filed Critical Seiko Epson Corp

2011-05-23 Priority to JP2011114818A priority Critical patent/JP5223947B2/ja

2011-11-24 Publication of JP2011236426A publication Critical patent/JP2011236426A/ja

2012-04-26 Publication of JP2011236426A5 publication Critical patent/JP2011236426A5/ja

2013-06-26 Application granted granted Critical

2013-06-26 Publication of JP5223947B2 publication Critical patent/JP5223947B2/ja

2024-08-30 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 144
239000006185 dispersion Substances 0.000 claims description 126
-1 acetylene glycol Chemical compound 0.000 claims description 113
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 91
229920000642 polymer Polymers 0.000 claims description 82
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 76
239000004094 surface-active agent Substances 0.000 claims description 56
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 52
125000003118 aryl group Chemical group 0.000 claims description 28
239000003086 colorant Substances 0.000 claims description 15
150000001875 compounds Chemical class 0.000 claims description 9
125000000962 organic group Chemical group 0.000 claims description 5
239000000976 ink Substances 0.000 description 191
238000011156 evaluation Methods 0.000 description 144
239000000049 pigment Substances 0.000 description 100
238000000034 method Methods 0.000 description 38
239000002245 particle Substances 0.000 description 30
238000007639 printing Methods 0.000 description 29
229920001296 polysiloxane Polymers 0.000 description 27
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 25
238000005259 measurement Methods 0.000 description 25
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230000000694 effects Effects 0.000 description 22
238000003860 storage Methods 0.000 description 22
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NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 20
239000004815 dispersion polymer Substances 0.000 description 19
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 17
MYONAGGJKCJOBT-UHFFFAOYSA-N benzimidazol-2-one Chemical compound C1=CC=CC2=NC(=O)N=C21 MYONAGGJKCJOBT-UHFFFAOYSA-N 0.000 description 17
239000002270 dispersing agent Substances 0.000 description 16
238000004519 manufacturing process Methods 0.000 description 16
239000012860 organic pigment Substances 0.000 description 16
150000003839 salts Chemical class 0.000 description 16
RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 description 15
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COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 14
FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 description 14
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SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 8
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HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 8
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JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 7
238000003786 synthesis reaction Methods 0.000 description 7
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NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 6
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LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000011324 bead Substances 0.000 description 6
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
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 6
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 6
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 5
125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 5
235000010443 alginic acid Nutrition 0.000 description 5
229920000615 alginic acid Polymers 0.000 description 5
150000004781 alginic acids Chemical class 0.000 description 5
239000002518 antifoaming agent Substances 0.000 description 5
230000000740 bleeding effect Effects 0.000 description 5
150000002009 diols Chemical class 0.000 description 5
230000000704 physical effect Effects 0.000 description 5
239000000243 solution Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 description 4
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229920000858 Cyclodextrin Polymers 0.000 description 4
GUBGYTABKSRVRQ-CUHNMECISA-N D-Cellobiose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-CUHNMECISA-N 0.000 description 4
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