JP2011157450A

JP2011157450A - 水性顔料分散液及び記録液

水性顔料分散液及び記録液 Download PDF

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Publication number: JP2011157450A
Authority: JP; Japan
Prior art keywords: meth; pigment; polymer; acrylate; dispersion
Prior art date: 2010-01-29
Legal status : Pending

Application number

JP2010019213A

Other languages

English (en)

Japanese (ja)

Other versions

JP2011157450A5 (https=

Inventor

Ai Ogura

あい小倉

Shinichiro Imai

真一郎今井

Terutoshi Sato

輝聴佐藤

Reika Hai

麗華裴

Current Assignee

Mitsubishi Chemical Corp

Original Assignee

Mitsubishi Chemical Corp

Priority date

2010-01-29

Filing date

2010-01-29

Publication date

2011-08-18

2010-01-29 Application filed by Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp

2010-01-29 Priority to JP2010019213A priority Critical patent/JP2011157450A/ja

2011-08-18 Publication of JP2011157450A publication Critical patent/JP2011157450A/ja

2013-07-11 Publication of JP2011157450A5 publication Critical patent/JP2011157450A5/ja

Status Pending legal-status Critical Current

Links

239000000049 pigment Substances 0.000 title claims abstract description 190
239000006185 dispersion Substances 0.000 title claims abstract description 128
239000007788 liquid Substances 0.000 title abstract description 44
229920000642 polymer Polymers 0.000 claims abstract description 106
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 43
239000000203 mixture Substances 0.000 claims description 38
239000006229 carbon black Substances 0.000 claims description 35
238000000034 method Methods 0.000 claims description 30
125000000129 anionic group Chemical group 0.000 claims description 20
239000011164 primary particle Substances 0.000 claims description 11
238000010521 absorption reaction Methods 0.000 claims description 9
125000001165 hydrophobic group Chemical group 0.000 claims description 7
239000003550 marker Substances 0.000 abstract description 10
238000004062 sedimentation Methods 0.000 abstract description 10
-1 acryl Chemical group 0.000 description 89
239000000178 monomer Substances 0.000 description 85
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 76
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 74
229940048053 acrylate Drugs 0.000 description 74
239000000839 emulsion Substances 0.000 description 37
235000019241 carbon black Nutrition 0.000 description 33
239000000976 ink Substances 0.000 description 33
241000557626 Corvus corax Species 0.000 description 30
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 30
239000002245 particle Substances 0.000 description 29
239000002904 solvent Substances 0.000 description 26
238000006116 polymerization reaction Methods 0.000 description 24
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
239000007864 aqueous solution Substances 0.000 description 22
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 22
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 20
239000000243 solution Substances 0.000 description 19
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 16
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 16
229940047670 sodium acrylate Drugs 0.000 description 16
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
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239000004094 surface-active agent Substances 0.000 description 14
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 13
239000003086 colorant Substances 0.000 description 13
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229910052757 nitrogen Inorganic materials 0.000 description 12
239000000047 product Substances 0.000 description 12
150000003839 salts Chemical class 0.000 description 12
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239000002202 Polyethylene glycol Substances 0.000 description 11
239000000654 additive Substances 0.000 description 11
229920001577 copolymer Polymers 0.000 description 11
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239000011734 sodium Substances 0.000 description 11
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239000003795 chemical substances by application Substances 0.000 description 9
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239000012986 chain transfer agent Substances 0.000 description 8
230000000694 effects Effects 0.000 description 8
235000011187 glycerol Nutrition 0.000 description 8
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 8
239000000126 substance Substances 0.000 description 8
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 7
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239000002585 base Substances 0.000 description 6
239000011324 bead Substances 0.000 description 6
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 6
235000014113 dietary fatty acids Nutrition 0.000 description 6
238000009826 distribution Methods 0.000 description 6
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238000010526 radical polymerization reaction Methods 0.000 description 6
238000000108 ultra-filtration Methods 0.000 description 6
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JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 5
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125000000217 alkyl group Chemical group 0.000 description 5
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238000005160 1H NMR spectroscopy Methods 0.000 description 4
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239000002253 acid Substances 0.000 description 4
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SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 4
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125000004122 cyclic group Chemical group 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
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RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
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