US3434890A - Composition and process for forming patina - Google Patents
Composition and process for forming patina Download PDFInfo
- Publication number
- US3434890A US3434890A US725204A US3434890DA US3434890A US 3434890 A US3434890 A US 3434890A US 725204 A US725204 A US 725204A US 3434890D A US3434890D A US 3434890DA US 3434890 A US3434890 A US 3434890A
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- United States
- Prior art keywords
- water
- patina
- amine
- organic solvent
- solution
- 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
- 241001311547 Patina Species 0.000 title description 36
- 239000000203 mixture Substances 0.000 title description 32
- 238000000034 method Methods 0.000 title description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 239000003960 organic solvent Substances 0.000 description 23
- 235000019441 ethanol Nutrition 0.000 description 19
- -1 inorganic acid salt Chemical class 0.000 description 17
- 150000003141 primary amines Chemical class 0.000 description 15
- HZAXFHJVJLSVMW-UHFFFAOYSA-N monoethanolamine hydrochloride Natural products NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- PMUNIMVZCACZBB-UHFFFAOYSA-N 2-hydroxyethylazanium;chloride Chemical compound Cl.NCCO PMUNIMVZCACZBB-UHFFFAOYSA-N 0.000 description 10
- 239000000956 alloy Substances 0.000 description 10
- 229910045601 alloy Inorganic materials 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 10
- 239000002184 metal Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 7
- 229920001800 Shellac Polymers 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 7
- 229940113147 shellac Drugs 0.000 description 7
- 235000013874 shellac Nutrition 0.000 description 7
- 239000004208 shellac Substances 0.000 description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 229910017053 inorganic salt Inorganic materials 0.000 description 5
- 238000005507 spraying Methods 0.000 description 4
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000005909 ethyl alcohol group Chemical group 0.000 description 3
- 239000011253 protective coating Substances 0.000 description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 2
- IKJAVHKRVPYFOD-UHFFFAOYSA-N 2-hydroxyethylazanium;bromide Chemical compound Br.NCCO IKJAVHKRVPYFOD-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- IZBZQUREHISXFJ-UHFFFAOYSA-N 2-[4-chloro-5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetic acid Chemical compound CC1=C(Cl)C(C(F)(F)F)=NN1CC(O)=O IZBZQUREHISXFJ-UHFFFAOYSA-N 0.000 description 1
- IXAZNYYEGLSHOS-UHFFFAOYSA-N 2-aminoethanol;phosphoric acid Chemical compound NCCO.OP(O)(O)=O IXAZNYYEGLSHOS-UHFFFAOYSA-N 0.000 description 1
- IQGWPPQNIZBTBM-UHFFFAOYSA-N 2-aminoethanol;sulfuric acid Chemical compound NCCO.OS(O)(=O)=O IQGWPPQNIZBTBM-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- WJYIASZWHGOTOU-UHFFFAOYSA-N Heptylamine Chemical compound CCCCCCCN WJYIASZWHGOTOU-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical class CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 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
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- HCFPRFJJTHMING-UHFFFAOYSA-N ethane-1,2-diamine;hydron;chloride Chemical compound [Cl-].NCC[NH3+] HCFPRFJJTHMING-UHFFFAOYSA-N 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PHFDTSRDEZEOHG-UHFFFAOYSA-N hydron;octan-1-amine;chloride Chemical compound Cl.CCCCCCCCN PHFDTSRDEZEOHG-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical compound CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/02—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using non-aqueous solutions
Definitions
- My invention is concerned with an improved process for forming patina and to novel compositions therefor.
- Natural patina and the desirable virtues thereof from a decorative and protective standpoint have long been known. Because of a number of disadvantages in the natural process of producing patina as well as in the properties of natural patina, extensive efforts have been made over a period of many years to develop processes for artificially producing patina, for instance, on newly laid copper roofs and similar copper surfaces with a number of objectives in view including the production of a patina simulating natural patina in a short period of time by chemical procedures. Such efforts have been characterized by indifferent success.
- the process of producing artificial patina which is perhaps best known is one which involves first carefully cleaning the copper or copper-base alloy surface to remove dirt, oil and grease therefrom, then spraying the cleaned surface with an aqueous ammoniacal solution of ammonium sulfate and copper sulfate, some five or six sprayings with alternate dryings between sprayings being carried out.
- the development of color depends upon suitable weather conditions, ideal weather conditions following the afore said treatment being a moderate to heavy dew, a light mist or fog, or other condition of high atmospheric moisture content with a relative humidity of 80% or more. Not infrequently, the foregoing process does not produce successful results.
- artificial patina is produced rapidly and in a simple manner, which provides good resemblance to natural patina, and, when the process is carried out in the specified manner, consistently good results are obtained which are essentially independent of weather conditions and, therefore,not generally subject to the vagaries of weather.
- the surface to be treated namely, copper or copper-base alloy such as brass or bronze
- This cleaning step can be carried out with hot water or detergent solutions.
- acid or alkaline cleaners can be utilized, it is preferred to use alkaline cleaners but, in any event, the cleaned metal surface should be carefully rinsed with water to insure removal of any adhering acid or alkaline material.
- the patina coloring compositions described below can be used to clean the metal surface by rubbing said surface with a cloth dampened with the said compositions.
- the cleaned metal surface is then contacted with a solution, in a volatile water-miscible or water-soluble organic solvent (hereafter called volatile water-soluble organic solvent) of an inorganic salt of a primary amine containing not more than 12 carbon atoms, said solution advantageously containing a minor proportion of water.
- a volatile water-miscible or water-soluble organic solvent hereafter called volatile water-soluble organic solvent
- the contact may be effected in any suitable manner as, for instance, by spraying, by dipping, by brushing or by rubbing with a cloth wet with said solution.
- the volatile Water-soluble organic solvent may be removed by evaporation by standing at lower than room temperature but, more advantageously, at temperatures of the order of 70 to degrees F. It is preferred to use said slightly elevated temperatures since, at lower temperatures, there is a tendency toward streakiness.
- patina formation will usually take place in from 5 to 10 minutes, at somewhat elevated temperatures, for instance '70 to 90 degrees F., patina formation commonly occurs in about a minute or two depending upon the particular composition utilized. in certain instances, if patina formation does not occur within about 5 minutes, depending upon temperature, a second coating may be applied and, after drying, the coated metal is allowed to stand until patina formation takes place. It may be noted, here, and as stated above, that patina formation pursuant to my present invention is in no way dependent upon atmospheric or weather conditions but only on temperature considerations which may be simply controlled as desired.
- volatile water-soluble organic solvents can be utilized in the compositions of my invention, as, for example, lower alcohols and ketones such as acetone, I find it especially advantageous to use monohydric aliphatic alcohols such as methyl alcohol, isopropyl alcohol and especially ethyl alcohol, and mixtures of volatile water-soluble organic solvents.
- volatile water-soluble organic solvents I mean those which have a boiling point of not in excess of about 200 degrees F. at atmospheric pressure. I find it particularly desirable to utilize those volatile water-soluble organic solvents which have boiling points in the range of to degrees F.
- the primary amines whose inorganic salts are used in the compositions of my invention are advantageously soluble in the volatile water-soluble organic solvent utilized or, where water is incorporated in the composition, in said organic solvent-water solution, but, in any event, the inorganic acid salts of said amines must be soluble in said organic solvent or organic solvent-water solution.
- water-soluble aliphatic primary amines or aliphatic hydroxy primary amines such as monoethanolamine, monoisopropanolamine, ethylene diamine, diethylene triamine, ethyl amine, propyl amine, isopropylamine, amyl amine, hexyl amine, cyclohexylamine, heptyl amine, octyl amine, nonyl amine, decyl amine, undecyl amine, dodecyl amine, 2-amino-2- methyl-l propanol and the like, although aromatic primary amines such as benzyl amine and aniline can be used but are not preferred. I have found that monoethanolamine is outstandingly satisfactory for the purposes of my invention.
- the acids which are used to form the salts of the aforesaid amines in the compositions of my invention are of inorganic character and include, by way of example, hydrochloric acid, hydrobromic acid, hydrofluoric acid, sulfuric acid, nitric acid and phosphoric acids.
- the nature and color of the patina which is obtained by the practice of my invention, and the speed with which such patina forms, are influenced by both the particular amine utilized and by the particular inorganic acid employed in conjunction therewith.
- amine salts such as monoethanolamine sulfate or monoethanolamine orthophosphate are utilized, the coloration obtained is of relatively dull bluish or greenish character which does not fully desirably simulate natural patina.
- salts of monoethanolamine and hydrochloric acid or hydrobromic acid or hydrofluoric acid, especially monoethanolamine hydrochloride are exceptionally satisfactory and their use represents particularly important, though limited, embodiments of my invention.
- the inorganic acid salts of the primary amines can be preformed and then incorporated With the volatile watersoluble organic solvent, and water where water is used in the compositions, to form a solution, with or without shellac or similar ingredients, or, alternatively, the inorganic acid and the primary amine can be added as such to the aforesaid organic solvent, or organic solvent-water solution, and admixed to form the inorganic acid salt of the primary amine in situ in the composition.
- compositions of my invention may, and advantageously do, include a minor proportion of water which may range from about 2% to 20%, particularly desirably from 5 to 12%, by weight of the composition.
- a minor proportion of water which may range from about 2% to 20%, particularly desirably from 5 to 12%, by weight of the composition.
- the use of water in the compositions aids in the production of a coloring or shade of patina more closely resembling natural patina.
- the water need not, however, be included in the composition since the water may be supplied by a water-moistened or water-wetted surface of the copper or copper-base alloy upon which the patina is to be formed.
- the volatile water-soluble organic solvent will constitute the major ingredient, ranging in proportions from about 60 to 95%, particularly from 75 to 90%, by weight of the composition.
- the inorganic acid salt of the amine constitutes a minor ingredient of the compositions, being present generally in proportions of about 2 to by weight of the compositions, with from 5 to 12% representing a particularly preferred range.
- patina-forming compositions a small proportion, for instance, 3 to 7%, preferably about 4%, by weigh-t of the composition, of shellac or similar resin since this provides for greater adhesion of the composition to the metal surface and tends to inhibit washing off of the coating composition in case of rain occurring before patina formation occurs, and it also aids in causing better adherence of the patina to the metal surface after it is formed.
- a transparent protective coating to the metal surface after the patina or color has formed.
- Suitable protective coatings are, in general, transparent synthetic plastics and resins such as the methacrylates, cellulose esters such as cellulose acetobutyrates, polyvinylidene chlorides, chlorinated rubbers, and the like. I find particularly satisfactory chlorinated rubbers, an illustrative example of which is Parlon (Hercules Powder Co.) in the form of a toluene or xylene solution which may be sprayed on the patina, the organic solvent evaporating rapidly and leaving a transparent protective coating on the patina.
- Parlon Hercules Powder Co.
- Example 1 Parts Ethyl alcohol -a 100 Water 10 Monoethanolamine hydrochloride 10
- Example 2 Ethyl alcohol 100 Water 10 Monoethanolamine hydrochloride l0 Shellac 5
- Example 3 Ethyl alcohol 100 Water 12 Monoethanolamine hydrobromide 11
- Example 4 Methyl alcohol 100 Monoisopropanolamine hydrochloride 8 Water 10
- Example 5 Ethyl alcohol 100 Ethylenediamine hydrochloride 8 Water 10
- Example 6 Ethyl alcohol 100 Monoethanolamine hydrochloride 10
- Example 7 Ethyl alcohol 100 Monoethanolamine hydrobromide l0 Shellac 3
- Example 8 Ethyl alcohol 100 Octyl amine hydrochloride 10
- Example 9 Ethyl alcohol 100 Dodecyl amine hydrochloride 10
- the term coppenbase alloy is used to include copper as Well as copper-base alloys which are susceptible to patina formation.
- a process for forming patina which comprises wetting a copper-base alloy with a solution containing as essential ingredients, by weight, from about 60 to of volatile water-soluble organic solvent, and from about 2 to 20% of inorganic acid salt of a primary amine containing not more than 12 carbon atoms, and allowing the solution to stand in contact with said alloy until patina formation occurs.
- inorganic salt is a member selected from the group consisting of hydrochloric, hydrobromic and hydrofluoric acid salts of said amine.
- Ethyl alcohol 100 Monoethanolamine hydrochloride 5-12 Water 5-12 Shellac 3-7 9.
- a composition for forming patina on a copper-base alloy comprising a solution containing as essential ingreclients, by weight, from about 60 to 95% of volatile water-soluble organic solvent, and from about 2 to 20% of inorganic salt of a primary amine containing not more than 12 carbon atoms.
- a composition according to claim 9 in which the organic solvent is an aliphatic alcohol containing from 1 to 3 carbon atoms, and in which the inorganic salt of the primary amine is a hydrohalide salt of a water-soluble hydroxy primary amine, said hydrohalide being selected from the group consisting of hydrochloride, hydrobromide and hydrofluoride.
- a composition according to claim 13 which includes about 5 to 12 parts water.
- a composition according to claim 14 which includes about 3 to 7 parts shellac.
- composition according to claim 15 in which the solution contains, by weight, about 100 parts of ethyl alcohol, about 10 parts Water, about 10 parts monoethanolamine hydrochloride, and about 5 parts shellac.
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- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Paints Or Removers (AREA)
Description
United States Patent US. Cl. 148--6.14 16 Claims ABSTRACT OF THE DISCLOSURE Formation of patina by wetting a copper-base alloy with a solution ocntaining a predominant proportion of a volatile water-soluble organic solvent and a minor proportion of an inorganic acid salt of a primary amine, for instance, monoethanolamine hydrochloride, and allowing the solution to stand in contact with said alloy until patina formation occurs.
This application is a continuation-in-part of application Ser. No. 364,266, now abandoned, filed May 1, 1964.
My invention is concerned with an improved process for forming patina and to novel compositions therefor.
Natural patina and the desirable virtues thereof from a decorative and protective standpoint have long been known. Because of a number of disadvantages in the natural process of producing patina as well as in the properties of natural patina, extensive efforts have been made over a period of many years to develop processes for artificially producing patina, for instance, on newly laid copper roofs and similar copper surfaces with a number of objectives in view including the production of a patina simulating natural patina in a short period of time by chemical procedures. Such efforts have been characterized by indifferent success. At the present time, the process of producing artificial patina which is perhaps best known is one which involves first carefully cleaning the copper or copper-base alloy surface to remove dirt, oil and grease therefrom, then spraying the cleaned surface with an aqueous ammoniacal solution of ammonium sulfate and copper sulfate, some five or six sprayings with alternate dryings between sprayings being carried out. The development of color depends upon suitable weather conditions, ideal weather conditions following the afore said treatment being a moderate to heavy dew, a light mist or fog, or other condition of high atmospheric moisture content with a relative humidity of 80% or more. Not infrequently, the foregoing process does not produce successful results.
In accordance with my present invention, artificial patina is produced rapidly and in a simple manner, which provides good resemblance to natural patina, and, when the process is carried out in the specified manner, consistently good results are obtained which are essentially independent of weather conditions and, therefore,not generally subject to the vagaries of weather.
In the practice of my invention, the surface to be treated, namely, copper or copper-base alloy such as brass or bronze, should first be cleaned to remove any dirt, dust, oil or grease. This cleaning step can be carried out with hot water or detergent solutions. While acid or alkaline cleaners can be utilized, it is preferred to use alkaline cleaners but, in any event, the cleaned metal surface should be carefully rinsed with water to insure removal of any adhering acid or alkaline material. Instead of using such cleaners, the patina coloring compositions described below can be used to clean the metal surface by rubbing said surface with a cloth dampened with the said compositions.
ice
The cleaned metal surface is then contacted with a solution, in a volatile water-miscible or water-soluble organic solvent (hereafter called volatile water-soluble organic solvent) of an inorganic salt of a primary amine containing not more than 12 carbon atoms, said solution advantageously containing a minor proportion of water. The contact may be effected in any suitable manner as, for instance, by spraying, by dipping, by brushing or by rubbing with a cloth wet with said solution. The volatile Water-soluble organic solvent may be removed by evaporation by standing at lower than room temperature but, more advantageously, at temperatures of the order of 70 to degrees F. It is preferred to use said slightly elevated temperatures since, at lower temperatures, there is a tendency toward streakiness. Generally, only a single coating on the metal is required and the patina will appear within a very few minutes, depending upon the temperature to which the coated metal surface is subjected. At room temperature or thereabouts, patina formation will usually take place in from 5 to 10 minutes, at somewhat elevated temperatures, for instance '70 to 90 degrees F., patina formation commonly occurs in about a minute or two depending upon the particular composition utilized. in certain instances, if patina formation does not occur within about 5 minutes, depending upon temperature, a second coating may be applied and, after drying, the coated metal is allowed to stand until patina formation takes place. It may be noted, here, and as stated above, that patina formation pursuant to my present invention is in no way dependent upon atmospheric or weather conditions but only on temperature considerations which may be simply controlled as desired.
While various volatile water-soluble organic solvents can be utilized in the compositions of my invention, as, for example, lower alcohols and ketones such as acetone, I find it especially advantageous to use monohydric aliphatic alcohols such as methyl alcohol, isopropyl alcohol and especially ethyl alcohol, and mixtures of volatile water-soluble organic solvents. By volatile water-soluble organic solvents, I mean those which have a boiling point of not in excess of about 200 degrees F. at atmospheric pressure. I find it particularly desirable to utilize those volatile water-soluble organic solvents which have boiling points in the range of to degrees F.
The primary amines whose inorganic salts are used in the compositions of my invention are advantageously soluble in the volatile water-soluble organic solvent utilized or, where water is incorporated in the composition, in said organic solvent-water solution, but, in any event, the inorganic acid salts of said amines must be soluble in said organic solvent or organic solvent-water solution. The primary amines which are preferably employed, generally speaking, contain not more than l2 carbon atoms, are of aliphatic character and they maybe straight chain or branched chain. Especially preferred are water-soluble aliphatic primary amines or aliphatic hydroxy primary amines such as monoethanolamine, monoisopropanolamine, ethylene diamine, diethylene triamine, ethyl amine, propyl amine, isopropylamine, amyl amine, hexyl amine, cyclohexylamine, heptyl amine, octyl amine, nonyl amine, decyl amine, undecyl amine, dodecyl amine, 2-amino-2- methyl-l propanol and the like, although aromatic primary amines such as benzyl amine and aniline can be used but are not preferred. I have found that monoethanolamine is outstandingly satisfactory for the purposes of my invention.
The acids which are used to form the salts of the aforesaid amines in the compositions of my invention are of inorganic character and include, by way of example, hydrochloric acid, hydrobromic acid, hydrofluoric acid, sulfuric acid, nitric acid and phosphoric acids. The nature and color of the patina which is obtained by the practice of my invention, and the speed with which such patina forms, are influenced by both the particular amine utilized and by the particular inorganic acid employed in conjunction therewith. Thus, for example, when amine salts such as monoethanolamine sulfate or monoethanolamine orthophosphate are utilized, the coloration obtained is of relatively dull bluish or greenish character which does not fully desirably simulate natural patina. I have found that salts of monoethanolamine and hydrochloric acid or hydrobromic acid or hydrofluoric acid, especially monoethanolamine hydrochloride, are exceptionally satisfactory and their use represents particularly important, though limited, embodiments of my invention.
The inorganic acid salts of the primary amines can be preformed and then incorporated With the volatile watersoluble organic solvent, and water where water is used in the compositions, to form a solution, with or without shellac or similar ingredients, or, alternatively, the inorganic acid and the primary amine can be added as such to the aforesaid organic solvent, or organic solvent-water solution, and admixed to form the inorganic acid salt of the primary amine in situ in the composition. I find it more desirable 'to perform the salt and add it to the organic solvent, or organic solvent-water solution, with stirring and, if desired, slight heating to hasten solubility if necessary.
The compositions of my invention, as stated above, may, and advantageously do, include a minor proportion of water which may range from about 2% to 20%, particularly desirably from 5 to 12%, by weight of the composition. The use of water in the compositions aids in the production of a coloring or shade of patina more closely resembling natural patina. The water need not, however, be included in the composition since the water may be supplied by a water-moistened or water-wetted surface of the copper or copper-base alloy upon which the patina is to be formed.
While the proportions of the other ingredients in the compositions of my invention are variable within reasonable limits, generally speaking, the volatile water-soluble organic solvent will constitute the major ingredient, ranging in proportions from about 60 to 95%, particularly from 75 to 90%, by weight of the composition. The inorganic acid salt of the amine constitutes a minor ingredient of the compositions, being present generally in proportions of about 2 to by weight of the compositions, with from 5 to 12% representing a particularly preferred range.
It is also desirable to include in the patina-forming compositions a small proportion, for instance, 3 to 7%, preferably about 4%, by weigh-t of the composition, of shellac or similar resin since this provides for greater adhesion of the composition to the metal surface and tends to inhibit washing off of the coating composition in case of rain occurring before patina formation occurs, and it also aids in causing better adherence of the patina to the metal surface after it is formed. In this same connection, although rain does not too adversely affect the patina, it is desirable to apply a transparent protective coating to the metal surface after the patina or color has formed. Suitable protective coatings are, in general, transparent synthetic plastics and resins such as the methacrylates, cellulose esters such as cellulose acetobutyrates, polyvinylidene chlorides, chlorinated rubbers, and the like. I find particularly satisfactory chlorinated rubbers, an illustrative example of which is Parlon (Hercules Powder Co.) in the form of a toluene or xylene solution which may be sprayed on the patina, the organic solvent evaporating rapidly and leaving a transparent protective coating on the patina.
The following examples are illustrative of compositions falling within the scope of my invention. Other specific embodiments will readily occur to those skilled in the art in the light of the guiding teachings and principles disclosed herein. All parts listed are by weight.
4 Example 1 Parts Ethyl alcohol -a 100 Water 10 Monoethanolamine hydrochloride 10 Example 2 Ethyl alcohol 100 Water 10 Monoethanolamine hydrochloride l0 Shellac 5 Example 3 Ethyl alcohol 100 Water 12 Monoethanolamine hydrobromide 11 Example 4 Methyl alcohol 100 Monoisopropanolamine hydrochloride 8 Water 10 Example 5 Ethyl alcohol 100 Ethylenediamine hydrochloride 8 Water 10 Example 6 Ethyl alcohol 100 Monoethanolamine hydrochloride 10 Example 7 Ethyl alcohol 100 Monoethanolamine hydrobromide l0 Shellac 3 Example 8 Ethyl alcohol 100 Octyl amine hydrochloride 10 Example 9 Ethyl alcohol 100 Dodecyl amine hydrochloride 10 For simplicity of expression in the claims, the term coppenbase alloy is used to include copper as Well as copper-base alloys which are susceptible to patina formation.
What is claimed is:
1. A process for forming patina which comprises wetting a copper-base alloy with a solution containing as essential ingredients, by weight, from about 60 to of volatile water-soluble organic solvent, and from about 2 to 20% of inorganic acid salt of a primary amine containing not more than 12 carbon atoms, and allowing the solution to stand in contact with said alloy until patina formation occurs.
2. A process according to claim 1 in which the organic solvent is an alcohol, and the primary amine is an aliphatic amine.
3. A process according to claim 2 in which the inorganic salt is a member selected from the group consisting of hydrochloric, hydrobromic and hydrofluoric acid salts of said amine.
4. A process according to claim 1 in which the organic solvent is a water-soluble aliphatic alcohol containing from 1 to 3 carbon atoms, and in which said solution con tains from 5 to 12% water, and from 5 to 12% of hydrohalide salt of a water-soluble hydroxy primary amine, said hydrohalide being selected from the group consisting of hydrochloride, hydrobromide and hydrofluoride.
5. A process according to claim 1 in which the organic solvent is ethyl alcohol and in which the inorganic salt of the primary amine is monoethanolamine hydrochloride.
6. A process according to claim 1 in which the organic solvent is ethyl alcohol, and in which said solution contains from 5 to 12% water, and from 5 to 12% of a hydrochloric acid salt of a water-soluble hydroxy primary amine.
7. A process according to claim 1 in which said solution contains the following ingredients in substantially the stated proportions by weight to each other:
Ethyl alcohol 100 Monoethanolamine hydrochloride 5-12 Water 5-12 8. A process according to claim 1 in which said solution contains the following ingredients in substantially the stated proportions by Weight to each other:
Ethyl alcohol 100 Monoethanolamine hydrochloride 5-12 Water 5-12 Shellac 3-7 9. A composition for forming patina on a copper-base alloy comprising a solution containing as essential ingreclients, by weight, from about 60 to 95% of volatile water-soluble organic solvent, and from about 2 to 20% of inorganic salt of a primary amine containing not more than 12 carbon atoms.
10. A composition according to claim 9 in which the organic solvent is an aliphatic alcohol containing from 1 to 3 carbon atoms, and in which the inorganic salt of the primary amine is a hydrohalide salt of a water-soluble hydroxy primary amine, said hydrohalide being selected from the group consisting of hydrochloride, hydrobromide and hydrofluoride.
11. A composition according to claim in which the hydrohalide is a hydrochloride and in which said Watersoluble hydroxy primary amine hydrochloride comprises from 5 to 12% of the solution, said solution also containing from 5 to 12% of water, said percentages being by weight of said solution.
12. A composition according to claim 9 in which the organic solvent is ethyl alcohol and in which the inorganic acid salt of the primary amine is a water-soluble hydroxy primary amine hydrochloride, said solution also containing a minor amount of water.
13. A composition according to claim 12 in which said solution contains, by weight, about parts of ethyl alcohol and in which the hydroxy primary amine is monoethanolamine, the monoethanolamine hydrochloride comprising from 5 to 12 parts, by weight, of said solution.
14. A composition according to claim 13 which includes about 5 to 12 parts water.
15. A composition according to claim 14 which includes about 3 to 7 parts shellac.
16. A composition according to claim 15 in which the solution contains, by weight, about 100 parts of ethyl alcohol, about 10 parts Water, about 10 parts monoethanolamine hydrochloride, and about 5 parts shellac.
References Cited UNITED STATES PATENTS 2,166,971 7/1939 Schoudt et al. 265-578 ALFRED L. LEAVITT, Primary Examiner.
A. GRIMALDI, Assistant Examiner.
US. Cl. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72520468A | 1968-04-29 | 1968-04-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3434890A true US3434890A (en) | 1969-03-25 |
Family
ID=24913576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US725204A Expired - Lifetime US3434890A (en) | 1968-04-29 | 1968-04-29 | Composition and process for forming patina |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3434890A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5160381A (en) * | 1991-06-26 | 1992-11-03 | Fumigation Maritime Ltee | Method for forming artificially and rapidly patina on copper, products thereof and solutions therefor |
| US5858122A (en) * | 1994-11-14 | 1999-01-12 | The Furukawa Electric Co., Ltd. | Materials capable of readily developing natural patina and process for producing the same |
| US6183570B1 (en) * | 1998-04-16 | 2001-02-06 | Nihon Parkerizing Co., Ltd. | Surface treatment process of metallic material and metallic material obtained thereby |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2166971A (en) * | 1932-09-14 | 1939-07-25 | Ig Farbenindustrie Ag | Production of amines |
-
1968
- 1968-04-29 US US725204A patent/US3434890A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2166971A (en) * | 1932-09-14 | 1939-07-25 | Ig Farbenindustrie Ag | Production of amines |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5160381A (en) * | 1991-06-26 | 1992-11-03 | Fumigation Maritime Ltee | Method for forming artificially and rapidly patina on copper, products thereof and solutions therefor |
| US5858122A (en) * | 1994-11-14 | 1999-01-12 | The Furukawa Electric Co., Ltd. | Materials capable of readily developing natural patina and process for producing the same |
| US6183570B1 (en) * | 1998-04-16 | 2001-02-06 | Nihon Parkerizing Co., Ltd. | Surface treatment process of metallic material and metallic material obtained thereby |
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