US2110792A - Process for electrodeposition of silver and products obtained therefrom - Google Patents

Process for electrodeposition of silver and products obtained therefrom Download PDF

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US2110792A
US2110792A US70396A US7039636A US2110792A US 2110792 A US2110792 A US 2110792A US 70396 A US70396 A US 70396A US 7039636 A US7039636 A US 7039636A US 2110792 A US2110792 A US 2110792A
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silver
deposit
cyanide
thio
electrodeposition
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US70396A
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Egeberg Birger
Promisel Nathan
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International Silver Co
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International Silver Co
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    • 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
    • C25D3/46Electroplating: Baths therefor from solutions of silver
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9265Special properties
    • Y10S428/927Decorative informative
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/934Electrical process
    • Y10S428/935Electroplating
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12861Group VIII or IB metal-base component
    • Y10T428/12896Ag-base component
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12993Surface feature [e.g., rough, mirror]

Definitions

  • This invention relates to electrodeposits of silver and similar metals, including silver alloys, and to a, process 01" electrodeposition thereof:
  • the standard bath is composed of silver cyanide, anexcess of alkali cyanide over'that required todissolve the silver cyanide, alkali carbonate and. water.
  • an electric current of suitable characteristics is passed, the current passing into the solution through silver anodes of high purity, through the solution depositing silver on the articles to be plated which constitute the cathodes, and then out of the bath through'the cathodes.
  • the principal object of the. present invention accordingly is to provide a deposit or coating of silver that has as deposited an inherent, smooth, uniform, highly lustrous character even for the thickest commercial coatings.
  • Another object of the invention is to provide a process for the production of such a deposit or coating which will do away with at least some of the objections to carbon-disulphide and other brlghteners heretofore employed.
  • Certain of the compounds which constitute brighteners in accordance with the invention may be represented by the chemical formula x as where X is NH: or substituted NH: in which one or both hydrogen atoms are replaced by the substituent radicals methyl, ethyl, acetyl or N112, and where Y is NI-h, SNHQR, SNHMR): or SM in which R is the methyl or ethyl radical, and M an alkali metal.
  • the proportions of the brightener may vary from minute amounts for example 0.01 g/l to large quantities for example 100 g/l, depending upon the particular substance and the attendant conditions.
  • a silver deposit is secured superior in luster to any such deposits or coatings heretofore produced.
  • the deposits and plating bath also have to a much less extent the disadvantages enumerated above for carbon-disulphide and in some cases these disadvantages are completely eliminated.
  • Example 1 An electrolytic bath employing thio-urea as a brightener is as follows:
  • lustrous silver deposits may be obtained at a current density of 6 amperes per sq. ft. of cathode surface.
  • Example 2 Another example employing acetyl-thio-urea NH-C OCH! is as follows:
  • the electrolytic bath contains:
  • Example 3 Another example employing mono-methyl- ,ammonium salt of mono-methyl-thiol-thionocarbamic acid At a temperature of 80 F. lustrous silver deposits may be obtained at a current density of 6 amperes per sq. ft. of cathode surface.
  • Example 4 An example employing potassium thiocyanate CNSK is as follows:
  • the electrolytic bath contains: Silver cyanide grams 25 Potassium cyaniden do 45 Potassium carbonate do 20 Potassium thiocyanate do 20 Water liter 1 At a temperature of 80 F. lustrous silver deposits may be obtained at a-current density of 6 amperes per sq. ft. of cathode surface.
  • Example 5 An example employing urea NH: is as follows:
  • the electrolytic bath contains:
  • thio-cyanates, thio-carbamates, thio-ureas and urea described above may be prepared by known methods.
  • Certain of the above mentioned brighteners for example, thiourea and urea, are substantially non-volatile, and the deposits resulting from their use are substantially uniform and approach mirror brightness. Being of such high luster they require little or no polishing. With these substances the current density, temperature, agitation and solution composition may be varied to the same extent as these factors vary in ordinary plating practice and it is not necessary, as in the case of carbon-disulphide, to adopt any extreme precautions to produce the deposit. These materials may be consumed during electrolysis to some extent but in any case their replenishment is easy to take care of. No more frequent additions of these materials are necessary than required for the silver cyanide, alkali cyanide or carbonate of the bath. The range of concentration of the materials as notedmay be varied and accordingly the control of the concentration is not difllcult.
  • a process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing a thio-urea as a brightener to form a bright deposit of silver therefrom.
  • a process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing acetyl-thio-urea as a brightener to form a bright deposit of silver therefrom.
  • a process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing a mono-methyl-ammonium salt of mono-methyl-thiol-thiono-carbamic acid as a brightener to form a bright deposit of silver therefrom.
  • a process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing a thio-semi-carbazide as a brightener to form a bright deposit of silver therefrom.
  • a metal base having a surface electrodeposit of silver characterized by high and substantially uniform luster as deposited and requiring thereby a minimum of polishing, said deposit being obtained from a silver cyanide plating bath containing a mono-methyl-ammonium salt of monomethyl-thiol-thiono-carbamic acid as a brightener.
  • a process for the electrodeposition of silver which comprises: electrolyzing a silver cyanide plating bath containing a brightener having the chemical formula where X is a member of the group consisting of NH: and substituted NH: in which the substituents for hydrogen are methyl, ethyl, acetyl or NH:, and where Y is a member of the group consisting of NH:, SNHaR, SNH2(R)2 and SM in which R is methyl or ethyl and M an alkali' where'X is a member of the group consisting of NH: and substituted NH: in which the substituents for hydrogen are methyl, ethyl, acetyl or NH:, and where Y is a member of the group consisting of NH:, SNHaR, SNH:(R): and SM in which R is methyl or ethyl, and M an alkali metal, said substituting groups being such as not to make the resulting compound
  • a metal base having a surface electrodeposit of silver characterized by high and substantially uniform luster as deposited and requiring thereby a minimum of polishing, said deposit being obtained from a silver cyanide plating bath containing thio-semi-carbazide as a brightener.

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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)

Description

Patented Mar. 8, 1938 PATENT, OFFICE p flraocnss roa ;auto'raonrzrosrrrou or i .snmaa AND THEREFROM PRODUCTS OBTAINED mm: Egebcrg and Nathan PromiscLJMerlden,
Com, assignors to International Silver Company, Meriden, Conn, a corporation of New Jersey No Drawing.
Application March 23, 1936, Serial N0. 70,396 i i 10 Olaima. (01. 204-16) This invention relates to electrodeposits of silver and similar metals, including silver alloys, and to a, process 01" electrodeposition thereof:
In the present accepted commercial practice of 5' electroplating silver coatings, the standard bath is composed of silver cyanide, anexcess of alkali cyanide over'that required todissolve the silver cyanide, alkali carbonate and. water. Through this solution an electric current of suitable characteristics is passed, the current passing into the solution through silver anodes of high purity, through the solution depositing silver on the articles to be plated which constitute the cathodes, and then out of the bath through'the cathodes. Under proper conditions of current, temperature, agitation and maintenance of a proper concentration. of they electrolyte, acrystalline, nonlustrous matte white deposit. .of silverimay be secured at-the cathode. 'Bufiing or burnishing, 20 sometimes both, of such a deposit is,therefore, necessaryto secure a bright surface. This bufling and burnishing is costly andwasteful and accordinglyhighly undesirable. It is, therefore, common practice to add to the above plating 25 bath a brightener which will give the deposit, as it is made in the bath, a slightly. lustrous appearance. For producing such a deposit, carbon-disulphide has been proposed and used commercially for nearly 100 years. A number of other 3 brighteners have been also proposed such as gums, sugars, sodium thiosulphate, tellurium and selenium compounds and others. The only one in extensive commercial use, however, is carbondisulphide and the other proposed brighteners 35 have never come into extensive commercial use. Carbon-disulphide although known and used for nearlya century has certain well-recognized disadvantages which may be briefly summarized as follows: Even under the best conditions the 40 deposit is not, satisfactory and. frequently lacks any appreciable luster. It is, moreover, usually not uniform over the entire plated surface unless extreme precautions are taken. The deposit is sensitive to plating conditions in that the quan- 5 tityoi carbon-disulphide present, the current density, temperature, agitation and solution composition must all be adjusted and maintained within closely balanced limits. The carbondisulphide limits are far narrower than required by the other components of the solution, namely,
the silver cyanide, alkali cyanide, carbonate and water. One diillculty in maintaining the proper quantity of carbon-disulphide present is that it is volatile at room temperature and this, in addition to its disappearance due to electrolysis, '5'
causes it to vanish rapidly from the solution. making frequent additions necessary. Consequently, the precautions which have to be taken in dealing with this material are numerous. It is a fact that where many individual plating solutions including carbon-disulphide are used. even with the best of control there are always certain solutions which perform unsatisiactorily andfrom which dull deposits are obtained, and
even in solutions giving semi-lustrous deposits, there are always variations in appearance from vat to vat and even from section to section on the same article. In general. in employing this material, trial-and-error methods 01' plating have to be employed to secure the semi-lustrous de- 2 posits.- Departure from conditions so determined may result in deposits the luster of which is actually inferior to those obtained from solutions containing no carbon-disulphide whatsoever. In addition. we have found with carbon-disulphide that only a relatively thin plating of semi-lustro'us character can be obtained, in that, with increasing thickness orme deposit, the deposit changes from the semi-lustrous appearance to,
eventually, a dull-white appearance.
The principal object of the. present invention accordingly is to provide a deposit or coating of silver that has as deposited an inherent, smooth, uniform, highly lustrous character even for the thickest commercial coatings. Another object of the invention is to provide a process for the production of such a deposit or coating which will do away with at least some of the objections to carbon-disulphide and other brlghteners heretofore employed. In accordance with our invention we have found that highly lustrous deposits or platings of silver may be produced under proper conditions of ingredient proportions and other characteristics of the solution and current employed, by electrolyzing a cyanide silver bath containing silver cyanide, alkali cyanide, and alkali carbonate in the presence'of a brightener comprisingany of several groups of chemical compounds, including derivatives of thio-carbamic acids, particularly so thio-carbamates, thio-ureas, thio-cyanates, urea or alkali metal cyanates, these substances, particularly the thio-cyanates, being such as not to produce ammonia since we find that the production of ammonia in our electrolytic baths interferes with the proper luster.
Certain of the compounds which constitute brighteners in accordance with the invention may be represented by the chemical formula x as where X is NH: or substituted NH: in which one or both hydrogen atoms are replaced by the substituent radicals methyl, ethyl, acetyl or N112, and where Y is NI-h, SNHQR, SNHMR): or SM in which R is the methyl or ethyl radical, and M an alkali metal.
The proportions of the brightener may vary from minute amounts for example 0.01 g/l to large quantities for example 100 g/l, depending upon the particular substance and the attendant conditions. By proper adjustment of the plating conditions a silver deposit is secured superior in luster to any such deposits or coatings heretofore produced. The deposits and plating bath also have to a much less extent the disadvantages enumerated above for carbon-disulphide and in some cases these disadvantages are completely eliminated. I
The following are preferred examples of baths and methods for carrying out the invention as we now prefer to practice it. It is understood that the invention is not to be considered as limited to these examples except as indicated in the appended claims.
Example 1 An electrolytic bath employing thio-urea as a brightener is as follows:
At a temperature of F. lustrous silver deposits may be obtained at a current density of 6 amperes per sq. ft. of cathode surface.
Example 2 Another example employing acetyl-thio-urea NH-C OCH! is as follows:
The electrolytic bath contains:
Silver cyanide grams.. 25 Potassium cyanide do 45 Potassium carbonate do 20 Acetyl-thiourea do 45 Water i liter 1 At a temperature 0580" F. lustrous silver deposits may be, obtained at a current density of 6 amperes per sq. ft. of cathode surface.
Example 3 Another example employing mono-methyl- ,ammonium salt of mono-methyl-thiol-thionocarbamic acid At a temperature of 80 F. lustrous silver deposits may be obtained at a current density of 6 amperes per sq. ft. of cathode surface.
Example 4 An example employing potassium thiocyanate CNSK is as follows:
The electrolytic bath contains: Silver cyanide grams 25 Potassium cyaniden do 45 Potassium carbonate do 20 Potassium thiocyanate do 20 Water liter 1 At a temperature of 80 F. lustrous silver deposits may be obtained at a-current density of 6 amperes per sq. ft. of cathode surface.
Example 5 An example employing urea NH: is as follows:
The electrolytic bath contains:
Silver cyanide grams 25 Potassium cyanide do.. 45 Potassiumcarbonate do 20 'Urea do 45 Water -..liter 1 At a temperature of 80 F. lustrous'silver deposits may be obtained at a current density of 6 amperes per sq. ft. of cathode surface.
Other substances which may be satisfactorily employed coming under the formula mentioned include- Thio-semi-carbazide NHCaHs B-NHrCt I Mono-methyl-ammonium salt or potassium salt of thioletbionocarbamic acid turnout The baths may be used immediately upon being prepared but we ordinarily prefer to allow them to age for two or three days before use.
The thio-cyanates, thio-carbamates, thio-ureas and urea described above may be prepared by known methods.
Certain of the above mentioned brighteners, for example, thiourea and urea, are substantially non-volatile, and the deposits resulting from their use are substantially uniform and approach mirror brightness. Being of such high luster they require little or no polishing. With these substances the current density, temperature, agitation and solution composition may be varied to the same extent as these factors vary in ordinary plating practice and it is not necessary, as in the case of carbon-disulphide, to adopt any extreme precautions to produce the deposit. These materials may be consumed during electrolysis to some extent but in any case their replenishment is easy to take care of. No more frequent additions of these materials are necessary than required for the silver cyanide, alkali cyanide or carbonate of the bath. The range of concentration of the materials as notedmay be varied and accordingly the control of the concentration is not difllcult.
We claim:
1. A process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing a thio-urea as a brightener to form a bright deposit of silver therefrom.-
2. A process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing acetyl-thio-urea as a brightener to form a bright deposit of silver therefrom.
3. A process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing a mono-methyl-ammonium salt of mono-methyl-thiol-thiono-carbamic acid as a brightener to form a bright deposit of silver therefrom.
4. A process for the electrodeposition of silver which comprises electrolyzing a silver cyanide bath containing a thio-semi-carbazide as a brightener to form a bright deposit of silver therefrom.
5. As a new article of manufacture. a metal base having a surface electrodeposit of silver characterized by high and substantially uniform luster as deposited and requiring thereby a minimum of polishing, said deposit being obtained from a silver cyanide plating bath containing thiourea as a brightener.
6. As a new article of manufacture, a metal base having a surface electrodeposit of silver characterized by high and substantially uniform luster as deposited and requiring thereby a minimum of polishing, said deposit being obtained from a silver cyanide plating bath containing acetyl-thio-urea as a brightener.
7.As a new article of manufacture, a metal base having a surface electrodeposit of silver characterized by high and substantially uniform luster as deposited and requiring thereby a minimum of polishing, said deposit being obtained from a silver cyanide plating bath containing a mono-methyl-ammonium salt of monomethyl-thiol-thiono-carbamic acid as a brightener.
8. A process for the electrodeposition of silver which comprises: electrolyzing a silver cyanide plating bath containing a brightener having the chemical formula where X is a member of the group consisting of NH: and substituted NH: in which the substituents for hydrogen are methyl, ethyl, acetyl or NH:, and where Y is a member of the group consisting of NH:, SNHaR, SNH2(R)2 and SM in which R is methyl or ethyl and M an alkali' where'X is a member of the group consisting of NH: and substituted NH: in which the substituents for hydrogen are methyl, ethyl, acetyl or NH:, and where Y is a member of the group consisting of NH:, SNHaR, SNH:(R): and SM in which R is methyl or ethyl, and M an alkali metal, said substituting groups being such as not to make the resulting compound insoluble in the cyanide plating bath and not forming a substance substantially alkaline in water or producing ammonia during the process of electrolysis, 10. As a new article of manufacture, a metal base having a surface electrodeposit of silver characterized by high and substantially uniform luster as deposited and requiring thereby a minimum of polishing, said deposit being obtained from a silver cyanide plating bath containing thio-semi-carbazide as a brightener.
BIRGER EGEBERGQ NATHAN PROMISEL.
US70396A 1936-03-23 1936-03-23 Process for electrodeposition of silver and products obtained therefrom Expired - Lifetime US2110792A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2429970A (en) * 1944-01-11 1947-10-28 Du Pont Silver plating
US2440672A (en) * 1942-10-24 1948-05-04 Gen Motors Corp Electroplating bath for silver
US2555375A (en) * 1948-11-13 1951-06-05 Battelle Development Corp Process of plating bright silver alloy
US2666738A (en) * 1950-09-15 1954-01-19 Hanson Van Winkle Munning Co Bright silver plating
US2771380A (en) * 1954-08-02 1956-11-20 Burgess Battery Co Method of plating copper particles with silver
US2799633A (en) * 1956-05-29 1957-07-16 Sel Rex Precious Metals Inc Method and electrolyte for producing bright gold
US3165456A (en) * 1960-11-21 1965-01-12 Minnesota Mining & Mfg Developer
US3362895A (en) * 1964-11-23 1968-01-09 Sel Rex Corp Electrodeposition of silver

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2440672A (en) * 1942-10-24 1948-05-04 Gen Motors Corp Electroplating bath for silver
US2429970A (en) * 1944-01-11 1947-10-28 Du Pont Silver plating
US2555375A (en) * 1948-11-13 1951-06-05 Battelle Development Corp Process of plating bright silver alloy
US2666738A (en) * 1950-09-15 1954-01-19 Hanson Van Winkle Munning Co Bright silver plating
US2771380A (en) * 1954-08-02 1956-11-20 Burgess Battery Co Method of plating copper particles with silver
US2799633A (en) * 1956-05-29 1957-07-16 Sel Rex Precious Metals Inc Method and electrolyte for producing bright gold
US3165456A (en) * 1960-11-21 1965-01-12 Minnesota Mining & Mfg Developer
US3362895A (en) * 1964-11-23 1968-01-09 Sel Rex Corp Electrodeposition of silver

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