US3081238A - Electrolytic treatment of metal surfaces - Google Patents
Electrolytic treatment of metal surfaces Download PDFInfo
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- US3081238A US3081238A US758747A US75874758A US3081238A US 3081238 A US3081238 A US 3081238A US 758747 A US758747 A US 758747A US 75874758 A US75874758 A US 75874758A US 3081238 A US3081238 A US 3081238A
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- metal surfaces
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- 229910052751 metal Inorganic materials 0.000 title claims description 29
- 239000002184 metal Substances 0.000 title claims description 29
- 238000000034 method Methods 0.000 claims description 26
- 230000007797 corrosion Effects 0.000 claims description 23
- 238000005260 corrosion Methods 0.000 claims description 23
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 20
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 14
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 12
- 238000000576 coating method Methods 0.000 claims description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 10
- 230000003213 activating effect Effects 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 239000011780 sodium chloride Substances 0.000 claims description 6
- 101100459267 Crotalus durissus terrificus CRO3 gene Proteins 0.000 claims 1
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 239000010408 film Substances 0.000 description 15
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 12
- 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 12
- 210000003298 dental enamel Anatomy 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 229910019142 PO4 Inorganic materials 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 7
- 235000021317 phosphate Nutrition 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 238000007654 immersion Methods 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 3
- 230000001464 adherent effect Effects 0.000 description 3
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 3
- 230000002950 deficient Effects 0.000 description 3
- 230000001627 detrimental effect Effects 0.000 description 3
- -1 e.g. Substances 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000001449 anionic compounds Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- 229940117975 chromium trioxide Drugs 0.000 description 2
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 description 2
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910001412 inorganic anion Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 238000007761 roller coating Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009924 canning Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910001430 chromium ion Inorganic materials 0.000 description 1
- BFGKITSFLPAWGI-UHFFFAOYSA-N chromium(3+) Chemical compound [Cr+3] BFGKITSFLPAWGI-UHFFFAOYSA-N 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000003716 rejuvenation Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Images
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
- C25D11/38—Chromatising
Definitions
- This invention relates to a process of applying a durable protective coating to the surface of a ferrous metal, such as iron, steel and the blackplate used in the canning and container industries, by cathodic treatment in a chromic acid solution.
- the purpose of the coating is (1) to enhance the corrosion resistance of the metal, (2) to provide a base for an adherent organic film, e.g., paint, lacquer or enamel, and (3) to reduce the underfihn corrosion of the painted surface.
- A'further object of this invention is to provide a rapid process for applying i this coating, in particular one adapted to continuous operation in a high-speed production line.
- Another object is to provide a continuous process that is easy to operate and simple to control. For example, it is highly desirable from a production standpoint that the various treating 4 baths be stable and long lived, and thus not subject to :frequent adjustment of composition or dumping.
- Still another object of the invention is to provide a process for which the installation and operating costs of the required apparatus'is low, so that, in combination with the Y high line speed and the eflectiveness of the resulting prod uct, a competitive advantage in the trade will result. 7
- the phosphate films used for metal protection without further coating are generally relatively thick; although effective in'resisting corrosion, they are extremely slow of deposition, brittle and not applicable where there is to be any appreciable deformation of the metal such as bending, drawing, forming, etc.
- the thinner phosphate films, used as a base for paint, are not so subject to rupture from deformation and they are cheaper to apply; but they do not afford a degree of protection against corrosion that is often necessary.
- Chromate films are usually thin, protective and adherent, although not always offering as good a' bond for paint as the phosphate type. They are applied under a very wide range-of conditions of composition, pH, temperature and current density.
- mate or dichroniate ion from either chromic acid or its alkali salts the solutions usually contain an inorganic anion such as phosphate or borate, added as the acid or a salt.
- inorganic anions such a nitrate, chloride of fluoride-have been used as well as the complex fluorides, fluosilicate, fluoborate, etc.
- organic acid anions are added. Often a portion of the hexavalent chromium in solution is reducedto the trivalent state by reaction with some organic material, for example sugar,
- a unique feature of my process lies in the fact that rust spots on the original strip are reduced to metal during Rust on blackplate is an ever present difficulty and cannot be prevented commercially in any economical way.
- the commercial advantage of a process which negates the unsightly appearance and corrosion initiating tendencies of rust on strip is very great.
- the protective film produced by the process of this invention is complex in nature and its chemical nature is not known definitely. It is an inorganic, non-metallic film which may contain hydrated chromic oxide with retained hexavalent chromium, possibly in the form of The appearance of the film may The protection of the base metal afforded by the film is of a very high order, much superior to that from films of comparable thickness cathodically applied in chromic acid baths in the presence of phosphate, borate, or trivalent chromium ion.
- F-iGURE 1 illustrates diagrammatically an apparatus for carrying out my process continuously for treating a moving strip of blackplate'in accordance with my invention.
- the steel strip if not already free from oil, grease and dirt is cleaned by any conventional method, such as cleaning in hot alkaline solution either with or without benefit of electrolytic action.
- the clean metal strip '10 is continuously uncoiled from the pay-oft reel 5, passed over guide roll 6, into tank 1 which contains an acid solution, preferably sulfuric acid, over lower guide roll EG'bGiWCfiIl a pair of squeegee or wringer rolls 7, and over guide roll 8.
- the strip 10 continuously passes over guide roll 9, through chamber 2 where it is rinsed with Water from spray nozzles 14, over guide roll 31, then between additional water spray nozzles 14a, then between squeegee rolls 13 and over guide roll 12.
- the conditions of the acid pretreatment result in a mild action, but either ovcrtreating or undertreating is to be avoided.
- immersion for one second at 60 C. for 3 seconds at 40 C. is satisfactory, although immersion times varying from about one second to about five seconds may be used in baths containing from about 0.5% to about by weight and at temperatures varying from about 20 C. to about 90 C.
- the immersion time will vary inversely with the acid concentration and the tem- .perature.
- the strip 10 is then immediately given the cathodic treatment in a bath in tank 3 containing about-100 to about 500 g. CrO per liter.
- the current density may range from about 200 to about 800 amperes per sq. ft., and the time of thetreatment from about 1 second to about 5 seconds.
- the strip 10 continuously passes over metal roll connected to the negative pole of a DC. generator 16, then between spaced anodes 19 connected to the positive pole of the generator 16 and immersed in the electrolytic bath in tank 3, then over guide roll 32, also immersed in the bath, then upwardly between another pair of spaced anodes 19a, then between squeegee rolls 17 and over guide roll 150, also connected to the negative pole of the generator 16.
- the electrolytic bath temperature is not a critical factor in the production of my protective surface film, I prefer to use a temperature falling in the range from about 20 C. to about 70 C., more specifically from about 45 C. to about 60 C. Below about 45 C. the electrolysis is ineffective in reducing rust, as heretofore described, and above about 60 C. the cost of heating the bath and difiiculties of handling the noxious fumes militate against the commercial utility of my process.
- the strip 10 passes immediately and continuously over guide roll 21, between water spray nozzles 22 in chamber 4, over guide roll 24, between water spray nozzles 22a, then between squeegee rolls 23 and over guide rolls 30 and 31.
- the strip 10 then passes through a hot air dryer 35, over a guide roll 36 and is coiled up on take-up reel 37.
- the activating acid pretreatment previous to the electrolytic bath is essential. If the strip is given no pretreatment, though initially clean and bright, the product is quite deficient in corrosion resistance, particularly when enamelled, as measured by the chloride-peroxide immersion test described above. At the completion of this test the rinsed and dried panels are inspected for rust, and the adhesion of the enamel is evaluated by applying pressure sensitive tape to the surface and quickly jerking it away. Deficient adhesion results in the rem-oval of. some enamel with the tape.
- Unpretreated panels those given an alkaline pretreatment, and those given an oxidizing pretreatment either in solution, as in nitric acid or ammonium persulfate, ,or by heating at a somewhat elevated temper.- ature, are all appreciably deficient compared to those pretreated in sulfuric acid.
- the deficiency exhibits itself in a greatly increased number of rust spots and a loss of enamel adhesion.
- the electrolytic process of this invention requires an active oxide-free surface, such as that imparted to commercial blackplate by a mild treatment in sulfuric acid and rinsing.
- a more drastic acid treatment such as the usual pickling is again detrimental, presumably due to the carbides, carbon and non-metallic inclusions left in and on the roughened surface.
- Acids other than sulfuric may be used, but oxidation must be avoided and the electrolytic treatment must follow immediately. Exposure to the liquid of the electrolytic bath prior to the passage of current is detrimental to the product and must be avoided. Also, after electrolysis, the strip must be rinsed immediately. A delay results in a lowered corrosion resistance of the product.
- the chromic acid bath of this invention operates at a very low pH, preferably less than unity.
- Alkali ions in small amounts can be tolerated, but major amounts are detrimental to corrosion resistance.
- the bath cannot be made up from an alkali dichromate.
- one side of the treated steel panel corresponding to the inside of the can is often enamelled to minimize the extent of attack by the can contents and the other side of the panel, to save the cost, is not.
- the outside of the can must have suitable protection against rusting during storage in the atmosphere.
- a thin film of oil applied over the surface treated by the process of this-invention imparts to the surface an abnormally high degree of rust resistance. Any one of a number of oils can be used, the dictate being largely one of cost.
- Cottonseed oil performs very well and can be applied by spraying, preferably with electrostatic aid, or by dipping or roller coating with appropriate solvent dilution so that the final oil film is very thin. Natural or synthetic resin solutions or emulsions may also be used.
- Clean blackplatc is passed from the uncoiler into an aqueous bath in tank 1 of 5% sulfuric acid at 50 C. where it receives a 1 second treatment. It is then rinsed with water sprays and immediately immersed as a cathode in an electrolytic bath in tank 3 containing 200 g. per liter of chromium trioxide free of impurities at a temperature of 50 C. using a current density of 400 amp. per sq. ft. for 2 seconds. The treated blackplate strip is then immediately rinsed again by water sprays and is passed between squeegee rolls. It is dried by warm air and coiled.
- the chromic acid bath does not deteriorate during use other than through loss of chromic acid due to the cathode reaction and drag-out. Only the periodic addition of chromic acid is necessary in order to maintain the initial concentration of the bath.
- This invention is applicable to iron and steel, particularly the blackplate used by the container industry. All component parts of the process are very rapid and lend themselves to a high speed production line.
- the treated strip is found to have superior durable corrosion resistance both before and after the application of a tightly adhering film of paint, varnish, lacquer, or enamel.
- the electrolytic bath contains no reducing agents and is therefore chemically stable and long lived. The control of this bathis simple and the process as a whole is easy to operate. The low cost of all processing chemicals, the extremely high production line speed, and the high quality of the product of my process result in a great commercial advantage.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Treatment Of Metals (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
I March 12, 1963 R. w. GURRY 3,081,238 ELECTROLYTIC TREATMENT OF METAL SURFACES Filed Sept. 3, 1 958 United States Patent 3,081,238 ELETROLYTIC TREATMENT OF METAL SURFACES Robert W. Garry, Berwyn, Pa, assignor to Quaker Chemical Corporation, a corporation of Pennsylvania Filed Sept. 3, 1958, Ser. No. 758,747 4 Claims. (Cl. 204-34) This invention relates to a process of applying a durable protective coating to the surface of a ferrous metal, such as iron, steel and the blackplate used in the canning and container industries, by cathodic treatment in a chromic acid solution. The purpose of the coating is (1) to enhance the corrosion resistance of the metal, (2) to provide a base for an adherent organic film, e.g., paint, lacquer or enamel, and (3) to reduce the underfihn corrosion of the painted surface.
This application is a continuation-in-part of application Serial No. 665,140, filed June 12, 1957, now abandoned.
his an object of this invention toprovide an effective means of applying such a corrosion-resistant, enamel-adhering coating to'the metal surface. A'further object of this invention is to provide a rapid process for applying i this coating, in particular one adapted to continuous operation in a high-speed production line. Another object is to provide a continuous process that is easy to operate and simple to control. For example, it is highly desirable from a production standpoint that the various treating 4 baths be stable and long lived, and thus not subject to :frequent adjustment of composition or dumping. Still another object of the invention is to provide a process for which the installation and operating costs of the required apparatus'is low, so that, in combination with the Y high line speed and the eflectiveness of the resulting prod uct, a competitive advantage in the trade will result. 7
It .is often desirable to protect ferrous metal surfaces against the formation of objectionable corrosion products during further processing, storage or actual use. It is also often desirable to increase the paint-bonding ability of ferrous metal surfaces and the corrosion resistance of the painted surface. All of these purposes can be accomplishedby application to the metal surface of a suitable film, whichimparts bothcorrosion resistance and 1 paint-bonding properties. Hitherto certain types of films have been found effective, notably phosphates and chromates, These are usually applied by contact with, or electrolysis in, aqueous solutions of a wide variety of compositions.
The phosphate films used for metal protection without further coating are generally relatively thick; although effective in'resisting corrosion, they are extremely slow of deposition, brittle and not applicable where there is to be any appreciable deformation of the metal such as bending, drawing, forming, etc. The thinner phosphate films, used as a base for paint, are not so subject to rupture from deformation and they are cheaper to apply; but they do not afford a degree of protection against corrosion that is often necessary.
Chromate films are usually thin, protective and adherent, although not always offering as good a' bond for paint as the phosphate type. They are applied under a very wide range-of conditions of composition, pH, temperature and current density. mate or dichroniate ion from either chromic acid or its alkali salts, the solutions usually contain an inorganic anion such as phosphate or borate, added as the acid or a salt. Other inorganic anions such a nitrate, chloride of fluoride-have been used as well as the complex fluorides, fluosilicate, fluoborate, etc. Sometimes organic acid anions are added. Often a portion of the hexavalent chromium in solution is reducedto the trivalent state by reaction with some organic material, for example sugar,
In addition to the chroreducing agents.
the cathodic treatment.
3,081,233 Patented Mar. 12, 1963 i'ice .glycerine, alcohol, or the like. Cathodic treatment in a bath containing chromic acid has also been suggested in Patent 1,827,247, but the conditions given fail to produce a satisfactory coating at a rate necessary for a modern continuous treating line.
I have found that a thin, adherent paint-bonding film imparting very superior corrosion resistance to steel strip can be applied at an extremely rapid rate by a process involving an activating acid pretreatment, rinsing, cathodic treatment in an aqueous bath containing only chromic acid, rinsing, and drying. Each of these steps is necessary and constitutes an integral part of the process as a whole.
By the process of this invention an electrolytic treatment as short as one second produces a coating with ex cellent corrosion resistance and enamel adherence. it will be apparent that the process of my invention is simple and easy to control. The chromic acid bath is chemically stable and has a long life, inasmuch as it contains no It is readily rejuvenated by the addition of chromium trioxide.
A unique feature of my process lies in the fact that rust spots on the original strip are reduced to metal during Rust on blackplate is an ever present difficulty and cannot be prevented commercially in any economical way. The commercial advantage of a process which negates the unsightly appearance and corrosion initiating tendencies of rust on strip is very great.
,No other known process for the chemical treatment of steel can accomplish this.
The protective film produced by the process of this invention is complex in nature and its chemical nature is not known definitely. It is an inorganic, non-metallic film which may contain hydrated chromic oxide with retained hexavalent chromium, possibly in the form of The appearance of the film may The protection of the base metal afforded by the film is of a very high order, much superior to that from films of comparable thickness cathodically applied in chromic acid baths in the presence of phosphate, borate, or trivalent chromium ion. When steel panels treate cathodically in chromic acid solution were coated with enamel, baked, scratched diagonally from corner to corner, and subjected to corrosion test by immersion for 18 hours in a solution containing 3% NaCl and 0.3% H 0 at F., the surface was extremely well inhibited against corrosion, including the scratches which were cut deeply into the base metal. The adhesion of the enamel was perfect after test, even immediately adjacent to the scratch. There was no underfilrn corrosion. Panels prepared in the same manner except with added phosphate, borate, or chromic ion in the electrolytic solution showed much more corrosion as well as some loss of adhesion. The enamel, applied by dipping and draining, or by roller coating so as to obtain an even coat, was a phenolic type baking enamel. The panels were cured for 10 minutes at 386 F.
Further details and advantages of my invention are given in the following explanation and accompanying drawing, wherein F-iGURE 1 illustrates diagrammatically an apparatus for carrying out my process continuously for treating a moving strip of blackplate'in accordance with my invention.
According to my invention the steel strip, if not already free from oil, grease and dirt is cleaned by any conventional method, such as cleaning in hot alkaline solution either with or without benefit of electrolytic action. Referring to FIGURE 1, the clean metal strip '10 is continuously uncoiled from the pay-oft reel 5, passed over guide roll 6, into tank 1 which contains an acid solution, preferably sulfuric acid, over lower guide roll EG'bGiWCfiIl a pair of squeegee or wringer rolls 7, and over guide roll 8.
After the acid pretreatment, the strip 10 continuously passes over guide roll 9, through chamber 2 where it is rinsed with Water from spray nozzles 14, over guide roll 31, then between additional water spray nozzles 14a, then between squeegee rolls 13 and over guide roll 12. The conditions of the acid pretreatment result in a mild action, but either ovcrtreating or undertreating is to be avoided. In a solution containing of sulfuric acid by weight, immersion for one second at 60 C. for 3 seconds at 40 C. is satisfactory, although immersion times varying from about one second to about five seconds may be used in baths containing from about 0.5% to about by weight and at temperatures varying from about 20 C. to about 90 C. In general, the immersion time will vary inversely with the acid concentration and the tem- .perature.
The strip 10 is then immediately given the cathodic treatment in a bath in tank 3 containing about-100 to about 500 g. CrO per liter. The current density may range from about 200 to about 800 amperes per sq. ft., and the time of thetreatment from about 1 second to about 5 seconds. The strip 10 continuously passes over metal roll connected to the negative pole of a DC. generator 16, then between spaced anodes 19 connected to the positive pole of the generator 16 and immersed in the electrolytic bath in tank 3, then over guide roll 32, also immersed in the bath, then upwardly between another pair of spaced anodes 19a, then between squeegee rolls 17 and over guide roll 150, also connected to the negative pole of the generator 16.
Although the electrolytic bath temperature is not a critical factor in the production of my protective surface film, I prefer to use a temperature falling in the range from about 20 C. to about 70 C., more specifically from about 45 C. to about 60 C. Below about 45 C. the electrolysis is ineffective in reducing rust, as heretofore described, and above about 60 C. the cost of heating the bath and difiiculties of handling the noxious fumes militate against the commercial utility of my process.
After the electrolytic treatment in tank 3, the strip 10 passes immediately and continuously over guide roll 21, between water spray nozzles 22 in chamber 4, over guide roll 24, between water spray nozzles 22a, then between squeegee rolls 23 and over guide rolls 30 and 31. The strip 10 then passes through a hot air dryer 35, over a guide roll 36 and is coiled up on take-up reel 37.
In carrying out the process of this invention, the activating acid pretreatment previous to the electrolytic bath is essential. If the strip is given no pretreatment, though initially clean and bright, the product is quite deficient in corrosion resistance, particularly when enamelled, as measured by the chloride-peroxide immersion test described above. At the completion of this test the rinsed and dried panels are inspected for rust, and the adhesion of the enamel is evaluated by applying pressure sensitive tape to the surface and quickly jerking it away. Deficient adhesion results in the rem-oval of. some enamel with the tape. Unpretreated panels, those given an alkaline pretreatment, and those given an oxidizing pretreatment either in solution, as in nitric acid or ammonium persulfate, ,or by heating at a somewhat elevated temper.- ature, are all appreciably deficient compared to those pretreated in sulfuric acid. The deficiency exhibits itself in a greatly increased number of rust spots and a loss of enamel adhesion. The electrolytic process of this invention requires an active oxide-free surface, such as that imparted to commercial blackplate by a mild treatment in sulfuric acid and rinsing. A more drastic acid treatment such as the usual pickling is again detrimental, presumably due to the carbides, carbon and non-metallic inclusions left in and on the roughened surface. Acids other than sulfuric may be used, but oxidation must be avoided and the electrolytic treatment must follow immediately. Exposure to the liquid of the electrolytic bath prior to the passage of current is detrimental to the product and must be avoided. Also, after electrolysis, the strip must be rinsed immediately. A delay results in a lowered corrosion resistance of the product.
The chromic acid bath of this invention operates at a very low pH, preferably less than unity. Alkali ions in small amounts can be tolerated, but major amounts are detrimental to corrosion resistance. For example, the bath cannot be made up from an alkali dichromate.
Higher temperatures and higher concentrations of chromic acid within the limits of this invention favor the reduction of rust on the metal strip during cathodic treatment as heretofore described.
In the manufacture of food containers, one side of the treated steel panel corresponding to the inside of the can is often enamelled to minimize the extent of attack by the can contents and the other side of the panel, to save the cost, is not. Thus, the outside of the can must have suitable protection against rusting during storage in the atmosphere. It has been found that a thin film of oil applied over the surface treated by the process of this-invention imparts to the surface an abnormally high degree of rust resistance. Any one of a number of oils can be used, the dictate being largely one of cost. Cottonseed oil performs very well and can be applied by spraying, preferably with electrostatic aid, or by dipping or roller coating with appropriate solvent dilution so that the final oil film is very thin. Natural or synthetic resin solutions or emulsions may also be used.
If such 'an oiling step is added to the process of this invention, it is inserted between the hot air drier and the take-up reel. Also, in the event that oil, grease or dirt is present on the initial blackplate strip, this is removed by an alkaline cleaning unit, either electrolytic or otherwise, inserted in the line between the pay-off reel and the pretreating bath.
The following is an illustrative example of carrying out the process of my invention. Clean blackplatc is passed from the uncoiler into an aqueous bath in tank 1 of 5% sulfuric acid at 50 C. where it receives a 1 second treatment. It is then rinsed with water sprays and immediately immersed as a cathode in an electrolytic bath in tank 3 containing 200 g. per liter of chromium trioxide free of impurities at a temperature of 50 C. using a current density of 400 amp. per sq. ft. for 2 seconds. The treated blackplate strip is then immediately rinsed again by water sprays and is passed between squeegee rolls. It is dried by warm air and coiled.
The chromic acid bath does not deteriorate during use other than through loss of chromic acid due to the cathode reaction and drag-out. Only the periodic addition of chromic acid is necessary in order to maintain the initial concentration of the bath.
This invention is applicable to iron and steel, particularly the blackplate used by the container industry. All component parts of the process are very rapid and lend themselves to a high speed production line. The treated strip is found to have superior durable corrosion resistance both before and after the application of a tightly adhering film of paint, varnish, lacquer, or enamel. The electrolytic bath contains no reducing agents and is therefore chemically stable and long lived. The control of this bathis simple and the process as a whole is easy to operate. The low cost of all processing chemicals, the extremely high production line speed, and the high quality of the product of my process result in a great commercial advantage.
I claim:
1. The process of reducing rust on and imparting to a continuously moving strip of ferrous metal a durable rust resistant coating resistant for 18 hours to corrosion by an aqueous solution containing 3 sodium chloride and 6.3% hydrogen peroxide at a temperature of 75 C. which consists essentially of continuously activating the surfaces of said strip in a dilute aqueous bath of sulfuric acid for a few seconds, immediately rinsing the metal surfaces with water, immediately thereafter immersing the moving ferrous metal surfaces in an electrolytic bath as a cathode, said bath consisting essentially of water and 100 to 500 gms. CrO per liter and having a temperature of between 45 and 60 C., subjecting the metal surfaces to a current density between 200 and 800 amp. per sq. ft. for l to 5 seconds, then immediately rinsing the coated metal surfaces in water for a few seconds and drying the coated ferrous metal.
2. The process of reducing rust on and imparting to a continuously moving strip of blackplate a durable rust resistant coating resistant for 18 hours to corrosion by an aqueous solution containing 3% sodium chloride and 0.3% hydrogen peroxide at a temperature of 75 C. which consists essentially of subjecting the moving surfaces of the blackplate to the activating action of an aqueous bath of 5% sulfuric acid at about 60 C. for 1 second, immediately rinsing the blackplate with water, immediately thereafter cathodically treating the moving blackplate strip in an electrolytic bath consisting essentially of water and 200 gms. pure CrO per liter at a temperature of 50 C. and current density of about 400 amp. per sq. ft. for 2 seconds, immediately rinsing the coated surfaces of the blackplate with water, then squeegeeing the surfaces of the blackplate, and drying the coated ferrous metal.
3. The process of reducing rust on and imparting to a continuously moving strip of ferrous metal a durable rust resistant coating resistant for 18 hours to corrosion by an aqueous solution containing 3% sodium chloride and 0.3% hydrogen peroxide at a temperature of 75" C.
which consists essentially of continuously activating the surfaces of said strip in a dilute bath of sulfuric acid for a few seconds, immediately thereafter depositing upon said moving surfaces an inorganic, nonmetallic coating by subjecting said surfaces to cathodic treatment in an aqueous bath at a temperature of between from about 20 to about C. consisting essentially of water and 1.00 to 500 gm. per liter of CrO at a current density of 260 to 800 amp. per sq. ft. for 1 to 5 seconds, and thereafter immediately rinsing said coated surfaces and drying the coated ferrous metal.
4. The process of reducing rust on and imparting to a continuously moving strip of ferrous metal a durable rust resistant coating resistant for 18 hours to corrosion by an aqueous solution containing 3% sodium chloride and 0.3% hydrogen peroxide at a temperature of C. which consists essentially of continuously activating the surfaces of said strip in a dilute bath of sulfuric acid for a few seconds, immediately rinsing the treated strip, immediately thereafter cathodically treating the moving strip in an electrolytic bath consisting essentially of water and 200 gms. pure CrO per liter at a temperature of 50 C. and current density of about 400 amp. per sq. ft. for 2 seconds, immediately rinsing the coated surfaces of the strip with water, then squeegeeing the surfaces of the strip, and drying the coated ferrous metal.
References Cited in the file of this patent UNITED STATES PATENTS 1,745,912 Richardson Feb. 4, 1930 1,827,247 Mason Oct. 13, 1931 2,392,871 Wick Ian. 15, 1946 2,733,199 Wick Ian. 31, 1956 2,780,592 Wick Feb. 5, 1957 2,812,297 Stareck et a1. Nov. 5, 1957
Claims (1)
1. THE PROCESS OF REDUCING RUST ON AND IMPARTING TO A CONTINUOUSLY MOVING STRIP OF FERROUS METAL A DURABLE RUST RESISTANT COATING RESISTANT FOR 18 HOURS TO CORROSION BY AN AQUEOUS SOLUTION CONTANING 3% SODIUM CHLORIDE AND 0.3% HYDROGEN PEROXIDE AT A TEMPERATURE OF 75* C. WHICH CONSISTS ESSENTIALLY OF CONTINUOUSLY ACTIVATING THE SURFACES OF SAIS STRIP IN A DILUTE AQUEOUS BATH OF SULFURIC ACID FOR A FEW SECONDS, IMMEDIATELY RINSING THE METAL SURFACES WITH WATER, IMMEDIATELY THEREAFTER IMMERSING THE MOVING FERROUS METAL SURFACES IN AN ELECTROLYTIC BATH AS A CATHODE, SAID BATH CONSISTING ESSENTIALLY OF WATER AND 100 TO 500 GMS. CRO3 PER LITER AND HAVING A TEMPERATURE OF BETWEEN 45 AND 60* C., SUBJECTING THE METAL SURFACES TO A CURRENT DENSITY BETWEEN 200 AND 800 AMP. PER SQ. FT. FOR 1 TO 5 SECONDS, THEN IMMEDIATELY RINSING THE COATED METAL SURFACES IN WATER FOR A FEW SECONDS AND DRYING THE COATED FERROUS METAL.
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US758747A US3081238A (en) | 1958-09-03 | 1958-09-03 | Electrolytic treatment of metal surfaces |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US758747A US3081238A (en) | 1958-09-03 | 1958-09-03 | Electrolytic treatment of metal surfaces |
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US3081238A true US3081238A (en) | 1963-03-12 |
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US758747A Expired - Lifetime US3081238A (en) | 1958-09-03 | 1958-09-03 | Electrolytic treatment of metal surfaces |
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3138548A (en) * | 1961-04-11 | 1964-06-23 | Inland Steel Co | Tin plate treatment |
US3278401A (en) * | 1966-01-12 | 1966-10-11 | Nat Steel Corp | Method of treating tin-containing surfaces |
US3288691A (en) * | 1962-06-13 | 1966-11-29 | Yawata Iron & Steel Co | Method of electrolytically chemically treating metals |
US3296100A (en) * | 1962-05-09 | 1967-01-03 | Yawata Iron & Steel Co | Process for producing anticorrosive surface treated steel sheets and product thereof |
US3337431A (en) * | 1962-11-10 | 1967-08-22 | Toyo Kohan Co Ltd | Electrochemical treatment of metal surfaces |
US3523067A (en) * | 1968-05-27 | 1970-08-04 | Canada Steel Co | Selective galvanizing of steel strip |
US3532608A (en) * | 1967-09-29 | 1970-10-06 | United States Steel Corp | Method of treating steel and electrolyte therefor |
US3535213A (en) * | 1967-12-20 | 1970-10-20 | Yawata Seitetsu Kk | Method of surface-treating metals |
US3755117A (en) * | 1970-05-26 | 1973-08-28 | Int Nickel Co | Coating stainless steels |
US4388169A (en) * | 1980-10-09 | 1983-06-14 | Nippon Steel Corporation | Apparatus for surface treatment of a steel strip |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1745912A (en) * | 1923-05-03 | 1930-02-04 | Westinghouse Lamp Co | Chromium-coated wire and method of manufacture |
US1827247A (en) * | 1927-10-18 | 1931-10-13 | Western Electric Co | Method of protecting metal surfaces |
US2392871A (en) * | 1939-07-08 | 1946-01-15 | Richard M Wick | Chromium plating |
US2733199A (en) * | 1956-01-31 | Electrolytic treatment of metal | ||
US2780592A (en) * | 1951-08-22 | 1957-02-05 | Bethlehem Steel Corp | Electrolytic treatment of metal surfaces |
US2812297A (en) * | 1953-03-13 | 1957-11-05 | Metal & Thermit Corp | Method of preventing etching by chromic acid chromium plating baths |
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1958
- 1958-09-03 US US758747A patent/US3081238A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2733199A (en) * | 1956-01-31 | Electrolytic treatment of metal | ||
US1745912A (en) * | 1923-05-03 | 1930-02-04 | Westinghouse Lamp Co | Chromium-coated wire and method of manufacture |
US1827247A (en) * | 1927-10-18 | 1931-10-13 | Western Electric Co | Method of protecting metal surfaces |
US2392871A (en) * | 1939-07-08 | 1946-01-15 | Richard M Wick | Chromium plating |
US2780592A (en) * | 1951-08-22 | 1957-02-05 | Bethlehem Steel Corp | Electrolytic treatment of metal surfaces |
US2812297A (en) * | 1953-03-13 | 1957-11-05 | Metal & Thermit Corp | Method of preventing etching by chromic acid chromium plating baths |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3138548A (en) * | 1961-04-11 | 1964-06-23 | Inland Steel Co | Tin plate treatment |
US3296100A (en) * | 1962-05-09 | 1967-01-03 | Yawata Iron & Steel Co | Process for producing anticorrosive surface treated steel sheets and product thereof |
US3288691A (en) * | 1962-06-13 | 1966-11-29 | Yawata Iron & Steel Co | Method of electrolytically chemically treating metals |
US3337431A (en) * | 1962-11-10 | 1967-08-22 | Toyo Kohan Co Ltd | Electrochemical treatment of metal surfaces |
US3278401A (en) * | 1966-01-12 | 1966-10-11 | Nat Steel Corp | Method of treating tin-containing surfaces |
US3532608A (en) * | 1967-09-29 | 1970-10-06 | United States Steel Corp | Method of treating steel and electrolyte therefor |
US3535213A (en) * | 1967-12-20 | 1970-10-20 | Yawata Seitetsu Kk | Method of surface-treating metals |
US3523067A (en) * | 1968-05-27 | 1970-08-04 | Canada Steel Co | Selective galvanizing of steel strip |
US3755117A (en) * | 1970-05-26 | 1973-08-28 | Int Nickel Co | Coating stainless steels |
US4388169A (en) * | 1980-10-09 | 1983-06-14 | Nippon Steel Corporation | Apparatus for surface treatment of a steel strip |
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