Classifications

• • C—CHEMISTRY; METALLURGY
  • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
  • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
  • C25D3/00—Electroplating: Baths therefor
  • C25D3/02—Electroplating: Baths therefor from solutions
  • C25D3/46—Electroplating: Baths therefor from solutions of silver

Definitions

• This invention relates to the electrodeposition of silver from aqueous electrolytes in which the silver is present mainly as a complex cyanide, and more particularly to electrolytes for bright silver plating.
• the silver deposit formed is not mirror bright, and needs at least some mechanical polishing for adequate appearance.
• the cathode current density range in which fully bright deposits can be obtained is rather narrow so that a coating of uniform appearance cannot be produced on deeply recessed objects.
• the brightener is a complex organic compound which cannot be purified at practical cost.
• the commercial product therefore contains by-products which are at best inert and at worst reduce the brightening effect.
• the amount and nature of the by-products cannot be held constant from one batch to the next so that difficulties in dosing the brightener are experienced by the plater.
• the primary object of the invention is the provision of uniformly bright silver electrodeposits directly from a cyanide type plating bath on complexly shaped objects in a convenient and simple manner.
• R may be lower alkoxy or NHR
• R" is hydrogen, lower alkyl, phenyl, halophenyl, lower alkyl phenyl, or lower alkoxy phenyl.
• R is hydrogen or lower alkyl
• X is oxygen, sulfur, or the imino group (NH), but R is difierent from amino when X is sulfur.
• the compounds of the invention are equally effective when added to a plating bath in the form of the free acid or in the form of a soluble salt such as the silver salt, an alkali metal salt, or more specifically a salt of sodium or potassium, or as a salt of ammonium or its alkyl deriva- 3,580,821 Patented May 25, 1971 "ice tives.
• the brightening effect is due solely to the anionic component.
• Example 1 50 ml. of a l-molar solution of potassium hydroxide in ethanol (0.05 mole KOH) were heated with 0.05 mole methylthiosemicarbazide. At 40 C., a solution of 0.07 mole carbon disulfide in 0.5 mole ethanol was added, and the resulting mixture was vigorously refluxed for ten minutes. Upon cooling to 40 C., a crystalline precipitate of Compound C was formed. It was recovered by suction filtration and purified by dissolving the crystals in a little water and adding ethanol to induce crystallization.
• the compounds of the invention are added to otherwise conventional cyanide silver plating solutions in amounts that may vary between 3 milligrams and 3 grams per liter, preferably between 10 milligrams and 1 gram per liter, depending on the brightener employed and operating conditions. They dissolve readily. Optimum amounts, which usually are not critical, are readily determined in Hull cell tests.
• the plating solutions employed typically contain 20 to 50 g./l. silver in the form of a complex cyanide, 50- 200 g./l. free cyanide as the potassium salt or an equivalent amount of the sodium salt, and -100 g./l.
• K 00 They may further contain known organic and inorganic secondary brightening agents such as thiocarbonates (sodium trithiocarbonate or ethylene trithiocarbonate), xanthogenates (potassium xanthogenate), thiocarbamates (ammonium thiocarbamate), organic selenium compounds (piazselenole), also inorganic selenium compounds (potassium selenocyanate or sodium selenite), and compounds of metals of Group Va of the Periodic System such as antimony compounds.
• thiocarbonates sodium trithiocarbonate or ethylene trithiocarbonate
• xanthogenates potassium xanthogenate
• thiocarbamates ammonium thiocarbamate
• organic selenium compounds piazselenole
• compounds of metals of Group Va of the Periodic System such as antimony compounds.
• Surfactants and colloids conventionally employed in cyanide type silver plating baths are fully compatible with
• the brighteners of the invention are most eifective at temperatures between about and 35 0., best results being achieved most readily at about C. Good brightness is found in cathode areas in which the actual current density is between 0.05 to 3 amps./dm. full brightness being usually available from 0.1 to 2. amps/dmfl.
• EXAMPLE 3 A conventional silver plating solution containing 30 g./l. sodium silver dicyanide and 100 g./l. free sodium cyanide produced dull electrodeposits over the entire operating range of a standard Hull cell. When 20 mg./l. Compound B were dissolved in the bath, a fully bright deposit of silver was obtained from approximately 0.1 to approximately 4 amps./dm.
• a silver plating electrolyte was prepared to the following composition:
• EXAMPLE 6 A silver plating electrolyte containing 35 g./l. silver in the form of potassium silver dicyanide g./l. free potassium cyanide 30 g./l. potassium carbonate yielded mat deposits at all current densities. Fully bright deposits over the entire range of usual cathode current densities (0.1-4 amps./dm. and partly to less than 0.1 amp./dm. were achieved by the addition of any one of the brighteners E,J,K,L,M,N,O, or P in an amount of 150 mg./l. and in the presence of 1 g./l. of polypotassium sulfonaphthyl methylene or other wetting agents.
• the electrolytes of the invention have been found to be particularly useful in the electrodeposition of thin silver coatings on hollowware over a layer of bright nickel. No mechanical polishing was found to be necessary.
• cups, dishes and similar articles made from copper or copper alloys were carefully cleaned and electrolytically degreased. They were then electroplated with bright nickel, rinsed well, pickled, flash silvered for 5 seconds at about 5 amps./dm. and transferred without rinsing to a silver plating bath of'the invention in which they were coated at an average current density of 1 amp./dm. with cathode agitation.
• Mirror bright silver deposits free from haze were obtained at coating thickness of as small as 1 micrometer.
• An aqueous alkaline silver plating bath containing silver in the form of a complex cyanide, free cyanide, and an amount of an acid of the formula or of a dissolved salt of said acid, in said formula R being lower alkoxy or NHR"; R" being hydrogen, lower alkyl, phenyl, halophenyl, lower alkyl phenyl, or lower alkoxy phenyl; R being hydrogen or lower alkyl; and X being oxygen, sulfur, or imino; R being different from NH when X is sulfur; said amount being between 3 milligrams and 3 grams per liter of said bath.
• a method of electrodepositing bright silver on a conductive object which comprises making said object the cathode in the bath defined in claim 1.
• a method of preparing a bright silver plating solution which comprises adding 3 milligrams to 3 grams per liter of an acid of the formula or of a water soluble salt of said acid to an aqueous plating bath containing, per liter, 20 to 50 grams silver as a complex cyanide, 50-200 grams free alkali metal cyanide, and 0 to 100 grams alkali metal carbonate, in said formula R being lower alkoxy'or NHR"; R" being hydrogen, lower alkyl, phenyl, halophenyl, lower alkyl phenyl, or lower alkoxy phenyl; R being hydrogen or lower alkyl; and X being oxygen, sulfur, or imino; R being different from NH when X is sulfur.

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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 And Plating Baths Therefor (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
• Chemically Coating (AREA)
• Adhesives Or Adhesive Processes (AREA)

Applications Claiming Priority (1)

Publications (1)

Family

ID=5700952

Family Applications (1)

Country Status (11)

Cited By (6)

Families Citing this family (1)

• 1969
  • 1969-06-11 ES ES368263A patent/ES368263A1/es not_active Expired
  • 1969-06-12 CH CH899169A patent/CH525285A/de not_active IP Right Cessation
  • 1969-06-17 GB GB30590/69A patent/GB1272839A/en not_active Expired
  • 1969-06-23 JP JP44049611A patent/JPS495818B1/ja active Pending
  • 1969-06-24 US US838040A patent/US3580821A/en not_active Expired - Lifetime
  • 1969-06-24 SE SE08951/69A patent/SE354676B/xx unknown
  • 1969-06-24 AT AT599669A patent/AT286055B/de not_active IP Right Cessation
  • 1969-06-26 FR FR6921468A patent/FR2016105A1/fr not_active Withdrawn
  • 1969-06-26 NO NO2658/69A patent/NO122048B/no unknown
  • 1969-06-27 BE BE735288D patent/BE735288A/xx not_active IP Right Cessation
  • 1969-06-27 NL NL6909961A patent/NL6909961A/xx unknown

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