US2030236A - Colored oxide film of aluminum - Google Patents
Colored oxide film of aluminum Download PDFInfo
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- US2030236A US2030236A US710376A US71037634A US2030236A US 2030236 A US2030236 A US 2030236A US 710376 A US710376 A US 710376A US 71037634 A US71037634 A US 71037634A US 2030236 A US2030236 A US 2030236A
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- US
- United States
- Prior art keywords
- oxide film
- aluminium
- blue
- tints
- acid
- 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 - Lifetime
Links
- 229910052782 aluminium Inorganic materials 0.000 title description 30
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title description 30
- 239000004411 aluminium Substances 0.000 description 28
- 239000000956 alloy Substances 0.000 description 11
- 229910045601 alloy Inorganic materials 0.000 description 11
- 239000000975 dye Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 238000004043 dyeing Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 150000001845 chromium compounds Chemical class 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 235000005811 Viola adunca Nutrition 0.000 description 4
- 240000009038 Viola odorata Species 0.000 description 4
- 235000013487 Viola odorata Nutrition 0.000 description 4
- 235000002254 Viola papilionacea Nutrition 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- 239000005749 Copper compound Substances 0.000 description 3
- 244000172533 Viola sororia Species 0.000 description 3
- 150000001399 aluminium compounds Chemical class 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 150000001880 copper compounds Chemical class 0.000 description 3
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 150000002736 metal compounds Chemical class 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- AQSOTOUQTVJNMY-UHFFFAOYSA-N 7-(dimethylamino)-4-hydroxy-3-oxophenoxazin-10-ium-1-carboxylic acid;chloride Chemical compound [Cl-].OC(=O)C1=CC(=O)C(O)=C2OC3=CC(N(C)C)=CC=C3[NH+]=C21 AQSOTOUQTVJNMY-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 240000007829 Haematoxylum campechianum Species 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001869 cobalt compounds Chemical class 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002506 iron compounds Chemical class 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
- VWVRASTUFJRTHW-UHFFFAOYSA-N 2-[3-(azetidin-3-yloxy)-4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group O=C(CN1C=C(C(OC2CNC2)=N1)C1=CN=C(NC2CC3=C(C2)C=CC=C3)N=C1)N1CCC2=C(C1)N=NN2 VWVRASTUFJRTHW-UHFFFAOYSA-N 0.000 description 1
- GNKCWVPIWVNYKN-SFQUDFHCSA-N 5-[(e)-(3-carboxy-5-methyl-4-oxocyclohexa-2,5-dien-1-ylidene)-(2,6-dichloro-3-sulfophenyl)methyl]-2-hydroxy-3-methylbenzoic acid Chemical compound C1=C(C(O)=O)C(=O)C(C)=C\C1=C(C=1C(=C(C=CC=1Cl)S(O)(=O)=O)Cl)\C1=CC(C)=C(O)C(C(O)=O)=C1 GNKCWVPIWVNYKN-SFQUDFHCSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 241000134400 Cotinus coggygria Species 0.000 description 1
- 244000163122 Curcuma domestica Species 0.000 description 1
- 235000003392 Curcuma domestica Nutrition 0.000 description 1
- AFSDNFLWKVMVRB-UHFFFAOYSA-N Ellagic acid Chemical compound OC1=C(O)C(OC2=O)=C3C4=C2C=C(O)C(O)=C4OC(=O)C3=C1 AFSDNFLWKVMVRB-UHFFFAOYSA-N 0.000 description 1
- ATJXMQHAMYVHRX-CPCISQLKSA-N Ellagic acid Natural products OC1=C(O)[C@H]2OC(=O)c3cc(O)c(O)c4OC(=O)C(=C1)[C@H]2c34 ATJXMQHAMYVHRX-CPCISQLKSA-N 0.000 description 1
- 229920002079 Ellagic acid Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241001366278 Leptotes marina Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 241001300834 Pictetia aculeata Species 0.000 description 1
- 241000759219 Rhamnus saxatilis Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000012932 acetate dye Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 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 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000012730 carminic acid Nutrition 0.000 description 1
- 239000004106 carminic acid Substances 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
- 235000005487 catechin Nutrition 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- FFUMCSDSJNSMQH-HEXQVDJKSA-K chromoxane cyanin R Chemical compound [Na+].[Na+].[Na+].C1=C(C([O-])=O)C(=O)C(C)=C\C1=C(C=1C(=CC=CC=1)S([O-])(=O)=O)\C1=CC(C)=C(O)C(C([O-])=O)=C1 FFUMCSDSJNSMQH-HEXQVDJKSA-K 0.000 description 1
- 229950001002 cianidanol Drugs 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
- 229940097267 cobaltous chloride Drugs 0.000 description 1
- 229940080423 cochineal Drugs 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- 235000003373 curcuma longa Nutrition 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 1
- 235000004132 ellagic acid Nutrition 0.000 description 1
- 229960002852 ellagic acid Drugs 0.000 description 1
- 229960004887 ferric hydroxide Drugs 0.000 description 1
- XHEFDIBZLJXQHF-UHFFFAOYSA-N fisetin Chemical compound C=1C(O)=CC=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 XHEFDIBZLJXQHF-UHFFFAOYSA-N 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- ADAUKUOAOMLVSN-UHFFFAOYSA-N gallocyanin Chemical compound [Cl-].OC(=O)C1=CC(O)=C(O)C2=[O+]C3=CC(N(C)C)=CC=C3N=C21 ADAUKUOAOMLVSN-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- IEECXTSVVFWGSE-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Fe+3] IEECXTSVVFWGSE-UHFFFAOYSA-M 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- FAARLWTXUUQFSN-UHFFFAOYSA-N methylellagic acid Natural products O1C(=O)C2=CC(O)=C(O)C3=C2C2=C1C(OC)=C(O)C=C2C(=O)O3 FAARLWTXUUQFSN-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000010446 mirabilite Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- ORFSSYGWXNGVFB-UHFFFAOYSA-N sodium 4-amino-6-[[4-[4-[(8-amino-1-hydroxy-5,7-disulfonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-5-hydroxynaphthalene-1,3-disulfonic acid Chemical compound COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N=NC3=C(C4=C(C=C3)C(=CC(=C4N)S(=O)(=O)O)S(=O)(=O)O)O)OC)N=NC5=C(C6=C(C=C5)C(=CC(=C6N)S(=O)(=O)O)S(=O)(=O)O)O.[Na+] ORFSSYGWXNGVFB-UHFFFAOYSA-N 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000004897 thiazines Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 235000013976 turmeric Nutrition 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/04—Anodisation of aluminium or alloys based thereon
- C25D11/18—After-treatment, e.g. pore-sealing
- C25D11/24—Chemical after-treatment
- C25D11/243—Chemical after-treatment using organic dyestuffs
Definitions
- This invention relates to the dyeing of an oxide film of aluminium or an alloy thereof with an organic dyestuff containing a metal in complex combination.
- the oxide film of aluminium or an alloy thereof may be obtained by electrolytic oxidation, such as in a bath containing sulfuric acid, oxalic acid, ammonium bicarbonate or chromic acid.
- dyestuiis containing a metal in complex combination there may be used the mono-metal compounds, for instance the chromium, copper, nickel, cobalt, titanium, vanadium, manganese or iron compound of monoor p'oly-azo-dyestufis; also the poly-metal compounds of these dyestuffs or the complex metal compounds of anthraquinone derivatives, triarylmethane dyestuffs, azines, thiazines or oxazines; also the complex metal compounds of natural organic dyestufis, I
- the oxide film of the aluminium or its alloy may be dyed in various manners; for example, the film may be treated with a solution of a dyestufi containing the metal in complex combination in water, alcohol, acetone, pyridine, an oil varnish, parafiin oil or a fat; such a solution may be sprayed on to the oxide film or painted on it; or the dyestuff containing the metal may be printed in the form of a paste on the oxide film.
- the dye-bath may be neutral and may contain additions such as Glaubers salt; or it may be acid, containing mineral acid or organic acid.
- the temperature of the dye-bath may vary within wide limits; for obtaining the best results, however, it is in many cases of advantage to suit the temperature of the dye-bath to the degree of hydration of the oxide film, in such a manner that films of a weaker degree of hydration are dyed at a higher temperature and films of a stronger degree of hydration at a lower temperature.
- the invention comprises also the dyeing of the oxide film of aluminium or an alloy thereof simultaneously with the production of the film.
- This modification has the advantage that there is only one stage in the process.
- the dyestufi containing the metal in complex combination may be produced in the dye-bath, still further simplifying the procedure.
- the present process there are obtained new compositions of matter consisting of oxide films of aluminium and organic dyestuffs containing complexly bound metal. These compositions of matter show very vivid tints which are very uniform and possess excellent iaetness properties.
- a dye-bath is prepared by dissolving the copper compound of the azo-dyestufi of the formula from diazotized 5-nitro-2-amlno-1-phenol and- 2-phenylamino-5-hydroxynaphthalene 7 sulphonic acid to the extent of 2-10 parts per litre of water, at 40 C.
- the corresponding chromium compound of this dyestufl is used, there is obtained a blue oxide film; the cobalt compound of the same dyestufi. dyes the film grey blue while the aluminium compound and also the nickel compound produces a blue violet.
- Emmple 3 The dyestuif containing chromium and copper obtained from the disazo dyestuii of the formula no nos-- NH son: on
- Example 4 A dye-bath is prepared from 5 parts of the chromium compound of the sulfonated dyestufl of the formula HOOC CODE from 1 mol. 2:6-dichioro-benza1dehyde and 2 moi. ortho-cresotinic acid per litre of liquor. Aiready in the cold, and better at 50 C. this bath colors the immersed oxidized aluminium a vivid blue.
- Reddish-blue tints are obtained by using the chromium compound of the dyestufi! Chromazurol S (Schultz, Farbstofitabellen, 5th edition, No. 554) and the chromium compound of Eriochrome Cyanine R (Schultz, Farbstoiftabellen, 5th edition, No. 553).
- Example 5 To 1000 parts of an oxalic acid bath of 3 per cent. strength, which is to be used for producing an anodic film of aluminum (Zeltschrift fiir eiektr. Chemie, vol. 37, pages 721-724), there are OzNHI added 5 parts of the chromium compound of the azo-dyestuff of the formula from diazotized 4i-chloro-2-amino-i-phenol-6- .sulfonic acid and 1-phenyl-3-methyl-5-pyrazolone in aqueous solution. During the subsequent anodic treatment there is produced on pure aluminimum an oxide layer which is colored red.
- Example 6 A dye-bath is prepared with 4 parts of the chromium compound from 1:2:4z5z6z8-hexahydroxyanthraquinone-3z'l-disulfonic acid of the formula on 0 on HO- SOIH H OH
- Example 7 superficially oxidized aluminium is immersed in an aqueous suspension of 10 percent. strength oi 1:2:5:B-tetrahydroxyanthraquirione ot the formula at 40.
- C At the same time there is added an aqueous solution of copper sulphate and the liquid is boiled for 1 hour. At the end of this time the aluminium is colored stronguniform, very fast'violet tints.
- Example s superficially oxidized aluminium is immersed at ordinary temperature in an alcoholioor acetonic solution of 0.5 per cent. strength of the nickeliferous dyestufi from the aao-estufi of the formula OH 0H from diazotized d-chloro-Z-amino-bphenol and A superficially oxidized aluminium is immersed for half-an-hour at 40-45 C. in an aqueous alcoholic or acetonic solution of 1-10 per cent.
- the chromiferous azo-dyestufi from diazotized i-nitro-Z-amino-l-phenol-fi sulphonic acid and acetonacetic acid anilide or the cupriferous dyestuff from diazotized l-amino-Z-hydrcxynaphthalenei-sulfonic acid and l-hydroxynaphthalene, or the chromiferous azo-dyestuif from diazotized 4-nitro-2-amino-l-phenol 6 sulfonic acid and 2-hydroxynaphthalene, or the cobaltiferous dyestuff from diazotized -nitro-Z-amino- L-phenol and Z-aminonaphthalene, or the ferruginous dyestufi from dia'zotized 4-chloro-2- amino-l-phenol and Z-hydroxy-naphthalene is used in like manner for dyeing an oxide film of aluminium, the latter is dyed yellow
- Example 10 2 parts oi. the cobalt compound of Gallocyanine DH made by heating Gallocyanine DH (Schultz, Farbstofftabellen, 5th edition, No. 626) with a cobaltous chloride solution are dissolved in water and an oxide film of aluminium is dyed with the solution at 60 C. Blue tints are obtained.
- Blue tints are also produced by dyeing the oxide film of aluminium or an alloy thereof with Gallocyanine Blue G (Schultz, Farbstofltabellen,
- Example 11 water and the solution is used for dyeing an oxide film of aluminium at a raised temperature; fast marine blue tints are obtained.
- Example 12 3 parts of logwood (Schultz, Farhstofitabellen, 5th edition, No. 938) are converted into the 00m plex iron compound by heating them in parts of water with 3 parts glycerine and 0.5 part of freshly precipitated ferric hydroxide.
- Example 13 3 parts of old fustic extract (Schultz, rlostofitabellen, 5th edition, No. 925) are converted into the complex aluminium compound by boiling them for half-an-hour in 100 parts of water containing 2 parts of aluminium hydroxide. t yellow tints are obtained by dyeing an oxide film of aluminium or an alloy thereof with this solution.
- a new composition of matter consisting of two components, viz. an electrolytically-produced oxide film of aluminium and azo-dyestufis containing a metal in complex combination, which composition of matter shows very vivid tints which are very uniform and possess excellent fastness properties.
- composition of matter consisting of two components, viz. an eiectroiyticaiiy n-produc oxide iilm of aluminium and monoazo-dyestnita containing chromium in complex combination, which composition of matter shows very vivid tints which are very uniform and possess excei- 5 lent i'astness properties.
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- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Description
Patented Feb. 11, 1936 COLORED OXIDE FILM OF ALUMINIIM Walter Anderau, Basel, Switzerland, assignor to Society of Chemical Industry in Basic, Basel,
Switzerland No Drawing. Application February 8, 1934, Serial No. 710 376. In Switzerland February 16, 1933 8 Qlaims.
This invention relates to the dyeing of an oxide film of aluminium or an alloy thereof with an organic dyestuff containing a metal in complex combination.
The oxide film of aluminium or an alloy thereof may be obtained by electrolytic oxidation, such as in a bath containing sulfuric acid, oxalic acid, ammonium bicarbonate or chromic acid.
As dyestuiis containing a metal in complex combination there may be used the mono-metal compounds, for instance the chromium, copper, nickel, cobalt, titanium, vanadium, manganese or iron compound of monoor p'oly-azo-dyestufis; also the poly-metal compounds of these dyestuffs or the complex metal compounds of anthraquinone derivatives, triarylmethane dyestuffs, azines, thiazines or oxazines; also the complex metal compounds of natural organic dyestufis, I
such as those of young fustic, old rustic, Persian berries, turmeric, quacitron, ellagic acid, cochineal, logwood or catechin.
The oxide film of the aluminium or its alloy may be dyed in various manners; for example, the film may be treated with a solution of a dyestufi containing the metal in complex combination in water, alcohol, acetone, pyridine, an oil varnish, parafiin oil or a fat; such a solution may be sprayed on to the oxide film or painted on it; or the dyestuff containing the metal may be printed in the form of a paste on the oxide film. The dye-bath may be neutral and may contain additions such as Glaubers salt; or it may be acid, containing mineral acid or organic acid. The temperature of the dye-bath may vary within wide limits; for obtaining the best results, however, it is in many cases of advantage to suit the temperature of the dye-bath to the degree of hydration of the oxide film, in such a manner that films of a weaker degree of hydration are dyed at a higher temperature and films of a stronger degree of hydration at a lower temperature.
The invention comprises also the dyeing of the oxide film of aluminium or an alloy thereof simultaneously with the production of the film. This modification has the advantage that there is only one stage in the process.
Furthermore, the dyestufi containing the metal in complex combination may be produced in the dye-bath, still further simplifying the procedure. According to the present process there are obtained new compositions of matter consisting of oxide films of aluminium and organic dyestuffs containing complexly bound metal. These compositions of matter show very vivid tints which are very uniform and possess excellent iaetness properties.
The following examples illustrate the inventim. the parts being by weight:-
Example 1 10 parts of the chromiferous azo-dyestufl ob= tai'ned by chroming the azo-dyestufl of the formula I on I Y A dye-bath is prepared by dissolving the copper compound of the azo-dyestufi of the formula from diazotized 5-nitro-2-amlno-1-phenol and- 2-phenylamino-5-hydroxynaphthalene 7 sulphonic acid to the extent of 2-10 parts per litre of water, at 40 C.
By immersing the oxidized surface of aluminium in this bath there is obtained in a short time a strong blue-violet tint.
If instead of the copper compound, the corresponding chromium compound of this dyestufl is used, there is obtained a blue oxide film; the cobalt compound of the same dyestufi. dyes the film grey blue while the aluminium compound and also the nickel compound produces a blue violet.
Emmple 3 The dyestuif containing chromium and copper obtained from the disazo dyestuii of the formula no nos-- NH son: on
OaNH:
from 7 7' disulfo-5:5'-dihydroxy-2:2'-dinaphthylamine and 2 mol. of diazotized 2-amino-1-hydroxy-i-sulfaminobenzene in a bath of 2-10 per cent. strength at 60-65 C. colors an oxide film of aluminium very fast. strong blue-violet tints.
When the dyeing is conducted with the cupriferous azo-dyestuff obtained from the disazo-dyestun of the formula.
from 2 mol. diazotized i-hydroxy-2-amino-4-suifaminobenzene and 1 mol. of the product of the action of phosgene on z-amino-t's-hydroxynapthalene- 'l-sulfonic acid, there is obtained a blui'sh-.
red oxide film, whereas the cupriferous disazodyestufi' from 2 mol. diazotized 1-hydroxy-2- amino-4-sulfaminobenzene and 1 mol. 7:7'-disulfa-5 5'-dihydroxy-2 2'-dinaphthylamine dyes the oxide film of aluminium blue violet tints. Pure blue tints are obtained by using the cupriferous azc-dyestufi obtained from the disazo-dyestuff of the formula OH NH:
H NH:
from 1 mol. tetrazotized 4:4'-diamino-3:3-dicarboxydiphenyl and 2 mol. 1-amino-8-hydr0xynaphthalene-3 G-disulfonic acid.
Example 4 A dye-bath is prepared from 5 parts of the chromium compound of the sulfonated dyestufl of the formula HOOC CODE from 1 mol. 2:6-dichioro-benza1dehyde and 2 moi. ortho-cresotinic acid per litre of liquor. Aiready in the cold, and better at 50 C. this bath colors the immersed oxidized aluminium a vivid blue.
Reddish-blue tints are obtained by using the chromium compound of the dyestufi! Chromazurol S (Schultz, Farbstofitabellen, 5th edition, No. 554) and the chromium compound of Eriochrome Cyanine R (Schultz, Farbstoiftabellen, 5th edition, No. 553).
Example 5 To 1000 parts of an oxalic acid bath of 3 per cent. strength, which is to be used for producing an anodic film of aluminum (Zeltschrift fiir eiektr. Chemie, vol. 37, pages 721-724), there are OzNHI added 5 parts of the chromium compound of the azo-dyestuff of the formula from diazotized 4i-chloro-2-amino-i-phenol-6- .sulfonic acid and 1-phenyl-3-methyl-5-pyrazolone in aqueous solution. During the subsequent anodic treatment there is produced on pure aluminimum an oxide layer which is colored red.
Example 6 A dye-bath is prepared with 4 parts of the chromium compound from 1:2:4z5z6z8-hexahydroxyanthraquinone-3z'l-disulfonic acid of the formula on 0 on HO- SOIH H OH Example 7 superficially oxidized aluminium is immersed in an aqueous suspension of 10 percent. strength oi 1:2:5:B-tetrahydroxyanthraquirione ot the formula at 40. C. At the same time there is added an aqueous solution of copper sulphate and the liquid is boiled for 1 hour. At the end of this time the aluminium is colored stronguniform, very fast'violet tints.
Example s superficially oxidized aluminium is immersed at ordinary temperature in an alcoholioor acetonic solution of 0.5 per cent. strength of the nickeliferous dyestufi from the aao-estufi of the formula OH 0H from diazotized d-chloro-Z-amino-bphenol and A superficially oxidized aluminium is immersed for half-an-hour at 40-45 C. in an aqueous alcoholic or acetonic solution of 1-10 per cent. strength of the chromiierous and niclzeiiferous dyestufi obtained from the azo-dyestuff of the formula on on from diazotized *l-nitro 2 amino-l-phenol and resorcinol; the aluminium is colored a strong red. c
If the chromiferous azo-dyestufi from diazotized i-nitro-Z-amino-l-phenol-fi sulphonic acid and acetonacetic acid anilide or the cupriferous dyestuff from diazotized l-amino-Z-hydrcxynaphthalenei-sulfonic acid and l-hydroxynaphthalene, or the chromiferous azo-dyestuif from diazotized 4-nitro-2-amino-l-phenol 6 sulfonic acid and 2-hydroxynaphthalene, or the cobaltiferous dyestuff from diazotized -nitro-Z-amino- L-phenol and Z-aminonaphthalene, or the ferruginous dyestufi from dia'zotized 4-chloro-2- amino-l-phenol and Z-hydroxy-naphthalene is used in like manner for dyeing an oxide film of aluminium, the latter is dyed yellow, violet, brown or violet brown or black.
Example 10 2 parts oi. the cobalt compound of Gallocyanine DH made by heating Gallocyanine DH (Schultz, Farbstofftabellen, 5th edition, No. 626) with a cobaltous chloride solution are dissolved in water and an oxide film of aluminium is dyed with the solution at 60 C. Blue tints are obtained.
Blue tints are also produced by dyeing the oxide film of aluminium or an alloy thereof with Gallocyanine Blue G (Schultz, Farbstofltabellen,
5th edition, No. 637), in presence of sodium aluminate, that is to say with the complex aluminium compound of Gallccyanine Blue G.
Example 11 water and the solution is used for dyeing an oxide film of aluminium at a raised temperature; fast marine blue tints are obtained.
The copper compound obtained by treating Indochromine T with copper acetate dyes an oxide film on aluminium vivid blue tints.
Example 12 3 parts of logwood (Schultz, Farhstofitabellen, 5th edition, No. 938) are converted into the 00m plex iron compound by heating them in parts of water with 3 parts glycerine and 0.5 part of freshly precipitated ferric hydroxide.
An oxide film of aluminium dyed for til minutes in this solution is colored deep black.
Example 13 3 parts of old fustic extract (Schultz, rlostofitabellen, 5th edition, No. 925) are converted into the complex aluminium compound by boiling them for half-an-hour in 100 parts of water containing 2 parts of aluminium hydroxide. t yellow tints are obtained by dyeing an oxide film of aluminium or an alloy thereof with this solution.
What I claim is:--
1. Process of coloring an electrolytically=produced oxide film of aluminium or of an alloy thereof, consisting in treating the oxide film oi aluminium or of an alloy thereof with organic dyestuffs containing a metal in complex combt nation.
2. Process of coloring an electrolytically-produced oxide film of aluminium or of an alloy thereof, consisting in treating the oxide film of aluminium or of an alloy thereof with azo-dyastufis containing a, metal in complex combination.
3. Process of coloring an electrolytically produced oxide film of aluminium or of an alloy thereof, consisting in treating the oxide film of stuffs containing a metal in complex combination, which composition of matter shows very vivid tints which are very uniform and possess excellent fastness properties.
6. A new composition of matter consisting of two components, viz. an electrolytically-produced oxide film of aluminium and azo-dyestufis containing a metal in complex combination, which composition of matter shows very vivid tints which are very uniform and possess excellent fastness properties.
lent fastness properties.
8. A new composition of matter consisting of two components, viz. an eiectroiyticaiiy n-produc oxide iilm of aluminium and monoazo-dyestnita containing chromium in complex combination, which composition of matter shows very vivid tints which are very uniform and possess excei- 5 lent i'astness properties.
. WALTER ANDERAU.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH2030236X | 1933-02-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2030236A true US2030236A (en) | 1936-02-11 |
Family
ID=4567203
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US710376A Expired - Lifetime US2030236A (en) | 1933-02-16 | 1934-02-08 | Colored oxide film of aluminum |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2030236A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2814576A (en) * | 1952-01-30 | 1957-11-26 | Ciba Ltd | Process for producing fast dyeings on anodically oxidized aluminium |
| US2960420A (en) * | 1959-01-23 | 1960-11-15 | Mitchell Bradford Chemical Co | Method and composition for blackening metal articles |
| US2989427A (en) * | 1959-04-08 | 1961-06-20 | Allied Chem | Dyeing of aluminum and/or aluminum alloys |
| US3019143A (en) * | 1959-10-21 | 1962-01-30 | Du Pont | Process of coloring anodized aluminum |
| US3291651A (en) * | 1957-06-21 | 1966-12-13 | Ciba Ltd | Dyeing anodized aluminum with cobaltiferous azo-dyestuffs |
| US3874902A (en) * | 1974-05-28 | 1975-04-01 | Stauffer Chemical Co | Method of neutralizing surface color caused by anodizing aluminum alloys |
| US4416816A (en) * | 1972-06-28 | 1983-11-22 | Sandoz Ltd. | 1:2 Chromium complex of 1-amino-2-(3',5'-dinitro-2'-hydroxyphenylazo)-4-sulfonaphthalene and alkali metal salts thereof |
-
1934
- 1934-02-08 US US710376A patent/US2030236A/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2814576A (en) * | 1952-01-30 | 1957-11-26 | Ciba Ltd | Process for producing fast dyeings on anodically oxidized aluminium |
| US3291651A (en) * | 1957-06-21 | 1966-12-13 | Ciba Ltd | Dyeing anodized aluminum with cobaltiferous azo-dyestuffs |
| US2960420A (en) * | 1959-01-23 | 1960-11-15 | Mitchell Bradford Chemical Co | Method and composition for blackening metal articles |
| US2989427A (en) * | 1959-04-08 | 1961-06-20 | Allied Chem | Dyeing of aluminum and/or aluminum alloys |
| US3019143A (en) * | 1959-10-21 | 1962-01-30 | Du Pont | Process of coloring anodized aluminum |
| US4416816A (en) * | 1972-06-28 | 1983-11-22 | Sandoz Ltd. | 1:2 Chromium complex of 1-amino-2-(3',5'-dinitro-2'-hydroxyphenylazo)-4-sulfonaphthalene and alkali metal salts thereof |
| US4469485A (en) * | 1972-06-28 | 1984-09-04 | Sandoz Ltd. | Use of the 1:2 chromium complex of 1-amino-2-(3', 5'-dinitro-2'-hydroxyphenylazo)-4-sulfonaphthalene and alkali metal salts thereof for dyeing polyamides and oxide layers on aluminum and aluminum alloys |
| US3874902A (en) * | 1974-05-28 | 1975-04-01 | Stauffer Chemical Co | Method of neutralizing surface color caused by anodizing aluminum alloys |
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