US2788292A - Method of treating chromium surfaces - Google Patents
Method of treating chromium surfaces Download PDFInfo
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- US2788292A US2788292A US549511A US54951155A US2788292A US 2788292 A US2788292 A US 2788292A US 549511 A US549511 A US 549511A US 54951155 A US54951155 A US 54951155A US 2788292 A US2788292 A US 2788292A
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- Prior art keywords
- chromium
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- coating
- steel
- nickel
- Prior art date
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- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 title claims description 37
- 229910052804 chromium Inorganic materials 0.000 title claims description 36
- 239000011651 chromium Substances 0.000 title claims description 36
- 238000000034 method Methods 0.000 title claims description 20
- 238000000576 coating method Methods 0.000 claims description 38
- 238000005260 corrosion Methods 0.000 claims description 34
- 230000007797 corrosion Effects 0.000 claims description 34
- 239000011248 coating agent Substances 0.000 claims description 30
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 claims description 19
- 238000007747 plating Methods 0.000 claims description 16
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 12
- 150000001845 chromium compounds Chemical class 0.000 claims description 8
- 239000011780 sodium chloride Substances 0.000 claims description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 58
- 229910052759 nickel Inorganic materials 0.000 description 29
- 229910000831 Steel Inorganic materials 0.000 description 23
- 239000010959 steel Substances 0.000 description 23
- 230000002401 inhibitory effect Effects 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 7
- 239000010953 base metal Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000007654 immersion Methods 0.000 description 5
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 3
- 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 3
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- ABXXWVKOBZHNNF-UHFFFAOYSA-N chromium(3+);dioxido(dioxo)chromium Chemical compound [Cr+3].[Cr+3].[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O ABXXWVKOBZHNNF-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282337 Nasua nasua Species 0.000 description 1
- 229910018487 Ni—Cr Inorganic materials 0.000 description 1
- JOSWYUNQBRPBDN-UHFFFAOYSA-P ammonium dichromate Chemical compound [NH4+].[NH4+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O JOSWYUNQBRPBDN-UHFFFAOYSA-P 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 1
- 238000007739 conversion coating Methods 0.000 description 1
- IQKQUSLYXMWMQZ-UHFFFAOYSA-N copper;oxido-(oxido(dioxo)chromio)oxy-dioxochromium Chemical compound [Cu+2].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O IQKQUSLYXMWMQZ-UHFFFAOYSA-N 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
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- -1 ferrous metals Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- PLHASFSAGNOMLM-UHFFFAOYSA-N nickel(2+);oxido-(oxido(dioxo)chromio)oxy-dioxochromium Chemical compound [Ni+2].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O PLHASFSAGNOMLM-UHFFFAOYSA-N 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- KHADWTWCQJVOQO-UHFFFAOYSA-N zinc;oxido-(oxido(dioxo)chromio)oxy-dioxochromium Chemical compound [Zn+2].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KHADWTWCQJVOQO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/24—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing hexavalent chromium compounds
Definitions
- Another object of the invention is the provision of a substantially invisible corrosion inhibiting coating on the plated surface of a metal article.
- Still another object is to provide a corrosion inhibiting coating on the plated surface of the article which is ahodic to the plating.
- a still further object is to provide a corrosion inhibiting coating on the plated surface of the article which is anodic to the base metal portion of the article.
- Yet another object is the provision of a process for economically and efliciently forming a corrosion inhibitihg coating on a plated metal article.
- Still another object is the provison of an abrasion rcsi'sta'rlt corrosion inhibiting coating on an article of the above type.
- the invention is more particularly directed toward the inhibiting of rust and corrosion on steel articles having a layer of nickel plate thereon and a layer of chromium plate over the nickel, it is also applicable to steel articles having chromium plated directly thereand is in fact applicable to numerous metal base articles plated with chromium or nickel and chromium, or plated with chromium or nickel and chromium ov'er platin'gs of other metals.
- the coating is invisible in the sense that it does not appreciably alter the a pearance of the outer plate, and the methods used to obtain the corrosion inhibiting coating may be so controlled as to attain this result.
- the exact nature of the coating is not definitely known, it is reasoned that it is probably chromium chromate, or that it includes chromium chromate, and is not a conversion coating, but rather one that is formed entirely from the ingredients of a treating bath.
- the invention contemplates treatment of articles of the above type in hexavalent chromium containing solutions, and preferably solutions having a pH below 7. More specifically, chromic acid baths, ahd dichromate solutions such as sodium dichromate, potassium dichromate, nickel dichromate, ammonium dichro mate, copper dichromate, Zinc dichromate, and calcium dichrornate were found to provide satisfactory coatings, although some of these materials are more satisfactory than others from an economic standpoint.
- corrosion inhibiting coatings of the above type can be applied to chromium and to nickel and chromium plated articles by immersion in baths of various hexavalent chromium containing solutions such as those containing various dichromates.
- factors such as solution concentration, pH, bath temperature, and time, are all controlled in such a manner as to give the desired result.
- the immersion process can also be so controlled as to produce corrosion inhibiting chromium compound coatings which are substantially invisible and which do not appreciably change the nor mal appearance of the plating. No complicated or eitpensive apparatus is required for the practice of this process, and it is therefore particularly adapted to the treatment of articles in small lots.
- the composition of the coatihg is not definitely known, but it has been found, for example, that the effectiveness of the coating is unaffected by dipping for 1 minute, after treatment in a 10 gm. per liter solution of chromic acid, while dipping for 1 minute in a concentrated chromic acid solution destroys the effecti ness of the coating, and presumably destroys the coati g itself.
- the coating is subject to removal or partial removal when subjected to vigorous scrubbirig with line abrasive cleaners such as light magnesium oxide, but as will be shown by tests to be described hereinafter, treated articles cleaned with light magnesium oxide were found to be far more resistant to corrosion than similarly cleaned untreated articles.
- ferrous base articles plated with nickel and thereafter with chromium and subsequently treated as above are anodic to steel, and that the articles maintain this anodic characteristic over long periods of time. Test pieces aged for six months after treatment were still anodic, On the other hand, articles which have been subjected to salt spray tests gradually lose this characteristic. Tests have indicated that articles treated by the immersion process have coatings which. appear to be highly resistant to abrasion.
- test piecs treated Numerou exposure tests were made on test piecs treated. In the tests to be described by way of example, all of the test pieces were of steel, and were plated first with bright nickel and then with bright chromium. Nickel plate thicknesses of about .6063 and about .6068 inch were included in the tests. The chromium plating conditions were the same for all the tests given, and the thickness of the chromium was on the order of .00001 inch.
- Test pieces having .0003 nickel plate with chromium plate thereon are given the immersion treatment. All the treated pieces were immersed in a gm. per liter sodium dichromate solution at 200 F. for 2 hours. Untreated pieces having .0003 nickel plate and chromium plate thereover showed over 100 rust spots after 24 hours in the salt spray. The treated pieces showed 6 spots at the end of 120 hours. Like untreated pieces having an .0008 nickel plate showed 60 spots at the end of 48 hours in the salt spray while like pieces treated as above showed no spots after 48 hours and 3 spot after l20 hours. All of these test pieces were also cleaned with magnesium Oxide prior to the salt spray test.
- Test pieces of steel having .0093 nickel plate and chromium plate thereover were treated by immersion in a 5 gm. per liter solution of sodium dichromate at 200 F. for 2 hours, and tested in comparison with like untreated pieces by exposing them to the weather on the roof of a building for 6 months. At the end of 10 weeks the untreated pieces showed over 100 rust spots. No spots appeared on the treated pieces. At the end of 6 months the untreated pieces were in very bad condition, while an average of i rust spot was found on the treated pieces. In this test none of the pieces were cleaned with abrasive cleaner prior to exposure.
- Tests were also made on similar test pieces of steel plated with copper and then with chromium, as well as with copper, nickel and chromium in the order named.
- Tests were also conducted to determine the conditions of operation required for satisfactory treatment, these tests relating to time of treatment, solution concentration, pH of the bath, and solution temperature.
- the method of increasing the corrosion resistance greases of a steel article having a plating of chromium thereon which is normally cathodic to the steel of the article when immersed in a sodium chloride solution which comprises forming a coating over the chromium plating which is anodic to the steel of the article by immersing the article in a solution containing hexavalent chromium until a coating of chromium compound is formed thereon.
- T he method of increasing the corrosion resistance of a steel article having a plating of chromium thereon which is normally cathodic to the steel of the article when immersed in. a sodium chloride solution, which comprises forming a coating over the chromium plating which is anodic to the steel of the article by immersing the article in a solution containing hexavalent chromium until a coating of chromium compound is formed thereon, and rinsing the article to remove the hexavalent chromium containing solution therefrom.
- the method of increasing the corrosion resistance of a steel article having a layer of nickel plate thereon and a layer of chromium plate on the nickel layer, the layer of chromium being normally cathodic to the steel of the article when immersed in a sodium chloride solution which comprises forming a coating over the chromium plating which is anodic to the steel of the article by immersing the article in a bath containing hexavalent chromium in solution until the coating is formed thereon and thereafter removing the article from the bath and rinsing the article to remove the hexavalent chromium containing solution therefrom.
- the method of increasing the corrosion resistance of a steel article having a layer of nickel plate thereon and a layer of chromium plate on the nickel layer, the layer of chromium being normally cathodic to the steel of the article when immersed in a sodium chloride solution which comprises immersing the article in a hexavalent chromium solution until a coating of chromium compound is formed thereon, and thereafter removing and rinsing the article to remove the hexavalent chromium solution therefrom, the article being removed from the bath prior to the formation of an appreciable visible film of said compound thereon.
- the method of forming a corrosion inhibiting coating on an article having a base member of ferrous metal and a layer of chromium plate thereover which comprises immersing the article in a solution containing hexavalent chromium until a coating of chromium compound is formed thereon, and thereafter removing the article from the bath and rinsing the article to remove the hexavalent chromium solution therefrom.
- the method of forming a corrosion inhibiting coating on an article having a base member of ferrous metal, a layer of nickel plate on the base member and a layer of chromium plate on the nickel layer which comprises immersing the article in a bath containing hexa valent chromium in solution until a coating is formed thereon which is anodic to the chromium layer, the nickel layer, and the base metal, and thereafter removing the 5 article from the bath and rinsing the article to remove the hexavalent chromium containing solution therefrom.
- the method of forming a corrosion inhibiting coating on an article having a base member of ferrous metal, a layer of nickel plate on the base metal, and a layer of chromium plate on the nickel plate layer which comprises immersing the article in a hexavalent chromium solution until a coating of a chromium compound is formed thereon, and thereafter removing and rinsing the article to remove the hexavalent chromium solution therefrom, the article being removed from the bath prior to the formation of an appreciably visible film of said compound thereon.
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- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Treatment Of Metals (AREA)
Description
United States stem:
William C. Gie'sker, Oakville, Conn, and Richard K.
Britton, Sidney, N. Y., assignors to The Autoyre Company, Inc., Oakville, Conn., a corporation of Connecticut N0 Drawing. Original application October 15, 1951,
Serial No. 251,462, new Patent No. 2,744 2,915, dated May 22, 1956. Divided and this application November 28, 1955, Serial No. 549,511
13 Claims. (Cl.- 117-71) This invention relates to the treatment of metal articles to prevent or retard corrosion, and more particularly to the treatment of articles formed of ferrous metals and having nickel and chrome plate coatings thercover. This application is a division of our earlier file copending application entitled Metal Treatment and Article, Serial #251,462, filed October 15, 1951, now Patent No. 2,746,915.
Difliculty has been experienced in the past with articles of this type due to the formation of numerous rust or corrosion spots on the surface thereof after a short period of time. Although the reasons for this corrosion are not too well established, there are, particularly in the case of nickel plating, two schools of thought at the present time, :1 assuming that there are pores present in the plating itself which expose the base metal and thus permit corrosion thereof, and the other holding that the plating is initially substantially continuous but subject to a pit type of corrosion which rapidly penetrates the coating, with resultant corrosion of the base metal. Previous attempts to eliminate corrosion of such plated articles have been directed toward elimination of the initial pores in the plating, While one of the primary objects of the present invention is the provision of a coating which will minimize either the pit type of corrosion or corrosion due to initial pits in the plating.
Another obiect of the invention is the provision of a substantially invisible corrosion inhibiting coating on the plated surface of a metal article.
Still another object is to provide a corrosion inhibiting coating on the plated surface of the article which is ahodic to the plating.
A still further object is to provide a corrosion inhibiting coating on the plated surface of the article which is anodic to the base metal portion of the article.
Yet another object is the provision of a process for economically and efliciently forming a corrosion inhibitihg coating on a plated metal article.
Still another object is the provison of an abrasion rcsi'sta'rlt corrosion inhibiting coating on an article of the above type.
These and other novel objects and features of the invention will be apparent to those skilled in the art in the light of the folio ng description, but it is to be understood the description is not to be considered as defining the limits of the invention, reference being bad for this purpose to the appended claims.
Although the invention is more particularly directed toward the inhibiting of rust and corrosion on steel articles having a layer of nickel plate thereon and a layer of chromium plate over the nickel, it is also applicable to steel articles having chromium plated directly thereand is in fact applicable to numerous metal base articles plated with chromium or nickel and chromium, or plated with chromium or nickel and chromium ov'er platin'gs of other metals. in the preferred form the coating is invisible in the sense that it does not appreciably alter the a pearance of the outer plate, and the methods used to obtain the corrosion inhibiting coating may be so controlled as to attain this result.
While opinions vary as to the nature of the action which results in the formation of corrosion, and particularly of rust spots on steel articles plated with nickel followed by a plate of chromium, it is generally agreed that in chromium plate, there are a large number of is or pores. These cracks or pores apparently ex pose the nickel underneath, and it has been determined by tests that in untreated articles, corrosion of the nickel occurs at these cracks and eventually extends underneath the chromium plate. This corrosion forms holes in the nickel plate, the steel is attacked, and rust spots appear on the article. Thus it is apparent that as long as the plating is protected against the formation of corroded holes by the coating, the base metal regardless of its nature, is also protected.
It has been found that untreated nickel and nickel chromium plated steel articles are normally cathodic to steel when immersed in a sodium chloride solution, and it was reasoned that a coating on the article which rendered the latter anodic to steel, might, under the influence corrosive agents, reduce corrosion forming" galvanic action, or be eaten away in preference to the other metals present, thus protecting the articles against corrosion. it was found that through the means to be described, substantially invisible and apparently anodic chromium compound coatings having the above characteristics could be formed on articles of the above type, and that these coatings were apparently .anodic to steel and very effective in preventing corrosion of the articles, due to sacrificial or other inhibiting action. While the exact nature of the coating is not definitely known, it is reasoned that it is probably chromium chromate, or that it includes chromium chromate, and is not a conversion coating, but rather one that is formed entirely from the ingredients of a treating bath.
in general, the invention contemplates treatment of articles of the above type in hexavalent chromium containing solutions, and preferably solutions having a pH below 7. More specifically, chromic acid baths, ahd dichromate solutions such as sodium dichromate, potassium dichromate, nickel dichromate, ammonium dichro mate, copper dichromate, Zinc dichromate, and calcium dichrornate were found to provide satisfactory coatings, although some of these materials are more satisfactory than others from an economic standpoint.
It has been found that corrosion inhibiting coatings of the above type can be applied to chromium and to nickel and chromium plated articles by immersion in baths of various hexavalent chromium containing solutions such as those containing various dichromates. Here as will be noted from the examples to be given, factors such as solution concentration, pH, bath temperature, and time, are all controlled in such a manner as to give the desired result. The immersion process can also be so controlled as to produce corrosion inhibiting chromium compound coatings which are substantially invisible and which do not appreciably change the nor mal appearance of the plating. No complicated or eitpensive apparatus is required for the practice of this process, and it is therefore particularly adapted to the treatment of articles in small lots.
As indicated heretofore, the composition of the coatihg is not definitely known, but it has been found, for example, that the effectiveness of the coating is unaffected by dipping for 1 minute, after treatment in a 10 gm. per liter solution of chromic acid, while dipping for 1 minute in a concentrated chromic acid solution destroys the effecti ness of the coating, and presumably destroys the coati g itself. Also the coating is subject to removal or partial removal when subjected to vigorous scrubbirig with line abrasive cleaners such as light magnesium oxide, but as will be shown by tests to be described hereinafter, treated articles cleaned with light magnesium oxide were found to be far more resistant to corrosion than similarly cleaned untreated articles. it is also noted that ferrous base articles plated with nickel and thereafter with chromium and subsequently treated as above are anodic to steel, and that the articles maintain this anodic characteristic over long periods of time. Test pieces aged for six months after treatment were still anodic, On the other hand, articles which have been subjected to salt spray tests gradually lose this characteristic. Tests have indicated that articles treated by the immersion process have coatings which. appear to be highly resistant to abrasion.
Numerou exposure tests were made on test piecs treated. In the tests to be described by way of example, all of the test pieces were of steel, and were plated first with bright nickel and then with bright chromium. Nickel plate thicknesses of about .6063 and about .6068 inch were included in the tests. The chromium plating conditions were the same for all the tests given, and the thickness of the chromium was on the order of .00001 inch.
Test pieces having .0003 nickel plate with chromium plate thereon are given the immersion treatment. All the treated pieces were immersed in a gm. per liter sodium dichromate solution at 200 F. for 2 hours. Untreated pieces having .0003 nickel plate and chromium plate thereover showed over 100 rust spots after 24 hours in the salt spray. The treated pieces showed 6 spots at the end of 120 hours. Like untreated pieces having an .0008 nickel plate showed 60 spots at the end of 48 hours in the salt spray while like pieces treated as above showed no spots after 48 hours and 3 spot after l20 hours. All of these test pieces were also cleaned with magnesium Oxide prior to the salt spray test.
Test pieces of steel having .0093 nickel plate and chromium plate thereover were treated by immersion in a 5 gm. per liter solution of sodium dichromate at 200 F. for 2 hours, and tested in comparison with like untreated pieces by exposing them to the weather on the roof of a building for 6 months. At the end of 10 weeks the untreated pieces showed over 100 rust spots. No spots appeared on the treated pieces. At the end of 6 months the untreated pieces were in very bad condition, while an average of i rust spot was found on the treated pieces. In this test none of the pieces were cleaned with abrasive cleaner prior to exposure.
Tests were also made on similar test pieces of steel plated with copper and then with chromium, as well as with copper, nickel and chromium in the order named.
Tests were also conducted to determine the conditions of operation required for satisfactory treatment, these tests relating to time of treatment, solution concentration, pH of the bath, and solution temperature.
It was found desirable to use a treatment time of about 2 hours for good results in a 50 gm. per liter sodium dichromate solution at 190 to 212 F. having a pH of about 4.5. However, articles were successfully treated in solutions having pH values of from 2.5 to 7. The use of lower temperatures results in satisfactory coatings but the time required for treatment is materially increased. It was found, however, that the corrosion inhibiting films could be formed in solutions having a hexavalent chromium concentration of .l to 150 gm. per liter, and temperatures as low as 70 F. could he used.
While the invention has been described with considerable particularity, it is to be understood that variations and modifications will suggest themselves to those skilled in the art, and reference is accordingly had to the appended claims for a definition of the limits of the invention.
What is claimed is:
1. The method of increasing the corrosion resistance greases of a steel article having a plating of chromium thereon which is normally cathodic to the steel of the article when immersed in a sodium chloride solution, which comprises forming a coating over the chromium plating which is anodic to the steel of the article by immersing the article in a solution containing hexavalent chromium until a coating of chromium compound is formed thereon.
2. The method as set forth in claim 1, wherein the hexavalent chromium concentration of the solution is of the order of .l to gm. per liter.
3. he method as set forth in claim 1, wherein the pH of the solution is maintained between 2.5 and 7.0.
4. The method set forth in claim 1, wherein the solution is maintained within a temperature range of approxima ely 70 to 212 F. and the article is immersed in the tion for at least 30 minutes.
5. T he method of increasing the corrosion resistance of a steel article having a plating of chromium thereon which is normally cathodic to the steel of the article when immersed in. a sodium chloride solution, which comprises forming a coating over the chromium plating which is anodic to the steel of the article by immersing the article in a solution containing hexavalent chromium until a coating of chromium compound is formed thereon, and rinsing the article to remove the hexavalent chromium containing solution therefrom.
6. The method as set forth in claim 5, wherein the hexavalent chromium concentration of the solution is of the order of .l to 150 gm. per liter.
7. The method as set forth in claim 5, wherein the pH of the solution is maintained between 2.5 and 7.0.
8. The method set forth in claim 5, wherein the solution is maintained within a temperature range of approximately 70 to 212 F. and the article is immersed in the solution for at least 30 minutes.
9. The method of increasing the corrosion resistance of a steel article having a layer of nickel plate thereon and a layer of chromium plate on the nickel layer, the layer of chromium being normally cathodic to the steel of the article when immersed in a sodium chloride solution, which comprises forming a coating over the chromium plating which is anodic to the steel of the article by immersing the article in a bath containing hexavalent chromium in solution until the coating is formed thereon and thereafter removing the article from the bath and rinsing the article to remove the hexavalent chromium containing solution therefrom.
10. The method of increasing the corrosion resistance of a steel article having a layer of nickel plate thereon and a layer of chromium plate on the nickel layer, the layer of chromium being normally cathodic to the steel of the article when immersed in a sodium chloride solution, which comprises immersing the article in a hexavalent chromium solution until a coating of chromium compound is formed thereon, and thereafter removing and rinsing the article to remove the hexavalent chromium solution therefrom, the article being removed from the bath prior to the formation of an appreciable visible film of said compound thereon.
11. The method of forming a corrosion inhibiting coating on an article having a base member of ferrous metal and a layer of chromium plate thereover, which comprises immersing the article in a solution containing hexavalent chromium until a coating of chromium compound is formed thereon, and thereafter removing the article from the bath and rinsing the article to remove the hexavalent chromium solution therefrom.
12. The method of forming a corrosion inhibiting coating on an article having a base member of ferrous metal, a layer of nickel plate on the base member and a layer of chromium plate on the nickel layer, which comprises immersing the article in a bath containing hexa valent chromium in solution until a coating is formed thereon which is anodic to the chromium layer, the nickel layer, and the base metal, and thereafter removing the 5 article from the bath and rinsing the article to remove the hexavalent chromium containing solution therefrom.
13. The method of forming a corrosion inhibiting coating on an article having a base member of ferrous metal, a layer of nickel plate on the base metal, and a layer of chromium plate on the nickel plate layer, which comprises immersing the article in a hexavalent chromium solution until a coating of a chromium compound is formed thereon, and thereafter removing and rinsing the article to remove the hexavalent chromium solution therefrom, the article being removed from the bath prior to the formation of an appreciably visible film of said compound thereon.
No references cited.
Claims (1)
1. THE METHOD OF INCREASING THE CORROSION RESISTANCE OF A STEEL ARTICLE HAVING A PLATING OF CHROMIUM THEREON WHICH IS NORMALLY CATHODIC TO THE STEEL OF THE ARTICLE WHEN IMMERSED IN A SODIUM CHLORIDE SOLUTION, WHICH COMPRISES FORMING A COATING OVER THE CHROMIUM PLATING WHICH IS ANODIC TO THE STEEL OF THE ARTICLE BY IMMERSING THE ARTICLE IN A SOLUTION CONTAINING HEXAVALENT CHROMIUM UNTIL A COATING OF CHROMIUM COMPOUND IS FORMED THEREON.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US549511A US2788292A (en) | 1951-10-15 | 1955-11-28 | Method of treating chromium surfaces |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US251462A US2746915A (en) | 1951-10-15 | 1951-10-15 | Electrolytic metal treatment and article |
| US549511A US2788292A (en) | 1951-10-15 | 1955-11-28 | Method of treating chromium surfaces |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2788292A true US2788292A (en) | 1957-04-09 |
Family
ID=26941633
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US549511A Expired - Lifetime US2788292A (en) | 1951-10-15 | 1955-11-28 | Method of treating chromium surfaces |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2788292A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2924539A (en) * | 1956-10-26 | 1960-02-09 | Midwest Mfg Corp | Wetting compound for colored aluminum anodized surfaces |
| US2938813A (en) * | 1955-11-02 | 1960-05-31 | Yawata Iron & Steel Co | Insulated coating for silicon steel sheet |
| US2975073A (en) * | 1958-02-06 | 1961-03-14 | Dow Chemical Co | Corrosion resistance of electroless nickel plate |
| US2991205A (en) * | 1957-12-13 | 1961-07-04 | Allegheny Ludlum Steel | Method of improving corrosion resistance of stainless steel |
| US3900601A (en) * | 1973-09-28 | 1975-08-19 | Ppg Industries Inc | Treatment of thin metallic films for increased durability |
| US5730809A (en) * | 1994-11-09 | 1998-03-24 | Enthone-Omi, Inc. | Passivate for tungsten alloy electroplating |
-
1955
- 1955-11-28 US US549511A patent/US2788292A/en not_active Expired - Lifetime
Non-Patent Citations (1)
| Title |
|---|
| None * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2938813A (en) * | 1955-11-02 | 1960-05-31 | Yawata Iron & Steel Co | Insulated coating for silicon steel sheet |
| US2924539A (en) * | 1956-10-26 | 1960-02-09 | Midwest Mfg Corp | Wetting compound for colored aluminum anodized surfaces |
| US2991205A (en) * | 1957-12-13 | 1961-07-04 | Allegheny Ludlum Steel | Method of improving corrosion resistance of stainless steel |
| US2975073A (en) * | 1958-02-06 | 1961-03-14 | Dow Chemical Co | Corrosion resistance of electroless nickel plate |
| US3900601A (en) * | 1973-09-28 | 1975-08-19 | Ppg Industries Inc | Treatment of thin metallic films for increased durability |
| US5730809A (en) * | 1994-11-09 | 1998-03-24 | Enthone-Omi, Inc. | Passivate for tungsten alloy electroplating |
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