US2110792A - Process for electrodeposition of silver and products obtained therefrom - Google Patents
Process for electrodeposition of silver and products obtained therefrom Download PDFInfo
- Publication number
- 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
- Authority
- US
- United States
- Prior art keywords
- silver
- deposit
- cyanide
- thio
- electrodeposition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910052709 silver Inorganic materials 0.000 title description 27
- 239000004332 silver Substances 0.000 title description 27
- 238000000034 method Methods 0.000 title description 12
- 238000004070 electrodeposition Methods 0.000 title description 7
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 26
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 24
- LFAGQMCIGQNPJG-UHFFFAOYSA-N silver cyanide Chemical compound [Ag+].N#[C-] LFAGQMCIGQNPJG-UHFFFAOYSA-N 0.000 description 18
- 229940098221 silver cyanide Drugs 0.000 description 17
- 238000007747 plating Methods 0.000 description 15
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 14
- 239000002932 luster Substances 0.000 description 9
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 8
- 239000003513 alkali Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000002659 electrodeposit Substances 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 238000005498 polishing Methods 0.000 description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
- IPCRBOOJBPETMF-UHFFFAOYSA-N N-acetylthiourea Chemical compound CC(=O)NC(N)=S IPCRBOOJBPETMF-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical class NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 3
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- 229940093956 potassium carbonate Drugs 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 235000011181 potassium carbonates Nutrition 0.000 description 3
- 150000003567 thiocyanates Chemical class 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 2
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 2
- 229940116357 potassium thiocyanate Drugs 0.000 description 2
- -1 silver alloys Chemical class 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 2
- 150000003585 thioureas Chemical class 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004133 Sodium thiosulphate Substances 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 229940065287 selenium compound Drugs 0.000 description 1
- 150000003343 selenium compounds Chemical class 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 150000003560 thiocarbamic acids Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/46—Electroplating: Baths therefor from solutions of silver
-
- 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
- Y10S428/927—Decorative informative
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/934—Electrical process
- Y10S428/935—Electroplating
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—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
- Y10T428/12993—Surface 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.
Landscapes
- 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.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70396A US2110792A (en) | 1936-03-23 | 1936-03-23 | Process for electrodeposition of silver and products obtained therefrom |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70396A US2110792A (en) | 1936-03-23 | 1936-03-23 | Process for electrodeposition of silver and products obtained therefrom |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2110792A true US2110792A (en) | 1938-03-08 |
Family
ID=22095043
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US70396A Expired - Lifetime US2110792A (en) | 1936-03-23 | 1936-03-23 | Process for electrodeposition of silver and products obtained therefrom |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2110792A (en) |
Cited By (8)
| 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 |
-
1936
- 1936-03-23 US US70396A patent/US2110792A/en not_active Expired - Lifetime
Cited By (8)
| 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 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3769182A (en) | Bath and method for electrodepositing tin and/or lead | |
| US2436316A (en) | Bright alloy plating | |
| US2176668A (en) | Silver plating process | |
| US4234396A (en) | Chromium plating | |
| US3661730A (en) | Process for the formation of a super-bright solder coating | |
| US2735809A (en) | Mirror bright silver plating | |
| US3730853A (en) | Electroplating bath for depositing tin-lead alloy plates | |
| US2110792A (en) | Process for electrodeposition of silver and products obtained therefrom | |
| US4554219A (en) | Synergistic brightener combination for amorphous nickel phosphorus electroplatings | |
| US2658032A (en) | Electrodeposition of bright copper-tin alloy | |
| FR2557892A1 (en) | ACID SOLUTION FOR ELECTROLYTIC COATING OF ZINC AND ZINC ALLOY, AND METHOD FOR USING THE SAME | |
| US4605474A (en) | Alkaline cyanide bath for electrolytic deposition of copper-tin-alloy coatings | |
| US2732336A (en) | Electroplating composition for copper | |
| US3149057A (en) | Acid gold plating | |
| US3691027A (en) | Method of producing corrosion resistant chromium plated articles | |
| US2511395A (en) | Process for the electrodeposition of tin alloys | |
| US2125229A (en) | Electrodeposition of metals | |
| US2555375A (en) | Process of plating bright silver alloy | |
| US2862861A (en) | Copper cyanide plating process and solution therefor | |
| US2876178A (en) | Electrodepositing copper | |
| US3522155A (en) | Method of electrodepositing a tinbismuth alloy and compositions therefor | |
| US3580821A (en) | Bright silver electroplating | |
| US2751341A (en) | Electrodeposition of lead and lead alloys | |
| US3617452A (en) | Gold plating | |
| US4297179A (en) | Palladium electroplating bath and process |