NL8702089A - Dispergeermiddel. - Google Patents

Dispergeermiddel. Download PDF

Info

Publication number: NL8702089A
Authority: NL; Netherlands
Prior art keywords: monomers; group; mol; methacrylate; dispersant
Prior art date: 1987-09-04

Application number

NL8702089A

Other languages

English (en)

Dutch (nl)

Original Assignee

Efka Chemicals Bv

Priority date (The priority date 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 date listed.)

1987-09-04

Filing date

1987-09-04

Publication date

1989-04-03

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=19850552&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NL8702089(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1987-09-04 Application filed by Efka Chemicals Bv filed Critical Efka Chemicals Bv

1987-09-04 Priority to NL8702089A priority Critical patent/NL8702089A/nl

1988-08-30 Priority to DE3885567T priority patent/DE3885567T3/de

1988-08-30 Priority to AT88201843T priority patent/ATE97143T1/de

1988-08-30 Priority to ES88201843T priority patent/ES2067466T5/es

1988-08-30 Priority to EP88201843A priority patent/EP0311157B2/de

1988-08-31 Priority to CA000576206A priority patent/CA1339180C/en

1988-09-02 Priority to JP63221205A priority patent/JP2843985B2/ja

1989-03-02 Priority to KR1019890002635A priority patent/KR960006215B1/ko

1989-04-03 Publication of NL8702089A publication Critical patent/NL8702089A/nl

1995-06-07 Priority to US08/482,008 priority patent/US5688858A/en

Links

239000000178 monomer Substances 0.000 claims abstract description 80
239000002270 dispersing agent Substances 0.000 claims abstract description 50
229920000642 polymer Polymers 0.000 claims abstract description 27
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 19
125000000217 alkyl group Chemical group 0.000 claims abstract description 13
238000006116 polymerization reaction Methods 0.000 claims abstract description 11
150000003839 salts Chemical class 0.000 claims abstract description 8
NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 7
230000008878 coupling Effects 0.000 claims abstract description 7
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 7
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 7
238000004132 cross linking Methods 0.000 claims abstract description 4
238000006880 cross-coupling reaction Methods 0.000 claims abstract description 3
125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 3
239000000049 pigment Substances 0.000 claims description 25
150000001875 compounds Chemical class 0.000 claims description 17
239000006185 dispersion Substances 0.000 claims description 16
238000000576 coating method Methods 0.000 claims description 12
239000000976 ink Substances 0.000 claims description 10
239000007787 solid Substances 0.000 claims description 10
239000007795 chemical reaction product Substances 0.000 claims description 8
239000007788 liquid Substances 0.000 claims description 8
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 6
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 5
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 4
KZTWONRVIPPDKH-UHFFFAOYSA-N 2-(piperidin-1-yl)ethanol Chemical compound OCCN1CCCCC1 KZTWONRVIPPDKH-UHFFFAOYSA-N 0.000 claims description 4
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims description 3
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 3
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 3
VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 claims description 3
GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 claims description 3
RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 claims description 3
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims description 3
HXXJMMLIEYAFOZ-UHFFFAOYSA-N (1-methylpiperidin-2-yl)methanol Chemical compound CN1CCCCC1CO HXXJMMLIEYAFOZ-UHFFFAOYSA-N 0.000 claims description 2
YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 claims description 2
BDHGFCVQWMDIQX-UHFFFAOYSA-N 1-ethenyl-2-methylimidazole Chemical compound CC1=NC=CN1C=C BDHGFCVQWMDIQX-UHFFFAOYSA-N 0.000 claims description 2
ZFDABCDCTKLGOK-UHFFFAOYSA-N 1-piperidin-1-ylpropan-2-amine Chemical compound CC(N)CN1CCCCC1 ZFDABCDCTKLGOK-UHFFFAOYSA-N 0.000 claims description 2
VMRYMOMQCYSPHS-UHFFFAOYSA-N 2-(azepan-1-yl)ethanol Chemical compound OCCN1CCCCCC1 VMRYMOMQCYSPHS-UHFFFAOYSA-N 0.000 claims description 2
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 2
KKFDCBRMNNSAAW-UHFFFAOYSA-N 2-(morpholin-4-yl)ethanol Chemical compound OCCN1CCOCC1 KKFDCBRMNNSAAW-UHFFFAOYSA-N 0.000 claims description 2
DHYLZDVDOQLEAQ-UHFFFAOYSA-N 2-O-methylcytosine Chemical compound COC1=NC=CC(N)=N1 DHYLZDVDOQLEAQ-UHFFFAOYSA-N 0.000 claims description 2
PQAMFDRRWURCFQ-UHFFFAOYSA-N 2-ethyl-1h-imidazole Chemical compound CCC1=NC=CN1 PQAMFDRRWURCFQ-UHFFFAOYSA-N 0.000 claims description 2
WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims description 2
AMSDWLOANMAILF-UHFFFAOYSA-N 2-imidazol-1-ylethanol Chemical compound OCCN1C=CN=C1 AMSDWLOANMAILF-UHFFFAOYSA-N 0.000 claims description 2
LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 claims description 2
ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 claims description 2
WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 claims description 2
CJNRGSHEMCMUOE-UHFFFAOYSA-N 2-piperidin-1-ylethanamine Chemical compound NCCN1CCCCC1 CJNRGSHEMCMUOE-UHFFFAOYSA-N 0.000 claims description 2
FUOZJYASZOSONT-UHFFFAOYSA-N 2-propan-2-yl-1h-imidazole Chemical compound CC(C)C1=NC=CN1 FUOZJYASZOSONT-UHFFFAOYSA-N 0.000 claims description 2
XPQIPUZPSLAZDV-UHFFFAOYSA-N 2-pyridylethylamine Chemical compound NCCC1=CC=CC=N1 XPQIPUZPSLAZDV-UHFFFAOYSA-N 0.000 claims description 2
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 2
KDHWOCLBMVSZPG-UHFFFAOYSA-N 3-imidazol-1-ylpropan-1-amine Chemical compound NCCCN1C=CN=C1 KDHWOCLBMVSZPG-UHFFFAOYSA-N 0.000 claims description 2
UIKUBYKUYUSRSM-UHFFFAOYSA-N 3-morpholinopropylamine Chemical compound NCCCN1CCOCC1 UIKUBYKUYUSRSM-UHFFFAOYSA-N 0.000 claims description 2
FVZXYJDGVYLMDB-UHFFFAOYSA-N 3-pyridin-2-ylpropan-1-ol Chemical compound OCCCC1=CC=CC=N1 FVZXYJDGVYLMDB-UHFFFAOYSA-N 0.000 claims description 2
ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 claims description 2
KZHGPDSVHSDCMX-UHFFFAOYSA-N 6-methoxy-1,3-benzothiazol-2-amine Chemical compound COC1=CC=C2N=C(N)SC2=C1 KZHGPDSVHSDCMX-UHFFFAOYSA-N 0.000 claims description 2
CMVNWVONJDMTSH-UHFFFAOYSA-N 7-bromo-2-methyl-1h-quinazolin-4-one Chemical compound C1=CC(Br)=CC2=NC(C)=NC(O)=C21 CMVNWVONJDMTSH-UHFFFAOYSA-N 0.000 claims description 2
KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims description 2
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 2
239000002202 Polyethylene glycol Substances 0.000 claims description 2
IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 claims description 2
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 2
LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 claims description 2
RWIVICVCHVMHMU-UHFFFAOYSA-N n-aminoethylmorpholine Chemical compound NCCN1CCOCC1 RWIVICVCHVMHMU-UHFFFAOYSA-N 0.000 claims description 2
KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 claims description 2
HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 claims description 2
229920001223 polyethylene glycol Polymers 0.000 claims description 2
229920001451 polypropylene glycol Polymers 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 claims description 2
TXQWFIVRZNOPCK-UHFFFAOYSA-N pyridin-4-ylmethanamine Chemical compound NCC1=CC=NC=C1 TXQWFIVRZNOPCK-UHFFFAOYSA-N 0.000 claims description 2
HBCQSNAFLVXVAY-UHFFFAOYSA-N pyrimidine-2-thiol Chemical compound SC1=NC=CC=N1 HBCQSNAFLVXVAY-UHFFFAOYSA-N 0.000 claims description 2
XLSZMDLNRCVEIJ-UHFFFAOYSA-N 4-methylimidazole Chemical compound CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 claims 2
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims 1
ZXTHWIZHGLNEPG-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC=C1 ZXTHWIZHGLNEPG-UHFFFAOYSA-N 0.000 claims 1
BXGYBSJAZFGIPX-UHFFFAOYSA-N 2-pyridin-2-ylethanol Chemical compound OCCC1=CC=CC=N1 BXGYBSJAZFGIPX-UHFFFAOYSA-N 0.000 claims 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims 1
KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 claims 1
XBRDBODLCHKXHI-UHFFFAOYSA-N epolamine Chemical compound OCCN1CCCC1 XBRDBODLCHKXHI-UHFFFAOYSA-N 0.000 claims 1
ZNAOFAIBVOMLPV-UHFFFAOYSA-N hexadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(C)=C ZNAOFAIBVOMLPV-UHFFFAOYSA-N 0.000 claims 1
MYSWGNHLJGOCPT-UHFFFAOYSA-N methyl prop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C=C MYSWGNHLJGOCPT-UHFFFAOYSA-N 0.000 claims 1
239000011230 binding agent Substances 0.000 description 10
239000000203 mixture Substances 0.000 description 8
239000002904 solvent Substances 0.000 description 6
239000000047 product Substances 0.000 description 5
238000010168 coupling process Methods 0.000 description 4
238000005859 coupling reaction Methods 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
-1 butyl ethyl Chemical group 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000009826 distribution Methods 0.000 description 3
238000005189 flocculation Methods 0.000 description 3
230000016615 flocculation Effects 0.000 description 3
239000001023 inorganic pigment Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000012860 organic pigment Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
238000003795 desorption Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
239000004922 lacquer Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
239000003973 paint Substances 0.000 description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
230000008569 process Effects 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
239000008096 xylene Substances 0.000 description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
WRXNJTBODVGDRY-UHFFFAOYSA-N 2-pyrrolidin-1-ylethanamine Chemical compound NCCN1CCCC1 WRXNJTBODVGDRY-UHFFFAOYSA-N 0.000 description 1
VYDWQPKRHOGLPA-UHFFFAOYSA-N 5-nitroimidazole Chemical compound [O-][N+](=O)C1=CN=CN1 VYDWQPKRHOGLPA-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
238000012662 bulk polymerization Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000003999 initiator Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
235000013980 iron oxide Nutrition 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
229940119545 isobornyl methacrylate Drugs 0.000 description 1
238000005259 measurement Methods 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
125000003367 polycyclic group Chemical group 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
238000007348 radical reaction Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
239000002002 slurry Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000006467 substitution reaction Methods 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
229920001567 vinyl ester resin Polymers 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- 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
- 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
- C08F226/00—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 a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F226/06—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 a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
- 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
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0084—Dispersions of dyes
- C09B67/0085—Non common dispersing agents
- C09B67/009—Non common dispersing agents polymeric dispersing agent
- 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
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/16—Amines or polyamines

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)

NL8702089A 1987-04-09 1987-09-04 Dispergeermiddel. NL8702089A (nl)

Priority Applications (9)

Application Number	Priority Date	Filing Date	Title
NL8702089A NL8702089A (nl)	1987-09-04	1987-09-04	Dispergeermiddel.
DE3885567T DE3885567T3 (de)	1987-09-04	1988-08-30	Dispergiermittel.
AT88201843T ATE97143T1 (de)	1987-09-04	1988-08-30	Dispergiermittel.
ES88201843T ES2067466T5 (es)	1987-09-04	1988-08-30	Dispersante.
EP88201843A EP0311157B2 (de)	1987-09-04	1988-08-30	Dispergiermittel
CA000576206A CA1339180C (en)	1987-09-04	1988-08-31	Dispersant
JP63221205A JP2843985B2 (ja)	1987-09-04	1988-09-02	重合体分散剤
KR1019890002635A KR960006215B1 (ko)	1987-09-04	1989-03-02	분산제
US08/482,008 US5688858A (en)	1987-04-09	1995-06-07	Dispersant

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8702089		1987-09-04
NL8702089A NL8702089A (nl)	1987-09-04	1987-09-04	Dispergeermiddel.

Publications (1)

Publication Number	Publication Date
NL8702089A true NL8702089A (nl)	1989-04-03

Family

ID=19850552

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8702089A NL8702089A (nl)	1987-04-09	1987-09-04	Dispergeermiddel.

Country Status (9)

Country	Link
US (1)	US5688858A (de)
EP (1)	EP0311157B2 (de)
JP (1)	JP2843985B2 (de)
KR (1)	KR960006215B1 (de)
AT (1)	ATE97143T1 (de)
CA (1)	CA1339180C (de)
DE (1)	DE3885567T3 (de)
ES (1)	ES2067466T5 (de)
NL (1)	NL8702089A (de)

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US5425900A (en) *	1990-12-27	1995-06-20	Efka-Chemicals B.V.	Dispersing agents, their use and solids coated therewith
EP0520586B1 (de) *	1991-06-26	1996-09-11	Efka-Chemicals B.V.	Dispergiermittel, ihre Verwendung und damit beschichtete Feststoffe
US5264481A (en) *	1991-11-22	1993-11-23	Westvaco Corporation	Hydroxyacrylic modified inks
DE4218539A1 (de) *	1992-06-05	1993-12-09	Basf Ag	Polymere, katalytisch wirksame Verbindungen, ihre Herstellung sowie ihre Verwendung als Katalysatoren bei der Herstellung von Urethdiongruppen enthaltenden Polyisocyanaten
DE4445498A1 (de) *	1994-12-20	1996-06-27	Roehm Gmbh	Universell verträgliche Pigmentdispergatoren
US5527614A (en) *	1994-12-21	1996-06-18	Basf Corporation	Pigment dispersants with primary amine functionality suitable for use in cathodic electrocoat compositions
DE19721728C2 (de) *	1997-05-24	2001-07-12	Byk Chemie Gmbh	Dispergiermittel für Pigmente oder Füllstoffe auf der Basis von Acrylsäurealkylester-Polymeren, Verwendung und Verfahren zur Herstellung
DE19732251B4 (de) *	1997-07-26	2004-07-29	Byk-Chemie Gmbh	Versalzungsprodukte von Polyaminen und deren Einsatz als Dispergiermittel für Pigmente und Füllstoffe
DE19904603A1 (de)	1999-02-05	2000-08-10	Goldschmidt Ag Th	Aminoxidgruppen enthaltende Maleinsäureanhydrid-Copolymere und ihre Verwendung als Dispergiermittel für Pigmente oder Füllstoffe
DE19941031A1 (de) *	1999-08-28	2001-03-01	Byk Chemie Gmbh	Verzweigte, Imidazolgruppen enthaltende Polymere, sowie deren Herstellung und Verwendung
US6586552B2 (en) *	2001-04-09	2003-07-01	E. I. Du Pont De Nemours And Company	Aminoazole-blocked isocyanate components
US6956084B2 (en)	2001-10-04	2005-10-18	Bridgestone Corporation	Nano-particle preparation and applications
DE10232908A1 (de)	2002-07-19	2004-01-29	Goldschmidt Ag	Verwendung organfunktionell modifizierter, Phenylderivate enthaltender Polysiloxane als Dispergier- und Netzmittel für Füllstoffe und Pigmente in wässrigen Pigmentpasten und Farb- oder Lackformulierungen
JP2005240000A (ja) *	2003-06-23	2005-09-08	Nippon Shokubai Co Ltd	顔料分散組成物及び感光性樹脂組成物
DE502004000446D1 (de)	2004-02-20	2006-05-24	Goldschmidt Gmbh	Verfahren zur Herstellung von homogenen, lagerstabilen Pasten, Farben, Lacken unter Mitverwendung ionischer Flüssigkeiten als Dispergierhilfsmittel
JP4803029B2 (ja)	2004-04-30	2011-10-26	株式会社湯山製作所	薬品供給システム
DE102004041536A1 (de) *	2004-08-27	2006-03-02	Merck Patent Gmbh	Verwendung von statistischen Copolymeren
KR101121761B1 (ko) *	2004-11-23	2012-03-23	세종대학교산학협력단	안료 또는 비수용성 염료의 분산 안정성을 증진시키는분산제의 제조방법 및 그를 이용하여 제조된 분산액
US7910022B2 (en)	2006-09-15	2011-03-22	Performance Indicator, Llc	Phosphorescent compositions for identification
US20060172135A1 (en)	2004-12-20	2006-08-03	Satish Agrawal	Layered envirochromic materials, applications and methods of preparation thereof
DE102005003299A1 (de)	2005-01-24	2006-07-27	Goldschmidt Gmbh	Nanopartikel für die Herstellung von Polyurethanschaum
JP4963803B2 (ja) *	2005-07-01	2012-06-27	富士フイルム株式会社	インク組成物、画像形成方法及び印刷物
BRPI0710724A2 (pt) *	2006-04-26	2012-01-31	Basf Se	método para aplicar um revestimento de controle de corrosão a uma superfìcie metálica, artigo conformado, copolìmero, e, preparação para aplicar um revestimento de controle de corrosão a uma superfìcie metálica
KR101472867B1 (ko) *	2006-06-02	2014-12-15	후지필름 가부시키가이샤	안료 분산 조성물, 광경화성 조성물, 이것을 사용하여제조된 컬러필터 및 컬러필터의 제조방법
US7547894B2 (en)	2006-09-15	2009-06-16	Performance Indicator, L.L.C.	Phosphorescent compositions and methods for identification using the same
ES2308901B1 (es) *	2006-09-22	2009-10-30	Consejo Superior De Investigaciones Cientificas	Sistemas que contienen nanoparticulas magneticas y polimeros, como nanocomposites y ferrofluidos, y sus aplicaciones.
JP5123539B2 (ja)	2007-03-06	2013-01-23	大日精化工業株式会社	共重合体およびその使用
CN101677937A (zh) *	2007-04-05	2010-03-24	巴斯夫欧洲公司	包含所选共聚物的防晒剂和个人护理组合物
EP2152230A2 (de) *	2007-04-05	2010-02-17	Basf Se	Sonnenschutzzusammensetzungen mit einem random-terpolymer
US7842128B2 (en)	2007-09-13	2010-11-30	Performance Indicatior LLC	Tissue marking compositions
US8039193B2 (en)	2007-09-13	2011-10-18	Performance Indicator Llc	Tissue markings and methods for reversibly marking tissue employing the same
DE102007045230A1 (de) *	2007-09-21	2009-04-09	Clariant International Limited	Polycarboxylatether als Dispergiermittel für anorganische Pigmentformulierungen
US8772371B2 (en)	2008-05-09	2014-07-08	Basf Se	Pearlescent pigments coated with a metal oxide/hydroxide layer and an acrylic copolymer
US20100104610A1 (en) *	2008-10-01	2010-04-29	Dueva-Koganov Olga V	Color cosmetics comprising a random terpolymer
US8501053B2 (en)	2008-10-02	2013-08-06	Basf Se	Multi color, photoactive, color changing compositions and UV dosimeters
US20100129303A1 (en) *	2008-10-17	2010-05-27	Dueva-Koganov Olga V	Sunscreen and personal care compositions comprising a random terpolymer
DE102012000414B4 (de)	2012-01-12	2014-03-20	Thyssenkrupp Rasselstein Gmbh	Verfahren zur Passivierung von Weißblech, sowie verzinntes Stahlband oder -blech
WO2019092036A1 (de)	2017-11-07	2019-05-16	Clariant Plastics & Coatings Ltd	Dispergiermittel für pigmente in nicht wässrigen farbmittelpräparationen

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DE945091C (de) *	1953-08-30	1956-06-28	Basf Ag	Schutzkolloide, Emulgier- bzw. Dispergiermittel
US2721852A (en) *	1954-02-05	1955-10-25	Eastman Kodak Co	Interpolymers of vinylpyridines or vinylquinolines, acrylic esters, acrylic amides and styrenes, and hydrosols thereof
GB883750A (en) *	1958-10-14	1961-12-06	Kurashiki Rayon Kk	Method of manufacturing stable polymerized emulsion
FR1250783A (fr) *	1959-01-28	1961-01-13	Basf Ag	Dispersions aqueuses, stables, et procédé pour leur production
US4302561A (en) *	1980-07-07	1981-11-24	Ppg Industries, Inc.	Pigment dispersants for coating compositions
JPS6092360A (ja) *	1983-10-27	1985-05-23	Kansai Paint Co Ltd	水性顔料分散液
JPS60188473A (ja) *	1984-03-08	1985-09-25	Kansai Paint Co Ltd	水性顔料分散液
US5134187A (en) *	1987-06-26	1992-07-28	Kansai Paint Co., Ltd.	Cationic aqueous pigment dispersion

1987
- 1987-09-04 NL NL8702089A patent/NL8702089A/nl not_active Application Discontinuation
1988
- 1988-08-30 ES ES88201843T patent/ES2067466T5/es not_active Expired - Lifetime
- 1988-08-30 AT AT88201843T patent/ATE97143T1/de not_active IP Right Cessation
- 1988-08-30 DE DE3885567T patent/DE3885567T3/de not_active Expired - Lifetime
- 1988-08-30 EP EP88201843A patent/EP0311157B2/de not_active Expired - Lifetime
- 1988-08-31 CA CA000576206A patent/CA1339180C/en not_active Expired - Fee Related
- 1988-09-02 JP JP63221205A patent/JP2843985B2/ja not_active Expired - Lifetime
1989
- 1989-03-02 KR KR1019890002635A patent/KR960006215B1/ko not_active IP Right Cessation
1995
- 1995-06-07 US US08/482,008 patent/US5688858A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP0311157B2 (de)	2001-05-23
JPH01164429A (ja)	1989-06-28
CA1339180C (en)	1997-07-29
DE3885567D1 (de)	1993-12-16
EP0311157A1 (de)	1989-04-12
ES2067466T3 (es)	1995-04-01
JP2843985B2 (ja)	1999-01-06
DE3885567T2 (de)	1994-03-24
DE3885567T3 (de)	2001-10-18
KR900014027A (ko)	1990-10-22
ATE97143T1 (de)	1993-11-15
US5688858A (en)	1997-11-18
EP0311157B1 (de)	1993-11-10
KR960006215B1 (ko)	1996-05-11
ES2067466T5 (es)	2001-10-16

Legal Events

Date	Code	Title	Description
1989-04-03	A1B	A search report has been drawn up
1990-05-01	BV	The patent application has lapsed

Publication	Publication Date	Title
NL8702089A (nl)	1989-04-03	Dispergeermiddel.
EP2115023B1 (de)	2012-01-04	Polyamin-polyacrylat-dispergiermittel
EP1155060B1 (de)	2009-08-05	Pigmentzusammensetzung enthaltend atrp polymere
JP5164835B2 (ja)	2013-03-21	分散剤およびその組成物
KR101252371B1 (ko)	2013-04-08	안료 분산액, 블록 폴리머 및 그 제조방법
JP2019056126A (ja)	2019-04-11	縮合芳香族イミドアンカー基を有するアクリル系分散剤
TWI734738B (zh)	2021-08-01	具有提升化學及熱穩定性之含多胺基的高分子分散劑
MXPA02003499A (es)	2002-09-02	Dispersantes de pigmentos con copolimeros en bloque acrilicos que contienen grupos heterociclicos.
KR101858681B1 (ko)	2018-05-16	분산제 조성물
KR20200103729A (ko)	2020-09-02	스티렌 말레아미드 블록 공중합체 안료 분산제
JP2010528146A (ja)	2010-08-19	グラフトコポリマーおよびその組成物
MXPA01005950A (en)	2001-12-13	Pigment composition containing atrp polymers