KR900014027A - 분산제 - Google Patents
분산제 Download PDFInfo
- Publication number
- KR900014027A KR900014027A KR1019890002635A KR890002635A KR900014027A KR 900014027 A KR900014027 A KR 900014027A KR 1019890002635 A KR1019890002635 A KR 1019890002635A KR 890002635 A KR890002635 A KR 890002635A KR 900014027 A KR900014027 A KR 900014027A
- Authority
- KR
- South Korea
- Prior art keywords
- monomers
- dispersant
- methacrylate
- group
- imidazole
- Prior art date
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- 239000002270 dispersing agent Substances 0.000 title claims 21
- 239000000178 monomer Substances 0.000 claims 22
- 239000000049 pigment Substances 0.000 claims 5
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N 4-methylimidazole Chemical compound CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 claims 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 3
- 239000007788 liquid Substances 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- KZTWONRVIPPDKH-UHFFFAOYSA-N 2-(piperidin-1-yl)ethanol Chemical compound OCCN1CCCCC1 KZTWONRVIPPDKH-UHFFFAOYSA-N 0.000 claims 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 2
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 claims 2
- KDHWOCLBMVSZPG-UHFFFAOYSA-N 3-imidazol-1-ylpropan-1-amine Chemical compound NCCCN1C=CN=C1 KDHWOCLBMVSZPG-UHFFFAOYSA-N 0.000 claims 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 2
- 230000008878 coupling Effects 0.000 claims 2
- 239000006185 dispersion Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- 238000006116 polymerization reaction Methods 0.000 claims 2
- 239000007787 solid Substances 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- HXXJMMLIEYAFOZ-UHFFFAOYSA-N (1-methylpiperidin-2-yl)methanol Chemical compound CN1CCCCC1CO HXXJMMLIEYAFOZ-UHFFFAOYSA-N 0.000 claims 1
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 claims 1
- BDHGFCVQWMDIQX-UHFFFAOYSA-N 1-ethenyl-2-methylimidazole Chemical compound CC1=NC=CN1C=C BDHGFCVQWMDIQX-UHFFFAOYSA-N 0.000 claims 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims 1
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims 1
- NUIPOEWADWHGSP-UHFFFAOYSA-N 1-hydroxypropyl 2-methylprop-2-enoate Chemical compound CCC(O)OC(=O)C(C)=C NUIPOEWADWHGSP-UHFFFAOYSA-N 0.000 claims 1
- ZFDABCDCTKLGOK-UHFFFAOYSA-N 1-piperidin-1-ylpropan-2-amine Chemical compound CC(N)CN1CCCCC1 ZFDABCDCTKLGOK-UHFFFAOYSA-N 0.000 claims 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims 1
- DHYLZDVDOQLEAQ-UHFFFAOYSA-N 2-O-methylcytosine Chemical compound COC1=NC=CC(N)=N1 DHYLZDVDOQLEAQ-UHFFFAOYSA-N 0.000 claims 1
- PQAMFDRRWURCFQ-UHFFFAOYSA-N 2-ethyl-1h-imidazole Chemical compound CCC1=NC=CN1 PQAMFDRRWURCFQ-UHFFFAOYSA-N 0.000 claims 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims 1
- 229940095095 2-hydroxyethyl acrylate Drugs 0.000 claims 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 claims 1
- AMSDWLOANMAILF-UHFFFAOYSA-N 2-imidazol-1-ylethanol Chemical compound OCCN1C=CN=C1 AMSDWLOANMAILF-UHFFFAOYSA-N 0.000 claims 1
- -1 2-mer Topyrimidine Chemical compound 0.000 claims 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical group CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 claims 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 claims 1
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 claims 1
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 claims 1
- FUOZJYASZOSONT-UHFFFAOYSA-N 2-propan-2-yl-1h-imidazole Chemical compound CC(C)C1=NC=CN1 FUOZJYASZOSONT-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
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 1
- FVZXYJDGVYLMDB-UHFFFAOYSA-N 3-pyridin-2-ylpropan-1-ol Chemical compound OCCCC1=CC=CC=N1 FVZXYJDGVYLMDB-UHFFFAOYSA-N 0.000 claims 1
- VYDWQPKRHOGLPA-UHFFFAOYSA-N 5-nitroimidazole Chemical compound [O-][N+](=O)C1=CN=CN1 VYDWQPKRHOGLPA-UHFFFAOYSA-N 0.000 claims 1
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- 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 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- DDIAIYSZCJDKOD-QACDDLKQSA-N NCCCC12C(C=CC=3C[C@@H]4[C@@H]5C=C[C@@H]([C@@H]([C@@]5(C13)CCN4C)O2)O)O Chemical compound NCCCC12C(C=CC=3C[C@@H]4[C@@H]5C=C[C@@H]([C@@H]([C@@]5(C13)CCN4C)O2)O)O DDIAIYSZCJDKOD-QACDDLKQSA-N 0.000 claims 1
- IOOXLMIGPXXEHO-SOEQMCAUSA-N O[C@H]([C@@H]1OC2(CCO)C(O)C=C3)C=C[C@H]4[C@]5([H])N(C)CC[C@@]41C2=C3C5 Chemical compound O[C@H]([C@@H]1OC2(CCO)C(O)C=C3)C=C[C@H]4[C@]5([H])N(C)CC[C@@]41C2=C3C5 IOOXLMIGPXXEHO-SOEQMCAUSA-N 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 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 claims 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 claims 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 238000004132 cross linking Methods 0.000 claims 1
- 238000006880 cross-coupling reaction Methods 0.000 claims 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 claims 1
- XBRDBODLCHKXHI-UHFFFAOYSA-N epolamine Chemical compound OCCN1CCCC1 XBRDBODLCHKXHI-UHFFFAOYSA-N 0.000 claims 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-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
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 claims 1
- 229940119545 isobornyl methacrylate Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- RWIVICVCHVMHMU-UHFFFAOYSA-N n-aminoethylmorpholine Chemical compound NCCN1CCOCC1 RWIVICVCHVMHMU-UHFFFAOYSA-N 0.000 claims 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920001451 polypropylene glycol Polymers 0.000 claims 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims 1
- SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 claims 1
- TXQWFIVRZNOPCK-UHFFFAOYSA-N pyridin-4-ylmethanamine Chemical compound NCC1=CC=NC=C1 TXQWFIVRZNOPCK-UHFFFAOYSA-N 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 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)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (17)
- 분산제로서 사용하기에 적합한 중합체로서, (A) 다음 화학식을 가진 하나 또는 그 이상의 단량체 0 내지 80몰%(여기서 R¹, R², R³ 및 R⁴는 서로 동일하거나 서로 상이하며, 수소원자 또는, 알킬을 대표함, (B) 다음 화학식을 가진 하나 또는 그 이상의 단량체 0 내지 70몰%여기서 R5, R6 및 R7은 서로 동일하거나, 서로 상이하며, 수소원자 또는 알킬을 대표하는 것이고, R8은 알킬 또는 치환된 알킬이며, 알킬기인 R8은 -0-기에 의해 삽입할 수 있음, (C) 최소한 하나의 염기성 링 질소원자를 가진 복소환기를 함유하거나, 또는 중합후에 이러한 복소환기를 부착시킨, 하나 또는 그 이상의 단량체 5 내지 50몰%, (D) 교차 연결 또는 커플링(결합)에 대해 반응성이 있는 하나 또는 그 이상의 기를 함유하는 하나 또는 그 이상의 단량체 0내지 10몰%, 및, (E) 상기 A 내지 D번의 군에 속하진 않은 하나 또는 그 이상의 단량체 0내지 20몰%(아크릴레이트기를 포함하는 단령체와 상기 A군의 단량체 및 그 유기성 염의 사용량은 최소한 20몰 %임).등으로 부터 형성한, 분산제로서 사용하기에 적합한 중합체.
- 제1항에 있어서, 상기 B군의 단량체들의 사용량은 최소한 20몰 %인 것을 특징으로 하는 분산제.
- 제1항 또는 제2항에 있어서, A군의 단량체 5내지 15몰 %, B군의 단량체 25내지 70몰 %, C군의 단량체 25내지 40몰 %, D군의 단량체 0내지 5몰 %, E군의 단량체 0내지 5몰 %등으로 구성되는 것을 특징으로 하는 분산제.
- 제1항 내지 제3항에 있어서, 상기 A군의 단량체들은 비닐틀루엔, 스티렌 및 α메틸 스티렌으로부터 선택되는 것을 특징으로 하는 분산제.
- 제1항 내지 제4항에 있어서, 상기 B군의 단량체들은, 메틸 메타 크릴레이트, 에틸 메타클릴레이트, n-부틸 메타크릴 레이트, 이소부틸 메타크릴레이트, 헥실메타크릴레이트, 2-에틸 헥실 메타크릴레이트, 디메틸 아미노 에틸 메타크릴레이트, 사이클로 헥실 메타크릴레이트, 메틸아크릴레이트, 이소보닐 메타클릴레이트, 에틸 아크릴레이트, 부틸 아크릴레이트,2-에틸 헥실 아크릴 레이트, 세틸메타크릴레이트, 스테아릴메타 크릴레이트, 베헤닐 메타크릴레이트, 플리프로필렌 글리클 모노메타크릴레이트, 플리에틸렌 글리클 모노메타크릴레이트, 및 EP-PO모노메타 크릴레이트, 등으로 부터 선택되는 것을 특징으로 하는 분산제.
- 제1항 내지 제5항에 있어서, 상기 C군의 단량체들은, 최소한 하나의 염기성 링 질소원자를 가진 복소환기를 포함하는 단량체들로 구성되는 것을 특징으로 하는 분산제.
- 제6항에 있어서, 상기 단량체 들은 비닐 이미다졸, 비닐피리딘, 2-메틸-N-비닐이미다졸, 비닐 피롤리돈, 및 비닐카바졸 등으로 부터 선택되는 것을 특징으로 하는 분산제.
- 제1항 내지 제5항에 있어서, 상기 C군의 단량체들은, 중합후에 최소한 하나의 염기성 링 질소원자를 가진 복소환기를 포함하는 화합물이 부착된 단량체들로 구성되는 것을 특징으로 하는 분산제.
- 제8항에 있어서, 상기 단량체들은 1-하이드록시 에틸아크릴레이트, 2-하이드록시 프로필 아크릴레이트, 글리시딜 메타크릴레이트, 2-하이드록시 에틸 메타 크릴레이트, 1-하이드록시프로필 메타크릴레이트, 아크릴산, 메타크릴산 및 상기 물질들의 알콕실화된 반응 물질등으로 부터 선택되는 것을 특징으로 하는 분산제.
- 제8항 또는 제9항에 있어서, 상기 부착된 화합물은 1-(2-하이드륵시-에틸)-피롤리딘, 2-(1-피롤리딘)-에틸아민, 2-(1-피페리딜)-에틸아민, 1-(2-하이드륵시 에틸)-피페리딘, 1-(2-아미노프로필)-피페리딘, N-(2-하이드륵시 에틸)-헤사메틸렌-이민, 4-(2-하이드륵시 에틸)-모플린, 2-(4-모플리닐)-에틸아민, 4-(3-아미노프로필)-모플린, 1-(2-하이드륵시에틸)-피페라진, 1-(2-아미노에틸)-피페라진, 1-(2-하이드륵시에틸)-2-아킬이미다졸린, 1-(3-아미노프로필)-이미다졸 (2-하이드륵시에틸)-2-알킬이미다졸린, 1-(3-아미노프로필)-이미다졸, (2-하이드륵시 에틸)-피라딘, (3-하이드록시프로필)-피리딘, (하이드륵시메틸)-피리딘, N-메틸-2-하이드록시메틸-피페리딘, 1-(2-하이드록시 에틸)-이미다졸, 2-아미노-6-메특시 벤조티아졸, 4-아미노 메틸-피리딘, 4-아미노-2-메특시 피리미딘, 2-메르캅토 피리미딘, 2-메르캅토-벤즈 이미다졸, 3-아미노-1, 2, 4-트리아졸, 2-이소프로필-이미다졸, 2-에틸-이미다졸, 4-메틸-이미다졸, 2-메틸이미다졸, 2-에틸-4-메틸-이미다졸, 2-페닐-이미다졸, 및4-니트로-이미다졸 등으로부터 선택되는 것을 특징으로 하는 분산제.
- 제1항 내지 제10항에 있어서, 상기 D군의 단량체의 함량은 0몰 %이상이며, 이 단량체들은, 2-하이드록시-에틸-아크릴레이트, 2-하이드록시프로필 아크릴레이트, 글리시딘 메타크릴레이트, 2-하이드록시에틸 메타크릴레이트, 2-하이드록시 프로필 메타크릴레이트, 아크릴산, 및 상기 화합물들의 알콕실화된 반응물질 등으로부터 선택되는 것을 특징으로 하는 분산제.
- 분산제의 용도로서, 피막제 및 인쇄잉크의 생산에 사용하는 것을 목적으로 하는 제1항 내지 제11항의 분산제의 용도.
- 제12항에 있어서, 색소표면(BET) 매㎡당1 내지 10㎎의 분산제를 사용하는 것을 특징으로 하는 분산제의 용도.
- 분말형 고체로서, 액상 시스템에 첨가하는 것을 목표로 하고, 상기 제1항내지 제11항의 분산제로서 피막시킨 분말형 고체.
- 제14항에 있어서, 분산제의 함량은 색소 표면 매㎡당1 내지 10㎎범위로 된 것을 특징으로 하는 분말형 고체.
- 색소 분말체로서, 주로 하나 또는 그 이상의 색소와, 상기 제1항 내지 제11항의 분산제와, 그리고 물과, 그리고/또는 비수성 액체로 구성되는 색소 분산체.
- 제16항에 있어서, 주로 10 내지 70중량 %의 색소, 1내지 10중량%의 분산제, 및 20 내지 89중량%의 물, 및/또는 비수성 액체 등으로 구성되는 것을 특징으로 하는 색소 분산체.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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 (2)
| Publication Number | Publication Date |
|---|---|
| KR900014027A true KR900014027A (ko) | 1990-10-22 |
| KR960006215B1 KR960006215B1 (ko) | 1996-05-11 |
Family
ID=19850552
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019890002635A KR960006215B1 (ko) | 1987-09-04 | 1989-03-02 | 분산제 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5688858A (ko) |
| EP (1) | EP0311157B2 (ko) |
| JP (1) | JP2843985B2 (ko) |
| KR (1) | KR960006215B1 (ko) |
| AT (1) | ATE97143T1 (ko) |
| CA (1) | CA1339180C (ko) |
| DE (1) | DE3885567T3 (ko) |
| ES (1) | ES2067466T5 (ko) |
| NL (1) | NL8702089A (ko) |
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| US5425900A (en) * | 1990-12-27 | 1995-06-20 | Efka-Chemicals B.V. | Dispersing agents, their use and solids coated therewith |
| ES2095389T3 (es) * | 1991-06-26 | 1997-02-16 | Efka Chemicals Bv | Agentes dispersantes, su utilizacion y solidos recubiertos con estos. |
| 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 |
| CN1950275B (zh) | 2004-04-30 | 2010-10-06 | 株式会社汤山制作所 | 药品供给系统 |
| 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 |
| US20060159925A1 (en) | 2004-12-20 | 2006-07-20 | Satish Agrawal | High-intensity, persistent thermochromic compositions and objects, and methods for creating the same |
| US7910022B2 (en) | 2006-09-15 | 2011-03-22 | Performance Indicator, Llc | Phosphorescent compositions for identification |
| 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 |
| CA2648483A1 (en) * | 2006-04-26 | 2007-11-08 | Basf Se | Method for the application of corrosion-resistant layers to metallic surfaces |
| 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 |
| WO2008122517A2 (en) * | 2007-04-05 | 2008-10-16 | Basf Se | Sunscreen compositions comprising a random terpolymer |
| US20080247975A1 (en) * | 2007-04-05 | 2008-10-09 | Dueva-Koganov Olga V | Sunscreen and personal care compositions comprising a select copolymer |
| US8039193B2 (en) | 2007-09-13 | 2011-10-18 | Performance Indicator Llc | Tissue markings and methods for reversibly marking tissue employing the same |
| US7842128B2 (en) | 2007-09-13 | 2010-11-30 | Performance Indicatior LLC | Tissue marking compositions |
| DE102007045230A1 (de) * | 2007-09-21 | 2009-04-09 | Clariant International Limited | Polycarboxylatether als Dispergiermittel für anorganische Pigmentformulierungen |
| EP2274382A1 (en) | 2008-05-09 | 2011-01-19 | 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 |
| ES2400585T3 (es) | 2008-10-02 | 2013-04-10 | Basf Se | Composiciones de color cambiante, multicolor, fotoactivas, y dosímetros de UV |
| 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 DE DE3885567T patent/DE3885567T3/de not_active Expired - Lifetime
- 1988-08-30 EP EP88201843A patent/EP0311157B2/en not_active Expired - Lifetime
- 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
- 1988-08-31 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 |
|---|---|
| ES2067466T5 (es) | 2001-10-16 |
| KR960006215B1 (ko) | 1996-05-11 |
| NL8702089A (nl) | 1989-04-03 |
| ATE97143T1 (de) | 1993-11-15 |
| CA1339180C (en) | 1997-07-29 |
| DE3885567T3 (de) | 2001-10-18 |
| EP0311157A1 (en) | 1989-04-12 |
| DE3885567T2 (de) | 1994-03-24 |
| ES2067466T3 (es) | 1995-04-01 |
| US5688858A (en) | 1997-11-18 |
| EP0311157B2 (en) | 2001-05-23 |
| EP0311157B1 (en) | 1993-11-10 |
| JP2843985B2 (ja) | 1999-01-06 |
| DE3885567D1 (de) | 1993-12-16 |
| JPH01164429A (ja) | 1989-06-28 |
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