US2705830A - Coated metal objects - Google Patents
Coated metal objects Download PDFInfo
- Publication number
- US2705830A US2705830A US238569A US23856951A US2705830A US 2705830 A US2705830 A US 2705830A US 238569 A US238569 A US 238569A US 23856951 A US23856951 A US 23856951A US 2705830 A US2705830 A US 2705830A
- Authority
- US
- United States
- Prior art keywords
- silver
- coat
- base
- melting point
- metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910052751 metal Inorganic materials 0.000 title description 28
- 239000002184 metal Substances 0.000 title description 28
- 229910052709 silver Inorganic materials 0.000 claims description 55
- 239000004332 silver Substances 0.000 claims description 55
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 49
- 238000002844 melting Methods 0.000 claims description 22
- 230000008018 melting Effects 0.000 claims description 22
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 6
- 239000011148 porous material Substances 0.000 description 17
- 150000003839 salts Chemical class 0.000 description 14
- 229910021607 Silver chloride Inorganic materials 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- -1 halogen salt Chemical class 0.000 description 7
- 230000000717 retained effect Effects 0.000 description 6
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 4
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 3
- 229910021612 Silver iodide Inorganic materials 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229940045105 silver iodide Drugs 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000009518 sodium iodide Nutrition 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229940096017 silver fluoride Drugs 0.000 description 1
- REYHXKZHIMGNSE-UHFFFAOYSA-M silver monofluoride Chemical compound [F-].[Ag+] REYHXKZHIMGNSE-UHFFFAOYSA-M 0.000 description 1
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
-
- 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
- C25D5/48—After-treatment of electroplated surfaces
-
- 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
- Y10S428/923—Physical dimension
- Y10S428/924—Composite
- Y10S428/926—Thickness of individual layer specified
-
- 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
-
- 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
- Y10T428/12007—Component of composite having metal continuous phase interengaged with nonmetal continuous phase
-
- 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
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12896—Ag-base component
-
- 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
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12951—Fe-base component
Definitions
- This invention relates to metal coating, and more particularly to the application of an extremely thin metal coating to a base which completely seals the base against the outside.
- This method essentially consists in applying an extremely thin, though porous, metal coat to the base, and polarizing the coated object in a suitable electrolyte solution to form on the surface of a porous metal coating a film of a compound of such properties that it can be subsequently fused, thereby sealing the pores in the porous metal coating.
- one of the principal objects of my invention is the formation of a metal coat of extreme thinness, whose pores are sealed by a compound of the coating metal.
- a further object of my invention is the electrochemical formation of a fusible salt on the surface of an extremely thin metal coat, with subsequent fusion to seal the pores of the coat.
- Another object of my invention is a saving in the cost of noble metals used for coating a base material.
- a further object of my invention is the provision of an extremely thin non-porous coat on a base, which coat consists of a metal and of a water-insoluble salt of such metal, the color of the salt resembling the color of the metal so as to give the appearance of a homogeneous film.
- the base is first coated with a thin coat of the coating metal, preferably but not necessarily by electrodeposition.
- the coat is intentionally of such thinness that it is not free from pores.
- the coat may be kept below a thickness of .0015 inch, which latter thickness is commonly considered to be the lower limit for a non-porous electrodeposited silver coat.
- the electrolytic bath is a solution of an ionizable compound whose negative ions or radicals are capable of combining with the coating metal at the anode to form a water-insoluble fusible salt.
- a suitable electrolytic bath is a water solution of hydrochloric acid or of sodium chloride which, upon passage of the current through the system, results in the formation of silver chloride on the silver coat.
- corresponding halogen salt may be formed by combination with the silver coat at the anode; inasmuch as silver chloride, silver iodide, and silver bromide are water-insoluble and fusible, they are suitable for the purpose of my invention.
- silver fluoride is water-soluble, and consequently a fluoride solution is unsuitable for use as an electrolytic bath for the purpose of my invention.
- the coated article which forms the anode, is withdrawn after part of the metal has been converted into the corresponding salt.
- the coated article is then subjected to a temperature above the melting point of the salt where the melting point of the salt is below that of the metal, or to a temperature above the melting point of the metal where the melting point of the salt is above the melting point of the metal.
- the elevated temperature is kept below the melting point of the metal itself; this exposure causes the salt to melt and to flow into the pores of the thin metal coat.
- the metal itself when heated above its melting point will evenly fill out the inter stices between the electrochemically formed salt deposit.
- a non-porous coat is found to have formed on the base. It may be buffed or burnished to give it a metallic appearance.
- Example I A porous silver coat of a thickness of the order of .0005 to .00075 inch is electrodeposited. upon steel.
- the coated object is immersed into an electrolytic bath consisting of a water solution of 50 cc. of concentrated hydrochloric acid in 450 cc. of water (or in a 10% sodium chloride solution in water).
- the coated object is polarized as the anode, and a current of .4 amp/sq. dcm. is permitted to flow through the system for 10 minutes at room temperature.
- the coated object is then removed, and a very thin film of silver chloride will be found to have formed on the silver coat.
- the coated object is washed, dried, and heated to a temperature of 455 C.
- Example II A steel base is electro-coated with silver, as in Example I, and immersed in an electrolytic bath consisting of a 15% solution of sodium bromide in water. The same process is followed as in Example I. Sodium bromide forms on the silver coat. Upon heat fusion of the silver bromide at a temperature of or somewhat above 434 C. (the melting point of silver bromide), a yellowish film is formed due to the yellow color of the silver bromide. A metallic luster can be obtained by butting or burnishing.
- Example 111 is carried out by using a 20% solution of sodium iodide as the electrolytic bath. After removal from the bath, the silverand silver iodide-covered object is heated to about 552 C., at which temperature the silver iodide fuses. The object is removed from the source of heat before any appreciable amount of the fused silver iodide has decomposed. Appearance and after-treatment of the object are the same as in Example II.
- a metallic coated article comprising a base having a higher melting point than silver, a thin porous silver coat on said base, said silver coat being of a thinness of less than about .0015 inch, and a water-insoluble fused silver salt having a lower melting point than said metallic base, said silver salt being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
- a metallic coated article comprising a base having a higher melting point than silver, a thin porous silver coat on said base, said silver coat being of a thinness of less than about .0015 inch, and a water-insoluble fused silver salt having a lower melting point than said metallic base and resembling the color of silver, said silver salt being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
- a metallic coated article comprising a base having a higher melting point than silver, and a continuous silver and water-insoluble fused silver halide coat of a thickness of less than .0015 inch on said base, said silver having pores, and said fused silver halide being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
- a metallic coated article comprising a base having a higher melting point than silver, and a continuous non-porous silver and water-insoluble fused silver halide coat of a thickness of the order of about .0005 to .00075 inch on said base, said silver having pores, and said fused silver halide being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
- a metallic coated article comprising a base having a higher melting point than silver, a thin porous silver coat on said base, said silver coat being of a thinness of less than about .0015 inch, and fused silver chloride on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
- a coated article comprising a ferrous base, and a continuous non-porous silver and water-insoluble fused silver halide coat of a thinness of less than .0015 inch on said ferrous base, said silver having pores, and said fused silver halide being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
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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)
- Electroplating Methods And Accessories (AREA)
Description
United States Patent F COATED METAL OBJECTS Hiram S. Lukens, Philadelphia, Pa., assignor to the United States of America as represented by the Secretary of War No Drawing. Original application July 1, 1947, Se-
rial No. 758,467. Divided and this application June 15, 1951, Serial No. 238,569
7 Claims. (Cl. 29-195) This application is a division of my copending ap plication Serial No. 758,467, filed July 1, 1947, for Metal Coating, now Patent No. 2,583,581.
This invention relates to metal coating, and more particularly to the application of an extremely thin metal coating to a base which completely seals the base against the outside.
It is well known in the art to protect a base from the outside by applying thereto a thin coat of a non-oxidizable or slowly oxidizable metal. An outstanding example of this is the application of a silver coat to an iron or steel base. By electrodeposition, thin nonporous coats of a thickness of the order of .0015 inch may be formed. However, if the coat is still thinner. it fails to protect the base because of the existence of pores in a coat below such thickness.
I have discovered a method for sealing the pores of an extremely thin metal coat, which makes possible the employment of a coat having only one-third to onehalf the thickness of what has heretofore been considered the minimum thickness for complete protection of the base. This method essentially consists in applying an extremely thin, though porous, metal coat to the base, and polarizing the coated object in a suitable electrolyte solution to form on the surface of a porous metal coating a film of a compound of such properties that it can be subsequently fused, thereby sealing the pores in the porous metal coating.
Consequently, one of the principal objects of my invention is the formation of a metal coat of extreme thinness, whose pores are sealed by a compound of the coating metal.
A further object of my invention is the electrochemical formation of a fusible salt on the surface of an extremely thin metal coat, with subsequent fusion to seal the pores of the coat.
Another object of my invention is a saving in the cost of noble metals used for coating a base material.
A further object of my invention is the provision of an extremely thin non-porous coat on a base, which coat consists of a metal and of a water-insoluble salt of such metal, the color of the salt resembling the color of the metal so as to give the appearance of a homogeneous film.
Further objects and advantages of my invention will appear as the description of my process, the product produced thereby, and of several preferred examples proceeds.
In accordance with my invention, the base is first coated with a thin coat of the coating metal, preferably but not necessarily by electrodeposition. The coat is intentionally of such thinness that it is not free from pores. Thus, in the case of an electrodeposited silver coat, the coat may be kept below a thickness of .0015 inch, which latter thickness is commonly considered to be the lower limit for a non-porous electrodeposited silver coat. I then immerse the coated article in an electrolytic bath and connect it as the anode. The electrolytic bath is a solution of an ionizable compound whose negative ions or radicals are capable of combining with the coating metal at the anode to form a water-insoluble fusible salt. Thus, in the case of a silver-coated article, a suitable electrolytic bath is a water solution of hydrochloric acid or of sodium chloride which, upon passage of the current through the system, results in the formation of silver chloride on the silver coat. By selecting a solution of anothei Patented Apr. 12, 1955 salide such as sodium bromide or sodium iodide, the
corresponding halogen salt may be formed by combination with the silver coat at the anode; inasmuch as silver chloride, silver iodide, and silver bromide are water-insoluble and fusible, they are suitable for the purpose of my invention. On the other hand, silver fluoride is water-soluble, and consequently a fluoride solution is unsuitable for use as an electrolytic bath for the purpose of my invention.
After a brief passage of the current through the systern, the coated article, which forms the anode, is withdrawn after part of the metal has been converted into the corresponding salt. The coated article is then subjected to a temperature above the melting point of the salt where the melting point of the salt is below that of the metal, or to a temperature above the melting point of the metal where the melting point of the salt is above the melting point of the metal. In the former case, i. e., where the melting point of the salt is below the melting point of the metal, the elevated temperature is kept below the melting point of the metal itself; this exposure causes the salt to melt and to flow into the pores of the thin metal coat. In the latter case, i. e., where the melting point of the salt is above that of the metal, the metal itself when heated above its melting point will evenly fill out the inter stices between the electrochemically formed salt deposit.
After cooling, a non-porous coat is found to have formed on the base. It may be buffed or burnished to give it a metallic appearance.
Among numerous uses for my invention may be mentioned, for instance, the electroplating of silverware? The following specific examples illustrate various ways in which my invention may be practiced, but are not to be deemed to constitute an exclusive enumeration of the materials or methods suitable for the purposes of my invention.
Example I A porous silver coat of a thickness of the order of .0005 to .00075 inch is electrodeposited. upon steel. The coated object is immersed into an electrolytic bath consisting of a water solution of 50 cc. of concentrated hydrochloric acid in 450 cc. of water (or in a 10% sodium chloride solution in water). The coated object is polarized as the anode, and a current of .4 amp/sq. dcm. is permitted to flow through the system for 10 minutes at room temperature. The coated object is then removed, and a very thin film of silver chloride will be found to have formed on the silver coat. The coated object is washed, dried, and heated to a temperature of 455 C. (the melting point of silver chloride) or somewhat above, but below the melting point of silver (960.5 C.). The silver chloride becomes limpid and flows into the pores of the silver coat. The object is then removed from the source of heat and permitted to cool. Upon cooling, a non-porous, very thin film of silver and silver chloride of a metallic or white color, depending on the thickness of the fused silver chloride, has been formed upon the base. Any excess silver chloride is removed by burnishing or buffing, which gives the entire article a pleasing, silverlike metallic appearance.
Example II A steel base is electro-coated with silver, as in Example I, and immersed in an electrolytic bath consisting of a 15% solution of sodium bromide in water. The same process is followed as in Example I. Sodium bromide forms on the silver coat. Upon heat fusion of the silver bromide at a temperature of or somewhat above 434 C. (the melting point of silver bromide), a yellowish film is formed due to the yellow color of the silver bromide. A metallic luster can be obtained by butting or burnishing.
Example 111 Example II is carried out by using a 20% solution of sodium iodide as the electrolytic bath. After removal from the bath, the silverand silver iodide-covered object is heated to about 552 C., at which temperature the silver iodide fuses. The object is removed from the source of heat before any appreciable amount of the fused silver iodide has decomposed. Appearance and after-treatment of the object are the same as in Example II.
Obviously, other metals and salts may be used to carry out my invention in accordance with the principle set forth in this specification. It is necessary that the salt formed on the coat be water-insoluble, to prevent deterioration of the coat by leaching. The composition and concentration of the electrolytic bath may be varied to suit specific requirements of each individual case. My invention is thus not restricted to any specific materials or quantities, or duration and density of the current flow during the electrochemical treatment as set forth in the foregoing examples, but encompasses all such variations of my inventive thought as will readily occur to the expert. I thus intend to claim my invention broadly, and to be limited only by the appended claims.
I claim:
1. A metallic coated article comprising a base having a higher melting point than silver, a thin porous silver coat on said base, said silver coat being of a thinness of less than about .0015 inch, and a water-insoluble fused silver salt having a lower melting point than said metallic base, said silver salt being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
2. A metallic coated article comprising a base having a higher melting point than silver, a thin porous silver coat on said base, said silver coat being of a thinness of less than about .0015 inch, and a water-insoluble fused silver salt having a lower melting point than said metallic base and resembling the color of silver, said silver salt being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
, non-porous 3. A metallic coated article comprising a base having a higher melting point than silver, and a continuous silver and water-insoluble fused silver halide coat of a thickness of less than .0015 inch on said base, said silver having pores, and said fused silver halide being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
4. A metallic coated article comprising a base having a higher melting point than silver, and a continuous non-porous silver and water-insoluble fused silver halide coat of a thickness of the order of about .0005 to .00075 inch on said base, said silver having pores, and said fused silver halide being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
5. A metallic coated article comprising a base having a higher melting point than silver, a thin porous silver coat on said base, said silver coat being of a thinness of less than about .0015 inch, and fused silver chloride on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
6. A coated article comprising a ferrous base, and a continuous non-porous silver and water-insoluble fused silver halide coat of a thinness of less than .0015 inch on said ferrous base, said silver having pores, and said fused silver halide being on the exterior of said silver coat and being retained in and closing the pores of said silver coat.
7. A metallic coated article according to claim 1, wherein said base is ferrous.
References Cited in the file of this patent UNITED STATES PATENTS 2,378,588 Skehan June 19, 1945 2,391,039 Schaefer Dec. 18, 1945 2,422,323 Waltman June 17, 1947 2,491,837 Smith-Johannsen Dec. 20, 1949 2,583,581 Lukens Jan. 29, 1952
Claims (1)
1. A METALLIC COATED ARTICLE COMPRISING A BASE HAVING A HIGHER MELTING POINT THAN SILVER, A THIN POROUS SILVER COAT ON SAID BASE, SAID SILVER COAT BEING OF A THINNESS OF LESS THAN ABOUT .0015 INCH, AND A WATER-IN SOLUBLE FUSED SILVER SALT HAVING A LOWER MELTING POINT THAN SAID METALLIC BASE, SAID SILVER SALT BEING ON THE EXTERIOR OF SAID SILVER COAT AND BEING RETIANED IN AND CLOSING THE PORES OF SAID SILVER COAT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US238569A US2705830A (en) | 1947-07-01 | 1951-06-15 | Coated metal objects |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US758467A US2583581A (en) | 1947-07-01 | 1947-07-01 | Metal coating |
| US238569A US2705830A (en) | 1947-07-01 | 1951-06-15 | Coated metal objects |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2705830A true US2705830A (en) | 1955-04-12 |
Family
ID=26931779
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US238569A Expired - Lifetime US2705830A (en) | 1947-07-01 | 1951-06-15 | Coated metal objects |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2705830A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3353134A (en) * | 1964-08-17 | 1967-11-14 | Amphenol Corp | Resistive element and variable resistor |
| US3475143A (en) * | 1965-02-10 | 1969-10-28 | Ionics | Metal to metal bonds with cuprous halide melts |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2378588A (en) * | 1942-03-14 | 1945-06-19 | Machlett Lab Inc | Method of making bearings |
| US2391039A (en) * | 1942-04-23 | 1945-12-18 | Cleveland Graphite Bronze Co | Method of coating metal articles |
| US2422323A (en) * | 1944-11-24 | 1947-06-17 | Nat Steel Corp | Method of producing sheets and the products obtained |
| US2491837A (en) * | 1948-08-31 | 1949-12-20 | Gen Electric | Manufacture of ice |
| US2583581A (en) * | 1947-07-01 | 1952-01-29 | Hiram S Lukens | Metal coating |
-
1951
- 1951-06-15 US US238569A patent/US2705830A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2378588A (en) * | 1942-03-14 | 1945-06-19 | Machlett Lab Inc | Method of making bearings |
| US2391039A (en) * | 1942-04-23 | 1945-12-18 | Cleveland Graphite Bronze Co | Method of coating metal articles |
| US2422323A (en) * | 1944-11-24 | 1947-06-17 | Nat Steel Corp | Method of producing sheets and the products obtained |
| US2583581A (en) * | 1947-07-01 | 1952-01-29 | Hiram S Lukens | Metal coating |
| US2491837A (en) * | 1948-08-31 | 1949-12-20 | Gen Electric | Manufacture of ice |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3353134A (en) * | 1964-08-17 | 1967-11-14 | Amphenol Corp | Resistive element and variable resistor |
| US3475143A (en) * | 1965-02-10 | 1969-10-28 | Ionics | Metal to metal bonds with cuprous halide melts |
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