SK6972002A3 - Pigment composition containing dispersing agent based on modified block copolymers, process for producing thereof and use - Google Patents
Pigment composition containing dispersing agent based on modified block copolymers, process for producing thereof and use Download PDFInfo
- Publication number
- SK6972002A3 SK6972002A3 SK697-2002A SK6972002A SK6972002A3 SK 6972002 A3 SK6972002 A3 SK 6972002A3 SK 6972002 A SK6972002 A SK 6972002A SK 6972002 A3 SK6972002 A3 SK 6972002A3
- Authority
- SK
- Slovakia
- Prior art keywords
- alkyl
- carbon atoms
- group
- groups
- substituted
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 84
- 239000000049 pigment Substances 0.000 title claims abstract description 71
- 229920001400 block copolymer Polymers 0.000 title claims abstract description 70
- 239000002270 dispersing agent Substances 0.000 title claims abstract description 23
- 238000000034 method Methods 0.000 title description 52
- 230000008569 process Effects 0.000 title description 21
- 150000003839 salts Chemical class 0.000 claims abstract description 45
- 239000008199 coating composition Substances 0.000 claims abstract description 27
- 239000001023 inorganic pigment Substances 0.000 claims abstract description 11
- 239000012860 organic pigment Substances 0.000 claims abstract description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 247
- 125000000217 alkyl group Chemical group 0.000 claims description 205
- -1 2-imidazolyl Chemical group 0.000 claims description 147
- 229920000642 polymer Polymers 0.000 claims description 94
- 239000002253 acid Substances 0.000 claims description 83
- 239000000178 monomer Substances 0.000 claims description 70
- 125000001424 substituent group Chemical group 0.000 claims description 53
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 51
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 48
- 125000003545 alkoxy group Chemical group 0.000 claims description 46
- 238000006116 polymerization reaction Methods 0.000 claims description 46
- 125000005907 alkyl ester group Chemical group 0.000 claims description 40
- 150000001875 compounds Chemical class 0.000 claims description 37
- 238000002360 preparation method Methods 0.000 claims description 35
- 239000006185 dispersion Substances 0.000 claims description 34
- 150000002148 esters Chemical class 0.000 claims description 33
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 32
- 150000003254 radicals Chemical class 0.000 claims description 30
- 125000004429 atom Chemical group 0.000 claims description 28
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 27
- 239000003999 initiator Substances 0.000 claims description 27
- 125000001931 aliphatic group Chemical group 0.000 claims description 26
- 125000003118 aryl group Chemical group 0.000 claims description 26
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 25
- 239000011230 binding agent Substances 0.000 claims description 24
- 229910052799 carbon Inorganic materials 0.000 claims description 24
- 239000000460 chlorine Substances 0.000 claims description 23
- 229910052757 nitrogen Inorganic materials 0.000 claims description 23
- 239000002245 particle Substances 0.000 claims description 23
- 150000001735 carboxylic acids Chemical group 0.000 claims description 22
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 21
- 239000003054 catalyst Substances 0.000 claims description 20
- 150000003009 phosphonic acids Chemical group 0.000 claims description 20
- 239000012634 fragment Substances 0.000 claims description 19
- 125000003277 amino group Chemical group 0.000 claims description 18
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 18
- 150000003460 sulfonic acids Chemical group 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 16
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 125000003010 ionic group Chemical group 0.000 claims description 15
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- 125000006168 tricyclic group Chemical group 0.000 claims description 15
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 14
- 125000004185 ester group Chemical group 0.000 claims description 14
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 13
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 13
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 12
- 150000007513 acids Chemical class 0.000 claims description 12
- 125000002091 cationic group Chemical group 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 238000010526 radical polymerization reaction Methods 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 11
- 239000001301 oxygen Chemical group 0.000 claims description 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 11
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims description 10
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 claims description 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 239000000945 filler Substances 0.000 claims description 9
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 9
- 239000003505 polymerization initiator Substances 0.000 claims description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 239000006096 absorbing agent Substances 0.000 claims description 8
- 125000000129 anionic group Chemical group 0.000 claims description 8
- 239000003381 stabilizer Substances 0.000 claims description 8
- 150000003440 styrenes Chemical class 0.000 claims description 8
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical group C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims description 7
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 7
- 150000001412 amines Chemical group 0.000 claims description 7
- YLFIGGHWWPSIEG-UHFFFAOYSA-N aminoxyl Chemical compound [O]N YLFIGGHWWPSIEG-UHFFFAOYSA-N 0.000 claims description 7
- 125000002950 monocyclic group Chemical group 0.000 claims description 7
- 239000003973 paint Substances 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
- 125000002619 bicyclic group Chemical group 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
- 230000000977 initiatory effect Effects 0.000 claims description 6
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- 150000003926 acrylamides Chemical class 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 5
- 150000001721 carbon Chemical group 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 5
- 239000004611 light stabiliser Substances 0.000 claims description 5
- 238000005956 quaternization reaction Methods 0.000 claims description 5
- 229910052717 sulfur Chemical group 0.000 claims description 5
- 239000011593 sulfur Chemical group 0.000 claims description 5
- 239000011701 zinc Substances 0.000 claims description 5
- QHVBLSNVXDSMEB-UHFFFAOYSA-N 2-(diethylamino)ethyl prop-2-enoate Chemical compound CCN(CC)CCOC(=O)C=C QHVBLSNVXDSMEB-UHFFFAOYSA-N 0.000 claims description 4
- BEWCNXNIQCLWHP-UHFFFAOYSA-N 2-(tert-butylamino)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(C)(C)C BEWCNXNIQCLWHP-UHFFFAOYSA-N 0.000 claims description 4
- KDAKDBASXBEFFK-UHFFFAOYSA-N 2-(tert-butylamino)ethyl prop-2-enoate Chemical compound CC(C)(C)NCCOC(=O)C=C KDAKDBASXBEFFK-UHFFFAOYSA-N 0.000 claims description 4
- LBSXSAXOLABXMF-UHFFFAOYSA-N 4-Vinylaniline Chemical compound NC1=CC=C(C=C)C=C1 LBSXSAXOLABXMF-UHFFFAOYSA-N 0.000 claims description 4
- GQWAOUOHRMHSHL-UHFFFAOYSA-N 4-ethenyl-n,n-dimethylaniline Chemical compound CN(C)C1=CC=C(C=C)C=C1 GQWAOUOHRMHSHL-UHFFFAOYSA-N 0.000 claims description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000004423 acyloxy group Chemical group 0.000 claims description 4
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- 125000002521 alkyl halide group Chemical group 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 239000004014 plasticizer Substances 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 4
- 125000001302 tertiary amino group Chemical group 0.000 claims description 4
- 125000006686 (C1-C24) alkyl group Chemical group 0.000 claims description 3
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 claims description 3
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 3
- 125000005041 acyloxyalkyl group Chemical group 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 3
- 125000004984 dialkylaminoalkoxy group Chemical group 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 125000005439 maleimidyl group Chemical class C1(C=CC(N1*)=O)=O 0.000 claims description 3
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims description 3
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 3
- 150000004760 silicates Chemical class 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 239000013008 thixotropic agent Substances 0.000 claims description 3
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical class [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000002966 varnish Substances 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 claims description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 2
- 235000000177 Indigofera tinctoria Nutrition 0.000 claims description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 239000005083 Zinc sulfide Substances 0.000 claims description 2
- 238000010669 acid-base reaction Methods 0.000 claims description 2
- 238000007259 addition reaction Methods 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 230000006229 amino acid addition Effects 0.000 claims description 2
- 125000002431 aminoalkoxy group Chemical group 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 150000004056 anthraquinones Chemical class 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 229910052980 cadmium sulfide Inorganic materials 0.000 claims description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 claims description 2
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 2
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 claims description 2
- 229940097275 indigo Drugs 0.000 claims description 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 claims description 2
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 claims description 2
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims description 2
- OBJNZHVOCNPSCS-UHFFFAOYSA-N naphtho[2,3-f]quinazoline Chemical class C1=NC=C2C3=CC4=CC=CC=C4C=C3C=CC2=N1 OBJNZHVOCNPSCS-UHFFFAOYSA-N 0.000 claims description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims description 2
- 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 claims description 2
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical group S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 229910000165 zinc phosphate Inorganic materials 0.000 claims description 2
- 229910052984 zinc sulfide Inorganic materials 0.000 claims description 2
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 claims description 2
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 2
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 claims 1
- MLMGJTAJUDSUKA-UHFFFAOYSA-N 2-ethenyl-1h-imidazole Chemical group C=CC1=NC=CN1 MLMGJTAJUDSUKA-UHFFFAOYSA-N 0.000 claims 1
- IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical group [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 claims 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 125000002843 carboxylic acid group Chemical group 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 150000004338 hydroxy anthraquinones Chemical class 0.000 claims 1
- 239000010954 inorganic particle Substances 0.000 claims 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 claims 1
- 229910001465 mixed metal phosphate Inorganic materials 0.000 claims 1
- 239000011146 organic particle Substances 0.000 claims 1
- 150000002979 perylenes Chemical class 0.000 claims 1
- 235000011007 phosphoric acid Nutrition 0.000 claims 1
- 150000003016 phosphoric acids Chemical class 0.000 claims 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims 1
- 229910052727 yttrium Inorganic materials 0.000 claims 1
- 239000000976 ink Substances 0.000 abstract description 6
- 239000004922 lacquer Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 57
- 239000011248 coating agent Substances 0.000 description 29
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 24
- 239000011347 resin Substances 0.000 description 22
- 229920005989 resin Polymers 0.000 description 22
- 238000000227 grinding Methods 0.000 description 21
- 239000002904 solvent Substances 0.000 description 20
- 239000002585 base Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 17
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 17
- 229920001577 copolymer Polymers 0.000 description 15
- 239000007787 solid Substances 0.000 description 13
- 238000005227 gel permeation chromatography Methods 0.000 description 12
- 239000003960 organic solvent Substances 0.000 description 12
- 229920000877 Melamine resin Polymers 0.000 description 10
- 239000010949 copper Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000011572 manganese Substances 0.000 description 9
- 238000007639 printing Methods 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 9
- 229910052723 transition metal Inorganic materials 0.000 description 9
- 239000004793 Polystyrene Substances 0.000 description 8
- 239000012964 benzotriazole Substances 0.000 description 8
- 238000001723 curing Methods 0.000 description 8
- 239000003446 ligand Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 150000003624 transition metals Chemical class 0.000 description 8
- 150000001350 alkyl halides Chemical group 0.000 description 7
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 7
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 125000005843 halogen group Chemical group 0.000 description 7
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- BUGISVZCMXHOHO-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]-2-[[1-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCC(CO)(CO)NC(=O)C(C)(C)N=NC(C)(C)C(=O)NC(CO)(CO)CO BUGISVZCMXHOHO-UHFFFAOYSA-N 0.000 description 1
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- CATWEXRJGNBIJD-UHFFFAOYSA-N n-tert-butyl-2-methylpropan-2-amine Chemical compound CC(C)(C)NC(C)(C)C CATWEXRJGNBIJD-UHFFFAOYSA-N 0.000 description 1
- ZPBSAMLXSQCSOX-UHFFFAOYSA-N naphthalene-1,3,6-trisulfonic acid Chemical compound OS(=O)(=O)C1=CC(S(O)(=O)=O)=CC2=CC(S(=O)(=O)O)=CC=C21 ZPBSAMLXSQCSOX-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
- RNVAPPWJCZTWQL-UHFFFAOYSA-N octadecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 RNVAPPWJCZTWQL-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- XQAABEDPVQWFPN-UHFFFAOYSA-N octyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=CC=CC3=N2)=C1O XQAABEDPVQWFPN-UHFFFAOYSA-N 0.000 description 1
- DMFXLIFZVRXRRR-UHFFFAOYSA-N octyl 3-[3-tert-butyl-5-(5-chlorobenzotriazol-2-yl)-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O DMFXLIFZVRXRRR-UHFFFAOYSA-N 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- SGNLDVYVSFANHW-UHFFFAOYSA-N pentane-2,4-dione;zirconium Chemical compound [Zr].CC(=O)CC(C)=O SGNLDVYVSFANHW-UHFFFAOYSA-N 0.000 description 1
- LLYCMZGLHLKPPU-UHFFFAOYSA-N perbromic acid Chemical class OBr(=O)(=O)=O LLYCMZGLHLKPPU-UHFFFAOYSA-N 0.000 description 1
- 230000008447 perception Effects 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical class OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 125000005544 phthalimido group Chemical group 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940068886 polyethylene glycol 300 Drugs 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- MCGNHPJOLQGCFY-UHFFFAOYSA-N pyridine-2,3-dicarboxylic acid pyridine-2,5-dicarboxylic acid Chemical compound OC(=O)c1ccc(nc1)C(O)=O.OC(=O)c1cccnc1C(O)=O MCGNHPJOLQGCFY-UHFFFAOYSA-N 0.000 description 1
- 150000003235 pyrrolidines Chemical class 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- KQYLUTYUZIVHND-UHFFFAOYSA-N tert-butyl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)C KQYLUTYUZIVHND-UHFFFAOYSA-N 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C09D153/00—Coating compositions based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/005—Modified block copolymers
-
- 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
- C09B67/006—Preparation of organic pigments
- C09B67/0063—Preparation of organic pigments of organic pigments with only macromolecular substances
-
- 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
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
- C09D11/037—Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
-
- 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
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- 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
- C09D11/324—Inkjet printing inks characterised by colouring agents containing carbon black
- C09D11/326—Inkjet printing inks characterised by colouring agents containing carbon black characterised by the pigment dispersant
-
- 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
- C09D153/00—Coating compositions based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D153/005—Modified block copolymers
-
- 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
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/45—Anti-settling agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2438/00—Living radical polymerisation
- C08F2438/02—Stable Free Radical Polymerisation [SFRP]; Nitroxide Mediated Polymerisation [NMP] for, e.g. using 2,2,6,6-tetramethylpiperidine-1-oxyl [TEMPO]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Paints Or Removers (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01810504 | 2001-05-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK6972002A3 true SK6972002A3 (en) | 2003-05-02 |
Family
ID=8183925
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK697-2002A SK6972002A3 (en) | 2001-05-21 | 2002-05-17 | Pigment composition containing dispersing agent based on modified block copolymers, process for producing thereof and use |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6849679B2 (de) |
| EP (1) | EP1275689B1 (de) |
| JP (1) | JP4307014B2 (de) |
| KR (1) | KR100866070B1 (de) |
| CN (1) | CN1282706C (de) |
| AR (1) | AR035980A1 (de) |
| AT (1) | ATE299908T1 (de) |
| AU (1) | AU784704B2 (de) |
| BR (1) | BR0201869B1 (de) |
| CA (1) | CA2387010A1 (de) |
| CZ (1) | CZ296348B6 (de) |
| DE (1) | DE60205068T2 (de) |
| ES (1) | ES2245724T3 (de) |
| MX (1) | MXPA02005079A (de) |
| SK (1) | SK6972002A3 (de) |
| TW (1) | TWI230175B (de) |
| ZA (1) | ZA200203956B (de) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200407363A (en) * | 2001-11-29 | 2004-05-16 | Ciba Sc Holding Ag | Pigment compositions with modified ATRP copolymer dispersants |
| EP1558658B1 (de) * | 2002-11-07 | 2012-12-19 | Rhodia Chimie | Copolymer mit kontrollierter struktur mit einem amphoteren oder zwitterionischen teil |
| FR2859209B1 (fr) * | 2003-08-29 | 2007-11-30 | Rhodia Chimie Sa | Copolymere a structure controlee presentant une partie amphotere ou zwitterionique |
| WO2004090030A1 (en) * | 2003-04-08 | 2004-10-21 | Ciba Specialty Chemicals Holding Inc. | Light stabilising polymer dispersants in pigment dispersions |
| EP1629054A1 (de) * | 2003-06-03 | 2006-03-01 | Ciba SC Holding AG | Verfahren zur herstellung von pigmentkonzentraten zur verwendung in strahlungshärtbaren beschichtungen |
| JP2005139251A (ja) * | 2003-11-05 | 2005-06-02 | Canon Inc | ブロック共重合体、それ含有するポリマー含有組成物、インク組成物、インク付与方法および装置 |
| KR100561409B1 (ko) * | 2003-12-23 | 2006-03-16 | 삼성전자주식회사 | 수계 시스템내 안료 입자를 위한 블록 공중합체 분산제,이를 포함한 잉크 조성물 |
| JP2006167674A (ja) * | 2004-12-20 | 2006-06-29 | Toyo Ink Mfg Co Ltd | 顔料分散剤 |
| CN100577692C (zh) * | 2005-01-11 | 2010-01-06 | 西巴特殊化学品控股有限公司 | 用受控自由基聚合方法制备的均聚物和共聚物的后改性方法 |
| US20060204732A1 (en) * | 2005-03-08 | 2006-09-14 | Fuji Photo Film Co., Ltd. | Ink composition, inkjet recording method, printed material, method of producing planographic printing plate, and planographic printing plate |
| JP5204371B2 (ja) * | 2005-06-06 | 2013-06-05 | 富士フイルム株式会社 | インクジェット記録用インク組成物およびこれを用いた平版印刷版の作製方法 |
| JP4799972B2 (ja) * | 2005-09-12 | 2011-10-26 | 富士フイルム株式会社 | インク組成物、インクジェット記録方法、平版印刷版の製造方法、及び平版印刷版 |
| DE602006010495D1 (de) * | 2005-09-27 | 2009-12-31 | Fujifilm Corp | Tintenzusammensetzung, Tintenstrahldruckverfahren, Herstellungsverfahren für eine Flachdruckplatte und Flachdruckplatte |
| JP4896502B2 (ja) * | 2005-11-22 | 2012-03-14 | 富士フイルム株式会社 | インク組成物、インクジェット記録方法、平版印刷版の製造方法、及び平版印刷版 |
| US7897322B2 (en) * | 2005-12-28 | 2011-03-01 | Fujifilm Corporation | Ink composition, inkjet recording method, producing method of planographic printing plate, and planographic printing plate |
| TW200730547A (en) * | 2006-01-03 | 2007-08-16 | Byk Chemie Gmbh | Copolymers comprising three segments of different ion density, processes for preparing them and use thereof |
| EP2022829B1 (de) * | 2006-04-21 | 2013-06-12 | Nippon Sheet Glass Company, Limited | Photolumineszierendes pigment, verfahren zur herstellung des pigments und das pigment enthaltende wässrige harzzusammensetzung |
| KR101416681B1 (ko) | 2006-07-06 | 2014-07-08 | 시바 홀딩 인크 | 전기영동 이동성 유기 착색제를 포함하는 캡슐화 분산액 |
| JP5425623B2 (ja) * | 2006-07-11 | 2014-02-26 | チバ ホールディング インコーポレーテッド | カラーフィルター組成物 |
| EP2058374B1 (de) * | 2006-08-29 | 2013-03-27 | Nippon Sheet Glass Company, Limited | Perlglanzpigment |
| DE102006048144A1 (de) * | 2006-10-10 | 2008-04-17 | Byk-Chemie Gmbh | Netz- und Dispergiermittel basierend auf Mischungen von strukturierten Copolymeren |
| DE102006062441A1 (de) * | 2006-12-27 | 2008-07-03 | Byk-Chemie Gmbh | Modifizierte Kammcopolymere |
| JP4793360B2 (ja) * | 2007-02-26 | 2011-10-12 | 大日本印刷株式会社 | カラーフィルタ用ネガ型レジスト組成物、およびこれを用いたカラーフィルタ、液晶表示装置 |
| WO2008130040A1 (ja) * | 2007-04-18 | 2008-10-30 | Nippon Sheet Glass Company, Limited | 光輝性顔料およびそれを用いた化粧用組成物 |
| CN101668819B (zh) * | 2007-04-27 | 2012-11-21 | 日本板硝子株式会社 | 光亮性颜料、含有其的光亮性涂料组合物及汽车外板涂敷物 |
| KR101386207B1 (ko) * | 2007-06-01 | 2014-04-21 | 주식회사 케이씨씨 | 안료 분산액 및 그의 제조방법 |
| KR101443928B1 (ko) * | 2007-06-21 | 2014-09-29 | 미쓰비시 가가꾸 가부시키가이샤 | 안료 분산액, 컬러 필터용 착색 조성물, 컬러 필터, 액정 표시 장치 및 유기 el 디스플레이 |
| US8270063B2 (en) | 2007-09-07 | 2012-09-18 | Basf Se | Encapsulated dispersions comprising electrophoretically mobile organic colorants |
| US8409708B2 (en) * | 2007-10-18 | 2013-04-02 | Nippon Sheet Glass Company, Limited | Bright pigment |
| CN102015911B (zh) | 2008-01-17 | 2015-11-25 | 巴斯夫欧洲公司 | 聚合毛发染料 |
| DE102008007713A1 (de) * | 2008-02-04 | 2009-08-06 | Byk-Chemie Gmbh | Netz- und Dispergiermittel |
| JP5374903B2 (ja) * | 2008-03-31 | 2013-12-25 | 大日本印刷株式会社 | カラーフィルタ用ネガ型レジスト組成物、カラーフィルタ及び液晶表示装置 |
| JP4835718B2 (ja) * | 2008-03-31 | 2011-12-14 | 大日本印刷株式会社 | カラーフィルタ用ネガ型レジスト組成物、カラーフィルタ及び液晶表示装置 |
| WO2009156277A1 (en) * | 2008-06-23 | 2009-12-30 | Basf Se | Pigment dispersants with modified copolymers |
| KR101252371B1 (ko) * | 2008-08-05 | 2013-04-08 | 고쿠리츠 다이가쿠 호진 교토 다이가쿠 | 안료 분산액, 블록 폴리머 및 그 제조방법 |
| JP4877352B2 (ja) * | 2008-08-26 | 2012-02-15 | 大日本印刷株式会社 | カラーフィルタ用ネガ型レジスト組成物、カラーフィルタ及び液晶表示装置 |
| JP4900346B2 (ja) * | 2008-08-27 | 2012-03-21 | 大日本印刷株式会社 | カラーフィルタ用顔料分散液、カラーフィルタ用ネガ型レジスト組成物、カラーフィルタ及び液晶表示装置 |
| JP4826614B2 (ja) * | 2008-09-30 | 2011-11-30 | 大日本印刷株式会社 | カラーフィルタ用顔料分散液、カラーフィルタ用ネガ型レジスト組成物、カラーフィルタ及び液晶表示装置 |
| DE102009040068A1 (de) | 2008-11-24 | 2010-05-27 | Byk-Chemie Gmbh | Zusammensetzungen umfassend Glycidylether-Copolymere |
| US8674006B2 (en) | 2009-01-19 | 2014-03-18 | BASF SE Ludwigshafen | Black pigment dispersion |
| WO2010108672A2 (de) * | 2009-03-25 | 2010-09-30 | Byk-Chemie Gmbh | Zusammensetzung umfassend stabile polyolmischungen |
| JP5001326B2 (ja) * | 2009-03-31 | 2012-08-15 | 大日本印刷株式会社 | カラーフィルタ用ネガ型レジスト組成物、カラーフィルタ及び液晶表示装置 |
| JP5625302B2 (ja) * | 2009-09-30 | 2014-11-19 | 大日本印刷株式会社 | カラーフィルター用青色顔料分散液、カラーフィルター用青色感光性樹脂組成物、カラーフィルター、及び液晶表示装置 |
| WO2011085775A1 (de) | 2009-12-22 | 2011-07-21 | Byk-Chemie Gmbh | Zusammensetzung umfassend stabile polyolmischungen |
| JP2012003225A (ja) | 2010-01-27 | 2012-01-05 | Fujifilm Corp | ソルダーレジスト用重合性組成物及びソルダーレジストパターンの形成方法 |
| US8459787B2 (en) * | 2010-10-29 | 2013-06-11 | Eastman Kodak Company | Aqueous inkjet printing fluid compositions |
| JP5417364B2 (ja) | 2011-03-08 | 2014-02-12 | 富士フイルム株式会社 | 固体撮像素子用硬化性組成物、並びに、これを用いた感光層、永久パターン、ウエハレベルレンズ、固体撮像素子、及び、パターン形成方法 |
| DE102011005493A1 (de) * | 2011-03-14 | 2012-09-20 | Evonik Rohmax Additives Gmbh | Estergruppen-umfassende Copolymere und deren Verwendung in Schmiermitteln |
| DE102011014250A1 (de) * | 2011-03-17 | 2012-09-20 | Clariant International Ltd. | Pulverlackzusammensetzung zum Strukturieren und Texturieren von Lackoberflächen |
| WO2013038974A1 (en) | 2011-09-14 | 2013-03-21 | Fujifilm Corporation | Colored radiation-sensitive composition for color filter, pattern forming method, color filter and method of producing the same, and solid-state image sensor |
| WO2013060708A1 (en) * | 2011-10-25 | 2013-05-02 | Basf Se | Use of comb or block copolymers as soil antiredeposition agents and soil release agents in laundry processes |
| JP5934664B2 (ja) | 2012-03-19 | 2016-06-15 | 富士フイルム株式会社 | 着色感放射線性組成物、着色硬化膜、カラーフィルタ、着色パターン形成方法、カラーフィルタの製造方法、固体撮像素子、及び画像表示装置 |
| JP5775479B2 (ja) | 2012-03-21 | 2015-09-09 | 富士フイルム株式会社 | 着色感放射線性組成物、着色硬化膜、カラーフィルタ、パターン形成方法、カラーフィルタの製造方法、固体撮像素子、及び画像表示装置 |
| SG11201504182RA (en) | 2012-11-30 | 2015-06-29 | Fujifilm Corp | Curable resin composition, production method of image sensor chip using the same, and image sensor chip |
| WO2014084289A1 (ja) | 2012-11-30 | 2014-06-05 | 富士フイルム株式会社 | 硬化性樹脂組成物、これを用いたイメージセンサチップの製造方法及びイメージセンサチップ |
| JP6170673B2 (ja) | 2012-12-27 | 2017-07-26 | 富士フイルム株式会社 | カラーフィルタ用組成物、赤外線透過フィルタ及びその製造方法、並びに赤外線センサー |
| CN105473628B (zh) | 2013-06-24 | 2019-04-12 | 比克化学股份有限公司 | 粘合增强添加剂和含有该添加剂的涂布组合物 |
| JP6162084B2 (ja) | 2013-09-06 | 2017-07-12 | 富士フイルム株式会社 | 着色組成物、硬化膜、カラーフィルタ、カラーフィルタの製造方法、固体撮像素子、画像表示装置、ポリマー、キサンテン色素 |
| CN105916895B (zh) * | 2014-01-17 | 2019-04-19 | 欧尼克斯荷兰有限公司 | 改善了开放时间的水性涂料组合物 |
| CN104387841A (zh) * | 2014-11-11 | 2015-03-04 | 合肥皖为电气设备工程有限责任公司 | 一种添加聚乙烯蜡的新型印刷油墨及其制作方法 |
| CN104387846A (zh) * | 2014-11-11 | 2015-03-04 | 合肥皖为电气设备工程有限责任公司 | 一种性价比高的印刷油墨及其制作方法 |
| WO2016122563A1 (en) | 2015-01-30 | 2016-08-04 | Hewlett-Packard Development Company, L.P. | Radiation curable binder dispersion |
| CN105237694B (zh) * | 2015-11-17 | 2018-06-29 | 深圳市长辉新材料科技有限公司 | 一种丙烯酸酯嵌段共聚物及其制备方法和应用 |
| WO2018127375A1 (en) | 2017-01-03 | 2018-07-12 | Byk-Chemie Gmbh | (meth)acrylic copolymers as rheological additives in drilling fluids and drilling fluids comprising such copolymers |
| US11591482B2 (en) | 2017-07-20 | 2023-02-28 | Sun Chemical Corporation | High speed water-based inks containing alcohol tolerant latexes |
| KR101896967B1 (ko) | 2017-08-21 | 2018-09-19 | 아이씨이아이우방(주) | 침염 연속식 황화 염색용 분산균염제 조성물, 이를 이용한 분산균염제 및 이의 제조방법 |
| CN111344319B (zh) * | 2017-11-15 | 2022-12-23 | 毕克化学有限公司 | 嵌段共聚物 |
| WO2019174021A1 (en) * | 2018-03-16 | 2019-09-19 | Dow Global Technologies Llc | Aqueous coating compositions and methods for improving freeze/thaw stability of aqueous coating compositions |
| EP4177396A1 (de) * | 2018-09-28 | 2023-05-10 | Daikin Industries, Ltd. | Oberflächenbehandlungsmittel enthaltend ein nichtfluoriertes blockcopolymer |
| TWI689531B (zh) * | 2018-12-20 | 2020-04-01 | 財團法人紡織產業綜合研究所 | 耐隆纖維及耐隆的製作方法 |
| CN113692431B (zh) * | 2019-04-18 | 2023-07-04 | 巴斯夫欧洲公司 | 胺分散剂 |
| EP3959274B1 (de) * | 2019-04-26 | 2023-06-07 | BYK-Chemie GmbH | Nichtpigmentierte dispergiermittelzusammensetzung |
| JP7299069B2 (ja) * | 2019-05-29 | 2023-06-27 | サカタインクス株式会社 | カラーフィルター用顔料分散組成物及びカラーフィルター用顔料分散レジスト組成物 |
| JP7338300B2 (ja) * | 2019-07-30 | 2023-09-05 | セイコーエプソン株式会社 | 高分子分散剤、色材分散液及びインク組成物 |
| JP7237166B2 (ja) | 2019-08-29 | 2023-03-10 | 富士フイルム株式会社 | 組成物、膜、近赤外線カットフィルタ、パターン形成方法、積層体、固体撮像素子、赤外線センサ、画像表示装置、カメラモジュール、及び、化合物 |
| WO2022015323A1 (en) | 2020-07-17 | 2022-01-20 | Hewlett-Packard Development Company, L.P. | White inkjet ink |
| CN113308169B (zh) * | 2021-05-13 | 2022-06-17 | 浙江省海洋开发研究院 | 一种基于石墨烯分散性好的水性环氧富锌涂料 |
| CN119081486A (zh) * | 2024-09-27 | 2024-12-06 | 广东嘉盛环保高新材料股份有限公司 | 一种高分子纳米隔热颜色水性面漆及其制备方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4812517A (en) * | 1987-12-28 | 1989-03-14 | E. I. Du Pont De Nemours And Company | Dispersants resistant to color change |
| JP2673114B2 (ja) * | 1995-04-21 | 1997-11-05 | 東洋インキ製造株式会社 | 着色剤組成物 |
| DE69829588T2 (de) | 1997-01-10 | 2006-01-19 | E.I. Du Pont De Nemours And Co., Wilmington | Farblose wässrige Ammoniumsulfidlösung |
| JPH11209558A (ja) * | 1998-01-28 | 1999-08-03 | Dainippon Printing Co Ltd | 光重合性顔料分散剤、感光性着色組成物及び遮光層用組成物 |
| SG82601A1 (en) | 1998-03-09 | 2001-08-21 | Ciba Sc Holding Ag | 1-alkoxy-polyalkyl-piperidine derivatives and their use as polymerization regulators |
| CA2341384A1 (en) | 1998-09-29 | 2000-04-06 | Ciba Specialty Chemicals Holding Inc. | Process for the preparation of polymers containing n->o terminal groups |
| US6204319B1 (en) * | 1998-10-30 | 2001-03-20 | E.I. Du Pont De Nemours And Company | Aqueous coating compositions |
| DE69941226D1 (de) | 1998-12-31 | 2009-09-17 | Ciba Holding Inc | Pigmentzusammensetzung enthaltend atrp polymere |
| US6316564B1 (en) * | 1999-10-07 | 2001-11-13 | E. I. Du Pont De Nemours And Company | Acrylic block copolymer pigment dispersants containing heterocyclic groups |
-
2002
- 2002-04-23 US US10/128,836 patent/US6849679B2/en not_active Expired - Lifetime
- 2002-05-14 AT AT02405386T patent/ATE299908T1/de not_active IP Right Cessation
- 2002-05-14 ES ES02405386T patent/ES2245724T3/es not_active Expired - Lifetime
- 2002-05-14 DE DE60205068T patent/DE60205068T2/de not_active Revoked
- 2002-05-14 EP EP02405386A patent/EP1275689B1/de not_active Revoked
- 2002-05-17 CA CA002387010A patent/CA2387010A1/en not_active Abandoned
- 2002-05-17 SK SK697-2002A patent/SK6972002A3/sk unknown
- 2002-05-17 AR ARP020101837A patent/AR035980A1/es active IP Right Grant
- 2002-05-17 ZA ZA200203956A patent/ZA200203956B/xx unknown
- 2002-05-20 CZ CZ20021755A patent/CZ296348B6/cs not_active IP Right Cessation
- 2002-05-20 CN CNB021201242A patent/CN1282706C/zh not_active Expired - Lifetime
- 2002-05-20 TW TW091110523A patent/TWI230175B/zh not_active IP Right Cessation
- 2002-05-20 BR BRPI0201869-1A patent/BR0201869B1/pt not_active IP Right Cessation
- 2002-05-21 KR KR1020020028230A patent/KR100866070B1/ko not_active Expired - Lifetime
- 2002-05-21 JP JP2002145725A patent/JP4307014B2/ja not_active Expired - Lifetime
- 2002-05-21 AU AU42377/02A patent/AU784704B2/en not_active Ceased
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| AR035980A1 (es) | 2004-07-28 |
| AU4237702A (en) | 2002-11-28 |
| KR100866070B1 (ko) | 2008-10-31 |
| TWI230175B (en) | 2005-04-01 |
| CA2387010A1 (en) | 2002-11-21 |
| CZ296348B6 (cs) | 2006-02-15 |
| MXPA02005079A (es) | 2002-12-05 |
| CN1386794A (zh) | 2002-12-25 |
| EP1275689B1 (de) | 2005-07-20 |
| ES2245724T3 (es) | 2006-01-16 |
| KR20020089192A (ko) | 2002-11-29 |
| US20030105201A1 (en) | 2003-06-05 |
| CN1282706C (zh) | 2006-11-01 |
| EP1275689A1 (de) | 2003-01-15 |
| AU784704B2 (en) | 2006-06-01 |
| ZA200203956B (en) | 2003-03-13 |
| JP2003049110A (ja) | 2003-02-21 |
| DE60205068D1 (de) | 2005-08-25 |
| ATE299908T1 (de) | 2005-08-15 |
| US6849679B2 (en) | 2005-02-01 |
| CZ20021755A3 (cs) | 2003-01-15 |
| DE60205068T2 (de) | 2006-06-01 |
| JP4307014B2 (ja) | 2009-08-05 |
| BR0201869A (pt) | 2003-03-25 |
| BR0201869B1 (pt) | 2012-06-26 |
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