DE2429762C2 - Farbstoffhaltige Glanzpigmente - Google Patents
Farbstoffhaltige GlanzpigmenteInfo
- Publication number
- DE2429762C2 DE2429762C2 DE2429762A DE2429762A DE2429762C2 DE 2429762 C2 DE2429762 C2 DE 2429762C2 DE 2429762 A DE2429762 A DE 2429762A DE 2429762 A DE2429762 A DE 2429762A DE 2429762 C2 DE2429762 C2 DE 2429762C2
- Authority
- DE
- Germany
- Prior art keywords
- dye
- pigments
- pigment
- aluminum
- dyes
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000000049 pigment Substances 0.000 title claims description 122
- 239000002932 luster Substances 0.000 title claims description 17
- 239000000975 dye Substances 0.000 claims description 79
- -1 aluminum ions Chemical class 0.000 claims description 35
- 239000002245 particle Substances 0.000 claims description 31
- 239000010445 mica Substances 0.000 claims description 28
- 229910052618 mica group Inorganic materials 0.000 claims description 28
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 26
- 229910052782 aluminium Inorganic materials 0.000 claims description 22
- 239000000243 solution Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 21
- 230000015572 biosynthetic process Effects 0.000 claims description 12
- 229910044991 metal oxide Inorganic materials 0.000 claims description 12
- 150000004706 metal oxides Chemical class 0.000 claims description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000004922 lacquer Substances 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 238000005859 coupling reaction Methods 0.000 claims description 6
- 239000000987 azo dye Substances 0.000 claims description 5
- 239000013522 chelant Substances 0.000 claims description 5
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 241000123069 Ocyurus chrysurus Species 0.000 claims description 3
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
- 239000010936 titanium Substances 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 30
- 239000002253 acid Substances 0.000 description 23
- 239000000725 suspension Substances 0.000 description 18
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 16
- 239000000047 product Substances 0.000 description 15
- 238000000576 coating method Methods 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 244000172533 Viola sororia Species 0.000 description 7
- 230000009918 complex formation Effects 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 240000007817 Olea europaea Species 0.000 description 6
- 229910010413 TiO 2 Inorganic materials 0.000 description 6
- 239000008367 deionised water Substances 0.000 description 6
- 229910021641 deionized water Inorganic materials 0.000 description 6
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 6
- 229910052737 gold Inorganic materials 0.000 description 6
- 239000010931 gold Substances 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 238000001556 precipitation Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000004408 titanium dioxide Substances 0.000 description 6
- 239000008366 buffered solution Substances 0.000 description 5
- 239000002738 chelating agent Substances 0.000 description 5
- 239000002537 cosmetic Substances 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 5
- AKEUNCKRJATALU-UHFFFAOYSA-N 2,6-dihydroxybenzoic acid Chemical compound OC(=O)C1=C(O)C=CC=C1O AKEUNCKRJATALU-UHFFFAOYSA-N 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 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 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229950011260 betanaphthol Drugs 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 3
- 229910001112 rose gold Inorganic materials 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- FMRLRBCECZNJNN-UHFFFAOYSA-N 1,2,5-trihydroxyanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1O FMRLRBCECZNJNN-UHFFFAOYSA-N 0.000 description 2
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 2
- UIAFKZKHHVMJGS-UHFFFAOYSA-N 2,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1O UIAFKZKHHVMJGS-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- GSGBLSFZYUSSSY-UHFFFAOYSA-N 6-amino-5-hydroxynaphthalene-1-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC2=C(O)C(N)=CC=C21 GSGBLSFZYUSSSY-UHFFFAOYSA-N 0.000 description 2
- 239000005725 8-Hydroxyquinoline Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 235000005811 Viola adunca Nutrition 0.000 description 2
- 240000009038 Viola odorata Species 0.000 description 2
- 235000013487 Viola odorata Nutrition 0.000 description 2
- 235000002254 Viola papilionacea Nutrition 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 2
- 229940092714 benzenesulfonic acid Drugs 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 229930002875 chlorophyll Natural products 0.000 description 2
- 235000019804 chlorophyll Nutrition 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- QWPVOAUJFKGLQA-UHFFFAOYSA-N flavopurpurin Chemical compound OC1=CC=C2C(=O)C3=CC(O)=CC=C3C(=O)C2=C1O QWPVOAUJFKGLQA-UHFFFAOYSA-N 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 2
- 229960003540 oxyquinoline Drugs 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000001052 yellow pigment Substances 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- NEVTZWLESVDYDA-UHFFFAOYSA-N 1,2,4,5,7,8-hexahydroxyanthracene-9,10-dione Chemical compound C1=C(O)C(O)=C2C(=O)C3=C(O)C(O)=CC(O)=C3C(=O)C2=C1O NEVTZWLESVDYDA-UHFFFAOYSA-N 0.000 description 1
- MCFGSXGJGCXNBP-UHFFFAOYSA-N 1,2,5,8-tetrahydroanthracene-9,10-dione Chemical compound O=C1C(CC=CC2)=C2C(=O)C2=C1C=CCC2 MCFGSXGJGCXNBP-UHFFFAOYSA-N 0.000 description 1
- KPQISZIQPSSIKA-UHFFFAOYSA-N 1,2-dihydroxy-4-nitroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC([N+]([O-])=O)=C3C(=O)C2=C1 KPQISZIQPSSIKA-UHFFFAOYSA-N 0.000 description 1
- BZXQYVXALVZAIF-UHFFFAOYSA-N 1-[(2-hydroxyphenyl)methylamino]anthracene-9,10-dione Chemical compound OC1=CC=CC=C1CNC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O BZXQYVXALVZAIF-UHFFFAOYSA-N 0.000 description 1
- AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 description 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- RUDINRUXCKIXAJ-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,14-heptacosafluorotetradecanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RUDINRUXCKIXAJ-UHFFFAOYSA-N 0.000 description 1
- XIAYFENBYCWHGY-UHFFFAOYSA-N 2-[2,7-bis[[bis(carboxymethyl)amino]methyl]-3-hydroxy-6-oxoxanthen-9-yl]benzoic acid Chemical compound C=12C=C(CN(CC(O)=O)CC(O)=O)C(=O)C=C2OC=2C=C(O)C(CN(CC(O)=O)CC(=O)O)=CC=2C=1C1=CC=CC=C1C(O)=O XIAYFENBYCWHGY-UHFFFAOYSA-N 0.000 description 1
- AGXCADFSYJNMEG-UHFFFAOYSA-N 2-[[5-[1-[3-[[bis(carboxymethyl)amino]methyl]-4-hydroxy-2-methyl-5-propan-2-ylphenyl]-3-oxo-2-benzofuran-1-yl]-2-hydroxy-6-methyl-3-propan-2-ylphenyl]methyl-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CC1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3C(=O)O2)C=2C(=C(CN(CC(O)=O)CC(O)=O)C(O)=C(C(C)C)C=2)C)=C1C AGXCADFSYJNMEG-UHFFFAOYSA-N 0.000 description 1
- QHKMTHBQSIKVAC-UHFFFAOYSA-N 2-[[5-[1-[3-[[bis(carboxymethyl)amino]methyl]-4-hydroxyphenyl]-3-oxo-2-benzofuran-1-yl]-2-hydroxyphenyl]methyl-(carboxymethyl)amino]acetic acid Chemical compound C1=C(O)C(CN(CC(O)=O)CC(=O)O)=CC(C2(C3=CC=CC=C3C(=O)O2)C=2C=C(CN(CC(O)=O)CC(O)=O)C(O)=CC=2)=C1 QHKMTHBQSIKVAC-UHFFFAOYSA-N 0.000 description 1
- IYZPEGVSBUNMBE-UHFFFAOYSA-N 2-[[5-[1-[3-[[carboxylatomethyl(carboxymethyl)azaniumyl]methyl]-4-hydroxy-5-methylphenyl]-3-oxo-2-benzofuran-1-yl]-2-hydroxy-3-methylphenyl]methyl-(carboxymethyl)azaniumyl]acetate Chemical compound OC(=O)CN(CC(O)=O)CC1=C(O)C(C)=CC(C2(C3=CC=CC=C3C(=O)O2)C=2C=C(CN(CC(O)=O)CC(O)=O)C(O)=C(C)C=2)=C1 IYZPEGVSBUNMBE-UHFFFAOYSA-N 0.000 description 1
- OKYOTYMRDBFYNX-UHFFFAOYSA-N 2-[[5-[3-[3-[[carboxymethyl(methyl)amino]methyl]-4-hydroxy-5-methylphenyl]-1,1-dioxo-2,1$l^{6}-benzoxathiol-3-yl]-2-hydroxy-3-methylphenyl]methyl-methylamino]acetic acid Chemical compound CC1=C(O)C(CN(CC(O)=O)C)=CC(C2(C3=CC=CC=C3S(=O)(=O)O2)C=2C=C(CN(C)CC(O)=O)C(O)=C(C)C=2)=C1 OKYOTYMRDBFYNX-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- JJRXZSDRNHMASN-UHFFFAOYSA-N 2-hydroxy-3-[(2-hydroxyphenyl)methylideneamino]-5-nitrobenzenesulfonic acid Chemical compound OC1=C(C=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O)C=CC=C1 JJRXZSDRNHMASN-UHFFFAOYSA-N 0.000 description 1
- UCTREIIEJSFTDI-UHFFFAOYSA-N 3-aminonaphthalene-2,7-disulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C=C(S(O)(=O)=O)C(N)=CC2=C1 UCTREIIEJSFTDI-UHFFFAOYSA-N 0.000 description 1
- ZPZABHGHNSRYBU-UHFFFAOYSA-N 3-hydroxy-4-[(2-hydroxy-1H-naphthalen-2-yl)diazenyl]-7-nitronaphthalene-1-sulfonic acid Chemical compound OC1=C(C2=CC=C(C=C2C(=C1)S(=O)(=O)O)[N+](=O)[O-])N=NC1(CC2=CC=CC=C2C=C1)O ZPZABHGHNSRYBU-UHFFFAOYSA-N 0.000 description 1
- RJNYNDHYSJRRDW-UHFFFAOYSA-N 4-(pyridin-2-yldiazenyl)benzene-1,3-diol Chemical compound OC1=CC(O)=CC=C1N=NC1=CC=CC=N1 RJNYNDHYSJRRDW-UHFFFAOYSA-N 0.000 description 1
- MHKGJUOEEHNBLE-UHFFFAOYSA-N 4-[(2,4-dihydroxyphenyl)azo]benzenesulfonic acid Chemical compound OC1=CC(O)=CC=C1N=NC1=CC=C(S(O)(=O)=O)C=C1 MHKGJUOEEHNBLE-UHFFFAOYSA-N 0.000 description 1
- RRRCKIRSVQAAAS-UHFFFAOYSA-N 4-[3-(3,4-dihydroxyphenyl)-1,1-dioxo-2,1$l^{6}-benzoxathiol-3-yl]benzene-1,2-diol Chemical compound C1=C(O)C(O)=CC=C1C1(C=2C=C(O)C(O)=CC=2)C2=CC=CC=C2S(=O)(=O)O1 RRRCKIRSVQAAAS-UHFFFAOYSA-N 0.000 description 1
- RNAVBZRQFCASHH-UHFFFAOYSA-N 4-amino-1,2-dihydroxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=C(O)C=C2N RNAVBZRQFCASHH-UHFFFAOYSA-N 0.000 description 1
- RXCMFQDTWCCLBL-UHFFFAOYSA-N 4-amino-3-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(N)=C(O)C=C(S(O)(=O)=O)C2=C1 RXCMFQDTWCCLBL-UHFFFAOYSA-N 0.000 description 1
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 1
- UEUIKXVPXLWUDU-UHFFFAOYSA-N 4-diazoniobenzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=C([N+]#N)C=C1 UEUIKXVPXLWUDU-UHFFFAOYSA-N 0.000 description 1
- BOOUUBPSTITCCZ-UHFFFAOYSA-N 5-amino-3-[[5-[3-[(8-amino-1-hydroxy-3,6-disulfonaphthalen-2-yl)diazenyl]-4-hydroxyphenyl]sulfonyl-2-hydroxyphenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonic acid Chemical compound NC=1C=C(C=C2C=C(C(=C(C=12)O)N=NC=1C=C(C=CC=1O)S(=O)(=O)C1=CC(=C(C=C1)O)N=NC1=C(C2=C(C=C(C=C2C=C1S(=O)(=O)O)S(=O)(=O)O)N)O)S(=O)(=O)O)S(=O)(=O)O BOOUUBPSTITCCZ-UHFFFAOYSA-N 0.000 description 1
- BGBDMEPBLWJCHI-UHFFFAOYSA-N 5-methyl-2-[[4-(4-methyl-2-sulfoanilino)-9,10-dioxoanthracen-1-yl]amino]benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(C)=CC=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=CC=C(C)C=C1S(O)(=O)=O BGBDMEPBLWJCHI-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 240000001592 Amaranthus caudatus Species 0.000 description 1
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910002566 KAl(SO4)2·12H2O Inorganic materials 0.000 description 1
- 239000004235 Orange GGN Substances 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229910000004 White lead Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 239000008351 acetate buffer Substances 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
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- 125000002843 carboxylic acid group Chemical group 0.000 description 1
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- DGQLVPJVXFOQEV-NGOCYOHBSA-N carminic acid Chemical compound OC1=C2C(=O)C=3C(C)=C(C(O)=O)C(O)=CC=3C(=O)C2=C(O)C(O)=C1[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O DGQLVPJVXFOQEV-NGOCYOHBSA-N 0.000 description 1
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- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
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- JBBPTUVOZCXCSU-UHFFFAOYSA-L dipotassium;2',4',5',7'-tetrabromo-4,7-dichloro-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate Chemical compound [K+].[K+].O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(Br)=C([O-])C(Br)=C1OC1=C(Br)C([O-])=C(Br)C=C21 JBBPTUVOZCXCSU-UHFFFAOYSA-L 0.000 description 1
- RAGZEDHHTPQLAI-UHFFFAOYSA-L disodium;2',4',5',7'-tetraiodo-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate Chemical compound [Na+].[Na+].O1C(=O)C2=CC=CC=C2C21C1=CC(I)=C([O-])C(I)=C1OC1=C(I)C([O-])=C(I)C=C21 RAGZEDHHTPQLAI-UHFFFAOYSA-L 0.000 description 1
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- CPSYWNLKRDURMG-UHFFFAOYSA-L hydron;manganese(2+);phosphate Chemical compound [Mn+2].OP([O-])([O-])=O CPSYWNLKRDURMG-UHFFFAOYSA-L 0.000 description 1
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- 230000007246 mechanism Effects 0.000 description 1
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- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
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- KVOIJEARBNBHHP-UHFFFAOYSA-N potassium;oxido(oxo)alumane Chemical compound [K+].[O-][Al]=O KVOIJEARBNBHHP-UHFFFAOYSA-N 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- BBNQQADTFFCFGB-UHFFFAOYSA-N purpurin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC(O)=C3C(=O)C2=C1 BBNQQADTFFCFGB-UHFFFAOYSA-N 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
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- 229940051201 quinoline yellow Drugs 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000010979 ruby Substances 0.000 description 1
- 229910001750 ruby Inorganic materials 0.000 description 1
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- 238000000926 separation method Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- COEZWFYORILMOM-UHFFFAOYSA-M sodium 4-[(2,4-dihydroxyphenyl)diazenyl]benzenesulfonate Chemical compound [Na+].OC1=CC(O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 COEZWFYORILMOM-UHFFFAOYSA-M 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- FNXKBSAUKFCXIK-UHFFFAOYSA-M sodium;hydrogen carbonate;8-hydroxy-7-iodoquinoline-5-sulfonic acid Chemical class [Na+].OC([O-])=O.C1=CN=C2C(O)=C(I)C=C(S(O)(=O)=O)C2=C1 FNXKBSAUKFCXIK-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 235000012756 tartrazine Nutrition 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- UJMBCXLDXJUMFB-GLCFPVLVSA-K tartrazine Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-GLCFPVLVSA-K 0.000 description 1
- 229960000943 tartrazine Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
- DKBXPLYSDKSFEQ-UHFFFAOYSA-L turquoise gll Chemical compound [Na+].[Na+].[Cu+2].N1=C(N=C2[N-]3)[C]4C(S(=O)(=O)[O-])=CC=CC4=C1N=C([N-]1)C4=CC=CC(S([O-])(=O)=O)=C4C1=NC(C=1C4=CC=CC=1)=NC4=NC3=C1[C]2C=CC=C1 DKBXPLYSDKSFEQ-UHFFFAOYSA-L 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- ORZHVTYKPFFVMG-UHFFFAOYSA-N xylenol orange Chemical compound OC(=O)CN(CC(O)=O)CC1=C(O)C(C)=CC(C2(C3=CC=CC=C3S(=O)(=O)O2)C=2C=C(CN(CC(O)=O)CC(O)=O)C(O)=C(C)C=2)=C1 ORZHVTYKPFFVMG-UHFFFAOYSA-N 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
- 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
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/0015—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings
- C09C1/0021—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings comprising a core coated with only one layer having a high or low refractive index
-
- 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
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/0015—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
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- 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
- C09C2200/00—Compositional and structural details of pigments exhibiting interference colours
- C09C2200/10—Interference pigments characterized by the core material
- C09C2200/102—Interference pigments characterized by the core material the core consisting of glass or silicate material like mica or clays, e.g. kaolin
-
- 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
- C09C2200/00—Compositional and structural details of pigments exhibiting interference colours
- C09C2200/30—Interference pigments characterised by the thickness of the core or layers thereon or by the total thickness of the final pigment particle
- C09C2200/301—Thickness of the core
-
- 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
- C09C2200/00—Compositional and structural details of pigments exhibiting interference colours
- C09C2200/30—Interference pigments characterised by the thickness of the core or layers thereon or by the total thickness of the final pigment particle
- C09C2200/303—Thickness of a layer with low refractive material
-
- 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
- C09C2200/00—Compositional and structural details of pigments exhibiting interference colours
- C09C2200/40—Interference pigments comprising an outermost surface coating
- C09C2200/401—Inorganic protective coating
-
- 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
- C09C2200/00—Compositional and structural details of pigments exhibiting interference colours
- C09C2200/40—Interference pigments comprising an outermost surface coating
- C09C2200/402—Organic protective coating
- C09C2200/403—Low molecular weight materials, e.g. fatty acids
- C09C2200/404—Low molecular weight materials, e.g. fatty acids comprising additional functional groups, e.g. -NH2, -C=C- or -SO3
-
- 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
- C09C2220/00—Methods of preparing the interference pigments
- C09C2220/10—Wet methods, e.g. co-precipitation
- C09C2220/103—Wet methods, e.g. co-precipitation comprising a drying or calcination step after applying each layer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2429762A DE2429762C2 (de) | 1974-06-21 | 1974-06-21 | Farbstoffhaltige Glanzpigmente |
| GB2593675A GB1464060A (en) | 1974-06-21 | 1975-06-18 | Coloured lustrous pigments |
| FR7519088A FR2275536A1 (fr) | 1974-06-21 | 1975-06-18 | Pigments brillants contenant des colorants |
| US05/588,504 US4084983A (en) | 1974-06-21 | 1975-06-19 | Dyed lustrous pigments |
| ES438743A ES438743A1 (es) | 1974-06-21 | 1975-06-20 | Procedimiento para la obtencion de pigmentos brillantes con-teniendo colorantes. |
| JP50076430A JPS5936663B2 (ja) | 1974-06-21 | 1975-06-21 | 染料含有光沢顔料およびその製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2429762A DE2429762C2 (de) | 1974-06-21 | 1974-06-21 | Farbstoffhaltige Glanzpigmente |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2429762A1 DE2429762A1 (de) | 1976-01-15 |
| DE2429762C2 true DE2429762C2 (de) | 1984-08-30 |
Family
ID=5918572
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2429762A Expired DE2429762C2 (de) | 1974-06-21 | 1974-06-21 | Farbstoffhaltige Glanzpigmente |
Country Status (6)
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2928287A1 (de) * | 1979-07-13 | 1981-01-29 | Merck Patent Gmbh | Perlglanzpigmente, verfahren zu ihrer herstellung und ihre verwendung |
| IT1153467B (it) * | 1982-02-22 | 1987-01-14 | Montefluos Spa | Pigmenti compositi e processo per la loro preparazione |
| IT1154630B (it) * | 1982-12-06 | 1987-01-21 | Montedison Spa | Pigmenti gialli compositi fotostabili e processo per la loro preparazione |
| DE3334598A1 (de) * | 1983-09-24 | 1985-04-18 | Merck Patent Gmbh | Witterungsbestaendige perlglanzpigmente |
| JPS60241372A (ja) * | 1984-05-16 | 1985-11-30 | Hitachi Ltd | 画像読取り装置 |
| JPS61264816A (ja) * | 1985-05-17 | 1986-11-22 | Kawamura Denki Sangyo Kk | 光パルス受信回路 |
| CA1269365A (en) * | 1985-06-24 | 1990-05-22 | Howard W. Clark | Insoluble pigments and preparation thereof |
| JPH0611871B2 (ja) * | 1985-10-25 | 1994-02-16 | メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 有機顔料附着薄片状顔料とその製造法 |
| JPH0611870B2 (ja) * | 1986-06-27 | 1994-02-16 | 徳山曹達株式会社 | 無機化合物／染料複合体粒子 |
| FR2605011B1 (fr) * | 1986-10-10 | 1988-12-30 | Rhone Poulenc Chimie | Pigments colores, notamment pigments magnetiques, leurs procedes de preparation et leurs applications, notamment a la preparation de poudres de developpement. |
| US4755229A (en) * | 1987-02-09 | 1988-07-05 | The Mearl Corporation | Colored micaceous pigments |
| JPH07117537B2 (ja) * | 1987-09-11 | 1995-12-18 | 株式会社トクヤマ | 免疫診断用試薬 |
| FI78924C (fi) * | 1988-01-22 | 1989-10-10 | Kemira Oy | Faergaemnes- eller faergpigmenthaltigt paerlemopigment och ett foerfarande foer dess framstaellning. |
| JPH0234669A (ja) * | 1988-07-22 | 1990-02-05 | Kao Corp | 染料含有光沢顔料の製造法 |
| US4968351A (en) * | 1988-11-02 | 1990-11-06 | The Mearl Corporation | Nacreous pigments colored by adsorbed dyes |
| US5106420A (en) * | 1989-10-27 | 1992-04-21 | J. M. Huber Corporation | Mineral based coloring pigments |
| US5587011A (en) * | 1989-10-27 | 1996-12-24 | J. M. Huber Corporation | Optically whitened clay pigments |
| US5106421A (en) * | 1989-10-27 | 1992-04-21 | J. M. Huber Corporation | Mineral dye pigments |
| US5091011A (en) * | 1990-03-12 | 1992-02-25 | The Mearl Corporation | Light and moisture resistant metal oxide-coated mica pigments |
| US5156889A (en) * | 1990-03-12 | 1992-10-20 | The Mearl Corporation | Process for stabilizing metal oxide-coated mica pigments against light and moisture |
| DE4009567A1 (de) * | 1990-03-24 | 1991-09-26 | Merck Patent Gmbh | Beschichtung mit organischen farbstoffen |
| DE4131447A1 (de) * | 1991-09-21 | 1993-03-25 | Basf Ag | Farbige, kristalline alumophosphate und/oder silicoalumophosphate vom ael-typ |
| US5286290A (en) * | 1992-04-16 | 1994-02-15 | Avonite, Inc. | Filler and artificial stone made therewith |
| US5532029A (en) * | 1993-05-13 | 1996-07-02 | Fuerst; Ronnie S. | Materials and methods utilizing a temporary visual indicator |
| US5567420A (en) * | 1994-11-16 | 1996-10-22 | Mceleney; John | Lotion which is temporarily colored upon application |
| DE19525503A1 (de) † | 1995-07-13 | 1997-01-16 | Basf Ag | Goniochromatische Glanzpigmente auf Basis transparenter, nichtmetallischer, plättchenförmiger Substrate |
| US6001167A (en) * | 1996-08-06 | 1999-12-14 | Engelhard Corporation | Pigment compositions |
| US5885342A (en) * | 1997-05-09 | 1999-03-23 | Engelhard Corporation | Blended nacreous pigments, colorants and adjuvants |
| US6107244A (en) * | 1997-10-15 | 2000-08-22 | Nashua Corporation | Verification methods employing thermally--imageable substrates |
| DE19831869A1 (de) * | 1998-07-16 | 2000-01-20 | Merck Patent Gmbh | Farbgebung mit Perlglanzpigmenten im Lebensmittel- und Pharmabereich |
| US6007797A (en) * | 1998-08-06 | 1999-12-28 | Ipa, Llc | Disappearing color sunscreen compositions |
| DE19858460A1 (de) | 1998-12-18 | 2000-06-21 | Basf Ag | Wäßrige metalleffektpigmenthaltige Beschichtungszusammensetzungen |
| US6143280A (en) * | 1999-05-18 | 2000-11-07 | J. M. Huber Corporation | Color containing silica resistant to dye migration and method of making the same |
| JP2001302942A (ja) * | 2000-02-14 | 2001-10-31 | Miyoshi Kasei Kk | 新規複合粉体及びこれを配合した化粧料 |
| US6471762B1 (en) | 2000-08-23 | 2002-10-29 | Engelhard Corp. | Bonded metal-hydroxide-organic composite polymer films on lamellar pigments |
| US6533858B1 (en) | 2000-10-10 | 2003-03-18 | Engelhard Corporation | Effect pigments with improved colorant adhesion |
| JP2003063932A (ja) * | 2001-08-24 | 2003-03-05 | Catalysts & Chem Ind Co Ltd | 化粧料用改質無機微粒子およびそれを配合した化粧料 |
| US6630019B2 (en) | 2001-08-31 | 2003-10-07 | J. M. Huber Corporation | Calcium phosphate colorants and method for making same |
| DE10204336A1 (de) * | 2002-02-01 | 2003-08-14 | Merck Patent Gmbh | Verwendung von Mehrschichtpigmenten im Lebensmittel- und Pharmabereich |
| DE10204789A1 (de) | 2002-02-06 | 2003-08-14 | Merck Patent Gmbh | Inhibitoren des Integrins alpha¶v¶beta6 |
| US7189454B2 (en) * | 2003-05-19 | 2007-03-13 | Engelhard Corporation | Carbon coated high luster materials |
| US7507285B2 (en) | 2004-05-11 | 2009-03-24 | Basf Corporation | Aluminum effect pigment blends |
| US7118622B2 (en) * | 2004-05-19 | 2006-10-10 | Engelhard Corporation | Organic dyes suitable for use in drugs and cosmetics laked onto a platy titanium dioxide pigment |
| ATE501222T1 (de) | 2004-08-23 | 2011-03-15 | Basf Se | Verfahren zur herstellung von blättchenförmigen pigmenten basierend auf aluminium und sioz (z=0.7-2.0) |
| CA2619439A1 (en) * | 2005-08-09 | 2007-02-22 | Soane Laboratories, Llc. | Dye-attached and/or surface-modified pigments |
| US20070108418A1 (en) * | 2005-08-09 | 2007-05-17 | Soane Laboratories, Llc | Hair hold formulations |
| CA2641309A1 (en) | 2006-02-03 | 2007-08-16 | Nanopaper Llc | Functionalization of paper components with an amine-containing polymer |
| US20090165976A1 (en) * | 2006-02-03 | 2009-07-02 | Nanopaper, Llc | Expansion agents for paper-based materials |
| EP2011836B1 (en) | 2006-03-27 | 2013-03-06 | Nippon Sheet Glass Company, Limited | Bright pigment with gold tone, and cosmetic, paint, ink or resin composition containing the same. |
| KR20090008242A (ko) * | 2006-04-07 | 2009-01-21 | 니혼 이타가라스 가부시키가이샤 | 광휘성 안료 및 그 제조 방법, 이 광휘성 안료를 포함하는 화장료, 도료, 잉크, 또는 수지 조성물 |
| US9045643B2 (en) | 2006-04-21 | 2015-06-02 | Nippon Sheet Glass Company Limited | Bright pigment, method for producing the pigment, and waterborne resin composition containing the pigment |
| KR20090064381A (ko) | 2006-08-29 | 2009-06-18 | 니혼 이타가라스 가부시키가이샤 | 진주 광택 안료 |
| US7820563B2 (en) * | 2006-10-23 | 2010-10-26 | Hawaii Nanosciences, Llc | Compositions and methods for imparting oil repellency and/or water repellency |
| JP2008255012A (ja) * | 2007-03-30 | 2008-10-23 | Kose Corp | 口唇化粧料 |
| US9107834B2 (en) | 2007-04-18 | 2015-08-18 | Nippon Sheet Glass Company, Limited | Bright pigment and cosmetic composition using the same |
| US8440014B2 (en) | 2007-04-27 | 2013-05-14 | Nippon Sheet Glass Company, Limited | Bright pigment, and bright coating composition and automotive body coating each containing the same |
| ATE497997T1 (de) | 2007-07-12 | 2011-02-15 | Basf Se | Interferenzpigmente auf basis von perlitschuppen |
| US8409708B2 (en) | 2007-10-18 | 2013-04-02 | Nippon Sheet Glass Company, Limited | Bright pigment |
| WO2011051122A1 (en) | 2009-10-28 | 2011-05-05 | Basf Se | Pigments with improved sparkling effect |
| DE102009051171A1 (de) | 2009-10-29 | 2011-05-05 | Merck Patent Gmbh | Pigmente |
| CN102741358B (zh) | 2010-02-04 | 2015-11-25 | 巴斯夫欧洲公司 | 具有改进闪光效应的颜料组合物 |
| US8475846B2 (en) * | 2010-03-09 | 2013-07-02 | Basf Corporation | Colored micaceous pigments having bismuth oxychloride appearance and performance effects |
| WO2012110858A1 (en) * | 2011-02-14 | 2012-08-23 | Indian Institute Of Technology Kanpur | Doped aluminum oxides |
| CN102746716A (zh) * | 2012-07-12 | 2012-10-24 | 杭州弗沃德精细化工有限公司 | 超细着色云母颜料的制备工艺 |
| EP2883923B1 (en) * | 2012-08-07 | 2017-05-10 | Nippon Paint Automotive Coatings Co., Ltd. | Photoluminescent coating composition, method for forming multilayer coating using same, and multilayer coating |
| US9011893B2 (en) * | 2012-11-14 | 2015-04-21 | U.S. Cosmetics Corporation | Aluminum hydroxide pigments having improved coloring capability |
| US9168209B2 (en) | 2013-03-13 | 2015-10-27 | Johnson & Johnson Consumer Inc. | Pigmented skin-care compositions |
| US9168393B2 (en) | 2013-03-13 | 2015-10-27 | Johnson & Johnson Consumer Inc. | Pigmented skin-care compositions |
| US9320687B2 (en) | 2013-03-13 | 2016-04-26 | Johnson & Johnson Consumer Inc. | Pigmented skin-care compositions |
| US9168394B2 (en) | 2013-03-13 | 2015-10-27 | Johnson & Johnson Consumer Inc. | Pigmented skin-care compositions |
| WO2014186510A1 (en) | 2013-05-15 | 2014-11-20 | Reedy International Corporation | Colorized micron sized free flowing fillers |
| KR101541009B1 (ko) * | 2013-10-28 | 2015-08-03 | 씨큐브 주식회사 | 식물성 천연 염료를 이용한 유색 광택 안료 및 그 제조 방법 |
| US10689518B2 (en) | 2014-07-25 | 2020-06-23 | Merck Patent Gmbh | Colored effect pigments |
| US11034841B2 (en) | 2014-11-24 | 2021-06-15 | Basf Corporation | Carbon black in effect pigments |
| EP3400440B1 (en) | 2016-01-08 | 2024-01-03 | Siemens Healthcare Diagnostics Inc. | Water color pigment solutions for use with reflectance-based diagnostic analyzers |
| DE102017002554A1 (de) | 2017-03-17 | 2018-09-20 | Merck Patent Gmbh | Effektpigmente |
| DE102017011800A1 (de) | 2017-12-20 | 2019-06-27 | Merck Patent Gmbh | Effektpigmente |
| CN110408240A (zh) * | 2019-06-28 | 2019-11-05 | 广西新晶科技有限公司 | 一种纳米无机-有机包膜的云母粉体及其制备方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2053208A (en) * | 1934-12-13 | 1936-09-01 | Merrimac Chemical Co | Color lake |
| US2772984A (en) * | 1952-07-12 | 1956-12-04 | Allied Chem & Dye Corp | Pigment |
| US2935481A (en) * | 1955-04-20 | 1960-05-03 | Monsanto Chemicals | Water-soluble fluorescent dye-coated hydrophobic silica and process of making the same |
| US3036059A (en) * | 1957-05-16 | 1962-05-22 | Sandoz Ag | Lakes of monoazo dyestuffs |
| US2984635A (en) * | 1957-06-03 | 1961-05-16 | Monsanto Chemicals | Composition comprising alumina particles coated with polymer of ethylenically unsaturated monomer |
| DE1192353B (de) * | 1957-11-26 | 1965-05-06 | Faberge Inc Eine Ges Nach Den | Verfahren zur Herstellung eines gefaerbten, feinteiligen, perlmuttartigen Materials |
| GB1000531A (en) * | 1961-05-24 | 1965-08-04 | Huber Corp J M | Colored pigments |
| US3087828A (en) * | 1961-06-28 | 1963-04-30 | Du Pont | Nacreous pigment compositions |
| US3342617A (en) * | 1965-08-12 | 1967-09-19 | Du Pont | Nacreous pigment compositions |
| US3477866A (en) * | 1966-02-07 | 1969-11-11 | Inca Inks | Pigment composition and method of manufacture |
| US3632395A (en) * | 1968-02-01 | 1972-01-04 | Parker Pen Co | Article having light-resistant simulated anodized aluminum coating |
| BE759469A (fr) * | 1969-11-29 | 1971-05-26 | Merck Patent Gmbh | Pigment a brillant nacre et leurs procedes de |
| US3740244A (en) * | 1970-05-16 | 1973-06-19 | Asahi Chemical Ind | Process for producing colored pearl essences |
| US3716388A (en) * | 1970-09-11 | 1973-02-13 | Sandoz Ag | Coloring compositions |
| US3917887A (en) * | 1974-01-24 | 1975-11-04 | Sandoz Ag | Process for dyeing oxide layers on aluminum and aluminum alloys |
-
1974
- 1974-06-21 DE DE2429762A patent/DE2429762C2/de not_active Expired
-
1975
- 1975-06-18 FR FR7519088A patent/FR2275536A1/fr active Granted
- 1975-06-18 GB GB2593675A patent/GB1464060A/en not_active Expired
- 1975-06-19 US US05/588,504 patent/US4084983A/en not_active Expired - Lifetime
- 1975-06-20 ES ES438743A patent/ES438743A1/es not_active Expired
- 1975-06-21 JP JP50076430A patent/JPS5936663B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1464060A (en) | 1977-02-09 |
| JPS5117910A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-02-13 |
| FR2275536B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-10-13 |
| FR2275536A1 (fr) | 1976-01-16 |
| DE2429762A1 (de) | 1976-01-15 |
| ES438743A1 (es) | 1977-05-16 |
| US4084983A (en) | 1978-04-18 |
| JPS5936663B2 (ja) | 1984-09-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| 8125 | Change of the main classification | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition |