US34470A - Improvement in process of electroplating iron and other metals with copper - Google Patents
Improvement in process of electroplating iron and other metals with copper Download PDFInfo
- Publication number
- US34470A US34470A US34470DA US34470A US 34470 A US34470 A US 34470A US 34470D A US34470D A US 34470DA US 34470 A US34470 A US 34470A
- Authority
- US
- United States
- Prior art keywords
- copper
- iron
- metals
- improvement
- cyanide
- 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
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title description 38
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title description 33
- 229910052802 copper Inorganic materials 0.000 title description 31
- 239000010949 copper Substances 0.000 title description 31
- 229910052742 iron Inorganic materials 0.000 title description 19
- 238000000034 method Methods 0.000 title description 13
- 239000002184 metal Substances 0.000 title description 8
- 229910052751 metal Inorganic materials 0.000 title description 8
- 150000002739 metals Chemical class 0.000 title description 7
- 238000009713 electroplating Methods 0.000 title description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 6
- 238000000151 deposition Methods 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 229910021653 sulphate ion Inorganic materials 0.000 description 3
- 235000011149 sulphuric acid Nutrition 0.000 description 3
- 239000001117 sulphuric acid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 230000002939 deleterious effect Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000007096 poisonous effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- LEKPFOXEZRZPGW-UHFFFAOYSA-N copper;dicyanide Chemical compound [Cu+2].N#[C-].N#[C-] LEKPFOXEZRZPGW-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
Images
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
- C25D3/38—Electroplating: Baths therefor from solutions of copper
- C25D3/40—Electroplating: Baths therefor from solutions of copper from cyanide baths, e.g. with Cu+
Definitions
- Wi'naww [72067242 04 1- %/a %M% EWMM v UNITED STATES PATENT OFFICE.
- A is a vessel of glass or of any other suitable material which will not suli'erdecomposition when'brought in contact with the agents employed and will permit the contained solution. to be warmed.
- This vessel I partially fill with a strong solution of cyanide of potassa, two pounds or there about being dissolved in one gallon of water, the temperature of the solution being raised to about 150 Fahrenheit.
- Into this bath I injectoduce the two poles-of a galvanic battery of sufficient strength to do the work.
- Bunsen battery as representedin the drawing, in which B is a glass vessel containing sulphuric acid and water; 0, the zinc to which isattached a copper wire, b.
- B is a glass vessel containing sulphuric acid and water;
- the zinc to which isattached a copper wire, b Within the zinc cylinder 0 is placed the porous cup D, which is partially filled with nitric acid,- and into which is introduced a block, E, of carbon.
- f to which is attached a large plate of copper, g, (the anode,) and to the wire b is attached the iron cathode'lt.
- the copper plate g and the iron plate h are both inserted into the bath in the vessel A, when, by the action of the galvanic current, the copper of the plate 9 is dissolved off. This action is permitted to go on until the solution in the vessel A is sufficiently saturated with copper, which will be indicated bya good deposit of copper on the iron plate h.
- the ar ticle to be plated is now introduced into the bath A in contact with the pole b of the battery, when the copper is deposited upon it, the
- the strength of the current required to commeuce the deposition of the copper upon the iron will depend upon the amount of surface to be coated. In general four Bunsen cups of one pint capacity are required to commence the deposition of the copper upon a surface of one square foot of iron. After the iron is once coated with copper and the deposition becomes one of copper upon copper it is simply necessary that-the surface of zinc in the battery be about equal to the surface on which the deposit is being made. Were a less-powerful current employed at the commencement of theoperation the copper which would be deposited would not adhere to the iron.
- W This process may be employed in depositing copper upon other substances than iron, but is particularly advantageous and economical in plating iron with copper.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (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
J. E. WALGOTT. ELEOTROPLATING IRON WITH COPPER.
No. 34,470. Patented Feb. 18, 1862.
Wi'naww: [72067242 04 1- %/a %M% EWMM v UNITED STATES PATENT OFFICE.
JABEZ E. WALOOTT, OF BOSTON, MASSAOHUSETTS, AS SIGNOR TO WILLIAM HOOPER BLAOKLER, OF SAME PLACE.
IMPROVEMENT lN PROCESS OF ELECTROPLAIlNG IRON AND OTHER METALS WITH'COPPER.
Specification forming part of Letters Patent No. 34,470, dated February 18, 1862.
To all whom it may concern Be it known that I, JABEZ E. WALGOTT, of Boston, in the county of Suffolk and State of Massachusetts, hay e invented a new and Improved Process of ltlectroplatin g with Copper, of which the following is a full, clear, and exact description, reference being had to the aceompan yin g drawing, making part of this specification, in which is represented the apparatus which I employ in carrying out my invention.
Where sulphate of copper is employed for the purpose of electroplating with copper, if the metal (iron for example) be soluble in sulphuric acid .it will be corroded by the acid and the copper will not adhere to it; but even with metals that are not liable to be corroded by the acid the process is an exceedingly slow one, and in consequence very expensive.
For the purpose of plating iron with copper in order to secure the adhesion of the two metals and to prevent the corrosion of the iron, it has heretofore been necessary to employ a solution composed of a mixture of cyanide copper and cyanide of pot-assa; but this process is without any practical utility in the arts, first, on account ofits great expense secondly, on account of the poisonous fumes which are given off while it is going on, and which are very deleterious to the health of the operatives. A process, therefore, by which copper may be deposited upon and made to adhere to the surface of iron and other metals soluble in sulphuric acid without the use of sulphate or of cyanide of copper, and which shall be less expensive than where either of these substances is used, and also free from the poisonous effects before spoken of, is a great desideratuin in the arts. This desideratum is attained and the before-mentioned inconveniences, as well as the great expense heretofore incurred, are avoided by my improved process, which I will now proceed more particularly todescribe.
Iam aware that a weak solution of cyanide of potassa in water, in connection with a galvanic current, has been employed for the purpose of plating with silver and some of the other metals 3 but such process has proved en'- tirely inapplicable and unavailing for the purpose of plating iron with copper. In the course of extensive experiments I have discovered that by th'eemployment of a solution of fused cyanide of p'otassa of great 'stren gth in connection with a powerful galvanic.
current I am enabled to plate iron and other metals rapidly and economically with copper without the employment of either sulphate or cyanide of copper and without danger or ineonvenienceto the workmen.
To enable others skilled in the art to understand my improved process, I will proceed to describe the mannerinwhich I have carried it out.
In the accompanying drawing, A is a vessel of glass or of any other suitable material which will not suli'erdecomposition when'brought in contact with the agents employed and will permit the contained solution. to be warmed. This vessel I partially fill with a strong solution of cyanide of potassa, two pounds or there about being dissolved in one gallon of water, the temperature of the solution being raised to about 150 Fahrenheit. Into this bath I .introduce the two poles-of a galvanic battery of sufficient strength to do the work. As this depends in a measure on the size of the bath and of the articles to be plated, no definite rule as to the strength of thecurrent can be given-for all cases; but a very strong current being required I use a Bunsen battery, as representedin the drawing, in which B is a glass vessel containing sulphuric acid and water; 0, the zinc to which isattached a copper wire, b. Within the zinc cylinder 0 is placed the porous cup D, which is partially filled with nitric acid,- and into which is introduced a block, E, of carbon. To this block is connected another copper wire, f, to which is attached a large plate of copper, g, (the anode,) and to the wire b is attached the iron cathode'lt. The battery now being in operation, the copper plate g and the iron plate h are both inserted into the bath in the vessel A, when, by the action of the galvanic current, the copper of the plate 9 is dissolved off. This action is permitted to go on until the solution in the vessel A is sufficiently saturated with copper, which will be indicated bya good deposit of copper on the iron plate h. The ar ticle to be plated is now introduced into the bath A in contact with the pole b of the battery, when the copper is deposited upon it, the
supply of copper being" kept up in the bath by 7 being dissolved 01f from the plate g. The operation may thus be continued uninterruptedly until the article being operated upon has been plated to the required thickness with copper.
The strength of the current required to commeuce the deposition of the copper upon the iron will depend upon the amount of surface to be coated. In general four Bunsen cups of one pint capacity are required to commence the deposition of the copper upon a surface of one square foot of iron. After the iron is once coated with copper and the deposition becomes one of copper upon copper it is simply necessary that-the surface of zinc in the battery be about equal to the surface on which the deposit is being made. Were a less-powerful current employed at the commencement of theoperation the copper which would be deposited would not adhere to the iron.
The important result which I have attained consists in the fact that the copper deposited by my process adheres as firmly to the iron as in any of the previously-known processes, while the cost of theoperation is so reduced and the operation is so divested of any deleterious effects upon the workmen that it can be madeof practical value in the arts.
W This process may be employed in depositing copper upon other substances than iron, but is particularly advantageous and economical in plating iron with copper.
What I claim as my invention, and desire to secure by Letters Patent, is-
The above-described process of electroplating with copper, substantially as described.
J. E. W'ALGOTT.
Witnesses: v
'lnos, R. ROAGH, EDMUND MASSON.
Publications (1)
Publication Number | Publication Date |
---|---|
US34470A true US34470A (en) | 1862-02-18 |
Family
ID=2104055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US34470D Expired - Lifetime US34470A (en) | Improvement in process of electroplating iron and other metals with copper |
Country Status (1)
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US (1) | US34470A (en) |
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0
- US US34470D patent/US34470A/en not_active Expired - Lifetime
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