US2851766A - Plural metallic coatings on uranium and method of applying same - Google Patents
Plural metallic coatings on uranium and method of applying same Download PDFInfo
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- US2851766A US2851766A US572094A US57209445A US2851766A US 2851766 A US2851766 A US 2851766A US 572094 A US572094 A US 572094A US 57209445 A US57209445 A US 57209445A US 2851766 A US2851766 A US 2851766A
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/34—Pretreatment of metallic surfaces to be electroplated
- C25D5/46—Pretreatment of metallic surfaces to be electroplated of actinides
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- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21C—NUCLEAR REACTORS
- G21C3/00—Reactor fuel elements and their assemblies; Selection of substances for use as reactor fuel elements
- G21C3/02—Fuel elements
- G21C3/04—Constructional details
- G21C3/16—Details of the construction within the casing
- G21C3/20—Details of the construction within the casing with coating on fuel or on inside of casing; with non-active interlayer between casing and active material with multiple casings or multiple active layers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E30/00—Energy generation of nuclear origin
- Y02E30/30—Nuclear fission reactors
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/934—Electrical process
- Y10S428/935—Electroplating
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/939—Molten or fused coating
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/12743—Next to refractory [Group IVB, VB, or VIB] metal-base component
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/12764—Next to Al-base component
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12806—Refractory [Group IVB, VB, or VIB] metal-base component
- Y10T428/12826—Group VIB metal-base component
- Y10T428/12847—Cr-base component
Definitions
- Metallic chromium has many desirable properties as a' structural or coating metal. In some cases, however, its corroson resistance is inadequate and application of other metals possessing greater resistance to the specific corrosive elements involved is desirable. In other cases the chromium exerts undesirable electro-chemical effects andapplication of coatings to overcome these effects may benecessary.
- chromium plate ings In the protection of metallic uranium, chromium plate ings have very beneficial properties for preventing diifusion of metallic uranium. However, for some purposes the metallic uranium is not adequately protected from corrosive influences by the chromium alone. Hence it is desirable to apply metallic coatings to the chromium platings.
- the chromium platings have been found to be particularly refractory to wetting by other coating metals. As a consequence only poor, incomplete coatings are obtained when coating of the chromium platings by'lowmelting hot-dip coating metals is attempted.
- An object of the present invention is the application of' adherent metallic coatings to chromium surfaces.
- a further object is the provision of corrosion-resistant protectilve coatings on chromium platings.
- a still further object is the protection of metallic uranium by means (if-chromium platings coated with hot-dip coatings.
- chromium surfaces are coated by applying coating metals consisting of or containing aluminum.
- coating metals consisting of or containing aluminum.
- the proportion of aluminum necessary to accomplish the purposes of the invention is not large.
- zinc coatings containing as little as 1% of aluminum have been applied successfully.
- coatings containing more than 99% of aluminum also may be applied.
- the process is particularly applicable to bright chromium electroplatings on metallic uranium.
- Most suitable conditions for applying the coatings will vary depending upon the composition of the coating metal employed. Thus temperatures from 450 C. or less to 750 C. or more may be used, depending upon the melting point of the metal to be applied. In the application of zinc coatings containing from 1% to 5% of aluminum, temperatures from 150 to 650 C. may be used, the lower temperatures ures between 600 C. and 750 C.
- the hot-dip coatings may be applied with or without fiux.
- Alkali-metal halide fluxes especially those containing small proportions of alkali-metal fluoride, have een found to be particularly satisfactory.
- the use of such fluxes is not essential to the production f adherent coatings.
- the invention is useful for the application of hot-dip coatings to serve as final protective coatings and also to serve as bonding means to unite the chromium surfaces with other metals.
- zinc coatings may serve as a base for solder bonds to other metals.
- a particularly suitable combination involves the application of lowmelting' aluminum-silicon alloys to metallic aluminum sheaths.
- the chromium may be applied directly tothe uranium or over a light coating of another metal, such as nickel or copper, as described in greater detail in my U. S. patent applications, Serial No. 572,093, entitled Nickel Coatings and Method of' Applying,'filed January 9, 1945, and Serial No. 571,673, entitled Copper Coatings and Method of. Applying, filed January 6, 1945.
- the metallic uranium preferably is prepared for the application of the coatings by an etchant treatment of the. metal surface with an aqueous etching solution containing chloride ions, i. e., a hydrochloric acid solution or a molten hydrate of ferric chloride.
- an aqueous etching solution containing chloride ions i. e., a hydrochloric acid solution or a molten hydrate of ferric chloride.
- Particularly satisfactory treatments of this type involve anodic pickling of the metal in trichloracetic acid solution, for example an aqueous solution containing 45% to 50% of trichloracetic acid, or in aqueous phosphoric acid solution containing about /z% of hydrochloric acid, to remove a one-half to one mil layer of the surface metal.
- Prior to the etchant treatment metal may be cleaned by sandblasting, pumice-scrubbing, treating with organic solvents to remove grease or oily impurities, or treating with a chemical solvent for the oxide film on the metal.
- Aque- 011s nitric acid solutions containing from 30% to 55% HNO by Weight are especially useful for this purpose.
- An additional short treatment with this reagent should be applied after the etchant treatment in order to remove the coating of oxide or oxychloride from the etched. metal surface.
- Example 1 A metallic uranium rod is pickled in aqueous 15% trichloracetic acid solution at about 55 C. while a current is passed through the solution with the rod connected as anode for 10 minutes at a current density of 50 amperes per square foot. The rod is then rinsed with cold water, dipped for four minutes in aqueous 35% HN 0 solution, rinsed again and electroplated in a chromic acid bath containing 400 grams per liter of chromic acid at 50 C. and 250 amperes per sq. ft. current density until a chromium layer about 0.001" thick is formed (about 1 hour). A conforming lead anode spaced about one inch from the rod is used.
- the freshly plated rod is then dipped into a molten zinc bath containing 1% ofaluminum at 600 C. for approximately seconds.
- the rod is removed from the bath, shaken to free it from excess molten metal, placed on smooth Transite (asbestos cement) rollers and rolled slowly in air until the coating solidifies.
- a firmly adherent zinc-aluminum coating is obtained on the chromium-plated. rod.
- Example 2 A rod plated and coated as in Example 1, upon removal. from the zinc bath, is spun at high speed for 5 seconds to remove excess metal and is then dipped for 10 seconds into a molten aluminum-silicon alloy comprising 88 parts of aluminum and 12 parts of silicon at 638 C. The rod is withdrawn and cooled on rollers as in Example 1. A firmly adherent coating of aluminum-silicon alloy over zinc is obtained on the chromium-plated uranium rod.
- the zinc bath has an important function of heating the rod to a temperature approaching that of the aluminum-silicon bath and thus facilitating application of this alloy.
- Example 3 A chromium-plated rod prepared as in Example 1 is dipped through a halide flux (prepared by first mixing 53 parts of potassium chloride, 42 parts of lithium chloride and parts of sodium chloride and adding to the mixture parts of sodium fluoride) into a zinc bath of 99% zinc and 1% aluminum at a temperature of about 660 C. The rod is held in this bath for 1 minute, then removed, spun to remove excess metal, and dipped for 4 seconds directly into an aluminum-silicon alloy containing 88% aluminum and 12% silicon at 640 C. for 4 seconds. The rod is removed from this alloy and rolled until cool as in the preceding examples.
- a halide flux prepared by first mixing 53 parts of potassium chloride, 42 parts of lithium chloride and parts of sodium chloride and adding to the mixture parts of sodium fluoride
- Example 4 A rod, chromium plated as in Example 1, is dipped through a halide fiux of the same composition as used in Example 3 into a molten zinc bath consisting of 95% zinc and 5% aluminum'at 650 C. The rod is held in this bath for about 75 seconds, withdrawn, centrifuged for 5 seconds, and passed through a flux of the same composition into an 88% aluminum 12% silicon alloy at 640 C. After 2 seconds in this bath the rod is withdrawn and plunged into a preheated aluminum can containing a small amount of aluminum-silicon at 600 C. Upon cooling the assembly the aluminum can is firmly united by the aluminum-silicon alloy and zinc to the chromium-plated rod.
- Example 5 A uranium rod, electroplated as in Example 1, is dipped for 30 seconds into molten aluminum 2S at a temperature of about 750 C. The molten aluminum is covered by a flux prepared by adding parts of NaF to 100 parts of a 53% KCl, 42% LiCl, 5% NaCl mixture. The coating is cooled on rollers as in Example 1. A continuous aluminum coating on the chromium-plated rod is thus obtained.
- Example 6 A machined cylindrical uranium rod about 8 inches long and 1 /3 inches in diameter is prepared for electroplating by dipping in trichlorethene to remove grease, sand-blasting lightly, dipping in aqueous 35% I-INO at 30 C. for 4 minutes, rinsing with cold water, etching by anodic treatment in aqueous 50% trichloracetic acid solution at between 50 C. and 60 C. for 10 minutes at 50 amperes per square foot current density, rinsing with cold water, dipping for 4 minutes in cold aqueous 35% HNO solution to clean the etched metal surface, and rinsing in cold water.
- the cleaned, etched metal rod is immediately electroplated in a copper pyrophosphate electroplating bath, comprising 75 grams per liter of copper as pyrophosphate, at a current density of amperes per square foot at 60 C. with air agitation until a copper plating about 0.0005 inch thick is formed (about minutes).
- the copper-plated rod is rinsed with water and then electroplated in a chromic acid bath, containing 400 grams per liter of chromic acid and 4 grams per liter of sulfuric acid at 50 C. and 250 amperes per sq. ft. current density until a chromium layer 0.0005 inch thick has formed (about 30 minutes).
- a concentric lead anode comprising an expanded metal cylinder having a diameter about 2 inches greater than the rod is used.
- the freshly chromium-plated rod is rinsed to remove electroplating solution, dried, and dipped directly into a sodium-modified 88% aluminum 12% silicon alloy at 640 C. for 50 seconds. It is then removed from the alloy, shaken free of excess metal, and placed on smooth Transite rollers where it is rolled in contact with air at room temperature until it has cooled.
- Example 7 The process of the preceding example is repeated except that the copper electroplating step is conducted for only about 2 minutes to produce a copper coating about 0.00003 inch thick and the uranium rod covered with this flash coating is electroplated in a chromic acid bath, to a thickness of 0.0008 inch chromium and then hot dipped as in Example 6. An equally adherent aluminum-silicon alloy coating affording adequate protection for the uranium rod is obtained.
- Example 8 A metallic uranium rod prepared for electroplating as in Example 6 is electroplated in a nickel sulfate electroplating bath, comprising 240 grams of NiSO .7H O, 45 grams of NiCl .6H O, and 30 grams of H 30 at a current density of 25 amperesper sq. ft. at 40 C. until a nickel plating about 0.0001 inch thick is formed (about 5 minutes).
- the plated rod is then rinsed in water and electroplated in an aqueous solution containing 400 grams per liter of chromic acid and 4 grams per liter of sulfuric acid at 50 C. until a chromium plating 0.0005 inch thick has been built up.
- a concentric lead anode comprising an expanded metal cylinder having a diameter about 2 inches greater than the rod is used.
- the chromium-plated rod is rinsed, dried and dipped in aluminum-silicon as in Example 6. After rolling and cooling, a uniform adherent coating is obtained on the rod.
- Example 9 The process of the preceding example is repeated except that the nickel electroplating step is conducted for only about 45 seconds to apply a nickel coating 0.000015 inch thick and the chromium electroplating step is conducted for about one hour to apply a chromium plating 0.001 inch thick. As in the preceding example a firmly adherent coating is obtained afiording adequate protection for the uranium rod.
- hot-dip coatings of other aluminum alloys such as copper-modified aluminum and magnesiumaluminum alloys may be applied to chromium platings on uranium and other metals.
- the methodof protectively coating uranium, which comprises applying a chromium plating to the uranium and bonding the chromium plating by means of molten aluminum-silicon alloy to an aluminum sheath.
- the method of protectively coating uranium which comprises applying a flash coating of a metal of the group consisting of copper and nickel, applying a chromium plating thereover, and bonding the chromium plating by means of molten aluminum-silicon alloy to an aluminum sheath.
- a molten metal of the group consisting of aluminum and aluminum-containing alloys by passing said chromiumplated article thru a molten halide flux containing from 10 to 15 parts of NaF added to parts of a 53% KCl,"
- the method of protectively coating a uranium article which comprises applying a chromium plating thereto by electrolysis from a chromic acid bath, passing said chromium plated article thru a molten halide flux containing from to parts of NaF added to 100 parts of a 53% KCl, 42% LiCl, 5% NaCl mixture into a molten metal bath consisting of 99% to zinc and 1% to 5% aluminum, and then applying to the surface of said coated article molten aluminum containing a minor proportion of silicon by passing said coated article thru a molten halide flux containing from 10 to 15 parts of NaF added to parts of a 53% KCl, 42% LiCl, 5% NaCl mixture into a molten bath'of an 88% aluminum 12% silicon alloy.
- a uranium article having a chromium plating over which there is a bonding layer consisting of an aluminumsilicon alloy containing about 12% of silicon and an aluminum sheath, said bonding layer lying between said chromium plating and said aluminum sheath.
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Description
2,851,766 Patented Sept. 16, 1958 MEETALLIC COATINGS N AND METHOD OF APPLYING SAME 8' Claims. (Cl. 29-194) This invention relates to the application of metallic coatings to chromium surfaces.
Metallic chromium has many desirable properties as a' structural or coating metal. In some cases, however, its corroson resistance is inadequate and application of other metals possessing greater resistance to the specific corrosive elements involved is desirable. In other cases the chromium exerts undesirable electro-chemical effects andapplication of coatings to overcome these effects may benecessary.
In the protection of metallic uranium, chromium plate ings have very beneficial properties for preventing diifusion of metallic uranium. However, for some purposes the metallic uranium is not adequately protected from corrosive influences by the chromium alone. Hence it is desirable to apply metallic coatings to the chromium platings. The chromium platings have been found to be particularly refractory to wetting by other coating metals. As a consequence only poor, incomplete coatings are obtained when coating of the chromium platings by'lowmelting hot-dip coating metals is attempted.
An object of the present invention is the application of' adherent metallic coatings to chromium surfaces. A further object, is the provision of corrosion-resistant protectilve coatings on chromium platings. A still further object is the protection of metallic uranium by means (if-chromium platings coated with hot-dip coatings. Other objects will appear from the following description of the invention.
In accordance with my invention chromium surfaces are coated by applying coating metals consisting of or containing aluminum. I have found that the aluminum wets the chromium and provides a firm bond between the chromium and the coating metal. The proportion of aluminum necessary to accomplish the purposes of the invention is not large. Thus zinc coatings containing as little as 1% of aluminum have been applied successfully. On the other hand coatings containing more than 99% of aluminum also may be applied. The process is particularly applicable to bright chromium electroplatings on metallic uranium. Most suitable conditions for applying the coatings will vary depending upon the composition of the coating metal employed. Thus temperatures from 450 C. or less to 750 C. or more may be used, depending upon the melting point of the metal to be applied. In the application of zinc coatings containing from 1% to 5% of aluminum, temperatures from 150 to 650 C. may be used, the lower temperatures ures between 600 C. and 750 C.
The hot-dip coatings may be applied with or without fiux. Alkali-metal halide fluxes, especially those containing small proportions of alkali-metal fluoride, have een found to be particularly satisfactory. However, the use of such fluxes is not essential to the production f adherent coatings.
The invention is useful for the application of hot-dip coatings to serve as final protective coatings and also to serve as bonding means to unite the chromium surfaces with other metals. Thus zinc coatings may serve as a base for solder bonds to other metals. A particularly suitable combination involves the application of lowmelting' aluminum-silicon alloys to metallic aluminum sheaths.
In the application of the invention to the coating of metallic uranium, the chromium may be applied directly tothe uranium or over a light coating of another metal, such as nickel or copper, as described in greater detail in my U. S. patent applications, Serial No. 572,093, entitled Nickel Coatings and Method of' Applying,'filed January 9, 1945, and Serial No. 571,673, entitled Copper Coatings and Method of. Applying, filed January 6, 1945.
The metallic uraniumpreferably is prepared for the application of the coatings by an etchant treatment of the. metal surface with an aqueous etching solution containing chloride ions, i. e., a hydrochloric acid solution or a molten hydrate of ferric chloride. Particularly satisfactory treatments of this type involve anodic pickling of the metal in trichloracetic acid solution, for example an aqueous solution containing 45% to 50% of trichloracetic acid, or in aqueous phosphoric acid solution containing about /z% of hydrochloric acid, to remove a one-half to one mil layer of the surface metal. Prior to the etchant treatment metal may be cleaned by sandblasting, pumice-scrubbing, treating with organic solvents to remove grease or oily impurities, or treating with a chemical solvent for the oxide film on the metal. Aque- 011s nitric acid solutions containing from 30% to 55% HNO by Weight are especially useful for this purpose. An additional short treatment with this reagent should be applied after the etchant treatment in order to remove the coating of oxide or oxychloride from the etched. metal surface.
The following examples further illustrate the inven tion. Unless otherwise indicated, quantities are expressed in terms of weight.
Example 1 A metallic uranium rod is pickled in aqueous 15% trichloracetic acid solution at about 55 C. while a current is passed through the solution with the rod connected as anode for 10 minutes at a current density of 50 amperes per square foot. The rod is then rinsed with cold water, dipped for four minutes in aqueous 35% HN 0 solution, rinsed again and electroplated in a chromic acid bath containing 400 grams per liter of chromic acid at 50 C. and 250 amperes per sq. ft. current density until a chromium layer about 0.001" thick is formed (about 1 hour). A conforming lead anode spaced about one inch from the rod is used. The freshly plated rod is then dipped into a molten zinc bath containing 1% ofaluminum at 600 C. for approximately seconds. The rod is removed from the bath, shaken to free it from excess molten metal, placed on smooth Transite (asbestos cement) rollers and rolled slowly in air until the coating solidifies. A firmly adherent zinc-aluminum coating is obtained on the chromium-plated. rod.
Example 2 A rod plated and coated as in Example 1, upon removal. from the zinc bath, is spun at high speed for 5 seconds to remove excess metal and is then dipped for 10 seconds into a molten aluminum-silicon alloy comprising 88 parts of aluminum and 12 parts of silicon at 638 C. The rod is withdrawn and cooled on rollers as in Example 1. A firmly adherent coating of aluminum-silicon alloy over zinc is obtained on the chromium-plated uranium rod.
In this example the zinc bath has an important function of heating the rod to a temperature approaching that of the aluminum-silicon bath and thus facilitating application of this alloy.
Example 3 A chromium-plated rod prepared as in Example 1 is dipped through a halide flux (prepared by first mixing 53 parts of potassium chloride, 42 parts of lithium chloride and parts of sodium chloride and adding to the mixture parts of sodium fluoride) into a zinc bath of 99% zinc and 1% aluminum at a temperature of about 660 C. The rod is held in this bath for 1 minute, then removed, spun to remove excess metal, and dipped for 4 seconds directly into an aluminum-silicon alloy containing 88% aluminum and 12% silicon at 640 C. for 4 seconds. The rod is removed from this alloy and rolled until cool as in the preceding examples.
Example 4 A rod, chromium plated as in Example 1, is dipped through a halide fiux of the same composition as used in Example 3 into a molten zinc bath consisting of 95% zinc and 5% aluminum'at 650 C. The rod is held in this bath for about 75 seconds, withdrawn, centrifuged for 5 seconds, and passed through a flux of the same composition into an 88% aluminum 12% silicon alloy at 640 C. After 2 seconds in this bath the rod is withdrawn and plunged into a preheated aluminum can containing a small amount of aluminum-silicon at 600 C. Upon cooling the assembly the aluminum can is firmly united by the aluminum-silicon alloy and zinc to the chromium-plated rod.
Example 5 A uranium rod, electroplated as in Example 1, is dipped for 30 seconds into molten aluminum 2S at a temperature of about 750 C. The molten aluminum is covered by a flux prepared by adding parts of NaF to 100 parts of a 53% KCl, 42% LiCl, 5% NaCl mixture. The coating is cooled on rollers as in Example 1. A continuous aluminum coating on the chromium-plated rod is thus obtained.
Example 6 A machined cylindrical uranium rod about 8 inches long and 1 /3 inches in diameter is prepared for electroplating by dipping in trichlorethene to remove grease, sand-blasting lightly, dipping in aqueous 35% I-INO at 30 C. for 4 minutes, rinsing with cold water, etching by anodic treatment in aqueous 50% trichloracetic acid solution at between 50 C. and 60 C. for 10 minutes at 50 amperes per square foot current density, rinsing with cold water, dipping for 4 minutes in cold aqueous 35% HNO solution to clean the etched metal surface, and rinsing in cold water.
The cleaned, etched metal rod is immediately electroplated in a copper pyrophosphate electroplating bath, comprising 75 grams per liter of copper as pyrophosphate, at a current density of amperes per square foot at 60 C. with air agitation until a copper plating about 0.0005 inch thick is formed (about minutes). The copper-plated rod is rinsed with water and then electroplated in a chromic acid bath, containing 400 grams per liter of chromic acid and 4 grams per liter of sulfuric acid at 50 C. and 250 amperes per sq. ft. current density until a chromium layer 0.0005 inch thick has formed (about 30 minutes). For the chromium plating step a concentric lead anode comprising an expanded metal cylinder having a diameter about 2 inches greater than the rod is used.
The freshly chromium-plated rod is rinsed to remove electroplating solution, dried, and dipped directly into a sodium-modified 88% aluminum 12% silicon alloy at 640 C. for 50 seconds. It is then removed from the alloy, shaken free of excess metal, and placed on smooth Transite rollers where it is rolled in contact with air at room temperature until it has cooled.
Example 7 The process of the preceding example is repeated except that the copper electroplating step is conducted for only about 2 minutes to produce a copper coating about 0.00003 inch thick and the uranium rod covered with this flash coating is electroplated in a chromic acid bath, to a thickness of 0.0008 inch chromium and then hot dipped as in Example 6. An equally adherent aluminum-silicon alloy coating affording adequate protection for the uranium rod is obtained.
Example 8 A metallic uranium rod prepared for electroplating as in Example 6 is electroplated in a nickel sulfate electroplating bath, comprising 240 grams of NiSO .7H O, 45 grams of NiCl .6H O, and 30 grams of H 30 at a current density of 25 amperesper sq. ft. at 40 C. until a nickel plating about 0.0001 inch thick is formed (about 5 minutes). The plated rod is then rinsed in water and electroplated in an aqueous solution containing 400 grams per liter of chromic acid and 4 grams per liter of sulfuric acid at 50 C. until a chromium plating 0.0005 inch thick has been built up. A concentric lead anode comprising an expanded metal cylinder having a diameter about 2 inches greater than the rod is used. The chromium-plated rod is rinsed, dried and dipped in aluminum-silicon as in Example 6. After rolling and cooling, a uniform adherent coating is obtained on the rod.
Example 9 The process of the preceding example is repeated except that the nickel electroplating step is conducted for only about 45 seconds to apply a nickel coating 0.000015 inch thick and the chromium electroplating step is conducted for about one hour to apply a chromium plating 0.001 inch thick. As in the preceding example a firmly adherent coating is obtained afiording adequate protection for the uranium rod.
In a similar manner hot-dip coatings of other aluminum alloys such as copper-modified aluminum and magnesiumaluminum alloys may be applied to chromium platings on uranium and other metals. 7
It will be understood that I intend to include variations and modifications of the invention and that the preceding examples are illustrations only and in no wise to be construed as limitations upon the invention, the scope of Which is defined in the appended claims, wherein:
I claim:
1. The methodof protectively coating uranium, which comprises applying a chromium plating to the uranium and bonding the chromium plating by means of molten aluminum-silicon alloy to an aluminum sheath.
2. The method of protectively coating uranium, which comprises applying a flash coating of a metal of the group consisting of copper and nickel, applying a chromium plating thereover, and bonding the chromium plating by means of molten aluminum-silicon alloy to an aluminum sheath.
3. A uranium article having a chromium plating on a flash plating of the group consisting of nickel and copper and bonded to an aluminum sheath by means of an aluminum-silicon alloy containing about 12% of silicon.
a molten metal of the group consisting of aluminum and aluminum-containing alloys by passing said chromiumplated article thru a molten halide flux containing from 10 to 15 parts of NaF added to parts of a 53% KCl,"
42% LiCl, 5% NaCl mixture into a bath of said molten metal.
5. The method of protectively coating a uranium article which comprises applying a chromium plating thereto by electrolysis from a chromic acid bath, passing said chromium plated article thru a molten halide flux containing from to parts of NaF added to 100 parts of a 53% KCl, 42% LiCl, 5% NaCl mixture into a molten metal bath consisting of 99% to zinc and 1% to 5% aluminum, and then applying to the surface of said coated article molten aluminum containing a minor proportion of silicon by passing said coated article thru a molten halide flux containing from 10 to 15 parts of NaF added to parts of a 53% KCl, 42% LiCl, 5% NaCl mixture into a molten bath'of an 88% aluminum 12% silicon alloy.
6. A uranium article having a chromium plating over which is firmly bonded a metal coating of the group consisting of aluminum and aluminum-containing alloys.
7. A uranium article having a chromium plating over which is firmly bonded an adherent metal coating consisting of an alloy of aluminum with a minor proportion of silicon.
81 A uranium article having a chromium plating over which there is a bonding layer consisting of an aluminumsilicon alloy containing about 12% of silicon and an aluminum sheath, said bonding layer lying between said chromium plating and said aluminum sheath.
References Cited in the file of this patent UNITED STATES PATENTS 1,128,059 Schoop Feb. 9, 1915 1,607,676 Jirotka Nov. 23, 1926 1,764,132 Wehr et al June 17, 1930 2,048,552 Johnson July 21, 1936 2,075,477 Smith Mar. 30, 1937 FOREIGN PATENTS 93,967 Austria Aug. 25, 1923 305,544 Great Britain Feb. 6, 1929
Claims (2)
1. THE METHOD OF PROTECTIVELY COATING URANIUM, WHICH COMPRISES APPLYING A CHROMIUM PLATING TO THE URANIUM AND BONDING THE CHROMIUM PLATING BY MEANS OF MOLTEN ALUMIUM-SILICON ALLOY TO AN ALUMINUM SHEATH.
6. A URANIUM ARTICLE HAVING A CHROMIUM PLATING OVER WHICH IS FIRMLY BONDED A METAL COATING OF THE GROUP CONSISTING OF ALUMIMUM AND ALUMINUM-CONTAINING ALLOYS.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US572094A US2851766A (en) | 1945-01-09 | 1945-01-09 | Plural metallic coatings on uranium and method of applying same |
GB2594/46A GB858301A (en) | 1945-01-09 | 1946-01-25 | This invention relates to the application of metallic coatings to chromium plated uranium surfaces |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US572094A US2851766A (en) | 1945-01-09 | 1945-01-09 | Plural metallic coatings on uranium and method of applying same |
Publications (1)
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US2851766A true US2851766A (en) | 1958-09-16 |
Family
ID=24286324
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US572094A Expired - Lifetime US2851766A (en) | 1945-01-09 | 1945-01-09 | Plural metallic coatings on uranium and method of applying same |
Country Status (2)
Country | Link |
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US (1) | US2851766A (en) |
GB (1) | GB858301A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2884364A (en) * | 1946-05-14 | 1959-04-28 | Elmer W Rebol | Method of electroplating on uranium |
US2902423A (en) * | 1956-02-02 | 1959-09-01 | Emmeth A Luebke | Neutronic reactor producing thermoelectric power |
US3288636A (en) * | 1962-10-27 | 1966-11-29 | Interatom | Process for coating uranium alloy members |
US3493476A (en) * | 1965-11-01 | 1970-02-03 | Avco Corp | Sulfidation and oxidation resistant coating |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3270413A (en) * | 1963-12-02 | 1966-09-06 | Ca Atomic Energy Ltd | Process for producing a diffusionless bond between metals |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1128059A (en) * | 1911-08-07 | 1915-02-09 | Metals Coating Company Of America | Method of plating or coating with metallic coatings. |
AT93967B (en) * | 1919-10-23 | 1923-08-25 | Internat General Elek C Compan | Process for treating the surface of metals. |
US1607676A (en) * | 1924-10-29 | 1926-11-23 | Firm Dr Otto Sprenger Patentve | Process for obtaining metal coatings on articles of aluminum and aluminum alloys |
GB305544A (en) * | 1928-02-06 | 1930-04-03 | Metallgesellschaft Aktiengesellschaft | |
US1764132A (en) * | 1926-09-13 | 1930-06-17 | American Rolling Mill Co | Heat-resistant metal sheet |
US2048552A (en) * | 1934-12-19 | 1936-07-21 | Johnson Steel & Wire Company I | Method of making rust resisting metal plated wire |
US2075477A (en) * | 1935-02-11 | 1937-03-30 | Corning Glass Works | Glass closure for metal containers and method of making it |
-
1945
- 1945-01-09 US US572094A patent/US2851766A/en not_active Expired - Lifetime
-
1946
- 1946-01-25 GB GB2594/46A patent/GB858301A/en not_active Expired
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1128059A (en) * | 1911-08-07 | 1915-02-09 | Metals Coating Company Of America | Method of plating or coating with metallic coatings. |
AT93967B (en) * | 1919-10-23 | 1923-08-25 | Internat General Elek C Compan | Process for treating the surface of metals. |
US1607676A (en) * | 1924-10-29 | 1926-11-23 | Firm Dr Otto Sprenger Patentve | Process for obtaining metal coatings on articles of aluminum and aluminum alloys |
US1764132A (en) * | 1926-09-13 | 1930-06-17 | American Rolling Mill Co | Heat-resistant metal sheet |
GB305544A (en) * | 1928-02-06 | 1930-04-03 | Metallgesellschaft Aktiengesellschaft | |
US2048552A (en) * | 1934-12-19 | 1936-07-21 | Johnson Steel & Wire Company I | Method of making rust resisting metal plated wire |
US2075477A (en) * | 1935-02-11 | 1937-03-30 | Corning Glass Works | Glass closure for metal containers and method of making it |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2884364A (en) * | 1946-05-14 | 1959-04-28 | Elmer W Rebol | Method of electroplating on uranium |
US2902423A (en) * | 1956-02-02 | 1959-09-01 | Emmeth A Luebke | Neutronic reactor producing thermoelectric power |
US3288636A (en) * | 1962-10-27 | 1966-11-29 | Interatom | Process for coating uranium alloy members |
US3493476A (en) * | 1965-11-01 | 1970-02-03 | Avco Corp | Sulfidation and oxidation resistant coating |
Also Published As
Publication number | Publication date |
---|---|
GB858301A (en) | 1961-01-11 |
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