USRE29239E - Ternary alloys - Google Patents

Ternary alloys Download PDF

Info

Publication number
USRE29239E
USRE29239E US05/614,349 US61434975A USRE29239E US RE29239 E USRE29239 E US RE29239E US 61434975 A US61434975 A US 61434975A US RE29239 E USRE29239 E US RE29239E
Authority
US
United States
Prior art keywords
alloys
metal
chromium
chloride
cobalt
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
Application number
US05/614,349
Inventor
Jacob Hyner
Robert A. Michelson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Whyco Chromium Co Inc
Original Assignee
Whyco Chromium Co Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US431025A external-priority patent/US3881919A/en
Application filed by Whyco Chromium Co Inc filed Critical Whyco Chromium Co Inc
Priority to US05/614,349 priority Critical patent/USRE29239E/en
Application granted granted Critical
Publication of USRE29239E publication Critical patent/USRE29239E/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/56Electroplating: Baths therefor from solutions of alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C13/00Alloys based on tin

Definitions

  • This invention relates to new and improved ternary alloys, to aqueous electrolytic baths from which the alloys are deposited, and to a process for forming the alloys.
  • an object of the invention is to provide a new and improved alloy which not only provides a chromium-like brightness and tarnish resistance, but also provides color stability and hardness superior to that found in any of the alloying metals individually.
  • Still another object of the invention is to provide new and improved electrolytic plating baths which are easily formulated and from which ternary alloys can be efficiently deposited on a wide variety of substrates to give coatings which are hard, bright, tarnish resistant and which have good color stability.
  • Another object is to provide a new and improved process whereby tin, cobalt and a third metal are electrolytically co-deposited to form a hard, bright coating which is stable and highly resistant to tarnishing.
  • a new and improved ternary alloy consisting essentially of about 40- 90 wt. % tin, about 10- 50 wt. % cobalt and about 1- 28 wt. % of a third metal selected from Periodic Group II B , III A or VI B .
  • Third metals include zinc, cadmium, indium, antimony or chromium, of which zinc, indium and chromium are preferred.
  • the third metals may be present in the alloy singly or in admixtures of two or more.
  • the plating baths of the invention are aqueous and highly acidic, and contain compounds providing stannous ions, cobaltous ions and ions of the third metal or metals to be deposited.
  • the ternary alloys are efficiently co-deposited from the baths at a temperature of about 50°- 85° C. and current density of about 5- 45 A/ft. 2 .
  • the alloys exhibit a hardness, chromium-like brightness and color stability which make them useful as coatings on a wide variety of substrates.
  • the ternary alloys of the invention are electrodeposited from highly acidic, aqueous baths of pH of about 1- 3.
  • a mineral acid is utilized for this purpose, such as a hydro-halide or a sulfur acid.
  • Preferred acids are hydrochloric and fluoboric acids since such acids provide anions in common with anions of preferred compounds of the metals to be deposited, and thus promote stability of the baths and good control of electrodeposition therefrom.
  • the metals to be deposited are present in the baths as ionic compounds, the anions of the compounds and other conditions being chosen such that the compounds are substantially completely soluble in the aqueous medium. Accordingly, the compounds may be present as halides, sulfates, or otherwise but preferably the compounds will have anions common to the anions of the acid utilized to provide the high acidity. Since hydrochloric and fluoboric acids are the preferred acids, the preferred metal compounds will be the chlorides and fluoborates of the metals.
  • the metal compounds may be dispersed and dissolved in the aqueous medium in any suitable manner with heating and agitation, as needed. Sequence of admixture is not critical although the usual precautions with highly acidic solutions should be exercised. However, dispersion and electroplating are each benefited by somewhat elevated temperature of the bath, of the order of about 50°- 85° C.
  • hydrochloric acid (37% solution) at a concentration of about 40- 150 mils./l., ammonium hydroxide (28% solution) in the range of about 10- 50 mls./l. and ammonium bifluoride, about 20- 400 g./l., to provide the requisite acidity and bath stability.
  • tin compound is a fluoborate
  • fluoboric acid in place of hydrochloric acid.
  • concentrations of these and other ingredients in the bath may then range as follows:
  • Indium chloride as a substitute for zinc chloride preferably is utilized at a concentration of about 5- 35 g./l. and chromium chloride as a substitute for either of the foregoing compounds is effective at a concentration of about 5- 55 g./l.
  • Electrodeposition including the cell form of electrolytic arrangement and type of substrate to be coated, control of concentration and rejuvenation of the baths, are well known in the art and do not require further description.
  • Hull cell may be utilized.
  • the current density preferred for efficient electrodeposition is about 5- 45 A/ft. 2 .
  • the percentage of each metal in the ternary alloy will vary in direct proportion to the concentration of each metal in the plating bath. To a lesser extent the percentage of each metal in the alloy will also vary in accordance with electroplating conditions such as temperature, current density and pH. It is believed that the new alloy exists as Sn 2 (Co, X) or (Sn, X) 2 (Co, X) where X is the third metal.
  • the resultant ternary alloys are analogous to tin-nickel and tin-cobalt with respect to tarnish resistance, the alloys exhibit not only chromium-like brightness but also consistently good color and color stability. Moreover, while the ternary alloys resist corrosion essentially to the same extent as chromium, they have a higher resistance than chromium to strong alkali under a superimposed anodic potential, that is, whereas chromium will dissolve if made anodic in a caustic solution, the ternary alloys of the invention are not affected. The alloys of the invention therefore are more resistant to chloride attack than chromium and will resist salt spray and salt water contact better than chromium.
  • the plating baths may contain auxiliary reagents for various purposes in accordance with the understanding in the art.
  • auxiliary reagents are ammonium chloride, gluconic acid, thiourea, fluorides such as ammonium bifluoride, sodium fluoride and potassium titanium fluoride, and various surfactants and the like such as alkyl aryl sodium sulfonate.
  • fluorides such as ammonium bifluoride, sodium fluoride and potassium titanium fluoride
  • surfactants and the like such as alkyl aryl sodium sulfonate.
  • Such reagents generally are useful in minor amounts, for example, about 0.01 to about 10 grams per liter of plating bath, to obtain their known benefits.
  • the ternary alloys may be co-deposited electrolytically upon a wide variety of substrates, including metals such as steel, brass and zinc, as well as ceramics and plastics, in accordance with techniques well known in the art for coating such substrates.
  • aqueous plating bath formulations and conditions of electrodeposition are intended as further illustration of the invention but are not necessarily limited of the scope of the invention except as set forth in the claims. All parts and percentages in these examples as well as in the foregoing specification are by weight unless otherwise indicated.
  • the ternary alloy deposited has an approximate composition: tin, 40- 90%; cobalt, 10- 50%; third metal, 1- 28%.

Abstract

Bright, tarnish resistant and color stable ternary alloys of about 40 - 90% of tin, about 10 - 50% cobalt and about 1 - 28% of a third metal of Periodic Group IIB, IIIB or VIB. Typical third metals are zinc, cadmium, indium, antimony or chromium. The alloys are electrodeposited from aqueous acidic baths at a temperature of about 50 - 85° C and current density of about 5 - 45 A/ft.

Description

BACKGROUND OF THE INVENTION
This invention relates to new and improved ternary alloys, to aqueous electrolytic baths from which the alloys are deposited, and to a process for forming the alloys.
Various alloys have been developed in efforts to duplicate the superior color of chromium and alloys containing substantial amounts of chromium, while also providing the corrosion resistance and tarnish resistance required when the alloy is to be used as a protective coating. Accordingly, the prior art teaches the addition of brightening agents to plating baths for the electro-deposition of tin-nickel binary alloys, as in U.S. Pat. No. 3,141,836 --Seyb et al, or the careful control of plating conditions, also in the deposition of nickel-tin binary alloys, such as the highly acidic baths in U.S. Pat. No. 2,926,124-- Taylor et al. In another approach cobalt-tin binary alloys have been studied with respect to close similarities in corrosion resistance to nickel-tin alloys. Clarke et al, "An Electrodeposited Bright Tin-Cobalt Intermetallic Compound, CoSn," Transactions of the Institute of Metal Finishing, 1972, Volume 50.
Despite the usefulness of such alloys from the standpoint of tarnish and corrosion resistance, those of such alloys which initially exhibited brightness similar to that of chromium did not maintain the good color. Moreover, results in obtaining hardness, brightness, tarnish resistance and color stability have not been consistent. Such properties tend to be overly sensitive to specific process conditions and therefore are difficult to reproduce on a commercial scale.
OBJECTS AND SUMMARY
Accordingly, an object of the invention is to provide a new and improved alloy which not only provides a chromium-like brightness and tarnish resistance, but also provides color stability and hardness superior to that found in any of the alloying metals individually.
Still another object of the invention is to provide new and improved electrolytic plating baths which are easily formulated and from which ternary alloys can be efficiently deposited on a wide variety of substrates to give coatings which are hard, bright, tarnish resistant and which have good color stability.
Another object is to provide a new and improved process whereby tin, cobalt and a third metal are electrolytically co-deposited to form a hard, bright coating which is stable and highly resistant to tarnishing.
These and other objects, features and advantages of the invention will be apparent from the description which follows.
In summary outline, the foregoing and other objects are achieved in a new and improved ternary alloy consisting essentially of about 40- 90 wt. % tin, about 10- 50 wt. % cobalt and about 1- 28 wt. % of a third metal selected from Periodic Group IIB, IIIA or VIB. Third metals include zinc, cadmium, indium, antimony or chromium, of which zinc, indium and chromium are preferred. The third metals may be present in the alloy singly or in admixtures of two or more. The plating baths of the invention are aqueous and highly acidic, and contain compounds providing stannous ions, cobaltous ions and ions of the third metal or metals to be deposited. The ternary alloys are efficiently co-deposited from the baths at a temperature of about 50°- 85° C. and current density of about 5- 45 A/ft.2. In addition to the tarnish resistance expected in alloys containing tin and cobalt, the alloys exhibit a hardness, chromium-like brightness and color stability which make them useful as coatings on a wide variety of substrates.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The ternary alloys of the invention are electrodeposited from highly acidic, aqueous baths of pH of about 1- 3. A mineral acid is utilized for this purpose, such as a hydro-halide or a sulfur acid. Preferred acids are hydrochloric and fluoboric acids since such acids provide anions in common with anions of preferred compounds of the metals to be deposited, and thus promote stability of the baths and good control of electrodeposition therefrom.
The metals to be deposited are present in the baths as ionic compounds, the anions of the compounds and other conditions being chosen such that the compounds are substantially completely soluble in the aqueous medium. Accordingly, the compounds may be present as halides, sulfates, or otherwise but preferably the compounds will have anions common to the anions of the acid utilized to provide the high acidity. Since hydrochloric and fluoboric acids are the preferred acids, the preferred metal compounds will be the chlorides and fluoborates of the metals.
The metal compounds may be dispersed and dissolved in the aqueous medium in any suitable manner with heating and agitation, as needed. Sequence of admixture is not critical although the usual precautions with highly acidic solutions should be exercised. However, dispersion and electroplating are each benefited by somewhat elevated temperature of the bath, of the order of about 50°- 85° C.
As chlorides the following ranges of concentrations of the metal compounds in the baths are effective:
______________________________________                                    
cobalt chloride     about 20-400 g./l.                                    
stannous chloride   about 10-100 g./l.                                    
zinc chloride       about 10-175 g./l.                                    
______________________________________                                    
To the baths containing the foregoing concentrations of metal compounds may be added hydrochloric acid (37% solution) at a concentration of about 40- 150 mils./l., ammonium hydroxide (28% solution) in the range of about 10- 50 mls./l. and ammonium bifluoride, about 20- 400 g./l., to provide the requisite acidity and bath stability.
When the tin compound is a fluoborate, it is preferred to use fluoboric acid in place of hydrochloric acid. The concentrations of these and other ingredients in the bath may then range as follows:
______________________________________                                    
cobalt chloride      about 100-300 g./l.                                  
stannous fluoborate (50% solution)                                        
                     about 25-75 mls./l.                                  
fluoboric acid       about 75-225 g./l.                                   
ammonium hydroxide (28% solution)                                         
                     about 25-150 mls./l.                                 
zinc chloride        about 10-135 g./l.                                   
______________________________________                                    
Indium chloride as a substitute for zinc chloride preferably is utilized at a concentration of about 5- 35 g./l. and chromium chloride as a substitute for either of the foregoing compounds is effective at a concentration of about 5- 55 g./l.
Other conditions of electrodeposition, including the cell form of electrolytic arrangement and type of substrate to be coated, control of concentration and rejuvenation of the baths, are well known in the art and do not require further description. For example, the well known Hull cell may be utilized. The current density preferred for efficient electrodeposition is about 5- 45 A/ft.2.
Generally, the percentage of each metal in the ternary alloy will vary in direct proportion to the concentration of each metal in the plating bath. To a lesser extent the percentage of each metal in the alloy will also vary in accordance with electroplating conditions such as temperature, current density and pH. It is believed that the new alloy exists as Sn2 (Co, X) or (Sn, X)2 (Co, X) where X is the third metal.
While the resultant ternary alloys are analogous to tin-nickel and tin-cobalt with respect to tarnish resistance, the alloys exhibit not only chromium-like brightness but also consistently good color and color stability. Moreover, while the ternary alloys resist corrosion essentially to the same extent as chromium, they have a higher resistance than chromium to strong alkali under a superimposed anodic potential, that is, whereas chromium will dissolve if made anodic in a caustic solution, the ternary alloys of the invention are not affected. The alloys of the invention therefore are more resistant to chloride attack than chromium and will resist salt spray and salt water contact better than chromium.
The plating baths may contain auxiliary reagents for various purposes in accordance with the understanding in the art. Among such auxiliary reagents are ammonium chloride, gluconic acid, thiourea, fluorides such as ammonium bifluoride, sodium fluoride and potassium titanium fluoride, and various surfactants and the like such as alkyl aryl sodium sulfonate. Such reagents generally are useful in minor amounts, for example, about 0.01 to about 10 grams per liter of plating bath, to obtain their known benefits.
The ternary alloys may be co-deposited electrolytically upon a wide variety of substrates, including metals such as steel, brass and zinc, as well as ceramics and plastics, in accordance with techniques well known in the art for coating such substrates.
The following examples of aqueous plating bath formulations and conditions of electrodeposition are intended as further illustration of the invention but are not necessarily limited of the scope of the invention except as set forth in the claims. All parts and percentages in these examples as well as in the foregoing specification are by weight unless otherwise indicated. In each example the ternary alloy deposited has an approximate composition: tin, 40- 90%; cobalt, 10- 50%; third metal, 1- 28%.
______________________________________                                    
EXAMPLE 1                                                                 
______________________________________                                    
Composition of aqueous bath                                               
Cobalt Chloride       20-400 g./l.                                        
Stannous Chloride     10-100 g./l.                                        
Ammonium Bifluoride   20-400 g./l.                                        
Hydrochloric Acid (37%)                                                   
                      40-150 mls./l.                                      
Ammonium Hydroxide (28%)                                                  
                      10-50 mls./l.                                       
Zinc Chloride         15-175 g./l.                                        
  Plating Conditions                                                      
  Temperature of bath 60-80° C.                                    
  Current density     10-30 A/ft..sup.2                                   
  pH of bath           1-3                                                
______________________________________                                    
EXAMPLE 2                                                                 
______________________________________                                    
Composition of aqueous bath                                               
Cobalt Chloride       20-400 g./l.                                        
Stannous Chloride     10-100 g./l.                                        
Ammonium Bifluoride   20-400 g./l.                                        
Hydrochloric Acid (37%)                                                   
                      40-150 mls./l.                                      
Ammonium Hydroxide (28%)                                                  
                      10-50 mls./l.                                       
Indium Chloride        5-35 g./l.                                         
  Plating Conditions                                                      
  Temperature         60-80° C.                                    
  Current density     10-30 A/ft..sup.2                                   
  pH of bath           1-3                                                
______________________________________                                    
EXAMPLE 3                                                                 
______________________________________                                    
Composition of aqueous bath                                               
Cobalt Chloride       20-400 g./l.                                        
Stannous Chloride     10-100 g./l.                                        
Ammonium Bifluoride   20-400 g./l.                                        
Hydrochloric Acid (37%)                                                   
                      40-150 mls./l.                                      
Ammonium Hydroxide (28%)                                                  
                      10-50 mls./l.                                       
Chromium Chloride      5-55 g./l.                                         
  Plating Conditions                                                      
  Temperature         60-80°  C.                                   
  Current density     10-30 A/ft..sup.2                                   
  pH of bath           1-3                                                
______________________________________                                    
EXAMPLE 4                                                                 
______________________________________                                    
Composition of aqueous bath                                               
Cobalt Chloride       100-300 g./l.                                       
Stannous Fluoborate (50%)                                                 
                       25-75 mls./1.                                      
Fluoboric Acid         75-225 g./l.                                       
Ammonium Hydroxide (28%)                                                  
                       25-150 mls./l.                                     
Zinc Chloride          10-g./l.                                           
  Plating Conditions                                                      
  Temperature         50-85° C.                                    
  Current density      5-45 A/ft..sup.2                                   
  pH                   1-3                                                
______________________________________                                    
EXAMPLE 5                                                                 
______________________________________                                    
Composition of aqueous bath                                               
Cobalt Chloride       100-300 g./l.                                       
Stannous Fluoborate (50%)                                                 
                       25-75 mls./l.                                      
Fluoboric Acid         75-225 g./l.                                       
Ammonium Hydroxide (28%)                                                  
                       25-150 mls./l.                                     
Chromium Chloride      10-75 g./l.                                        
  Plating Conditions                                                      
  Temperature         50-85° C.                                    
  Current density      5-45 A/ft..sup.2                                   
  pH                   1-3                                                
______________________________________                                    
EXAMPLE 6                                                                 
______________________________________                                    
Composition of aqueous bath                                               
Cobalt Chloride       100-300 g./l.                                       
Stannous Fluoborate (50%)                                                 
                       25-75 mls./l.                                      
Fluoboric Acid         75-225 g./l.                                       
Ammonium Hydroxide (28%)                                                  
                       25-150 mls./l.                                     
Indium Chloride        5-35 g./l.                                         
  Plating Conditions                                                      
  Temperature         50-85° C.                                    
  Current density       5-45 A/ft..sup.2                                  
  pH                   1-3                                                
______________________________________                                    

Claims (2)

What is claimed is:
1. A bright, tarnish resistant and color stable ternary alloy consisting essentially of about
40- 90 wt. % tin
10- 50 wt. % cobalt
1- 28 wt. % third metal
wherein said third metal is antimony.Iadd., zinc .Iaddend.or a metal of Periodic Group .[.IIB,.]. IIIA or VIB. .[.2. A ternary alloy as in claim 1 wherein said third metal is zinc, cadmium, indium, or
chromium..]. 3. A ternary alloy as in claim 1 wherein said third metal is zinc, indium or chromium.
US05/614,349 1974-01-07 1975-09-17 Ternary alloys Expired - Lifetime USRE29239E (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US05/614,349 USRE29239E (en) 1974-01-07 1975-09-17 Ternary alloys

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US431025A US3881919A (en) 1974-01-07 1974-01-07 Ternary alloys
US05/614,349 USRE29239E (en) 1974-01-07 1975-09-17 Ternary alloys

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US431025A Reissue US3881919A (en) 1974-01-07 1974-01-07 Ternary alloys

Publications (1)

Publication Number Publication Date
USRE29239E true USRE29239E (en) 1977-05-31

Family

ID=27028857

Family Applications (1)

Application Number Title Priority Date Filing Date
US05/614,349 Expired - Lifetime USRE29239E (en) 1974-01-07 1975-09-17 Ternary alloys

Country Status (1)

Country Link
US (1) USRE29239E (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4331518A (en) 1981-01-09 1982-05-25 Vulcan Materials Company Bismuth composition, method of electroplating a tin-bismuth alloy and electroplating bath therefor
US5333550A (en) * 1993-07-06 1994-08-02 Teledyne Mccormick Selph Tin alloy sheath material for explosive-pyrotechnic linear products
US5501154A (en) * 1993-07-06 1996-03-26 Teledyne Industries, Inc. Substantially lead-free tin alloy sheath material for explosive-pyrotechnic linear products

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2853382A (en) * 1957-07-24 1958-09-23 John V Klochkov Alloy compositions
US3856513A (en) * 1972-12-26 1974-12-24 Allied Chem Novel amorphous metals and amorphous metal articles
US3871836A (en) * 1972-12-20 1975-03-18 Allied Chem Cutting blades made of or coated with an amorphous metal

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2853382A (en) * 1957-07-24 1958-09-23 John V Klochkov Alloy compositions
US3871836A (en) * 1972-12-20 1975-03-18 Allied Chem Cutting blades made of or coated with an amorphous metal
US3856513A (en) * 1972-12-26 1974-12-24 Allied Chem Novel amorphous metals and amorphous metal articles

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4331518A (en) 1981-01-09 1982-05-25 Vulcan Materials Company Bismuth composition, method of electroplating a tin-bismuth alloy and electroplating bath therefor
US5333550A (en) * 1993-07-06 1994-08-02 Teledyne Mccormick Selph Tin alloy sheath material for explosive-pyrotechnic linear products
US5501154A (en) * 1993-07-06 1996-03-26 Teledyne Industries, Inc. Substantially lead-free tin alloy sheath material for explosive-pyrotechnic linear products

Similar Documents

Publication Publication Date Title
US3966564A (en) Method of electrodepositing an alloy of tin, cobalt and a third metal and electrolyte therefor
US3940319A (en) Electrodeposition of bright tin-nickel alloy
US2926124A (en) Tin nickel alloy plating process and composition
US3881919A (en) Ternary alloys
JPS608315B2 (en) Tin/gold electroplating aqueous bath
JPS60169588A (en) Acidic zinc plating bath, acidic zinc alloy plating bath and process
US4297177A (en) Method and composition for electrodepositing palladium/nickel alloys
USRE29239E (en) Ternary alloys
US3892638A (en) Electrolyte and method for electrodepositing rhodium-ruthenium alloys
US4014761A (en) Bright acid zinc plating
US2181773A (en) Brass plating
US4772362A (en) Zinc alloy electrolyte and process
JPS6141999B2 (en)
US4048023A (en) Electrodeposition of gold-palladium alloys
US5176813A (en) Protection of lead-containing anodes during chromium electroplating
CA1062513A (en) Ternary alloys
US4297179A (en) Palladium electroplating bath and process
CA1078776A (en) Baths for electrodeposition of ternary alloys
NO137760B (en) PROCEDURES FOR THE PREPARATION OF A GALVANIC PRECIPITATION OF AN IRON ALLOY CONTAINING NICKEL OR NICKEL AND COBOLT, AND WATER PLATING SOLUTION FOR PERFORMING THE PROCEDURE.
US4634505A (en) Process and bath for the electrolytic deposition of gold-tin alloy coatings
US4411744A (en) Bath and process for high speed nickel electroplating
US3984291A (en) Electrodeposition of tin-lead alloys and compositions therefor
AU638512B2 (en) Protection of lead-containing anodes during chromium electroplating
US3374156A (en) Electro-depositing stainless steel coatings on metal surfaces
US3890210A (en) Method and electrolyte for electroplating rhodium-rhenium alloys