US3057049A - Alloy and composite stock - Google Patents
Alloy and composite stock Download PDFInfo
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- US3057049A US3057049A US732437A US73243758A US3057049A US 3057049 A US3057049 A US 3057049A US 732437 A US732437 A US 732437A US 73243758 A US73243758 A US 73243758A US 3057049 A US3057049 A US 3057049A
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- silver
- layer
- alloy
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- weight
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/01—Layered products comprising a layer of metal all layers being exclusively metallic
- B32B15/018—Layered products comprising a layer of metal all layers being exclusively metallic one layer being formed of a noble metal or a noble metal alloy
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C5/00—Alloys based on noble metals
- C22C5/06—Alloys based on silver
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/18—Cells with non-aqueous electrolyte with solid electrolyte
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/18—Cells with non-aqueous electrolyte with solid electrolyte
- H01M6/182—Cells with non-aqueous electrolyte with solid electrolyte with halogenide as solid electrolyte
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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
- Y10S428/9265—Special properties
- Y10S428/929—Electrical contact feature
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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
- Y10S428/936—Chemical deposition, e.g. electroless plating
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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
- Y10S428/938—Vapor deposition or gas diffusion
-
- 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.]
- Y10T428/12535—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
- Y10T428/12583—Component contains compound of adjacent metal
-
- 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
- Y10T428/12972—Containing 0.01-1.7% carbon [i.e., steel]
Definitions
- This invention relates to alloys and to composite stock incorporating these alloys, these alloys and the composite stock being useful in forming components of solid-electrolyte batteries.
- the components of this type of battery are, in many cases, formed by a layer of silver adhered to a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride.
- the silver layer acts as the anode of the battery, and the silver halide layer as the electrolyte thereof.
- the silver halide layer can be formed by heating a section of silver in an atmosphere of the halide vapor whereby the exposed surface of the silver becomes tarnished with a layer of the silver halide.
- the surface of the silver layer opposite that to which the silver halide layer is adhered can be bonded to a base layer of corrosion-resistant metal such as stainless steel preferably of the austenitic type, Monel and Inconel. Monel is a line of high nickel-copper alloys and Inconel is a high nickel-chromium-iron alloy; both of these being registered trademarks of the International Nickel Co., Inc., of New York, New York.
- an object of this invention is to provide new and improved alloys and composite stock incorporating said alloys, these being useful in forming components of a solid-electrolyte battery.
- a further object of this invention is to provide such alloys which exhibit improved adherence to silver bromide, silver iodide and silver chloride.
- a further object is to provide such composite stock which includes alayer of one of said silver halides and an improved silver alloy layer, the two layers having improved adherence therebetween.
- a further object is to provide such an alloy and such composite stock capable of being mechanically worked without deleterious effect.
- the invention accordingly comprises the elements, combination of elements, features of structure, arrangements of parts, the ingredients, combinations of ingredients, the proportions thereof, and features of composition which will be exemplified in the structures and products hereinafter described, and the scope of the application of which will be indicated in the following claims.
- an improved silver-base alloy is substituted for the above-mentioned pure silver layer, the silver-base layer consisting essentially of from an effective trace to 0.75% by weight of cobalt, from 0% to 0.15% by weight of copper and the remainder silver.
- No perceptible improvement in the adherence between the silver halide layer and the silver-base alloy layer (due to the presence of the cobalt) has been detected when the percentage of cobalt in the latter layer was less than ice 0.05%, and this is, therefore, what is meant by the term effective trace as used herein.
- the upper limit of 0.75 by weight of cobalt as set forth herein is determined by the fact that this is the highest percentage of cobalt attainable in the alloy.
- the alloy of this invention is produced by conventional melting and mixing techniques, and when an excess of 0.75% of cobalt is melted and mixed with silver, all of the excess cobalt rises to the surface of the melt.
- a layer of pure silver provided with an adhered layer of silver iodide by tarnishing in the manner described above does not exhibit these improved qualities.
- This improved adherence is important for the reason, among others, that the composite material should be capable of being provided in strip form and subsequently worked (such as by stamping out pieces from the strip) without damage to the composite stock. Best results from the standpoint of effective adherence at a minimum cost are obtained when the percentage by weight of the cobalt in the alloy is 0.20.
- the silver base alloy according to this invention includes cobalt with or without copper, both in the above-stated percentage ranges, and the remainder silver except for the inclusion of impurities and agents which do not deleteriously affect the alloy in the environment of a solid-electrolyte battery or in the environment of other electrical applications (such, for example, as transistors).
- An example of an agent which can be incorporated into the silver halide layer is cadmium bromide as disclosed in US. Patent Re. 24,408 to A. I. hack et al.
- cobalt is practically insoluble in silver, and when alloyed therewith the cobalt precipitates out at the boundaries of the silver grains.
- an alloy of this invention consisting essentially of silver and cobalt is heated in an atmosphere of halide vapor, the chemical reaction of the halide with the silver in the alloy layer i promoted and proceeds along the grain boundaries at a faster rate (as compared, for example, with pure silver) due to the presence of the cobalt.
- cobalt acts as a graingrowth inhibitor whereby advancement of the chemical reaction along the grain boundaries is enhanced due to the presence of more and finer grains of the silver.
- the interface between two layers formed by tarnishing a layer of pure silver in an atmosphere of iodine is smooth as compared with the interface resulting from so tarnishing, for example, a layer of three nines fine silver which contains a significant amount of copper less than the maximum of the range for copper according to this invention (and an insignificant, if any, amount of cobalt). It is believed that this indicates the effect of an alteration of the silver by the copper similar to that as theorized above with respect to cobalt with the result of apparently an even greater degree of preferential grain boundary attack by the halide. Whatever the mechanics of the cause may be, the effect of incorporating copper along with cobalt in the silver as described above is further to increase the degree of adherence between the layers.
- the result of the preferential grain boundary attack by the halide, absent or present the copper is a multitude of microscopic anchors extending along the grain boundaries into the silver-alloy layer from the silver halide layer; these anchors being responsible, in part, for the improved adherence between the two layers. Also, due to the rough interface resulting between the two layers, the interfacial area is increased correspondingly increasing the degree of adherence therebetween. The presence of the above-described anchors and rough interface is apparent by examination of metallographically prepared transverse cross-sections of the composite stock of this invention.
- a length of the aboveidentified silver-base alloy according to this invention is so solid-phase bonded to a length of corrosion-resistant metal such as austenitic stainless steel, this composite is then rolled to the desired gauge with intermediate annealing steps, if necessary, and the silver halide layer is formed on the exposed surface of the silver-base alloy layer by heating the composite and exposing it to an atmosphere of the respective halid vapor.
- the silver base alloy layer incorporates copper as well as cobalt, all as described above, the advantage of an even greater adherence between the silverbase alloy and the silver halide layers results along with the added advantage that the quality of the bond between the silver-base alloy layer and the corrosion-resistant, metal, base layer is improved.
- the layer of silver halide can be provided in adhered relation to the anode-forming layer in producing the composite stock according to this invention by methods other than tarnishing as described above.
- the alternative methods 4 disclosed in US. Patent No. Re. 24,408 to A. I. hack et al. could be used.
- Composite stock comprising a layer of a silver selected from the grounp consisting of silver iodide, silver bromide and silver chloride adhered to a layer formed of an alloy consisting essentially of from 0.05% to 0.75% by weight of cobalt, up to 0.15% by weight of copper, and the remainder silver.
- Composite stock comprising a layer of silver iodide adhered to a layer formed of an alloy consisting essentially of from 0.05% to 0.75% by weight of cobalt, up to 0.15 by weight of copper, and the remainder silver.
- Composite stock comprising a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride adhered to a layer formed of an alloy consisting essentially of 0.20% by weight of cobalt and the remainder silver.
- Composite stock comprising an intermediate layer formed of an alloy consisting essentially of from 0.05 to 0.75% by weight of cobalt, up to 0.15 by weight of copper and the remainder silver; said intermediate layer being adhered at one surface thereof to a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride; and said intermediate layer being bonded at the opposite surface thereof to a corrosion-resistant, metal, base layer.
- Composite stock comprising an intermediate layer formed of an alloy consisting essentially of from 0.05% to 0.75% by Weight of cobalt, up to 0.15% by weight of copper and the remainder silver; said intermediate layer being adhered at one surface thereof to a layer of silver iodide; and said intermediate layer being bonded at the opposite surface thereof to a corrosion-resistant, metal, base layer.
- Composite stock comprising a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride adhered to a layer of an alloy consisting essentially of from 0.05% to 0.75% by weight of cobalt and the remainder silver.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
- Hybrid Cells (AREA)
- Laminated Bodies (AREA)
Description
United States Patent 3,057,049 ALLOY AND (IOMPOSITE STOCK Heinz R. Piiurnm, Plainvilie, and Joseph J. Buchinski,
Wrentham, Mass, assignors to Texas Instruments Incorporated, Dallas, Tex., a corporation of Delaware No Drawing. Filed May 2, 1958, Ser. No. 732,437 7 Claims. (Q1. 29195) This invention relates to alloys and to composite stock incorporating these alloys, these alloys and the composite stock being useful in forming components of solid-electrolyte batteries.
The components of this type of battery are, in many cases, formed by a layer of silver adhered to a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride. The silver layer acts as the anode of the battery, and the silver halide layer as the electrolyte thereof. The silver halide layer can be formed by heating a section of silver in an atmosphere of the halide vapor whereby the exposed surface of the silver becomes tarnished with a layer of the silver halide. The surface of the silver layer opposite that to which the silver halide layer is adhered can be bonded to a base layer of corrosion-resistant metal such as stainless steel preferably of the austenitic type, Monel and Inconel. Monel is a line of high nickel-copper alloys and Inconel is a high nickel-chromium-iron alloy; both of these being registered trademarks of the International Nickel Co., Inc., of New York, New York.
Among the difiiculties which present themselves in providing the components of a battery of the above-described type, is that of obtaining a satisfactory degree of adherence between the silver halide layer and the silver layer. Also, it is important, in many cases, that any modification of the silver layer to improve the adherence between the latter and the silver halide layer not have the effect of preventing or deterring the formation of an adequate bond between the silver layer and the corrosion-resistant, metal, base layer.
Accordingly, an object of this invention is to provide new and improved alloys and composite stock incorporating said alloys, these being useful in forming components of a solid-electrolyte battery.
A further object of this invention is to provide such alloys which exhibit improved adherence to silver bromide, silver iodide and silver chloride.
A further object is to provide such composite stock which includes alayer of one of said silver halides and an improved silver alloy layer, the two layers having improved adherence therebetween.
A further object is to provide such an alloy and such composite stock capable of being mechanically worked without deleterious effect.
Other objects will be in part obvious and in part pointed out hereinafter.
The invention accordingly comprises the elements, combination of elements, features of structure, arrangements of parts, the ingredients, combinations of ingredients, the proportions thereof, and features of composition which will be exemplified in the structures and products hereinafter described, and the scope of the application of which will be indicated in the following claims.
According to this invention, an improved silver-base alloy is substituted for the above-mentioned pure silver layer, the silver-base layer consisting essentially of from an effective trace to 0.75% by weight of cobalt, from 0% to 0.15% by weight of copper and the remainder silver. No perceptible improvement in the adherence between the silver halide layer and the silver-base alloy layer (due to the presence of the cobalt) has been detected when the percentage of cobalt in the latter layer was less than ice 0.05%, and this is, therefore, what is meant by the term effective trace as used herein. The upper limit of 0.75 by weight of cobalt as set forth herein is determined by the fact that this is the highest percentage of cobalt attainable in the alloy. In this regard, the alloy of this invention is produced by conventional melting and mixing techniques, and when an excess of 0.75% of cobalt is melted and mixed with silver, all of the excess cobalt rises to the surface of the melt.
The addition of cobalt to silver, the former within the range of from an effective trace to 0.75% by weight, substantially improves the adherence thereto of the silver halide layer. The magnitude of this improved adherence is evidenced by back and forth bending and creasing of a strip of composite stock formed by heating a strip of the silver-base alloy of this invention in an atmosphere of iodine vapor to provide a layer of the silver-base alloy tarnished with a layer of silver iodide. When this composite stock is so bent and creased, there is no flaking or other damage to the silver halide layer, the two layers otherwise remain intact, and these layers remain uniformly adhere-d to each other. In contradistinction thereto, a layer of pure silver provided with an adhered layer of silver iodide by tarnishing in the manner described above does not exhibit these improved qualities. This improved adherence is important for the reason, among others, that the composite material should be capable of being provided in strip form and subsequently worked (such as by stamping out pieces from the strip) without damage to the composite stock. Best results from the standpoint of effective adherence at a minimum cost are obtained when the percentage by weight of the cobalt in the alloy is 0.20.
The improved results noted above with respect to the addition of cobalt to the silver-base alloy are obtained whether or not copper in a range up to 0.15 by weight is incorporated into the alloy. It has been found, however, that when copper is included in the range of up to 0.15 by weight, an even better adherence between the silver halide and the silver-base alloy layers is obtained, along with an improvement in the quality of the bond between the silver-base alloy layer and the base metal layer.
It will be understood that the silver base alloy according to this invention includes cobalt with or without copper, both in the above-stated percentage ranges, and the remainder silver except for the inclusion of impurities and agents which do not deleteriously affect the alloy in the environment of a solid-electrolyte battery or in the environment of other electrical applications (such, for example, as transistors). An example of an agent which can be incorporated into the silver halide layer is cadmium bromide as disclosed in US. Patent Re. 24,408 to A. I. Hack et al. Conventional commercially fine silver or three nines fine silver is well suited for the addition thereto of cobalt in the percentage range stated above to provide an improved alloy according to the invention, it being noted that ordinarily this material incorporates a quantity of copper within the percentage range named above. The impurities present in commercially or three nines fine silver have been found to have no ill effect on the silver alloy of this invention.
Theorizing, it is believed that these improved results may be accounted for, at least in part, as follows. First, cobalt is practically insoluble in silver, and when alloyed therewith the cobalt precipitates out at the boundaries of the silver grains. When an alloy of this invention consisting essentially of silver and cobalt is heated in an atmosphere of halide vapor, the chemical reaction of the halide with the silver in the alloy layer i promoted and proceeds along the grain boundaries at a faster rate (as compared, for example, with pure silver) due to the presence of the cobalt. Additionally, cobalt acts as a graingrowth inhibitor whereby advancement of the chemical reaction along the grain boundaries is enhanced due to the presence of more and finer grains of the silver.
The interface between two layers formed by tarnishing a layer of pure silver in an atmosphere of iodine is smooth as compared with the interface resulting from so tarnishing, for example, a layer of three nines fine silver which contains a significant amount of copper less than the maximum of the range for copper according to this invention (and an insignificant, if any, amount of cobalt). It is believed that this indicates the effect of an alteration of the silver by the copper similar to that as theorized above with respect to cobalt with the result of apparently an even greater degree of preferential grain boundary attack by the halide. Whatever the mechanics of the cause may be, the effect of incorporating copper along with cobalt in the silver as described above is further to increase the degree of adherence between the layers.
In any case, the result of the preferential grain boundary attack by the halide, absent or present the copper, is a multitude of microscopic anchors extending along the grain boundaries into the silver-alloy layer from the silver halide layer; these anchors being responsible, in part, for the improved adherence between the two layers. Also, due to the rough interface resulting between the two layers, the interfacial area is increased correspondingly increasing the degree of adherence therebetween. The presence of the above-described anchors and rough interface is apparent by examination of metallographically prepared transverse cross-sections of the composite stock of this invention.
In forming a composite article comprising an intermediate layer of the silver-base alloy according to this invention adhered at one surface to a layer of one of silver iodide, silver chloride and silver bromide, and bonded at its opposite surface to a layer of corrosion-resistant metal, the latter is solid-phase bonded to th silver-base alloy layer by the method disclosed and claimed in US. Patent No. 2,691,815 granted on October 19, 1954, to Boessenkool et al. By way of example, a length of the aboveidentified silver-base alloy according to this invention is so solid-phase bonded to a length of corrosion-resistant metal such as austenitic stainless steel, this composite is then rolled to the desired gauge with intermediate annealing steps, if necessary, and the silver halide layer is formed on the exposed surface of the silver-base alloy layer by heating the composite and exposing it to an atmosphere of the respective halid vapor. It has been found that when the silver base alloy layer incorporates copper as well as cobalt, all as described above, the advantage of an even greater adherence between the silverbase alloy and the silver halide layers results along with the added advantage that the quality of the bond between the silver-base alloy layer and the corrosion-resistant, metal, base layer is improved.
It is to be noted that the layer of silver halide can be provided in adhered relation to the anode-forming layer in producing the composite stock according to this invention by methods other than tarnishing as described above. By way of example, the alternative methods 4 disclosed in US. Patent No. Re. 24,408 to A. I. Hack et al. could be used.
In view of the above, it will be seen that the several objects of the invention are achieved and other advantageous results attained.
As many changes could be made in the above constructions Without departing from the scope of the invention, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
We claim:
1. Composite stock comprising a layer of a silver selected from the grounp consisting of silver iodide, silver bromide and silver chloride adhered to a layer formed of an alloy consisting essentially of from 0.05% to 0.75% by weight of cobalt, up to 0.15% by weight of copper, and the remainder silver.
2. Composite stock comprising a layer of silver iodide adhered to a layer formed of an alloy consisting essentially of from 0.05% to 0.75% by weight of cobalt, up to 0.15 by weight of copper, and the remainder silver.
3. Composite stock comprising a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride adhered to a layer formed of an alloy consisting essentially of 0.20% by weight of cobalt and the remainder silver.
4-. Composite stock comprising an intermediate layer formed of an alloy consisting essentially of from 0.05 to 0.75% by weight of cobalt, up to 0.15 by weight of copper and the remainder silver; said intermediate layer being adhered at one surface thereof to a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride; and said intermediate layer being bonded at the opposite surface thereof to a corrosion-resistant, metal, base layer.
5. Composite stock comprising an intermediate layer formed of an alloy consisting essentially of from 0.05% to 0.75% by Weight of cobalt, up to 0.15% by weight of copper and the remainder silver; said intermediate layer being adhered at one surface thereof to a layer of silver iodide; and said intermediate layer being bonded at the opposite surface thereof to a corrosion-resistant, metal, base layer.
6. Composite stock comprising a layer of a silver halide selected from the group consisting of silver iodide, silver bromide and silver chloride adhered to a layer of an alloy consisting essentially of from 0.05% to 0.75% by weight of cobalt and the remainder silver.
7. The composite stock as set forth in claim 6 wherein said alloy layer is bonded to a corrosion-resistant, metal, base layer.
References Cited in the file of this patent UNITED STATES PATENTS 1,362,455 Wallen et al. Dec. 14, 1920 1,612,782 Vogt et al. Dec. 28, 1926 2,151,905 Emmert Mar. 28, 1939 2,241,816 Hensel et al May 13, 1941 2,445,962 Mell July 27, 1948
Claims (1)
- 4. COMPOSIT STOCK COMPRISING AN INTERMEDIATE LAYER FORMED OF AN ALLOY CONSISTING ESSENTIALLY OF FROM 0.05% TO 0.75% BY WEIGHT OF COBALT, UP TO 0.15% BY WEIGHT OF COPPER AND THE REMAINDER SILVER; AND INTERMEDIATE LAYER BEING ADHERED AT ONE SURFACE THEREOF TO A LAYER OF A SILVER HALIDE SELECTED FROM THE GROUP CONSISTING OF SILVER IODIDE, SILVER BROMIDE AND SILVER CHLORIDE; AND SAID INTERMDEIATE LAYER BEING BONDED AT THE OPPOSITE SURFACE THEREOF TO CORROSION-RESISTANT, METAL, BASE LAYER.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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US732437A US3057049A (en) | 1958-05-02 | 1958-05-02 | Alloy and composite stock |
GB13045/59A GB914853A (en) | 1958-05-02 | 1959-04-16 | Silver-base alloy and composite stock made therefrom |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US732437A US3057049A (en) | 1958-05-02 | 1958-05-02 | Alloy and composite stock |
Publications (1)
Publication Number | Publication Date |
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US3057049A true US3057049A (en) | 1962-10-09 |
Family
ID=24943503
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US732437A Expired - Lifetime US3057049A (en) | 1958-05-02 | 1958-05-02 | Alloy and composite stock |
Country Status (2)
Country | Link |
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US (1) | US3057049A (en) |
GB (1) | GB914853A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3262159A (en) * | 1963-05-22 | 1966-07-26 | Us Rubber Co | Molding apparatus and process for making same |
US3293737A (en) * | 1963-05-22 | 1966-12-27 | Us Rubber Co | Process for making mold for vacuum-forming materials |
US3331656A (en) * | 1961-11-22 | 1967-07-18 | Bruck Stephen Desiderius | Chemically crimping nylon fibers through formation of disulfide bonds therein |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1362455A (en) * | 1919-10-23 | 1920-12-14 | Leo T Wallen | Point for electrical contacts of ignition apparatus |
US1612782A (en) * | 1923-12-19 | 1926-12-28 | Lee S Smith & Son Mfg Company | Dental alloy and process of making the same |
US2151905A (en) * | 1937-09-29 | 1939-03-28 | Mallory & Co Inc P R | Electric contact combination |
US2241816A (en) * | 1940-01-16 | 1941-05-13 | Mallory & Co Inc P R | Silver electric contact |
US2445962A (en) * | 1944-08-24 | 1948-07-27 | Rca Corp | Method of forming silver sulfide coatings |
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1958
- 1958-05-02 US US732437A patent/US3057049A/en not_active Expired - Lifetime
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1959
- 1959-04-16 GB GB13045/59A patent/GB914853A/en not_active Expired
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1362455A (en) * | 1919-10-23 | 1920-12-14 | Leo T Wallen | Point for electrical contacts of ignition apparatus |
US1612782A (en) * | 1923-12-19 | 1926-12-28 | Lee S Smith & Son Mfg Company | Dental alloy and process of making the same |
US2151905A (en) * | 1937-09-29 | 1939-03-28 | Mallory & Co Inc P R | Electric contact combination |
US2241816A (en) * | 1940-01-16 | 1941-05-13 | Mallory & Co Inc P R | Silver electric contact |
US2445962A (en) * | 1944-08-24 | 1948-07-27 | Rca Corp | Method of forming silver sulfide coatings |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3331656A (en) * | 1961-11-22 | 1967-07-18 | Bruck Stephen Desiderius | Chemically crimping nylon fibers through formation of disulfide bonds therein |
US3262159A (en) * | 1963-05-22 | 1966-07-26 | Us Rubber Co | Molding apparatus and process for making same |
US3293737A (en) * | 1963-05-22 | 1966-12-27 | Us Rubber Co | Process for making mold for vacuum-forming materials |
Also Published As
Publication number | Publication date |
---|---|
GB914853A (en) | 1963-01-09 |
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