USRE20306E - Method for gold plating - Google Patents

Method for gold plating Download PDF

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Publication number
USRE20306E
USRE20306E US20306DE USRE20306E US RE20306 E USRE20306 E US RE20306E US 20306D E US20306D E US 20306DE US RE20306 E USRE20306 E US RE20306E
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gold
article
plating
bath
hydrochloric acid
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/34Pretreatment of metallic surfaces to be electroplated
    • C25D5/36Pretreatment of metallic surfaces to be electroplated of iron or steel
    • 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
    • C25D3/48Electroplating: Baths therefor from solutions of gold

Definitions

  • the principal object of the invention is to provide a gold plating method which will produce a plate tenaciously adhering to the base metal.
  • alloys for certain. purposes may contain in the'neighborhood of 18% chromium, about 8% nickel, 2 molybdenum, and the balance iron and incidental impurities.
  • chromium steel alloys are ordinarily considered to be rendered corrosion resistant or stainless by virtue of the formation, on the surface of the alloy, of a non-metallic oxide film.
  • This non-metallic film forms on the surface of the alloy very quickly upon exposure to the atmosphere, and, apparently, it is this film which has heretofore made it very dimcult, if not impossible, to secure an adherent gold plate.
  • .chlorlc acid is not essential.
  • the articles are first formed from the chromium alloy steel and, after thorough cleaning,- as by an al-) kaline wash, I proceed as follows:
  • the action of the bath may be accelerated by electrolysis and may contain from about 25% to about 50% hydrochloric acid.
  • this treatment which apparently destroys the oxide film
  • I preferably rinse the articles in a dilute acid wash.
  • this wash may contain from about 10% to about hydrochloric acid.
  • the articles are transferred very quickly to an electroplating bath, and it 'is to be noted that the rapidity of transfer is useful when following these steps for the reason that the relatively low strength of the hydrochloric acid wash is only sufficient to prevent the reformation of the oxide film for a relatively short period of time.
  • the hydrochloric acid rinse or wash is relatively low in concentration in order to avoid carrying large quantities of hydrochloric acid into the plating bath' and thus building up the acid content of the plating bath beyond the preferable figure.
  • the bath may be composed of the following ingredients in the approximate proportions indicated:
  • the plating bath has at least a 10 slight acid reaction is important in preventing reformation of the oxide filmbefore some metal has been deposited.-
  • the success of this gold plating operation is apparently due to the presence in the platingbath throwing powerof the plating solution.
  • the quantity of free hydrocyanic acid present is not critical.
  • the bath should contain sufilcient to give a slight acid reaction to litmus, and the quantity may be carried up at least to an amount equivalent to that which will combine with the gold present. Having initially prepared a bath with the proportions of ingredients listed above,I prefer to renew the supply of hydrocyanic acid either by adding an additional supply of sodium cyanide at periodic intervals or in some other equivalent manner.
  • the brilliance of the deposit may be observed.
  • additional cyanide should be added.
  • the gold plating solution may also be prepared from other gold salts.
  • gold chloride may be employed, although in this instance also it is necessary to use hydrochloric acid and cyanide so as to ensure the presence of free hydrocyan ic acid.
  • the articles may be removed from the bath'and the film of oxide, of course, will not reform.
  • the articles may be used in this condition, although I prefer to add a second gold plate in one of the common types of alkaline baths, such as a cyanide bath.
  • a suitable alkaline bath may contain about ounce sodiumgold cyanide and about 2 ounces sodium cyanide per gallon at of water.
  • the articles are first treated with acid to remove the non-metallic or oxide film, and thereafter the plating is accomplished by electro- 00 deposition in a novel type of electroplating bath and in a manner which prevents reformation of any film until a direct bondingof the plate to the metal is secured. Where a direct bonding is obtained, of course, the oxide film cannot reform.
  • the foreg'oing procedure is effective for the purposes here involved, including the prevention of tarnishing or corrosion, may not be fully understood, I have found in actual practice that a highly adherent gold plate is deposited in the presence of free hydrocyanic acid.
  • the final product is one which is not subject to tarnishing or corrosion. It might seem that since the protective film-is removed and replaced by a plate which is well known to be porous, the final product would be subject to difficulties similar to those encountered with prior gold plated articles where the base metal was not of a type which produces an oxide film. I have found, however, that articles plated in accordance with my improved process are not subject to corrosion and the reason for this may be that the oxide film reforms in the pores of the plating. I have also noticed that where wear occurs in an article plated in accordance with this invention so as to expose the alloy, the oxide film immediately reforms on the exposed surface.
  • the method of gold plating a so-called stainless steel article which includes the steps of dissolving the oxide film normally present on the article, and electrodepositing gold from an acid gold plating solution containing free hydrocyanic acid.
  • the method of gold plating a so'-called stainless steel article on the surface of which a nonmetallic oxide film normally forms which includes the steps of subjecting the article to a concentrated hydrochloric acid solution, washing the article in a dilute hydrochloric acid solution, and electrolytically depositing a gold plate on the article from a plating bath containing. approximately the following proportions of ingredients: to each gallon of water, 1 pint of concentrated hydrochloric acid, 8 ounces sodium cyanide. and ounce sodium gold cyanide.
  • the method of gold plating a so-called stainless steel article on the surface of which a nonmetallic oxide film normally forms f which includes the steps of subjecting the article to a concentrated hydrochloric acid solution, washing the article in a dilute hydrochloric acid solution, and electrolytically depositing a gold plate on the article from a plating bath containing water, hydrochloric acid, sodium cyanide, and sodium gold cyanide.
  • the method of gold plating a so-called stainless steel article on the surface of which a nonmetallic oxide film normally forms which method includes the steps of subjecting the article to hydrochloric acid, and electrolytically depositing a goldplate on the article from a plating bath containing a gold salt, hydrochloric acid and sodium cyanide.
  • the method of gold plating a so-calied stainless steel article on the surface of which a nonmetallic oxide film normally forms which method includes the steps of subjecting the article to'hydrochloric acid, and electrolytically depositing a gold plate on the article from a plating bath containing hydrochloric acid, sodium cyanide, and sodium gold cyanide.
  • the method of gold plating a so-called stainless steel article on the surface of which a nonmetallic film normally forms includes the steps of subjecting the article to an acid solution capable of dissolving said film, rinsing the article to remove the excess acid, and electrolytically depositing gold thereon from a plating solution containing free hydrocyanic acid.
  • the method of gold plating a so-called stain- I I 20,300 leeeateelortlcleonthesurfaceofwhlchanonmetnllic fllm normally forms, which-method includeathestepeofsuhiectingtheerticletoehath capable of dissolving said film, rinsing the article. end electrolytically depositing gold thereon from a. gold plating solution containing tree hydrocyenic ecid.

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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

Reie'sued Mar. 23, 1937 UNITED STATES PATENT OFFICE 20,306 METHOD Fon GOLD m'rmc.
Hiram S. Lukens, Philadelphia, Pa., assignor to 0. Howard Hunt Pen Company, Camden, N. 1.,
a corporation of New Jersey 1936, Serial No. 94,469
8 Claims. (Cl. 204-12) This invention relates to a method for gold plating and is especially concerned with the plating of a chromium alloy steel. The application, furthermore, is a continuation of my copending apzplication Serial No. 707,502, filed January 20th,
The principal object of the invention is to provide a gold plating method which will produce a plate tenaciously adhering to the base metal. In
this connection, it should be understood that heretofore it has been very diflicult, if not impossible, to produce a satisfactory gold plating on a chrome alloy steel, such as the so-called corrosion resistant steel alloys which are usually chiefly comprised of chromium, nickel and iron with the addition of smaller amounts of other elements which are added for the purpose of still further increasing the corrosion resistance or other properties of the product. As a specific example of the composition, it might be noted that alloys for certain. purposes, for example for the production of pen points, may contain in the'neighborhood of 18% chromium, about 8% nickel, 2 molybdenum, and the balance iron and incidental impurities.
Before discussing the method steps themselves, it might be noted that chromium steel alloys are ordinarily considered to be rendered corrosion resistant or stainless by virtue of the formation, on the surface of the alloy, of a non-metallic oxide film. This non-metallic film forms on the surface of the alloy very quickly upon exposure to the atmosphere, and, apparently, it is this film which has heretofore made it very dimcult, if not impossible, to secure an adherent gold plate.
In accordance with the method steps disclosed in my copending application above referred to, I apparently secure direct bonding of the plate 40 to the base metal, without the interposition of an oxide film. Thus, even though the oxide film has been eliminated and replaced, so to speak, by the gold plate, the resulting article is one which is not subjectto tarnishing or corrosion. It will 45 be seen, therefore, that even though the very thing which is usually considered to provide the protection for a metal of the type in question has been removed, the articles are not subject to the difllculties heretofore encountered. In this way, 5 I am enabled to produce an article (such, for instance, as a pen point) having the appearance and some of the characteristics of gold, and this article under conditions of normal use will not corrode or tarnish and is, of course, much less ex- 55 pensive than a solid gold article.
.chlorlc acid is not essential.
In carrying out the method as described inmy copending application above referred to, the articles are first formed from the chromium alloy steel and, after thorough cleaning,- as by an al-) kaline wash, I proceed as follows:
I subject the articles to the action of a bath capable of removing the oxide film such as a hydrochloric acid bath in suflicient concentration to accomplish the result. The action of the bath may be accelerated by electrolysis and may contain from about 25% to about 50% hydrochloric acid.
Subsequent to this treatment, which apparently destroys the oxide film, I preferably rinse the articles in a dilute acid wash. By way of example, this wash may contain from about 10% to about hydrochloric acid. Subsequent to the washing, the articles are transferred very quickly to an electroplating bath, and it 'is to be noted that the rapidity of transfer is useful when following these steps for the reason that the relatively low strength of the hydrochloric acid wash is only sufficient to prevent the reformation of the oxide film for a relatively short period of time.
Further with reference to the foregoing point, the hydrochloric acid rinse or wash is relatively low in concentration in order to avoid carrying large quantities of hydrochloric acid into the plating bath' and thus building up the acid content of the plating bath beyond the preferable figure.
With reference to the above, it should be noted that the washing of the articles in dilute hydro- In fact, I may even eliminate this wash entirely or substitute a water wash, especially where it is convenient to transfer the articles very rapidly from the strong hydrochloric bath to the water wash and from thereto the plating bath. In accordance with my understanding of the action which takes place, the important factor when treating the articles in this way to remove the oxide film is to carry on the several steps in such manner as to provide for the electrodeposition of some metal before the oxide film has had time or opportunity to reform to any appreciable extent.
As to'the plating itself, I first employ a plating bath of the acid type produced, forexample, in accordance withthe disclosure of my copending application above referred to. That is, the bath may be composed of the following ingredients in the approximate proportions indicated:
Concentrated hydrochloric acid pt 1 f Sodium cyanide 0z 8 Sodium gold cyanide oz 4 Water gal 1 A bath made up in this way is slightly acid or, in other words, has a relatively low hydrogen ion concentration, and I find that this is preferable, although, if desired, the acidity may be reduced 6 until the bath approaches neutrality, or increased until the bath becomes almost a concentrated hydrochloric acid bath containing a little gold and cyanide.
The fact that the plating bath has at least a 10 slight acid reaction is important in preventing reformation of the oxide filmbefore some metal has been deposited.- In addition, I have found that the success of this gold plating operation is apparently due to the presence in the platingbath throwing powerof the plating solution. I have shown by tests that the quantity of free hydrocyanic acid presentis not critical. Preferably, the bath should contain sufilcient to give a slight acid reaction to litmus, and the quantity may be carried up at least to an amount equivalent to that which will combine with the gold present. Having initially prepared a bath with the proportions of ingredients listed above,,I prefer to renew the supply of hydrocyanic acid either by adding an additional supply of sodium cyanide at periodic intervals or in some other equivalent manner. As a guide in determining when additional sodium cyanide is necessary, the brilliance of the deposit may be observed. When the deposit noticeably loses its brilliance, additional cyanide should be added. Ordinarily, in an average plating bath of fifteen gallons capacity, it is sufficient to add a few ounces of sodium cyanide for each .500 gross of pens plated.
40 It will be understood that the gold plating solution may also be prepared from other gold salts. For example, gold chloride may be employed, although in this instance also it is necessary to use hydrochloric acid and cyanide so as to ensure the presence of free hydrocyan ic acid.
After this initial gold plating step, the articles may be removed from the bath'and the film of oxide, of course, will not reform. The articles may be used in this condition, although I prefer to add a second gold plate in one of the common types of alkaline baths, such as a cyanide bath.
By way 'of example, a suitable alkaline bath may contain about ounce sodiumgold cyanide and about 2 ounces sodium cyanide per gallon at of water.
In summarizing the foregoing steps, it will be seen that the articles are first treated with acid to remove the non-metallic or oxide film, and thereafter the plating is accomplished by electro- 00 deposition in a novel type of electroplating bath and in a manner which prevents reformation of any film until a direct bondingof the plate to the metal is secured. Where a direct bonding is obtained, of course, the oxide film cannot reform. 05 While all of the reasons why theforeg'oing procedure is effective for the purposes here involved, including the prevention of tarnishing or corrosion, may not be fully understood, I have found in actual practice that a highly adherent gold plate is deposited in the presence of free hydrocyanic acid. Even though the non-metallic corrosion proof film has been removed and replaced by a gold plate, thefinal product is one which is not subject to tarnishing or corrosion. It might seem that since the protective film-is removed and replaced by a plate which is well known to be porous, the final product would be subject to difficulties similar to those encountered with prior gold plated articles where the base metal was not of a type which produces an oxide film. I have found, however, that articles plated in accordance with my improved process are not subject to corrosion and the reason for this may be that the oxide film reforms in the pores of the plating. I have also noticed that where wear occurs in an article plated in accordance with this invention so as to expose the alloy, the oxide film immediately reforms on the exposed surface.
In any event, my improved article, as a matter of fact, is not subject to noticeable corrosion under normal conditions of service.
The numerous objects of the invention will be apparent to those skilled in the art although it might be mentioned that durability of the plating and resistance to tarnishing and corrosion are the most outstanding advantages.
I claim:
1. The method of gold plating a so-called stainless steel article which includes the steps of dissolving the oxide film normally present on the article, and electrodepositing gold from an acid gold plating solution containing free hydrocyanic acid.-
2. The method of gold plating a so'-called stainless steel article on the surface of which a nonmetallic oxide film normally forms which includes the steps of subjecting the article to a concentrated hydrochloric acid solution, washing the article in a dilute hydrochloric acid solution, and electrolytically depositing a gold plate on the article from a plating bath containing. approximately the following proportions of ingredients: to each gallon of water, 1 pint of concentrated hydrochloric acid, 8 ounces sodium cyanide. and ounce sodium gold cyanide.
3. The method of gold plating a so-called stainless steel article on the surface of which a nonmetallic oxide film normally forms fwhich includes the steps of subjecting the article to a concentrated hydrochloric acid solution, washing the article in a dilute hydrochloric acid solution, and electrolytically depositing a gold plate on the article from a plating bath containing water, hydrochloric acid, sodium cyanide, and sodium gold cyanide.
4. The method of gold plating a so-called stainless steel article on the surface of which a nonmetallic oxide film normally forms, which method includes the steps of subjecting the article to hydrochloric acid, and electrolytically depositing a goldplate on the article from a plating bath containing a gold salt, hydrochloric acid and sodium cyanide.
5. The method of gold plating a so-calied stainless steel article on the surface of which a nonmetallic oxide film normally forms, which method includes the steps of subjecting the article to'hydrochloric acid, and electrolytically depositing a gold plate on the article from a plating bath containing hydrochloric acid, sodium cyanide, and sodium gold cyanide.
6. The method of gold plating a so-called stainless steel article on the surface of which a nonmetallic film normally forms, which method includes the steps of subjecting the article to an acid solution capable of dissolving said film, rinsing the article to remove the excess acid, and electrolytically depositing gold thereon from a plating solution containing free hydrocyanic acid.
7. The method of gold plating a so-called stain- I I 20,300 leeeateelortlcleonthesurfaceofwhlchanonmetnllic fllm normally forms, which-method includeathestepeofsuhiectingtheerticletoehath capable of dissolving said film, rinsing the article. end electrolytically depositing gold thereon from a. gold plating solution containing tree hydrocyenic ecid.
8. The method of gold plating a. so-called stainless steel article which includes the steps of dissolving the oxide fllm normally present on the article and electro-depositing gold from an'acid gold plating solution containing hydrochloric acid 5 end sodium cyanide; v HIRAM 8. LUKENS.
US20306D 1935-05-13 Method for gold plating Expired USRE20306E (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2491126A (en) * 1944-08-02 1949-12-13 Emi Ltd Method of electroplating on chromium or chromium-iron alloys
US2812299A (en) * 1949-05-05 1957-11-05 Birle & Co K G Electrolytic deposition of gold and gold alloys
US3502548A (en) * 1966-10-24 1970-03-24 Ernest H Lyons Jr Method of electroplating gold on chromium

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2472786A (en) * 1943-08-21 1949-06-14 Sylvania Electric Prod Method of pickling metal contact surfaces
US4046644A (en) * 1976-05-24 1977-09-06 American Standard Inc. Process for forming a gold-chromium alloy from an electrodeposited gold-chromium surface

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2491126A (en) * 1944-08-02 1949-12-13 Emi Ltd Method of electroplating on chromium or chromium-iron alloys
US2812299A (en) * 1949-05-05 1957-11-05 Birle & Co K G Electrolytic deposition of gold and gold alloys
US3502548A (en) * 1966-10-24 1970-03-24 Ernest H Lyons Jr Method of electroplating gold on chromium

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