KR960010726A - 교반-혼입형 유기 안료 - Google Patents
교반-혼입형 유기 안료 Download PDFInfo
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- KR960010726A KR960010726A KR1019950029769A KR19950029769A KR960010726A KR 960010726 A KR960010726 A KR 960010726A KR 1019950029769 A KR1019950029769 A KR 1019950029769A KR 19950029769 A KR19950029769 A KR 19950029769A KR 960010726 A KR960010726 A KR 960010726A
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- pigment
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- 239000012860 organic pigment Substances 0.000 title claims abstract 16
- 239000000049 pigment Substances 0.000 claims abstract 66
- 239000000203 mixture Substances 0.000 claims abstract 16
- 238000000034 method Methods 0.000 claims abstract 13
- 239000002245 particle Substances 0.000 claims abstract 13
- 239000011256 inorganic filler Substances 0.000 claims abstract 10
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract 10
- 239000011368 organic material Substances 0.000 claims abstract 8
- 238000004040 coloring Methods 0.000 claims abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 6
- 239000010445 mica Substances 0.000 claims 5
- 229910052618 mica group Inorganic materials 0.000 claims 5
- 238000002156 mixing Methods 0.000 claims 4
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 claims 4
- 229920005989 resin Polymers 0.000 claims 4
- 239000011347 resin Substances 0.000 claims 4
- 239000000454 talc Substances 0.000 claims 4
- 229910052623 talc Inorganic materials 0.000 claims 4
- MTKKGHVQPVOXIL-UHFFFAOYSA-N 3h-isoindol-1-amine Chemical compound C1=CC=C2C(N)=NCC2=C1 MTKKGHVQPVOXIL-UHFFFAOYSA-N 0.000 claims 3
- 229920000877 Melamine resin Polymers 0.000 claims 3
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims 3
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-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
- -1 aliphatic 1,2-diol Chemical class 0.000 claims 3
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims 3
- 150000004056 anthraquinones Chemical class 0.000 claims 3
- 239000011248 coating agent Substances 0.000 claims 3
- 238000000576 coating method Methods 0.000 claims 3
- 238000001035 drying Methods 0.000 claims 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 2
- 229920000180 alkyd Polymers 0.000 claims 2
- 239000004202 carbamide Substances 0.000 claims 2
- 229920002678 cellulose Polymers 0.000 claims 2
- VPWFPZBFBFHIIL-UHFFFAOYSA-L disodium 4-[(4-methyl-2-sulfophenyl)diazenyl]-3-oxidonaphthalene-2-carboxylate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 VPWFPZBFBFHIIL-UHFFFAOYSA-L 0.000 claims 2
- 238000000227 grinding Methods 0.000 claims 2
- 229920000728 polyester Polymers 0.000 claims 2
- 229920002635 polyurethane Polymers 0.000 claims 2
- 239000004814 polyurethane Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 238000001694 spray drying Methods 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 claims 1
- MBSOHMUBMHZCGE-UHFFFAOYSA-N 9h-carbazole;dioxazine Chemical compound O1ON=CC=C1.C1=CC=C2C3=CC=CC=C3NC2=C1 MBSOHMUBMHZCGE-UHFFFAOYSA-N 0.000 claims 1
- 239000004925 Acrylic resin Substances 0.000 claims 1
- 229920000178 Acrylic resin Polymers 0.000 claims 1
- 239000005995 Aluminium silicate Substances 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 239000004952 Polyamide Substances 0.000 claims 1
- 239000004642 Polyimide Substances 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 239000004793 Polystyrene Substances 0.000 claims 1
- 229910010413 TiO 2 Inorganic materials 0.000 claims 1
- 235000012211 aluminium silicate Nutrition 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 229920003086 cellulose ether Polymers 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 claims 1
- 229920003244 diene elastomer Polymers 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 239000010459 dolomite Substances 0.000 claims 1
- 229910000514 dolomite Inorganic materials 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 claims 1
- 239000003623 enhancer Substances 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 150000002191 fatty alcohols Chemical class 0.000 claims 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims 1
- 150000003949 imides Chemical class 0.000 claims 1
- 235000019239 indanthrene blue RS Nutrition 0.000 claims 1
- 230000001788 irregular Effects 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 125000005395 methacrylic acid group Chemical group 0.000 claims 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 1
- OBJNZHVOCNPSCS-UHFFFAOYSA-N naphtho[2,3-f]quinazoline Chemical compound C1=NC=C2C3=CC4=CC=CC=C4C=C3C=CC2=N1 OBJNZHVOCNPSCS-UHFFFAOYSA-N 0.000 claims 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 claims 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims 1
- 229920001643 poly(ether ketone) Polymers 0.000 claims 1
- 229920002492 poly(sulfone) Polymers 0.000 claims 1
- 229920002647 polyamide Polymers 0.000 claims 1
- 229920000515 polycarbonate Polymers 0.000 claims 1
- 239000004417 polycarbonate Substances 0.000 claims 1
- 229920000647 polyepoxide Polymers 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 229920001721 polyimide Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 229920000098 polyolefin Polymers 0.000 claims 1
- 229920002223 polystyrene Polymers 0.000 claims 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims 1
- 239000004810 polytetrafluoroethylene Substances 0.000 claims 1
- 229920001291 polyvinyl halide Polymers 0.000 claims 1
- 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 1
- 239000005060 rubber Substances 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 229920005573 silicon-containing polymer Polymers 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 235000012424 soybean oil Nutrition 0.000 claims 1
- 239000003549 soybean oil Substances 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 229920001169 thermoplastic Polymers 0.000 claims 1
- 239000004416 thermosoftening plastic Substances 0.000 claims 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 claims 1
- 239000013058 crude material Substances 0.000 abstract 1
Classifications
-
- 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
- C09B67/0001—Post-treatment of organic pigments or dyes
- C09B67/0022—Wet grinding of pigments
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- 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
- 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
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
본 발명은 평균 입도 0.5 내지 25㎛인 비-소판 형태의 입자를 주성분으로 함유하는 유기 안료 조원료이고(거나) 평균 입도 0.01 내지 25㎛인 유기 안료 및 무기 충전제 안료를 주성분으로 함유하는 안료 조성물인 교반-혼입형 안료의 착색 유효랑을 고분자량 유기 물질 중으로 균질하게 분산시키는 것으로 이루어진 고분자량 유기 물질의 착색 방법을 개시하고 있다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (20)
- 평균 입도 0.5 내지 25㎛ 범위내인 비-소판 형태의 안료 입자를 주성분으로 함유하지만 카르바졸 디옥사진 조원료는 아닌 유기 교반-혼입형 안료이거나, 또는 무기 충전제 안료 0.1 내지 50중량부 및 유기 안료 50 내지 99.9 중량부로 이루어지며(여기서, 무기 충전제 안료 및 유기 안료의 중량부의 총합은 100임) 유기 안료의 평균 입도가 0.01 내지 25㎛범위 내인 안료 조성물인 교반-혼입형 안료를 고분자량 유기 물질의 현탁액 또는 용액 중으로 교반 혼입시킴으로써 고분자량의 유기 물질 내에 교반-혼입형 안료의 유효 착색량을 균질하게 분산시키는 것으로 이루어진 고분자량 유기 물질의 착색 방법.
- 제1항에 있어서, 유기 교반-혼입형 안료 또는 유기 안료가 아조, 아조메틴, 메틴, 안트라퀴논, 프탈로시아닌, 페리논, 페릴렌, 디케토피롤로피롤, 티오인디고, 이미노이소인돌린, 이미노이소인돌리논, 퀴나크리돈, 플라반트론, 인단트롤, 안트라피리미딘 또는 퀴노프탈론 안료 조원료 또는 조절된 안료, 바람직하게는 디케토피롤로피롤, 퀴나크리돈, 안트라퀴논, 프탈로시아닌, 안단트론 또는 이미노이소인 돌리논 안료 조원료 또는 조절된 안료인 방법.
- 제1항에 있어서, 유기 교반-혼입형 안료 또는 안료 조성물이 분무-건조법 또는 유동층 건조법에 의해 그의 프레스케익으로부터 제조된 것인 방법.
- 제1항에 있어서, 유기 교반-혼입형 안료 또는 안료 조성물이 분무-건조법, 유동층 건조법 또는 트레이-건조법에 이은 초미세 분쇄법 또는 에어-제트 분쇄법에 의해 그의 프레스케익으로부터 제조된 것인 방법.
- 제1항에 있어서, 유기 교반-혼입형 안료 또는 유기 안료가 씨. 아이. 피그먼트 레드 202, 씨. 아이. 피그먼트 바이올렛 19, 씨. 아이. 피그먼트 레드 122, 씨 아이, 피그먼트 레드 179, 씨. 아이. 피그먼트 레드 170, 씨. 아이. 피그먼트 레드 177, 씨. 아이. 피그먼트 레드 144, 씨 아이, 피그먼트 브라운 23, 씨. 아이. 피그먼트 오렌지 61, 씨. 아이. 피그먼트 레드 254, 씨. 아이. 피그먼트 레드 255, 씨 아이, 피그먼트 레드 264, 씨. 아이. 피그먼트 옐로우 109, 씨. 아이. 피그먼트 옐로우 110, 씨. 아이. 피그먼트 블루 15, 씨. 아이, 피그먼트 블루 60, 씨. 아이. 피그먼트 오렌지 73 및 씨. 아이. 피그먼트 오렌지 71 또는 상응하는 안료 조원료인 방법.
- 제1항에 있어서, 유기 교반-혼입형 안료의 평균 입도가 2 내지 15㎛의 범위내, 바람직하게는 2.5 내지 10㎛의 범위 내인 방법.
- 제1항에 있어서, 유기 교반-혼입형 안료가 불규칙형, 입방형, 침상형 또는 막대형의 입자를 주성분으로 함유하는 방법.
- 제1항에 있어서, 유기 안료의 평균 입도가 0.1 내지 3㎛범위 내인 방법.
- 제1항에 있어서, 안료 조성물이 유기 안료 65 내지 95중량부 및 무기 충전제 안료 5 내지 35중량부로 이루어진 방법.
- 제1항에 있어서, 무기 충전제 안료가 운모, 카올린, 활석 및 천연 또는 합성 실리카로 이루어진 군, 바람직하게는 천연의 백운모, 활석 또는 그의 혼합물로 이루어진 군으로부터 선택된 것인 방법.
- 제10항에 있어서, 상기 운모 안료가 금속 산화물, 바람직하게는 TiO2, ZrO2, Fe2O3또는 Cr2O3또는 그의 혼합물로 피복된 운모인 방법.
- 제1항에 있어서, 무기 충전제 안료의 평균 입도가 1.0 내지 50㎛ 범위내, 바람직하게는 1.2 내지 30㎛범위 내인 방법.
- 제1항에 있어서, 안료 조성물이 탄소 원자가 적어도 12개인 지방산, 아이드, 에스테르 또는 그의 염, 지방족 1,2-디올, 에폭시화 대두유, 에톡실화 지방 알코올, 왁스, 수지 산 및 수지 산 염, 또는 그의 염, 바람직하게는 로진(rosin) 산 또는 로진 산 염, 가장 바람직하게는 수불용성 로진 산 염으로부터 선택된 조직-개선제 0.05 내지 20중량부, 바람직하게는 1 내지 10중량부를 더 포함하는 방법.
- 제1항에 있어서, 고분자량 유기 물질이 셀룰로오스 에테르, 셀룰로오스 에스테르, 폴리우레탄, 폴리에스테르, 폴리카르보네이트, 폴리올레핀, 폴리스티렌, 폴리술폰, 폴리아미드, 폴리시클로아미드, 폴리이미드, 폴리에테르, 폴리에테르 케톤, 폴리비닐 할라이드, 폴리테트라플루오로에틸렌, 아크릴계 및 메타크릴계 중합체, 고무, 실리콘 중합체, 페놀/포름알데히드 수지, 멜라민/포름알데히드 수지, 우레아/포름알데히드 수지, 에폭시 수지, 디엔 고무 및 그의 공중합체로 이루어진 군으로부터 선택된 코팅 또는 잉크 시스템인 방법.
- 제1항에 있어서, 고분자량 유기 물질이 바람직하게는 아크릴계 알키드, 에폭시, 페놀계, 멜라민, 우레아, 폴리에스테르, 폴리우레탄, 차단된 이소시아네이트, 벤조구아나민 또는 셀룰로오스 에스테르 수지, 또는 그의 조합물인 열-경화성 또는 가교결합성 반응성 코팅 시스템이거나 또는 아크릴계/멜라민, 알키드/멜라민 또는 열가소성 아크릴계 수지인 용매 또는 수함유 코팅 시스템인 방법.
- (a)무기 충전제 안료 0.1 내지 50중량부, (b)평균 입도 0.01 내지 25㎛ 범위내인 입자를 주성분으로 함유하는 유기 안료 50 내지 99.9 중량부, 및 임의로는 또한 (c)조직-개선제 0.05 내지 20중량부 (여기서, 무기 충전제 안료와 유기 안료의 중량부의 총합은 100임)로 이루어진 교반-혼입형 안료 조성물.
- 제16항에 있어서, 무기 충전제 안료가 운모 또는 활석이고, 바람직하게는 유기 안료가 디케토피롤로피롤 안료인 교반-혼입형 안료 조성물.
- 제16항에 있어서, 유기 안료가 디케토피롤로피롤 안료 1 내지 99중량% 및 아조, 퀴나프탈론, 안트라퀴논, 이미노이소인돌린, 이미노이소인돌론, 프탈로시아닌 또는 퀴나크리돈 안료 1 내지 99중량%로 이루어진 안료 혼합물인 교반-혼입형 안료 조성물.
- 제16항에 있어서, 무기 충전제 안료가 운모 또는 활석이고, 유기 안료가 씨. 아이. 피그먼트 레드 254, 씨. 아이. 피그먼트 레드 255, 씨. 아이. 피그먼트 레드 264 및 씨. 아이. 피그먼트 오렌지 73인 교반-혼입형 안료 조성물.
- 제16항에 있어서, 유기 안료가 씨. 아이. 피그먼트 레드 202, 씨. 아이. 피그먼트 레드 122 또는 씨. 아이. 피그먼트 바이올렛 19 또는 상응하는 안료 조원료인 교반-혼입형 안료 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/305,549 US5584922A (en) | 1994-09-14 | 1994-09-14 | Stir-in organic pigments |
| US08/305549 | 1994-09-14 | ||
| US08/305,549 | 1994-09-14 | ||
| US08/475,165 | 1995-06-07 | ||
| US08/475,165 US5554217A (en) | 1994-09-14 | 1995-06-07 | Stir-in organic pigments |
| US08/475165 | 1995-06-07 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR960010726A true KR960010726A (ko) | 1996-04-20 |
| KR100375023B1 KR100375023B1 (ko) | 2003-11-17 |
Family
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019950029769A KR100375023B1 (ko) | 1994-09-14 | 1995-09-13 | 교반-혼입형유기안료 |
| KR1019950029993A KR100375022B1 (ko) | 1994-09-14 | 1995-09-14 | 유기안료와특정입자크기의충전재를포함하는새로운안료조성물 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019950029993A KR100375022B1 (ko) | 1994-09-14 | 1995-09-14 | 유기안료와특정입자크기의충전재를포함하는새로운안료조성물 |
Country Status (3)
| Country | Link |
|---|---|
| US (3) | US5584922A (ko) |
| KR (2) | KR100375023B1 (ko) |
| TW (2) | TW396193B (ko) |
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1995
- 1995-06-07 US US08/475,165 patent/US5554217A/en not_active Expired - Fee Related
- 1995-06-07 US US08/475,163 patent/US5667580A/en not_active Expired - Fee Related
- 1995-08-26 TW TW084108897A patent/TW396193B/zh not_active IP Right Cessation
- 1995-08-29 TW TW084108979A patent/TW440580B/zh active
- 1995-09-13 KR KR1019950029769A patent/KR100375023B1/ko not_active IP Right Cessation
- 1995-09-14 KR KR1019950029993A patent/KR100375022B1/ko not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100471036B1 (ko) * | 2002-05-30 | 2005-03-08 | 현대자동차주식회사 | 차량용 흑색 피막제 |
Also Published As
| Publication number | Publication date |
|---|---|
| US5584922A (en) | 1996-12-17 |
| TW440580B (en) | 2001-06-16 |
| KR960010791A (ko) | 1996-04-20 |
| US5667580A (en) | 1997-09-16 |
| KR100375022B1 (ko) | 2004-02-11 |
| US5554217A (en) | 1996-09-10 |
| TW396193B (en) | 2000-07-01 |
| KR100375023B1 (ko) | 2003-11-17 |
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