AU2012204141B2 - Methods and compositions for acid treatment of a metal surface - Google Patents
Methods and compositions for acid treatment of a metal surface Download PDFInfo
- Publication number
- AU2012204141B2 AU2012204141B2 AU2012204141A AU2012204141A AU2012204141B2 AU 2012204141 B2 AU2012204141 B2 AU 2012204141B2 AU 2012204141 A AU2012204141 A AU 2012204141A AU 2012204141 A AU2012204141 A AU 2012204141A AU 2012204141 B2 AU2012204141 B2 AU 2012204141B2
- Authority
- AU
- Australia
- Prior art keywords
- acid
- aluminum
- etching
- per liter
- grams per
- 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.)
- Ceased
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- 238000000034 method Methods 0.000 title claims abstract description 70
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 42
- 239000002184 metal Substances 0.000 title claims abstract description 42
- 238000010306 acid treatment Methods 0.000 title description 3
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 68
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- 238000005530 etching Methods 0.000 claims abstract description 36
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- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 18
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- 235000019838 diammonium phosphate Nutrition 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 7
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- QSQIGGCOCHABAP-UHFFFAOYSA-N hexacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC6=CC=CC=C6C=C5C=C4C=C3C=C21 QSQIGGCOCHABAP-UHFFFAOYSA-N 0.000 description 1
- PKIFBGYEEVFWTJ-UHFFFAOYSA-N hexaphene Chemical compound C1=CC=C2C=C3C4=CC5=CC6=CC=CC=C6C=C5C=C4C=CC3=CC2=C1 PKIFBGYEEVFWTJ-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 150000002467 indacenes Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000014413 iron hydroxide Nutrition 0.000 description 1
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
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- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- RRSMHQNLDRCPQG-UHFFFAOYSA-N methanamine;hydrofluoride Chemical compound [F-].[NH3+]C RRSMHQNLDRCPQG-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- PFTXKXWAXWAZBP-UHFFFAOYSA-N octacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC6=CC7=CC8=CC=CC=C8C=C7C=C6C=C5C=C4C=C3C=C21 PFTXKXWAXWAZBP-UHFFFAOYSA-N 0.000 description 1
- OVPVGJFDFSJUIG-UHFFFAOYSA-N octalene Chemical compound C1=CC=CC=C2C=CC=CC=CC2=C1 OVPVGJFDFSJUIG-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- WTFQBTLMPISHTA-UHFFFAOYSA-N octaphene Chemical compound C1=CC=C2C=C(C=C3C4=CC5=CC6=CC7=CC=CC=C7C=C6C=C5C=C4C=CC3=C3)C3=CC2=C1 WTFQBTLMPISHTA-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LSQODMMMSXHVCN-UHFFFAOYSA-N ovalene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3C5=C6C(C=C3)=CC=C3C6=C6C(C=C3)=C3)C4=C5C6=C2C3=C1 LSQODMMMSXHVCN-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N penta-1,3-diene Chemical compound CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 1
- GUVXZFRDPCKWEM-UHFFFAOYSA-N pentalene Chemical compound C1=CC2=CC=CC2=C1 GUVXZFRDPCKWEM-UHFFFAOYSA-N 0.000 description 1
- JQQSUOJIMKJQHS-UHFFFAOYSA-N pentaphene Chemical compound C1=CC=C2C=C3C4=CC5=CC=CC=C5C=C4C=CC3=CC2=C1 JQQSUOJIMKJQHS-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- XDJOIMJURHQYDW-UHFFFAOYSA-N phenalene Chemical compound C1=CC(CC=C2)=C3C2=CC=CC3=C1 XDJOIMJURHQYDW-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- DIJNSQQKNIVDPV-UHFFFAOYSA-N pleiadene Chemical compound C1=C2[CH]C=CC=C2C=C2C=CC=C3[C]2C1=CC=C3 DIJNSQQKNIVDPV-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LNKHTYQPVMAJSF-UHFFFAOYSA-N pyranthrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC3=C(C=CC=C4)C4=CC4=CC=C1C2=C34 LNKHTYQPVMAJSF-UHFFFAOYSA-N 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- FMKFBRKHHLWKDB-UHFFFAOYSA-N rubicene Chemical compound C12=CC=CC=C2C2=CC=CC3=C2C1=C1C=CC=C2C4=CC=CC=C4C3=C21 FMKFBRKHHLWKDB-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- BFXAWOHHDUIALU-UHFFFAOYSA-M sodium;hydron;difluoride Chemical compound F.[F-].[Na+] BFXAWOHHDUIALU-UHFFFAOYSA-M 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
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- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- ing And Chemical Polishing (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Abstract
The invention relates to compositions and methods that are useful in etching a metal surface. In particular, the invention relates to novel acid compositions and methods of using such compositions in etching an aluminum surface prior to anodizing to dissolve impurities, imperfections, scale, and oxide. The composition is effective in maintaining its etching capacity and in removing smut produced by the etching of an aluminum surface as well as in general cleaning.
Description
P/00101 1 Regulation 3.2 AUSTRALIA Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Invention Title: Methods and compositions for acid treatment of a metal surface The following statement is a full description of this invention, including the best method of performing it known to us: METHODS AND COMPOSITIONS FOR ACID TREATMENT OF A METAL SURFACE I. FIELD OF THE INVENTION [00011 The invention relates to compositions and methods that are useful in etching a metal surface. In particular, the invention relates to novel acid compositions and methods of using such compositions in etching an aluminum surface prior to anodizing to dissolve impurities, imperfections, scale, and oxide. The composition is effective in maintaining its etching capacity and in removing smut produced by the etching of an aluminum surface as well as in general cleaning. I. BACKGROUND OF THE INVENTION [0002] Articles made of aluminum or aluminum alloy, are customarily manufactured by a metal-forming operation called drawing and ironing. In the course of this and similar metal-forming operations a lubricant oil is applied to the surface of the metal being deformed, and some abraded aluminum particles and other contaminates (usually referred to as "smut") adhere to the metal surface, especially to the inner walls of such beverage containers. The surfaces are protected by subsequent chemical-conversion coating and/or paint coating techniques. Therefore, the above-mentioned lubricant oil or smut must be removed, by cleaning, from the metal surfaces before the chemical-conversion coating. [00031 This surface cleaning is normally applied by means of an acidic cleaning agent, which appropriately etches the metal surfaces. The currently used acidic cleaning agents used for smut-removal have generally been ones containing chromic acid or hydrofluoric acid. Especially, the cleaning agent containing the hydrofluoric acid is superior in enabling the low-temperature acidic cleaning (e.g., up to 50 "C.). [00041 U.S. Pat. Nos. 4,728,456 and 4,851,148 disclose a cleaning agent including an acidic cleaning agent of pH 2 or below prepared from sulfuric acid and nitric -IA acid containing little or no fluoric ions with the addition of ferric ions serving an accelerator instead of fluoride ions, and a method for controlling the oxidation-reduction potential of the cleaning bath to control the ferric ion concentration in the bath, respectively. [00051 PCT published application WO 9301332-Al discloses an acidic cleaning solution containing sulfuric acid and/or nitric acid and ferric ions serving as an accelerator for etching instead of fluoride ions, and further containing oxidized ion of diphenylarnine having color-change potential (that is, at a transition of a certain potential, color becomes transparent) in the vicinity of standard oxidation-reduction potential (+0.77 +/- 0.09 V) where ferric ions (Fe 3 *) are changed into ferrous ions (Fe 2 +), oxidized ions of diphenylbenzidine and oxidized ions of sulfonic diphenylamine, and the cleaning process for controlling the ferric ion concentration by controlling the color-change point. 100061 U.S. Pat. No. 3,607,484 discloses is a corrosion liquid consisting of sulfuric acid aqueous solution with the addition of metals (ions of Cu, Fe, Ni, Co, Sn, Zn, etc.) having a smaller ionization tendency than aluminum and 7 g ion/l of at least one selected from halogen ions (F~, Br~, T) besides CT, P0 4 3 , pyrophosphoric ion, pentaphasphoric ion and so on. [00071 Japanese Patent Publication No. 47-39823 discloses a corrosion liquid containing 0.1 to 7.0 g ion/l of at least one of CT, F~, Br, I, phosphoric ion, pyrophosphoric ion, pentaphosphoric ion and so on. [00081 Generally, the etching reaction of aluminum within the acidic cleaning solution includes an anode reaction in which aluminum is changed into aluminum ions (A13') and a cathode reaction in which H in the cleaning solution is reduced into 1/2 H 2 . Thus, the addition of ferric ions (Fe 3 *) into the acidic cleaning solution simultaneously causes a cathode action for reducing Fe 3 * into Fe 2 + and the reduction of H, which accelerates the etching reaction of aluminum. 100091 Further, the oxidizing agent is used to control the oxidation-reduction potential to control the ferric ion concentration within the bath, thereby suppressing the Fe2+ concentration which increases accordingly as the etching reaction advances and oxidizing the Fe 2 + into Fe 3 '. -2- 10010] It is hbieWver known that the oxidizing agent typically acts to oxidize and decompose the surfactant. Therefore, the addition of an oxidizing agent into an acidic cleaning aqueous solution containing a surfactant for improving the degreasing ability may cause accumulation of oxidized decomposed substance within the cleaning bath, which will lead to a reduction in the degreasing ability on the aluminum surfaces. On the contrary, the addition of excessive oxidizing agent in order to maintain the degreasing ability will increase the operating cost. [00111 In PCT published application WO 91 19830-Al there is proposed an "acidic liquid composition and process for cleaning aluminum" containing a mineral acid selected from the group of phosphoric acid, sulfuric acid, and nitric acid, multiply charged metallic ions, surfactant, and oxidizing agent for oxidizing the multiply charged metallic ions which were reduced during the cleaning operation, with the addition of 0.05 to 5 g/l of a C 2 to Clo glycol for suppressing the decomposing reaction of surfactant due to the oxidizing agent. [0012] In the case of using the acidic cleaning agent disclosed in U.S. Pat Nos. 4,728,456 and 4,851,148, however, the treatment must be made at a higher temperature (70 *C. to 80 "C) than the temperature (up to 50 "C) of acidic cleaning by means of acidic cleaning agent containing fluoric ions in order to obtain the same effect as theFacidic cleaning by the acidic-cleaning agent containing fluoride ions, which will be economically disadvantageous. Since a multiplicity of Fe 3 + ions are contained, a precipitation derived from ferric ions is produced, and in particular, iron hydroxide which is in the form of a precipitate may adhere to the heater section. Also, in the case of WO 9301332-Al, it is necessary to perform acidic cleaning at high temperature, which will be economically disadvantageous. 100131 The corrosion liquid disclosed in U.S. Pat No. 3,607,484 and Japanese Patent Publication No. 47-39823 mainly aims to etch the aluminum alloy by electrodeposition in order to form a photoengraving. In the case of coexisting with the copper ion, as disclosed by U.S. Pat. No. 3,607,484, the oxidation reduction potential is over 1.08 V in the etching treatment. Therefore, the use of Br ions as halogen ions besides CI would lead to the reaction. 2Br -> Br 2 -3 - +2e, which leads to the production of harmful bromine gas. Thus, exclusive treatment facility must be provided, which will be economically disadvantageous. In addition, these corrosion liquids contain 56 g/1l or more of bromide ions for its object in the examples, which is different in the object of etching from the present invention. 5 [0014] In the acidic cleaning aqueous solution disclosed in WO 9119830-Al, the content of a C 2 to CIO glycol for the suppression of decomposition reaction of surfactant by the oxidizing agent is 0.05 to 5 g/1 (namely, 50 to 5000 ppm) within the acidic cleaning aqueous solution, and hence the glycol compounds do not solely have the etching accelerating effect. Reversely, a large volume of addition will increase the effective ingredients, which 10 will increase the load of liquid waste treatment. [0015] The present invention was conceived in view of the above conventional problems. The present invention seeks to provide an acidic cleaning solution for aluminum and aluminum alloy and its cleaning process. Reference to any prior art in the specification is not, and should not be taken as, an 15 acknowledgment, or any form of suggestion, that this prior art forms part of the common general knowledge in Australia or any other jurisdiction or that this prior art could reasonably be expected to be ascertained, understood and regarded as relevant by a person skilled in the art. III. SUMMARY OF THE INVENTION 20 [0016] Alkaline etch is the most popular and common etch process prior to sulfuric acid anodizing. The present invention encompasses novel methods of etching a metal, preferably aluminum, to dissolve impurities, imperfections, scale and oxide from the metal surface, preferably an aluminum surface. The method also provides a technique to remove or minimize extrusion lines to produce a uniform texture and better appearance for the 25 finished product. [0017] It has now been discovered that an aluminum alloy may be etched in an acid solution at a temperature from about 70 OF to about 200 OF, preferably from about 70 OF to about 150 OF. The etch composition of the present invention encompasses an aqueous, acidic solution comprising at least one organic acid, at least one acid salt, at least one surfactant, 30 at least one grain refiner, and at least one fluoride salt or a combination thereof. The etch
A
composition can optionally further comprise at least one mineral acid. The methods of the invention provide compositions with a uniform texture. [0018] In one embodiment the invention encompasses a composition for etching a metal, preferably aluminum or aluminum alloy, comprising an aqueous acidic solution 5 comprising one or more organic acids, fluoride ion compounds, such as for example a fluoride salt, one or more grain refiners, and one or more surfactants. Optionally the composition comprises one or more mineral acids. [0019] In another embodiment the invention encompasses a composition for etching a metal, preferably aluminum or aluminum alloy, comprising ammonium bifluoride, hydrofluoric 10 acid, glycolic acid, and a surfactant. [0020] In yet another embodiment the invention encompasses a method of treating the surface of a metal, preferably aluminum or aluminum alloy, which comprises treating the metal (preferably the aluminum or aluminum alloy) with a composition comprising an aqueous acidic solution comprising one or more organic acids, fluoride ion compounds, such as for 15 example a fluoride salt, one or more grain refiners, and one or more surfactants. The method further encompasses optionally treating with one or more mineral acids. The present invention also relates to a composition comprising: (i) one or more fluoride ion compounds selected from the group consisting of hydrofluoric acid, hydrofluorosilsilic acid, fluoroboric acid, ammonium bifluoride, 20 sodium fluoride, and potassium fluoride; (ii) one or more surfactants; and (iii) one or more grain refiners selected from the group consisting of diammonium phosphate, ammonium phosphate, and sodium phosphate. The present invention also relates to an aqueous composition comprising: 25 (i) one or more fluoride ion compounds selected from the group consisting of hydrofluoric acid, hydrofluorosilsilic acid, fluoroboric acid, ammonium bifluoride, sodium fluoride, and potassium fluoride; (ii) one or more surfactants; and (iii) one or more grain refiners selected from the group consisting of diammonium 30 phosphate, ammonium phosphate, and sodium phosphate.
The present invention also relates to an acid etch bath comprising: (i) one or more fluoride ion compounds selected from the group consisting of hydrofluoric acid, hydrofluorosilsilic acid, fluoroboric acid, ammonium bifluoride, sodium fluoride, and potassium fluoride; 5 (ii) one or more grain refiners selected from the group consisting of diammonium phosphate, ammonium phosphate, and. sodium phosphate; (iii) water; and (iv) aluminum metal or an aluminum metal alloy. The present invention also relates to a composition consisting of: 10 (i) about 10 to about 200 grams per liter of a fluoride ion compound selected from the group consisting of hydrofluoric acid, hydrofluorosilsilic acid, fluoroboric acid, ammonium bifluoride, sodium fluoride, and potassium fluoride; (ii) about 1 to about 50 grams per liter of a grain refiner selected from the group consisting of diammonium phosphate, ammonium phosphate, and sodium 15 phosphate; (iii) water. IV. DETAILED DESCRIPTION OF THE INVENTION A. Definitions. [0021] As used herein and unless otherwise indicated, the term "alkyl" or alkyll group" means a 20 saturated, monovalent, unbranched (i.e., linear) or branched hydrocarbon chain. An alkyll group" further means a monovalent group selected from (Ci-Cs)alkyl, (C 2
-C
8 )alkenyl, and
(C
2 -Cs)alkynyl, optionally substituted with one or two suitable substituents. Preferably, the hydrocarbon chain of a hydrocarbon group is from 1 to 6 carbon atoms in length, referred to herein as "(Ci-C 6 )hydrocarbon." Examples of alkyl groups or hydrocarbon groups 25 include, but are not limited to, (CI-C6)alkyl groups, such as methyl, ethyl, propyl, isopropyl, 2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl, 3-methyl-1-butyl, 2 methyl-3-butyl, 2,2-dimethyl-1-propyl, 2-methyl-i-pentyl, 3-methyl-1-pentyl, 4-methyl-i pentyl, 2-methyl-2-pentyl, 3-methyl-2- ~pentyf~ 4:metiyl-2-pentyl, 2,2-diinethyl-1-butyl, 3,3-dimethyl- I-butyl, 2 ethyl-l-butyl, butyl, isobutyl, t-butyl, pentyl, isopentyl, neopentyl, and hexyl, and longer alkyl groups, such as heptyl, and octyl. An alkyl group can be unsubstituted or substituted with one or two suitable substituents. [0022] As used herein and unless otherwise indicated, the term "aryl" refers to a monovalent aromatic hydrocarbon group derived by the removal of one hydrogen atom from a single carbon atom of a parent aromatic ring system (e.g., removal of a -H atom from benzene). Typical aryl groups include, but are not limited to, groups derived from aceanthrylene, acenaphthylene, acephenanithrylene, anthracene, azulene, benzene, chrysene, coronene, fluoranthene, fluorene, hexacene, hexaphene, hexalene, as-indacene, s indacene, indane, indene, naphthalene, octacene, octaphene, octalene, ovalene, penta-2,4-diene, pentacene, pentalene, pentaphene, perylene, phenalene, phenanthrene, picene, pleiadene, pyrene, pyranthrene, rubicene, triphenylene, trinaphthalene and the like. Preferably, an aryl group comprises from 6 to 24 carbon atoms. [0023] As used herein and unless otherwise indicated, the term "etching" or "etch" will be understood by persons of ordinary skill in the art to include, but not be limited to cleaning of an aluminum or aluminum alloy surface, dissolving impurities, imperfections, scale or oxide from an aluminum or aluminum alloy surface. [00241 As used herein and unless otherwise indicated, the term "fluoride salt(s)" and "fluoride ion compounds" are used interchangeably and will be understood by persons of ordinary skill in the art to include, but not be limited to, fluoride salts and bifluoride salts including metal salts, ammonium salts and quaternary ammonium salts. Illustrative examples of the fluoride metal salts include those which have high solubility, such as potassium fluorides, sodium fluoride, potassium hydrogen fluoride, sodium hydrogen fluoride and the like. Examples of the ammonium salts encompassed by the invention include, but are not limited to, ammonium fluoride and ammonium hydrogen fluoride (ammonium hydrogen fluoride). Examples of the quaternary ammonium salts encompassed by the invention include, but are not limited to, tetramethyl -6ammonium fluoride, methylamine hydrofluoride, 2-hydroxyethyltrimethylarnronium fluoride, tetramethylarnmonuum hydrogen fluoride. [00251 As used herein and unless otherwise indicated, the term "grain refiner" refers to any material that is added to a metal or alloy because of its high melting temperature that 5 enhances the physical properties of the metal or alloy. Illustrative examples of grain refiners include, but are not limited to, sodium, potassium, or ammonium salts. Particular examples of grain refiners include, but are not limited to sodium phosphate, ammonium phosphate, or diammonium phosphate or mixtures thereof. [0026] As used herein and unless otherwise indicated, the term "organic acid" includes, but is not 10 limited to, acetic acid, propionic acid, butyric acid, isobutyric, valeric acid, caproic acid, caprylic acid, monochloroacetic acid, dichloroacetic acid, trichloroacetic acid, monofiuoroacetic acid, difluoroacetic acid, trifluoroacetic acid, alpha-chlorobutyric acid, beta-chlorobutyric acid, gamma-chlorobutyric acid, lactic acid, glycolic acid, pyruvic acid, glyoxalic acid, acrylic acid and like monocarboxylic acids, methanesulfonic acid, 15 toluenesulfonic acid and like sulfonic acids, oxalic acid, succinic acid, adipic acid, tartaric acid, citric acid and like polycarboxylic acids. As used herein, except where the context requires otherwise, the term "comprise" and variations of the term, such as "comprising", "comprises" and "comprised", are not intended to exclude other additives, components, integers or steps. 20 B. Compositions of the Invention 10027] In one embodiment the invention encompasses novel aqueous acidic compositions for treating the surface of a metal. In an illustrative embodiment, the compositions are useful for treating a surface prior to anodizing the surface. In another embodiment, the compositions are useful for etching a surface to dissolve impurities, imperfections, scale 25 and/or oxide from the metal surface. In a preferred embodiment, the metal surface is an aluminum or aluminum alloy surface. The compositions are also useful for removing or minimizing extrusion line to produce a uniform texture and better appearance for the finished surface. [0028] In another embodiment, the compositions of the invention comprise one or more fluoride 30 ion compounds, one or more organic acids, and one or more surfactants or combinations thereof. The composition optionally comprises one or more grain refiners and/or one or more mineral acids. [00291 Another embodiment of the invention encompasses an aqueous, acidic solution comprising one or more grain refiners, one or more fluoride ion compounds, such as for example a fluoride salt, one or more grain refiners, and one or more surfactants. The composition optionally comprises one or more organic acids and/or one or more mineral acids. [00301 In another embodiment, the compositions of the invention have a pH from about 2.0 to about 5.0, preferably from about 3.0 to about 4.0. In an illustrative embodiment, the compositions overcome limitations of alkaline etch solutions. [00311 In another illustrative embodiment, the organic acid of the invention includes, but is not limited to, oxalic acid or glycolic acid or mixtures thereof. Preferably, the organic acid is present in an amount from about I to about 30 grams per liter, more preferably from about 2.5 to about 25 grams per liter, and even more preferably from about 5 to about 20 grams per liter. [0032] In another illustrative embodiment, the surfactant of the invention includes, but is not limited to, nonionic surfactant, an amphoteric surfactant, or a synergistic surfactant. Preferably, the surfactant comprises salts of alkyl aryl sulfonates, alkyl sulfonates, alkyl ether sulfates, alkyl sulfates, alkyl taurates, alkyl sulfosuccinates, hydrocarbon derivatives, abietic acid derivatives, ethoxylated primary alcohols, and modified polyethoxylated alcohols, individually or in combinations of two or more. Preferably, the surfactant is present in an amount from about 1 to about 3 grams per liter. _ [0033] In another illustrative embodiment, the fluoride ion compound of the invention includes, but is not limited to, hydrofluoric acid, hydrofluorosilic acid, or fluoroboric acid or mixtures thereof. In another preferred embodiment, the fluoride ion compound is a fluoride salt. Preferred fluoride salts include, but are not limited to, sodium fluoride, potassium fluoride, ammonium bifluoride or mixtures thereof. Preferably, the fluoride ion compound is present in an amount from about 5 to about 225 grams per liter, preferably from about 10 to -8about 200 grams per liter, more preferably from about 20 to about 80 grams per liter, and even more preferably from about 60 to about 70 grams per liter. [0034] In another illustrative embodiment, the grain refiner of the invention includes, but is not limited to, sodium phosphate, ammonium phosphate, or diammonium phosphate or a mixture thereof. In an illustrative embodiment, the composition comprises a single grain refiner. In another illustrative embodiment, the composition comprises combinations of two or more grain refiners. In an illustrative embodiment, the grain refiner is present in.an amount of from about 1 to about 50 grams per liter, preferably from about 5 to about 30 grams per liter, and more preferably from about 10 to about 20 grams per liter. 10035] In another illustrative embodiment, the mineral acid of the invention is hydrofluoric acid, nitric acid, sulfuric acid, or phosphoric acid or mixtures thereof. Preferably, the mineral acid is present in an amount from about 20 to about 100 grams per liter, more preferably from about 30 to about 90 grams per liter and even more preferably from about 40 to about 80 grams per liter. [00361 In a particular embodiment, the invention encompasses a composition for etching aluminum or aluminum alloy, comprising ammonium bifluoride, hydrofluoric acid, glycolic acid, and surfactant. C. Methods of the Invention [0037] Another embodiment of the invention encompasses a method of treating the surface of a metal, preferably aluminum or aluminum allow, which comprises treating the metal (preferably aluminum or aluminum allow) with a composition comprising a one or more fluoride ion compounds, one or more mineral acids, one or more organic acids and one or more surfactants. [0038] In an illustrative embodiment, the treatment is done at a solution temperature of about 60 "F to about 200 *F, preferably at a solution temperature of about 70 *F to about 150 *F, and more preferably at a solution temperature of about 100 *F to about 120 *F. Preferably, the treatment is done from about 0.5 to -9about 15 minutes, preferably from about i to about 10 minutes, and more preferably from about 3 to about 5 minutes. [0039] In one embodiment the invention encompasses a novel method for treating the surface of a metal comprising contacting the surface of the metal with an aqueous acidic composition. In an illustrative embodiment, the methods are useful for treating a surface prior to anodizing the surface. In another embodiment, the methods are useful for etching a surface to dissolve impurities, imperfections, scale and/or oxide from the metal surface. In a preferred embodiment, the metal surface is an aluminum or aluminum alloy surface. The methods are also useful for removing or minimizing extrusion line to produce a uniform texture and better appearance for the finished surface. [00401 In another embodiment, the methods of the invention comprise contacting a metal surface, preferably aluminum or aluminum alloy, with one or more fluoride ion compounds, one or more organic acids, and one or more surfactants or combinations thereof. The methods optionally comprise contacting the metal surface with one or more grain refiners and/or one or more mineral acids. [00411 Another embodiment of die invention encompasses a method for treating a metal surface, preferably aluminum or aluminum alloy comprising contacting the metal surface with one or more grain refiners, one or more fluoride ion compounds, such as for example a fluoride salt, one or more grain refiners, and one or more surfactants. The method optionally comprises treating a metal surface with one or more organic acids and/or one or more mineral acids. [0042] In another embodiment, the methods of the invention encompass contacting a metal surface with a composition of the invention having a pH from about 2.0 to about 5.0, preferably from about 3.0 to about 4.0. In an illustrative embodiment, the methods overcome limitations of alkaline etch solutions. [00431 In another illustrative embodiment, the organic acid encompassed by the method for treating a metal surface, preferably aluminum or aluminum alloy, include, but are not limited to, oxalic acid or glycolic acid or mixtures thereof. -10- Preferably, the organic acid is present in an amount from about I to about 30 grams per liter, more preferably from about 2.5 to about 25 grams per liter, and even more preferably from about 5 to about 20 grams per liter. [00441 In another illustrative embodiment, the surfactants encompassed by the method for treating a metal surface, preferably aluminum or aluminum alloy, include, but are not limited to, a nonionic surfactant, an amphoteric surfactant, or a synergistic surfactant. Preferably, the surfactant comprises salts of alkyl aryl sulfonates, alkyl sulfonates, alkyl ether sulfates, alkyl sulfates, alkyl taurates, alkyl sulfosuccinates, hydrocarbon derivatives, abietic acid derivatives, ethoxylated primary alcohols, and modified polyethoxylated alcohols, individually or in combinations of two or more. Preferably, the surfactant is present in an amount from about I to about 3 grams per liter. [0045] In another illustrative embodiment, the fluoride ions encompassed by the method for treating a metal surface, preferably aluminum or aluminum alloy, include, but are not limited to, hydrofluoric acid, hydrofluorosilic acid, or fluoroboric acid or mixtures thereof. In another preferred embodiment, the fluoride ion compound is a fluoride salt. Preferred fluoride salts include, but are not limited to, sodium fluoride, potassium fluoride, ammonium bifluoride or mixtures thereof. Preferably, the fluoride ion compound is present in an amount from- about 5 to about 2-25 grams- per liter, preferably from about 10-to about 200 grams per liter, more preferably from about 20 to about 80 grams per liter, and even more preferably from about 60 to about 70 grams per liter. [00461 In another illustrative embodiment, the grain refiners encompassed by the method for treating a metal surface, preferably aluminum or aluminum alloy, include, but are not limited to, sodium phosphate, ammonium phosphate, or diammonium phosphate or a mixture thereof. In an illustrative embodiment, the method comprises a single grain refiner. In another illustrative embodiment, the method comprises combinations of two or more grain refiners. In an illustrative embodiment, the grain refiner is present in an amount of from about I to about 50 grams per liter, preferably from about 5 to about 30 grams per liter, and more preferably from about 10 to about 20 grams per liter. -11 - 100471 In another illustrative embodiment, the mineral acid encompassed by the method for treating a metal surface, preferably aluminum or aluminum alloy, include, but are not limited to, hydrofluoric acid, nitric acid, sulfuric acid, or phosphoric acid or mixtures thereof. Preferably, the mineral acid is present in an amount from about 20 to about 100 grams per liter, more preferably from about 30 to about 90 grams per liter and even more preferably from about 40 to about 80 grams per liter. [0048] In a particular embodiment, the invention encompasses a method for etching aluminum or aluminum alloy, comprising contacting the aluminum or aluminum alloy with ammonium bifluoride, hydrofluoric acid, glycolic acid, and surfactant. [0049] An illustrative acidic liquid aluminum etching agent with a robust, durable cleaning activity can be obtained by preparing the acidic liquid aluminum cleaner as follows: 100501 A mineral acid is exemplified by sulfuric acid, nitric acid, phosphoric acid, and the like, and at least one selection therefrom should be added. The preferable concentrations are as follows: about 80 g/L for phosphoric acid, about 80 g/L for sulfuric acid, and about 80 g/L for nitric acid. The mineral acid may take the form of a single acid or may comprise a combination of two or more acids, which is freeliselected within a range, which does not adversely affect the surface cleaning performance. Such mixed acids are exemplified by tricomponent mixed acids of 3 to 10 g/L phosphoric acid, 5 to 15 g/L sulfuric acid, and 0.5 to 2 g/L nitric acid, and by bicomponent mixed acid&of 10 to 20 g/L sulfuric acid and 0.5 to 2 g/L nitric acid. [00511 Through the use of these mineral acids, the pH preferably does not exceed 2.0 and more preferably is 0.6 to 2. Preferably, no particular restriction is placed on the lower pH limit. [00521 The surfactant component preferably is a hydrocarbon derivative, abietic acid derivatives, ethoxylated primary alcohols, and modified polyethoxylated alcohols, and these may be used singly or in combinations of two or more. The preferable concentration is 0.1 to 10 g/L and more preferably 0.5 to 3 g/L. -12- [0053] in addition, aluminum ions are eluted during cleaning with the acidic liquid cleaner according to the present invention, and this may reduce its cleaning efficiency. Accordingly, as a countermeasure in response to this, optionally a chelating agent, which sequesters the aluminum ions may also be present. Chelating agents useable for this purpose are exemplified by citric acid, oxalic acid, tartaric acid, gluconic acid, and the like. [0054] The acidic liquid aluminum cleaner prepared according to the present invention is highly effective f or the removal of smut and scale from aluminum and aluminum alloy as well as for the etching of same. [0055] The practice of the invention may be further appreciated from the following working and comparison examples, which are meant to provide illustrative embodiments and are in no way intended to limit the scope of the invention. V. EXAMPLES A. Example 1 [00561 Aluminum test specimens of 6063-T5 aluminum alloy were cleaned in acid cleaner, rinse then etched in the following acid etch composition: [00571 Hydrofluoric Acid 49% 7.5 g/L [00581 Fluoroboric Acid 49% . 5.0 g/L [00591 Ammonium Bifluoride 60.0 g/L [00601 Sodium Phosphate 15.0 g/L [00611 Surfactant 1.0 g/L [00621 The Solution pH was adjusted to 3.4. [00631 Test samples were etched in the above solution for 1.0, 3.0 and 5.0 minutes respectively. The etched samples were subjected to rinse, deox, rinse, dry off and weight loss taken before and after etch were performed on all test samples to determine the aluminum dissolution or removal rate. For comparison, a controlled aluminum specimen was acid cleaned, rinse then etched in aqueous - 13 alkaliiie etech bafi for 5.0 and 10.0 minutes respectively at a temperature of 145*- 1500 F. [0064] The etch bath contained 90.0 g/L sodium hydroxide, 100.00 g/L dissolved aluminum and 2.0 % volume of Houghton no-dump/long life etchant additives. As with the acid etched samples, all alkaline etched samples were subjected to rinse, deox, rinse, dry off and weight loss taken before and after etch. [0065] All acid and alkaline etched samples were anodized as follows: [0066] 1. Rinse Room Temperature [0067] 2. Deox Houghton A-1745 at 7.0% volume for 1.0 min. [0068] 3. Rinse Room Temperature [0069] 4. Anodizing Sulfuric Acid 180 g/L [00701 Aluminum 10 g/L [0071] Current Density 18 amps per sq.ft. [0072] Bath Temperature 720 F. [00731 Anodizing Time 30 min. [00741 Coating Thickness 0.7 mil [0075] 5. Rinse Room Temperature [0076] 6. Seal A-620 (Houghton Mid-Temp. Seal) 3% volume at 180 *F. for 10.0 min. [0077] 7. Rinse [0078] 8. Dry off [0079] Results from illustrative embodiments of the invention compared to a base alkaline etch are described in Table (1). [0080] Aluminum removal is measured in grams per square foot of aluminum removal (i.e., g/ft). All anodized samples were carefully evaluated for the quality of the etch by visual examinations and by the gloss reading using reflectometer at 600 angle. -14- Table 3 Etch Bath Temp. (*F) Al Removed (g/ft 2 ) Time (min.) Gloss Acid 115 0.70 1.0 6.2 Acid 115 1.17 3.0 5.9 Acid 115 1.42 5.0 4.9 Alkaline 145 5.4 5.0 18.1 Alkaline 145 10.5 10.0 9.4 D. Example 2 [00811 Aluminum test specimens of 6063-T5 aluminum alloy were etched in the following acid bath. [0082] Hydrofluoric acid 49% 10.0 g/L [00831 Ammonium bifluoride 80.0 g/L [00841 Diammonium phosphate 30.0 g/L [00851 Surfactant 200.0 ppm - [0086] pH - - 3:4-:.6 [00871 Aluminum removal rate was performed as in Example (1). All samples were anodized the same as Example (1) and the finished samples were evaluated using same method as in Example (1). Results from Examples (2) are described in Table (2). Table 4 Etch Bath Temp. (*F) Al Removed (g/ft' Time (mi.) Gloss Acid 110 0.85 2.0 6.0 Acid 110 1.51 6.0 4.8 Acid 110 1.53 10.0 4.2 -15- E. Example 3 100881 Aluminum test specimens of 6063 - Ts aluminum alloy that contained high zinc content at 0.1% in its alloy were etched separately in the following etch baths. [0089] Acid Etch Bath [00901 Bath composition same as in example (2) [00911 Bath temperature 1100 F. [0092] Etch time 5.0 minutes [0093] Alkaline Etch Bath [00941 Sodium Hydroxide 8.0 oz/gal [00951 Aluminum 100.0 g/L [00961 Temperature 145.00 F. [00971 Etch Time 10.0 minutes [0098] After etch all samples were subjected to rinse, deox, rinse, dry off and carefully evaluated. F. Results [00991 Alkaline etched samples had very rough or galVaniingproblem while acid etched parts had uniform matt finish. G. Test Results [001001 1. The compositions and methods of the invention comprising the acid etch compositions produce excellent uniform matte finish. [00101] 2. The compositions and methods of the invention comprising the acid etch compositions are more effective than alkaline etch in hiding extrusion lines, scratches or defects than alkaline etch. [001021 3. The compositions and methods of the invention comprising the acid etch compositions produce lower gloss reading than alkaline etch. - 16- [00103] 4. The compositions and methods of the invention comprising the acid etch compositions operates at lower bath temperature and unlike alkaline etch does not require cooling. [00104] 5. The compositions and methods of the invention comprising the acid etch compositions reduces etch time to 3.0 -5.0 minutes compared to 9 15 minutes in case of alkaline etch [001051 6. The compositions and methods of the invention comprising the acid etch compositions produce less aluminum removal 0.5 -1.5 gr/ft vs 9.0 13.0 gr/ff in case of alkaline etch. [00106] 7. The compositions and methods of the invention comprising the acid etch compositions reduce waster. Due to the fact that 1.0 lb. of aluminum is removed in the etch process results in 20.0 lbs. of waste sludge, therefore acid etch presents significant waste sludge reduction. [001071 8. The compositions and methods of the invention comprising the acid etch compositions parts are easy to rinse and require less rinse tanks than alkaline etch. This presents less water consumption. [00108] 9. The compositions and methods of the invention comprising the acid etch compositions are more effective in preventing pitting prior to anodizing. [00109] 10. The compositions and methods of the invention comprising the acid etch compositions are not sensitive to zinc content in the aluminum alloy as in the case of alkaline etch. High zinc content results in a rough finish or galvanizing defect. [00110] The invention described and claimed herein is not to be limited in scope by the specific embodiments herein disclosed, since these embodiments are intended as illustrations of several aspects of the invention. Any equivalent embodiments are intended to be within the scope of this invention. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. -17-
Claims (22)
1. A composition for etching metal consisting essentially of: (a) about 20 to about 80 grams per liter of ammonium bifluoride; (b) about 1 to about 50 grams per liter of diammonium phosphate; and 5 (c) water.
2. A composition for etching metal consisting of: (a) about 20 to about 80 grams per liter of ammonium bifluoride; (b) about 1 to about 50 grams per liter of diammonium phosphate; and (c) water. 10
3. The composition according to claim 1 or 2, which has a pH of about 2 to about 5.
4. The composition according to claim 1 or 2, consisting of about 5 to about 30 grams per liter of diammonium phosphate.
5. The composition according to claim 1 or 2, consisting of about 10 to about 20 grams per liter of diammonium phosphate. 15
6. The composition according to claim 1 or 2, consisting of about 60 to 70 grams per liter of ammonium bifluoride.
7. A method of etching aluminum, said method comprising contacting said aluminum with a composition according to any one of claims 1 to 6.
8. The method according to claim 7, wherein said etching is performed in about 1 to about 20 3 minutes.
9. The method according to claim 8, wherein said etching is performed in about 0.5 to about 10 minutes.
10. The method according to any one of claims 7 to 9, wherein said etching is performed at a pH of about 2 to about 5. 25
11. The method according to any one of claims 7 to 10, further comprising rinsing the etched aluminum. 18
12. The method according to any one of claims 7 to 11, wherein said aluminum is an aluminum alloy.
13. The method according to any one of claims 7 to 12, wherein the etched aluminum is resistant to pitting. 5
14. The method according to any one of claims 7 to 13, wherein the etch aluminum bath does not require cooling.
15. The method according to any one of claims 7 to 14, wherein the etched aluminum has a uniform matte finish when analyzed using a reflectometer at a 600 angle.
16. The method according to any one of claims 7 to 15, wherein extrusion lines on said 10 etched aluminum are removed or minimized.
17. The method according to any one of claims 7 to 16, which results in a significant reduction of waste products from the aluminum etching process.
18. The method according to any one of claims 7 to 17, wherein said etching removes about 0.5 to about 1.5 gr/ft 2 of aluminum. 15
19. The method according to any one of claims 7 to 18, which results in a reduction of water consumption in the aluminum etching process.
20. The method according to any one of claims 7 to 19, wherein said etching is performed at a composition temperature of 70 'F to 150 'F.
21. The method according to claim 20, wherein said etching is performed at a temperature 20 of about 100 'F to about 125 'F.
22. A composition according to claim 1 or claim 2, substantially as herein described. 19
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